CN118558097A - Pet sand peculiar smell deodorant and preparation method thereof - Google Patents
Pet sand peculiar smell deodorant and preparation method thereof Download PDFInfo
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- CN118558097A CN118558097A CN202410494518.9A CN202410494518A CN118558097A CN 118558097 A CN118558097 A CN 118558097A CN 202410494518 A CN202410494518 A CN 202410494518A CN 118558097 A CN118558097 A CN 118558097A
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- 239000004576 sand Substances 0.000 title claims abstract description 52
- 239000002781 deodorant agent Substances 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title abstract description 18
- 239000002808 molecular sieve Substances 0.000 claims abstract description 58
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims abstract description 58
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 23
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000000126 substance Substances 0.000 claims abstract description 23
- 239000010457 zeolite Substances 0.000 claims abstract description 23
- 239000003463 adsorbent Substances 0.000 claims abstract description 22
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims abstract description 18
- 239000002250 absorbent Substances 0.000 claims abstract description 18
- 230000002745 absorbent Effects 0.000 claims abstract description 18
- 239000011943 nanocatalyst Substances 0.000 claims abstract description 17
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229960000892 attapulgite Drugs 0.000 claims abstract description 12
- 229910052625 palygorskite Inorganic materials 0.000 claims abstract description 12
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims abstract description 10
- 239000001110 calcium chloride Substances 0.000 claims abstract description 10
- 229910001628 calcium chloride Inorganic materials 0.000 claims abstract description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 10
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims abstract description 9
- 235000017557 sodium bicarbonate Nutrition 0.000 claims abstract description 9
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229960004889 salicylic acid Drugs 0.000 claims abstract description 7
- 235000014655 lactic acid Nutrition 0.000 claims abstract description 5
- 239000004310 lactic acid Substances 0.000 claims abstract description 5
- 239000012629 purifying agent Substances 0.000 claims abstract description 5
- 235000011148 calcium chloride Nutrition 0.000 claims abstract description 3
- 230000001877 deodorizing effect Effects 0.000 claims description 19
- 239000003054 catalyst Substances 0.000 claims description 18
- 241000282326 Felis catus Species 0.000 claims description 16
- 239000007790 solid phase Substances 0.000 claims description 15
- 238000001035 drying Methods 0.000 claims description 12
- 229910052709 silver Inorganic materials 0.000 claims description 10
- 239000004332 silver Substances 0.000 claims description 10
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000011259 mixed solution Substances 0.000 claims description 8
- 101710134784 Agnoprotein Proteins 0.000 claims description 7
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 7
- 239000008103 glucose Substances 0.000 claims description 7
- -1 silver ions Chemical class 0.000 claims description 7
- 230000032683 aging Effects 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 238000011068 loading method Methods 0.000 claims description 5
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 5
- 238000009210 therapy by ultrasound Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 6
- 230000000694 effects Effects 0.000 abstract description 11
- 238000004332 deodorization Methods 0.000 abstract description 9
- 230000006378 damage Effects 0.000 abstract description 4
- 230000002045 lasting effect Effects 0.000 abstract description 4
- 238000003912 environmental pollution Methods 0.000 abstract description 3
- 230000001954 sterilising effect Effects 0.000 abstract description 3
- 238000004659 sterilization and disinfection Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 30
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 15
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 15
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 15
- 239000007789 gas Substances 0.000 description 9
- 238000001914 filtration Methods 0.000 description 7
- 238000005406 washing Methods 0.000 description 6
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 4
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 230000003213 activating effect Effects 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 235000013527 bean curd Nutrition 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000010419 pet care Methods 0.000 description 2
- 229910052573 porcelain Inorganic materials 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- 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
- B01D53/02—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 by adsorption, e.g. preparative gas chromatography
-
- 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
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/52—Hydrogen sulfide
-
- 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
- B01D53/46—Removing components of defined structure
- B01D53/54—Nitrogen compounds
-
- 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
- B01D53/46—Removing components of defined structure
- B01D53/54—Nitrogen compounds
- B01D53/58—Ammonia
-
- 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
- B01D53/81—Solid phase processes
-
- 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
- B01D53/8603—Removing sulfur compounds
- B01D53/8612—Hydrogen sulfide
-
- 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
- B01D53/8621—Removing nitrogen compounds
-
- 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
- B01D53/8621—Removing nitrogen compounds
- B01D53/8634—Ammonia
-
- 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
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/03—Catalysts comprising molecular sieves not having base-exchange properties
-
- 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
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/30—Sulfur compounds
- B01D2257/304—Hydrogen sulfide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/40—Nitrogen compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/40—Nitrogen compounds
- B01D2257/406—Ammonia
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
The application discloses a pet sand peculiar smell deodorant and a preparation method thereof, and belongs to the technical field of materials. The raw materials of the pet sand peculiar smell purifying agent comprise the following components: 20-70% of physical adsorbent, 10-50% of chemical absorbent, 5-30% of nano catalyst and 100% of total weight; the physical adsorbent is at least one selected from a 5A zeolite molecular sieve, a Beta zeolite molecular sieve and attapulgite; the chemical absorbent is at least one selected from salicylic acid, lactic acid, baking soda and calcium chloride; the nano catalyst is selected from Ag-delta-MnO 2 molecular sieve and/or Ag-OMS-2 molecular sieve. The three components of the purifying agent are used according to a specific mass ratio, so that good effects of quick deodorization and lasting deodorization can be obtained; has obvious effect of eliminating the peculiar smell of the pets, long duration, no generation of harmful substances, no environmental pollution, no damage to the pets and human bodies and sterilization effect.
Description
Technical Field
The application belongs to the technical field of materials, and particularly relates to a pet sand peculiar smell deodorant and a preparation method thereof.
Background
With the continuous development of China economic society and the continuous improvement of income level of people, china pet industry enters into the expansion period of Bobo. High quality pet care will be a trend and clean care products for pets will also become a necessity for life for pet care people. Malodour is one of the biggest pain points for pets, often the malodour originating mainly in the mouth, skin hair, faeces and saliva. The components of the catalyst mainly comprise trimethylamine, hydrogen sulfide and ammonia.
The existing deodorizing products in the market at present mainly comprise deodorizing spray, cat litter and other products. The deodorizing spray can achieve the effect of rapidly eliminating peculiar smell by directly spraying the space and the pet body, but the spraying product is not suitable for deodorizing the peculiar smell of the pet sand, and the conventional liquid spray can cause the pet sand to form agglomerations and lead the pet sand to be wet and moldy.
The cat litter product is a pet deodorization product which is widely applied at present, and the cat litter product mainly comprises bean curd soil cat litter, bentonite cat litter, crystal cat litter, pine cat litter and the like. The bean curd soil cat litter has the defects of easiness in breeding bacterial parasites in wet weather and high price, and has a common deodorizing effect on trimethylamine, hydrogen sulfide and ammonia gas; the bentonite cat litter has the advantages of large dust, light weight, easy maintenance in the jaw seam of the cat and common deodorizing effect, and needs to be cleaned frequently. Therefore, a product capable of removing pet sand odor in a targeted manner is lacking in the prior art.
Disclosure of Invention
In view of the above, the application provides a pet sand peculiar smell deodorant and a preparation method thereof, and mainly aims to solve the technical problem that the odor gas such as trimethylamine, hydrogen sulfide and ammonia gas in the pet sand is difficult to purify.
In one aspect, the application provides a pet sand peculiar smell deodorant, which comprises the following raw materials of physical adsorbent, chemical absorbent and nano catalyst;
Wherein the physical adsorbent is at least one selected from a 5A zeolite molecular sieve, a Beta zeolite molecular sieve and attapulgite clay;
the chemical absorbent is at least one selected from salicylic acid, lactic acid, baking soda and calcium chloride;
The nano catalyst is selected from Ag-delta-MnO 2 molecular sieve and/or Ag-OMS-2 molecular sieve.
Optionally, the physical adsorbent is used in an amount of 20wt% to 70wt%, the chemical absorbent is used in an amount of 10wt% to 50wt%, and the nano catalyst is used in an amount of 5wt% to 30wt%, and the total amount is 100wt%.
Optionally, the physical adsorbent is used in an amount of 30wt% to 60wt%, the chemical absorbent is used in an amount of 20wt% to 50wt%, and the nano catalyst is used in an amount of 10wt% to 30wt%, and the total amount is 100wt%.
Optionally, the physical adsorbent is used in an amount of 20% -70%, and can be selected from any value or a range value between any two of 20%, 30%, 40%, 50%, 60%, 70%; the dosage of the chemical absorbent is between 10% and 50%, and can be selected from any value or range value between any two of 10%, 20%, 30%, 40% and 50%; the amount of the nano catalyst is between 5% and 30%, and can be any value or range value between any two of 5%, 10%, 15%, 20%, 25% and 30%.
Preferably, the physical adsorbent is a combination of a 5A zeolite molecular sieve and attapulgite.
Preferably, the chemical absorbent is a combination of salicylic acid and calcium chloride.
The raw materials of the application are available in the market in the prior art.
Optionally, the preparation process of the Ag-delta-MnO 2 molecular sieve comprises the following steps:
S1: KMnO 4 and glucose are mixed and heated and crystallized for 3.5 to 4.5 hours at the temperature of 650 to 750 ℃ to obtain a solid phase delta-MnO 2 carrier;
S2: immersing the solid phase delta-MnO 2 carrier in an aqueous solution containing silver nitrate, carrying out ultrasonic treatment, stirring, aging, stirring at the temperature of 75-85 ℃ until the water of the mixed solution is evaporated to dryness, loading active components on the solid phase delta-MnO 2, and continuously drying for 4.5-5.5 hours at the temperature of 95-105 ℃; and then the mixture is moved to the air condition and baked for 4.5 to 5.5 hours at the temperature of 350 to 450 ℃ to obtain the Ag-delta-MnO 2 molecular sieve catalyst taking silver ions as active components.
Optionally, the molar ratio of KMnO 4 to glucose is 2.5-3.5:1.
Optionally, the mass content of the active component silver ions in the Ag-delta-MnO 2 molecular sieve catalyst is 8-12%.
Optionally, the preparation process of the Ag-OMS-2 molecular sieve comprises the following steps: KMnO 4、Mn(Ac)2·4H2 O and AgNO 3 are mixed, subjected to hydrothermal reaction at 75-85 ℃ and crystallized for 3.5-4.5 hours to obtain a crystallized product, and the crystallized product is purified and dried to obtain Ag-OMS-2.
Optionally, the mole ratio of KMnO 4、Mn(Ac)2·4H2 O to AgNO 3 is (2.5-3.5): 1 (1.2-1.8).
Optionally, the preparation process of the Ag-delta-MnO 2 molecular sieve catalyst comprises the following steps: mixing KMnO 4 with glucose, crystallizing at 700deg.C for 4 hr; filtering, washing and drying the crystallized sample to obtain a solid phase delta-MnO 2 carrier; immersing solid phase delta-MnO 2 serving as a carrier in aqueous solution containing silver nitrate, carrying out ultrasonic treatment, stirring, aging, stirring the mixed solution at 80 ℃, evaporating the water in the mixed solution to dryness, loading active components on the solid phase delta-MnO 2, and continuously drying at 100 ℃ for 5 hours; then moving to the air condition and roasting for 5 hours at 400 ℃; roasting delta-MnO 2 containing silver active components to obtain an Ag-delta-MnO 2 molecular sieve catalyst taking silver ions as active components;
Optionally, the silver ion active component is 10% by mass.
Optionally, the preparation process of the Ag-delta-MnO 2 molecular sieve catalyst comprises the following steps: 9.489g (0.06 mol) of KMnO 4 and 3.603g (0.02 mol) of glucose were mixed and charged into a mortar, stirred at room temperature for 0.5 hours, and then transferred into a porcelain week, and crystallized at 700℃for 4 hours. Filtering, washing and drying the crystallized sample to obtain a solid phase delta-MnO 2 carrier; immersing solid phase delta-MnO 2 serving as a carrier in an aqueous solution containing silver nitrate, carrying out ultrasonic treatment for 30 minutes, stirring for 4 hours, and aging overnight; stirring the mixed solution at 80 ℃ by using a glass rod, evaporating water in the mixed solution to dryness, uniformly loading active components on a solid phase delta-MnO 2, and continuously drying at 100 ℃ for 5 hours; then the mixture is moved into a muffle furnace under the air condition and baked for 5 hours at 400 ℃; roasting delta-MnO 2 containing silver active components to obtain a catalyst taking silver ions as active components; the mass content of the active component is 10%.
Optionally, the preparation process of the Ag-OMS-2 molecular sieve catalyst comprises the following steps: KMnO 4、Mn(Ac)2·4H2 O and AgNO 3 were mixed, reacted hydrothermally, and crystallized at 80 ℃ for 4 hours; filtering, washing and drying the crystallized sample to obtain the Ag-OMS-2.
Optionally, the preparation process of the Ag-OMS-2 molecular sieve catalyst comprises the following steps: 9.489g (0.06 mol) of KMnO 4,22.059g(0.09mol)Mn(Ac)2·4H2 O and 5.096g (0.03 mol) of AgNO 3 were mixed and added to a mortar, stirred at room temperature for 10 minutes, then transferred to a hydrothermal reaction kettle, and crystallized at 80 ℃ for 4 hours; filtering and washing the crystallized sample, and continuously drying at 80 ℃ for 4 hours to obtain the Ag-OMS-2.
The pet sand peculiar smell deodorant provided by the application is solid particles, and the particle size is not particularly limited, so long as the pet sand peculiar smell deodorant is suitable for being easily mixed with cat sand particles.
The physical adsorbent in the purifying agent is mainly used for adsorbing peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the chemical absorbent is mainly used for rapidly fixing the peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the nano catalyst is mainly used for activating oxygen in air, and continuously reacts with molecules of pet odor gas such as trimethylamine, hydrogen sulfide, ammonia gas and the like through the catalysis to generate nontoxic and harmless small molecular gas, so that the purpose of thoroughly eliminating the odor is achieved.
When the three components of the purifying agent are used according to a specific mass ratio, better effects of quick deodorization and lasting deodorization can be obtained; has obvious effect of eliminating the peculiar smell of the pets, long duration, no generation of harmful substances, no environmental pollution, no damage to the pets and human bodies and sterilization effect.
In a second aspect, the application provides a method for preparing the pet sand peculiar smell deodorant, which comprises the following steps:
Mixing and crushing the physical adsorbent, the chemical absorbent and the nano deodorizing catalyst according to a raw material formula to obtain the pet sand peculiar smell deodorant.
Preferably, the preparation method further comprises the steps of filtering and packaging the obtained nano deodorizing catalyst.
The preparation method of the pet sand peculiar smell deodorant provided by the application has the advantages of simple process, easiness in operation and lower raw material cost, and is suitable for large-scale industrial production.
In a third aspect, the present application provides the above-described pet litter, wherein the raw materials of the pet litter include the above-described pet litter odor deodorizer and pet litter.
Optionally, the pet litter is cat litter.
The pet sand peculiar smell deodorant provided by the application can be mixed with cat sand raw materials according to a certain proportion (the proportion can be adjusted according to actual conditions), and can be prepared into novel nano deodorizing cat sand for use.
Compared with the prior art, the application has the following beneficial effects:
(1) The pet sand peculiar smell deodorant provided by the application comprises three components of a physical adsorbent, a chemical absorbent and a nano deodorizing catalyst, wherein the physical adsorbent is mainly used for adsorbing peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the chemical absorbent is mainly used for rapidly fixing the peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the nano catalyst is mainly used for activating oxygen in air, and reacting with trimethylamine, hydrogen sulfide, ammonia gas and other pet peculiar smell to generate nontoxic and harmless micromolecular gas; the three components are mutually cooperated to obtain good effects of quickly eliminating and permanently eliminating the peculiar smell of the pet.
(2) The preparation process provided by the application adopts nontoxic and harmless components, and can not cause harm to human bodies and pets, and the preparation method is simple and easy to implement.
Detailed Description
The application will be further illustrated with reference to specific examples. The following description is given of several embodiments of the present application and is not intended to limit the application in any way, and although the application is disclosed in the preferred embodiments, it is not intended to limit the application, and any person skilled in the art will make some changes or modifications with the technical content disclosed in the above description equivalent to the equivalent embodiments without departing from the scope of the technical solution of the present application.
Unless otherwise indicated, all starting materials in the examples of the present application were purchased commercially and used without any particular treatment.
The preparation method of the nano catalyst is as follows.
The preparation process of the Ag-delta-MnO 2 molecular sieve catalyst comprises the following steps: 9.489g (0.06 mol) of KMnO 4 and 3.603g (0.02 mol) of glucose were mixed and charged into a mortar, stirred at room temperature for 0.5 hours, and then transferred into a porcelain week, and crystallized at 700℃for 4 hours. Filtering, washing and drying the crystallized sample to obtain a solid phase delta-MnO 2 carrier; immersing solid phase delta-MnO 2 serving as a carrier in an aqueous solution containing silver nitrate, carrying out ultrasonic treatment for 30 minutes, stirring for 4 hours, and aging overnight; stirring the mixed solution at 80 ℃ by using a glass rod, evaporating water in the mixed solution to dryness, uniformly loading active components on a solid phase delta-MnO 2, and continuously drying at 100 ℃ for 5 hours; then the mixture is moved into a muffle furnace under the air condition and baked for 5 hours at 400 ℃; roasting delta-MnO 2 containing silver active components to obtain a catalyst taking silver ions as active components; the mass content of the active component is 10%.
The preparation process of the Ag-OMS-2 molecular sieve catalyst comprises the following steps: 9.489g (0.06 mol) of KMnO 4,22.059g(0.09mol)Mn(Ac)2·4H2 O and 5.096g (0.03 mol) of AgNO 3 were mixed and added to a mortar, stirred at room temperature for 10 minutes, then transferred to a hydrothermal reaction kettle, and crystallized at 80 ℃ for 4 hours; filtering and washing the crystallized sample, and continuously drying at 80 ℃ for 4 hours to obtain the Ag-OMS-2.
Example 1
Mixing 30wt% of 5A zeolite molecular sieve, 40wt% of salicylic acid and 30wt% of Ag-delta-MnO 2 molecular sieve, extruding by using a strip extruder, and drying to obtain the pet sand peculiar smell deodorant.
Example 2
40Wt% of 5A zeolite molecular sieve, 30wt% of lactic acid and 30wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded by a strip extruder and dried, and then the pet sand peculiar smell deodorant is obtained.
Example 3
50Wt% of 5A zeolite molecular sieve, 20wt% of baking soda and 30wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded by a strip extruder and dried, and then the pet sand peculiar smell deodorant is obtained.
Example 4
60 Weight percent of beta zeolite molecular sieve, 20 weight percent of calcium chloride and 20 weight percent of Ag-OMS-2 molecular sieve are mixed, extruded by a strip extruder and dried to obtain the pet sand peculiar smell deodorant.
Example 5
60 Weight percent of attapulgite, 35 weight percent of baking soda and 5 weight percent of Ag-OMS-2 molecular sieve are mixed, extruded by a strip extruder and dried to obtain the pet sand peculiar smell deodorant.
Example 6
30Wt% of 5A zeolite molecular sieve, 20wt% of attapulgite, 20wt% of salicylic acid, 20wt% of calcium chloride, 5wt% of Ag-OMS-2 molecular sieve and 5wt% of Ag-delta-MnO 2 are mixed, extruded and dried by using an extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 7
10Wt% of beta zeolite molecular sieve, 20wt% of attapulgite, 20wt% of baking soda, 20wt% of calcium chloride, 15wt% of Ag-OMS-2 molecular sieve and 15wt% of Ag-delta-MnO 2 are mixed, extruded and dried by using a strip extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 8
20Wt% of beta zeolite molecular sieve, 20wt% of 5A zeolite molecular sieve, 20wt% of attapulgite, 20wt% of calcium chloride and 20wt% of Ag-OMS-2 molecular sieve are mixed, extruded and dried by using a strip extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 9
20Wt% of beta zeolite molecular sieve, 20wt% of 5A zeolite molecular sieve, 20wt% of attapulgite, 20wt% of calcium chloride and 20wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded and dried by using a strip extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 10
20Wt% of beta zeolite molecular sieve, 20wt% of 5A zeolite molecular sieve, 20wt% of attapulgite, 20wt% of baking soda and 20wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded and dried by using a strip extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 11
10Wt% of beta zeolite molecular sieve, 10wt% of 5A zeolite molecular sieve, 10wt% of attapulgite, 30wt% of baking soda, 20wt% of Ag-OMS-2 molecular sieve and 20wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded and dried by using an extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Example 12
20Wt% of beta zeolite molecular sieve, 10wt% of 5A zeolite molecular sieve, 10wt% of attapulgite, 10wt% of salicylic acid, 10wt% of lactic acid, 10wt% of baking soda, 10wt% of calcium chloride, 10wt% of Ag-OMS-2 molecular sieve and 10wt% of Ag-delta-MnO 2 molecular sieve are mixed, extruded and dried by using a strip extruder, and then mixed to obtain the pet sand peculiar smell deodorant.
Test case
Referring to QB/T2761 2006, 50g of the nano deodorant prepared in examples 1-12 is respectively placed in a closed cabin of 1m 3, then mixed liquid prepared from hexanal, n-heptanal, octanal, nonanal, isovaleric acid, trimethylamine, hydrogen sulfide and ammonia water is placed in the closed cabin according to the volume ratio of 6.5:4.6:2.8:11.4:1:1:1, the mixed liquid simulated pet odor prepared from hexanal, n-heptanal, octanal, nonanal, isovaleric acid, trimethylamine, hydrogen sulfide and ammonia water is placed in the closed cabin, the mixed TVOC concentration is kept at 10ppm, the evaluation is carried out after 12h of treatment, and the mixed TVOC concentration (ppm) is measured at 0h, 1h, 2h, 3h, 4h, 5h, 6h, 7h, 8h, 9h, 10h, 11h and 12h respectively, and the results are shown in Table 1:
TABLE 1 detection results of residual concentration of odor
Group of | 0h | 1h | 2h | 3h | 4h | 5h | 6h | 7h | 8h | 9h | 10h | 11h | 12h |
Background value | 0 | 9.68 | 9.57 | 9.43 | 9.32 | 9.26 | 9.18 | 9.13 | 9.09 | 9.06 | 9.03 | 9.01 | 8.99 |
Example 1 | 0 | 0.28 | 0.17 | 0.08 | 0.03 | 0.02 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 2 | 0 | 0.25 | 0.13 | 0.11 | 0.02 | 0.02 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 3 | 0 | 0.24 | 0.12 | 0.05 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 4 | 0 | 0.86 | 0.56 | 0.43 | 0.31 | 0.15 | 0.07 | 0.04 | 0.03 | 0.03 | 0.03 | 0.02 | 0.02 |
Example 5 | 0 | 1.75 | 0.98 | 0.75 | 0.56 | 0.32 | 0.21 | 0.11 | 0.09 | 0.07 | 0.06 | 0.02 | 0.01 |
Example 6 | 0 | 0.88 | 0.58 | 0.47 | 0.29 | 0.14 | 0.08 | 0.05 | 0.03 | 0.03 | 0.02 | 0.02 | 0.01 |
Example 7 | 0 | 0.23 | 0.15 | 0.08 | 0.02 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 8 | 0 | 0.75 | 0.49 | 0.13 | 0.09 | 0.05 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 9 | 0 | 0.78 | 0.46 | 0.18 | 0.09 | 0.05 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 10 | 0 | 0.72 | 0.47 | 0.13 | 0.11 | 0.04 | 0.03 | 0.03 | 0.02 | 0.02 | 0.02 | 0.01 | 0.01 |
Example 11 | 0 | 0.15 | 0.03 | 0.03 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
Example 12 | 0 | 0.74 | 0.48 | 0.14 | 0.08 | 0.05 | 0.03 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 |
As can be seen from the data in table 1: the concentration of the odor gas in examples 1-12 can be reduced from the original value of 9.68 to below 0.15-1.75 within 1h, and the average is reduced to below 0.05 times of the original value, so that the cat litter deodorant has very good deodorizing effects on trimethylamine, hydrogen sulfide and ammonia gas only within 1h, and after 10h deodorizing treatment, the odor gas is reduced to below 0.001 times of the original value on average, and the deodorizing effects are stable at 11h and 12 h. The original gas concentration is about 93% after 12 hours of standing without professional deodorizing treatment. As is apparent from comparison, the targeted deodorant of the present application can treat almost all the odorous gases, and has a very remarkable deodorizing effect.
The pet sand peculiar smell deodorant prepared by the application has very high-efficiency and lasting capability of eliminating peculiar smell pollutants of pets, can reduce the peculiar smell of the pets in the closed cabin to be below the standard within 1 hour, and has no rebound; at the same time, the selection of the types of physical adsorbent and chemical absorbent can also obviously improve the elimination capability of the nano deodorizing catalyst.
The principle of the pet sand peculiar smell deodorant of the application comprises the following aspects: the physical adsorbent is mainly used for adsorbing peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the chemical absorbent is mainly used for rapidly fixing the peculiar smell of pets such as trimethylamine, hydrogen sulfide, ammonia gas and the like; the nano catalyst is mainly used for activating oxygen in air, and reacting with trimethylamine, hydrogen sulfide, ammonia and other pet peculiar smell to generate nontoxic and harmless micromolecular gas.
When the three components of the pet sand peculiar smell deodorant are used according to a specific mass ratio, better effects of quick deodorization and lasting deodorization can be obtained; has obvious effect of eliminating the peculiar smell of the pets, long duration, no generation of harmful substances, no environmental pollution, no damage to the pets and human bodies and sterilization effect.
The solid granular deodorant provided by the application can be mixed with solid pet sand for use, can be used for deodorization, is safe and non-irritating to pets, and can be reused; deodorization spraying is often adopted in the prior art, the product is not suitable for pet sand, and liquid spraying can form agglomerations on the pet sand and can cause the pet sand to be wet and moldy.
While the application has been described in terms of preferred embodiments, it will be understood by those skilled in the art that various changes and modifications can be made without departing from the scope of the application, and it is intended that the application is not limited to the specific embodiments disclosed.
Claims (10)
1. The pet sand peculiar smell deodorant is characterized by comprising the following raw materials: physical adsorbents, chemical adsorbents, and nanocatalysts;
Wherein the physical adsorbent is at least one selected from a 5A zeolite molecular sieve, a Beta zeolite molecular sieve and attapulgite clay;
the chemical absorbent is at least one selected from salicylic acid, lactic acid, baking soda and calcium chloride;
The nano catalyst is selected from Ag-delta-MnO 2 molecular sieve and/or Ag-OMS-2 molecular sieve.
2. A pet sand odor eliminating agent as defined in claim 1, wherein said physical adsorbent is used in an amount of 20-70 wt%, said chemical absorbent is used in an amount of 10-50 wt%, and said nanocatalyst is used in an amount of 5-30 wt%, totaling 100wt%.
3. The pet sand odor eliminating agent according to claim 1, wherein the amount of the physical adsorbent is 30wt% -60 wt%, the amount of the chemical absorbent is 20wt% -50 wt%, and the amount of the nano catalyst is 10wt% -30 wt%, totaling 100wt%;
preferably, the amount of the physical adsorbent is 45-50 wt%, the amount of the chemical adsorbent is 25-35 wt%, and the amount of the nano catalyst is 15-25 wt%.
4. The pet sand odor eliminating agent as defined in claim 1, wherein the Ag-delta-MnO 2 molecular sieve is prepared by the following steps:
S1: KMnO 4 and glucose are mixed and heated and crystallized for 3.5 to 4.5 hours at the temperature of 650 to 750 ℃ to obtain a solid phase delta-MnO 2 carrier;
S2: immersing the solid phase delta-MnO 2 carrier in an aqueous solution containing silver nitrate, carrying out ultrasonic treatment, stirring, aging, stirring at the temperature of 75-85 ℃ until the water of the mixed solution is evaporated to dryness, loading active components on the solid phase delta-MnO 2, and continuously drying for 4.5-5.5 hours at the temperature of 95-105 ℃; and then the mixture is moved to the air condition and baked for 4.5 to 5.5 hours at the temperature of 350 to 450 ℃ to obtain the Ag-delta-MnO 2 molecular sieve catalyst taking silver ions as active components.
5. The pet litter odor control deodorant of claim 4 wherein the molar ratio of KMnO 4 to said glucose is from 2.5 to 3.5:1.
6. The pet sand peculiar smell deodorant according to claim 4, wherein the mass content of the active component silver ions in the Ag-delta-MnO 2 molecular sieve catalyst is 8-12%.
7. The pet sand odor eliminator as claimed in claim 1, wherein the Ag-OMS-2 molecular sieve is prepared by the steps of: KMnO 4、Mn(Ac)2·4H2 O and AgNO 3 are mixed, subjected to hydrothermal reaction at 75-85 ℃ and crystallized for 3.5-4.5 hours to obtain a crystallized product, and the crystallized product is purified and dried to obtain Ag-OMS-2.
8. The pet litter odor eliminating agent according to claim 7, wherein the mole ratio of KMnO 4、Mn(Ac)2·4H2 O to AgNO 3 is (2.5-3.5): 1 (1.2-1.8).
9. A method for preparing a pet litter deodorizing agent as set forth in any one of claims 1 to 8, comprising the steps of:
and mixing and crushing the physical adsorbent, the chemical absorbent and the nano catalyst according to a raw material formula to obtain the pet sand peculiar smell purifying agent.
10. A nano deodorizing pet sand, characterized in that the raw materials of the pet sand comprise the deodorizing agent for pet sand and the pet sand according to any one of claims 1 to 8; preferably, the pet litter is cat litter.
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