AU670988B2 - Ester cured no-bake foundry binder system - Google Patents
Ester cured no-bake foundry binder systemInfo
- Publication number
- AU670988B2 AU670988B2 AU56062/94A AU5606294A AU670988B2 AU 670988 B2 AU670988 B2 AU 670988B2 AU 56062/94 A AU56062/94 A AU 56062/94A AU 5606294 A AU5606294 A AU 5606294A AU 670988 B2 AU670988 B2 AU 670988B2
- Authority
- AU
- Australia
- Prior art keywords
- foundry
- binder system
- resin
- epoxy resin
- weight
- 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.)
- Ceased
Links
- 239000011230 binding agent Substances 0.000 title claims description 53
- 150000002148 esters Chemical class 0.000 title claims description 27
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 54
- 239000003822 epoxy resin Substances 0.000 claims description 41
- 229920000647 polyepoxide Polymers 0.000 claims description 41
- 229920005989 resin Polymers 0.000 claims description 36
- 239000011347 resin Substances 0.000 claims description 36
- 229920003987 resole Polymers 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 27
- 239000003637 basic solution Substances 0.000 claims description 26
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 24
- 239000004848 polyfunctional curative Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 19
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 14
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 12
- 239000002585 base Substances 0.000 claims description 11
- 239000004202 carbamide Substances 0.000 claims description 11
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 9
- 239000007795 chemical reaction product Substances 0.000 claims description 8
- 229920001568 phenolic resin Polymers 0.000 claims description 8
- -1 urea modified phenolic resin Chemical class 0.000 claims description 8
- 239000005011 phenolic resin Substances 0.000 claims description 7
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 238000005058 metal casting Methods 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000004593 Epoxy Substances 0.000 claims description 4
- 238000007493 shaping process Methods 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000000376 reactant Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 22
- 239000004576 sand Substances 0.000 description 20
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 16
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000002156 mixing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000001299 aldehydes Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000001733 carboxylic acid esters Chemical class 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 3
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 150000002118 epoxides Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 150000005677 organic carbonates Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-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
- IJWIRZQYWANBMP-UHFFFAOYSA-N 4-[2-(4-hydroxy-3-propan-2-ylphenyl)propan-2-yl]-2-propan-2-ylphenol Chemical compound C1=C(O)C(C(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)C)=C1 IJWIRZQYWANBMP-UHFFFAOYSA-N 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- GSCLMSFRWBPUSK-UHFFFAOYSA-N beta-Butyrolactone Chemical compound CC1CC(=O)O1 GSCLMSFRWBPUSK-UHFFFAOYSA-N 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- WZRZKFUVOSDSBQ-UHFFFAOYSA-N butane-1,2-diol;carbonic acid Chemical compound OC(O)=O.CCC(O)CO WZRZKFUVOSDSBQ-UHFFFAOYSA-N 0.000 description 1
- ANQJWUKLNGHYIP-UHFFFAOYSA-N butane-1,3-diol;carbonic acid Chemical compound OC(O)=O.CC(O)CCO ANQJWUKLNGHYIP-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- CHYOCNJYMLMTNE-UHFFFAOYSA-N carbonic acid;pentane-1,2-diol Chemical compound OC(O)=O.CCCC(O)CO CHYOCNJYMLMTNE-UHFFFAOYSA-N 0.000 description 1
- MEYBCCDNSNEEGP-UHFFFAOYSA-N carbonic acid;pentane-1,3-diol Chemical compound OC(O)=O.CCC(O)CCO MEYBCCDNSNEEGP-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052609 olivine Inorganic materials 0.000 description 1
- 239000010450 olivine Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- IYMSIPPWHNIMGE-UHFFFAOYSA-N silylurea Chemical compound NC(=O)N[SiH3] IYMSIPPWHNIMGE-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
-
- 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
- B22C1/2246—Condensation polymers of aldehydes and ketones
- B22C1/2253—Condensation polymers of aldehydes and ketones with phenols
-
- 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
- B22C1/226—Polyepoxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97796492A | 1992-11-18 | 1992-11-18 | |
US977964 | 1992-11-18 | ||
PCT/US1993/011031 WO1994011132A1 (en) | 1992-11-18 | 1993-11-15 | Ester cured no-bake foundry binder system |
Publications (2)
Publication Number | Publication Date |
---|---|
AU5606294A AU5606294A (en) | 1994-06-08 |
AU670988B2 true AU670988B2 (en) | 1996-08-08 |
Family
ID=25525688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU56062/94A Ceased AU670988B2 (en) | 1992-11-18 | 1993-11-15 | Ester cured no-bake foundry binder system |
Country Status (9)
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3324718B2 (ja) | 1993-04-30 | 2002-09-17 | 花王株式会社 | 鋳型製造用粘結剤−硬化剤キット |
US5621037A (en) * | 1994-02-18 | 1997-04-15 | Young-Keun Hong | Rubber solution and rubber concrete using the same |
GB2322062B (en) * | 1997-02-15 | 2001-05-02 | Padley G W Holdings Ltd | Improvements in and relating to food products |
WO2001029133A1 (en) * | 1999-10-20 | 2001-04-26 | Kingspan Industrial Insulation Limited | Cellular plastic material based on phenolic resin |
WO2005013852A2 (en) * | 2003-08-07 | 2005-02-17 | Dynamic Spine, Inc. | Intervertebral prosthetic device and associated devices and methods for implanting the intervertebral prosthetic device |
WO2005072236A2 (en) * | 2004-01-29 | 2005-08-11 | Ashland Inc. | Compostion and process for inhibiting the movement of free flowing particles |
DE102014106178A1 (de) | 2014-05-02 | 2015-11-05 | Ask Chemicals Gmbh | Verfahren zum schichtweisen Aufbau von Körpern umfassend feuerfesten Formgrundstoff und Resole und Formen oder Kerne hergestellt nach diesem Verfahren |
DE102014106177A1 (de) * | 2014-05-02 | 2015-11-05 | Ask Chemicals Gmbh | Formstoffmischung enthaltend Resole und amorphes Siliciumdioxid, aus diesen hergestellte Formen und Kerne und Verfahren zu deren Herstellung |
US20170174813A1 (en) * | 2015-12-18 | 2017-06-22 | Ha-International, Llc | Compositions and Methods for Modified Ester-Curatives and Reduction of Formaldehyde Emission and Odor in Ester-Cured Phenolic Binder Systems |
DE102016123661A1 (de) | 2016-12-07 | 2018-06-07 | Ask Chemicals Gmbh | Alkalische Resolbinder mit verbesserter Fließfähigkeit |
DE102019135605A1 (de) | 2019-12-20 | 2021-06-24 | Ask Chemicals Gmbh | Verfahren zum schichtweisen Aufbau von Körpern umfassend feuerfesten Formgrundstoff und Resole, nach diesem Verfahren hergestellte dreidimensionale Körper sowie ein Bindemittel für den 3-dimensionalen Aufbau von Körpern |
CN113651557A (zh) * | 2021-08-30 | 2021-11-16 | 常州高鼎新材料科技有限公司 | 矿物铸件制备配方 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4596840A (en) * | 1984-03-31 | 1986-06-24 | Hoechst Aktiengesellschaft | Mixture for the production of acid-resistant sealing materials and impregnating materials, a process for their preparation and their use |
US4980394A (en) * | 1988-01-12 | 1990-12-25 | Borden (Uk) Limited | Foundry moulding composition |
WO1993003096A1 (en) * | 1991-08-09 | 1993-02-18 | Darchem Engineering Limited | Blast, impact and fire resistant composite material |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3404118A (en) * | 1964-01-30 | 1968-10-01 | Ashland Oil Inc | Reactive modifiers for thermosetting resins |
US4732920A (en) * | 1981-08-20 | 1988-03-22 | Graham John W | High strength particulates |
US4508765A (en) * | 1981-10-20 | 1985-04-02 | International Paint Public Limited Company | Synthetic resins and coating compositions containing them |
JPS58147464A (ja) * | 1982-02-26 | 1983-09-02 | Hitachi Chem Co Ltd | 塗料用材料 |
GB8404595D0 (en) * | 1984-02-22 | 1984-03-28 | Foseco Int | Foundry sand compositions |
JPH0629315B2 (ja) * | 1985-05-29 | 1994-04-20 | ユニチカ株式会社 | 微小球状樹脂組成物及びその製造法 |
US4761441A (en) * | 1985-07-01 | 1988-08-02 | Cl Industries, Inc. | Acid-curable compositions comprising mixtures of furan and epoxy resins and use in preparing formed, shaped, filled bodies |
BR8806482A (pt) * | 1988-04-08 | 1990-07-31 | Acme Resin Corp | Processo para producao de artigo modelado com areia aglutinada com resina; processo para producao de agregados de areia; solucao aglutinante; e composicao de mistura mestra |
US4988745A (en) * | 1989-04-27 | 1991-01-29 | Acme Resin Corporation | Ester hardeners for phenolic resin binder systems |
DK0577733T3 (da) * | 1991-03-27 | 1996-06-03 | Minteq International Inc | Vibrationsbar, harpiksbundet, ildfast sammensætning |
-
1993
- 1993-10-26 TW TW082108895A patent/TW256851B/zh active
- 1993-11-10 ZA ZA938380A patent/ZA938380B/xx unknown
- 1993-11-15 EP EP94901490A patent/EP0668803A4/en not_active Withdrawn
- 1993-11-15 BR BR9307458-1A patent/BR9307458A/pt not_active IP Right Cessation
- 1993-11-15 CA CA002149115A patent/CA2149115A1/en not_active Abandoned
- 1993-11-15 WO PCT/US1993/011031 patent/WO1994011132A1/en not_active Application Discontinuation
- 1993-11-15 JP JP6512419A patent/JPH08506054A/ja active Pending
- 1993-11-15 AU AU56062/94A patent/AU670988B2/en not_active Ceased
-
1994
- 1994-06-16 US US08/260,620 patent/US5405881A/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4596840A (en) * | 1984-03-31 | 1986-06-24 | Hoechst Aktiengesellschaft | Mixture for the production of acid-resistant sealing materials and impregnating materials, a process for their preparation and their use |
US4980394A (en) * | 1988-01-12 | 1990-12-25 | Borden (Uk) Limited | Foundry moulding composition |
WO1993003096A1 (en) * | 1991-08-09 | 1993-02-18 | Darchem Engineering Limited | Blast, impact and fire resistant composite material |
Also Published As
Publication number | Publication date |
---|---|
US5405881A (en) | 1995-04-11 |
AU5606294A (en) | 1994-06-08 |
TW256851B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1995-09-11 |
ZA938380B (en) | 1994-06-13 |
BR9307458A (pt) | 1999-10-13 |
CA2149115A1 (en) | 1994-05-26 |
JPH08506054A (ja) | 1996-07-02 |
EP0668803A4 (en) | 1995-11-02 |
EP0668803A1 (en) | 1995-08-30 |
WO1994011132A1 (en) | 1994-05-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5424376A (en) | Ester cured no-bake foundry binder system | |
AU670988B2 (en) | Ester cured no-bake foundry binder system | |
US4780489A (en) | Modifiers for aqueous basic solutions of phenolic resole resins | |
US4495316A (en) | Acid-curable fluoride-containing no-bake foundry resins | |
BG64942B1 (bg) | Свързващо средство за получаване на леярски сърцаи леярски форми на полиуретанова основа | |
US5607986A (en) | Heat cured foundry mixes and their use | |
US7125914B2 (en) | Heat-cured furan binder system | |
US5376696A (en) | Foundry mixes based upon reclaimed sand | |
US4766949A (en) | Hot box process for preparing foundry shapes | |
KR20020092374A (ko) | 푸란 자경성 주형 결합제 및 그의 용도 | |
CA1339905C (en) | Ester hardeners for phenolic resin binder systems | |
US5036116A (en) | Ester hardeners for phenolic resin binder systems | |
US6326418B1 (en) | Acid-curable, refractory particulate material composition for forming mold | |
WO1997018913A1 (en) | Cold-box process for preparing foundry shapes | |
JPS6228041A (ja) | 鋳物用粘結剤組成物 | |
JP2504660B2 (ja) | 有機エステル硬化型鋳物砂用硬化剤組成物及びこれを用いた鋳型の製造方法 | |
JP2542144B2 (ja) | 有機エステル硬化型鋳物砂用粘結剤組成物及びこれを用いた鋳型の製造方法 | |
WO1992001016A1 (en) | Three component foundry binder system | |
JPH0550177A (ja) | 鋳物砂用樹脂組成物 | |
JP2892468B2 (ja) | 鋳物砂用粘結剤組成物 | |
JP2831825B2 (ja) | 鋳物砂用粘結剤組成物 | |
WO2000050186A1 (en) | No-bake ester cured molding mixes | |
JP3197973B2 (ja) | 鋳物砂用組成物 | |
JPH0573496B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JPS6228042A (ja) | 鋳型用粘結剤樹脂組成物 |