JP2018515414A - 石膏含有組成物 - Google Patents
石膏含有組成物 Download PDFInfo
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- JP2018515414A JP2018515414A JP2017556947A JP2017556947A JP2018515414A JP 2018515414 A JP2018515414 A JP 2018515414A JP 2017556947 A JP2017556947 A JP 2017556947A JP 2017556947 A JP2017556947 A JP 2017556947A JP 2018515414 A JP2018515414 A JP 2018515414A
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- 239000000203 mixture Substances 0.000 title claims abstract description 48
- 229910052602 gypsum Inorganic materials 0.000 title claims abstract description 31
- 239000010440 gypsum Substances 0.000 title claims abstract description 31
- 239000000178 monomer Substances 0.000 claims abstract description 124
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims abstract description 61
- 229920000642 polymer Polymers 0.000 claims abstract description 55
- 239000011230 binding agent Substances 0.000 claims abstract description 26
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 25
- 239000000945 filler Substances 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 78
- -1 hydroxypropyl Chemical group 0.000 claims description 68
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 63
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 24
- 150000002148 esters Chemical class 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 229910052925 anhydrite Inorganic materials 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
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- 238000006477 desulfuration reaction Methods 0.000 claims description 7
- 230000023556 desulfurization Effects 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 239000003546 flue gas Substances 0.000 claims description 6
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 5
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- 239000011505 plaster Substances 0.000 claims description 3
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical group OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 claims description 3
- HZAZCFXDTQTSIP-UHFFFAOYSA-N (3-ethenoxy-2-hydroxypropyl) dihydrogen phosphate Chemical compound C=COCC(O)COP(O)(O)=O HZAZCFXDTQTSIP-UHFFFAOYSA-N 0.000 claims description 2
- DPXGHLJSGPBFGC-UHFFFAOYSA-N 4-ethenoxybutyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCCOC=C DPXGHLJSGPBFGC-UHFFFAOYSA-N 0.000 claims description 2
- AGNYGVJOJNYJMS-UHFFFAOYSA-N but-3-enyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCC=C AGNYGVJOJNYJMS-UHFFFAOYSA-N 0.000 claims description 2
- KJLQJEWLKADPDQ-UHFFFAOYSA-N but-3-enylphosphonic acid Chemical compound OP(O)(=O)CCC=C KJLQJEWLKADPDQ-UHFFFAOYSA-N 0.000 claims description 2
- BNKAXGCRDYRABM-UHFFFAOYSA-N ethenyl dihydrogen phosphate Chemical compound OP(O)(=O)OC=C BNKAXGCRDYRABM-UHFFFAOYSA-N 0.000 claims description 2
- RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 claims description 2
- NCTNGTZTRXYGQK-UHFFFAOYSA-N (1-ethenoxy-3-phosphonooxypropan-2-yl) dihydrogen phosphate Chemical compound OP(O)(=O)OCC(OP(O)(O)=O)COC=C NCTNGTZTRXYGQK-UHFFFAOYSA-N 0.000 claims 1
- 125000004946 alkenylalkyl group Chemical group 0.000 claims 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims 1
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- 239000000243 solution Substances 0.000 description 37
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- 235000011132 calcium sulphate Nutrition 0.000 description 17
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 13
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 12
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 12
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 11
- 239000011976 maleic acid Substances 0.000 description 11
- 239000002270 dispersing agent Substances 0.000 description 10
- 239000003999 initiator Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 229940043430 calcium compound Drugs 0.000 description 9
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- 239000003054 catalyst Substances 0.000 description 9
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- HMBNQNDUEFFFNZ-UHFFFAOYSA-N 4-ethenoxybutan-1-ol Chemical compound OCCCCOC=C HMBNQNDUEFFFNZ-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 7
- 229940052303 ethers for general anesthesia Drugs 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 238000010526 radical polymerization reaction Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- FLJPGEWQYJVDPF-UHFFFAOYSA-L caesium sulfate Chemical compound [Cs+].[Cs+].[O-]S([O-])(=O)=O FLJPGEWQYJVDPF-UHFFFAOYSA-L 0.000 description 4
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 150000003949 imides Chemical class 0.000 description 4
- 229920005646 polycarboxylate Polymers 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 3
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920000388 Polyphosphate Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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- 125000004185 ester group Chemical group 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- RAFRTSDUWORDLA-UHFFFAOYSA-N phenyl 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1 RAFRTSDUWORDLA-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003008 phosphonic acid esters Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 229910000345 rubidium hydrogen sulfate Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([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])C([H])([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])[H] 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229960000834 vinyl ether Drugs 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
- 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
- C04B28/14—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 calcium sulfate cements
- C04B28/145—Calcium sulfate hemi-hydrate with a specific crystal form
- C04B28/146—Calcium sulfate hemi-hydrate with a specific crystal form alpha-hemihydrate
-
- 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
- C04B24/16—Sulfur-containing compounds
- C04B24/161—Macromolecular compounds comprising sulfonate or sulfate groups
- C04B24/163—Macromolecular compounds comprising sulfonate or sulfate groups obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/165—Macromolecular compounds comprising sulfonate or sulfate groups obtained by reactions only involving carbon-to-carbon unsaturated bonds containing polyether side chains
-
- 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
- C04B28/14—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 calcium sulfate cements
- C04B28/145—Calcium sulfate hemi-hydrate with a specific crystal form
- C04B28/147—Calcium sulfate hemi-hydrate with a specific crystal form beta-hemihydrate
-
- 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
- C04B28/14—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 calcium sulfate cements
- C04B28/16—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 calcium sulfate cements containing anhydrite, e.g. Keene's cement
-
- 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
- C04B28/14—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 calcium sulfate cements
- C04B28/16—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 calcium sulfate cements containing anhydrite, e.g. Keene's cement
- C04B28/165—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 calcium sulfate cements containing anhydrite, e.g. Keene's cement containing synthetic anhydrite
-
- 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
- C08F28/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
- C08F28/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur by a bond to sulfur
- C08F28/04—Thioethers
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- 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
- C04B2111/00612—Uses not provided for elsewhere in C04B2111/00 as one or more layers of a layered structure
- C04B2111/0062—Gypsum-paper board like materials
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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
- C04B2111/60—Flooring materials
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- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
A)硫酸カルシウムをベースとする少なくとも1種のバインダーと、
B)モノマーの重合によって得られる少なくとも1種のポリマーと
を含む組成物であって、当該モノマーが、一般式(I)
R1、R2およびR3は、同じであるかまたは異なっており、かつ互いに無関係に、HまたはCH3であり、
R4は、直鎖または分枝鎖のC1〜C30−アルキレンであり、
R5およびR6は、同じであるかまたは異なっており、かつ互いに無関係に、H、C1〜C20−アルキル、C3〜C15−シクロアルキル、アリール、−CH2−O−C1〜C20−アルキルまたは−CH2−O−C2〜C20−アルケニルであり、ここで、R5とR6は、一緒になってC3〜C6−アルキレンを形成してもよく、
R7は、H、C1〜C4−アルキルまたは
R8は、C1〜C22−アルキルまたはC2〜C22−アルケニルであり、かつ
nは、2〜200の整数である]の不飽和化合物を含む、前記組成物によって解決された。
C1〜C22−アルキル:22個までの炭素原子を有する直鎖もしくは分枝鎖の炭化水素基、例えばC1〜C10−アルキルまたはC11〜C22−アルキル、好ましくはC1〜C10−アルキル、例えばC1〜C3−アルキル、例えばメチル、エチル、プロピル、イソプロピル、またはC4〜C6−アルキル、n−ブチル、sec−ブチル、tert−ブチル、1,1−ジメチルエチル、ペンチル、2−メチルブチル、1,1−ジメチルプロピル、1,2−ジメチルプロピル、2,2−ジメチルプロピル、1−エチルプロピル、ヘキシル、2−メチルペンチル、3−メチルペンチル、1,1−ジメチルブチル、1,2−ジメチルブチル、1,3−ジメチルブチル、2,2−ジメチルブチル、2,3−ジメチルブチル、3,3−ジメチルブチル、2−エチルブチル、1,1,2−トリメチルプロピル、1,2,2−トリメチルプロピル、1−エチル−1−メチルプロピル、1−エチル−2−メチルプロピル、またはC7〜C10−アルキル、例えばヘプチル、オクチル、2−エチルヘキシル、2,4,4−トリメチルペンチル、1,1,3,3−テトラメチルブチル、ノニルもしくはデシルおよびそれらの異性体。
(1)カルボン酸基を含むモノエチレン性不飽和のモノマーまたはその無水物もしくは塩、例えばアクリル酸、メタクリル酸、マレイン酸またはマレイン酸無水物など、
(2)リン酸基またはホスホン酸基を含むモノエチレン性不飽和のモノマーまたはその塩、例えばヒドロキシエチル(メタ)アクリレート、ヒドロキシプロピル(メタ)アクリレートまたはヒドロキシブチル(メタ)アクリレートと(ポリ)リン酸とのエステルなど、
(3)スルホン酸基を含むモノエチレン性不飽和のモノマーまたはその塩、例えば、ビニルスルホン酸または2−アクリルアミド−2−メチルプロパンスルホン酸など、
(4)(メタ)アクリル酸ヒドロキシアルキルエステル、例えばヒドロキシエチルアクリレートまたはヒドロキシプロピルアクリレートなど、
(5)ポリアルコキシ基を含むモノエチレン性不飽和のモノマー、例えば(イソ)プレニルアルコキシレート、(メタ)アリルアルコキシレート、ヒドロキシブチルビニルエーテルアルコキシレートまたは(メタ)アクリル酸アルコキシレートなど
からなる群から選択される少なくとも1種のモノマーを含む。
この実施形態の場合、不飽和化合物(I)、更なるモノマーおよび開始剤の一部のみが反応容器に最初に装入され、ここで、最初に装入されるモノマーの量は、モノマーの意図された総量の25重量%、好ましくは総量の10重量%を超えるべきではなく、さらに、最初に装入されるモノマーのモル比は、ポリマー中での意図された比に従って選択されるべきである。差違(偏差)は、一般に、意図された比の±20%以下、好ましくは±10%以下であるべきである。特に好ましくは、最初に装入されるモノマーの比は、所望のモノマー比に対応する。
a.一般式(II)
b.工程a.において形成されたポリマーを、一般式(III)
を含み、ここで、記号および添え字は、上掲の意味を有する。
i)硫酸塩化合物0.1〜6モル/l、好ましくは0.5〜2モル/l、特に0.6〜1モル/l、
ii)カルシウム化合物0.1〜10モル/l、好ましくは3〜8モル/l、特に4〜6モル/l。
GPC溶離液中のポリマー濃度が0.5重量%となるように、GPC溶離液にコポリマー溶液を溶解させることによって分子量測定のためのサンプル調製を行った。その後、この溶液をポリエーテルスルホン膜および0.45μmの孔径を有するシリンジフィルターユニットに通して濾過した。この濾液の注入量は50〜100μlであった。
Shodex OHpak SB 804HQおよび802.5HQ
(PHMゲル、8×300mm、pH4.0〜7.5)
溶離液:0.05M 水性ギ酸アンモニウム/メタノール混合物=80:20(体積部)
流速:0.5ml/分
温度:50℃
注入:50〜100μl
検出:RIおよびUV
水酸基価(OHN)=12.1mgKOH/g(理論値:9.3mgKOH/g)
PEG含量:2.0重量%
84重量%のVME−135 EOと16重量%のHEMA−Pとのコポリマー
実験装置は、1000mlの二重壁反応器、サーモスタット、プロペラ撹拌器を備えた撹拌モーター、温度センサー、pHプローブおよびN2供給導管から成る。反応器に水172.80gおよびVME−135 EO 106.38gを加える。引き続きN2を導入して酸素を置換する。サーモスタットをT=75℃に設定して反応器の内容物を加熱する。
約60℃で、水104.6g中のHEMA−P 19.79gを添加する。約1.0〜1.5のpH値が生じる。その後、約3のpH値を設定するために50%濃度のNaOH7.05gを添加する.HEMA−P溶液の添加中に温度は50℃にまで低下する。引き続き、反応器の内容物を60℃に加熱する。次いで、水11.3g中のWako VA−044(2,2’−アゾビス[2−(2−イミダゾリン−2−イル)プロパン]ジヒドロクロリド)1.26gを添加する。3時間の反応時間後、反応器の内容物を25℃に冷却する。
形成された帯黄色のわずかに濁った生成物は、約2.5のpH値および33重量%の固体含量を有する。ポリマーの平均モル質量(Mw)は29000g/モルである。多分散度は1.35である。
結果を表2にまとめる。
94.9重量%のVME−135 EOと5.1重量%のアクリル酸とのコポリマー
実験装置は、1000mlの二重壁反応器、サーモスタット、プロペラ撹拌器を備えた撹拌モーター、温度センサー、pHプローブおよびN2供給導管から成る。反応器に水172.80gおよびVME−135 EO 106.38gを加える。引き続きN2を導入して酸素を置換する。サーモスタットをT=40℃に設定して反応器の内容物を加熱する。
アクリル酸5.78g(99.5%濃度)と水30.36gとから成る溶液1および水10.09g中のWako VA−044(2,2’−アゾビス[2−(2−イミダゾリン−2−イル)プロパン]ジヒドロクロリド)1.12gから成る溶液2を製造する。
残留溶液1に3−メルカプトプロピオン酸0.57gを加える。
0.6mlの溶液2を反応器に添加する。
サーモスタットをT=78℃に設定し、引き続き反応器の内容物を約60℃に加熱する。
約60℃および約4.0のpH値で、残りの溶液1を11.5ml/hの速度で180分間にわたって添加し始め、残りの溶液2を2.7ml/hの速度で240分間にわたって添加し始める。
添加開始から10分後(約65℃の内部温度)に、サーモスタットを70℃に設定する。
続けて、後反応のためにさらに120分間撹拌し、次いで、反応器の内容物を25℃に冷却する。NaOH6.66g(50%濃度)を用いて約3.0のpH値を約8.4に設定する。
結果を表3にまとめる。
実験装置は、1000mlの二重壁反応器、サーモスタット、プロペラ撹拌器を備えた撹拌モーター、温度センサー、pHプローブおよびN2供給導管から成る。
反応器に水170.0gおよびVOB−135 EO 202.12gを加える。引き続きN2を導入して酸素を置換する。サーモスタットをT=40℃に設定して反応器の内容物を加熱する。
約35℃で、水87.72中のHEMA−P(99.99%濃度)37.59gを添加する。約1.5のpH値が生じる。その後、約3のpH値を設定するためにNaOH10.20g(50%濃度)を添加する.サーモスタットをT=75℃に設定して反応器の内容物をさらに加熱する。約65℃で、水21.6g中のWako VA−044(2,2’−アゾビス[2−(2−イミダゾリン−2−イル)プロパン]ジヒドロクロリド)2.40gを添加する。
15分後、サーモスタットをT=70℃に設定する。
3時間の反応時間後、反応器の内容物を20℃に冷却する。反応器の内容物を、NaOH20.16g(50%濃度)を用いてpH値を約8.1に設定する。
撹拌器、pH電極、温度計、酸化還元電極、N2注入口を備えたガラス反応器に、脱イオン水108.7gおよびVOB−135 EO 112.5gを最初に装入し、重合開始温度15℃に冷却する(初期装入物)。
別個の供給容器中で、HEA−P 22.12gを脱イオン水199.08gおよびNaOH9.7g(50%濃度)と均一に混合する(溶液A)。並行して、亜硫酸ナトリウム、2−ヒドロキシ−2−スルフィナト酢酸の二ナトリウム塩および2−ヒドロキシ−2−スルホナト酢酸の二ナトリウム塩(Brueggemann GmbHのBrueggolit FF6)の混合物の水中6%溶液を製造する(溶液B)。撹拌および冷却しながら、まず109.53gの溶液Aを初期装入物に加え、その後、3−メルカプトプロピオン酸(MPS)0.77gを残りの溶液Aに加える。引き続き、3−メルカプトプロピオン酸0.14gおよび硫酸鉄(II)七水和物(FeSO4)0.089gを初期装入物の溶液に連続的に加える。これを、引き続きNaOH(50%濃度)を用いて5.3の出発pHに設定する。
初期装入物の混合物に過酸化水素0.75g(水中で30%濃度の溶液)を添加することにより、反応を開始させる。同時に、撹拌した装入物への溶液Aおよび溶液Bの添加を開始する。溶液Aを30分間にわたり添加する。並行して、溶液Bを13.5ml/hの一定の配量速度で、溶液中に過酸化物がもはや検出され得なくなるまで添加する。引き続き、得られたポリマー溶液を50%濃度の水酸化ナトリウム溶液を用いてpH値を6.5に設定する。
得られたコポリマーは、溶液中に生じ、これは29.3重量%の固体含量を有する。コポリマーの平均モル質量(Mw)は40400g/モルであり、多分散度は1.6である。
合成例からの分散剤を、適切な試験系において石膏可塑剤としてのその特性について調べる。
排煙脱硫からのβ型半水和物300gをまず、促進剤としての微粉砕された硫酸カルシウム二水和物(石膏)とともに予めホモジナイズして187gの水に振りかけた。分散剤は事前に混練水に混ぜ入れる。引き続き、この混合物のバッチを15秒間放置する。その後、ホバートミキサーによりIIの設定(285回転/分)でさらに15秒間にわたり撹拌し始める。60秒後に持ち上げられるシリンダー(h=10cm、d=5cm)の充填後、スランプフローの測定を行う。硬化時間を、いわゆるナイフカット法(DIN EN 13279−2)により測定する。
Claims (15)
- A)硫酸カルシウムをベースとする少なくとも1種のバインダーと、
B)モノマーの重合によって得られる少なくとも1種のポリマーと
を含む組成物であって、前記モノマーが、一般式(I)
R1、R2およびR3は、同じであるかまたは異なっており、かつ互いに無関係に、HまたはCH3であり、
R4は、直鎖または分枝鎖のC1〜C30−アルキレンであり、
R5およびR6は、同じであるかまたは異なっており、かつ互いに無関係に、H、C1〜C20−アルキル、C3〜C15−シクロアルキル、アリール、−CH2−O−C1〜C20−アルキルまたは−CH2−O−C2〜C20−アルケニルであり、ここで、R5とR6は、一緒になってC3〜C6−アルキレンを形成してもよく、
R7は、H、C1〜C4−アルキルまたは
R8は、C1〜C22−アルキルまたはC2〜C22−アルケニルであり、かつ
nは、2〜200の整数である]の不飽和化合物を含む、前記組成物。 - R4が、C2〜C4−アルキレン基であり、R5およびR6が、同じであるかまたは異なっており、かつ互いに無関係に、H、−CH3、−CH2−CH3、−C3〜C11−アルキル、−C12−C22−アルキル、フェニル、−CH2−O−C1〜C10−アルキルまたは−CH2−O−C2〜C10−アルケニルから選択される基であり、R7が、HまたはC1〜C4−アルキルであり、かつnが、5〜140である、請求項1記載の組成物。
- nが、60〜140である、請求項4記載の組成物。
- 前記ポリマーが、一般式(I)の化合物とは異なる少なくとも1種の更なるモノマーを前記ポリマー中に含む、請求項1から5までのいずれか1項記載の組成物。
- 前記少なくとも1種の更なるモノマーが、少なくとも1個の酸基を含む少なくとも1種のモノエチレン性不飽和モノマーであり、ここで、前記酸基は、完全にまたは部分的に中和されていてよい、請求項6記載の組成物。
- 前記酸基が、カルボン酸基、スルホン酸基、リン酸基およびホスホン酸基からなる群から選択される少なくとも1個の酸基である、請求項7記載の組成物。
- 前記ポリマーが、ビニルホスホン酸、ヒドロキシエチル(メタ)アクリレート、ヒドロキシプロピル(メタ)アクリレートまたはヒドロキシブチル(メタ)アクリレートと(ポリ)リン酸とのエステル、リン酸モノビニルエステル、アリルホスホン酸、リン酸モノアリルエステル、3−ブテニルホスホン酸、リン酸(モノ−3−ブテニル)エステル、リン酸モノ(4−ビニルオキシブチル)エステル、リン酸モノ(2−ヒドロキシ−3−ビニルオキシプロピル)エステル、リン酸モノ(1−ホスホノオキシメチル−2−ビニルオキシエチル)エステル、リン酸モノ(3−アリルオキシ−2−ヒドロキシプロピル)エステル、リン酸モノ−2−(アリルオキシ−1−ホスホノオキシメチルエチル)エステル、2−ヒドロキシ−4−ビニルオキシメチル−1,3,2−ジオキサホスホール、2−ヒドロキシ−4−アリルオキシメチル−1,3,2−ジオキサホスホールおよびそれらの塩からなる群から選択される、リン酸基またはホスホン酸基を有する少なくとも1種のモノマーを含む、請求項8記載の組成物。
- 前記ポリマー中に、モノマーの総量を基準として、前記一般式(I)の不飽和化合物5〜99.9重量%が含まれている、請求項1から9までのいずれか1項記載の組成物。
- 前記ポリマー中に、それぞれモノマーの総量を基準として、前記一般式(I)の不飽和化合物5〜99.9重量%と、更なるモノエチレン性不飽和モノマー95〜0.1重量%とが含まれている、請求項1から9までのいずれか1項記載の組成物。
- 前記硫酸カルシウムをベースとするバインダーが、α型半水和物、α/β型半水和物、β型半水和物、天然硬石膏、合成硬石膏、排煙脱硫から得られる硬石膏および/またはそれらの2種以上の混合物である、請求項1から11までのいずれか1項記載の組成物。
- 前記組成物が、乾燥質量を基準として、A)硫酸カルシウムをベースとする少なくとも1種のバインダー少なくとも10重量%と、B)少なくとも1種のポリマー0.005〜5重量%とを含む、請求項1から12までのいずれか1項記載の組成物。
- 請求項1から13までのいずれか1項記載の組成物の硬化によって製造された成形体。
- 前記成形体が、石膏プラスターボード、石膏ウォールボード、スクリードまたはナイフフィラーである、請求項14記載の成形体。
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