CA1169181A - Polyisocyanate reaction products - Google Patents
Polyisocyanate reaction productsInfo
- Publication number
- CA1169181A CA1169181A CA000390828A CA390828A CA1169181A CA 1169181 A CA1169181 A CA 1169181A CA 000390828 A CA000390828 A CA 000390828A CA 390828 A CA390828 A CA 390828A CA 1169181 A CA1169181 A CA 1169181A
- Authority
- CA
- Canada
- Prior art keywords
- article
- polyisocyanate
- chrome
- shavings
- chrome shavings
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000005056 polyisocyanate Substances 0.000 title claims abstract description 33
- 229920001228 polyisocyanate Polymers 0.000 title claims abstract description 28
- 239000007795 chemical reaction product Substances 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 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 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 3
- 239000002245 particle Substances 0.000 abstract description 13
- 239000010985 leather Substances 0.000 abstract description 9
- 239000000047 product Substances 0.000 abstract description 6
- 239000012948 isocyanate Substances 0.000 description 10
- 150000002513 isocyanates Chemical class 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 239000011093 chipboard Substances 0.000 description 9
- 125000005442 diisocyanate group Chemical group 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000003063 flame retardant Substances 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- -1 polycarboxyl groups Polymers 0.000 description 5
- 239000004035 construction material Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- 229920001184 polypeptide Polymers 0.000 description 3
- 102000004196 processed proteins & peptides Human genes 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 102000008186 Collagen Human genes 0.000 description 2
- 108010035532 Collagen Proteins 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 229920001436 collagen Polymers 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012974 tin catalyst Substances 0.000 description 2
- 238000009966 trimming Methods 0.000 description 2
- SZBXTBGNJLZMHB-UHFFFAOYSA-N 1-chloro-2,4-diisocyanatobenzene Chemical class ClC1=CC=C(N=C=O)C=C1N=C=O SZBXTBGNJLZMHB-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 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
- 239000013638 trimer Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
- C08G18/6415—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63 having nitrogen
- C08G18/6446—Proteins and derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21163680A | 1980-12-01 | 1980-12-01 | |
| US211,636 | 1980-12-01 | ||
| US06/317,171 US4380474A (en) | 1980-12-01 | 1981-11-03 | Polyisocyanate reaction products |
| US317,171 | 1981-11-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1169181A true CA1169181A (en) | 1984-06-12 |
Family
ID=26906322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000390828A Expired CA1169181A (en) | 1980-12-01 | 1981-11-24 | Polyisocyanate reaction products |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4380474A (en:Method) |
| KR (1) | KR830007763A (en:Method) |
| AT (1) | AT379160B (en:Method) |
| AU (1) | AU549362B2 (en:Method) |
| BR (1) | BR8107716A (en:Method) |
| CA (1) | CA1169181A (en:Method) |
| DE (1) | DE3147407A1 (en:Method) |
| ES (1) | ES507561A0 (en:Method) |
| FR (1) | FR2495054A1 (en:Method) |
| GB (1) | GB2088423B (en:Method) |
| IN (1) | IN156593B (en:Method) |
| IT (1) | IT1172115B (en:Method) |
| NZ (1) | NZ199027A (en:Method) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4536430A (en) * | 1982-05-26 | 1985-08-20 | Krecke Edmond D | Process for the production of leather base material |
| DE4439656A1 (de) * | 1994-11-07 | 1996-05-09 | Ralf Gerhard Schenke Fa Dr | Verfahren zur Verwertung von Altmaterialien |
| US6180192B1 (en) * | 1997-03-24 | 2001-01-30 | Wood Waste Energy, Inc. | Solids produced from ash and process for producing the same |
| US7199168B2 (en) * | 2002-02-13 | 2007-04-03 | Bayer Materialscience Llc | Process for making cellular composites using polymeric isocyanates as binders for hollow filler particles |
| US20070184742A1 (en) * | 2005-10-20 | 2007-08-09 | Sustainable Solutions, Inc., (SSI) Corp. of Delaware | Composite leather material |
| US8057775B2 (en) | 2008-04-22 | 2011-11-15 | Us Synthetic Corporation | Polycrystalline diamond materials, methods of fabricating same, and applications using same |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1079705A (fr) * | 1949-05-30 | 1954-12-02 | Ici Ltd | Matières composées à base de cuir |
| US2808398A (en) * | 1953-10-05 | 1957-10-01 | Forward Frederick Bruce | Process for the preparation of leather dust |
| US3428592A (en) * | 1966-05-24 | 1969-02-18 | Du Pont | Polyisocyanate emulsions |
| US3505169A (en) * | 1966-12-05 | 1970-04-07 | Wyandotte Chemicals Corp | Reconstituted leather and method for producing it |
| US4060384A (en) * | 1976-09-09 | 1977-11-29 | Seton Company | Manufacture of leather |
-
1981
- 1981-11-03 US US06/317,171 patent/US4380474A/en not_active Expired - Lifetime
- 1981-11-13 GB GB8134278A patent/GB2088423B/en not_active Expired
- 1981-11-13 AU AU77490/81A patent/AU549362B2/en not_active Expired - Fee Related
- 1981-11-23 NZ NZ199027A patent/NZ199027A/en unknown
- 1981-11-23 KR KR1019810004524A patent/KR830007763A/ko not_active Ceased
- 1981-11-24 CA CA000390828A patent/CA1169181A/en not_active Expired
- 1981-11-27 BR BR8107716A patent/BR8107716A/pt unknown
- 1981-11-30 ES ES507561A patent/ES507561A0/es active Granted
- 1981-11-30 FR FR8122376A patent/FR2495054A1/fr active Pending
- 1981-11-30 DE DE19813147407 patent/DE3147407A1/de not_active Withdrawn
- 1981-11-30 IT IT49799/81A patent/IT1172115B/it active
- 1981-11-30 AT AT0514881A patent/AT379160B/de not_active IP Right Cessation
- 1981-12-11 IN IN1411/CAL/81A patent/IN156593B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATA514881A (de) | 1985-04-15 |
| NZ199027A (en) | 1984-07-06 |
| GB2088423A (en) | 1982-06-09 |
| AT379160B (de) | 1985-11-25 |
| ES8305077A1 (es) | 1983-03-16 |
| BR8107716A (pt) | 1982-08-31 |
| AU7749081A (en) | 1982-06-10 |
| GB2088423B (en) | 1984-09-12 |
| AU549362B2 (en) | 1986-01-23 |
| FR2495054A1 (fr) | 1982-06-04 |
| IN156593B (en:Method) | 1985-09-14 |
| DE3147407A1 (de) | 1982-07-01 |
| US4380474A (en) | 1983-04-19 |
| KR830007763A (ko) | 1983-11-07 |
| IT8149799A0 (it) | 1981-11-30 |
| IT1172115B (it) | 1987-06-18 |
| ES507561A0 (es) | 1983-03-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4359507A (en) | Mixed ethylene and propylene carbonate-containing organic polyisocyanate adhesive binder composition | |
| US4522975A (en) | Select NCO-terminated, uretdione group-containing polyurethane prepolymers and lignocellulosic composite materials prepared therefrom | |
| CA2244190C (en) | Method of producing press-moulding materials with polyisocyanate binders and using latent, heat-activable catalysts | |
| US4414361A (en) | Organic polyisocyanate-cyclic alkylene carbonate adhesive binder compositions | |
| US4293456A (en) | Process for the production of polyurethane plastics | |
| US4032483A (en) | Manufacture of polyurethanes from bark | |
| US4362827A (en) | Manufacture of chipboard | |
| HU176537B (en) | Method for producing plates and pressed form bodies | |
| CA1335311C (en) | Polyurethane and process for preparing same | |
| DE2031160B2 (de) | Verfahren zur impraegnierung von schaumstoffen mit polyurethanen | |
| US4327195A (en) | Polyurethane containing polypeptides | |
| EP0346059A2 (en) | Composite materials | |
| US20060231968A1 (en) | Protein-modified isocyanate-functional adhesive binder for cellulosic composite materials | |
| US4496684A (en) | Uretdione group-containing polyurethane oligomers and aqueous dispersions thereof | |
| US4344798A (en) | Organic polyisocyanate-dialkyl carbonate adhesive binder compositions | |
| GB2370577A (en) | Binder resin including parting agent and synergist and process of making lignocellulosic articles | |
| CA1169181A (en) | Polyisocyanate reaction products | |
| US4361662A (en) | Organic polyisocyanate-alkylene oxide adhesive composition for preparing lignocellulosic composite products | |
| CA1300328C (en) | Laminated composite of a rigid polyurethane modified polyisocyanurate substrate and metal, plastic, cellulose, glass, ceramic or combinations thereof | |
| JPH11503476A (ja) | リグノセルロース系材料の結合方法 | |
| US3075930A (en) | Expanded polyurethane plastic containing zein and process for preparing same | |
| EP0464781B1 (en) | Process for the preparation of aqueous polyisocyanate emulsions and emulsions obtained thereby | |
| CA1331247C (en) | Isocyanate-polyester polyol binder for manufacture of lignocellulosic composites | |
| NO309869B1 (no) | Polyisocyanat-blanding samt anvendelse derav | |
| GB1585074A (en) | Process for the manufacture of cellulose-polyurethane materials |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |