RU2012128922A - Смолы - Google Patents
Смолы Download PDFInfo
- Publication number
- RU2012128922A RU2012128922A RU2012128922/04A RU2012128922A RU2012128922A RU 2012128922 A RU2012128922 A RU 2012128922A RU 2012128922/04 A RU2012128922/04 A RU 2012128922/04A RU 2012128922 A RU2012128922 A RU 2012128922A RU 2012128922 A RU2012128922 A RU 2012128922A
- Authority
- RU
- Russia
- Prior art keywords
- aldehyde
- oil
- crosslinking agent
- resin
- volatile
- Prior art date
Links
- 239000011347 resin Substances 0.000 title claims abstract 24
- 229920005989 resin Polymers 0.000 title claims abstract 24
- 239000003431 cross linking reagent Substances 0.000 claims abstract 33
- 238000000034 method Methods 0.000 claims abstract 22
- 239000007859 condensation product Substances 0.000 claims abstract 17
- 239000003921 oil Substances 0.000 claims abstract 15
- 235000019198 oils Nutrition 0.000 claims abstract 15
- 239000008158 vegetable oil Substances 0.000 claims abstract 7
- 235000015112 vegetable and seed oil Nutrition 0.000 claims abstract 5
- -1 C-C monoaldehyde) Chemical class 0.000 claims abstract 4
- 244000226021 Anacardium occidentale Species 0.000 claims abstract 3
- 235000020226 cashew nut Nutrition 0.000 claims abstract 3
- 238000004519 manufacturing process Methods 0.000 claims abstract 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract 3
- 235000019483 Peanut oil Nutrition 0.000 claims abstract 2
- 235000019484 Rapeseed oil Nutrition 0.000 claims abstract 2
- 235000019486 Sunflower oil Nutrition 0.000 claims abstract 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000010775 animal oil Substances 0.000 claims abstract 2
- 239000004359 castor oil Substances 0.000 claims abstract 2
- 235000019438 castor oil Nutrition 0.000 claims abstract 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract 2
- 238000007037 hydroformylation reaction Methods 0.000 claims abstract 2
- 239000000944 linseed oil Substances 0.000 claims abstract 2
- 235000021388 linseed oil Nutrition 0.000 claims abstract 2
- 239000007788 liquid Substances 0.000 claims abstract 2
- 239000008164 mustard oil Substances 0.000 claims abstract 2
- 239000004006 olive oil Substances 0.000 claims abstract 2
- 235000008390 olive oil Nutrition 0.000 claims abstract 2
- 238000005949 ozonolysis reaction Methods 0.000 claims abstract 2
- 239000000312 peanut oil Substances 0.000 claims abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract 2
- 235000013824 polyphenols Nutrition 0.000 claims abstract 2
- 230000002829 reductive effect Effects 0.000 claims abstract 2
- 239000003549 soybean oil Substances 0.000 claims abstract 2
- 235000012424 soybean oil Nutrition 0.000 claims abstract 2
- 239000002600 sunflower oil Substances 0.000 claims abstract 2
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract 2
- 239000002383 tung oil Substances 0.000 claims abstract 2
- 235000013311 vegetables Nutrition 0.000 claims abstract 2
- 150000001299 aldehydes Chemical class 0.000 claims 41
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 claims 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- 230000000694 effects Effects 0.000 claims 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims 2
- 239000012670 alkaline solution Substances 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 239000002131 composite material Substances 0.000 claims 2
- 238000004132 cross linking Methods 0.000 claims 2
- 239000000839 emulsion Substances 0.000 claims 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 claims 2
- 239000007787 solid Substances 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 2
- 125000005457 triglyceride group Chemical group 0.000 claims 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 239000003377 acid catalyst Substances 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000005456 glyceride group Chemical group 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 229920005610 lignin Polymers 0.000 claims 1
- 229940098779 methanesulfonic acid Drugs 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000010466 nut oil Substances 0.000 claims 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 claims 1
- 229960001553 phloroglucinol Drugs 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- 235000018553 tannin Nutrition 0.000 claims 1
- 229920001864 tannin Polymers 0.000 claims 1
- 239000001648 tannin Substances 0.000 claims 1
- 239000013638 trimer Substances 0.000 claims 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 16
- 239000004971 Cross linker Substances 0.000 abstract 5
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 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
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
-
- 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
- C08G6/00—Condensation polymers of aldehydes or ketones only
-
- 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
-
- 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
-
- 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
- C08G8/26—Condensation polymers of aldehydes or ketones with phenols only from mixtures of aldehydes and ketones
-
- 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
- C08G8/28—Chemically modified polycondensates
-
- 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
- C08G8/28—Chemically modified polycondensates
- C08G8/32—Chemically modified polycondensates by organic acids or derivatives thereof, e.g. fatty oils
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Engineering & Computer Science (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0921666.4 | 2009-12-10 | ||
| GB0921666A GB0921666D0 (en) | 2009-12-10 | 2009-12-10 | Resins |
| PCT/GB2010/002257 WO2011070332A1 (en) | 2009-12-10 | 2010-12-10 | Resins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2012128922A true RU2012128922A (ru) | 2014-01-20 |
Family
ID=41666924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2012128922/04A RU2012128922A (ru) | 2009-12-10 | 2010-12-10 | Смолы |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9139681B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2510025A1 (cg-RX-API-DMAC7.html) |
| KR (1) | KR20120104595A (cg-RX-API-DMAC7.html) |
| AU (1) | AU2010329686A1 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112012014067A2 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2820148A1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB0921666D0 (cg-RX-API-DMAC7.html) |
| IN (1) | IN2012DN06062A (cg-RX-API-DMAC7.html) |
| RU (1) | RU2012128922A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2011070332A1 (cg-RX-API-DMAC7.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2694035C2 (ru) * | 2014-07-17 | 2019-07-08 | Кнауф Инзулацьон Спрл | Улучшенные связующие композиции и их применения |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2517338B (en) | 2012-05-03 | 2020-03-25 | Virdia Inc | A method for fractionating a liquid sample |
| CN105377958B (zh) * | 2013-05-03 | 2019-01-01 | 威尔迪亚公司 | 用于处理木质纤维素材料的方法 |
| CN105358608B (zh) | 2013-05-03 | 2018-11-16 | 威尔迪亚公司 | 用于制备热稳定的木质素级分的方法 |
| CA2954274C (en) | 2014-07-09 | 2024-02-13 | Virdia, Inc. | Methods for separating and refining lignin from black liquor and compositions thereof |
| US9791012B1 (en) | 2016-04-20 | 2017-10-17 | King Abdulaziz University | Thermo-set resin composition for brake pads, method of preparation, and brake pad assembly |
| KR102220941B1 (ko) * | 2016-10-13 | 2021-02-25 | (주)엘지하우시스 | 열경화성 수지 조성물 및 이의 제조방법 |
| GB2586914B (en) * | 2020-06-29 | 2021-09-01 | Nexgen Tree Shelters Ltd | Tree shelter |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB950623A (en) | 1959-10-14 | 1964-02-26 | Philips Electrical Ind Ltd | Improvements in or relating to laminated products |
| US3112329A (en) * | 1962-03-08 | 1963-11-26 | Everett H Pryde | Unsaturated aldehyde oils and method for preparing the same |
| US4588613A (en) | 1984-10-10 | 1986-05-13 | Formosa Plastics Corporation | Process for reducing polymer buildup |
| EP1131277B1 (en) * | 1998-11-25 | 2005-07-13 | Cambridge Biopolymers Limited | Method of modifying components present in cashew nut shell liquid |
| ATE284856T1 (de) | 1999-06-18 | 2005-01-15 | Cambridge Biopolymers Ltd | Oxidative spaltung ungesättigter öle sowie daraus hergestellte produkte |
| GB0129590D0 (en) | 2001-12-11 | 2002-01-30 | Cambridge Biopolymers Ltd | Oil Ozonolysis |
| GB2392163A (en) | 2002-08-20 | 2004-02-25 | Univ Sheffield | Soluble phenol-aldehyde condensate |
| CN100347213C (zh) * | 2005-11-25 | 2007-11-07 | 华南理工大学 | 一种环氧植物油改性酚醛树脂及其制备方法与应用 |
| US7538236B2 (en) * | 2006-01-04 | 2009-05-26 | Suresh Narine | Bioplastics, monomers thereof, and processes for the preparation thereof from agricultural feedstocks |
| WO2008073729A2 (en) | 2006-12-11 | 2008-06-19 | Dow Global Technologies Inc. | Aldehyde and alcohol compositions derived from seed oils |
-
2009
- 2009-12-10 GB GB0921666A patent/GB0921666D0/en not_active Ceased
-
2010
- 2010-12-10 US US13/514,781 patent/US9139681B2/en not_active Expired - Fee Related
- 2010-12-10 RU RU2012128922/04A patent/RU2012128922A/ru not_active Application Discontinuation
- 2010-12-10 IN IN6062DEN2012 patent/IN2012DN06062A/en unknown
- 2010-12-10 WO PCT/GB2010/002257 patent/WO2011070332A1/en not_active Ceased
- 2010-12-10 KR KR20127017870A patent/KR20120104595A/ko not_active Ceased
- 2010-12-10 CA CA 2820148 patent/CA2820148A1/en not_active Abandoned
- 2010-12-10 EP EP10790468A patent/EP2510025A1/en not_active Withdrawn
- 2010-12-10 BR BR112012014067A patent/BR112012014067A2/pt not_active IP Right Cessation
- 2010-12-10 AU AU2010329686A patent/AU2010329686A1/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2694035C2 (ru) * | 2014-07-17 | 2019-07-08 | Кнауф Инзулацьон Спрл | Улучшенные связующие композиции и их применения |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2010329686A1 (en) | 2012-08-02 |
| BR112012014067A2 (pt) | 2016-07-05 |
| WO2011070332A4 (en) | 2011-09-15 |
| KR20120104595A (ko) | 2012-09-21 |
| US20130116386A1 (en) | 2013-05-09 |
| IN2012DN06062A (cg-RX-API-DMAC7.html) | 2015-09-18 |
| US9139681B2 (en) | 2015-09-22 |
| WO2011070332A1 (en) | 2011-06-16 |
| GB0921666D0 (en) | 2010-01-27 |
| EP2510025A1 (en) | 2012-10-17 |
| CA2820148A1 (en) | 2011-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2012128922A (ru) | Смолы | |
| Dugmore et al. | Valorisation of biowastes for the production of green materials using chemical methods | |
| Esposito et al. | Redefining biorefinery: the search for unconventional building blocks for materials | |
| Dabral et al. | Mechanistic studies of base-catalysed lignin depolymerisation in dimethyl carbonate | |
| Chikkali et al. | Refining of plant oils to chemicals by olefin metathesis | |
| Jeong et al. | Levulinic acid production by two-step acid-catalyzed treatment of Quercus mongolica using dilute sulfuric acid | |
| CO6420318A2 (es) | Preparación sin disolvente de polioles por ozonólisis | |
| Farmer et al. | Platform molecules | |
| RU2018134925A (ru) | Получение мономеров из лигнина в процессе деполимеризации содержащей лигноцеллюлозу композиции | |
| KR102422984B1 (ko) | 재생 가능하게 유도된 폴리아마이드 및 이의 제조 방법 | |
| Deruer et al. | Thiazolylidene‐Catalyzed Cleavage of Methyl Oleate‐Derived α‐Hydroxy Ketone to the Corresponding Free Aldehydes | |
| Škulcová et al. | Deep eutectic solvents as medium for pretreatment of biomass | |
| SI2922885T1 (en) | A process for making polymers analogous to phenol formaldehyde resins | |
| Škulcova et al. | Green solvents based on choline chloride for the extraction of spruce bark (Picea abies) | |
| US20160002851A1 (en) | Process Operations for Biomass Fractionation | |
| Shen et al. | Catalytic Synthesis of Diphenolic Acid from Levulinic Acid over Bronsted Acidic Ionic Liquids. | |
| Thébault et al. | Naturally occurring phenolic sources for industrial applications | |
| Adhikari et al. | Production of novolac resin after partial substitution of phenol from bio-oil | |
| Abbina et al. | Emergence of sustainable approaches for functional materials: Cashew nut shell liquid and other relevant crop-based renewable resources | |
| US9775347B2 (en) | Methods to convert lignin to phenolic and carboxylate compounds | |
| Agblevor et al. | Pyrolytic conversion of olive mill wastewater sludge to biofuels using red mud as catalyst | |
| de Souza et al. | Biomass-derived polyurethanes for sustainable future | |
| Inkrod et al. | Characteristics of lignin extracted from pararubber wood sawdust via organosolv fractionation | |
| El-Azazy et al. | Lignin and lignocellulosic materials: a glance on the current opportunities for energy and sustainability | |
| Schneider et al. | Oleochemical biorefinery |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20160115 |