CN111359579A - Preparation method of antibacterial diatomite wall material - Google Patents
Preparation method of antibacterial diatomite wall material Download PDFInfo
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- CN111359579A CN111359579A CN202010242452.6A CN202010242452A CN111359579A CN 111359579 A CN111359579 A CN 111359579A CN 202010242452 A CN202010242452 A CN 202010242452A CN 111359579 A CN111359579 A CN 111359579A
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 56
- 239000000463 material Substances 0.000 title claims abstract description 50
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims abstract description 22
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims abstract description 14
- 235000011114 ammonium hydroxide Nutrition 0.000 claims abstract description 14
- 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 abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 14
- 238000005245 sintering Methods 0.000 claims abstract description 14
- 229910001961 silver nitrate Inorganic materials 0.000 claims abstract description 12
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims abstract description 8
- 239000007864 aqueous solution Substances 0.000 claims abstract description 8
- 239000000243 solution Substances 0.000 claims abstract description 8
- 239000011812 mixed powder Substances 0.000 claims abstract description 7
- 239000002002 slurry Substances 0.000 claims abstract description 7
- 238000002791 soaking Methods 0.000 claims abstract description 7
- 238000003756 stirring Methods 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 6
- 239000011230 binding agent Substances 0.000 claims abstract description 5
- 239000000843 powder Substances 0.000 claims description 9
- 239000005909 Kieselgur Substances 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- 239000000440 bentonite Substances 0.000 claims description 6
- 229910000278 bentonite Inorganic materials 0.000 claims description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical group O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 5
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 3
- 239000000292 calcium oxide Substances 0.000 claims description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 3
- 239000000395 magnesium oxide Substances 0.000 claims description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 3
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 239000001099 ammonium carbonate Substances 0.000 claims description 2
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 2
- 229920000609 methyl cellulose Polymers 0.000 claims description 2
- 239000001923 methylcellulose Substances 0.000 claims description 2
- 244000275012 Sesbania cannabina Species 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 claims 1
- 239000004599 antimicrobial Substances 0.000 claims 1
- 238000001179 sorption measurement Methods 0.000 abstract description 15
- 230000000694 effects Effects 0.000 abstract description 8
- 230000001954 sterilising effect Effects 0.000 abstract description 6
- 238000004659 sterilization and disinfection Methods 0.000 abstract description 5
- 230000000052 comparative effect Effects 0.000 description 20
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 6
- 241000219782 Sesbania Species 0.000 description 5
- 229910001923 silver oxide Inorganic materials 0.000 description 5
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Substances [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 238000003905 indoor air pollution Methods 0.000 description 3
- 229910052746 lanthanum Inorganic materials 0.000 description 3
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000206761 Bacillariophyta Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- UKHWJBVVWVYFEY-UHFFFAOYSA-M silver;hydroxide Chemical compound [OH-].[Ag+] UKHWJBVVWVYFEY-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 238000004887 air purification Methods 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000002195 synergetic effect Effects 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/10—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
- B01J20/14—Diatomaceous earth
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/04—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
- B01J20/041—Oxides or hydroxides
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
- B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Toxicology (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
The invention provides a preparation method of an antibacterial diatomite wall material, which is characterized by comprising the following steps: the preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps: (a) 80-93 parts by mass of diatomite, 5-10 parts by mass of alkaline earth metal oxide, 1-5 parts by mass of binder and 1-5 parts by mass of pore-enlarging agent are mixed at a high speed according to the proportion; (b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of silver nitrate and lanthanum nitrate, continuously stirring at 50-80 ℃, and slowly dropwise adding ammonia water solution for 4 hours to form slurry-like mixture; (c) and sintering the slurry mixture at a high temperature and crushing to obtain the wall material. According to the method, the diatomite is modified, so that the prepared diatomite has strong adsorption capacity and a sterilization effect.
Description
Technical Field
The invention belongs to the field of building materials, and particularly relates to a preparation method of an antibacterial diatomite wall material.
Background
The diatomite wall material (or named diatom ooze and diatom ooze wall material) is a powdery functional wall surface painting material prepared by taking diatomite as a main material and matching with various other inorganic mineral materials and functional additives through a certain production process. As a novel interior wall finishing material appearing in the building material market in recent years, compared with traditional mainstream interior wall finishing materials such as emulsion paint and wallpaper, the diatomite wall material has the functions of humidity regulation, antibiosis, mildew prevention, air purification, fire prevention, flame retardation, heat preservation, heat insulation and the like, and has no environmental pollution, safety and safety from the material composition aspect, meets the requirement of circular economy, meets the development trend of paint, and has very good application prospect.
The diatomite wall material has multiple functionalities, and is the main characteristic of being different from the common coating. The diatomite wall materials in the prior art mainly comprise the following components: 1. a large amount of rubber powder-cured diatomaceous earth was used. The middle rubber powder of the diatomite wall material can block the micropores of the diatoms, so that the diatoms lose the humidity adjusting function, and therefore, the diatomite wall material is easy to mildew in a humid environment and has poor flame retardant effect when encountering fire. The diatomite wall material is easy to identify: spraying water to the wall surface by using a watering can, wherein the sprayed water flows quickly; then the mixture is burnt by a flame gun, and black smoke and peculiar smell can be generated. 2. Clay-based solidified diatomaceous earth. The diatomite wall material has the characteristics of reduction into mud when meeting water, strong humidity adjusting capability and good fireproof performance. However, the diatomite wall material has low surface strength, is easy to pulverize, and cannot be used in a particularly humid environment.
The indoor air pollution phenomenon is widely existed in various closed buildings such as living rooms at present, and severe indoor air brings serious harm to human health. The world environment held in Washington in 1997 indicates that indoor air pollution is more severe than outdoor air pollution. The problem of indoor air pollution is highly regarded in many countries of the world, and research work on indoor environment quality has been conducted in europe, north america, japan, and the like from the 20 th century to the 80 th century.
The dust floating in the air can carry a large amount of bacteria, so when the diatomite is used for purifying the air dust, if the diatomite has a certain antibacterial property, the air quality is greatly improved, and the diatomite is beneficial to body health.
Compared with the prior art, the invention has the advantages of low price, simple preparation, and adsorption capacity and sterilization effect on indoor polluted gas.
Disclosure of Invention
The invention aims to provide a preparation method of an antibacterial diatomite wall material, which modifies diatomite to enable the prepared diatomite to have strong adsorption capacity and a sterilization effect.
The invention provides a preparation method of an antibacterial diatomite wall material, which is characterized by comprising the following steps:
(a) 80-93 parts by mass of diatomite, 5-10 parts by mass of alkaline earth metal oxide, 1-5 parts by mass of binder and 1-5 parts by mass of pore-enlarging agent are mixed at a high speed according to the proportion;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of silver nitrate and lanthanum nitrate, continuously stirring at 50-80 ℃, and slowly dropwise adding ammonia water solution for 4 hours to form slurry-like mixture;
(c) and sintering the slurry mixture at a high temperature and crushing to obtain the wall material.
Further, the sintering temperature is 500-600 ℃.
Further, the alkaline earth metal oxide is one or more of calcium oxide, aluminum oxide and magnesium oxide.
Further wherein the binder is bentonite and/or acid clay.
Further, the pore-expanding agent is one or a mixture of ammonium carbonate, methyl cellulose and sesbania powder.
Further, the concentration of the aqueous ammonia solution is 25 mass%, and the amount of the aqueous ammonia solution added is 5 to 10 parts by mass.
Further, the molar concentration of the silver nitrate in the mixed water solution is 0.2-0.5mol/L, and the molar concentration of the lanthanum nitrate is 0.02-0.05 mol/L.
The invention also provides a method for purifying indoor air, which uses the prepared antibacterial diatomite wall material. The diatomite wall material is used for the wall surface coating through a conventional method, and has the effects of purifying air and sterilizing.
The sintering temperature is 500-600 ℃. The purpose of high temperature is to decompose the rare earth complex to form metal oxide, which is further combined with the carrier diatomite, thereby increasing the loading capacity and enhancing the adsorption capacity. Meanwhile, the pore-expanding agent and other residual substances in the molecular sieve powder can be decomposed, the diameter of the pore passage is increased, and the specific surface area is increased.
The alkaline earth metal may comprise one or more of calcium oxide, aluminum oxide, magnesium oxide. The alkaline earth metal oxide has the function of providing enough hydroxyl groups, and after the alkaline earth metal oxide is compounded with diatomite, the alkaline earth metal oxide can fully absorb harmful gas small molecules such as formaldehyde and the like which react with the hydroxyl groups based on the hydroxyl-rich structure.
After ammonia water is added, silver nitrate and lanthanum nitrate react to form silver hydroxide sol, the silver hydroxide sol is decomposed into nano silver oxide under the high-temperature condition, and the nano silver oxide sol is fully compounded with diatomite powder to form a nano silver oxide coating on the surface. The nano silver oxide can play an antibacterial role and kill harmful bacteria in the air. Meanwhile, the lanthanum nitrate can also form nano lanthanum oxide, and the nano lanthanum oxide has a broader spectrum light excitation effect and can further activate the sterilization effect of the nano silver oxide. The amount of lanthanum nitrate should not be too much, and too much will have a slight radioactivity, preferably at a molar concentration of 0.02-0.05 mol/L.
The raw materials of the invention are simple and easy to obtain, the preparation process is simple and convenient, the industrial production can be realized by using conventional equipment, the requirements on reaction conditions and formula proportion are low, and the invention is suitable for large-scale popularization and application.
According to the preparation method of the antibacterial diatomite wall material, the diatomite is modified, so that the prepared diatomite has strong adsorption capacity and a sterilization effect.
Detailed Description
The present invention is further described below with reference to examples, but the scope of the present invention is not limited by these examples. The scope of the invention is set forth in the claims.
The preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps:
(a) 80-93 parts by mass of diatomite, 5-10 parts by mass of alumina, 1-5 parts by mass of bentonite and 1-5 parts by mass of sesbania powder are mixed at a high speed according to the proportion;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of 0.2-0.5mol/L silver nitrate and 0.02-0.05mol/L lanthanum nitrate, continuously stirring at 50-80 ℃, and slowly dripping 5-10 parts by mass of 25 mass% ammonia water solution for 4 hours to form slurry-like mixture;
(c) sintering the slurry mixture at the sintering temperature of 500-600 ℃, and crushing to obtain the wall material.
Diatomaceous earth was diatomaceous earth C499 available from heshi wall chemical industry.
Example 1
The preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps:
(a) 86 parts of diatomite, 8 parts of alumina, 3 parts of bentonite and 3 parts of sesbania powder by mass are mixed at a high speed according to the proportion;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of 0.3mol/L silver nitrate and 0.03mol/L lanthanum nitrate, continuously stirring at 65 ℃ and slowly dropwise adding 8 parts by mass of 25 mass% ammonia water solution for 4 hours to form slurry-like mixture;
(c) and sintering the slurry mixture at the sintering temperature of 550 ℃, and crushing to obtain the wall material.
Example 2
The preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps:
(a) 93 parts by mass of diatomite, 5 parts by mass of alumina, 1 part by mass of bentonite and 1 part by mass of sesbania powder are mixed at a high speed according to the mixture ratio;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of 0.2mol/L silver nitrate and 0.02mol/L lanthanum nitrate, continuously stirring at 80 ℃ and slowly dropwise adding 10 parts by mass of 25 mass% ammonia water solution for 4 hours to form slurry-like mixture;
(c) and sintering the slurry mixture at the sintering temperature of 600 ℃, and crushing to obtain the wall material.
Example 3
The preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps:
(a) 80 parts by mass of diatomite, 10 parts by mass of alumina, 5 parts by mass of bentonite and 5 parts by mass of sesbania powder are mixed at a high speed according to the mixture ratio;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of 0.5mol/L silver nitrate and 0.05mol/L lanthanum nitrate, continuously stirring at 50 ℃, and slowly dropwise adding 5 parts by mass of 25 mass% ammonia water solution for 4 hours to form slurry-like mixture;
(c) and sintering the slurry mixture at the sintering temperature of 500 ℃ and then crushing to obtain the wall material.
Comparative example 1
The test was performed directly using diatomaceous earth.
Comparative example 2
Prepared according to the method of example 1 except that no metal oxide is added.
Comparative example 3
Prepared according to the method of example 1 except that lanthanum nitrate was not added.
Comparative example 4
Prepared according to the method of example 1, except that the lanthanum nitrate concentration is 0.1 mol/L.
Comparative example 5
Prepared according to the method of example 1, except that no silver nitrate was added.
Comparative example 6
Prepared according to the method of example 1, except that the concentration of silver nitrate is 1 mol/L.
Comparative example 7
The preparation was carried out in accordance with the procedure of example 1, by directly adding an aqueous ammonia solution to the mixture in step 2, and then calcining and pulverizing the mixture.
Adsorption measurement of the adsorbent:
the method for testing the adsorption capacity of the adsorbing material to toluene and formaldehyde comprises the steps of respectively introducing toluene gas and formaldehyde gas in a nitrogen bubbling mode in a 1 cubic meter glass box until the concentration of harmful gas is 100ppm, adding 1g of adsorbing material to be tested, and adsorbing until the adsorbing material is saturated, namely, achieving adsorption balance, wherein the toluene and formaldehyde gas is not continuously introduced during the period.
And (3) carrying out tests according to GB/T21510-.
The results are as follows
TABLE 1 measurement results
Example 1 | Example 2 | Example 3 | Comparative example 1 | Comparative example 2 | Comparative example 3 | Comparative example 4 | Comparative example 5 | Comparative example 6 | Comparative example 7 | |
Adsorption Rate/(ppm/h) | 87 | 83 | 80 | 51 | 71 | 77 | 72 | 73 | 79 | 67 |
Adsorption capacity/(ppm) | 457 | 442 | 438 | 319 | 411 | 413 | 427 | 413 | 431 | 382 |
Antibacterial rate | 98 | 97 | 95 | 15 | 87 | 72 | 97 | 55 | 98 | 73 |
According to the results of the performance test, comparative example 1 and comparative example 1,
in comparative example 2, it was found that the adsorption material further supported with a metal oxide can increase the adsorption rate and adsorption capacity by a certain amount and promote the improvement of antibacterial properties. Comparing example 1 with comparative examples 3 and 4, it is found that the antibacterial rate can be significantly improved by introducing lanthanum element, but the performance is not further improved by excessive loading lanthanum element. Comparing example 1 with comparative examples 5 and 6, it is found that the antibacterial rate can be remarkably improved by introducing silver element, but the performance is not further improved by excessive silver element loading. Comparing example 1 and comparative example 7, slowly dropwise add aqueous ammonia and heat reaction 4 hours, can let the load of silver and lanthanum more fully even to improve synergistic bactericidal effect, and have and let the combined material more even more fine and close, thereby improve adsorption rate and adsorption capacity.
Those of ordinary skill in the art will understand that: the invention is not to be considered as limited to the specific embodiments thereof, but is to be understood as being modified in all respects, all changes and equivalents that come within the spirit and scope of the invention.
Claims (8)
1. The preparation method of the antibacterial diatomite wall material is characterized by comprising the following steps:
(a) 80-93 parts by mass of diatomite, 5-10 parts by mass of alkaline earth metal oxide, 1-5 parts by mass of binder and 1-5 parts by mass of pore-enlarging agent are mixed at a high speed according to the proportion;
(b) soaking the mixed powder into 100 parts by mass of mixed aqueous solution of silver nitrate and lanthanum nitrate, continuously stirring at 50-80 ℃, and slowly dropwise adding ammonia water solution for 4 hours to form slurry-like mixture;
(c) and sintering the slurry mixture at a high temperature and crushing to obtain the wall material.
2. The method for preparing the antibacterial diatomite wall material as claimed in claim 1, wherein the sintering temperature is 500-600 ℃.
3. The method for preparing the antibacterial diatomite wall material according to claim 1, wherein the alkaline earth metal oxide is one or more of calcium oxide, aluminum oxide and magnesium oxide.
4. The method of making an antimicrobial diatomaceous earth wall material of claim 1, wherein the binder is bentonite and/or acid clay.
5. The method for preparing the antibacterial diatomite wall material according to claim 1, wherein the pore-enlarging agent is one or a mixture of ammonium carbonate, methylcellulose and sesbania powder.
6. The method for producing an antibacterial diatomaceous earth wall material according to claim 1, wherein the concentration of the aqueous ammonia solution is 25 mass%, and the amount of the aqueous ammonia solution added is 5 to 10 parts by mass.
7. The method for preparing the antibacterial diatomite wall material according to claim 1, wherein the molar concentration of silver nitrate in the mixed aqueous solution is 0.2-0.5mol/L, and the molar concentration of lanthanum nitrate is 0.02-0.05 mol/L.
8. A method for purifying indoor air using the antibacterial diatomite wall material prepared according to claims 1-7.
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