CN115041003A - High-efficiency aldehyde-removing spray and preparation method thereof - Google Patents
High-efficiency aldehyde-removing spray and preparation method thereof Download PDFInfo
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- 239000007921 spray Substances 0.000 title claims abstract description 105
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- 238000001179 sorption measurement Methods 0.000 claims abstract description 23
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 claims abstract description 21
- 150000007524 organic acids Chemical class 0.000 claims abstract description 21
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000004202 carbamide Substances 0.000 claims abstract description 20
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000011159 matrix material Substances 0.000 claims abstract description 19
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 15
- 239000003899 bactericide agent Substances 0.000 claims abstract description 15
- 239000002270 dispersing agent Substances 0.000 claims abstract description 11
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 239000002994 raw material Substances 0.000 claims abstract description 8
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims description 24
- 229920001661 Chitosan Polymers 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 15
- 238000003756 stirring Methods 0.000 claims description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- 229960003080 taurine Drugs 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000006185 dispersion Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 230000006196 deacetylation Effects 0.000 claims description 5
- 238000003381 deacetylation reaction Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 3
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 170
- 239000003795 chemical substances by application Substances 0.000 abstract description 17
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract description 9
- 238000005286 illumination Methods 0.000 abstract description 3
- 150000001299 aldehydes Chemical class 0.000 description 57
- 230000000052 comparative effect Effects 0.000 description 18
- 230000000694 effects Effects 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 7
- 229910021641 deionized water Inorganic materials 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 125000003172 aldehyde group Chemical group 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000002349 favourable effect Effects 0.000 description 6
- 238000000889 atomisation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000011941 photocatalyst Substances 0.000 description 2
- 239000000419 plant extract Substances 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- KHSLHYAUZSPBIU-UHFFFAOYSA-M benzododecinium bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 KHSLHYAUZSPBIU-UHFFFAOYSA-M 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- FAFWKDXOUWXCDP-UHFFFAOYSA-N ethenylurea Chemical compound NC(=O)NC=C FAFWKDXOUWXCDP-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/72—Organic compounds not provided for in groups B01D53/48 - B01D53/70, e.g. hydrocarbons
-
- 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
- B01D53/77—Liquid phase processes
- B01D53/78—Liquid phase processes with gas-liquid contact
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
- B01D2257/708—Volatile organic compounds V.O.C.'s
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
The application discloses an efficient aldehyde-removing spray and a preparation method thereof, relates to the field of aldehyde-removing agents, and aims to solve the problems that the existing aldehyde-removing spray is harsh in use condition and low in aldehyde-removing efficiency. The efficient aldehyde-removing spray is prepared from the following raw materials in percentage by weight: 1-2% of water-soluble adsorption matrix, 0.1-0.5% of ethylene urea, 0.4-0.8% of urea, 1.0-1.5% of carbazide, 2-4% of organic acid, 3-4% of bactericide, 0.1-0.3% of dispersing agent and the balance of solvent. The formaldehyde-removing spray has no requirements on illumination and the like, has low requirements on formaldehyde-removing conditions, and can quickly remove formaldehyde. Meanwhile, for low-concentration formaldehyde, the formaldehyde removing spray can reduce the concentration of the low-concentration formaldehyde to be below 0.1mg/m3 within 30min, and meets the requirement of national standard on indoor living environment.
Description
Technical Field
The application relates to the field of aldehyde removal agents, in particular to an efficient aldehyde removal spray and a preparation method thereof.
Background
Most of house decoration, furniture manufacturing, cabinet manufacturing, and articles in a vehicle use a substance containing formaldehyde. However, formaldehyde is a highly toxic substance, and in order to protect human health, it is necessary to perform an aldehyde removal treatment on a house which has been just finished, a furniture cabinet which has been just manufactured, an article in a vehicle, and the like, so as to reduce the concentration of formaldehyde to below a safe concentration.
The formaldehyde removing spray is a common medicament capable of removing formaldehyde, and comprises the following types: (1) a photocatalyst; (2) a biological enzyme; (3) plant extract. The main raw material of the photocatalyst method is nano titanium dioxide, but the aldehyde removal effect in the internal environment with insufficient light is not ideal. The biological enzyme method has harsh use conditions and the catalytic capability is easily influenced by the environment. The plant extract method has limited formaldehyde adsorption capacity and slow effect.
Therefore, an aldehyde-removing spray which has low requirement on the use condition and can rapidly remove formaldehyde is needed.
Disclosure of Invention
In order to solve the problems that the existing aldehyde removing spray has harsh use conditions and low aldehyde removing efficiency, the application provides the high-efficiency aldehyde removing spray and the preparation method thereof.
In a first aspect, the application provides an efficient aldehyde removal spray, which adopts the following technical scheme:
an efficient aldehyde-removing spray is prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1 to 2 percent
Ethylene urea: 0.1 to 0.5 percent
Urea: 0.4 to 0.8 percent
Carbohydrazide: 1.0 to 1.5 percent
Organic acid: 2 to 4 percent of
And (3) bactericide: 3 to 4 percent
Dispersing agent: 0.1 to 0.3 percent
Solvent: and (4) the balance.
The water-soluble adsorption matrix is made of water-soluble substances with adsorption effect such as carboxymethyl chitosan and carboxymethyl cellulose, and can adsorb harmful substances in the captured air, such as formaldehyde. The ethylene urea and the urea contain active groups which can react with aldehyde groups, and have good elimination effect on aldehyde substances; the carbazide has strong reducibility and can quickly neutralize aldehyde groups; the organic acid can catalyze the reaction of the ethylene urea, the urea and the carbazide with the aldehyde group, thereby quickly eliminating the aldehyde substance and being beneficial to improving the aldehyde removal efficiency of the aldehyde removal spray. Meanwhile, the formaldehyde removing spray has no requirements on illumination and the like, and can also remove low-concentration formaldehyde to reduce the indoor formaldehyde concentration to 0.1mg/m 3 The requirements of national standards on indoor living environment are met.
Optionally, the high-efficiency aldehyde-removing spray is prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1 to 1.5 percent
Ethylene urea: 0.3 to 0.4 percent
Urea: 0.5 to 0.8 percent
Carbohydrazide: 1.2 to 1.3 percent
Organic acid: 2.5 to 3.2 percent
And (3) bactericide: 3 to 4 percent of
Dispersing agent: 0.15-0.25%
Solvent: and (4) the balance.
Through adopting above-mentioned technical scheme, when the weight percent content of each component of except that aldehyde spray is in above-mentioned within range, except that aldehyde spray has the advantage that atomization effect is good and adsorption efficiency is excellent concurrently, be favorable to adsorbing fast and decomposing formaldehyde, further improve except that aldehyde efficiency of aldehyde spray. Wherein, for low-concentration formaldehyde, the formaldehyde removing spray can reduce the concentration of the formaldehyde to 0.1mg/m within 15min 3 The following.
Optionally, the high-efficiency aldehyde-removing spray is prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1.26 percent
Ethylene urea: 0.345 percent
Urea: 0.6 percent
Carbohydrazide: 1.26 percent
Organic acid: 2.835 percent
And (3) bactericide: 3.5 percent
Dispersing agent: 0.2 percent of
Solvent: 90 percent.
By adopting the technical scheme, when the components of the aldehyde-removing spray are prepared into the aldehyde-removing spray according to the weight percentage, the aldehyde-removing efficiency of the aldehyde-removing spray is highest.
Optionally, the organic acid is taurine.
Through adopting above-mentioned technical scheme, taurine is chooseed for use to the organic acid, can not only improve the smell of removing the aldehyde spray for the people can not produce the impression that produces the thorn in the environment of spraying this application except that the aldehyde spray, and simultaneously, when the organic acid adopted taurine, still was favorable to the extension to remove the effective function time of aldehyde spray.
Optionally, the viscosity of the water-soluble adsorption matrix is 100-200 mpa.s.
By adopting the technical scheme, when the viscosity of the water-soluble adsorption matrix is 100-200mPa.s, the formaldehyde removing spray can better adsorb formaldehyde, is favorable for obtaining the formaldehyde removing spray with good atomization effect, and is favorable for further improving the formaldehyde removing efficiency of the formaldehyde removing spray.
Optionally, the water-soluble adsorption matrix is carboxymethyl chitosan.
By adopting the technical scheme, when the carboxymethyl chitosan is selected as the water-soluble adsorption matrix, the carboxymethyl chitosan has the sterilization effect, so that the effective period of the formaldehyde-removing spray can be prolonged.
Optionally, the degree of deacetylation of the carboxymethyl chitosan is greater than or equal to 90%.
By adopting the technical scheme, when the deacetylation degree of the carboxymethyl chitosan is greater than or equal to 90%, the water solubility of the carboxymethyl chitosan is improved, and the components can be promoted to be uniformly mixed.
Optionally, the dispersant is any one or a combination of several of ethylene glycol, propylene glycol and hexylene glycol.
Through adopting above-mentioned technical scheme, ethylene glycol, propylene glycol, hexanediol all are the micro molecule alcohols, can promote the dispersion of removing each component of aldehyde spray on the one hand, can also form one deck shallow film on the surface of removing the aldehyde spray simultaneously, this shallow film can not hinder formaldehyde and get into in removing the aldehyde spray for formaldehyde can with remove the effective component reaction in the aldehyde spray, can also delay the efflorescence that volatilizees of effective component in removing the aldehyde spray simultaneously, thereby the effective function time of extension aldehyde spray.
Optionally, the bactericide is any one or a combination of ethanol and a quaternary ammonium salt bactericide.
By adopting the technical scheme, the ethanol, the quaternary ammonium salt bactericide and the like can kill bacteria, reduce the breeding of the bacteria and be beneficial to prolonging the effective period of the aldehyde-removing spray. The quaternary ammonium salt bactericide can be any one or a combination of dodecyl trimethyl ammonium chloride, dodecyl dimethyl benzyl ammonium chloride and dodecyl dimethyl benzyl ammonium bromide.
Optionally, the solvent is deionized water.
The solvent is mainly used for dissolving components such as a water-soluble adsorption matrix, ethylene urea, carbazide, organic acid and the like, and deionized water, pure water and the like can be selected for reducing the introduction of impurities.
In a second aspect, the preparation method of the high-efficiency aldehyde-removing spray provided by the application adopts the following technical scheme:
the preparation method of the high-efficiency aldehyde-removing spray comprises the following steps:
s1, uniformly mixing the bactericide, the dispersing agent and the solvent to prepare a dispersion liquid;
s2, adding the water-soluble adsorption matrix and the ethylene urea into the dispersion liquid, stirring at a stirring speed of 1000-2000r/min until the mixture is dissolved uniformly, adjusting the stirring speed to 50-100r/min, adding the carbazide, the urea and the organic acid, stirring until the mixture is completely transparent, filtering and subpackaging to obtain the aldehyde-removing spray.
Through adopting above-mentioned technical scheme, the aldehyde spray that removes that the preparation obtained viscosity is even, the active ingredient reserve volume is big, can not block up the shower nozzle simultaneously, still has better atomization effect, is favorable to formaldehyde and removes the abundant contact of aldehyde spray to improve the adsorption rate of removing the aldehyde spray to formaldehyde, make the active ingredient in removing the aldehyde spray decompose the formaldehyde fast.
To sum up, the aldehyde-removing spray of the application at least has the following beneficial effects:
1. the formaldehyde removing spray agent can adsorb and grab harmful substances in the air, such as formaldehyde, through the water-soluble adsorption matrix. The ethylene urea and the urea contain active groups which can react with aldehyde groups, and have good elimination effect on aldehyde substances; the carbazide has strong reducibility and can quickly neutralize aldehyde groups; the organic acid can catalyze the reaction of the ethylene urea, the urea and the carbazide with the aldehyde group, thereby quickly eliminating the aldehyde substance and being beneficial to improving the aldehyde removal efficiency of the aldehyde removal spray.
2. The formaldehyde-removing spray in the application has no requirements on illumination and the like, has low requirements on the formaldehyde-removing condition, and can quickly remove formaldehyde.
3. The formaldehyde removing spray can reduce the formaldehyde concentration of low-concentration formaldehyde to 0.1mg/m within 30min 3 The requirements of national standards on indoor living environment are met.
4. The method for preparing the aldehyde-removing spray can prepare the aldehyde-removing spray which is uniform, has large retention amount of effective components, can not block the spray head and has good atomization effect, and is favorable for improving the aldehyde-removing efficiency of the aldehyde-removing spray.
Detailed Description
The present application will be described in further detail with reference to examples and comparative examples.
Examples
Examples 1 to 5
The weight percentages of the components in the high-efficiency aldehyde-removing spray in the examples 1-5 refer to the following table 1:
TABLE 1 weight percents of the components of the high-efficiency aldehyde-removing spray in examples 1-5
Among them, the carboxymethyl chitosan in examples 1 to 5 had a deacetylation degree of 90% and a viscosity of 200 mPa.s.
The preparation method of the high-efficiency aldehyde removal spray in the embodiments 1 to 5 comprises the following steps:
s1, adding deionized water into the stirring kettle, starting stirring, adding alcohol and ethylene glycol into the deionized water, and uniformly stirring to obtain a dispersion liquid;
s2, adding water-soluble chitin and ethylene urea into the dispersion, stirring for 20min at a stirring speed of 1000r/min, adjusting the stirring speed to 100r/min, adding carbazide, urea and taurine, stirring until the mixture is completely transparent, and filtering and subpackaging to obtain the aldehyde-removing spray.
Example 6
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, taurine was replaced by an equal amount of acetic acid.
Example 7
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, taurine was replaced by citric acid in equal amounts.
Example 8
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, the degree of deacetylation of carboxymethyl chitosan was 90%, and the viscosity was 100 mpa.s.
Example 9
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, carboxymethyl chitosan was replaced with equal amount of sodium carboxymethyl cellulose.
Example 10
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, the alcohol was replaced by an equal amount of dodecyltrimethylammonium chloride.
Example 11
An efficient aldehyde-removing spray agent is different from the spray agent in example 3 in that:
in this example, the ethylene glycol was replaced with an equal amount of propylene glycol.
Comparative example
Comparative example 1
An aldehyde-removing spray differing from example 3 in that:
the weight percentage of the carboxymethyl chitosan is 3.5 percent, and the weight percentage of the deionized water is 87.76 percent.
Comparative example 2
An aldehyde-removing spray differing from example 3 in that:
ethylene urea and urea were replaced with equal amounts of carbazide.
Comparative example 3
An aldehyde-removing spray differing from example 3 in that:
the urea and carbazide were replaced with equal amounts of ethylene urea.
Comparative example 4
An aldehyde-removing spray differing from example 3 in that:
equal amount of urea is used to replace both ethylene urea and carbazide.
Comparative example 5
An aldehyde-removing spray differing from example 3 in that:
taurine was replaced with an equal amount of deionized water.
Performance test
Aldehyde removal efficiency test:
1. in a closed climate box with 300X 250mm, 3g of formaldehyde-free acrylic plate sprayed with atomized formaldehyde-removing spray agent is placed in the box, then a cotton swab is used for adsorbing formaldehyde solution to release formaldehyde in the box, and the initial concentration C of formaldehyde in the box 0 About 10 ppm. Continuously monitoring with formaldehyde detector, and recording concentration data C of formaldehyde after 1h 1 Concentration data C of formaldehyde after 8h 8 And calculating the aldehyde removal rate y after the aldehyde removal spray agent is used for 1 hour 1 The aldehyde removal rate y after 8h 8 Recorded in table 2 below.
2. In a closed climate chamber with 300X 250mm, formaldehyde is released in the chamber by adsorbing formaldehyde solution with cotton swabs, the initial concentration C of formaldehyde 0 About 0.5mg/m 3 Then 0.5g of aldehyde-removing spray is sprayed into the box. Continuously monitoring with formaldehyde detector, and recording concentration data C of formaldehyde after 15min 15 Concentration data C of formaldehyde after 30min 30 Recorded in table 3 below.
Performance test data
TABLE 2 aldehyde removal efficiency of the aldehyde-removing spray in examples 1-11 and comparative examples 1-5 for high concentration formaldehyde
TABLE 3 aldehyde removal efficiency of the aldehyde-removing spray in examples 1-11 and comparative examples 1-5 for low-concentration formaldehyde
Sample (I) | C0(mg/m3) | C15(mg/m3) | C30(mg/m3) |
Example 1 | 0.52 | 0.12 | 0.08 |
Example 2 | 0.49 | 0.08 | 0.04 |
Example 3 | 0.58 | 0.04 | 0.02 |
Example 4 | 0.48 | 0.07 | 0.03 |
Example 5 | 0.53 | 0.13 | 0.07 |
Example 6 | 0.56 | 0.18 | 0.09 |
Example 7 | 0.50 | 0.11 | 0.08 |
Example 8 | 0.49 | 0.08 | 0.04 |
Example 9 | 0.47 | 0.09 | 0.05 |
Example 10 | 0.51 | 0.04 | 0.03 |
Example 11 | 0.52 | 0.05 | 0.02 |
Comparative example 1 | 0.54 | 0.20 | 0.13 |
Comparative example 2 | 0.50 | 0.18 | 0.16 |
Comparative example 3 | 0.49 | 0.22 | 0.19 |
Comparative example 4 | 0.52 | 0.25 | 0.20 |
Comparative example 5 | 0.48 | 0.45 | 0.42 |
Combining the data in the table 2 and the table 3 and combining the examples 1 to 11, the formaldehyde removing spray prepared by the method can not only rapidly remove high-concentration formaldehyde, but also rapidly reduce the formaldehyde content of low-concentration formaldehyde to 0.1mg/m 3 The requirements of national standards on indoor living environment can be met.
As can be seen by comparing example 3 with comparative example 1 and combining the data in tables 2 and 3, when the amount of carboxymethyl chitosan exceeds 2%, the aldehyde removing efficiency of the aldehyde removing spray decreases for both high and low concentrations of formaldehyde. The reasons may be that excessive carboxymethyl chitosan may affect the atomization effect of the aldehyde-removing spray, which results in poor dispersibility of the aldehyde-removing spray, and the efficiency of the water-soluble adsorption matrix for adsorbing formaldehyde is reduced, which results in a reduction in the decomposition rate of carbohydrazide, vinylurea and urea on formaldehyde.
Comparing example 3 with comparative examples 2 to 4 and combining the data in tables 2 and 3, it can be seen that when the single carbohydrazide, ethylene urea or urea is used instead of the combination of carbohydrazide, ethylene urea and urea, the aldehyde removing efficiency of the aldehyde removing spray is reduced, and the aldehyde removing spray can not be used for removing aldehyde within 30min to reach a concentration range of 0.5mg/m 3 The low concentration formaldehyde on the left and right is reduced to 0.1mg/m 3 The following.
As can be seen by comparing example 3 with comparative example 5 and by combining the data in tables 2 and 3, when taurine was replaced with an equal amount of deionized water, the aldehyde removing spray had a greatly reduced aldehyde removing efficiency for high concentration formaldehyde, and at the same time, the aldehyde removing spray did not substantially work for low concentration formaldehyde.
Comparative example 3 andas can be seen from examples 6 and 7 in combination with the data in table 2, when taurine is used as the organic acid, the aldehyde removal rate after 1 hour is 90.8%, and the aldehyde removal rate after 8 hours is 99.5%; when the organic acid adopts acetic acid, the aldehyde removing rate after 1h of the aldehyde removing spray is 89.5%, the aldehyde removing rate after 8h is 91.2%, when the organic acid adopts citric acid, the aldehyde removing rate after 1h of the aldehyde removing spray is 89.8%, and the aldehyde removing rate after 8h is 91.9%. In addition, the data in table 3 show that when taurine is used as the organic acid, the formaldehyde concentration of the formaldehyde can be reduced to 0.1mg/m within 15min when the formaldehyde removing spray is used for treating low-concentration formaldehyde 3 The following. Namely, when the organic acid in the formaldehyde removing spray adopts taurine, the formaldehyde removing efficiency of the formaldehyde removing spray to low-concentration formaldehyde is improved.
The present embodiment is only for explaining the present application, and it is not limited to the present application, and those skilled in the art can make modifications of the present embodiment without inventive contribution as needed after reading the present specification, but all of them are protected by patent law within the scope of the claims of the present application.
Claims (10)
1. The efficient aldehyde-removing spray is characterized by being prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1 to 2 percent
Ethylene urea: 0.1 to 0.5 percent
Urea: 0.4 to 0.8 percent
Carbohydrazide: 1.0 to 1.5 percent
Organic acid: 2 to 4 percent of
And (3) bactericide: 3 to 4 percent of
Dispersing agent: 0.1 to 0.3 percent
Solvent: and (4) the balance.
2. The high-efficiency aldehyde-removing spray as claimed in claim 1, which is characterized in that: the feed is prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1 to 1.5 percent
Ethylene urea: 0.3 to 0.4 percent
Urea: 0.5 to 0.8 percent
Carbohydrazide: 1.2 to 1.3 percent
Organic acid: 2.5 to 3.2 percent
And (3) bactericide: 3 to 4 percent of
Dispersing agent: 0.15-0.25%
Solvent: and (4) the balance.
3. The high-efficiency aldehyde-removing spray as claimed in claim 1, which is characterized in that: the feed is prepared from the following raw materials in percentage by weight:
water-soluble adsorption matrix: 1.26 percent
Ethylene urea: 0.345 percent
Urea: 0.6 percent
Carbohydrazide: 1.26 percent
Organic acid: 2.835 percent
And (3) bactericide: 3.5 percent
Dispersing agent: 0.2 percent of
Solvent: 90 percent.
4. The high-efficiency aldehyde-removing spray according to any one of claims 1 to 3, which is characterized in that: the organic acid is taurine.
5. The high-efficiency aldehyde-removing spray as claimed in claim 4, which is characterized in that: the viscosity of the water-soluble adsorption matrix is 100-200mPa.
6. The efficient aldehyde-removing spray as claimed in claim 5, wherein: the water-soluble adsorption matrix is carboxymethyl chitosan.
7. The high-efficiency aldehyde-removing spray as claimed in claim 6, which is characterized in that: the degree of deacetylation of the carboxymethyl chitosan is greater than or equal to 90%.
8. The high-efficiency aldehyde-removing spray according to any one of claims 1 to 3, which is characterized in that: the dispersing agent is any one or a combination of more of ethylene glycol, propylene glycol and hexanediol.
9. The high-efficiency aldehyde-removing spray according to any one of claims 1 to 3, which is characterized in that: the bactericide is any one or a composition of more of ethanol and quaternary ammonium salt bactericide.
10. The preparation method of the high-efficiency aldehyde-removing spray of any one of claims 1 to 9, which is characterized by comprising the following steps:
s1, uniformly mixing the bactericide, the dispersing agent and the solvent to prepare a dispersion liquid;
s2, adding the water-soluble adsorption matrix and the ethylene urea into the dispersion liquid, stirring at a stirring speed of 1000-2000r/min until the mixture is dissolved uniformly, adjusting the stirring speed to 50-100r/min, adding the carbazide, the urea and the organic acid, stirring until the mixture is completely transparent, filtering and subpackaging to obtain the aldehyde-removing spray.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116764600A (en) * | 2023-07-14 | 2023-09-19 | 佛山市三水日邦化工有限公司 | Formaldehyde-purifying antibacterial agent, and preparation method and application thereof |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11347109A (en) * | 1998-06-05 | 1999-12-21 | Toyo Riken Kk | Formaldehyde absorbent |
JP2002273145A (en) * | 2001-03-15 | 2002-09-24 | Mariko Koizumi | Formaldehyde scavenger, method for treating woody plate, and woody plate |
JP4061331B1 (en) * | 2006-09-25 | 2008-03-19 | 三木理研工業株式会社 | Aldehyde remover |
CN101954167A (en) * | 2010-08-24 | 2011-01-26 | 杭州茂龙环保科技有限公司 | Composite long-acting formaldehyde remover and preparation method thereof |
CN106139892A (en) * | 2015-04-16 | 2016-11-23 | 杭州笨鸟环保科技有限公司 | A kind of environment-friendly highly efficient formaldehyde scavenger |
DE102017200833A1 (en) * | 2017-01-19 | 2018-07-19 | SinoHephaestus Solution GmbH | formaldehyde scavenger |
CN108404618A (en) * | 2018-06-01 | 2018-08-17 | 江苏敖广日化集团股份有限公司 | A kind of formaldehyde eliminating agent and preparation method thereof |
CN109925852A (en) * | 2019-03-20 | 2019-06-25 | 北京菲迪可环保科技有限公司 | A method of except formaldehyde composition and removal formaldehyde |
CN110403541A (en) * | 2019-06-28 | 2019-11-05 | 浙江维度环保科技有限公司 | A kind for the treatment of air indoor taste removal construction technology |
CN111249173A (en) * | 2020-01-20 | 2020-06-09 | 小佩网络科技(上海)有限公司 | Deodorizing and purifying concentrated solution and preparation method and application thereof |
CN111701424A (en) * | 2020-06-24 | 2020-09-25 | 浙江农林大学 | High-efficiency aldehyde removing agent and preparation method thereof |
CN112675700A (en) * | 2020-12-29 | 2021-04-20 | 上海纳米技术及应用国家工程研究中心有限公司 | Preparation method of weak-light photocatalyst composite formaldehyde-removing spray, product and application thereof |
CN114288848A (en) * | 2021-12-30 | 2022-04-08 | 佛山市三水日邦化工有限公司 | Smell purifying agent and preparation method thereof |
CN114588767A (en) * | 2022-03-16 | 2022-06-07 | 北京森态环保科技有限公司 | Environment-friendly efficient formaldehyde removing agent and preparation method thereof |
-
2022
- 2022-06-28 CN CN202210739544.4A patent/CN115041003B/en active Active
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11347109A (en) * | 1998-06-05 | 1999-12-21 | Toyo Riken Kk | Formaldehyde absorbent |
JP2002273145A (en) * | 2001-03-15 | 2002-09-24 | Mariko Koizumi | Formaldehyde scavenger, method for treating woody plate, and woody plate |
JP4061331B1 (en) * | 2006-09-25 | 2008-03-19 | 三木理研工業株式会社 | Aldehyde remover |
CN101954167A (en) * | 2010-08-24 | 2011-01-26 | 杭州茂龙环保科技有限公司 | Composite long-acting formaldehyde remover and preparation method thereof |
CN106139892A (en) * | 2015-04-16 | 2016-11-23 | 杭州笨鸟环保科技有限公司 | A kind of environment-friendly highly efficient formaldehyde scavenger |
DE102017200833A1 (en) * | 2017-01-19 | 2018-07-19 | SinoHephaestus Solution GmbH | formaldehyde scavenger |
CN108404618A (en) * | 2018-06-01 | 2018-08-17 | 江苏敖广日化集团股份有限公司 | A kind of formaldehyde eliminating agent and preparation method thereof |
CN109925852A (en) * | 2019-03-20 | 2019-06-25 | 北京菲迪可环保科技有限公司 | A method of except formaldehyde composition and removal formaldehyde |
CN110403541A (en) * | 2019-06-28 | 2019-11-05 | 浙江维度环保科技有限公司 | A kind for the treatment of air indoor taste removal construction technology |
CN111249173A (en) * | 2020-01-20 | 2020-06-09 | 小佩网络科技(上海)有限公司 | Deodorizing and purifying concentrated solution and preparation method and application thereof |
CN111701424A (en) * | 2020-06-24 | 2020-09-25 | 浙江农林大学 | High-efficiency aldehyde removing agent and preparation method thereof |
CN112675700A (en) * | 2020-12-29 | 2021-04-20 | 上海纳米技术及应用国家工程研究中心有限公司 | Preparation method of weak-light photocatalyst composite formaldehyde-removing spray, product and application thereof |
CN114288848A (en) * | 2021-12-30 | 2022-04-08 | 佛山市三水日邦化工有限公司 | Smell purifying agent and preparation method thereof |
CN114588767A (en) * | 2022-03-16 | 2022-06-07 | 北京森态环保科技有限公司 | Environment-friendly efficient formaldehyde removing agent and preparation method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116764600A (en) * | 2023-07-14 | 2023-09-19 | 佛山市三水日邦化工有限公司 | Formaldehyde-purifying antibacterial agent, and preparation method and application thereof |
CN116764600B (en) * | 2023-07-14 | 2024-02-23 | 佛山市三水日邦化工有限公司 | Formaldehyde-purifying antibacterial agent, and preparation method and application thereof |
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