Solid magnetic heavy metal ion separation material and preparation method thereof

A technology for separating heavy metal ions and materials, applied in the fields of alkali metal compounds, chemical instruments and methods, alkali metal oxides/hydroxides, etc., can solve the problems of high manufacturing cost, small adsorption capacity, poor adaptability, etc., and achieve improved Uniformity and stability, the uniformity of the coating layer, and the effect of improving stability

Active Publication Date: 2018-05-22
HUNAN UNIV OF SCI & TECH
View PDF5 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are some disadvantages in the developed adsorption materials, such as natural adsorption materials are limited by their own structure, the adsorption capacity is generally not large, and it is easy to produce a large amount of solid waste containing heavy metals; synthetic adsorption materials, such as carbonaceous adsorption materials Generally small, while synthetic resins, synthetic porous materials and synthetic nanomaterials generally have complex preparation processes and high manufacturing costs; bioabsorbent materials have problems such as selectivity to heavy metals, poor adaptability, and difficult breeding of strains.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Solid magnetic heavy metal ion separation material and preparation method thereof
  • Solid magnetic heavy metal ion separation material and preparation method thereof
  • Solid magnetic heavy metal ion separation material and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] (1) Get 2.0g of ferric oxide microspheres with an average particle size of 435nm and 100mL of absolute ethanol into a 250mL three-necked flask with a dropping funnel, reflux condenser and mechanical stirring, then add 4.10g of quality Triethylenetetramine with a percentage concentration of 95.0%, mechanically stirred for 3 hours with the aid of ultrasonic waves. Raise the temperature to 60°C, and slowly add 2.4 mL of epichlorohydrin with a concentration of 99.0% by mass dropwise. After the dropwise addition, continue to react for another 3 h, cool to room temperature, and then adsorb and separate the solid matter with a magnet.

[0029] (2) Transfer the solid matter separated in step (1) into a 250mL three-necked flask with a dropping funnel, a reflux condenser and a mechanical stirrer, add 100mL toluene, and ultrasonically assisted mechanically stir for 3h, then pass through the dripping Slowly add a 5.0% chloroform solution prepared by 0.36mL glutaraldehyde into the f...

Embodiment 2

[0032] (1) Get 2.0g of ferric oxide microspheres with an average particle size of 340nm and 90mL of absolute ethanol and join them in a 250mL three-necked flask with a dropping funnel, reflux condenser and mechanical stirring, then add 4.50g of quality Triethylenetetramine with a percentage concentration of 95.0%, mechanically stirred for 2.5 hours with the aid of ultrasonic waves. Raise the temperature to 55°C, slowly add 2.6mL of epichlorohydrin with a mass percent concentration of 99.0% dropwise, and continue the reaction for 2.5h after the dropwise addition, cool to room temperature, and then adsorb and separate the solid matter with a magnet.

[0033] (2) transfer the solid matter separated in step (1) into a 250mL three-necked flask with a dropping funnel, a reflux condenser and a mechanical stirrer, add 90mL toluene, and ultrasonically assisted mechanically stir for 2h, then pass the dripping Slowly add 7.0% chloroform solution prepared by 0.33mL glutaraldehyde into the...

Embodiment 3

[0036] (1) Get 2.0g of ferric oxide microspheres with an average particle size of 218nm and 80mL of absolute ethanol into a 250mL three-necked flask with a dropping funnel, reflux condenser and mechanical stirring, then add 5.00g of quality Triethylenetetramine with a percentage concentration of 95.0%, mechanically stirred for 3 hours with the aid of ultrasonic waves. The temperature was raised to 50°C, and 2.97 mL of epichlorohydrin with a concentration of 99.0% by mass was slowly added dropwise. After the dropwise addition was completed, the reaction was continued for another 3 h, cooled to room temperature, and then the solid matter was adsorbed and separated by a magnet.

[0037] (2) Transfer the solid matter separated in step (1) into a 250mL three-necked flask with a dropping funnel, a reflux condenser and a mechanical stirrer, add 100mL toluene, and ultrasonically assisted mechanically stir for 3h, then pass through the dripping Slowly add a 10.0% chloroform solution pr...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
Login to view more

Abstract

The invention relates to a solid magnetic heavy metal ion separation material and a preparation method of the separation material. Epoxy chloropropane and triethylene tetramine perform a polymerization reaction in the presence of a ferroferric oxide microsphere to generate linear high polymer chains; the surface of the ferroferric oxide microsphere absorbs and is wound with the linear high polymerchains in situ; the high polymer chains are further cross-linked by using glutaric dialdehyde in methylbenzene, so that the surface of the ferroferric oxide microsphere is coated with the high polymer chains stably; an iminodiacetic acid group is connected to a high polymer chain net on the surface of the ferroferric oxide microsphere via a dialdehyde substance, so that the surface of the ferroferric oxide microsphere is coated with the high polymer chain net containing rich active groups such as -N(CH2COO-)2, -NH2, -NH- and -OH; the trapping and absorbing capacity on heavy metals is greatlyimproved; the material has excellent magnetic separation performance; the subsequent separation is simple; continuous absorption and separation operation can be achieved; and the material is convenient in industrial application and popularization.

Description

technical field [0001] The invention relates to the field of heavy metal wastewater treatment, in particular to a solid magnetic heavy metal ion separation material and a preparation method thereof. Background technique [0002] Water pollution by toxic heavy metals has become a major global environmental problem. Fertilizer production, pesticide manufacturing, leather production, mineral mining, smelting and processing, material surface finishing and battery manufacturing will all produce a large amount of wastewater containing heavy metals, which seriously threatens the safety of the water environment and people's health. In response to the increasingly serious threat of heavy metal pollution, a variety of heavy metal wastewater treatment methods have been developed, such as traditional chemical precipitation, chelation flocculation, coagulation / flocculation, ferrite, ion exchange, enhanced ultrafiltration, Ion flotation, electrodialysis, electrodeposition and adsorptio...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): B01J20/26B01J20/28B01J20/30C02F1/28C02F101/20
CPCB01J20/06B01J20/267B01J20/28009B01J20/28016C02F1/288C02F2101/20
Inventor 刘立华胡博强赵露薛建荣唐安平周智华
Owner HUNAN UNIV OF SCI & TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products