CA1076730A - Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau - Google Patents

Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau

Info

Publication number: CA1076730A
Authority: CA; Canada
Prior art keywords: curtain; composition; diol; phenol; adhesive
Prior art date: 1976-04-01
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

Application number

CA249,342A

Other languages

English (en)

Inventor

Paul Robitschek

Norman A. Chappelie

John W. Lorimer

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Chembond Corp

Original Assignee

Chembond Corp

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.)

1976-04-01

Filing date

1976-04-01

Publication date

1980-04-29

1976-04-01 Application filed by Chembond Corp filed Critical Chembond Corp

1976-04-01 Priority to CA249,342A priority Critical patent/CA1076730A/fr

1980-04-29 Application granted granted Critical

1980-04-29 Publication of CA1076730A publication Critical patent/CA1076730A/fr

Status Expired legal-status Critical Current

Links

239000000853 adhesive Substances 0.000 title claims abstract description 67
230000001070 adhesive effect Effects 0.000 title claims abstract description 66
LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical compound CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-UHFFFAOYSA-N 0.000 title claims abstract description 19
238000007766 curtain coating Methods 0.000 title claims abstract description 15
229920003987 resole Polymers 0.000 title 1
239000000203 mixture Substances 0.000 claims abstract description 62
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 41
150000002009 diols Chemical class 0.000 claims abstract description 33
239000007788 liquid Substances 0.000 claims abstract description 27
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 12
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 7
239000000945 filler Substances 0.000 claims abstract description 7
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 7
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims abstract description 5
239000000654 additive Substances 0.000 claims description 31
230000000996 additive effect Effects 0.000 claims description 27
229920005989 resin Polymers 0.000 claims description 23
239000011347 resin Substances 0.000 claims description 23
229920001568 phenolic resin Polymers 0.000 claims description 17
239000007787 solid Substances 0.000 claims description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
-1 phenol aldehyde Chemical class 0.000 claims description 9
239000002562 thickening agent Substances 0.000 claims description 7
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 claims description 6
239000000463 material Substances 0.000 claims description 5
239000011120 plywood Substances 0.000 abstract description 15
238000004519 manufacturing process Methods 0.000 abstract description 8
239000000758 substrate Substances 0.000 abstract description 4
239000011248 coating agent Substances 0.000 abstract description 2
238000000576 coating method Methods 0.000 abstract description 2
239000003292 glue Substances 0.000 description 26
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
238000009740 moulding (composite fabrication) Methods 0.000 description 14
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 12
239000000047 product Substances 0.000 description 12
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 11
238000000034 method Methods 0.000 description 10
150000002170 ethers Chemical class 0.000 description 9
238000009736 wetting Methods 0.000 description 9
239000000243 solution Substances 0.000 description 8
239000002023 wood Substances 0.000 description 8
239000000470 constituent Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
235000011121 sodium hydroxide Nutrition 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
241000209140 Triticum Species 0.000 description 5
235000021307 Triticum Nutrition 0.000 description 5
240000008042 Zea mays Species 0.000 description 5
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
235000002017 Zea mays subsp mays Nutrition 0.000 description 5
235000005822 corn Nutrition 0.000 description 5
235000013312 flour Nutrition 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 4
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
239000000126 substance Substances 0.000 description 4
CSHOPPGMNYULAD-UHFFFAOYSA-N 1-tridecoxytridecane Chemical compound CCCCCCCCCCCCCOCCCCCCCCCCCCC CSHOPPGMNYULAD-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
239000004606 Fillers/Extenders Substances 0.000 description 3
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical class CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
150000001299 aldehydes Chemical class 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
235000013824 polyphenols Nutrition 0.000 description 3
235000017550 sodium carbonate Nutrition 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
238000012360 testing method Methods 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
239000003513 alkali Substances 0.000 description 2
239000008280 blood Substances 0.000 description 2
210000004369 blood Anatomy 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
238000013329 compounding Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229960004279 formaldehyde Drugs 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
CRMIJUGSUHPVNT-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne Chemical compound CC(C)CC(C)C#CC(C)CC(C)C CRMIJUGSUHPVNT-UHFFFAOYSA-N 0.000 description 1
IHJUECRFYCQBMW-UHFFFAOYSA-N 2,5-dimethylhex-3-yne-2,5-diol Chemical compound CC(C)(O)C#CC(C)(C)O IHJUECRFYCQBMW-UHFFFAOYSA-N 0.000 description 1
ZWNMRZQYWRLGMM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diol Chemical compound CC(C)(O)CCC(C)(C)O ZWNMRZQYWRLGMM-UHFFFAOYSA-N 0.000 description 1
NUYADIDKTLPDGG-UHFFFAOYSA-N 3,6-dimethyloct-4-yne-3,6-diol Chemical compound CCC(C)(O)C#CC(C)(O)CC NUYADIDKTLPDGG-UHFFFAOYSA-N 0.000 description 1
PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 description 1
CUUQUEAUUPYEKK-UHFFFAOYSA-N 4-ethyloct-1-yn-3-ol Chemical compound CCCCC(CC)C(O)C#C CUUQUEAUUPYEKK-UHFFFAOYSA-N 0.000 description 1
XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000004439 Isononyl alcohol Substances 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
239000002313 adhesive film Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000005456 alcohol based solvent Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003518 caustics Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
DPWCXHJKJXRDBZ-UHFFFAOYSA-N dec-5-yne-4,7-diol Chemical compound CCCC(O)C#CC(O)CCC DPWCXHJKJXRDBZ-UHFFFAOYSA-N 0.000 description 1
230000002950 deficient Effects 0.000 description 1
238000013461 design Methods 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
VOOLKNUJNPZAHE-UHFFFAOYSA-N formaldehyde;2-methylphenol Chemical compound O=C.CC1=CC=CC=C1O VOOLKNUJNPZAHE-UHFFFAOYSA-N 0.000 description 1
229920005546 furfural resin Polymers 0.000 description 1
BTDWSZJDLLLTMI-UHFFFAOYSA-N hex-2-yn-1-ol Natural products CCCC#CCO BTDWSZJDLLLTMI-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 description 1
229960002238 methylpentynol Drugs 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
MWKFXSUHUHTGQN-UHFFFAOYSA-N n-decyl alcohol Natural products CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
238000011017 operating method Methods 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
229960004063 propylene glycol Drugs 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229940070376 protein Drugs 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000002481 rotproofing Substances 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000000926 separation method Methods 0.000 description 1
DGSDBJMBHCQYGN-UHFFFAOYSA-M sodium;2-ethylhexyl sulfate Chemical compound [Na+].CCCCC(CC)COS([O-])(=O)=O DGSDBJMBHCQYGN-UHFFFAOYSA-M 0.000 description 1
HHURSJAUVYNJBT-UHFFFAOYSA-M sodium;heptadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCCOS([O-])(=O)=O HHURSJAUVYNJBT-UHFFFAOYSA-M 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
239000001570 sorbitan monopalmitate Substances 0.000 description 1
229940031953 sorbitan monopalmitate Drugs 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
150000003739 xylenols Chemical class 0.000 description 1

Landscapes

Adhesives Or Adhesive Processes (AREA)
Veneer Processing And Manufacture Of Plywood (AREA)

CA249,342A 1976-04-01 1976-04-01 Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau Expired CA1076730A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA249,342A CA1076730A (fr)	1976-04-01	1976-04-01	Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA249,342A CA1076730A (fr)	1976-04-01	1976-04-01	Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau

Publications (1)

Publication Number	Publication Date
CA1076730A true CA1076730A (fr)	1980-04-29

Family

ID=4105610

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA249,342A Expired CA1076730A (fr)	1976-04-01	1976-04-01	Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau

Country Status (1)

Country	Link
CA (1)	CA1076730A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2022152946A1 (fr)	2021-01-18	2022-07-21	Foresa Technologies, S.L.U.	Formulation de résine phénol-formaldéhyde et adhésif pour couchage à nappe

1976
- 1976-04-01 CA CA249,342A patent/CA1076730A/fr not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2022152946A1 (fr)	2021-01-18	2022-07-21	Foresa Technologies, S.L.U.	Formulation de résine phénol-formaldéhyde et adhésif pour couchage à nappe

Legal Events

Date	Code	Title	Description
1997-04-29	MKEX	Expiry
2024-02-20	MKEX	Expiry	Effective date: 19970429

Publication	Publication Date	Title
DE60016493T2 (de)	2005-11-03	Verwendung von anionischen oder cationischen Weichmachern mit sulfonierten Polyestern in Heissschmelzformulierungen
DE60220085T2 (de)	2008-01-10	Verfahren zum Verkleben von Materialien auf Holzbasis
US3966658A (en)	1976-06-29	Liquid phenol-aldehyde adhesive for use in curtain-coating adhesive applicators
SE1950773A1 (en)	2020-12-25	Process for preparing a bonding resin
AU2002339807A1 (en)	2003-07-03	Method of gluing wood based materials
AU2002339806A1 (en)	2003-07-03	Method of gluing wood based materials
US7452442B2 (en)	2008-11-18	Gluing wood based materials with melaminic amino resin and resorcinol or tannin resin
US3947425A (en)	1976-03-30	Rapid curing, hydrophilic resin compositions
US4182732A (en)	1980-01-08	Thermosetting phenolic resin coating and adhesive compositions
US3661814A (en)	1972-05-09	Phenol-formaldehyde adhesive resins by addition of polyhydric alcohols
WO1993003111A1 (fr)	1993-02-18	Adhesif aqueux
US3949149A (en)	1976-04-06	Process for the production of wood materials having high resistance to hot water, said materials containing phenol-aldehyde resin and alkylene carbonate hardener
AU2017252245B2 (en)	2019-11-28	Incorporation of boron complex into resin
US20070149657A1 (en)	2007-06-28	Corrugating adhesives for bonding coated papers and methods for bonding coated papers
US20040102546A1 (en)	2004-05-27	Corrugating adhesives for bonding coated papers and methods for bonding coated papers
US3074897A (en)	1963-01-22	Aqueous alkaline adhesive comprising phenol-formaldehyde condensate and homopolymers of ethylene oxide
US4034012A (en)	1977-07-05	Acetone-formaldehyde-resorcinol resin compositions and adhesives prepared therefrom
US2886540A (en)	1959-05-12	Phenol-formaldehyde-ketone condensate and starch composition
JP2001115120A (ja)	2001-04-24	段ボール用耐水接着剤
US2890182A (en)	1959-06-09	Method of increasing pot life of adhesive compositions containing an amylaceous component, a phenolic compound, and an aldehyde
US3591535A (en)	1971-07-06	High molecular weight/low molecular weight phenol-formaldehyde curtain coating adhesive composition
JP2645321B2 (ja)	1997-08-25	レゾルシノール系樹脂接着剤組成物
US1989150A (en)	1935-01-29	Glue
US2930772A (en)	1960-03-29	Adhesive ingredient and process
US2375195A (en)	1945-05-08	Coating and method of preparing same

CA1076730A - Adhesif de resol de phenolaldehyde en milieu aqueux contenant des derives de tetramethyldecynediol pour l'enduction en rideau - Google Patents

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Links

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Priority Applications (1)

Applications Claiming Priority (1)

Publications (1)

Family

ID=4105610

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

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