NL8303003A - Bescherming van oplossingen, emulsies en dispersies in water. - Google Patents

Bescherming van oplossingen, emulsies en dispersies in water. Download PDF

Info

Publication number: NL8303003A
Authority: NL; Netherlands
Prior art keywords: water; reaction; quaternary ammonium; protected; ammonium compound
Prior art date: 1983-06-20

Application number

NL8303003A

Other languages

English (en)

Dutch (nl)

Original Assignee

Buckman Labor Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-06-20

Filing date

1983-08-29

Publication date

1985-01-16

1983-08-29 Application filed by Buckman Labor Inc filed Critical Buckman Labor Inc

1985-01-16 Publication of NL8303003A publication Critical patent/NL8303003A/nl

Links

XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 22
239000000839 emulsion Substances 0.000 title claims description 20
239000006185 dispersion Substances 0.000 title description 9
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 36
238000000034 method Methods 0.000 claims description 19
235000010299 hexamethylene tetramine Nutrition 0.000 claims description 18
239000004312 hexamethylene tetramine Substances 0.000 claims description 18
229960004011 methenamine Drugs 0.000 claims description 18
238000006243 chemical reaction Methods 0.000 claims description 14
239000000243 solution Substances 0.000 claims description 14
239000003973 paint Substances 0.000 claims description 13
150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 9
239000000725 suspension Substances 0.000 claims description 9
230000015556 catabolic process Effects 0.000 claims description 6
229940106681 chloroacetic acid Drugs 0.000 claims description 6
238000006731 degradation reaction Methods 0.000 claims description 6
244000005700 microbiome Species 0.000 claims description 6
-1 aluminum compound Chemical class 0.000 claims description 5
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 5
239000002173 cutting fluid Substances 0.000 claims description 5
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 claims description 4
150000002366 halogen compounds Chemical class 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 claims description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
230000002906 microbiologic effect Effects 0.000 claims description 3
239000011591 potassium Chemical group 0.000 claims description 3
229910052700 potassium Inorganic materials 0.000 claims description 3
230000001681 protective effect Effects 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Chemical group 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
238000005520 cutting process Methods 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
239000007788 liquid Substances 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
239000007900 aqueous suspension Substances 0.000 claims 2
229910052782 aluminium Inorganic materials 0.000 claims 1
230000002401 inhibitory effect Effects 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
239000000203 mixture Substances 0.000 description 9
239000007787 solid Substances 0.000 description 9
239000000758 substrate Substances 0.000 description 9
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
238000011081 inoculation Methods 0.000 description 8
239000000047 product Substances 0.000 description 8
150000003242 quaternary ammonium salts Chemical class 0.000 description 8
159000000000 sodium salts Chemical class 0.000 description 7
239000012266 salt solution Substances 0.000 description 6
241000894006 Bacteria Species 0.000 description 5
239000003223 protective agent Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000001993 wax Substances 0.000 description 5
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
238000011534 incubation Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229920002472 Starch Polymers 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
150000002825 nitriles Chemical class 0.000 description 3
239000006916 nutrient agar Substances 0.000 description 3
235000019645 odor Nutrition 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
235000019698 starch Nutrition 0.000 description 3
229920001817 Agar Polymers 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
239000008272 agar Substances 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000003599 detergent Substances 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
WBJINCZRORDGAQ-UHFFFAOYSA-N ethyl formate Chemical compound CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
235000018102 proteins Nutrition 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000002002 slurry Substances 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000008107 starch Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
239000004408 titanium dioxide Substances 0.000 description 2
JUIKUQOUMZUFQT-UHFFFAOYSA-N 2-bromoacetamide Chemical compound NC(=O)CBr JUIKUQOUMZUFQT-UHFFFAOYSA-N 0.000 description 1
AUHYZQCEIVEMFH-UHFFFAOYSA-N 2-bromopropanamide Chemical compound CC(Br)C(N)=O AUHYZQCEIVEMFH-UHFFFAOYSA-N 0.000 description 1
MONMFXREYOKQTI-UHFFFAOYSA-N 2-bromopropanoic acid Chemical compound CC(Br)C(O)=O MONMFXREYOKQTI-UHFFFAOYSA-N 0.000 description 1
OEZPDHRXGCLGKB-UHFFFAOYSA-N 2-chloropropanamide Chemical compound CC(Cl)C(N)=O OEZPDHRXGCLGKB-UHFFFAOYSA-N 0.000 description 1
GAWAYYRQGQZKCR-UHFFFAOYSA-N 2-chloropropionic acid Chemical compound CC(Cl)C(O)=O GAWAYYRQGQZKCR-UHFFFAOYSA-N 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
244000063299 Bacillus subtilis Species 0.000 description 1
235000014469 Bacillus subtilis Nutrition 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
229920002261 Corn starch Polymers 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
241000588747 Klebsiella pneumoniae Species 0.000 description 1
229920000388 Polyphosphate Polymers 0.000 description 1
241000588767 Proteus vulgaris Species 0.000 description 1
241000589517 Pseudomonas aeruginosa Species 0.000 description 1
241001103617 Pseudomonas aeruginosa ATCC 15442 Species 0.000 description 1
241001138501 Salmonella enterica Species 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
229940037003 alum Drugs 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
238000006065 biodegradation reaction Methods 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000011109 contamination Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
239000010730 cutting oil Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
239000000976 ink Substances 0.000 description 1
239000002054 inoculum Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920001206 natural gum Polymers 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
229940007042 proteus vulgaris Drugs 0.000 description 1
238000005956 quaternization reaction Methods 0.000 description 1
238000007789 sealing Methods 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000004753 textile Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment

Landscapes

Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Zoology (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Environmental Sciences (AREA)
Hydrology & Water Resources (AREA)
Environmental & Geological Engineering (AREA)
Water Supply & Treatment (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Paints Or Removers (AREA)

NL8303003A 1983-06-20 1983-08-29 Bescherming van oplossingen, emulsies en dispersies in water. NL8303003A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US50558283		1983-06-20
US06/505,582 US4505831A (en)	1983-06-20	1983-06-20	Method of preservation of aqueous systems by addition to said systems of quaternary ammonium salts of hexamethylenetetramine

Publications (1)

Publication Number	Publication Date
NL8303003A true NL8303003A (nl)	1985-01-16

Family

ID=24010927

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8303003A NL8303003A (nl)	1983-06-20	1983-08-29	Bescherming van oplossingen, emulsies en dispersies in water.

Country Status (19)

Country	Link
US (1)	US4505831A (fr)
JP (1)	JPS604107A (fr)
AR (1)	AR231694A1 (fr)
AU (1)	AU555164B2 (fr)
BE (1)	BE897629A (fr)
BR (1)	BR8306152A (fr)
CA (1)	CA1202433A (fr)
DE (1)	DE3332160A1 (fr)
ES (1)	ES8702879A1 (fr)
FI (1)	FI73575C (fr)
FR (1)	FR2547484B1 (fr)
GB (1)	GB2141704B (fr)
IT (1)	IT1200930B (fr)
MX (1)	MX166140B (fr)
NL (1)	NL8303003A (fr)
NO (1)	NO160893C (fr)
NZ (1)	NZ205424A (fr)
PH (1)	PH19046A (fr)
SE (1)	SE8304591L (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4650866A (en) *	1986-03-06	1987-03-17	Buckman Laboratories, Inc.	Process of preparing 1-methyl-3,5,7-triaza-1-azoniatricyclodecane halides
US5245031A (en) *	1988-03-29	1993-09-14	Buckman Laboratories International, Inc.	1-methyl-3,5,7-triaza-1-azoniatricyclodecane compounds, a method for preparing these compounds, their use in the control of microorganisms in aqueous systems, and their use in the inhibition of corrosion
US4920107A (en) *	1988-03-29	1990-04-24	Buckman Laboratories International, Inc.	1-methyl-3,5,7-triaza-1-azoniatricyclodecane compounds, a method for preparing these compounds, and their use in the control of microorganisms in aqueous systems
US5061797A (en) *	1988-03-29	1991-10-29	Buckman Laboratories International, Inc.	1-methyl-3,5,7-triaza-1-azoniatricyclodecane compounds
US4892583A (en) *	1988-11-04	1990-01-09	Buckman Laboratories International, Inc.	1-Methyl-3,5,7-triaza-1-azoniatricyclodecane triiodide, a method of preparation, and its use in the control of microorganisms in aqueous systems
US5023332A (en) *	1988-11-04	1991-06-11	Buckman Laboratories International, Inc.	1-methyl-3,5,7-triaza-1-azoniatricyclodecane triiodide
NZ254769A (en) *	1992-08-03	1996-02-27	Henkel Kgaa	Lubricant and lubricant solution; based on fatty amines and contains at least one linear polyamine derivative of a fatty amine
RU2259955C1 (ru) *	2004-07-06	2005-09-10	Волгоградский государственный технический университет (ВолгГТУ)	Способ очистки природных и сточных вод от взвешенных веществ и микроорганизмов
US9131683B2 (en)	2011-09-30	2015-09-15	The Sherwin-Williams Company	High quality antimicrobial paint composition

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2264999A (en) *	1939-07-15	1941-12-02	Standard Oil Co	Manufacture of lubricants
US3228829A (en) *	1963-11-04	1966-01-11	Dow Chemical Co	Preservation of aqueous dispersions
US3244710A (en) *	1963-12-23	1966-04-05	Dow Chemical Co	Iodine complexes of hexamethylene-tetramine quaternary salts
US3624254A (en) *	1970-03-05	1971-11-30	Dow Chemical Co	Hexamethylenetetramine adducts with haloacetonitriles
US3624253A (en) *	1970-03-05	1971-11-30	Dow Chemical Co	Hexamethylenetetramine adducts with haloacetic acid esters
US3928607A (en) *	1973-10-05	1975-12-23	Cosan Chem Corp	Antibacterial composition and method employing a certain hexamethylenetetramine adduct
US4160089A (en) *	1973-10-18	1979-07-03	Aquila S.P.A.	Utilization of orthophosphoric esters for the production of aqueous fluids for working metals
US3936451A (en) *	1974-08-27	1976-02-03	United States Pipe And Foundry Company	Process for producing salts of hexamethylenetetramine
CH615696A5 (fr) *	1975-08-05	1980-02-15	Alusuisse
US4188386A (en) *	1977-11-07	1980-02-12	Meggle Milchindustrie Gmbh & Co. Kg	Compositions containing thiocyanic acid and hexamethylene-tetramine, production process and administration thereof as bactericide and mycocide

1983
- 1983-06-20 US US06/505,582 patent/US4505831A/en not_active Expired - Lifetime
- 1983-08-23 NO NO833028A patent/NO160893C/no unknown
- 1983-08-24 SE SE8304591A patent/SE8304591L/xx unknown
- 1983-08-26 AR AR294019A patent/AR231694A1/es active
- 1983-08-29 NL NL8303003A patent/NL8303003A/nl not_active Application Discontinuation
- 1983-08-30 NZ NZ205424A patent/NZ205424A/en unknown
- 1983-08-31 BE BE0/211428A patent/BE897629A/fr not_active IP Right Cessation
- 1983-08-31 CA CA000435809A patent/CA1202433A/fr not_active Expired
- 1983-09-05 AU AU18724/83A patent/AU555164B2/en not_active Ceased
- 1983-09-06 DE DE19833332160 patent/DE3332160A1/de not_active Ceased
- 1983-09-07 ES ES525436A patent/ES8702879A1/es not_active Expired
- 1983-09-09 FI FI833233A patent/FI73575C/fi not_active IP Right Cessation
- 1983-09-27 MX MX198864A patent/MX166140B/es unknown
- 1983-10-05 FR FR838315853A patent/FR2547484B1/fr not_active Expired
- 1983-10-11 JP JP58189788A patent/JPS604107A/ja active Pending
- 1983-11-09 BR BR8306152A patent/BR8306152A/pt not_active IP Right Cessation
- 1983-11-29 IT IT49403/83A patent/IT1200930B/it active
1984
- 1984-01-26 GB GB08402067A patent/GB2141704B/en not_active Expired
- 1984-02-03 PH PH30197A patent/PH19046A/en unknown

Also Published As

Publication number	Publication date
IT8349403A0 (it)	1983-11-29
SE8304591L (sv)	1984-12-21
ES525436A0 (es)	1987-01-16
SE8304591D0 (sv)	1983-08-24
CA1202433A (fr)	1986-03-25
BR8306152A (pt)	1985-02-20
FI73575B (fi)	1987-07-31
FR2547484A1 (fr)	1984-12-21
US4505831A (en)	1985-03-19
NO160893B (no)	1989-03-06
GB2141704A (en)	1985-01-03
NO160893C (no)	1989-06-14
FI73575C (fi)	1987-11-09
FI833233A0 (fi)	1983-09-09
FR2547484B1 (fr)	1989-04-07
GB2141704B (en)	1987-08-05
BE897629A (fr)	1983-12-16
NZ205424A (en)	1986-06-11
AU555164B2 (en)	1986-09-11
NO833028L (no)	1984-12-21
PH19046A (en)	1985-12-11
IT1200930B (it)	1989-01-27
JPS604107A (ja)	1985-01-10
AU1872483A (en)	1985-01-03
FI833233L (fi)	1984-12-21
ES8702879A1 (es)	1987-01-16
AR231694A1 (es)	1985-02-28
GB8402067D0 (en)	1984-02-29
DE3332160A1 (de)	1984-12-20
MX166140B (es)	1993-12-21

Legal Events

Date	Code	Title
1988-08-01	BA	A request for search or an international-type search has been filed
1988-08-01	BB	A search report has been drawn up
1988-10-03	BC	A request for examination has been filed
1991-04-02	BV	The patent application has lapsed

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