Citation: CAO Xiao-feng, ZHANG Qi, JIANG Dong, LIU Qi-ying, MA Long-long, WANG Tie-jun, LI De-bao. Influence of calcination temperature on the performance of Ni/La(III) catalyst in the hydrogenolysis of sorbitol to low-carbon glycols[J]. Journal of Fuel Chemistry and Technology, ;2015, 43(8): 970-979. shu

Influence of calcination temperature on the performance of Ni/La(III) catalyst in the hydrogenolysis of sorbitol to low-carbon glycols

  • Corresponding author: JIANG Dong,  LIU Qi-ying, 
  • Received Date: 26 January 2015
    Available Online: 23 March 2015

    Fund Project: 国家自然科学基金(51376185) (51376185)国家重点基础研究发展规划(973计划,2012CB215304) (973计划,2012CB215304)国家高技术研究发展计划(863计划,2012AA101806) (863计划,2012AA101806)广东省自然科学基金(S2013010011612)。 (S2013010011612)

  • Nanorod-shaped La(OH)3 support was prepared by hydrothermal method, over which the supported Ni/La(III) catalysts were obtained through wet impregnation method; the influence of calcination temperature on the performance of Ni/La(III) catalyst in the hydrogenolysis of sorbitol to low-carbon glycols was then investigated by means of XRD, SEM/EDS, BET, H2-TPR-MS, CO/CO2-TPD-MS, ICP-AES and TG. The results revealed that the Ni/La(III) catalysts are highly active for sorbitol hydrogenolysis; the yield of low-carbon glycols reaches 53% after reaction at 220℃ and 4 MPa H2 for 1.5 h. The catalyst calcined at low temperature (500℃) is mainly in the form of NiO/La2O2CO3, which may transform into La2NiO4-La2O3 with the increase of calcination temperature. The basicity is a crucial factor for the hydrogenolysis activity; high calcionation temperature may enhance the basicity of the catalysts and then improve their hydrogenolysis activity, whereas the calcination temperature has little effect on the products selectivity. However, NiO/La2O2CO3 exhibits better hydrothermal stability than La2NiO4-La2O3 for sorbitol hydrogenolysis. The deactivation of catalysts can be attributed to the separation of active Ni particles from the support and the agglomeration of the active species, which may reduce the amount of the active metal sites and destroy the catalyst structure.
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