NO137191B - CEMENT PRODUCTS. - Google Patents
CEMENT PRODUCTS. Download PDFInfo
- Publication number
- NO137191B NO137191B NO161769A NO161769A NO137191B NO 137191 B NO137191 B NO 137191B NO 161769 A NO161769 A NO 161769A NO 161769 A NO161769 A NO 161769A NO 137191 B NO137191 B NO 137191B
- Authority
- NO
- Norway
- Prior art keywords
- parts
- cement
- product
- organic polyisocyanate
- cement products
- Prior art date
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- 239000004568 cement Substances 0.000 title claims description 21
- 239000005056 polyisocyanate Substances 0.000 claims description 13
- 229920001228 polyisocyanate Polymers 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 6
- 235000012239 silicon dioxide Nutrition 0.000 claims description 6
- 239000011396 hydraulic cement Substances 0.000 claims description 5
- 229920005862 polyol Polymers 0.000 claims description 5
- 150000003077 polyols Chemical class 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 2
- 235000011089 carbon dioxide Nutrition 0.000 claims description 2
- 239000000306 component Substances 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 42
- 239000000047 product Substances 0.000 description 30
- 239000000203 mixture Substances 0.000 description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000004576 sand Substances 0.000 description 6
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 5
- 150000002513 isocyanates Chemical class 0.000 description 5
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 5
- 239000011398 Portland cement Substances 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 3
- 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 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000010440 gypsum Substances 0.000 description 3
- 229910052602 gypsum Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- KOKPBCHLPVDQTK-UHFFFAOYSA-N 4-methoxy-4-methylpentan-2-one Chemical compound COC(C)(C)CC(C)=O KOKPBCHLPVDQTK-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- AGWMJKGGLUJAPB-UHFFFAOYSA-N aluminum;dicalcium;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Ca+2].[Ca+2].[Fe+3] AGWMJKGGLUJAPB-UHFFFAOYSA-N 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- 235000012241 calcium silicate Nutrition 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- JHLNERQLKQQLRZ-UHFFFAOYSA-N calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 2
- 239000001175 calcium sulphate Substances 0.000 description 2
- 235000011132 calcium sulphate Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- HOOWDPSAHIOHCC-UHFFFAOYSA-N dialuminum tricalcium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[Al+3].[Al+3].[Ca++].[Ca++].[Ca++] HOOWDPSAHIOHCC-UHFFFAOYSA-N 0.000 description 2
- BCAARMUWIRURQS-UHFFFAOYSA-N dicalcium;oxocalcium;silicate Chemical compound [Ca+2].[Ca+2].[Ca]=O.[O-][Si]([O-])([O-])[O-] BCAARMUWIRURQS-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 235000019976 tricalcium silicate Nutrition 0.000 description 2
- 229910021534 tricalcium silicate Inorganic materials 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- MXHKJQTYOAFPBY-UHFFFAOYSA-N 2-(2,3-dihydroxypropoxycarbonyl)benzoic acid Chemical class OCC(O)COC(=O)C1=CC=CC=C1C(O)=O MXHKJQTYOAFPBY-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000011400 blast furnace cement Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 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
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000011381 foam concrete Substances 0.000 description 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 239000011431 lime mortar Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011404 masonry cement Substances 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- 239000011412 natural cement Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011271 tar pitch Substances 0.000 description 1
Classifications
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
- C08G18/6476—Bituminous materials, e.g. asphalt, coal tar, pitch; derivatives thereof
-
- 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
- C04B24/24—Macromolecular compounds
- C04B24/28—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/282—Polyurethanes; Polyisocyanates
-
- 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
-
- 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
- C04B28/28—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 organic polyacids, e.g. polycarboxylate cements, i.e. ionomeric systems
-
- 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
- C08G18/08—Processes
- C08G18/088—Removal of water or carbon dioxide from the reaction mixture or reaction components
- C08G18/0885—Removal of water or carbon dioxide from the reaction mixture or reaction components using additives, e.g. absorbing agents
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/302—Water
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/36—Hydroxylated esters of higher fatty acids
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/54—Polycondensates of aldehydes
- C08G18/542—Polycondensates of aldehydes with phenols
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
-
- 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
- C04B2111/60—Flooring materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Civil Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Saccharide Compounds (AREA)
Description
Foreliggende oppfinnelse vedrører nye sementprodukter The present invention relates to new cement products
som f.eks. er egnet til gulv. like for example. is suitable for floors.
Det har vist seg at hurtig-herdende sementblandinger kan oppnås ved å tilsette organiske polyisocyanatmaterialer til vanlige hydrauliske sement/sand/vann-blandinger. Disse blandinger kan være oppskummede eller i alt vesentlig ikke-oppskummede produkter. It has been found that rapid-hardening cement mixtures can be obtained by adding organic polyisocyanate materials to ordinary hydraulic cement/sand/water mixtures. These mixtures can be foamed or substantially non-foamed products.
I henhold til foreliggende oppfinnelse tilveiebringes således sementprodukter fremstilt ved at en hydraulisk sement, According to the present invention, cement products produced by a hydraulic cement,
et kiselsyreholdig fyllstoff, vann og komponenter inneholdende et organisk polyisocyanat og eventuelt oppløsningsmidler eller fortynningsmidler blandes sammen og får herde. Produktene karakteriseres ved at komponentene inneholdende organisk polyisocyanat omfatter et organisk polyisocyanat og en polyol, idet det organiske polyisocyanat er til stede i en mengde som er tilstrekkelig til å tilveiebringe et overskudd av isocyanatgrupper i forhold til hydroksylgruppene i polyolene. a silicic acid-containing filler, water and components containing an organic polyisocyanate and possibly solvents or diluents are mixed together and allowed to harden. The products are characterized in that the components containing organic polyisocyanate comprise an organic polyisocyanate and a polyol, the organic polyisocyanate being present in an amount sufficient to provide an excess of isocyanate groups in relation to the hydroxyl groups in the polyols.
Uttrykket "hydraulisk sement" som her anvendes, skal The term "hydraulic cement" used here shall
forstås å omfatte den klasse av bygningsmaterialer som anvendes i blanding med vann og derefter herder som følge av fysiske eller is understood to include the class of building materials that are used in a mixture with water and then harden as a result of physical or
kjemiske endringer som forbruker det tilstedeværende vann. Foruten vanlig Portland-sement omfatter slike hydrauliske sementer følgende stoffer: 1. Hurtigherdende sementer som er karakterisert med høye aluminiumoksydinnhold. 2. Lav-varme-sementer som er karakterisert ved høye prosent-innhold av dikalsiumsilikat og tetrakalsiumaluminoferritt og.lave prosentmengder av trikalsiumsilikat og trikalsiumaluminat. 3. Sulfatmotstandsdyktige sementer som er karakterisert ved usedvanlig høye prosentmengder av trikalsiumsilikat og dikalsiumsilikat og usedvanlig lave prosentmengder av trikalsiumaluminat og tetrakalsiumaluminoferritt. 4. Portland-masovnsement som er karakterisert ved en blanding av Portland-sementklinkere og granulert slagg. 5. Murverkssementer som er karakterisert ved blandinger av Portland-sement og et eller flere av følgende stoffer: hydrati-sert kalk, granulert slagg, pulverisert kalksten, kolloidal leire, diatomejord eller andre findelte former for kiselsyre, kalsiumstea-rat og parafin. 6. Naturlige sementer som er karakterisert ved materiale som fåes fra avleiringer i Lehigh Valley, U.S-A. 7. Kalksementer som er karakterisert ved kalsiumoksyd i ren form eller uren form og hva enten det inneholder eller ikke noe leir-aktig materiale. 8. Gipssement som er karakterisert ved tilsetning av 5-10 % brent gips til kalk. 9. Pussolansement som er karakterisert ved en blanding av pussolanjord, trass-kiselgur, pimpesten, tuffsten, santorinjord eller granulert slagg med kalkmørtel. 10. Kalsiumsulfatsementer som er karakterisert ved slike som er basert på hydratisering av kalsiumsulfat og omfatter gips, Keene's sement og Parian-sement. chemical changes that consume the water present. In addition to ordinary Portland cement, such hydraulic cements include the following substances: 1. Quick-hardening cements that are characterized by high aluminum oxide contents. 2. Low-heat cements which are characterized by high percentages of dicalcium silicate and tetracalcium aluminoferrite and low percentages of tricalcium silicate and tricalcium aluminate. 3. Sulfate-resistant cements which are characterized by exceptionally high percentages of tricalcium silicate and dicalcium silicate and exceptionally low percentages of tricalcium aluminate and tetracalcium aluminoferrite. 4. Portland blast furnace cement which is characterized by a mixture of Portland cement clinkers and granulated slag. 5. Masonry cements which are characterized by mixtures of Portland cement and one or more of the following substances: hydrated lime, granulated slag, powdered limestone, colloidal clay, diatomaceous earth or other finely divided forms of silicic acid, calcium stearate and paraffin. 6. Natural cements characterized by material obtained from deposits in the Lehigh Valley, U.S.A. 7. Lime cements which are characterized by calcium oxide in pure form or impure form and whether or not it contains any clay-like material. 8. Gypsum cement which is characterized by the addition of 5-10% burnt gypsum to lime. 9. Pussolan cement which is characterized by a mixture of puzzolan soil, trass diatomaceous earth, pumice stone, tuff stone, santorini soil or granulated slag with lime mortar. 10. Calcium sulphate cements which are characterized by those based on the hydration of calcium sulphate and include gypsum, Keene's cement and Parian cement.
Som kiselsyreholdige fyllstoffer som kan anvendes skal nevnes sand og kiselsyreprodukter med lavt leireinnhold, fortrinns-vis vasket og som har en partikkelstørrelse som i det vesentlige er innenfor området 3,8 cm-200 B.S.siktstørreIse. Størrelser uten-for disse grenser kan imidlertid anvendes for spesielle formål. Silicic acid-containing fillers that can be used include sand and silicic acid products with a low clay content, preferably washed and which have a particle size that is essentially within the range of 3.8 cm-200 B.S. dry ice. Sizes outside these limits can, however, be used for special purposes.
Som organiske polyisocyanater som kan anvendes skal nev- As organic polyisocyanates that can be used, nev-
nes tolylendiisocyanat og difenylmetandiisocyanat, også uretedion eller isocyanuratpolymerer iav disse, og polyuretaner med isocyanat- nes tolylene diisocyanate and diphenylmethane diisocyanate, also uretedione or isocyanurate polymers of these, and polyurethanes with isocyanate
grupper i endestilling erholdt ved reaksjon av et overskudd av et organisk diisocyanat med en polyfunksjonell isocyanat-reaktiv forbindelse, som f.eks. en glykol eller en høyere flerverdig alko-hol, aminoalkohol eller polyamin, en polyester, polyesteramid eller polyeter. groups in the terminal position obtained by reaction of an excess of an organic diisocyanate with a polyfunctional isocyanate-reactive compound, such as e.g. a glycol or a higher polyhydric alcohol, amino alcohol or polyamine, a polyester, polyesteramide or polyether.
Det er å foretrekke også å tilsette en isocyanat-reaktiv organisk forbindelse til produktene ifølge oppfinnelsen, for-trinnsvis en toverdig eller treverdig polyeter med en ekvivalentvekt av 100 till500, men flerverdige alkoholer, aminoalkoholer, polyaminer, polyestere og polyesteramider kan også anvendes. Oppløsningsmidler og fortynningsmidler kan også tilsettes. It is preferable to also add an isocyanate-reactive organic compound to the products according to the invention, preferably a divalent or trivalent polyether with an equivalent weight of 100 to 500, but polyhydric alcohols, amino alcohols, polyamines, polyesters and polyester amides can also be used. Solvents and diluents may also be added.
Produktene kan alt efter sin fluiditet før herdnina anvendes som selv-utjevnende gulvbelegg eller gulvbelegg som må glattes eller utjevnes ved hjelp av en murskje, og produktene er langt bedre enn vanlige sementgulvbelegg eller andre kjente harpiks-sammenbundne sementgulvbeleggprodukter, som følge av sin herdningshastighet. Ved hjelp av oppfinnelsen er det mulig å fremstille gulv eller gulvbelegg som er tilstrekkelig stabile til å gå på innen 1 time etter fremstillingen og som motstår fall-vektslagprøve av DEF 1083, metode 17 efter bare 24 timers herdning. Depending on their fluidity before hardening, the products can be used as self-leveling floor coverings or floor coverings that must be smoothed or leveled with a trowel, and the products are far better than ordinary cement floor coverings or other known resin-bonded cement floor covering products, as a result of their curing speed. With the help of the invention, it is possible to produce floors or floor coverings which are sufficiently stable to be walked on within 1 hour of production and which withstand the drop-weight impact test of DEF 1083, method 17 after only 24 hours of curing.
Oppfinnelsen skal klargjøres ved de følgende eksempler hvor deler er basert på vekt. The invention shall be clarified by the following examples where parts are based on weight.
Eksempel 1 Example 1
100 deler Portland-sement og 100 deler av en 70 %'s opp-løsning av et polyisocyanat (erholdt som beskrevet nedenfor) blandes sammen og deretter innblandes 100 deler sand av 30-200 B.S.-siktstørrelse, 25 deler vann og 10 deler av en oksypropylert glycerol med et hydroksyltall av 535 mg KOH/g. 100 parts of Portland cement and 100 parts of a 70% solution of a polyisocyanate (obtained as described below) are mixed together and then mixed with 100 parts of sand of 30-200 B.S. sieve size, 25 parts of water and 10 parts of a oxypropylated glycerol with a hydroxyl number of 535 mg KOH/g.
Det fåes et hurtig-herdende flytende produkt som når det utspres i et lag av en tykkelse av ca. 1,3 cm, stivner hurtig og er tilstrekkelig fast til at man kan gå på det efter 2-2% time. A fast-hardening liquid product is obtained which, when spread in a layer with a thickness of approx. 1.3 cm, hardens quickly and is sufficiently firm that you can walk on it after 2-2% hours.
Polyisocyanatet som anvendes kan fåes ved å opphete en blanding av tolylendiisocyanat (1 mol), trimetylolpropan (.0,197 mol) og butylenglykol (0,159 mol) i 2 timer: ved 60°C i nærvær av halvparten av den samlede vekt av en lrlELanding.av 6-etoksyetyl-acetat og xylen. 0,029 mol av en oksypropylert glycerol med molekylvekt 3000 tilsettes og opphetningen fortsettes i 4 timer ved 60°C. Tilstrekkelig xylen tilsettes derpå for å gi oppløsningen et innhold av faste stoffer av 70 %. The polyisocyanate used can be obtained by heating a mixture of tolylene diisocyanate (1 mol), trimethylolpropane (.0.197 mol) and butylene glycol (0.159 mol) for 2 hours: at 60°C in the presence of half the total weight of a lrlELanding.of 6-ethoxyethyl acetate and xylene. 0.029 mol of an oxypropylated glycerol with a molecular weight of 3000 is added and the heating is continued for 4 hours at 60°C. Sufficient xylene is then added to give the solution a solids content of 70%.
Eksempel 2 Example 2
Hvis den oksypropylerte glycerol som ble anvendt i eksempel 1 (avsnitt 1) erstattes med 10 deler av et oksypropylert trietanolamin av molekylvekt 320, så fåes det ennu hurtigere herdende produkter. If the oxypropylated glycerol that was used in example 1 (section 1) is replaced with 10 parts of an oxypropylated triethanolamine of molecular weight 320, even faster curing products are obtained.
Dette produkt er tilstrekkelig hårdt til at man kan gå på det etter 1 time etter utspredningen. This product is sufficiently hard to walk on after 1 hour of spreading.
Eksempel 3 Example 3
gir et produkt som man kan gå på 1 time etter utspredningen. gives a product that can be walked on 1 hour after spreading.
Isocyanatet som anvendes er det produkt som fåes ved å la reagere 1 mol tolylendiisocyanat, 0,22 mol glycerol og 0,18 mol dietylenglykol i en tredjedel av den samlede vekt av etylacetat ved 75-80°C i 3 timer. The isocyanate used is the product obtained by reacting 1 mol of tolylene diisocyanate, 0.22 mol of glycerol and 0.18 mol of diethylene glycol in one third of the total weight of ethyl acetate at 75-80°C for 3 hours.
Eksempel 4 Example 4
Hvis isocyanatet. som ble anvendt i eksempel 3 erstattes med 60 deler av det produkt som fåes ved å la kulltjærebek som inneholder 2 vektprosent av hydroksylgrupper (eller deres ekvivalent av isocyanat-reaktive grupper) reagere med difenylmetandiisocyanat (6,5 ekvivalenter) som en 85 %'s oppløsning i 2-metyl-2-metoksy-pentan-4-on ved 90°C i 4 timer, så kan man gå på det resulterende produkt 1 time etter utspredningen. If the isocyanate. which was used in Example 3 is replaced by 60 parts of the product obtained by reacting coal tar pitch containing 2% by weight of hydroxyl groups (or their equivalent of isocyanate-reactive groups) with diphenylmethane diisocyanate (6.5 equivalents) as an 85% solution in 2-methyl-2-methoxy-pentan-4-one at 90°C for 4 hours, then you can walk on the resulting product 1 hour after spreading.
Eksempel 5 Example 5
Dette produkt kan man gå på 1 time etter utspredningen. This product can be used 1 hour after spreading.
Eksempel 6 ~ Example 6 ~
Dette produkt kan man gå på ca. 30 minutter etter utspredningen. This product can be used for approx. 30 minutes after the spread.
Eksempel 7 Example 7
Hvis tolylendiisocyanatet som ble anvendt i eksempel 6 erstattes med 200 deler av den følgende blanding, så fåes det et lignende hurtig-herdende produkt. If the tolylene diisocyanate used in example 6 is replaced by 200 parts of the following mixture, a similar fast-hardening product is obtained.
Et polyetylen/propylen (7r3)adipat av molekylvekt ca. 1000 kondenseres med 1,43 ekvivalenter av tolylendiisocyanat og det resulterende produkt (1 del) blandes med 1 del av en isocya-nuratpolymer av tolylendiisocyanat av NCO-verdi 14,8 % i 0,5 deler av 2-metyl-2-metoksy-pentan-4-on og 1,5 deler butylacetat. A polyethylene/propylene (7r3) adipate of molecular weight approx. 1000 is condensed with 1.43 equivalents of tolylene diisocyanate and the resulting product (1 part) is mixed with 1 part of an isocyanurate polymer of tolylene diisocyanate of NCO value 14.8% in 0.5 parts of 2-methyl-2-methoxy- pentan-4-one and 1.5 parts of butyl acetate.
Eksempel 8 Example 8
2 vektdeler av sement blandes inn i 100 deler av polyisocyanatet som ble anvendt i eksempel 1, og til denne blanding tilsettes under ytterligere sammenblanding 198 deler sand, 25 deler vann og 10 deler oksypropylert glycerol med OH-verdi 535 2 parts by weight of cement are mixed into 100 parts of the polyisocyanate that was used in example 1, and to this mixture are added, during further mixing, 198 parts of sand, 25 parts of water and 10 parts of oxypropylated glycerol with an OH value of 535
mg KOH/g. mg KOH/g.
Det fåes et uretansammenbundet oppskummet betongprodukt som er tilstrekkelig hårdt til at man kan gå på det etter ca. 5-6 timer. A urethane-bonded foamed concrete product is obtained that is sufficiently hard to walk on after approx. 5-6 hours.
Eksempel 9 Example 9
100 vektdeler sement blandes inn i 43 deler av en 75 %'s oppløsning i etylglykolacetat/xylen (lii) av et reaksjonsprodukt av heksametylendiisocyanat, og vann og med et isocyanatinnhold av ca. 16 %. Til denne blanding tilsettes under videre omrøring 100 deler sand, 20 deler vann og 10 deler oksypropylert glycerol med OH-tall 535 mg KOH/g. Det fåes et hurtigtørkende uretansammenbundet betongprodukt som er tilstrekkelig hårdt til at man kan gå på det etter 1-1% time. 100 parts by weight of cement are mixed into 43 parts of a 75% solution in ethyl glycol acetate/xylene (lii) of a reaction product of hexamethylene diisocyanate, and water and with an isocyanate content of approx. 16%. 100 parts of sand, 20 parts of water and 10 parts of oxypropylated glycerol with an OH number of 535 mg KOH/g are added to this mixture with further stirring. A fast-drying urethane-bonded concrete product is obtained which is sufficiently hard to walk on after 1-1% hours.
Eksempel 10 Example 10
100 deler sement blandes inn i 50 deler av en 75 %'s opp- 100 parts of cement are mixed into 50 parts of a 75%
løsning i etylglykolacetat/xylen (1:1) av et reaksjonsprodukt av heksametylendiisocyanat, trimetylolpropan og 1:3 butandiol med et isocyanatinnhold av ca. 12 %. Til denne blanding tilsettes under ytterligere sammenblanding 100 deler sand, 25 deler vann og 10 deler oksypropylert glycerol med et OH-tall av 535 mg KOH/g. Det fåes et hurtigtørkende uretansammenbundet betongprodukt som er tilstrekkelig hårdt til at man kan gå på det etter l-l%time. solution in ethyl glycol acetate/xylene (1:1) of a reaction product of hexamethylene diisocyanate, trimethylolpropane and 1:3 butanediol with an isocyanate content of approx. 12%. 100 parts of sand, 25 parts of water and 10 parts of oxypropylated glycerol with an OH number of 535 mg KOH/g are added to this mixture during further mixing. A quick-drying urethane-bonded concrete product is obtained which is sufficiently hard to walk on after 1-1% hours.
Eksempel 11 Example 11
Hvis den oksypropylerte glycerol som ble anvendt i eksempel 1 erstattes med 30 deler av en polyester som fåes ved å kon-densere sammen 1,3-butylenglykol, heksantriol og adipinsyre i mol-forholdet 3:lt3 og med et syretall under 3 mg KOH/g, så fåes det et selv-utjevnende produkt som herder i løpet av ca. 1 time. If the oxypropylated glycerol used in example 1 is replaced with 30 parts of a polyester obtained by condensing together 1,3-butylene glycol, hexanetriol and adipic acid in the molar ratio 3:lt3 and with an acid number below 3 mg KOH/ g, then a self-leveling product is obtained which hardens within approx. 1 hour.
Eksempel 12 Example 12
Hvis den oksypropylerte glycerol som ble anvendt i eksempel 1 erstattes med 30 deler av en oppløsning av et polyesteramid-polyuretan-kondenseringsprodukt fremstilt som beskrevet nedenfor, så fåes et produkt som krever utspredning og somherder i løpet av 30-60 minutter. If the oxypropylated glycerol used in example 1 is replaced with 30 parts of a solution of a polyesteramide-polyurethane condensation product prepared as described below, a product is obtained which requires spreading and which hardens within 30-60 minutes.
Oppløsningen av polyesteramid/polyuretan-kondenserings-produktet som anvendes i dette eksempel fremstilles ved følgende fremgangsmåte r The solution of the polyesteramide/polyurethane condensation product used in this example is prepared by the following method r
Et polyesteramid fremstilles ved å opphete en blanding A polyester amide is prepared by heating a mixture
av 4330 deler adipinsyre, 1820 deler etylenglykol, 177 deler dietylenglykol og 113 deler monoetanolamin ved 240°C, under tilbakeløp inntil det fåes et syretall av 2,0 til 3,0 mg KOH/g og produktet har en molekylvekt av 1850. of 4330 parts adipic acid, 1820 parts ethylene glycol, 177 parts diethylene glycol and 113 parts monoethanolamine at 240°C, under reflux until an acid number of 2.0 to 3.0 mg KOH/g is obtained and the product has a molecular weight of 1850.
En blanding av 1533 deler av det ovennevnte polyesteramid, 2108 deler metyletylketon, 2,08 deler vann, 10,75 deler etylenglykol, 0,77 deler dimetylaminopyridin og 188,5 deler av en 80r20-blanding av 2,4- og 2,6-tolylendiisocyanater omrøres ved 57 til 63°C inntil viskositeten av en prøve målt ved 25°C når en verdi mellom 100 og 140 poise. 13,5 deler metanol tilsettes derpå og blandingen omrøres ved samme temperatur i 3 timer. 0,38 deler salicylsyre tilsettes derpå og blandingen omrøres ved samme temperatur i 1 time og avkjøles derpå. Polyesteramid-polyuretanoppløs-ningen som man får på denne måte er da ferdig for bruk. A mixture of 1533 parts of the above polyesteramide, 2108 parts of methyl ethyl ketone, 2.08 parts of water, 10.75 parts of ethylene glycol, 0.77 parts of dimethylaminopyridine and 188.5 parts of an 80r20 mixture of 2.4- and 2.6 -tolylene diisocyanates are stirred at 57 to 63°C until the viscosity of a sample measured at 25°C reaches a value between 100 and 140 poise. 13.5 parts of methanol are then added and the mixture is stirred at the same temperature for 3 hours. 0.38 parts of salicylic acid are then added and the mixture is stirred at the same temperature for 1 hour and then cooled. The polyesteramide-polyurethane solution obtained in this way is then ready for use.
Mengden av vann som er angitt, er den totalt tilstedeværende, idet den faktiske mengde som tilsettes beregnes under hensyn-tagen til små mengder som er tilstede i oppløsningsmidlet. The amount of water indicated is the total amount present, as the actual amount added is calculated taking into account small amounts present in the solvent.
Eksempel 13 Example 13
Hvis den oksypropylerte glycerol som anvendes i eksempel If the oxypropylated glycerol used in example
1 erstattes med 30 deler av en 50 vekt/vekt-prosents oppløsning i xylen av et dehydratisert risinusolje-modifisert glycerylftalathar-piks (et ikke-tørkende alkydharpiks) så fåes et meget tykt produkt som krever utspredning, men som herder i løpet av ca. 30 minutter. 1 is replaced with 30 parts of a 50 wt/wt percent solution in xylene of a dehydrated castor oil-modified glyceryl phthalate tar pitch (a non-drying alkyd resin), then a very thick product is obtained which requires spreading, but which hardens within approx. 30 minutes.
Eksempel 14 Example 14
Hvis den oksypropylerte glycerol som anvendes i eksempel If the oxypropylated glycerol used in example
1 erstattes med 30 deler av en 50 vekt/vekt-prosents oppløsning i toluen av et reaksjonsprodukt fra opphetning av glycerol, palme-kjerneoljefettsyrer, jordnøttoljefettsyrer, stearinsyre og ftal-syreanhydrid (en tørkende alkydharpiks) så fåes et meget tykt produkt som krever utspredning, men som herder i løpet av ca. 30 minutter. 1 is replaced by 30 parts of a 50 wt/wt percent solution in toluene of a reaction product from heating glycerol, palm kernel oil fatty acids, peanut oil fatty acids, stearic acid and phthalic anhydride (a drying alkyd resin), then a very thick product is obtained which requires spreading, but which hardens within approx. 30 minutes.
Eksempel 15 Example 15
Hvis den oksypropylerte glycerol som anvendes i eksempel If the oxypropylated glycerol used in example
1 erstattes med 42 deler av en 50 vekt/vekt-prosents oppløsning i metyletylketon av en polyeterharpiks erholdt ved reaksjon av dife-nylolpropan med epiklorhydrin slik at det resulterende produkt har et hydroksyltall av ca. 130 mg KOH/g, så fåes et produkt som er lett hellbart og selv-utjevnende, og som herder tilstrekkelig hårdt til at man kan gå på det etter 5-6 timer. 1 is replaced by 42 parts of a 50% by weight solution in methyl ethyl ketone of a polyether resin obtained by reaction of diphenylolpropane with epichlorohydrin so that the resulting product has a hydroxyl number of approx. 130 mg KOH/g, then a product is obtained which is easy to pour and self-levelling, and which hardens sufficiently hard to be walked on after 5-6 hours.
Eksempel 16 Example 16
gir et selv-utjevnende produkt som herder i løpet av ca. 1 time. provides a self-leveling product that hardens within approx. 1 hour.
Difenylmetandiisocyanat-forpolymeroppløsningen som anvendes i dette eksempel, fåes på følgende måte: 100 deler oksypropylert glycerol med molekylvekt ca. 1000 (hydroksyltall 165 mg KOH/g) blandes med 25 deler av en opp-løsningsmiddelblanding bestående av 70 vektprosent tørr cykloheksa-non og 30 vektprosent xylen. 205 deler av et kommersielt tilgjen-gelig 4,4'-diisocyanat-difenylmetan med et NCO-innhold av 30,0 %, oppløses i ytterligere 50 deler av oppløsningsmiddelblandingen og de to oppløsninger blandes og lagres i en tørr, lukket beholder i 3 dager, hvorefter forpolymeren er ferdig til bruk. The diphenylmethane diisocyanate prepolymer solution used in this example is obtained in the following way: 100 parts of oxypropylated glycerol with a molecular weight of approx. 1000 (hydroxyl number 165 mg KOH/g) is mixed with 25 parts of a solvent mixture consisting of 70 weight percent dry cyclohexanone and 30 weight percent xylene. 205 parts of a commercially available 4,4'-diisocyanate-diphenylmethane with an NCO content of 30.0%, is dissolved in a further 50 parts of the solvent mixture and the two solutions are mixed and stored in a dry, closed container for 3 days, after which the prepolymer is ready for use.
Claims (3)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GB2262468A GB1192864A (en) | 1968-05-13 | 1968-05-13 | New Cement Compositions |
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Publication Number | Publication Date |
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NO137191B true NO137191B (en) | 1977-10-10 |
NO137191C NO137191C (en) | 1978-01-18 |
Family
ID=10182455
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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NO161769A NO137191C (en) | 1968-05-13 | 1969-04-18 | CEMENT PRODUCTS. |
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BE (1) | BE732602A (en) |
BR (1) | BR6908756D0 (en) |
CA (1) | CA944369A (en) |
DK (1) | DK143225C (en) |
ES (1) | ES367121A1 (en) |
FI (1) | FI54593C (en) |
FR (1) | FR2008417A1 (en) |
GB (1) | GB1192864A (en) |
NL (1) | NL167942C (en) |
NO (1) | NO137191C (en) |
PL (1) | PL79568B1 (en) |
SE (1) | SE415350B (en) |
Families Citing this family (20)
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US4211680A (en) * | 1968-05-13 | 1980-07-08 | Imperial Chemical Industries Limited | Quick-set compositions of hydraulic cement, silica, water, polyisocyanate and polyol |
US4127548A (en) | 1970-03-18 | 1978-11-28 | Imperial Chemical Industries Limited | Cement compositions |
US4273908A (en) * | 1979-05-07 | 1981-06-16 | Blount David H | Process for the production of poly (polyisocyanate-polyol-alkali metal silicate solid |
USRE31340E (en) * | 1970-09-11 | 1983-08-09 | Process for the production of poly (polyisocyanate-polyol-alkali metal silicate) solid | |
US3772051A (en) * | 1971-07-29 | 1973-11-13 | Ici Ltd | Decorative flooring surfaces |
US3951885A (en) * | 1971-11-01 | 1976-04-20 | Thompson Chemicals, Inc. | Method of making magnesium oxychloride cement cofoamed with synthetic resin |
DE2310559C3 (en) * | 1973-03-02 | 1975-09-11 | Bayer Ag, 5090 Leverkusen | Foam concrete, a process for its manufacture and its use for the manufacture of building elements |
AU1562276A (en) * | 1975-08-07 | 1978-01-12 | Ici Ltd | Quick setting compositions |
NO762677L (en) * | 1975-08-29 | 1977-03-01 | Ici Ltd | |
DE2546181B2 (en) * | 1975-10-15 | 1979-03-08 | Hoechst Ag, 6000 Frankfurt | Process for the production of gypsum foam and structural elements made therefrom |
DE2743884A1 (en) * | 1977-09-29 | 1979-04-12 | Bischofsheim Chemie Anlagen | PROCESS FOR MANUFACTURING FOAMED OR NON-FOAMED MASSES |
DE2756399A1 (en) * | 1977-12-17 | 1979-06-28 | Basf Ag | METHOD FOR MANUFACTURING COMPOSITE BODIES |
DE2842582A1 (en) * | 1978-09-29 | 1980-08-21 | Bischofsheim Chemie Anlagen | METHOD FOR PRODUCING FOAMED OR UNFOAMED MASSES |
GB2127838B (en) * | 1982-10-01 | 1986-03-19 | Mohamed Mohamed Abdul Metikes | A moulding compostion |
DE3414807A1 (en) * | 1984-04-19 | 1985-10-31 | Bayer Ag, 5090 Leverkusen | METHOD FOR PRODUCING CHEMICAL-RESISTANT COATINGS OF SURFACES |
JPH0678520B2 (en) * | 1986-04-08 | 1994-10-05 | 清水建設株式会社 | Water stop method for concrete structure |
JPH0755851B2 (en) * | 1987-02-20 | 1995-06-14 | 宇部興産株式会社 | High-strength cement hardened body and method for producing the same |
DE19654429A1 (en) * | 1996-12-24 | 1998-06-25 | Bayer Ag | Water-dispersible polyisocyanate mixtures as additives for concrete |
US8083851B2 (en) | 2006-12-29 | 2011-12-27 | Sciessent Llc | Antimicrobial cements and cementitious compositions |
CN113396133B (en) * | 2019-02-12 | 2023-09-22 | Sika技术股份公司 | Multicomponent composition for producing polyurethane/urea cement mixed systems |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2902388A (en) * | 1957-06-27 | 1959-09-01 | Allied Chem | Hydraulic cement-polyurethane compositions useful for coating, sealing, patching, and surfacing |
GB893273A (en) * | 1957-08-28 | 1962-04-04 | Dunlop Rubber Co | Improvements relating to articles comprising solid reaction products derived from organic isocyanates and the like |
BE638157A (en) * | 1961-11-13 | 1900-01-01 | ||
US3354099A (en) * | 1964-03-10 | 1967-11-21 | Frederick C Stegeman | Polyurethane-hydraulic cement compositions and process for manufacturing the same |
FR1486644A (en) * | 1966-07-13 | 1967-06-30 | thermally insulating construction element for the building |
-
1968
- 1968-05-13 GB GB2262468A patent/GB1192864A/en not_active Expired
-
1969
- 1969-04-17 PL PL13301869A patent/PL79568B1/en unknown
- 1969-04-18 NO NO161769A patent/NO137191C/en unknown
- 1969-04-30 CA CA050,209A patent/CA944369A/en not_active Expired
- 1969-05-06 BE BE732602A patent/BE732602A/xx not_active IP Right Cessation
- 1969-05-06 DK DK247569A patent/DK143225C/en not_active IP Right Cessation
- 1969-05-12 ES ES367121A patent/ES367121A1/en not_active Expired
- 1969-05-12 NL NL6907292A patent/NL167942C/en not_active IP Right Cessation
- 1969-05-12 SE SE6906686A patent/SE415350B/en unknown
- 1969-05-13 FR FR6915475A patent/FR2008417A1/en active Pending
- 1969-05-13 FI FI141069A patent/FI54593C/en active
- 1969-05-13 BR BR20875669A patent/BR6908756D0/en unknown
Also Published As
Publication number | Publication date |
---|---|
BE732602A (en) | 1969-11-06 |
FI54593B (en) | 1978-09-29 |
NL6907292A (en) | 1969-11-17 |
SE415350B (en) | 1980-09-29 |
SU430539A3 (en) | 1974-05-30 |
NO137191C (en) | 1978-01-18 |
GB1192864A (en) | 1970-05-20 |
FI54593C (en) | 1979-01-10 |
NL167942B (en) | 1981-09-16 |
CA944369A (en) | 1974-03-26 |
DK143225B (en) | 1981-07-27 |
BR6908756D0 (en) | 1973-05-03 |
DE1924468A1 (en) | 1970-08-27 |
ES367121A1 (en) | 1971-04-01 |
DK143225C (en) | 1981-11-30 |
PL79568B1 (en) | 1975-06-30 |
NL167942C (en) | 1982-02-16 |
FR2008417A1 (en) | 1970-01-23 |
DE1924468B2 (en) | 1975-10-23 |
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