SE449954B - Bindemedelskomposition for framstellning av gjutformar, gjutformningskomposition samt forfarande for framstellning av en gjutform och forfarande for gjutning av metallforemal - Google Patents

Bindemedelskomposition for framstellning av gjutformar, gjutformningskomposition samt forfarande for framstellning av en gjutform och forfarande for gjutning av metallforemal

Info

Publication number: SE449954B
Authority: SE; Sweden
Prior art keywords: weight; casting; composition according; oil; phenolic resin
Prior art date: 1979-05-14

Application number

SE8003483A

Other languages

English (en)

Swedish (sv)

Other versions

SE8003483L (sv

Inventor

J J Gardikes

Original Assignee

Ashland Oil Inc

Priority date (The priority date 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 date listed.)

1979-05-14

Filing date

1980-05-08

Publication date

1987-06-01

1980-05-08 Application filed by Ashland Oil Inc filed Critical Ashland Oil Inc

1980-11-15 Publication of SE8003483L publication Critical patent/SE8003483L/

1987-06-01 Publication of SE449954B publication Critical patent/SE449954B/sv

Links

239000000203 mixture Substances 0.000 title claims description 136
238000005266 casting Methods 0.000 title claims description 50
238000000034 method Methods 0.000 title claims description 12
238000002360 preparation method Methods 0.000 title description 6
229920001568 phenolic resin Polymers 0.000 claims description 64
239000005011 phenolic resin Substances 0.000 claims description 64
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 57
239000011230 binding agent Substances 0.000 claims description 53
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 52
229920001228 polyisocyanate Polymers 0.000 claims description 48
239000005056 polyisocyanate Substances 0.000 claims description 48
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 45
239000000463 material Substances 0.000 claims description 40
239000003921 oil Substances 0.000 claims description 32
235000019198 oils Nutrition 0.000 claims description 32
229920005989 resin Polymers 0.000 claims description 29
239000011347 resin Substances 0.000 claims description 29
229910052782 aluminium Inorganic materials 0.000 claims description 21
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 21
150000002989 phenols Chemical class 0.000 claims description 21
229910052751 metal Inorganic materials 0.000 claims description 20
239000002184 metal Substances 0.000 claims description 20
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 claims description 18
238000001035 drying Methods 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 13
229920003986 novolac Polymers 0.000 claims description 12
239000000853 adhesive Substances 0.000 claims description 11
230000001070 adhesive effect Effects 0.000 claims description 11
239000004215 Carbon black (E152) Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
239000007788 liquid Substances 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 10
229930195733 hydrocarbon Natural products 0.000 claims description 9
239000000944 linseed oil Substances 0.000 claims description 9
235000021388 linseed oil Nutrition 0.000 claims description 9
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 8
238000002844 melting Methods 0.000 claims description 8
230000008018 melting Effects 0.000 claims description 8
150000002148 esters Chemical class 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
238000000465 moulding Methods 0.000 claims description 6
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 5
229910000077 silane Inorganic materials 0.000 claims description 5
239000003549 soybean oil Substances 0.000 claims description 5
235000012424 soybean oil Nutrition 0.000 claims description 5
239000002023 wood Substances 0.000 claims description 5
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 4
239000007859 condensation product Substances 0.000 claims description 4
238000004132 cross linking Methods 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 3
239000004848 polyfunctional curative Substances 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
230000004048 modification Effects 0.000 claims description 2
238000012986 modification Methods 0.000 claims description 2
230000008569 process Effects 0.000 claims description 2
150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
239000008158 vegetable oil Substances 0.000 claims description 2
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 56
239000004576 sand Substances 0.000 description 40
239000012948 isocyanate Substances 0.000 description 28
239000002904 solvent Substances 0.000 description 27
150000002513 isocyanates Chemical class 0.000 description 26
-1 hydrocarbon radicals Chemical class 0.000 description 25
150000001299 aldehydes Chemical class 0.000 description 11
239000003849 aromatic solvent Substances 0.000 description 10
125000003118 aryl group Chemical group 0.000 description 10
239000002245 particle Substances 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 9
235000013824 polyphenols Nutrition 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000002798 polar solvent Substances 0.000 description 8
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 8
238000005495 investment casting Methods 0.000 description 7
239000003960 organic solvent Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 6
239000011256 inorganic filler Substances 0.000 description 6
229910003475 inorganic filler Inorganic materials 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
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 5
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 5
QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 5
239000006061 abrasive grain Substances 0.000 description 5
125000001931 aliphatic group Chemical group 0.000 description 5
229910010293 ceramic material Inorganic materials 0.000 description 5
FSCIDASGDAWVED-UHFFFAOYSA-N dimethyl hexanedioate;dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC.COC(=O)CCCCC(=O)OC FSCIDASGDAWVED-UHFFFAOYSA-N 0.000 description 5
HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 5
229920003987 resole Polymers 0.000 description 5
OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 4
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
235000019441 ethanol Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
150000002739 metals Chemical class 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
239000011819 refractory material Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
238000007792 addition Methods 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
238000009835 boiling Methods 0.000 description 3
210000000988 bone and bone Anatomy 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000010439 graphite Substances 0.000 description 3
229910002804 graphite Inorganic materials 0.000 description 3
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 3
239000003350 kerosene Substances 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
238000010992 reflux Methods 0.000 description 3
229910052726 zirconium Inorganic materials 0.000 description 3
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 2
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 2
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
VTCDZPUMZAZMSB-UHFFFAOYSA-N 3,4,5-trimethoxyphenol Chemical compound COC1=CC(O)=CC(OC)=C1OC VTCDZPUMZAZMSB-UHFFFAOYSA-N 0.000 description 2
YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-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
TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-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
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
229910001369 Brass Inorganic materials 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
229910000881 Cu alloy Inorganic materials 0.000 description 2
UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
229910001060 Gray iron Inorganic materials 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
239000003082 abrasive agent Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
239000010951 brass Substances 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000000470 constituent Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
229920006037 cross link polymer Polymers 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 2
XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 2
230000003628 erosive effect Effects 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
239000012046 mixed solvent Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 2
229910052609 olivine Inorganic materials 0.000 description 2
239000010450 olivine Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
229910010271 silicon carbide Inorganic materials 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 1
XRUGBBIQLIVCSI-UHFFFAOYSA-N 2,3,4-trimethylphenol Chemical compound CC1=CC=C(O)C(C)=C1C XRUGBBIQLIVCSI-UHFFFAOYSA-N 0.000 description 1
ZYPDJSJJXZWZJJ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-piperidin-4-yloxypyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)OC1CCNCC1 ZYPDJSJJXZWZJJ-UHFFFAOYSA-N 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
NGFPWHGISWUQOI-UHFFFAOYSA-N 2-sec-butylphenol Chemical compound CCC(C)C1=CC=CC=C1O NGFPWHGISWUQOI-UHFFFAOYSA-N 0.000 description 1
ZDZYGYFHTPFREM-UHFFFAOYSA-N 3-[3-aminopropyl(dimethoxy)silyl]oxypropan-1-amine Chemical compound NCCC[Si](OC)(OC)OCCCN ZDZYGYFHTPFREM-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
OAHMVZYHIJQTQC-UHFFFAOYSA-N 4-cyclohexylphenol Chemical compound C1=CC(O)=CC=C1C1CCCCC1 OAHMVZYHIJQTQC-UHFFFAOYSA-N 0.000 description 1
ILASIIGKRFKNQC-UHFFFAOYSA-N 4-methoxy-3-methylphenol Chemical compound COC1=CC=C(O)C=C1C ILASIIGKRFKNQC-UHFFFAOYSA-N 0.000 description 1
ZNPSUQQXTRRSBM-UHFFFAOYSA-N 4-n-Pentylphenol Chemical compound CCCCCC1=CC=C(O)C=C1 ZNPSUQQXTRRSBM-UHFFFAOYSA-N 0.000 description 1
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
OGRAOKJKVGDSFR-UHFFFAOYSA-N 6-Oxy-pseudocumol Natural products CC1=CC(C)=C(C)C(O)=C1 OGRAOKJKVGDSFR-UHFFFAOYSA-N 0.000 description 1
229910052580 B4C Inorganic materials 0.000 description 1
229910052582 BN Inorganic materials 0.000 description 1
PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
IYAHYZQOYHDKNN-UHFFFAOYSA-N COC(=O)c1c(C)c(Cc2c(O)c(C(O)=O)c(C)c3Oc4c(OC(=O)c23)c(C)cc(O)c4C=O)c(O)c(C)c1O Chemical compound COC(=O)c1c(C)c(Cc2c(O)c(C(O)=O)c(C)c3Oc4c(OC(=O)c23)c(C)cc(O)c4C=O)c(O)c(C)c1O IYAHYZQOYHDKNN-UHFFFAOYSA-N 0.000 description 1
MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 1
BIECHDFOWIXSMP-UHFFFAOYSA-N Furfuric acid Natural products CC1=C(O)C(C(=O)OC)=C(C)C(CC=2C=3OC(=O)C4=C(C)C=C(O)C(C=O)=C4OC=3C(C)=C(C(O)=O)C=2O)=C1O BIECHDFOWIXSMP-UHFFFAOYSA-N 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
241000208202 Linaceae Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
241000556720 Manga Species 0.000 description 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
GVZLNOOLGIOOEC-UHFFFAOYSA-N [2,4,4-trimethyl-5-(2-methylpropanoyloxy)pentyl] 2-methylpropanoate Chemical compound CC(C)C(=O)OCC(C)CC(C)(C)COC(=O)C(C)C GVZLNOOLGIOOEC-UHFFFAOYSA-N 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
238000007605 air drying Methods 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
FYXKZNLBZKRYSS-UHFFFAOYSA-N benzene-1,2-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC=C1C(Cl)=O FYXKZNLBZKRYSS-UHFFFAOYSA-N 0.000 description 1
YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
238000007664 blowing Methods 0.000 description 1
INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
230000008859 change Effects 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
229910052593 corundum Inorganic materials 0.000 description 1
239000010431 corundum Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
229910001610 cryolite Inorganic materials 0.000 description 1
150000001913 cyanates Chemical class 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
229910001651 emery Inorganic materials 0.000 description 1
WSEQXVZVJXJVFP-FQEVSTJZSA-N escitalopram Chemical compound C1([C@]2(C3=CC=C(C=C3CO2)C#N)CCCN(C)C)=CC=C(F)C=C1 WSEQXVZVJXJVFP-FQEVSTJZSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
229940013317 fish oils Drugs 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000010436 fluorite Substances 0.000 description 1
239000002223 garnet Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
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 description 1
239000010460 hemp oil Substances 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910000464 lead oxide Inorganic materials 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
150000001247 metal acetylides Chemical class 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 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
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000004767 nitrides Chemical class 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
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 1
235000006408 oxalic acid Nutrition 0.000 description 1
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 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
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
238000010944 pre-mature reactiony Methods 0.000 description 1
238000003825 pressing Methods 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
239000011342 resin composition Substances 0.000 description 1
238000007790 scraping Methods 0.000 description 1
238000013458 shaking study Methods 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
229910021332 silicide Inorganic materials 0.000 description 1
IYMSIPPWHNIMGE-UHFFFAOYSA-N silylurea Chemical compound NC(=O)N[SiH3] IYMSIPPWHNIMGE-UHFFFAOYSA-N 0.000 description 1
238000005245 sintering Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
239000004246 zinc acetate Substances 0.000 description 1

Classifications

- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02M—APPARATUS FOR CONVERSION BETWEEN AC AND AC, BETWEEN AC AND DC, OR BETWEEN DC AND DC, AND FOR USE WITH MAINS OR SIMILAR POWER SUPPLY SYSTEMS; CONVERSION OF DC OR AC INPUT POWER INTO SURGE OUTPUT POWER; CONTROL OR REGULATION THEREOF
- H02M7/00—Conversion of AC power input into DC power output; Conversion of DC power input into AC power output
- H02M7/42—Conversion of DC power input into AC power output without possibility of reversal
- H02M7/44—Conversion of DC power input into AC power output without possibility of reversal by static converters
- H02M7/48—Conversion of DC power input into AC power output without possibility of reversal by static converters using discharge tubes with control electrode or semiconductor devices with control electrode
- 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
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/54—Polycondensates of aldehydes
- C08G18/542—Polycondensates of aldehydes with phenols
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/6547—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen the low-molecular compounds being compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02M—APPARATUS FOR CONVERSION BETWEEN AC AND AC, BETWEEN AC AND DC, OR BETWEEN DC AND DC, AND FOR USE WITH MAINS OR SIMILAR POWER SUPPLY SYSTEMS; CONVERSION OF DC OR AC INPUT POWER INTO SURGE OUTPUT POWER; CONTROL OR REGULATION THEREOF
- H02M7/00—Conversion of AC power input into DC power output; Conversion of DC power input into AC power output
- H02M7/42—Conversion of DC power input into AC power output without possibility of reversal
- H02M7/44—Conversion of DC power input into AC power output without possibility of reversal by static converters
- H02M7/48—Conversion of DC power input into AC power output without possibility of reversal by static converters using discharge tubes with control electrode or semiconductor devices with control electrode
- H02M7/505—Conversion of DC power input into AC power output without possibility of reversal by static converters using discharge tubes with control electrode or semiconductor devices with control electrode using devices of a thyratron or thyristor type requiring extinguishing means
- H02M7/515—Conversion of DC power input into AC power output without possibility of reversal by static converters using discharge tubes with control electrode or semiconductor devices with control electrode using devices of a thyratron or thyristor type requiring extinguishing means using semiconductor devices only

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Mechanical Engineering (AREA)
Materials Engineering (AREA)
Power Engineering (AREA)
Mold Materials And Core Materials (AREA)
Polyurethanes Or Polyureas (AREA)
Compositions Of Macromolecular Compounds (AREA)
Phenolic Resins Or Amino Resins (AREA)
Dry Formation Of Fiberboard And The Like (AREA)
Adhesives Or Adhesive Processes (AREA)

SE8003483A 1979-05-14 1980-05-08 Bindemedelskomposition for framstellning av gjutformar, gjutformningskomposition samt forfarande for framstellning av en gjutform och forfarande for gjutning av metallforemal SE449954B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/039,016 US4268425A (en)	1979-05-14	1979-05-14	Phenolic resin-polyisocyanate binder systems containing a drying oil and use thereof

Publications (2)

Publication Number	Publication Date
SE8003483L SE8003483L (sv)	1980-11-15
SE449954B true SE449954B (sv)	1987-06-01

Family

ID=21903205

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8003483A SE449954B (sv)	1979-05-14	1980-05-08	Bindemedelskomposition for framstellning av gjutformar, gjutformningskomposition samt forfarande for framstellning av en gjutform och forfarande for gjutning av metallforemal

Country Status (25)

Country	Link
US (1)	US4268425A (pt)
JP (2)	JPS5922614B2 (pt)
KR (1)	KR830002434B1 (pt)
AR (1)	AR226557A1 (pt)
AT (1)	AT382096B (pt)
AU (1)	AU518833B2 (pt)
BE (1)	BE883311A (pt)
BR (1)	BR8002997A (pt)
CA (1)	CA1159585A (pt)
CH (1)	CH647250A5 (pt)
DE (1)	DE3018466C2 (pt)
DK (1)	DK170552B1 (pt)
ES (1)	ES8105169A1 (pt)
FR (1)	FR2456759A1 (pt)
GB (1)	GB2050400B (pt)
IT (1)	IT1131180B (pt)
MA (1)	MA18830A1 (pt)
MX (1)	MX155006A (pt)
NL (1)	NL180670C (pt)
NO (1)	NO155383C (pt)
PH (1)	PH15844A (pt)
PT (1)	PT71228A (pt)
SE (1)	SE449954B (pt)
TR (1)	TR20865A (pt)
ZA (1)	ZA802813B (pt)

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US4514316A (en) *	1983-06-29	1985-04-30	Acme Resin Corporation	Polyisocyanate compositions useful for polyurethane binders
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US5021539A (en) *	1989-03-24	1991-06-04	Acme Resin Corporation	Alkaline benzylic ether phenolic resin binders
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US5238976A (en) *	1990-06-15	1993-08-24	Borden, Inc.	Process to enhance the tensile strength of reclaimed sand bonded with ester cured alkaline phenolic resin
US5447968A (en) *	1993-07-23	1995-09-05	Ashland Inc.	Polyurethane-forming binder systems containing 2,2'-dipyridyl, 1,10-phenanthroline, and their substituted alkyl derivatives
DE4327292C2 (de) *	1993-08-13	1996-04-25	Ashland Suedchemie Kernfest	Bindemittel zur Herstellung von Gießereikernen und -formen und ihre Verwendung
SI0771599T2 (en) *	1995-11-01	2004-04-30	Huettenes-Albertus	Binder based on polyurethanes for producing foundry mould and core compositions
BR9601454C1 (pt) *	1996-03-25	2000-01-18	Paulo Roberto Menon	Processo para produção de luvas exotérmicas e isolantes.
US6133340A (en) *	1996-03-25	2000-10-17	Ashland Inc.	Sleeves, their preparation, and use
DE19617938A1 (de) *	1996-04-27	1997-11-06	Chemex Gmbh	Speisereinsätze und deren Herstellung
DE19647368A1 (de) *	1996-11-15	1998-05-20	Inst Neue Mat Gemein Gmbh	Verbundwerkstoffe
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US6017978A (en) *	1998-02-28	2000-01-25	Ashland Inc.	Polyurethane forming no-bake foundry binders
US6013695A (en) *	1998-09-30	2000-01-11	Ashland Inc.	Foundry binders containing modified polyisocyanates
IT1313280B1 (it) *	1999-08-02	2002-07-17	Cavenaghi Spa	Sistemi leganti per fonderia.
US6365646B1 (en)	1999-12-08	2002-04-02	Borden Chemical, Inc.	Method to improve humidity resistance of phenolic urethane foundry binders
AU2002243322A1 (en) *	2000-11-03	2002-06-24	Ashland Inc.	Foundry binder systems which contain a silane-modified polyisocyanate
US20050250874A1 (en) *	2004-05-04	2005-11-10	Ha-International, Llc	Phenolic urethane foundry binder
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
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1979
- 1979-05-14 US US06/039,016 patent/US4268425A/en not_active Expired - Lifetime
1980
- 1980-05-01 AU AU57980/80A patent/AU518833B2/en not_active Ceased
- 1980-05-02 CA CA000351168A patent/CA1159585A/en not_active Expired
- 1980-05-05 MA MA19026A patent/MA18830A1/fr unknown
- 1980-05-06 GB GB8015031A patent/GB2050400B/en not_active Expired
- 1980-05-08 SE SE8003483A patent/SE449954B/sv not_active IP Right Cessation
- 1980-05-09 DK DK205680A patent/DK170552B1/da not_active IP Right Cessation
- 1980-05-12 ZA ZA00802813A patent/ZA802813B/xx unknown
- 1980-05-12 PT PT71228A patent/PT71228A/pt unknown
- 1980-05-13 ES ES491435A patent/ES8105169A1/es not_active Expired
- 1980-05-13 CH CH3743/80A patent/CH647250A5/de not_active IP Right Cessation
- 1980-05-13 NL NLAANVRAGE8002759,A patent/NL180670C/xx not_active IP Right Cessation
- 1980-05-13 PH PH24016A patent/PH15844A/en unknown
- 1980-05-13 KR KR1019800001875A patent/KR830002434B1/ko active
- 1980-05-13 NO NO801411A patent/NO155383C/no unknown
- 1980-05-13 AT AT0255880A patent/AT382096B/de not_active IP Right Cessation
- 1980-05-14 MX MX182328A patent/MX155006A/es unknown
- 1980-05-14 DE DE3018466A patent/DE3018466C2/de not_active Expired
- 1980-05-14 FR FR8010935A patent/FR2456759A1/fr not_active Withdrawn
- 1980-05-14 TR TR20865A patent/TR20865A/xx unknown
- 1980-05-14 JP JP55062928A patent/JPS5922614B2/ja not_active Expired
- 1980-05-14 AR AR281039A patent/AR226557A1/es active
- 1980-05-14 BE BE0/200627A patent/BE883311A/fr not_active IP Right Cessation
- 1980-05-14 IT IT22054/80A patent/IT1131180B/it active
- 1980-05-14 BR BR8002997A patent/BR8002997A/pt not_active IP Right Cessation
1981
- 1981-06-10 JP JP56088324A patent/JPS599253B2/ja not_active Expired

Also Published As

Publication number	Publication date
FR2456759A1 (fr)	1980-12-12
JPS564622A (en)	1981-01-19
SE8003483L (sv)	1980-11-15
ZA802813B (en)	1981-06-24
GB2050400B (en)	1983-04-13
PH15844A (en)	1983-04-08
NO155383B (no)	1986-12-15
PT71228A (en)	1980-06-01
IT1131180B (it)	1986-06-18
GB2050400A (en)	1981-01-07
NL180670C (nl)	1987-04-01
KR830002824A (ko)	1983-05-30
MA18830A1 (fr)	1980-12-31
JPS5922614B2 (ja)	1984-05-28
NL8002759A (nl)	1980-11-18
CH647250A5 (de)	1985-01-15
MX155006A (es)	1988-01-19
TR20865A (tr)	1982-11-09
ES491435A0 (es)	1981-05-16
DK205680A (da)	1980-11-15
BE883311A (fr)	1980-09-01
NO155383C (no)	1987-03-25
JPS599253B2 (ja)	1984-03-01
NO801411L (no)	1980-11-17
DE3018466A1 (de)	1980-11-20
DE3018466C2 (de)	1984-12-13
BR8002997A (pt)	1980-12-23
IT8022054A0 (it)	1980-05-14
JPS5728650A (en)	1982-02-16
NL180670B (nl)	1986-11-03
AT382096B (de)	1987-01-12
AU518833B2 (en)	1981-10-22
ATA255880A (de)	1986-06-15
AU5798080A (en)	1980-11-20
DK170552B1 (da)	1995-10-23
AR226557A1 (es)	1982-07-30
US4268425A (en)	1981-05-19
ES8105169A1 (es)	1981-05-16
CA1159585A (en)	1983-12-27
KR830002434B1 (ko)	1983-10-26

Publication	Publication Date	Title
SE449954B (sv)	1987-06-01	Bindemedelskomposition for framstellning av gjutformar, gjutformningskomposition samt forfarande for framstellning av en gjutform och forfarande for gjutning av metallforemal
US4540724A (en)	1985-09-10	Phenolic resin-polyisocyanate binder systems containing a phosphorus halide and use thereof
CA1277795C (en)	1990-12-11	Phenolic resin polyisocyanate binder systems containing a phosphorus based acid
EP0183782B1 (en)	1991-09-11	Phenolic resin-polyisocyanate binder systems
KR910003431B1 (ko)	1991-05-31	유기할로겐 인산염을 함유한 페놀계수지-폴리이소시아네이트의 결합제 조성물과 그것을 이용한 주물용 조성물 및 주형의 제법
US4982781A (en)	1991-01-08	No-bake process for preparing foundry shapes for casting low melting metal castings
US4946876A (en)	1990-08-07	Polyurethane-forming foundry binders containing a polyester polyol
US5101001A (en)	1992-03-31	Polyurethane-forming foundry binders and their use
US4852629A (en)	1989-08-01	Cold-box process for forming foundry shapes which utilizes certain carboxylic acids as bench life extenders
US4760101A (en)	1988-07-26	Polyurethane-forming binder compositions containing certain carboxylic acids as bench life extenders
WO1999043455A1 (en)	1999-09-02	Polyurethane forming no-bake foundry binders
WO1991016157A1 (en)	1991-10-31	Polyurethane-forming foundry binders containing a polyether polyol
WO1989007626A1 (en)	1989-08-24	Low solids polyurethane-forming foundry binders for cold-box process
US6883587B2 (en)	2005-04-26	Polyisocyanate compositions and their use
WO1989006576A1 (en)	1989-07-27	Phenolic resin compositions and their use in foundry binders
WO1988003541A1 (en)	1988-05-19	Polyurethane-forming binder compositions containing certain phosphonic dihalides as bench life extenders

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