期刊文献+

pH调节剂对溶液燃烧法制备纳米LaFeO_3的影响 被引量:1

Effect of pH regulator on nanocrystalline LaFeO_3 Prepared by solution combustion synthesis
在线阅读 下载PDF
导出
摘要 以硝酸镧和硝酸铁为氧化剂,柠檬酸为燃料,采用溶液燃烧法制备了钙钛矿型LaFeO3。通过XRD和SEM表征,分别研究了以乙二胺和NaOH溶液为pH调节剂,前驱物溶液在不同pH值条件下,对制备的纳米LaFeO3粉体的晶相组成和微观形貌的影响。结果表明:前驱物溶液pH值对燃烧产物的晶相组成、晶粒大小和微观相貌都有显著的影响。乙二胺调节前驱物溶液pH值为3至12时,在300℃燃烧条件下获得为无定形产物,而在600℃均可制得纯相LaFeO3纳米晶体。NaOH溶液为pH调节剂,前驱物溶液在pH值5至13范围内,在300℃的条件下均能制得纯相LaFeO3纳米晶体;其中pH=7的中性环境中产物为蓬松多孔网状纳米结构,具有最大的晶粒尺30.5 nm,而在酸性和碱性环境中制得的产物均为无规则颗粒的聚集体。 Perovskite compound LaFeO3 was prepared by solution combustion synthesis using lanthanum nitrate and ferric nitrate as oxidants,citric acid as organic fuel.Effect of pH value of precursor solution on phase composition and morphology of LaFeO3 employing ethylenediamine and NaOH solution as pH regulator,respectively,was investigated by using X-ray diffraction(XRD)and scanning electron microscope(SEM).The results showed that the pH regulator and the pH value of precursor solution had significant effect on the phase composition,crystallite size and morphology of LaFeO3.When the pH value of precursor solution was adjusted to the range of 3-12 by ethylenediamine,only amorphous products were obtained at 300 ℃,while pure phase LaFeO3 could be obtained at 600 ℃.In contrast to this,using NaOH solution as pH regulator,pure phase LaFeO3 could be obtained in the pH range of 5 to 13 at 300 ℃,and the LaFeO3 nanocrystal prepared at pH=7 had a net-like porous structure with the largest crystallite size of 30.5 nm.However,under the acidic and basic conditions,the obtained LaFeO3 products were an aggregate of irregular particles.
机构地区 暨南大学化学系
出处 《化学研究与应用》 CAS CSCD 北大核心 2011年第6期779-783,共5页 Chemical Research and Application
关键词 PH调节剂 溶液燃烧合成 LAFEO3 pH value solution combustion synthesis LaFeO3
作者简介 联系人简介:杨骏(1967-),男,副教授,主要从事无机材料合成及多相催化研究。Email:tyangi@jnu.edu.cn
  • 相关文献

参考文献19

  • 1Sun L H, Qin H W, Cao E S, Zhao M, Gao F, Hu J F. Gassensing properties of perovskite La0.875 Ba0.125 FeO3 nanocrystalline powders [ J ]. J. Phys. Chem. Solids, 2011,72 : 29 -33.
  • 2Parida K M, Reddy K H, Martha S, Das D P, Biswal N. Fabrication of nanoerystalline LaFeO3 : An efficient sol-gel auto-combustion assisted visible light responsive photoeatalyst for water decomposition [ J ]. Int. J. Hydrogen. Energ,2010,35:12161-12168.
  • 3钟慧琼,杨骏,张渊明.制备方法对LaFeO_3可见光光催化活性的影响[J].中国有色金属学报,2009,19(1):160-166. 被引量:9
  • 4Yang J, Zhong H Q, Li M, Zhang L Z, Zhang Y M. Markedly enhancing the visible photocatalytic activity of LaFeO3 by post-treatment in molten salt[ J]. React. Kinet. Catal. Lett. 2009,97:269-274.
  • 5Li S, Jing L, Fu W, Yang L, Xin B, Fu H. Photoindueed charge property of nanosized perovskite-type LaFeO3 and its relationships with photocatalytic activity under visible irradiation [J]. Mater Res Bull 2007,42:203-212.
  • 6Yang M, Xu A, Du H, Sun C, Li C. Removal of salicylic acid on perovskite-type oxide LaFeO3 catalyst in catalytic wet air oxidation process[J]. J Hazard Mater,2007,139: 86 -92.
  • 7Sadakane M, Horiuchi T, Kato N, Sasaki K, Ueda W, Preparation of three-dimensionally ordered macroporous perovskite-type lanthanum-iron-oxide LaFeO3 with tunable pore diameters:high porosity and photonic property[ J ]. J. Solid State Chem. 2010,183 : 1365-1371.
  • 8Li F T, Liu Y, Liu R H, Sun Z M, Zhao D S, Kou C G. Preparation of Ca-doped LaFeO3 nanopowders in a reverse microemulsion and their visible light photocatalytic activity [J]. Mater. Lett. 2010,64:223-225.
  • 9Furukawa M, Iseya T, Itoh S, Anzai A, Sato K, Kurihara M, Sakamoto M, Aono H, Sadaoka Y, Hamakawa S, Hoshi Y, Mizukami F. Effect of preparation techniques of LaFeO3 Perovskite-type oxide on its surface morphologies [ J ] J. Ceramic Soc. Japan. 2007,115 (10) :640-642.
  • 10Shabbir G, Qureshi A H, Saeed K. Nano-crystalline LaFeO3 powders synthesized by the citrate-gel method [ J ]. Mater Lett,2006 ;60 : 3706-3709.

二级参考文献53

  • 1关鲁雄,李家元,王婷,李娟,钟文毅.掺杂铜和钒的纳米二氧化钛的光催化性能[J].中南大学学报(自然科学版),2006,37(4):731-736. 被引量:31
  • 2雷波,徐悦华,郭来秋,罗海燕.Ce-TiO_2/硅藻土的制备、表征及其光催化活性[J].中国有色金属学报,2007,17(5):795-799. 被引量:12
  • 3HOFFMANN M R, MARTIN S T, CHOI W, BAHNEMANN D W. Environmental applications of semiconductor photocatalysis [J]. Chem Rev, 1995, 95: 69-96.
  • 4SCHWITZGEBEL J, EKERDT J G, GERISCHTER H, HELLER A. Role of the oxygen molecule and the photogenerated electron in TiO2-photocatalyzed air oxidation reactions[J]. J Plays Chem, 1995, 99: 5633-5638.
  • 5CARP O, HUISMAN C L, RELLER A. Photoinduced reactivity of titanium dioxide[J]. Prog Solid State Chem, 2004, 32: 33-177.
  • 6LITTER M I. Heterogeneous photocatalysis transition metal ions in photocatalytic system[J]. Appl Catal B: Environ, 1999, 23: 89-114.
  • 7KIEBLING D, SCHNEIDER R, KRAAK E HAFTENDORN M, WENDT G. Perovskite-type oxides-catalysts for the total oxidation of chlorinated hydrocarbons [J ]. Appl Catal B: Environ, 1998, 19: 143-151.
  • 8YIN J, ZOU Z G, YE J H. Photophysical and photocatalytic properties of MIno.sNbo.503 (M =Ca, Sr, and Ba)[J]. J Phys Chem B, 2003, 107: 61-65.
  • 9JING L Q, xu z L, SUN X J, SHANG J, CAI W M. The surface properties and photocatalytic activities of ZnO ultrafine particles[J]. Appl Surf Sci, 2001, 180: 308-314.
  • 10LI X Z, LI F B, YANG C L, GE W K. Photocatalytic activity of WOx-TiO2 under visible light irradiation[J]. J Photoch Photobio A: Chem, 2001, 141: 209-217.

共引文献60

同被引文献5

引证文献1

二级引证文献1

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