欢迎登录材料期刊网

材料期刊网

高级检索

利用石墨型氮化碳(C3N4)和氨硼烷(NH3BH3,AB)球磨制备了AB-C3N4体系,发现C3N4的加入使AB放氢反应温度明显降低,但是副产物氨气浓度有所升高.因此,利用LiBH4改性的C3N4 (LC3N4)同AB球磨合成出了AB-LC3N4体系,并采用X射线衍射、程序升温脱附-质谱联用、热重-差热分析及核磁共振等技术考察了该体系的脱氢性能.结果表明,由于LC3N4的加入,AB的放氢反应温度明显降低,放氢反应速率加快,放氢诱导期缩短,同时抑制了副产物无机苯的生成.另外,C3N4的化学修饰也降低了AB-LC3N4放氢过程中生成氨气的浓度.动力学分析和核磁共振结果表明,AB-LC3N4分解过程依然遵循NH3BH2NH3BH4诱导的氨硼烷自分解机理.

参考文献

[1] Rosi NL.;Eckert J.;Eddaoudi M.;Vodak DT.;Kim J.;O'Keeffe M.;Yaghi OM. .Hydrogen storage in microporous metal-organic frameworks[J].Science,2003(5622):1127-1129.
[2] Bogdanovi(c) B;Schwickardi M .[J].Journal of Alloys and Compounds,1997,253-254:1.
[3] Chen P;Xiong ZT;Luo JZ;Lin JY;Tan KL .Interaction of hydrogen with metal nitrides and imides[J].Nature,2002(6913):302-304.
[4] Wolf G.;Baitalow F.;Hoffmann FP.;Baumann J. .Calorimetric process monitoring of thermal decomposition of B-N-H compounds[J].Thermochimica Acta: An International Journal Concerned with the Broader Aspects of Thermochemistry and Its Applications to Chemical Problems,2000(1/2):19-25.
[5] Hu M G;Geanangel R A;Wendlandt W W .[J].Thermochimica Acta,1978,23:249.
[6] Gutowska A;Li L;Shin Y;Wang C M,Li X S,Linehan J C,Smith R S,Kay B D,Schmid B,Shaw W,Gutowski M,Autrey T .[J].Angewandte Chemie International Edition,2005,44:3578.
[7] He T;Xiong Z T;Wu G T;Chu H L Wu C Z Zhang T Chen P .[J].Chemistry of Materials,2009,21:2315.
[8] Denney M C;Pons V;Hebden T J;Heinekey D M Goldberg K I .[J].Journal of the American Chemical Society,2006,128:12048.
[9] Bluhm M E;Bradley M G;Butterick R Ⅲ;Kusari U Sneddon L G .[J].Journal of the American Chemical Society,2006,128:7748.
[10] Stephens F H;Baker R T;Matus M H;Grant D J,Dixon D A .[J].Angewandte Chemie International Edition,2007,46:746.
[11] Neiner D;Luedtke A;Karkamkar A;Shaw W Wang J L Browning N D Autrey T Kauzlarich S M .[J].JPhys Chem C,2010,114:13935.
[12] Feaver A;Sepehri S;Shamberger P;Stowe A Autrey T Cao G Z .[J].Journal of Physical Chemistry B,2007,111:7469.
[13] Zhao J Z;Shi J F;Zhang X W;Cheng F Y Liang J Tao Z L Chen J .[J].Advanced Materials,2010,22:394.
[14] Ramachandran PV;Gagare PD .Preparation of ammonia borane in high yield and purity, methanolysis, and regeneration[J].Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics,2007(19):7810-7817.
[15] Wang, Y.;Yao, J.;Li, H.;Su, D.;Antonietti, M. .Highly selective hydrogenation of phenol and derivatives over a pd@carbon nitride catalyst in aqueous media[J].Journal of the American Chemical Society,2011(8):2362-2365.
[16] Pinkerton F E;Meisner G P;Meyer M S;Balogh M P Kundrat M D .[J].Journal of Physical Chemistry B,2005,109:6.
[17] Matsumoto S;Xie E Q;Izumi F .[J].Diamond and Related Materials,1999,8:1175.
[18] Heldebrant D J;Karkamkar A;Hess N J;Bowden M Rassat S Zheng F Rappe K Autrey T .[J].Chemistry of Materials,2008,20:5332.
[19] Kang X D;Fang Z Z;Kong L Y;Cheng H M Yao X D Lu G Q Wang P .[J].Advanced Materials,2008,20:2756.
[20] Stowe AC;Shaw WJ;Linehan JC;Schmid B;Autrey T .In situ solid state B-11 MAS-NMR studies of the thermal decomposition of ammonia borane: mechanistic studies of the hydrogen release pathways from a solid state hydrogen storage material[J].Physical chemistry chemical physics: PCCP,2007(15):1831-1836.
[21] Jürgens B;Irran E;Senker J;Kroll P Müller H Schnick W .[J].Journal of the American Chemical Society,2003,125:10288.
[22] Jüürgens B .[D].Munich:University of Munich (Germany,2004.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%