CN102114412B - Chitosan-grafted and modified attapulgite clay absorbing material and preparation method thereof - Google Patents

Chitosan-grafted and modified attapulgite clay absorbing material and preparation method thereof Download PDF

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CN102114412B
CN102114412B CN 201110021514 CN201110021514A CN102114412B CN 102114412 B CN102114412 B CN 102114412B CN 201110021514 CN201110021514 CN 201110021514 CN 201110021514 A CN201110021514 A CN 201110021514A CN 102114412 B CN102114412 B CN 102114412B
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attapulgite
chitosan
attapulgite clay
dialdehyde
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CN102114412A (en
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彭勇刚
纪俊玲
汪媛
陶永新
姚超
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Liyang Chang Technology Transfer Center Co., Ltd.
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Changzhou University
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Abstract

The invention relates to a chitosan-grafted and modified attapulgite clay absorbing material and a preparation method thereof, belonging to the technical field of new materials. The chitosan-grafted and modified attapulgite clay absorbing material is prepared by using chitosan and organic attapulgite clay as raw materials through dialdehyde crosslinking. The preparation method comprises the steps of: modifying the attapulgite clay by adopting an aminosilane coupling agent to prepare the organic attapulgite clay; then, dispersing the organic attapulgite clay into a dialdehyde solution, stirring at a temperature of 30 DEG C for 3-4h to prepare the dialdehyde modified attapulgite clay; then dropping a chitosan solution in a dialdehyde-modified attapulgite clay suspension, reacting at a temperature of 30-45 DEG C for 3-5h, reducing with a reducing agent at room temperature under the alkalinity condition, fully washing with deionized water, drying in vacuum, grinding and screening to obtain the chitosan-grafted and modified attapulgite clay. The chitosan is bonded on the surface of the attapulgite clay in a covalent bond manner, thus the bonding firmness of the chitosan and the attapulgite clay is greatly improved. The chitosan-grafted and modified attapulgite clay prepared with the method provided by the invention has better absorbing property to various dyes.

Description

Attapulgite modified sorbing material of a kind of chitosan graft and preparation method thereof
Technical field
The invention belongs to new material technology field, relate to a kind of organic surface modifying method of attapulgite, be specially the preparation method of the attapulgite modified sorbing material of a kind of chitosan graft.
Background technology
Attapulgite is that a kind of porous type chain stratiform contains Shuifu County's zeopan class clay mineral, and its theoretical chemistry formula is Si 8Mg 5O 20(OH) 2(H 2O) 44H 2O, the skeleton structure of attapulgite is the 3 D stereo shape, interconnect and form by sharing the summit by silicon-oxy tetrahedron and magnalium octahedron, zeolite cavity and hole run through total, be a kind of porous mineral matter, crystal structure inside has a large amount of zeolite channels, and crystals zeolite cavity size is consistent, make its effect with molecular sieve, can be used for the absorption of various industrial wastewaters.For improving the absorption property of attapulgite, usually need to carry out suitable modification to it.Method of modifying commonly used mainly contains: acid activation modification, high-temperature roasting modification and organically-modified.Acid activation modification and high-temperature roasting modification mainly are that partial impurities makes the open and enlarged-diameter in attapulgite duct in the attapulgite by removing, and specific area increases, and absorption property strengthens.The organically-modified electronegative characteristic of attapulgite's surface of mainly utilizing, adopt cationic surfactant to its modification, as: Wang Xingguo etc. adopt the attapulgite modified absorption for phenol of cationic surfactant (publication number: CN1793242A, a kind of preparation method of attapulgite of cationic surfactant modification); Chen Tiantian etc. adopt long-chain alkylguanidine-modified attapulgite to be used for the absorption (publication number: CN101538047A, the preparation method of long-chain alkylguanidine-modified attapulgite) of waste water from dyestuff.
Shitosan is that chitin is hydrolyzed and sloughs the derivative that generates behind the part acetyl group under alkali condition, a large amount of the dissociating-NH of containing in the molecule 2,-OH can borrow hydrogen bond, ionic bond to form and have similar cancellated cage type molecule, and metal ion, dye molecule are had good absorption property.
Adopting attapulgite and shitosan is that raw material prepares composite adsorbing material and can give full play to both advantages, simultaneously, can improve significantly that shitosan sorbing material settling property in solution is poor, separation difficulty, the defective that easily runs off in acid solution.The mode that the people such as Li Zengxin, Yin Jingzhou once adopted dipping on attapulgite, is made solid compound adsorbent with chitosan loaded, is used for absorption (the attapulgite load shitosan absorption waste water Cd of heavy metal ions in wastewater 2+Research, nonmetallic ore, the 4th phase in 2008; The absorption of Heavy Metal Ions on Attapulgite Modified by Chitosan, chemical industry environmental protection, the 3rd phase in 2007).
Said method mainly is to cationic interchangeability according to attapulgite, utilize shitosan characteristic with positive charge in acid solution, with chitosan loaded on attapulgite, the combination of shitosan and attapulgite is that shitosan is in the physical absorption of attapulgite's surface, both are not in conjunction with firm, and the performance of material is not high.
Summary of the invention:
For overcoming the deficiencies in the prior art, the invention provides the preparation method of the attapulgite modified sorbing material of a kind of chitosan graft, the method is utilized the reactivity of active amino in attapulgite's surface silicon hydroxyl and the chitosan molecule, mode by chemical bonding with chitosan graft to attapulgite, can significantly improve shitosan at the binding strength of attapulgite's surface, give full play to both absorption properties.
The technical scheme that realizes above-mentioned purpose is: the attapulgite modified sorbing material of chitosan graft makes by dialdehyde is crosslinked take shitosan, organic attapulgite soil as raw material; Wherein its molecular weight of used shitosan is 1.1-2.5 * 10 5, deacetylation is 75-95%; Used organic attapulgite soil is that dialdehyde is attapulgite modified; Wherein the attapulgite modified mass ratio of shitosan and dialdehyde is: 1:1-1:2, used dialdehyde are glyoxal or glutaraldehyde.
The preparation method of the attapulgite modified sorbing material of chitosan graft provided by the invention, carry out according to following step:
(1) the attapulgite powder is scattered in the organic solvent with solid-liquid mass ratio 1:10-1:30, ultrasonic dispersion 10-30min drips amino silicane coupling agent, 70-100 ℃ of reaction 6-10h; After reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets silane coupler modified organic attapulgite soil;
(2) above-mentioned silane coupler modified organic attapulgite soil being scattered in is in the 5% dialdehyde solution in mass, and the solid-liquid mass ratio is 1:10-1:25, and 30 ℃ are stirred 3-4h, filter, deionized water is repeatedly washed, vacuum drying, and it is attapulgite modified namely to get dialdehyde;
(3) shitosan being dissolved in quality counts and is made into quality in 1% acetum and volume ratio is the chitosan-acetic acid solution of 0.5%-1.5%, stir 3h, being added drop-wise to quality and volume ratio is in the attapulgite modified suspension of 1-2% dialdehyde, stirring also is heated to 30-45 ℃, reaction 3-5h, centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, add reducing agent room temperature reduction 10-12h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft.
Wherein the used organic solvent of step (1) is toluene or dimethylbenzene.
Wherein the used amino silicane coupling agent of step (1) is: a kind of in gamma-aminopropyl-triethoxy-silane, γ-aminopropyltrimethoxysilane, N-β-(aminoethyl)-γ-aminopropyl methyl dimethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-gamma-aminopropyl-triethoxy-silane, γ-aminopropyl methyldiethoxysilane, the γ-aminopropyl methyl dimethoxysilane, wherein the mass ratio of amino silicane coupling agent and attapulgite is 1:1.
Wherein the used dialdehyde of step (2) is glyoxal or glutaraldehyde.
Wherein the used reducing agent of step (3) is sodium borohydride or sodium cyanoborohydride, the concentration 3mol/L of reducing agent; The attapulgite modified mass ratio of shitosan and dialdehyde is 1:1-1:2.
Wherein used its molecular weight of shitosan of step (3) is 1.1-2.5 * 10 5, deacetylation is 75-95%.
As shown from the above technical solution: the present invention at first introduces amino by amino silicane coupling agent in inorganic attapulgite's surface; Then, adopt dialdehyde as crosslinking agent, the amino on the chitosan molecule and attapulgite modified surface amino groups is crosslinked, thus the covalent bond of realization shitosan and attapulgite.
The attapulgite modified sorbing material advantage of chitosan graft of the present invention is:
(1) adopt natural high polymer that attapulgite is carried out graft modification, environmental protection.
(2) mode by covalent bond arrives attapulgite's surface with chitosan graft, and both adhesions are strong, and sorbing material separates in solution easily.
(3) chitosan graft is attapulgite modified all has good absorption property to various dyestuffs.
The specific embodiment
Employed term among the present invention unless other explanation is arranged, generally has the implication that those of ordinary skills understand usually.
Below in conjunction with specific embodiment, the present invention is described in further detail.Should be understood that these embodiment just in order to demonstrate the invention, but not limit the scope of the invention by any way.
Embodiment 1
The 10g attapulgite is scattered in the 100mL toluene, ultrasonic dispersion 30min under the stirring condition, drips the 10g gamma-aminopropyl-triethoxy-silane, after dripping, be heated to 70 ℃, reaction 10h is after reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets silane coupler modified organic attapulgite soil.
It is in 5% glutaraldehyde solution in mass that gained organic attapulgite soil is dispersed in 150mL, behind 30 ℃ of reaction 3h, filter, and after deionized water is repeatedly washed, vacuum drying, it is attapulgite modified namely to get aldehyde radical.
The 1g shitosan is dissolved in quality counts that to be made into quality and volume ratio in 1% acetum be 0.5% chitosan-acetic acid solution, stir 3h, being added drop-wise to 100mL quality and volume ratio is in the 1% aldehyde radical attapulgite suspension, stirring also is heated to 30 ℃, behind the reaction 5h, and centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, use 3mol/LNaBH 4Solution room temperature reduction 12h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft.
Embodiment 2
The 10g attapulgite is scattered in the 300mL dimethylbenzene, ultrasonic dispersion 10min under the stirring condition, drips 10g γ-aminopropyl methyl dimethoxysilane, after dripping, be heated to 100 ℃, behind the reaction 6h, after reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets attapulgite modified by silane coupling agent.
It is in 5% glyoxal solution in mass that gained organic attapulgite soil is dispersed in 250mL, behind 30 ℃ of reaction 4h, filter, and after deionized water is repeatedly washed, vacuum drying, it is attapulgite modified namely to get aldehyde radical.
The 1g shitosan is dissolved in quality counts that to be made into quality and volume ratio in 1% acetum be 1.5% chitosan-acetic acid solution, stir 3h, being added drop-wise to 100mL quality and volume ratio is in the 2% aldehyde radical attapulgite suspension, stirring also is heated to 45 ℃, behind the reaction 3h, and centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, use 3mol/LNaBH 4Solution room temperature reduction 10h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft.
Embodiment 3
The 10g attapulgite is scattered in the 200mL toluene, and ultrasonic dispersion 20min under the stirring condition, drips the 10g γ-aminopropyltrimethoxysilane, after dripping, be heated to 80 ℃, behind the reaction 8h, after reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets attapulgite modified by silane coupling agent.
It is in 5% glutaraldehyde solution in mass that the gained attapulgite modified by silane coupling agent is dispersed in 100mL, behind 30 ℃ of reaction 4h, filter, and after deionized water is repeatedly washed, vacuum drying, it is attapulgite modified namely to get aldehyde radical.
The 1g shitosan is dissolved in quality counts that to be made into quality and volume ratio in 1% acetum be 1% chitosan-acetic acid solution, stir 3h, being added drop-wise to 100mL quality and volume ratio is in the 1.5% aldehyde radical attapulgite suspension, stirring also is heated to 40 ℃, behind the reaction 4h, and centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, use 3mol/LNaBH 3(CN) solution room temperature reduction 10h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft.
Embodiment 4
The 10g attapulgite is scattered in the 250mL dimethylbenzene, ultrasonic dispersion 20min under the stirring condition, drips 10gN-β-(aminoethyl)-γ-aminopropyl methyl dimethoxysilane, after dripping, be heated to 90 ℃, behind the reaction 7h, after reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets attapulgite modified by silane coupling agent.
It is in 5% glyoxal solution in mass that the gained attapulgite modified by silane coupling agent is dispersed in 200mL, behind 30 ℃ of reaction 3h, filter, and after deionized water is repeatedly washed, vacuum drying, it is attapulgite modified namely to get aldehyde radical.
The 1g shitosan is dissolved in quality counts that to be made into quality and volume ratio in 1% acetum be 1% chitosan-acetic acid solution, stir 3h, being added drop-wise to 100mL quality and volume ratio is in the 1% aldehyde radical attapulgite suspension, stirring also is heated to 35 ℃, behind the reaction 4h, and centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, use 3mol/LNaBH 3(CN) solution room temperature reduction 12h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft.
Test one
Dye Adsorption experiment: select active yellow 3 R S, reactive red 3BS, weak acid brilliant blue 2R, acid green B, C.I. disperse yellow 54, C.I. disperse red 60, C.I. Disperse Blue-56 to be mixed with respectively 500 mgL -1Dye wastewater.Measure dye wastewater sample 50 mL in conical flask, add respectively 0.2 g attapulgite (attapulgite wherein comprises the attapulgite modified and concave convex rod original soil of chitosan graft), be placed into vibration 180 min in 25 ℃ of constant temperature oscillators, then centrifugation, get supernatant liquor, in the maximum absorption wave strong point, the concentration of dyestuff when the initial sum of measuring each water sample reaches balance is calculated as follows the adsorbance of dyestuff with spectrophotometer.
Adsorbance
Figure 123440DEST_PATH_IMAGE002
In the formula: C 0Original concentration (the mgL of-dye solution -1); C eEquilibrium concentration (the mgL of-dye solution -1); The volume of V-dye solution (L); The dosage (g) that m-chitosan graft is attapulgite modified.
Embodiment 1,2,3,4 products therefroms and concave convex rod original soil are carried out various Dye Adsorption experiments, and the result is as follows:
The attapulgite modified absorption property to various dyestuffs of table 1
Figure 417411DEST_PATH_IMAGE003
Can find out from the experimental result of upper table, compare with the concave convex rod original soil, attapulgite modified to reactive dye (active yellow 3 R S, reactive red 3BS), acid dyes (weak acid brilliant blue 2R, acid green B), disperse dyes (C.I. disperse yellow 54, C.I. absorption property Disperse Blue-56, C.I. disperse red 60) significantly improves.

Claims (2)

1. the attapulgite modified sorbing material of chitosan graft is characterized in that making by dialdehyde is crosslinked take shitosan, organic attapulgite soil as raw material; Wherein its molecular weight of used shitosan is 2.5 * 10 5, deacetylation is 75-95%; Used organic attapulgite soil is that dialdehyde is attapulgite modified; Wherein the attapulgite modified mass ratio of shitosan and dialdehyde is: 1:1-1:2, used dialdehyde are glyoxal or glutaraldehyde;
Carry out according to following step: (1) is scattered in the attapulgite powder in the organic solvent with solid-liquid mass ratio 1:10-1:30, and ultrasonic dispersion 10-30min drips amino silicane coupling agent, 70-100 ℃ of reaction 6-10h; After reaction finishes, desolventizing, vacuum drying, grinding is sieved, and namely gets silane coupler modified organic attapulgite soil; (2) above-mentioned silane coupler modified organic attapulgite soil being scattered in is in the 5% dialdehyde solution in mass, and the solid-liquid mass ratio is 1:10-1:25, and 30 ℃ are stirred 3-4h, filter, and deionized water is repeatedly washed, vacuum drying, and it is attapulgite modified namely to get dialdehyde; (3) shitosan being dissolved in quality counts and is made into quality in 1% acetum and volume ratio is the chitosan-acetic acid solution of 0.5%-1.5%, stir 3h, being added drop-wise to quality and volume ratio is in the attapulgite modified suspension of 1-2% dialdehyde, stirring also is heated to 30-45 ℃, reaction 3-5h, centrifugation, fully washing, remove the not shitosan of covalent cross-linking, under alkali condition, add reducing agent room temperature reduction 10-12h, after deionized water is fully washed, vacuum drying, grinding is sieved, and it is attapulgite modified namely to get chitosan graft;
Wherein the used amino silicane coupling agent of step (1) is: a kind of in gamma-aminopropyl-triethoxy-silane, γ-aminopropyltrimethoxysilane, N-β-(aminoethyl)-γ-aminopropyl methyl dimethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-gamma-aminopropyl-triethoxy-silane, γ-aminopropyl methyldiethoxysilane, the γ-aminopropyl methyl dimethoxysilane, and wherein the mass ratio of amino silicane coupling agent and attapulgite is 1:1;
Wherein the used reducing agent of step (3) is sodium borohydride or sodium cyanoborohydride, the concentration 3mol/L of reducing agent.
2. the attapulgite modified sorbing material of chitosan graft according to claim 1 is characterized in that wherein the used organic solvent of step (1) is toluene or dimethylbenzene.
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