CN108164281B - Open spontaneous multi-functional water-permeable brick of generation negative oxygen ion and preparation method thereof - Google Patents
Open spontaneous multi-functional water-permeable brick of generation negative oxygen ion and preparation method thereof Download PDFInfo
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- CN108164281B CN108164281B CN201810012029.XA CN201810012029A CN108164281B CN 108164281 B CN108164281 B CN 108164281B CN 201810012029 A CN201810012029 A CN 201810012029A CN 108164281 B CN108164281 B CN 108164281B
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- floor tile
- waste material
- permeable brick
- wall
- mesh
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- 239000011449 brick Substances 0.000 title claims abstract description 80
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 52
- 239000001301 oxygen Substances 0.000 title claims abstract description 52
- 230000002269 spontaneous effect Effects 0.000 title claims abstract description 41
- 238000002360 preparation method Methods 0.000 title description 26
- 150000001875 compounds Chemical class 0.000 claims abstract description 68
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000002699 waste material Substances 0.000 claims abstract description 38
- 238000010521 absorption reaction Methods 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims description 86
- 239000000463 material Substances 0.000 claims description 54
- 239000004744 fabric Substances 0.000 claims description 48
- 150000002500 ions Chemical class 0.000 claims description 45
- -1 oxygen ion Chemical class 0.000 claims description 45
- 238000010304 firing Methods 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 38
- 238000003756 stirring Methods 0.000 claims description 31
- 238000000889 atomisation Methods 0.000 claims description 30
- 229910000245 dravite Inorganic materials 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 229910052656 albite Inorganic materials 0.000 claims description 14
- 239000004615 ingredient Substances 0.000 claims description 12
- 238000005245 sintering Methods 0.000 claims description 9
- 239000011651 chromium Substances 0.000 claims description 7
- 238000000748 compression moulding Methods 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 230000006835 compression Effects 0.000 claims description 6
- 238000007906 compression Methods 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- 239000011265 semifinished product Substances 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 4
- 230000005484 gravity Effects 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000004886 process control Methods 0.000 claims description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 3
- PNEFIWYZWIQKEK-UHFFFAOYSA-N carbonic acid;lithium Chemical compound [Li].OC(O)=O PNEFIWYZWIQKEK-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 238000004332 deodorization Methods 0.000 abstract description 3
- 230000020477 pH reduction Effects 0.000 abstract description 3
- 230000001954 sterilising effect Effects 0.000 abstract description 3
- 239000012466 permeate Substances 0.000 abstract description 2
- 239000003570 air Substances 0.000 description 40
- 239000000047 product Substances 0.000 description 32
- 239000000919 ceramic Substances 0.000 description 26
- 239000002245 particle Substances 0.000 description 24
- 150000001450 anions Chemical class 0.000 description 23
- 235000013339 cereals Nutrition 0.000 description 23
- 238000004519 manufacturing process Methods 0.000 description 22
- 230000008569 process Effects 0.000 description 21
- 229920002472 Starch Polymers 0.000 description 17
- 239000008107 starch Substances 0.000 description 17
- 235000019698 starch Nutrition 0.000 description 17
- 238000012360 testing method Methods 0.000 description 15
- 239000007791 liquid phase Substances 0.000 description 13
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 13
- 229910052613 tourmaline Inorganic materials 0.000 description 12
- 239000011032 tourmaline Substances 0.000 description 12
- 229940070527 tourmaline Drugs 0.000 description 12
- 230000035699 permeability Effects 0.000 description 11
- 229910052808 lithium carbonate Inorganic materials 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000010433 feldspar Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 238000005265 energy consumption Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 7
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000001976 improved effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 239000007767 bonding agent Substances 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 230000035515 penetration Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 238000003916 acid precipitation Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- 229940092782 bentonite Drugs 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000010865 sewage Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000000725 suspension 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 2
- 239000002253 acid Substances 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000000498 ball milling Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052705 radium Inorganic materials 0.000 description 2
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- HUPNQNOWXCVQSW-UHFFFAOYSA-N 2h-pyran-4-carboxamide Chemical compound NC(=O)C1=CCOC=C1 HUPNQNOWXCVQSW-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- ONCZQWJXONKSMM-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical group O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] ONCZQWJXONKSMM-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000003837 high-temperature calcination Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 210000000697 sensory organ Anatomy 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229940080314 sodium bentonite Drugs 0.000 description 1
- 229910000280 sodium bentonite Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/06—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances
- C04B38/063—Preparing or treating the raw materials individually or as batches
- C04B38/0635—Compounding ingredients
- C04B38/0645—Burnable, meltable, sublimable materials
-
- 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
-
- 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
- C04B33/1324—Recycled material, e.g. tile dust, stone waste, spent refractory material
-
- 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
- C04B2235/3201—Alkali metal oxides or oxide-forming salts thereof
- C04B2235/3203—Lithium oxide 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
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
-
- 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
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
- C04B2235/3472—Alkali metal alumino-silicates other than clay, e.g. spodumene, alkali feldspars such as albite or orthoclase, micas such as muscovite, zeolites such as natrolite
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- 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
- C04B2235/447—Phosphates or phosphites, e.g. orthophosphate or hypophosphite
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
-
- 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
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
The invention discloses a kind of open spontaneous multi-functional water-permeable bricks of generation negative oxygen ion, and the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion includes precoat and initial bed, and the precoat includes following components in percentage by weight：The 90-93% Wall or floor tile waste material grain compound hydrosol A of A, 7-10%, the initial bed includes following components in percentage by weight：The water absorption rate of 90-93% Wall or floor tile waste material grain B, 7-10% compound hydrosol B, the Wall or floor tile waste material grain A and Wall or floor tile waste material grain B are less than 3%.The open spontaneous multi-functional water-permeable brick of generation negative oxygen ion of the invention can in time permeate the ground rainwater, can efficiently generate negative oxygen ion, improve air quality, mitigate haze pollution, have deodorization to water body, mitigate the rainwater of acidification and have sterilizing function.
Description
Technical field
The invention belongs to technical field of inorganic non-metal ceramic, and in particular to and it is a kind of that rainwater can permeate the ground in time, and
Negative oxygen ion can be efficiently generated, air quality is improved, mitigates haze pollution, has deodorization to water body, mitigate the rainwater of acidification and have
Multi-functional water-permeable brick of sterilizing function and preparation method thereof.
Background technique
Ceramic water-permeable brick uses floor tile waste material, former as main production after multiple stage crushing, processing, classification
Material, this solves the problems, such as a large amount of solid wastes that floor tile manufacturing enterprise generates.Meanwhile ceramic water-permeable brick has preferably
Compression strength, flexural strength and water penetration (be significantly better than baking-free type using cement and denatured resin as the seepy material of cohesive body
And floor tile), there are also good ageing-resistant, weather resistance, high temperature resistant, resistance to soiling and wearabilities.The face that ceramic water-permeable brick is showed
Color is the inorganic chemical industry colorant using ceramic body, has many advantages, such as not fugitive color, extensively the welcome by market, simultaneously
Also at one of the main seepy material in national popularization sponge city.
The water-permeable brick of the sold circulation of domestic production at present and market, major function is mainly permeable, to solution heavy rain
Caused urban waterlogging, urban ground " sponge effect " play the role of it is very big, to reducing noise, mitigate city " tropical island effect " etc.
There is certain booster action.
Patent CN1336349A discloses a kind of ceramic water-permeable brick and its production method, major ingredient are：Useless Wall or floor tile grain 70-
90%, feldspar powder 8-20%, cellulose 1-5%, sawdust 1-5% and appropriate amount of water.The production method of ceramic water-permeable brick is：(1) match
Material：Useless floor brick material is pulverized and sieved into 4-60 mesh, sawdust is sieved 20-60 mesh, and 10 times of water weight of cellulose are impregnated, and obtains viscosity 400-
600 degree, feldspar powder pulverizes and sieves 200-250 mesh；Useless Wall or floor tile grain, feldspar powder, cellulose, sawdust is added by formula, adds
Suitable water stirs evenly；(2) base：It is squeezed into base by predetermined size, that is, is formed, carries out 100-130 DEG C of drying, 50- later
After 70 minutes obtain 0.5% or less aqueous adobe, after calcined 100-140 minutes under the conditions of 1100-1300 DEG C.
In patent CN1336349A, it is to be added in aggregate to generate viscosity using cellulose bubble liquid, is molding viscosity
Material, the effect of the feldspar powder of addition are to generate melting in high-temperature calcination and ceramic tile particle is bonded together generation intensity, are added
The effect for entering sawdust is the water penetration for generating communication type channel when generating gap and burning and gas-exhausting after sawdust burns and improving product.
But this method has some disadvantages：The viscosity of the cellulosic pulp obtained with infusion method is difficult to control, and causes to expect in production
Viscosity is unstable, and the thickness deviation of product is larger when leading to pressing fabric.Meanwhile sawdust and solid fuel, it is being rapidly fired to
When the gas that generates of moment easily lead to adobe burst apart in exhaust, cause waste product.The method is only suitable for the push plate being burnt at a slow speed
Kiln or tunnel oven, and it is burnt into energy consumption height, product quality is difficult to control.
Patent CN1232738A discloses a kind of manufacturing method of water-permeable brick, and ceramic aggregate is broken, sieve, adhesive is nothing
Two kinds of machine clay A, B, aggregate press 4-7 mesh aggregate 85-94% using Unglazed ceramic matter brick red brick, and adhesive is viscous for low temperature high viscosity
Soil, mixing mixing, compression moulding, pressure 150-250kgf/cm2, and various color bricks are made using primary or secondary material distributing.It adopts
Main technique is：With the aggregate (accounting for 70-85% greater than 10 mesh) for being greater than 4 mesh, molding adhesive is low temperature high viscosity clay,
Bonding agent low temperature itself, in 1150-1250 DEG C of high temperature firing, ceramic aggregate particle is bonded together after bonding agent melting and
Intensity is generated, not using other fluxing agents, process for calcining and firing period do not illustrate.The simple process, but producing
In, with ceramic tile particle higher temperature required for congruent melting phenomenon occurs for bonding agent itself, and the flexural strength difficulty of product is more than 7.0Mpa/
cm2, relative energy consumption is higher.
Patent CN101182185A discloses a kind of outdoor water-permeable brick and preparation method thereof, and main technique is：Using pottery
The useless brick of porcelain is broken for the particle for being greater than 0 less than 100 mesh, by 6-8 mesh<5%, 8-30 mesh are 85-90%, and being greater than 30 mesh is 5-15%
Mass mixing, add the adhesive and water of 5wt%, be made mud, be added in mold, use 90-110pa/mm2Pressure compacting
Molding, tunnel oven is burnt at 1160-1220 DEG C, and total firing period is 26-29 hours.In that patent, swelling is mainly used
Soil is adhesive, and no other fluxing agents, directly use low temperature bentonite as fluxing agent in ingredient.Because tunnel oven mode is burnt
It is long at the time, ceramic tile grain surface soften at high temperature after be added bentonite it is fluxing, can obtain higher resistance to compression flexural strength and
Compared with the product of high water-permeability, it is most apparent the disadvantage is that tunnel oven the link of kiln loading vehicle is difficult to realize automate in process of production,
A large amount of manpower and material resources are needed, and firing time is too long, energy consumption is high.The temperature difference of upper, middle and lower is difficult to control in another tunnel oven calcining kiln,
The color difference of product is difficult to control, and surface bulky grain has relatively good mobility when cloth, and the little particle that compares is in pressing fabric
When it is easily separated, uneven, appearance chromatic difference is big, texture is poor.
Patent CN1919564A discloses a kind of production method of environment friendly composite ceramic water-permeable brick, and this method is with can
The industrial residue of combustion things is bottom aggregate, and grain composition is：10-20 mesh 55-65% and 20-30 mesh 35-40%, mixing are added
A certain proportion of high-temperature agglomerant and organic binder C.M.C, agitated, aging, molding, roast and obtain finished product drying.Though
Right this method utilizes industrial residue, and manufacture water-permeable passage obtains higher-strength and good when using combustible being pore former and exhaust
The product of good water penetration, in process of production, it is necessary to which by dry process, and large amount of organic carbonization, burning must expire
The process that foot discharges slowly, is suitable only for the production method that firing period is more than 12 hours or more.
Patent CN103771864B disclose it is a kind of using in-situ preparation high-temperature agglomerant preparation ceramic water-permeable brick and its
Preparation method is mainly technically characterized by introducing soluble-salt in the aggregate of water-permeable brick, and bone is added in form of an aqueous solutions
In material, it is uniformly mixed more difficult to solve the problems, such as to be added in solid form, and also eliminates the problem of preparing high-temperature agglomerant,
Simplify the link of production.But soluble-salt used is metal monovalent salt and divalent salts, and additional amount is less than 5% in aqueous solution
When, when being actually added into the salt quality in aggregate than being only 0.175%, and a large amount of water soluble salts be added, the alkalinity enhancing of aqueous solution,
The viscosity that molding adhesive can largely be destroyed, causes molding blank bonding poor, and green strength is low and model easy to stick when suppressing
At surface defect.Breakage is easily caused in compacting demoulding, mobile process, and additional amount is reduced, though it can guarantee low temperature bonding agent
Viscosity, but fluxing action is decreased obviously, can only improve melting by improving firing temperature, firing temperature will to 1170 DEG C-
1230 DEG C, cause firing energy consumption higher.
Currently, the method for domestic production ceramic water-permeable brick, is broadly divided into two major classes：(1) inorganic Low binder is used.It is main
Wanting ingredient is sodium bentonite and calcium-base bentonite, and reinforcing body hypothermia feldspar, (fusing point of low temperature feldspar is wanted as high temperature fluxing agent
It asks at 1150 DEG C or less)；(2) molding adhesive is used as using polysaccharide solution (concentration 50wt%), is made with aqueous metal salt
For high temperature fluxing agent.Although the product being prepared has preferable compression strength, flexural strength and coefficient of permeability, generally it is burnt into
Temperature need to reach 1170 DEG C or more, and for firing time at 6-29 hours, the energy consumption cost of firing accounted for 30% or more product cost, and
And yield is lower (35~100mm of product thickness), largely constrains the dosage in bigger market, and its function is only saturating
Water, reduces city " tropical island effect " and fainter sound absorption function at aqueous (gap is aqueous), and when permeable, evaporation water can not
Make certain processing to water body, it cannot be to the apparent improvement result of ambient air quality.
The negative ion ceramic ceramic tile of currently available technology production, is all made of tourmaline powder or combined type tourmaline powder or combined type
Rare earth tourmaline powder (hereinafter referred to as negative ion powder).Its preparation process is two classes：
(1) unglazed tile, polished bricks part are directly added negative ion powder in formula, ingredient, mud are made by ball milling
0.2~2.5mm powder particles are made by spray drying in slurry, mud, low by compacting, drying, high temperature firing acquisition water absorption rate
In 0.5% floor tile.Due to tourmaline powder sheet as black, short, bristly hair or beard is red or brown based on, be added in ceramic batch, firing
The aesthetics that carcass can be seriously affected after product, so additional amount is restricted.Separately because unglazed floor tiles, polished bricks, glazed tile etc. are burnt
Cheng Houwei dense body, specific gravity are 2.6~2.8g/cm3, water absorption rate is both needed to 0.5% hereinafter, and the negative ion powder quilt that is added
It is completely encapsulated in inside the carcass of complete vitreous, it is few (by addition that surface can expose aerial anionic particle
The granule size of weight percent when negative ion powder can calculate), and the liquid that ceramic tile is formed in high-temperature sintering process
It meets and immerses inside negative ion powder crystal structure, and physical-chemical reaction and variation have occurred therewith, destroy to a certain extent
The unidirectional polar axis of negative ion powder, can reduce the ability of negative ion powder launching electronics, also just reduce and to generate negative oxygen ion
Ability.Other direction, because negative ion powder is completely wrapped in inside the ceramic tile carcass of vitreous, the water absorption rate of ceramic tile is 0.5%
(it is considered that not absorbing water substantially) below has also just broken off the approach that negative ion powder directly contacts water body and air, in very great Cheng
Approach and ability that negative ion powder generates the negative oxygen ion of higher concentration are limited on degree, belong to closed transmitting anion.
(2) glazed tile class：Glazed tile, which refers to, applies the glaze layer that a layer thickness is 0.3-3.0mm on floor tile surface.And it bears
Ion powder, by being manually incorporated in glaze, by ball milling, is sieved, is made containing anion during preparing glaze slip
The glaze slip of powder.In process of production, glaze slip is allowed to be attached to ceramic adobe surface with the mode for getting rid of glaze or leaching glaze, glaze spraying, through overdrying
After dry, after 1180-1250 DEG C of high temperature firing melts, the complete vitreous of glaze paint forms compact structure, water absorption rate is less than 0.05%
Complete vitreous glazed layer, final negative ion powder is completely wrapped in inside glaze layer, and glazed layer is melted in high temperature sintering
It needs to be completely formed the full liquid phase compared with low viscosity in the process, stronger physical-chemical reaction has occurred in liquid phase and negative ion powder, right
The erosion of negative ion powder is bigger, is easier to weaken the ability of negative ion powder launching electronics.Likewise, negative ion powder is sealed completely
Closure is rolled in silicate glass body, can not directly contact wetting and air, the concentration of the negative oxygen ion of generation all can only compared with
Low level, can only be in 1300/cm3Within.
Currently, water-permeable brick function in the market is mainly permeable, have a single function, is not able to satisfy the need of city continuous development
It wants.Compound hydrosol is equably sprayed onto water-permeable brick particles of aggregates surface using spray-on process by the present invention, and is relatively evenly attached to
Aggregate surface prepares multi-functional water-permeable brick.The water-permeable brick of preparation is not only able to satisfy every basic function needed for sponge city and refers to
Mark, while the haze to large and medium-sized city, air pollution, acid rain penetrate into ground with rainwater to the pollution of earth's surface, ground sanitary sewage
Foul smell taste generated after topsoil etc. has clear improvement and assists improvement result, and the negative aeroion in especially increase city is dense
Degree allows the square in city and pavement can spontaneous generation anion.
Summary of the invention
Rainwater can be permeated the ground in time the object of the present invention is to provide a kind of, can efficiently generate negative oxygen ion, improved empty
Makings amount mitigates haze pollution, has deodorization to water body, mitigates the rainwater of acidification and the multi-functional water-permeable brick with sterilizing function.
The technical solution adopted by the present invention is that：A kind of open spontaneous multi-functional water-permeable brick of generation negative oxygen ion, it is described to open
Putting the spontaneous multi-functional water-permeable brick of generation negative oxygen ion of formula includes precoat and initial bed, and the precoat includes following weight percent
The component of ratio：
Wall or floor tile waste material grain A 90-93%,
Compound hydrosol A 7-10%,
The initial bed includes following components in percentage by weight：
Wall or floor tile waste material grain B 90-93%,
Compound hydrosol B 7-10%；
The water absorption rate of the Wall or floor tile waste material grain A and Wall or floor tile waste material grain B are less than 3%.
Preferably, the Wall or floor tile waste material grain A mixes shape by the Wall or floor tile waste material grain of the granular-grade of following weight percent
At：
10-16 mesh Wall or floor tile waste material grain 75-85%,
16-60 mesh Wall or floor tile waste material grain 15-25%.
In addition, the needs of fabric view color, can additionally incorporate required inorganic ceramic colorant.
Preferably, the Wall or floor tile waste material grain B mixes shape by the Wall or floor tile waste material grain of the granular-grade of following weight percent
At：
3-10 mesh Wall or floor tile waste material grain 40-50%,
10-16 mesh Wall or floor tile waste material grain 15-30%,
16-60 mesh Wall or floor tile waste material grain 20-35%.
Preferably, the compound hydrosol A includes following components in percentage by weight：
Preferably, the compound hydrosol B includes following components in percentage by weight：
Wherein, each component that the compound hydrosol B of the compound hydrosol A of precoat and initial bed is used is as follows：Water
For industrial tap water；Converted starch is manufactured by Foshan starch factory industrialness；Lithium carbonate fine powder is industrial tailing, carbonic acid lithium content
It is 50~60%, fineness 25-320 mesh；Albite fine powder fineness is 250-300 mesh, Na2O content > 6.7% (ingredient ratio)；Phosphorus
Sour trisodium is industrial products, is used as diluent, influence liquidity, and have fluxing action；The fineness 1200-1500 of negative ion powder
Mesh.
The compound hydrosol A of precoat and the compound hydrosol B of initial bed (are free of negative ion powder, then save addition
The step of negative ion powder) specific preparation method it is as follows：
1) prepare a high-velocity fluid dispersator, revolving speed can be in 1500-3000 revs/min of variable frequency adjustment, according to need
It adjusts；
2) lithium carbonate superfine powder and sodium will be added after water, converted starch and tertiary sodium phosphate in proportion ingredient stirring 5-10 minutes
Feldspar superfine powder after being stirred for 5-8 minutes, is added negative ion powder, then 5-8 minutes, is sieved with 120 mesh, can obtain mobility
And the good compound hydrosol of suspension.
Wherein, the sticky control standard of converted starch is：By water:Converted starch=4:1 weight ratio stirs evenly, and control is viscous
Degree is qualified between 6000-9000；Lithium carbonate, albite, the negative ion powder of addition are fine powder, are substantially insoluble in water, institute
Must be uniformly dispersed in converted starch, just be added after abundant aquation, guarantee that the fine powder being added does not have agglomeration.
The compound hydrosol A of the precoat of preparation and the compound hydrosol B of initial bed meet following index：
(1) specific gravity of compound hydrosol is by production actual needs control in 1.70-2.0g/cm3Between, mobility grace
The test of lattice viscosity apparatus, controlled between 40-50 seconds；
(2) suspension：The compound hydrosol prepared, with diameter of phi 100, high 50cm glass tank in be added to height be
The hydrosol of 45cm stands 24 hours, with the naked eye observes glass tank bottom whether subject to sediment, is not allow for sediment.
Preferably, the specific gravity of the compound hydrosol A and compound hydrosol B is 1.70-2.0g/cm3, viscosity 40-50
Second.
Preferably, the purity 50-60% of the lithium carbonate fine powder, fineness are 250-320 mesh；The albite fine powder it is thin
Degree is 250-300 mesh, Na2O content > 6.7%.
Preferably, the negative ion powder by weight percent following raw material：Dravite 12-18%, iron dravite
12-18%, chromium dravite 12-18%, hokutolite 48-56% are mixed, and the fineness of the negative ion powder is 1200-1500
Mesh.It is furthermore preferred that following raw material of the negative ion powder by weight percent：Dravite 16%, iron dravite 16%, chromium
Dravite 16%, hokutolite 52% mix.
The negative ion powder that the present invention uses is obtained with natural purified tourmaline and Peitou stone ore hybrid process.It is various
The anion emission ability of crude tourmaline and hokutolite is widely different because of the mineral structure of itself difference.Generally polishing
Floor tile throws glaze floor tile, is only suitable on interior glazed tile with light or white as far as possible tourmaline powder, and brown, dirty-green, black
Because the color development of the base glaze to brick has larger impact, unsuitable large scale uses the tourmaline powder of color.And (Inner Mongol goes out Peitou mountain flour
Produce) it is coffee color, there is faint radium element, infrared ray can be emitted, after the two is combined, the ability of transmitting anion
It is strengthened.
The anion-generating material that the present invention uses is the mixed of dravite, iron tourmaline, chromium U.S. tourmaline and hokutolite
Zoarium is machined to 1200-1500 mesh fineness by air-flow crushing, and specific composition and structure are respectively：
(1) dravite：NaMg3Al6B3Si6O27(O,OH,F)4Etc. shaft-like, brown.
(2) iron dravite：(Na,k)(Mg,Fe)3Fe6B3Si16O27(O,OH,F)4Etc. shaft-like, short cylinder black.
(3) chromium dravite：NaMg3(Cr5,Al)B3Si16O27(OH)4Pyramid shape, dirty-green.
(4) hokutolite：PbBa4(SO4)5Precipitating crystalline contains micro radium element, coffee-like.
By weight above 4 kinds of raw materials, dravite 16%, iron dravite 16%, chromium dravite 16%, Peitou
The mixing of 52% ratio of stone obtains fineness through air-flow crushing and uses in 1200-1500 mesh super fine or every kind of separate machined at micro mist
Weight ratio obtains after mixing in the above ratio.
Preferably, the precoat with a thickness of 12-18mm, the degree of the initial bed is 35-45mm.
The present invention also provides the methods for preparing the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion, including following step
Suddenly：
1) the Wall or floor tile waste material grain B of initial bed is subjected to ingredient in proportion, carries out horizontal batch, using pressure atomization with
The mode that compressed air secondary-atomizing mode combines adds compound hydrosol B, carries out the broken stirring of horizontal distributing, is sent into certainly
Dynamic bottom material feeder is stand-by, obtains bottom material；
2) the Wall or floor tile waste material grain A of precoat is subjected to ingredient in proportion, carries out horizontal batch, using pressure atomization with
The mode that compressed air secondary-atomizing mode combines adds compound hydrosol A, carries out the broken stirring of horizontal distributing, is sent into certainly
Dynamic fabric feeder is stand-by, obtains fabric；
3) bottom material is sent into press and carries out a cloth, fabric is sent into press and carries out secondary material distributing, compression moulding takes off
Mould obtains water-permeable brick semi-finished product；
4) water-permeable brick semi-finished product are placed on and carry out heating firing, it is cooling to get more to open spontaneous generation negative oxygen ion
Function water-permeable brick.
Wherein, the addition of compound hydrosol is added using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Enter, the total amount being added is automatically controlled with quantitative flow measurement mode, and spray-on process can equably be sprayed onto compound hydrosol permeable
Brick particles of aggregates surface, and relatively evenly it is attached to aggregate surface.
Preferably, compound hydrosol A is added with the mode that compressed air secondary-atomizing mode combines using pressure atomization
When with compound hydrosol B, the condition of control is：Nozzle diameter Φ 2.5~Φ 3.0mm, 0.5~0.6mpa of pressure；Compressed air
Pressure is 0.4~0.6mpa.
Wherein pressure atomization pressurization contracting air atomizing principle is：With special spray gun, spray gun nozzle aperture is 2.0~Φ of Φ
2.5mm is forced into 0.5~0.6mpa pressure with stainless steel alkali prevention, antifouling pump, sprays to be formed all less than 0.10mm water through rifle nozzle
The mist of pearl, then be atomized with 0.4~0.6mpa pressure compressed air, droplet is carried out secondary-atomizing, keeps compound hydrosol abundant
Atomization forms 0.05mm misty hydrosol below, is easy to be uniformly adhered aggregate surface (spraying into hydrosol while stirring).
Final realize allows the smallest negative ion powder of partial size to be uniformly adhered the outermost layer in aggregate.Lithium carbonate powder and albite in powder granularity compared with
Negative ion powder is big, and momentum is big when spraying from spray gun, is first attached to aggregate surface, negative ion powder is just attached to lithium carbonate and albite grain table
Face, final negative ion powder are exposed to outer layer, form Open architecture.
Preferably, it is 2000-2900 revs/min that horizontal distributing, which is crushed the revolving speed of whipping process control, the pressure of compression moulding
Power control is 17-27Mpa, and heating sintering process control is：First stage, firing temperature are 50-200 DEG C, time 15-
30min；Second stage, firing temperature are 200-450 DEG C, time 15-30min；Phase III, firing temperature 450-700
DEG C, time 25-40min；Fourth stage, firing temperature are 900-1030 DEG C, time 35-45min；5th stage, firing
Temperature is 1030-1050 DEG C, time 40-60min.
The preparation of open type multifunctional water-permeable brick is integrated by multiple requirements such as the functions, cost and decoration of water-permeable brick
Considering, uses secondary material distributing mode in preparation process, it is contemplated that cost performance factor, bottom are added without colorant and negative ion powder, and
Surface layer should assurance function, while meeting decoration, the requirement such as sense organ again, therefore different from bottom material.Raw material aggregate is to use water absorption rate
Wall or floor tile waste material less than 3% is crushed, separate storage to quality obtains.
More specifically, the technological process of production of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion is as follows：
The present invention adds compound hydrosol with the mode that compressed air secondary-atomizing mode combines using pressure atomization, can
To realize that compound hydrosol is uniformly adhered to water-permeable brick aggregate surface, that is, may be implemented in compound hydrosol it is various at
Part can relatively evenly disperse to be attached to particles of aggregates surface.
The preparation process of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion carries out the broken stirring of horizontal distributing, this
It is the weight and specific surface area of the relatively fine particle coarse grained weight in because having thinner particle (- 60 mesh of 16 mesh) in aggregate
It differs greatly with specific surface area, fine grained will appear agglomeration in part in level stirring, therefore it is broken to design horizontal distributing
Broken blender, principle is the speeder that 2000-2900 revs/min of revolving speed is used during Horizontal stirring, what is reunited
Thinner powder ball impact dispersion, while in shattering process, by that biggish particle will not be smashed.
Compression moulding uses fully automatic hydraulic press, after the pressure compacting of pressure 17-27Mpa, in compound hydrosol
Converted starch solution generates cohesive force, suppresses required shape and thickness, but its cohesive force is weaker, can only use vacuum mechanical-arm
It takes out.
Roller kilns continuous burnt：Product firing period be 4.0-6.5 hour, depending on product specifications, thickness and it is different, be burnt into most
High-temperature is 1030-1050 DEG C.Detailed process and time are as follows：
A：From starting into 50-200 DEG C of section of kiln, required time 15-30 minutes, main function was product preheating, and quickly
The free water section in product is allowed to be discharged.
B：From 200-450 DEG C of section, required time 15-30 minutes, converted starch fast dewatering, in particles of aggregates part from
By water and most of constitution water discharge, converted starch starts to solidify, and the contraction of 0.2-0.4% occurs in product, from 350 DEG C or so,
Converted starch is carbonized, and partial oxidation combustion, and CO is discharged2, for negative ion powder open connection provide gap and
Channel.
C：From 450-700 DEG C of section, required time 25-40 minutes, the aggregate of product had the thermal expansion of 0.1-0.3%, but
Voidage inside product is 20-40%, will not influence the integrality of product, and since 630 DEG C, lithium carbonate particle starts
Fusing, and gradually generate liquid phase.As the temperature rises with the continuity of time, Li2CO3The liquid phase that melt generates can penetrate into week
Side, in conjunction with albite particle, while the anion particle that part is wrapped up can reveal.
D：900-1030 DEG C of section, required time 35-45 minutes.Li2CO3The liquid phase and albite particle that melt generates are sent out
Raw congruent melting generates more liquid phases, and as temperature increases, the time increases, liquid phase can spread, be immersed in ceramic tile aggregate surface, open
Begin that congruent melting occurs with aggregate surface, while the negative ion powder wrapped up can be revealed further.
E：1030-1050 DEG C of section, required time 40-60 minutes.Surface softens ceramic tile aggregate at high temperature, and produces before
Eutectic reaction occurs for raw liquid phase, and liquid phase part penetrates into aggregate micro-crack, interpenetrates, and forms the wire type of local point type
Melting is coupled.(particles of aggregates is irregular polyhedrons, is substantially point contact between bulky grain.)
It is fired by high temperature, Li2CO3Liquid phase, and the adhesive attachment for passing through liquid phase with aggregate are formed completely with albite micro mist
To together, after rapid cooling, liquid phase solidifies the contraction for becoming solid-state again, and having 1-2% again.At this time at high temperature by liquid phase
Closed channel can become the channel of aperture again, and a part that anionic particle is closed package can be exposed (negative again
The melting temperature of ion is greater than 1310 DEG C).
Cooling procedure control is as follows：
DEG C A.1050~710 DEG C：It is quickly cooled down：It is directly sent into normal temperature air with blower, is quickly cooled down after heat exchange, institute
Take time is 3~10 minutes.
B. 20-40 minutes required from 710-450 DEG C.Slowly cool to 450 DEG C from 710 DEG C, because aggregate can generate it is biggish
It shrinks, it is necessary to control the rate of cooling, otherwise product is also easy to produce more micro-crack, directly cracks when serious, while to ensure
Product surface and the center temperature difference are unable to 50 DEG C of size.
C. 10-15 minutes required from 450-100 DEG C.It can be quickly cooled down, roller tables means of transportation Temperature fall is used after kiln discharge
To after 60 DEG C or less, pick, packaging.
The present invention during the preparation process, increases pressure atomization and adds with the mode that compressed air secondary-atomizing mode combines
The step of the step of adding compound hydrosol and horizontal distributing are crushed stirring, can ensure that product properties and functional stabilization.
In addition, the present invention can be prepared by the way of a cloth as another kind selection of the invention, i.e., bottom material,
The identical material of fabric, selected bottom material, the material of fabric are as described above.
The beneficial effects of the invention are as follows：
(1) the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion of the invention can be 1000-1050 DEG C in lower temperature
Sintering in range prepares properties and is significantly better than national standard, the efficient generating negative ions of energy multifunction road water-permeable bricks；
(2) compound hydrosol is added with the mode that compressed air secondary-atomizing mode combines using pressure atomization, to big
The feasibility and stability of production have effective guarantee, while can be uniformly adhered to aggregate surface most end form for negative ion powder
At Open architecture, effective method and physical environment are provided；
(3) in process of production, the negative ion powder partially wrapped up, because the burning of converted starch can expose again
Most surface forms open connection again, can be effectively facilitated the efficient generation of anion；
(4) method of the invention can be effectively reduced firing temperature in the case where guaranteeing that product properties is significantly better than national standard
Degree 100-250 DEG C, the firing efficiency of product when energy consumption is effectively reduced, and improving production, shorten firing period, comprehensive energy consumption compared with
Other methods reduce by 20% or more, and yield can be improved 20% or more, are to solve current sintered type water-permeable brick firing period length, yield
Low effective way and method；
(5) the multi-functional water-permeable brick of the present invention, water penetration, water-retaining property are its basic function, and bigger advantage is energy
Anion, that is, negative oxygen ion are efficiently generated, beneficial environment is provided to the health of people, anion, which diffuses into air, to be had
Can quickly in conjunction with the positively charged particle in air, particle loses can quickly reunite after positive charge after be deposited to ground, be
Solve effective product of city haze.Meanwhile having certain neutralization to the water body for contacting, permeating, energy large area is to acid
Property rainwater (acid rain in city accounts for 80% or more) play the role of weakening acid and neutralize, and have decomposition to the foul smell of sewage generation
And inhibiting effect.
Detailed description of the invention
Fig. 1 is the structural schematic diagram of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion of embodiment 1-7 preparation；
Fig. 2 is the structural schematic diagram of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion prepared by embodiment 9；
Fig. 3 is the structural schematic diagram of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion prepared by embodiment 10.
Specific embodiment
Aggregate described in embodiment 1-10 is the Wall or floor tile waste material grain of corresponding mesh number.
Embodiment 1
Fabric is prepared with compound hydrosol：50kg(A1)
Specific formula：
Bottom material is prepared with compound hydrosol：50kg(B1)
Specific formula：
| Water | 75% | 37.5kg |
| Converted starch | 7% | 3.5kg |
| Lithium carbonate powder | 11.9% | 5.95kg |
| Albite in powder | 6% | 3.0kg |
| Tertiary sodium phosphate | 0.1% | 0.05kg |
The compound hydrosol A of precoat and the compound hydrosol B of initial bed (are free of negative ion powder, then save addition
The step of negative ion powder) specific preparation method it is as follows：
1) prepare a high-velocity fluid dispersator, revolving speed can be in 1500-3000 revs/min of variable frequency adjustment, as needed
It adjusts；
2) lithium carbonate superfine powder and sodium will be added after water, converted starch and tertiary sodium phosphate in proportion ingredient stirring 5-10 minutes
Feldspar superfine powder after being stirred for 5-8 minutes, is added negative ion powder, then 5-8 minutes, is sieved with 120 mesh, can obtain mobility
And the good compound hydrosol of suspension.
Take precoat aggregate 100kg
10~16 mesh, 75% 75kg
16~60 mesh, 25% 25kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol atomization of 8kgA1, and carry out that horizontal distributing is broken to stir evenly, manually breaks up conglomeration caused by subdivision.
Take initial bed aggregate 400kg
3~10 mesh, 50% 200kg
10~16 mesh, 20% 80kg
16~60 mesh, 30% 120kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 32kgB1, and carry out that horizontal distributing is broken to stir evenly, breaks up conglomeration caused by subdivision.
With 100 × 200mm mold：Bottom material adds fabric 0.55kg after adding 1.5kg, cloth even again, is persistently added with 5000kg pressure
Pressure is after 8 seconds, demoulding.60 are pressed altogether, complete semi-finished product is obtained and is placed on high temperature backing plate, with 1050 DEG C of maximum temperature, when firing
Between 270 minutes (4.5 hours), obtain the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion.Measurement result is as follows：
Flexural strength：8.7Mpa
Coefficient of permeability：2.5cm/s
2212/cm of anion generation concentration3
Radionuclide test：γ=0.71 I ra=0.5, I (meet national standard A class, can indoor use)
Note：Radionuclide national standard A class：γ≤1.3 Ira≤1.0, I.
Embodiment 2
Take fabric aggregate 100kg
10~16 mesh, 82% 82kg
16~60 mesh, 18% 18kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 8kg A1, and carry out that horizontal distributing is broken to stir evenly, breaks up conglomeration caused by subdivision.
Take bottom material aggregate 400kg
3~10 mesh, 46% 184kg
10~16 mesh, 20% 80kg
16~60 mesh, 34% 136kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 32kg B1, and carry out that horizontal distributing is broken to stir evenly, breaks up conglomeration caused by subdivision.
With 100 × 200 molds：Bottom material adds 1.6kg cloth even, and fabric adds 0.45kg cloth even, is taken off after pressure pressure maintaining 8 seconds with 5 tons
Mould and being placed on high temperature backing plate is pressed 60 times altogether, with 1050 DEG C of maximum sintering temperature, firing period 270 minutes, is obtained open
The spontaneous multi-functional water-permeable brick of generation negative oxygen ion.Measure referring mainly to for the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion
Mark：
Flexural strength：9.1Mpa
Coefficient of permeability：2.3cm/s
2016/cm of anion generation concentration3
Radionuclide test：γ=0.72 Ira=0.51, I (meets and uses A class in national standard room).
Embodiment 3
Prepare precoat compound hydrosol (A2) 50kg, specific formula:
| Water | 60% | 30kg |
| Converted starch | 3.85% | 1.925kg |
| Lithium carbonate powder | 3% | 1.5kg |
| Albite in powder | 3% | 1.5kg |
| Tertiary sodium phosphate | 0.15% | 0.075kg |
| Negative ion powder | 30% | 15kg |
After being prepared as described in Example 1 with process, it is stirred for after standing 24 hours stand-by.
Prepare bottom material compound hydrosol 50kg (B2), specific formula：
Take the total 100kg of fabric aggregate
10~16 mesh, 80% 80kg
16~60 mesh, 20% 20kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 8kg A2, and carry out that horizontal distributing is broken to stir evenly, breaks up conglomeration caused by subdivision.
Take bottom material aggregate 400kg
3~10 mesh, 45% 180kg
10~16 mesh, 20% 80kg
16~60 mesh, 35% 140kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 32kg B2, and carry out that horizontal distributing is broken to stir evenly, manually breaks up conglomeration caused by subdivision, be made
Bottom material.
With 100 × 200mm mold：Bottom material addition 1.5kg cloth is even, and 0.55kg is added in fabric, is persistently added with 5000kg pressure
Pressure 6~10 seconds, is placed on high temperature on backing plate and presses altogether 60 times, with 1030 DEG C of maximum sintering temperature, firing period 270 minutes after demoulding
(4.5 hours) high-temperature holding time 45 minutes are fired into the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion.Measurement knot
Fruit：
Flexural strength 9.2Mpa (30 average)
Coefficient of permeability 2.2cm/s (10 average)
1870/cm of anion generation concentration3
Radionuclide test：γ=0.78 Ira=0.53, I (national standard A class requires Ira≤1.0, γ≤1.3 I).
Embodiment 4
Fabric preparation：Take aggregate 100kg
10~16 mesh 70%
16~60 mesh 30%
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 8kg A2, and carry out that horizontal distributing is broken to stir evenly, manually breaks up conglomeration caused by subdivision,
Bottom material preparation：Take aggregate 400kg
3~10 mesh, 50% 200kg
10~16 mesh, 25% 100kg
16~60 mesh, 25% 200kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 32kg B2, and carry out that horizontal distributing is broken to stir evenly, manually breaks up conglomeration caused by subdivision, be made
Bottom material.
With 100 × 200mm mold：Bottom material adds 1.5kg cloth even, and fabric adds 0.55kg cloth even, with 5000kg pressure keep 8~
10 seconds, press 60 altogether, with 1030 DEG C of maximum sintering temperature, firing period 270 minutes, 1030 DEG C soaking time 45 minutes, roller-way
Kiln firing, obtains the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion, tests product major parameter：
Flexural strength 9.4Mpa (10 average)
Coefficient of permeability 2.1cm/s (10 average)
1792/cm of anion generation concentration3
Radionuclide limitation：γ=0.78 IIra=0.53, I.
Embodiment 5
Fabric compound hydrosol (A3) 30kg is prepared, is formulated as follows：
| Water | 56% | 16.8kg |
| Converted starch | 4% | 1.2kg |
| Lithium carbonate powder | 3% | 0.9kg |
| Albite in powder | 3% | 0.9kg |
| Tertiary sodium phosphate | 0.2% | 0.06kg |
| Negative ion powder | 33.8% | 10.14kg |
After preparing as described in Example 1 with process, 24 hours abundant aquations are preferably placed, for use.
Bottom material compound hydrosol (B3) 30kg is prepared, is formulated as follows：
| Water | 70% | 21kg |
| Converted starch | 9.85% | 2.955kg |
| Lithium carbonate powder | 10% | 3kg |
| Albite in powder | 10% | 3kg |
| Tertiary sodium phosphate | 0.15% | 0.045kg |
After preparing as described in Example 1 with process, 24 hours abundant aquations are stood, for use.
Ingredient preparation：Take fabric aggregate 50kg
10~16 mesh, 80% 40kg
16~60 mesh, 20% 10kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 4.0kg A3, and carry out that horizontal distributing is broken to stir evenly, manually breaks up conglomeration caused by subdivision.
Bottom material preparation：Total 200kg
3~10 mesh, 40% 80kg
10~16 mesh, 25% 50kg
16~60 mesh, 35% 70kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add 18kg B3 complex hydrosol, and carry out that horizontal distributing is broken to stir evenly, breaks up fine powder conglomeration.
With 300 × 300mm mold：Bottom material adds 7.3kg, and cloth is flat, and fabric uses pressure 25Mpa pressure after adding 2.75kg cloth flat,
Pressure maintaining 8~10 seconds, extruded article thickness 55.5mm sucted high temperature backing plate with vacuum chuck, 12 was pressed altogether, in 1050 DEG C of highests
Temperature is burnt into, obtains the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion for firing time 300 minutes.Test its main indicator：
Flexural strength 8.3Mpa
Coefficient of permeability 2.2cm/s
2020/cm of anion release concentration3
Radionuclide test：γ=0.91 Ira=0.72, I.
Embodiment 6
Fabric preparation：Take the total 50kg of fabric aggregate
10~16 mesh, 78% 39kg
16~60 mesh, 22% 11kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 5.0kg A3, and carry out that horizontal distributing is broken to stir evenly, manually breaks up fine powder conglomeration.
Bottom material preparation：Take the total 200kg of bottom material
3~10 mesh, 50% 100kg
10~16 mesh, 30% 60kg
16~60 mesh, 20% 40kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 18kg B3, and carry out that horizontal distributing is broken to stir evenly, is stirred for 10 points after manually breaing up fine powder conglomeration
Clock, until naked-eye observation is without fine powder conglomeration.
With 200 × 400mm mold：Bottom material adds 5.8kg, and cloth is flat, adds fabric 2.3kg cloth and puts down, is added with 200 t hydraulic press
Pressure, brick face are in fact 250kg/cm by pressure2, the brick shape of 400 × 200 × 55mm is made afterwards, presses 15 altogether, is moved with vacuum chuck
Upper high temperature backing plate is burnt into roller kilns in 1050 DEG C of maximum temperatures, and firing period is 300 minutes, and firing obtains open spontaneous
Generate the multi-functional water-permeable brick of negative oxygen ion.Its main indicator is tested：
Flexural strength 7.8Mpa
Coefficient of permeability 2.7cm/s
2350/cm of anion release concentration3
Radionuclide test：γ=0.90 Ira=0.73, I.
Embodiment 7
Fabric compound hydrosol (A4) 30kg is prepared, is formulated as follows
After preparing as described in Example 1 with process, 120 meshes are crossed, stand 24 hours, abundant aquation, for use.
Bottom material is prepared with compound hydrosol 50kg (B4)
| Water | 71.95% | 35.975kg |
| Converted starch | 8% | 4.0kg |
| Lithium carbonate powder | 10% | 5kg |
| Albite in powder | 10% | 5kg |
| Tertiary sodium phosphate | 0.05% | 0.025kg |
After preparing as described in Example 1 with process, 120 meshes are crossed, stand 24 hours, abundant aquation, for use.
Fabric preparation：Take total 60kg fabric
10~16 mesh, 75% 45kg
16~60 mesh, 25% 15kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol body of 6kg A4, and carry out that horizontal distributing is broken to stir evenly, and break up fine powder conglomeration, is stirred for mixing 5
Minute.
Bottom material preparation：The total 100kg of bottom material aggregate is taken, wherein
3~10 mesh, 50% 50kg
10~16 mesh, 30% 30kg
16~60 mesh, 20% 20kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 10kg B4, and carry out that horizontal distributing is broken to stir evenly, and breaks up fine powder conglomeration.
With 600 × 300mm mold, add bottom material 15kg, cloth is flat, then plus fabric 5.2kg, cloth is flat, with 1500T hydraulic press, uses
It is placed on high temperature backing plate after the pressure maintaining of 27Mpa pressure 5~8 seconds with vacuum chuck taking-up, presses 5 altogether.Afterwards with roller kilns in highest
1030 DEG C of temperature, 300 minute period firing, obtains the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion, tests its main function
It can index：
Flexural strength 9.2Mpa
Coefficient of permeability 2.7cm/s
2430/cm of anion release concentration3
Radionuclide test：γ=1.07 Ira=0.78, I.
Structural schematic diagram such as Fig. 1 institute of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion of embodiment 1-7 preparation
Show, including precoat and initial bed.
Embodiment 8
Using a distributing mode, i.e. bottom material, the identical material of fabric, aggregate 200kg is taken, wherein
3~10 mesh, 50% 100kg
10~16 mesh, 20% 40kg
16~60 mesh, 30% 60kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 18kg A1, and carry out that horizontal distributing is broken to stir evenly, and manually breaks up fine powder conglomeration, and again
Stirring 5 minutes, naked-eye observation is without obvious fine powder conglomeration.
With 200 × 100mm mold, 2.2kg material is added, cloth is flat, with 25mpa pressure compression moulding, presses 50 altogether, places
On high temperature backing plate, with 1050 DEG C of maximum temperature, it is burnt within firing period 240 minutes, obtains open spontaneous generation negative oxygen ion
Multi-functional water-permeable brick.To its major function index test：
Flexural strength 8.4Mpa
Coefficient of permeability 2.4cm/s
2590/cm of anion release concentration3
Radionuclide test：γ=1.08 Ira=0.83, I.
Embodiment 9
Using a distributing mode, i.e. bottom material, the identical material of fabric, aggregate 100kg is taken, wherein
10~16 mesh, 80% 80kg
16~60 mesh, 20% 20kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 10kg A2, and carry out that horizontal distributing is broken to stir evenly, manually breaks up fine powder conglomeration, be stirred for 5 points
Clock, naked-eye observation is without obvious fine powder conglomeration.
With 200 × 100mm mold, 2.1kg material is added, presses 30 altogether, is placed on high temperature backing plate, with maximum temperature 1050
DEG C, it was burnt within the period 240 minutes, obtains the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion.Its main indicator is tested：
Flexural strength 10.3Mpa
Coefficient of permeability 3.1cm/s
2670/cm of anion release concentration3
Radionuclide test：γ=0.97 Ira=0.80, I.
The structural schematic diagram of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion prepared by embodiment 9 is as shown in Figure 2.
Embodiment 10
Using a distributing mode, i.e. bottom material, the identical material of fabric, aggregate 100kg is taken, wherein
3~10 mesh, 40% 40kg
10~16 mesh, 30% 30kg
16~60 mesh, 30% 30kg
After progress horizontal batch is uniform, sprayed using pressure atomization with the mode that compressed air secondary-atomizing mode combines
Add the compound hydrosol of 10kg A4, and carry out that horizontal distributing is broken to stir evenly, manually breaks up fine powder conglomeration, be stirred for 5 points
Clock, naked-eye observation is without obvious fine powder conglomeration.
With 300 × 300 molds, 10.5kg material is added, after the compacting of 27mpa pressure, vacuum chuck is placed on high temperature backing plate
On, press 6 altogether, with 1030 DEG C of maximum sintering temperature, firing period is 270 minutes, be burnt into the open spontaneous negative oxygen of generation from
The multi-functional water-permeable brick of son.It is to its major function index test result：
Flexural strength 9.7Mpa
Coefficient of permeability 3.5cm/s
2890/cm of anion release concentration3
Radionuclide test：γ=1.17 Ira=0.93, I (in the limitation of national standard A class).
Structural schematic diagram such as Fig. 3 institute of the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion prepared by embodiment 10
Show.
The spontaneous generation anion of product of the present invention energy, with the moisture and moisture in water-permeable brick gap (voidage 20~40%)
Son directly contacts, and anion can be efficiently generated, due to the O in air2N in molecular proportion air2Molecule and CO2Molecule has more
Compatibility, the anion of generation is preferentially and O2Molecule combines and forms negative oxygen ion.According to the World Health Organization and various countries' medical research,
Negative oxygen ion to the health of human body have " air vitamin " title, now because densely populated in city, industrial waste gas and motor-driven
Tail gas discharge is serious, and the negative oxygen ion in environment is more and more low, the major part of the particle (PM2.5) to suspend in air be band just
Charge, because of the principle that there is a natural attraction between the sexes, negative oxygen ion can in time, fully with positively charged particle ining conjunction with, formed after neutralization reunion,
Sedimentation can effectively reduce haze, improve because of air quality.During another rainwater penetrates into surface soil through water-permeable brick, because of tourmaline
Particle generates hydrolysis, can produce the alkalescent of PH7~8.5, has to the surface rain in the big or middle city of current 80% acid rain
Improved effect, separately plays the role of decomposition to dirty Organic substance in water, plays the role of improvement to sewage deodorizing.
Separately due to using in the street crossing face of road both sides, pedestrian's walking steps down in water-permeable brick surface and generates pressure, can produce
Piezoelectric effect.What the vehicle walked on road generated can propose the vibration on both sides pavement and the sound wave impact of noise road pavement
The ability of high-negative ion powder (compound tourmaline powder) launching electronics, to urban air-quality is improved, pedestrian is breathed to higher concentration
Negative oxygen ion play the role of it is positive.The present invention provides can significantly improve air matter in current big or middle urban public environment
Amount, the product for reducing haze concentration, and be can spontaneous permanent generation anion and generate the negative oxygen ion of higher concentration (simultaneously
The consumption energy is not needed).
Energy is permanent while meeting the seepy material that sponge city uses for product, automatically generates negative oxygen ion, can be effective
While reducing PM2.5, the negative oxygen ion of the title of vitamin in air is increased, wholesome street crossing is provided to human body
Or square, market prospects will be more and more wide, the economic benefit of production can also have lasting guarantee.
Claims (8)
1. a kind of open spontaneous multi-functional water-permeable brick of generation negative oxygen ion, which is characterized in that the open spontaneous generation is negative
The multi-functional water-permeable brick of oxonium ion includes precoat and initial bed, and the precoat includes following components in percentage by weight：
Wall or floor tile waste material grain A 90-93%,
Compound hydrosol A 7-10%,
The initial bed includes following components in percentage by weight：
Wall or floor tile waste material grain B 90-93%,
Compound hydrosol B 7-10%；
The water absorption rate of the Wall or floor tile waste material grain A and Wall or floor tile waste material grain B are less than 3%；
The compound hydrosol A includes following components in percentage by weight：
The compound hydrosol B includes following components in percentage by weight：
2. the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion according to claim 1, which is characterized in that the wall
Floor tile waste material grain A is mixed to form by the Wall or floor tile waste material grain of the granular-grade of following weight percent：
10-16 mesh Wall or floor tile waste material grain 75-85%,
16-60 mesh Wall or floor tile waste material grain 15-25%.
3. the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion according to claim 1, which is characterized in that the wall
Floor tile waste material grain B is mixed to form by the Wall or floor tile waste material grain of the granular-grade of following weight percent：
3-10 mesh Wall or floor tile waste material grain 40-50%,
10-16 mesh Wall or floor tile waste material grain 15-30%,
16-60 mesh Wall or floor tile waste material grain 20-35%.
4. the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion according to claim 1, which is characterized in that described multiple
The specific gravity of Heshui solution A and compound hydrosol B are 1.70-2.0g/cm3, Engler viscosity is 40-50 seconds.
5. the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion according to claim 1, which is characterized in that the carbon
Sour lithium fine powder is the industrial tailing that carbonic acid lithium content is 50-60%, and fineness is 250-320 mesh；The fineness of the albite fine powder
For 250-300 mesh, Na2O content > 6.7%.
6. the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion according to claim 1, which is characterized in that described negative
Ion powder by weight percent following raw material：Dravite 12-18%, iron dravite 12-18%, chromium dravite 12-
18%, hokutolite 48-56% is mixed, and the fineness of the negative ion powder is 1200-1500 mesh.
7. the method for preparing the open spontaneous multi-functional water-permeable brick of generation negative oxygen ion described in any one of claim -1-6,
It is characterized by comprising the following steps：
1) the Wall or floor tile waste material grain B of initial bed is subjected to ingredient in proportion, carries out horizontal batch, using pressure atomization and compression
The mode that air secondary atomizing type combines adds compound hydrosol B, carries out the broken stirring of horizontal distributing, is sent into automatic bottom
Expect that feeder is stand-by, obtains bottom material；
2) the Wall or floor tile waste material grain A of precoat is subjected to ingredient in proportion, carries out horizontal batch, using pressure atomization and compression
The mode that air secondary atomizing type combines adds compound hydrosol A, carries out the broken stirring of horizontal distributing, is sent into automatic top
Expect that feeder is stand-by, obtains fabric；
3) bottom material is sent into press and carries out a cloth, fabric is sent into press and carries out secondary material distributing, compression moulding, demoulding obtains
To water-permeable brick semi-finished product；
4) water-permeable brick semi-finished product are put into kiln and carry out heating firing, it is cooling to get more to open spontaneous generation negative oxygen ion
Function water-permeable brick.
8. the method according to the description of claim 7 is characterized in that the revolving speed that horizontal distributing is crushed whipping process control is
2000-2900 revs/min, the pressure control of compression moulding is 17-27Mpa, and heating sintering process control is：First stage, firing
Temperature is 50-200 DEG C, time 15-30min；Second stage, firing temperature are 200-450 DEG C, time 15-30min；The
Three stages, firing temperature are 450-700 DEG C, time 25-40min；Fourth stage, firing temperature are 900-1030 DEG C, the time
For 35-45min；5th stage, firing temperature are 1030-1050 DEG C, time 40-60min；It is empty using pressure atomization and compression
When the mode that gas secondary-atomizing mode combines adds compound hydrosol A and compound hydrosol B, the condition of control is：Nozzle holes
Diameter Φ 2.5~Φ 3.0mm, 0.5~0.6mpa of pressure；Compressed air pressure is 0.4~0.6mpa.
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| CN109673406B (en) * | 2018-12-05 | 2020-12-08 | 四川农业大学 | Construction method of moso bamboo forest health-care system |
| CN111875367A (en) * | 2020-08-07 | 2020-11-03 | 广西净雨环保科技有限公司 | Preparation method of waterproof granite-like plate |
| CN116262661A (en) * | 2021-12-13 | 2023-06-16 | 广东金裕福建材有限公司 | Negative ion ceramic tile with air purification and peculiar smell removal functions and production process thereof |
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| CN1336349A (en) * | 2001-08-31 | 2002-02-20 | 庞伟 | permeable ceramic brick and its production process |
| CN104003755A (en) * | 2014-05-21 | 2014-08-27 | 佛山市东鹏陶瓷有限公司 | Process for preparing ventilating brick by using polishing waste residue |
| CN104860670A (en) * | 2015-05-04 | 2015-08-26 | 安徽省亚欧陶瓷有限责任公司 | Hematite health care ceramic tile and preparation method thereof |
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Effective date of registration: 20210728 Address after: 529400 Enping Ganghua Ceramics Co., Ltd., Encheng north suburb industrial zone, Enping City, Jiangmen City, Guangdong Province Patentee after: GUANGDONG CLERAIN ENVIRONMENTAL SCI-TECH Co.,Ltd. Address before: 543000 in Guangxi Xindu Ceramics Co., Ltd. (No. A3, Ceramic Industrial Park), beside the second class road of Tangdong, Tengzhou Town, Tengxian County, Wuzhou City, Guangxi Zhuang Autonomous Region Patentee before: Guangxi Jingyu Environmental Protection Technology Co.,Ltd. |
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