Title of Invention

A PROCESS FOR PRODUCING ETHYLENE FROM ETHANOL COMBINING THE CATALYTIC CONVERSION OF HYDROCARBONS

Abstract

A process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons: an ethanol feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, and a coked catalyst and an target product of ethylene are obtained after separating the reaction stream; a hydrocarbon feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, a spent catalyst and an oil vapor are obtained after separating the reaction stream, and the oil vapor is further separated to give the products such as gas, gasoline and the like; a part or all of the coked catalyst and a part or all of the spent catalyst enter the regenerator for the coke-burning regeneration, and the regenerated catalyst is divided into two portions, wherein one portion returns to be contacted with the hydrocarbon feedstock, and the other portion, after cooling, returns to be contacted with ethanol feedstock. This process not only reasonably utilizes the excessive thermal energy of the hydrocarbon conversion, but also solves the problem of beat supply for the conversion of ethanol, thus ensuring the continuous catalytic conversion of ethanol and generating enormous economic benefits. For the catalytic conversion of the ethanol, the content of ethylene is 95 vol% or more in the gas product; and the conversion of ethylene is not less than 99%. For the catalytic conversion of the hydrocarbons, the yield for the light olefins increases slightly by at least 2 mol%.

Full Text

Form 2 THE PATENTS ACT, 1970 (39 of 1970) & THE PATENT RULES, 2003 COMPLETE SPECIFICATION (Section 10 and Rule 13) TITLE OF THE INVENTION:- "A PROCESS FOR PRODUCING ETHYLENE FROM ETHANOL COMBINING THE CATALYTIC CONVERSION OF HYDROCARBONS" APPLICANTS:- 1. Name : - China Petroleum & Chemical Corporation Nationality : - Chinese (CN) Address : - 6a, Huixin Dong Street, Chaoyang District, Beijing 100 029, P. R. China (CN) 2. Name : - Research Institute of Petroleum Processing, Sinopec Nationality : - Chinese (CN) Address : - 18 Xueyuan Road, Haidian District, Beijing 100 083 P. R. China (CN) 3. PREAMBLE OF THE DESCRIPTION:- The following specification particularly describes the invention and the manner in which it is to be performed. FIELD OF THE INVENTION The present invention relates to a process for producing ethylene from ethanol, more particular, to a process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons. BACKGROUND OF THE INVENTION The global petroleum supply-demand contradiction is increasingly prominent at the beginning of the 21st century. Along with the increased demand for various petroleum and petrochemical products, the price of crude oil in the market is continuously increased. This situation leads to persisting high market-prices of important chemical products such as light olefins (especially ethylene and propylene) and light ethers (such as dimethyl ether, ethyl ether, etc), using petroleum and petrochemical products as feedstock. Therefore, it is one choice of solving these problems to seek for another substituting feedstock such as by-product ethanol from agriculture and forestry, and methanol prepared from natural gas or coal to produce light olefins and light ethers. The process for preparing ethylene from ethanol is to carry out the dehydration reaction CH3CH2OH -> CH2=CH2 + H20 at I40-400°C with a suitable catalyst. At the beginning of 1980's, India and Brazil built up industry-scale devices for converting ethanol to ethylene, using Si02-Al203 as catalyst and adopting fixed bed and fluidized bed reactors altogether. For the balance of heat, an additional fuel will be added when the catalyst is regenerated. The process disclosed in US 6,441,261 is to convert oxygenates (methanol, etc) to light olefins, e.g. ethylene and propylene, on a silicoaluminophosphate molecular sieve catalyst under a relative high pressure. US 6,303,839 and US 5,914,433 convert oxygenates (methanol, etc) to light olefins and fractionate out the propylene and/or butene therein for cracking, thereby enhancing the yield of ethylene and propylene. Although the above processes also use fluidized bed operation, it is seen from the data of the examples that the yield of coke is only 2%. With a low yield of coke, the heat of the system is difficult to be balanced, and an external heat supply is generally needed. US 6,049,017 increases the yield of light olefins by separating the product containing C4 components and converting them to ethylene and propylene on a non-molecular sieve catalyst. This process may be used in the catalytic cracking or the methanol dehydration for producing ethylene and propylene. 2 US 4,148,835 uses a shape-selective molecular sieve catalyst and derivatives thereof to convert alcohols (especially methanol) to a product mainly containing light olefins, but this patent does not mention of the process. The ethanol dehydration reaction is an endothermic reaction, and is conducted at a certain temperature. Although coke deposition may occur during the reaction, the amount of the coke is insufficient to balance the heat of the process. In summary, all the prior arts provide the heat in a manner of supplying an external fuel, making the process too complicated or the energy consumption too high. SUMMARY OF THE INVENTION Based on the prior art, the object of the present invention is to provide'a process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons. According to the present invention, the process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons comprises the following steps: (1) An ethanol feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, and a coked catalyst and a target product of ethylene are obtained after separating the reaction stream; (2) A hydrocarbon feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, a spent catalyst and an oil vapor are obtained after separating the reaction stream, and the oil vapor is further separated to give the products such as gas, gasoline and the like; (3) Apart or all of the coked catalyst in step (1) and a part or all of the spent catalyst in step (2) enter a regenerator for the coke-burning regeneration, and the regenerated catalyst is divided into two portions, wherein one portion returns to step (2), and the other portion returns to step (1) after cooling. The ethanol content in the ethanol feedstock in the present invention is 50-100 wt%, preferably 70-100 wt%, and more preferably 90-100 wt%. A small amount of impurities such as water and methanol may be contained in the ethanol feedstock. Said hydrocarbon feedstock is selected from the group consisting of Cj+ hydrocarbons, crude oil, gasoline, diesel oil, vacuum gas oil, coker gas oil, deasphalted oil, hydrogenaled bottom, atmospheric residuum, vacuum residuum and mixtures thereof; and it is preferably selected from the group consisting of vacuum gas oil, coker gas oil, deasphalted oil, hydrogenated bottom, atmospheric residuum, vacuum residuum and mixtures thereof. Said Y-zeolite containing catalyst may contain a Y-zeolite and an optional other molecular sieve, but not contain inorganic oxides and clay, wherein the weight ratio of the other 3 molecular sieve to the Y-zeolite is 0-10. Said Y-zeolite containing catalyst preferably contains inorganic oxides and/or clay, a Y-zeolite, and an optional other molecular sieve, wherein the weight ratio of the other molecular sieve to the Y-zeolite is 0-10, and the total weight of the other molecular sieve and the Y-zeolite comprises 10-60% of the catalyst. Said Y-zeolite includes Y-type zeolite and their derivative or modified zeolites, and is selected from the group consisting of Y, HY; REY, REHY, USY, REUSY and mixtures thereof. Said other molecular sieve is one or more selected from meso porous zeolites, Beta-zeolites, and SAPO-molecular sieves. Said meso porous zeolite includes ZRP series (rare earth-modified). ZSP series (iron-modified), ZSM series zeolites and their derivative or modified zeolites. For the more detailed description of ZRP, a reference may be made to US 5,232,675. Said ZSM series zeolite is selected from the group consisting of ZSM-5, ZSM-11, ZSM-12, ZSM-22, ZSM-23, ZSM-35, ZSM38, ZSM-48, and other zeolites having a similar structure. For more detailed description of ZSM-5, a reference may be made to US 3,702,886. A more preferred Y-zeolite containing catalyst contains Y-zeolites, meso porous zeolites, inorganic oxides, and clay, wherem the weight ratio of the meso porous zeolite to the Y-zeolite is 0.1-10, and the total weight of the meso porous zeolite and the Y-zeolite accounts for 10-60% of total weight of the catalyst. Said inorganic oxide is selected from the group consisting of alumina, silica, amorphous silica-alumina and mixtures thereof. The clay is kaolin and/or halloysite. The reaction conditions in step (1) are a temperature of 200-450°C, preferably 250-400°C, a pressure (gauge) of 0-0.8 MPa, a weight ratio of the catalyst to the ethanol feedstock of 0.05-20, and a weight hourly space velocity of 0.05-10 h"1, preferably 0.1-5 h'1. The reaction conditions in step (2) are a temperature of 400-700°C, preferably 450-600°C, a pressure (gauge) of 0-0.8 MPa, a weight ratio of the catalyst to the hydrocarbon feedstock of 1-30, and a contact time of 1-10 seconds. The catalytic conversion process in step (2) comprises conventional catalytic cracking .processes and various family processes such as the DCC process, CPP process, MIP process, MIP-CGP process, MGD process, MGG process, ARGG process, SHMP process and the like. The proportion of the coked catalyst in step (1) subjected to coke-burning is 0.5-100%, preferably 5-60%, more preferably 8-40% by the total weight of the coked catalyst. When a portion of the coked catalyst in step (1) enters the regenerator for the coke-burning regeneration, the remaining coked catalyst returns to step (1) and/or step (2), and said portion of the coked catalyst subjected to coke-burning comprises 0.5-99%, preferably 5-60%, more preferably 8-40%) by the total weight of the coked catalyst. 4 The proportion of the spent catalyst in step (2) subjected to coke-burning is 1-100%. preferably 50-100%, more preferably 80-100% by the total weight of the spent catalyst. When a portion of the spent catalyst in step (2) enters the regenerator for the coke-burning regeneration, the remaining spent catalyst returns to step (1). and said portion of the spent catalyst comprises 1-99%, preferably 50-99%, more preferably 80-99% by the total weight of the spent catalyst. The regeneration in step (3) is one-stage regeneration or two-stage regeneration, and said regenerated catalyst is a partially regenerated catalyst (i.e. semi-regenerated catalyst) and/or a full regenerated catalyst. The weight ratio of the coked catalyst and the spent catalyst entering the regenerator for the coke-burning regeneration is no more than 1.0, preferably no more than 0.5. more preferably no more than 0.2. The reactors used in step (1) and step (2) are both catalyst-movable reactors, and are selected from the group consisting of a fluidized bed, a riser, a descending transfer line reactor, a moving bed, a composite reactor of riser and fluidized bed, a composite reactor of riser and descending transfer line, a composite reactor of two or more risers, a composite reactor of two or more fluidized beds, a composite reactor of two or more descending transfer lines, and a composite reactor of two or more moving beds. Each of the above reactors may be divided into two or more reaction zones. The preferred reactor in step (1) is a fluidized bed, more preferably a dense-phase fluidized bed. The preferred reactor in step (2) is a riser. Said riser is one or more selected from an iso-diameter riser, an equal-velocity riser, and various variable-diameter risers. Said fluidized bed is one or more selected from a fixed fluidized bed, a particulate fluidization bed, a bubbling bed, a turbulent bed, a quick bed. a transfer bed, and a dense-phase fluidized bed. \ An existing catalytic cracking reactor may be used as the aforesaid reactor. Alternatively, a necessary modification may be made to an existing catalytic cracking reactor. Also the reactors having a similar structure and function to an existing catalytic cracking reactor can be used. The product separation device may be the same one shared in Step (1) and Step (2), or the product separation device used in Step (1) is different from that in Step (2). The excessive ethanol separated in step (1) may return to step (1). The C/ light hydrocarbons separated in step (2) may return to step (1) and/or step (2). The regenerated catalyst returning to the reactor of step (1) is first cooled down to 200-450°C in a direct heat exchange mode or an indirect heat exchange mode. The direct heat exchange mode is to carry out heat exchange by directly contacting the regenerated catalyst with the air having a relatively low temperature. The air is a part or all of the air compressed by an air compressor and delivered to the regenerator, that is, the high temperature thermal energy 5 from a portion of regenerated catalyst is used to preheat the air entering the regenerator. The direct heat exchanger is in a type of fluidized bed or riser, and the cooled catalyst separated by a cyclone separator enters the catalytic conversion reactor of ethanol after stripping off the gas impurities (nitrogen, oxygen, carbon dioxide and the like) with the hot steam. The indirect heat exchange mode is to use an indirect heat exchanger, wherein the hot catalyst passes through the tube side and the steam passes through the shell side. The process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons according to the present invention, not only reasonably utilizes the excessive thermal energy of the hydrocarbon conversion, but also solves the problem of heat supply for the conversion of ethanol, thus ensuring the continuous catalytic conversion of ethanol and generating enormous economic benefits. For the catalytic conversion of the ethanol, the content of ethylene is 95 vol% or more in the gas product; and the conversion of ethylene is not less than 99%. For the catalytic conversion of the hydrocarbons, the yield for the light olefins increases slightly by at least 2 mol%. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic flowsheet of the process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons according to an embodiment of the present invention. PREFERRED EMBODIMENTS OF THE INVENTION The process of the present invention will be further illustrated in reference to the drawing, but the present invention is not limit thereto. Fig. 1 is a schematic flowsheet of the process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons according to an embodiment of the present invention. An ethanol feedstock from line 1 is introduced into the reactor 2 and contacted with a Y-zeolite containing regenerated catalyst from line 14 to react at 200-450°C, under a pressure (gauge) of 0-0.8MPa, at a weight ratio of the catalyst to ethanol feedstock of 0.05-20, with a weight hourly space velocity of 0.1-10 h"'. A coked catalyst and a product stream are obtained after separating the reaction stream. The product stream is withdrawn through the line 3 and further separated to give the target product of ethylene. The coked catalyst may be partially or completely introduced into the regenerator 5 through the line 4 for the coke-burning regeneration, and a portion of the coked catalyst may return to the reactor 2 sequentially through the lines 15 and 14 or return to the reactor 7 sequentially through the lines 17 and 10. 6 The hydrocarbon feedstock from line 6 is introduced into the reactor 7 and contacted with a Y-zeolite containing regenerated catalyst from the line 10 to react at 400-700°C, under a pressure (gauge) of 0-0.8MPa, at a weight ratio of the catalyst to the hydrocarbon feedstock of 1-30, with a contact time of 1-10 s. A spent catalyst and an oil vapor are obtained after separating the reaction stream, wherein the oil vapor is withdrawn through the line 8 and further separated to give the products such as gas, gasoline, diesel oil and the like (not shown in the figure). After stripping, the spent catalyst is completely or partially introduced into the regenerator 5 through the line 9 for the coke-burning regeneration, and a portion of the spent catalyst may return to the reactor 2 sequentially through the lines 16 and 14. The weight ratio of the coked catalyst and the spent catalyst entering the regenerator 5 for the coke-burning regeneration is no more than 1.0, preferably no more than 0.5, more preferably no more than 0,2. The regenerated catalyst, which is coke-burning regenerated in the regenerator 5, is divided into two portions, wherein one portion returns to the reactor 7 through line 10, and the other portion sequentially enters the heat exchanger 13 through the line 12, cools therein, and then returns to the reactor 2 through the line 14. The process of the present invention will further be illustrated by the following examples, but the present invention is not limit thereto. Example 1 The ethanol feedstock and hydrocarbon feedstock used in this example were an ethanol feedstock containing 95% ethanol brewed from grains and vacuum gas oil (VGO), respectively, and the properties of VGO are shown in Table 1. The catalyst used in this example was CGP-1 (containing 25 wt% of REY-zeoIite, 10 wt% of ZSP-zeoIite, and the balanced support, all based on the total weight of the catalyst) produced by SINOPEC Catalyst Company Qilu Division. The ethanol feedstock was introduced into a fluidized bed reactor and contacted with the CGP-1 catalyst to react at 340°C. under a pressure (gauge) of 0.1 MPa, at a weight ratio of the catalyst to the ethanol feedstock (catalyst/alcohol ratio) of 1, with a weight hourly space velocity of 1.0 h' .A coked catalyst and a product stream were obtained after separating the product stream. The product stream was further separated to give the target product of ethylene. The product distribution is shown in Table 2. The coked catalyst was divided into two portions, wherein 20 wt% of the coked catalyst was introduced into the regenerator for the coke-burning regeneration, and the remaining 80 wt% of the coked catalyst retuned to the fluidized bed reactor through the inner recycle. 7 The preheated VGO was injected into a riser reactor after the steam atomization at a weight ratio of the steam to VGO was 0.1:1. VGO was contacted with the hot CGP-1 catalyst in the riser to react at 500°C, under a pressure (gauge) of 0.1 MPa, at a weight ratio of the catalyst to VGO (catalyst/oil ratio) of 6, with a reaction time of 3 seconds. The mixture of the oil vapor and the catalyst rose along the riser to the outlet of the riser. The reaction product and the spent catalyst were separated. The reaction product was introduced into the settler and then into the subsequent separation system to further separate into various products. The product distribution is shown in Table 2. The spent catalyst entered the stripper under the action of gravity to strip with the steam, and it was then introduced into the regenerator for the coke-burning regeneration. 20 wt% of the coked catalyst and all the spent catalyst were regenerated in the regenerator, wherein the weight ratio of the coked catalyst and the spent catalyst entering the regenerator for the coke-burning regeneration is about 0.02. After the regeneration, the regenerated catalyst were divided into two portions, wherein 85 wt% of the regenerated catalyst, having a temperature of 660°C, retuned to the riser for the recycling use, and the remaining 15 wt% of the regenerated catalyst was cooled down to 410°C and retuned to the fluidized bed for the recycling use. The testing results demonstrated that by combining the catalytic conversion of ethanol and the catalytic conversion of hydrocarbons, the heat between the two conversions can be balanced, and there is no need for the external ruel or other heat sources. For the catalytic conversion of the ethanol, the content of ethylene is as high as 95.79 vol% in the gas product; and the conversion of ethylene is as high as 99%. Further, the inventors also found that: (1) The catalytic conversion of ethanol had not any effect on the crystalline phase of the catalyst CGP-1; and in comparison of the catalyst's acidity prior to the catalytic conversion, the catalyst's acidity decreased slightly after the catalytic conversion; and (2) For the catalytic conversion of the hydrocarbons, the yield for the light products increases slightly by 2 mol% by combining the catalytic conversion of ethanol and the catalytic conversion of the hydrocarbons, the reason for which is believed that the catalyst's acidity is decreased. Example 2 In this example, the ethanol feedstock is identical to that of Example 1; and the hydrocarbon feedstock is an atmospheric residuum. The properties of the atmospheric residuum are shown in Table 1. The catalyst used in this example was MMC-2 (containing 10 8 wt% of USY-zeolite, 20 wt% of ZSM-5 zeolite, and the balanced support, all based on the total weight of the catalyst) produced by SINOPEC Catalyst Company Qilu Division. The ethanol feedstock was introduced into a fluidized bed reactor and contacted with the MMC-2 catalyst to react at 360°C, under a pressure (gauge) of 0.1 MPa, at a weight ratio of the catalyst to the ethanol feedstock (catalyst/alcohol ratio) of 5, with a weight hourly space velocity of 1.5 h"1. A coked catalyst and a product stream were obtained after separating the reaction stream. The product stream was further separated to give the target product of ethylene. The product distribution is shown in Table 2. The coked catalyst was divided into two portions, wherein 30 wt% of the coked catalyst was introduced into the regenerator for the coke-burning regeneration, and the remaining 70 wt% of the coked catalyst retuned to the fluidized bed reactor through the inner recycle. The preheated atmospheric residuum was injected into a riser reactor after the steam atomization at a weight ratio of the steam to the atmospheric residuum was 0.1:1. The atmospheric residuum was contacted with the hot MMC-2 catalyst in the riser to react at 550°C, under a pressure (gauge) of 0.1 MPa, at a weight ratio of the catalyst to the atmospheric residuum (catalyst/oil ratio) of 8, with a reaction time of 4 seconds. The mixture of the oil vapor and the catalyst rose along the riser to the outlet of the riser. The reaction product and the spent catalyst were separated. The reaction product was introduced into the settler and then into the subsequent separation system to further separate into various products. The product distribution is shown in Table 2. The spent catalyst entered the stripper under the action of gravity to strip with the steam, and it was then introduced into the regenerator for the coke-burning regeneration. 30 wt% of the coked catalyst and all the spent catalyst were regenerated in the regenerator, wherein the weight ratio of the coked catalyst and the spent catalyst entering the regenerator for the coke-burning regeneration is about 0.02. After the regeneration, the regenerated catalyst were divided into two portions, wherein 80 wt% of the regenerated catalyst, having a temperature of 680°C, retuned to the riser for the recycling use, and the remaining 20 wt% of the regenerated catalyst was cooled down to 410°C and retuned to the fluidized bed for the recycling use. The testing results demonstrated that by combining the catalytic conversion of ethanol and the catalytic conversion of hydrocarbons, the heat between the two conversions can be balanced, and there is no need for the external fuel or other heat sources. For the catalytic conversion of the ethanol, the content of ethylene is as high as 98.3 vol% in the gas product; and the conversion of ethylene is as high as 99.1%. Further, the inventors also found that: 9 (1) The catalytic conversion of ethanol had not any effect on the crystalline phase of the catalyst MMC-2; and in comparison of the catalyst's acidity prior to the catalytic conversion, the catalyst's acidity decreased slightly after the catalytic conversion; and (2) For the catalytic conversion of the hydrocarbons, the yield for the light products increases slightly by 2 mol% by combining the catalytic conversion of ethanol and the catalytic conversion of the hydrocarbons, the reason for which is believed that the catalyst's acidity is decreased. 10 Table 1 Feedstock Properties VGO Atmospheric residuum Density (20°C), g/cmj 0.9526 0.9387 Sulfur content, ppm 11000 12000 Nitrogen content, ppm 916 647 Carbon residue, m% 12.4 9.2 C, m% 86.3 85.95 H, m% 11.52 11.83 Kinetic viscosity. mm2/s 80°C 1102.3 325.1 100°C 650.7 129.5 Freezing point, °C 45 35 True boiling point, °C >450 >350 Vanadium, ppm 2.1 1.7 Nickel, ppm 42 30 II Table 2 Example 1 2 Catalyst type CGP-1 MMC-2 Catalytic conversion of ethanol Reaction conditions Temperature, °C 340 360 Pressure (gauge), MPa 0.1 0.1 Catalyst/alcohol ratio 1 5 WHSV,h'1 1.0 1.5 Product distribution, vol% Ethylene 95.79 98.32 Propylene 1.18 0.29 Iso-butane 0.72 0.15 Total pentane 0.45 0 Total pentene 0.25 0.31 C(,+ hydrocarbons 0.54 0.53 Conversion of ethanol, % 99.1 99.5 Selectivity to ethylene, % 98 98.3 Carbon base ethylene yield*, m% 89.52 99.78 Catalytic conversion of hydrocarbons Reaction conditions Temperature, °C 500 550 Pressure (gauge). MPa 0.1 0.1 Catalyst/oil ratio 6 6 Time on stream, s 3 3 Product distribution, wt% Dry gas 10.56 3.17 LPG 44.78 18.04 Gasoline 21.32 48.26 Diesel oil 6.89 18.73 Heavy oil 3.18 4.56 Coke 13.28 7.24 * Carbon base ethylene yield = Carbon content in the target product/ carbon content in the ethanol feedstock 12 Claims 1. A process for producing ethylene from ethanol combining the catalytic conversion of hydrocarbons, characterized in that said process comprises the following steps: (1) An ethanol feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, and a coked catalyst and a target product of ethylene are obtained after separating the reaction stream; (2) A hydrocarbon feedstock is contacted with a Y-zeolite containing catalyst to give a product stream, a spent catalyst and an oil vapor are obtained after separating the reaction stream, and the oil vapor is further separated; (3) Apart or all of the coked catalyst in step (1) and a part or ail of the spent catalyst in step (2) enter a regenerator for the coke-burning regeneration, and the regenerated catalyst is divided into two portions, wherein one portion returns to step (2) and the other portion returns to step (1) after cooling. 2. The process according to claim 1, characterized in that the content of the ethanol in said ethanol feedstock is 50-100% by weight. 3. The process according to claim 1, characterized in that the content of the ethanol in said ethanol feedstock is 70-100% by weight. 4. The process according to claim 1, characterized in that the content of the ethanol in said ethanol feedstock is 90-100% by weight. 5. The process according to claim 1, characterized in that said hydrocarbon feedstock is selected from the group consisting of C4+ hydrocarbons, crude oil, gasoline, diesel oil, vacuum gas oil, coker gas oil, deasphalted oil, hydrogenated bottom, atmospheric residuum, vacuum residuum and mixtures thereof. 6. The process according to claim 1, characterized in that said hydrocarbon feedstock is selected from the group consisting of vacuum gas oil, coker gas oil, deasphalted oil, hydrogenated bottom, atmospheric residuum, vacuum residuum and mixtures thereof. 7. The process according to claim 1, characterized in that said Y-zeolite containing catalyst comprises a Y-zeoJite and an optional other molecular sieve, but not contain inorganic oxides and clay. i3 8. The process according to claim 1, characterized in that said Y-zeolite containing catalyst comprises a Y-zeolite, an optional other molecular sieve, and inorganic oxides and/or clay. 9. The process according to claim 7 or 8, characterized in that said other molecular sieve is one or more selected from meso porous zeolites, Beta-zeolites, and SAPO-molecular sieves. 10. The process according to claim 7 or 8, characterized in that the weight ratio of said other molecular sieve to the Y-zeolite is 0-10. 11. The process according to claim 1, characterized in that said Y-zeolite containing catalyst contains Y-zeolites, meso porous zeolites, inorganic oxides, and clay. 12. The process according to claim 11, characterized in that the weight ratio of said meso porous zeolite to the Y-zeolite is 0.1-10, and the total weight of the meso porous zeolite and the Y-zeolite accounts for 10-50% of total weight of the catalyst. 13. The process according to claim 1, 7 or 8, characterized in that said Y-zeolite is selected from the group consisting of Y, HY, REY, REHY, USY, REUSY and mixtures thereof. 14. The process according to claim 9 or 11, characterized in that said meso porous zeolite includes ZRP series, ZSP series, and ZSM series zeolites, as well as their derivative or modified zeolites. 15. The process according to claim 7 or 8, characterized in that said inorganic oxide is selected from the group consisting of alumina, silica, amorphous silica-alumina, and mixtures thereof, and the clay is kaolin clay and/or halloysite. 16. The process according to claim 1, characterized in that the reaction conditions in step (1) are a temperature of 200-450°C, a gauge pressure of 0-0.8 MPa, a weight ratio of the catalyst to the ethanol feedstock of 0.05-20, and a weight hourly space velocity of 0^05-10 h"1. 17. The process according to claim 16, characterized in that the reaction conditions in step (1) are a temperature of 250-400°C, and a weight hourly space velocity of 0.1 -5 h"1. 18. The process according to claim 1, characterized in that the reaction conditions in step (2) are a temperature of 400-700°C, a gauge pressure of 0-0.8 MPa. a weight ^ ratio of the catalyst to the hydrocarbon feedstock of 1-30, and a contact time of I-10 seconds. 19. The process according to claim 18, characterized in that the reaction conditions in step (2) are a temperature of 450-600°C. 20. The process according to claim 1, characterized in that the proportion of the coked catalyst in step (1) subjected to coke-burning is 0.5-100% by the total weight of the coked catalyst. 21. The process according to claim 1 or 20, characterized in that when a portion of the coked catalyst in step (1) enters the regenerator for the coke-burning regeneration, the remaining coked catalyst returns to step (1) and/or step (2)5 and said portion of the coked catalyst comprises 0.5-99% by the total weight of the coked catalyst. 22. The process according to claim 1, characterized in that the proportion of the spent catalyst in step (2) subjected to coke-burning is 1-100% by the total weight of the spent catalyst. 23. The process according to claim 1 or 22, characterized in that when a portion of the spent catalyst in step (2) enters the regenerator for the coke-burning regeneration, the remaining spent catalyst returns to step (1), and said portion of the spent catalyst comprises 1-99% by the total weight of the spent catalyst 24. The process according to claim 1, characterized in that the regeneration in step (3) is one-stage regeneration or two-stage regeneration, and said regenerated catalyst is a partially regenerated catalyst and/or a full regenerated catalyst. 25. The process according to claim 1, characterized in that the reactors used in step (1) and step (2) are both catalyst-movable reactors, and are selected from the group consisting of a fluidized bed, a riser, a descending transfer line reactor, a moving bed, a composite reactor of riser and fluidized bed, a composite reactor of riser and descending transfer line, a composite reactor of two or more risers, a composite reactor of two or more fluidized beds, a composite reactor of two or more descending transfer lines, and a composite reactor of two or more moving beds; and each of the above reactors can be divided into two or more reaction zones. 26. The process according to claim 1, characterized in that the reactor in step (1) is a fluidized bed, and the reactor in step (2) is a riser. 27. The process according to claim 25 or 26, characterized in that said riser is one or more selected from an iso-diameter riser, an equal-velocity riser, and various variable-diameter riser; and said fluidized bed is one or more selected from a fixed 15 fluidized bed, a particulate fluidization bed, a bubbling bed, a turbulent bed, a quick bed, a transfer bed, and a dense-phase fluidized bed. 28. The process according to claim 1, characterized in that the regenerated catalyst returning to the reactor of step (1) is first cooled down to 200-450°C in a direct heat exchange mode or an indirect heat exchange mode. 29. The process according to claim 28, characterized in that said direct heat exchange mode is to carry out heat exchange by directly contacting the regenerated catalyst with the air having a relatively low temperature, and the direct heat exchanger is in a type of fluidized bed or riser; and the indirect heat exchange mode is to use an indirect heat exchanger, wherein the hot catalyst passes through the tube side and the steam passes through the shell side. 30. The process according to claim 1, characterized in that the weight ratio of the coked catalyst and the spent catalyst entering the regenerator for the coke-burning regeneration is no more than 1.0. Dated:- 10thFebruary 2009 JehangirGuJabbhai & Billmoria & Daruwalla TEHEMTAN N.DARU WALLA Constituted patent Agents Attorney for the Applicants 16

Documents:

327-mumnp-2009-abstract.doc

327-mumnp-2009-abstract.pdf

327-MUMNP-2009-CLAIMS(AMENDED)-(26-6-2013).pdf

327-MUMNP-2009-CLAIMS(MARKED COPY)-(26-6-2013).pdf

327-mumnp-2009-claims.doc

327-mumnp-2009-claims.pdf

327-MUMNP-2009-CORRESPONDENCE(10-8-2009).pdf

327-MUMNP-2009-CORRESPONDENCE(31-5-2010).pdf

327-mumnp-2009-correspondence.pdf

327-mumnp-2009-description(complete).doc

327-mumnp-2009-description(complete).pdf

327-mumnp-2009-drawing.pdf

327-mumnp-2009-form 1.pdf

327-MUMNP-2009-FORM 18(31-5-2010).pdf

327-mumnp-2009-form 2(title page).pdf

327-mumnp-2009-form 2.doc

327-mumnp-2009-form 2.pdf

327-mumnp-2009-form 26.pdf

327-MUMNP-2009-FORM 3(10-8-2009).pdf

327-MUMNP-2009-FORM 3(26-6-2013).pdf

327-MUMNP-2009-FORM 3(31-5-2010).pdf

327-mumnp-2009-form 3.pdf

327-mumnp-2009-form 5.pdf

327-MUMNP-2009-OTHER DOCUMENT(26-6-2013).pdf

327-mumnp-2009-pct-ib-373.pdf

327-mumnp-2009-pct-isa-210.pdf

327-mumnp-2009-pct-isa-237.pdf

327-MUMNP-2009-REPLY TO EXAMINATION REPORT(26-6-2013).pdf

327-mumnp-2009-wo international publication report a1.pdf

abstract1.jpg