乙二醛交联壳寡糖水热制备介孔碳及其表征

廖雯琪1,2, 王梦1,2, 史连军3, 秦红3, 潘红艳1,2,3*, 林倩1,2*

化工新型材料 ›› 2020, Vol. 48 ›› Issue (12) : 111 -115.

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化工新型材料 ›› 2020, Vol. 48 ›› Issue (12) : 111-115. DOI: 10.19817/j.cnki.issn 1006-3536.2020.12.027
科学研究

乙二醛交联壳寡糖水热制备介孔碳及其表征

    廖雯琪1,2, 王梦1,2, 史连军3, 秦红3, 潘红艳1,2,3*, 林倩1,2*
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Preparation and characterization of mesoporous carbon prepared by GL/COS

  • Liao Wenqi1,2, Wang Meng1,2, Shi Lianjun3, Qin Hong3, Pan Hongyan1,2,3, Lin Qian1,2
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摘要

首次选用交联剂乙二醛,以壳寡糖为碳氮源、F127为软模板,用低浓度水热合成法制备孔径均匀的介孔碳。采用热重、N2吸附/脱附和小角X射线衍射等表征手段分析介孔碳的性质,探讨了乙二醛用量、F127与壳寡糖质量比及原料添加顺序对介孔碳孔结构的影响。结果表明:N成功掺杂到介孔碳中,其质量分数为4.84%;乙二醛添加量2mL、原料中F127与壳寡糖的质量比为0.333、碳源滴加到模板中时,所制备的介孔碳孔径主要分布在5~10nm之间,平均孔径约7.62nm,其比表面积和介孔孔容分别为473m2/g和0.37cm3/g,有望提高材料的吸附性能。

Abstract

First the cross-linking agent glyoxal(GL) was selected,homogeneous mesoporous carbon was prepared by low concentration hydrothermal synthesis method which using chitosan-oligosaccharide(COS) as C—N source,F127 as soft template.The influence of GL amount,the mass ratio of F127 to COS and the order of adding raw materials on pore structure of porous carbon was investigated by using TG,BET,XRD,SEM and XPS.The results shown that nitrogen was successfully doped in-situ into mesoporous carbon materials,and its content was 4.84 % and the uniform carbon was prepared as follows: the amount of GL was 2mL,the value of F127/COS was 0.333,and the carbon source was dropped into the template,the pore size was mainly distributed between 5~10nm,the average pore size of mesoporous carbons was about 7.6nm.The specific surface area and mesopore volume were 473m2/g and 0.37cm3/g.The addition of GL improved the pore structure of the materials.

关键词

乙二醛 / 壳寡糖 / 均匀孔径 / 水热法

Key words

glyoxal / chitosan-oligosaccharide / uniform pore size / hydrothermal synthesis method

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乙二醛交联壳寡糖水热制备介孔碳及其表征[J]. 化工新型材料, 2020, 48(12): 111-115 DOI:10.19817/j.cnki.issn 1006-3536.2020.12.027

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参考文献

[1] Davis M E.Ordered porous materials for emerging applications[J].ChemInform,2010,33(40):813-821.
[2] Lee S Y,Jang D I,Bae S T,et al.Facile synthesis of nitrogen-enriched mesoporous carbon for carbon dioxide capture[J].International Journal of Hydrogen Energy,2014,39(23):12347-12352.
[3] Ravat V,Nongwe I,Coville N J.N-doped ordered mesoporous carbon supported PdCo nanoparticles for the catalytic oxidation of benzyl alcohol[J].Microporous and Mesoporous Materials,2016,225:224-231.
[4] Zhao X,Liu Y,Manuel J,et al.Nitrogen-doped mesoporous carbon:a top-down strategy to promote sulfur ommobilization for lithium-sulfur batteries[J].Chem Sus Chem,2015,8(19):3234-3241.
[5] Romero A,Alonso E,Sastre Á,et al.Conversion of biomass into sorbitol:cellulose hydrolysis on MCM-48 and d-glucose hydrogenation on Ru/MCM-48[J].Microporous and Mesoporous Materials,2016,224:1-8.
[6] Mitome T,Hirota Y,Uchida Y,et al.Porous structure and pore size control of mesoporous carbons using a combination of a soft-templating method and a solvent evaporation technique[J].Colloids and Surfaces A:Physicochemical and Engineering Aspects,2016,494:180-185.
[7] Che S,Lund K,Tatsumi T,et al.Direct observation of 3D mesoporous structure by scanning electron microscopy (SEM):SBA-15 silica and CMK-5 carbon[J].Angewandte Chemie-International Edition,2003,42(19):2182-2185.
[8] Domard A.A perspective on 30 years research on chitin and chitosan[J].Carbohydrate Polymers,2011,84(2):696-703.
[9] Rinaudo M.Chitin and chitosan:properties and applications[J].Progress in Polymer Science,2006,31(7):603-632.
[10] Przekora A,Ginalska G.Biological properties of novel chitosan-based composites for medical application as bone substitute[J].Central European Journal of Biology,2014,9(6):634-641.
[11] Nikpour M R,Rabiee S M,Jahanshahi M.Synthesis and characterization of hydroxyapatite/chitosan nanocomposite materials for medical engineering applications[J].Composites Part B:Engineering,2012,43(4):1881-1886.
[12] Chun Y,Yong S H I.Preparation and characterization of chitosan-derived mesoporous carbon materials through template method[J].Applied Chemical Industry,2017,46(8):1485-1489.
[13] Wang M,Pan H Y,Yang C L,et al.Preparation and characterization of in-situ nitrogen doped mesoporous carbons with large pore[J].Rengong Jingti Xuebao/Journal of Synthetic Crystals,2019,48(9):1726-1733.
[14] Herou S,Ribadeneyra M C,Madhu R,et al.Ordered mesoporous carbons from lignin:a new class of biobased electrodes for supercapacitors[J].Green Chemistry,2019,21(3):550-559.
[15] Andreoli S,Benito P,Solmi M V,et al.Insights into the synthesis and surface functionalization of mesoporous carbon for catalytic applications[J].Chemistry Select,2017,2(25):7590-7596.
[16] Wang X,Pan H,Lin Q,et al.One-step synthesis of nitrogen-doped hydrophilic mesoporous carbons from chitosan-based triconstituent system for drug release[J].Nanoscale Research Letters,2019,14(1):259-271.
[17] Chong J,Zhu X,Huang W,et al.The fabrication of size-tunable nitrogen-doped dual-mesoporous carbon nanospheres with excellent thermal stability via colloidal silica driving co-assembly strategy[J].Carbon,2018,126:156-158.
[18] Zhao L,Baccile N,Gross S,et al.Sustainable nitrogen-doped carbonaceous materials from biomass derivatives[J].Carbon,2010,48(13):3778-3787.
[19] Liu R,Shi Y,Wan Y,et al.Triconstituent co-assembly to ordered mesostructured polymer-silica and carbon-silica nanocomposites and large-pore mesoporous carbons with high surface areas[J].Journal of the American Chemical Society,2006,128(2):11652-11662.
[20] 刘蕾.新型微孔和介孔碳材料的合成及其催化/吸附性能[D].天津:南开大学,2012.
[21] Meng Y,Gu D,Zhang F,et al.A family of highly ordered mesoporous polymer resin and carbon structures from organic-organic self-assembly[J].Chemistry of Materials,2006,18(18):4447-4464.
[22] Gorgulho H F,Gonçalves F,Pereira M F R,et al.Synthesis and characterization of nitrogen-doped carbon xerogels[J].Carbon,2009,47(8):2032-2039.

基金资助

贵州省科技厅基金项目(黔科合LH字[2017]7254号);贵州省科技支撑计划项目[批准(2018)2192]

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