PH27024A - Spray dried phenol - formaldehyde resin composition - Google Patents

Spray dried phenol - formaldehyde resin composition Download PDF

Info

Publication number: PH27024A
Authority: PH; Philippines
Prior art keywords: resin; powdered; spray; phenol; powder
Prior art date: 1989-07-26

Application number

PH40875A

Other languages

English (en)

Inventor

Shui-Tung Chiu

Original Assignee

Borden 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.)

1989-07-26

Filing date

1990-07-20

Publication date

1993-02-01

1990-07-20 Application filed by Borden Inc filed Critical Borden Inc

1993-02-01 Publication of PH27024A publication Critical patent/PH27024A/en

Links

239000007921 spray Substances 0.000 title claims description 51
229920001568 phenolic resin Polymers 0.000 title claims description 6
239000011342 resin composition Substances 0.000 title description 3
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 title description 2
229920005989 resin Polymers 0.000 claims description 186
239000011347 resin Substances 0.000 claims description 186
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 41
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 22
238000001694 spray drying Methods 0.000 claims description 21
239000002245 particle Substances 0.000 claims description 16
150000001875 compounds Chemical class 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 10
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 9
150000001639 boron compounds Chemical class 0.000 claims description 9
229910052796 boron Inorganic materials 0.000 claims description 7
239000011734 sodium Substances 0.000 claims description 6
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 5
-1 phenol aldehyde Chemical class 0.000 claims description 5
229910052708 sodium Inorganic materials 0.000 claims description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 3
150000001642 boronic acid derivatives Chemical class 0.000 claims description 3
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 claims description 3
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 3
VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 claims description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
LGURYBCSJPXHTF-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)ethyl benzoate Chemical compound ClC1=CC(Cl)=CC=C1OCCOC(=O)C1=CC=CC=C1 LGURYBCSJPXHTF-UHFFFAOYSA-N 0.000 claims 1
229930040373 Paraformaldehyde Natural products 0.000 claims 1
235000010678 Paulownia tomentosa Nutrition 0.000 claims 1
240000002834 Paulownia tomentosa Species 0.000 claims 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims 1
229920002866 paraformaldehyde Polymers 0.000 claims 1
229920003987 resole Polymers 0.000 claims 1
239000000843 powder Substances 0.000 description 59
FWZTTZUKDVJDCM-CEJAUHOTSA-M disodium;(2r,3r,4s,5s,6r)-2-[(2s,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;iron(3+);oxygen(2-);hydroxide;trihydrate Chemical compound O.O.O.[OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 FWZTTZUKDVJDCM-CEJAUHOTSA-M 0.000 description 18
238000004519 manufacturing process Methods 0.000 description 18
229960004279 formaldehyde Drugs 0.000 description 14
235000019256 formaldehyde Nutrition 0.000 description 13
210000000569 greater omentum Anatomy 0.000 description 13
238000006243 chemical reaction Methods 0.000 description 12
229910021538 borax Inorganic materials 0.000 description 11
238000000034 method Methods 0.000 description 11
239000004328 sodium tetraborate Substances 0.000 description 11
235000010339 sodium tetraborate Nutrition 0.000 description 11
239000007787 solid Substances 0.000 description 11
235000012431 wafers Nutrition 0.000 description 11
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 10
239000004327 boric acid Substances 0.000 description 10
239000007788 liquid Substances 0.000 description 9
239000002023 wood Substances 0.000 description 9
238000009826 distribution Methods 0.000 description 8
238000001035 drying Methods 0.000 description 8
239000004615 ingredient Substances 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
150000001299 aldehydes Chemical class 0.000 description 6
241001459693 Dipterocarpus zeylanicus Species 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
239000013068 control sample Substances 0.000 description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
102100028255 Renin Human genes 0.000 description 4
108090000783 Renin Proteins 0.000 description 4
239000011575 calcium Substances 0.000 description 4
229910052791 calcium Inorganic materials 0.000 description 4
238000002156 mixing Methods 0.000 description 4
MOWNZPNSYMGTMD-UHFFFAOYSA-N oxidoboron Chemical compound O=[B] MOWNZPNSYMGTMD-UHFFFAOYSA-N 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
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 4
238000011282 treatment Methods 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
235000011114 ammonium hydroxide Nutrition 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
239000008188 pellet Substances 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
238000003825 pressing Methods 0.000 description 3
239000000523 sample Substances 0.000 description 3
102100039981 Hairy and enhancer of split-related protein HELT Human genes 0.000 description 2
101001034987 Homo sapiens Hairy and enhancer of split-related protein HELT Proteins 0.000 description 2
241000282322 Panthera Species 0.000 description 2
YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
241000183024 Populus tremula Species 0.000 description 2
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 2
UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical compound CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 2
238000010306 acid treatment Methods 0.000 description 2
230000032683 aging Effects 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
239000000378 calcium silicate Substances 0.000 description 2
229910052918 calcium silicate Inorganic materials 0.000 description 2
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
239000002274 desiccant Substances 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000010410 layer Substances 0.000 description 2
PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 2
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 description 2
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 description 2
229920003986 novolac Polymers 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
150000004686 pentahydrates Chemical class 0.000 description 2
230000036647 reaction Effects 0.000 description 2
238000003860 storage Methods 0.000 description 2
239000010875 treated wood Substances 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
YSGQGNQWBLYHPE-CFUSNLFHSA-N (7r,8r,9s,10r,13s,14s,17s)-17-hydroxy-7,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-one Chemical compound C1C[C@]2(C)[C@@H](O)CC[C@H]2[C@@H]2[C@H](C)CC3=CC(=O)CC[C@@H]3[C@H]21 YSGQGNQWBLYHPE-CFUSNLFHSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
JIGWWGDIEUWCOR-UHFFFAOYSA-N 3-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-6-fluorodibenzothiophene 5,5-dioxide Chemical compound C1=C2S(=O)(=O)C=3C(F)=CC=CC=3C2=CC=C1N1CCN2CCC1CC2 JIGWWGDIEUWCOR-UHFFFAOYSA-N 0.000 description 1
JULDKEYYPIYHLQ-UHFFFAOYSA-N 3-hydroxy-2-[[2-[(3-hydroxy-4-oxopyran-2-yl)methyl-methylamino]ethyl-methylamino]methyl]pyran-4-one Chemical compound O1C=CC(=O)C(O)=C1CN(C)CCN(C)CC=1OC=CC(=O)C=1O JULDKEYYPIYHLQ-UHFFFAOYSA-N 0.000 description 1
NGHVIOIJCVXTGV-ALEPSDHESA-N 6-aminopenicillanic acid Chemical compound [O-]C(=O)[C@H]1C(C)(C)S[C@@H]2[C@H]([NH3+])C(=O)N21 NGHVIOIJCVXTGV-ALEPSDHESA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
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241000356604 Beara Species 0.000 description 1
241000270299 Boa Species 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
101100440699 Drosophila melanogaster corto gene Proteins 0.000 description 1
102100023630 E3 ubiquitin-protein ligase ZNF598 Human genes 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
241001539176 Hime Species 0.000 description 1
101000976468 Homo sapiens E3 ubiquitin-protein ligase ZNF598 Proteins 0.000 description 1
101000635799 Homo sapiens Run domain Beclin-1-interacting and cysteine-rich domain-containing protein Proteins 0.000 description 1
241000511976 Hoya Species 0.000 description 1
208000022120 Jeavons syndrome Diseases 0.000 description 1
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
241000489861 Maximus Species 0.000 description 1
241000252067 Megalops atlanticus Species 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
101100328463 Mus musculus Cmya5 gene Proteins 0.000 description 1
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244000234179 Myrtus ugni Species 0.000 description 1
235000012093 Myrtus ugni Nutrition 0.000 description 1
UGJBHEZMOKVTIM-UHFFFAOYSA-N N-formylglycine Chemical compound OC(=O)CNC=O UGJBHEZMOKVTIM-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
241001282736 Oriens Species 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
241001237728 Precis Species 0.000 description 1
OOPDAHSJBRZRPH-UHFFFAOYSA-L Pyrvinium pamoate Chemical compound C1=CC2=CC(N(C)C)=CC=C2[N+](C)=C1C=CC(=C1C)C=C(C)N1C1=CC=CC=C1.C1=CC2=CC(N(C)C)=CC=C2[N+](C)=C1C=CC(=C1C)C=C(C)N1C1=CC=CC=C1.C12=CC=CC=C2C=C(C([O-])=O)C(O)=C1CC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 OOPDAHSJBRZRPH-UHFFFAOYSA-L 0.000 description 1
101100009350 Rattus norvegicus Depp gene Proteins 0.000 description 1
102100030852 Run domain Beclin-1-interacting and cysteine-rich domain-containing protein Human genes 0.000 description 1
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PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
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240000004668 Valerianella locusta Species 0.000 description 1
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230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
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229940060515 aleve Drugs 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
NTBYNMBEYCCFPS-UHFFFAOYSA-N azane boric acid Chemical class N.N.N.OB(O)O NTBYNMBEYCCFPS-UHFFFAOYSA-N 0.000 description 1
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ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
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238000006482 condensation reaction Methods 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000012792 core layer Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
235000013367 dietary fats Nutrition 0.000 description 1
RSCACTKJFSTWPV-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;pentahydrate Chemical compound O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 RSCACTKJFSTWPV-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
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238000001704 evaporation Methods 0.000 description 1
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239000010520 ghee Substances 0.000 description 1
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QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
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UOJMTSCORVQOHS-UHFFFAOYSA-N pachypodol Natural products COc1cc(ccc1O)C2=C(C)C(=O)c3c(O)cc(C)cc3O2 UOJMTSCORVQOHS-UHFFFAOYSA-N 0.000 description 1
239000003415 peat Substances 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
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239000004014 plasticizer Substances 0.000 description 1
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229940072033 potash Drugs 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
JVUYWILPYBCNNG-UHFFFAOYSA-N potassium;oxido(oxo)borane Chemical compound [K+].[O-]B=O JVUYWILPYBCNNG-UHFFFAOYSA-N 0.000 description 1
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
RIUWBIIVUYSTCN-UHFFFAOYSA-N trilithium borate Chemical class [Li+].[Li+].[Li+].[O-]B([O-])[O-] RIUWBIIVUYSTCN-UHFFFAOYSA-N 0.000 description 1
239000003643 water by type Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/122—Pulverisation by spraying
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
- 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
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
- C08J2361/04—Condensation polymers of aldehydes or ketones with phenols only
- C08J2361/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Dry Formation Of Fiberboard And The Like (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Adhesives Or Adhesive Processes (AREA)

PH40875A 1989-07-26 1990-07-20 Spray dried phenol - formaldehyde resin composition PH27024A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/385,571 US4950433A (en)	1989-07-26	1989-07-26	Method of spray drying phenol-formaldehyde resin compositions

Publications (1)

Publication Number	Publication Date
PH27024A true PH27024A (en)	1993-02-01

Family

ID=23521973

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH40875A PH27024A (en)	1989-07-26	1990-07-20	Spray dried phenol - formaldehyde resin composition

Country Status (7)

Country	Link
US (1)	US4950433A (fr)
JP (1)	JP3027398B2 (fr)
AU (1)	AU629659B2 (fr)
CA (1)	CA1337614C (fr)
MY (1)	MY109483A (fr)
NZ (1)	NZ234626A (fr)
PH (1)	PH27024A (fr)

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US5207954A (en) *	1989-09-25	1993-05-04	Union Carbide Chemicals & Plastics Technology Corporation	Method of making coreactable powdered coatings
US5145913A (en) *	1990-08-02	1992-09-08	Borden, Inc.	Retarders for curing phenolic resole resins
US5262495A (en) *	1990-08-02	1993-11-16	Borden, Inc.	Retarders for curing phenolic resole resins containing an aggregate material
US5096983A (en) *	1990-08-02	1992-03-17	Borden, Inc.	Method for making a phenolic resole resin composition having extended work life
NL9201461A (nl) *	1992-08-17	1994-03-16	Dsm Nv	Werkwijze voor de bereiding van een fenol-formaldehydehars.
US5693085A (en)	1994-04-29	1997-12-02	Scimed Life Systems, Inc.	Stent with collagen
US6023855A (en) *	1996-11-27	2000-02-15	The United States Of America As Represented By The Secretary Of Agriculture	Air-assisted wiping device
US6627131B2 (en) *	2001-02-09	2003-09-30	Georgia-Pacific Resins, Inc.	Method for introducing an additive to a composite panel
US6818707B2 (en) *	2002-01-08	2004-11-16	Borden Chemical, Inc.	Spray dried phenolic resole molding powder with crystalline phenolic compounds
US6608162B1 (en)	2002-03-15	2003-08-19	Borden Chemical, Inc.	Spray-dried phenol formaldehyde resins
US7064175B2 (en) *	2002-04-26	2006-06-20	Mitanic, Inc.	Adhesive system containing tannin for binding lignocellulosic materials
DE10314466A1 (de) *	2003-03-28	2004-10-14	Basf Ag	Verfahren zur Herstellung von kondensierten Harzen in Pulverform
EP1649322A4 (fr)	2003-07-17	2007-09-19	Honeywell Int Inc	Films de planarisation pour dispositifs et applications en microelectronique avancee et procedes de production desdits films
US7141195B2 (en) *	2003-09-05	2006-11-28	Weyerhaeuser Co.	Process for making engineered lignocellulosic-based panels
US20050054807A1 (en) *	2003-09-05	2005-03-10	Weyerhaeuser Company	Low-nitrogen content phenol-formaldehyde resin
US20060128886A1 (en) *	2004-12-14	2006-06-15	Winterowd Jack G	Low-nitrogen content phenol-formaldehyde resin
WO2008113181A1 (fr) *	2007-03-21	2008-09-25	Alberta Research Council Inc.	Résines modifiées par de l'argile de phyllosilicate pour des panneaux composites à base de fibres lignocellulosiques
US8569430B2 (en)	2009-12-09	2013-10-29	Georgia-Pacific Chemicals Llc	Method of spray drying phenol-formaldehyde resin
CN102443181B (zh) *	2011-10-24	2013-04-10	太仓力达莱特精密工业有限公司	一种热固性硼酚醛树脂粉末的制备方法
CN103409841B (zh) *	2013-07-30	2015-11-04	中原工学院	硼酸改性高邻位酚醛纤维的制备方法

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1138589A (fr) *	1979-04-20	1982-12-28	Krishan K. Sudan	Liant de resine phenolique au lignosulfonate
FR2599746B1 (fr) *	1986-06-05	1989-01-13	Charbonnages Ste Chimique	Nouvelles compositions resineuses a base de resines phenoliques
FR2633630B1 (fr) *	1988-06-30	1992-05-22	Norsolor Sa	Compositions resineuses a base de resines phenoliques

1989
- 1989-07-26 US US07/385,571 patent/US4950433A/en not_active Expired - Lifetime
- 1989-09-13 CA CA000611262A patent/CA1337614C/fr not_active Expired - Lifetime
1990
- 1990-06-22 MY MYPI90001060A patent/MY109483A/en unknown
- 1990-07-05 AU AU58733/90A patent/AU629659B2/en not_active Ceased
- 1990-07-20 PH PH40875A patent/PH27024A/en unknown
- 1990-07-24 NZ NZ234626A patent/NZ234626A/xx unknown
- 1990-07-26 JP JP2198955A patent/JP3027398B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JP3027398B2 (ja)	2000-04-04
MY109483A (en)	1997-02-28
JPH03163136A (ja)	1991-07-15
US4950433A (en)	1990-08-21
CA1337614C (fr)	1995-11-21
AU5873390A (en)	1991-02-07
NZ234626A (en)	1991-11-26
AU629659B2 (en)	1992-10-08

Publication	Publication Date	Title
PH27024A (en)	1993-02-01	Spray dried phenol - formaldehyde resin composition
US6608162B1 (en)	2003-08-19	Spray-dried phenol formaldehyde resins
US3919134A (en)	1975-11-11	Thermal insulation of mineral fiber matrix bound with phenolic resin
EP0793680B1 (fr)	1998-10-14	Resine phenol-aldehyde modifiee et procede pour sa production
FI114462B (fi)	2004-10-29	Veden- ja tulenkestäviä materiaaleja ja menetelmiä niiden valmistamiseksi
EP0013447B1 (fr)	1983-05-18	Fabrication de panneaux de copeaux de bois
US4433120A (en)	1984-02-21	Liquid phenolic resin composition and method for waferboard manufacture
US5646219A (en)	1997-07-08	Method of preparing binder system and product thereof
US4960826A (en)	1990-10-02	Melamine-containing resole resitol and resite compositions
CS256385B2 (en)	1988-04-15	Method of urea formaldehyde resin preparation with superlow formaldehyde-urea molecular ratio
US3932334A (en)	1976-01-13	Calcia catalyzed resins
US5047275A (en)	1991-09-10	Spray dried phenol-formaldehyde resin compositions
US5847058A (en)	1998-12-08	Alkylresorcinol modified phenol-aldehyde resol resin and binder system, and method of making same
USRE30375E (en)	1980-08-19	Calcia catalyzed resins
US3185654A (en)	1965-05-25	Composition containing resole and lignin in free acid form and process for preparing same
US5367040A (en)	1994-11-22	Precure resistant thermoset resin for molded wood composites
US5916966A (en)	1999-06-29	Stabilized phenolic resin melamine dispersions and methods of making same
US4052359A (en)	1977-10-04	Dilutable resole resin solutions having stabilized dispersed inert salts
WO2019189410A1 (fr)	2019-10-03	Liant pour produits à base de fibres inorganiques, procédé de fabrication dudit liant et procédé de fabrication d'un produit à base de fibres inorganiques
US5019618A (en)	1991-05-28	Spray dried phenol-formaldehyde resin compositions
US5290843A (en)	1994-03-01	Phenolic resins for reinforced composites
CA1049174A (fr)	1979-02-20	Liants phenol-acetone-formol pour produits forestiers imputrescibles
US3471420A (en)	1969-10-07	Acetone-formaldehyde and phenol-acetone-formaldehyde resins extended with animal blood or soy flour and oil-in-water emulsion
FI113274B (fi)	2004-03-31	Sideaineita lignoselluloosapitoisten muotokappaleiden valmistamiseksi
EP1597294A1 (fr)	2005-11-23	Copolymeres phenol uree/melamine formaldehyde, leur procede de production et leur utilisation