CN106639236B - A kind of elastic brick for toilet floor and its making method - Google Patents
A kind of elastic brick for toilet floor and its making method Download PDFInfo
- Publication number
- CN106639236B CN106639236B CN201611065034.4A CN201611065034A CN106639236B CN 106639236 B CN106639236 B CN 106639236B CN 201611065034 A CN201611065034 A CN 201611065034A CN 106639236 B CN106639236 B CN 106639236B
- Authority
- CN
- China
- Prior art keywords
- parts
- powder
- weight
- modified
- mixed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000011449 brick Substances 0.000 title claims abstract description 65
- 238000000034 method Methods 0.000 title claims description 24
- 229920002635 polyurethane Polymers 0.000 claims abstract description 37
- 239000004814 polyurethane Substances 0.000 claims abstract description 37
- 239000000853 adhesive Substances 0.000 claims abstract description 3
- 230000001070 adhesive effect Effects 0.000 claims abstract description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 193
- 239000000843 powder Substances 0.000 claims description 106
- 239000000377 silicon dioxide Substances 0.000 claims description 99
- 239000003822 epoxy resin Substances 0.000 claims description 51
- 229920000647 polyepoxide Polymers 0.000 claims description 51
- 239000000203 mixture Substances 0.000 claims description 48
- 239000003607 modifier Substances 0.000 claims description 46
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 44
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 34
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 33
- -1 polypropylene Polymers 0.000 claims description 30
- 229910020648 KH550 Inorganic materials 0.000 claims description 29
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 claims description 29
- 229910001863 barium hydroxide Inorganic materials 0.000 claims description 29
- 238000002156 mixing Methods 0.000 claims description 29
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 28
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 24
- 229910052782 aluminium Inorganic materials 0.000 claims description 24
- 239000011521 glass Substances 0.000 claims description 23
- 229920001451 polypropylene glycol Polymers 0.000 claims description 22
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 21
- 230000008569 process Effects 0.000 claims description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 20
- 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 claims description 20
- 239000000945 filler Substances 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 20
- 239000001301 oxygen Substances 0.000 claims description 20
- 239000002808 molecular sieve Substances 0.000 claims description 18
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 18
- 229910052624 sepiolite Inorganic materials 0.000 claims description 17
- 235000019355 sepiolite Nutrition 0.000 claims description 17
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 238000005245 sintering Methods 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 13
- 229920000120 polyethyl acrylate Polymers 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 10
- 239000002699 waste material Substances 0.000 claims description 10
- 239000004743 Polypropylene Substances 0.000 claims description 9
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 9
- 229920001155 polypropylene Polymers 0.000 claims description 9
- 239000001632 sodium acetate Substances 0.000 claims description 9
- 235000017281 sodium acetate Nutrition 0.000 claims description 9
- 239000004927 clay Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 8
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 7
- 239000000292 calcium oxide Substances 0.000 claims description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 7
- 238000001914 filtration Methods 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 229910021487 silica fume Inorganic materials 0.000 claims description 7
- 239000003245 coal Substances 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- 230000003014 reinforcing effect Effects 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 5
- 239000004113 Sepiolite Substances 0.000 claims description 5
- 229920002472 Starch Polymers 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 5
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 5
- 239000003365 glass fiber Substances 0.000 claims description 5
- 239000008103 glucose Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 5
- 229910017604 nitric acid Inorganic materials 0.000 claims description 5
- 239000003921 oil Substances 0.000 claims description 5
- 239000008107 starch Substances 0.000 claims description 5
- 235000019698 starch Nutrition 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 238000007654 immersion Methods 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 239000004005 microsphere Substances 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 230000007423 decrease Effects 0.000 claims 1
- 239000011325 microbead Substances 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 239000002893 slag Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 16
- 238000002360 preparation method Methods 0.000 abstract description 13
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 11
- 230000006378 damage Effects 0.000 abstract description 4
- 208000027418 Wounds and injury Diseases 0.000 abstract description 3
- 208000014674 injury Diseases 0.000 abstract description 3
- 239000004615 ingredient Substances 0.000 description 42
- 235000019441 ethanol Nutrition 0.000 description 28
- 230000002708 enhancing effect Effects 0.000 description 27
- 239000000654 additive Substances 0.000 description 26
- 230000000996 additive effect Effects 0.000 description 26
- 239000004135 Bone phosphate Substances 0.000 description 24
- 235000012239 silicon dioxide Nutrition 0.000 description 23
- 238000003756 stirring Methods 0.000 description 16
- 239000003595 mist Substances 0.000 description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- 230000004048 modification Effects 0.000 description 10
- 238000012986 modification Methods 0.000 description 10
- 239000013078 crystal Substances 0.000 description 8
- 230000006837 decompression Effects 0.000 description 8
- 230000018044 dehydration Effects 0.000 description 8
- 238000006297 dehydration reaction Methods 0.000 description 8
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 239000011863 silicon-based powder Substances 0.000 description 8
- 239000011159 matrix material Substances 0.000 description 7
- 239000004844 aliphatic epoxy resin Substances 0.000 description 6
- 239000006004 Quartz sand Substances 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 229910052681 coesite Inorganic materials 0.000 description 5
- 229910052906 cristobalite Inorganic materials 0.000 description 5
- 229910052682 stishovite Inorganic materials 0.000 description 5
- 229910052905 tridymite Inorganic materials 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 229910052863 mullite Inorganic materials 0.000 description 4
- 125000003367 polycyclic group Chemical group 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000010257 thawing Methods 0.000 description 4
- 238000010792 warming Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 210000000085 cashmere Anatomy 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 229910001691 hercynite Chemical group 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 241000208340 Araliaceae Species 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 208000037656 Respiratory Sounds Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000011468 face brick Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F15/00—Flooring
- E04F15/02—Flooring or floor layers composed of a number of similar elements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/1305—Organic additives
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/131—Inorganic additives
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/132—Waste materials; Refuse; Residues
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/132—Waste materials; Refuse; Residues
- C04B33/135—Combustion residues, e.g. fly ash, incineration waste
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/132—Waste materials; Refuse; Residues
- C04B33/138—Waste materials; Refuse; Residues from metallurgical processes, e.g. slag, furnace dust, galvanic waste
-
- 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
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/16—Lean materials, e.g. grog, quartz
-
- 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
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4045—Mixtures of compounds of group C08G18/58 with other macromolecular compounds
-
- 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
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4812—Mixtures of polyetherdiols with polyetherpolyols having at least three hydroxy groups
-
- 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
- C08G18/48—Polyethers
- C08G18/4829—Polyethers containing at least three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/06—Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/28—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/02—Ingredients treated with inorganic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
- C08K9/06—Ingredients treated with organic substances with silicon-containing 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3215—Barium oxides or oxide-forming salts 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/44—Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
- C04B2235/442—Carbonates
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/48—Organic compounds becoming part of a ceramic after heat treatment, e.g. carbonising phenol resins
- C04B2235/483—Si-containing organic compounds, e.g. silicone resins, (poly)silanes, (poly)siloxanes or (poly)silazanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/60—Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Ceramic Engineering (AREA)
- Medicinal Chemistry (AREA)
- Structural Engineering (AREA)
- Dispersion Chemistry (AREA)
- Materials Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Inorganic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Road Paving Structures (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Floor Finish (AREA)
Abstract
Several bonding pits are distributed on the upper surface of brick body in a kind of elastic brick and preparation method thereof for accomodation ground, including brick body, and longitudal section of each bonding pit is isosceles trapezoid, and its width is gradually reduced from bottom to top;A strata urethane elastic layer is equipped on the upper surface of brick body, and the elastic polyurethane layer is filled into bonding pit, the surface of elastic polyurethane layer is plane, and has been densely covered with the arc-shaped protrusions of massage effect thereon.The present invention not only acts as anti-skidding effect by the way that a strata urethane elastic layer is arranged on the brick body surface that bakes, prevents from falling down and resulting tumble injury, and improves comfort when walking;The surface of brick body is equipped with the big bonding pit in the small top in bottom, so that elastic polyurethane layer be enable to be filled into bonding pit, improves the adhesive strength of the two;Arc-shaped protrusions are distributed in elastic polyurethane layer surface, can play to foot and massage anti-skidding effect.
Description
Technical field
The present invention relates to the floor tile in the field of building materials, specifically a kind of elastic brick for accomodation ground
And preparation method thereof.
Background technique
Floor tile is a kind of floor decorative material, is also floor tile, and most of floor tile is fired with clay, ruler
Very little specification and shape are also varied, have many advantages, such as that matter is hard, pressure resistance is wear-resisting, can be moisture-proof, and some has after glazing treatment
Decoration function is chiefly used in the ground and floor of public building and civil buildings.
In actual life, the floor of toilet and wall substantially all use floor tile and face brick to be filled in finishing
Decorations cause ground to be easy to slip due to the ground of toilet often wet water, and surface is used to have the ground of decorative pattern or lines
Although brick aesthetics is relatively good, step on and uncomfortable.
Summary of the invention
The elastic brick and preparation method thereof that the object of the present invention is to provide a kind of for accomodation ground, the floor tile by
One layer of polyurethane elastomer is arranged in the tile surface that bakes, not only acts as anti-skidding effect, prevents from falling down and tumble injury, Er Qieti
Comfort when high walking.
The present invention to realize the above-mentioned technical purpose used by technical solution are as follows: a kind of elasticity for accomodation ground
Several bonding pits are distributed on the upper surface of brick body in brick, including brick body, and longitudal section of each bonding pit is isosceles ladder
Shape, and its width is gradually reduced from bottom to top;A strata urethane elastic layer, and the poly- ammonia are equipped on the upper surface of brick body
Ester elastomer layer is filled into bonding pit, and the surface of elastic polyurethane layer is plane, and has been densely covered with the arc of massage effect thereon
Shape protrusion;
The elastic polyurethane layer is mixed by the B component of component A and component A weight 50-60%, wherein according to weight
Than, component A is mixed by 12-14 parts of polyoxypropylene, 7-8 parts of polyether-tribasic alcohol and 5-6 parts of triisocyanate,
B component is by 7-8 parts of polyoxypropylene, 4-5 parts of polyether-tribasic alcohol, 2-3 parts of polyethyl acrylate, 5-6 parts of epoxy
Resin, 3-4 parts of silica solution and 5-6 parts of modified filler are made, the modified filler by 2-3 parts modified abandoned molecular sieve,
4-6 parts of modified meerschaum suede powder, 10-12 parts of modification hollow glass micropearl and the mixing of 3-5 parts of modified manometer silicon dioxide
It forms, the modified abandoned molecular sieve is that discarded molecular sieve is first added to mass concentration is 20-25%, temperature is 80-90 DEG C
Immersion treatment 2h in dilute nitric acid solution is then filtered and dry and obtain under conditions of 350 DEG C, the modified meerschaum suede powder with
Modified hollow glass micropearl refers to respectively that the surface of commercially available sepiolite cashmere powder and hollow glass micropearl and its weight 3-5% is modified
Filtering dries to obtain agent I stands 1-2h after mixing after, and surface modifier I used is pressed by KH550, ethyl alcohol, acetone and barium hydroxide
It is mixed according to the ratio of weight ratio 3-4:80:2-3:1-2;The modified manometer silicon dioxide is by commercially available nanometer titanium dioxide
The surface modifier II of silicon and its weight 3-5% is mixed to get, which is pressed by barium hydroxide, sodium carbonate and KH550
It is mixed according to the ratio of weight ratio 3-4:1-2:30;
Brick body is by major ingredient, the additive of major ingredient weight 5-6%, the enhancing powder of major ingredient weight 3-4% and major ingredient weight
The aluminum filament of 12-13% and diameter no more than 1mm is fired, and according to weight ratio, the major ingredient is by 12-14 parts of gangue
Powder, 23-24 parts of clay, 7-8 parts of shale powder, 11-12 parts of clinker and 5-6 parts of iron ore waste residue composition, additive is by 4-5
The calcium oxide and 1-2 parts of montmorillonite powder of part mix, and the enhancing powder is no more than quartz sand, the 2- of 1mm by 6-7 parts of partial sizes
The modified aluminas micro mist of 3 parts of SILICA FUME and 1-1.2 part obtains after mixing;The modified aluminas micro mist is will to aoxidize
Aluminium micro mist and the surface modifier of its weight 3-5% are mixed to get, which is pressed by barium hydroxide, sodium carbonate and KH550
It is mixed according to the ratio of weight ratio 3-4:1-2:30.
The preparation method of the elastic polyurethane layer the following steps are included:
1) component A is prepared, it is spare;
Polyoxypropylene, polyether-tribasic alcohol and triisocyanate are weighed according to above-mentioned ratio respectively, then by polycyclic
Ethylene Oxide ether carries out decompression dehydration under conditions of vacuum degree is 0.096MPa, after its moisture content is less than 0.1%, is cooled to 60
DEG C, load weighted polyether-tribasic alcohol is added thereto under stirring conditions, is warming up to 85-90 DEG C, is stirred to react 2h, then drops
Temperature is to 40 DEG C, then load weighted triisocyanate is added thereto, is uniformly mixed and obtains component A;
2) B component is prepared, it is spare;
Respectively according to above-mentioned ratio weigh polyoxypropylene, polyether-tribasic alcohol, polyethyl acrylate, epoxy resin,
Silica solution and modified filler, then by polyoxypropylene under conditions of vacuum degree is 0.096MPa decompression dehydration to moisture content
Less than 0.1%, epoxy resin is then added thereto, after epoxy resin thawing, is cooled to 50 DEG C, then successively adds thereto
Enter polyether-tribasic alcohol, polyethyl acrylate, silica solution and modified filler, stirs evenly and obtain B component;
3) when in use, component A and the B component of its weight 50-60% are mixed and obtain elastic polyurethane layer.
According to weight ratio, the epoxy resin is by 3 parts of bisphenol A type epoxy resin, 1 part of aliphatic epoxy resin, 0.5
The polypropylene fibre, 0.5 part of modified manometer silicon dioxide and 0.5 part of modified silicasol of part are made, the modified Nano two
Silica is to be mixed to get commercially available nano silica and the surface modifier II of its weight 3-5%, and surface modifier II is by hydrogen
Barium monoxide, sodium carbonate and KH550 are mixed according to the ratio of weight ratio 3-4:1-2:30;The modified silicasol is commercially available
The silicon powder of silica solution weight 2-3%, the crystal whisker of hexa potassium titanate and silica solution weight of silica solution weight 1-2% are sequentially added in silica solution
The sodium acetate of 0.8-1% is measured, the mixture that 1-2h is obtained then is stirred under the conditions of 70-80 DEG C.
Also containing 0.4 part of glass fiber in the epoxy resin.
Also containing 0.3 part of nano aluminium oxide in the epoxy resin.
The preparation method of the epoxy resin the following steps are included:
1) modified manometer silicon dioxide and modified silicasol are prepared respectively, it is spare;
The modified manometer silicon dioxide is to mix commercially available nano silica and the surface modifier II of its weight 3-5%
Conjunction obtains, surface modifier II by barium hydroxide, sodium carbonate and KH550 according to weight ratio 3-4:1-2:30 ratio mixing and
At;
The modified silicasol is the silicon powder that silica solution weight 2-3% is sequentially added in commercially available silica solution, silica solution weight
The crystal whisker of hexa potassium titanate of 1-2% and the sodium acetate of silica solution weight 0.8-1% are measured, then 1-2h is stirred under the conditions of 70-80 DEG C and obtains
The mixture arrived;
2) each component is weighed according to the ratio, after then melting bisphenol A type epoxy resin, is added weighs thereto
Good aliphatic epoxy resin and polypropylene fibre stirs after melting completely, then is added thereto modified made from step 1)
Nano silica and modified silicasol, obtain epoxy resin after mixing evenly.
Also it is no more than 300 microns of talcum powder in the enhancing powder containing 1-1.2 parts of partial sizes.
Also containing 1-2 parts of basalt powder in the additive.
The production method of the above-mentioned elastic brick for accomodation ground, comprising the following steps:
1) modified aluminas micro mist is prepared, it is spare;
The surface modifier of alumina powder and its weight 3-5% is mixed to get, the surface modifier by barium hydroxide,
Sodium carbonate and KH550 are mixed according to the ratio of weight ratio 3-4:1-2:30;
2) composition major ingredient, additive and each raw material mixing for enhancing powder and grinding are weighed respectively according to above-mentioned requirement to thin
Degree is no more than 100 microns, so that major ingredient powder, additive and enhancing powder is made, it is spare;
The aluminum filament that diameter is no more than 1mm is weighed, it is spare;
3) major ingredient powder made from step 2, additive and enhancing powder are mixed, then sequentially adds major ingredient powder weight thereto
The water of 40-50% and the mix liquid of major ingredient powder weight 3-5% are measured, mix uniformly obtains pug, and after pug is aged 6-8 days, standby
With;
The mix liquid is that gutter oil, starch and glucose are mixed according to the ratio that weight ratio is 10:1:1;
4) it takes the weighed aluminum filament of step 2 to mix uniform with the pug mix after being aged in step 3) afterwards, is then made
Adobe, and 90-110 DEG C at a temperature of dry, it is spare;
5) adobe after drying in step 4) is sintered, brick body is obtained after natural cooling, then on the surface of brick body
A strata urethane elastic layer is laid with to get product is arrived;
The sintering is divided into preheating section, warming-up section and furnace zone three parts, wherein preheating section is to instigate in-furnace temperature from normal
Temperature is uniformly increased to 350 DEG C in 3h, and keeps temperature 1-2h, in the process, oxygen content in furnace is kept to be not higher than 4%;
The warming-up section refers to, in-furnace temperature is made uniformly to be increased to 950 DEG C in 4h from 350 DEG C, and keeps temperature 1-2h,
In the process, oxygen content in furnace is kept to be not less than 45%;
The furnace zone refers to, in-furnace temperature is made uniformly to be increased to 1550 DEG C in 2h from 950 DEG C, and keeps temperature 3-
4h keeps oxygen content in furnace to be not less than 35% in the process.
Contain modified abandoned molecular sieve in the present invention, in the modified filler of elastic polyurethane layer, modified meerschaum suede powder, change
Property hollow glass micropearl and modified manometer silicon dioxide, these types of substance can be dispersed in polyurethane matrix, on the one hand,
Modified abandoned molecular sieve and modified meerschaum suede powder have very big internal surface area, are the micro mists with microcellular structure, these
Microcellular structure can effectively cut down the transmitting of vibration and absorb moisture, on the other hand be to make hollow glass micropearl table in modifying process
Both face is grafted a large amount of silicone hydroxyl, these groups are connected hollow glass micropearl and matrix by chemically reacting, guarantee
With good interface binding power, when by external force, by stress shape is occurred material for hollow glass micropearl particle in the material
Become, destroy etc., to absorb impact energy, impact property is improved, while crazing can also be caused, crack extension is terminated, one
Determine the shear yielding for causing matrix under morphosis, to consume a large amount of impact energy, and can preferably transmit and be born
External force improves compressive strength, bending strength, the impact strength of elastic polyurethane layer;
When making modified manometer silicon dioxide in the present invention, allows and receive as catalyst using barium hydroxide and sodium carbonate mixing
The SiO of meter level2The surface of particle, to contain a certain number of oxygen-containing functional groups, can be increased and receive by the effect of hydroxyl
Meter level SiO2The related surface compatability of particle, in nanoscale SiO2When particle and remaining raw material are sufficiently mixed, because of SiO2Particle
Very little, and large specific surface area, the structure of imperceptibility increase rest materials and its contact area, make SiO2Particle can be
It is evenly dispersed in material, consequently facilitating SiO2Chemical bonding or physical bond occurs at high temperature with remaining substance.In addition,
The nanoscale SiO of even dispersion2Be equivalent to " anchor point ", the reinforcing matrix generated under hot environment can be made in connection, by
To external impacts effect under, the effect of " stress concentrations " can be generated so that surrounding some matrixes " surrender " and absorption compared with
Furthermore more work of deformations can also generate " pinning-is climbed up and over " effect, increase the crackle resistance suffered in extension, and consumption becomes
Shape function, so that its toughness be made to increase;
Epoxy resin in elastic polyurethane layer of the invention is by bisphenol A type epoxy resin, aliphatic epoxy resin, poly- third
Alkene fiber, modified manometer silicon dioxide and modified silicasol are made, and improve the toughness of material.It is molten that modified silicon is added in system
Glue particle and modified manometer silicon dioxide can substantially improve the mechanical property and thermal property of material, while also found and be modified
The addition of silica solution particle is to the raising of the tensile property of component mixing, product in preparation process and the final interpenetrating of product
Form is advantageous;
In the present invention, to fire coal gangue powder, clay, shale powder, clinker and the iron ore waste residue of floor tile as major ingredient, wherein
The SiO contained2Mullite is generated with oxidation reactive aluminum, to form mullite reinforcement in floor tile;During the sintering process, oxygen
Change aluminium and hercynite structure can be generated in iron oxide, to enhance its intensity;Calcium oxide and montmorillonite powder in additive
Sintering temperature can be effectively reduced;Mix is carried out with special mix liquid before firing, so that its stickiness and plasticity obtain
Enhancing;
Enhance the quartz sand and the double ginsengs of SILICA FUME in powder, can in improvement system particle it is tightly packed, modified aluminas is micro-
Powder activity is big, and even dispersion greatly improves its filling rate, three kinds of materials realize compound volcano ash effect, right in whole system
The compression strength for improving material has very strong effect;
During the sintering process, aluminum filament melts and is filled in the hole of part brick body of the invention, acts not only as
The skeleton of brick body enhances its intensity, and during the sintering process, and a part of aluminaization forms aluminium oxide to closely tie with floor tile
It closes, enhances the intensity and globality of floor tile.
The utility model has the advantages that compared with the existing, the invention has the following advantages that
1) the elasticity brick not only acts as anti-skidding work by the way that a strata urethane elastic layer is arranged on the brick body surface baked
With preventing from falling down and resulting tumble injury, and improve comfort when walking;The surface of brick body is equipped with bottom little Ding
The big bonding pit in portion improves the adhesive strength of the two so that elastic polyurethane layer be enable to be filled into bonding pit;Poly- ammonia
Arc-shaped protrusions are distributed in ester elastomer layer surface, can play to foot and massage anti-skidding effect;
4) present invention in, in the modified filler of elastic polyurethane layer containing modified abandoned molecular sieve, modified meerschaum suede powder,
Modified hollow glass micropearl and modified manometer silicon dioxide, these types of substance can be dispersed in polyurethane matrix, a side
Face, modified abandoned molecular sieve and modified meerschaum suede powder have very big internal surface area, are the micro mists with microcellular structure, this
Pore structure can effectively cut down the transmitting of vibration and absorb moisture slightly, on the other hand be to make hollow glass micropearl in modifying process
The a large amount of silicone hydroxyl of surface grafting, these groups are connected hollow glass micropearl and matrix by chemically reacting, and guarantee two
Person has good interface binding power, and when by external force, hollow glass micropearl particle is occurred by stress material in the material
Deformation, destruction etc. improve impact property, while can also cause crazing to absorb impact energy, terminate crack extension,
The shear yielding for causing matrix under certain morphosis, to consume a large amount of impact energy, and can preferably transmit and be born
External force, improve elastic polyurethane layer compressive strength, bending strength, impact strength;
3) present invention is to fire coal gangue powder, clay, shale powder, clinker and the iron ore waste residue of floor tile as major ingredient, wherein
The SiO contained2Mullite is generated with oxidation reactive aluminum, to form mullite reinforcement in floor tile;During the sintering process, oxygen
Change aluminium and hercynite structure can be generated in iron oxide, to enhance its intensity;Calcium oxide and montmorillonite powder in additive
Sintering temperature can be effectively reduced;Mix is carried out with special mix liquid before firing, so that its stickiness and plasticity obtain
Enhancing;
4) during the sintering process, aluminum filament melts and is filled in the hole of part brick body of the invention, can not only make
Enhance its intensity for the skeleton of brick body, and during the sintering process, a part of aluminaization forms aluminium oxide to close with floor tile
In conjunction with enhancing the intensity and globality of floor tile.
Detailed description of the invention
Fig. 1 is the structural diagram of the present invention;
Appended drawing reference: 1, brick body, 101, bonding pit, 2, elastic polyurethane layer, 201, arc-shaped protrusions.
Specific embodiment
The present invention is further elaborated combined with specific embodiments below.
Embodiment 1
As shown, a kind of elastic brick for accomodation ground, including brick body 1, if being distributed on the upper surface of brick body 1
Dry bonding pit 101, the longitudal section of each bonding pit 101 is isosceles trapezoid, and its width gradually contracts from bottom to top
It is small;A strata urethane elastic layer 2 is equipped on the upper surface of brick body 1, and the elastic polyurethane layer 2 is filled into bonding pit 101
Interior, the surface of elastic polyurethane layer 2 is plane, and has been densely covered with the arc-shaped protrusions 201 of massage effect thereon;
The elastic polyurethane layer 2 is mixed by the B component of component A and component A weight 50%, wherein according to weight
Than, component A is mixed by 12 parts of polyoxypropylene, 7 parts of polyether-tribasic alcohol and 5 parts of triisocyanate, B component by
7 parts of polyoxypropylene, 4 parts of polyether-tribasic alcohol, 2 parts of polyethyl acrylate, 5 parts of epoxy resin, 3 parts of silica solution
Modified filler with 5 parts is made, and the modified filler is by 2 parts of modified abandoned molecular sieve, 4 parts of modified meerschaum suede powder, 10
The modification hollow glass micropearl and 3 parts of modified manometer silicon dioxide of part mix, and the modified abandoned molecular sieve is first will
Discarded molecular sieve is added to immersion treatment 2h in the dilute nitric acid solution that mass concentration is 20%, temperature is 80 DEG C, then filtering and
Drying obtains under conditions of 350 DEG C, and the modified meerschaum suede powder and modified hollow glass micropearl refer to commercially available Hai Pao respectively
Filtering dries to obtain aminanthine powder and hollow glass micropearl stand 1h after mixing with the surface modifier I of its weight 3% after, table used
Face modifying agent I is mixed by KH550, ethyl alcohol, acetone and barium hydroxide according to the ratio of weight ratio 3:80:2:1;The modification
Nano silica is to be mixed to get the surface modifier II of commercially available nano silica and its weight 3%, and the surface is modified
Agent II is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3:1:30;
Brick body 1 is by major ingredient, the additive of major ingredient weight 5%, the enhancing powder of major ingredient weight 3% and major ingredient weight 12%
And diameter fires no more than the aluminum filament of 1mm, according to weight ratio, the major ingredient by 12 parts coal gangue powder, 23 parts
Clay, 7 parts of shale powder, 11 parts of clinker and 5 parts of iron ore waste residue composition, additive are taken off by 4 parts of calcium oxide and 1 part of illiteracy
Mountain flour mixes, the enhancing powder by 6 parts of partial sizes no more than the quartz sand of 1mm, 2 parts of SILICA FUME and 1 part it is modified oxidized
Aluminium micro mist obtains after mixing;The modified aluminas micro mist is to mix alumina powder and the surface modifier of its weight 3%
Conjunction obtains, which is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3:1:30;
The production method of the above-mentioned elastic brick for accomodation ground, comprising the following steps:
1) modified aluminas micro mist is prepared, it is spare;
Alumina powder and the surface modifier of its weight 3% are mixed to get, the surface modifier is by barium hydroxide, carbon
Sour sodium and KH550 are mixed according to the ratio of weight ratio 3:1:30;
2) composition major ingredient, additive and each raw material mixing for enhancing powder and grinding are weighed respectively according to above-mentioned requirement to thin
Degree is no more than 100 microns, so that major ingredient powder, additive and enhancing powder is made, it is spare;
The aluminum filament that diameter is no more than 1mm is weighed, it is spare;
3) major ingredient powder made from step 2, additive and enhancing powder are mixed, then sequentially adds major ingredient powder weight thereto
The water of amount 40% and the mix liquid of major ingredient powder weight 3%, mix uniformly obtain pug, and after pug is aged 6 days, spare;
The mix liquid is that gutter oil, starch and glucose are mixed according to the ratio that weight ratio is 10:1:1;
4) it takes the weighed aluminum filament of step 2 to mix uniform with the pug mix after being aged in step 3) afterwards, is then made
Adobe, and 90 DEG C at a temperature of dry, it is spare;
5) adobe after drying in step 4) is sintered, brick body 1 is obtained after natural cooling, then in the table of brick body 1
Face is laid with a strata urethane elastic layer 2 to get product is arrived;
The sintering is divided into preheating section, warming-up section and furnace zone three parts, wherein preheating section is to instigate in-furnace temperature from normal
Temperature is uniformly increased to 350 DEG C in 3h, and keeps temperature 1h, in the process, oxygen content in furnace is kept to be not higher than 4%;
The warming-up section refers to, in-furnace temperature is made uniformly to be increased to 950 DEG C in 4h from 350 DEG C, and keeps temperature 1h,
During this, oxygen content in furnace is kept to be not less than 45%;
The furnace zone refers to, in-furnace temperature is made uniformly to be increased to 1550 DEG C in 2h from 950 DEG C, and keeps temperature 3h,
In the process, oxygen content in furnace is kept to be not less than 35%.
The above are the basic embodiments of the present embodiment, can be further optimized, improve and limit on the basis of above:
Such as, the elastic polyurethane layer 2 preparation method the following steps are included:
1) component A is prepared, it is spare;
Polyoxypropylene, polyether-tribasic alcohol and triisocyanate are weighed according to above-mentioned ratio respectively, then by polycyclic
Ethylene Oxide ether carries out decompression dehydration under conditions of vacuum degree is 0.096MPa, after its moisture content is less than 0.1%, is cooled to 60
DEG C, load weighted polyether-tribasic alcohol is added thereto under stirring conditions, is warming up to 85 DEG C, is stirred to react 2h, then cools down
To 40 DEG C, then load weighted triisocyanate is added thereto, is uniformly mixed and obtains component A;
2) B component is prepared, it is spare;
Respectively according to above-mentioned ratio weigh polyoxypropylene, polyether-tribasic alcohol, polyethyl acrylate, epoxy resin,
Silica solution and modified filler, then by polyoxypropylene under conditions of vacuum degree is 0.096MPa decompression dehydration to moisture content
Less than 0.1%, epoxy resin is then added thereto, after epoxy resin thawing, is cooled to 50 DEG C, then successively adds thereto
Enter polyether-tribasic alcohol, polyethyl acrylate, silica solution and modified filler, stirs evenly and obtain B component;
3) when in use, the B component of component A and its weight 50% is mixed and obtains elastic polyurethane layer 2;
For another example, according to weight ratio, the epoxy resin is by 3 parts of bisphenol A type epoxy resin, 1 part of aliphatic epoxy tree
Rouge, 0.5 part of polypropylene fibre, 0.5 part of modified manometer silicon dioxide and 0.5 part of modified silicasol are made, the modification
Nano silica is to be mixed to get the surface modifier II of commercially available nano silica and its weight 3%, surface modifier II
It is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3:1:30;The modified silicasol is commercially available
The silicon powder of silica solution weight 2%, the crystal whisker of hexa potassium titanate of silica solution weight 1% and silica solution weight are sequentially added in silica solution
0.8% sodium acetate then stirs the mixture that 1h is obtained under the conditions of 70 DEG C;
Further, the epoxy resin preparation method the following steps are included:
1) modified manometer silicon dioxide and modified silicasol are prepared respectively, it is spare;
The modified manometer silicon dioxide is to mix commercially available nano silica with the surface modifier II of its weight 3%
It obtains, surface modifier II is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3:1:30;
The modified silicasol is the silicon powder that silica solution weight 2% is sequentially added in commercially available silica solution, silica solution weight
1% crystal whisker of hexa potassium titanate and the sodium acetate of silica solution weight 0.8% then stir the mixture that 1h is obtained under the conditions of 70 DEG C;
2) each component is weighed according to the ratio, after then melting bisphenol A type epoxy resin, is added weighs thereto
Good aliphatic epoxy resin and polypropylene fibre stirs after melting completely, then is added thereto modified made from step 1)
Nano silica and modified silicasol, obtain epoxy resin after mixing evenly.
Further, also containing 0.4 part of glass fiber in the epoxy resin;
Further, also containing 0.3 part of nano aluminium oxide in the epoxy resin;
For another example, also it is no more than 300 microns of talcum powder in the enhancing powder containing 1 part of partial size;
Finally, also containing 1 part of basalt powder in the additive.
Embodiment 2
As shown, a kind of elastic brick for accomodation ground, including brick body 1, if being distributed on the upper surface of brick body 1
Dry bonding pit 101, the longitudal section of each bonding pit 101 is isosceles trapezoid, and its width gradually contracts from bottom to top
It is small;A strata urethane elastic layer 2 is equipped on the upper surface of brick body 1, and the elastic polyurethane layer 2 is filled into bonding pit 101
Interior, the surface of elastic polyurethane layer 2 is plane, and has been densely covered with the arc-shaped protrusions 201 of massage effect thereon;
The elastic polyurethane layer 2 is mixed by the B component of component A and component A weight 60%, wherein according to weight
Than, component A is mixed by 14 parts of polyoxypropylene, 8 parts of polyether-tribasic alcohol and 6 parts of triisocyanate, B component by
8 parts of polyoxypropylene, 5 parts of polyether-tribasic alcohol, 3 parts of polyethyl acrylate, 6 parts of epoxy resin, 4 parts of silica solution
Modified filler with 6 parts is made, and the modified filler is by 3 parts of modified abandoned molecular sieve, 6 parts of modified meerschaum suede powder, 12
The modification hollow glass micropearl and 5 parts of modified manometer silicon dioxide of part mix, and the modified abandoned molecular sieve is first will
Discarded molecular sieve be added to mass concentration be 25%, immersion treatment 2h in dilute nitric acid solution at a temperature of 90 °C, then filtering and
Drying obtains under conditions of 350 DEG C, and the modified meerschaum suede powder and modified hollow glass micropearl refer to commercially available Hai Pao respectively
Filtering dries to obtain aminanthine powder and hollow glass micropearl stand 2h after mixing with the surface modifier I of its weight 5% after, table used
Face modifying agent I is mixed by KH550, ethyl alcohol, acetone and barium hydroxide according to the ratio of weight ratio 4:80:3:2;The modification
Nano silica is to be mixed to get the surface modifier II of commercially available nano silica and its weight 5%, and the surface is modified
Agent II is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 4:2:30;
Brick body 1 is by major ingredient, the additive of major ingredient weight 6%, the enhancing powder of major ingredient weight 4% and major ingredient weight 13%
And diameter fires no more than the aluminum filament of 1mm, according to weight ratio, the major ingredient by 14 parts coal gangue powder, 24 parts
Clay, 8 parts of shale powder, 12 parts of clinker and 6 parts of iron ore waste residue composition, additive are taken off by 5 parts of calcium oxide and 2 parts of illiteracy
Mountain flour mixes, and the enhancing powder is no more than quartz sand, 3 parts of SILICA FUME and 1.2 parts of the modification oxygen of 1mm by 7 parts of partial sizes
Change aluminium micro mist to obtain after mixing;The modified aluminas micro mist is by the surface modifier of alumina powder and its weight 5%
It is mixed to get, which is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 4:2:30;
The production method of the above-mentioned elastic brick for accomodation ground, comprising the following steps:
1) modified aluminas micro mist is prepared, it is spare;
Alumina powder and the surface modifier of its weight 5% are mixed to get, the surface modifier is by barium hydroxide, carbon
Sour sodium and KH550 are mixed according to the ratio of weight ratio 4:2:30;
2) composition major ingredient, additive and each raw material mixing for enhancing powder and grinding are weighed respectively according to above-mentioned requirement to thin
Degree is no more than 100 microns, so that major ingredient powder, additive and enhancing powder is made, it is spare;
The aluminum filament that diameter is no more than 1mm is weighed, it is spare;
3) major ingredient powder made from step 2, additive and enhancing powder are mixed, then sequentially adds major ingredient powder weight thereto
The water of amount 50% and the mix liquid of major ingredient powder weight 5%, mix uniformly obtain pug, and after pug is aged 8 days, spare;
The mix liquid is that gutter oil, starch and glucose are mixed according to the ratio that weight ratio is 10:1:1;
4) it takes the weighed aluminum filament of step 2 to mix uniform with the pug mix after being aged in step 3) afterwards, is then made
Adobe, and 110 DEG C at a temperature of dry, it is spare;
5) adobe after drying in step 4) is sintered, brick body 1 is obtained after natural cooling, then in the table of brick body 1
Face is laid with a strata urethane elastic layer 2 to get product is arrived;
The sintering is divided into preheating section, warming-up section and furnace zone three parts, wherein preheating section is to instigate in-furnace temperature from normal
Temperature is uniformly increased to 350 DEG C in 3h, and keeps temperature 2h, in the process, oxygen content in furnace is kept to be not higher than 4%;
The warming-up section refers to, in-furnace temperature is made uniformly to be increased to 950 DEG C in 4h from 350 DEG C, and keeps temperature 2h,
During this, oxygen content in furnace is kept to be not less than 45%;
The furnace zone refers to, in-furnace temperature is made uniformly to be increased to 1550 DEG C in 2h from 950 DEG C, and keeps temperature 4h,
In the process, oxygen content in furnace is kept to be not less than 35%.
The above are the basic embodiments of the present embodiment, can be further optimized, improve and limit on the basis of above:
Such as, the elastic polyurethane layer 2 preparation method the following steps are included:
1) component A is prepared, it is spare;
Polyoxypropylene, polyether-tribasic alcohol and triisocyanate are weighed according to above-mentioned ratio respectively, then by polycyclic
Ethylene Oxide ether carries out decompression dehydration under conditions of vacuum degree is 0.096MPa, after its moisture content is less than 0.1%, is cooled to 60
DEG C, load weighted polyether-tribasic alcohol is added thereto under stirring conditions, is warming up to 90 DEG C, is stirred to react 2h, then cools down
To 40 DEG C, then load weighted triisocyanate is added thereto, is uniformly mixed and obtains component A;
2) B component is prepared, it is spare;
Respectively according to above-mentioned ratio weigh polyoxypropylene, polyether-tribasic alcohol, polyethyl acrylate, epoxy resin,
Silica solution and modified filler, then by polyoxypropylene under conditions of vacuum degree is 0.096MPa decompression dehydration to moisture content
Less than 0.1%, epoxy resin is then added thereto, after epoxy resin thawing, is cooled to 50 DEG C, then successively adds thereto
Enter polyether-tribasic alcohol, polyethyl acrylate, silica solution and modified filler, stirs evenly and obtain B component;
3) when in use, the B component of component A and its weight 60% is mixed and obtains elastic polyurethane layer 2;
For another example, according to weight ratio, the epoxy resin is by 3 parts of bisphenol A type epoxy resin, 1 part of aliphatic epoxy tree
Rouge, 0.5 part of polypropylene fibre, 0.5 part of modified manometer silicon dioxide and 0.5 part of modified silicasol are made, the modification
Nano silica is to be mixed to get the surface modifier II of commercially available nano silica and its weight 5%, surface modifier II
It is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 4:2:30;The modified silicasol is commercially available
The silicon powder of silica solution weight 3%, the crystal whisker of hexa potassium titanate of silica solution weight 2% and silica solution weight 1% are sequentially added in silica solution
Sodium acetate, 2h obtained mixture is then stirred under the conditions of 80 DEG C;
Further, the epoxy resin preparation method the following steps are included:
1) modified manometer silicon dioxide and modified silicasol are prepared respectively, it is spare;
The modified manometer silicon dioxide is to mix commercially available nano silica with the surface modifier II of its weight 5%
It obtains, surface modifier II is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 4:2:30;
The modified silicasol is the silicon powder that silica solution weight 3% is sequentially added in commercially available silica solution, silica solution weight
2% crystal whisker of hexa potassium titanate and the sodium acetate of silica solution weight 1% then stir the mixture that 2h is obtained under the conditions of 80 DEG C;
2) each component is weighed according to the ratio, after then melting bisphenol A type epoxy resin, is added weighs thereto
Good aliphatic epoxy resin and polypropylene fibre stirs after melting completely, then is added thereto modified made from step 1)
Nano silica and modified silicasol, obtain epoxy resin after mixing evenly.
Further, also containing 0.4 part of glass fiber in the epoxy resin;
Further, also containing 0.3 part of nano aluminium oxide in the epoxy resin;
For another example, also it is no more than 300 microns of talcum powder in the enhancing powder containing 1.2 parts of partial sizes;
Finally, also containing 2 parts of basalt powder in the additive.
Embodiment 3
As shown, a kind of elastic brick for accomodation ground, including brick body 1, if being distributed on the upper surface of brick body 1
Dry bonding pit 101, the longitudal section of each bonding pit 101 is isosceles trapezoid, and its width gradually contracts from bottom to top
It is small;A strata urethane elastic layer 2 is equipped on the upper surface of brick body 1, and the elastic polyurethane layer 2 is filled into bonding pit 101
Interior, the surface of elastic polyurethane layer 2 is plane, and has been densely covered with the arc-shaped protrusions 201 of massage effect thereon;
The elastic polyurethane layer 2 is mixed by the B component of component A and component A weight 55%, wherein according to weight
Than component A is mixed by 13 parts of polyoxypropylene, 7.5 parts of polyether-tribasic alcohol and 5.5 parts of triisocyanate, B group
Part is by 7.5 parts of polyoxypropylene, 4.5 parts of polyether-tribasic alcohol, 2.5 parts of polyethyl acrylate, 5.5 parts of asphalt mixtures modified by epoxy resin
Rouge, 3.5 parts of silica solution and 5.5 parts of modified filler are made, the modified filler by 2.5 parts modified abandoned molecular sieve, 5 parts
Modified meerschaum suede powder, 11 parts of modification hollow glass micropearl and 4 parts of modified manometer silicon dioxide mix, it is described to change
Property discarded molecular sieve be that first discarded molecular sieve is added in the dilute nitric acid solution that mass concentration is 22.5%, temperature is 85 DEG C to soak
Bubble processing 2h, then filters and dry and obtain under conditions of 350 DEG C, the modified meerschaum suede powder and to be modified hollow glass micro-
Pearl refers to commercially available sepiolite cashmere powder and hollow glass micropearl are mixed with the surface modifier I of its weight 4% respectively after stand 1.5h
Filtering dries to obtain afterwards, and surface modifier I used is by KH550, ethyl alcohol, acetone and barium hydroxide according to weight ratio 3.5:80:
2.5:1.5 ratio mix;The modified manometer silicon dioxide is by commercially available nano silica and its weight 4%
Surface modifier II is mixed to get, and the surface modifier II is by barium hydroxide, sodium carbonate and KH550 according to weight ratio 3.5:1.5:
30 ratio mixes;
Brick body 1 is by major ingredient, the additive of major ingredient weight 5.5%, the enhancing powder of major ingredient weight 3.5% and major ingredient weight
12.5% and diameter fired no more than the aluminum filament of 1mm, according to weight ratio, the major ingredient by 13 parts coal gangue powder,
23.5 parts of clay, 7.5 parts of shale powder, 11.5 parts of clinker and 5.5 parts of iron ore waste residue composition, additive is by 4.5 parts
Calcium oxide and 1.5 parts of montmorillonite powder mix, and the enhancing powder is no more than the quartz sand of 1mm, 2.5 parts by 6.5 parts of partial sizes
SILICA FUME and 1.1 parts of modified aluminas micro mist obtain after mixing;The modified aluminas micro mist is that aluminium oxide is micro-
Powder and the surface modifier of its weight 4% are mixed to get, and the surface modifier is by barium hydroxide, sodium carbonate and KH550 according to weight
Ratio than 3.5:1.5:30 mixes;
The production method of the above-mentioned elastic brick for accomodation ground, comprising the following steps:
1) modified aluminas micro mist is prepared, it is spare;
Alumina powder and the surface modifier of its weight 4% are mixed to get, the surface modifier is by barium hydroxide, carbon
Sour sodium and KH550 are mixed according to the ratio of weight ratio 3.5:1.5:30;
2) composition major ingredient, additive and each raw material mixing for enhancing powder and grinding are weighed respectively according to above-mentioned requirement to thin
Degree is no more than 100 microns, so that major ingredient powder, additive and enhancing powder is made, it is spare;
The aluminum filament that diameter is no more than 1mm is weighed, it is spare;
3) major ingredient powder made from step 2, additive and enhancing powder are mixed, then sequentially adds major ingredient powder weight thereto
The water of amount 45% and the mix liquid of major ingredient powder weight 4%, mix uniformly obtain pug, and after pug is aged 7 days, spare;
The mix liquid is that gutter oil, starch and glucose are mixed according to the ratio that weight ratio is 10:1:1;
4) it takes the weighed aluminum filament of step 2 to mix uniform with the pug mix after being aged in step 3) afterwards, is then made
Adobe, and 100 DEG C at a temperature of dry, it is spare;
5) adobe after drying in step 4) is sintered, brick body 1 is obtained after natural cooling, then in the table of brick body 1
Face is laid with a strata urethane elastic layer 2 to get product is arrived;
The sintering is divided into preheating section, warming-up section and furnace zone three parts, wherein preheating section is to instigate in-furnace temperature from normal
Temperature is uniformly increased to 350 DEG C in 3h, and keeps temperature 1.5h, in the process, oxygen content in furnace is kept to be not higher than 4%;
The warming-up section refers to, in-furnace temperature is made uniformly to be increased to 950 DEG C in 4h from 350 DEG C, and keeps temperature 1.5h,
In the process, oxygen content in furnace is kept to be not less than 45%;
The furnace zone refers to, so that in-furnace temperature is uniformly increased to 1550 DEG C in 2h from 950 DEG C, and keep the temperature
3.5h keeps oxygen content in furnace to be not less than 35% in the process.
The above are the basic embodiments of the present embodiment, can be further optimized, improve and limit on the basis of above:
Such as, the elastic polyurethane layer 2 preparation method the following steps are included:
1) component A is prepared, it is spare;
Polyoxypropylene, polyether-tribasic alcohol and triisocyanate are weighed according to above-mentioned ratio respectively, then by polycyclic
Ethylene Oxide ether carries out decompression dehydration under conditions of vacuum degree is 0.096MPa, after its moisture content is less than 0.1%, is cooled to 60
DEG C, load weighted polyether-tribasic alcohol is added thereto under stirring conditions, is warming up to 88 DEG C, is stirred to react 2h, then cools down
To 40 DEG C, then load weighted triisocyanate is added thereto, is uniformly mixed and obtains component A;
2) B component is prepared, it is spare;
Respectively according to above-mentioned ratio weigh polyoxypropylene, polyether-tribasic alcohol, polyethyl acrylate, epoxy resin,
Silica solution and modified filler, then by polyoxypropylene under conditions of vacuum degree is 0.096MPa decompression dehydration to moisture content
Less than 0.1%, epoxy resin is then added thereto, after epoxy resin thawing, is cooled to 50 DEG C, then successively adds thereto
Enter polyether-tribasic alcohol, polyethyl acrylate, silica solution and modified filler, stirs evenly and obtain B component;
3) when in use, the B component of component A and its weight 55% is mixed and obtains elastic polyurethane layer 2;
For another example, according to weight ratio, the epoxy resin is by 3 parts of bisphenol A type epoxy resin, 1 part of aliphatic epoxy tree
Rouge, 0.5 part of polypropylene fibre, 0.5 part of modified manometer silicon dioxide and 0.5 part of modified silicasol are made, the modification
Nano silica is to be mixed to get the surface modifier II of commercially available nano silica and its weight 4%, surface modifier II
It is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3.5:1.5:30;The modified silicasol be
It is molten that the silicon powder of silica solution weight 2.5%, the crystal whisker of hexa potassium titanate of silica solution weight 1.5% and silicon are sequentially added in commercially available silica solution
The sodium acetate of glue weight 0.9% then stirs the mixture that 1.5h is obtained under the conditions of 75 DEG C;
Further, the epoxy resin preparation method the following steps are included:
1) modified manometer silicon dioxide and modified silicasol are prepared respectively, it is spare;
The modified manometer silicon dioxide is to mix commercially available nano silica with the surface modifier II of its weight 4%
It obtains, surface modifier II is mixed by barium hydroxide, sodium carbonate and KH550 according to the ratio of weight ratio 3.5:1.5:30;
The modified silicasol is the silicon powder that silica solution weight 2.5% is sequentially added in commercially available silica solution, silica solution weight
The crystal whisker of hexa potassium titanate of amount 1.5% and the sodium acetate of silica solution weight 0.9%, then stirred under the conditions of 75 DEG C 1.5h obtain it is mixed
Close object;
2) each component is weighed according to the ratio, after then melting bisphenol A type epoxy resin, is added weighs thereto
Good aliphatic epoxy resin and polypropylene fibre stirs after melting completely, then is added thereto modified made from step 1)
Nano silica and modified silicasol, obtain epoxy resin after mixing evenly.
Further, also containing 0.4 part of glass fiber in the epoxy resin;
Further, also containing 0.3 part of nano aluminium oxide in the epoxy resin;
For another example, also it is no more than 300 microns of talcum powder in the enhancing powder containing 1.1 parts of partial sizes;
Finally, also containing 1.5 parts of basalt powder in the additive.
Claims (7)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201611065034.4A CN106639236B (en) | 2016-11-28 | 2016-11-28 | A kind of elastic brick for toilet floor and its making method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201611065034.4A CN106639236B (en) | 2016-11-28 | 2016-11-28 | A kind of elastic brick for toilet floor and its making method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106639236A CN106639236A (en) | 2017-05-10 |
| CN106639236B true CN106639236B (en) | 2019-02-26 |
Family
ID=58812865
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201611065034.4A Expired - Fee Related CN106639236B (en) | 2016-11-28 | 2016-11-28 | A kind of elastic brick for toilet floor and its making method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106639236B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111517829B (en) * | 2020-05-27 | 2022-06-03 | 广西欧神诺陶瓷有限公司 | A kind of anti-slip antibacterial ceramic tile and preparation method thereof |
| CN115849944B (en) * | 2022-12-21 | 2023-08-11 | 江苏恒尚节能科技股份有限公司 | Aerated concrete block for building curtain wall and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103387649A (en) * | 2013-08-08 | 2013-11-13 | 常熟市中腾塑胶有限公司 | Method for preparing all plastic polyurethane plastic floor |
| CN104211895A (en) * | 2014-09-18 | 2014-12-17 | 东莞市雄林新材料科技股份有限公司 | Flame-retardant wear-resistant pressure-resistant polyurethane floor material and preparation method thereof |
| CN105176366A (en) * | 2015-07-17 | 2015-12-23 | 河南科技大学 | Preparation method of wear-resistant anti-microbial coating for sports equipment |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100472741C (en) * | 2005-02-21 | 2009-03-25 | 日东电工株式会社 | Manufacturing method of semiconductor device |
-
2016
- 2016-11-28 CN CN201611065034.4A patent/CN106639236B/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103387649A (en) * | 2013-08-08 | 2013-11-13 | 常熟市中腾塑胶有限公司 | Method for preparing all plastic polyurethane plastic floor |
| CN104211895A (en) * | 2014-09-18 | 2014-12-17 | 东莞市雄林新材料科技股份有限公司 | Flame-retardant wear-resistant pressure-resistant polyurethane floor material and preparation method thereof |
| CN105176366A (en) * | 2015-07-17 | 2015-12-23 | 河南科技大学 | Preparation method of wear-resistant anti-microbial coating for sports equipment |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106639236A (en) | 2017-05-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106760400B (en) | A kind of bumper and absorbing shock type floor tile and preparation method thereof | |
| CN106116688B (en) | Method for manufacturing ceramic of multi-layer structure | |
| CN106630939A (en) | Light-weight porous floor tile and manufacturing method thereof | |
| CN106639236B (en) | A kind of elastic brick for toilet floor and its making method | |
| CN111003991A (en) | Light high-strength silicate ceramsite concrete | |
| CN109678445A (en) | A kind of desulfurized gypsum 3D printing alkali-activated carbonatite cementitious material and its application method | |
| CN106519354B (en) | A kind of special shockproof support device of surveying instrument | |
| CN103030352A (en) | Tile glue for ceramic thin plate | |
| CN106916554B (en) | A kind of one pack system vitrified brick gum | |
| CN106632976A (en) | Elastic vibration-absorptive material for gymnasium floor, and preparation method of elastic vibration-absorptive material | |
| CN108516813A (en) | A kind of graphene ceramic tile | |
| CN118495917A (en) | A high-strength ceramic brick and its preparation method and application | |
| CN105175007B (en) | A kind of light-weight insulating brick | |
| CN106431458B (en) | The method that tailings in vanadium extraction prepares porous ceramics | |
| CN109608180A (en) | A decorative wall panel and its one-time firing method and application | |
| WO2006125287B1 (en) | Natural aluminosilicate composites and aggregates synthesized in alkaline environment and their manufacturing process | |
| CN108854014A (en) | A kind of boxing body-building sandbag | |
| CN107936901A (en) | A kind of novel flexible polyurethane glue for tile and preparation method thereof | |
| CN108529946A (en) | High-strength lightweight concrete and preparation method thereof | |
| CN106608724A (en) | Floor tile with sound absorbing function and preparation method thereof | |
| CN113135773B (en) | Silicon-based porous ceramic for high-pressure slip casting and preparation method thereof | |
| CN106589899A (en) | Elastic material laid on ground of indoor gym | |
| CN106758679B (en) | A kind of floor tile and preparation method thereof being laid with for outdoor plastic cement race track | |
| CN106554745A (en) | Acoustic mastic and preparation method thereof is built in a kind of environment-friendly type anophelifuge one-component epoxy resin capital construction | |
| TWI385127B (en) | Composite material of paper slag sludge and inorganic polymer and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20190226 |