Deodorizing composition and application thereof
Technical Field
The application provides a deodorant composition and application thereof.
Background
Daily life garbage is always accompanied with the release of odor. The odor of the garbage is generated by the decomposition of organic components in the garbage by bacteria. 75 to 80 percent of the domestic garbage is organic matters, and mainly comprises peels, vegetable stalks, leftovers/vegetables, skins, hairs, viscera, fat, excrement, leftovers/blood water, leaves, waste paper, flowers and plants, organisms of animals and fishes and certain water. In the process of natural digestion, the odor is generated under the action of aerobic/anaerobic fermentation and the like, and especially in hot weather, the odor becomes more serious due to the accelerated fermentation action. The chemical components contained in these odors include inorganic substances such as hydrogen sulfide and ammonia, and organic compounds such as volatile fatty acids, thiols, amines, aldehydes, phenols, ketones, ethers, and nitrogen-containing heterocyclic compounds.
These compounds can cause toxicity to various degrees to human body in respiration, digestion, cardiovascular, endocrine and nervous systems, wherein aromatic compounds such as benzene, toluene, styrene, etc. can also cause human body to be distorted and cancerized. In addition, a large amount of odor is generated in livestock farms, bio-fertilizer plants, municipal sewage treatment stations, septic tanks, public toilets and other places, which affects human health. These sources of odor not only harm the workers involved, but also affect the lives of the residents nearby. Therefore, deodorization is a key technology related to public health.
Currently, common methods for treating industrial malodors include a washing method, a chemical cleaning method, an activated carbon adsorption method, an ozone oxidation method, an electrostatic deodorization method, a soil deodorization method, a combustion method, a biological deodorization method, and the like. However, these methods have problems of poor deodorizing ability and poor deodorizing effect.
Disclosure of Invention
One of the applications provides a deodorizing composition, which comprises plant vinegar, glycerol, a surfactant, water, eucommia ulmoides leaf extract and/or folium artemisiae argyi extract, and further comprises the following components: wintergreen oil and/or citral.
In a specific embodiment, the plant vinegar is selected from at least one of wood vinegar, bamboo vinegar and grass vinegar.
In one embodiment, the surfactant is tween-80 and/or OP-10.
In a specific embodiment, the content of the plant vinegar is 2% to 5%, the content of the folium cortex eucommiae extract is 1% to 5%, the content of the folium artemisiae argyi extract is 1% to 5%, the content of the glycerol is 1% to 5%, the content of the surfactant is 2% to 4%, the content of the water is 75% to 92%, the content of the wintergreen oil is 1% to 4%, and the content of the citral is 1% to 4% by volume.
In a specific embodiment, the content of the plant vinegar is 3%, the content of the folium cortex eucommiae extract is 2.5%, the content of the folium artemisiae argyi extract is 2.5%, the content of the glycerol is 2%, the content of the surfactant is 3%, the content of the water is 85%, and the content of the wintergreen oil is 2% by volume.
In a specific embodiment, the content of the plant vinegar is 4%, the content of the folium cortex eucommiae extract is 2.5%, the content of the folium artemisiae argyi extract is 2.5%, the content of the glycerol is 2%, the content of the surfactant is 3%, the content of the water is 84%, and the content of the citral is 2% by volume.
In one embodiment, the plant vinegar is a pyrolysis product of plant material under high temperature anoxic conditions.
In one embodiment, the detailed preparation process of wood vinegar comprises the following steps: the wood chips are placed in a closed carbonization furnace and heated at 350-400 ℃. Crude pyroligneous liquor produced from wood is collected by cooling until pyroligneous liquor is no longer produced. Refining the crude wood vinegar solution by atmospheric distillation, and collecting distillation components at 60 deg.C-100 deg.C to obtain refined wood vinegar solution with pH of 1.5-3.7 and density of 1.001g/ml or more.
In a specific embodiment, the folium cortex eucommiae extract is prepared by extracting folium cortex eucommiae with 40-60 v% ethanol aqueous solution, concentrating under reduced pressure, passing through a D101 type macroporous resin column, eluting with 30-50 v% ethanol aqueous solution, and evaporating ethanol to obtain a first concentrated solution, wherein the first concentrated solution contains 3-6% by mass of geniposide.
In one embodiment, the detailed process of obtaining the folium cortex eucommiae extract is as follows: adding folium Eucommiae and 40-60 v% ethanol water solution into an extraction tank, wherein the mass (kg)/volume ratio (L) of folium Eucommiae and ethanol is 1: 5-1: 7, reflux-heating (boiling) for 1-3 hr to obtain extractive solution, concentrating under reduced pressure of-0.25 to-0.75 Mpa until the concentration solution is 0.5 to 1 times of folium Eucommiae mass, passing through D101 type macroporous resin, washing the column with 8 to 10 times of folium Eucommiae mass distilled water, eluting with 30 v% to 50 v% ethanol water solution, and (3) detecting the content of the geniposide in the eluent on line, stopping eluting after the mass content of the component in the eluent is lower than 0.5%, and performing evaporation concentration on the eluent to obtain a first concentrated solution (eucommia ulmoides leaf extracting solution), wherein the first concentrated solution contains 3-6% of the geniposide by mass.
In a specific embodiment, the folium artemisiae argyi extract is prepared by extracting folium artemisiae argyi with 40-60 v% ethanol aqueous solution, concentrating under reduced pressure, passing through an AB-8 type macroporous resin column, eluting with 50-70 v% ethanol aqueous solution, and evaporating ethanol to obtain a second concentrated solution, wherein the second concentrated solution contains 4-6% by mass of chlorogenic acid.
In one embodiment, the detailed process for obtaining the folium artemisiae argyi extract is as follows: adding folium Artemisiae Argyi and 40-60 v% ethanol water solution into extraction tank, wherein the mass (kg)/volume ratio (L) of folium Eucommiae to 50% ethanol is 1: 5-1: 7, reflux-heating (boiling) for 1-3 hr to obtain extractive solution, concentrating under reduced pressure of-0.25 to-0.75 Mpa until the concentrated solution is 0.5 to 1 times of folium Artemisiae Argyi mass, passing the concentrated solution through AB-8 type macroporous resin, washing the column with 8 to 10 times of folium Artemisiae Argyi mass of distilled water, eluting with 50 v% to 70 v% ethanol water solution, and (3) detecting the content of chlorogenic acid in the eluent on line, stopping elution after the mass content of the component in the eluent is lower than 0.5%, and performing evaporation concentration on the eluent to obtain a second concentrated solution (folium artemisiae argyi extract), wherein the second concentrated solution contains 4-6% by mass of chlorogenic acid.
A second aspect of the invention provides the use of a deodorant composition according to any one of the first to third aspects of the invention in a landfill, a waste transfer station, a public toilet, a municipal septic tank, a body of black and odorous water, an organic fertilizer plant and a livestock farm.
The beneficial effect of this application:
the present application has obtained a deodorizing composition with a very good deodorizing effect, which is particularly suitable for refuse landfills, refuse transfer stations, public toilets, municipal septic tanks, black and odorous water bodies, organic fertilizer plants or livestock farms.
Detailed Description
The present invention is further illustrated by the following examples, which are intended to be purely exemplary of the invention and are not to be construed as limiting the invention in any way.
The reagents used in the present application are commercially available unless otherwise specified.
The wood vinegar can be obtained commercially or prepared by itself.
The detailed preparation process of the wood vinegar comprises the following steps: 100kg of wood chips are placed in a closed carbonization furnace, and the wood chips are heated at a temperature of not higher than 400 ℃ of the temperature at which tar is generated, so that crude wood vinegar is produced. The heating was stopped so that pyroligneous acid was no longer produced. The crude pyroligneous liquor produced by wood is obtained by cooling and collecting. The crude pyroligneous liquor is refined by atmospheric distillation. Collecting distillation fraction at 60 deg.C to 100 deg.C to obtain refined pyroligneous acid solution with pH of 2.0 and density of 1.001g/ml
The detailed preparation process of the eucommia ulmoides leaf extract comprises the following steps: adding 10kg of folium cortex eucommiae and 50L of ethanol with the volume content of 50% into an extraction tank, refluxing, heating and extracting for 2 hours to obtain an extracting solution, concentrating to 5L under reduced pressure (-0.5MPa), passing the concentrated solution through D101 type macroporous resin, washing a column with 100L of distilled water, eluting with 50% of ethanol with the volume content, detecting the content of geniposidic acid in an eluent on line, stopping eluting after the mass content of the component in the eluent is lower than 0.5%, evaporating and concentrating the eluent until the mass content of the geniposidic acid in the concentrated solution is 5%, thus obtaining the folium cortex eucommiae extracting solution. Cooling and then standby.
The detailed preparation process of the folium artemisiae argyi extract comprises the following steps: adding 10kg of folium artemisiae argyi and 50L of ethanol with the volume content of 40% into an extraction tank, refluxing, heating and extracting for 2 hours to obtain an extracting solution, concentrating to 5L under reduced pressure (-0.5MPa), passing the concentrated solution through AB-8 type macroporous resin, washing a column with 100L of distilled water, eluting with 50% of ethanol with the volume content, detecting the content of chlorogenic acid in an eluent on line, stopping elution after the mass content of the component in the eluent is lower than 0.5%, evaporating and concentrating the eluent until the mass content of the chlorogenic acid in the concentrated solution is 4%, thus obtaining the folium artemisiae argyi extracting solution. Cooling and then standby.
The contents of the components in the following formulations are by volume.
Example 1
The preparation method comprises the following steps: by volume, 1% of wintergreen oil, 801% of tween-tween, 101% of OP-101%, 2% of wood vinegar, 1% of glycerol, 1% of folium cortex eucommiae extract, 1% of folium artemisiae argyi extract and 92% of water.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 2
The preparation method comprises the following steps: by volume, 4% of wintergreen oil, 4% of tween-802%, OP-102%, 4% of wood vinegar, 3% of glycerol, 5% of folium cortex eucommiae extract, 5% of folium artemisiae argyi extract and water: 75 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 3
The preparation method comprises the following steps: by volume, 2% of wintergreen oil, 801.5% of tween-801, 101.5% of OP, 3% of wood vinegar, 2% of glycerol, 2.5% of folium cortex eucommiae extract, 2.5% of folium artemisiae argyi extract and water: 85 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 4
The preparation method comprises the following steps: by volume, 1% of citral, 801% of tween-tween, OP-101%, 3% of wood vinegar, 1% of glycerol, 1% of folium cortex eucommiae extract, 1% of folium artemisiae argyi extract and water: 91 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 5
The preparation method comprises the following steps: by volume, 4% of citral, 802% of tween-tween, OP-102%, 5% of wood vinegar, 5% of glycerol, 5% of folium cortex eucommiae extract, 5% of folium artemisiae argyi extract and water: 78 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 6
The preparation method comprises the following steps: by volume, 2% of citral, 801.5% of tween-tween, 101.5% of OP-101, 4% of wood vinegar, 2% of glycerol, 2.5% of folium cortex eucommiae extract, 2.5% of folium artemisiae argyi extract and water: 84 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 7
The preparation method comprises the following steps: by volume, 2.5% of eucommia ulmoides extract, 2% of wintergreen oil, 801.5% of tween-OP-101.5%, 3% of wood vinegar, 2% of glycerol and water: 90 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 8
The preparation method comprises the following steps: by volume, 2.5% of eucommia ulmoides extract, 2% of citral, 801.5% of tween-OP-101.5%, 4% of wood vinegar, 2% of glycerol and water: 89 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 9
The preparation method comprises the following steps: by volume, 2.5% of folium artemisiae argyi extract, 2% of wintergreen oil, 801.5% of tween-OP-101.5%, 3% of wood vinegar, 2% of glycerol and water: 90 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Example 10
The preparation method comprises the following steps: by volume, 2.5% of folium artemisiae argyi extract, 2% of citral, 801.5% of tween-OP-101.5%, 4% of wood vinegar, 2% of glycerol and water: 89 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Comparative example 1
The preparation method comprises the following steps: by volume, 2% of wintergreen oil, 801.5% of tween-801, 101.5% of OP, 3% of wood vinegar, 2% of glycerol and water: 90 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
Comparative example 2
The preparation method comprises the following steps: by volume, citral 2%, tween-801.5%, OP-101.5%, wood vinegar 4%, glycerol 2%, water: 89 percent.
Diluting by 10 times, spraying onto the exposed surface of the odor source at a ratio of 100mL/m2Spraying is carried out.
The deodorizing effect was measured by a three-point comparison odor bag method in the measurement of air quality odor (GB/T14675-1993), and the results are shown in Table 1.
From the results shown in Table 1, it can be seen from the comparison of the deodorizing effects of the formulations of examples 1 to 10 with those of the formulations of comparative examples 1 and 2 that the deodorizing solutions after the addition of the extract solutions of eucommia ulmoides leaves and the extract solution of artemisia argyi leaves are significantly superior to the formulations containing only pyroligneous acid in terms of both immediate air odor removal and continuation of the deodorizing effect. Therefore, the eucommia ulmoides leaf extract and the folium artemisiae argyi extract play a key role in the aspect of deodorization effect. Particularly, as can be seen from the comparison of the deodorizing effects of the formulations of examples 1 to 6 and the deodorizing effects of the formulations of examples 7 to 10, when the extract of eucommia ulmoides leaves and the extract of artemisia argyi coexist in the formulation, a synergistic effect is generated between the two extracts, and the deodorizing effect of the formulation is improved. Further, from the results of the examples, it is found that the effect is most preferable when the content of the extract liquid of eucommia ulmoides leaf and the extract liquid of artemisia leaf is 2.5% in the examples, because the content is not as large as possible but is in a range of one from 1% to 5% in the range of the use range of the extract liquid of eucommia ulmoides leaf and the extract liquid of artemisia leaf.
TABLE 1
While the present application has been described with reference to specific embodiments, those skilled in the art will appreciate that various changes can be made without departing from the true spirit and scope of the present application. In addition, many modifications may be made to adapt a particular situation, material, composition of matter, and method to the objective, spirit and scope of the present application. All such modifications are intended to be included within the scope of the claims of this application.