SK1598A3 - Polymer material, process for its production and use thereof - Google Patents

Polymer material, process for its production and use thereof Download PDF

Info

Publication number: SK1598A3
Authority: SK; Slovakia
Prior art keywords: oil; acid; anhydride; weight; polycarboxylic
Prior art date: 1995-07-05

Application number

SK15-98A

Other languages

English (en)

Slovak (sk)

Inventor

Uwe Schonfeld

Original Assignee

Preform Gmbh

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.)

1995-07-05

Filing date

1996-07-05

Publication date

1998-09-09

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7766089&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK1598(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-07-05 Application filed by Preform Gmbh filed Critical Preform Gmbh

1998-09-09 Publication of SK1598A3 publication Critical patent/SK1598A3/sk

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
239000002657 fibrous material Substances 0.000 description 3
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
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
235000005979 Citrus limon Nutrition 0.000 description 1
244000131522 Citrus pyriformis Species 0.000 description 1
240000000491 Corchorus aestuans Species 0.000 description 1
235000011777 Corchorus aestuans Nutrition 0.000 description 1
235000010862 Corchorus capsularis Nutrition 0.000 description 1
229930185597 Euphorbia lathyris Natural products 0.000 description 1
241001553700 Euphorbia lathyris Species 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
239000002879 Lewis base Substances 0.000 description 1
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
239000003822 epoxy resin Substances 0.000 description 1
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
239000004615 ingredient Substances 0.000 description 1
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
229910052627 muscovite Inorganic materials 0.000 description 1
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
239000001944 prunus armeniaca kernel oil Substances 0.000 description 1
238000004064 recycling Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000007017 scission Effects 0.000 description 1
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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Ceramic Engineering (AREA)
Materials Engineering (AREA)
Structural Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Epoxy Resins (AREA)
Polyesters Or Polycarbonates (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Graft Or Block Polymers (AREA)
Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Extrusion Moulding Of Plastics Or The Like (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Paints Or Removers (AREA)

SK15-98A 1995-07-05 1996-07-05 Polymer material, process for its production and use thereof SK1598A3 (en)

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 (2)

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
SK244-99U SK2738U (sk)	1995-07-05	1996-07-05	Polymérny materiál a jeho použitie

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SK244-99U SK2738U (sk)	1995-07-05	1996-07-05	Polymérny materiál a jeho použitie

Country Status (24)

Country	Link
EP (1)	EP0836627B2 (da)
JP (1)	JP2000501119A (da)
KR (1)	KR19990028734A (da)
CN (1)	CN1103791C (da)
AT (1)	ATE207092T1 (da)
AU (1)	AU713023B2 (da)
BG (1)	BG63603B1 (da)
BR (1)	BR9609342A (da)
CA (1)	CA2224714A1 (da)
CZ (1)	CZ417797A3 (da)
DE (2)	DE19627165C2 (da)
DK (1)	DK0836627T3 (da)
EA (1)	EA000565B1 (da)
ES (1)	ES2165508T5 (da)
HU (1)	HUP9802994A3 (da)
MX (1)	MX9800135A (da)
NZ (1)	NZ312082A (da)
PL (1)	PL324348A1 (da)
PT (1)	PT836627E (da)
SI (1)	SI9620102A (da)
SK (2)	SK1598A3 (da)
TR (1)	TR199701758T1 (da)
UA (1)	UA49837C2 (da)
WO (1)	WO1997002307A1 (da)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
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
DE60116638T9 (de) *	2000-05-24	2012-01-12	Armstrong Dlw Ag	Auf erneuerbaren Rohmaterialien basierende Zusammensetzung
EP1178065A1 (en) *	2000-08-03	2002-02-06	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
US8058361B2 (en) *	2007-03-30	2011-11-15	Toray Industries, Inc.	Polymer and a film or sheet containing the same
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
DE102011001539B4 (de) *	2011-03-24	2026-02-12	meyer-POLYCRETE GmbH	Polymerbeton und Verfahren zur Herstellung von Polymerbeton
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
CN103797721B (zh)	2011-09-09	2015-11-25	住友电气工业株式会社	供电系统和连接器
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
US9556293B2 (en)	2012-10-15	2017-01-31	Iowa State University Research Foundation, Inc.	Polyisocyanates from fused bicyclic polyols and polyurethanes therefrom
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
US11396578B2 (en)	2018-04-21	2022-07-26	Natural Fiber Wielding, Inc.	Curative
KR102538880B1 (ko) *	2018-04-21	2023-06-05	네추럴 파이버 웰딩 인코포레이티드	경화제
US12247098B2 (en)	2018-04-21	2025-03-11	Natural Fiber Welding, Inc.	Curative
US10882951B2 (en)	2018-04-21	2021-01-05	Natural Fiber Welding, Inc.	Curative and method
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
US11987690B2 (en) *	2021-01-28	2024-05-21	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
EP4594389A1 (en) *	2022-09-26	2025-08-06	Fondazione Istituto Italiano di Tecnologia	Method for constructing a covering of a substrate and composite material comprising that covering
CN117428882A (zh) *	2023-10-16	2024-01-23	德华兔宝宝装饰新材股份有限公司	一种复合阻燃地板的制备工艺

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DD51985A (da) *
DD48687A (da) †
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 (da) *	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
CA2038936A1 (en) *	1989-08-09	1991-02-10	Rainer Frische	Method of producing plastics from crude fats and oils
US5151485A (en) *	1990-11-21	1992-09-29	The Dow Chemical Company	Advanced epoxy compositions, curable compositions and cured products

1996
- 1996-07-05 BR BR9609342-0A patent/BR9609342A/pt unknown
- 1996-07-05 ES ES96922761T patent/ES2165508T5/es not_active Expired - Lifetime
- 1996-07-05 DK DK96922761T patent/DK0836627T3/da active
- 1996-07-05 SK SK15-98A patent/SK1598A3/sk unknown
- 1996-07-05 PL PL96324348A patent/PL324348A1/xx unknown
- 1996-07-05 EP EP96922761A patent/EP0836627B2/de not_active Expired - Lifetime
- 1996-07-05 DE DE19627165A patent/DE19627165C2/de not_active Expired - Fee Related
- 1996-07-05 CZ CZ974177A patent/CZ417797A3/cs unknown
- 1996-07-05 SI SI9620102A patent/SI9620102A/sl unknown
- 1996-07-05 PT PT96922761T patent/PT836627E/pt unknown
- 1996-07-05 KR KR1019980700032A patent/KR19990028734A/ko not_active Ceased
- 1996-07-05 CN CN96196748A patent/CN1103791C/zh not_active Expired - Fee Related
- 1996-07-05 TR TR97/01758T patent/TR199701758T1/xx unknown
- 1996-07-05 SK SK244-99U patent/SK2738U/sk unknown
- 1996-07-05 CA CA002224714A patent/CA2224714A1/en not_active Abandoned
- 1996-07-05 WO PCT/DE1996/001243 patent/WO1997002307A1/de not_active Ceased
- 1996-07-05 DE DE59607956T patent/DE59607956D1/de not_active Expired - Lifetime
- 1996-07-05 UA UA97126299A patent/UA49837C2/uk unknown
- 1996-07-05 HU HU9802994A patent/HUP9802994A3/hu unknown
- 1996-07-05 AU AU63530/96A patent/AU713023B2/en not_active Ceased
- 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 EA EA199800004A patent/EA000565B1/ru not_active IP Right Cessation
- 1996-07-05 NZ NZ312082A patent/NZ312082A/xx unknown
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
MX9800135A (es)	1998-11-29
SK2738U (sk)	2001-01-18
ES2165508T5 (es)	2005-12-01
SI9620102A (sl)	1998-10-31
DE59607956D1 (de)	2001-11-22
EP0836627B1 (de)	2001-10-17
KR19990028734A (ko)	1999-04-15
CN1195357A (zh)	1998-10-07
UA49837C2 (uk)	2002-10-15
ES2165508T3 (es)	2002-03-16
BR9609342A (pt)	2002-04-30
EA000565B1 (ru)	1999-12-29
ATE207092T1 (de)	2001-11-15
BG63603B1 (bg)	2002-06-28
WO1997002307A1 (de)	1997-01-23
AU713023B2 (en)	1999-11-18
HUP9802994A3 (en)	2000-04-28
DE19627165C2 (de)	1999-02-25
PT836627E (pt)	2002-02-28
CN1103791C (zh)	2003-03-26
EP0836627B2 (de)	2005-06-01
BG102153A (en)	1998-08-31
HUP9802994A2 (hu)	1999-04-28
DK0836627T3 (da)	2001-11-19
CZ417797A3 (cs)	1998-05-13
AU6353096A (en)	1997-02-05
PL324348A1 (en)	1998-05-25
TR199701758T1 (xx)	1998-03-21
NZ312082A (en)	2000-04-28
EP0836627A1 (de)	1998-04-22
EA199800004A1 (ru)	1998-08-27
CA2224714A1 (en)	1997-01-23
DE19627165A1 (de)	1997-01-09
JP2000501119A (ja)	2000-02-02

Publication	Publication Date	Title
CZ417797A3 (cs)	1998-05-13	Polymerní materiál, způsob jeho přípravy a použití
DE2512170C3 (de)	1981-06-11	Verfahren zur Herstellung von gegebenenfalls schaumförmigem, harten anorganisch-organischem Verbundmaterial
DE2536319B2 (de)	1978-02-09	Haertbare masse und verfahren zu deren haertung
DE2325090A1 (de)	1974-11-28	Anorganisch-organische kunststoffe
WO2001002469A1 (de)	2001-01-11	Verfahren zur herstellung von faserverbundwerkstoffen
EP0644861B1 (de)	1997-10-01	Dämmstoff auf basis von altrohstoffen und faserigen rohstoffen sowie verfahren zu dessen herstellung
US20010023276A1 (en)	2001-09-20	Polymeric material, method for its manufacture, and its utilization
WO2000006632A1 (de)	2000-02-10	Verbundwerkstoffe auf der basis nachwachsender rohstoffe
EP0160270B1 (de)	1989-03-15	Verfahren zum Herstellen von Formteilen durch Verpressen von faserigem Material unter gleichzeitiger Verklebung
RU2126808C1 (ru)	1999-02-27	Эпоксидная композиция для покрытия полов
WO2022073078A1 (en)	2022-04-14	Composite products comprising coffee grounds and the manufacture thereof
HRP970014A2 (en)	1999-04-30	Polymer material, process for its production and the use thereof
DE2351820A1 (de)	1975-04-17	Isolierende klebe-, dichtungs- und spachtelmassen
JPS59138214A (ja)	1984-08-08	発泡性防火組成物およびそれから製造された構造要素
EP0374522B1 (en)	1995-01-25	Binding compositions for fire-retarded ligno-cellulosic composites and process for preparing them
HK1014969A (en)	1999-10-08	Polymer material, process for its production and use thereof
DE2314515A1 (de)	1974-10-03	Schmelzmassen
KR0128130B1 (ko)	1998-04-16	접착성 및 제진성이 우수한 복합형 제진재료 제조방법
CA2306577A1 (en)	2000-10-26	Composite molding compound additive
JPH02127043A (ja)	1990-05-15	特殊繊維シート材料
EA007980B1 (ru)	2007-02-27	Экологически чистая водостойкая древесно-минерально-полимерная композиция
EP1854836A1 (de)	2007-11-14	Verfahren zum Umwandlung von umweltschädlichen und/oder gesundheitschädigenden Reststoffen in Formkörper für die Verwendung im Baubereich
WO2004048288A1 (de)	2004-06-10	Verfahren zur herstellung eines formkörpers aus einem hydratisierbaren mineralischem werkstoff und einem füllstoff
KR20060020374A (ko)	2006-03-06	석분을 함유하는 접착용 에폭시 수지 조성물 및 이의 제조방법
PL162053B1 (pl)	1993-08-31	Sposób wytwarzania lekkich, trudno palnych kompozytów polimerowych