• 综合
  • 标题
  • 关键词
  • 摘要
  • 学者
  • 期刊-刊名
  • 期刊-ISSN
  • 会议名称
搜索

作者:

Ouyang, Teng (Ouyang, Teng.) | Zhai, Chengwei (Zhai, Chengwei.) | Sun, Jihong (Sun, Jihong.) (学者:孙继红) | Panezai, Hamida (Panezai, Hamida.) | Bai, Shiyang (Bai, Shiyang.)

收录:

EI Scopus SCIE

摘要:

Nanosol precursor was obtained via hydrothermal pre-crystallization time periods of 6, 60 and 102 h at 423 K. Different amounts of nanosol precursor with different crystallization time periods were added to the hydrothermal synthesis system as structural promoter (SP) to synthesize clinoptilolite. The various characterizations such as XRD, SEM, BET, FT-IR, TG-DSC, ICP, UV-Raman, and element analysis were employed to investigate the structural and textural characteristics and potential applications of synthetic clinoptilolites in CH4/N-2 separation. Their activation energies of induction (E-n) and growth (E-g) periods during crystallization intervals were calculated according to Arrhenius equation, where the former being much larger than the latter proved that nucleation is the key in the synthesis of clinoptilolite. The E-n value gradually decreased with increasing amount of the SP and its pre-crystallization time interval, which further revealed that the addition of SP with the shortened crystallization time is beneficial in the formation of crystal nuclei. However, the amount of SP significantly altered the particle size, extent of impurities (phillipsite), and thermal stability of the clinoptilolite. The results demonstrated that pure clinoptilolite could be successfully synthesized in a short time period at low temperature. Particularly, the ion exchange performance and CH4/N-2 separation capacity of clinoptilolite synthesized with the additive SP (3 wt %) in the pre-crystallization interval of 60 h were found almost in similarity with the clinoptilolite prepared without SP, showing a promising adsorbent for kinetic separation of CH4/N-2.

关键词:

CH4/N-2 separation Clinoptilolite Hydrothermal synthesis Ion exchange performance Structural promoter

作者机构:

  • [ 1 ] [Ouyang, Teng]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China
  • [ 2 ] [Zhai, Chengwei]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China
  • [ 3 ] [Sun, Jihong]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China
  • [ 4 ] [Panezai, Hamida]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China
  • [ 5 ] [Bai, Shiyang]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China

通讯作者信息:

  • 孙继红

    [Sun, Jihong]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China;;[Bai, Shiyang]Beijing Univ Technol, Dept Chem & Chem Engn, Beijing Key Lab Green Catalysis & Separat, 100 PingLeYuan, Beijing 100124, Peoples R China

电子邮件地址:

查看成果更多字段

相关关键词:

来源 :

MICROPOROUS AND MESOPOROUS MATERIALS

ISSN: 1387-1811

年份: 2020

卷: 294

5 . 2 0 0

JCR@2022

ESI学科: MATERIALS SCIENCE;

ESI高被引阀值:37

JCR分区:1

被引次数:

WoS核心集被引频次: 12

SCOPUS被引频次: 13

ESI高被引论文在榜: 0 展开所有

万方被引频次:

中文被引频次:

近30日浏览量: 2

在线人数/总访问数:313/2923251
地址:北京工业大学图书馆(北京市朝阳区平乐园100号 邮编:100124) 联系我们:010-67392185
版权所有:北京工业大学图书馆 站点建设与维护:北京爱琴海乐之技术有限公司