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A kind of preparation method of magnetic bentonite

A technology of bentonite and sodium bentonite, applied in chemical instruments and methods, inorganic chemistry, non-metallic elements, etc., can solve the problems of cumbersome steps and high cost, and achieve the effects of low preparation cost, low production threshold and environmental friendliness

Active Publication Date: 2016-09-14
UNIV OF JINAN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The present invention aims at the shortcomings of high cost and complicated steps of the existing hydrothermal preparation method of magnetic bentonite, thereby providing a method for directly synthesizing magnetic bentonite in one step

Method used

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  • A kind of preparation method of magnetic bentonite
  • A kind of preparation method of magnetic bentonite
  • A kind of preparation method of magnetic bentonite

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] (1) Add 2.0 g FeCl 3 ∙6H 2 O was dissolved in 40 mL of ethylene glycol, and then 6.0 g of NaAc∙3H was added 2 O, form a transparent solution, then add 20 mL of ethylenediamine, add 0.08 g of sodium bentonite powder, and stir magnetically for 30 min; a well-mixed yellow-brown suspension is obtained (sodium bentonite powder is fully dispersed);

[0030] (2) Encapsulate the above mixture in a polytetrafluoroethylene reactor, heat and react at 180 °C for 8 h, and cool to room temperature after the reaction is completed;

[0031] (3) Wash the obtained black solid several times with distilled water (to remove impurities), and magnetically separate (the specific operation is to use a magnet to separate the magnetic substance (ie, magnetic bentonite) from the washed solid-liquid mixture, and discard the distilled water), drying, grinding, and passing through a 200-mesh sieve to obtain magnetic bentonite MB1;

[0032] At room temperature, add 0.2g MB1 to 25mL 100mg / L basic fu...

Embodiment 2

[0034] (1) Add 2.0 g FeCl 3 ∙6H 2 O was dissolved in 40 mL of ethylene glycol, and then 6.0 g of NaAc∙3H was added 2 0, form a transparent solution, then add 20 mL of ethylenediamine, add 0.2 g of sodium bentonite powder, and magnetically stir for 30 minutes; the sodium bentonite powder is fully dispersed to obtain a fully mixed yellow-brown suspension;

[0035] (2) Encapsulate the above mixture in a polytetrafluoroethylene reactor, heat and react at 190 °C for 10 h, and cool to room temperature after the reaction is completed;

[0036] (3) The obtained black solid was washed several times with distilled water, magnetically separated, dried, ground, and passed through a 200-mesh sieve to obtain magnetic bentonite MB2;

[0037] At room temperature, add 0.2g MB2 to 25mL 100mg / L basic fuchsin solution, shake for 90min, the adsorption rate reaches 98.36%; add 0.05g MB2 to 25mL 300mg / L basic fuchsin solution, shake for 90min, the The rate reached 68.34%.

Embodiment 3

[0039] (1) Mix 6.0 g NaAc∙3H 2 O and 2.0 g FeCl 3 ∙6H 2 O was dissolved in 40 mL of ethylene glycol to form a transparent solution, then 10 mL of ethylenediamine was added, 0.4 g of sodium bentonite powder was added, and magnetically stirred for 30 min; a fully mixed yellow-brown suspension was obtained;

[0040] (2) Encapsulate the above mixture in a polytetrafluoroethylene reactor, heat and react at 200 °C for 8 h, and cool to room temperature after the reaction is complete;

[0041] (3) The obtained black solid was washed several times with distilled water, magnetically separated, dried, ground, and passed through a 200-mesh sieve to obtain magnetic bentonite MB3;

[0042] At room temperature, add 0.2g MB3 to 25mL 100mg / L basic fuchsin solution, shake for 90min, the adsorption rate reaches 99.51%; add 0.05g MB3 to 25mL 300mg / L basic fuchsin solution, shake for 90min, the The rate reached 88.69%.

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Abstract

The invention relates to a preparation method of magnetic bentonite and belongs to the technical field of inorganic materials. The preparation method comprises the following steps of mixing FeCl3.6H2O, NaAc.3H2O, glycol, ethene diamine and sodium-based bentonite powder to obtain a tawny suspension liquid, packaging the tawny suspension liquid in a Teflon reactor, carrying a reaction process at a temperature of 180-200 DEG C for 8h or more, taking black solids, and carrying out washing, magnetic separation, drying, grinding and sieving to obtain the magnetic bentonite material. The magnetic bentonite is directly synthesized by a one-step hydrothermal method. The preparation method is free of water as a medium, only needs a small amount of an organic solvent, is simple, can be controlled easily, has a low preparation cost and a low industrialization production threshold, and can be industrialized easily. The magnetic bentonite contains a bentonite characteristic diffraction peak, has superparamagetism of magnetic nanoparticles and has good effects of adsorption of a part of dye pollutants and organic pollutants in water.

Description

technical field [0001] The invention relates to a preparation method of magnetic bentonite, which belongs to the technical field of inorganic material preparation. Background technique [0002] Bentonite belongs to layered aluminosilicate clay minerals, which can expand between layers and have large cation exchange capacity, and its main component is montmorillonite. Montmorillonite is a mineral material composed of aluminum-oxygen octahedron and silicon-oxygen tetrahedron. Its general chemical formula is: E x (H 2 O) 4 {(Al 2 -Mg x )[Si 4 o 10 ](OH) 2}. Among them, low-valent ions (Mg 2+ ) can replace Si in 4+ and Al 3+ , resulting in excess negative charges between the structural layers, which can better absorb cations. Moreover, bentonite has the characteristics of large surface area and strong ion exchange capacity. [0003] The controllable interlayer structure and modifiable surface properties of bentonite make it have technological characteristics such as...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01B33/40
Inventor 闫良国李双郝元峰单然然于海琴杜斌魏东李合莲
Owner UNIV OF JINAN