PH26826A - Latently curable binder compositions which contain cure enhancing agents - Google Patents

Latently curable binder compositions which contain cure enhancing agents Download PDF

Info

Publication number: PH26826A
Authority: PH; Philippines
Prior art keywords: curing agent; resin; binder composition; resin solution; weight
Prior art date: 1987-09-30

Application number

PH37170A

Other languages

English (en)

Inventor

Richard D Stratton

David A Perry

Original Assignee

Perkins Ind Inc

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.)

1987-09-30

Filing date

1988-07-04

Publication date

1992-11-05

1988-07-04 Application filed by Perkins Ind Inc filed Critical Perkins Ind Inc

1992-11-05 Publication of PH26826A publication Critical patent/PH26826A/en

Links

239000000203 mixture Substances 0.000 title claims description 137
239000003795 chemical substances by application Substances 0.000 title claims description 86
239000011230 binding agent Substances 0.000 title claims description 83
230000002708 enhancing effect Effects 0.000 title description 4
238000001723 curing Methods 0.000 claims description 87
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 81
229920005989 resin Polymers 0.000 claims description 63
239000011347 resin Substances 0.000 claims description 63
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 53
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 41
229920001568 phenolic resin Polymers 0.000 claims description 39
239000007787 solid Substances 0.000 claims description 38
238000000034 method Methods 0.000 claims description 37
239000005011 phenolic resin Substances 0.000 claims description 31
239000002023 wood Substances 0.000 claims description 29
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 27
230000008569 process Effects 0.000 claims description 26
RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 26
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 24
238000004519 manufacturing process Methods 0.000 claims description 21
URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims description 20
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 18
239000007788 liquid Substances 0.000 claims description 18
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 10
239000004202 carbamide Substances 0.000 claims description 10
150000002148 esters Chemical group 0.000 claims description 10
235000013773 glyceryl triacetate Nutrition 0.000 claims description 10
230000009257 reactivity Effects 0.000 claims description 10
229960002622 triacetin Drugs 0.000 claims description 10
238000001816 cooling Methods 0.000 claims description 9
239000001087 glyceryl triacetate Substances 0.000 claims description 9
238000010438 heat treatment Methods 0.000 claims description 9
239000012978 lignocellulosic material Substances 0.000 claims description 9
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 8
229940099112 cornstarch Drugs 0.000 claims description 8
150000002596 lactones Chemical class 0.000 claims description 8
239000011734 sodium Substances 0.000 claims description 8
229910052708 sodium Inorganic materials 0.000 claims description 8
229920002261 Corn starch Polymers 0.000 claims description 7
239000008120 corn starch Substances 0.000 claims description 7
239000004576 sand Substances 0.000 claims description 7
238000013019 agitation Methods 0.000 claims description 6
150000001299 aldehydes Chemical class 0.000 claims description 6
238000001879 gelation Methods 0.000 claims description 6
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 5
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
239000011819 refractory material Substances 0.000 claims description 4
229910052845 zircon Inorganic materials 0.000 claims description 4
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 4
229920002522 Wood fibre Polymers 0.000 claims description 3
229930188620 butyrolactone Natural products 0.000 claims description 3
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 3
RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 claims description 3
150000005677 organic carbonates Chemical class 0.000 claims description 3
239000002025 wood fiber Substances 0.000 claims description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
150000001733 carboxylic acid esters Chemical class 0.000 claims description 2
239000000395 magnesium oxide Substances 0.000 claims description 2
229960003742 phenol Drugs 0.000 claims 11
239000003513 alkali Substances 0.000 claims 7
241000478345 Afer Species 0.000 claims 1
150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
239000007795 chemical reaction product Substances 0.000 claims 1
239000007859 condensation product Substances 0.000 claims 1
125000000524 functional group Chemical group 0.000 claims 1
229910052609 olivine Inorganic materials 0.000 claims 1
239000010450 olivine Substances 0.000 claims 1
HTYIXCKSEQQCJO-UHFFFAOYSA-N phenaglycodol Chemical compound CC(C)(O)C(C)(O)C1=CC=C(Cl)C=C1 HTYIXCKSEQQCJO-UHFFFAOYSA-N 0.000 claims 1
239000000243 solution Substances 0.000 description 39
238000007792 addition Methods 0.000 description 29
229940032159 propylene carbonate Drugs 0.000 description 19
239000011120 plywood Substances 0.000 description 18
238000006243 chemical reaction Methods 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
239000000853 adhesive Substances 0.000 description 12
230000001070 adhesive effect Effects 0.000 description 12
230000005484 gravity Effects 0.000 description 12
239000000499 gel Substances 0.000 description 11
229960004279 formaldehyde Drugs 0.000 description 10
238000003860 storage Methods 0.000 description 9
230000000717 retained effect Effects 0.000 description 8
239000000084 colloidal system Substances 0.000 description 7
239000003292 glue Substances 0.000 description 7
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 6
239000000835 fiber Substances 0.000 description 6
235000013824 polyphenols Nutrition 0.000 description 6
229940095050 propylene Drugs 0.000 description 6
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000004606 Fillers/Extenders Substances 0.000 description 5
-1 cresole Chemical compound 0.000 description 5
239000000463 material Substances 0.000 description 5
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
239000002253 acid Substances 0.000 description 4
230000009471 action Effects 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
239000002245 particle Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
238000004026 adhesive bonding Methods 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
230000008901 benefit Effects 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
230000003247 decreasing effect Effects 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
235000013312 flour Nutrition 0.000 description 3
239000010410 layer Substances 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
239000011591 potassium Substances 0.000 description 3
TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 description 2
OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
239000000919 ceramic Substances 0.000 description 2
150000005690 diesters Chemical class 0.000 description 2
238000009826 distribution Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000006260 foam Substances 0.000 description 2
239000013505 freshwater Substances 0.000 description 2
238000007731 hot pressing Methods 0.000 description 2
230000007774 longterm Effects 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000002365 multiple layer Substances 0.000 description 2
QEVHRUUCFGRFIF-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C(C5=CC=C(OC)C=C5N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 QEVHRUUCFGRFIF-MDEJGZGSSA-N 0.000 description 2
229920003987 resole Polymers 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
239000007858 starting material Substances 0.000 description 2
235000012431 wafers Nutrition 0.000 description 2
WLNBMPZUVDTASE-HXIISURNSA-N (2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanal;sulfuric acid Chemical compound [O-]S([O-])(=O)=O.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO WLNBMPZUVDTASE-HXIISURNSA-N 0.000 description 1
JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
JFMGYULNQJPJCY-UHFFFAOYSA-N 4-(hydroxymethyl)-1,3-dioxolan-2-one Chemical compound OCC1COC(=O)O1 JFMGYULNQJPJCY-UHFFFAOYSA-N 0.000 description 1
KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
229920000049 Carbon (fiber) Polymers 0.000 description 1
241000543381 Cliftonia monophylla Species 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241000490229 Eucephalus Species 0.000 description 1
241001640034 Heteropterys Species 0.000 description 1
241000283986 Lepus Species 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
102100028255 Renin Human genes 0.000 description 1
108090000783 Renin Proteins 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
239000000292 calcium oxide Substances 0.000 description 1
ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
229960005286 carbaryl Drugs 0.000 description 1
CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
239000004917 carbon fiber Substances 0.000 description 1
CHYOCNJYMLMTNE-UHFFFAOYSA-N carbonic acid;pentane-1,2-diol Chemical compound OC(O)=O.CCCC(O)CO CHYOCNJYMLMTNE-UHFFFAOYSA-N 0.000 description 1
239000000306 component Substances 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000011094 fiberboard Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
FOXPDHYHTBBLBU-UHFFFAOYSA-N formaldehyde;phenol;potassium Chemical compound [K].O=C.OC1=CC=CC=C1 FOXPDHYHTBBLBU-UHFFFAOYSA-N 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
230000002427 irreversible effect Effects 0.000 description 1
ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000003607 modifier Substances 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
239000000123 paper Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
238000003908 quality control method Methods 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000002964 rayon Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical class CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)
Adhesives Or Adhesive Processes (AREA)
Phenolic Resins Or Amino Resins (AREA)

PH37170A 1987-09-30 1988-07-04 Latently curable binder compositions which contain cure enhancing agents PH26826A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US10266587A	1987-09-30	1987-09-30

Publications (1)

Publication Number	Publication Date
PH26826A true PH26826A (en)	1992-11-05

Family

ID=22291026

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH37170A PH26826A (en)	1987-09-30	1988-07-04	Latently curable binder compositions which contain cure enhancing agents

Country Status (4)

Country	Link
JP (1)	JP2785912B2 (fr)
AU (1)	AU600601B2 (fr)
CA (1)	CA1330604C (fr)
PH (1)	PH26826A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19854207A1 (de)	1998-11-24	2000-05-25	Wacker Chemie Gmbh	Verfahren zur Herstellung von schnellhärtenden, mit Phenolharz gebundenen Formkörpern
NL1037314C2 (nl) *	2009-09-23	2011-03-28	Jakob Gerrit Hendrik Pannekoek	Olivijn coating.
CN119566216B (zh) *	2024-11-19	2026-01-16	沈阳工业大学	无机粘结剂砂硬化工艺方法及应用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU553707B2 (en) *	1982-04-27	1986-07-24	Borden (Uk) Limited	Impregnated filter paper
EP0259042A3 (fr) *	1986-09-03	1989-01-25	Borden, Inc.	Procédé pour lier des matériaux lignocellulosiques
US4758478A (en) *	1986-09-30	1988-07-19	Daisy Nick K	Fast curing phenolic resins and bonding methods employing same

1988
- 1988-05-18 CA CA 567126 patent/CA1330604C/fr not_active Expired - Fee Related
- 1988-07-04 PH PH37170A patent/PH26826A/en unknown
- 1988-09-29 JP JP63242623A patent/JP2785912B2/ja not_active Expired - Lifetime
- 1988-09-29 AU AU22974/88A patent/AU600601B2/en not_active Ceased

Also Published As

Publication number	Publication date
AU600601B2 (en)	1990-08-16
AU2297488A (en)	1989-04-06
JP2785912B2 (ja)	1998-08-13
JPH01132650A (ja)	1989-05-25
CA1330604C (fr)	1994-07-05

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US8241415B2 (en)	2012-08-14	Wax formulations for lignocellulosic products, methods of their manufacture and products formed therefrom
US4758478A (en)	1988-07-19	Fast curing phenolic resins and bonding methods employing same
US4098770A (en)	1978-07-04	Spray-dried phenolic adhesives
EP1288237A2 (fr)	2003-03-05	Procédé de préparation d'un liqueur noire a base d'une resine phenol formaldehyde thermodurcissable
JP3027398B2 (ja)	2000-04-04	硬化可能なフェノール―アルデヒド噴霧乾燥粉末の製造法
US2574784A (en)	1951-11-13	Phenolic adhesive and method of bonding wood plies
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US4082903A (en)	1978-04-04	Tree foliage extenders and fillers for wood adhesives
US2962459A (en)	1960-11-29	Composition comprising phenolic resin and cellulosic material coated with petroleum hydrocarbon and process for preparing board therefrom
US5047275A (en)	1991-09-10	Spray dried phenol-formaldehyde resin compositions
US5446089A (en)	1995-08-29	Resorcinol-glutaraldehyde resin as an accelerator for curing phenol-formaldehyde resins
US3839251A (en)	1974-10-01	Phenolic resin and process for making same
US3793113A (en)	1974-02-19	Adhesive compositions and method of making plywood
US4977231A (en)	1990-12-11	Phenolic resin containing a latent hardening agent comprising the carbamate reaction product of a cyclic
US4968773A (en)	1990-11-06	Process for the preparation of urea-formaldehyde resins
US20060094853A1 (en)	2006-05-04	Modified phenol-formaldehyde resole resins, methods of manufacture, methods of use, and articles formed therefrom
US2889241A (en)	1959-06-02	Phenolic resin composition and means for controlling viscosity of same
US2781328A (en)	1957-02-12	Phenolic resin glue compositions containing hydrolyzed ligno-cellulosic degradation products
PH26826A (en)	1992-11-05	Latently curable binder compositions which contain cure enhancing agents
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
US3074897A (en)	1963-01-22	Aqueous alkaline adhesive comprising phenol-formaldehyde condensate and homopolymers of ethylene oxide
US3268460A (en)	1966-08-23	Adhesive and method of making the same
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US3267053A (en)	1966-08-16	Phenol-formaldehyde resin compositions
US2781327A (en)	1957-02-12	Phenolic resin glue compositions containing modified bark phloem flour