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Synthesis of Pt/mesoporous SiC-15 and its catalytic performance for sulfuric acid decomposition
Catalysis Today ( IF 5.3 ) Pub Date : 2017-09-18 , DOI: 10.1016/j.cattod.2017.09.026
Hassnain Abbas Khan , Prakash Natarajan , Kwang-Deog Jung

Sulfuric acid (SA) decomposition is one of the key reactions in the sulfur-iodine (SI) cycle to produce hydrogen. Catalysts for the SA decomposition should be active and stable in a wide temperature range of 550–850 °C to absorb latent heat generated from a thermal solar heat or a very high temperature nuclear reactor. Here, mesoporous mSiC-15 is prepared using the SBA-15 template. TEM analysis shows that the morphology of the mSiC-15 has the replica structure of SBA-15. Pt/SBA-15 and Pt/mSiC-15 catalysts are prepared by impregnation and the catalytic activity is examined under the reaction condition of 650–850 °C and a GHSV of 76,000 mL/gcat/h. The Pt/mSiC-15 catalyst is relatively stable for 50 h at 850 °C, while the Pt/SBA-15 was severely deactivated. The Pt amounts on the Pt/SBA-15 and Pt/mSiC-15 catalysts decreased from 0.73 and 0.80 wt% at initial reaction time to 0.39 and 0.68 wt% after 12 h reaction, respectively. The Pt loss during the SA reaction is main cause of deactivation, which is caused by the evaporation of Pt oxides under O2 environment produced during the SA decomposition. It is observed that the Pt particles are embedded in porous SiO2 (Pt/mSiO2), which is transformed from Pt/mSiC-15 during the SA decomposition for 6 h. The Pt/mSiC-15 was relatively active and stable for the SA decomposition and the Pt loss was minimized by the structural change from Pt/mSiC-15 to Pt/mSiO2 after 6 h.



中文翻译:

Pt /介孔SiC-15的合成及其催化硫酸分解的性能

硫酸(SA)分解是硫碘(SI)循环中产生氢的关键反应之一。用于SA分解的催化剂应在550-850°C的宽温度范围内保持活性且稳定,以吸收太阳热或高温核反应堆产生的潜热。在此,使用SBA-15模板制备了介孔mSiC-15。TEM分析表明,mSiC-15的形态具有SBA-15的复制结构。通过浸渍制备Pt / SBA-15和Pt / mSiC-15催化剂,并在650–850°C和GHSV为76,000 mL / g cat的反应条件下检查催化活性。/H。Pt / mSiC-15催化剂在850°C下相对稳定50小时,而Pt / SBA-15则严重失活。Pt / SBA-15和Pt / mSiC-15催化剂上的Pt量分别从初始反应时间的0.73和0.80 wt%降低到12 h反应后的0.39和0.68 wt%。SA反应期间的Pt损失是失活的主要原因,这是由于在SA分解过程中在O 2环境下Pt氧化物的蒸发引起的。观察到,Pt颗粒嵌入多孔SiO 2(Pt / mSiO 2)中,在SA分解6 h时,其从Pt / mSiC-15转变。Pt / mSiC-15对SA分解相对活跃且稳定,并且通过从Pt / mSiC-15到Pt / mSiO的结构变化将Pt损失最小化2后6小时。

更新日期:2017-09-18
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