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TiO_2/N-琥珀酰壳聚糖复合材料的制备及表征 被引量:1

Synthesis and Characterization of TiO_2/N-succinyl-chitosan Composite
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摘要 以N-琥珀酰壳聚糖与TiO2复合制备了TiO2/N-琥珀酰壳聚糖复合材料。采用透射电镜(TEM)、傅里叶红外光谱(FTIR)、紫外-可见光谱(UV-Vis)、X射线衍射(XRD)、粒径及Zeta电位分析对复合材料进行表征。结果表明,TiO2表面羟基与N-琥珀酰壳聚糖分子中的羟基、酰胺、羧基相互作用形成了稳定的复合材料;复合材料中TiO2晶型呈锐钛矿型;复合材料平均粒径为50nm,Zeta电位达39mV;紫外-可见光谱显示,复合材料的光响应范围拓宽到可见光区,且对光的吸收能力显著增强,但在模拟太阳光下其光催化效率较TiO2有所下降。 TiO2/ N-succinyl-chitosan composite was prepared by compositing TiO2 and N-succinylchitosan. The composite was characterized by transmission electron microscopy( TEM),fourier infrared spectrum( FTIR),ultraviolet-visible spectra( UV-Vis),X-ray diffraction( XRD),particle size and Zeta potential analysis. The results showed that stable composite was formed by interaction of the surface hydroxyl groups of TiO2 with hydroxyl,amide and carboxyl groups of N-succinyl-chitosan. TiO2 of the composite was anatase. The average particle size of the composite was 50 nm and Zeta potential was 39 mV. Ultraviolet-visible spectra revealed that light response range of the composite was widened to visible region and the light absorption capacity significantly enhanced,but its photocatalytic efficiency was lower than TiO2 under simulated sunlight.
出处 《精细化工》 EI CAS CSCD 北大核心 2016年第3期277-282,共6页 Fine Chemicals
基金 山西省自然科学基金(2015011012)~~
关键词 光敏剂 N-琥珀酰壳聚糖 TIO2 TiO2/N-琥珀酰壳聚糖复合材料 功能材料 photosensitizer N-succinyl-chitosan TiO2 TiO2/N-succinyl-chitosan composite functional materials
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  • 1Hou Z Y,Zhang Y X, Deng K R,et al. UV-emitting upconversion- based TiO2 photosensitizing nanoplatform: near-infrared light mediated in vivo photodynamic therapy via mitochondria-involved apoptosis pathway[ J]. ACS Nano,2015,9(3 ) :2584 -2599.
  • 2Di Corato R, B6alle G, Kolosnjaj-Tabi J, et al. Combining magnetic hyperthermia and photodynamic therapy for tumor ablation with photoresponsive magnetic liposomes [ J~. ACS Nano, 2015,9 (3) : 2904 -2916.
  • 3邓春月,龙莹莹,刘厦,陈章宝,李翀.生物素介导的胰腺癌靶向聚合物胶束制备及其用于光动力治疗的初步研究[J].药学学报,2015,50(8):1038-1044. 被引量:7
  • 4Freyre-Fonseca V, Delgado-Buenrostro N L, Guti~rrez-Cirlos E B, et al. Titanium dioxide nanoparticles impair lung mitochondrial function [ J ]. Toxicology Letters,2011,202 (2) : 111 - 119.
  • 5Saquih Q, A1-Khedhairy A A, Siddiqui M A, et al. Titanium dioxide nanoparticles induced cytotoxicity, oxidative stress and DNA damage in human amnion epithelial (WISH) cells[ J]. Toxicology in Vitro,2012,26(2) :351 -361.
  • 6Sha B Y,Gao W,Wang S Q,et al. Cytotoxicity of titanium dioxide nanoparticles differs in four liver ceils from human and rat [ J ]. Composites Part B-Engineering,2011,42 ( 8 ) :2136 - 2144.
  • 7Chen X Q, Liu Y Y, Shi H F, et al. Carboxymethyl chitosan coating to block photocatalytic activity of TiO2 nanoparticles [ J 1. Textile Research Journal, 2010,80 ( 20 ) :2214 - 2222.
  • 8Mukhopadhyay P, Bhattacharya S, Nandy A, et al. Assessment of in vivo chronic toxicity of chitosan and its derivates used as oral insulin carriers [ J 1. Toxicology Research, 20 l 5,4 ( 2 ) : 281 - 290.
  • 9Muzzarelli R, Weexk M, FiliPPiin O, et al. Characteristic properties of N-carboxybutyl chitosan [ J ]. Carbohydrate Polymers, 1989,11 (30) :7 -20.
  • 10Kamiyama K, Onishi H, Machida Y. Biodisposition characteristics of N-succinylchitosan and glycol-chitosan in normal and tumor- bearing mice[J]. Biological & Pharmaceutical Bulletin, 1999,22 (2) :179 -186.

二级参考文献19

  • 1许晨,卢灿辉.壳聚糖季铵化衍生物的吸湿性与保湿性[J].应用化学,1996,13(5):94-96. 被引量:44
  • 2Roberts GAF. Chitin chemistry[M]. London: Macmillan Press, 1992.
  • 3Tang L-G, Hon D N-S . Chelation of chitosan derivatives with zinc ions Ⅱ: Association complexes of Zn2+ onto O,N-carboxymethyl chitosan[J]. J Appl Polym Sci, 2001, 79:1476-1485.
  • 4Quignard F, Choplin A, Domard A . Chitosan: A natural polymeric support of catalysts for the synthesis of fine chemicals[J]. Langmair, 2000, 16:9106-9108.
  • 5Kato Y, Onishi H, Machida Y . Lactosaminated and intact N-succinyl-chitosans as drug carriers in liver metastasis[J]. International J Pharmace, 2001,226:93-106.
  • 6Muzzarelli RAA, Tanfani F, Emanuelli M, et al. N-(carboxymethylidene)chitosans and N-(carboxymethyl)chitosans: Novel chelating polyampholytes obtained from chitosan glyoxylate[J]. Carbohydr Res, 1982,107:199-214.
  • 7Kubota N, Tatsumoto N, Sano T, et al. A simple preparation of half N-acetylated chitosan highly soluble in water and aqueous organic solvents[J]. Carbohydr Res, 2000, 324(4):268-274.
  • 8Hirano S, Sakaguchi T, Kuramitsu K, et al. N-Alanyl and some N-(N'-aryl)glycyl derivatives of chitosan[J]. Carbohydr Polym, 1992, 19:135-138.
  • 9Hirano S, Ohe Y, Ono H. Selective N-acylation of chitosan [J]. Carbohydr Res,1976,47:315-320.
  • 10ROBERTS G A F.Chitin Chemistry[M].London:Macmillan Press,1992:79.

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