RU2001114505A - SUITABLE FOR REPEATED DISPERSION IN WATER GRANULES CONTAINING ACTIVE SUBSTANCE IN LIQUID VIEW - Google Patents
SUITABLE FOR REPEATED DISPERSION IN WATER GRANULES CONTAINING ACTIVE SUBSTANCE IN LIQUID VIEWInfo
- Publication number
- RU2001114505A RU2001114505A RU2001114505/04A RU2001114505A RU2001114505A RU 2001114505 A RU2001114505 A RU 2001114505A RU 2001114505/04 A RU2001114505/04 A RU 2001114505/04A RU 2001114505 A RU2001114505 A RU 2001114505A RU 2001114505 A RU2001114505 A RU 2001114505A
- Authority
- RU
- Russia
- Prior art keywords
- paragraphs
- granules according
- monomer
- radical
- cooh
- Prior art date
Links
- 239000008187 granular material Substances 0.000 title claims 29
- 239000000126 substance Substances 0.000 title claims 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims 6
- 239000007788 liquid Substances 0.000 title claims 2
- 239000006185 dispersion Substances 0.000 title 1
- -1 alkyl radical Chemical class 0.000 claims 18
- 239000000178 monomer Substances 0.000 claims 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 13
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 12
- 150000003254 radicals Chemical class 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 9
- 229920000642 polymer Polymers 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 7
- 125000004122 cyclic group Chemical group 0.000 claims 6
- 239000002736 nonionic surfactant Substances 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 5
- 125000001931 aliphatic group Chemical group 0.000 claims 5
- 125000004432 carbon atoms Chemical group C* 0.000 claims 5
- 238000001035 drying Methods 0.000 claims 5
- 125000005842 heteroatoms Chemical group 0.000 claims 4
- 150000002430 hydrocarbons Chemical class 0.000 claims 4
- 230000002209 hydrophobic Effects 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 claims 4
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N Methyl radical Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- 150000008064 anhydrides Chemical class 0.000 claims 3
- 239000000839 emulsion Substances 0.000 claims 3
- TUSBCMPNIOJUBX-UHFFFAOYSA-N 2,3,3-trimethylpent-1-ene Chemical compound CCC(C)(C)C(C)=C TUSBCMPNIOJUBX-UHFFFAOYSA-N 0.000 claims 2
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 claims 2
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methylpent-1-ene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-UHFFFAOYSA-N 0.000 claims 2
- RYKZRKKEYSRDNF-UHFFFAOYSA-N 3-methylidenepentane Chemical compound CCC(=C)CC RYKZRKKEYSRDNF-UHFFFAOYSA-N 0.000 claims 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-Methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims 2
- 230000000875 corresponding Effects 0.000 claims 2
- 150000004676 glycans Polymers 0.000 claims 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims 2
- 229920001184 polypeptide Polymers 0.000 claims 2
- 229920001282 polysaccharide Polymers 0.000 claims 2
- 239000005017 polysaccharide Substances 0.000 claims 2
- 150000004804 polysaccharides Polymers 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-Dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 claims 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- IJFYMXHTVPNBRP-UHFFFAOYSA-N 2,3-bis(2-phenylethyl)phenol Chemical class C=1C=CC=CC=1CCC=1C(O)=CC=CC=1CCC1=CC=CC=C1 IJFYMXHTVPNBRP-UHFFFAOYSA-N 0.000 claims 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical class CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims 1
- 229960005261 Aspartic Acid Drugs 0.000 claims 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 claims 1
- 240000008886 Ceratonia siliqua Species 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical class C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- 240000005497 Cyamopsis tetragonoloba Species 0.000 claims 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N DL-aspartic acid Chemical compound OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 claims 1
- 229920002307 Dextran Polymers 0.000 claims 1
- 229920000926 Galactomannan Polymers 0.000 claims 1
- 229960002989 Glutamic Acid Drugs 0.000 claims 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 229920002774 Maltodextrin Polymers 0.000 claims 1
- 239000005913 Maltodextrin Substances 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N Methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- JNYAEWCLZODPBN-CTQIIAAMSA-N Sorbitan Chemical class OCC(O)C1OCC(O)[C@@H]1O JNYAEWCLZODPBN-CTQIIAAMSA-N 0.000 claims 1
- 229920002472 Starch Polymers 0.000 claims 1
- 229940032147 Starch Drugs 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 125000004948 alkyl aryl alkyl group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 235000003704 aspartic acid Nutrition 0.000 claims 1
- 125000004429 atoms Chemical group 0.000 claims 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical class CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 229960002086 dextran Drugs 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- 235000013305 food Nutrition 0.000 claims 1
- 235000013922 glutamic acid Nutrition 0.000 claims 1
- 239000004220 glutamic acid Substances 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- 239000002563 ionic surfactant Substances 0.000 claims 1
- 229940035034 maltodextrin Drugs 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 150000002823 nitrates Chemical class 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 125000005245 nitryl group Chemical group [N+](=O)([O-])* 0.000 claims 1
- 125000004430 oxygen atoms Chemical group O* 0.000 claims 1
- 239000003973 paint Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 230000000379 polymerizing Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M propionate Chemical class CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- 239000008107 starch Substances 0.000 claims 1
- 235000019698 starch Nutrition 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 150000003626 triacylglycerols Chemical class 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 239000003643 water by type Substances 0.000 claims 1
- 229920001285 xanthan gum Polymers 0.000 claims 1
- 239000000230 xanthan gum Substances 0.000 claims 1
- 229940082509 xanthan gum Drugs 0.000 claims 1
- 235000010493 xanthan gum Nutrition 0.000 claims 1
Claims (26)
(R1)(R1)-С= (CR1)-COOH (I)
в которой радикалы R1, одинаковые или разные, обозначают атом водорода, C1-С10-углеводородный радикал, который может содержать группу -СООН, группу -СООН; и по меньшей мере одного мономера формулы III:
CH2= C(R3)-C(O)-O-[CH2CH(R4)O] m-[CH(R5)CH2O] n-R6
в которой R3 обозначает атом водорода или радикал метил;
R4 и R5, одинаковые или разные, обозначают атом водорода или алкильный радикал с 1-4 атомами углерода;
R6 обозначает радикал алкил, арил, алкиларил или арилалкил, содержащие от 1 до 30, преимущественно от 8 до 30, атомов углерода;
n равно от 2 до 100, преимущественно от 6 до 100;
m равно от 0 до 50, при условии, что n больше или равно m, а их сумма составляет от 2 до 100, преимущественно от 6 до 100;
и возможно по меньшей мере одного мономера формулы II
(R2)(R2)-С= СН2 (II)
в которой радикалы R2, одинаковые или разные, обозначают атом водорода, нормальный или разветвленный алифатический или циклический C1-С10-радикал.2. Granules under item 1, characterized in that the polymer (i) is obtained by polymerization of at least one monomer of formula I
(R 1 ) (R 1 ) -C = (CR 1 ) -COOH (I)
in which the radicals R 1 , identical or different, denote a hydrogen atom, a C 1 -C 10 -hydrocarbon radical, which may contain a group -COOH, a group -COOH; and at least one monomer of formula III:
CH 2 = C (R 3 ) -C (O) -O- [CH 2 CH (R 4 ) O] m - [CH (R 5 ) CH 2 O] n -R 6
in which R 3 denotes a hydrogen atom or a methyl radical;
R 4 and R 5 , the same or different, represent a hydrogen atom or an alkyl radical with 1-4 carbon atoms;
R 6 is an alkyl, aryl, alkylaryl or arylalkyl radical containing from 1 to 30, preferably from 8 to 30, carbon atoms;
n is from 2 to 100, preferably from 6 to 100;
m is from 0 to 50, provided that n is greater than or equal to m, and their sum is from 2 to 100, preferably from 6 to 100;
and possibly at least one monomer of formula II
(R 2 ) (R 2 ) -C = CH 2 (II)
in which the radicals R 2 , identical or different, denote a hydrogen atom, a normal or branched aliphatic or cyclic C 1 -C 10 radical.
(R1)(R1)-C= C(R1)-COOH (I)
в которой радикалы R1, одинаковые или разные, обозначают атом водорода или C1-С10-углеводородный радикал, который может содержать группу -СООН, группу -СООН; и по меньшей мере одного мономера формулы II'
(R2)(R2)-С= СН2 (II')
в которой радикалы R2, одинаковые или разные, обозначают атом водорода, нормальный или разветвленный алифатический или циклический, насыщенный или этиленовоненасыщенный С2-С10-радикал при условии, что оба радикала не могут быть атомами водорода.3. Granules under item 1, characterized in that the polymer (i) is obtained by polymerization: at least one monomer of the formula I
(R 1 ) (R 1 ) -C = C (R 1 ) -COOH (I)
in which the radicals R 1 , which are the same or different, designate a hydrogen atom or a C 1 -C 10 -hydrocarbon radical, which may contain a group -COOH, a group -COOH; and at least one monomer of formula II ′
(R 2 ) (R 2 ) -C = CH 2 (II ')
in which the radicals R 2 , identical or different, denote a hydrogen atom, a normal or branched aliphatic or cyclic, saturated or ethylenically unsaturated C 2 -C 10 radical, provided that both radicals cannot be hydrogen atoms.
(R11)HC= C(R12)-COOH
в которой R11 обозначает атом водорода, группу -СООН или группу -(СН2)n-COOH, в которой n равно от 1 до 4, или радикал C1-C4-алкил; R12 обозначает атом водорода, группу-(CH2)m-COOH, в которой m равно от 1 до 4, или С1-С4-алкильный радикал.4. Granules according to any one of paragraphs. 1-3, characterized in that the monomer I of polymer (i) or (ii) is monocarboxylic or polycarboxylic acid or carboxylic anhydride corresponding to the following formula:
(R 11 ) HC = C (R 12 ) -COOH
in which R 11 represents a hydrogen atom, a —COOH group, or a - (CH 2 ) n —COOH group in which n is from 1 to 4, or a C 1 -C 4 alkyl radical; R 12 represents a hydrogen atom, a group - (CH 2 ) m —COOH, in which m is from 1 to 4, or a C 1 -C 4 alkyl radical.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9813682A FR2785198B1 (en) | 1998-10-30 | 1998-10-30 | WATER REDISPERSABLE GRANULES COMPRISING AN ACTIVE MATERIAL IN LIQUID FORM |
FR98/13682 | 1998-10-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2001114505A true RU2001114505A (en) | 2003-04-20 |
RU2218363C2 RU2218363C2 (en) | 2003-12-10 |
Family
ID=9532213
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2001114505/04A RU2218363C2 (en) | 1998-10-30 | 1999-11-02 | Water-redispersible granules containing active substance in liquid state |
Country Status (16)
Country | Link |
---|---|
US (1) | US6841613B1 (en) |
EP (1) | EP1141097B1 (en) |
JP (1) | JP3493001B2 (en) |
KR (1) | KR100432922B1 (en) |
CN (1) | CN1174032C (en) |
AT (1) | ATE297431T1 (en) |
AU (1) | AU757233B2 (en) |
BR (1) | BR9914971A (en) |
CA (1) | CA2349673C (en) |
DE (1) | DE69925755T2 (en) |
ES (1) | ES2241329T3 (en) |
FR (1) | FR2785198B1 (en) |
NO (1) | NO20012117L (en) |
PL (1) | PL348120A1 (en) |
RU (1) | RU2218363C2 (en) |
WO (1) | WO2000026280A1 (en) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10018812A1 (en) * | 2000-04-15 | 2001-10-25 | Cognis Deutschland Gmbh | Nonionic surfactant granulate, used in surfactant, cosmetic or pharmaceutical formulation or laundry or other detergent, is obtained by granulating and simultaneously drying aqueous surfactant paste in presence of organic polymeric carrier |
FR2815550B1 (en) * | 2000-10-20 | 2003-08-29 | Rhodia Chimie Sa | GRANULES OBTAINED BY DRYING A MULTIPLE EMULSION |
US7001872B2 (en) | 2001-06-11 | 2006-02-21 | Halliburton Energy Services, Inc. | Subterranean formation treating fluid and methods of fracturing subterranean formations |
FR2827193B1 (en) * | 2001-07-12 | 2004-04-23 | Rhodia Chimie Sa | GRANULES OBTAINED BY EMULSION DRYING COMPRISING A POLYMER AND A CONTROL AGENT |
ITMI20012366A1 (en) * | 2001-11-09 | 2003-05-09 | Farmatron Ltd | THERAPEUTIC SYSTEMS STABILIZED WITH IMMEDIATE RELEASE AND / OR MODIFIED FOR THE ORAL ADMINISTRATION OF ACTIVE AND / OR EXCIPIENT PRINCIPLES AND / OR WINGS |
FR2834225B1 (en) * | 2001-12-27 | 2004-09-24 | Rhodia Chimie Sa | GRANULES OBTAINED BY DRYING AN EMULSION COMPRISING A POLYMER AND A BONE OR BONE DERIVATIVE |
US20040116824A1 (en) * | 2002-10-01 | 2004-06-17 | L'oreal | Evaluation or diagnostic kit |
FR2845069B1 (en) | 2002-10-01 | 2005-05-27 | Oreal | APPLICATOR COMPRISING AT LEAST TWO PRODUCTS STORED SEPARATELY |
FR2852312B1 (en) * | 2003-03-10 | 2007-04-06 | Rhodia Chimie Sa | A METHOD FOR INCREASING THE HYDROFUGATION OF MINERAL BINDER COMPOSITIONS AND THE COMPOSITIONS WHICH MAY BE OBTAINED BY THIS METHOD AND THEIR USES |
FR2870673B1 (en) * | 2004-05-28 | 2006-07-14 | Rhodia Chimie Sa | SOLID FORMULATION COMPRISING A PHYTOSANITARY PRODUCT |
MX2007002957A (en) * | 2004-09-14 | 2007-05-23 | Bayer Cropscience Gmbh | Emulsifiable granules formulations with boron containing fertilisers. |
FR2878170B1 (en) * | 2004-11-22 | 2007-07-20 | Rhodia Chimie Sa | DRY EMULSION, PROCESS FOR PREPARING THE SAME, AND USES THEREOF |
GB0500956D0 (en) * | 2005-01-18 | 2005-02-23 | Unilever Plc | Improvements relating to emulsions |
CN103053516B (en) * | 2006-07-26 | 2015-07-15 | 陶氏农业科学公司 | A method of retarding crystal growth of cloquintocet-mexyl aquo-complex |
EP2061583B1 (en) * | 2006-09-14 | 2019-04-10 | Yissum Research Development Company, of The Hebrew University of Jerusalem | Organic nanoparticles obtained from microemulsions by solvent evaporation |
AR063704A1 (en) | 2006-09-14 | 2009-02-11 | Makhteshim Chem Works Ltd | PESTICIDE NANOPARTICLES OBTAINED OBTAINED FROM MICROEMULSIONS AND NANOEMULSIONS |
DE102006053894B4 (en) | 2006-11-14 | 2010-07-22 | Beiersdorf Ag | Cosmetic preparation and its concentrate with improved drying properties |
US8491212B2 (en) | 2008-03-17 | 2013-07-23 | Laboratoire Naturel Paris, Llc | Multi-functional applicator |
US8881894B2 (en) | 2008-08-21 | 2014-11-11 | Sonovia Holdings Llc | Multiple-compartment applicator |
ES2609984T3 (en) | 2012-03-02 | 2017-04-25 | Basf Se | Process for the preparation of an emulsifiable granule by mixing a pesticide emulsion with a solid dispersant and extruding the resulting paste |
KR101372943B1 (en) | 2012-06-26 | 2014-03-12 | 주식회사경농 | Method for preparing emulsifiable solid agrochemical composition comprising an inorganic salt |
DE102013208942A1 (en) * | 2013-05-15 | 2014-11-20 | Evonik Industries Ag | Superabsorbent polymers with fast absorption properties and process for its preparation |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0216297B1 (en) * | 1985-09-25 | 1991-07-03 | Mitsubishi Kasei Corporation | Water repellent composition |
FR2740360B1 (en) | 1995-10-25 | 1997-12-26 | Rhone Poulenc Chimie | WATER REDISPERSABLE GRANULES COMPRISING AN ACTIVE MATERIAL IN LIQUID FORM |
GB9211708D0 (en) * | 1992-06-03 | 1992-07-15 | Unilever Plc | Cosmetic composition |
FR2740462B1 (en) * | 1995-10-25 | 1997-12-19 | Rhone Poulenc Chimie | WATER REDISPERSABLE POWDER COMPOSITION OF FILM-FORMING POLYMERS PREPARED FROM ETHYLENICALLY UNSATURATED MONOMERS |
FR2740461B1 (en) * | 1995-10-25 | 1997-12-19 | Rhone Poulenc Chimie | WATER REDISPERSABLE POWDER COMPOSITION OF FILM-FORMING POLYMERS PREPARED FROM ETHYLENICALLY UNSATURATED MONOMERS |
FR2740357B1 (en) * | 1995-10-25 | 1997-11-28 | Rhone Poulenc Chimie | WATER REDISPERSABLE GRANULES COMPRISING A LIQUID-ACTIVE MATERIAL AND A NON-IONIC ALCOXYL SURFACTANT |
FR2774311B1 (en) | 1998-02-02 | 2000-03-17 | Rhodia Chimie Sa | WATER-DISPERSABLE GRANULES COMPRISING A HYDROPHOBIC ACTIVE MATERIAL |
US6624136B2 (en) | 1998-02-02 | 2003-09-23 | Rhodia Chimie | Water-dispersible granules comprising a fragrance in a water-soluble or water-dispersible matrix, and process for their preparation |
-
1998
- 1998-10-30 FR FR9813682A patent/FR2785198B1/en not_active Expired - Fee Related
-
1999
- 1999-11-02 WO PCT/FR1999/002667 patent/WO2000026280A1/en active IP Right Grant
- 1999-11-02 JP JP2000579663A patent/JP3493001B2/en not_active Expired - Fee Related
- 1999-11-02 DE DE69925755T patent/DE69925755T2/en not_active Expired - Lifetime
- 1999-11-02 CN CNB998138533A patent/CN1174032C/en not_active Expired - Fee Related
- 1999-11-02 KR KR10-2001-7005381A patent/KR100432922B1/en not_active IP Right Cessation
- 1999-11-02 US US09/830,766 patent/US6841613B1/en not_active Expired - Lifetime
- 1999-11-02 ES ES99950895T patent/ES2241329T3/en not_active Expired - Lifetime
- 1999-11-02 AU AU63490/99A patent/AU757233B2/en not_active Ceased
- 1999-11-02 RU RU2001114505/04A patent/RU2218363C2/en not_active IP Right Cessation
- 1999-11-02 EP EP99950895A patent/EP1141097B1/en not_active Expired - Lifetime
- 1999-11-02 CA CA002349673A patent/CA2349673C/en not_active Expired - Fee Related
- 1999-11-02 BR BR9914971-0A patent/BR9914971A/en not_active IP Right Cessation
- 1999-11-02 PL PL99348120A patent/PL348120A1/en not_active IP Right Cessation
- 1999-11-02 AT AT99950895T patent/ATE297431T1/en not_active IP Right Cessation
-
2001
- 2001-04-27 NO NO20012117A patent/NO20012117L/en not_active Application Discontinuation
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