HU223611B1 - Kötõanyagrendszer poliuretánalapú magok és öntõformák készítéséhez - Google Patents
Kötõanyagrendszer poliuretánalapú magok és öntõformák készítéséhez Download PDFInfo
- Publication number
- HU223611B1 HU223611B1 HU0104315A HUP0104315A HU223611B1 HU 223611 B1 HU223611 B1 HU 223611B1 HU 0104315 A HU0104315 A HU 0104315A HU P0104315 A HUP0104315 A HU P0104315A HU 223611 B1 HU223611 B1 HU 223611B1
- Authority
- HU
- Hungary
- Prior art keywords
- phenolic resin
- mold
- binder system
- weight
- resin component
- Prior art date
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- 239000011230 binding agent Substances 0.000 title claims abstract description 45
- 239000004814 polyurethane Substances 0.000 title description 4
- 229920002635 polyurethane Polymers 0.000 title description 4
- 230000008018 melting Effects 0.000 title 1
- 238000002844 melting Methods 0.000 title 1
- 239000005011 phenolic resin Substances 0.000 claims abstract description 44
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 39
- -1 fatty acid ester Chemical class 0.000 claims abstract description 36
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 30
- 239000000194 fatty acid Substances 0.000 claims abstract description 30
- 229930195729 fatty acid Natural products 0.000 claims abstract description 30
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000002904 solvent Substances 0.000 claims abstract description 28
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 22
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 238000000465 moulding Methods 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 27
- 150000002989 phenols Chemical class 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 238000005266 casting Methods 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 150000005676 cyclic carbonates Chemical class 0.000 claims description 4
- 150000003997 cyclic ketones Chemical class 0.000 claims description 4
- 239000003495 polar organic solvent Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 2
- 238000011049 filling Methods 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 abstract description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract description 2
- 238000005058 metal casting Methods 0.000 abstract description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 23
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 150000004665 fatty acids Chemical class 0.000 description 10
- 239000004576 sand Substances 0.000 description 9
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- 239000003849 aromatic solvent Substances 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
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- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
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- 239000011347 resin Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
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- 125000001424 substituent group Chemical group 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- 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
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
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- 239000000779 smoke Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VTCDZPUMZAZMSB-UHFFFAOYSA-N 3,4,5-trimethoxyphenol Chemical compound COC1=CC(O)=CC(OC)=C1OC VTCDZPUMZAZMSB-UHFFFAOYSA-N 0.000 description 2
- FDQQNNZKEJIHMS-UHFFFAOYSA-N 3,4,5-trimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1C FDQQNNZKEJIHMS-UHFFFAOYSA-N 0.000 description 2
- XQDNFAMOIPNVES-UHFFFAOYSA-N 3,5-Dimethoxyphenol Chemical compound COC1=CC(O)=CC(OC)=C1 XQDNFAMOIPNVES-UHFFFAOYSA-N 0.000 description 2
- LPCJHUPMQKSPDC-UHFFFAOYSA-N 3,5-diethylphenol Chemical compound CCC1=CC(O)=CC(CC)=C1 LPCJHUPMQKSPDC-UHFFFAOYSA-N 0.000 description 2
- HMNKTRSOROOSPP-UHFFFAOYSA-N 3-Ethylphenol Chemical compound CCC1=CC=CC(O)=C1 HMNKTRSOROOSPP-UHFFFAOYSA-N 0.000 description 2
- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 description 2
- MBGGFXOXUIDRJD-UHFFFAOYSA-N 4-Butoxyphenol Chemical compound CCCCOC1=CC=C(O)C=C1 MBGGFXOXUIDRJD-UHFFFAOYSA-N 0.000 description 2
- ZSBDGXGICLIJGD-UHFFFAOYSA-N 4-phenoxyphenol Chemical compound C1=CC(O)=CC=C1OC1=CC=CC=C1 ZSBDGXGICLIJGD-UHFFFAOYSA-N 0.000 description 2
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000006004 Quartz sand Substances 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 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 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
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- 150000003512 tertiary amines Chemical class 0.000 description 2
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
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- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
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- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 1
- HRUHVKFKXJGKBQ-UHFFFAOYSA-N 3,5-dibutylphenol Chemical compound CCCCC1=CC(O)=CC(CCCC)=C1 HRUHVKFKXJGKBQ-UHFFFAOYSA-N 0.000 description 1
- PEZSSBYAUDZEMO-UHFFFAOYSA-N 3,5-dicyclohexylphenol Chemical compound C=1C(O)=CC(C2CCCCC2)=CC=1C1CCCCC1 PEZSSBYAUDZEMO-UHFFFAOYSA-N 0.000 description 1
- LKVFCSWBKOVHAH-UHFFFAOYSA-N 4-Ethoxyphenol Chemical compound CCOC1=CC=C(O)C=C1 LKVFCSWBKOVHAH-UHFFFAOYSA-N 0.000 description 1
- CHQPRDVSUIJJNP-NSCUHMNNSA-N 4-[(e)-but-2-enyl]phenol Chemical compound C\C=C\CC1=CC=C(O)C=C1 CHQPRDVSUIJJNP-NSCUHMNNSA-N 0.000 description 1
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- CYYZDBDROVLTJU-UHFFFAOYSA-N 4-n-Butylphenol Chemical compound CCCCC1=CC=C(O)C=C1 CYYZDBDROVLTJU-UHFFFAOYSA-N 0.000 description 1
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- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
- B22C1/22—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
- B22C1/22—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
- B22C1/2233—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B22C1/2273—Polyurethanes; Polyisocyanates
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mold Materials And Core Materials (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19850833A DE19850833C2 (de) | 1998-11-04 | 1998-11-04 | Bindemittelsystem zur Herstellung von Kernen und Gießformen auf Polyurethanbasis, deren Verwendung und Verfahren zur Herstellung eines Gießformteils auf Polyurethanbasis |
| PCT/EP1999/008419 WO2000025957A1 (de) | 1998-11-04 | 1999-11-04 | Bindemittelsystem zur herstellung von kernen und giessformen auf polyurethanbasis |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| HUP0104315A2 HUP0104315A2 (hu) | 2002-03-28 |
| HUP0104315A3 HUP0104315A3 (en) | 2002-05-28 |
| HU223611B1 true HU223611B1 (hu) | 2004-10-28 |
Family
ID=7886667
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU0104315A HU223611B1 (hu) | 1998-11-04 | 1999-11-04 | Kötõanyagrendszer poliuretánalapú magok és öntõformák készítéséhez |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP1137500B9 (cs) |
| KR (1) | KR100871534B1 (cs) |
| AT (1) | ATE262387T1 (cs) |
| AU (1) | AU757432B2 (cs) |
| BG (1) | BG64942B1 (cs) |
| BR (1) | BR9915076A (cs) |
| CA (1) | CA2349878C (cs) |
| CZ (1) | CZ296809B6 (cs) |
| DE (2) | DE19850833C2 (cs) |
| DK (1) | DK1137500T3 (cs) |
| ES (1) | ES2217841T3 (cs) |
| HU (1) | HU223611B1 (cs) |
| NO (1) | NO20012166L (cs) |
| PL (1) | PL191929B1 (cs) |
| TR (1) | TR200101240T2 (cs) |
| WO (1) | WO2000025957A1 (cs) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004057671B4 (de) * | 2004-11-29 | 2007-04-26 | Hüttenes-Albertus Chemische Werke GmbH | Phenol-Formaldehydharze und Verfahren zu deren Herstellung |
| DE102006037288B4 (de) * | 2006-08-09 | 2019-06-13 | Ask Chemicals Gmbh | Formstoffmischung enthaltend Cardol und/oder Cardanol in Gießereibindemitteln auf Polyurethanbasis, Verfahren zur Herstellung eines Formkörpers sowie Verwendung desselben |
| ES2739455T3 (es) | 2007-01-22 | 2020-01-31 | Arkema France | Proceso para fabricar núcleos conformados de fundición y para colar metales |
| DE102007031376A1 (de) | 2007-07-05 | 2009-01-08 | GTP Schäfer Gießtechnische Produkte GmbH | Alternatives Cold-Box-Verfahren mit Rohölen |
| DE102008007181A1 (de) | 2008-02-01 | 2009-08-06 | Ashland-Südchemie-Kernfest GmbH | Verwendung von verzweigten Alkandiolcarbonsäurediestern in Gießereibindemitteln auf Polyurethanbasis |
| DE102008025311A1 (de) | 2008-05-27 | 2009-12-03 | Ashland-Südchemie-Kernfest GmbH | Geruchs- und schadstoffadsorbierende Beschichtungsmasse für den kastengebundenen Metallguss |
| DE102010032734A1 (de) | 2010-07-30 | 2012-02-02 | Ashland-Südchemie-Kernfest GmbH | Bindemittelsystem auf Polyurethanbasis zur Herstellung von Kernen und Gießformen unter Verwendung cyclischer Formale, Formstoffmischung und Verfahren |
| DE102010046981A1 (de) | 2010-09-30 | 2012-04-05 | Ashland-Südchemie-Kernfest GmbH | Bindemittel enthaltend substituierte Benzole und Napthaline zur Herstellung von Kernen und Formen für den Metallguss, Formstoffmischung und Verfahren |
| DE102010051567A1 (de) | 2010-11-18 | 2012-05-24 | Ashland-Südchemie-Kernfest GmbH | Bindemittel auf Polyurethanbasis zur Herstellung von Kernen und Gießformen unter Verwendung von Isocyanaten enthaltend eine Urethonimin- und/oder Carbodiimid-Gruppe, eine Formstoffmischung enthaltend das Bindemittel und ein Verfahren unter Verwendung des Bindemittels |
| DE102013004663B4 (de) | 2013-03-18 | 2024-05-02 | Ask Chemicals Gmbh | Bindemittelsystem, Formstoffmischung enthaltend dasselbe, Verfahren zur Herstellung der Formstoffmischung, Verfahren zur Herstellung eines Gießformteils oder Gießkerns, Gießformteil oder Gießkern sowie Verwendung des so erhältlichen Gießformteils oder Gießkerns für den Metallguss |
| DE102013004661A1 (de) | 2013-03-18 | 2014-09-18 | Ask Chemicals Gmbh | Verwendung von Carbonsäuren und Fettaminen in PU-Bindemitteln zur Herstellung von Kernen und Formen für den Metallguss |
| DE102013004662A1 (de) | 2013-03-18 | 2014-09-18 | Ask Chemicals Gmbh | Verwendung von Monoestern epoxidierter Fettsäuren in PU-Bindemitteln zur Herstellung von Kernen und Formen für den Metallguss |
| DE102014110189A1 (de) | 2014-07-18 | 2016-01-21 | Ask Chemicals Gmbh | CO-Katalysatoren für Polyurethan-Coldbox-Bindemittel |
| DE102014117284A1 (de) | 2014-11-25 | 2016-05-25 | Ask Chemicals Gmbh | Polyurethan-Bindemittelsystem zur Herstellung von Kernen und Gießformen, Formstoffmischung enthaltend das Bindemittel und ein Verfahren unter Verwendung des Bindemittels |
| DE102015102952A1 (de) | 2015-03-02 | 2016-09-08 | Ask Chemicals Gmbh | Verfahren zur Aushärtung von Polyurethan-Bindemitteln in Formstoffmischungen durch Einleiten tertiärer Amine und Lösungsmittel und Kit zur Durchführung des Verfahrens |
| DE102015107016A1 (de) | 2015-05-05 | 2016-06-23 | Ask Chemicals Gmbh | Verfahren zur Reduzierung von freiem Formaldehyd in Benzylether-Harzen |
| BR112018008817B1 (pt) | 2015-10-30 | 2022-06-21 | ASK Chemicals LLC | Sistema aglutinante para mistura de material de moldagem, bem como mistura de material de moldagem e método para produção de molde ou núcleo para fundição de metal fundido |
| DE102016115947A1 (de) | 2016-08-26 | 2018-03-01 | Ask Chemicals Gmbh | Verfahren zum schichtweisen Aufbau von Formkörpern mit einem Phenolharz-Polyurethan-basiertem Bindersystem |
| DE102016123621A1 (de) | 2016-12-06 | 2018-06-07 | Ask Chemicals Gmbh | Polyurethan Bindemittel mit verbesserter Fließfähigkeit |
| DE102016125700A1 (de) | 2016-12-23 | 2018-06-28 | Ask Chemicals Gmbh | Bindemittel auf Basis von Phenolharzen vom Benzylethertyp enthaltend freies Phenol und freie Hydroxybenzylalkohole |
| DE102016125702A1 (de) | 2016-12-23 | 2018-06-28 | Ask Chemicals Gmbh | Komponentenystem zur Herstellung von Kernen und Formen |
| DE102017112681A1 (de) | 2017-06-08 | 2018-12-13 | Ask Chemicals Gmbh | Verfahren zur Herstellung von dreidimensional geschichteten Formkörpern |
| DE102018100694A1 (de) | 2018-01-12 | 2019-07-18 | Ask Chemicals Gmbh | Formaldehydreduziertes Phenolharzbindemittel |
| DE102020003562A1 (de) | 2020-06-15 | 2021-12-16 | Ask Chemicals Gmbh | Verfahren zum schichtweisen Aufbau eines ausgehärteten dreidimensionalen Formkörpers, Formkörper, welcher dadurch erhalten werden kann, sowie dessen Verwendung |
| DE102020118314A1 (de) | 2020-07-10 | 2022-01-13 | Ask Chemicals Gmbh | Mittel zur Reduzierung von Sandanhaftungen |
| DE102021003265A1 (de) | 2021-06-24 | 2022-12-29 | Ask Chemicals Gmbh | Beschichteter körniger stoff, verfahren zum beschichten eines körnigen stoffs und verwendung eines bindemittels zum beschichten eines körnigen stoffs |
| DE102021003264A1 (de) | 2021-06-24 | 2022-12-29 | Ask Chemicals Gmbh | Zwei-komponenten-polyurethanzusammensetzungen |
| EP4389789A1 (en) | 2022-12-21 | 2024-06-26 | Prefere Resins Holding GmbH | Use of hydroxybenzoic acid to modify a benzyl ether type resin |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4657950A (en) * | 1984-10-12 | 1987-04-14 | Acme Resin Corporation | Refractory binders |
| US4546124A (en) * | 1984-10-12 | 1985-10-08 | Acme Resin Corporation | Polyurethane binder compositions |
| US4848442A (en) * | 1984-10-12 | 1989-07-18 | Acme Resin Corporation | Resin binders for foundry sand cores and molds |
| US5101001A (en) * | 1989-12-21 | 1992-03-31 | Ashland Oil, Inc. | Polyurethane-forming foundry binders and their use |
| DE4135572A1 (de) * | 1991-10-29 | 1993-05-06 | Bayer Ag, 5090 Leverkusen, De | Hydrophobe polyurethan-systeme |
| GB2267524B (en) * | 1992-06-04 | 1995-07-12 | Chas Braithwaite | Cycle parking fixture |
| DE4327292C2 (de) * | 1993-08-13 | 1996-04-25 | Ashland Suedchemie Kernfest | Bindemittel zur Herstellung von Gießereikernen und -formen und ihre Verwendung |
| WO1998002473A1 (en) * | 1996-07-17 | 1998-01-22 | Ashland Inc. | Benzylic ether phenolic resole resins, their preparation, and uses |
-
1998
- 1998-11-04 DE DE19850833A patent/DE19850833C2/de not_active Expired - Fee Related
-
1999
- 1999-11-04 WO PCT/EP1999/008419 patent/WO2000025957A1/de not_active Ceased
- 1999-11-04 CA CA002349878A patent/CA2349878C/en not_active Expired - Fee Related
- 1999-11-04 KR KR1020017005623A patent/KR100871534B1/ko not_active Expired - Fee Related
- 1999-11-04 DK DK99957988T patent/DK1137500T3/da active
- 1999-11-04 EP EP99957988A patent/EP1137500B9/de not_active Expired - Lifetime
- 1999-11-04 HU HU0104315A patent/HU223611B1/hu not_active IP Right Cessation
- 1999-11-04 ES ES99957988T patent/ES2217841T3/es not_active Expired - Lifetime
- 1999-11-04 AT AT99957988T patent/ATE262387T1/de active
- 1999-11-04 DE DE59908972T patent/DE59908972D1/de not_active Expired - Lifetime
- 1999-11-04 AU AU15509/00A patent/AU757432B2/en not_active Ceased
- 1999-11-04 TR TR2001/01240T patent/TR200101240T2/xx unknown
- 1999-11-04 BR BR9915076-0A patent/BR9915076A/pt not_active Application Discontinuation
- 1999-11-04 CZ CZ20011334A patent/CZ296809B6/cs not_active IP Right Cessation
- 1999-11-04 PL PL348642A patent/PL191929B1/pl unknown
-
2001
- 2001-05-02 NO NO20012166A patent/NO20012166L/no not_active Application Discontinuation
- 2001-06-01 BG BG105554A patent/BG64942B1/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CZ20011334A3 (cs) | 2002-05-15 |
| HUP0104315A2 (hu) | 2002-03-28 |
| KR20010113634A (ko) | 2001-12-28 |
| CA2349878C (en) | 2009-06-09 |
| WO2000025957A1 (de) | 2000-05-11 |
| AU1550900A (en) | 2000-05-22 |
| NO20012166D0 (no) | 2001-05-02 |
| PL191929B1 (pl) | 2006-07-31 |
| DE19850833C2 (de) | 2001-06-13 |
| ATE262387T1 (de) | 2004-04-15 |
| PL348642A1 (en) | 2002-06-03 |
| NO20012166L (no) | 2001-06-11 |
| KR100871534B1 (ko) | 2008-12-05 |
| EP1137500B1 (de) | 2004-03-24 |
| BR9915076A (pt) | 2001-10-23 |
| DK1137500T3 (da) | 2004-05-10 |
| TR200101240T2 (tr) | 2001-10-22 |
| BG64942B1 (bg) | 2006-10-31 |
| DE19850833A1 (de) | 2000-05-11 |
| HUP0104315A3 (en) | 2002-05-28 |
| AU757432B2 (en) | 2003-02-20 |
| DE59908972D1 (de) | 2004-04-29 |
| EP1137500B9 (de) | 2005-12-14 |
| ES2217841T3 (es) | 2004-11-01 |
| CZ296809B6 (cs) | 2006-06-14 |
| EP1137500A1 (de) | 2001-10-04 |
| CA2349878A1 (en) | 2000-05-11 |
| BG105554A (en) | 2001-12-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HFG4 | Patent granted, date of granting |
Effective date: 20040903 |
|
| MM4A | Lapse of definitive patent protection due to non-payment of fees |