JP5219315B2 - 抑制剤の組み合わせの使用、樹脂組成物、反応性樹脂モルタル、2成分モルタル組成物、2成分モルタル組成物の化学固定用途への使用、並びに2成分モルタル組成物を収容するパトローネ、カートリッジ、及び薄膜袋 - Google Patents
抑制剤の組み合わせの使用、樹脂組成物、反応性樹脂モルタル、2成分モルタル組成物、2成分モルタル組成物の化学固定用途への使用、並びに2成分モルタル組成物を収容するパトローネ、カートリッジ、及び薄膜袋 Download PDFInfo
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- JP5219315B2 JP5219315B2 JP2012131028A JP2012131028A JP5219315B2 JP 5219315 B2 JP5219315 B2 JP 5219315B2 JP 2012131028 A JP2012131028 A JP 2012131028A JP 2012131028 A JP2012131028 A JP 2012131028A JP 5219315 B2 JP5219315 B2 JP 5219315B2
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- straight chain
- resin
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- 229920005989 resin Polymers 0.000 title claims description 94
- 239000011347 resin Substances 0.000 title claims description 94
- 239000004570 mortar (masonry) Substances 0.000 title claims description 67
- 239000011342 resin composition Substances 0.000 title claims description 48
- 239000000203 mixture Substances 0.000 title claims description 41
- 239000000126 substance Substances 0.000 title claims description 40
- 239000010409 thin film Substances 0.000 title claims 3
- 239000003112 inhibitor Substances 0.000 title description 55
- 150000001875 compounds Chemical class 0.000 claims description 96
- 238000001879 gelation Methods 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 24
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 22
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 239000000654 additive Substances 0.000 claims description 13
- 239000003085 diluting agent Substances 0.000 claims description 13
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 11
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 claims description 11
- 230000009257 reactivity Effects 0.000 claims description 10
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 8
- NCPSFAHJUGJPHA-UHFFFAOYSA-N 2-(dimethylamino)-4,6-dimethylpyrimidin-5-ol Chemical compound CN(C)C1=NC(C)=C(O)C(C)=N1 NCPSFAHJUGJPHA-UHFFFAOYSA-N 0.000 claims description 8
- 230000000996 additive effect Effects 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- YEPCZOWQAYSIBD-UHFFFAOYSA-N 2-(dimethylamino)pyrimidin-5-ol Chemical compound CN(C)C1=NC=C(O)C=N1 YEPCZOWQAYSIBD-UHFFFAOYSA-N 0.000 claims description 6
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 6
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- 150000002431 hydrogen Chemical group 0.000 claims description 5
- 150000002484 inorganic compounds Chemical class 0.000 claims description 5
- 229910010272 inorganic material Inorganic materials 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 3
- SBBJBEPNVNFNSZ-UHFFFAOYSA-N 4,6-dimethyl-2-octoxypyrimidine Chemical compound CC1=NC(=NC(=C1)C)OCCCCCCCC SBBJBEPNVNFNSZ-UHFFFAOYSA-N 0.000 claims description 3
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- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 125000005447 octyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims 1
- 238000001723 curing Methods 0.000 description 40
- -1 nitroxy radical Chemical class 0.000 description 37
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 30
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- 239000004593 Epoxy Substances 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 5
- 239000004342 Benzoyl peroxide Substances 0.000 description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 4
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- LTXJLQINBYSQFU-UHFFFAOYSA-N pyrimidin-5-ol Chemical class OC1=CN=CN=C1 LTXJLQINBYSQFU-UHFFFAOYSA-N 0.000 description 4
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- 239000000057 synthetic resin Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- GPGBDDNRYPDIFA-UHFFFAOYSA-N 4,6-dimethyl-2-octoxypyrimidin-5-ol Chemical compound CCCCCCCCOC1=NC(C)=C(O)C(C)=N1 GPGBDDNRYPDIFA-UHFFFAOYSA-N 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- 239000001530 fumaric acid Substances 0.000 description 3
- 230000002779 inactivation Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
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- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical class C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 2
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical class OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 description 2
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- 229930185605 Bisphenol Natural products 0.000 description 2
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N Methyl ethyl ketone Natural products CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
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- 150000004645 aluminates Chemical class 0.000 description 2
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- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
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- 238000004040 coloring Methods 0.000 description 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
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- 239000007788 liquid Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
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- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
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- BOKBKEJKCYRLKG-UHFFFAOYSA-N 2-octoxypyrimidin-5-ol Chemical compound C(CCCCCCC)OC1=NC=C(C=N1)O BOKBKEJKCYRLKG-UHFFFAOYSA-N 0.000 description 1
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- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
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- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
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- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 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
- 239000011324 bead Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000440 bentonite Chemical class 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical class O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000004359 castor oil Chemical class 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- DJKGDNKYTKCJKD-UHFFFAOYSA-N chlorendic acid Chemical compound ClC1=C(Cl)C2(Cl)C(C(=O)O)C(C(O)=O)C1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-UHFFFAOYSA-N 0.000 description 1
- SURLGNKAQXKNSP-DBLYXWCISA-N chlorin Chemical compound C\1=C/2\N/C(=C\C3=N/C(=C\C=4NC(/C=C\5/C=CC/1=N/5)=CC=4)/C=C3)/CC\2 SURLGNKAQXKNSP-DBLYXWCISA-N 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000010941 cobalt Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical class [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229910052571 earthenware Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Chemical class CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000013035 low temperature curing Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Chemical class 0.000 description 1
- 239000001923 methylcellulose Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
- HKJNHYJTVPWVGV-UHFFFAOYSA-N n,n-diethyl-4-methylaniline Chemical compound CCN(CC)C1=CC=C(C)C=C1 HKJNHYJTVPWVGV-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
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229910021426 porous silicon Inorganic materials 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021081 unsaturated fats Nutrition 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/02—Alcohols; Phenols; Ethers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
-
- 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
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/12—Nitrogen containing compounds organic derivatives of hydrazine
- C04B24/128—Heterocyclic nitrogen compounds
-
- 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
-
- 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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
- C04B28/06—Aluminous cements
-
- 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
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
- C04B40/0039—Premixtures of ingredients
-
- 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
- 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
- C04B40/0658—Retarder inhibited mortars activated by the addition of accelerators or retarder-neutralising agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
-
- 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
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member
-
- 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
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Mechanical Engineering (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Polymerisation Methods In General (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Description
「A成分」と同義なものとして使用する。
[実施例1]
反応性樹脂モルタルの作成のために、976.1gのメタクリレート樹脂に対して、4.06gの3,5−ジ−tert−ブチル−4−ヒドロキシアニソール(TBA)と、2.89gの2-(ジメチルアミノ)−4,6−ジメチルピリミジン−5−オール(Me2N−PymOH)とを加え、一様な溶液が得られるまで攪拌する。この配合は、約1:1の抑制剤比率に対応する。引き続き真空中で72.4gの発熱性珪酸(Aerosil R202(登録商標);Evonik Degussa GmbH製)482.68gと、アルミン酸塩セメントと、868.82gの石英砂F32とをディゾルバーを使って、一様なペーストになるまで樹脂溶液中に分散させた。
メタクリレート樹脂のための硬化剤として、ベンゾイル過酸化物の40%水分散液10重量%と、脱ミネラル化された水14重量%とを混ぜて、次いで、その中に40μmの平均粒径を有する石英砂53重量%と、平均粒径0.8μmを有する粘土22重量%とを分散させ、更に1重量%の発熱性の珪酸を加えて濃縮した。
[比較例1]
[比較例2]
[実施例2]
反応性樹脂モルタルに加える抑制剤が、2.38gの2,6−ジ−tert−ブチル−4−メチルフェノール(BHT)と、0.27gの4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オール(C8O-PymOH)とであることだけが実施例1と異なるよう試料を作成した。この量は、両抑制剤のモル比BHT:C8O−PymOHが10:1であることに対応する。
反応性樹脂モルタルに加える抑制剤が、3.07gの2,6−ジ−tert−ブチル−4−メチルフェノール(BHT)のみであることだけが実施例1と異なるよう試料を作成した。
反応性樹脂モルタルに加える抑制剤が、9.84gの4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オール(C8O−PymOH)のみであることだけが実施例1と異なるよう試料を作成した。
2:同様のドリル穴で、−5℃で固定、硬化
3:同様のドリル穴で、+40℃で固定、硬化
4:同様のドリル穴で、24時間、室温で固定、硬化したあと、24時間80℃に加熱し、更に80℃で引き抜きを実行
* :2,6−ジ−tert−ブチル−4−メチルフェノール
**:4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オール
Claims (23)
- ラジカル重合可能な化合物をベースとした樹脂組成物の反応性とゲル化時間との調整のための、下記の化合物(I)と、下記の化合物(II)との組み合わせの使用
- 前記化合物(I)において、R1およびR2はそれぞれ、相互に独立であって、水素あるいは、分岐鎖または直鎖C1〜C8のアルキル基である、請求項1に記載の使用。
- 前記化合物(I)において、R1およびR2はそれぞれ、相互に独立であって、水素またはメチルである、請求項2に記載の使用。
- 前記化合物(I)が、2−(ジメチルアミノ)ピリミジン−5−オール、2−(ジメチルアミノ)−4,6−ジメチルピリミジン−5−オールまたは4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オールである、請求項3に記載の使用。
- 前記化合物(II)が、2,6−ジ−tert-ブチル−4−メチルフェノールまたは3,5−ジ−tert−ブチル−4−ヒドロキシアニソールである、請求項1〜4のいずれか1項に記載の使用。
- 前記、化合物(I)と化合物(II)との組み合わせが、2−(ジメチルアミノ)ピリミジン−5−オールと、2,6−ジ−tert−ブチル−4−メチルフェノールとの組み合わせ(III−1)、2−(ジメチルアミノ)−4,6−ジメチルピリミジン−5−オールと、3,5−ジ−tert−ブチル−4−ヒドロキシアニソールとの組み合わせ(III−2)、または、4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オールと、2,6−ジ−tert−ブチル−4−メチルフェノールとの組み合わせ(III−3)である、請求項5に記載の使用。
- 前記化合物(I)の、前記化合物(II)に対するモル比が、1:1〜1:10である、請求項1〜6のいずれか1項に記載の使用。
- 少なくとも1種のラジカル重合可能な化合物と、反応性とゲル化時間の調整のための助剤(c)とを含有し、前記助剤(c)は、下記の化合物(I)と、下記の化合物(II)とを組み合わせたものである樹脂組成物
- 前記化合物(I)において、R1およびR2はそれぞれ、相互に独立であって、水素あるいは、分岐鎖または直鎖C1−C8−アルキル基である、請求項8に記載の樹脂組成物。
- 前記化合物(I)において、R1およびR2はそれぞれ、相互に独立であって、水素またはメチルである、請求項9に記載の樹脂組成物。
- 前記化合物(I)が、2−(ジメチルアミノ)ピリミジン−5−オール、2−(ジメチルアミノ)−4,6−ジメチルピリミジン−5−オールまたは4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オールである、請求項10に記載の樹脂組成物。
- 前記化合物(II)が、2,6−ジ−tert-ブチル−4−メチルフェノールまたは3,5−ジ−tert−ブチル−4−ヒドロキシアニソールである、請求項8〜11のいずれか1項に記載の樹脂組成物。
- 前記助剤(c)が、2−(ジメチルアミノ)ピリミジン−5−オールと、2,6−ジ−tert−ブチル−4−メチル−フェノールとの組み合わせ(III−1)、2−(ジメチルアミノ)−4,6−ジメチルピリミジン−5−オールと、3,5−ジ−tert−ブチル−4−ヒドロキシアニソールとの組み合わせ(III−2)、または、4,6−ジメチル−2−(オクチルオキシ)ピリミジン−5−オールと、2,6−ジ−tert−ブチル−4−メチルフェノールとの組み合わせ((III−3)である、請求項12に記載の樹脂組成物。
- 前記化合物(I)の、前記化合物(II)に対するモル比が、1:1〜1:10である、請求項8〜13のいずれか1項に記載の樹脂組成物。
- 樹脂組成物が更に硬化物質のための促進剤を含む、請求項8〜14のいずれか1項に記載の樹脂組成物。
- 反応性希釈剤を含有する請求項8〜15のいずれか1項に記載の樹脂組成物。
- 請求項8〜15のいずれか1項に記載の樹脂組成物と無機の添加剤とを含む反応性樹脂モルタル。
- A成分としての、請求項17に記載の反応性樹脂モルタルと、A成分とは反応しないよう離された、B成分としての、硬化剤とを含む2成分モルタル組成物。
- 前記硬化剤が硬化物質として無機または有機の過酸化物を含む、請求項18に記載の2成分モルタル組成物。
- 前記硬化剤が無機の添加剤を含む、請求項18または19に記載の2成分モルタル組成物。
- A成分が、反応性樹脂モルタルの他に、水硬性の、または重縮合可能なもう1つの無機化合物を付加的に含有し、B成分が硬化物質の他にさらに水を含有する、請求項18〜20のいずれか1項に記載の2成分モルタル組成物。
- 請求項18〜21のいずれか1項に記載の2成分モルタル組成物の化学固定用途への使用。
- 請求項18〜21のいずれか1項に記載の2成分モルタル組成物を収容するパトロ−ネ、カートリッジまたは薄膜袋であって、内部に前記反応性樹脂モルタルまたは硬化剤を収容する、互いに分離した2以上のチャンバを備えることを特徴とするパトロ−ネ、カートリッジまたは薄膜袋。
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DE102011077254A DE102011077254B3 (de) | 2011-06-09 | 2011-06-09 | Verwendung einer Inhibitorkombination, Harzmischung, Reaktionsharzmörtel, Zweikomponenten - Mörtelsystem und dessen Verwendung sowie Patrone, Kartusche oder Folienbeutel enthaltend ein Zweikomponenten - Mörtelsystem |
DE102011077254.5 | 2011-06-09 |
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JP2012131028A Expired - Fee Related JP5219315B2 (ja) | 2011-06-09 | 2012-06-08 | 抑制剤の組み合わせの使用、樹脂組成物、反応性樹脂モルタル、2成分モルタル組成物、2成分モルタル組成物の化学固定用途への使用、並びに2成分モルタル組成物を収容するパトローネ、カートリッジ、及び薄膜袋 |
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US (2) | US8735475B2 (ja) |
EP (1) | EP2532632B1 (ja) |
JP (1) | JP5219315B2 (ja) |
AU (1) | AU2012203362B2 (ja) |
CA (1) | CA2779431C (ja) |
DE (1) | DE102011077254B3 (ja) |
ES (1) | ES2647591T3 (ja) |
RU (1) | RU2597701C2 (ja) |
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HUE038828T2 (hu) * | 2013-02-20 | 2018-11-28 | Polycare Research Tech Gmbh & Co Kg | Polimer beton és eljárás ennek elõállítására |
EP2796433A1 (de) * | 2013-04-22 | 2014-10-29 | HILTI Aktiengesellschaft | Reaktionsharz-Zusammensetzung sowie deren Verwendung |
AU2017217194B2 (en) | 2016-02-08 | 2019-03-14 | Shell Internationale Research Maatschappij B.V. | Method for providing zonal isolation in an underground wellbore |
EP3424971A1 (de) | 2017-07-03 | 2019-01-09 | HILTI Aktiengesellschaft | Urethanmethacrylat-verbindungen enthaltende reaktivharze, reaktivharzkomponenten sowie reaktivharz-systeme und deren verwendung |
CN108203285A (zh) * | 2018-03-27 | 2018-06-26 | 奥泰利新技术集团有限公司 | 一种环氧树脂灌浆材料及其制备方法 |
EP3851424A1 (de) | 2020-01-14 | 2021-07-21 | Hilti Aktiengesellschaft | Verwendung von reaktionsharzmischungen mit vordefinierter polarität zur einstellung der gelzeit einer mörtelmasse sowie verfahren zur einstellung der gelzeit einer mörtelmasse |
EP4001327A1 (de) | 2020-11-11 | 2022-05-25 | Hilti Aktiengesellschaft | Zweikomponenten-mörtelmasse |
DE102023118527A1 (de) | 2022-11-10 | 2024-05-16 | Fischerwerke Gmbh & Co. Kg | Hochleistungsmörtel mit TBX und Analogen |
WO2024099783A1 (de) | 2022-11-10 | 2024-05-16 | Fischerwerke Gmbh & Co. Kg | Hochleistungsmörtel mit tbx und analogen |
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DE102011077248B3 (de) * | 2011-06-09 | 2012-09-27 | Hilti Aktiengesellschaft | Verwendung eines Inhibitors, Harzmischung, Reaktionsharzmörtel, Zweikomponenten - Mörtelsystem und dessen Verwendung sowie Patrone, Kartusche oder Folienbeutel enthaltend ein Zweikomponenten - Mörtelsystem |
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2011
- 2011-06-09 DE DE102011077254A patent/DE102011077254B3/de not_active Expired - Fee Related
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2012
- 2012-05-15 EP EP12168008.6A patent/EP2532632B1/de not_active Not-in-force
- 2012-05-15 ES ES12168008.6T patent/ES2647591T3/es active Active
- 2012-06-05 CA CA2779431A patent/CA2779431C/en not_active Expired - Fee Related
- 2012-06-07 AU AU2012203362A patent/AU2012203362B2/en not_active Ceased
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- 2012-06-08 RU RU2012123717/04A patent/RU2597701C2/ru not_active IP Right Cessation
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RU2012123717A (ru) | 2013-12-20 |
EP2532632A2 (de) | 2012-12-12 |
RU2597701C2 (ru) | 2016-09-20 |
US20140224424A1 (en) | 2014-08-14 |
CA2779431A1 (en) | 2012-12-09 |
EP2532632A3 (de) | 2016-01-27 |
ES2647591T3 (es) | 2017-12-22 |
US8735475B2 (en) | 2014-05-27 |
DE102011077254B3 (de) | 2012-09-20 |
JP2012255152A (ja) | 2012-12-27 |
AU2012203362A1 (en) | 2013-01-10 |
AU2012203362B2 (en) | 2013-08-15 |
US20130123393A1 (en) | 2013-05-16 |
EP2532632B1 (de) | 2017-08-16 |
CA2779431C (en) | 2013-05-21 |
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