MXPA00002058A - Monomeros de vinilo basados en azucar y copolimeros utiles en adhesivos que se forman nuevamente en pasta papelera y otras aplicacio - Google Patents
Monomeros de vinilo basados en azucar y copolimeros utiles en adhesivos que se forman nuevamente en pasta papelera y otras aplicacioInfo
- Publication number
- MXPA00002058A MXPA00002058A MXPA00002058A MXPA00002058A MX PA00002058 A MXPA00002058 A MX PA00002058A MX PA00002058 A MXPA00002058 A MX PA00002058A MX PA00002058 A MXPA00002058 A MX PA00002058A
- Authority
- MX
- Mexico
- Prior art keywords
- alkyl
- mixture
- apg
- maleic acid
- group
- Prior art date
Links
- 239000000178 monomer Substances 0.000 title claims abstract description 56
- 229920001577 copolymer Polymers 0.000 title claims abstract description 39
- 239000000853 adhesive Substances 0.000 title claims abstract description 28
- 229920002554 vinyl polymer Polymers 0.000 title claims abstract description 28
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 26
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title claims abstract description 26
- 235000000346 sugar Nutrition 0.000 title description 27
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 61
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 238000004806 packaging method and process Methods 0.000 claims abstract description 8
- 238000004513 sizing Methods 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- 239000012860 organic pigment Substances 0.000 claims abstract description 5
- 230000014759 maintenance of location Effects 0.000 claims abstract description 4
- 239000002952 polymeric resin Substances 0.000 claims abstract description 4
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 4
- 239000002023 wood Substances 0.000 claims abstract description 4
- 238000004026 adhesive bonding Methods 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 51
- 238000000034 method Methods 0.000 claims description 48
- 230000008569 process Effects 0.000 claims description 33
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 29
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 28
- 238000006243 chemical reaction Methods 0.000 claims description 25
- 239000011976 maleic acid Substances 0.000 claims description 23
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 22
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 16
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 14
- -1 maleic acid ester Chemical class 0.000 claims description 11
- WQZGKKKJIJFFOK-DVKNGEFBSA-N alpha-D-glucose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-DVKNGEFBSA-N 0.000 claims description 10
- 150000003138 primary alcohols Chemical class 0.000 claims description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 8
- 230000032050 esterification Effects 0.000 claims description 7
- 238000005886 esterification reaction Methods 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 238000007334 copolymerization reaction Methods 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 6
- 239000011087 paperboard Substances 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- 150000001720 carbohydrates Chemical class 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 3
- 239000011111 cardboard Substances 0.000 claims description 3
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims description 3
- 125000002347 octyl 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])[H] 0.000 claims description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
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- 150000003254 radicals Chemical class 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 6
- 238000010557 suspension polymerization reaction Methods 0.000 claims 1
- 150000002688 maleic acid derivatives Chemical class 0.000 abstract description 6
- 239000002245 particle Substances 0.000 description 34
- 239000000123 paper Substances 0.000 description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 229910001868 water Inorganic materials 0.000 description 23
- 238000004064 recycling Methods 0.000 description 21
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 20
- 238000005755 formation reaction Methods 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 239000000835 fiber Substances 0.000 description 14
- 230000001464 adherent effect Effects 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 238000005481 NMR spectroscopy Methods 0.000 description 10
- 239000000523 sample Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 238000005188 flotation Methods 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
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- 230000035484 reaction time Effects 0.000 description 8
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- 239000000356 contaminant Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- 230000008030 elimination Effects 0.000 description 6
- 238000003379 elimination reaction Methods 0.000 description 6
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- RNAMYOYQYRYFQY-UHFFFAOYSA-N 2-(4,4-difluoropiperidin-1-yl)-6-methoxy-n-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine Chemical compound N1=C(N2CCC(F)(F)CC2)N=C2C=C(OCCCN3CCCC3)C(OC)=CC2=C1NC1CCN(C(C)C)CC1 RNAMYOYQYRYFQY-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
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- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 5
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/12—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by acids having the group -X-C(=X)-X-, or halides thereof, in which each X means nitrogen, oxygen, sulfur, selenium or tellurium, e.g. carbonic acid, carbamic acid
-
- 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
- C08F218/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F218/02—Esters of monocarboxylic acids
- C08F218/04—Vinyl esters
- C08F218/08—Vinyl acetate
-
- 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
-
- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/12—Esters of phenols or saturated alcohols
- C08F222/20—Esters containing oxygen in addition to the carboxy oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/38—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing crosslinkable groups
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
- Saccharide Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/920,911 US5872199A (en) | 1997-08-29 | 1997-08-29 | Sugar based vinyl monomers and copolymers useful in repulpable adhesives and other applications |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MXPA00002058A true MXPA00002058A (es) | 2001-08-01 |
| MX246640B MX246640B (enExample) | 2007-06-25 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA00002058 MXPA00002058A (es) | 1997-08-29 | 2000-02-28 | Monomeros de vinilo basados en azucar y copolimeros utiles en adhesivos que se forman nuevamente en pasta papelera y otras aplicacio |
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|---|---|
| US (2) | US5872199A (enExample) |
| EP (1) | EP1007529B1 (enExample) |
| JP (1) | JP3648160B2 (enExample) |
| KR (1) | KR100343267B1 (enExample) |
| CN (1) | CN1160365C (enExample) |
| AT (1) | ATE217005T1 (enExample) |
| AU (1) | AU725193B2 (enExample) |
| BR (1) | BR9811427A (enExample) |
| CA (1) | CA2301622C (enExample) |
| DE (1) | DE69805186T2 (enExample) |
| DK (1) | DK1007529T3 (enExample) |
| ES (1) | ES2175748T3 (enExample) |
| MX (1) | MXPA00002058A (enExample) |
| PT (1) | PT1007529E (enExample) |
| WO (1) | WO1999011670A2 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US5872199A (en) * | 1997-08-29 | 1999-02-16 | Lions Adhesives, Inc. | Sugar based vinyl monomers and copolymers useful in repulpable adhesives and other applications |
| US6300442B1 (en) * | 1997-12-10 | 2001-10-09 | Isp Investments Inc. | Process for making a cosmetically or pharmaceutically-acceptable emulsion or gel composition |
| US6355734B1 (en) * | 1999-08-20 | 2002-03-12 | Ecosynthetix Inc. | Resin-fortified sugar-based vinyl emulsion copolymers and methods of preparing the same |
| US6723802B2 (en) * | 2001-08-24 | 2004-04-20 | Board Of Trustees Of Michigan State University | Epoxy resin and polyglycoside based polymers and process for the preparation thereof |
| US20050133181A1 (en) * | 2003-12-22 | 2005-06-23 | Weyerhaeuser Company | Paper product and method of making |
| US20050133182A1 (en) * | 2003-12-22 | 2005-06-23 | Weyerhaeuser Company | Paper product and method of making field |
| JP4911285B2 (ja) * | 2006-03-13 | 2012-04-04 | Ｊｓｒ株式会社 | ブロック共重合体およびその製造方法 |
| US20080020961A1 (en) | 2006-07-21 | 2008-01-24 | Rodrigues Klin A | Low Molecular Weight Graft Copolymers |
| US8674021B2 (en) | 2006-07-21 | 2014-03-18 | Akzo Nobel N.V. | Sulfonated graft copolymers |
| US20110030710A1 (en) * | 2007-06-15 | 2011-02-10 | Kesselman Joshua D | Rolling paper structures for creating smoking articles and adhesives comprising hemp additive for same |
| GB2451883A (en) * | 2007-08-16 | 2009-02-18 | Sustainable Adhesive Products | Fully biodegradable adhesives |
| GB2463735A (en) * | 2008-09-30 | 2010-03-31 | Paul Howard James Roscoe | Fully biodegradable adhesives |
| BR112012001605B1 (pt) | 2009-07-31 | 2021-02-23 | Akzo Nobel Chemicals International B.V | composição de formulação, composição método de inibição da sistema aquoso 1/102 co polímero inibidora formação de híbrido aniônico, de incrustação e incrustação em um sistema aquoso |
| US8283304B2 (en) * | 2009-10-14 | 2012-10-09 | S.C. Johnson & Son, Inc. | Green compositions containing synergistic blends of surfactants and linkers |
| CN102651977B (zh) | 2009-12-10 | 2014-08-20 | 陶氏环球技术有限责任公司 | 制备稳定的淀粉分散体的方法 |
| US9080290B2 (en) * | 2010-10-08 | 2015-07-14 | Ecosynthetix Ltd. | Use of biobased sugar monomers in vinyl copolymers as latex binders and compositions based thereon |
| SG11201401383WA (en) | 2011-11-04 | 2014-08-28 | Akzo Nobel Chemicals Int Bv | Graft dendrite copolymers, and methods for producing the same |
| CN103945828A (zh) | 2011-11-04 | 2014-07-23 | 阿克佐诺贝尔化学国际公司 | 混杂树枝状共聚物、其组合物及其制备方法 |
| US8937140B2 (en) * | 2012-03-26 | 2015-01-20 | Empire Technology Development Llc | Adhesives and methods for their manufacture and use |
| US9126922B2 (en) | 2012-03-26 | 2015-09-08 | Empire Technology Development Llc | Methods and systems for the production of diesters from triacylglyceride esters |
| KR20140143837A (ko) | 2012-04-09 | 2014-12-17 | 애버리 데니슨 코포레이션 | 재생가능한 자원을 기반으로 한 감압 접착제, uv 경화 및 관련 방법 |
| CN102747651A (zh) * | 2012-06-08 | 2012-10-24 | 太仓市新星轻工助剂厂 | 一种涂布纸胶粘剂及其制备方法 |
| CN103214619B (zh) * | 2012-12-27 | 2015-09-23 | 南通斯恩特纺织科技有限公司 | 一种氨基糖基超分散剂及其制备方法 |
| WO2015160794A1 (en) * | 2014-04-14 | 2015-10-22 | Ecosynthetix Ltd. | Bio-based nanoparticle and composite materials derived therefrom |
| CN104559849B (zh) * | 2014-11-25 | 2016-08-24 | 桐乡嘉力丰实业股份有限公司 | 一种墙纸壁画胶及其制备方法 |
| CN107793518A (zh) * | 2016-09-07 | 2018-03-13 | 中国石油化工股份有限公司 | 中和剂在控制eva弹性体乳液的乳液粒径中的应用 |
| CN106433512B (zh) * | 2016-09-29 | 2019-06-21 | 江南大学 | 一种通过淀粉氧化偶联糊化制备的墙纸胶 |
| CN107868629A (zh) * | 2017-12-14 | 2018-04-03 | 安徽猛牛彩印包装有限公司 | 一种塑料薄膜用淀粉粘合剂及其制备方法 |
| CN107868628A (zh) * | 2017-12-14 | 2018-04-03 | 安徽猛牛彩印包装有限公司 | 一种用于塑料薄膜的粘合胶料制备方法 |
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| US3839318A (en) * | 1970-09-27 | 1974-10-01 | Rohm & Haas | Process for preparation of alkyl glucosides and alkyl oligosaccharides |
| JPS49116104A (enExample) * | 1973-03-12 | 1974-11-06 | ||
| JPS60252664A (ja) * | 1984-05-28 | 1985-12-13 | Nippon Paint Co Ltd | 塗料組成物 |
| US4713436A (en) | 1986-04-04 | 1987-12-15 | A. E. Staley Manufacturing Company | Glycoside-containing polyester preparation process |
| US4806275A (en) | 1986-09-05 | 1989-02-21 | A. E. Staley Manufacturing Company | Ionic derivatives of alkyl mono and polyglycosides |
| US5003057A (en) * | 1988-12-23 | 1991-03-26 | Henkel Kommanditgesellschaft Auf Aktien | Process for production of glycosides |
| DE4006192A1 (de) | 1990-02-28 | 1991-08-29 | Huels Chemische Werke Ag | Verfahren zur herstellung von kohlenhydrattensiden |
| US5266690A (en) | 1991-12-19 | 1993-11-30 | Henkel Corporation | Preparation of alkylpolyglycosides |
| US5449763A (en) | 1991-10-10 | 1995-09-12 | Henkel Corporation | Preparation of alkylpolyglycosides |
| EP0608371B1 (en) | 1991-10-15 | 1997-12-03 | Avery Dennison Corporation | Improvement in repulpable pressure-sensitive adhesive compositions |
| US5554745A (en) * | 1992-05-14 | 1996-09-10 | National Starch And Chemical Investment Holding Corporation | Aldehyde cationic derivatives of galactose containing polysaccharides used as paper strength additives |
| AU3546395A (en) | 1994-09-09 | 1996-03-27 | Ryobi North America, Inc. | Attachment system for battery powered tool |
| GB9500886D0 (en) | 1995-01-18 | 1995-03-08 | Cerester Holding B V | Alkylpolyglycosides with a high degree of polymerisation and a process for the preparation thereof |
| US5580940A (en) * | 1995-04-12 | 1996-12-03 | Lions Adhesives, Inc. | Biodegradable diacrylates and adhesives based thereon |
| US5872199A (en) * | 1997-08-29 | 1999-02-16 | Lions Adhesives, Inc. | Sugar based vinyl monomers and copolymers useful in repulpable adhesives and other applications |
-
1997
- 1997-08-29 US US08/920,911 patent/US5872199A/en not_active Expired - Lifetime
-
1998
- 1998-08-12 ES ES98939357T patent/ES2175748T3/es not_active Expired - Lifetime
- 1998-08-12 PT PT98939357T patent/PT1007529E/pt unknown
- 1998-08-12 WO PCT/US1998/016718 patent/WO1999011670A2/en not_active Ceased
- 1998-08-12 CA CA002301622A patent/CA2301622C/en not_active Expired - Fee Related
- 1998-08-12 BR BR9811427-1A patent/BR9811427A/pt not_active IP Right Cessation
- 1998-08-12 KR KR20007002147A patent/KR100343267B1/ko not_active Expired - Fee Related
- 1998-08-12 AU AU87804/98A patent/AU725193B2/en not_active Ceased
- 1998-08-12 JP JP2000508707A patent/JP3648160B2/ja not_active Expired - Fee Related
- 1998-08-12 AT AT98939357T patent/ATE217005T1/de not_active IP Right Cessation
- 1998-08-12 DK DK98939357T patent/DK1007529T3/da active
- 1998-08-12 CN CNB98808676XA patent/CN1160365C/zh not_active Expired - Fee Related
- 1998-08-12 EP EP98939357A patent/EP1007529B1/en not_active Expired - Lifetime
- 1998-08-12 DE DE69805186T patent/DE69805186T2/de not_active Expired - Lifetime
- 1998-09-03 US US09/145,937 patent/US6242593B1/en not_active Expired - Lifetime
-
2000
- 2000-02-28 MX MXPA00002058 patent/MXPA00002058A/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| PT1007529E (pt) | 2002-10-31 |
| CA2301622C (en) | 2003-11-04 |
| WO1999011670A3 (en) | 1999-07-29 |
| AU8780498A (en) | 1999-03-22 |
| AU725193B2 (en) | 2000-10-05 |
| DE69805186D1 (de) | 2002-06-06 |
| US5872199A (en) | 1999-02-16 |
| EP1007529A2 (en) | 2000-06-14 |
| US6242593B1 (en) | 2001-06-05 |
| DK1007529T3 (da) | 2002-07-08 |
| JP3648160B2 (ja) | 2005-05-18 |
| ATE217005T1 (de) | 2002-05-15 |
| KR20010023501A (ko) | 2001-03-26 |
| CN1268952A (zh) | 2000-10-04 |
| CN1160365C (zh) | 2004-08-04 |
| MX246640B (enExample) | 2007-06-25 |
| WO1999011670A2 (en) | 1999-03-11 |
| KR100343267B1 (ko) | 2002-07-10 |
| CA2301622A1 (en) | 1999-03-11 |
| ES2175748T3 (es) | 2002-11-16 |
| EP1007529B1 (en) | 2002-05-02 |
| DE69805186T2 (de) | 2002-11-28 |
| JP2001514265A (ja) | 2001-09-11 |
| BR9811427A (pt) | 2000-11-21 |
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| FG | Grant or registration | ||
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