CS228905B2 - Method or manufacturing boards from particles - Google Patents

Method or manufacturing boards from particles Download PDF

Info

Publication number: CS228905B2
Authority: CS; Czechoslovakia
Prior art keywords: alkyl; particles; formula; polyisocyanate; compound
Prior art date: 1980-04-14

Application number

CS812452A

Other languages

Czech (cs)

English (en)

Inventor

William J Farrissev

Laughlin Alexander Mc

Reinhard H Richter

Curtis P Smith

Benjamin W Tucker

Original Assignee

Upjohn Co

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.)

1980-04-14

Filing date

1981-04-01

Publication date

1984-05-14

1981-04-01 Application filed by Upjohn Co filed Critical Upjohn Co

1982-09-14 Priority to CS826618A priority Critical patent/CS228940B2/cs

1984-05-14 Publication of CS228905B2 publication Critical patent/CS228905B2/cs

Links

239000002245 particle Substances 0.000 title claims abstract description 82
238000000034 method Methods 0.000 title claims description 76
238000004519 manufacturing process Methods 0.000 title description 9
239000005056 polyisocyanate Substances 0.000 claims abstract description 77
229920001228 polyisocyanate Polymers 0.000 claims abstract description 77
-1 hydrocarbylureido Chemical group 0.000 claims abstract description 63
238000002360 preparation method Methods 0.000 claims abstract description 37
239000000839 emulsion Substances 0.000 claims abstract description 26
229910019142 PO4 Inorganic materials 0.000 claims abstract description 25
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
125000000217 alkyl group Chemical group 0.000 claims abstract description 17
125000003118 aryl group Chemical group 0.000 claims abstract description 8
229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 5
125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
125000004423 acyloxy group Chemical group 0.000 claims abstract description 3
229910052794 bromium Inorganic materials 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 59
229920006389 polyphenyl polymer Polymers 0.000 claims description 28
150000001875 compounds Chemical class 0.000 claims description 26
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 22
239000010452 phosphate Substances 0.000 claims description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
238000006243 chemical reaction Methods 0.000 claims description 15
239000003995 emulsifying agent Substances 0.000 claims description 13
239000000463 material Substances 0.000 claims description 13
JVDAQRSNKWBATO-UHFFFAOYSA-N 1-[chloro(dodecoxy)phosphoryl]oxydodecane Chemical compound CCCCCCCCCCCCOP(Cl)(=O)OCCCCCCCCCCCC JVDAQRSNKWBATO-UHFFFAOYSA-N 0.000 claims description 11
239000011541 reaction mixture Substances 0.000 claims description 8
239000000460 chlorine Substances 0.000 claims description 7
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
239000006185 dispersion Substances 0.000 claims description 6
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
LOLGINHRZSNUDZ-UHFFFAOYSA-N didodecyl methyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OC)OCCCCCCCCCCCC LOLGINHRZSNUDZ-UHFFFAOYSA-N 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
125000004437 phosphorous atom Chemical group 0.000 claims description 2
229910052698 phosphorus Inorganic materials 0.000 claims description 2
125000006413 ring segment Chemical group 0.000 claims description 2
125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
229910052736 halogen Inorganic materials 0.000 claims 1
150000002367 halogens Chemical class 0.000 claims 1
239000011230 binding agent Substances 0.000 abstract description 37
235000021317 phosphate Nutrition 0.000 abstract description 23
230000015572 biosynthetic process Effects 0.000 abstract description 3
150000003013 phosphoric acid derivatives Chemical class 0.000 abstract description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 3
150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract description 2
125000002587 enol group Chemical group 0.000 abstract description 2
RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 abstract 2
125000002252 acyl group Chemical group 0.000 abstract 1
125000001769 aryl amino group Chemical group 0.000 abstract 1
125000004104 aryloxy group Chemical group 0.000 abstract 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 abstract 1
125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
239000003795 chemical substances by application Substances 0.000 description 23
239000011093 chipboard Substances 0.000 description 22
239000000243 solution Substances 0.000 description 17
239000002023 wood Substances 0.000 description 16
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
238000002156 mixing Methods 0.000 description 12
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 12
229920005989 resin Polymers 0.000 description 11
239000011347 resin Substances 0.000 description 11
238000012360 testing method Methods 0.000 description 10
230000000704 physical effect Effects 0.000 description 9
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 9
244000019397 Pinus jeffreyi Species 0.000 description 8
235000013267 Pinus ponderosa Nutrition 0.000 description 8
235000013269 Pinus ponderosa var ponderosa Nutrition 0.000 description 8
235000013268 Pinus ponderosa var scopulorum Nutrition 0.000 description 8
239000000706 filtrate Substances 0.000 description 8
238000003825 pressing Methods 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
238000005452 bending Methods 0.000 description 6
238000010438 heat treatment Methods 0.000 description 5
239000012948 isocyanate Substances 0.000 description 5
150000002513 isocyanates Chemical class 0.000 description 5
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000007858 starting material Substances 0.000 description 5
NVIKEGBHOVMMDC-UHFFFAOYSA-N 1-dichlorophosphoryloxydodecane Chemical compound CCCCCCCCCCCCOP(Cl)(Cl)=O NVIKEGBHOVMMDC-UHFFFAOYSA-N 0.000 description 4
229910000831 Steel Inorganic materials 0.000 description 4
MEESPVWIOBCLJW-KTKRTIGZSA-N [(z)-octadec-9-enyl] dihydrogen phosphate Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(O)(O)=O MEESPVWIOBCLJW-KTKRTIGZSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
238000001914 filtration Methods 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000000465 moulding Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
239000010959 steel Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
CGWCKAGBZVWKGT-UHFFFAOYSA-N 1-[chloro-(2-nonylphenoxy)phosphoryl]oxy-2-nonylbenzene Chemical compound CCCCCCCCCC1=CC=CC=C1OP(Cl)(=O)OC1=CC=CC=C1CCCCCCCCC CGWCKAGBZVWKGT-UHFFFAOYSA-N 0.000 description 3
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
239000012442 inert solvent Substances 0.000 description 3
229910010272 inorganic material Inorganic materials 0.000 description 3
239000011147 inorganic material Substances 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000000047 product Substances 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
WTMRVLJHCHPKDJ-PMDAXIHYSA-N (Z)-3-[chloro-[(9Z,28Z)-19-(1,2-dihydroxyethyl)heptatriaconta-9,28-dien-19-yl]oxyphosphoryl]oxy-3-[(Z)-octadec-9-enyl]henicos-12-ene-1,2-diol Chemical compound C(CCCCCCC\C=C/CCCCCCCC)C(C(O)CO)(CCCCCCCC\C=C/CCCCCCCC)OP(=O)(OC(C(O)CO)(CCCCCCCC\C=C/CCCCCCCC)CCCCCCCC\C=C/CCCCCCCC)Cl WTMRVLJHCHPKDJ-PMDAXIHYSA-N 0.000 description 2
SPURMHFLEKVAAS-UHFFFAOYSA-N 1-docosene Chemical compound CCCCCCCCCCCCCCCCCCCCC=C SPURMHFLEKVAAS-UHFFFAOYSA-N 0.000 description 2
HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
HMSWAIKSFDFLKN-UHFFFAOYSA-N Hexacosane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCC HMSWAIKSFDFLKN-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
YLGCLRBAPZRTHO-UHFFFAOYSA-N N-[diethylamino-(dodecylamino)phosphoryl]dodecan-1-amine Chemical compound C(C)N(P(=O)(NCCCCCCCCCCCC)NCCCCCCCCCCCC)CC YLGCLRBAPZRTHO-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
FCZCIXQGZOUIDN-UHFFFAOYSA-N ethyl 2-diethoxyphosphinothioyloxyacetate Chemical compound CCOC(=O)COP(=S)(OCC)OCC FCZCIXQGZOUIDN-UHFFFAOYSA-N 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
239000011368 organic material Substances 0.000 description 2
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
150000003018 phosphorus compounds Chemical class 0.000 description 2
239000011120 plywood Substances 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
238000012545 processing Methods 0.000 description 2
238000010992 reflux Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
229920001187 thermosetting polymer Polymers 0.000 description 2
239000003039 volatile agent Substances 0.000 description 2
239000002699 waste material Substances 0.000 description 2
AFSHUZFNMVJNKX-LLWMBOQKSA-N 1,2-dioleoyl-sn-glycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-LLWMBOQKSA-N 0.000 description 1
OVIBXFDXRSJJSX-CLFAGFIQSA-N 1,3-bis[(z)-octadec-9-enoxy]propan-2-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCC(O)COCCCCCCCC\C=C/CCCCCCCC OVIBXFDXRSJJSX-CLFAGFIQSA-N 0.000 description 1
ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical class O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
DKJBREHOVWISMR-UHFFFAOYSA-N 1-chloro-2,3-diisocyanatobenzene Chemical compound ClC1=CC=CC(N=C=O)=C1N=C=O DKJBREHOVWISMR-UHFFFAOYSA-N 0.000 description 1
YAYNEUUHHLGGAH-UHFFFAOYSA-N 1-chlorododecane Chemical compound CCCCCCCCCCCCCl YAYNEUUHHLGGAH-UHFFFAOYSA-N 0.000 description 1
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000609240 Ambelania acida Species 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000189148 Juniperus occidentalis Species 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
IGGUPRCHHJZPBS-UHFFFAOYSA-N Nonacosane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCC IGGUPRCHHJZPBS-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
108010011935 Poly 18 antigen Proteins 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
229920002396 Polyurea Polymers 0.000 description 1
235000004443 Ricinus communis Nutrition 0.000 description 1
229920000147 Styrene maleic anhydride Polymers 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000010828 animal waste Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
239000010905 bagasse Substances 0.000 description 1
125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
ITVPBBDAZKBMRP-UHFFFAOYSA-N chloro-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound OP(O)(Cl)=O ITVPBBDAZKBMRP-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
BJZIAVRHKGVWOH-UHFFFAOYSA-N dibenzoyloxyphosphanyl benzoate Chemical class C=1C=CC=CC=1C(=O)OP(OC(=O)C=1C=CC=CC=1)OC(=O)C1=CC=CC=C1 BJZIAVRHKGVWOH-UHFFFAOYSA-N 0.000 description 1
JTXUVYOABGUBMX-UHFFFAOYSA-N didodecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCC JTXUVYOABGUBMX-UHFFFAOYSA-N 0.000 description 1
LBNBTSGMGZSOFX-UHFFFAOYSA-N didodecyl octyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCC)OCCCCCCCCCCCC LBNBTSGMGZSOFX-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
238000004821 distillation Methods 0.000 description 1
125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000001035 drying Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
238000007731 hot pressing Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000010954 inorganic particle Substances 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000010534 mechanism of action Effects 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000002557 mineral fiber Substances 0.000 description 1
125000002819 montanyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QHMGJGNTMQDRQA-UHFFFAOYSA-N n-Dotriacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC QHMGJGNTMQDRQA-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
ZYURHZPYMFLWSH-UHFFFAOYSA-N n-octacosane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCC ZYURHZPYMFLWSH-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
QEXZDYLACYKGOM-UHFFFAOYSA-N octacos-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCC=C QEXZDYLACYKGOM-UHFFFAOYSA-N 0.000 description 1
125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000123 paper Substances 0.000 description 1
BDWBGSCECOPTTH-UHFFFAOYSA-N pentacos-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC=C BDWBGSCECOPTTH-UHFFFAOYSA-N 0.000 description 1
125000002460 pentacosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
IMACFCSSMIZSPP-UHFFFAOYSA-N phenacyl chloride Chemical compound ClCC(=O)C1=CC=CC=C1 IMACFCSSMIZSPP-UHFFFAOYSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000011495 polyisocyanurate Substances 0.000 description 1
229920000582 polyisocyanurate Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000012552 review Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000010904 stalk Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000010902 straw Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
ZDLBWMYNYNATIW-UHFFFAOYSA-N tetracos-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCC=C ZDLBWMYNYNATIW-UHFFFAOYSA-N 0.000 description 1
229940095068 tetradecene Drugs 0.000 description 1
125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
WMZHDICSCDKPFS-UHFFFAOYSA-N triacontene Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C WMZHDICSCDKPFS-UHFFFAOYSA-N 0.000 description 1
SJDSOBWGZRPKSB-UHFFFAOYSA-N tricos-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCC=C SJDSOBWGZRPKSB-UHFFFAOYSA-N 0.000 description 1
125000002469 tricosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000004584 weight gain Effects 0.000 description 1
235000019786 weight gain Nutrition 0.000 description 1
239000002916 wood waste Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
- 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/06—Polymer mixtures characterised by other features having improved processability or containing aids for moulding methods
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Polyurethanes Or Polyureas (AREA)
Dry Formation Of Fiberboard And The Like (AREA)
Laminated Bodies (AREA)
Adhesives Or Adhesive Processes (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compositions Of Macromolecular Compounds (AREA)

CS812452A 1980-04-14 1981-04-01 Method or manufacturing boards from particles CS228905B2 (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CS826618A CS228940B2 (cs)	1980-04-14	1982-09-14	Pojivová směs pro částicové desky

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/139,872 US4257996A (en)	1980-04-14	1980-04-14	Process for preparing particle board and polyisocyanate-phosphorus compound release agent composition therefor

Publications (1)

Publication Number	Publication Date
CS228905B2 true CS228905B2 (en)	1984-05-14

Family

ID=22488675

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS812452A CS228905B2 (en)	1980-04-14	1981-04-01	Method or manufacturing boards from particles

Country Status (30)

Country	Link
US (1)	US4257996A (fi)
JP (1)	JPS5950510B2 (fi)
KR (1)	KR830001964B1 (fi)
AT (1)	AT369024B (fi)
AU (1)	AU537997B2 (fi)
BE (1)	BE888395A (fi)
BR (1)	BR8102135A (fi)
CA (1)	CA1166382A (fi)
CH (1)	CH652641A5 (fi)
CS (1)	CS228905B2 (fi)
DD (1)	DD158251A5 (fi)
DE (1)	DE3111562C2 (fi)
DK (1)	DK153298C (fi)
ES (1)	ES8302534A1 (fi)
FI (1)	FI71758C (fi)
FR (1)	FR2480176A1 (fi)
GB (1)	GB2075037B (fi)
GR (1)	GR74521B (fi)
HU (1)	HU196082B (fi)
IL (1)	IL62351A (fi)
IN (1)	IN152663B (fi)
IT (1)	IT1170868B (fi)
NL (1)	NL8101809A (fi)
NO (1)	NO153973C (fi)
NZ (1)	NZ196470A (fi)
PH (1)	PH17540A (fi)
PT (1)	PT72776B (fi)
SE (1)	SE441995B (fi)
TR (1)	TR21069A (fi)
ZA (1)	ZA812044B (fi)

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US4528154A (en) *	1983-06-15	1985-07-09	Atlantic Richfield Company	Preparation of molded lignocellulosic compositions using an emulsifiable polyisocyanate binder and an emulsifiable carboxy functional siloxane internal release agent
DE3328662A1 (de) *	1983-08-09	1985-02-21	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von presswerkstoffen mit polyisocyanat-bindemitteln unter mitverwendung von latenten, waermeaktivierbaren katalysatoren
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US5302330A (en) *	1993-06-08	1994-04-12	Harold Umansky	Method for the manufacture of waferboard
US5554438A (en) *	1994-07-22	1996-09-10	Imperial Chemical Industries, Plc	Self-release binder system
AU3960701A (en)	1999-12-23	2001-07-03	Sorin Cezar Cosofret	Composition functioning as a binding agent and as a combat factor against ascensional humidity in building and method to apply
US6586504B1 (en) *	2000-04-26	2003-07-01	P & M Signs	Wood and plastic composite material and methods for making same
US6478998B1 (en)	2000-09-13	2002-11-12	Borden Chemical, Inc.	Hybrid phenol-formaldehyde and polymeric isocyanate based adhesive and methods of synthesis and use
US6451101B1 (en)	2000-12-29	2002-09-17	Basf Corporation	Parting agent for an isocyanate wood binder
US6464820B2 (en)	2000-12-29	2002-10-15	Basf Corporation	Binder resin and synergist composition including a parting agent and process of making lignocellulosic
US6458238B1 (en)	2000-12-29	2002-10-01	Basf Corporation	Adhesive binder and synergist composition and process of making lignocellulosic articles
US7018461B2 (en) *	2002-02-22	2006-03-28	Cellulose Solutions, Llc	Release agents
DE10215053A1 (de) *	2002-04-05	2003-10-23	Bayer Ag	Polyurethan-Dispersionen auf Basis von Fettsäuredialkanolamiden
US20050242459A1 (en) *	2004-04-29	2005-11-03	Savino Thomas G	Lignocellulosic composite material and method for preparing the same
PT103693B (pt) *	2007-03-19	2009-07-28	Univ Tras Os Montes E Alto Dou	Processo de aglomeração de partículas dos sectores da madeira e da cortiça
PT103702B (pt) *	2007-03-27	2009-06-08	Univ Tras Os Montes E Alto Dou	Processo de aglomeração de fibras de madeira para a produção de placas ou painéis de aglomerado
DE102009047764A1 (de) *	2009-12-10	2011-06-16	Evonik Goldschmidt Gmbh	Trennmittel und Verwendung zur Herstellung von Kompositformkörpern
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US4005034A (en) *	1973-10-25	1977-01-25	Stauffer Chemical Company	Poly(haloethyl-ethyleneoxy) phosphoric acid ester polymers as flame retardant agents
US4024088A (en) *	1974-12-23	1977-05-17	Union Carbide Corporation	Compositions and methods useful in forming polyether polyurethanes having release properties
US4100328A (en) *	1976-06-04	1978-07-11	Basf Wyandotte Corporation	Binder composition and process for preparing pressure molded cellulosic articles
FI64639C (fi) *	1978-09-27	1983-12-12	Unilever Nv	Bleknings- och rengoeringskomposition
IN152487B (fi) *	1978-09-29	1984-01-28	Upjohn Co

1980
- 1980-04-14 US US06/139,872 patent/US4257996A/en not_active Expired - Lifetime
1981
- 1981-03-10 GB GB8107581A patent/GB2075037B/en not_active Expired
- 1981-03-11 NZ NZ196470A patent/NZ196470A/xx unknown
- 1981-03-12 IL IL62351A patent/IL62351A/xx unknown
- 1981-03-24 DE DE3111562A patent/DE3111562C2/de not_active Expired
- 1981-03-26 ZA ZA00812044A patent/ZA812044B/xx unknown
- 1981-03-30 AT AT0147981A patent/AT369024B/de not_active IP Right Cessation
- 1981-03-31 PT PT72776A patent/PT72776B/pt unknown
- 1981-04-01 CS CS812452A patent/CS228905B2/cs unknown
- 1981-04-01 HU HU81844A patent/HU196082B/hu unknown
- 1981-04-01 PH PH25456A patent/PH17540A/en unknown
- 1981-04-02 AU AU69031/81A patent/AU537997B2/en not_active Ceased
- 1981-04-02 IN IN372/CAL/81A patent/IN152663B/en unknown
- 1981-04-02 IT IT48189/81A patent/IT1170868B/it active
- 1981-04-08 CH CH2372/81A patent/CH652641A5/de not_active IP Right Cessation
- 1981-04-09 FI FI811097A patent/FI71758C/fi not_active IP Right Cessation
- 1981-04-09 BR BR8102135A patent/BR8102135A/pt unknown
- 1981-04-09 SE SE8102284A patent/SE441995B/sv not_active IP Right Cessation
- 1981-04-10 JP JP56054252A patent/JPS5950510B2/ja not_active Expired
- 1981-04-10 ES ES501267A patent/ES8302534A1/es not_active Expired
- 1981-04-10 TR TR21069A patent/TR21069A/xx unknown
- 1981-04-13 FR FR8107385A patent/FR2480176A1/fr active Granted
- 1981-04-13 GR GR64675A patent/GR74521B/el unknown
- 1981-04-13 NL NL8101809A patent/NL8101809A/nl not_active Application Discontinuation
- 1981-04-13 CA CA000375379A patent/CA1166382A/en not_active Expired
- 1981-04-13 NO NO811277A patent/NO153973C/no unknown
- 1981-04-13 KR KR1019810001247A patent/KR830001964B1/ko active
- 1981-04-13 DK DK167081A patent/DK153298C/da not_active IP Right Cessation
- 1981-04-13 BE BE0/204466A patent/BE888395A/fr not_active IP Right Cessation
- 1981-04-13 DD DD81229196A patent/DD158251A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
ES501267A0 (es)	1983-02-01
CA1166382A (en)	1984-04-24
NL8101809A (nl)	1981-11-02
DE3111562A1 (de)	1982-04-08
CH652641A5 (de)	1985-11-29
GR74521B (fi)	1984-06-29
KR830001964B1 (ko)	1983-09-29
GB2075037B (en)	1984-03-14
KR830004965A (ko)	1983-07-23
HU196082B (en)	1988-09-28
FI811097L (fi)	1981-10-15
FR2480176B1 (fi)	1984-01-13
NO153973B (no)	1986-03-17
IT1170868B (it)	1987-06-03
NZ196470A (en)	1983-06-14
IN152663B (fi)	1984-03-03
NO153973C (no)	1986-06-25
BR8102135A (pt)	1982-01-12
PT72776A (en)	1981-04-01
TR21069A (tr)	1983-06-16
GB2075037A (en)	1981-11-11
AT369024B (de)	1982-11-25
IL62351A (en)	1984-10-31
AU537997B2 (en)	1984-07-26
JPS5950510B2 (ja)	1984-12-08
SE8102284L (sv)	1981-10-15
DK153298C (da)	1988-11-14
ZA812044B (en)	1982-04-28
ATA147981A (de)	1982-04-15
JPS56157337A (en)	1981-12-04
DK167081A (da)	1981-10-15
US4257996A (en)	1981-03-24
SE441995B (sv)	1985-11-25
FI71758C (fi)	1987-02-09
PT72776B (en)	1982-03-24
DD158251A5 (de)	1983-01-05
PH17540A (en)	1984-09-19
FR2480176A1 (fr)	1981-10-16
DK153298B (da)	1988-07-04
FI71758B (fi)	1986-10-31
IT8148189A0 (it)	1981-04-02
IL62351A0 (en)	1981-05-20
AU6903181A (en)	1981-10-22
DE3111562C2 (de)	1985-06-05
NO811277L (no)	1981-10-15
BE888395A (fr)	1981-10-13
ES8302534A1 (es)	1983-02-01

Publication	Publication Date	Title
CS228905B2 (en)	1984-05-14	Method or manufacturing boards from particles
US4257995A (en)	1981-03-24	Process for preparing particle board and polyisocyanate-phosphorus compound release agent composition therefor
GB2031914A (en)	1980-04-30	Particle boards
EP0095594B1 (en)	1986-08-27	Stable aqueous polyisocyanate emulsions
FI70245C (fi)	1986-09-15	Foerfarande foer framstaellning av spaonskivor genom att anvaenda ett polyisocyanatbindemedel tillsammans med ett p-innehaollande inre slaeppmedel
JPH0118068B2 (fi)	1989-04-03
CS228940B2 (cs)	1984-04-16	Pojivová směs pro částicové desky
CA1123817A (en)	1982-05-18	Polymeric isocyanate binder with internal release agent
US4480070A (en)	1984-10-30	Compositions and process
KR820001949B1 (ko)	1982-10-21	파티클보드의 제조방법
AT383132B (de)	1987-05-25	Verfahren zum herstellen von aus teilchenfoermigen stoffen bestehenden platten