期刊文献+

具有层状碱金属盐结构的氢氧化氨基苯甲酸锌的制备及表征 被引量:2

Hydrothermal synthesis and characterization of layered hydroxide zinc aminobenzoate compounds with structure of layered basic metal salts
下载PDF
导出
摘要 以自制的β-Zn(OH)2和氨基苯甲酸为原料,水热合成了具有层状碱金属盐(LBMS)结构的氢氧化氨基苯甲酸锌化合物。通过XRD、TG-DTA、SEM和TEM分析研究了合成产物的结构、形貌和热稳定性,探讨了合成条件对水热反应产物的影响及合成产物在有机溶剂中的剥离反应。当o-NH2C6H4COOH/Zn的摩尔比为1.2,水热温度70℃下反应12h时,得到的层状物具有板块状粒子特征,层间距为1.33nm;当m-NH2C6H4COOH/Zn的摩尔比为1.8,水热温度40℃下反应24h时,得到的层状化合物具有纤维状粒子特征,层间距为1.08nm。合成的层状物在醇溶剂中可发生剥离反应,层状氢氧化邻氨基苯甲酸锌在正丁醇中的剥离量为0.12g.L-1,层状氢氧化间氨基苯甲酸锌在乙醇中的剥离量为0.18g·L-1。 Two types of layered hydroxide zinc aminobenzoate compounds with a basal spacing of 1.33nm and 1.08nm,and with structure of layered basic metal salts(LBMS)were prepared using β-Zn(OH)2 and aminobenzoic acid by hydrothermal reaction. XRD,TG-DTA,SEM and TEM were used to characterize the structure and particle morphology of the synthesized layered compounds. Meanwhile, the effect of the synthetic conditions on the obtained compounds and its exfoliation in different alcohol solvents were also investigated. When the molar ratio of x(o-NH2 C6 H4 COOH/Zn)was 1.2, the temperature of 70℃ and the reaction time for 12h, the layered phase showed plate-like particle morphology with a basal spacing of 1.33nm. When the molar ratio of x(m-NH2 C6 H4 COOH/Zn)was 1.8, the temperature of 40℃ and the reaction time for 24h, the layered phase showed strip-like particle morphology with a basal spacing of 1.08ram. Both the plate-like crystals and the strip-like crystals can all be exfoliated in alcohol solvents. The saturation concentration of the exfoliated samples were 0.12g/L for layered hydroxide zinc o-aminobenzoate compound in the n-butyl alcohol solvent and 0.18g/L for layered hydroxide zinc m-aminobenzoate compound in the alcohol solvent.
出处 《化工新型材料》 CAS CSCD 北大核心 2012年第8期103-106,共4页 New Chemical Materials
基金 陕西省重点实验室自然科学基金(05JS43) 陕西省教育厅自然科学基金(2010JK409)资助项目
关键词 层状氢氧化氨基苯甲酸锌 层状碱金属盐(LBMS) 水热合成 剥离反应 纳米单元片 layered hydroxide zinc aminobenzoate compound, layered basic metal salt, hydrothermal synthesis, exfoliation reaction, nanosheet
  • 相关文献

参考文献23

  • 1Johnsen R E,Wu Q L,Sjastacl A O,et al. [J]. J Phys Chem C, 2008,112(43) : 16733-16739.
  • 2Sasaki,T. [J]. J Ceramic Soc Jpn. ,2007,115(1137) : 9-16.
  • 3Li L, Ma R, Ebina Y, et al. [J]. Chem Mater, 2005,17 (17) : 4386-4391.
  • 4Ma R,Liu Z, Takada K, et al. [J]. J Am Chem Soc, 2007, 129 (16):5257-5263.
  • 5Takagaki A, Sugisawa M, Lu D, et al. [J]. J Am Chem Soc, 2003,125 (18) : 5479-5485.
  • 6Lei L, Vijayan R P,O' Hare D. [J]. J Mater Chem, 2001, 11 (12) : 3276-3280.
  • 7Tunney J J, Detellier C. [J]. J Mater Chem, 1996,6 (10) : 1679- 1685.
  • 8Inoue M,Kominami H,Kondo Y,et al. [J]. Chem Mater, 1997, 9(7) : 1614-1619.
  • 9Poul L, Jouini N, Fievet F J.[J]. Chem Mater, 2000,12 (10) :3123-3132.
  • 10Ogata S, Tasaka Y, Tagaya H, et al. [J]. Chem Lett, 1998,27 (3) :237 -240.

二级参考文献32

  • 1苗建英,赵立芳,刘宗怀.层状氢氧化苯甲酸锌的水热合成与表征[J].物理化学学报,2006,22(2):193-197. 被引量:2
  • 2Jose,M., Masahiro,Y.J.Am.Chem.Soc.,2001,123:741.
  • 3Nalwa,H.S.Handbook of nanostructured material and nanotechnology.San Diego:Academic Press,1999:Chap.1.
  • 4Morioka,H., Tagaya,H., Karasu,M., Kadokawa,J., Chiba,K.J.Solid State Chem.,1995,117:337.
  • 5Tunney,J.J., Detellier,C.J.Mater.Chem.,1996,6:1679.
  • 6Inoue,M., Kominami,H., Kondo,Y., Inui,T.Chem.Mater.,1997,9:1614.
  • 7Poul,L., Jouini,N., Fievet,F.Chem.Mater.,2000,12:3123.
  • 8Ogata,S., Tasaka,Y., Tagaya,H., Kadokawa,J., Chiba,K.Chem.Lett.,1998:237.
  • 9Ogata,S., Tagaya,H., Karasu,M., Kadokawa,J.J.Mater.Chem.,2000,10:321.
  • 10Reynolds,D.C., Look,D.C., Jogai,B., Hoelscher,J.E.J.Appl.Phys.,2000,88:2152.

共引文献14

同被引文献40

  • 1左春英,丁言镁,王建华.微波的生物非热效应的机理研究[J].沈阳师范大学学报(自然科学版),2005,23(3):254-257. 被引量:17
  • 2池建伟,张勇,魏振承.微波处理对香蕉多酚氧化酶活性的影响[J].广东农业科学,2006,33(11):86-88. 被引量:21
  • 3周本省.工业水处理技术[M].北京:化学工业出版社,2000..
  • 4Sakurai A,Toyoda S,Sakakibara M.Removal of bisphenol A by polymerization and precipitation method using Coprinus cinereus peroxidase[J].Biotechnol Lett,2001,23(12):995-998.
  • 5Klibanov A M,Morris E D,Felshin L M.Enzymatic removal of toxic phenols and anilines from waste waters[J].Appl Biochem,1980,4(2):414-421.
  • 6Gomez J,Bastid E,Hidalgo J,et al.Immobilization of peroxidase on glass beads:An improved alternative for phenol removal[J].Enzyme Microb Tech,2006,39(5):1016-1022.
  • 7Cheng J,Yu S M,Zuo P.Horseradish peroxidase immobilized on aluminum-pillared interlayered clay for the catalytic oxidation of phenolic waster[J].Water Res,2006,40(2):283-290.
  • 8Ai Z H,Yang P,Lu X H.Degradation of 4-chlorophenol by microwave irradiation enhanced advanced oxidation processes[J].Chemosphere,2005,60(6):824-827.
  • 9Renzo C,Francesco D.The enhancing effect of low power microwaves on phenol oxidation by the Fenton process[J].J Environ Chem Eng,2013,1(4):1292-1300.
  • 10Ince N H,Tezcanli G,Belen R K,et al.Ultrasound as a catalyzer of aqueous reaction systems:the state of the art and environmental application[J].Appl Cat B:Environ,2001,29(3):167-176.

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部