TW200415179A - Rheology-improving adhesion promoters for PVC plastisols - Google Patents

Rheology-improving adhesion promoters for PVC plastisols Download PDF

Info

Publication number: TW200415179A
Authority: TW; Taiwan
Prior art keywords: scope; patent application; adhesion promoter; acid; plastic
Prior art date: 2002-08-21

Application number

TW92122712A

Other languages

English (en)

Chinese (zh)

Inventor

Jorg Volle

Christa Broll

Alfred Kruse

Original Assignee

Vantico Gmbh

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.)

2002-08-21

Filing date

2003-08-19

Publication date

2004-08-16

2003-08-19 Application filed by Vantico Gmbh filed Critical Vantico Gmbh

2004-08-16 Publication of TW200415179A publication Critical patent/TW200415179A/zh

Links

239000002318 adhesion promoter Substances 0.000 title claims abstract description 56
229920001944 Plastisol Polymers 0.000 title abstract 5
239000004999 plastisol Substances 0.000 title abstract 5
150000004665 fatty acids Chemical class 0.000 claims abstract description 16
229920000768 polyamine Polymers 0.000 claims abstract description 16
-1 amine compound Chemical class 0.000 claims abstract description 15
235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 15
229930195729 fatty acid Natural products 0.000 claims abstract description 15
239000000194 fatty acid Substances 0.000 claims abstract description 15
238000000034 method Methods 0.000 claims abstract description 14
229920001281 polyalkylene Polymers 0.000 claims abstract description 9
238000002360 preparation method Methods 0.000 claims abstract description 9
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 7
229920003023 plastic Polymers 0.000 claims description 61
239000004033 plastic Substances 0.000 claims description 61
239000002253 acid Substances 0.000 claims description 19
229920000915 polyvinyl chloride Polymers 0.000 claims description 16
239000004800 polyvinyl chloride Substances 0.000 claims description 16
239000002002 slurry Substances 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 12
239000000853 adhesive Substances 0.000 claims description 11
238000000576 coating method Methods 0.000 claims description 11
239000000463 material Substances 0.000 claims description 11
239000004014 plasticizer Substances 0.000 claims description 9
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 8
239000004593 Epoxy Substances 0.000 claims description 8
230000001070 adhesive effect Effects 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 8
150000007513 acids Chemical class 0.000 claims description 7
239000011248 coating agent Substances 0.000 claims description 7
239000000945 filler Substances 0.000 claims description 6
238000010438 heat treatment Methods 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 5
229920006395 saturated elastomer Polymers 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
229920001577 copolymer Polymers 0.000 claims description 3
239000000178 monomer Substances 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
150000001735 carboxylic acids Chemical class 0.000 claims 2
AZWLGPJBVAQRHW-UHFFFAOYSA-N 4-aminobutane-1,3-diol Chemical compound NCC(O)CCO AZWLGPJBVAQRHW-UHFFFAOYSA-N 0.000 claims 1
239000005062 Polybutadiene Substances 0.000 claims 1
229920002873 Polyethylenimine Polymers 0.000 claims 1
125000004122 cyclic group Chemical group 0.000 claims 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims 1
238000006471 dimerization reaction Methods 0.000 claims 1
229920002857 polybutadiene Polymers 0.000 claims 1
150000003141 primary amines Chemical class 0.000 claims 1
239000002689 soil Substances 0.000 claims 1
238000005829 trimerization reaction Methods 0.000 claims 1
239000011347 resin Substances 0.000 abstract description 5
229920005989 resin Polymers 0.000 abstract description 5
238000009833 condensation Methods 0.000 abstract description 3
230000005494 condensation Effects 0.000 abstract description 3
229920000962 poly(amidoamine) Polymers 0.000 description 15
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 12
150000001412 amines Chemical class 0.000 description 8
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 8
239000000047 product Substances 0.000 description 6
230000000052 comparative effect Effects 0.000 description 5
150000001991 dicarboxylic acids Chemical class 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000009472 formulation Methods 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
239000013008 thixotropic agent Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
230000002411 adverse Effects 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000000539 dimer Substances 0.000 description 3
239000010410 layer Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000000758 substrate Substances 0.000 description 3
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
238000007259 addition reaction Methods 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
125000002636 imidazolinyl group Chemical group 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
230000035515 penetration Effects 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
239000002985 plastic film Substances 0.000 description 2
229920006255 plastic film Polymers 0.000 description 2
230000000717 retained effect Effects 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
239000013638 trimer Substances 0.000 description 2
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
GBURUDXSBYGPBL-UHFFFAOYSA-N 2,2,3-trimethylhexanedioic acid Chemical compound OC(=O)C(C)(C)C(C)CCC(O)=O GBURUDXSBYGPBL-UHFFFAOYSA-N 0.000 description 1
GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 1
BVCAMTKLEXJPLH-UHFFFAOYSA-N 2-(2h-pyridin-1-yl)ethanamine Chemical compound NCCN1CC=CC=C1 BVCAMTKLEXJPLH-UHFFFAOYSA-N 0.000 description 1
KFUSXMDYOPXKKT-UHFFFAOYSA-N 2-[(2-methylphenoxy)methyl]oxirane Chemical compound CC1=CC=CC=C1OCC1OC1 KFUSXMDYOPXKKT-UHFFFAOYSA-N 0.000 description 1
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
XPQIPUZPSLAZDV-UHFFFAOYSA-N 2-pyridylethylamine Chemical compound NCCC1=CC=CC=N1 XPQIPUZPSLAZDV-UHFFFAOYSA-N 0.000 description 1
ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
101100025919 Mus musculus Ncoa6 gene Proteins 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
229910052776 Thorium Inorganic materials 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
229920006397 acrylic thermoplastic Polymers 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000008602 contraction Effects 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000005611 electricity Effects 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
229920001038 ethylene copolymer Polymers 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000011049 filling Methods 0.000 description 1
RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
150000007857 hydrazones Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
238000003402 intramolecular cyclocondensation reaction Methods 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
230000005923 long-lasting effect Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
TWOKQHDORBJKRS-UHFFFAOYSA-N n'-[2-[2-(ethylamino)ethylamino]ethyl]ethane-1,2-diamine Chemical compound CCNCCNCCNCCN TWOKQHDORBJKRS-UHFFFAOYSA-N 0.000 description 1
DOSSJECCMHEIPN-UHFFFAOYSA-N n'-[2-[2-aminoethyl(ethyl)amino]ethyl]-n'-ethylethane-1,2-diamine Chemical compound NCCN(CC)CCN(CC)CCN DOSSJECCMHEIPN-UHFFFAOYSA-N 0.000 description 1
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
238000011022 operating instruction Methods 0.000 description 1
OZHOHTGAQOJLCS-UHFFFAOYSA-N oxalic acid;propanoic acid Chemical compound CCC(O)=O.OC(=O)C(O)=O OZHOHTGAQOJLCS-UHFFFAOYSA-N 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
150000002927 oxygen compounds Chemical class 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
229910052702 rhenium Inorganic materials 0.000 description 1
WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
- C09J5/02—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving pretreatment of the surfaces to be joined
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/34—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of 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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/12—Polyester-amides
- 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
- C09J2477/00—Presence of polyamide

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Adhesives Or Adhesive Processes (AREA)

TW92122712A 2002-08-21 2003-08-19 Rheology-improving adhesion promoters for PVC plastisols TW200415179A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10238275		2002-08-21

Publications (1)

Publication Number	Publication Date
TW200415179A true TW200415179A (en)	2004-08-16

Family

ID=31895569

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW92122712A TW200415179A (en)	2002-08-21	2003-08-19	Rheology-improving adhesion promoters for PVC plastisols

Country Status (3)

Country	Link
AU (1)	AU2003268943A1 (fr)
TW (1)	TW200415179A (fr)
WO (1)	WO2004018543A2 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1076030A (en) *	1963-01-30	1967-07-19	Gen Mills Inc	Improvements in or relating to copolyamides

2003
- 2003-08-18 WO PCT/EP2003/050381 patent/WO2004018543A2/fr not_active Ceased
- 2003-08-18 AU AU2003268943A patent/AU2003268943A1/en not_active Abandoned
- 2003-08-19 TW TW92122712A patent/TW200415179A/zh unknown

Also Published As

Publication number	Publication date
WO2004018543A3 (fr)	2004-04-22
WO2004018543A2 (fr)	2004-03-04
AU2003268943A1 (en)	2004-03-11

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EP0442700B1 (fr)	1996-01-03	Compositions de résine thermofusibles durcissables à deux composants
US5612448A (en)	1997-03-18	Curable adhesive compositions containing polyamide resins
CA1271293A (fr)	1990-07-03	Composition adhesive
JPH0768498B2 (ja)	1995-07-26	ホットメルト接着剤およびその製造方法
US4409373A (en)	1983-10-11	Adhesive compositions based upon thermoplastic polyamides
KR20100014868A (ko)	2010-02-11	프라이머 조성물 및 접착성 기재
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KR20150113174A (ko)	2015-10-07	방식 도료 조성물, 방식 도막 및 기재의 방식방법
SE439319B (sv)	1985-06-10	Sett att framstella overdrag pa och hopklistringar av metalliska material samt polyvinylklorid-plastisol till anvendning vid settet
CN102459488B (zh)	2013-11-06	水性粘接剂组合物
JPH0578641A (ja)	1993-03-30	２成分型硬化性ホツトメルト樹脂組成物
JPH09509978A (ja)	1997-10-07	ポリアミド熱溶融型接着剤
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