Progresses in the Preparation of Coke Resistant Ni‐based Catalyst for Steam and CO2 Reforming of Methane

蒸汽重整 焦炭 甲烷转化炉 甲烷 催化作用 合成气 二氧化碳重整 合成气制汽油 化学工程 制氢 催化重整 碳纤维 化学 材料科学 废物管理 有机化学 复合材料 复合数 工程类
作者
Changjun Liu,Jingyun Ye,Jiaojun Jiang,Yun‐Xiang Pan
出处
期刊:Chemcatchem [Wiley]
卷期号:3 (3): 529-541 被引量:587
标识
DOI:10.1002/cctc.201000358
摘要

Abstract Steam reforming of methane is an extremely important process for the hydrogen and syngas production. Nickel‐based catalysts have been extensively employed in the industrial process of steam reforming because of their high activity, low cost, and the plentiful supply of Nickel. Nickel‐based catalysts have also shown high activity for CO 2 reforming of methane, which has been considered as a good option, with consumption of a significant amount of carbon dioxide. However, a major challenge is that Ni catalysts have a high thermodynamic potential for coke formation during reforming reactions. For steam reforming, coke formation induces deactivation of the catalyst, especially if the carbon forms as carbon filaments. The filamentous carbon material has a high mechanical strength and can cause mechanical deformation of the catalyst. For CO 2 reforming, coke formation over Ni catalyst is even more serious and leads to rapid deactivation of the catalyst. It is highly desired to design and synthesize a coke resistant Ni catalyst not only for reforming of methane, but also for reforming of other hydrocarbons (including biomass derived hydrocarbons). Herein we summarize the very recent progresses in the design, synthesis, and characterization of coke resistant Ni catalysts for steam and CO 2 reforming of methane. The progresses in the use of promoters, in the effect of supporting materials and in the preparation methods have been discussed. The thermal stability, regeneration, and future development of coke resistant Ni catalysts for these processes are also briefly addressed.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
热热带汤完成签到,获得积分10
1秒前
初景发布了新的文献求助10
1秒前
万能图书馆应助FuTing采纳,获得10
2秒前
molihuakai应助汉皇高祖采纳,获得30
2秒前
翟文艳发布了新的文献求助10
3秒前
777完成签到 ,获得积分10
5秒前
爆米花应助xtx采纳,获得10
5秒前
大知闲闲应助贲耷采纳,获得10
6秒前
东方发布了新的文献求助10
6秒前
今后应助zhongkaizhao采纳,获得10
6秒前
完美世界应助呆桃采纳,获得10
8秒前
whitelex77完成签到 ,获得积分10
9秒前
丘比特应助腼腆的妖妖采纳,获得10
9秒前
10秒前
10秒前
七月兔完成签到,获得积分10
10秒前
思念变成王年年完成签到,获得积分10
10秒前
ambition完成签到,获得积分10
10秒前
11秒前
小马甲应助合适乐萱采纳,获得10
11秒前
12秒前
张欢馨应助dg_fisher采纳,获得10
13秒前
张欢馨应助dg_fisher采纳,获得10
13秒前
科目三应助dg_fisher采纳,获得10
13秒前
SciGPT应助dg_fisher采纳,获得10
13秒前
13秒前
彩色金针菇完成签到,获得积分10
14秒前
FashionBoy应助dg_fisher采纳,获得10
14秒前
研友_VZG7GZ应助dg_fisher采纳,获得10
14秒前
chenhouhan发布了新的文献求助20
14秒前
香蕉觅云应助dg_fisher采纳,获得10
14秒前
aa发布了新的文献求助10
14秒前
Nole应助dg_fisher采纳,获得30
14秒前
Y888888应助dg_fisher采纳,获得30
14秒前
14秒前
博修发布了新的文献求助10
14秒前
翟文艳完成签到,获得积分10
15秒前
15秒前
妮妮完成签到 ,获得积分20
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
APA handbook of comparative psychology: Basic concepts, methods, neural substrate, and behavior 1000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7609892
求助须知:如何正确求助?哪些是违规求助? 9185563
关于积分的说明 19677196
捐赠科研通 7183581
什么是DOI,文献DOI怎么找? 3270335
关于科研通互助平台的介绍 2434013
邀请新用户注册赠送积分活动 2264893