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SAPO-5
JOURNAL OF POROUS MATERIALS · 2015 ·Vol. 22 ·期 3 ·577-584 · IF 1.108

Hierarchically structured SAPO-5 molecular sieve catalysts with tailored mesoporosity for alkylation reaction

Zhao Xinhong,Wen Juanjuan,Zhao Jiangbo,Li An,Li Guixian,Wang Xiaolai

Hierarchically structured SAPO-5 molecular sieve was synthesized by microwave-assisted ionothermal method in eutectic mixture solvent. Their porous texture and acid properties were characterized by nitrogen physisorption, SEM, TEM and NH 3 -TPD. The results show that the mesoporous volume of SAPO-5 can be tuned via simply varying the degree of supersaturation, the type of mineralizer or replacing partly succinic acid with sebacic acid. A lower degree of supersaturation and using ammonium fluoride as a mineralizer favor the synthesis of SAPO-5 with large mesoporous volume. Notably, the introduction of sebacic acid can lead to three-level micro-meso-macroporous structure (sample C1). Five typical samples were selected as catalysts and tested in the alkylation of benzene with benzyl alcohol. Among all catalysts, the sample C1, whose aspect ratio is the lowest, exhibited the best catalytic activity, giving a 91 % benzyl alcohol conversion. The diffraction peak intensity ratio of I 002 /I 100 was proposed to be a good indicator in fabricating a highly active SAPO-5 catalyst for this reaction.

CAS / MDL: 112945-52-5
研究领域: 化学工程 · 材料科学
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Nanomaterials · 2025 ·Vol. 15 ·期 5 ·321 · IF 4.3

BiOBr/Coal Gangue-Based SAPO-5 Molecular Sieve Nanocomposite for Enhanced Adsorption and Photocatalytic Degradation of Methylene Blue

Boyang Xu,Jie Chen,Kai Wang,Pengfei Li,Le Kang,Huiling Du,Qianqian Liu,Xiaoqing Lian

The accumulation of organic pollutants and solid waste is one of the major environmental challenges faced globally. Establishing an efficient recycling system for solid waste and designing cost-effective, high-performance photocatalysts are urgent tasks for the removal of organic pollutants from water. This study utilizes coal gangue as the precursor to synthesize a coal gangue-based phosphorus–silicon–aluminum molecular sieve (SAPO-5) via hydrothermal synthesis. The resulting material was then composited with bismuth oxybromide (BiOBr) to form a novel BiOBr/coal gangue-based SAPO-5 nanocomposite. When the mass ratio of BiOBr to coal gangue-based SAPO-5 molecular sieve is 0.3, the synthesized nanocomposite exhibits excellent adsorption and photocatalytic performance for the removal of methylene blue, achieving a removal rate of 97.8% and the mineralization rate of 57.4% within 30 min. The superior performance can be attributed to the optimal pore size, rapid charge transfer rate, and high photogenerated charge density of the BiOBr/coal gangue-based SAPO-5 nanocomposite. The novel BiOBr/coal gangue-based SAPO-5 molecular sieve nanocomposite catalyst presents a new approach for the harmless treatment of organic dye wastewater and the high-value utilization of coal gangue.

研究领域: 环境科学 · 材料科学
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Materials · 2019 ·Vol. 12 ·期 23 ·3948 · IF 2.972

Enhanced Visible-Light Photocatalytic Performance of SAPO-5-Based g-C3N4 Composite for Rhodamine B (RhB) Degradation

Lingfang Qiu,Zhiwei Zhou,Mengfan Ma,Ping Li,Jinyong Lu,Yingying Hou,Xiangshu Chen,Shuwang Duo

Novel visible-light responded aluminosilicophosphate-5 (SAPO-5)/g-C3N4composite has been easily constructed by thermal polymerization for the mixture of SAPO-5, NH4Cl, and dicyandiamide. The photocatalytic activity of SAPO-5/g-C3N4is evaluated by degrading RhB (30 mg/L) under visible light illumination (λ > 420 nm). The effects of SAPO-5 incorporation proportion and initial RhB concentration on the photocatalytic performance have been discussed in detail. The optimized SAPO-5/g-C3N4composite shows promising degradation efficiency which is 40.6% higher than that of pure g-C3N4. The degradation rate improves from 0.007 min−1to 0.022 min−1, which is a comparable photocatalytic performance compared with other g-C3N4-based heterojunctions for dye degradation. The migration of photo-induced electrons from g-C3N4to the Al site of SAPO-5 should promote the photo-induced electron-hole pairs separation rate of g-C3N4efficiently. Furthermore, the redox reactions for RhB degradation occur on the photo-induced holes in the g-C3N4and Al sites in SAPO-5, respectively. This achievement not only improves the photocatalytic activity of g-C3N4efficiently, but also broadens the application of SAPOs in the photocatalytic field.Keywords:g-C3N4;SAPO-5;composite;photocatalytic;visible light

CAS / MDL: 81-88-9
研究领域: 材料科学 · 环境科学 · 化学
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JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS · 2021 · IF 3.995

Enhanced aromatic selectivity using the core–shell synergistic effects of HZSM-5/SAPO-5 zeolites in isobutane conversion

Ruizhen Zhang,Jie Wang,Lina Han,Jiancheng Wang,Liangfu Zhao

HZSM-5 molecular sieves are efficient catalysts in the aromatization of light hydrocarbons and the fabrication of HZSM-5-based core–shell composites has become an important strategy to improve their catalytic performance due to the simultaneous modification of the acidity and pore structures in the catalyst. In this paper, HZSM-5/SAPO-5 (CSZP and CSZC) were synthesized via a two-stage crystallization process using PDDA and CTAB as modifiers of HZSM-5, respectively. The structure, acidity, and the weight of carbon deposition of the resulting molecular sieves catalysts were characterized using various methods and their catalytic behavior in isobutane aromatization investigated. The results show that CSZP exhibits a perfect core–shell structure with a uniform and thin shell composed of nano-SAPO-5, while CSZC has an irregular coat configuration with HZSM-5 covered by a rough and thick shell consisting of flaky micro-SAPO-5 crystals. The introduction of SAPO-5 via an in-situ synthesis decreases the Brønsted acidity of the catalysts to different extents and provides a large number of intergranular mesopores due to the stacking of SAPO-5 on the surface of HZSM-5, which is favorable toward improving the BTEX selectivity (benzene, toluene, ethylbenzene, and xylene) and catalytic stability over CSZP and CSZC. Meanwhile, CSZP has more competitive advantages than CSZC in promoting the mass transfer efficiency due to its significantly thinner shell than CSZC, which combined with its moderate acidity and appropriate mesopore structure result in its excellent selectivity and stability during the aromatization of isobutane.

CAS / MDL: 26062-79-3
研究领域: 化学工程 · 催化科学
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2025 · IF 3.7

Enhanced activity and stability of SAPO-5 zeolite supported RuMn catalyst for aqueous-phase selective hydrodeoxygenation of guaiacol to cyclohexanol

Mengting Chen,Minjie Zhu,Tingyu Zhou,Qifeng Zhong,Meihua Zhang,Yingxin Liu,Zuojun Wei

SAPO-5 zeolite supported RuMn was a highly efficient catalyst for the aqueous-phase selective hydrodeoxygenation of guaiacol to cyclohexanol. The optimal catalyst achieved a high cyclohexanol yield of 93.7% at full guaiacol conversion under mild conditions, with a high TOF of 920 h -1 . Moreover, the catalyst displayed remarkable performance for the hydrogenation of phenol to cyclohexanol, where a 100% yield of cyclohexanol was obtained at a phenol-to-Ru molar ratio of about 17900. In particular, the catalyst exhibited excellent recyclability and could be recycled for 20 times without obvious activity loss. The as-prepared RuMn/SAPO-5 catalyst exhibited higher performance than most of the reported Ru-based catalysts.

研究领域: 催化化学 · 能源化学
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Journal of CO2 Utilization · 2018 · IF 5.503

Highly selective conversion of CO2 to lower hydrocarbons (C2-C4) over bifunctional catalysts composed of In2O3-ZrO2 and zeolite

Jianyang Wang,Anfeng Zhang,Xiao Jiang,Chunshan Song,Xinwen Guo

Although many researchers have reported CO 2 hydrogenation to various C1 chemicals, it is still challenging to directly and selectively convert CO 2 to C 2 -C 4 hydrocarbons in terms of overcoming the extreme inertness of CO 2 and a high C C coupling barrier. In the present work, we report an efficient integration of methanol-synthesis and the methanol-to-hydrocarbons with the bifunctional catalyst component of In 2 O 3 -ZrO 2 and SAPO-5. These tandem reactions exhibit an excellent relative selectivity of C 2 -C 4 (83%) with a suppressed CH 4 relative selectivity less than 3% at T = 300 °C. A detailed analysis indicates that the partially reduced indium oxide surface (In 2 O 3 -ZrO 2 ) can better activate CO 2 and promote the synthesis of methanol than In 2 O 3 alone, and C C coupling is subsequently manipulated within the confined acidic pores of SAPO-5 according to XRD, H 2 -TPR, CO 2 -TPD, SEM and TEM. Furthermore, the proximity of two components and the content of Si also play an important role in such outstanding selectivity to C 2 -C 4 . Our study paves a new path for the direct synthesis of lower hydrocarbons.

CAS / MDL: 1314-23-4
研究领域: 化学工程 · 催化化学 · 能源化学
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CHEMICAL PHYSICS LETTERS · 2021 · IF 2.328

Flowerlike hierarchical SAPO-5 molecular sieve composed of loosely aggregating uniformly primary nano-rods-like AFI crystals

Quanhua Wang,Sai Li,Yanchao Liu,Lichen Zhang,Jiajun Zheng,Binbin Fan,Shuwei Chen,Wenlin Li,Ruifeng Li

Flowerlike hierarchical SAPO-5 molecular sieve was fabricated by a hydrothermally dynamic crystallization route using tetrapropyl-ammoniuhydroxide as a single structure-directing agent. The hierarchical SAPO-5 reveals high crystallinity, and large external surface areas validated by the XRD and N 2 adsorption-desorption. SEM and TEM indicate that the flowerlike hierarchical SAPO-5 is composed of loosely stacked primary nanorods with average diameter of 20 nm. FT-IR and EDS analyses show that as increasing crystallization time, more and more Si species are incorporated into the AFI crystals. Moreover, it is found that a dynamic crystallization condition is very mandatory toward the synthesis of a novel-flowerlike SAPO-5.

研究领域: 材料科学 · 化学 · 无机化学 · 催化 · 纳米材料 · 多孔材料
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