Thermochemical Synthesis of Molybdenum Carbide on the Basis of the (NH4)6Mo7O24-NH4NO3-C6H12N4 System

被引:0
作者
Podbolotov, K. B. [1 ]
Egorova, Yu. A. [1 ]
Dogotar', L. V. [1 ]
Vasilevich, S. V. [2 ]
Asadchii, A. N. [3 ]
机构
[1] Natl Acad Sci Belarus, Inst Phys & Technol, Minsk 220084, BELARUS
[2] Belarusian State Acad Aviat, Minsk 220096, BELARUS
[3] Natl Acad Sci Belarus, Power Engn Inst, Minsk 220072, BELARUS
关键词
molybdenum carbide; molybdenum; molybdenum oxides; solution combustion synthesis; thermal reduction; TRANSITION-METAL CARBIDES; HYDROGEN-PRODUCTION; MO2C; CATALYSTS; METHANOL;
D O I
10.1134/S0020168524701528
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Data on the thermochemical synthesis of molybdenum carbide on the basis of the (NH4)(6)Mo7O24-NH4NO3-C6H12N4 system at different component ratios have been reported. Thermodynamic computations have been performed to establish composition regions for probable exothermic reactions to produce molybdenum carbide: 10-20 moles of ammonium nitrate per 1 mole of ammonium molybdate and the ratio of reducing agent to oxidizing agent (phi) equal to 1.5-4.0. It has been found that the reaction in ammonium molybdate-ammonium nitrate-urotropin system includes several stages, the main exothermic reaction is observed after temperature of 120-180 degrees C is reached. Molybdenum carbide forms at phi >= 6.5 after thermal treatment at 1000 degrees C under inert atmosphere. The reaction leads to fine crystalline structure of particles with size of 100-200 nm. The obtained materials based on molybdenum carbide show catalytic activity in the conversion of products of incomplete combustion of biofuel (pyrolysis resins). Addition of the obtained materials to pyrolysis resin in 1/10 ratio enhances its conversion (rate parameter increases by 2-10 times), reduces average process temperature by 50-100 degrees C, and decreases activation energy from 82 to 52-65 kJ/mol.
引用
收藏
页码:1205 / 1215
页数:11
相关论文
共 34 条
[1]   Kinetic model of indole HDN over molybdenum carbide:: influence of potassium on early and late denitrogenation pathways [J].
Adamski, G ;
Dyrek, K ;
Kotarba, A ;
Sojka, Z ;
Sayag, C ;
Djéga-Mariadassou, G .
CATALYSIS TODAY, 2004, 90 (1-2) :115-119
[2]   Alternative catalytic materials: carbides, nitrides, phosphides and amorphous boron alloys [J].
Alexander, Anne-Marie ;
Hargreaves, Justin S. J. .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (11) :4388-4401
[3]   Hydrogenation and ring opening of naphthalene on bulk and supported Mo2C catalysts [J].
Ardakani, Shahrzad Jooya ;
Liu, Xuebin ;
Smith, Kevin J. .
APPLIED CATALYSIS A-GENERAL, 2007, 324 :9-19
[4]   Hydrogen production in the decomposition and steam reforming of methanol on Mo2C/carbon catalysts [J].
Barthos, Robert ;
Solymosi, Frigyes .
JOURNAL OF CATALYSIS, 2007, 249 (02) :289-299
[5]   BAND-STRUCTURE OF TRANSITION-METAL COMPOUNDS [J].
CALAIS, JL .
ADVANCES IN PHYSICS, 1977, 26 (06) :847-885
[6]   Synthesis, characterization and application of nano-structured Mo2C thin films [J].
Chen, HY ;
Chen, L ;
Lu, Y ;
Hong, Q ;
Chua, HC ;
Tang, SB ;
Lin, J .
CATALYSIS TODAY, 2004, 96 (03) :161-164
[7]   In situ preparation of oxide-based supported catalysts by solution combustion synthesis [J].
Dinka, P ;
Mukasyan, AS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (46) :21627-21633
[8]   Controlling combustion wave propagation for transition metal/alloy/cermet foam synthesis [J].
Erri, Peter ;
Nader, Jose ;
Varma, Arvind .
ADVANCED MATERIALS, 2008, 20 (07) :1243-+
[9]   Hydrodeoxygenation of solvolysed lignocellulosic biomass by unsupported MoS2, MoO2, Mo2C and WS2 catalysts [J].
Grilc, M. ;
Veryasov, G. ;
Likozar, B. ;
Jesih, A. ;
Levec, J. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2015, 163 :467-477
[10]   Molybdenum Carbide-Catalyzed Conversion of Renewable Oils into Diesel-like Hydrocarbons [J].
Han, Junxing ;
Duan, Jinzhao ;
Chen, Ping ;
Lou, Hui ;
Zheng, Xiaoming .
ADVANCED SYNTHESIS & CATALYSIS, 2011, 353 (14-15) :2577-2583