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FUEL · 2022 · IF 8.035

A highly efficient SAPO-34 catalyst for improving light olefins in methanol conversion: Insight into the role of hierarchical porosities and tailoring acid properties based on in situ NH3-poisoning

Quanhua Wang,Wenwen Zhang,Xiaosen Ma,Yanchao Liu,Lichen Zhang,Jiajun Zheng,Yan Wang,Wenlin Li,Binbin Fan,Ruifeng Li

Hierarchical SAPO-34 zeolites with tunable porosity were hydrothermally synthesized by modulating the Si/Al molar ratios of the gel precursors, and the morphologies of SAPO-34 crystals gradually evolve from well-dispersed ultra-small nanocrystals to compactly polycrystalline aggregates, and to analogous polycrystallinites but adhered with minute amorphous debris by increasing the Si/Al ratio ranging from 0.20 to 0.67. The catalytic tests during methanol-to-olefins (MTO) reaction indicate that the Hier-SAPO-34-0.20 (Si/Al = 0.20) catalyst constructed by loosely nano-sized crystals centered at 50 nm presents prominent catalytic performances with about 2.5 times prolonged catalytic longevity and around 10 % improvement for the selectivity toward light olefins (ethylene and propylene) as compared to a reference catalyst. More interestingly, when Hier-SAPO-34-0.20 catalyst was in situ pretreated with NH 3 flowing, the selectivity of light olefins can be greatly increased by 18.1 % at the initial stage and the corresponding even selectivity with time-on-stream can be elevated by 6.9 %. It founds that in situ NH 3 -poisoned catalysts with improved light olefins selectivity are also suitable for ZSM-5 zeolite. These results reveal that the weakened strong acid sites modified by NH 3 -poisoning play a pivotal role in suppressing the undesired hydrogen transfer reactions and thus giving a high selectivity for light olefins. This work highlights the importance of acidity fine-tailoring by in-situ NH 3 -poisoning strategy on hierarchical zeolites for the improvement of light olefin selectivity, which would be valuable guidance for industrial applications.

CAS / MDL: 109-89-7 167114-91-2
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APPLIED CATALYSIS A-GENERAL · 2021 · IF 5.706

Excellent low-temperature NH3-SCR of NO activity and resistance to H2O and SO2 over WaCeOx (a = 0.06, 0.12, 0.18, 0.24) catalysts: Key role of acidity derived from tungsten addition

Huansheng Tan,Shibo Ma,Xiaoyu Zhao,Yushi Li,Chen Zhao,Yujun Zhu

Bimetallic W a CeO x (a = 0.06, 0.12, 0.18, 0.24) catalysts were synthesized for selective catalytic reduction of NO x with NH 3 (NH 3 -SCR). The influences of W on structure, activity and surface properties were investigated by XRF, XRD, Raman, TEM, N 2 adsorption-desorption, H 2 -TPR, O 2 /NH 3 /SO 2 -TPD, XPS, and in-situ DRIFTS. The characterization results show that the W/Ce ratio has a great effect on the NH 3 -SCR activity. The different catalytic activities of W a CeO x are mainly attributed to the acidity change, especially the increase of B-acid content plays a major role in enhancing low temperature activity. W 0.18 CeO x exhibits excellent low-temperature NH 3 -SCR activity, SO 2 /H 2 O resistance and N 2 selectivity with a broad activity window (190–490 °C) with 5%H 2 O. Moreover, good activity window (235–460 °C) can be maintained even the catalyst treated with 5% H 2 O at 800 °C for 12 h, showing especial hydrothermal stability. Thus, it can be summarized that W 0.18 CeO x is regarded as outstanding catalyst for low-temperature NH 3 -SCR of NO.

CAS / MDL: 12333-11-8 10294-41-4
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