Zn Modification of Pd/TiO2/Ti Catalyst for CO Oxidation

催化作用 傅里叶变换红外光谱 吸附 扫描电子显微镜 程序升温还原 无机化学 氧化还原 化学 材料科学 核化学 分析化学(期刊) 化学工程 物理化学 生物化学 工程类 色谱法 复合材料
作者
Payam Samadi,Michal J. Binczarski,Waldemar Maniukiewicz,Aleksandra Pawlaczyk,Jacek Rogowski,E. Szubiakiewicz,M. I. Szynkowska,I. Witońska
出处
期刊:Materials [MDPI AG]
卷期号:16 (3): 1216-1216 被引量:6
标识
DOI:10.3390/ma16031216
摘要

The main goal of this study was to modify the activity of Pd/TiO2/Ti catalyst in the reaction of CO oxidation by the addition of Zn. Plasma electrolytic oxidation (PEO) of Ti wire was conducted to produce a uniform porous layer of TiO2. A mixture of Pd and Zn was then introduced by means of adsorption. After reduction treatment, the activity of the samples was examined by oxidation of 5% CO in a temperature range from 80–350 °C. Model catalysts with sufficient amounts of the metals for physico-chemical investigation were prepared to further investigate the reaction between Pd and Zn during CO oxidation. The structures and compositions of the samples were investigated using scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS), time-of-flight secondary ion mass spectrometry (TOF-SIMS), inductively coupled plasma mass spectrometry (ICP-MS), Fourier transform infrared (FTIR), and X-ray diffraction (XRD). Modification of Pd/TiO2/Ti catalyst by Zn with a Pd:Zn atomic ratio of 2:1 decreased the temperature of complete CO oxidation from 220 °C for Pd/TiO2/Ti to 180 °C for Pd-Zn/TiO2/Ti. The temperature of 50% CO conversion on Pd-Zn(2:1)/TiO2/Ti was around 55 °C lower than in the reaction on monometallic Pd catalyst. The addition of Zn to the Pd catalyst lowered the binding energy of CO on the surface and improved the dissociative adsorption of oxygen, facilitating the oxidation of CO. FTIR showed that the bridging form of adsorbed CO is preferred on bimetallic systems. Analysis of the surface compositions of the samples (SEM-EDS, TOF-SIMS) showed higher amounts of oxygen on the bimetallic systems.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
汉堡包应助xmy采纳,获得10
1秒前
cizzz完成签到,获得积分10
1秒前
mayocoh发布了新的文献求助10
1秒前
Cclaaa完成签到 ,获得积分10
2秒前
意未清完成签到,获得积分10
2秒前
3秒前
啊啊啊啊完成签到,获得积分10
4秒前
jack发布了新的文献求助10
4秒前
野性的枕头应助呆呆采纳,获得10
4秒前
明明就完成签到 ,获得积分10
5秒前
大模型应助坦率曼寒采纳,获得10
6秒前
8秒前
8秒前
hou发布了新的文献求助10
9秒前
10秒前
demon发布了新的文献求助10
10秒前
11秒前
doctorw完成签到,获得积分0
11秒前
雪落年轮完成签到,获得积分10
11秒前
一一发布了新的文献求助10
11秒前
11秒前
Akim应助王里走采纳,获得10
12秒前
彭于晏应助端庄的白开水采纳,获得10
13秒前
13秒前
orixero应助亦玉采纳,获得10
13秒前
冬虫夏草完成签到,获得积分10
14秒前
caoju完成签到 ,获得积分10
14秒前
赘婿应助housii采纳,获得10
15秒前
情怀应助科研通管家采纳,获得10
16秒前
浮游应助科研通管家采纳,获得10
16秒前
浮游应助科研通管家采纳,获得10
16秒前
半个丸子发布了新的文献求助10
16秒前
zhonglv7应助科研通管家采纳,获得10
16秒前
慕青应助科研通管家采纳,获得10
16秒前
16秒前
大模型应助科研通管家采纳,获得10
16秒前
派大星应助科研通管家采纳,获得20
16秒前
香蕉觅云应助科研通管家采纳,获得10
16秒前
客服小祥应助科研通管家采纳,获得10
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
On the Angular Distribution in Nuclear Reactions and Coincidence Measurements 1000
Vertébrés continentaux du Crétacé supérieur de Provence (Sud-Est de la France) 600
A complete Carnosaur Skeleton From Zigong, Sichuan- Yangchuanosaurus Hepingensis 四川自贡一完整肉食龙化石-和平永川龙 600
FUNDAMENTAL STUDY OF ADAPTIVE CONTROL SYSTEMS 500
微纳米加工技术及其应用 500
Nanoelectronics and Information Technology: Advanced Electronic Materials and Novel Devices 500
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 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5308436
求助须知:如何正确求助?哪些是违规求助? 4453578
关于积分的说明 13857553
捐赠科研通 4341263
什么是DOI,文献DOI怎么找? 2383753
邀请新用户注册赠送积分活动 1378386
关于科研通互助平台的介绍 1346379