CN110871017A - Preparation for removing volatile organic compound, application thereof and method for removing volatile organic compound - Google Patents

Preparation for removing volatile organic compound, application thereof and method for removing volatile organic compound Download PDF

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Publication number
CN110871017A
CN110871017A CN201811004054.XA CN201811004054A CN110871017A CN 110871017 A CN110871017 A CN 110871017A CN 201811004054 A CN201811004054 A CN 201811004054A CN 110871017 A CN110871017 A CN 110871017A
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cyclodextrin
volatile organic
preparation
organic compounds
soil
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CN110871017B (en
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冯婕
王岽
李博伟
胡艳华
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/14Separation 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 absorption
    • B01D53/1487Removing organic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/14Separation 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 absorption
    • B01D53/1493Selection of liquid materials for use as absorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09CRECLAMATION OF CONTAMINATED SOIL
    • B09C1/00Reclamation of contaminated soil
    • B09C1/08Reclamation of contaminated soil chemically
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/58Treatment of water, waste water, or sewage by removing specified dissolved compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2252/00Absorbents, i.e. solvents and liquid materials for gas absorption
    • B01D2252/20Organic absorbents
    • B01D2252/202Alcohols or their derivatives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2252/00Absorbents, i.e. solvents and liquid materials for gas absorption
    • B01D2252/20Organic absorbents
    • B01D2252/205Other organic compounds not covered by B01D2252/00 - B01D2252/20494
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2252/00Absorbents, i.e. solvents and liquid materials for gas absorption
    • B01D2252/50Combinations of absorbents
    • B01D2252/504Mixtures of two or more absorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/70Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
    • B01D2257/708Volatile organic compounds V.O.C.'s
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/30Organic compounds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Water Supply & Treatment (AREA)
  • Organic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Soil Sciences (AREA)
  • Processing Of Solid Wastes (AREA)

Abstract

The invention relates to the field of environmental management and discloses a preparation for removing volatile organic compounds, application and a method for removing the volatile organic compounds, wherein the preparation comprises the following components in parts by weight: (2-50) the cyclodextrin and/or its derivative and a surfactant; the method comprises the following steps: (1) preparing the preparation; (2) adding the preparation to the place to be treated so that the concentration of the volatile organic compounds at the place to be treated is lower than 18 mg/L; the method for removing the volatile organic compounds can be applied to air, water and soil, has good treatment effect and high speed, and the used medicament is green and environment-friendly, does not produce secondary pollution in the process, and is simple and convenient and wide in application range.

Description

Preparation for removing volatile organic compound, application thereof and method for removing volatile organic compound
Technical Field
The invention relates to the field of environmental management, in particular to a preparation for removing volatile organic compounds, application thereof and a method for removing the volatile organic compounds.
Background
Volatile Organic Compounds (VOCs) are abbreviated as VOCs, and VOCs in the general sense are commanding organic compounds; but the definition in the environmental protection sense refers to an active class of volatile organic compounds, namely, volatile organic compounds which can cause harm. With the rapid development of industry, nearly 60 million tons of organic matters in China cause soil-underground water system pollution through various ways every year. The VOC can cause serious pollution to surrounding air while polluting soil and underground water, and when the VOC in the air reaches a certain value, symptoms such as headache, nausea, vomiting, hypodynamia and the like can be caused, and even convulsion, coma, liver, kidney, brain and nervous system are caused in serious cases, so that serious consequences such as hypomnesis and the like are caused. And the disturbance to the polluted area is large in the process of remediation and treatment, along with the air flow, large-area VOC pollution can be caused if the control cannot be carried out in time, sometimes, the VOC pollution range is larger than that of the polluted area of soil and underground water, and great harm exists.
The traditional VOC air purification usually adopts physical adsorption or filtration technology for air treatment, and the purification devices have certain limitations on air purification, have low physical adsorption capacity, are easy to saturate and need to continuously replace an adsorbent; the filtering technology has the advantages of limited catalyst, small contact area with air, slow reaction and unstable treatment effect, and the two methods only aim at the VOC in the air and do not treat the VOC source, so that the VOC source cannot be fundamentally cut off.
CN103639184A discloses a method for circularly remediating organic contaminated soil by using cyclodextrin eluent, which comprises the following steps: (1) adding the organic contaminated soil into cyclodextrin eluent with the concentration of 100-500 mu mol/L to form a soil-eluent mixture with the organic contaminated soil content of 20-40g/L, and eluting the soil-eluent mixture at the temperature of 15-35 ℃; (2) carrying out centrifugal separation on the eluted soil-eluent mixture, and determining the concentration of organic pollutants in the filtrate; (3) placing the filtrate obtained in the step (2) under an ultraviolet lamp, and irradiating until the concentration of organic pollutants in the filtrate is less than or equal to 5% of the concentration of the organic pollutants determined in the step (2), so as to obtain regenerated cyclodextrin eluent; repeating steps (1) - (3) using the regenerated cyclodextrin eluent instead of the cyclodextrin eluent in step (1). The method transfers organic pollutants from the soil to the eluent, a large amount of eluent is generated, the eluent is complex to process and is easy to cause secondary pollution, organic matters in the soil are also taken away by the eluent in the process of eluting the pollutants, the influence on the soil is large, and the effect of the cyclodextrin and the derivatives thereof on removing the VOC is not involved in the patent.
Therefore, there is a need in the art to remove volatile organic compounds from various environments by a simple, rapid, and efficient method.
Disclosure of Invention
The invention aims to overcome the problems of complex operation of VOC removal and limited VOC removal environment in the prior art, and provides a volatile organic compound removal method and application thereof.
The inventor of the invention finds in research that compared with other types of cyclodextrin, the cyclodextrin in the preparation of the invention is β -cyclodextrin, the volatile organic compound is better removed, in addition, after the surfactant is added, the volatile organic compound is obviously improved, and when the weight ratio of the cyclodextrin to the surfactant is 100 (9-12), the preparation can achieve better effect on removing the volatile organic compound.
In order to achieve the above object, a first aspect of the present invention provides a formulation having a function of removing volatile organic compounds, the formulation comprising, in a weight ratio of 100: (2-50) cyclodextrin and/or its derivative and a surfactant.
A second aspect of the present invention provides a method of removing volatile organic compounds, the method comprising the steps of:
(1) preparing the preparation of the invention;
(2) and adding the preparation to the place to be treated so that the concentration of the volatile organic compounds at the place to be treated is lower than 18 mg/L.
In a third aspect the invention provides the use of a method according to the invention for the removal of volatile organic compounds.
Through the technical scheme, the method for removing the volatile organic compounds has the following advantages:
the preparation used by the method does not generate waste gas, waste liquid and waste residue in the using process, and the removed volatile organic compounds are difficult to separate from the inclusion compound formed by the preparation, so that secondary pollution to the environment is avoided;
(II) the operation is simple, large-scale equipment is not needed, the treatment speed is high, the effect is obvious, and the volatile organic compounds can be fundamentally removed;
(III) the method for removing the volatile organic compounds is slightly influenced by environmental factors, can be used for removing the volatile organic compounds in different environments, and is particularly suitable for soil and air.
Detailed Description
The endpoints of the ranges and any values disclosed herein are not limited to the precise range or value, and such ranges or values should be understood to encompass values close to those ranges or values. For ranges of values, between the endpoints of each of the ranges and the individual points, and between the individual points may be combined with each other to give one or more new ranges of values, and these ranges of values should be considered as specifically disclosed herein.
The invention provides a preparation with a function of removing volatile organic compounds, which comprises the following components in a weight ratio of 100: (2-50) the cyclodextrin and/or its derivative and the surfactant, preferably, the weight ratio of the cyclodextrin and/or its derivative and the surfactant is 100: (5-20), more preferably 100: (9-12).
In the present invention, the formulation may further include water, and the formulation is formulated into a solution or a suspension with water. When used to remove volatile organic compounds other than water (e.g., volatile organic compounds in soil and/or air), the formulation preferably contains water, thereby allowing the formulation to disperse more uniformly and provide better treatment. In particular, when the preparation is used for removing volatile organic compounds from soil having a water content of 20% or less and/or air having a humidity of 50% or less, the preparation preferably contains water.
In the water-containing formulation of the present invention, the concentration of the cyclodextrin and/or its derivative may be 15 to 60 g/L; preferably 30-50g/L (31g/L, 32g/L, 33g/L, 34g/L, 35g/L, 36g/L, 37g/L, 38g/L, 39g/L, 40g/L, 41g/L, 42g/L, 43g/L, 44g/L, 45g/L, 46g/L, 47g/L, 48g/L, 49g/L or any value therebetween).
In the present invention, the cyclodextrin and/or its derivative is commercially available, and preferably at least one of α -cyclodextrin, β -cyclodextrin, γ -cyclodextrin, hydroxypropyl- β -cyclodextrin, carboxymethyl- β -cyclodextrin, hydroxyethyl- β -cyclodextrin and sulfonated- β -cyclodextrin, and preferably β -cyclodextrin.
In the present invention, since cyclodextrin is stable in an alkaline medium, the pH of the preparation is 7 to 12, preferably 7 to 8, and in the present invention, an alkaline pH adjusting agent may be added to adjust the pH.
According to the invention, the cyclodextrin is of a molecular structure with 'inner hydrophobicity and outer hydrophilicity', so that the cyclodextrin becomes a biological model molecule similar to an enzyme, the cyclodextrin has unique inclusion performance, has the characteristics of no toxic or side effect, low price and easiness in obtaining, and due to the excellent characteristics of the structure of the cyclodextrin, the preparation disclosed by the invention forms an inclusion after absorbing an organic volatile compound, and the formed inclusion does not need to be further treated.
In the invention, the surfactant has hydrophilic and lipophilic groups, can be directionally arranged on the surface of the solution, can obviously reduce the surface tension of the solution, has an interaction promoting effect with the cyclodextrin, and can further improve the inclusion performance of the cyclodextrin.
In the present invention, the surfactant may be selected from at least one of ionic surfactants, nonionic surfactants, amphoteric surfactants, and nonionic surfactants, preferably anionic surfactants and/or nonionic surfactants, and more preferably at least one of sodium dodecylbenzenesulfonate, sodium dodecylsulfate, and triton.
In the present invention, the preparation may further comprise C2-C6The alcohol of (a), preferably the alcohol is a monohydric alcohol, more preferably ethanol and/or isopropanol, and the addition of the alcohol can reduce the repulsion between the polarities of the surfactant molecules, make the surfactant molecules more compact, and simultaneously have a solubilizing effect on the volatile organic compounds, thereby facilitating the dissolution of the volatile organic compounds from the contaminants and promoting the inclusion of the contaminants by the cyclodextrin. Preferably, the weight ratio between the cyclodextrin and/or its derivative and the alcohol is 100: (1-10), more preferably 100: (2-5) according to a preferred embodiment of the invention, the addition of the formulation comprising an alcohol to the site to be treated makes it possible to bring the concentration of volatile organic compounds to be treated to less than 8 mg/L.
According to the most preferred embodiment of the invention, the preparation contains β -cyclodextrin, sodium dodecyl sulfate surfactant, ethanol and water, the preparation contains β -cyclodextrin of 30-40g/L, and the weight ratio of β -cyclodextrin, sodium dodecyl sulfate and ethanol is 100 (9-12) to (2-5).
In a second aspect the present invention provides a method of removing volatile organic compounds, the method comprising the steps of:
(1) preparing the preparation of the invention;
(2) and adding the preparation to the place to be treated so that the concentration of the volatile organic compounds at the place to be treated is lower than 18 mg/L.
In the present invention, the place to be treated is not particularly limited, and may be at least one of soil, air and water, for example, when the place to be treated is soil and/or air, the water content in soil is less than or equal to 20%, and when the humidity in air is less than or equal to 50%, the preparation may be prepared into a solution or suspension with a certain concentration by using water, and the preparation is directly added to the place to be treated; when the site to be treated is water or when the water content of the soil and/or the soil in the air of the site to be treated is greater than 20% and the humidity of the air is greater than 50%, the preparation may be a mixture (powder) of cyclodextrin and/or its derivative, a surfactant and an alcohol, but in view of maximizing the utilization rate of the preparation, according to a preferred embodiment of the present invention, the preparation is a solution or a suspension, that is, a preparation containing water.
In the present invention, it is preferable that the addition is performed at room temperature without heat treatment of the treatment site or the preparation. The specific adding mode has no special requirement, when the added preparation is powder, a raising and scattering mode can be adopted, and when the preparation is solution or suspension, a spraying (by means of a spray can and the like) mode can be adopted.
In the invention, the adding mode is intermittent, the area of the part to be treated is taken as a calculation unit, and the adding amount (excluding water) of the preparation on a dry basis can be 0.5-15g/m2The time interval between two adjacent adding times can be 2-10min each time. Wherein the area of the to-be-treated part is the sum of the areas of the contact surfaces of the pollution source and the air.
Preferably, the dosage of the formulation (excluding water) on a dry basis may be from 4 to 8g/m2The time interval between two adjacent adding times can be 2-5min each time.
In the invention, when the concentration of the volatile organic compound at the position to be treated is higher than 300mg/L, the adding amount of the preparation ensures that the adding total amount of the cyclodextrin and/or the derivative thereof is more than 50g/m2
Or, the said to-be-treatedWhen the concentration of the volatile organic compound is 100-300mg/L, the dosage of the preparation ensures that the total dosage of the cyclodextrin and/or the derivative thereof is 30-50g/m2
Or when the concentration of the volatile organic compound at the position to be treated is lower than 100mg/L, the adding amount of the preparation ensures that the adding total amount of the cyclodextrin and/or the derivative thereof is 15-30g/m2
In the present invention, the number of the addition is not particularly limited as long as the VOC can be reduced to less than 18mg/L, preferably less than 8mg/L, and more preferably less than 3 mg/L. According to a preferred embodiment of the invention, the dosage per time is 50-200mL/m2The adding times are 7-15 times, and more preferably, the adding times are 7-12 times.
In a third aspect the invention provides the use of a formulation according to the invention for the removal of volatile organic compounds.
In the present invention, the application range of the preparation is not particularly limited, and the preparation can be used as long as it is used in an environment (a place to be treated) contaminated with a volatile organic compound, and for example, can be applied to air, soil and water contaminated with a volatile organic compound.
The present invention will be described in detail below by way of examples. In the following examples of the present invention,
the air humidity (namely the air humidity in the ground triangular flask) is measured by a GBT 11605-2005 humidity measuring method;
the water content of the soil is measured by a drying method (drying to constant weight at 105 ℃ in an oven),
wherein the moisture content (%) ═ soil wet weight (g) -soil dry weight (g)) × 100/soil wet weight (g);
the VOC value in the air of the ground triangular flask is measured by a VOC detector (Miniralite-PGM 7300, America China Rary (RAE) model);
the VOC value in the soil is measured by a headspace/gas chromatography-mass spectrometry (gas chromatography-mass spectrometer, Nippon Shimadzu model GCMS-TQ8030 of the manufacturer) for measuring volatile organic compounds in the soil and sediments by HJ 642-2013;
the concentration of petroleum hydrocarbon in the soil is measured by an infrared photometry (an infrared oil measuring instrument, a model JLGG-129U of a northern optical analyzer in Jilin city, a manufacturer) for measuring HJ soil petroleum;
the raw material β -cyclodextrin is purchased from Tianjin Guangfu Fine chemical research institute and is analytically pure;
raw materials α -cyclodextrin and gamma-cyclodextrin were purchased from Aladdin reagent company and were analytically pure;
raw materials of sulfonated- β -cyclodextrin, hydroxypropyl- β -cyclodextrin and carboxymethyl- β -cyclodextrin are all purchased from national medicine group chemical reagent company Limited and are analytically pure;
in the following examples, unless otherwise specified, various raw materials used were commercially available and were analytically pure.
Example 1
And respectively measuring VOC values of air (the humidity is 35%) and a soil sample (the water content is 0%) in the ground triangular flask and the concentration of petroleum hydrocarbon in the soil sample by taking the soil sample as a pollution source.
1) Weighing β -cyclodextrin 4g, sodium dodecyl sulfate 0.4g and ethanol 0.2g, dissolving in water, diluting to 100mL to obtain a preparation with pH of 7.2, and shaking uniformly for later use;
2) weighing 10g of soil sample polluted by petroleum hydrocarbon, placing the soil sample into a 100mL ground triangular flask, sealing, shaking uniformly and flatly paving the flask for about 25cm2Standing;
3) the VOC value in the air in the ground triangular flask when the preparation was not sprayed was measured to be 128.6mg/L, and the VOC value in the soil and the petroleum hydrocarbon concentration in the soil sample were measured, the results are shown in Table 1;
4) spraying 0.3mL of the preparation prepared in the step 1) into a ground triangular flask and fully and uniformly stirring;
5) standing for 2 minutes, and measuring the VOC value in the gas in the ground triangular flask;
6) the procedure of step 4) and step 5) was repeated, and after spraying the formulation of step 1) 8 times in total, the VOC values of the air and soil samples in the ground flask and the petroleum hydrocarbon concentration in the soil samples were measured, and the results are shown in table 1.
Example 2
And respectively measuring VOC values of air (humidity is 40%) and a soil sample (water content is 0%) in the ground triangular flask and the concentration of petroleum hydrocarbon in the soil sample by taking the soil sample as a pollution source.
1) Weighing 4.5g of β -cyclodextrin, 0.5g of sodium dodecyl sulfate and 0.1g of ethanol, dissolving in water, and fixing the volume to 100mL to obtain a preparation with the pH value of 7, and shaking uniformly for later use;
2) weighing 10g of soil sample polluted by petroleum hydrocarbon, placing the soil sample into a 100mL ground triangular flask, sealing, shaking uniformly and flatly paving the flask for about 25cm2Standing;
3) the VOC value in the air in the ground triangular flask when the preparation is not sprayed is determined to be 209.2mg/L, and the VOC value in the soil and the petroleum hydrocarbon concentration in the soil sample are determined, and the results are shown in Table 1;
4) spraying 0.3mL of the preparation prepared in the step 1) into a ground triangular flask and fully and uniformly stirring;
5) standing for 5 minutes, and measuring the VOC value in the gas in the ground triangular flask;
6) the procedure of step 4) and step 5) was repeated, and after spraying the formulation of step 1) 9 times in total, the VOC values of the air and soil samples in the ground flask and the petroleum hydrocarbon concentration in the soil samples were measured, and the results are shown in table 1.
Example 3
And respectively measuring VOC values of air (humidity is 45%) and a soil sample (water content is 0%) in the ground triangular flask and the concentration of petroleum hydrocarbon in the soil sample by taking the soil sample as a pollution source.
1) Weighing β -cyclodextrin 5g, sodium dodecyl sulfate 0.45g and ethanol 0.15g, dissolving in water, diluting to 100mL to obtain a preparation with pH of 7.7, and shaking uniformly for later use;
2) weighing 10g of soil sample polluted by petroleum hydrocarbon, placing the soil sample into a 100mL ground triangular flask, sealing, shaking uniformly and flatly paving the flask for about 25cm2Standing;
3) the VOC value in the air in the ground triangular flask when the preparation was not sprayed was determined to be 310.6mg/L, and the VOC value in the soil and the petroleum hydrocarbon concentration in the soil sample were determined, the results are shown in Table 1;
4) spraying 0.3mL of the preparation prepared in the step 1) into a ground triangular flask and fully and uniformly stirring;
5) standing for 5 minutes, and measuring the VOC value in the gas in the ground triangular flask;
6) the procedure of step 4) and step 5) was repeated, and after spraying the formulation of step 1) 9 times in total, the VOC values of the air and soil samples in the ground flask and the petroleum hydrocarbon concentration in the soil samples were measured, and the results are shown in table 1.
Example 4
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the surfactant added was sodium dodecylbenzenesulfonate, and the results are shown in Table 1.
Example 5
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the alcohol added was isopropanol, and the results are shown in Table 1.
Example 6
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that α -cyclodextrin was added as the cyclodextrin, and the results are shown in Table 1.
Example 7
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the cyclodextrin added was sulfonated- β -cyclodextrin, the results of which are shown in Table 1.
Example 8
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the cyclodextrin added was gamma-cyclodextrin, and the results are shown in Table 1.
Example 9
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that hydroxypropyl- β -cyclodextrin was added, and the results are shown in Table 1.
Example 10
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the cyclodextrin added was carboxymethyl- β -cyclodextrin, the results of which are shown in Table 1.
Example 11
The soil samples and air in the ground flask were freed of volatile organic compounds by the method of example 1, except that the surfactant added was fatty alcohol polyoxyethylene ether.
Example 12
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the alcohol added was n-propanol.
Example 13
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that β -cyclodextrin was added in an amount of 2g to the formulated formulation, and the results are shown in Table 1.
Example 14
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that 0.2g of sodium lauryl sulfate was used in the formulation, and the results are shown in Table 1.
Example 15
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that the amount of ethanol added to the formulated formulation was 0.05g, as shown in Table 1.
Example 16
The soil sample and the air in the ground flask were freed of volatile organic compounds by the method of example 1, except that 0.13mL of volatile organic compounds was added to the soil sample in the ground flask each time, and the results are shown in Table 1.
Example 17
Soil samples and air in ground flasks were freed of volatile organic compounds by the method of example 1, except that no ethanol was added, and the results are shown in Table 1.
Example 18
The soil sample and the air in the ground triangular flask were freed of volatile organic compounds by the method of example 1, except that no water was added to the preparation, the soil sample had a water content of 25% and the air had a humidity of 55%, and the specific procedure was as follows:
1) weighing 96mg of β -cyclodextrin, 9.6mg of sodium dodecyl sulfate and 4.8mg of ethanol, and uniformly mixing for later use;
2) weighing 10g of soil sample polluted by petroleum hydrocarbon, placing the soil sample into a 100mL ground triangular flask, sealing, shaking uniformly and flatly paving the flask for about 25cm2Standing;
3) measuring the VOC value in the air in the ground triangular flask when the preparation is not added to be 128.6mg/L, and measuring the VOC value in the soil and the petroleum hydrocarbon concentration in the soil sample, wherein the results are shown in Table 1;
4) adding the preparation prepared in the step 1) into a ground triangular flask and fully and uniformly stirring;
5) after standing for 5 minutes, the VOC values of the air and soil samples in the ground flask and the petroleum hydrocarbon concentration in the soil samples were measured, and the results are shown in table 1.
Comparative example 1
The soil samples and air in the ground flask were freed of volatile organic compounds by the method of example 1, except that β -cyclodextrin was not added to the formulation, and the results are shown in Table 1.
Comparative example 2
The soil samples and air in the ground flask were freed of volatile organic compounds by the method of example 1, except that the surfactant sodium lauryl sulfate was not added to the formulation, and the results are shown in Table 1.
TABLE 1
Figure BDA0001783610750000121
Figure BDA0001783610750000131
The results in table 1 show that, according to the preparation and the method for removing volatile organic compounds provided by the present invention, firstly, the VOC value in the air can be reduced to below 3mg/L after 8-10 times of addition in examples 1-3, and the removal rate of the volatile organic compounds in the air can reach above 97%;
secondly, as can be seen from example 1, example 4 and example 11, the removal effect of the volatile organic compound of which the surfactant is sodium dodecyl benzene sulfonate is the best, as can be seen from example 1, example 5 and example 12, the removal effect of the volatile organic compound of which the alcohol is ethanol is the best, and as can be seen from example 1 and examples 6-10, the removal effect of the volatile organic compound of which the cyclodextrin is β -cyclodextrin is the best;
again, it can be seen from examples 1-3 and examples 13-15 that β -cyclodextrin, surfactant and alcohol in examples 1-3 had the best removal effect when the concentration ratio of (9-12) to (2-5) was within the preferred range of 100, and that β -cyclodextrin, surfactant and alcohol had the best removal effect when the concentration ratio of (9-12) to (2-5) was within the range of 100 and β -cyclodextrin was 40-50g/L as seen from examples 1-15;
finally, as can be seen from examples 1 and 16, the dosage of the preparation is 4-8g/m2When the content is within the range, the removal effect of the volatile organic compound is best; as can be seen from examples 1 and 17, the formulations with ethanol added had the best VOC removal; it can be seen from examples 1 and 18 that the formulations with the addition of water have the best removal of volatile organic compounds.
In addition, the preparation and the method for removing the volatile organic compounds can reduce the content of the volatile organic compounds and petroleum hydrocarbon in the polluted soil sample, and the preparation is non-toxic and harmless, does not need large-scale equipment in the treatment method, is simple in operation method, and has good popularization and application values.
The preferred embodiments of the present invention have been described above in detail, but the present invention is not limited thereto. Within the scope of the technical idea of the invention, many simple modifications can be made to the technical solution of the invention, including combinations of various technical features in any other suitable way, and these simple modifications and combinations should also be regarded as the disclosure of the invention, and all fall within the scope of the invention.

Claims (10)

1. A preparation having a function of removing volatile organic compounds, which comprises, by weight, 100: (2-50) cyclodextrin and/or its derivative and a surfactant.
2. The formulation according to claim 1, wherein the formulation further comprises water, preferably the concentration of the cyclodextrin and/or its derivatives is 15-60 g/L.
3. The formulation of claim 2, wherein the concentration of the cyclodextrin and/or its derivative is 30-50 g/L.
4. The VOC-inhibiting agent as claimed in claim 1, wherein the cyclodextrin and/or its derivative is at least one selected from the group consisting of α -cyclodextrin, β -cyclodextrin, γ -cyclodextrin, hydroxypropyl- β -cyclodextrin, carboxymethyl- β -cyclodextrin, hydroxyethyl- β -cyclodextrin and sulfonated- β -cyclodextrin, preferably β -cyclodextrin.
5. The formulation according to claim 1, wherein the surfactant is selected from at least one of ionic, non-ionic, amphoteric and non-ionic surfactants, preferably anionic and/or non-ionic surfactants, more preferably at least one of sodium dodecylbenzene sulfonate, sodium dodecyl sulfate and polyoxyethylene-8-octylphenyl ether.
6. A method for removing volatile organic compounds, the method comprising the steps of:
(1) formulating the formulation of any one of claims 1-5;
(2) and adding the preparation to the place to be treated so that the concentration of the volatile organic compounds at the place to be treated is lower than 18 mg/L.
7. The method according to claim 1, wherein the dosing in step (2) is intermittent, and the dosage of the preparation is 0.5-15g/m on a dry basis2The time interval between two adjacent adding times is 2-10min each time.
8. The method according to claim 1, wherein the dosing in step (2) is intermittent, and the dosage of the preparation is 4-8g/m on a dry basis2The time interval between two adjacent adding times is 2-5min each time.
9. The method according to claim 1, wherein the formulation is added in such an amount that the total amount of cyclodextrin and/or its derivatives added is greater than 50g/m at a concentration of volatile organic compounds higher than 300mg/L at the site to be treated2
Or when the concentration of the volatile organic compound at the position to be treated is 100-300mg/L, the adding amount of the preparation ensures that the adding total amount of the cyclodextrin and/or the derivative thereof is 30-50g/m2
Or when the concentration of the volatile organic compound at the position to be treated is lower than 100mg/L, the adding amount of the preparation ensures that the adding total amount of the cyclodextrin and/or the derivative thereof is 15-30g/m2
10. Use of a formulation according to any one of claims 1 to 5 for the removal of volatile organic compounds.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114085674A (en) * 2020-08-24 2022-02-25 中国石油化工股份有限公司 VOC (volatile organic compound) pollution repairing agent and application thereof and method for repairing VOC polluted environment
CN114618266A (en) * 2020-12-10 2022-06-14 中国石油天然气股份有限公司 Solubilization absorbent, preparation method thereof and organic waste gas treatment method
CN115245727A (en) * 2021-04-25 2022-10-28 中国石油天然气股份有限公司 High-performance VOCs absorbent and preparation method and application thereof

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5615975A (en) * 1995-07-14 1997-04-01 Sandoz Ltd. Method for remediation of volatile organic contaminated soils
CN1261785A (en) * 1997-06-09 2000-08-02 普罗克特和甘保尔公司 Method for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins and perfume
CN1398267A (en) * 1999-12-16 2003-02-19 伊斯曼化学公司 Cyclodextrin ethers
CN1522787A (en) * 2003-09-05 2004-08-25 �Ϻ���ͨ��ѧ Method of removing polycyclic arene from gas phase
CN1531587A (en) * 2000-06-30 2004-09-22 Detergent compositions comprising cyclodextrin glucanotrasferase enzyme
CN103599924A (en) * 2013-11-29 2014-02-26 浙江大学 Novel desorbent for processing diesel polluted soil and preparation method thereof
CN103801180A (en) * 2012-11-12 2014-05-21 镇江新元素医药科技有限公司 Air purifier
CN106139891A (en) * 2015-04-08 2016-11-23 江苏瑞丰科技实业有限公司 VOC high-efficient purification spray in car
CN106538926A (en) * 2016-10-26 2017-03-29 华南理工大学 A kind of water soluble Chinese cassia tree aldehyde sustained release inclusion compound and preparation method thereof
CN107149852A (en) * 2017-07-24 2017-09-12 朱友富 A kind of chloride volatile organic compounds handling process
WO2017175143A1 (en) * 2016-04-05 2017-10-12 Innonix Technologies, Incorporated Compositions for reducing inhalation of toxic air pollution components
CN107899370A (en) * 2017-11-17 2018-04-13 北京沃太斯环保科技发展有限公司 A kind of absorbent for removing VOC gas and preparation method thereof

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5615975A (en) * 1995-07-14 1997-04-01 Sandoz Ltd. Method for remediation of volatile organic contaminated soils
CN1261785A (en) * 1997-06-09 2000-08-02 普罗克特和甘保尔公司 Method for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins and perfume
CN1398267A (en) * 1999-12-16 2003-02-19 伊斯曼化学公司 Cyclodextrin ethers
CN1531587A (en) * 2000-06-30 2004-09-22 Detergent compositions comprising cyclodextrin glucanotrasferase enzyme
CN1522787A (en) * 2003-09-05 2004-08-25 �Ϻ���ͨ��ѧ Method of removing polycyclic arene from gas phase
CN103801180A (en) * 2012-11-12 2014-05-21 镇江新元素医药科技有限公司 Air purifier
CN103599924A (en) * 2013-11-29 2014-02-26 浙江大学 Novel desorbent for processing diesel polluted soil and preparation method thereof
CN106139891A (en) * 2015-04-08 2016-11-23 江苏瑞丰科技实业有限公司 VOC high-efficient purification spray in car
WO2017175143A1 (en) * 2016-04-05 2017-10-12 Innonix Technologies, Incorporated Compositions for reducing inhalation of toxic air pollution components
CN106538926A (en) * 2016-10-26 2017-03-29 华南理工大学 A kind of water soluble Chinese cassia tree aldehyde sustained release inclusion compound and preparation method thereof
CN107149852A (en) * 2017-07-24 2017-09-12 朱友富 A kind of chloride volatile organic compounds handling process
CN107899370A (en) * 2017-11-17 2018-04-13 北京沃太斯环保科技发展有限公司 A kind of absorbent for removing VOC gas and preparation method thereof

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
FOURMENTIN等: "cyclodextrins: A new efficient absorbent to treat watse gas streams", 《CHEMOSPHERE》 *
庄一廷等: ""环糊精在环境治理中的应用"", 《福建环境》 *
庄一廷等: "环糊精在环境治理中的应用", 《福建环境》 *
廖波: "环糊精与表面活性剂增效电动力学法修复石油污染土壤", 《科学技术与工程》 *
李兆敏: "《泡沫流体油气开采技术研究进展》", 31 July 2009, 中国石油大学出版社 *
郭书海等: "《污染土壤电动修复原理与技术》", 31 December 2017, 中国环境出版社 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114085674A (en) * 2020-08-24 2022-02-25 中国石油化工股份有限公司 VOC (volatile organic compound) pollution repairing agent and application thereof and method for repairing VOC polluted environment
CN114618266A (en) * 2020-12-10 2022-06-14 中国石油天然气股份有限公司 Solubilization absorbent, preparation method thereof and organic waste gas treatment method
CN114618266B (en) * 2020-12-10 2023-07-25 中国石油天然气股份有限公司 Solubilizing absorbent, preparation method thereof and treatment method of organic waste gas
CN115245727A (en) * 2021-04-25 2022-10-28 中国石油天然气股份有限公司 High-performance VOCs absorbent and preparation method and application thereof

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