Title of Invention

OXYGEN PRODUCTION PROCESS USING THREE-STAGE PRESSURE SWING ADSORPTION PLANTS

Abstract A process for producing oxygen by using of three-stage pressure swing adsorption plants, wherein the process is used to separate nitrogen and oxygen from a feed air stream, the product can be oxygen or nitrogen or both of them. The process utilizes three-stage pressure swing adsorption plants which are serially connected. In the first stage, carbon dioxide, water and part of nitrogen are removed and nitrogen is concentrated. In the second stage, nitrogen is further separated from the effluent intermediate gas from the adsorption step in the adsorption towers of the first stage and oxygen is concentrated to the desired concentration. In the third stage, nitrogen and argon are further separated from the effluent oxygen-enriched mixture gas from the adsorption step in the adsorption towers of the second stage and the concentration of oxygen is raised to 95V% or more. In the first stage, the adsorption towers go through the steps in turn in a cycle: Adsorption(A), Purge(P'), evacuation(VC), countercurrent pressure equalization rising of the second stage gas(2ER), purge gas pressurization(R'), final pressurization(FR); In the second stage, the adsorption towers go through the steps in turn in a cycle: Adsorption(A), countercurrent pressure equalization falling(BD'), final pressurization(FR); In the third stage, the adsorption towers go through the steps in turn in a cycle: Adsorption(A), Oxygen product purge(P'), Oxygen product depressurization(D), Purge gas pressurization(R').
Full Text

BACKGROUND OF THE INVENTION
1. Field of the invention
The present invention relates to a oxygen production process using three-stage pressure swing
adsorption plants.
2. Description of the Related Art
At present, patent literatures and documents in relation to a method of making pure oxygen from
air with three-stage pressure-swing adsorption technique have not been published at home and
abroad. All of methods of making pure (or enriched) oxygen from air known in the art adopted
the two-stage pressure-swing adsorption device. For example, CN1252322A, US4190424,
US4595083 and US5395427, etc.. In the art, the concentration of oxygen was higher in the
adsorption tower before performing desorption-blowdown step. The investment and the
electricity consumption of the whole oxygen-making device were very high because the recovery
of oxygen was low.
SUMMARY OF THE INVENTION
The target of the present invention is to supply a method of making oxygen with three-stage
pressure-swing adsorption device. This method can overcome the technical problems of prior art
mentioned above. Comparing with prior art, this method can reduce investment and electricity
consumption greatly and increase oxygen recovery of the whole device.
The present invention adopts the three-stage pressure-swing adsorption device to separate
oxygen and nitrogen from air. The production can be pure oxygen or pure nitrogen or both of
them. The method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the
adsorption tower in the adsorption step of the first stage and increase the concentration of oxygen
up to the desired level, and the third stage pressure-swing adsorption device is used to further

remove the nitrogen and argon in oxygen-enriched gas mixture which is discharged from the
adsorption tower in the adsorption step of the second stage and increase the concentration of
oxygen up to above 95V%. The adsorption tower of the first stage sequentially undergoes the
following steps in one circulation period: adsorption A, purge P', evacuation VC, the second
stage gas backward equalization repressurization 2ER, purge gas repressurization R', final
repressurization FR. The adsorption tower of the second stage sequentially undergoes the
following steps in one circulation period: adsorption A, backward equalization depressurization
BD', final repressurization FR. The adsorption tower of the third stage sequentially undergoes
the following steps in one circulation period: adsorption A, oxygen product purge P', oxygen
product depressurization D, and purge gas repressurization R'.
The adsorption tower of the second stage adds the cocurrent equalization depressurization ED
step after the adsorption A step, and adds the backward repressurization ER step after the
backward equalization depressurization BD' step in the meantime; the gas mixture of the
repressurization ER step comes from the depressurization ED step;
and/or
the adsorption tower of the third stage adds the cocurrent equalization depressurization ED step
after the adsorption A step, and adds the backward repressurization ER step after the purge gas
repressurization R' step in the meantime; the gas mixture of the repressurization ER step comes
from the depressurization ED step.
The adsorption tower of the first stage adds the two-end equalization depressurization 2ED' step
after the adsorption A step, and adds the two-end equalization repressurization 2ER' step after
the second stage gas backward equalization repressurization 2ER step in the meantime; the gas
mixture of the two-end equalization repressurization 2ER' step comes from the equalization
depressurization 2ED' step.
The adsorption tower of the third stage adds evacuation VC step after the oxygen product
depressurization D step.
The adsorption tower of the first stage adds backward depressurization BD step after the purge P'
step.
The gas mixture discharged from the backward equalization depressurization BD' step in the
adsorption tower of the second stage enters into the buffer vessel V until pressure balance; in the
meantime, the adsorption tower of the first stage is connected with the buffer vessel V, while
proceeding the second stage gas backward equalization repressurization 2ER, until pressure

balance.
The average concentration of oxygen in outlet gas ,which comes from the adsorption tower in the
adsorption step of the first stage ,is 21 ~ 80 V % .
The average concentration of oxygen in outlet gas ,which comes from the adsorption tower in the
adsorption step of the first stage ,is 21 - 25 V % .
The pressure of adsorption step A of three-stage pressure-swing adsorption device is
0.001 ~0.6Mpa(g);
or
the pressure of adsorption step A of the first stage and the second stage pressure-swing
adsorption device is 0.001 ~ 0.05Mpa(g); the pressure of adsorption step A of the third stage
pressure-swing adsorption device is 0.1 ~ 0.6Mpa(g).
The adsorbents which are packed in the adsorption tower of the first stage are activated alumina
and molecular sieve from the bottom up; the adsorbent which is packed in the adsorption tower
of the second stage is molecular sieve only; and the adsorbent which is packed in the adsorption
tower of the third stage is oxygen adsorption equilibrium adsorbent or selective adsorbent of
oxygen by adsorption kinetics.
The frequency of the backward equalization depressurization ED' step in the adsorption tower of
the second stage and the frequency of the second stage gas backward equalization
repressurization 2ER step in the adsorption tower of the first stage are more than or equal to 1.
The frequency of the backward equalization depressurization ED' step in the adsorption tower of
the second stage and the frequency of the second stage gas backward equalization
repressurization 2ER step in the adsorption tower of the first stage are 3-7.
The present invention adopts the three-stage pressure-swing adsorption device to separate
oxygen and nitrogen from air. The production can be pure oxygen or pure nitrogen or both of
them. The method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the
adsorption tower in the adsorption step of the first stage and increase the concentration of oxygen
up to the desired level. The adsorption tower of the first stage sequentially undergoes the

following steps in one circulation period: adsorption A, two-end equalization depressurization
2ED', purge P', backward depressurization BD, the second stage gas backward equalization
repressurization 2ER , two-end equalization repressurization 2ER', purge gas repressurization
R', final repressurization FR. The adsorption tower of the second stage sequentially undergoes
the following steps in one circulation period: adsorption A, cocurrent equalization
depressurization ED, backward equalization depressurization BD', backward equalization
repressurization ER, final repressurization FR. The adsorption tower of the third stage
sequentially undergoes the following steps in one circulation period: adsorption A, oxygen
product purge P', oxygen product depressurization D, and purge gas repressurization R'.
The pressure of adsorption A step of three-stage pressure-swing adsorption device is
0.2 - 0.6Mpa(g).
The present invention adopts the three-stage pressure-swing adsorption device to separate
oxygen and nitrogen from air. The production can be pure oxygen or pure nitrogen or both of
them. The method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the
adsorption tower in the adsorption step of the first stage and increase the concentration of oxygen
up to the desired level. The adsorption tower of the first stage sequentially undergoes the
following steps in one circulation period: adsorption A, two-end equalization depressurization
2ED', evacuation VC, the second stage gas backward equalization repressurization 2ER, two-end
equalization repressurization 2ER', final repressurization FR. The adsorption tower of the second
stage sequentially undergoes the following steps in one circulation period: adsorption A,
backward equalization depressurization BD', final repressurization FR. The adsorption tower of
the third stage sequentially undergoes the following steps in one circulation period: adsorption A,
oxygen product purge P', oxygen product depressurization D, and purge gas repressurization R'.
The present invention adopts the three-stage pressure-swing adsorption device to separate
oxygen and nitrogen from air. The production can be pure oxygen or pure nitrogen or both of
them. The method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the

adsorption tower in the adsorption step of the first stage and increase the concentration of oxygen
up to the desired level, and the third stage pressure-swing adsorption device is used to further
remove the nitrogen and argon in oxygen-enriched gas mixture which is discharged from the
adsorption tower in the adsorption step of the second stage and increase the concentration of
oxygen up to above 95V%. The adsorption tower of the first stage sequentially undergoes the
following steps in one circulation period: adsorption A, purge P', evacuation VC, the second
stage gas backward equalization repressurization 2ER, purge gas repressurization R', final
repressurization FR. The adsorption tower of the second stage sequentially undergoes the
following steps in one circulation period: adsorption A, backward equalization depressurization
BD', final repressurization FR. The adsorption tower of the third stage sequentially undergoes
the following steps in one circulation period: adsorption A, cocurrent equalization
depressurization ED, oxygen product depressurization D, an□ Backward equalization
repressurization ER.
The adsorption tower of the third stage adds the evacuation VC step after the oxygen product
depressurization D step.
The present invention adopts the three-stage pressure-swing adsorption device to separate
oxygen and nitrogen from air. The production can be pure oxygen or pure nitrogen or both of
them. The method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the
adsorption tower in the adsorption step of the first stage and increase the concentration of oxygen
up to the desired level, and the third stage pressure-swing adsorption device is used to further
remove the nitrogen and argon in oxygen-enriched gas mixture which is discharged from the
adsorption tower in the adsorption step of the second stage and increase the concentration of
oxygen up to above 95V%. The adsorption tower of the first stage sequentially undergoes the
following steps in one circulation period: adsorption A, purge P', evacuation VC, the second
stage gas backward equalization repressurization 2ER, purge gas repressurization R', final
repressurization FR. The adsorption tower of the second stage sequentially undergoes the
following steps in one circulation period: adsorption A, backward equalization depressurization
BD', final repressurization FR. The adsorption tower of the third stage sequentially undergoes
the following steps in one circulation period: adsorption A, cocurrent equalization

depressurization ED, evacuation VC, an□ Backward equalization repressurization ER.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is the working procedure scheme of technology steps for the first stage pressure-swing
adsorption device of example.
Fig.2 is the working procedure scheme of technology steps for the second stage pressure-swing
adsorption device of example.
Fig.3 is the working procedure scheme of technology steps for the third stage pressure-swing
adsorption device of example.
Fig.4 is the technology flow sheet of example 1.
DETAILED DESCRIPTION OF THE INVENTION
The raw material gas of the present invention is air and its typical components are shown in the
following table:

The present invention adopts the three-stage pressure-swing adsorption technique to produce the
enriched oxygen from air. The method adopts three-stage pressure-swing adsorption device
operating in series, wherein the first stage is used to remove gaseous water and carbon dioxide as
well as partial nitrogen. The average concentration of oxygen in outlet gas of the adsorption
tower in the adsorption step is 21 ~ 80% ( V ) . The adsorbents in the adsorption tower of the
first stage are activated alumina and molecular sieve from the bottom up. The second stage is
used to further remove the nitrogen in interim gas which is discharged from the adsorption tower
in the adsorption step of the first stage and increase the concentration of oxygen up to the desired
level. The adsorbent which is packed in the adsorption tower of the second stage is molecular
sieve. The third stage is used to further remove the nitrogen and argon in gas mixture which is
discharged from the adsorption tower in the adsorption step of the second stage and increase the

concentration of oxygen up to above 99.5V%. The adsorbent in the adsorption tower of the third
stage is carbon molecular sieve or oxygen adsorption equilibrium adsorbent. The pressure of
adsorption step A of three-stage pressure-swing adsorption device is 0.001 ~ 0.6Mpa(g). Each
adsorption tower of the three-stage pressure-swing adsorption device sequentially undergoes the
following steps in one circulation period:
The first stage :
□ Adsorption A
Feed air into the inlet of the adsorption tower in adsorption step, the adsorbents in the adsorption
tower adsorb selectively water, carbon dioxide and partial nitrogen, etc. in turn from the air. The
nonadsorbed partial nitrogen and weakly adsorbed argon, etc. are discharged from the outlet and
enter into the adsorption tower in adsorption step of the second stage. The total amount of
adsorbed water, carbon dioxide and partial nitrogen etc. increases gradually with the increase of
time. Stop feeding air when the adsorbents are saturated by the components mentioned above,
and the adsorption ends here.
□ Two-end Equalization Depressurization 2ED'
After the adsorption, the concentration of oxygen in the dead-space of the adsorption tower is
relatively higher and this part of oxygen should be recovered and reused. Thus, decrease the
pressure of the gas in the adsorption tower from both ends of top and bottom. The gas of dead-
space is discharged from the two ends of the adsorption tower and enters into the corresponding
adsorption tower of the first stage that has completed the second stage gas backward equalization
repressurization 2ER step to perform the two-end repressurization 2ER' step. The frequency of
two-end equalization depressurization 2ED' can be 1 or above (for example, 1 to 3 times).
After the adsorption, it can also perform the step of cocurrent equalization depressurization or
backward equalization depressurization only.
□ Purge P'
After the two-end equalization depressurization 2ED' step, replace the remained oxygen in the
adsorption tower out by feeding the gas got from evacuation VC step of the first stage from the
bottom of the adsorption tower. The gas mixture replaced from the adsorption tower enters into
the corresponding adsorption tower of the first stage that has completed the second stage gas
backward equalization repressurization 2ER step or the two-end equalization repressurization
2ER' step to perform the purge gas repressurization R' step.

□ Backward Depressurization BD
After purge P' step, this part of gas is backward vented to the atmosphere from the bottom of the
adsorption tower or act as product.
□ Evacuation VC
After purge P' step, pull out and blow off the water, carbon dioxide and nitrogen adsorbed by the
adsorbents from the bottom of the adsorption tower with the vacuum pump. This step enable the
absorbent to obtain the regeneration.
□ The Second Stage Gas Backward Equalization Repressurization 2ER
After evacuation VC step, the gas discharged from the adsorption tower of the second stage that
has completed the adsorption or the cocurrent equalization depressurization ED step enters into
the adsorption tower of the first stage that has complete□ Evacuation VC step, and lifts the
pressure of the adsorption tower. The frequency of the second stage gas backward equalization
repressurization 2ER can be 1 or above (for example, 1 to 7 times).
□ Two-end Equalization repressurization 2ER'
After the second stage gas backward equalization repressurization 2ER step, the gas discharged
from the two-end equalization depressurization 2ED' step of the first stage enters into the
adsorption tower from the inlet end and the outlet end, and lifts the pressure of the adsorption
tower gradually. The frequency of 2ER' and 2EDD is equal. The gas of 2ER' comes from 2EDD
gas of different adsorption tower every time. The 2ER' step of the adsorption tower of the first
stage is different from the general equalization repressurization ER step. In the general ER step,
the gas enters at the outlet end of the adsorption tower. By contrast, in the 2ER' step of the
adsorption tower of the first stage, the gas enters at the inlet end and the outlet end of the
adsorption tower.
□ Purge Gas Repressurization R'
After the 2ER' step or the 2ER step, the pressure of the adsorption tower is increased by the gas
discharged from the outlet of the adsorption tower in the purge P' step of the first stage.
□ Final Repressurization FR
After the R' step, the pressure of the adsorption tower is increased from the top with the gas
discharged from the outlet of the adsorption tower in the adsorption step or with the raw material
air until the adsorption pressure.
The second stage:
□ Adsorption A

Feed the outlet gas of the adsorption tower in the adsorption step of the first stage into the
adsorption tower in the adsorption step of the second stage. The adsorbent of the adsorption
tower adsorbs selectively nitrogen. The weakly adsorbed oxygen and argon etc. are discharged
from the outlet end and enter into enriched oxygen buffer vessel or the next step. The total
amount of adsorbed nitrogen increases gradually with the increase of time. Stop feeding gas
when the adsorbent is saturated by nitrogen and the adsorption ends here. The concentration of
oxygen in the outlet gas should be controlled in the level of production required.
□ Cocurrent Equalization depressurization ED
After the adsorption, the dead-space gas in the adsorption tower is discharged from the outlet and
enters into the corresponding adsorption tower of the second stage that has completed the
backward equalization depressurization BD' step to increase the pressure. The pressure of the
two towers can be equal or not, to satisfy the requirement of the concentration of the enriched
oxygen in production. The frequency of ED can be 1 or above (for example, 1 to 3 times).
□ Backward Equalization Depressurization BD'
After adsorption or ED step, perform the second stage gas backward equalization
repressurization 2ER step directly for several times with the gas discharge□ Backward from the
bottom of the adsorption tower for the adsorption tower of the first stage that has completed VC
step. The frequency of BD' can be 1 or above (for example, 1 to 7 times).
When performing 2ER mentioned above, we can also discharge backward the gas in the
adsorption tower into a buffer vessel at first, and then transfer it into the adsorption tower that
has completed VC step in first stage to perform the 2ER step. The number of the buffer vessels
equals to the frequency of BD' step.
□ Backward Repressurization ER
After backward equalization depressurization BD' step, the gas discharged from the ED step
enters into the adsorption tower at the outlet end, and increases the pressure of the adsorption
tower.
□ Final Repressurization FR
The gas discharged from the outlet of the adsorption tower in the adsorption step is used to
increase the pressure of the adsorption tower from the top until the adsorption pressure.
The third stage :
□ Adsorption A
Feed oxygen-enriched gas mixture into the inlet of the adsorption tower in adsorption step, the

adsorbent in the adsorption tower adsorbs selectively oxygen, etc. in turn from the oxygen-
enriched gas mixture. The nonadsorbed nitrogen or argon, etc. are discharged from the outlet to
. vent to the atmosphere or serve as other use. The total amount of adsorbed oxygen etc. increases
gradually with the increase of time. Stop feeding gas when the adsorbent is saturated by oxygen
mentioned above, and the adsorption ends here.
□ Cocurrent Equalization depressurization ED
After the adsorption, the dead-space gas in the adsorption tower is discharged from the outlet and
enters into the corresponding adsorption tower of the third stage that has completed the purge gas
repressurization R' step to increase the pressure. The pressure of the two towers can be equal or
not, to satisfy the requirement of the concentration of oxygen in production. The frequency of
ED can be 1 or above (for example, 1 to 3 times).
□ Purge P'
After the cocurrent equalization depressurization ED step, replace the remained nitrogen and
argon in the adsorption tower out by feeding the compressive product oxygen from the bottom of
the adsorption tower; the product oxygen comes from the adsorption tower of the third stage that
has completed purge P' step. The gas mixture replaced from the adsorption tower enters into the
corresponding adsorption tower of the third stage that has completed the depressurization D step
or the evacuation VC step to perform the purge gas repressurization R' step.
(4) Oxygen Product Depressurization D
After the purge P' step, this part of gas is discharged from the adsorption tower. One part of the
gas acts as product, the other part of the gas is pressurized to purge the adsorbent in the
adsorption tower.
□ Evacuation VC
After the purge P' step or the cocurrent equalization depressurization ED step or the oxygen
product depressurization D step, the pure oxygen adsorbed by the adsorbent is pulled out from
the bottom of the adsorption tower with the vacuum pump and enters into the next step. This step
enable the absorbent to obtain the regeneration at the same time.
(6) Purge Gas Repressurization R'
After the oxygen product depressurization D step or the evacuation VC step, the pressure of the
adsorption tower is increased by the gas discharged from the outlet of the other adsorption tower
in the purge P' step of the third stage.
(7) Backward Equalization Repressurization ER

After the oxygen product depressurization D step or the purge gas repressurization R' step or the
evacuation VC step, the gas discharged from the cocurrent equalization depressurization ED step
enters into the adsorption tower from the outlet, and lifts the pressure of the adsorption tower.
Example 1
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product). The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).
The components of air in this example are as following:

pressure : 0.6 MPa ( G )
As shown in the Fig.4,the first stage pressure-swing adsorption device is composed of four
adsorption towers 1A ~ 1D; the adsorbents in the adsorption tower of the first stage are activated
alumina and molecular sieve in turn from the bottom up; single tower is simultaneously in an
adsorption step and the equalizing pressure step performs once in the working procedure; do the
creation of vacuum on the adsorption tower through the vacuum pipe-line G15 using the vacuum
pump P1. The second stage pressure-swing adsorption device is composed of four adsorption
towers 2A ~ 2D; the adsorbent in the adsorption tower of the second stage is molecular sieve;
single tower is simultaneously in an adsorption step and the equalizing pressure step performs
once in the working procedure. The third stage pressure-swing adsorption device is composed of
four adsorption towers 3A ~ 3D; the adsorbent in the adsorption tower of the third stage is
carbon molecular sieve or oxygen adsorption equilibrium adsorbent; single tower is

simultaneously in an adsorption step and purge-depressurization is performed in the working
procedure. This example adopts three-stage pressure-swing adsorption device mentioned above
operating in series. The first stage is used to remove the gaseous water, carbon dioxide and
partial nitrogen in the air, the second stage pressure-swing adsorption device is used to further
remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level,
and the third stage pressure-swing adsorption device is used to further remove the nitrogen and
argon in gas mixture which is discharged from the adsorption tower in the adsorption step of the
second stage and increase the concentration of oxygen up to above 99.5V%.
The air enters into the adsorption tower in adsorption step of the first stage. The adsorbents in the
adsorption tower adsorb selectively vaporous water, carbon dioxide and partial nitrogen etc. in
turn from the air. The nonadsorbed partial nitrogen, weakly adsorbed oxygen and argon etc. are
discharged from the outlet and enter into the adsorption tower in adsorption step of the second
stage. The molecular sieve in the adsorption tower of the second stage adsorbs selectively
nitrogen. The weakly adsorbed oxygen and argon etc. are discharged from the outlet and enter
i
into buffer vessel of oxygen-enriched product. The third stage pressure-swing adsorption device
is used to further remove the nitrogen and argon in gas mixture which is discharged from the
adsorption tower in the adsorption step of the second stage and increase the concentration of
oxygen up to above 99.5V%. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ;
the adsorption tower of the first stage sequentially undergoes the following steps in one
circulation period: adsorption A , purge P' ,evacuation VC , the second stage gas backward
equalization repressurization 2ER , purge gas repressurization R', final repressurization FR. The
concentration of oxygen in the outlet gas discharged from the adsorption tower in the adsorption
step of the second stage should be controlled at about 70-95% ( V ) ; the adsorption tower of
the second stage sequentially undergoes the following steps in one circulation period: adsorption
A, backward equalization depressurization BD', and Final repressurization FR. The third stage
pressure-swing adsorption device is used to increase the concentration of oxygen in the outlet gas
discharged from the adsorption tower in the adsorption step of the second stage up to 99.5V%.
The adsorption tower of the third stage sequentially undergoes the following steps in one
circulation period: adsorption A, oxygen product purge P', oxygen product depressurization D,

and purge gas repressurization R'.
Taking the adsorption tower 1A as an example and crossing reference to Fig.l and Fig.4, we
demonstrate the steps of the adsorption tower of the first stage in one circulation period in this
example:
(1) Adsorption A
By now, the adsorption tower 1A has completed FR step. The air enters into the adsorption tower
1A through the pipeline G11 by opening the sequence valves 11A, 12A. In tower 1A, the
adsorbents adsorb selectively water, carbon dioxide and partial nitrogen etc. in turn from the air.
The nonadsorbed partial nitrogen and weakly adsorbed argon, etc. are discharged from the outlet
and enter into the adsorption tower in adsorption step of the second stage. The total amount of
adsorbed water, carbon dioxide and partial nitrogen etc. increases gradually with the increase of
time. Stop feeding air when the adsorbents are saturated by the components mentioned above,
and the adsorption ends here. Close the sequence valves 11A, 12A. The concentration of nitrogen
in the outlet gas should be controlled at 70-78 %(V).
(2) Purge P'
After the adsorption step, the outlet gas from the vacuum pump enters into the adsorption tower
1C through the pipeline G16 and G14 to perform the purge gas repressurization step (abbr. R')
by opening the sequence valve's 16A, 14A and 14C. When the concentration of nitrogen in the
adsorption tower 1A meets the requirement, close 16A, 14A and 14C.
(3)Evacuation VC
After the purge P' step, open the sequence valve 15A, the adsorbed water, carbon dioxide and
nitrogen are taken out from the bottom of the adsorption tower with vacuum pump to vent to the
atmosphere or act as product, and the absorbents are regenerated at the same time.
(4)The Second Stage Gas Backward Equalization Repressurization 2ER
After the evacuation VC step, open the sequence valves 25a, 14A and KV8. The gas of the BD'
step in the adsorption tower 2a of the second stage enters into the adsorption tower 1A to
increase the pressure of the adsorption tower 1 A.
(5)Final Repressurization FR
After the 2ER step, open the sequence valves KV6 and 13A. The outlet gas from the adsorption
tower in the adsorption step enters from the top of the adsorption tower 1A to increase the
pressure of it. When the pressure of the adsorption tower 1A reaches near the adsorption

pressure, close KV6 and 13 A.
Thus, the adsorption tower 1A has completed a circulation period and can enter into the next
circulation again. The circulation steps of the adsorption tower 1B~ 1D are the same as tower
1A, but the operating time is staggered each other, see also Fig. 1 and Fig.4.
Taking the adsorption tower 2a as an example and crossing reference to Fig.2 and Fig.4, we
demonstrate the steps of the adsorption tower of the second stage in one circulation period in this
example now:
(1) Adsorption A
By now, the adsorption tower 2a has completed the FR step. The interim gas mixture enters into
the adsorption tower 2a through the pipeline G21 by opening the sequence valves 21a, 22a. In
tower 2a, the outlet gas from the adsorption tower in adsorption step of the first stage enters into
the adsorption tower in adsorption step of the second stage. The adsorbent in the adsorption
tower adsorbs selectively nitrogen. The weakly adsorbed oxygen and argon, etc. are discharged
from the outlet and enter into enriched oxygen buffer vessel or the next step. The total amount of
adsorbed nitrogen increases gradually with the increase of time. Stop feeding gas when the
adsorbent is saturated by nitrogen, and the adsorption ends here. Close 21a, 22a.
(2) Backward Equalization Depressurization BD'
After the adsorption step, open the sequence valves 25a, 14A and KV8. The gas in the adsorption
tower 2a enters into the adsorption tower 1A backward to increase the pressure of it.
(3) Final Repressurization FR
After the BD' step, open the sequence valves KV7 and 23a. The outlet gas from the adsorption
tower in the adsorption step enters from the top of the adsorption tower 2a to increase the
pressure of it. When the pressure of the adsorption tower 2a reaches near the adsorption pressure,
close KV7 and 23 a.
Thus, the adsorption tower 2a has completed a circulation period and can enter into the next
circulation again. The circulation steps of the adsorption tower 2b~ 2h are the same as 2a, but the
operating time is staggered each other, see also Fig.2 and Fig.4.
Taking the adsorption tower 3A as an example and crossing reference to Fig.3 and Fig.4, we
demonstrate the steps of the adsorption tower of the third stage in one circulation period in this
example:

(1)AdsorptionA
By now, the adsorption tower 3A has completed R' step. The oxygen-enriched gas enters into the
adsorption tower 3A through the pipeline G31 by opening the sequence valve 31 A. When the
pressure of the adsorption tower 3 A is increased to the adsorption pressure, open the sequence
valve 32A. In tower 3A, the adsorbent adsorbs selectively oxygen in turn from the oxygen-
enriched gas mixture. The nonadsorbed nitrogen or argon, etc. are discharged from the outlet to
vent to the atmosphere or serve as other use. The total amount of adsorbed oxygen increases
gradually with the increase of time. Stop feeding gas when the adsorbent is saturated by oxygen
mentioned above, and the adsorption ends here. Close the sequence valves 31 A, 32A. The
concentration of oxygen in the outlet gas should be controlled at 5-50 %(V).
(2) Purge P'
After the adsorption step, the outlet gas from the compressor enters into the adsorption tower 3C
through the pipeline G36 and G33 to perform the purge gas repressurization step (abbr. R') by
opening the sequence valves 36A, 34A and 34C. When the concentration of oxygen in the outlet
gas mixture of the adsorption tower 3A meets the requirement, close 36A, 34A and 34C.
(3) Oxygen Product Depressurization D
After the purge P' step, by opening the sequence valves 33A,36B, 34B and 34D at first, the
oxygen product is discharged from the adsorption tower and is pressurized to the adsorption
pressure to purge the adsorption tower 3B. And then the oxygen product is discharged from the
adsorption tower and enters into the next step by opening the sequence valve 35A at the end of
purging.
(4) Purge Gas Repressurization R'
After the oxygen product depressurization D step, the outlet gas discharged from the adsorption
tower 3C in the purge P' step lifts the pressure of the adsorption tower by opening the sequence
valve 34A-
Thus, the adsorption tower 3A has completed a circulation period and can enter into the next
circulation again. The circulation steps of the adsorption tower 3B~ 3D are the same as tower
3A, but the operating time is staggered each other, see also Fig.3 and Fig.4.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 2

The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product). The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5 % (V).
The components of air in this example are as following:

Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1 ,purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about

93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER, final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %( v).
Example 3
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).
The components of air in this example are as following:

Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular

sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1 ,purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER, final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, cocurrent equalization depressurization ED, oxygen product
purge P', oxygen product depressurization D, purge gas repressurization R', backward
equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 4
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~23%o ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption

tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).
The components of air in this example are as following:

Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, first backward equalization depressurization B1D',
second Backward equalization depressurization B2D', third Backward equalization
depressurization B3D', final repressurization FR. The third stage is used to further remove the

nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, cocurrent equalization depressurization ED, oxygen product
purge P', oxygen product depressurization D, purge gas repressurization R', backward
equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 5
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).
The components of air in this example are as following:

Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the

adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A
,two-end equalization depressurization2ED', purge P' ,evacuation VC , third second stage gas
backward equalization repressurization 2ER3, second second stage gas backward equalization
repressurization 2ER2, first second stage gas backward equalization repressurization 2ER1, two-
end equalization repressurization 2ER',purge gas repressurization R', final repressurization FR.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the second stage should be controlled at about 93% ( V ) ; the adsorption
tower of the second stage sequentially undergoes the following steps in one circulation period:
adsorption A, cocurrent equalization depressurization ED, first backward equalization
depressurization B1D', second Backward equalization depressurization B2D', third Backward
equalization depressurization B3D', backward equalization repressurization ER, final
repressurization FR. The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V). The adsorption tower of the
third stage sequentially undergoes the following steps in one circulation period: adsorption A,
oxygen product purge P', oxygen product depressurization D, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %( v), and the recovery of oxygen is above 99.5 %(v).
Example 6:
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 - 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).


Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A
,two-end equalization depressurization2ED', purge P' ,evacuation VC , third second stage gas
backward equalization repressurization 2ER3, second second stage gas backward equalization
repressurization 2ER2, first second stage gas backward equalization repressurization 2ER1, two-
end equalization repressurization 2ER',purge gas repressurization R', final repressurization FR.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the second stage should be controlled at about 93% ( V ) ; the adsorption
tower of the second stage sequentially undergoes the following steps in one circulation period:
adsorption A, first backward equalization depressurization B1D', second Backward equalization
depressurization B2D', third Backward equalization depressurization B3D', final repressurization
FR. The third stage is used to further remove the nitrogen and argon in gas mixture which is
discharged from the adsorption tower in the adsorption step of the second stage and increase the
concentration of oxygen up to above 99.5%(V). The adsorption tower of the third stage
sequentially undergoes the following steps in one circulation period: adsorption A, cocurrent

equalization depressurization ED, oxygen product purge P', oxygen product depressurization D,
purge gas repressurization R', backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %( v).
Example 7
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A

,two-end equalization depressurization2ED', purge P' ,evacuation VC , third second stage gas
backward equalization repressurization 2ER3, second second stage gas backward equalization
repressurization 2ER2, first second stage gas backward equalization repressurization 2ER1, two-
end equalization repressurization2ER', purge gas repressurization R', final repressurization FR.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the second stage should be controlled at about 93% ( V ) ; the adsorption
tower of the second stage sequentially undergoes the following steps in one circulation period:
adsorption A, cocurrent equalization depressurization ED, first backward equalization
depressurization B1D', second Backward equalization depressurization B2D', third Backward
equalization depressurization B3D', backward equalization repressurization ER ,final
repressurization FR. The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V). The adsorption tower of the
third stage sequentially undergoes the following steps in one circulation period: adsorption A,
cocurrent equalization depressurization ED, oxygen product purge P', oxygen product
depressurization D, purge gas repressurization R', backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 8
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 -23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).



Pressure : 0.1 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER ,final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, evacuation VC, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the

concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 9
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 -23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%>(V).

Pressure : 0.1MPa( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , second stage gas backward equalization repressurization 2ER, purge
gas repressurization R', final repressurization FR. The concentration of oxygen in the outlet gas
discharged from the adsorption tower in the adsorption step of the second stage should be

controlled at about 70-95% ( V ) ; the adsorption tower of the second stage sequentially
undergoes the following steps in one circulation period: adsorption A, backward equalization
depressurization BD' , final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, evacuation VC, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 10
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove

the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER ,fmal repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, cocurrent equalization depressurization ED, oxygen product
purge P', oxygen product depressurization D, evacuation VC, purge gas repressurization R',
backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 11
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.

oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.2 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
two-end equalization depressurization 2ED', purge P' ,evacuation VC , third second stage gas
backward equalization repressurization 2ER3, second second stage gas backward equalization
repressurization 2ER2, first second stage gas backward equalization repressurization 2ER1, two-
end equalization repressurization 2ER', purge gas repressurization R', final repressurization FR.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the second stage should be controlled at about 93% ( V ) ; the adsorption
tower of the second stage sequentially undergoes the following steps in one circulation period:
adsorption A, first backward equalization depressurization B1D', second backward equalization
depressurization B2D', third backward equalization depressurization B3D', final repressurization
FR. The third stage is used to further remove the nitrogen and argon in gas mixture which is

discharged from the adsorption tower in the adsorption step of the second stage and increase the
concentration of oxygen up to above 99.5%(V). The adsorption tower of the third stage
sequentially undergoes the following steps in one circulation period: adsorption A, cocurrent
equalization depressurization ED, oxygen product purge P', oxygen product depressurization D,
evacuation VC, purge gas repressurization R', backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 12
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.

The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
two-end equalization depressurization 2ED',backward depressurization BD, purge P' ,evacuation
VC , third second stage gas backward equalization repressurization 2ER3, second second stage
gas backward equalization repressurization 2ER2, first second stage gas backward equalization
repressurization 2ER1, two-end equalization repressurization 2ER', purge gas repressurization
R', final repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
. backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER and Final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 13
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 -23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).


Pressure : 0.5 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
repressurization ER and Final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in

one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, purge gas repressurization R'. The gas from the first backward equalization depressurization
step B1D' of the adsorption tower of the second stage is discharged into the buffer vessel V1 to
perform pressure equalization , and then the buffer vessel V1 equalizes with the adsorption
tower in the first backward equalization repressurization step 2ER1 of the first stage; the gas
from the second Backward equalization depressurization step B2D' of the adsorption tower of the
second stage is discharged into the buffer vessel V2 to perform pressure equalization , and then
the buffer vessel V2 equalizes with the adsorption tower in the second Backward equalization
repressurization step 2ER2 of the first stage; the gas from the third Backward equalization
depressurization step B3D' of the adsorption tower of the second stage is discharged into the
buffer vessel V3 to perform pressure equalization , and then the buffer vessel V3 equalizes with
the adsorption tower in the third Backward equalization repressurization step 2ER3 of the first
stage.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 14
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 -23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).


Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 - 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, first backward equalization depressurization B1D',
second Backward equalization depressurization B2D', third Backward equalization
depressurization B3D', final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, purge gas repressurization R'. The gas from the first backward equalization depressurization
step B1D' of the adsorption tower of the second stage is discharged into the buffer vessel V1 to
perform pressure equalization , and then the buffer vessel V1 equalizes with the adsorption
tower in the first backward equalization repressurization step 2ER1 of the first stage; the gas
from the second Backward equalization depressurization step B2D' of the adsorption tower of the

second stage is discharged into the buffer vessel V2 to perform pressure equalization , and then
the buffer vessel V2 equalizes with the adsorption tower in the second Backward equalization
repressurization step 2ER2 of the first stage; the gas from the third Backward equalization
depressurization step B3D' of the adsorption tower of the second stage is discharged into the
buffer vessel V3 to perform pressure equalization , and then the buffer vessel V3 equalizes with
the adsorption tower in the third Backward equalization repressurization step 2ER3 of the first
stage.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 15
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove

the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
two-end equalization depressurization2ED',purge P', backward depressurization BD, third
second stage gas backward equalization repressurization 2ER3, second second stage gas
backward equalization repressurization 2ER2, first second stage gas backward equalization
repressurization 2ER1, two-end equalization repressurization2ER',purge gas repressurization R',
final repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, cocurrent equalization depressurization ED, first
backward equalization depressurization B1D', second Backward equalization depressurization
B2D', third Backward equalization depressurization B3D', backward equalization
depressurization ER, final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, oxygen product purge P', oxygen product depressurization
D, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).
Example 16
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.

oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.1 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
two-end equalization depressurization2ED',evacuation VC , third second stage gas backward
equalization repressurization 2ER3, second second stage gas backward equalization
repressurization 2ER2, first second stage gas backward equalization repressurization 2ER1, two-
end equalization repressurization2ER',final repressurization FR. The concentration of oxygen in
the outlet gas discharged from the adsorption tower in the adsorption step of the second stage
should be controlled at about 93% ( V ) ; the adsorption tower of the second stage sequentially
undergoes the following steps in one circulation period: adsorption A, first backward
equalization depressurization B1D', second Backward equalization depressurization B2D', third
Backward equalization depressurization B3D', final repressurization FR. The third stage is used
to further remove the nitrogen and argon in gas mixture which is discharged from the adsorption

tower in the adsorption step of the second stage and increase the concentration of oxygen up to
above 99.5%(V). The adsorption tower of the third stage sequentially undergoes the following
steps in one circulation period: adsorption A, oxygen product purge P', oxygen product
depressurization D, purge gas repressurization R'.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %( v).
Example 17
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 ~ 23% ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).

Pressure : 0.3 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the

adsorption step of the first stage should be controlled at 21 - 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, first backward equalization depressurization B1D',
second Backward equalization depressurization B2D', third Backward equalization
depressurization B3D', final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, cocurrent equalization depressurization ED, oxygen product
depressurization D, backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %( v).
Example 18
The feed gas of this example is air. The concentration of oxygen in the outlet gas discharged
from the adsorption tower in the adsorption step of the first stage should be controlled at
21 - 23%o ( V ) . The concentration of oxygen in the outlet gas discharged from the adsorption
tower in the adsorption step of the second stage should be controlled at about 93% ( V ) (viz.
oxygen-enriched product).The third stage is used to further remove the nitrogen and argon in gas
mixture which is discharged from the adsorption tower in the adsorption step of the second stage
and increase the concentration of oxygen up to above 99.5%(V).



Pressure : 0.5 MPa ( G )
The adsorbents in the adsorption tower of the first stage are activated alumina and molecular
sieve in turn from the bottom up. The adsorbent in the adsorption tower of the second stage is
molecular sieve. The adsorbent in the adsorption tower of the third stage is carbon molecular
sieve or oxygen adsorption equilibrium adsorbent. This example adopts three-stage pressure-
swing adsorption device mentioned above operating in series. The first stage is used to remove
the gaseous water, carbon dioxide and partial nitrogen in the air, and the second stage is used to
further remove the nitrogen in interim gas which is discharged from the adsorption tower in the
adsorption step of the first stage and increase the concentration of oxygen up to the desired level.
The concentration of oxygen in the outlet gas discharged from the adsorption tower in the
adsorption step of the first stage should be controlled at 21 ~ 23% ( V ) ; the adsorption tower of
the first stage sequentially undergoes the following steps in one circulation period: adsorption A,
purge P' ,evacuation VC , third second stage gas backward equalization repressurization 2ER3,
second second stage gas backward equalization repressurization 2ER2, first second stage gas
backward equalization repressurization 2ER1, purge gas repressurization R', final
repressurization FR. The concentration of oxygen in the outlet gas discharged from the
adsorption tower in the adsorption step of the second stage should be controlled at about
93% ( V ) ; the adsorption tower of the second stage sequentially undergoes the following steps
in one circulation period: adsorption A, first backward equalization depressurization B1D',
second Backward equalization depressurization B2D', third Backward equalization
depressurization B3D', final repressurization FR. The third stage is used to further remove the
nitrogen and argon in gas mixture which is discharged from the adsorption tower in the
adsorption step of the second stage and increase the concentration of oxygen up to above
99.5%(V). The adsorption tower of the third stage sequentially undergoes the following steps in
one circulation period: adsorption A, cocurrent equalization depressurization ED, evacuation VC,
backward equalization repressurization ER.
The result of this example is that the concentration of oxygen is above 99.5 %( v), the
concentration of nitrogen is above 99.9 %(v), and the recovery of oxygen is above 99.5 %(v).

INDUSTRIAL APPLICATION
The present invention can be applied to a wide range of the industrial field of chemical
engineering, petrochemical processing, pharmacy, building materials, environmental protection
and so on.

We claim,
1. A method of making oxygen with three-stage pressure-swing adsorption device, wherein oxygen
and nitrogen are separated from air; the production being enriched-oxygen and nitrogen at the
same time; the method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the adsorption
tower in the adsorption step of the first stage and increase the concentration of oxygen up to the
desired level, the adsorbents in the first and second stages both adsorbing selectively nitrogen and
the third stage pressure-swing adsorption device is used to further remove the nitrogen and argon in
oxygen-enriched gas mixture which is discharged from the adsorption tower in the adsorption step
of the second stage and increase the concentration of oxygen up to above 95 volume %; the
adsorption tower of the first stage sequentially undergoes the following steps in one circulation
period: adsorption A, purge P', evacuation VC, the second stage gas backward equalization
repressurization 2ER, purge gas repressurization R', final repressurization FR; the adsorption tower
of the second stage sequentially undergoes the following steps in one circulation period: adsorption
A, backward equalization depressurization BD', final repressurization FR; the adsorption tower of
the third stage sequentially undergoes the following steps in one circulation period: adsorption A,
oxygen product purge P', oxygen product depressurization D, and purge gas repressurization R'.
2. The method of claim 1, wherein the adsorption tower of the second stage adds the cocurrent
equalization depressurization ED step after the adsorption A step, and adds the backward
equalization repressurization ER step after the backward equalization depressurization BD' step
in the meantime; the gas mixture of the repressurization ER step comes from the depressurization
ED step;
and/or
the adsorption tower of the third stage adds the cocurrent equalization depressurization ED
step after the adsorption A step, and adds the backward equalization repressurization ER step after
the purge gas repressurization R' step in the meantime; the gas mixture of the repressurization ER
step comes from the depressurization ED step.
3. The method of claim 1 or 2, wherein the adsorption tower of the first stage adds the two-end
equalization depressurization 2ED' step after the adsorption A step, and adds the two-end
equalization repressurization 2ER' step after the second stage gas backward equalization
repressurization 2ER step in the meantime; the gas mixture of the two-end equalization
repressurization 2ER' step comes from the equalization depressurization 2ED' step.
4. The method of claim 1 or 2, wherein the adsorption tower of the third stage adds evacuation VC
step after the oxygen product depressurization D step.
5. The method of claim 3, wherein the adsorption tower of the third stage adds evacuation VC step
after the oxygen product depressurization D step.

6. The method of claim 3, wherein the adsorption tower of the first stage adds backward
depressurization BD step after the purge P' step.
7. The method of claim 1 or 2, wherein the gas mixture discharged from the backward equalization
depressurization BD' step in the adsorption tower of the second stage enters into the buffer vessel V
until pressure balance; in the meantime, the adsorption tower of the first stage is connected with the
buffer vessel V, while proceeding the second stage gas backward equalization repressurization 2ER,
until pressure balance.
8. The method of claim 3, wherein the gas mixture discharged from the backward equalization
depressurization BD' step in the adsorption tower of the second stage enters into the buffer vessel V
until pressure balance; in the meantime, the adsorption tower of the first stage is connected with the
buffer vessel V, while proceeding the second stage gas backward equalization repressurization 2ER,
until pressure balance.
9. The method of claim 4, wherein the gas mixture discharged from the backward equalization
depressurization BD' step in the adsorption tower of the second stage enters into the buffer vessel V
until pressure balance; in the meantime, the adsorption tower of the first stage is connected with the
buffer vessel V, while proceeding the second stage gas backward equalization repressurization 2ER,
until pressure balance.

10. The method of claim 1 or 2, wherein the average concentration of oxygen in outlet gas, which
comes from the adsorption tower in the adsorption step of the first stage, is 21 to 80 volume %.
11. The method of claim 3, wherein the average concentration of oxygen in outlet gas, which comes
from the adsorption tower in the adsorption step of the first stage, is 21 to 80 volume %.
12. The method of claim 4, wherein the average concentration of oxygen in outlet gas, which comes
from the adsorption tower in the adsorption step of the first stage, is 21 to 80 volume %.
13. The method of claim 10, wherein the average concentration of oxygen in outlet gas, which
comes from the adsorption tower in the adsorption step of the first stage, is 21 to 25 volume %.
14. The method of claim 11, wherein the average concentration of oxygen in outlet gas, which
comes from the adsorption tower in the adsorption step of the first stage, is 21 to 25 volume %.
15. The method of claim 12, wherein the average concentration of oxygen in outlet gas, which
comes from the adsorption tower in the adsorption step of the first stage, is 21 to 25 volume %.
16. The method of claim 1 or 2, wherein the pressure of adsorption step A of three-stage
pressure-swing adsorption device is 0.001 to 0.6MPa (g);
or

the pressure of adsorption step A of the first stage and the second stage pressure-swing
adsorption device is 0.001 to 0.05MPa(g); the pressure of adsorption step A of the third stage
pressure-swing adsorption device is 0.1 to 0.6MPa(g).
17. The method of claim 3,wherein the pressure of adsorption step A of three-stage pressure-swing
adsorption device is 0.001 to 0.6MPa(g);
or
the pressure of adsorption step A of the first stage and the second stage pressure-swing
adsorption device is 0.001 to 0.05MPa(g); the pressure of adsorption step A of the third stage
pressure-swing adsorption device is 0.1 to 0.6 MPa(g).
18. The method of claim 4, wherein the pressure of adsorption step A of three-stage pressure-swing
adsorption device is 0.001 to 0.6 MPa(g);
or
the pressure of adsorption step A of the first stage and the second stage pressure-swing
adsorption device is 0.001 to 0.05MPa(g); the pressure of adsorption step A of the third stage
pressure-swing adsorption device is 0.1 to 0.6MPa(g).
19. The method of claim 1 or 2, wherein the adsorbents which are packed in the adsorption tower of
the first stage are activated alumina and molecular sieve from the bottom up; the adsorbent which is
packed in the adsorption tower of the second stage is molecular sieve only; and the adsorbent which
is packed in the adsorption tower of the third stage is oxygen adsorption equilibrium adsorbent or
selective adsorbent of oxygen by adsorption kinetics.
20. The method of claim 3, wherein the adsorbents which are packed in the adsorption tower of the
first stage are activated alumina and molecular sieve from the bottom up; the adsorbent which is
packed in the adsorption tower of the second stage is molecular sieve only; and the adsorbent which
is packed in the adsorption tower of the third stage is oxygen adsorption equilibrium adsorbent or
selective adsorbent of oxygen by adsorption kinetics.
21. The method of claim 4, wherein the adsorbents which are packed in the adsorption tower of the
first stage are activated alumina and molecular sieve from the bottom up; the adsorbent which is
packed in the adsorption tower of the second stage is molecular sieve only; and the adsorbent which
is packed in the adsorption tower of the third stage is oxygen adsorption equilibrium adsorbent or
selective adsorbent of oxygen by adsorption kinetics.
22. The method of claim 1 or 2,wherein the frequency of the backward equalization
depressurization ED' step in the adsorption tower of the second stage and the frequency of the
second stage gas backward equalization repressurization 2ER step in the adsorption tower of the
first stage are more than or equal to 1.
23. The method of claim 3,wherein the frequency of the backward equalization depressurization
ED' step in the adsorption tower of the second stage and the frequency of the second stage gas

backward equalization repressurization 2ER step in the adsorption tower of the first stage are more
than or equal to 1.
24. The method of claim 4,wherein the frequency of the backward equalization depressurization
ED' step in the adsorption tower of the second stage and the frequency of the second stage gas
backward equalization repressurization 2ER step in the adsorption tower of the first stage are more
than or equal to 1.
25. The method of claim 18,wherein the frequency of the backward equalization depressurization
ED' step in the adsorption tower of the second stage and the frequency of the second stage gas
backward equalization repressurization 2ER step in the adsorption tower of the first stage are 3 to 7.
26. The method of claim 19,wherein the frequency of the backward equalization depressurization
ED' step in the adsorption tower of the second stage and the frequency of the second stage gas
backward equalization repressurization 2ER step in the adsorption tower of the first stage are 3 to 7.
27. The method of claim 20,wherein the frequency of the backward equalization depressurization
ED' step in the adsorption tower of the second stage and the frequency of the second stage gas
backward equalization repressurization 2ER step in the adsorption tower of the first stage are 3 to 7.
28. A method of making oxygen with three-stage pressure-swing adsorption device, wherein
oxygen and nitrogen are separated from air; the production being enriched-oxygen and nitrogen at
the same time; the method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the adsorption
tower in the adsorption step of the first stage and increase the concentration of oxygen up to the
desired level, the adsorbents in the first and second stages both adsorbing selectively nitrogen and
the third stage pressure-swing adsorption device is used to further remove the nitrogen and argon in
oxygen-enriched gas mixture which is discharged from the adsorption tower in the adsorption step
of the second stage and increase the concentration of oxygen up to above 95 volume %; the
adsorption tower of the first stage sequentially undergoes the following steps in one circulation
period: adsorption A, two-end equalization depressurization 2ED', purge P', backward
depressurization BD, the second stage gas backward equalization repressurization 2ER , two-end
equalization repressurization 2ER', purge gas repressurization R', final repressurization FR; the
adsorption tower of the second stage sequentially undergoes the following steps in one circulation
period: adsorption A, cocurrent equalization depressurization ED, backward equalization
depressurization BD', backward equalization repressurization ER, final repressurization FR; the
adsorption tower of the third stage sequentially undergoes the following steps in one circulation
period: adsorption A, oxygen product purge P', oxygen product depressurization D, and purge gas
repressurization R'.
29. The method of claim 28,wherein the pressure of adsorption A step of three-stage

pressure-swing adsorption device is 0.2 to 0.6MPa(g).
30. A method of making oxygen with three-stage pressure-swing adsorption device, wherein
oxygen and nitrogen are separated from air; the production being enriched-oxygen and nitrogen at
the same time; the method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the adsorption
tower in the adsorption step of the first stage and increase the concentration of oxygen up to the
desired level, the adsorbents in the first and second stages both adsorbing selectively nitrogen and
the third stage pressure-swing adsorption device is used to further remove the nitrogen and argon in
oxygen-enriched gas mixture which is discharged from the adsorption tower in the adsorption step
of the second stage and increase the concentration of oxygen up to above 95 volume %; the
adsorption tower of the first stage sequentially undergoes the following steps in one circulation
period: adsorption A, two-end equalization depressurization 2ED', evacuation VC, the second
stage gas backward equalization repressurization 2ER, two-end equalization repressurization 2ER',
final repressurization FR; the adsorption tower of the second stage sequentially undergoes the
following steps in one circulation period: adsorption A, backward equalization depressurization
BD', final repressurization FR; the adsorption tower of the third stage sequentially undergoes the
following steps in one circulation period: adsorption A, oxygen product purge P', oxygen product
depressurization D, and purge gas repressurization R'.
31. The method of claim 30, wherein the adsorption tower of the second stage adds the cocurrent
equalization depressurization ED step after the adsorption A step, and adds the backward
repressurization ER step after the backward equalization depressurization BD' step in the
meantime; the gas mixture of the repressurization ER step comes from the depressurization ED
step.
32. The method of claim 30 or 31, wherein the adsorption tower of the first stage adds the backward
depressurization BD step after the two-end equalization depressurization 2ED' step.

33. The method of claim 30 or 31, wherein the gas mixture discharged from the backward
equalization depressurization BD' step in the adsorption tower of the second stage enters into the
buffer vessel V until pressure balance; in the meantime, the adsorption tower of the first stage is
connected with the buffer vessel V, while proceeding the second stage gas backward equalization
repressurization 2ER, until pressure balance.
34. The method of claim 30 or 31,wherein the pressure of adsorption A step of three-stage
pressure-swing adsorption device is 0.005 to 0.6MPa(g).
35. A method of making oxygen with three-stage pressure-swing adsorption device, wherein
oxygen and nitrogen are separated from air; the production being enriched-oxygen and nitrogen at
the same time; the method adopts three-stage pressure-swing adsorption device operating in series,

wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the adsorption
tower in the adsorption step of the first stage and increase the concentration of oxygen up to the
desired level, the adsorbents in the first and second stages both adsorbing selectively nitrogen and
the third stage pressure-swing adsorption device is used to further remove the nitrogen and argon in
oxygen-enriched gas mixture which is discharged from the adsorption tower in the adsorption step
of the second stage and increase the concentration of oxygen up to above 95 volume %; the
adsorption tower of the first stage sequentially undergoes the following steps in one circulation
period: adsorption A, purge P', evacuation VC, the second stage gas backward equalization
repressurization 2ER, purge gas repressurization R', final repressurization FR; the adsorption tower
of the second stage sequentially undergoes the following steps in one circulation period: adsorption
A, backward equalization depressurization BD', final repressurization FR; the adsorption tower of
the third stage sequentially undergoes the following steps in one circulation period: adsorption A,
cocurrent equalization depressurization ED, oxygen product depressurization D, an□ Backward
equalization repressurization ER.
36. The method of claim 35, wherein the adsorption tower of the third stage adds the evacuation
VC step after the oxygen product depressurization D step.
37. The method of claim 35 or 36, wherein the adsorbents which are packed in the adsorption tower
of the first stage are activated alumina and molecular sieve from the bottom up; the adsorbent
which is packed in the adsorption tower of the second stage is molecular sieve only; and the
adsorbent which is packed in the adsorption tower of the third stage is oxygen adsorption
equilibrium adsorbent or selective adsorbent of oxygen by adsorption kinetics.
38. A method of making oxygen with three-stage pressure-swing adsorption device, wherein
oxygen and nitrogen are separated from air; the production being enriched-oxygen and nitrogen at
the same time; the method adopts three-stage pressure-swing adsorption device operating in series,
wherein the first stage pressure-swing adsorption device is used to remove carbon dioxide and
water as well as partial nitrogen and enrich nitrogen, the second stage pressure-swing adsorption
device is used to further remove the nitrogen in interim gas which is discharged from the adsorption
tower in the adsorption step of the first stage and increase the concentration of oxygen up to the
desired level, the adsorbents in the first and second stages both adsorbing selectively nitrogen and
the third stage pressure-swing adsorption device is used to further remove the nitrogen and argon in
oxygen-enriched gas mixture which is discharged from the adsorption tower in the adsorption step
of the second stage and increase the concentration of oxygen up to above 95 volume %; the
adsorption tower of the first stage sequentially undergoes the following steps in one circulation
period: adsorption A, purge P', evacuation VC, the second stage gas backward equalization
repressurization 2ER, purge gas repressurization R', final repressurization FR; the adsorption tower
of the second stage sequentially undergoes the following steps in one circulation period: adsorption
A, backward equalization depressurization BD', final repressurization FR; the adsorption tower of
the third stage sequentially undergoes the following steps in one circulation period: adsorption A,

cocurrent equalization depressurization ED, evacuation VC, and backward equalization
repressurization ER.



ABSTRACT


OXYGEN PRODUCTION PROCESS USING THREE-STAGE
PRESSURE SWING ADSORPTION PLANTS
A process for producing oxygen by using of three-stage pressure swing adsorption plants,
wherein the process is used to separate nitrogen and oxygen from a feed air stream, the
product can be oxygen or nitrogen or both of them. The process utilizes three-stage pressure
swing adsorption plants which are serially connected. In the first stage, carbon dioxide, water
and part of nitrogen are removed and nitrogen is concentrated. In the second stage, nitrogen is
further separated from the effluent intermediate gas from the adsorption step in the adsorption
towers of the first stage and oxygen is concentrated to the desired concentration. In the third
stage, nitrogen and argon are further separated from the effluent oxygen-enriched mixture gas
from the adsorption step in the adsorption towers of the second stage and the concentration of
oxygen is raised to 95V% or more. In the first stage, the adsorption towers go through the
steps in turn in a cycle: Adsorption(A), Purge(P'), evacuation(VC), countercurrent pressure
equalization rising of the second stage gas(2ER), purge gas pressurization(R'), final
pressurization(FR); In the second stage, the adsorption towers go through the steps in turn in
a cycle: Adsorption(A), countercurrent pressure equalization falling(BD'), final
pressurization(FR); In the third stage, the adsorption towers go through the steps in turn in a
cycle: Adsorption(A), Oxygen product purge(P'), Oxygen product depressurization(D), Purge
gas pressurization(R').

Documents:

00065-kolnp-2007-correspondence-1.1.pdf

00065-kolnp-2007-correspondence-1.2.pdf

00065-kolnp-2007-form-18.pdf

00065-kolnp-2007-p.a.pdf

0065-kolnp-2007 abstract.pdf

0065-kolnp-2007 claims.pdf

0065-kolnp-2007 correspondence others.pdf

0065-kolnp-2007 description (complete).pdf

0065-kolnp-2007 drawings.pdf

0065-kolnp-2007 form-1.pdf

0065-kolnp-2007 form-2.pdf

0065-kolnp-2007 form-3.pdf

0065-kolnp-2007 form-5.pdf

0065-kolnp-2007 international publication.pdf

0065-kolnp-2007 international search authority report.pdf

0065-kolnp-2007 pct form.pdf

0065-kolnp-2007 priority document.pdf

0065-KOLNP-2007-CORRESPONDENCE OTHERS 1.3.pdf

65-KOLNP-2007-(01-10-2012)-CORRESPONDENCE.pdf

65-KOLNP-2007-(14-03-2012)-ABSTRACT.pdf

65-KOLNP-2007-(14-03-2012)-AMANDED CLAIMS.pdf

65-KOLNP-2007-(14-03-2012)-AMANDED PAGES OF SPECIFICATION.pdf

65-KOLNP-2007-(14-03-2012)-CORRESPONDENCE.pdf

65-KOLNP-2007-(14-03-2012)-DESCRIPTION (COMPLETE).pdf

65-KOLNP-2007-(14-03-2012)-FORM-1.pdf

65-KOLNP-2007-(14-03-2012)-FORM-2.pdf

65-KOLNP-2007-(14-03-2012)-FORM-3.pdf

65-KOLNP-2007-(14-03-2012)-OTHERS.pdf

65-KOLNP-2007-(14-03-2012)-REPLY TO EXAMINATION REPORT.pdf

65-KOLNP-2007-(15-11-2011)-CORRESPONDENCE.pdf

65-KOLNP-2007-(15-11-2011)-ENGLISH TRANSLATION.pdf

65-KOLNP-2007-(29-03-2011)-EXAMINATION REPORT.pdf

65-KOLNP-2007-(29-09-2011)-EXAMINATION REPORT REPLY RECIEVED.pdf

65-KOLNP-2007-(29-09-2011)-FORM 3.pdf

65-KOLNP-2007-(29-09-2011)-OTHERS.pdf

65-KOLNP-2007-(30-09-2011)-CORRESPONDENCE.pdf

65-KOLNP-2007-(30-09-2011)-FORM 3.pdf

65-KOLNP-2007-CANCELLED PAGES.pdf

65-KOLNP-2007-CORRESPONDENCE 1.1.pdf

65-KOLNP-2007-CORRESPONDENCE.pdf

65-KOLNP-2007-CORRESPONDENCE_1.2.pdf

65-KOLNP-2007-FORM 18.pdf

65-KOLNP-2007-GRANTED-ABSTRACT.pdf

65-KOLNP-2007-GRANTED-CLAIMS.pdf

65-KOLNP-2007-GRANTED-DESCRIPTION (COMPLETE).pdf

65-KOLNP-2007-GRANTED-DRAWINGS.pdf

65-KOLNP-2007-GRANTED-FORM 1.pdf

65-KOLNP-2007-GRANTED-FORM 2.pdf

65-KOLNP-2007-GRANTED-FORM 3.pdf

65-KOLNP-2007-GRANTED-FORM 5.pdf

65-KOLNP-2007-GRANTED-SPECIFICATION-COMPLETE.pdf

65-KOLNP-2007-OTHERS1.1.pdf

65-KOLNP-2007-PA.pdf

65-KOLNP-2007-PRIORITY DOCUMENT.pdf

65-KOLNP-2007-TRANSLATED COPY OF PRIORITY DOCUMENT.pdf


Patent Number 255805
Indian Patent Application Number 65/KOLNP/2007
PG Journal Number 13/2013
Publication Date 29-Mar-2013
Grant Date 25-Mar-2013
Date of Filing 05-Jan-2007
Name of Patentee CHENGDU TIANLI CHEMICAL ENGINEERING TECHNOLOGY CO., LTD.
Applicant Address YULIN, 5 NORTHSTREET, CHENGDU CITY, SICHUAN PROVINCE, P.R. CHINA
Inventors:
# Inventor's Name Inventor's Address
1 SONG, YUWEN YULIN, 5 NORTHSTREET, CHENGDU CITY, SICHUAN PROVINCE, P.R. CHINA
PCT International Classification Number B01D53/047; C01B13/02
PCT International Application Number PCT/CN2005/000642
PCT International Filing date 2005-05-09
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 200410046599.9 2004-06-11 China