CA1124746A - Rubber latex compounds - Google Patents

Rubber latex compounds

Info

Publication number: CA1124746A
Authority: CA; Canada
Prior art keywords: latex; sulphosuccinamate; carbon atoms; group; compound according
Prior art date: 1977-12-14
Legal status (The legal status 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 status listed.): Expired

Application number

CA317,927A

Other languages

English (en)

French (fr)

Inventor

Henry Cowx

Jean-Luc Urbain

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Solvay Solutions UK Ltd

Original Assignee

Albright and Wilson Ltd

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.)

1977-12-14

Filing date

1978-12-14

Publication date

1982-06-01

1978-12-14 Application filed by Albright and Wilson Ltd filed Critical Albright and Wilson Ltd

1982-06-01 Application granted granted Critical

1982-06-01 Publication of CA1124746A publication Critical patent/CA1124746A/en

Status Expired legal-status Critical Current

Links

229920000126 latex Polymers 0.000 title claims abstract description 45
150000001875 compounds Chemical class 0.000 title claims abstract description 34
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 26
125000000217 alkyl group Chemical group 0.000 claims abstract description 24
239000007787 solid Substances 0.000 claims abstract description 12
239000006185 dispersion Substances 0.000 claims abstract description 9
125000002947 alkylene group Chemical group 0.000 claims abstract description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract description 5
229920006173 natural rubber latex Polymers 0.000 claims abstract 2
239000004816 latex Substances 0.000 claims description 36
BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical compound NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 claims description 34
239000006260 foam Substances 0.000 claims description 18
239000000203 mixture Substances 0.000 claims description 10
239000011343 solid material Substances 0.000 claims description 5
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
229920001971 elastomer Polymers 0.000 claims description 4
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
239000005060 rubber Substances 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 3
238000001035 drying Methods 0.000 claims description 3
239000000758 substrate Substances 0.000 claims description 3
239000002174 Styrene-butadiene Substances 0.000 claims description 2
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 2
239000011115 styrene butadiene Substances 0.000 claims description 2
229920003048 styrene butadiene rubber Polymers 0.000 claims description 2
239000004088 foaming agent Substances 0.000 abstract description 12
-1 alkyl alkoxy sulpho-succinamate Chemical compound 0.000 abstract description 9
238000005187 foaming Methods 0.000 abstract description 3
239000007864 aqueous solution Substances 0.000 abstract description 2
239000000463 material Substances 0.000 abstract description 2
239000012141 concentrate Substances 0.000 abstract 1
229920006174 synthetic rubber latex Polymers 0.000 abstract 1
239000000243 solution Substances 0.000 description 25
150000001412 amines Chemical class 0.000 description 14
238000003860 storage Methods 0.000 description 12
125000005055 alkyl alkoxy group Chemical group 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 8
BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 description 7
239000000047 product Substances 0.000 description 6
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 5
150000003141 primary amines Chemical class 0.000 description 5
230000002035 prolonged effect Effects 0.000 description 5
238000003756 stirring Methods 0.000 description 5
101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 description 4
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002253 acid Substances 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
239000011149 active material Substances 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
229920001821 foam rubber Polymers 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
125000000896 monocarboxylic acid group Chemical group 0.000 description 2
239000000376 reactant Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
241000894007 species Species 0.000 description 2
239000000126 substance Substances 0.000 description 2
229910021653 sulphate ion Inorganic materials 0.000 description 2
LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241001323490 Colias gigantea Species 0.000 description 1
PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
229920000388 Polyphosphate Polymers 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
238000005915 ammonolysis reaction Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
235000006708 antioxidants Nutrition 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000010009 beating Methods 0.000 description 1
125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003349 gelling agent Substances 0.000 description 1
235000021478 household food Nutrition 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
229960002900 methylcellulose Drugs 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
TYLSDQJYPYQCRK-UHFFFAOYSA-N sulfo 4-amino-4-oxobutanoate Chemical class NC(=O)CCC(=O)OS(O)(=O)=O TYLSDQJYPYQCRK-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
MHUJKPGMUBTQJM-UHFFFAOYSA-L zinc carboxylatooxymethanethioate Chemical compound C(=S)([O-])OC(=O)[O-].[Zn+2] MHUJKPGMUBTQJM-UHFFFAOYSA-L 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/30—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by mixing gases into liquid compositions or plastisols, e.g. frothing with air
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

CA317,927A 1977-12-14 1978-12-14 Rubber latex compounds Expired CA1124746A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB5193677		1977-12-14
GB51936/77		1977-12-14

Publications (1)

Publication Number	Publication Date
CA1124746A true CA1124746A (en)	1982-06-01

Family

ID=10462017

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA317,927A Expired CA1124746A (en)	1977-12-14	1978-12-14	Rubber latex compounds

Country Status (9)

Country	Link
AU (1)	AU527402B2 (it)
BE (1)	BE872755A (it)
CA (1)	CA1124746A (it)
DE (1)	DE2854087A1 (it)
DK (1)	DK560378A (it)
FR (2)	FR2422700A1 (it)
GB (1)	GB2091720B (it)
IT (1)	IT1109650B (it)
NL (1)	NL7812121A (it)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3512335A1 (de) *	1985-04-04	1986-10-16	Bayer Ag, 5090 Leverkusen	Verzweigte sulfosuccinamidsaeure-emulgatoren zur herstellung besonders scherstabiler dispersionen
US6602839B2 (en) *	2001-01-05	2003-08-05	Huntsman Petrochemical Corporation	Advanced sulfosuccinamate surfactants
US20040256596A1 (en) *	2001-11-28	2004-12-23	Nguyen Duy T	Sulfosuccinamate surfactants as deposition inhibitors

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE832200A (fr) *	1974-08-14	1975-12-01		Esters sulfosucciniques et procede de leur preparation

1978
- 1978-12-13 DK DK560378A patent/DK560378A/da not_active Application Discontinuation
- 1978-12-13 NL NL7812121A patent/NL7812121A/xx not_active Application Discontinuation
- 1978-12-14 DE DE19782854087 patent/DE2854087A1/de not_active Withdrawn
- 1978-12-14 IT IT69857/78A patent/IT1109650B/it active
- 1978-12-14 AU AU42561/78A patent/AU527402B2/en not_active Expired
- 1978-12-14 CA CA317,927A patent/CA1124746A/en not_active Expired
- 1978-12-14 GB GB8121089A patent/GB2091720B/en not_active Expired
- 1978-12-14 FR FR7835271A patent/FR2422700A1/fr active Granted
- 1978-12-14 BE BE192311A patent/BE872755A/xx not_active IP Right Cessation
1979
- 1979-06-05 FR FR7914346A patent/FR2422631A1/fr active Granted

Also Published As

Publication number	Publication date
IT1109650B (it)	1985-12-23
IT7869857A0 (it)	1978-12-14
DK560378A (da)	1979-06-15
AU527402B2 (en)	1983-03-03
DE2854087A1 (de)	1979-07-05
FR2422700B1 (it)	1983-09-09
FR2422631A1 (fr)	1979-11-09
BE872755A (fr)	1979-06-14
GB2091720B (en)	1983-01-06
AU4256178A (en)	1979-06-21
FR2422631B1 (it)	1982-11-12
NL7812121A (nl)	1979-06-18
FR2422700A1 (fr)	1979-11-09
GB2091720A (en)	1982-08-04

Legal Events

Date	Code	Title	Description
1999-06-01	MKEX	Expiry

Publication	Publication Date	Title
CS633990A2 (en)	1991-09-15	Herbicide
DE2048331A1 (de)	1972-04-06	Feste, pulverförmige bis kornige Mittel zur Herstellung von kaltwirksamen Bleich flotten, insbesondere von kaltwirksamen blei chenden Waschlaugen, und Verfahren zur Her stellung dieser Mittel
NO176175B (no)	1994-11-07	Preparat for bruk innen agrikultur
CA1111276A (en)	1981-10-27	Herbicidal compositions
CA1124746A (en)	1982-06-01	Rubber latex compounds
US2858250A (en)	1958-10-28	Pesticidal composition containing a water dispersible lignin sulfonic acid
KR920000888B1 (ko)	1992-01-30	살충제 수화제 및 그의 제조방법
US4266965A (en)	1981-05-12	2-(α-naphthoxy)-N,N-diethyl propionamide as an aqueous flowable concentrate
KR930005279B1 (ko)	1993-06-17	무수 살충제 조성물의 제조방법
US4231912A (en)	1980-11-04	Rubber latex compounds
US3945987A (en)	1976-03-23	Carbamide adducts of polymetalophosphamate
DE2207472A1 (de)	1972-09-14	Herstellung von Ammoniumpolyphosphaten
US2662841A (en)	1953-12-15	Water-insoluble salts of dithiocarbamic acid made rapidly water dispersible and compositions thereof
US5994271A (en)	1999-11-30	Herbicidal compositions, methods of preparation and methods of use
US3554912A (en)	1971-01-12	Basic aluminum salt fire extinguishing compositions
US2156790A (en)	1939-05-02	Wettable sulphur composition
US4765926A (en)	1988-08-23	Surfactant compositions and method therefor
US2683700A (en)	1954-07-13	Latex paints stabilized against freezing
JPH07252103A (ja)	1995-10-03	種子消毒用水和剤
US3032405A (en)	1962-05-01	Process for making alkali metal metaborates and compositions containing the same
US3130036A (en)	1964-04-21	Process for preparing flakes of sodium metaborate and mixtures thereof
EP0077233A1 (fr)	1983-04-20	Poudres mouillables de substances solides hydrophobes, leur préparation et adjuvants mouillants-dispersants et non moussants utilisables à cet effet
JPS6440585A (en)	1989-02-10	Production of aqueous emulsion of tackifier polymer
GB1578319A (en)	1980-11-05	Surface-active agent compositions and processes for manufacturing and using them
US2791563A (en)	1957-05-07	Method for preparation of 7-dialkylamino-4-methyl coumarin salts and compositions containing same