NO813455L - Lim paa basis av pvac-emulsjon og fremgangsmaate for dets fremstilling - Google Patents

Lim paa basis av pvac-emulsjon og fremgangsmaate for dets fremstilling

Info

Publication number: NO813455L
Authority: NO; Norway
Prior art keywords: weight; glue; polyvinyl alcohol; mixture; polymerization
Prior art date: 1980-10-16

Application number

NO813455A

Other languages

English (en)

Norwegian (no)

Inventor

Jean-Luc Schuppiser

Jean-Claude Daniel

Original Assignee

Rhone Poulenc Ind

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.)

1980-10-16

Filing date

1981-10-14

Publication date

1982-04-19

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26222032&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO813455(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1980-10-16 Priority claimed from FR8022108A external-priority patent/FR2492398A1/fr

1981-06-30 Priority claimed from FR8112812A external-priority patent/FR2508478A2/fr

1981-10-14 Application filed by Rhone Poulenc Ind filed Critical Rhone Poulenc Ind

1982-04-19 Publication of NO813455L publication Critical patent/NO813455L/no

Links

239000003292 glue Substances 0.000 title claims description 22
229920002689 polyvinyl acetate Polymers 0.000 title claims description 11
239000000839 emulsion Substances 0.000 title claims description 6
238000000034 method Methods 0.000 title claims description 5
238000004519 manufacturing process Methods 0.000 title claims description 3
239000000203 mixture Substances 0.000 claims description 34
238000006116 polymerization reaction Methods 0.000 claims description 33
239000000178 monomer Substances 0.000 claims description 32
229920002451 polyvinyl alcohol Polymers 0.000 claims description 31
235000019422 polyvinyl alcohol Nutrition 0.000 claims description 31
239000004816 latex Substances 0.000 claims description 28
229920000126 latex Polymers 0.000 claims description 28
239000004372 Polyvinyl alcohol Substances 0.000 claims description 27
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 27
239000004014 plasticizer Substances 0.000 claims description 17
229920000642 polymer Polymers 0.000 claims description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
229920001577 copolymer Polymers 0.000 claims description 14
150000002148 esters Chemical class 0.000 claims description 14
239000000853 adhesive Substances 0.000 claims description 13
230000001070 adhesive effect Effects 0.000 claims description 13
-1 dibenzoate Chemical compound 0.000 claims description 12
239000011118 polyvinyl acetate Substances 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 9
239000012986 chain transfer agent Substances 0.000 claims description 7
239000003995 emulsifying agent Substances 0.000 claims description 6
150000002763 monocarboxylic acids Chemical class 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
239000003999 initiator Substances 0.000 claims description 5
239000000084 colloidal system Substances 0.000 claims description 4
239000002245 particle Substances 0.000 claims description 4
230000001681 protective effect Effects 0.000 claims description 4
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 3
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 3
150000001298 alcohols Chemical class 0.000 claims description 3
150000001336 alkenes Chemical class 0.000 claims description 3
125000005907 alkyl ester group Chemical group 0.000 claims description 3
VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 claims description 3
150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 3
229920001519 homopolymer Polymers 0.000 claims description 3
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 claims description 3
229920001567 vinyl ester resin Polymers 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 claims description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 2
QCOAPBRVQHMEPF-UHFFFAOYSA-N bis(2-methylpropyl) butanedioate Chemical class CC(C)COC(=O)CCC(=O)OCC(C)C QCOAPBRVQHMEPF-UHFFFAOYSA-N 0.000 claims description 2
150000008282 halocarbons Chemical class 0.000 claims description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 2
URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims 2
SENMPMXZMGNQAG-UHFFFAOYSA-N 3,4-dihydro-2,5-benzodioxocine-1,6-dione Chemical compound O=C1OCCOC(=O)C2=CC=CC=C12 SENMPMXZMGNQAG-UHFFFAOYSA-N 0.000 claims 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims 1
239000001087 glyceryl triacetate Substances 0.000 claims 1
235000013773 glyceryl triacetate Nutrition 0.000 claims 1
125000005498 phthalate group Chemical class 0.000 claims 1
229960002622 triacetin Drugs 0.000 claims 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 16
239000007864 aqueous solution Substances 0.000 description 14
239000000243 solution Substances 0.000 description 12
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 10
229960002380 dibutyl phthalate Drugs 0.000 description 8
235000014113 dietary fatty acids Nutrition 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
239000005977 Ethylene Substances 0.000 description 5
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
235000017557 sodium bicarbonate Nutrition 0.000 description 5
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 4
NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 4
239000004160 Ammonium persulphate Substances 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
235000019395 ammonium persulphate Nutrition 0.000 description 3
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 3
239000011111 cardboard Substances 0.000 description 3
238000001816 cooling Methods 0.000 description 3
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000011148 porous material Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
VOMGOUBSTOBNLL-UHFFFAOYSA-N 2-(2,2,2-trichloroethoxycarbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCC(Cl)(Cl)Cl VOMGOUBSTOBNLL-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
239000004159 Potassium persulphate Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
229960001826 dimethylphthalate Drugs 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229920001038 ethylene copolymer Polymers 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
150000002688 maleic acid derivatives Chemical class 0.000 description 2
150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000004806 packaging method and process Methods 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
235000019394 potassium persulphate Nutrition 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
NEFDVAJLNQFZTD-UHFFFAOYSA-N 2,3-diacetyloxypropyl acetate;propane-1,2,3-triol Chemical compound OCC(O)CO.CC(=O)OCC(OC(C)=O)COC(C)=O NEFDVAJLNQFZTD-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
APWRLAZEMYLHKZ-UHFFFAOYSA-N 2-amino-5,6-dimethyl-1h-pyrimidin-4-one Chemical compound CC=1NC(N)=NC(=O)C=1C APWRLAZEMYLHKZ-UHFFFAOYSA-N 0.000 description 1
VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 description 1
HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
239000003139 biocide Substances 0.000 description 1
229950005228 bromoform Drugs 0.000 description 1
239000000872 buffer Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000011436 cob Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000007872 degassing Methods 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000000151 deposition Methods 0.000 description 1
150000008049 diazo compounds Chemical class 0.000 description 1
229940031769 diisobutyl adipate Drugs 0.000 description 1
238000009826 distribution Methods 0.000 description 1
YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
QTFKDEXLBIOHOQ-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate;ethenyl dodecanoate Chemical compound CC(C)(C)C(=O)OC=C.CCCCCCCCCCCC(=O)OC=C QTFKDEXLBIOHOQ-UHFFFAOYSA-N 0.000 description 1
GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000012943 hotmelt Substances 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
239000012768 molten material Substances 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
239000011087 paperboard Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000000047 product Substances 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
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
238000000196 viscometry Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/28—Processes for applying liquids or other fluent materials performed by transfer from the surfaces of elements carrying the liquid or other fluent material, e.g. brushes, pads, rollers
- 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
- C09J131/00—Adhesives based on homopolymers or 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; Adhesives based on derivatives of such polymers
- C09J131/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C09J131/04—Homopolymers or copolymers of vinyl acetate
- 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
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/003—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Adhesives Or Adhesive Processes (AREA)
Materials For Medical Uses (AREA)

NO813455A 1980-10-16 1981-10-14 Lim paa basis av pvac-emulsjon og fremgangsmaate for dets fremstilling NO813455L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8022108A FR2492398A1 (fr)	1980-10-16	1980-10-16	Colles a prise rapide a base de latex aqueux de polyacetate de vinyle plastifie et leur procede de preparation
FR8112812A FR2508478A2 (fr)	1981-06-30	1981-06-30	Colles a prise rapide a base de latex aqueux de copolymere d'acetate de vinyle plastifie et leur procede de fabrication

Publications (1)

Publication Number	Publication Date
NO813455L true NO813455L (no)	1982-04-19

Family

ID=26222032

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO813455A NO813455L (no)	1980-10-16	1981-10-14	Lim paa basis av pvac-emulsjon og fremgangsmaate for dets fremstilling

Country Status (8)

Country	Link
EP (1)	EP0050548B1 (fi)
DE (1)	DE3168353D1 (fi)
DK (1)	DK457281A (fi)
ES (1)	ES8302761A1 (fi)
FI (1)	FI813172L (fi)
MA (1)	MA19301A1 (fi)
NO (1)	NO813455L (fi)
PT (1)	PT73823B (fi)

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US6087425A (en) *	1994-02-18	2000-07-11	Rohm And Haas Company	Laminating adhesive composition
BR0313398A (pt)	2002-08-12	2005-06-28	Exxonmobil Chem Patents Inc	Composições de poliolefina plasticizada
US7271209B2 (en)	2002-08-12	2007-09-18	Exxonmobil Chemical Patents Inc.	Fibers and nonwovens from plasticized polyolefin compositions
US7998579B2 (en)	2002-08-12	2011-08-16	Exxonmobil Chemical Patents Inc.	Polypropylene based fibers and nonwovens
US8003725B2 (en)	2002-08-12	2011-08-23	Exxonmobil Chemical Patents Inc.	Plasticized hetero-phase polyolefin blends
US7531594B2 (en)	2002-08-12	2009-05-12	Exxonmobil Chemical Patents Inc.	Articles from plasticized polyolefin compositions
US8192813B2 (en)	2003-08-12	2012-06-05	Exxonmobil Chemical Patents, Inc.	Crosslinked polyethylene articles and processes to produce same
US8389615B2 (en)	2004-12-17	2013-03-05	Exxonmobil Chemical Patents Inc.	Elastomeric compositions comprising vinylaromatic block copolymer, polypropylene, plastomer, and low molecular weight polyolefin
WO2007011541A1 (en)	2005-07-15	2007-01-25	Exxonmobil Chemical Patents Inc.	Elastomeric compositions
DE102006037317A1 (de)	2006-08-08	2008-02-14	Celanese Emulsions Gmbh	Vinylestercopolymer-Dispersionen, Verfahren zu deren Herstellung und Verwendung
DE102007033595A1 (de)	2007-07-19	2009-01-22	Celanese Emulsions Gmbh	Polyvinylesterdispersionen, Verfahren zu deren Herstellung und deren Verwendung
DE102007033596A1 (de)	2007-07-19	2009-01-22	Celanese Emulsions Gmbh	Beschichtungsmittel mit hoher Bewitterungsbeständigkeit, Verfahren zu deren Herstellung und deren Verwendung

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1419673A (fr) *	1961-06-21	1965-12-03	Borden Co	émulsion aqueuse d'acétate de polyvinyle contenant de l'acide borique et de l'alcool polyvinylique
US3442845A (en) *	1966-11-04	1969-05-06	Borden Co	Hot and cold water redispersible polyvinyl acetate adhesives
JPS4840890B1 (fi) *	1970-03-05	1973-12-03

1981
- 1981-10-07 EP EP81401551A patent/EP0050548B1/fr not_active Expired
- 1981-10-07 DE DE8181401551T patent/DE3168353D1/de not_active Expired
- 1981-10-13 MA MA19502A patent/MA19301A1/fr unknown
- 1981-10-13 FI FI813172A patent/FI813172L/fi not_active Application Discontinuation
- 1981-10-14 NO NO813455A patent/NO813455L/no unknown
- 1981-10-15 PT PT73823A patent/PT73823B/pt unknown
- 1981-10-15 DK DK457281A patent/DK457281A/da not_active Application Discontinuation
- 1981-10-15 ES ES506256A patent/ES8302761A1/es not_active Expired

Also Published As

Publication number	Publication date
ES506256A0 (es)	1983-01-16
ES8302761A1 (es)	1983-01-16
PT73823B (fr)	1983-01-17
EP0050548B1 (fr)	1985-01-16
MA19301A1 (fr)	1982-07-01
FI813172L (fi)	1982-04-17
DK457281A (da)	1982-04-17
PT73823A (fr)	1981-11-01
DE3168353D1 (en)	1985-02-28
EP0050548A1 (fr)	1982-04-28

Publication	Publication Date	Title
DE3852325T2 (de)	1995-04-27	Vinylacetat-Ethylen-Copolymer-Emulsionen, hergestellt in Anwesenheit eines Stabilisiersystems eines Polyvinylalkohols mit niedrigem Molekulargewicht und eines oberflächenaktiven Mittels.
EP1088835B1 (en)	2004-12-22	Aqueous emulsion and method for producing it
NO813455L (no)	1982-04-19	Lim paa basis av pvac-emulsjon og fremgangsmaate for dets fremstilling
EP2898147B1 (en)	2020-06-10	Chlorofluoropolymer coated substrates and methods for producing the same
US4542182A (en)	1985-09-17	Latices of vinyl acetate/olefin copolymers
US3290265A (en)	1966-12-06	Three stage polymerization process for the production of polyvinyl chloride resins
US4542181A (en)	1985-09-17	Latices of vinyl acetate polymers
US4439574A (en)	1984-03-27	Process for the preparation of lattices of vinylacetate/olefin copolymers
EP0004795B1 (en)	1984-10-24	Method for producing vinyl chloride resins
US5939505A (en)	1999-08-17	High solids ethylene vinyl acetate emulsions
US3113114A (en)	1963-12-03	Initiator systems for acrylic polymerizations
US3094500A (en)	1963-06-18	Vinyl ester polymer emulsions containing polyvinyl alcohol
US4746705A (en)	1988-05-24	Vinyl chloride polymer composition containing (meth)acrylate-alpha methyl styrene copolymer
FI70907C (fi)	1986-10-27	Foerfarande foer framstaellning av vinylacetatpolymerers latexer
US3583959A (en)	1971-06-08	Heat-stable vinyl chloride-acetate resins prepared in the presence of olefins
US3027358A (en)	1962-03-27	Process for the production of copolymers of vinyl chloride and fumaric acid esters
US3843581A (en)	1974-10-22	Reducing heat-seal temperature requirements for coatings prepared from latexes of vinylidene chloride polymers
JPS63108016A (ja)	1988-05-12	変性ポリビニルアルコ−ル共重合体の製造法
NO864121L (no)	1987-04-21	Fremgangsmaate til fremstilling av polyvinylklorid.
US3884890A (en)	1975-05-20	Preparation of transparent and thermostable copolymers
US2851449A (en)	1958-09-09	Copolymers of trifluoroethyl vinyl ether and vinyl esters
JPS584736B2 (ja)	1983-01-27	エンカビニリデンケイキヨウジユウゴウタイジユシノアンテイカソセイブツ
JPS607644B2 (ja)	1985-02-26	塩化ビニリデン系共重合体樹脂の残存モノマ−の除去法
JPH09208631A (ja)	1997-08-12	塩化ビニル系重合体
FR2508478A2 (fr)	1982-12-31	Colles a prise rapide a base de latex aqueux de copolymere d'acetate de vinyle plastifie et leur procede de fabrication