Title of Invention

COMPOSITION AND METHOD FOR CONTROLLING BIOLOGICAL GROWTH USING STABILIZED SODIUM HYPOBROMITE IN SYNERGISTIC COMBINATION

Abstract A synergistic composition and method for controlling biological growth in industrial fluids are disclosed, wherein the composition comprises stabilized sodium hypobromite and at least one compound selected from the group consisting of coco alkyldimethylamine oxide, n-coco alkyltrimethylenediamine, tetra-alkyl phosphonium chloride, 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid and 4,5-dichloro-2-n-octyl-4-isothiazoline-3-one.
Full Text COMPOSITION AND METHOD FOR CONTROLLING BIOLOGICAL
GROWTH USING STABILIZED SODIUM HYPOBROMITE IN
SYNERGISTIC COMBINATIONS
FIELD OF THE INVENTION
This invention relates generally to biocides and,
more particularly, to a composition and method for
controlling biological growth using stabilized sodium
hypobromite in synergistic combinations.
BACKGROUND OF THE INVENTION
The proliferation of microorganisms and the
resultant formation of slime is a problem which commonly
occurs in aqueous systems. Problematic slime producing
microbes may include bacteria, fungi and algae. Slime
deposits typically occur in many industrial aqueous
systems including cooling water systems, pulp and paper
mill systems, petroleum operations, clay and pigment
slurries, recreational water systems, air washer systems,
decorative fountains, food, beverage, and industrial
process pasteurizers, sweetwater systems, gas scrubber
systems, latex systems, industrial lubricants, cutting
fluids, etc.
The proliferation of organisms such as mussels and
clams is also a problem which occurs in many water
systems. Growth of these organisms is a serious problem
in municipal and industrial water systems such as once-
through or recirculating cooling water systems, cooling
ponds, intake pipes, ballast water tanks and ship
reservoirs that draw water from infested bodies of water.
Biocides and antimicrobials are used to control
microbial growth in a number of different aqueous media.
As used herein, "control" is defined to-include both
inhibition and removal. If left untreated, microbes and
microbial biofilms (slimes) can cause deterioration of
cooling tower structures, loss in heat exchange
efficiency in a cooling system, aesthetic defects in
decorative fountains, promotion and acceleration of
corrosion on metal surfaces, increased down time, or
breaks in paper sheets in pulp and paper systems.
Bacterial slimes may also be objectionable as they relate
to cleanliness and sanitation in breweries, dairies, and
other industrial food and beverage process water systems.
The proliferation of microbial contamination in
lubricants and cutting fluids is a common problem due to
the elevated temperatures and unsanitary conditions found
in many metal working plants.
For many types of municipal and industrial water
systems, screening of intake water is often performed to
prevent the entrance of large objects, including mature
clams and mussels. This screening, however, does not
prevent the passage of jivenile macroinvertebrates.
These early life stages of the macroinvertebrates attach
within water systems and mature to a size and density
which cause fouling. This growth can cause severe
plugging and damage to the systems they colonize,
resulting in system down time and costly cleanings and
repairs. As a consequence of the deleterious effects of
uncontrolled biological growth and contamination in many
industrial processes, different biocides and
antimicrobials have been developed to aid in eliminating
and controlling biological growth.
Often, one biocide is insufficient to control
biological growth in the aqueous media. Biocides may act
in combination, i.e. synergistically, to yield better
biocidal performance as opposed to the efficacy obtained
when each biocide is used separately. Biocides may act
on the target organism in a number of different ways to
cause cell stress or death. The mechanisms by which
biocides exert biocidal activity depend upon a number of
factors which include the chemical properties of the
biocide, and the biochemical and physical characteristics
of the target organism. Some biocides target the cell
membrane or cell wall. Others target critical enzymes or
the cellular metabolic machinery which leads to cell
death or disruption of cellular replication.
The combination of two biocides may yield enhanced
efficacy beyond the cumulative or additive effect of the
two biocides. This likely reflects a synergistic
biocidal effect on some essential component(s) of the
cell for survival and sustained growth. A combination of
two biocides that are synergistic allows for the addition
of lesser amounts of the individual biocides to achieve
the desired level of control. This has both advantageous
environmental and economic impacts. It allows for
reduced discharge of potential environmental pollutants
and a more cost effective control program for diverse
industrial systems.
It is an object of the present invention to provide
novel biocidal compositions which provide enhanced
effectiveness for controlling the growth of both
microorganisms and macroorganisms in industrial fluids.
It is another object of this invention to provide an
improved method for controlling microorganisms and
macroorganisms in industrial fluids. It is an advantage
of the present invention that the biocidal compositions
permit a reduction in the amount of biocide required to
achieve acceptable biological control.
Important applications of the synergistic biocidal
compositions of the present invention include, but are
not limited to, controlling the growth of microorganisms
such as bacteria, fungi and algae, and macroorganisms
such as zebra mussels, blue mussels and the Asiatic clam
in aqueous media. The composition of the present
invention possesses unexpected synergistic activity
against microorganisms and macroorganisms.
Stabilized sodium hypobromite is less volatile and
more stable than other halogenated molecules such as
sodium hypochiorite and sodium hypobromite. Also, much
higher levels of available halogen for microbial
disinfection are attained using stabilized sodium
hypobromite than with other halogenated antimicrobials.
Further, stabilized sodium hypobromite yielded reduced
generation of adsorbable organic halogen (AOX) in
laboratory studies and process waters.
This invention provides superior biological control
by combining stabilized sodium hypobromite with at least
one compound selected from the group consisting of coco
alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1] heptane-2 , 3-dicarboxylic
acid and 4, 5-dichloro-2-n-octyl-4-isothiazoline-3-one .
The combination of the two biocides leads to unexpectedly
superior results, and allows for significantly less use
of either biocide compared to the necessary amount of
each individual biocide to achieve the same biocidal
performance. In addition to biocidal synergism, the use
of these biocide combinations may result in improved
removal of adherent biomass due to the biocidal
persistence of coco alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic
acid and 4, 5-dichloro-2-n-octyl-4-isothiazoline-3-one
coupled with the reactivity and biofilm removal
properties of- stabilized sodium hypobromite. As is well
known in the art, stabilized sodium hypobromite, coco
alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1]heptane-2, 3-dicarboxylic
acid and 4,5-dichloro-2-n-octyl-4-isothiazoline-3-one
exhibit biocidal activity when used alone. However, the
prior art does not teach or suggest the performance
advantages of the inventive combinations or the resulting
synergistic behavior.
SUMMARY OF THE INVENTION
The composition of the present invention comprises
stabilized sodium hypobromite and at least one compound
selected from the group consisting of coco
alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1] heptane-2, 3-dicarboxylic
acid and 4 , 5-dichloro-2-n-octyl-4-isothiazoline-3-one.
The inventive composition effectively controls
biological growth in industrial fluids.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to a composition
and method for controlling biological growth in
industrial fluids using stabilized sodium hypobromite in
synergistic combinations. In accordance with this
invention, stabilized sodium hypobromite is added to the
industrial fluid in combination with another compound.
Suitable compounds which may be used in combination with
the stabilized sodium hypobromite include, but are not
limited to, surfactants such as coco alkyldimethylamine
oxide and n-coco alkyltrimethylenediamine, and non-
oxidizing biocides such as tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1] heptane-2, 3-dicarboxylic
acid (also known as endothall) and 4,5-dichloro-2-n-
octyi-4-isothiazolin-3-one.
The biological growth may be microbiological or
macrobiological in nature. Microbiological growth
includes bacteria, fungi, algae and combinations thereof.
Macrobiological growth includes zebra mussels (Dreissena
polymorpha, Dreissena bugensis), blue mussels (Mytilus
edulis) , and the Asiatic clam (Corbicula fluminea) .
The stabilized sodium hypobromite may be sodium
hypobromite stabilized with sodium sulfamate. The sodium
hypobromite may be stabilized with an alkali metal
sulfamate, such as sodium sulfamate. Moreover, the
sodium hypobromite may also be stabilized with an acid
amide derivative selected from the group consisting of
carbonic acids, hydrogen cyanide, carboxylic acids, amino
acids, sulfuric acids, phosphoric acids and boric acids.
The industrial fluids include cooling waters; food,
beverage and industrial process waters; pulp and paper
mill systems; brewery pasteurizers; sweetwater systems;
air washer systems; oil field drilling fluids and muds;
petroleum recovery processes; industrial lubricants;
cutting fluids; heat transfer systems; gas scrubber
systems; latex systems; clay and pigment systems;
decorative fountains; water intake pipes; ballast water
tanks and ship reservoirs, among others.
The amount of stabilized sodium hypobromite may
range from about 0.05 ppm to about 1000 ppm total
residual oxidant (as chlorine) and the amount of the
compound selected from the group consisting of coco
alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic
acid and 4,5-dichloro-2-n-octyl-4-isothiazoline-3-one
ranges from about 0.05 ppm to about 1000 ppm active
ingredient (active ingredient refers to the amount of the
compound in the industrial fluid)-. "Total residual
oxidant" as used herein is defined as hypobromite or
hypobromous acid, expressed as chlorine, including
chemical combinations of those two compounds with ammonia
or organic nitrogen-containing compounds.
As used herein, the term "stabilized sodium
hypobromite" indicates NaOBr stabilized with sodium
sulfamate. However, NaOBr can be stabilized with other
stabilizers which includes the acid amide derivatives of
carbonic acids, hydrogen cyanide, carboxylic acids, amino
acids, sulfuric acids, phosphoric acids and boric acids.
Moreover, stabilizers can be selected from the group of
compounds having an N-H or NH2 group adjacent to an
electron withdrawing functional group such as C=O, S=O,
P=O, or B=O.
Stabilization of NaOBr is desirable to prevent
disproportionation into halates and halides upon storage.
As a result of stabilization, these biocides can be
stored more safely since less bromate is generated, fewer
organic molecules containing halogens are formed, and
volatility is reduced. A stabilized aqueous alkali or
alkaline earth metal hypobromite solution may be prepared
in the following fashion:
a. Mixing an aqueous solution of alkali or alkaline
earth metal hypochlorite having from about 5 percent to
about 70 percent available halogen as chlorine with a
water soluble bromide ion source;
b. Allowing the bromide ion source and the alkali
or alkaline earth metal hypochlorite to react to form a
0.5 to 70 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;
c. Adding to the unstabilized solution of alkali or
alkaline earth metal hypobromite an aqueous solution of
an alkali metal sulfamate in a quantity to provide a
molar ratio of alkali metal sulfamate to alkali or
alkaline earth metal hypobromite from about 0.5 to about
7; and
d. Recovering a stabilized aqueous alkali or
alkaline earth metal hypobromite solution.
The stabilized sodium hypobromite utilized herein
(STABREX®) is available from Nalco Chemical Company of
Naperville, IL.
The synergistic composition of this invention may be
added separately to an industrial fluid or may be
formulated as a simple mixture comprising its essential
ingredients.
It may be the case that the stabilized sodium
hypobromite will act synergistically against
microorganisms when combined with other non-oxidizing
biocides or surfactants. It is expected that the above
detailed description would also apply to a composition
and method for controlling macrobiological growth in
industrial fluids comprising a combination of stabilized
sodium hypobromite with other non-oxidizing biocides.
Examples of other non-oxidizing biocides include
glutaraldehyde, 2,2-dibromo-3-nitrilopropionamide
(DBNPA), 2-bromo-2-nitropropane-l,3 diol, 1-bromo-l-
(bromomethyl)-1,3-propanedicarbonitrile,
tetrachloroisophthalonitrile, alkyldimethylbenzylammonium
chloride (ADBAC), dimethyl dialkyl ammonium chloride,
poly (oxyethylene (dimethyliminio) ethylene (diemethyliminio)
ethylene dichloride, methylene bisthiocyanate (MBT), 2-
decylthioethanamine (DTEA) , tetrakishydroxymethyl
phosphonium sulfate (THPS), dithiocarbamate,
cyanodithioimidocarbonate, 2-methyl-5-nitroimidazole-1-
ethanol, 2-(2-bromo-2-nitroethenyl) furan (BNEF), beta-
bromo-beta-nitrostyrene (BNS), beta-nitrostyrene (NS),
beta-nitrovinyl furan (NVF) , 2-bromo-2-bromomethyl-
glutaronitrile (BBMGN), bis(trichloromethyl) sulfone, S-
(2-hydroxypropyl)thiomethanesulfonate, tetrahydro-3,5-
dimethyl-2H-l,3,5-hydrazine-2-thione, 2-
(thiocyanomethylthio)benzothiazole (TCTMB), 2-bromo-4"-
hydroxyacetophenone, 1,4-bis (bromoacetoxy) -2-butene,
bis(tributyltin)oxide (TBTO), copper sulfate, 2-(tert-
butylamino)-4-chloro-6-(ethylamino)-s-triazine,
dodecylguanidine acetate and dodecylguanadine
hydrochloride (DGH).
EXAMPLES
The following examples are intended to be
illustrative of the present invention and to teach one of
ordinary skill how to make and use the invention. These
examples are not intended to limit the invention or its
protection in any way.
Synergism was determined in each of the Examples
below by an industrially accepted method as described by
Kull, F.C., Eisman, P.C., Sylwestrowicz, H.D. and Mayer,
R.L. in Applied Microbiology, 9:538-541 (1961), using the
equation for the calculation of a synergy index
determined by:
Qa/QA + Qb/QB = Synergy Index (S.I.)
wherein
QA = concentration of compound A in parts per million
(ppm) acting alone, which produced an endpoint;
Qa = concentration of compound A in ppm, in the
mixture, which produced an endpoint;
Qs = concentration of compound B in ppm acting alone
which produced an endpoint;
Qb = concentration of compound B in ppm, in the
mixture, which produced an
endpoint.
When the sum of Qa/QA and Qb/QB is greater than 1.0,
antagonism is indicated. When the sum is equal to 1.0,
additivity is indicated, and when the sum is less than
1.0, synergy is demonstrated.
Example 1
Chloralla sorokiniana green algae were grown in
Proteose medium for three weeks, harvested by
centrifugation, and resuspended in synthetic cooling
water (pH 8.2). For the assay, 96-well tissue culture
microplate (FALCON® 3075) wells were prepared with 200 uL
of the indicated biocides in synthetic cooling water.
100 uL of a Chlorella sorokiniana cell suspension [10"
Colony Forming Units (CFU) per mL] were inoculated into
each microplate well providing a 300 uL total volume.
Microplates were covered with the provided lid and
incubated at 25°C for six days with 16 hour/8 hour
light/dark cycles (cool-white fluorescent lamps, 1255
lux) . Following incubation, the supernatant from each
microplate well was removed by aspiration and chlorophyll
was extracted from the remaining cells using
dimethylsulfoxide (DMSO) . The reduction in algae cell
chlorophyll content due to algicidal activity was
measured using the optical density at 650 ran (Beckman
Biomek® plate reader) of each extraction. As shown below
in Table 1, synergy was indicated.
Example 2
The test protocol described above in Example 1 was
utilized. However, for this example, the test inoculum
was 100 pL of Scenedesmus obliquus green algae (106
CFU/mL). As shown below in Table 2, synergy was
indicated.
harvested by centrifugation, and resuspended in synthetic
cooling water (pH 8.2). For the assay, 12-well tissue
culture microplate (FALCON®) wells were prepared with 4 mL
algae suspension (OD664nm, = 0.15) and dosed with the
indicated biocide. Plates were incubated at 25°C for 24
hours with continuous illumination. Following
incubation, a 1 mL sample from each microplate well was
removed and chlorophyll in each sample was measured using
extraction with 90% acetone and a standard trichromatic
spectrophotometric procedure [Standard Methods for the
Examination of Water and Wastewater, 19th edition (1995)].
The results are shown below in Table 3 and are reported
as percent reduction in chlorophyll relative to an
untreated control culture. Synergy was indicated.
While the present invention is described above in
connection with preferred or illustrative embodiments,
these embodiments are not intended to be exhaustive or
limiting of the invention. Rather, the invention is
intended to cover all alternatives, modifications and
equivalents included within its spirit and scope, as
defined by the appended claims.
WE CLAIM
1. A composition for controlling biological growth in
industrial fluids comprising effective amounts of
stabilized sodium hypobromite and at least one compound
selected from the group consisting of coco
alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic
acid and 4 , 5-dichloro-2-n-octyl-4-isothiazoline-3-one .
2. The composition of claim 1 wherein the biological
growth is microbiological growth.
3. The composition of claim 2 wherein the
microbiological growth is selected from the group
consisting of bacteria, fungi, algae and combinations
thereof.
4. The composition of claim 1 wherein the biological
growth is macrobiological growth.
5. The composition of claim 4 wherein the
macrobiological growth is selected from the group
consisting of zebra mussels, blue mussels and the Asiatic
clam.
6. The composition of claim 1 wherein the stabilized
sodium hypobromite is sodium hypobromite stabilized with
sodium sulfamate.
7. The composition of claim 6 wherein the sodium
hypobromite is stabilized
with an alkali metal sulfamate.
8. The composition of claim 6 wherein the sodium
hypobromite is stabilized with an acid amide derivative
selected from the group consisting of carbonic acids,
hydrogen cyanide, carboxylic acids, amino acids, sulfuric
acids, phosphoric acids and boric acids.
9. The composition of claim 1 wherein the industrial
fluids are selected from the group consisting of cooling
waters; food, beverage and industrial process waters;
pulp and paper mill systems; brewery pasteurizers;
sweetwater systems; air washer systems; oil field
drilling fluids and muds; petroleum recovery processes;
industrial lubricants; cutting fluids; heat transfer
systems; gas scrubber systems; latex systems; clay and
pigment systems; decorative fountains; water intake
pipes; ballast water tanks and ship reservoirs.
10. The composition of claim 1 wherein the amount of
stabilized sodium hypobromite
ranges from about 0.05 ppm to about 1000 ppm total
residual oxidant and the amount of the compound selected
from the group consisting of coco alkyldimethylamine
oxide, n-coco alkyltrimethylenediamine, tetra-alkyl
phosphonium chloride, 7-oxabicyclo [2.2.1] heptane-2, 3-
dicarboxylic acid and 4,5-dichloro-2-n-octyl-4-
isothiazoline-3-one ranges from about 0.05 ppm to about
1000 ppm active ingredient.
11. A method of controlling biological growth in an
industrial fluid which comprises the step of adding to
the industrial fluid effective biological growth
controlling amounts of stabilized sodium hypobromite and
at least one compared selected from the group consisting
of coco alkyldimethylamine oxide, n-coco
alkyltrimethylenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1] heptane-2, 3-dicarboxylic
acid and 4, 5-dichloro-2-n-octyl-4-isothiazoline-3-one.
12. The method of claim 11 wherein the biological growth
is microbiological growth.
13. The method of claim 12 wherein the microbiological
growth is selected from the group consisting of bacteria,
fungi, algae and combinations thereof.
14. The method of claim 11, wherein the biological growth is
macrobiological growth.
15. The method of claim 14, wherein the macrobiological growth is
selected from the group consisting of zebra mussels, blue mussels
and the Asiatic clam.
16.The method of claim 11, wherein the Industrial fluid Is selected
from the group consisting of : cooling waters; food, beverage and
industrial process waters; pulp and paper mill systems; brewery
pasteurizers; sweetwater systems; air washer systems; oi) field
drilling fluids and muds; petroleum recovery processes; Industrial
lubricants; cutting fluids; heat transfer systems; gas scrubber
systems; latex systems; clay and pigment systems; decorative
fountains; water intake pipes; ballast water tanks and ship
reservoirs.
17. The method of claim 11, wherein the amount of stabilized
sodium hypobromite ranges from about 0.05 ppm to about 1000
ppm total residual oxidant and the amountof the compound
selected from the group consisting of coco alkyldimethylarrine
oxide, n-coco alkyltrimethytenediamine, tetra-alkyl phosphonium
chloride, 7-oxabicyclo [2.2.1]heptane-2,3-dicarboxylic acid and
4,5-dlchioro-2-2-n-octyL-4-lsothiazollne-3-one ranges from about
0.05 ppm to about 1000 ppm active ingredient.
Composition and method for controlling biological
growth using stabilized sodium hypobtomite In
synerglstic combinations.
A synergistic composition and method for controlling biological
growth in Industrial fluids are disclosed, wherein the composition
comprises stabilized sodium hypobnomlte and at least one
compound selected from the group consisting of coco
alkyldimethylamine oxide, n-coco alkyltrimethyienedlamine, tetra-
alkyl phosphonium chloride, 7-oxablcyclo[2.2.1]heptane-2.3-
dicarboxylic acid and 4.5-dichloro-2-n-octy)-4-isothiazoline-3-one.

Documents:

IN-PCT-2002-143-KOL-FORM-27.pdf

in-pct-2002-143-kol-granted-abstract.pdf

in-pct-2002-143-kol-granted-assignment.pdf

in-pct-2002-143-kol-granted-claims.pdf

in-pct-2002-143-kol-granted-correspondence.pdf

in-pct-2002-143-kol-granted-description (complete).pdf

in-pct-2002-143-kol-granted-examination report.pdf

in-pct-2002-143-kol-granted-form 1.pdf

in-pct-2002-143-kol-granted-form 18.pdf

in-pct-2002-143-kol-granted-form 2.pdf

in-pct-2002-143-kol-granted-form 26.pdf

in-pct-2002-143-kol-granted-form 3.pdf

in-pct-2002-143-kol-granted-form 5.pdf

in-pct-2002-143-kol-granted-letter patent.pdf

in-pct-2002-143-kol-granted-reply to examination report.pdf

in-pct-2002-143-kol-granted-specification.pdf

in-pct-2002-143-kol-granted-translated copy of priority document.pdf


Patent Number 214000
Indian Patent Application Number IN/PCT/2002/143/KOL
PG Journal Number 04/2008
Publication Date 25-Jan-2008
Grant Date 23-Jan-2008
Date of Filing 29-Jan-2002
Name of Patentee NALCO CHEMICAL COMPANY
Applicant Address ONE NALCO CENTER, NAPERVILLE IL 60563-1198
Inventors:
# Inventor's Name Inventor's Address
1 COOPER, ANDREW, J. 309 TAFT DRIVE OSWEGO, IL 60543
2 DALLMIER, ANTHONY, W. 1683 KAUTZ ROAD, AURORA, IL 60504
3 KELLY, ROBERT, F. 260 MORGAN VALLEY DRIVE OSWEGO, IL 60543
4 MCCOY, WILLIAM, F. 735 THORNAPPLE DRIVE, NAPERVILLE, IL 60540
5 MA, XI 339 CLEMENTI AVENUE 3, NO.07-272 SINGAPORE MORGAN, OSWEGO, IL 60543
PCT International Classification Number A 01 N
PCT International Application Number PCT/US00/20962
PCT International Filing date 2000-08-01
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 09/373,288 1999-08-12 U.S.A.