Synthesis of uniform Ni nanoparticles encapsulated in ZSM–5 for selective hydrodeoxygenation of phenolics

加氢脱氧 催化作用 除氧 ZSM-5型 茴香醚 初湿浸渍 沸石 化学 吸附 纳米颗粒 环己烷 金属 无机化学 材料科学 化学工程 有机化学 选择性 纳米技术 工程类
作者
Sen Li,Longhui Guo,Xinyu He,Congzhen Qiao,Yajie Tian
出处
期刊:Renewable Energy [Elsevier BV]
卷期号:194: 89-99 被引量:53
标识
DOI:10.1016/j.renene.2022.05.052
摘要

Bio–oil as the promising renewable resources to replace fossil fuels, requires upgrading into deoxygenated fuel. Zeolite supported base metal catalysts have been deemed highly efficient for the hydrodeoxygenation (HDO) of bio–oil, but facing a degraded activity due to metal aggregation. In this study, uniform Ni nanoparticles (∼4 wt%) encapsulated in ZSM–5 zeolites ([email protected]–5s) were synthesized by a one–pot method for catalytic HDO of phenolic compounds. The Ni dispersion was found to be significantly enhanced in the [email protected]–5s catalysts after encapsulation compared with a catalyst prepared by wetness impregnation (Ni/ZSM–5), which is ascribed to the strong interaction between the Ni and the zeolite surface. The [email protected]–5s catalysts show higher HDO activities for phenolics than the Ni/ZSM–5 catalyst, owing to the enhanced adsorption and spillover of active hydrogen by the highly dispersed Ni species. [email protected]–5–50 (Si/Al of 50) gave cyclohexane yield of 91.6% at 250 °C, through sequenced hydrogenation and deoxygenation of anisole. Moreover, the [email protected]–5–100 (Si/Al of 100) with decreased acidities further gave an enhanced TOF value for the conversion of phenolics. From the FT–IR spectrum obtained for adsorbed anisole, the reduction of acidities is determined to facilitate the desorption of intermediates, which accelerates the initial hydrogenation.
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
恋空完成签到,获得积分10
刚刚
DrHHB应助ll_kyt采纳,获得50
刚刚
刚刚
乐观兔子完成签到,获得积分10
刚刚
慕青应助轩少的采纳,获得10
刚刚
1秒前
1秒前
Wu完成签到,获得积分10
1秒前
英俊的铭应助GeoY采纳,获得10
1秒前
smilling发布了新的文献求助10
1秒前
噜啦噜啦嘞完成签到,获得积分10
1秒前
1秒前
2秒前
与山发布了新的文献求助10
2秒前
2秒前
香蕉觅云应助斯文的梦露采纳,获得10
2秒前
SciGPT应助斯文的梦露采纳,获得10
2秒前
2秒前
2秒前
2秒前
3秒前
yk完成签到,获得积分10
3秒前
xxz完成签到,获得积分10
3秒前
3秒前
123完成签到,获得积分20
4秒前
fxs完成签到,获得积分10
4秒前
4秒前
赘婿应助霖槿采纳,获得10
4秒前
111发布了新的文献求助10
5秒前
molihuakai应助majun采纳,获得10
5秒前
如梦如幻91完成签到,获得积分10
5秒前
Loooong完成签到,获得积分0
6秒前
Huggige完成签到 ,获得积分10
6秒前
6秒前
宓风华完成签到,获得积分10
6秒前
KKK发布了新的文献求助10
6秒前
6秒前
6秒前
7秒前
Wu发布了新的文献求助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
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
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 7745408
求助须知:如何正确求助?哪些是违规求助? 9293421
关于积分的说明 20219198
捐赠科研通 7324898
什么是DOI,文献DOI怎么找? 3307854
关于科研通互助平台的介绍 2459854
邀请新用户注册赠送积分活动 2319150