SI9620102A - Polimerni material, postopek za njegovo proizvodnjo in njegova uporaba - Google Patents

Polimerni material, postopek za njegovo proizvodnjo in njegova uporaba Download PDF

Info

Publication number: SI9620102A
Authority: SI; Slovenia
Prior art keywords: oil; acid; acids; anhydride; weight
Prior art date: 1995-07-05

Application number

SI9620102A

Other languages

English (en)

Slovenian (sl)

Inventor

Uwe Schoenfeld

Original Assignee

Preform Raumgliederungssysteme 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

1998-10-31

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=SI9620102(A) "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 Raumgliederungssysteme Gmbh filed Critical Preform Raumgliederungssysteme Gmbh

1998-10-31 Publication of SI9620102A publication Critical patent/SI9620102A/sl

Links

238000000034 method Methods 0.000 title claims description 9
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239000002861 polymer material Substances 0.000 title abstract description 3
238000004519 manufacturing process Methods 0.000 title description 5
239000002253 acid Substances 0.000 claims abstract description 52
150000008065 acid anhydrides Chemical class 0.000 claims abstract description 30
239000007795 chemical reaction product Substances 0.000 claims abstract description 15
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 10
239000004593 Epoxy Substances 0.000 claims abstract description 6
239000002994 raw material Substances 0.000 claims abstract description 6
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239000000463 material Substances 0.000 claims description 58
239000000203 mixture Substances 0.000 claims description 40
239000003921 oil Substances 0.000 claims description 30
235000019198 oils Nutrition 0.000 claims description 30
150000007513 acids Chemical class 0.000 claims description 26
150000003626 triacylglycerols Chemical class 0.000 claims description 20
239000000835 fiber Substances 0.000 claims description 16
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239000000945 filler Substances 0.000 claims description 13
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
150000008064 anhydrides Chemical class 0.000 claims description 8
239000003054 catalyst Substances 0.000 claims description 8
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238000004132 cross linking Methods 0.000 claims description 8
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ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 5
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 4
QDPOOGQUCJJZAO-FCXRPNKRSA-N [(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate Chemical compound C1=C(O)C(O)=CC=C1\C=C\C(=O)OC(=O)\C=C\C1=CC=C(O)C(O)=C1 QDPOOGQUCJJZAO-FCXRPNKRSA-N 0.000 claims description 4
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YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 4
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JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 3
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239000003999 initiator Substances 0.000 claims description 3
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150000004760 silicates Chemical class 0.000 claims description 3
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239000010902 straw Substances 0.000 claims description 3
239000002383 tung oil Substances 0.000 claims description 3
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
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240000006240 Linum usitatissimum Species 0.000 claims description 2
235000004431 Linum usitatissimum Nutrition 0.000 claims description 2
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229920002230 Pectic acid Polymers 0.000 claims description 2
238000005299 abrasion Methods 0.000 claims description 2
150000001298 alcohols Chemical class 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 compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 2
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125000002619 bicyclic group Chemical group 0.000 claims description 2
239000012267 brine Substances 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
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238000006356 dehydrogenation reaction Methods 0.000 claims description 2
239000011094 fiberboard Substances 0.000 claims description 2
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229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
239000010468 hazelnut oil Substances 0.000 claims description 2
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239000004310 lactic acid Substances 0.000 claims description 2
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
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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
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239000003760 tallow Substances 0.000 claims description 2
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
229930185597 Euphorbia lathyris Natural products 0.000 description 1
241001553700 Euphorbia lathyris Species 0.000 description 1
WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
239000002879 Lewis base Substances 0.000 description 1
229910010082 LiAlH Inorganic materials 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
FSQUGILNTZXNCQ-UHFFFAOYSA-N N12CCC(CC1)CC2.C(C(C)C)O Chemical compound N12CCC(CC1)CC2.C(C(C)C)O FSQUGILNTZXNCQ-UHFFFAOYSA-N 0.000 description 1
LLUSUBJQCNHDSP-UHFFFAOYSA-N N12CCC(CC1)CC2.C(C)(C)O Chemical compound N12CCC(CC1)CC2.C(C)(C)O LLUSUBJQCNHDSP-UHFFFAOYSA-N 0.000 description 1
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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
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238000010521 absorption reaction Methods 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
150000001447 alkali salts Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000001541 aziridines Chemical class 0.000 description 1
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229910052601 baryte Inorganic materials 0.000 description 1
239000010428 baryte Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
RTSGJTANVBJFFJ-UHFFFAOYSA-N benzo[d][2]benzoxepine-5,7-dione Chemical compound O=C1OC(=O)C2=CC=CC=C2C2=CC=CC=C12 RTSGJTANVBJFFJ-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229910052797 bismuth Inorganic materials 0.000 description 1
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
230000008859 change Effects 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
238000005253 cladding Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
238000006352 cycloaddition reaction Methods 0.000 description 1
230000007547 defect Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000013461 design Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 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
238000004090 dissolution Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
QJWQYOHBMUQHGZ-UHFFFAOYSA-N ethanol;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound CCO.OC(=O)CC(O)(C(O)=O)CC(O)=O QJWQYOHBMUQHGZ-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000011152 fibreglass Substances 0.000 description 1
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
229940074391 gallic acid Drugs 0.000 description 1
235000004515 gallic acid Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
235000013922 glutamic acid Nutrition 0.000 description 1
239000004220 glutamic acid Substances 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
238000005098 hot rolling Methods 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910052738 indium Inorganic materials 0.000 description 1
APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
229910052909 inorganic silicate Inorganic materials 0.000 description 1
238000009434 installation Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000007527 lewis bases Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910003002 lithium salt Inorganic materials 0.000 description 1
159000000002 lithium salts Chemical class 0.000 description 1
238000011068 loading method Methods 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
BYVCTYDTPSKPRM-UHFFFAOYSA-N naphthalene-1-carbonyl naphthalene-1-carboxylate Chemical compound C1=CC=C2C(C(OC(=O)C=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 BYVCTYDTPSKPRM-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
230000037361 pathway Effects 0.000 description 1
229920001568 phenolic resin Polymers 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
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
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235000018102 proteins Nutrition 0.000 description 1
238000004064 recycling Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
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238000009416 shuttering Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000012360 testing method 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
230000009466 transformation Effects 0.000 description 1
FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 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
229920006337 unsaturated polyester resin Polymers 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
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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)

SI9620102A 1995-07-05 1996-07-05 Polimerni material, postopek za njegovo proizvodnjo in njegova uporaba SI9620102A (sl)

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
SI9620102A true SI9620102A (sl)	1998-10-31

Family

ID=7766089

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SI9620102A SI9620102A (sl)	1995-07-05	1996-07-05	Polimerni material, postopek za njegovo proizvodnjo in njegova uporaba

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
DE59607956D1 (de)	2001-11-22
EP0836627B1 (de)	2001-10-17
SK1598A3 (en)	1998-09-09
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

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DE2536319B2 (de)	1978-02-09	Haertbare masse und verfahren zu deren haertung
DE2512170A1 (de)	1976-09-23	Verfahren zur herstellung von anorganisch-organischen kunststoffen
DE2359611A1 (de)	1975-06-05	Verbundstoffe
WO2007050000A1 (en)	2007-05-03	Fire-resistant composition for coating, sealing and protection purposes
US20010023276A1 (en)	2001-09-20	Polymeric material, method for its manufacture, and its utilization
UA128796C2 (uk)	2024-10-23	Ізоляційний матеріал та спосіб його виробництва
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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
RU2521582C1 (ru)	2014-06-27	Состав для получения покрытий
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AT228113B (da)	1963-06-25
EP2246492A2 (de)	2010-11-03	Beschichtung von Befestigungselementen
DE102018115893A1 (de)	2019-01-17	Flamm- und/oder Brandschutzmittel und dessen Herstellung und Verwendung, für Anstrichmittel und darauf basierte Produkte sowie deren Vor- und Zwischenprodukte
HK1014969A (en)	1999-10-08	Polymer material, process for its production and use thereof
SU1544745A1 (ru)	1990-02-23	Полимерминеральна смесь
WO2009000323A1 (en)	2008-12-31	An adhesive composition comprising a polyol base part and an isocyanate hardener and the use thereof