SK1598A3 - Polymer material, process for its production and use thereof - Google Patents
Polymer material, process for its production and use thereof Download PDFInfo
- Publication number
- SK1598A3 SK1598A3 SK15-98A SK1598A SK1598A3 SK 1598 A3 SK1598 A3 SK 1598A3 SK 1598 A SK1598 A SK 1598A SK 1598 A3 SK1598 A3 SK 1598A3
- Authority
- SK
- Slovakia
- Prior art keywords
- oil
- acid
- anhydride
- weight
- polycarboxylic
- Prior art date
Links
- 239000002861 polymer material Substances 0.000 title claims abstract description 9
- 238000000034 method Methods 0.000 title claims description 11
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000002253 acid Substances 0.000 claims abstract description 52
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 14
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 150000008065 acid anhydrides Chemical class 0.000 claims abstract description 7
- 239000004593 Epoxy Substances 0.000 claims abstract description 6
- 125000004069 aziridinyl group Chemical group 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 68
- 239000000203 mixture Substances 0.000 claims description 43
- 239000003921 oil Substances 0.000 claims description 41
- 235000019198 oils Nutrition 0.000 claims description 35
- 150000008064 anhydrides Chemical class 0.000 claims description 34
- 150000003626 triacylglycerols Chemical class 0.000 claims description 25
- 150000007513 acids Chemical class 0.000 claims description 22
- 239000000835 fiber Substances 0.000 claims description 14
- 239000000945 filler Substances 0.000 claims description 12
- -1 acid anhydride anhydride anhydride Chemical class 0.000 claims description 11
- 229920003023 plastic Polymers 0.000 claims description 11
- 239000004033 plastic Substances 0.000 claims description 11
- 238000000465 moulding Methods 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
- 239000002023 wood Substances 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 239000003063 flame retardant Substances 0.000 claims description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 5
- 239000004359 castor oil Substances 0.000 claims description 5
- 235000019438 castor oil Nutrition 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 239000012973 diazabicyclooctane Substances 0.000 claims description 5
- 239000011094 fiberboard Substances 0.000 claims description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 5
- 239000000944 linseed oil Substances 0.000 claims description 5
- 235000021388 linseed oil Nutrition 0.000 claims description 5
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 claims description 5
- VFZDNKRDYPTSTP-UHFFFAOYSA-N 5,8,8-trimethyl-3-oxabicyclo[3.2.1]octane-2,4-dione Chemical compound O=C1OC(=O)C2(C)CCC1C2(C)C VFZDNKRDYPTSTP-UHFFFAOYSA-N 0.000 claims description 4
- LQOPXMZSGSTGMF-UHFFFAOYSA-N 6004-79-1 Chemical compound C1CC2C3C(=O)OC(=O)C3C1C2 LQOPXMZSGSTGMF-UHFFFAOYSA-N 0.000 claims description 4
- 241000221079 Euphorbia <genus> Species 0.000 claims description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N Lactic Acid Natural products CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 4
- 241000219745 Lupinus Species 0.000 claims description 4
- 235000019486 Sunflower oil Nutrition 0.000 claims description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical group OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 claims description 4
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 claims description 4
- YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
- 235000014571 nuts Nutrition 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical group OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical group OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 claims description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 4
- 239000003549 soybean oil Substances 0.000 claims description 4
- 235000012424 soybean oil Nutrition 0.000 claims description 4
- 239000002600 sunflower oil Substances 0.000 claims description 4
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical group OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 4
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- KAOMOVYHGLSFHQ-UTOQUPLUSA-N anacardic acid Chemical compound CCC\C=C/C\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O KAOMOVYHGLSFHQ-UTOQUPLUSA-N 0.000 claims description 3
- 235000014398 anacardic acid Nutrition 0.000 claims description 3
- ADFWQBGTDJIESE-UHFFFAOYSA-N anacardic acid 15:0 Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1C(O)=O ADFWQBGTDJIESE-UHFFFAOYSA-N 0.000 claims description 3
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 238000005253 cladding Methods 0.000 claims description 3
- 235000013312 flour Nutrition 0.000 claims description 3
- 239000010460 hemp oil Substances 0.000 claims description 3
- 239000003999 initiator Substances 0.000 claims description 3
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- 235000005713 safflower oil Nutrition 0.000 claims description 3
- 239000003813 safflower oil Substances 0.000 claims description 3
- 235000019512 sardine Nutrition 0.000 claims description 3
- 150000004760 silicates Chemical class 0.000 claims description 3
- 239000010902 straw Substances 0.000 claims description 3
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 claims description 2
- KLGKVMMWRDYKJM-UHFFFAOYSA-N 2,2-dimethylcyclobutane-1,3-dicarboxylic acid Chemical compound CC1(C)C(C(O)=O)CC1C(O)=O KLGKVMMWRDYKJM-UHFFFAOYSA-N 0.000 claims description 2
- SBDSLKNAJKQNNN-UHFFFAOYSA-N 2-[2-[2-(2-carboxyphenyl)acetyl]oxy-2-oxoethyl]benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CC(=O)OC(=O)CC1=CC=CC=C1C(O)=O SBDSLKNAJKQNNN-UHFFFAOYSA-N 0.000 claims description 2
- LNPQMDSMIGLHSR-UHFFFAOYSA-N 2-oxaspiro[3.5]non-5-ene-1,3-dione Chemical compound O=C1OC(=O)C11C=CCCC1 LNPQMDSMIGLHSR-UHFFFAOYSA-N 0.000 claims description 2
- HHCHLHOEAKKCAB-UHFFFAOYSA-N 2-oxaspiro[3.5]nonane-1,3-dione Chemical compound O=C1OC(=O)C11CCCCC1 HHCHLHOEAKKCAB-UHFFFAOYSA-N 0.000 claims description 2
- WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 claims description 2
- 235000019489 Almond oil Nutrition 0.000 claims description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical class [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- 241000273930 Brevoortia tyrannus Species 0.000 claims description 2
- 235000003301 Ceiba pentandra Nutrition 0.000 claims description 2
- 244000146553 Ceiba pentandra Species 0.000 claims description 2
- 235000019487 Hazelnut oil Nutrition 0.000 claims description 2
- 241001543245 Herklotsichthys lossei Species 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 claims description 2
- 235000008753 Papaver somniferum Nutrition 0.000 claims description 2
- 240000001090 Papaver somniferum Species 0.000 claims description 2
- 235000019483 Peanut oil Nutrition 0.000 claims description 2
- 229920002230 Pectic acid Polymers 0.000 claims description 2
- 235000004347 Perilla Nutrition 0.000 claims description 2
- 244000124853 Perilla frutescens Species 0.000 claims description 2
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- 238000005299 abrasion Methods 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 239000008168 almond oil Substances 0.000 claims description 2
- 239000010775 animal oil Substances 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical class [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 2
- 239000010426 asphalt Substances 0.000 claims description 2
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 229910052797 bismuth Inorganic materials 0.000 claims description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical class [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 150000001860 citric acid derivatives Chemical class 0.000 claims description 2
- 235000005687 corn oil Nutrition 0.000 claims description 2
- 239000002285 corn oil Substances 0.000 claims description 2
- 229910052593 corundum Inorganic materials 0.000 claims description 2
- 239000010431 corundum Substances 0.000 claims description 2
- 235000012343 cottonseed oil Nutrition 0.000 claims description 2
- 239000002385 cottonseed oil Substances 0.000 claims description 2
- ASJCSAKCMTWGAH-UHFFFAOYSA-N cyclopentane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCC1C(O)=O ASJCSAKCMTWGAH-UHFFFAOYSA-N 0.000 claims description 2
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 2
- MCQOWYALZVKMAR-UHFFFAOYSA-N furo[3,4-b]pyridine-5,7-dione Chemical compound C1=CC=C2C(=O)OC(=O)C2=N1 MCQOWYALZVKMAR-UHFFFAOYSA-N 0.000 claims description 2
- 229940074391 gallic acid Drugs 0.000 claims description 2
- 235000004515 gallic acid Nutrition 0.000 claims description 2
- 239000003365 glass fiber Substances 0.000 claims description 2
- 239000008169 grapeseed oil Substances 0.000 claims description 2
- 239000010468 hazelnut oil Substances 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 239000004021 humic acid Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- KHARCSTZAGNHOT-UHFFFAOYSA-N naphthalene-2,3-dicarboxylic acid Chemical compound C1=CC=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 KHARCSTZAGNHOT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004006 olive oil Substances 0.000 claims description 2
- 235000008390 olive oil Nutrition 0.000 claims description 2
- 239000012766 organic filler Substances 0.000 claims description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 claims description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 2
- 239000000312 peanut oil Substances 0.000 claims description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 2
- 150000003018 phosphorus compounds Chemical class 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 239000010453 quartz Substances 0.000 claims description 2
- 229960004889 salicylic acid Drugs 0.000 claims description 2
- 239000004576 sand Substances 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 2
- 239000008159 sesame oil Substances 0.000 claims description 2
- 235000011803 sesame oil Nutrition 0.000 claims description 2
- 239000011492 sheep wool Substances 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003784 tall oil Substances 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 150000003628 tricarboxylic acids Chemical class 0.000 claims description 2
- 239000002916 wood waste Substances 0.000 claims description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- 241001125046 Sardina pilchardus Species 0.000 claims 1
- 239000005862 Whey Substances 0.000 claims 1
- 102000007544 Whey Proteins Human genes 0.000 claims 1
- 108010046377 Whey Proteins Proteins 0.000 claims 1
- 239000010477 apricot oil Substances 0.000 claims 1
- 239000004020 conductor Substances 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- FQILZCAXBBSGEC-UHFFFAOYSA-N n-benzyl-n,2-dimethylaniline Chemical compound C=1C=CC=C(C)C=1N(C)CC1=CC=CC=C1 FQILZCAXBBSGEC-UHFFFAOYSA-N 0.000 claims 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 claims 1
- 239000003566 sealing material Substances 0.000 claims 1
- 238000005245 sintering Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
- 229910052760 oxygen Inorganic materials 0.000 description 10
- 239000001301 oxygen Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
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- 230000000977 initiatory effect Effects 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 3
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 2
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 2
- GVJRTUUUJYMTNQ-UHFFFAOYSA-N 2-(2,5-dioxofuran-3-yl)acetic acid Chemical group OC(=O)CC1=CC(=O)OC1=O GVJRTUUUJYMTNQ-UHFFFAOYSA-N 0.000 description 2
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 2
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 241001125048 Sardina Species 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- PIYNUZCGMLCXKJ-UHFFFAOYSA-N 1,4-dioxane-2,6-dione Chemical group O=C1COCC(=O)O1 PIYNUZCGMLCXKJ-UHFFFAOYSA-N 0.000 description 1
- CCFAKBRKTKVJPO-UHFFFAOYSA-N 1-anthroic acid Chemical compound C1=CC=C2C=C3C(C(=O)O)=CC=CC3=CC2=C1 CCFAKBRKTKVJPO-UHFFFAOYSA-N 0.000 description 1
- IHEDBVUTTQXGSJ-UHFFFAOYSA-M 2-[bis(2-oxidoethyl)amino]ethanolate;titanium(4+);hydroxide Chemical compound [OH-].[Ti+4].[O-]CCN(CC[O-])CC[O-] IHEDBVUTTQXGSJ-UHFFFAOYSA-M 0.000 description 1
- BOGVTNYNTGOONP-UHFFFAOYSA-N 3,4-dihydroxyoxolane-2,5-dione Chemical group OC1C(O)C(=O)OC1=O BOGVTNYNTGOONP-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical group CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical group C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- XUKLTPZEKXTPBT-UHFFFAOYSA-N 3-oxatricyclo[5.2.1.01,5]dec-5-ene-2,4-dione Chemical compound C1CC2C=C3C(=O)OC(=O)C13C2 XUKLTPZEKXTPBT-UHFFFAOYSA-N 0.000 description 1
- OXBPLZZVUNCKDI-UHFFFAOYSA-N 6-methyl-3-oxatricyclo[5.2.1.01,5]dec-5-ene-2,4-dione Chemical compound C1CC(C2)C(C)=C3C12C(=O)OC3=O OXBPLZZVUNCKDI-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
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- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
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- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
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- 241001553700 Euphorbia lathyris Species 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
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- 229910010082 LiAlH Inorganic materials 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 239000010428 baryte Substances 0.000 description 1
- 229910052601 baryte Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000006352 cycloaddition reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 description 1
- YGANSGVIUGARFR-UHFFFAOYSA-N dipotassium dioxosilane oxo(oxoalumanyloxy)alumane oxygen(2-) Chemical compound [O--].[K+].[K+].O=[Si]=O.O=[Al]O[Al]=O YGANSGVIUGARFR-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical group O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 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 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- MUTGBJKUEZFXGO-UHFFFAOYSA-N hexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21 MUTGBJKUEZFXGO-UHFFFAOYSA-N 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
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- 150000007517 lewis acids Chemical class 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
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- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000011049 pearl Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
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- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B26/00—Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
- C04B26/02—Macromolecular compounds
- C04B26/10—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B26/18—Polyesters; Polycarbonates
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/34—Epoxy compounds containing three or more epoxy groups obtained by epoxidation of an unsaturated polymer
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/027—Polycondensates containing more than one epoxy group per molecule obtained by epoxidation of unsaturated precursor, e.g. polymer or monomer
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
-
- 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
- C08L63/08—Epoxidised polymerised polyenes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/04—Non-macromolecular organic compounds
- C09K2200/0441—Carboxylic acids, salts, anhydrides or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/04—Non-macromolecular organic compounds
- C09K2200/0447—Fats, fatty oils, higher fatty acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
- C09K2200/0645—Macromolecular organic compounds, e.g. prepolymers obtained otherwise than by reactions involving carbon-to-carbon unsaturated bonds
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19524514 | 1995-07-05 | ||
| PCT/DE1996/001243 WO1997002307A1 (de) | 1995-07-05 | 1996-07-05 | Polymerwerkstoff, verfahren zu seiner herstellung und dessen verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK1598A3 true SK1598A3 (en) | 1998-09-09 |
Family
ID=7766089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK15-98A SK1598A3 (en) | 1995-07-05 | 1996-07-05 | Polymer material, process for its production and use thereof |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP0836627B2 (ko) |
| JP (1) | JP2000501119A (ko) |
| KR (1) | KR19990028734A (ko) |
| CN (1) | CN1103791C (ko) |
| AT (1) | ATE207092T1 (ko) |
| AU (1) | AU713023B2 (ko) |
| BG (1) | BG63603B1 (ko) |
| BR (1) | BR9609342A (ko) |
| CA (1) | CA2224714A1 (ko) |
| CZ (1) | CZ417797A3 (ko) |
| DE (2) | DE59607956D1 (ko) |
| DK (1) | DK0836627T3 (ko) |
| EA (1) | EA000565B1 (ko) |
| ES (1) | ES2165508T5 (ko) |
| HU (1) | HUP9802994A3 (ko) |
| MX (1) | MX9800135A (ko) |
| NZ (1) | NZ312082A (ko) |
| PL (1) | PL324348A1 (ko) |
| PT (1) | PT836627E (ko) |
| SI (1) | SI9620102A (ko) |
| SK (1) | SK1598A3 (ko) |
| TR (1) | TR199701758T1 (ko) |
| UA (1) | UA49837C2 (ko) |
| WO (1) | WO1997002307A1 (ko) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19834048A1 (de) * | 1998-07-30 | 2000-02-03 | Cognis Deutschland Gmbh | Verbundwerkstoffe auf der Basis nachwachsender Rohstoffe |
| DE19952364A1 (de) * | 1999-10-30 | 2001-07-19 | Cognis Deutschland Gmbh | Lagerstabile Prepregs auf Basis duroplastischer, oleochemischer Matrices |
| EP1178065A1 (en) * | 2000-08-03 | 2002-02-06 | DLW Aktiengesellschaft | Composition based on renewable raw materials |
| US6946541B2 (en) | 2000-05-24 | 2005-09-20 | Dlw Aktiengesellschaft | Composition based on renewable raw materials |
| DE10038034C2 (de) * | 2000-08-03 | 2003-07-17 | Moeller Plast Gmbh | Verfahren zur mechanischen Stabilisierung von Schäben |
| DE10132749A1 (de) * | 2001-07-03 | 2003-01-30 | Fraunhofer Ges Forschung | Faserverstärkter Werkstoff auf der Basis duroplastischer Polymere |
| DE10148672A1 (de) * | 2001-10-02 | 2003-04-24 | Cognis Deutschland Gmbh | Polyester |
| DE10237694A1 (de) * | 2002-08-15 | 2004-03-04 | Sai Automotive Sal Gmbh | Verfahren sowie Vorrichtung zum Herstellen von Formteilen |
| KR100540796B1 (ko) * | 2002-12-09 | 2006-01-11 | 학교법인 건국대학교 | 글리세롤과 지방산을 이용한 폴리우레탄-아마이드 접착제 |
| DE102006003762A1 (de) * | 2006-01-25 | 2007-07-26 | Dracowo Forschungs- Und Entwicklungs Gmbh | Leinölepoxid-basierte Faserverbundwerkstoffe |
| ITTV20060092A1 (it) | 2006-05-31 | 2007-12-01 | Luca Toncelli | Procedimento per la fabbricazione di manufatti in conglomerato di granulato di materiale lapideo e resina poliestere in forma di lastre o blocchi. |
| EP1884531A1 (en) * | 2006-07-30 | 2008-02-06 | Lonza Compounds GmbH & Co. KG | Sheet molding compounds (smc) comprising thermosetting resins based on renewable resources |
| 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 |
| WO2008120722A1 (ja) * | 2007-03-30 | 2008-10-09 | Toray Industries, Inc. | 重合体およびそれを含むフィルムまたはシート |
| DE102008063442B4 (de) * | 2008-12-31 | 2011-12-29 | Peter Klenert | Verfahren zur Herstellung von Polymerwerkstoffen |
| JP5322220B2 (ja) * | 2009-03-11 | 2013-10-23 | 中部電力株式会社 | 絶縁性高分子材料組成物 |
| BRPI0923991A2 (pt) | 2009-03-18 | 2018-05-29 | Cosentino, S.A. | painel ou laje de pedra artificial particularmente apropriado para uso interno e método de fabricação de painéis ou lajes de pedra artificiais |
| JP5366208B2 (ja) * | 2009-09-16 | 2013-12-11 | 中部電力株式会社 | 絶縁性高分子材料組成物及びその製造方法 |
| JP5547456B2 (ja) * | 2009-11-10 | 2014-07-16 | スリーエム イノベイティブ プロパティズ カンパニー | 一液型エポキシ樹脂組成物及びそれを用いた接着方法 |
| DE102011001539A1 (de) * | 2011-03-24 | 2012-09-27 | Meyer Rohr + Schacht Gmbh | Verbundwerkstoff |
| ITMI20110797A1 (it) * | 2011-05-10 | 2012-11-11 | Polynt S P A | Miscela indurente a bassa temperatura per resine epossidiche. |
| CN102352089B (zh) * | 2011-07-01 | 2013-03-20 | 中航复合材料有限责任公司 | 一种植物纤维增强生物质树脂薄层材料及其制备方法 |
| EP2755332B1 (en) | 2011-09-09 | 2017-04-26 | Sumitomo Electric Industries, Ltd. | Power supply system and connector |
| ITTV20110125A1 (it) * | 2011-09-20 | 2013-03-21 | Luca Toncelli | Processo per la preparazione di manufatti in conglomerato di granulato di materiale lapideo e resina con anidridi di origine terpenica |
| US8754152B2 (en) | 2011-10-21 | 2014-06-17 | King Abdulaziz City For Science And Technology | Efficient polymer composites based on natural wool |
| WO2014062625A1 (en) | 2012-10-15 | 2014-04-24 | Iowa State University Research Foundation, Inc. | Tackifier compounds and methods of using the same |
| KR101401097B1 (ko) * | 2013-02-25 | 2014-05-28 | 주식회사 웰데코 | 다기능 보호필름의 제조방법 |
| DE202013104133U1 (de) | 2013-09-11 | 2013-10-15 | Michael Sorge | Polymerwerkstoff auf Basis nachwachsender Rohstoffe |
| US10077257B2 (en) | 2015-04-06 | 2018-09-18 | Iowa State University Research Foundation, Inc. | Aziridinated triglycerides and polymers formed therefrom |
| US11760836B2 (en) | 2018-04-21 | 2023-09-19 | Natural Fiber Welding, Inc. | Curative |
| US10882951B2 (en) | 2018-04-21 | 2021-01-05 | Natural Fiber Welding, Inc. | Curative and method |
| KR102538880B1 (ko) * | 2018-04-21 | 2023-06-05 | 네추럴 파이버 웰딩 인코포레이티드 | 경화제 |
| JP7404086B2 (ja) * | 2020-01-31 | 2023-12-25 | サカタインクス株式会社 | ポリエステル樹脂、オフセット印刷用インキ組成物、印刷物、および印刷物の製造方法 |
| US20220235195A1 (en) * | 2021-01-28 | 2022-07-28 | The Goodyear Tire & Rubber Company | Fatty acid-modified vegetable oils in rubber compositions and tires |
| US11667775B2 (en) * | 2021-01-28 | 2023-06-06 | The Goodyear Tire & Rubber Company | Resin-modified vegetable oils in rubber compositions and tires |
| WO2024069417A1 (en) * | 2022-09-26 | 2024-04-04 | Fondazione Istituto Italiano Di Tecnologia | Method for constructing a covering of a substrate and composite material comprising that covering |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD48687A (ko) † | ||||
| DD51985A (ko) * | ||||
| US2935492A (en) * | 1956-04-30 | 1960-05-03 | Shell Oil Co | Process for curing material having internal epoxy groups and resulting products |
| CH486755A (de) * | 1965-11-09 | 1970-02-28 | Liebknecht Transformat | Verfahren zur Erhöhung der Kriechstromfestigkeit von Oberflächen elektrischer Isolierteile |
| US3507814A (en) * | 1967-01-13 | 1970-04-21 | Gen Tire & Rubber Co | Multifunctional aziridino compounds,polymeric products thereof and production processes |
| FR1548423A (ko) * | 1967-09-05 | 1968-12-06 | ||
| DE3246615A1 (de) * | 1982-12-16 | 1984-06-20 | Henkel KGaA, 4000 Düsseldorf | Alkydharze, enthaltend funktionelle epoxide |
| SU1696450A1 (ru) * | 1989-07-11 | 1991-12-07 | Предприятие П/Я А-1120 | Герметизирующий компаунд |
| JPH04501284A (ja) * | 1989-08-09 | 1992-03-05 | バッテレーインスティツウト エ．ファウ． | 原料油脂からプラスチックを製造する方法 |
| US5151485A (en) * | 1990-11-21 | 1992-09-29 | The Dow Chemical Company | Advanced epoxy compositions, curable compositions and cured products |
-
1996
- 1996-07-05 EA EA199800004A patent/EA000565B1/ru not_active IP Right Cessation
- 1996-07-05 HU HU9802994A patent/HUP9802994A3/hu unknown
- 1996-07-05 ES ES96922761T patent/ES2165508T5/es not_active Expired - Lifetime
- 1996-07-05 PL PL96324348A patent/PL324348A1/xx unknown
- 1996-07-05 DE DE59607956T patent/DE59607956D1/de not_active Expired - Lifetime
- 1996-07-05 CZ CZ974177A patent/CZ417797A3/cs unknown
- 1996-07-05 EP EP96922761A patent/EP0836627B2/de not_active Expired - Lifetime
- 1996-07-05 SI SI9620102A patent/SI9620102A/sl unknown
- 1996-07-05 CN CN96196748A patent/CN1103791C/zh not_active Expired - Fee Related
- 1996-07-05 AT AT96922761T patent/ATE207092T1/de not_active IP Right Cessation
- 1996-07-05 JP JP9504723A patent/JP2000501119A/ja active Pending
- 1996-07-05 AU AU63530/96A patent/AU713023B2/en not_active Ceased
- 1996-07-05 UA UA97126299A patent/UA49837C2/uk unknown
- 1996-07-05 TR TR97/01758T patent/TR199701758T1/xx unknown
- 1996-07-05 DE DE19627165A patent/DE19627165C2/de not_active Expired - Fee Related
- 1996-07-05 NZ NZ312082A patent/NZ312082A/xx unknown
- 1996-07-05 DK DK96922761T patent/DK0836627T3/da active
- 1996-07-05 KR KR1019980700032A patent/KR19990028734A/ko not_active Application Discontinuation
- 1996-07-05 PT PT96922761T patent/PT836627E/pt unknown
- 1996-07-05 BR BR9609342-0A patent/BR9609342A/pt unknown
- 1996-07-05 SK SK15-98A patent/SK1598A3/sk unknown
- 1996-07-05 WO PCT/DE1996/001243 patent/WO1997002307A1/de not_active Application Discontinuation
- 1996-07-05 CA CA002224714A patent/CA2224714A1/en not_active Abandoned
-
1997
- 1997-12-29 BG BG102153A patent/BG63603B1/bg unknown
-
1998
- 1998-01-07 MX MX9800135A patent/MX9800135A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2165508T5 (es) | 2005-12-01 |
| MX9800135A (es) | 1998-11-29 |
| UA49837C2 (uk) | 2002-10-15 |
| EA199800004A1 (ru) | 1998-08-27 |
| CN1195357A (zh) | 1998-10-07 |
| PL324348A1 (en) | 1998-05-25 |
| KR19990028734A (ko) | 1999-04-15 |
| DK0836627T3 (da) | 2001-11-19 |
| ATE207092T1 (de) | 2001-11-15 |
| CA2224714A1 (en) | 1997-01-23 |
| BR9609342A (pt) | 2002-04-30 |
| JP2000501119A (ja) | 2000-02-02 |
| EA000565B1 (ru) | 1999-12-29 |
| EP0836627A1 (de) | 1998-04-22 |
| CN1103791C (zh) | 2003-03-26 |
| DE19627165C2 (de) | 1999-02-25 |
| DE19627165A1 (de) | 1997-01-09 |
| SI9620102A (sl) | 1998-10-31 |
| EP0836627B2 (de) | 2005-06-01 |
| ES2165508T3 (es) | 2002-03-16 |
| PT836627E (pt) | 2002-02-28 |
| AU713023B2 (en) | 1999-11-18 |
| TR199701758T1 (xx) | 1998-03-21 |
| BG102153A (en) | 1998-08-31 |
| HUP9802994A3 (en) | 2000-04-28 |
| NZ312082A (en) | 2000-04-28 |
| CZ417797A3 (cs) | 1998-05-13 |
| HUP9802994A2 (hu) | 1999-04-28 |
| WO1997002307A1 (de) | 1997-01-23 |
| EP0836627B1 (de) | 2001-10-17 |
| AU6353096A (en) | 1997-02-05 |
| DE59607956D1 (de) | 2001-11-22 |
| BG63603B1 (bg) | 2002-06-28 |
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