Improved catalytic NO oxidation over Pt supported on sulfuric acid treated TiO2

被引:1
作者
Bae, Wo Bin [1 ]
Park, Jiseok [2 ]
Go, You Jin [2 ]
Byun, Sang Woo [2 ]
Shin, Hyeonwoo [2 ]
Kim, Young Jin [3 ]
Jang, Jun Hee [1 ]
Kang, Sung Bong [2 ,4 ]
机构
[1] Rowan Univ, Dept Chem Engn, Glassboro, NJ 08028 USA
[2] Gwangju Inst Sci & Technol, Sch Environm & Energy Engn, Gwangju 61005, South Korea
[3] Kyungpook Natl Univ, Dept Environm Engn, Daegu 41566, South Korea
[4] Gwangju Inst Sci & Technol, Res Ctr Innovat Energy & Carbon Optimized Synth Ch, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
Pt/TiO2; Sulfuric acid treatment; NO oxidation; Surface acidity; Dispersion and phase; PLATINUM OXIDE FORMATION; REDUCTION; PT/AL2O3; IMPACT; DISPERSION; PRECURSOR; STORAGE; CHARGE; OXYGEN; MODEL;
D O I
10.1016/j.seppur.2024.130033
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Promoting the formation of metallic Pt over the catalysts is the key to improving the NO reactivity. In general, TiO2 suppresses the oxidation of Pt by surface acidity and induces the formation of the metallic phase of Pt by PtTi interaction. However, the limited number of acidic sites (-OH) contributes to the formation of large Pt particles, which may lead to the formation of Pt2+ or Pt4+, resulting in performance degradation. In this study, we further formulated the acidic sites of the TiO2 with sulfuric acid treatment (SA-TiO2) to improve catalytic NO oxidation. During the SA treatment, the TiO2 surface is positively charged by the low pH, providing an environment for well-distributed sulfate. In the subsequent introduction of Pt, the increase in acidic sites for Pt adsorption greatly enhanced the dispersion of Pt. During this process, Pt formed bonds with sulfate as [Pt (NH3)4]-SO4. The surface species combined with SO4 and NH3 were decomposed during the calcination process, thereby inhibiting the oxidation of Pt, which promotes the formation of metallic Pt. As a result, highly reactive Pt0 and Pt2+ were further formulated by increasing the acidic sites of SA-TiO2, where the low-temperature NO oxidation performance was improved, regardless of the Pt loading (0.3 to 3 wt.%).
引用
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页数:10
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