CN1283742C - 多组分包和组合物以及其应用和所得的塑胶 - Google Patents
多组分包和组合物以及其应用和所得的塑胶 Download PDFInfo
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- CN1283742C CN1283742C CNB028076524A CN02807652A CN1283742C CN 1283742 C CN1283742 C CN 1283742C CN B028076524 A CNB028076524 A CN B028076524A CN 02807652 A CN02807652 A CN 02807652A CN 1283742 C CN1283742 C CN 1283742C
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- MILSYCKGLDDVLM-UHFFFAOYSA-N 2-phenylpropan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)C1=CC=CC=C1 MILSYCKGLDDVLM-UHFFFAOYSA-N 0.000 description 1
- WZHHYIOUKQNLQM-UHFFFAOYSA-N 3,4,5,6-tetrachlorophthalic acid Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O WZHHYIOUKQNLQM-UHFFFAOYSA-N 0.000 description 1
- FFWNCSWLUYKKKA-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1.NC1=CC=CC(O)=C1 FFWNCSWLUYKKKA-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- QOJBDGDYUVKQDS-UHFFFAOYSA-N 4-(3-piperazin-1-ylthiomorpholin-4-yl)morpholine Chemical compound N1(CCNCC1)C1N(CCSC1)N1CCOCC1 QOJBDGDYUVKQDS-UHFFFAOYSA-N 0.000 description 1
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 1
- DUJMVKJJUANUMQ-UHFFFAOYSA-N 4-methylpentanenitrile Chemical compound CC(C)CCC#N DUJMVKJJUANUMQ-UHFFFAOYSA-N 0.000 description 1
- YVPZFPKENDZQEJ-UHFFFAOYSA-N 4-propylcyclohexan-1-ol Chemical compound CCCC1CCC(O)CC1 YVPZFPKENDZQEJ-UHFFFAOYSA-N 0.000 description 1
- VNFYMAPAENTMMO-UHFFFAOYSA-N 5-chloro-2-methylquinoline Chemical compound ClC1=CC=CC2=NC(C)=CC=C21 VNFYMAPAENTMMO-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 1
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 1
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- KGWDUNBJIMUFAP-KVVVOXFISA-N Ethanolamine Oleate Chemical compound NCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KGWDUNBJIMUFAP-KVVVOXFISA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
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- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
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- DOFHXXBIPRPYSZ-UHFFFAOYSA-N [cyclohexyl(isocyanato)methyl]cyclohexane Chemical class C1CCCCC1C(N=C=O)C1CCCCC1 DOFHXXBIPRPYSZ-UHFFFAOYSA-N 0.000 description 1
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000003975 dentin desensitizing agent Substances 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
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- 239000010433 feldspar Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
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- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000003454 indenyl group Chemical class C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
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- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
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- SYWIXHZXHQDFOO-UHFFFAOYSA-N methyl n-phenyliminocarbamate Chemical compound COC(=O)N=NC1=CC=CC=C1 SYWIXHZXHQDFOO-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
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- YQYUUNRAPYPAPC-UHFFFAOYSA-N n,n-diethyl-2-methylaniline Chemical compound CCN(CC)C1=CC=CC=C1C YQYUUNRAPYPAPC-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- 150000002894 organic compounds Chemical class 0.000 description 1
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- 238000007254 oxidation reaction Methods 0.000 description 1
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- 239000012188 paraffin wax Substances 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
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- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
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- 150000008117 polysulfides Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000003469 silicate cement Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
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- PYHOFAHZHOBVGV-UHFFFAOYSA-N triazane Chemical compound NNN PYHOFAHZHOBVGV-UHFFFAOYSA-N 0.000 description 1
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- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 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
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/06—Inhibiting the setting, e.g. mortars of the deferred action type containing water in breakable containers ; Inhibiting the action of active ingredients
- C04B40/0641—Mechanical separation of ingredients, e.g. accelerator in breakable microcapsules
- C04B40/065—Two or more component mortars
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
- C08F290/147—Polyurethanes; Polyureas
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
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- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1021—Polyurethanes or derivatives thereof
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- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/44—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing organic binders only
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- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
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- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00715—Uses not provided for elsewhere in C04B2111/00 for fixing bolts or the like
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Abstract
Description
二苯基甲烷二异氰酸酯,在BDDMA中,60%用苯醌预加速和阻聚 | 3.4g |
干燥的玻璃珠(粒度150-200μm) | 3.5g |
叔丁基氨基乙基甲基丙烯酸酯 | 1.7g |
BDDMA | 0.5g |
石英砂(粒度1.2-1.8mm) | 4.0g |
二苯甲酰基过氧化物,50%,于二环己基邻苯二甲酸酯中 | 0.3g |
叔丁基氨基乙基甲基丙烯酸酯 | 55g |
石英砂 | 36g |
二氧化硅 | 6g |
二乙基苯胺 | 2g |
添加剂 | 0.5g |
氢醌 | 0.5g |
二苯基甲烷二异氰酸酯 | 97g |
二氧化硅 | 3g |
二苯甲酰基过氧化物 | 20g |
减敏剂 | 35g |
石膏 | 40g |
添加剂和着色剂 | 3g |
二氧化硅 | 2g |
二苯基甲烷二异氰酸酯 | 2.5g |
2-羟丙基甲基丙烯酸酯 | 1.43g |
DABCD(Air产品) | 0.03g |
氢醌 | 0.02g |
1,4-丁二醇甲基丙烯酸酯 | 1.43g |
二甲基苯胺 | 0.08g |
刚玉(粒度1-2mm) | 8.1g |
二苯甲酰基过氧化物 | 0.3g |
Claims (11)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE10115591A DE10115591A1 (de) | 2001-03-29 | 2001-03-29 | Mehrkomponentenkits und Kombinationen, ihre Verwendung und erhältliche Kunstmörtel |
DE10115591.3 | 2001-03-29 |
Publications (2)
Publication Number | Publication Date |
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CN1500129A CN1500129A (zh) | 2004-05-26 |
CN1283742C true CN1283742C (zh) | 2006-11-08 |
Family
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Application Number | Title | Priority Date | Filing Date |
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CNB028076524A Expired - Fee Related CN1283742C (zh) | 2001-03-29 | 2002-03-05 | 多组分包和组合物以及其应用和所得的塑胶 |
Country Status (15)
Country | Link |
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US (1) | US20040092656A1 (zh) |
EP (1) | EP1373429B1 (zh) |
JP (1) | JP2004523639A (zh) |
KR (1) | KR100580582B1 (zh) |
CN (1) | CN1283742C (zh) |
AT (1) | ATE515547T1 (zh) |
BR (1) | BR0208443A (zh) |
CZ (1) | CZ20032646A3 (zh) |
DE (1) | DE10115591A1 (zh) |
HU (1) | HUP0303951A3 (zh) |
NO (1) | NO20034195L (zh) |
PL (1) | PL364498A1 (zh) |
RU (1) | RU2003131684A (zh) |
SK (1) | SK11742003A3 (zh) |
WO (1) | WO2002079341A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110831995A (zh) * | 2017-07-03 | 2020-02-21 | 喜利得股份公司 | 包含氨基甲酸酯甲基丙烯酸酯化合物的反应性树脂、反应性树脂组分以及反应性树脂体系及其用途 |
Families Citing this family (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10260974A1 (de) * | 2002-12-24 | 2004-07-15 | Fischerwerke Artur Fischer Gmbh & Co. Kg | Spezialmörtel für Mehrkomponentensysteme |
DE102004008464A1 (de) | 2004-02-19 | 2005-09-15 | Fischerwerke Artur Fischer Gmbh & Co. Kg | Mehrkomponentenkit für Befestigungszwecke und dessen Verwendung |
DE102006030044A1 (de) * | 2006-06-29 | 2008-01-03 | Fischerwerke Artur Fischer Gmbh & Co. Kg | Schnellhärtendes chemisches Befestigungssystem und dessen Verwendung |
DE102006054471B4 (de) | 2006-11-18 | 2018-10-31 | Fischerwerke Gmbh & Co. Kg | Verwendung eines feinverteilte Gase beinhaltenden Mehrkomponenten-Kunstsharzsystems zur Befestigung von Befestigungselementen |
DE102006056306A1 (de) * | 2006-11-29 | 2008-06-05 | Fischerwerke Gmbh & Co. Kg | Methode zur Abdichtung |
DE102008018861A1 (de) | 2008-04-15 | 2009-12-17 | Fischerwerke Gmbh & Co. Kg | Verwendung definierter Kunstharze beim Befestigen von Schrauben und ähnlichen Verankerungsmitteln, entsprechende Verfahren und Kunstharze |
DE102009019898A1 (de) * | 2009-05-04 | 2010-11-11 | Fischerwerke Gmbh & Co. Kg | Mehrkomponenten-Kunstmörtel auf Basis silanterminierter Harze |
DE102009019899A1 (de) | 2009-05-04 | 2010-11-11 | Fischerwerke Gmbh & Co. Kg | Klebstoffe auf Basis silanterminierter Isocyanate |
DE102009040705A1 (de) | 2009-09-10 | 2011-03-24 | Heraeus Kulzer Gmbh | Vorrichtung zum halbautomatischen Dosieren zu mischender Komponenten |
DE102009059210A1 (de) | 2009-12-18 | 2011-06-22 | fischerwerke GmbH & Co. KG, 72178 | Radikalisch polymerisierbarer Befestigungsmörtel mit Silanzusätzen |
DE102010015981A1 (de) | 2010-03-16 | 2011-09-22 | Fischerwerke Gmbh & Co. Kg | Epoxidbasierter Befestigungsmörtel mit Silanzusätzen |
US9441147B2 (en) * | 2010-07-09 | 2016-09-13 | Halliburton Energy Services, Inc. | Hybrid cement set-on-command compositions |
DE102010060443A1 (de) | 2010-11-09 | 2012-05-10 | Fischerwerke Gmbh & Co. Kg | Harz für Kleb- und Beschichtungsstoffe auf Basis silanterminierter Harze mit mindestens zwei Edukten |
DE102010051818B3 (de) * | 2010-11-18 | 2012-02-16 | Hilti Aktiengesellschaft | Zweikomponenten-Mörtelmasse und ihre Verwendung |
DE102011053598A1 (de) | 2011-09-14 | 2013-03-14 | Fischerwerke Gmbh & Co. Kg | Chemisches Befestigungssystem und dessen Verwendung |
KR101322760B1 (ko) | 2011-12-07 | 2013-10-29 | 흥진산업(주) | 도로 보수용 조성물 및 그를 이용한 도로 보수 방법 |
DE102012216972B3 (de) | 2012-09-21 | 2013-09-19 | Hilti Aktiengesellschaft | Verwendung oberflächenfunktionalisierter Kieselsäuren als Additiv für Reaktionsharz-Zusammensetzungen sowie dieses enthaltende Harz- und Härter-Zusammensetzungen |
DE102012219479B4 (de) | 2012-10-24 | 2016-12-15 | Hilti Aktiengesellschaft | Reaktionsharz-Zusammensetzung und deren Verwendung |
EP2931782B1 (de) | 2012-12-11 | 2016-12-07 | fischerwerke GmbH & Co. KG | Epoxybasierte masse für befestigungszwecke, deren verwendung und die verwendung bestimmter komponenten |
EP2796433A1 (de) | 2013-04-22 | 2014-10-29 | HILTI Aktiengesellschaft | Reaktionsharz-Zusammensetzung sowie deren Verwendung |
WO2014202187A1 (de) | 2013-06-21 | 2014-12-24 | Fischerwerke Gmbh & Co. Kg | Neue flächig einsetzbare verklebungsmittel, deren herstellung und verwendung |
JP6327933B2 (ja) * | 2013-06-28 | 2018-05-23 | 株式会社クレハ | ダウンホールツール用ゴム部材、及びダウンホールツール、並びに炭化水素資源の回収方法 |
EP2824117A1 (de) * | 2013-07-09 | 2015-01-14 | HILTI Aktiengesellschaft | Reaktionsharz-Zusammensetzung und deren Verwendung |
EP2824155A1 (de) | 2013-07-09 | 2015-01-14 | HILTI Aktiengesellschaft | Reaktionsharz-Zusammensetzung und deren Verwendung |
EP2826797A1 (de) | 2013-07-18 | 2015-01-21 | HILTI Aktiengesellschaft | Härterkomponente, diese enthaltende Mörtelmasse und deren Verwendung |
EP2826796A1 (de) | 2013-07-18 | 2015-01-21 | HILTI Aktiengesellschaft | Verwendung einer Mehrkomponenten-Mörtelmasse auf Epoxid-Amin-Basis |
EP2829524A1 (de) | 2013-07-24 | 2015-01-28 | HILTI Aktiengesellschaft | Harzmischung, Reaktionsharz-Mörtel, Mehrkomponenten-Mörtelsystem und deren Verwendung |
DE102013109602A1 (de) | 2013-09-03 | 2015-03-05 | Fischerwerke Gmbh & Co. Kg | Chemisches Recycling von Polyestern, epoxybasierte Masse mit aminolysiertem Polyester als Härter, deren Verwendung und die Verwendung bestimmter Komponenten |
EP2851352A1 (de) | 2013-09-19 | 2015-03-25 | HILTI Aktiengesellschaft | Durch Frontalpolymerisation aushärtbarer Reaktionsharzmörtel und Verfahren zur Befestigung von Ankerstangen |
DE102013114061A1 (de) | 2013-12-16 | 2015-06-18 | Fischerwerke Gmbh & Co. Kg | Thiole und/oder Thiolester und Metallsalze als Härtersystem in Harzzusammensetzungen unter anderem für die Befestigungstechnik |
DE102015003221A1 (de) | 2014-04-11 | 2015-10-15 | Fischerwerke Gmbh & Co. Kg | CH-Acide Verbindungen und Metallsalze als Härtesystem, entsprechende Harzzusammensetzungen unter anderem für die Befestigungstechnik |
DE102014109355A1 (de) | 2014-07-04 | 2016-01-07 | Fischerwerke Gmbh & Co. Kg | Reaktivverdünner für die chemische Befestigung |
DE102015109125A1 (de) | 2014-07-04 | 2016-01-07 | Fischerwerke Gmbh & Co. Kg | Epoxidbasiertes Befestigungskunstmörtelsystem mit Siloxanoligomeren |
DE102014111651A1 (de) | 2014-08-12 | 2016-02-18 | Fischerwerke Gmbh & Co. Kg | Radikalisch härtbare Kunstharzmasse mit Siloxanoligomerzusätzen |
DE102015111484A1 (de) * | 2014-09-17 | 2016-03-17 | Fischerwerke Gmbh & Co. Kg | Härterzusammensetzung für additionspolymerisationsbasierte Befestigungskunstmörtelsysteme, dessen Verwendung und Herstellung |
DE102015115942A1 (de) | 2014-11-20 | 2016-05-25 | Fischerwerke Gmbh & Co. Kg | Mannich-Basen, deren Herstellung und ihre Verwendung als Härter beispielsweise in Kunstharzzusammensetzungen |
EP3034520A1 (de) | 2014-12-19 | 2016-06-22 | HILTI Aktiengesellschaft | Reaktionsharz-Zusammensetzung und deren Verwendung |
DE102015000875A1 (de) | 2015-01-23 | 2016-07-28 | Fischerwerke Gmbh & Co. Kg | Resorcinbasierte Mannichbasen und Silane in Kunstharzzusammensetzungen für Befestigungszwecke |
CN107787337B (zh) | 2015-06-26 | 2020-10-16 | 费希尔厂有限责任两合公司 | 作为固化剂体系中的引发剂的醛亚胺和酮亚胺和尤其用于固定技术的相应的树脂组合物 |
DE102015118134A1 (de) | 2015-10-23 | 2017-04-27 | Fischerwerke Gmbh & Co. Kg | Aldimine und Ketimine als Initiatoren in Härtersystemen und entsprechende Harzzusammensetzungen unter anderem für die Befestigungstechnik |
DE102015112457A1 (de) | 2015-07-30 | 2017-02-02 | Fischerwerke Gmbh & Co. Kg | Verwendung eines Ein-Komponentensystems zur Befestigung von Verankerungsmitteln |
DE102016110272A1 (de) | 2015-07-30 | 2017-02-02 | Fischerwerke Gmbh & Co. Kg | Verwendung eines Ein- oder Mehr-Komponentensystems zur Befestigung von Verankerungsmitteln |
DE102016117749A1 (de) | 2015-10-22 | 2017-04-27 | Fischerwerke Gmbh & Co. Kg | Vinylesterurethane wie Urethan(meth)acrylate auf Basis nachwachsender Rohstoffe beinhaltende Kunstharz- Befestigungssysteme |
DE102015118136A1 (de) | 2015-10-23 | 2017-04-27 | Fischerwerke Gmbh & Co. Kg | Aldehyde und Ketone als Initiatoren in Härtersystemen und entsprechende Harzzusammensetzungen unter anderem für die Befestigungstechnik |
EP3184499A1 (de) | 2015-12-21 | 2017-06-28 | HILTI Aktiengesellschaft | Reaktionsharz-zusammensetzung, mehrkomponenten-system und deren verwendung |
EP3272777A1 (de) | 2016-07-18 | 2018-01-24 | HILTI Aktiengesellschaft | Reaktionsharz-zusammensetzung auf basis von zuckermethacrylat und deren verwendung |
DE102016124075A1 (de) | 2016-12-12 | 2018-06-14 | Fischerwerke Gmbh & Co. Kg | Hybridbindemittel sowie dessen Verwendung |
EP3424969A1 (de) * | 2017-07-03 | 2019-01-09 | HILTI Aktiengesellschaft | Mischung von radikalisch härtbaren verbindungen und deren verwendung |
EP3424970A1 (de) | 2017-07-03 | 2019-01-09 | HILTI Aktiengesellschaft | Verzweigte urethanmethacrylat-verbindungen und deren verwendung |
EP3424900A1 (de) | 2017-07-03 | 2019-01-09 | HILTI Aktiengesellschaft | Epoxymethacrylat-verbindungen und deren verwendung |
EP3424968A1 (de) * | 2017-07-03 | 2019-01-09 | HILTI Aktiengesellschaft | Urethanmethacrylat-verbindungen und deren verwendung |
EP3428208A1 (de) | 2017-07-10 | 2019-01-16 | HILTI Aktiengesellschaft | Verfahren zur herstellung einer tempol-haltigen urethanharz-zusammensetzung mit lagerstabilität |
EP3450477B1 (de) | 2017-08-30 | 2020-11-04 | fischerwerke GmbH & Co. KG | Mehrkomponentige klebstoffsysteme und deren verwendung |
DE102018113577A1 (de) | 2017-08-30 | 2019-02-28 | Fischerwerke Gmbh & Co. Kg | Mehrkomponentige Klebstoffsysteme und deren Verwendung |
DE102019108150A1 (de) | 2018-04-11 | 2019-10-17 | Fischerwerke Gmbh & Co. Kg | Bestimmte Verbindungen als Beschleuniger für Imin/Metallsalz-initiierte radikalische Polymerisation ungesättigter Verbindungen und ihre Verwendung als Beschleuniger |
EP3587299A1 (de) | 2018-06-21 | 2020-01-01 | fischerwerke GmbH & Co. KG | Mehrkomponentige klebstoffsysteme und deren verwendung |
DE102019112375A1 (de) | 2018-06-21 | 2019-12-24 | Fischerwerke Gmbh & Co. Kg | Mehrkomponentige Klebstoffsysteme und deren Verwendung |
EP3587380A1 (de) | 2018-06-27 | 2020-01-01 | HILTI Aktiengesellschaft | Verwendung von alkylimidazolidon(meth)acrylaten als reaktivverdünner in einer reaktionsharz-zusammensetzung |
EP3623407A1 (de) | 2018-09-14 | 2020-03-18 | Hilti Aktiengesellschaft | Reaktiver amin-beschleuniger, diesen enthaltendes reaktivharz sowie deren verwendung |
EP3670612A1 (de) | 2018-12-18 | 2020-06-24 | Hilti Aktiengesellschaft | Verwendung von urethanmethacrylat-verbindungen in reaktivharz-zusammensetzungen |
EP3708591A1 (de) | 2019-03-15 | 2020-09-16 | Hilti Aktiengesellschaft | Beschleuniger-kombination |
EP3838862A1 (de) | 2019-12-18 | 2021-06-23 | Hilti Aktiengesellschaft | Verwendung einer reaktivharz-zusammensetzung für die chemische befestigung eines verankerungsmittels in einem bohrloch |
EP3838863A1 (de) | 2019-12-18 | 2021-06-23 | Hilti Aktiengesellschaft | Verwendung einer reaktivharz-zusammensetzung für die chemische befestigung eines verankerungsmittels in einem bohrloch |
DE102021114890A1 (de) | 2020-07-02 | 2022-01-05 | Fischerwerke Gmbh & Co. Kg | Spezielle Imine und ihre Edukte, sowie Verwendung bei der Härtung von Reaktivharzen durch Polyaddition oder radikalische Polymerisation |
EP3995525A1 (de) | 2020-11-10 | 2022-05-11 | Hilti Aktiengesellschaft | Monomer mit zwei polymerisierbaren gruppen (für romp und für radikalische polymerisation) und dessen verwendung |
EP3995524A1 (de) | 2020-11-10 | 2022-05-11 | Hilti Aktiengesellschaft | Dual cure system für die chemische befestigung eines verankerungsmittels in einem bohrloch |
EP4056607A1 (de) | 2021-03-12 | 2022-09-14 | Hilti Aktiengesellschaft | Reaktivverdünnermischung für die chemische befestigung |
EP4177229A1 (de) | 2021-11-09 | 2023-05-10 | Hilti Aktiengesellschaft | Ziegelmehl als füllstoff in mehrkomponenten-systemen für die chemische befestigung |
EP4177235A1 (de) | 2021-11-09 | 2023-05-10 | HILTI Aktiengesellschaft | Pulverisierte recyclingmaterialien als füllstoffe für mehrkomponenten-systeme zur chemischen befestigung |
EP4257570A1 (de) | 2022-04-06 | 2023-10-11 | Hilti Aktiengesellschaft | Verbindungen auf basis recyclierter verbindungen für mehrkomponenten-reaktivharzsysteme zur chemischen befestigung |
DE102023111046A1 (de) | 2022-05-18 | 2023-11-23 | Fischerwerke Gmbh & Co. Kg | Wässrige Aminosiloxan-Härter für Massen für Klebezwecke, entsprechende Massen und damit verbundene Verwendungen und Verfahren |
EP4279560A1 (de) | 2022-05-18 | 2023-11-22 | fischerwerke GmbH & Co. KG | Wässrige aminosiloxan-härter für massen für klebezwecke, entsprechende massen und damit verbundene verwendungen und verfahren |
WO2024099783A1 (de) | 2022-11-10 | 2024-05-16 | Fischerwerke Gmbh & Co. Kg | Hochleistungsmörtel mit tbx und analogen |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2848401A1 (de) * | 1978-11-08 | 1980-06-12 | Hoechst Ag | Haertbare massen und verfahren zu ihrer herstellung |
DE3932171A1 (de) * | 1989-09-27 | 1991-04-04 | Henkel Kgaa | Universalklebespachtel |
DE3940309A1 (de) | 1989-12-06 | 1991-06-13 | Hilti Ag | Moertelmasse |
DE3941441A1 (de) | 1989-12-15 | 1991-06-20 | Hilti Ag | Befestigungen an holzwerkstoffen |
NL9001181A (nl) * | 1990-05-22 | 1991-12-16 | Stamicarbon | Samenstelling voor toepassing in de resin injection moulding techniek, bevattende laagmoleculaire verbindingen die tesamen een hybride netwerk vormen. |
DE59200176D1 (de) * | 1992-02-05 | 1994-06-23 | Gerhard Kertscher Chemische Ba | Dauerelastische Mehrzweckmasse und Verfahren zur deren Herstellung. |
DE4233429A1 (de) | 1992-10-05 | 1994-04-07 | Basf Ag | Patrone oder Kartusche für die chemische Befestigungstechnik |
DE4304824A1 (de) | 1993-02-17 | 1994-08-18 | Upat Max Langensiepen Kg | Reaktionsharzmörtel für Zweikomponentensysteme |
DE19746170B4 (de) * | 1997-09-24 | 2004-04-15 | AKEMI Chem.-Techn. Spezialfabrik Erich Höntsch GmbH | Mehrkomponenten-Steinkitt |
-
2001
- 2001-03-29 DE DE10115591A patent/DE10115591A1/de not_active Ceased
-
2002
- 2002-03-05 WO PCT/EP2002/002383 patent/WO2002079341A1/de active Application Filing
- 2002-03-05 BR BR0208443-0A patent/BR0208443A/pt not_active IP Right Cessation
- 2002-03-05 US US10/472,433 patent/US20040092656A1/en not_active Abandoned
- 2002-03-05 SK SK1174-2003A patent/SK11742003A3/sk unknown
- 2002-03-05 PL PL02364498A patent/PL364498A1/xx not_active Application Discontinuation
- 2002-03-05 RU RU2003131684/04A patent/RU2003131684A/ru unknown
- 2002-03-05 KR KR1020037012555A patent/KR100580582B1/ko not_active IP Right Cessation
- 2002-03-05 CZ CZ20032646A patent/CZ20032646A3/cs unknown
- 2002-03-05 AT AT02724197T patent/ATE515547T1/de active
- 2002-03-05 EP EP02724197A patent/EP1373429B1/de not_active Expired - Lifetime
- 2002-03-05 HU HU0303951A patent/HUP0303951A3/hu unknown
- 2002-03-05 JP JP2002578348A patent/JP2004523639A/ja active Pending
- 2002-03-05 CN CNB028076524A patent/CN1283742C/zh not_active Expired - Fee Related
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2003
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110831995A (zh) * | 2017-07-03 | 2020-02-21 | 喜利得股份公司 | 包含氨基甲酸酯甲基丙烯酸酯化合物的反应性树脂、反应性树脂组分以及反应性树脂体系及其用途 |
CN110831995B (zh) * | 2017-07-03 | 2022-11-25 | 喜利得股份公司 | 包含氨基甲酸酯甲基丙烯酸酯化合物的反应性树脂、反应性树脂组分以及反应性树脂体系及其用途 |
Also Published As
Publication number | Publication date |
---|---|
KR100580582B1 (ko) | 2006-05-16 |
BR0208443A (pt) | 2004-03-02 |
EP1373429B1 (de) | 2011-07-06 |
HUP0303951A2 (hu) | 2004-03-01 |
NO20034195L (no) | 2003-11-28 |
CZ20032646A3 (cs) | 2003-12-17 |
HUP0303951A3 (en) | 2004-07-28 |
PL364498A1 (en) | 2004-12-13 |
DE10115591A1 (de) | 2002-10-02 |
CN1500129A (zh) | 2004-05-26 |
WO2002079341A1 (de) | 2002-10-10 |
KR20030097812A (ko) | 2003-12-31 |
SK11742003A3 (sk) | 2004-04-06 |
ATE515547T1 (de) | 2011-07-15 |
US20040092656A1 (en) | 2004-05-13 |
RU2003131684A (ru) | 2005-01-27 |
NO20034195D0 (no) | 2003-09-19 |
JP2004523639A (ja) | 2004-08-05 |
EP1373429A1 (de) | 2004-01-02 |
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