Abst'/> Novel inorganic precursors [Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/SiO_2 and Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/Al_2O_3 for Fischer-Tropsch synthesis
首页> 外文期刊>International journal of hydrogen energy >Novel inorganic precursors [Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/SiO_2 and Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/Al_2O_3 for Fischer-Tropsch synthesis
【24h】

Novel inorganic precursors [Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/SiO_2 and Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6]/Al_2O_3 for Fischer-Tropsch synthesis

机译:新型无机前体[Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6] / SiO_2和Co_(4.32)Zn_(1.68)(HCO_2)_(18)(C_2H_8N)_6] / Al_2O_3费-托合成

获取原文
获取原文并翻译 | 示例
       

摘要

AbstractThe silica- and alumina-supported Co–Zn catalysts were synthesized by thermal decomposition of new inorganic precursors [Co4.32Zn1.68(HCO2)18(C2H8N)6]/SiO2or Al2O3. A novel coordination polymer formulated as [Co4.32Zn1.68(HCO2)18(C2H8N)6] (1) was prepared using the solvothermal technique and characterized by elemental analysis, FT-infrared spectroscopy. Thermal stability of the complex1was investigated by thermogravimetric analysis and differential scanning calorimetry, and its structure was determined by single-crystal X-ray diffraction. Characterization of catalysts was carried out using powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and BET specific surface area. The catalysts were evaluated for Fischer–Tropsch synthesis (FTS) in the temperature range 200–300 °C. The results revealed that the synthesized catalysts have higher selectivity to the desired products at 260 °C. The performance of the catalysts was compared to those of catalysts constructed via impregnation method and the fabricated catalysts show higher activity and selectivity than the reference catalysts.Graphical abstractDisplay OmittedHighlightsThe Co–Zn catalysts were synthesized through new inorganic precursors.The synthesized catalysts are more active than impregnation reference samples.The fabricated catalysts have higher selectivity to olefins than reference samples.
机译: 摘要 通过热分解新的无机前体合成二氧化硅和氧化铝负载的Co-Zn催化剂[Co 4.32 1.68 (HCO 2 )< ce:inf loc =“ post”> 18 (C 2 H 8 N) 6 ] / SiO 2 或Al 2 O 3 。新型配位聚合物,配制成[Co 4.32 Zn 1.68 (HCO 2 18 (C 2 H 8 N) 6 ]( 1 )是使用溶剂热技术制备的,并通过元素分析,FT红外光谱进行了表征。通过热重分析和差示扫描量热法研究了配合物 1 的热稳定性,并通过单晶X射线衍射确定了其结构。使用X射线衍射(XRD)粉末,扫描电子显微镜(SEM)和BET比表面积对催化剂进行表征。在200–300°C的温度范围内对催化剂的费-托合成(FTS)进行了评估。结果表明,合成的催化剂在260°C下对所需产物具有更高的选择性。将该催化剂的性能与浸渍法制备的催化剂进行了比较,所制得的催化剂的活性和选择性均高于参比催化剂。 图形摘要 省略显示 突出显示 钴锌催化剂是通过新的无机前体合成的。 合成的催化剂比浸渍参考样品具有更高的活性。 与参考样品相比,制备的催化剂对烯烃的选择性更高。 /为什么:p>

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号