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A kind of preparation method of fiber membrane for oil-water separation

An oil-water separation and nanofiber membrane technology, applied in the fields of electrospinning and environmental protection, can solve the problems of low efficiency, poor separation effect, and single oil-water separation performance, and achieve a large adsorption capacity, small volume, and large specific surface area. Effect

Active Publication Date: 2021-04-02
BEIJING UNIV OF CHEM TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Most of the oil-water separation nanofiber membranes studied now use the interception method to separate oil and water, while the oil-absorbing type of oil-water separation is mostly oil-absorbing resin, which has a single oil-water separation performance, and the efficiency is not high, and the separation effect is poor.

Method used

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  • A kind of preparation method of fiber membrane for oil-water separation
  • A kind of preparation method of fiber membrane for oil-water separation
  • A kind of preparation method of fiber membrane for oil-water separation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Example 1: 5wt% SiCDs / SiO 2 Preparation of nanofibrous membranes

[0021] (1) Organosilane carbon dots (SiCDs) were synthesized by chemical hydrothermal synthesis. Dissolve 0.5g of anhydrous citric acid (CA) in distilled water, add 10mL of N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane (AEAPMS) and mix well, then add to the autoclave , the heating temperature was 180°C, and the heating time was 12h; the SiCDs solution was extracted and purified using a 5:1 (V / V) mixture of petroleum ether and ethyl acetate, and extracted three times; the SiCDs solution was extracted using a vacuum rotary evaporator. Concentrate and remove excess solvent to obtain organosilane carbon dots (SiCDs).

[0022] (2) Add 40.375mL of MTES solution and 80mL of absolute ethanol into a beaker, stir at room temperature, and mix thoroughly to form a MTES / ethanol solution;

[0023] (3) Divide 20mL of acetic acid aqueous solution with a pH value of 2.5 into 3 parts, and add each part to the MTE...

Embodiment 2

[0028] Example 2: 10wt% SiCDs / SiO 2 Preparation of nanofibrous membranes

[0029] (1) Organosilane carbon dots (SiCDs) were synthesized by chemical hydrothermal synthesis. Dissolve 0.5g of anhydrous citric acid (CA) in distilled water, add 10mL of N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane (AEAPMS) and mix well, then add to the autoclave , the heating temperature was 180°C, and the heating time was 12h; the SiCDs solution was extracted and purified using a 5:1 (V / V) mixture of petroleum ether and ethyl acetate, and extracted three times; the SiCDs solution was extracted using a vacuum rotary evaporator. Concentrate and remove excess solvent to obtain organosilane carbon dots (SiCDs).

[0030] (2) Add 38.25mL of MTES solution and 80mL of absolute ethanol into a beaker, stir at room temperature, and mix thoroughly to form a MTES / ethanol solution;

[0031] (3) Divide 20mL of acetic acid aqueous solution with a pH value of 2.5 into 3 parts, and add each part to the MTE...

Embodiment 3

[0036] Example 3: 20wt% SiCDs / SiO 2 Preparation of nanofibrous membranes

[0037] (1) Organosilane carbon dots (SiCDs) were synthesized by chemical hydrothermal synthesis. Dissolve 0.5g of anhydrous citric acid (CA) in distilled water, add 10mL of N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane (AEAPMS) and mix well, then add to the autoclave , the heating temperature was 180°C, and the heating time was 12h; the SiCDs solution was extracted and purified using a 5:1 (V / V) mixture of petroleum ether and ethyl acetate, and extracted three times; the SiCDs solution was extracted using a vacuum rotary evaporator. Concentrate and remove excess solvent to obtain organosilane carbon dots (SiCDs).

[0038] (2) Add 34mL of MTES solution and 80mL of absolute ethanol into a beaker, stir at room temperature, and mix thoroughly to form a MTES / ethanol solution;

[0039] (3) Divide 20mL of acetic acid aqueous solution with a pH value of 2.5 into 3 parts, and add each part to the MTES / e...

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Abstract

The invention discloses a preparation method of a fibrous membrane for oil-water separation. Anhydrous CA (citric acid) and AEAPMS (N-(beta-aminoethyl)-gamma-aminopropyl methyl dimethoxysilane) reactto form organosilane carbon dots (SiCDs), then, the SiCDs and organic matter MTES (methyltriethoxysilane) are subjected to a hydrolytic polycondensation reaction in a sol-gel process to produce SiCDs / SiO2 composite sol, wherein the mass percentage of the SiCDs in the composite sol is 1wt%-30wt%, and finally, the SiCDs / SiO2 composite sol is spun with an electrostatic spinning technology to obtain the SiCDs / SiO2 nanofibrous membrane. The nanofibrous membrane has excellent oil-water separation performance and can be applied to oil-water separation of sewage and wastewater containing oils.

Description

technical field [0001] The invention relates to oil-water separation treatment of oil-containing sewage and wastewater in life and production, and is mainly used in the field of environmental protection; meanwhile, it relates to the preparation of nanofiber membranes by using an electrospinning method, which belongs to the field of electrospinning. Background technique [0002] At present, a lot of sewage and wastewater containing oil will be produced every day in production and life. Because the treatment cost of oil-containing sewage and wastewater is too high, many factories do not treat them and discharge them directly to nature, which not only pollutes the environment, but also wastes a lot of oil resources and water resources, and is not conducive to economic development. Production and life have caused great harm. The main reason for not treating is that the treatment of domestic and industrial oily sewage and wastewater is technically difficult and the separation ef...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): D04H1/4382D04H1/728D01D5/00D01F1/10D01F9/08B01D17/022
CPCB01D17/0202D01D5/003D01D5/0061D01D5/0092D01F1/10D01F9/08D04H1/4382D04H1/728
Inventor 刘勇许志阳徐玉龙
Owner BEIJING UNIV OF CHEM TECH