The influence of carbon supports and their surface modification on aqueous phase highly selective hydrogenation of phenol to cyclohexanol over different Ni/carbon catalysts

环己醇 催化作用 环己酮 苯酚 活性炭 无机化学 化学 碳纤维 水溶液 碳纳米管 材料科学 化学工程 有机化学 吸附 纳米技术 复合材料 复合数 工程类
作者
Zhepeng Zhao,Xiangyi Long,Marcos Millán,Guanming Yuan,Zhengwei Cui,Zhijun Dong,Ye Cong,Zhang Jiang,Xuanke Li
出处
期刊:Carbon [Elsevier BV]
卷期号:213: 118227-118227 被引量:31
标识
DOI:10.1016/j.carbon.2023.118227
摘要

Cyclohexanol is an important feedstock in the chemical industry. Highly selective hydrogenation of phenols to cyclohexanol over non-noble metal catalysts remains a challenge. Herein, four distinctive carbon materials, carbon black (CB), activated carbon (AC), activated carbon fiber (ACF) and carbon nanotube (CNT) were selected as catalyst supports to load Ni nanoparticles for effective phenol hydrogenation. The results show that the phenol conversion and cyclohexanol selectivity in aqueous phase hydrogenation reaction at 180 °C for 2 h over 10 wt% Ni/AC catalyst could reach 99.7% and 94.8%, respectively. These values are better than those obtained over 10 wt% Ni/ACF, Ni/CNT and Ni/Al2O3. After surface modification of carbon supports, the catalytic activity and reuse effect of modified catalysts are significantly enhanced and the optimal temperature decreases to 150 °C. This is because that modified carbon supports have abundant surface functional groups so as to provide a high dispersion and stable anchor of ultrafine active Ni nanoparticles (∼12 nm). Phenol hydrogenation catalyzed by different Ni/carbon catalysts conforms to a first-order reaction, and their apparent activation energies are in a range of 49∼68 kJ mol−1 (49 corresponds to the modified catalyst Ni/MAC), which are markedly lower than that of Ni/Al2O3 (∼96 kJ mol−1). The potential mechanism of highly selective hydrogenation of phenol to cyclohexanol in this work is mainly controlled by the reaction kinetics, which is closely related to the different desorption abilities of cyclohexanone and cyclohexanol from the catalysts.
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
陈平安应助粗犷的月饼采纳,获得10
刚刚
凝雁完成签到,获得积分10
1秒前
Steven完成签到,获得积分10
1秒前
萌萌哒完成签到,获得积分10
1秒前
1秒前
马天宇发布了新的文献求助10
1秒前
有钱发布了新的文献求助10
2秒前
2秒前
帅气忆秋完成签到,获得积分10
2秒前
2秒前
蓝天应助屎上雕花采纳,获得10
2秒前
小新XIAO发布了新的文献求助10
3秒前
一汪发布了新的文献求助10
3秒前
细心的发布了新的文献求助10
3秒前
NexusExplorer应助晒晒太阳采纳,获得10
3秒前
3秒前
Shawn完成签到,获得积分10
4秒前
mhy完成签到 ,获得积分10
4秒前
ableyy完成签到,获得积分10
4秒前
Amor完成签到,获得积分10
5秒前
JamesPei应助粗暴的方盒采纳,获得10
5秒前
桐桐应助粗暴的方盒采纳,获得10
5秒前
快乐大炮发布了新的文献求助10
5秒前
FashionBoy应助粗暴的方盒采纳,获得10
5秒前
传奇3应助粗暴的方盒采纳,获得10
5秒前
上官若男应助粗暴的方盒采纳,获得10
5秒前
华仔应助粗暴的方盒采纳,获得10
5秒前
隐形曼青应助粗暴的方盒采纳,获得10
5秒前
领导范儿应助粗暴的方盒采纳,获得10
5秒前
我是老大应助粗暴的方盒采纳,获得10
5秒前
5秒前
槲寄生发布了新的文献求助10
5秒前
scjgf应助dzjin采纳,获得10
6秒前
zzzzz完成签到,获得积分10
6秒前
菜鸟应助zbx采纳,获得50
6秒前
panpan完成签到,获得积分10
6秒前
ty7500发布了新的文献求助10
6秒前
11完成签到,获得积分10
6秒前
直率谷蕊发布了新的文献求助10
6秒前
帅气的惜天完成签到,获得积分10
7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
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6159901
求助须知:如何正确求助?哪些是违规求助? 7988060
关于积分的说明 16603138
捐赠科研通 5268283
什么是DOI,文献DOI怎么找? 2810896
邀请新用户注册赠送积分活动 1791166
关于科研通互助平台的介绍 1658105