CO5221054A1 - Suspensiones acuosas de materiales minerales y sus usos . - Google Patents
Suspensiones acuosas de materiales minerales y sus usos .Info
- Publication number
- CO5221054A1 CO5221054A1 CO98040804A CO98040804A CO5221054A1 CO 5221054 A1 CO5221054 A1 CO 5221054A1 CO 98040804 A CO98040804 A CO 98040804A CO 98040804 A CO98040804 A CO 98040804A CO 5221054 A1 CO5221054 A1 CO 5221054A1
- Authority
- CO
- Colombia
- Prior art keywords
- group
- acrylic
- methacrylic
- esters
- maleic
- Prior art date
Links
- 229910052500 inorganic mineral Inorganic materials 0.000 title abstract 3
- 239000011707 mineral Substances 0.000 title abstract 3
- 239000000463 material Substances 0.000 title 1
- 239000000725 suspension Substances 0.000 title 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 4
- 150000002148 esters Chemical class 0.000 abstract 4
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 4
- 239000000178 monomer Substances 0.000 abstract 4
- 150000003254 radicals Chemical class 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 230000002209 hydrophobic effect Effects 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000007900 aqueous suspension Substances 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 abstract 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 abstract 2
- 150000003673 urethanes Chemical class 0.000 abstract 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 abstract 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 abstract 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- QNIRRHUUOQAEPB-UHFFFAOYSA-N 2-(prop-2-enoylamino)butane-2-sulfonic acid Chemical class CCC(C)(S(O)(=O)=O)NC(=O)C=C QNIRRHUUOQAEPB-UHFFFAOYSA-N 0.000 abstract 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical class CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 abstract 1
- BVEFYGKIBZZLDU-UHFFFAOYSA-N 2-methylprop-2-enamide;trimethyl(propyl)azanium Chemical class CC(=C)C(N)=O.CCC[N+](C)(C)C BVEFYGKIBZZLDU-UHFFFAOYSA-N 0.000 abstract 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 abstract 1
- UDXXYUDJOHIIDZ-UHFFFAOYSA-N 2-phosphonooxyethyl prop-2-enoate Chemical compound OP(O)(=O)OCCOC(=O)C=C UDXXYUDJOHIIDZ-UHFFFAOYSA-N 0.000 abstract 1
- BRWBXCPVJZQRHJ-UHFFFAOYSA-N 2-phosphonooxypropyl 2-methylprop-2-enoate Chemical compound OP(=O)(O)OC(C)COC(=O)C(C)=C BRWBXCPVJZQRHJ-UHFFFAOYSA-N 0.000 abstract 1
- ZWJWOOXWVLIPPX-UHFFFAOYSA-N 2-phosphonooxypropyl prop-2-enoate Chemical compound OP(=O)(O)OC(C)COC(=O)C=C ZWJWOOXWVLIPPX-UHFFFAOYSA-N 0.000 abstract 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 abstract 1
- QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 abstract 1
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229930016911 cinnamic acid Natural products 0.000 abstract 1
- 235000013985 cinnamic acid Nutrition 0.000 abstract 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 abstract 1
- 229940018557 citraconic acid Drugs 0.000 abstract 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 abstract 1
- YIOJGTBNHQAVBO-UHFFFAOYSA-N dimethyl-bis(prop-2-enyl)azanium Chemical class C=CC[N+](C)(C)CC=C YIOJGTBNHQAVBO-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- DOEXKUOGPAEBAD-UHFFFAOYSA-N ethyl n-(2-methylprop-2-enoyl)carbamate Chemical compound CCOC(=O)NC(=O)C(C)=C DOEXKUOGPAEBAD-UHFFFAOYSA-N 0.000 abstract 1
- IPZIVCLZBFDXTA-UHFFFAOYSA-N ethyl n-prop-2-enoylcarbamate Chemical compound CCOC(=O)NC(=O)C=C IPZIVCLZBFDXTA-UHFFFAOYSA-N 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- LDHQCZJRKDOVOX-IHWYPQMZSA-N isocrotonic acid Chemical compound C\C=C/C(O)=O LDHQCZJRKDOVOX-IHWYPQMZSA-N 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 abstract 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- -1 rent ilaryl Chemical group 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/10—Treatment with macromolecular organic compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
- C08F220/286—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety and containing polyethylene oxide in the alcohol moiety, e.g. methoxy polyethylene glycol (meth)acrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paper (AREA)
- Colloid Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
- Seasonings (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Una suspensión acuosa de substancias minerales que contiene un copolímero como agente dispesor y/o triturante de substancias minerales en suspensión acuosa, caracterizada en que dicho copolímero consiste de:a) por lo menos un monómero etilénicamente no saturado que tenga una función carboxílica, seleccionado entre los mono-ácidos tales como ácido acrílico, metacrílico, crotónico, isocrotónico o cinámico, los di ácidos tales como ácido itacónico, fumárico, maléico o citracónico, los anhídridos de ácido carboxílico tales como anhídrido maléico y los hemi - ésteres de di ácidos tales como los monoésteres en C1 a C4 de ácido maléico o itacónico, b) opcionalmente, por lo menos un monómero etilénicamente no saturado que tenga una función sulfónica, seleccionado entre los ácidos acrilamido-metil-propano-sulfónico, metalilsulfonato de sodio, ácido vinil sulfónico y ácido estireno sulfónico, o que tenga una función fosfórica seleccionada entre etileno glicol metacrilato fosfato, propileno glicol metacrilato fosfato, etileno glicol acrilato fosfato, propileno glicol acrilato fosfato y sus etoxilatos o mezclas de ellos, c) opcionalmente, por lo menos un monómero etilénicamente no saturado que tenga una función no carboxílica, seleccionado entre el grupo que comprende los ésteres de ácidos acrílicos o metacrílicos tales como metil, etil, butil, 2-etil-hexil acrilatos o metacrilatos, o acrilonitrilo, metacrilonitrilo, acetato de vinilo, estireno, metilestireno, diisobutileno, vinilpirrolidona, tinilcaprolactam, o alternativamente amidas no saturadas tales como acrilamida, metacrilamida o sus derivados sustitutos tales como dimetilaminopropil acrilamida o metacrilamida, los ésteres acrílicos o metacrílicos de glicol, metacrilamido-propil-trimetil-amonio clorado o sulfato, metacrilato de trimetil-amonio-etil-clorado o sulfato así como también sus contrapartes acrilamida quaternario y/o dimetildialilamonio clorado, d) por lo menos un monómero oxialkilatado actuante en la superficie que sea etilénicamente no saturado y que termine con una cadena hidrofóbica teniendo como fórmula general (I): - 3 -<EMI FILE="98040804_1" ID="1" IMF=JPEG >en la cual:m y p representan un número de unidades de óxido de alquileno menor o igual a 100,n representa un número de unidades de óxido de etileno menor o igual a 100q es un número por lo menos igual a 1 y tal que:O < q(n m p) < 100R1 es hidrógeno o el radical metil o etil,R2 es hidrógeno o el radical metil o etil,R representa el radical polimerizable no saturado perteneciente al grupo de los ésteres acrílico, metacrílico, maléico, itacónico, crotónico, vinilptálico así como también los uretanos no saturados tales como, acriluretano, metacriluretano, a-aAND#39 dimetil-m-isopropil-benciluretano-aliluretano.RAND#39 representa el radical hidrofóbico tales como el grupo tristirifenil así como también el grupo lineal o ramificado alquil, alquilaril, arilalquil, aril que tenga por lo menos 8 átomos de carbono o los dialquil aminos que tengan por lo menos 8 átomos cuando R representa los uretanos no saturados yRAND#39 representa radical hidrofóbico tales ocmo el tristirifenil así como también el grupo lineal o ramificado alquil, alquilaril, arilalquil, aril que tenga más de 30 átomos de carbono o los dialquilaminos que tengan por lo menos 22 átomos de carbono cuando R representa el radical polimerizable no saturado perteneciente al grupo de los ésteres acrílico, metacrílico, maléico, itacónico, crotónico o vinilptálico.El total de componentes (a), (b), (c) y (d) siendo igual a 100.Y en que este tenga una viscosidad específica máxima igual a 50 y preferiblemente no más de 25.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9709388A FR2766107B1 (fr) | 1997-07-18 | 1997-07-18 | Suspensions aqueuses de matieres minerales et leurs utilisations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5221054A1 true CO5221054A1 (es) | 2002-11-28 |
Family
ID=9509557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO98040804A CO5221054A1 (es) | 1997-07-18 | 1998-07-17 | Suspensiones acuosas de materiales minerales y sus usos . |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US6057398A (es) |
| EP (1) | EP0892111B8 (es) |
| JP (1) | JP4260930B2 (es) |
| KR (1) | KR19990014038A (es) |
| CN (1) | CN1116478C (es) |
| AT (1) | ATE403776T1 (es) |
| AU (1) | AU747463B2 (es) |
| BR (1) | BR9803713A (es) |
| CA (1) | CA2240859C (es) |
| CO (1) | CO5221054A1 (es) |
| CZ (1) | CZ299793B6 (es) |
| DE (1) | DE69839833D1 (es) |
| ES (1) | ES2312182T3 (es) |
| FR (1) | FR2766107B1 (es) |
| HU (1) | HU230125B1 (es) |
| ID (1) | ID20601A (es) |
| IN (1) | IN190671B (es) |
| MY (1) | MY119646A (es) |
| NO (1) | NO325269B1 (es) |
| NZ (1) | NZ331003A (es) |
| PL (1) | PL201874B1 (es) |
| PT (1) | PT892111E (es) |
| SI (1) | SI0892111T1 (es) |
| SK (1) | SK286491B6 (es) |
| TR (1) | TR199801401A2 (es) |
| ZA (1) | ZA986372B (es) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2766107B1 (fr) * | 1997-07-18 | 1999-08-20 | Pluss Stauffer Ag | Suspensions aqueuses de matieres minerales et leurs utilisations |
| FR2766106B1 (fr) * | 1997-07-18 | 2001-09-07 | Coatex Sa | Utilisation d'un copolymere a structure tensio-active comme agent dispersant et/ou d'aide au broyage |
| FR2792932B1 (fr) * | 1999-04-30 | 2001-07-06 | Coatex Sa | Nouveaux agents de type copolymeres acryliques a base d'urethanne pour ameliorer la maniabilite des liants hydrauliques, leur procede de preparation, les liants les contenant et leurs applications |
| US6660793B1 (en) * | 2000-06-15 | 2003-12-09 | E. I. Du Pont De Nemours And Company | Aqueous coating compositions having improved transparency |
| FR2810261B1 (fr) * | 2000-06-15 | 2002-08-30 | Coatex Sa | Utilisation de copolymeres faiblement anioniques comme agent dispersant et/ou d'aide au broyage de suspension aqueuse de matieres minerales, suspensions aqueuses obtenues et leurs utilisations |
| FR2815629B1 (fr) * | 2000-10-25 | 2003-09-05 | Coatex Sas | Procede pour ameliorer la resistance mecanique notamment "aux jeunes ages" des matrices cimentaires, matrices cimentaires obtenues et leurs utilisations |
| FR2815627B1 (fr) * | 2000-10-25 | 2003-09-05 | Coatex Sas | Procede pour ameliorer la resistance mecanique notamment "aux jeunes ages" des matrices cimentaires, matrices cimentaires ainsi obtenues et leurs utilisations |
| US20030073586A1 (en) * | 2001-10-03 | 2003-04-17 | Martin Crossman | Scale control composition for high scaling environments |
| KR100452558B1 (ko) * | 2001-11-20 | 2004-10-14 | 주식회사 엘지화학 | 공중합성 이온 단량체를 함유하는 종이 코팅용 라텍스 |
| FR2846972B1 (fr) | 2002-11-08 | 2005-02-18 | Omya Ag | Suspensions aqueuses de matieres minerales broyees, faiblement chargees ioniquement et leurs utilisations |
| FR2846971B1 (fr) * | 2002-11-08 | 2006-09-29 | Omya Ag | Utilisation d'un copolymere disposant d'au moins une fonction greffee alkoxy ou hydroxy polyalkylene glycol, comme agent ameliorant la brillance du papier et produits obtenus |
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| DE102007059736A1 (de) | 2007-12-12 | 2009-06-18 | Omya Development Ag | Oberflächenmineralisierte organische Fasern |
| FR2925077A1 (fr) * | 2007-12-17 | 2009-06-19 | Coatex Soc Par Actions Simplif | Epaississant acrylique a chaine hydrophobe et ramifiee pour sauce de couchage papetiere a retention d'eau amelioree |
| EP2075374A1 (fr) | 2007-12-17 | 2009-07-01 | Omya Development AG | Procédé de fabrication d'une sauce de couchage avec mise en oeuvre d'un epaississant acrylique à chaine hydrophobe ramifiée et sauce obtenue |
| EP2199348A1 (en) * | 2008-12-19 | 2010-06-23 | Omya Development AG | Process for manufacturing aqueous suspensions of mineral materials or dried mineral materials, the obtained products, as well as uses thereof |
| EP2208761B1 (en) * | 2009-01-16 | 2012-10-10 | Omya Development AG | Process to prepare self-binding pigment particles implementing acrylic comb copolymers with hydrophobic groups as coupling agents, self binding pigment particles and uses thereof |
| JP2011105853A (ja) * | 2009-11-17 | 2011-06-02 | Fimatec Ltd | 湿式粉砕助剤及び微粒重質炭酸カルシウム分散体 |
| CN102199248B (zh) * | 2010-03-26 | 2012-11-14 | 中国石油化工股份有限公司 | 三元丙烯腈共聚体及其制备方法 |
| CN102060950A (zh) * | 2010-11-22 | 2011-05-18 | 青岛科技大学 | 一种制备二甲基二烯丙基氯化铵均聚物和共聚物的方法 |
| ES2487639T3 (es) * | 2011-04-01 | 2014-08-22 | Omya International Ag | Híbrido de pigmentos autoaglutinantes |
| EP2505614B1 (en) | 2011-04-01 | 2013-11-13 | Omya International AG | Process for preparing self-binding pigment particles |
| DK2565236T3 (en) | 2011-08-31 | 2014-03-17 | Omya Int Ag | Self-binding pigment hybrid |
| AU2013230911B2 (en) | 2012-03-08 | 2016-02-25 | Hercules Incorporated | Viscosity suppression of associative thickeners using organophosphates |
| ES2550854T3 (es) * | 2012-06-28 | 2015-11-12 | Omya International Ag | Suspensión acuosa con alto contenido en sólidos de pigmentos y/o material de relleno y/o minerales en un entorno de pH acídico |
| US9145340B2 (en) | 2012-08-13 | 2015-09-29 | Verdesian Life Sciences, Llc | Method of reducing atmospheric ammonia in livestock and poultry containment facilities |
| US9961922B2 (en) | 2012-10-15 | 2018-05-08 | Verdesian Life Sciences, Llc | Animal feed and/or water amendments for lowering ammonia concentrations in animal excrement |
| US11254620B2 (en) | 2013-08-05 | 2022-02-22 | Verdesian Life Sciences U.S., Llc | Micronutrient-enhanced polymeric seed coatings |
| TW201522390A (zh) | 2013-08-27 | 2015-06-16 | 特級肥料產品公司 | 聚陰離子聚合物 |
| CA2923561C (en) | 2013-09-05 | 2022-05-03 | Verdesian Life Sciences, Llc | Polymer-boric acid compositions |
| US10519070B2 (en) | 2014-05-21 | 2019-12-31 | Verdesian Life Sciences U.S., Llc | Polymer soil treatment compositions including humic acids |
| US10822487B2 (en) | 2014-05-22 | 2020-11-03 | Verdesian Life Sciences Llc | Polymeric compositions |
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| CN109943102B (zh) * | 2019-04-09 | 2021-08-31 | 江西广源化工有限责任公司 | 一种涂布级超微细针状硅灰石的生产方法 |
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|---|---|---|---|---|
| US3567503A (en) * | 1969-09-30 | 1971-03-02 | Monsanto Co | Paper treated with copolymer compositions |
| AU527072B2 (en) * | 1978-11-27 | 1983-02-17 | Dow Chemical Company, The | Aqueous emulsion copolymer |
| EP0215565B1 (en) * | 1985-08-12 | 1991-07-24 | Ciba Specialty Chemicals Water Treatments Limited | Dispersing agents |
| SI9011099B (sl) * | 1989-06-06 | 1999-10-31 | Pluess - Staufer Ag | Visoko koncentrirana vodna suspenzija mineralov in/ali polnil in/ali pigmentov |
| FR2650594B1 (fr) * | 1989-08-04 | 1992-04-03 | Coatex Sa | Application aux suspensions aqueuses pigmentaires de carbonate de calcium d'un agent polycarboxylique a fonction phosphatee ou phosphonee inhibant l'effet de choc provoque par l'introduction d'un electrolyte sous forme concentree |
| GB9116523D0 (en) * | 1991-07-31 | 1991-09-11 | Raychem Sa Nv | Electrical component |
| FR2693203B1 (fr) * | 1992-07-01 | 1994-08-26 | Coatex Sas | Copolymère acrylique partiellement ou totalement hydrosoluble, réticulé ou non et son utilisation. |
| GB9320233D0 (en) * | 1993-10-01 | 1993-11-17 | Ecc Int Ltd | Paper coating pigment |
| GB9522228D0 (en) * | 1995-10-31 | 1996-01-03 | Ecc Int Ltd | Pigments for paper coating compositions |
| JPH09255740A (ja) * | 1996-03-26 | 1997-09-30 | Nof Corp | 三元共重合体 |
| FR2766107B1 (fr) * | 1997-07-18 | 1999-08-20 | Pluss Stauffer Ag | Suspensions aqueuses de matieres minerales et leurs utilisations |
-
1997
- 1997-07-18 FR FR9709388A patent/FR2766107B1/fr not_active Expired - Lifetime
-
1998
- 1998-07-11 SI SI9830912T patent/SI0892111T1/sl unknown
- 1998-07-11 AT AT98202339T patent/ATE403776T1/de active
- 1998-07-11 DE DE69839833T patent/DE69839833D1/de not_active Expired - Lifetime
- 1998-07-11 PT PT98202339T patent/PT892111E/pt unknown
- 1998-07-11 EP EP98202339A patent/EP0892111B8/fr not_active Expired - Lifetime
- 1998-07-11 ES ES98202339T patent/ES2312182T3/es not_active Expired - Lifetime
- 1998-07-15 NZ NZ331003A patent/NZ331003A/xx not_active IP Right Cessation
- 1998-07-15 SK SK969-98A patent/SK286491B6/sk not_active IP Right Cessation
- 1998-07-16 CZ CZ0224198A patent/CZ299793B6/cs not_active IP Right Cessation
- 1998-07-16 PL PL327527A patent/PL201874B1/pl unknown
- 1998-07-17 IN IN465BO1998 patent/IN190671B/en unknown
- 1998-07-17 NO NO19983310A patent/NO325269B1/no not_active IP Right Cessation
- 1998-07-17 ZA ZA986372A patent/ZA986372B/xx unknown
- 1998-07-17 BR BR9803713-7A patent/BR9803713A/pt not_active IP Right Cessation
- 1998-07-17 AU AU77304/98A patent/AU747463B2/en not_active Expired
- 1998-07-17 ID IDP981016A patent/ID20601A/id unknown
- 1998-07-17 JP JP20411098A patent/JP4260930B2/ja not_active Expired - Lifetime
- 1998-07-17 MY MYPI98003291A patent/MY119646A/en unknown
- 1998-07-17 CO CO98040804A patent/CO5221054A1/es not_active Application Discontinuation
- 1998-07-17 CA CA002240859A patent/CA2240859C/en not_active Expired - Lifetime
- 1998-07-17 CN CN98120256A patent/CN1116478C/zh not_active Expired - Lifetime
- 1998-07-17 HU HU9801624A patent/HU230125B1/hu unknown
- 1998-07-18 KR KR1019980029363A patent/KR19990014038A/ko not_active Application Discontinuation
- 1998-07-20 US US09/119,016 patent/US6057398A/en not_active Expired - Lifetime
- 1998-07-20 TR TR1998/01401A patent/TR199801401A2/xx unknown
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1999
- 1999-12-21 US US09/468,781 patent/US6414074B1/en not_active Expired - Lifetime
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