首页> 外文OA文献 >Synthesis and characterization of iridium/platinum-hzsm5 catalyst for isomerization of n-pentane
【2h】

Synthesis and characterization of iridium/platinum-hzsm5 catalyst for isomerization of n-pentane

机译:正戊烷异构化铱/铂-hzsm5催化剂的合成与表征

摘要

Catalytic isomerization of n-alkane has been one of the important processes in petrochemical refining industry to increase the octane number of gasoline. This study investigates the catalytic activity of Ir/Pt-HZSM5 for n-pentane isomerization. The potential of iridium (Ir) as a catalyst for n-pentane isomerization was preliminarily investigated by using Ir-HZSM5. The result showed that Ir has a great potential to be used as a promoter, hence as a co-promoter for Pt-HZSM5. Ir/Pt-HZSM5 was prepared by impregnation of Ir on 0.1wt% Pt-HZSM5. The catalyst was characterized with X-Ray Diffraction (XRD), Surface Area Analyzer, Fourier Transformation Infra Red (FTIR), Nuclear Magnetic Resonance (NMR), Electron Spin Resonance (ESR) and X-Ray Photoelectron Spectroscopy (XPS). The acidity was determined by 2,6-lutidine adsorbed FTIR spectroscopy, while the catalytic activity was carried out in a microcatalytic pulse reactor. The results showed that Ir in the form of IrO2 was bonded to perturbed silanol groups. The presence of 0.1 wt% Ir slightly increased the acidity of Pt-HZSM5 and selectivity of isopentane. Ir enhanced the formation of protonic acid sites which participate in the isomerization, and inhibited the formation of hydroxyl groups which may participate in the enhancement of the cracking reaction. An increase in Ir loading (0-2.0 wt%) continuously decreased the acid sites. At low Ir loading, cracking process proceed through dimerization-cracking step, whereas high Ir loading reduces the contribution of dimerization-cracking step and promotes the contribution of hydrogenolysis. An increase in Si/Al ratio (23-280) decreased the number of strong acid sites which led to a decrease in the activity towards n-pentane isomerization. From the Response Surface Methodology (RSM) experiments, the optimum conditions for the n-pentane isomerization over Ir/Pt-HZSM5 were at treatment temperature of 723 K, treatment time of 6 h, reaction temperature of 548 K and flow of hydrogen over weight of catalyst, F/W of 500 ml g-1 min-1 in which the predicted value for the n-pentane conversion, isopentane selectivity and isopentane yield was 63.0%, 98.2% and 61.9%, respectively. The catalytic activity studies confirmed that n-pentane isomerization over Ir/Pt-HZSM5 strongly depending on the promotive effect of hydrogen. Ir/Pt-HZSM5 exhibited high stability during the coke removal process which was shown by the high activity of Ir/Pt-HZSM5 in the n-pentane isomerization after 90 pulses (30 h).
机译:正构烷烃的催化异构化已成为石化炼油工业中提高汽油辛烷值的重要工艺之一。本研究研究了Ir / Pt-HZSM5对正戊烷异构化的催化活性。通过使用Ir-HZSM5,初步研究了铱(Ir)作为正戊烷异构化催化剂的潜力。结果表明,Ir具有很大的潜力用作启动子,因此可以作为Pt-HZSM5的共启动子。通过在0.1wt%的Pt-HZSM5上浸渍Ir来制备Ir / Pt-HZSM5。用X射线衍射(XRD),表面积分析仪,傅立叶变换红外(FTIR),核磁共振(NMR),电子自旋共振(ESR)和X射线光电子能谱(XPS)对催化剂进行了表征。通过2,6-二甲基吡啶吸附的FTIR光谱测定酸度,同时在微催化脉冲反应器中进行催化活性。结果表明,IrO2形式的Ir与受干扰的硅烷醇基键合。 0.1wt%Ir的存在稍微增加了Pt-HZSM5的酸度和异戊烷的选择性。 Ir增强了参与异构化的质子酸位点的形成,并抑制了可能参与裂化反应的增强的羟基的形成。 Ir负载量的增加(0-2.0wt%)连续降低了酸位。在低Ir负载下,裂化过程通过二聚化裂化步骤进行,而高Ir负载量则减少了二聚化裂化步骤的贡献,并促进了氢解作用。 Si / Al比(23-280)的增加减少了强酸位点的数量,这导致对正戊烷异构化的活性降低。根据响应表面方法学(RSM)实验,在Ir / Pt-HZSM5上进行正戊烷异构化的最佳条件是:处理温度为723 K,处理时间为6 h,反应温度为548 K,氢气流量超过重量催化剂的F / W为500ml g-1min-1,其中正戊烷转化率,异戊烷选择性和异戊烷产率的预测值分别为63.0%,98.2%和61.9%。催化活性研究证实,正戊烷在Ir / Pt-HZSM5上的异构化很大程度上取决于氢的促进作用。 Ir / Pt-HZSM5在除焦过程中表现出很高的稳定性,这表现为Ir / Pt-HZSM5在90个脉冲(30小时)后在正戊烷异构化中的高活性。

著录项

  • 作者

    Setiabudi Herma Dina;

  • 作者单位
  • 年度 2013
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

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