WO2006010777A1 - Utilisation de resines phenoliques modifiees dans des procedes de moulage en coquille - Google Patents
Utilisation de resines phenoliques modifiees dans des procedes de moulage en coquille Download PDFInfo
- Publication number
- WO2006010777A1 WO2006010777A1 PCT/ES2004/000300 ES2004000300W WO2006010777A1 WO 2006010777 A1 WO2006010777 A1 WO 2006010777A1 ES 2004000300 W ES2004000300 W ES 2004000300W WO 2006010777 A1 WO2006010777 A1 WO 2006010777A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phenolic resin
- modified
- fraction
- modified phenolic
- cashew nut
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 28
- 229920001568 phenolic resin Polymers 0.000 title claims abstract description 25
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 25
- 238000010112 shell-mould casting Methods 0.000 title claims abstract description 19
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title description 11
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000004576 sand Substances 0.000 claims abstract description 25
- 244000226021 Anacardium occidentale Species 0.000 claims abstract description 21
- 235000020226 cashew nut Nutrition 0.000 claims abstract description 21
- 238000000576 coating method Methods 0.000 claims abstract description 11
- 239000011248 coating agent Substances 0.000 claims abstract description 10
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- 229920003986 novolac Polymers 0.000 claims description 11
- 239000010466 nut oil Substances 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 7
- 235000019198 oils Nutrition 0.000 claims description 7
- 238000003723 Smelting Methods 0.000 claims description 2
- 235000019492 Cashew oil Nutrition 0.000 claims 3
- 239000010467 cashew oil Substances 0.000 claims 3
- 229940059459 cashew oil Drugs 0.000 claims 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 49
- 239000000377 silicon dioxide Substances 0.000 abstract description 13
- 238000005058 metal casting Methods 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 16
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 9
- 239000004312 hexamethylene tetramine Substances 0.000 description 8
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 238000005266 casting Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- 229910001141 Ductile iron Inorganic materials 0.000 description 2
- 229910001060 Gray iron Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JOLVYUIAMRUBRK-UHFFFAOYSA-N 11',12',14',15'-Tetradehydro(Z,Z-)-3-(8-Pentadecenyl)phenol Natural products OC1=CC=CC(CCCCCCCC=CCC=CCC=C)=C1 JOLVYUIAMRUBRK-UHFFFAOYSA-N 0.000 description 1
- YLKVIMNNMLKUGJ-UHFFFAOYSA-N 3-Delta8-pentadecenylphenol Natural products CCCCCCC=CCCCCCCCC1=CC=CC(O)=C1 YLKVIMNNMLKUGJ-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- JOLVYUIAMRUBRK-UTOQUPLUSA-N Cardanol Chemical compound OC1=CC=CC(CCCCCCC\C=C/C\C=C/CC=C)=C1 JOLVYUIAMRUBRK-UTOQUPLUSA-N 0.000 description 1
- FAYVLNWNMNHXGA-UHFFFAOYSA-N Cardanoldiene Natural products CCCC=CCC=CCCCCCCCC1=CC=CC(O)=C1 FAYVLNWNMNHXGA-UHFFFAOYSA-N 0.000 description 1
- 239000010369 Cascara Substances 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000556215 Frangula purshiana Species 0.000 description 1
- 239000000817 Petroleum-derived resin Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- PTFIPECGHSYQNR-UHFFFAOYSA-N cardanol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 description 1
- 229940058505 cascara Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000000916 dilatatory effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 229910001234 light alloy Inorganic materials 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000001393 microlithography Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000010935 stainless steel Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000003039 volatile agent Substances 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
- 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
- B22C1/24—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 oily or fatty substances; of distillation residues therefrom
-
- 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
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
-
- 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
Definitions
- the present invention relates to the field of the manufacture of molds and dies for foundry and, in particular, to the field of modified phenolic resins used in the manufacture thereof by means of shell molding processes.
- sand grains are used, generally of silica coated with a thermosetting resin film. Said particles are brought into contact with a hot metallic model whereby the resin softens and flows around the grains of sand to form a slightly adherent shell on the model. Once the desired shell thickness is obtained (depending on the contact time and the temperature of the model), the excess of non-adhered sand is removed. The model with the bonded shell is then cooked in order to finish the resin cure, thus forming a mold in thermosetting, self-supporting and rigid shell that adapts to The shape of the metal model. After curing, the hardened shell mold is demolished, this, the mold is separated from the model by, for example, the classic ejectors. A mold or male of sufficient three-dimensional precision is thus produced.
- thermosetting resins of phenolic type such as Novolaca resins are used, for example, to coat the grains of silica sand. Molds or males are thus obtained that have good thermal stability and that withstand the casting temperature. However, they can also exhibit excessive rigidity against the thermal shock of the liquid metal during casting.
- modified phenolic resins are used so that greater flexibility is achieved in the face of the thermal shock of the molten metal, thus avoiding the "cracking" effect by dilating the silica and getting the castings to have a perfect finish.
- phenolic resins for shell molding processes have been modified by adding a series of additives.
- a natural resin commercially called "Vinsol” whose availability is limited given its origin and, therefore, high price, and which also presents other inconveniences such as the production of fumes and odors.
- the modification of the phenolic resins by adding other products such as rosins, high molecular weight resins, petroleum-derived resins, etc.
- these additives have never become a real alternative due to deficiencies in thermal behavior.
- phenolic resins by modifying said phenolic resins by adding cashew nut shell oil, in English called cashew nut shell liquid (CNSL), or a fraction thereof, such as cardanol , so good or better results are obtained than with the phenolic resin modified with Vinsol in terms of the properties of plasticity and hot deformation of the foundry molds and males.
- CNSL cashew nut shell liquid
- Said phenolic resins modified with CNSL or fraction thereof also have a series of additional advantages in terms of the availability and cost of this very common natural product.
- phenolic resins modified with CNSL is known in the industry for various applications such as, for example, the preparation of brake linings and clutches, in the manufacture of photosensitive resins for microlithography (see international patent application WO 02 / 102867), in the preparation of refractory masses (see Spanish patent ES 2151262), etc.
- phenolic resins modified with CNSL for sand coating used to obtain molds and cast iron by means of shell molding procedures.
- the invention provides a new use of said phenolic resins modified with CNSL, or some of its components, specifically their use in shell molding processes.
- the present invention provides the use of a phenolic resin modified with cashew nut shell oil or faction thereof in a shell molding process.
- Another object of the present invention is a shell molding process in which said phenolic resin modified with cashew nut oil or fraction thereof is used in the step of coating the silica sand grains.
- Another object of the present invention is a mold or male for melting metals based on sand grains, generally of silica coated with a phenolic resin modified with cashew nut oil or fraction thereof.
- the present invention provides the use of a phenolic resin modified with cashew nut oil or fraction thereof in a shell molding process.
- cashew nut shell oil is refers to the oil extracted from the cashew nut shell or fraction thereof.
- the modified phenolic resin is a novolac resin.
- the percentage of CNSL in the modified phenolic resin is 1-50% by weight, preferably 5-20% by weight, by weight.
- the invention provides a process comprising a step of coating the silica sand grains with a modified phenolic resin, characterized in that said modified phenolic resin is a modified phenolic resin with nut shell oil of the cashew nut or fraction thereof.
- Said procedure basically comprises three stages:
- CNSL modified novolac resin As starting products, for example, a 100% phenol solution, a 37% formaldehyde solution and CNSL, which are commercial products, are used. For example, to obtain 100 kg of CNSL modified novolac resin, one can start from:
- Phenol and CNSL or derivatives are charged at a temperature of the order of 40-50 ° C.
- An acid catalyst organic, such as oxalic acid, or inorganic acid, such as sulfuric acid
- the formaldehyde is then gradually charged for 1 hour in a phenol / formaldehyde ratio of 1 to 80% by weight, preferably 5 to 15% by weight.
- the reaction is allowed to proceed for another hour at that temperature and, subsequently, evaporation is carried out at a temperature of the order of 130-140 0 C and a vacuum pressure of 700-760 mm in order to eliminate volatiles.
- the degree of polymerization can be controlled by controlling the refractive index, the softening point or the amount of free phenol or free formaldehyde.
- reaction conditions it is possible to work at different temperatures depending on the pressure conditions used.
- pressure conditions for example, at atmospheric pressure one works at 80-110 ° C, at depression at 80-100 ° C and at overpressure at 110-140 ° C.
- the resin thus prepared can be a solid resin (chopped, flaked, pearl or granulated), or a resin in liquid solution with organic solvents of the alcohol, acetone, etc. type, with a softening point of 70-100 ° C (typical values of 88-92 0 C) and with a free phenol amount of 0-6% by weight (typical values of 2-4% by weight).
- Hot coating The sand is heated at a sufficient temperature to melt the solid resin.
- Tempered coating The dissolved solid resin is added on the grains of sand at room temperature.
- a crosslinker such as hexamine (hexamethylenetetramine) is added, which catalyzes and fixes the novolac to the grain.
- hexamine hexamethylenetetramine
- novolac resins behave by themselves as thermoplastics, that is, they do not react in the presence of heat and require the extra contribution of formaldehyde to polymerize, the most widespread form being the addition of hexamine which, at temperatures of the order of 100 0 C, decomposes into ammonia and formaldehyde, thus facilitating the formation of diethylene amine and methylene bridges.
- the hot process is the most common of the three previously reviewed.
- the sand is heated, generally of silica, alone or with additives, up to temperature of 125-175 ° C and then introduced into a mixer.
- the novolac type resin is added until it is completely fused.
- water the mixture below 100 0 C.
- an amount of hexamine solution is introduced and the whole is subjected to depression with entrainment of water from the medium.
- the mixture is then dried and a release agent introduced, such as a metal stearate, preferably calcium, or a polyethylene wax.
- the mixture is broken down, cooled and sieved to be packaged or for immediate use.
- molds or taps are obtained for the smelting of metals for the production of parts for the automotive, railway, aeronautics, chemical, etc. industries.
- the invention provides a shell molding process characterized in that the modified phenolic resin employed is a novolac resin.
- the percentage of CNSL in the modified phenolic resin is 1-50% by weight. More specifically, it is 5-20% by weight.
- the invention provides a mold or male for casting. of metals based on sand grains coated with a phenolic resin modified with cashew nut oil.
- said mold or male is characterized in that the modified phenolic resin used in the coating of the sand grains thereof is a novolac resin.
- said mold or male is characterized in that the percentage of cashew nut oil in the modified phenolic resin is 1-50% by weight. More particularly, it is 5-20% by weight. 5
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/ES2004/000300 WO2006010777A1 (fr) | 2004-06-25 | 2004-06-25 | Utilisation de resines phenoliques modifiees dans des procedes de moulage en coquille |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/ES2004/000300 WO2006010777A1 (fr) | 2004-06-25 | 2004-06-25 | Utilisation de resines phenoliques modifiees dans des procedes de moulage en coquille |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006010777A1 true WO2006010777A1 (fr) | 2006-02-02 |
Family
ID=35785922
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/ES2004/000300 WO2006010777A1 (fr) | 2004-06-25 | 2004-06-25 | Utilisation de resines phenoliques modifiees dans des procedes de moulage en coquille |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006010777A1 (fr) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008017476A1 (fr) * | 2006-08-09 | 2008-02-14 | Ashland-Südchemie-Kernfest GmbH | Utilisation de dérivés de coquille de noix de cajou dans des liants pour fonderie à base de polyuréthanne |
WO2018185400A1 (fr) | 2017-04-04 | 2018-10-11 | Compagnie Generale Des Etablissements Michelin | Composition de caoutchouc a base de resine renforcante et d'un derive d'aminobenzoate |
CN110586847A (zh) * | 2019-10-08 | 2019-12-20 | 赵陆军 | 一种高温稳定型覆膜砂 |
US10853502B1 (en) | 2015-03-04 | 2020-12-01 | Micro Focus Llc | Systems and methods for reducing computational difficulty of cryptographic operations |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES8101944A1 (es) * | 1980-06-09 | 1980-12-16 | Borden Inc | Un procedimiento para preparar una composicion de moldeo pa-ra fundicion |
JPS63117060A (ja) * | 1986-11-04 | 1988-05-21 | Asahi Organic Chem Ind Co Ltd | 結合剤用粉末状フェノール系樹脂組成物 |
ES2168147T3 (es) * | 1997-05-22 | 2002-06-01 | Hatsunen Co Ltd | Procedimiento de produccion de un cuerpo exotermico de fundicion. |
-
2004
- 2004-06-25 WO PCT/ES2004/000300 patent/WO2006010777A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES8101944A1 (es) * | 1980-06-09 | 1980-12-16 | Borden Inc | Un procedimiento para preparar una composicion de moldeo pa-ra fundicion |
JPS63117060A (ja) * | 1986-11-04 | 1988-05-21 | Asahi Organic Chem Ind Co Ltd | 結合剤用粉末状フェノール系樹脂組成物 |
ES2168147T3 (es) * | 1997-05-22 | 2002-06-01 | Hatsunen Co Ltd | Procedimiento de produccion de un cuerpo exotermico de fundicion. |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Derwent World Patents Index; AN 1988-179489 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008017476A1 (fr) * | 2006-08-09 | 2008-02-14 | Ashland-Südchemie-Kernfest GmbH | Utilisation de dérivés de coquille de noix de cajou dans des liants pour fonderie à base de polyuréthanne |
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 |
US10853502B1 (en) | 2015-03-04 | 2020-12-01 | Micro Focus Llc | Systems and methods for reducing computational difficulty of cryptographic operations |
WO2018185400A1 (fr) | 2017-04-04 | 2018-10-11 | Compagnie Generale Des Etablissements Michelin | Composition de caoutchouc a base de resine renforcante et d'un derive d'aminobenzoate |
CN110586847A (zh) * | 2019-10-08 | 2019-12-20 | 赵陆军 | 一种高温稳定型覆膜砂 |
CN110586847B (zh) * | 2019-10-08 | 2020-11-24 | 青铜峡市瑞通支撑剂有限公司 | 一种高温稳定型覆膜砂 |
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