CN107096574A - Photocatalyst formaldehyde removing composition and preparation method thereof - Google Patents
Photocatalyst formaldehyde removing composition and preparation method thereof Download PDFInfo
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- CN107096574A CN107096574A CN201710312596.2A CN201710312596A CN107096574A CN 107096574 A CN107096574 A CN 107096574A CN 201710312596 A CN201710312596 A CN 201710312596A CN 107096574 A CN107096574 A CN 107096574A
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title claims abstract description 297
- 239000000203 mixture Substances 0.000 title claims abstract description 69
- 239000011941 photocatalyst Substances 0.000 title claims abstract description 58
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000000843 powder Substances 0.000 claims abstract description 29
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 27
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 25
- -1 yttrium modified nano-titanium dioxide Chemical class 0.000 claims abstract description 25
- 229910052779 Neodymium Inorganic materials 0.000 claims abstract description 22
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 22
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000002994 raw material Substances 0.000 claims abstract description 16
- 229910052746 lanthanum Inorganic materials 0.000 claims abstract description 14
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims abstract description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000002516 radical scavenger Substances 0.000 claims abstract description 7
- 239000000243 solution Substances 0.000 claims description 56
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 48
- 238000001035 drying Methods 0.000 claims description 31
- 238000009413 insulation Methods 0.000 claims description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 26
- 238000003756 stirring Methods 0.000 claims description 25
- NGDQQLAVJWUYSF-UHFFFAOYSA-N 4-methyl-2-phenyl-1,3-thiazole-5-sulfonyl chloride Chemical compound S1C(S(Cl)(=O)=O)=C(C)N=C1C1=CC=CC=C1 NGDQQLAVJWUYSF-UHFFFAOYSA-N 0.000 claims description 24
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 22
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 claims description 19
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 18
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 16
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims description 16
- CFYGEIAZMVFFDE-UHFFFAOYSA-N neodymium(3+);trinitrate Chemical compound [Nd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CFYGEIAZMVFFDE-UHFFFAOYSA-N 0.000 claims description 16
- 229910021529 ammonia Inorganic materials 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 13
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 claims description 12
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 11
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 11
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 11
- 229960005274 benzocaine Drugs 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 235000019270 ammonium chloride Nutrition 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 239000011592 zinc chloride Substances 0.000 claims description 9
- 238000001354 calcination Methods 0.000 claims description 8
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 8
- 239000011259 mixed solution Substances 0.000 claims description 8
- 239000002893 slag Substances 0.000 claims description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005642 Oleic acid Substances 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 239000004408 titanium dioxide Substances 0.000 claims description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229940102253 isopropanolamine Drugs 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 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 claims 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 claims 1
- RCEAADKTGXTDOA-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCCCC[Na] Chemical compound OS(O)(=O)=O.CCCCCCCCCCCC[Na] RCEAADKTGXTDOA-UHFFFAOYSA-N 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 235000019256 formaldehyde Nutrition 0.000 abstract description 87
- 238000005516 engineering process Methods 0.000 abstract description 6
- 239000004615 ingredient Substances 0.000 abstract description 4
- 231100000614 poison Toxicity 0.000 abstract description 4
- 230000007096 poisonous effect Effects 0.000 abstract description 4
- 238000012545 processing Methods 0.000 abstract description 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 18
- 150000001299 aldehydes Chemical class 0.000 description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 229910003074 TiCl4 Inorganic materials 0.000 description 6
- 238000000227 grinding Methods 0.000 description 6
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000000975 co-precipitation Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 206010012434 Dermatitis allergic Diseases 0.000 description 1
- 206010015946 Eye irritation Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 241001464837 Viridiplantae Species 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical class O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 231100000013 eye irritation Toxicity 0.000 description 1
- 231100000025 genetic toxicology Toxicity 0.000 description 1
- 230000001738 genotoxic effect Effects 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/38—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of titanium, zirconium or hafnium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/8668—Removing organic compounds not provided for in B01D53/8603 - B01D53/8665
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/66—Silver or gold
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/39—Photocatalytic properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2258/00—Sources of waste gases
- B01D2258/06—Polluted air
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Catalysts (AREA)
Abstract
The present invention relates to a kind of photocatalyst formaldehyde removing composition and preparation method thereof, described photocatalyst formaldehyde removing composition includes the raw material of following parts by weight:60 parts~80 parts of 40 parts~60 parts of nano titanium oxide activated carbon, 8 parts~15 parts of yttrium modified nano-titanium dioxide powder, 20 parts~35 parts of neodymium modified nano zinc oxide powder, 20 parts~35 parts of lanthanum modified nano zinc oxide powder, 40 parts~60 parts of formaldehyde scavenger, 30 parts~50 parts of Nano Silver and water.The formaldehyde removing composition of the present invention, preparation technology is simple, with low cost, and performance is stable, after the processing through the formaldehyde removing composition of the present invention, the burst size of methanal of glued board can be down to below 0.5mg/L by 10mg/L, and the aldehyde rate that disappears is high, and the formaldehyde removing composition of the present invention, the environment-protecting and non-poisonous non-secondary pollution of ingredient, formaldehyde efficiently can be forever removed, it is applied widely, with good commercial promise.
Description
Technical field
The invention belongs to technical field of chemistry and chemical engineering, and in particular to a kind of photocatalyst formaldehyde removing composition and its preparation
Method.
Background technology
It is various containing formaldehyde with the economic development and improvement of living standards, requirement more and more higher of the people to finishing
The building and ornament materials that raw material is made largely have entered into family, such as various sheet materials, furniture, coating and decorative textile product.According to
Know, the IAQ of current 80% family does not reach the requirement of national standard, wherein 90% is caused by formaldehyde.
Formaldehyde Pollution of Indoor Air has the characteristics that:Cycle is long, even if still there is formaldehyde problem in family of the finishing after 10 years;It is exceeded tight
Weight, in formaldehyde room, most of exceeded even exceeded more than 10 times 4~5 times, had.
Formaldehyde mainly has the following aspects to health hazard:Stimulation, the main harm of formaldehyde is shown as to skin
The stimulation of mucous membrane, formaldehyde is magma noxious material, can be combined with protein, high concentration suction when respiratory tract occur serious
Stimulate and oedema, Eye irritation, headache;Sensitization, direct skin contact formaldehyde can cause allergic dermatitis, color spot, necrosis,
Bronchial astehma can be induced during suction high-concentration formaldehyde.Mutagenesis, high-concentration formaldehyde or a kind of genotoxicity material.
Therefore the removal of research formaldehyde is imperative, and formaldehyde minimizing technology effectively, easy, economic is not only advantageous for people's
It is healthy, and it is also significant with environmental quality to be improved the quality of living for people.Although putting at home
Green plants, can serve the effect for removing formaldehyde, while also beautified living environment, but the limited sorption capacity of plant,
Individually by plant except formaldehyde and unrealistic, therefore many researchers are devoted to the exploitation, synthesis and application of formaldehyde elimination agent and ground
Study carefully.In the market formaldehyde scavenger class product mainly has chemical reaction type, catalyst breakdown type, disinfection agent of chlorine dioxide class, essence
The aqueous solution and formaldehyde sealing agent or paraffin, but most of formaldehyde clearance is relatively low, part can also cause secondary pollution.
The content of the invention
It is an object of the present invention to propose a kind of photocatalyst formaldehyde removing composition.
A kind of photocatalyst formaldehyde removing composition of the present invention, includes the raw material of following parts by weight:Nanometer titanium dioxide
40 parts~60 parts of titanium-activated carbon, 8 parts~15 parts of yttrium modified nano-titanium dioxide powder, 20 parts of neodymium modified nano zinc oxide powder
~35 parts, 20 parts~35 parts of lanthanum modified nano zinc oxide powder, 40 parts~60 parts of formaldehyde scavenger, 30 parts~50 parts of Nano Silver
With 60 parts~80 parts of water.
The formaldehyde removing composition of the present invention, preparation technology is simple, with low cost, and performance is stable, in the first through the present invention
Aldehyde is removed after the processing of composition, and the burst size of methanal of glued board can be down to below 0.5mg/L by 10mg/L, and the aldehyde rate that disappears is high, and
The formaldehyde removing composition of the present invention, the environment-protecting and non-poisonous non-secondary pollution of ingredient efficiently can forever remove formaldehyde, be applicable
Scope is wide, with good commercial promise.
In addition, photocatalyst formaldehyde removing composition according to the above embodiment of the present invention, can also have what is added as follows
Technical characteristic:
As the preferred embodiment of the present invention, the formaldehyde scavenger includes the raw material of following parts by weight:Polypropylene
It is 20 parts~45 parts of hydrazides, 3 parts~10 parts of 3- methyl -2- (N- methylaminos) pentane, 15 parts~30 parts of 4- imino group -2- pentanones, right
8 parts~15 parts of 10 parts~25 parts of benzocaine, 15 parts~35 parts of ammonium sulfate and ammonium chloride.
As the preferred embodiment of the present invention, described photocatalyst formaldehyde removing composition, including following parts by weight
Raw material:40 parts of nano titanium oxide-activated carbon, 15 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder
20 parts of end, 35 parts of lanthanum modified nano zinc oxide powder, 30 parts of Nano Silver, 80 parts of water, 20 parts of polyacrylic hydrazide, 3- methyl -2-
10 parts of (N- methylaminos) pentane, 4- imino groups -15 parts of 2 pentanone, 25 parts of ethylaminobenzoate, 15 parts of ammonium sulfate and chlorination
15 parts of ammonium.
As the preferred embodiment of the present invention, described photocatalyst formaldehyde removing composition, including following parts by weight
Raw material:60 parts of nano titanium oxide-activated carbon, 8 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder
35 parts of end, 20 parts of lanthanum modified nano zinc oxide powder, 50 parts of Nano Silver, 60 parts of water, 45 parts of polyacrylic hydrazide, 3- methyl -2-
3 parts of (N- methylaminos) pentane, 4- imino groups -30 parts of 2 pentanone, 10 parts of ethylaminobenzoate, 35 parts of ammonium sulfate and ammonium chloride
8 parts.
As the preferred embodiment of the present invention, described photocatalyst formaldehyde removing composition, including following parts by weight
Raw material:50 parts of nano titanium oxide-activated carbon, 12 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder
27 parts of end, 27 parts of lanthanum modified nano zinc oxide powder, 40 parts of Nano Silver, 70 parts of water, 32 parts of polyacrylic hydrazide, 3- methyl -2-
7 parts of (N- methylaminos) pentane, 4- imino groups -22 parts of 2 pentanone, 17 parts of ethylaminobenzoate, 25 parts of ammonium sulfate and chlorination
12 parts of ammonium.
It is another object of the present invention to the preparation method for proposing described photocatalyst formaldehyde removing composition.
The preparation method of described photocatalyst formaldehyde removing composition, comprises the following steps:S101:First by parts by weight
The water that number is 100 parts~150 parts of ethanol and parts by weight are 25 parts~30 parts is mixed, then be added dropwise parts by weight be 1 part~
5 parts of TiCl4, 24h~36h is stirred for, molar concentration is then added for 5mol/L~6mol/L ammoniacal liquor and adjusts solution
PH value is 6.8~7.2, then is baked to, be then heated to successively 280 DEG C~320 DEG C insulation 6h~8h, 480 DEG C~520 DEG C
6h~8h and 680 DEG C~720 DEG C insulation 6h~8h of insulation, then powder is ground into, it is 8 parts~15 parts to add parts by weight
Interfacial agent and parts by weight be 80 parts~120 parts of water, obtain dispersion soln, then into the dispersion soln plus
Enter the activated carbon that parts by weight are 10 parts~15 parts, stood after stirring, then filter, obtain filter residue, then the filter residue is done
It is dry and grind, obtain nano titanium oxide-activated carbon;S102:It is heavy to be added in 96 parts~120 parts of ethanol to parts by weight
The butyl titanate that number is 24 parts~45 parts is measured, butyl titanate solution is obtained, and it is 1.0~2.0 to adjust its pH value;By weight
The water that number is 48 parts~60 parts of ethanol and parts by weight are 3 parts~6 parts is mixed, and it is 32 parts~60 to add parts by weight
The yttrium nitrate of part, obtains yttrium nitrate solution;Then the yttrium nitrate solution is added in the butyl titanate solution, then stirred
Mix 30min~50min, then stand, obtain gel, then dry successively and grind the gel, be then heated to 650 DEG C~
700 DEG C of insulation 4h~6h, are then cooled to after room temperature and grind, obtain yttrium modified nano-titanium dioxide powder;S103:To mole
Concentration is 1.2mol/L~1.5mol/L ZnCl2Neodymium nitrate and weight of the parts by weight for 20 parts~35 parts are added in solution
Number is 20 parts~35 parts of lanthanum nitrate, and then stirring obtains mixed solution, and then adding molar concentration while stirring is
5mol/L~6mol/L ammonia spirit, until when solution ph is higher than 9.5, stopping adding ammoniacal liquor, is stirred for reacting 30min
~50min, obtains coprecipitated product, then cleans successively, dries, grinds the coprecipitated product, then is heated to 780
DEG C~800 DEG C of calcining 3h~5h, it is subsequently cooled to room temperature and is washed and ground successively, obtains neodymium modified nano-silica
Zinc powder;Wherein, ZnCl2Mol ratio with neodymium nitrate and lanthanum nitrate is 3:(1.5~2.5):(1.5~2.5);S104:By institute
State the product that step S101, the step S102 and the step S103 obtain to mix with surplus stock component, obtain photocatalyst
Formaldehyde removing composition.
As the preferred embodiment of the present invention, in the step S101, the temperature of the drying process is 100 DEG C
~110 DEG C, the dry time is 12h~14h;In the step S102, the temperature of the drying process is 60 DEG C~65
DEG C, drying time is 22h~26h;In the step S103, the temperature of the drying process is 70 DEG C~75 DEG C, is dried
Time is 22h~26h.
As the preferred embodiment of the present invention, in the step S101, the time of standing is 24h~28h;Institute
State in step S102, the time of standing is 24h~28h.
It is used as the preferred embodiment of the present invention, in the step S103, the ammonia for being 0.5mol/L with concentration during washing
The aqueous solution.
As the preferred embodiment of the present invention, in the step S101, the interfacial agent at least includes 12
Sodium alkyl sulfate, neopelex, oleic acid, calgon, polyethylene glycol, isopropanolamine and polyvinylpyrrolidine
One kind in ketone.
The additional aspect and advantage of the present invention will be set forth in part in the description, partly will from the following description
Become obvious, or recognized by the practice of the present invention.
Embodiment
Embodiments of the invention are described below in detail, the embodiment is exemplary, it is intended to for explaining the present invention,
And be not considered as limiting the invention.
It is an object of the present invention to propose a kind of photocatalyst formaldehyde removing composition.
A kind of photocatalyst formaldehyde removing composition of the present invention, includes the raw material of following parts by weight:Nanometer titanium dioxide
40 parts~60 parts of titanium-activated carbon, 8 parts~15 parts of yttrium modified nano-titanium dioxide powder, 20 parts of neodymium modified nano zinc oxide powder
~35 parts, 20 parts~35 parts of lanthanum modified nano zinc oxide powder, 40 parts~60 parts of formaldehyde scavenger, 30 parts~50 parts of Nano Silver
With 60 parts~80 parts of water.
The formaldehyde removing composition of the present invention, preparation technology is simple, with low cost, and performance is stable, in the first through the present invention
Aldehyde is removed after the processing of composition, and the burst size of methanal of glued board can be down to below 0.5mg/L by 10mg/L, and the aldehyde rate that disappears is high, and
The formaldehyde removing composition of the present invention, the environment-protecting and non-poisonous non-secondary pollution of ingredient efficiently can forever remove formaldehyde, be applicable
Scope is wide, with good commercial promise.
It is another object of the present invention to the preparation method for proposing described photocatalyst formaldehyde removing composition, specifically
Comprise the following steps:
S101:Ethanol that parts by weight are 100 parts~150 parts and water that parts by weight are 25 parts~30 parts are mixed first
Close, the TiCl that parts by weight are 1 part~5 parts is then added dropwise4, 24h~36h is stirred for, it is 5mol/L then to add molar concentration
~the 6mol/L ammoniacal liquor and pH value for adjusting solution is 6.8~7.2, then is baked to, 280 DEG C~320 is then heated to successively
DEG C insulation 6h~8h, 6h~8h and 680 DEG C~720 DEG C insulation 6h~8h of 480 DEG C~520 DEG C insulations, then are ground into powder
End, adds the water that parts by weight are 8 parts~15 parts of interfacial agent and parts by weight are 80 parts~120 parts, obtains scattered molten
Liquid, the activated carbon that parts by weight are 10 parts~15 parts is then added into the dispersion soln, stands, then filters after stirring,
Filter residue is obtained, then by the filter residue and drying and is ground, nano titanium oxide-activated carbon is obtained.
S102:The metatitanic acid fourth that parts by weight are 24 parts~45 parts is added into the ethanol that parts by weight are 96 parts~120 parts
Ester, obtains butyl titanate solution, and it is 1.0~2.0 to adjust its pH value;By parts by weight for 48 parts~60 parts ethanol with again
Measure number to mix for 3 parts~6 parts of water, add the yttrium nitrate that parts by weight are 32 parts~60 parts, obtain yttrium nitrate solution;
Then the yttrium nitrate solution is added in the butyl titanate solution, is stirred for 30min~50min, then stands, obtain
To gel, then dry successively and grind the gel, be then heated to 650 DEG C~700 DEG C insulation 4h~6h, be then cooled to
Ground after room temperature, obtain yttrium modified nano-titanium dioxide powder.
S103:To the ZnCl that molar concentration is 1.2mol/L~1.5mol/L2In solution add parts by weight be 20 parts~
35 parts of neodymium nitrate and parts by weight is 20 parts~35 parts of lanthanum nitrate, and then stirring obtains mixed solution, then in stirring
The ammonia spirit that molar concentration is 5mol/L~6mol/L is added simultaneously, until when solution pH value is higher than 9.5, stopping adding ammonia
Water, is stirred for reacting 30min~50min, obtains coprecipitated product, then cleans, dries successively, grinding the co-precipitation production
Thing, then 780 DEG C~800 DEG C calcining 3h~5h are heated to, it is subsequently cooled to room temperature and is washed and ground successively, obtains
To neodymium modified nano-silica zinc powder;Wherein, ZnCl2Mol ratio with neodymium nitrate and lanthanum nitrate is 3:(1.5~2.5):
(1.5~2.5).
S104:By the obtained product of the step S101, the step S102 and the step S103 and surplus stock group
Divide mixing, obtain photocatalyst formaldehyde removing composition.
The present invention is described in detail below by specific embodiment.
Embodiment 1
Embodiment 1 proposes a kind of photocatalyst formaldehyde removing composition, includes the raw material of following parts by weight:Nanometer two
40 parts of titanium oxide-activated carbon, 15 parts of yttrium modified nano-titanium dioxide powder, 20 parts of neodymium modified nano zinc oxide powder, lanthanum are modified
35 parts of nano-zinc oxide powder, 30 parts of Nano Silver, 80 parts of water, 20 parts of polyacrylic hydrazide, 3- methyl -2- (N- methylaminos) pentane
15 parts of 10 parts, 4- imino groups -15 parts of 2 pentanone, 25 parts of ethylaminobenzoate, 15 parts of ammonium sulfate and ammonium chloride.
The preparation method of the photocatalyst formaldehyde removing composition of embodiment 1, specifically includes following steps:
(1) ethanol that parts by weight are 100 parts is mixed with the water that parts by weight are 30 parts first, weight is then added dropwise
Number is 1 part of TiCl4, 36h is stirred for, ammoniacal liquor that molar concentration is 5mol/L is then added and adjusts the pH value of solution and be
7.2, then be baked to, 280 DEG C of insulation 8h, 8h and 680 DEG C of insulation 8h of 480 DEG C of insulations are then heated to successively, then are ground
Into powder, the water that parts by weight are 8 parts of neopelex and parts by weight are 120 parts is added, obtains scattered molten
Liquid, the activated carbon that parts by weight are 10 parts is then added into the dispersion soln, is stood after stirring, is then filtered, filtered
Slag, then by the filter residue and drying and grind, obtain nano titanium oxide-activated carbon;Wherein, the temperature of drying process is 100
DEG C, the dry time is 14h, and the time of standing is 24h.
(2) butyl titanate that parts by weight are 24 parts is added into the ethanol that parts by weight are 120 parts, metatitanic acid fourth is obtained
Ester solution, and it is 2.0 to adjust its pH value;The ethanol that parts by weight are 48 parts is mixed with the water that parts by weight are 6 parts, then added
Enter the yttrium nitrate that parts by weight are 32 parts, obtain yttrium nitrate solution;Then the yttrium nitrate solution is added to the metatitanic acid fourth
In ester solution, 50min is stirred for, is then stood, obtain gel, then dried successively and grind the gel, be then heated to
650 DEG C of insulation 6h, are then cooled to after room temperature and grind, obtain yttrium modified nano-titanium dioxide powder;Wherein, drying process
Temperature is 65 DEG C, and drying time is 22h, and the time of standing is 28h.
(3) to the ZnCl that molar concentration is 1.2mol/L2Neodymium nitrate and weight of the parts by weight for 35 parts are added in solution
Number is 20 parts of lanthanum nitrate, and then stirring obtains mixed solution, and it is 6mol/L that molar concentration is then added while stirring
Ammonia spirit, until solution ph be higher than 9.5 when, stop add ammoniacal liquor, be stirred for react 30min, obtain co-precipitation production
Thing, then cleans, dries, grinding the coprecipitated product successively, then is heated to 800 DEG C of calcining 3h, is subsequently cooled to room
Temperature is simultaneously washed and ground successively, obtains neodymium modified nano-silica zinc powder;Wherein, ZnCl2With neodymium nitrate and lanthanum nitrate
Mol ratio be 3:1.5: 2.5;Wherein, the temperature of the drying process is 70 DEG C, and the dry time is 26h.
(4) product and surplus stock component obtained the step (1), the step (2) and the step (3) is mixed
Close, obtain photocatalyst formaldehyde removing composition.
Embodiment 2
Embodiment 2 proposes a kind of photocatalyst formaldehyde removing composition, includes the raw material of following parts by weight:Nanometer two
60 parts of titanium oxide-activated carbon, 8 parts of yttrium modified nano-titanium dioxide powder, 35 parts of neodymium modified nano zinc oxide powder, lanthanum are modified
20 parts of nano-zinc oxide powder, 50 parts of Nano Silver, 60 parts of water, 45 parts of polyacrylic hydrazide, 3- methyl -2- (N- methylaminos) pentane 3
Part, 4- imino groups -30 parts of 2 pentanone, 10 parts of ethylaminobenzoate, 35 parts of ammonium sulfate and 8 parts of ammonium chloride.
The preparation method of the photocatalyst formaldehyde removing composition of embodiment 2, specifically includes following steps:
(1) ethanol that parts by weight are 150 parts is mixed with the water that parts by weight are 25 parts first, weight is then added dropwise
Number is 5 parts of TiCl4, 24h is stirred for, ammoniacal liquor that molar concentration is 6mol/L is then added and adjusts the pH value of solution and be
6.8, then be baked to, 320 DEG C of insulation 6h, 6h and 720 DEG C of insulation 6h of 520 DEG C of insulations are then heated to successively, then are ground
Into powder, the water that parts by weight are 15 parts of oleic acid and parts by weight are 80 parts is added, dispersion soln is obtained, then to described
It is 15 parts of activated carbon that parts by weight are added in dispersion soln, stands, then filters after stirring, obtains filter residue, then by the filter
Slag is dried and ground, and obtains nano titanium oxide-activated carbon;Wherein, the temperature of drying process is 110 DEG C, and the dry time is
12h, the time of standing is 28h.
(2) butyl titanate that parts by weight are 45 parts is added into the ethanol that parts by weight are 96 parts, butyl titanate is obtained
Solution, and it is 1.0 to adjust its pH value;The ethanol that parts by weight are 60 parts is mixed with the water that parts by weight are 3 parts, added
Parts by weight are 60 parts of yttrium nitrate, obtain yttrium nitrate solution;Then the yttrium nitrate solution is added to the butyl titanate
In solution, 30min is stirred for, is then stood, obtain gel, then dried successively and grind the gel, be then heated to 700
DEG C insulation 4h, be then cooled to after room temperature grind, obtain yttrium modified nano-titanium dioxide powder;Wherein, the temperature of drying process
For 60 DEG C, drying time is 26h, and the time of standing is 24h.
(3) to the ZnCl that molar concentration is 1.5mol/L2Neodymium nitrate and weight of the parts by weight for 20 parts are added in solution
Number is 35 parts of lanthanum nitrate, and then stirring obtains mixed solution, and it is 5mol/L that molar concentration is then added while stirring
Ammonia spirit, until solution ph be higher than 9.5 when, stop add ammoniacal liquor, be stirred for react 50min, obtain co-precipitation production
Thing, then cleans, dries, grinding the coprecipitated product successively, then is heated to 780 DEG C of calcining 5h, is subsequently cooled to room
Temperature is simultaneously washed and ground successively, obtains neodymium modified nano-silica zinc powder;Wherein, ZnCl2With neodymium nitrate and lanthanum nitrate
Mol ratio be 3: 2.5:1.5;Wherein, the temperature of the drying process is 75 DEG C, and the dry time is 22h.
(4) product and surplus stock component obtained the step (1), the step (2) and the step (3) is mixed
Close, obtain photocatalyst formaldehyde removing composition.
Embodiment 3
Embodiment 3 proposes a kind of photocatalyst formaldehyde removing composition, includes the raw material of following parts by weight:Nanometer two
50 parts of titanium oxide-activated carbon, 12 parts of yttrium modified nano-titanium dioxide powder, 27 parts of neodymium modified nano zinc oxide powder, lanthanum are modified
27 parts of nano-zinc oxide powder, 40 parts of Nano Silver, 70 parts of water, 32 parts of polyacrylic hydrazide, 3- methyl -2- (N- methylaminos) pentane 7
Part, 4- imino groups -22 parts of 2 pentanone, 17 parts of ethylaminobenzoate, 25 parts of ammonium sulfate and 12 parts of ammonium chloride.
The preparation method of the photocatalyst formaldehyde removing composition of embodiment 3, specifically includes following steps:
(1) ethanol that parts by weight are 125 parts is mixed with the water that parts by weight are 27 parts first, weight is then added dropwise
Number is 3 parts of TiCl4, 30h is stirred for, then addition molar concentration is 5.5mol/L ammoniacal liquor and adjusts the pH value of solution
For 7.0, then it is baked to, 300 DEG C of insulation 7h, 7h and 700 DEG C of insulation 7h of 500 DEG C of insulations is then heated to successively, then ground
Clay into power, add the water that parts by weight are 11 parts of polyvinylpyrrolidone and parts by weight are 100 parts, obtain scattered molten
Liquid, the activated carbon that parts by weight are 12 parts is then added into the dispersion soln, is stood after stirring, is then filtered, filtered
Slag, then by the filter residue and drying and grind, obtain nano titanium oxide-activated carbon;Wherein, the temperature of drying process is 105
DEG C, the dry time is 13h, and the time of standing is 26h.
(2) butyl titanate that parts by weight are 34 parts is added into the ethanol that parts by weight are 96 parts~120 parts, is obtained
Butyl titanate solution, and it is 1.5 to adjust its pH value;Ethanol that parts by weight are 54 parts and water that parts by weight are 5 parts are mixed
Close, add the yttrium nitrate that parts by weight are 48 parts, obtain yttrium nitrate solution;Then the yttrium nitrate solution is added to institute
State in butyl titanate solution, be stirred for 40min, then stand, obtain gel, then dry successively and grind the gel, then
680 DEG C of insulation 5h are heated to, is then cooled to after room temperature and grinds, obtain yttrium modified nano-titanium dioxide powder;Wherein, dry
The temperature of operation is 63 DEG C, and drying time is 24h, and the time of standing is 26h.
(3) to the ZnCl that molar concentration is 1.3mol/L2Neodymium nitrate and weight of the parts by weight for 27 parts are added in solution
Number is 27 parts of lanthanum nitrate, and then stirring obtains mixed solution, and then adding molar concentration while stirring is
5.5mol/L ammonia spirit, until when solution ph is higher than 9.5, stopping adding ammoniacal liquor, is stirred for reacting 40min, is total to
Precipitated product, then cleans, dries, grinding the coprecipitated product, then being heated to 790 DEG C of calcinings 4h, Ran Houleng successively
But washed to room temperature and successively and ground, obtain neodymium modified nano-silica zinc powder;Wherein, ZnCl2With neodymium nitrate and
The mol ratio of lanthanum nitrate is 3:2:2;Wherein, the temperature of the drying process is 72 DEG C, and the dry time is 24h.
(4) product and surplus stock component obtained the step (1), the step (2) and the step (3) is mixed
Close, obtain photocatalyst formaldehyde removing composition.
Comparative example 1
Comparative example 1 proposes a kind of photocatalyst formaldehyde removing composition, and comparative example 1 is differed only in embodiment 1,
Do not include nano titanium oxide-activated carbon, remaining raw material and the phase of embodiment 1 in the photocatalyst formaldehyde removing composition of comparative example 1
Together.
The preparation method of the photocatalyst formaldehyde removing composition of comparative example 1, specifically includes following steps:
(1) butyl titanate that parts by weight are 24 parts is added into the ethanol that parts by weight are 120 parts, metatitanic acid fourth is obtained
Ester solution, and it is 2.0 to adjust its pH value;The ethanol that parts by weight are 48 parts is mixed with the water that parts by weight are 6 parts, then added
Enter the yttrium nitrate that parts by weight are 32 parts, obtain yttrium nitrate solution;Then the yttrium nitrate solution is added to the metatitanic acid fourth
In ester solution, 50min is stirred for, is then stood, obtain gel, then dried successively and grind the gel, be then heated to
650 DEG C of insulation 6h, are then cooled to after room temperature and grind, obtain yttrium modified nano-titanium dioxide powder;Wherein, drying process
Temperature is 65 DEG C, and drying time is 22h, and the time of standing is 28h.
(2) to the ZnCl that molar concentration is 1.2mol/L2Neodymium nitrate and weight of the parts by weight for 35 parts are added in solution
Number is 20 parts of lanthanum nitrate, and then stirring obtains mixed solution, and it is 6mol/L that molar concentration is then added while stirring
Ammonia spirit, until solution ph be higher than 9.5 when, stop add ammoniacal liquor, be stirred for react 30min, obtain co-precipitation production
Thing, then cleans, dries, grinding the coprecipitated product successively, then is heated to 800 DEG C of calcining 3h, is subsequently cooled to room
Temperature is simultaneously washed and ground successively, obtains neodymium modified nano-silica zinc powder;Wherein, ZnCl2With neodymium nitrate and lanthanum nitrate
Mol ratio be 3:1.5: 2.5;Wherein, the temperature of the drying process is 70 DEG C, and the dry time is 26h.
(3) product for obtaining the step (1) and the step (2) is mixed with surplus stock component, obtains photocatalyst
Formaldehyde removing composition.
Comparative example 2
Comparative example 2 proposes a kind of photocatalyst formaldehyde removing composition, and comparative example 2 is differed only in embodiment 2,
In the photocatalyst formaldehyde removing composition of comparative example 2 not include yttrium modified nano-titanium dioxide powder, remaining raw material with contrast
Example 2 is identical.
The preparation method of the photocatalyst formaldehyde removing composition of comparative example 2, specifically includes following steps:
(1) ethanol that parts by weight are 150 parts is mixed with the water that parts by weight are 25 parts first, weight is then added dropwise
Number is 5 parts of TiCl4, 24h is stirred for, ammoniacal liquor that molar concentration is 6mol/L is then added and adjusts the pH value of solution and be
6.8, then be baked to, 320 DEG C of insulation 6h, 6h and 720 DEG C of insulation 6h of 520 DEG C of insulations are then heated to successively, then are ground
Into powder, the water that parts by weight are 15 parts of interfacial agent and parts by weight are 80 parts is added, dispersion soln is obtained, then
The activated carbon that parts by weight are 15 parts is added into the dispersion soln, stands, then filters after stirring, filter residue is obtained, then will
The filter residue and drying is simultaneously ground, and obtains nano titanium oxide-activated carbon;Wherein, the temperature of drying process is 110 DEG C, is dried
Time is 12h, and the time of standing is 28h.
(2) to the ZnCl that molar concentration is 1.5mol/L2Neodymium nitrate and weight of the parts by weight for 20 parts are added in solution
Number is 35 parts of lanthanum nitrate, and then stirring obtains mixed solution, and it is 5mol/L that molar concentration is then added while stirring
Ammonia spirit, until solution ph be higher than 9.5 when, stop add ammoniacal liquor, be stirred for react 50min, obtain co-precipitation production
Thing, then cleans, dries, grinding the coprecipitated product successively, then is heated to 780 DEG C of calcining 5h, is subsequently cooled to room
Temperature is simultaneously washed and ground successively, obtains neodymium modified nano-silica zinc powder;Wherein, ZnCl2With neodymium nitrate and lanthanum nitrate
Mol ratio be 3: 2.5:1.5;Wherein, the temperature of the drying process is 75 DEG C, and the dry time is 22h.
(3) product for obtaining the step (1) and the step (2) is mixed with surplus stock component, obtains photocatalyst
Formaldehyde removing composition.
Comparative example 3
Comparative example 3 proposes a kind of photocatalyst formaldehyde removing composition, and comparative example 3 is differed only in embodiment 3,
Do not include neodymium modified nano zinc oxide powder and lanthanum modified nano zinc oxide in the photocatalyst formaldehyde removing composition of comparative example 3
Powder, remaining raw material is identical with comparative example 3.
The preparation method of the photocatalyst formaldehyde removing composition of comparative example 3, specifically includes following steps:
(1) ethanol that parts by weight are 125 parts is mixed with the water that parts by weight are 27 parts first, weight is then added dropwise
Number is 3 parts of TiCl4, 30h is stirred for, then addition molar concentration is 5.5mol/L ammoniacal liquor and adjusts the pH value of solution
For 7.0, then it is baked to, 300 DEG C of insulation 7h, 7h and 700 DEG C of insulation 7h of 500 DEG C of insulations is then heated to successively, then ground
Clay into power, add the water that parts by weight are 11 parts of interfacial agent and parts by weight are 100 parts, obtain dispersion soln, so
The activated carbon that parts by weight are 12 parts is added in the backward dispersion soln, is stood after stirring, is then filtered, obtain filter residue, then
By the filter residue and drying and grind, obtain nano titanium oxide-activated carbon;Wherein, the temperature of drying process is 105 DEG C, is dried
Time be 13h, time of standing is 26h.
(2) butyl titanate that parts by weight are 34 parts is added into the ethanol that parts by weight are 96 parts~120 parts, is obtained
Butyl titanate solution, and it is 1.5 to adjust its pH value;Ethanol that parts by weight are 54 parts and water that parts by weight are 5 parts are mixed
Close, add the yttrium nitrate that parts by weight are 48 parts, obtain yttrium nitrate solution;Then the yttrium nitrate solution is added to institute
State in butyl titanate solution, be stirred for 40min, then stand, obtain gel, then dry successively and grind the gel, then
680 DEG C of insulation 5h are heated to, is then cooled to after room temperature and grinds, obtain yttrium modified nano-titanium dioxide powder;Wherein, dry
The temperature of operation is 63 DEG C, and drying time is 24h, and the time of standing is 26h.
(3) product for obtaining the step (1) and the step (2) is mixed with surplus stock component, obtains photocatalyst
Formaldehyde removing composition.
36 pieces of 30mm × 30mm × 5mm glued board is taken, 6 groups are divided into, each embodiment and comparative example is respectively applied
Photocatalyst formaldehyde removing composition, coating weight is 50g/m2, then air-dry, it is dry according to 9-11L as defined in GB/T17657-1999
Dry device method, under natural light, determines the burst size of methanal of glued board.As a result it is as shown in table 1.The aldehyde rate that disappears (%, quality)=reaction
The formaldehyde amount fallen/original content of formaldehyde=(original content of formaldehyde-residual formaldehyde content)/original content of formaldehyde.
Table 1:Formaldehyde removing aptitude tests result
As it can be seen from table 1 the aldehyde rate that disappears of 1-3 of embodiment of the present invention photocatalyst formaldehyde removing composition is 95%
Left and right and more than, after the photocatalyst formaldehyde removing compositions-treated by the present invention, the burst size of methanal of glued board significantly under
Drop, can be down to 0.5mg/L and following.And the aldehyde rate that disappears of comparative example 1-3 photocatalyst formaldehyde removing composition is 50% or so
And it is following, the aldehyde effect that disappears substantially is not so good as embodiment 1-3 photocatalyst formaldehyde removing composition.
To sum up, photocatalyst formaldehyde removing composition of the invention, preparation technology is simple, with low cost, and performance is stable,
After the processing of the photocatalyst formaldehyde removing composition of the present invention, the burst size of methanal of glued board can be down to by 10mg/L
Below 0.5mg/L, the aldehyde rate that disappears is high, and the photocatalyst formaldehyde removing composition of the present invention, and ingredient is environment-protecting and non-poisonous without secondary dirt
Dye, efficiently can forever remove formaldehyde, applied widely, with good commercial promise.
In the description of this specification, reference term " one embodiment ", " some embodiments ", " example ", " specifically show
The description of example " or " some examples " etc. means to combine specific features, structure, material or the spy that the embodiment or example are described
Point is contained at least one embodiment of the present invention or example.In this manual, to the schematic representation of above-mentioned term not
Identical embodiment or example must be directed to.Moreover, specific features, structure, material or the feature of description can be with office
Combined in an appropriate manner in one or more embodiments or example.In addition, in the case of not conflicting, this area
Technical staff can be carried out the feature of the not be the same as Example described in this specification or example and non-be the same as Example or example
With reference to and combination.
Although embodiments of the invention have been shown and described above, it is to be understood that above-described embodiment is example
Property, it is impossible to limitation of the present invention is interpreted as, one of ordinary skill in the art within the scope of the invention can be to above-mentioned
Embodiment is changed, changed, replacing and modification.
Claims (10)
1. a kind of photocatalyst formaldehyde removing composition, it is characterised in that include the raw material of following parts by weight:Nanometer titanium dioxide
40 parts~60 parts of titanium-activated carbon, 8 parts~15 parts of yttrium modified nano-titanium dioxide powder, 20 parts of neodymium modified nano zinc oxide powder
~35 parts, 20 parts~35 parts of lanthanum modified nano zinc oxide powder, 40 parts~60 parts of formaldehyde scavenger, 30 parts~50 parts of Nano Silver and
60 parts~80 parts of water.
2. photocatalyst formaldehyde removing composition according to claim 1, it is characterised in that the formaldehyde scavenger is included such as
The raw material of lower parts by weight:20 parts~45 parts of polyacrylic hydrazide, 3 parts~10 parts of 3- methyl -2- (N- methylaminos) pentane, 4- imido
8 parts of 15 parts~30 parts of base -2 pentanone, 10 parts~25 parts of ethylaminobenzoate, 15 parts~35 parts of ammonium sulfate and ammonium chloride~
15 parts.
3. photocatalyst formaldehyde removing composition according to claim 2, it is characterised in that include the original of following parts by weight
Material:40 parts of nano titanium oxide-activated carbon, 15 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder 20
Part, 35 parts of lanthanum modified nano zinc oxide powder, 30 parts of Nano Silver, 80 parts of water, 20 parts of polyacrylic hydrazide, 3- methyl -2- (N- first ammonia
Base) 15 parts of 10 parts of pentane, 4- imino groups -15 parts of 2 pentanone, 25 parts of ethylaminobenzoate, 15 parts of ammonium sulfate and ammonium chloride.
4. photocatalyst formaldehyde removing composition according to claim 2, it is characterised in that include the original of following parts by weight
Material:60 parts of nano titanium oxide-activated carbon, 8 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder 35
Part, 20 parts of lanthanum modified nano zinc oxide powder, 50 parts of Nano Silver, 60 parts of water, 45 parts of polyacrylic hydrazide, 3- methyl -2- (N- first ammonia
Base) 8 parts of 3 parts of pentane, 4- imino groups -30 parts of 2 pentanone, 10 parts of ethylaminobenzoate, 35 parts of ammonium sulfate and ammonium chloride.
5. photocatalyst formaldehyde removing composition according to claim 2, it is characterised in that include the original of following parts by weight
Material:50 parts of nano titanium oxide-activated carbon, 12 parts of yttrium modified nano-titanium dioxide powder, neodymium modified nano zinc oxide powder 27
Part, 27 parts of lanthanum modified nano zinc oxide powder, 40 parts of Nano Silver, 70 parts of water, 32 parts of polyacrylic hydrazide, 3- methyl -2- (N- first ammonia
Base) 12 parts of 7 parts of pentane, 4- imino groups -22 parts of 2 pentanone, 17 parts of ethylaminobenzoate, 25 parts of ammonium sulfate and ammonium chloride.
6. the preparation method of the photocatalyst formaldehyde removing composition described in claim any one of 1-5, it is characterised in that including such as
Lower step:
S101:The ethanol that parts by weight are 100 parts~150 parts is mixed with the water that parts by weight are 25 parts~30 parts first, so
The TiCl that parts by weight are 1 part~5 parts is added dropwise afterwards4, be stirred for 24h~36h, then add molar concentration be 5mol/L~
The 6mol/L ammoniacal liquor and pH value for adjusting solution is 6.8~7.2, then is baked to, 280 DEG C~320 DEG C is then heated to successively
6h~8h, 6h~8h and 680 DEG C~720 DEG C insulation 6h~8h of 480 DEG C~520 DEG C insulations are incubated, then are ground into powder, plus
Enter the interfacial agent that parts by weight are 8 parts~15 parts and the water that parts by weight are 80 parts~120 parts, obtain dispersion soln, so
The activated carbon that parts by weight are 10 parts~15 parts is added in the backward dispersion soln, is stood after stirring, is then filtered, filtered
Slag, then by the filter residue and drying and grind, obtain nano titanium oxide-activated carbon;
S102:The butyl titanate that parts by weight are 24 parts~45 parts is added into the ethanol that parts by weight are 96 parts~120 parts, is obtained
To butyl titanate solution, and it is 1.0~2.0 to adjust its pH value;Ethanol and parts by weight by parts by weight for 48 parts~60 parts
Mixed for 3 parts~6 parts of water, add the yttrium nitrate that parts by weight are 32 parts~60 parts, obtain yttrium nitrate solution;Then by institute
State yttrium nitrate solution to be added in the butyl titanate solution, be stirred for 30min~50min, then stand, obtain gel, then
Dry successively and grind the gel, be then heated to 650 DEG C~700 DEG C insulation 4h~6h, be then cooled to after room temperature and grind,
Obtain yttrium modified nano-titanium dioxide powder;
S103:To the ZnCl that molar concentration is 1.2mol/L~1.5mol/L2It is 20 parts~35 parts that parts by weight are added in solution
Neodymium nitrate and the lanthanum nitrate that parts by weight are 20 parts~35 parts, then stirring obtain mixed solution, then add while stirring
Enter the ammonia spirit that molar concentration is 5mol/L~6mol/L, until when solution ph is higher than 9.5, stopping adding ammoniacal liquor, then stir
Mix reaction 30min~50min, obtain coprecipitated product, then clean successively, dry, grind the coprecipitated product, then by its
780 DEG C~800 DEG C calcining 3h~5h are heated to, room temperature is subsequently cooled to and is washed and ground successively, neodymium modification is obtained and receives
Rice zinc oxide powder;Wherein, ZnCl2Mol ratio with neodymium nitrate and lanthanum nitrate is 3:(1.5~2.5):(1.5~2.5);
S104:The obtained product of the step S101, the step S102 and the step S103 and surplus stock component are mixed
Close, obtain photocatalyst formaldehyde removing composition.
7. the preparation method of photocatalyst formaldehyde removing composition according to claim 6, it is characterised in that in the step
In S101, the temperature of the drying process is 100 DEG C~110 DEG C, and the dry time is 12h~14h;In the step S102
In, the temperature of the drying process is 60 DEG C~65 DEG C, and drying time is 22h~26h;It is described dry in the step S103
The temperature of dry operation is 70 DEG C~75 DEG C, and the dry time is 22h~26h.
8. the preparation method of photocatalyst formaldehyde removing composition according to claim 6, it is characterised in that in the step
In S101, the time of standing is 24h~28h;In the step S102, the time of standing is 24h~28h.
9. the preparation method of photocatalyst formaldehyde removing composition according to claim 6, it is characterised in that in the step
In S103, the ammonia spirit for being 0.5mol/L with concentration during washing.
10. the preparation method of photocatalyst formaldehyde removing composition according to claim 6, it is characterised in that in the step
In rapid S101, the interfacial agent at least includes lauryl sodium sulfate, neopelex, oleic acid, hexa metaphosphoric acid
One kind in sodium, polyethylene glycol, isopropanolamine and polyvinylpyrrolidone.
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107488370A (en) * | 2017-09-25 | 2017-12-19 | 深圳飞阳环保科技有限公司 | The preparation method and metal ion Cleaning luminaire of a kind of new type purification material |
CN108187470A (en) * | 2017-12-05 | 2018-06-22 | 浙江师范大学 | Formaldehyde catching gel |
CN108970392A (en) * | 2018-07-05 | 2018-12-11 | 吴亚琴 | A kind of formaldehyde cleaning coating liquid |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104368325A (en) * | 2014-12-04 | 2015-02-25 | 东北林业大学 | Preparation method of formaldehyde-photodegrading honeycomb activated carbon |
CN105866183A (en) * | 2016-03-11 | 2016-08-17 | 北京大学 | Lanthanum-doped formaldehyde-sensitive material and preparation method thereof, and formaldehyde sensor |
CN106189390A (en) * | 2016-07-20 | 2016-12-07 | 王玲 | A kind of photocatalyst of titanium dioxide coating and film thereof, and preparation method |
CN106345287A (en) * | 2016-08-02 | 2017-01-25 | 保护伞环保科技成都有限公司 | Anion formaldehyde purifying agent |
CN106512941A (en) * | 2016-11-30 | 2017-03-22 | 安吉云界生物科技有限公司 | Composite nanometer titanium dioxide and active carbon adsorbent |
-
2017
- 2017-05-05 CN CN201710312596.2A patent/CN107096574A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104368325A (en) * | 2014-12-04 | 2015-02-25 | 东北林业大学 | Preparation method of formaldehyde-photodegrading honeycomb activated carbon |
CN105866183A (en) * | 2016-03-11 | 2016-08-17 | 北京大学 | Lanthanum-doped formaldehyde-sensitive material and preparation method thereof, and formaldehyde sensor |
CN106189390A (en) * | 2016-07-20 | 2016-12-07 | 王玲 | A kind of photocatalyst of titanium dioxide coating and film thereof, and preparation method |
CN106345287A (en) * | 2016-08-02 | 2017-01-25 | 保护伞环保科技成都有限公司 | Anion formaldehyde purifying agent |
CN106512941A (en) * | 2016-11-30 | 2017-03-22 | 安吉云界生物科技有限公司 | Composite nanometer titanium dioxide and active carbon adsorbent |
Non-Patent Citations (1)
Title |
---|
王雨群等: "人造板材甲醛清除剂研究进展", 《江苏建筑》 * |
Cited By (8)
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CN108187470A (en) * | 2017-12-05 | 2018-06-22 | 浙江师范大学 | Formaldehyde catching gel |
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CN108970392A (en) * | 2018-07-05 | 2018-12-11 | 吴亚琴 | A kind of formaldehyde cleaning coating liquid |
CN109529782A (en) * | 2018-12-28 | 2019-03-29 | 上海纳米技术及应用国家工程研究中心有限公司 | The preparation method and product of the mesoporous activated carbon of rich phosphorus richness nitrogen functional group and application |
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