CN117534326A - Preparation method of rock plate protection glaze and printed rock plate - Google Patents
Preparation method of rock plate protection glaze and printed rock plate Download PDFInfo
- Publication number
- CN117534326A CN117534326A CN202311700438.6A CN202311700438A CN117534326A CN 117534326 A CN117534326 A CN 117534326A CN 202311700438 A CN202311700438 A CN 202311700438A CN 117534326 A CN117534326 A CN 117534326A
- Authority
- CN
- China
- Prior art keywords
- glaze
- rock
- rock plate
- parts
- anhydrous
- 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.)
- Granted
Links
- 239000011435 rock Substances 0.000 title claims abstract description 85
- 238000002360 preparation method Methods 0.000 title claims abstract description 27
- 239000002270 dispersing agent Substances 0.000 claims abstract description 47
- 230000001681 protective effect Effects 0.000 claims abstract description 40
- 239000002994 raw material Substances 0.000 claims abstract description 30
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 26
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 25
- 238000005507 spraying Methods 0.000 claims abstract description 15
- 239000003960 organic solvent Substances 0.000 claims abstract description 14
- 238000005245 sintering Methods 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims description 31
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 30
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- 238000003756 stirring Methods 0.000 claims description 16
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- -1 acrylic compound Chemical class 0.000 claims description 14
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 14
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 14
- 238000000227 grinding Methods 0.000 claims description 11
- 239000004342 Benzoyl peroxide Substances 0.000 claims description 10
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
- 239000002202 Polyethylene glycol Substances 0.000 claims description 10
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 10
- 239000013530 defoamer Substances 0.000 claims description 10
- 229920001223 polyethylene glycol Polymers 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 8
- 239000000725 suspension Substances 0.000 claims description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims description 6
- XUPYJHCZDLZNFP-UHFFFAOYSA-N butyl butanoate Chemical compound CCCCOC(=O)CCC XUPYJHCZDLZNFP-UHFFFAOYSA-N 0.000 claims description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 6
- 239000004576 sand Substances 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 3
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 3
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 3
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 3
- HFZLSTDPRQSZCQ-UHFFFAOYSA-N 1-pyrrolidin-3-ylpyrrolidine Chemical compound C1CCCN1C1CNCC1 HFZLSTDPRQSZCQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011490 mineral wool Substances 0.000 claims 3
- 230000001133 acceleration Effects 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 238000007639 printing Methods 0.000 abstract description 7
- 230000000149 penetrating effect Effects 0.000 abstract description 4
- 230000002708 enhancing effect Effects 0.000 abstract description 2
- 238000006116 polymerization reaction Methods 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 21
- 238000000576 coating method Methods 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 16
- 150000003254 radicals Chemical class 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000010454 slate Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000012986 chain transfer agent Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 8
- 238000001556 precipitation Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 5
- 235000012211 aluminium silicate Nutrition 0.000 description 5
- 239000010433 feldspar Substances 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000010453 quartz Substances 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000010459 dolomite Substances 0.000 description 3
- 229910000514 dolomite Inorganic materials 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000010456 wollastonite Substances 0.000 description 3
- 229910052882 wollastonite Inorganic materials 0.000 description 3
- 229910021532 Calcite Inorganic materials 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 229910052656 albite Inorganic materials 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 235000019700 dicalcium phosphate Nutrition 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 2
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 1
- JMIVGVPHTRYNAJ-UHFFFAOYSA-N OC(=O)C(C)P(=O)=O Chemical compound OC(=O)C(C)P(=O)=O JMIVGVPHTRYNAJ-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 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 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/14—Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions
- C03C8/16—Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions with vehicle or suspending agents, e.g. slip
-
- 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
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/50—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
- C04B41/5022—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with vitreous 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
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/81—Coating or impregnation
- C04B41/85—Coating or impregnation with inorganic materials
- C04B41/86—Glazes; Cold glazes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/104—Esters of polyhydric alcohols or polyhydric phenols of tetraalcohols, e.g. pentaerythritol tetra(meth)acrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Structural Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
Abstract
本发明公开了一种岩板保护釉料及打印岩板的制备方法。所述岩板保护釉料,包括下述重量份原料:基础釉料35‑55份;有机溶剂45‑55份;消泡剂0.04‑0.12份;流平剂0.04‑0.08份;釉料无水分散剂4‑8份。所述打印岩板的制备方法,包括下述步骤:将所述岩板保护釉料喷涂至岩板坯体烧结。本发明在岩板保护釉料中引入了釉料无水分散剂,确保釉料中不含水分,从而减少釉料中水分渗透坯体的问题,提高了釉层与坯体之间的结合强度,增强了岩板的强度和耐久性。The invention discloses a rock plate protective glaze and a preparation method for printing rock plates. The rock plate protective glaze includes the following raw materials by weight: 35-55 parts of basic glaze; 45-55 parts of organic solvent; 0.04-0.12 parts of defoaming agent; 0.04-0.08 parts of leveling agent; glaze anhydrous 4-8 parts of dispersant. The preparation method of the printed rock plate includes the following steps: spraying the rock plate protective glaze to the rock plate body for sintering. The present invention introduces a glaze anhydrous dispersant into the rock plate protective glaze to ensure that the glaze does not contain moisture, thereby reducing the problem of moisture in the glaze penetrating into the green body and improving the bonding strength between the glaze layer and the green body. , enhancing the strength and durability of the rock slab.
Description
技术领域Technical field
本发明涉及岩板技术领域,尤其涉及一种岩板保护釉料及打印岩板的制备方法。The invention relates to the technical field of rock panels, and in particular to a rock panel protective glaze and a preparation method for printing rock panels.
背景技术Background technique
近年来,随着陶瓷喷墨技术在陶瓷行业的迅速兴起,陶瓷制造企业纷纷引进陶瓷数码喷墨打印机,取代传统的印花工艺,以满足市场需求。In recent years, with the rapid rise of ceramic inkjet technology in the ceramic industry, ceramic manufacturing companies have introduced ceramic digital inkjet printers to replace traditional printing processes to meet market demand.
然而,就目前的技术情境而言,岩板的加工通常采用数码喷釉工艺,即采用数码打印釉料的方法。然而,在现有的岩板保护釉料中,通常采用基础釉料、有机溶剂、消泡剂、流平剂以及含水分散剂等组成的基础配方。然而,这种岩板保护釉料本质上是一种含水悬浮液,其易于渗透进入岩板坯体的内部。由此引发的问题对产品的强度和耐久性产生了显著的负面影响。特别是在烧制过程中,这种渗透现象可能会导致开裂的发生,甚至会在最终成品中降低岩板的断裂模数,进而影响产品的整体强度和使用寿命。However, as far as the current technical situation is concerned, the processing of rock slabs usually adopts the digital glaze spraying process, that is, the method of digitally printing glaze. However, in existing slate protective glazes, a basic formula consisting of basic glaze, organic solvent, defoaming agent, leveling agent and aqueous dispersant is usually used. However, this slate protective glaze is essentially an aqueous suspension, which easily penetrates into the interior of the slate body. The resulting problems have a significant negative impact on the strength and durability of the product. Especially during the firing process, this penetration phenomenon may lead to the occurrence of cracking and even reduce the rupture modulus of the rock slab in the final product, thereby affecting the overall strength and service life of the product.
这种渗透现象带来的弱点严重制约了岩板制造过程中的质量和稳定性。因为含水分散剂的存在,涂布过程中岩板保护釉料更易渗透进入坯体的毛细孔和裂缝中,导致涂层与坯体之间的结合不够紧密,进而影响岩板的整体结构和性能。这在烧制过程中尤为显著,涂料的挥发和烧结过程可能导致水分蒸发,使涂层与坯体之间的粘结更加脆弱。这种现象进一步引发了岩板烧制过程中的开裂问题,破坏了产品的外观和品质。更为严重的是,这种问题可能会延续到最终成品中,导致岩板的强度不足,从而影响其在使用时的耐久性。The weaknesses brought about by this penetration phenomenon severely restrict the quality and stability of the rock slab manufacturing process. Due to the presence of aqueous dispersants, the protective glaze for rock slabs is more likely to penetrate into the capillary pores and cracks of the body during the coating process, resulting in an insufficiently tight bond between the coating and the body, thus affecting the overall structure and performance of the rock slab. . This is especially noticeable during the firing process. The volatilization of the coating and the sintering process may cause water to evaporate, making the bond between the coating and the body more fragile. This phenomenon further causes the problem of cracking during the firing process of rock slabs, destroying the appearance and quality of the product. What's more serious is that this problem may extend into the final product, resulting in insufficient strength of the rock slab, thus affecting its durability during use.
发明内容Contents of the invention
鉴于上述技术缺陷,迫切需要一种创新性的解决方案来克服这些技术难题。这种解决方案必须能够提升岩板保护釉料的制备和应用过程中的稳定性,确保涂层与坯体之间的良好结合,并在烧制和使用阶段保持稳定的性能。在这个技术背景下,本发明应运而生,通过引入釉料无水分散剂和相应的制备工艺,创新性地解决了岩板保护釉料制备过程中的核心问题。In view of the above technical shortcomings, an innovative solution is urgently needed to overcome these technical difficulties. This solution must be able to improve the stability during the preparation and application of the slate protective glaze, ensure a good bond between the coating and the body, and maintain stable performance during the firing and use stages. Against this technical background, the present invention emerged as the times require. By introducing an anhydrous dispersant for the glaze and a corresponding preparation process, it innovatively solves the core problem in the preparation process of the glaze for protecting rock slabs.
本发明所要解决的技术问题是提供了一种岩板保护釉料及打印岩板的制备方法。The technical problem to be solved by the present invention is to provide a rock plate protective glaze and a preparation method for printing rock plates.
本发明的具体技术方案为:The specific technical solutions of the present invention are:
本发明公开了一种岩板保护釉料,包括下述重量份原料:The invention discloses a rock plate protective glaze, which includes the following raw materials in parts by weight:
基础釉料35-55份;35-55 parts of basic glaze;
有机溶剂45-55份;45-55 parts of organic solvent;
消泡剂0.04-0.12份;Defoaming agent 0.04-0.12 parts;
流平剂0.04-0.08份;Leveling agent 0.04-0.08 parts;
釉料无水分散剂4-8份。4-8 parts of glaze water-free dispersant.
所述釉料无水分散剂,采用下述方法制备而成:The glaze anhydrous dispersant is prepared by the following method:
(1)将丙烯酸类化合物和苯乙烯加入N,N-二甲基甲酰胺中;(1) Add acrylic compounds and styrene to N,N-dimethylformamide;
(2)加入聚乙二醇二甲基丙烯酸酯;(2) Add polyethylene glycol dimethacrylate;
(3)加入甲基丙烯磺酸钠;(3) Add sodium methacrylate sulfonate;
(4)加入过氧化苯甲酰;(4) Add benzoyl peroxide;
(5)搅拌60-180分钟;(5) Stir for 60-180 minutes;
(6)冷却至室温。(6) Cool to room temperature.
优选地,一种釉料无水分散剂,采用下述方法制备而成:Preferably, a glaze anhydrous dispersant is prepared by the following method:
(1)70-80℃,氮气环境下,保持100-300转/分搅拌下,将50-60g丙烯酸类化合物和20-30g苯乙烯滴加到30-50gN,N-二甲基甲酰胺中;(1) At 70-80°C, in a nitrogen environment, add 50-60g acrylic compound and 20-30g styrene dropwise to 30-50g N,N-dimethylformamide while stirring at 100-300 rpm. ;
(2)滴加5-15g聚乙二醇二甲基丙烯酸酯;(2) Add 5-15g polyethylene glycol dimethacrylate dropwise;
(3)加入1-3g甲基丙烯磺酸钠,100-300转/分搅拌5-15分钟;(3) Add 1-3g sodium methacrylate sulfonate and stir at 100-300 rpm for 5-15 minutes;
(4)滴加1-3g过氧化苯甲酰;(4) Add 1-3g benzoyl peroxide dropwise;
(5)70-80℃,100-300转/分,搅拌60-180分钟;(5) 70-80℃, 100-300 rpm, stir for 60-180 minutes;
(6)冷却至室温,得到所述釉料无水分散剂。(6) Cool to room temperature to obtain the glaze anhydrous dispersant.
优选地,步骤中(1)、(2)和(4)的滴加速度均为0.2-1.0g/分钟。Preferably, the dropping speeds of steps (1), (2) and (4) are all 0.2-1.0g/minute.
优选地,所述丙烯酸类化合物为丙烯酸、甲基丙烯酸、四丙烯酸异戊四酯和季戊四醇三丙烯酸酯中的至少一种。Preferably, the acrylic compound is at least one of acrylic acid, methacrylic acid, isopentaerythrityl tetraacrylate and pentaerythritol triacrylate.
优选地,所述有机溶剂为甲醇、乙醇、乙二醇、二乙二醇、正丙醇、甘油、异丙醇、丙酮、丁醇、丁酮、丁二醇、环己酮、醋酸丁酯、丙酸丁酯、丁酸丁酯和二乙二醇单丁醚中的至少一种。Preferably, the organic solvent is methanol, ethanol, ethylene glycol, diethylene glycol, n-propanol, glycerin, isopropyl alcohol, acetone, butanol, butanone, butanediol, cyclohexanone, butyl acetate , at least one of butyl propionate, butyl butyrate and diethylene glycol monobutyl ether.
优选地,所述消泡剂为SN-DEFOAMER485消泡剂、SN-DEFOAMER77-P消泡剂、SN-Defoamer470消泡剂、巴斯夫Foamstar_SI2210消泡剂、日本信越KMZ-7752消泡剂、德国赢创TEGOFoamex805N消泡剂或TEGOFoamex810消泡剂中的至少一种。Preferably, the defoaming agent is SN-DEFOAMER485 defoaming agent, SN-DEFOAMER77-P defoaming agent, SN-Defoamer470 defoaming agent, BASF Foamstar_SI2210 defoaming agent, Japan's Shin-Etsu KMZ-7752 defoaming agent, Germany's Evonik At least one of TEGOFoamex805N defoamer or TEGOFoamex810 defoamer.
优选地,所述流平剂为流平剂BYK-333、流平剂BYK-358N、流平剂BYK-306或流平剂EFKA-3770中的至少一种。Preferably, the leveling agent is at least one of leveling agent BYK-333, leveling agent BYK-358N, leveling agent BYK-306 or leveling agent EFKA-3770.
本发明还公开了一种岩板保护釉料的制备方法,包括下述步骤:将有机溶剂、消泡剂、流平剂、釉料无水分散剂和基础釉料加入砂磨机中研磨均匀,得到悬浮液。The invention also discloses a method for preparing rock plate protective glaze, which includes the following steps: adding organic solvent, defoaming agent, leveling agent, glaze anhydrous dispersant and basic glaze into a sand mill and grinding evenly , to obtain a suspension.
优选地,直径0.5-1.5mm的氧化锆球作为研磨介质,砂磨时间2-8小时,研磨转速500-1500rpm。Preferably, zirconia balls with a diameter of 0.5-1.5 mm are used as grinding media, the sanding time is 2-8 hours, and the grinding speed is 500-1500 rpm.
本发明还公开了一种打印岩板的制备方法,包括下述步骤:将岩板保护釉料喷淋至岩板坯体,烧结。The invention also discloses a method for preparing a printed rock plate, which includes the following steps: spraying the rock plate protective glaze onto the rock plate body and sintering.
优选地,一种打印岩板的制备方法,包括下述步骤:采用喷墨机将岩板保护釉料喷涂于岩板坯体,控制喷涂量为20-80g/㎡,在1150-1250℃下烧结40-80min。Preferably, a method for preparing a printed rock board includes the following steps: using an inkjet machine to spray the rock board protective glaze onto the rock board body, controlling the spraying amount to 20-80g/㎡, at 1150-1250°C Sintering 40-80min.
本发明在岩板保护釉料中引入了釉料无水分散剂,确保釉料中不含水分,从而减少釉料中水分渗透坯体的问题,提高了釉层与坯体之间的结合强度,增强了岩板的强度和耐久性。The present invention introduces a glaze anhydrous dispersant into the rock plate protective glaze to ensure that the glaze does not contain moisture, thereby reducing the problem of moisture in the glaze penetrating into the green body and improving the bonding strength between the glaze layer and the green body. , enhancing the strength and durability of the rock slab.
具体实施方式Detailed ways
一种岩板保护釉料,包括下述重量份原料:A kind of rock plate protective glaze, including the following weight parts of raw materials:
基础釉料35-55份;35-55 parts of basic glaze;
有机溶剂45-55份;45-55 parts of organic solvent;
消泡剂0.04-0.12份;Defoaming agent 0.04-0.12 parts;
流平剂0.04-0.08份;Leveling agent 0.04-0.08 parts;
釉料无水分散剂4-8份。4-8 parts of glaze water-free dispersant.
所述釉料无水分散剂,采用下述方法制备而成:The glaze anhydrous dispersant is prepared by the following method:
(1)70-80℃,氮气环境下,保持100-300转/分搅拌下,将50-60g丙烯酸类化合物和20-30g苯乙烯滴加到30-50gN,N-二甲基甲酰胺中;(1) At 70-80°C, in a nitrogen environment, add 50-60g acrylic compound and 20-30g styrene dropwise to 30-50g N,N-dimethylformamide while stirring at 100-300 rpm. ;
丙烯酸类化合物和苯乙烯作为单体进行聚合反应,这些聚合物将成为分散剂的主要成分,影响其性能;Acrylic compounds and styrene are used as monomers for polymerization reactions. These polymers will become the main components of the dispersant and affect its performance;
N,N-二甲基甲酰胺主要起到溶解、混合和提供反应环境的作用;N,N-dimethylformamide mainly plays the role of dissolving, mixing and providing a reaction environment;
搅拌和加热至70-80℃有助于混合原材料,使其均匀分散;Stirring and heating to 70-80℃ helps mix the raw materials and make them evenly dispersed;
通入氮气可创建惰性气氛,防止反应体系受到氧化或其他干扰;Introducing nitrogen can create an inert atmosphere to prevent the reaction system from oxidation or other interference;
(2)滴加5-15g聚乙二醇二甲基丙烯酸酯;(2) Add 5-15g polyethylene glycol dimethacrylate dropwise;
聚乙二醇二甲基丙烯酸酯被用作交联剂,在聚合反应中引入交联点,增加材料的网络结构,提高材料的强度、稳定性和耐久性;Polyethylene glycol dimethacrylate is used as a cross-linking agent to introduce cross-linking points during the polymerization reaction, increase the network structure of the material, and improve the strength, stability and durability of the material;
(3)加入1-3g甲基丙烯磺酸钠,100-300转/分搅拌5-15分钟;(3) Add 1-3g sodium methacrylate sulfonate and stir at 100-300 rpm for 5-15 minutes;
甲基丙烯磺酸钠,作为链转移剂,在聚合反应中用于控制分子量的物质;引入到聚合反应中,通过捕获聚合活性中心,限制聚合链的生长,从而控制聚合物的分子量和分子量分布;Sodium methacrylate sulfonate, as a chain transfer agent, is used to control the molecular weight in polymerization reactions; it is introduced into the polymerization reaction to limit the growth of the polymer chain by capturing the polymerization active center, thereby controlling the molecular weight and molecular weight distribution of the polymer. ;
(4)滴加1-3g过氧化苯甲酰;(4) Add 1-3g benzoyl peroxide dropwise;
过氧化苯甲酰被用作自由基聚合反应的引发剂,在加热时会分解产生自由基,从而启动聚合反应;Benzoyl peroxide is used as an initiator for free radical polymerization. When heated, it decomposes to produce free radicals, thereby starting the polymerization reaction;
(5)70-80℃,100-300转/分,搅拌60-180分钟;(5) 70-80℃, 100-300 rpm, stir for 60-180 minutes;
控制温度在70-80℃有助于保持适宜的反应速率和产物质量;继续反应60-180分钟,确保聚合反应达到适当程度,形成所需的高分子聚合物;Controlling the temperature at 70-80°C will help maintain appropriate reaction rate and product quality; continue the reaction for 60-180 minutes to ensure that the polymerization reaction reaches an appropriate level and the required polymer is formed;
(6)冷却至室温,得到所述釉料无水分散剂。(6) Cool to room temperature to obtain the glaze anhydrous dispersant.
优选地,步骤中(1)、(2)和(4)的滴加速度均为0.2-1.0g/分钟。Preferably, the dropping speeds of steps (1), (2) and (4) are all 0.2-1.0g/minute.
优选地,所述丙烯酸类化合物为丙烯酸、甲基丙烯酸、四丙烯酸异戊四酯和季戊四醇三丙烯酸酯中的至少一种。Preferably, the acrylic compound is at least one of acrylic acid, methacrylic acid, isopentaerythrityl tetraacrylate and pentaerythritol triacrylate.
所述基础釉料,通常由两种主要类型的原材料组成,以实现涂层的特定性能和效果:(1)天然矿物原料:这些原材料来自地球的天然矿物资源,例如硅灰石、钠长石、石英、高岭土、烧滑石、长石、石灰石、白云石、锆英石等。它们可以用作填料或颜料,赋予涂层颜色、质感和装饰性。(2)无机非金属材料:这些原材料包括氧化锌、氧化铝、硅酸锆、氢氧化铝、磷酸氢钙、氟化镁等无机金属氧化物。它们在涂料中扮演重要角色,影响涂层的遮盖性、硬度、附着力和保护性能。这些原材料的组合和比例可以根据涂料的目标性能和所需效果进行调整,以实现最终的涂层质量。它们一起协同工作,为涂料提供所需的功能和特性。The basic glaze is usually composed of two main types of raw materials to achieve specific properties and effects of the coating: (1) Natural mineral raw materials: These raw materials come from the natural mineral resources of the earth, such as wollastonite, albite , quartz, kaolin, burnt talc, feldspar, limestone, dolomite, zircon, etc. They can be used as fillers or pigments to give color, texture and decorative properties to coatings. (2) Inorganic non-metallic materials: These raw materials include inorganic metal oxides such as zinc oxide, alumina, zirconium silicate, aluminum hydroxide, calcium hydrogen phosphate, magnesium fluoride, etc. They play an important role in coatings, affecting the coating's hiding, hardness, adhesion and protective properties. The combination and proportion of these raw materials can be adjusted according to the target performance and desired effect of the coating to achieve the final coating quality. They work together to provide the coating with the desired functionality and properties.
在本发明中可以采用本领域通用基础釉料配方即可,例如:In the present invention, common basic glaze formulas in this field can be used, for example:
所述基础釉料,由以下重量百分比的原料组成:10-20%钾长石粉、15-20%石英粉、15-25%高岭土、3-5%微铝粉、4-6%熟滑石粉、5-10%蔚州土、10-20%坪田洗泥和15-25%硅灰石。The basic glaze is composed of the following raw materials by weight: 10-20% potash feldspar powder, 15-20% quartz powder, 15-25% kaolin, 3-5% microaluminum powder, 4-6% cooked talc powder , 5-10% Yuzhou soil, 10-20% Pingtian washing mud and 15-25% wollastonite.
所述基础釉料,由以下重量百分比的原料组成:13-16%的三氧化二铝、67-75%的二氧化硅、2.5-5%的氧化钙、2-4.5%的氧化镁、3-5%的氧化钾和2-3%氧化钠。The basic glaze is composed of the following raw materials in weight percentages: 13-16% aluminum oxide, 67-75% silica, 2.5-5% calcium oxide, 2-4.5% magnesium oxide, 3 -5% potassium oxide and 2-3% sodium oxide.
所述基础釉料,由以下重量百分比的原料组成:长石15-25%、氢氧化铝4-10%、硅酸锆8-15%、石英粉23-37%、氧化锌2-6%、磷酸氢钙13-20%、氟化镁4-10%。The basic glaze is composed of the following raw materials in weight percentage: feldspar 15-25%, aluminum hydroxide 4-10%, zirconium silicate 8-15%, quartz powder 23-37%, zinc oxide 2-6% , calcium hydrogen phosphate 13-20%, magnesium fluoride 4-10%.
所述基础釉料,由以下重量百分比的原料组成:硅灰石10-12%、钠长石38-42%、高岭土5-10%、烧滑石3-5%、煅烧氧化锌3-4%、煅烧氧化铝11-14%和亮光熔块粉20-23%。The basic glaze is composed of the following raw materials in weight percentage: wollastonite 10-12%, albite 38-42%, kaolin 5-10%, burnt talc 3-5%, calcined zinc oxide 3-4% , calcined alumina 11-14% and bright frit powder 20-23%.
所述基础釉料,由以下重量份原料组成:石英31份、长石28份、方解石15份、白云石4份、滑石2.5份、氧化铝2份、氧化锌4.2份、高岭土2.3份、硅酸锆11份。The basic glaze is composed of the following raw materials by weight: 31 parts of quartz, 28 parts of feldspar, 15 parts of calcite, 4 parts of dolomite, 2.5 parts of talc, 2 parts of alumina, 4.2 parts of zinc oxide, 2.3 parts of kaolin, silicon 11 parts of zirconium acid.
所述有机溶剂为甲醇、乙醇、乙二醇、二乙二醇、正丙醇、甘油、异丙醇、丙酮、丁醇、丁酮、丁二醇、环己酮、醋酸丁酯、丙酸丁酯、丁酸丁酯和二乙二醇单丁醚中的至少一种。The organic solvent is methanol, ethanol, ethylene glycol, diethylene glycol, n-propanol, glycerol, isopropyl alcohol, acetone, butanol, methyl ethyl ketone, butanediol, cyclohexanone, butyl acetate, propionic acid At least one of butyl ester, butyl butyrate and diethylene glycol monobutyl ether.
所述消泡剂为本领域常用消泡剂,可以是SN-DEFOAMER485消泡剂、SN-DEFOAMER77-P消泡剂、SN-Defoamer470消泡剂、巴斯夫Foamstar_SI2210消泡剂、日本信越KMZ-7752消泡剂、德国赢创TEGOFoamex805N消泡剂或TEGOFoamex810消泡剂中的至少一种。The defoaming agent is a commonly used defoaming agent in this field, and can be SN-DEFOAMER485 defoaming agent, SN-DEFOAMER77-P defoaming agent, SN-Defoamer470 defoaming agent, BASF Foamstar_SI2210 defoaming agent, Japan Shin-Etsu KMZ-7752 defoaming agent Foaming agent, at least one of German Evonik TEGO Foamex805N defoaming agent or TEGO Foamex810 defoaming agent.
所述流平剂为本领域常用流平剂,如流平剂BYK-333、流平剂BYK-358N、流平剂BYK-306或流平剂EFKA-3770中的至少一种。The leveling agent is a commonly used leveling agent in this field, such as at least one of leveling agent BYK-333, leveling agent BYK-358N, leveling agent BYK-306 or leveling agent EFKA-3770.
本发明还公开了一种岩板保护釉料的制备方法,包括下述步骤:将有机溶剂、消泡剂、流平剂、釉料无水分散剂和基础釉料加入砂磨机中研磨均匀,得到悬浮液,即为本发明的岩板保护釉料。优选地,直径0.5-1.5mm的氧化锆球作为研磨介质,砂磨时间2-8小时,研磨转速500-1500rpm。The invention also discloses a method for preparing rock plate protective glaze, which includes the following steps: adding organic solvent, defoaming agent, leveling agent, glaze anhydrous dispersant and basic glaze into a sand mill and grinding them evenly , the suspension is obtained, which is the rock plate protective glaze of the present invention. Preferably, zirconia balls with a diameter of 0.5-1.5 mm are used as grinding media, the sanding time is 2-8 hours, and the grinding speed is 500-1500 rpm.
制备岩板保护釉料的过程包括以下关键步骤:首先,准备所需的原材料,包括有机溶剂、消泡剂、流平剂、釉料无水分散剂和基础釉料。接着,将这些原材料按照特定的配比添加到砂磨机中。砂磨机作为混合、搅拌和研磨设备,将原材料在其中进行充分的混合和搅拌,以实现均匀的分散状态。在砂磨机中经过一段时间的研磨和混合后,原材料彼此之间得以充分融合,形成一个均匀的悬浮液。这个步骤至关重要,因为它确保了各种成分的有效混合,从而保证了最终产品的一致性能。通过这个过程,原材料被充分混合并分散在有机溶剂中,形成了稳定的悬浮液。得到的悬浮液即为制备好的岩板保护釉料。这个悬浮液可以直接应用于岩板表面,以实现保护、装饰以及其他所需的性能。整个制备过程依次进行,确保了原材料的均匀分散,最终获得了高质量的岩板保护釉料。The process of preparing rock slab protective glaze includes the following key steps: First, prepare the required raw materials, including organic solvents, defoaming agents, leveling agents, glaze anhydrous dispersants and basic glazes. Then, these raw materials are added to the sand mill in specific proportions. Sand mill is used as a mixing, stirring and grinding equipment, in which the raw materials are fully mixed and stirred to achieve a uniform dispersion state. After a period of grinding and mixing in a sand mill, the raw materials are fully integrated with each other to form a uniform suspension. This step is crucial as it ensures the effective mixing of the various ingredients, thus guaranteeing consistent performance of the final product. Through this process, the raw materials are thoroughly mixed and dispersed in the organic solvent to form a stable suspension. The obtained suspension is the prepared rock plate protective glaze. This suspension can be applied directly to slate surfaces to achieve protection, decoration and other desired properties. The entire preparation process is carried out in sequence, ensuring the uniform dispersion of raw materials, and finally obtaining a high-quality rock slab protective glaze.
一种打印岩板的制备方法,包括下述步骤:采用喷墨机将岩板保护釉料喷涂于岩板坯体,控制喷涂量为20-80g/m2,在1150-1250℃下烧结40-80min。A method for preparing a printed rock plate, including the following steps: using an inkjet machine to spray the rock plate protective glaze on the rock plate body, controlling the spraying amount to 20-80g/ m2 , and sintering at 1150-1250°C for 40 -80min.
首先,选用喷墨机将事先准备好的岩板保护釉料喷涂在岩板坯体表面上。这一步旨在将釉料均匀地涂布于岩板表面,以实现保护和装饰的目的。喷涂过程需要注意控制喷涂量,即每平方米喷涂的釉料量,其范围在20-80g/平方米之间。在喷涂的过程中,需要精确控制喷涂量,以确保岩板表面获得均匀的涂层。喷涂量的控制与最终涂层的厚度和质量直接相关。喷涂量过多可能导致涂层不均匀或过厚,而喷涂量过少可能无法达到所需的保护效果。喷涂后的岩板坯体需要进入烧结过程,以将涂层与坯体融合并形成稳定的保护层。烧结温度在1150-1250℃之间,烧结时间为40-80分钟。在烧结过程中,涂层会与岩板坯体发生化学反应,同时固化和融合,从而形成结实的保护层。整个制备方法的目的是通过将岩板保护釉料喷涂在岩板坯体表面,然后在适当的温度下进行烧结,以实现对岩板的保护和装饰。喷涂量、烧结温度和时间的控制都对最终产品的质量和性能产生重要影响。经过喷涂和烧结后,岩板表面会形成一层保护性的涂层,这一层涂层可以提供岩板所需的保护功能,同时也能够实现装饰效果。整个制备过程需要精确控制各个参数,以获得高质量的打印岩板。First, use an inkjet machine to spray the pre-prepared rock slab protective glaze on the surface of the rock slab body. This step is intended to evenly apply the glaze to the surface of the slate for protection and decoration purposes. During the spraying process, attention needs to be paid to controlling the spraying amount, that is, the amount of glaze sprayed per square meter, which ranges from 20-80g/square meter. During the spraying process, the amount of spraying needs to be precisely controlled to ensure a uniform coating on the surface of the rock slab. The control of spray volume is directly related to the thickness and quality of the final coating. Applying too much may result in an uneven or thick coating, while applying too little may not provide the desired protection. The sprayed rock slab body needs to enter the sintering process to fuse the coating with the body and form a stable protective layer. The sintering temperature is between 1150-1250℃, and the sintering time is 40-80 minutes. During the sintering process, the coating reacts chemically with the slab body, solidifying and fusing at the same time to form a strong protective layer. The purpose of the entire preparation method is to protect and decorate the rock slab by spraying the rock slab protective glaze on the surface of the rock slab body and then sintering it at an appropriate temperature. The control of spray volume, sintering temperature and time all have an important impact on the quality and performance of the final product. After spraying and sintering, a protective coating will be formed on the surface of the rock slab. This layer of coating can provide the required protection function of the slab and also achieve a decorative effect. The entire preparation process requires precise control of various parameters to obtain high-quality printed rock slabs.
本发明的创新之处在于将釉料无水分散剂引入岩板保护釉料中,从而有效地消除了水分对釉料的影响。釉料无水分散剂的引入确保了釉料不含水分,因此在施加于岩板表面时,不会发生水分渗透到坯体内部的问题。这一关键特点解决了传统含水悬浮液釉料易渗透坯体的难题,从而避免了在烧制过程中可能导致的开裂现象。通过减少水分的渗透,岩板的整体强度得到了显著提升,因为釉料与坯体之间的结合强度得以增强,从而使得最终的岩板产品更具有耐久性和稳定性。The innovation of the present invention is that the glaze water-free dispersant is introduced into the rock plate protective glaze, thereby effectively eliminating the influence of moisture on the glaze. The introduction of the glaze water-free dispersant ensures that the glaze does not contain moisture, so when it is applied to the surface of the stone slab, there will be no problem of moisture penetrating into the interior of the body. This key feature solves the problem of traditional aqueous suspension glazes easily penetrating the body, thereby avoiding possible cracking during the firing process. By reducing moisture penetration, the overall strength of the slab is significantly improved because the bond between the glaze and the body is enhanced, making the final slab product more durable and stable.
此创新方案的优势不仅在于提高了岩板的强度和耐久性,还在于它为岩板行业带来了更为可靠和稳定的生产工艺。由于釉料无水分散剂的引入,生产过程中不再受制于水分含量的波动,从而避免了涂层均匀性和稳定性的问题。岩板制造企业可以更加可靠地控制生产过程,提高产品的一致性和质量。The advantage of this innovative solution is not only that it improves the strength and durability of the rock slabs, but also that it brings a more reliable and stable production process to the rock slab industry. Due to the introduction of water-free dispersants for glazes, the production process is no longer subject to fluctuations in moisture content, thereby avoiding problems with coating uniformity and stability. Slate manufacturing companies can more reliably control the production process, improving product consistency and quality.
在本发明实施例和对比例中,所采用的部分原材料具体介绍如下:In the examples and comparative examples of the present invention, some of the raw materials used are specifically introduced as follows:
基础釉料,由以下重量份原料组成:石英31份、长石28份、方解石15份、白云石4份、滑石2.5份、氧化铝2份、氧化锌4.2份、高岭土2.3份、硅酸锆11份。(参考至《卫生陶瓷原料与泥釉料配方徐熙武主编2018年版》),将上述各种原料按比例加入球磨机中,研磨48小时,过2000目筛,制成基础釉料。The basic glaze is composed of the following raw materials by weight: 31 parts of quartz, 28 parts of feldspar, 15 parts of calcite, 4 parts of dolomite, 2.5 parts of talc, 2 parts of alumina, 4.2 parts of zinc oxide, 2.3 parts of kaolin, and zirconium silicate 11 servings. (Refer to "Sanitary Ceramics Raw Materials and Mud Glaze Formulas, 2018 Edition edited by Xu Xiwu"). Add the above raw materials into a ball mill in proportion, grind for 48 hours, and pass through a 2000 mesh sieve to make a basic glaze.
甲氧聚乙二醇二甲基丙烯酸酯,MPEG400MA,购买自南通庄园化工有限公司。Methoxypolyethylene glycol dimethacrylate, MPEG400MA, was purchased from Nantong Zhuangzhuang Chemical Co., Ltd.
实施例1:Example 1:
A、釉料无水分散剂的制备:A. Preparation of water-free dispersant for glaze:
(1)70℃,氮气环境下,保持200转/分搅拌下,将55g丙烯酸类化合物和25g苯乙烯滴加到40gN,N-二甲基甲酰胺中;(1) At 70°C, in a nitrogen environment, add 55g of acrylic compound and 25g of styrene dropwise into 40g of N,N-dimethylformamide while maintaining stirring at 200 rpm;
(2)滴加10g聚乙二醇二甲基丙烯酸酯(PEGDMA2k);(2) Add 10g of polyethylene glycol dimethacrylate (PEGDMA2k) dropwise;
(3)加入2g甲基丙烯磺酸钠,200转/分搅拌10分钟;(3) Add 2g sodium methacrylate sulfonate and stir at 200 rpm for 10 minutes;
(4)滴加2g过氧化苯甲酰;(4) Add 2g benzoyl peroxide dropwise;
(5)75℃,200转/分,搅拌120分钟;(5) 75℃, 200 rpm, stir for 120 minutes;
(6)冷却至室温,得到透明粘稠状液态物质,即为本发明的釉料无水分散剂。(6) Cool to room temperature to obtain a transparent viscous liquid substance, which is the glaze anhydrous dispersant of the present invention.
其中,步骤中(1)、(2)和(4)滴加速度均为0.5g/分钟。Among them, the dropping speeds in steps (1), (2) and (4) are all 0.5g/minute.
所述丙烯酸类化合物为丙烯酸。The acrylic compound is acrylic acid.
B、岩板保护釉料的制备:B. Preparation of rock slab protective glaze:
将50重量份有机溶剂甘油、0.06重量份TEGOFoamex805N消泡剂、0.06重量份流平剂BYK-333、6重量份上述制备的釉料无水分散剂和45重量份上述制备的基础釉料加入砂磨机中研磨均匀,得到悬浮液,即为本发明的岩板保护釉料。其中采用直径1mm的氧化锆球作为研磨介质,砂磨时间5小时,研磨转速1000rpm。Add 50 parts by weight of organic solvent glycerin, 0.06 parts by weight of TEGO Foamex805N defoaming agent, 0.06 parts by weight of leveling agent BYK-333, 6 parts by weight of the glaze anhydrous dispersant prepared above and 45 parts by weight of the basic glaze prepared above. Grind evenly in a mill to obtain a suspension, which is the rock plate protective glaze of the present invention. Zirconia balls with a diameter of 1mm are used as grinding media, the sanding time is 5 hours, and the grinding speed is 1000rpm.
C、打印岩板的制备:C. Preparation of printed rock slabs:
采用喷墨机将上述制得的岩板保护釉料喷涂于岩板坯体,控制喷涂量为50g/m2,在1190℃下烧结60min,制得本发明的打印岩板。Use an inkjet machine to spray the rock plate protective glaze prepared above on the rock plate body, control the spraying amount to 50g/m 2 , and sinter at 1190°C for 60 minutes to prepare the printed rock plate of the present invention.
实施例2:Example 2:
与实施例1不同为:釉料无水分散剂的制备过程中,所述丙烯酸类化合物为甲基丙烯酸。The difference from Example 1 is that in the preparation process of the glaze anhydrous dispersant, the acrylic compound is methacrylic acid.
实施例3:Example 3:
与实施例1不同为:釉料无水分散剂的制备过程中,所述丙烯酸类化合物为四丙烯酸异戊四酯。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, the acrylic compound is isopentyl tetraacrylate.
实施例4:Example 4:
与实施例1不同为:釉料无水分散剂的制备过程中,所述丙烯酸类化合物为季戊四醇三丙烯酸酯。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, the acrylic compound is pentaerythritol triacrylate.
实施例5:Example 5:
与实施例1不同为:釉料无水分散剂的制备过程中,所述55g丙烯酸类化合物为25g甲基丙烯酸和30g季戊四醇三丙烯酸酯。The difference from Example 1 is that in the preparation process of the glaze anhydrous dispersant, the 55g acrylic compound is 25g methacrylic acid and 30g pentaerythritol triacrylate.
对比例1:Comparative example 1:
与实施例1不同为:釉料无水分散剂的制备过程中,N,N-二甲基甲酰胺替换为等重量的N-甲基吡咯烷酮。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, N,N-dimethylformamide was replaced by an equal weight of N-methylpyrrolidone.
对比例2:Comparative example 2:
与实施例1不同为:釉料无水分散剂的制备过程中,聚乙二醇二甲基丙烯酸酯(PEGDMA2k)替换为等重量的甲氧聚乙二醇二甲基丙烯酸酯。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, polyethylene glycol dimethacrylate (PEGDMA2k) was replaced by an equal weight of methoxypolyethylene glycol dimethacrylate.
对比例3:Comparative example 3:
与实施例1不同为:釉料无水分散剂的制备过程中,甲基丙烯磺酸钠替换为等重量的疏基丙酸。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, sodium methacrylate sulfonate was replaced by an equal weight of phosphopropionic acid.
对比例4:Comparative example 4:
与实施例1不同为:釉料无水分散剂的制备过程中,过氧化苯甲酰替换为等重量的偶氮二异丁氰。The difference from Example 1 is that during the preparation process of the glaze anhydrous dispersant, benzoyl peroxide was replaced by an equal weight of azobisisobutyl cyanide.
对比例5:Comparative example 5:
与实施例1不同为:釉料无水分散剂的制备过程中,N,N-二甲基甲酰胺替换为等重量的N-甲基吡咯烷酮;聚乙二醇二甲基丙烯酸酯(PEGDMA2k)替换为等重量的甲氧聚乙二醇二甲基丙烯酸酯;甲基丙烯磺酸钠替换为等重量的疏基丙酸;过氧化苯甲酰替换为等重量的偶氮二异丁氰。The difference from Example 1 is that: during the preparation process of the glaze anhydrous dispersant, N,N-dimethylformamide was replaced by an equal weight of N-methylpyrrolidone; polyethylene glycol dimethacrylate (PEGDMA2k) Replace with equal weight of methoxypolyethylene glycol dimethacrylate; replace sodium methacrylate sulfonate with equal weight of mercaptopropionic acid; replace benzoyl peroxide with equal weight of azobisisobutyl cyanide.
对比例6:Comparative example 6:
与实施例1不同为:岩板保护釉料的制备过程中,采用的分散剂为BSF公司PA25CL-FR分散剂(聚丙烯酸水溶液)。The difference from Example 1 is that in the preparation process of the rock plate protective glaze, the dispersant used is BSF Company. PA25CL-FR dispersant (polyacrylic acid aqueous solution).
空白例:Blank example:
未烧结且未喷涂釉料的岩板坯体。Unsintered and unglazed slate body.
测试例1:Test example 1:
岩板保护釉料沉淀率测试方法:Test method for sedimentation rate of slate protective glaze:
(1)将100g实施例及对比例所制得的岩板保护釉料分别加入干净的圆柱形玻璃瓶中;(1) Add 100g of the rock plate protective glaze prepared in the Examples and Comparative Examples into clean cylindrical glass bottles respectively;
(2)用盖子将玻璃瓶的瓶口封闭,以防止外部空气进入瓶内,从而保持内部环境的稳定性;(2) Seal the mouth of the glass bottle with a cap to prevent external air from entering the bottle, thereby maintaining the stability of the internal environment;
(3)把密封的玻璃瓶放置在恒定的环境中,温度设置为65±1℃,这是一个恒定的温度环境,以模拟釉料在高温条件下的稳定性;(3) Place the sealed glass bottle in a constant environment with the temperature set to 65±1°C. This is a constant temperature environment to simulate the stability of the glaze under high temperature conditions;
(4)让玻璃瓶在65±1℃的环境中静置10天;(4) Let the glass bottle stand in an environment of 65±1℃ for 10 days;
(5)静置期结束后,打开瓶盖轻轻倒出釉料后,再将玻璃瓶瓶口向下倒置5分钟,使得部分挂在瓶壁上的釉料滴落;(5) After the resting period, open the bottle cap and pour out the glaze gently, then turn the glass bottle upside down for 5 minutes to allow part of the glaze hanging on the bottle wall to drip;
(6)称量最终玻璃瓶的质量记为Y克,之前干净的玻璃瓶记为X克;(6) Weigh the final glass bottle and record it as Y grams, and the previously clean glass bottle as X grams;
(7)计算岩板保护釉料沉淀率=(Y-X)/100×100%。(7) Calculate the precipitation rate of the rock slab protective glaze = (Y-X)/100×100%.
沉淀率是一种比率,指的是在倒置试验后,与总釉料相比,最终附着在玻璃瓶的侧壁和内壁上的釉料的比例。沉淀率越低,表示釉料在特定条件下保持稳定性的能力更强,这表明该釉料更适合用于打印或喷涂在岩板上。这意味着这种釉料不太容易分离或沉淀,能够在高温环境下保持均匀分散,从而提供更好的质量和效果。Sedimentation rate is a ratio that refers to the proportion of glaze that ends up adhering to the side and inner walls of a glass bottle compared to the total glaze after an inversion test. The lower the settling rate, the greater the glaze's ability to remain stable under certain conditions, indicating that the glaze is more suitable for printing or spraying on rock slabs. This means the glaze is less likely to separate or settle and remains evenly dispersed in high-temperature environments, providing better quality and results.
表1岩板保护釉料沉淀率的测试结果Table 1 Test results of precipitation rate of rock plate protective glaze
实施例1至实施例5的岩板保护釉料沉淀率分别在6.2-9.5%之间。这些实施例的沉淀率相对较低,表明釉料在高温条件下能够保持较好的均匀分散性,不易分离或沉淀。这有助于确保打印或喷涂在岩板上的釉料质量和效果稳定。The precipitation rates of the rock plate protective glazes in Examples 1 to 5 are respectively between 6.2-9.5%. The precipitation rates of these examples are relatively low, indicating that the glaze can maintain good uniform dispersion under high temperature conditions and is not easy to separate or precipitate. This helps ensure the quality and consistency of glazes printed or sprayed onto rock slabs.
对比例1至对比例5的沉淀率分别在9.7-13.5%之间。相对于实施例,这些对比例的沉淀率较高,意味着这些配方的釉料在高温条件下更容易发生分离或沉淀,从而影响了其稳定性和质量。The precipitation rates of Comparative Examples 1 to 5 were respectively between 9.7-13.5%. Compared with the examples, the precipitation rates of these comparative examples are higher, which means that the glazes of these formulas are more likely to separate or precipitate under high temperature conditions, thus affecting their stability and quality.
综合来看,实施例的岩板保护釉料表现出更低的沉淀率,这反映了其在高温条件下保持稳定性的能力较强。这进一步证明了本发明引入的釉料无水分散剂对于提高岩板保护釉料的稳定性和质量具有积极作用,从而适用于打印或喷涂在岩板上,确保产品具有更好的质量和效果。Taken together, the rock plate protective glaze of the embodiment shows a lower precipitation rate, which reflects its strong ability to maintain stability under high temperature conditions. This further proves that the glaze water-free dispersant introduced in the present invention has a positive effect on improving the stability and quality of the rock plate protective glaze, so that it is suitable for printing or spraying on the rock plate, ensuring that the product has better quality and effect. .
测试例2:Test example 2:
将实施例及对比例所制得的打印岩板,采用《GBT 3810.4-2016陶瓷砖试验方法第4部分:断裂模数和破坏强度的测定》方法,进行断裂模数性能测试。The printed rock plates prepared in the Examples and Comparative Examples were tested for modulus of rupture performance using the method of "GBT 3810.4-2016 Ceramic Tile Test Methods Part 4: Determination of Modulus of Fracture and Destruction Strength".
表2打印岩板断裂模数性能的测试结果Table 2 Test results of fracture modulus performance of printed rock slabs
实施例1至实施例5的断裂模数范围在60.5-64.9MPa之间。这些实施例在采用本发明的岩板保护釉料后,显示出较高的断裂模数,表明岩板的抗弯曲和抗拉伸能力得到了增强,整体强度更高。The modulus of rupture of Examples 1 to 5 ranges from 60.5 to 64.9 MPa. These examples show a higher modulus of rupture after using the rock plate protective glaze of the present invention, indicating that the bending and tensile resistance of the rock plate is enhanced and the overall strength is higher.
对比例1至对比例5的断裂模数范围在55.7-59.9MPa之间。这些对比例使用了不同的成分,其断裂模数比实施例的结果低。这可能意味着一些对比配方在一定程度上也具有一定的强度性能,但明显不如本发明的实施例。The modulus of rupture of Comparative Examples 1 to 5 ranges from 55.7 to 59.9MPa. These comparative examples use different ingredients and have lower modulus of rupture than the results of the examples. This may mean that some comparative formulations also have certain strength properties to a certain extent, but are significantly inferior to the examples of the present invention.
对比例6的断裂模数为42.6MPa,这是所有测试中最低的值。这表明该对比例的配方对岩板的强度性能产生了较大的负面影响,可能由于成分选择过程中的某些问题。The modulus of rupture of Comparative Example 6 is 42.6MPa, which is the lowest value among all tests. This indicates that the formulation of this comparative example has a greater negative impact on the strength properties of the rock slab, possibly due to some issues in the ingredient selection process.
综合来看,本发明的实施例在断裂模数性能方面表现出明显的优势,具有更高的抗弯曲和抗拉伸能力。这进一步证实了引入釉料无水分散剂的岩板保护剂对于提高产品的整体强度和耐久性具有重要作用。Taken together, the embodiments of the present invention show obvious advantages in modulus of rupture performance and have higher bending resistance and tensile resistance. This further confirms that the introduction of slate protective agents as glaze water-free dispersants plays an important role in improving the overall strength and durability of the product.
在制备釉料无水分散剂的过程中,不同的原材料扮演着关键角色,共同构建了稳定的聚合反应环境,确保所制备的无水分散剂具备卓越的性能。以下是各个原材料的作用及其在实验数据中的表现:In the process of preparing the water-free dispersant for glazes, different raw materials play a key role, jointly building a stable polymerization reaction environment and ensuring that the prepared water-free dispersant has excellent performance. The following is the role of each raw material and its performance in experimental data:
丙烯酸类化合物和苯乙烯:作为单体参与聚合反应,形成分散剂的主要成分。这些成分的选择和聚合过程直接影响着最终的性能特征。实验数据表明,不同的丙烯酸类化合物在性能上存在差异,季戊四醇三丙烯酸酯>四丙烯酸异戊四酯>丙烯酸>甲基丙烯酸。Acrylic compounds and styrene: participate in the polymerization reaction as monomers and form the main components of the dispersant. The selection of these ingredients and the polymerization process directly affect the final performance characteristics. Experimental data show that different acrylic compounds have differences in performance, pentaerythritol triacrylate > isopenterythrityl tetraacrylate > acrylic acid > methacrylic acid.
N,N-二甲基甲酰胺:在反应中发挥溶解和混合的作用,同时提供了适宜的反应环境,促进其他原材料的反应进行。实验数据中显示,其效果明显优于N-甲基吡咯烷酮。N,N-dimethylformamide: plays the role of dissolving and mixing in the reaction, and provides a suitable reaction environment to promote the reaction of other raw materials. Experimental data show that its effect is significantly better than N-methylpyrrolidone.
氮气:引入氮气以创建惰性气氛,防止反应过程受到氧化或其他干扰,确保聚合反应在稳定的环境中进行。Nitrogen: Nitrogen is introduced to create an inert atmosphere, prevent the reaction process from oxidation or other interference, and ensure that the polymerization reaction proceeds in a stable environment.
聚乙二醇二甲基丙烯酸酯:引入交联点,形成复杂的网络结构。这有助于提高釉料的强度、稳定性和耐久性。实验数据中显示,其效果明显优于交联剂甲氧聚乙二醇二甲基丙烯酸酯。Polyethylene glycol dimethacrylate: introduces cross-linking points to form a complex network structure. This helps improve the strength, stability and durability of the glaze. Experimental data shows that its effect is significantly better than that of the cross-linking agent methoxypolyethylene glycol dimethacrylate.
甲基丙烯磺酸钠:作为链转移剂,调控聚合物分子量和分子量分布。它通过捕获聚合活性中心来限制聚合链的生长,实现对聚合反应的控制。实验数据中显示,其效果明显优于链转移剂疏基丙酸。Sodium methacrylate sulfonate: used as a chain transfer agent to control polymer molecular weight and molecular weight distribution. It limits the growth of polymer chains by capturing polymerization active centers to control polymerization reactions. Experimental data shows that its effect is significantly better than that of the chain transfer agent mercaptopropionic acid.
过氧化苯甲酰:作为自由基聚合反应的引发剂,通过加热分解产生自由基,启动聚合反应的链式增长。Benzoyl peroxide: As an initiator of free radical polymerization, it generates free radicals through thermal decomposition and initiates the chain growth of the polymerization reaction.
综上所述,这些不同的原材料在相互协作下,形成了稳定的聚合反应体系,成功实现了无水分散剂的制备。实验数据也进一步证实了各个原材料的作用在整个制备过程中的重要性,为岩板的质量和性能提供了坚实的基础。In summary, these different raw materials cooperate with each other to form a stable polymerization reaction system and successfully achieve the preparation of anhydrous dispersants. Experimental data also further confirmed the importance of each raw material in the entire preparation process, providing a solid foundation for the quality and performance of rock slabs.
进一步分析,甲基丙烯磺酸钠作为链转移剂在聚合反应中的作用原理涉及自由基聚合的机制。在自由基聚合中,聚合活性中心通过链转移反应来调节聚合物的分子量和分子量分布。链转移剂的作用是通过与自由基反应来捕获和稳定活性自由基,从而阻止自由基的继续反应,导致聚合链的生长受到限制。这一过程能够在一定程度上控制聚合物分子量的增长速率,从而影响聚合物的分子量分布。具体到甲基丙烯磺酸钠在制备无水分散剂的过程中的作用,它的分子结构中含有磺酸基团,这种基团在聚合反应中可以与自由基发生反应,形成稳定的中间产物,从而捕获和稳定自由基。在制备无水分散剂的聚合反应中,甲基丙烯磺酸钠可以与聚合反应中的自由基发生反应,从而抑制自由基的继续反应,限制聚合链的生长。这样一来,聚合反应的进行会受到控制,聚合物的分子量增长速率降低,从而影响聚合物的分子量分布。这种控制作用可以使得所得到的聚合物分子量分布更加均匀,有助于实现所需的聚合物性质。与此同时,与甲基丙烯磺酸钠相比,链转移剂疏基丙酸的效果较差,可能是因为其分子结构的特点导致了与聚合反应中的自由基反应的能力较弱,无法有效地稳定和捕获自由基,从而无法实现对聚合链生长的有效调控。总之,甲基丙烯磺酸钠作为链转移剂在聚合反应中通过与自由基的反应,捕获和稳定活性自由基,从而限制聚合链的生长,实现对聚合反应的控制,影响聚合物的分子量和分子量分布。这种机理解释了实验数据中显示甲基丙烯磺酸钠效果优于链转移剂疏基丙酸的现象。Further analysis shows that the working principle of sodium methacrylate sulfonate as a chain transfer agent in polymerization reactions involves the mechanism of free radical polymerization. In free radical polymerization, the polymerization active center adjusts the molecular weight and molecular weight distribution of the polymer through chain transfer reactions. The function of the chain transfer agent is to capture and stabilize active free radicals by reacting with free radicals, thereby preventing the continued reaction of free radicals and limiting the growth of the polymer chain. This process can control the growth rate of polymer molecular weight to a certain extent, thereby affecting the molecular weight distribution of the polymer. Specific to the role of sodium methacrylate sulfonate in the process of preparing anhydrous dispersants, its molecular structure contains sulfonic acid groups. This group can react with free radicals during the polymerization reaction to form a stable intermediate. products, thereby trapping and stabilizing free radicals. In the polymerization reaction for preparing anhydrous dispersants, sodium methacrylate sulfonate can react with free radicals in the polymerization reaction, thereby inhibiting the continued reaction of free radicals and limiting the growth of the polymer chain. In this way, the progress of the polymerization reaction will be controlled, and the molecular weight growth rate of the polymer will be reduced, thus affecting the molecular weight distribution of the polymer. This control can make the resulting polymer molecular weight distribution more uniform and help achieve the desired polymer properties. At the same time, compared with sodium methacrylate sulfonate, the chain transfer agent mercaptopropionic acid is less effective. This may be because its molecular structure has a weak ability to react with free radicals in the polymerization reaction and cannot Effectively stabilizes and traps free radicals, making it impossible to effectively regulate polymer chain growth. In short, sodium methacrylate sulfonate, as a chain transfer agent, captures and stabilizes active free radicals by reacting with free radicals during the polymerization reaction, thereby limiting the growth of the polymer chain, achieving control of the polymerization reaction, and affecting the molecular weight and molecular weight of the polymer. The molecular weight distribution. This mechanism explains the experimental data showing that sodium methacrylate sulfonate is more effective than the chain transfer agent mercaptopropionic acid.
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1370757A (en) * | 2001-02-22 | 2002-09-25 | 北京航空材料研究院 | Methd of composing ceramic powder with liquid gel |
CN102504124A (en) * | 2011-09-17 | 2012-06-20 | 深圳市五山建材实业有限公司 | Method for preparing polycarboxylic acid water reducing agent by using sodium methyl acryl sulfonate as chain transfer agent |
CN104211842A (en) * | 2014-08-22 | 2014-12-17 | 中科院广州化学有限公司南雄材料生产基地 | Novel zwitterionic polyelectrolyte dispersing agent as well as method and application thereof |
CN107628817A (en) * | 2017-08-29 | 2018-01-26 | 浙江攀盛冶金材料有限公司 | A kind of Environment-friendlyzirconium zirconium matter dry materials |
CN112322085A (en) * | 2020-09-15 | 2021-02-05 | 江苏固迈新材料技术有限公司 | PMMA waterproof coating for intercity high-speed railway and urban light rail concrete bridge |
CN113387582A (en) * | 2021-08-17 | 2021-09-14 | 佛山市三水区康立泰无机合成材料有限公司 | Glaze for ultrathin ceramic rock plate and preparation method and application thereof |
CN114621401A (en) * | 2022-04-26 | 2022-06-14 | 洛阳君江建材科技有限公司 | Dispersant for red mud slurrying |
-
2023
- 2023-12-12 CN CN202311700438.6A patent/CN117534326B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1370757A (en) * | 2001-02-22 | 2002-09-25 | 北京航空材料研究院 | Methd of composing ceramic powder with liquid gel |
CN102504124A (en) * | 2011-09-17 | 2012-06-20 | 深圳市五山建材实业有限公司 | Method for preparing polycarboxylic acid water reducing agent by using sodium methyl acryl sulfonate as chain transfer agent |
CN104211842A (en) * | 2014-08-22 | 2014-12-17 | 中科院广州化学有限公司南雄材料生产基地 | Novel zwitterionic polyelectrolyte dispersing agent as well as method and application thereof |
CN107628817A (en) * | 2017-08-29 | 2018-01-26 | 浙江攀盛冶金材料有限公司 | A kind of Environment-friendlyzirconium zirconium matter dry materials |
CN112322085A (en) * | 2020-09-15 | 2021-02-05 | 江苏固迈新材料技术有限公司 | PMMA waterproof coating for intercity high-speed railway and urban light rail concrete bridge |
CN113387582A (en) * | 2021-08-17 | 2021-09-14 | 佛山市三水区康立泰无机合成材料有限公司 | Glaze for ultrathin ceramic rock plate and preparation method and application thereof |
CN114621401A (en) * | 2022-04-26 | 2022-06-14 | 洛阳君江建材科技有限公司 | Dispersant for red mud slurrying |
Non-Patent Citations (1)
Title |
---|
(英)罗 菲(ROFFEY,C.G.)著;黄毓礼等译: "光聚合高分子材料及应用", 28 February 1990, 北京:科学技术文献出版社, pages: 205 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN118724616A (en) * | 2024-08-09 | 2024-10-01 | 广东兴辉陶瓷集团有限公司 | A bright hot-bent integrated rock plate basin and its manufacturing process |
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