GB1459843A - Contact adhesive - Google Patents
Contact adhesiveInfo
- Publication number
- GB1459843A GB1459843A GB1873074A GB1873074A GB1459843A GB 1459843 A GB1459843 A GB 1459843A GB 1873074 A GB1873074 A GB 1873074A GB 1873074 A GB1873074 A GB 1873074A GB 1459843 A GB1459843 A GB 1459843A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dispersion
- acrylate
- resole
- phenol
- latex
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000004821 Contact adhesive Substances 0.000 title abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 13
- 239000006185 dispersion Substances 0.000 abstract 13
- 229920003987 resole Polymers 0.000 abstract 8
- 239000004816 latex Substances 0.000 abstract 7
- 229920000126 latex Polymers 0.000 abstract 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 5
- 244000215068 Acacia senegal Species 0.000 abstract 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 4
- 229920000084 Gum arabic Polymers 0.000 abstract 4
- 239000000205 acacia gum Substances 0.000 abstract 4
- 235000010489 acacia gum Nutrition 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 229920005989 resin Polymers 0.000 abstract 4
- 239000011347 resin Substances 0.000 abstract 4
- 239000007787 solid Substances 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 239000005018 casein Substances 0.000 abstract 3
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 3
- 235000021240 caseins Nutrition 0.000 abstract 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 2
- -1 alkali metal salt Chemical class 0.000 abstract 2
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 2
- 229920001568 phenolic resin Polymers 0.000 abstract 2
- 239000005011 phenolic resin Substances 0.000 abstract 2
- 229920000058 polyacrylate Polymers 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- LQOUIUASQQPAGR-UHFFFAOYSA-N 2-[bis(hydroxymethyl)amino]ethanol Chemical compound OCCN(CO)CO LQOUIUASQQPAGR-UHFFFAOYSA-N 0.000 abstract 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004925 Acrylic resin Substances 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 229930185605 Bisphenol Natural products 0.000 abstract 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 229920002907 Guar gum Polymers 0.000 abstract 1
- IAJILQKETJEXLJ-SQOUGZDYSA-N L-guluronic acid Chemical group O=C[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O IAJILQKETJEXLJ-SQOUGZDYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- 241000282372 Panthera onca Species 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical group OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- AEMOLEFTQBMNLQ-YBSDWZGDSA-N d-mannuronic acid Chemical compound O[C@@H]1O[C@@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-YBSDWZGDSA-N 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 230000001804 emulsifying effect Effects 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 150000004676 glycans Chemical class 0.000 abstract 1
- 239000000665 guar gum Substances 0.000 abstract 1
- 235000010417 guar gum Nutrition 0.000 abstract 1
- 229960002154 guar gum Drugs 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000002952 polymeric resin Substances 0.000 abstract 1
- 239000005017 polysaccharide Substances 0.000 abstract 1
- 229920001282 polysaccharide Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 230000007704 transition Effects 0.000 abstract 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
- C09J133/00—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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Adhesive Tapes (AREA)
Abstract
1459843 Aqueous phenolic resin dispersion/ acrylate latex contact adhesives UNION CARBIDE CORP 29 April 1974 [30 April 1973] 18730/74 Headings C3R and C3P A contact adhesive composition comprises an aqueous mixed dispersion containing: (a) an alkyl acrylate polymer resin latex having a second order transition temperature not greater than 30‹ C.; and (b) an aqueous phenolic resole dispersion having a weight average M.Wt. of from 200 to 3000 and comprising either: (i) a first resole formed by the alkaline condensation of an aldehyde and a phenol and which is employed in the dispersion as solid particles suspended in water, substantially all of which have diameters of less than 60 microns; or (ii) a second resole comprising the alkaline condensed reaction product of formaldehyde and a difunctional phenol and having a labile formaldehyde content of from 0 to 12% wt., based on the weight of the second resole and wherein the second resole is employed in the dispersion as a solution in a water-immiscible organic solvent. The acrylate polymer preferably comprises at least 25% wt. of units derived from alkyl acrylates; and preferably has a mean average ultimate elongation of at least 500%. The first resole dispersion may be prepared by condensing at least one phenol selected from phenol itself, trifunctional monohydric mono- or dimeta-substituted C 1 -C 9 alkyl or alkoxy, or halo-phenols, and bisphenols with formaldehyde or furfural in the presence of an alkaline catalyst and optionally a mixture of gum arabic and at least one polysaccharide gum having mannose and galactose units or D-mannuronic and L-guluronic acid units. The second resole dispersion may be prepared by reacting a para-substituted phenol preferably a para-C 1 -C 12 alkyl-phenol with formaldehyde in the presence of an alkaline catalyst and emulsifying the resole formed with up to 50% wt. of a water-immiscible solvent e.g. an aromatic or aliphatic hydrocarbon, before adding it to water to form the dispersion optionally in the presence of an emulsifier such as an alkali metal salt of a C 12 -C 24 aliphatic fatty acid alone or together with the corresponding amine or ammonium salt or with casein, ammoniated casein and various gums. The composition preferably comprises 5-45 wt. per cent phenolic resin solids and 95-55 wt. per cent acrylate resin solids, based on the combined weight of the resins and optionally up to 50 wt. per cent of a filler or pigment determined on a solids basis of the total formulation. In the examples adhesives are prepared from (1) either (i) a latex copolymer of ethyl acrylate, acrylonitrile, acrylic acid and N-methylol acrylamide alone or in admixture with an acrylate latex copolymer (B) of vinyl acetate and isobutyl acrylate, or (ii) an acrylate latex prepared by adding an aqueous dispersion of a copolymer of ethylene and acrylic acid partially neutralized with N,N-dimethylolethanolamine to an acrylate copolymer latex of ethyl acrylate, methyl methacrylate and methacrylic acid and then heating, alone or in admixture with acrylate latex (B), and (2) either (i) a bisphenol-AHCHO resin aqueous dispersion prepared in presence of gum arabic and "Jaguar" (R.T.M.) gum, or (ii) a phenol-HCHO resin aqueous dispersion prepared in the presence of gum arabic and either guar gum or a gum comprising galactose units, or (iii) an aqueous dispersion of either p-tert-butylphenol-HCHO resin having a labile HCHO content of 6À3% wt., or an aqueous phenol-cresol-HCHO dispersion each containing oleic acid, NaOH, ammoniated casein, gum arabic and an organic solvent.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35567673A | 1973-04-30 | 1973-04-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1459843A true GB1459843A (en) | 1976-12-31 |
Family
ID=23398361
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1873074A Expired GB1459843A (en) | 1973-04-30 | 1974-04-29 | Contact adhesive |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS5014735A (en) |
| AU (1) | AU6836374A (en) |
| DE (1) | DE2420683B2 (en) |
| FR (1) | FR2227309B1 (en) |
| GB (1) | GB1459843A (en) |
| IT (1) | IT1010238B (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4543387A (en) * | 1983-02-21 | 1985-09-24 | Imperial Chemical Industries Plc | Aqueous latex copolymer compositions |
| US4543386A (en) * | 1983-02-21 | 1985-09-24 | Imperial Chemical Industries Plc | Vinylidene chloride copolymer aqueous latex composition |
| US4783499A (en) * | 1984-12-06 | 1988-11-08 | Imperial Chemical Industries Plc | Vinylidene chloride polymer aqueous latex compositions |
| EP0262376A3 (en) * | 1986-08-30 | 1989-10-11 | Basf Aktiengesellschaft | Aqueous binder dispersions for the preparation of spreading and coating compounds |
| US4975484A (en) * | 1985-05-10 | 1990-12-04 | E. I. Du Pont De Nemours And Company | Acrylic copolymer composition and adhesive coatings therefrom |
| US4980410A (en) * | 1985-05-10 | 1990-12-25 | E. I. Du Pont De Nemours And Company | Acrylic copolymer composition and adhesive coatings therefrom |
| US5418262A (en) * | 1991-12-09 | 1995-05-23 | Heraeus Kulzer Gmbh | Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it |
| WO2014134442A1 (en) * | 2013-03-01 | 2014-09-04 | Valspar Corporation | Aqueous coating compositions including phenolic resin(s) |
| TWI621675B (en) * | 2016-12-21 | 2018-04-21 | Adhesive composition, treated fabric and composite laminate | |
| US10486865B2 (en) | 2013-10-02 | 2019-11-26 | The Sherwin-Williams Company | Removable closure and coating system |
| US11377277B2 (en) | 2013-10-02 | 2022-07-05 | Swimc Llc | Removable closure and coating system |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53121038A (en) * | 1977-02-09 | 1978-10-23 | Nitto Electric Ind Co Ltd | Hot pressure-sensitive tapes or sheets |
| US4228055A (en) * | 1978-09-06 | 1980-10-14 | Ppg Industries, Inc. | Aqueous coating compositions containing flatting agents and low molecular weight polyethers |
| EP0553448A1 (en) * | 1991-12-09 | 1993-08-04 | Kettenbach GmbH & CO. KG | Surface conditioned impression tray |
-
1974
- 1974-04-29 IT IT7422074A patent/IT1010238B/en active
- 1974-04-29 FR FR7414853A patent/FR2227309B1/fr not_active Expired
- 1974-04-29 GB GB1873074A patent/GB1459843A/en not_active Expired
- 1974-04-29 AU AU68363/74A patent/AU6836374A/en not_active Expired
- 1974-04-29 DE DE19742420683 patent/DE2420683B2/en not_active Withdrawn
- 1974-04-30 JP JP49047805A patent/JPS5014735A/ja active Pending
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4543387A (en) * | 1983-02-21 | 1985-09-24 | Imperial Chemical Industries Plc | Aqueous latex copolymer compositions |
| US4543386A (en) * | 1983-02-21 | 1985-09-24 | Imperial Chemical Industries Plc | Vinylidene chloride copolymer aqueous latex composition |
| US4783499A (en) * | 1984-12-06 | 1988-11-08 | Imperial Chemical Industries Plc | Vinylidene chloride polymer aqueous latex compositions |
| US4975484A (en) * | 1985-05-10 | 1990-12-04 | E. I. Du Pont De Nemours And Company | Acrylic copolymer composition and adhesive coatings therefrom |
| US4980410A (en) * | 1985-05-10 | 1990-12-25 | E. I. Du Pont De Nemours And Company | Acrylic copolymer composition and adhesive coatings therefrom |
| EP0262376A3 (en) * | 1986-08-30 | 1989-10-11 | Basf Aktiengesellschaft | Aqueous binder dispersions for the preparation of spreading and coating compounds |
| US5418262A (en) * | 1991-12-09 | 1995-05-23 | Heraeus Kulzer Gmbh | Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it |
| WO2014134442A1 (en) * | 2013-03-01 | 2014-09-04 | Valspar Corporation | Aqueous coating compositions including phenolic resin(s) |
| US10358571B2 (en) | 2013-03-01 | 2019-07-23 | The Sherwin-Williams Company | Aqueous coating compositions including phenolic resin(s) |
| US11225586B2 (en) | 2013-03-01 | 2022-01-18 | Swimc Llc | Aqueous coating compositions including phenolic resin(s) |
| US10486865B2 (en) | 2013-10-02 | 2019-11-26 | The Sherwin-Williams Company | Removable closure and coating system |
| US11377277B2 (en) | 2013-10-02 | 2022-07-05 | Swimc Llc | Removable closure and coating system |
| TWI621675B (en) * | 2016-12-21 | 2018-04-21 | Adhesive composition, treated fabric and composite laminate |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5014735A (en) | 1975-02-17 |
| FR2227309A1 (en) | 1974-11-22 |
| IT1010238B (en) | 1977-01-10 |
| DE2420683B2 (en) | 1977-10-06 |
| DE2420683A1 (en) | 1974-11-07 |
| FR2227309B1 (en) | 1978-01-20 |
| AU6836374A (en) | 1975-10-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |