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SAPO-34
Catalysts · 2021 ·Vol. 11 ·期 5 ·616 · IF 4.146

Ionothermal Synthesis of Triclinic SAPO-34 Zeolites

Li Han,Xinxin Yan,Lulu Guo,Yanan Duan,Zheng Wang,Tianliang Lu,Jun Xu,Yuzhong Zhan,Jianfeng Wang

A triclinic SAPO-34 molecular sieve was synthesized ionothermally. The as-synthesized products were characterized by powder X-ray diffraction (XRD), scanning electron microscope (SEM), nuclear magnetic resonance (NMR), fourier infrared spectrometer (FT-IR) and thermogravimetric (TG) analyses. The formation mechanism of the hierarchical porous triclinic SAPO-34 zeolites and the factors affecting the morphology of the SAPO-34 molecular sieve were investigated. The results show that the formation mechanism of the hierarchical pores is in accordance with Ostwald ripening theory, and the accumulation of grains constitutes the existence of mesopores and macropores. The crystallization temperature, ionic liquid type, and organic amines can effectively change the morphology and crystallinity of the SAPO-34 molecular sieve. The crystallization temperature, ionic liquid and template have great influence on the (111) crystal plane, thus affecting the morphology of the molecular sieve. Moreover, it can be proven through NMR and TG analyses that ionic liquids and organic amines can be used as structure directing agents together.

研究领域: 材料科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

CO2 hydrogenation to lower olefins over Mn2O3-ZnO/SAPO-34 tandem catalysts

Jun Mou,Xingqi Fan,Fei Liu,Xiaodan Wang,Tianxiang Zhao,Peng Chen,Ziwei Li,Chunliang Yang,Jianxin Cao

The direct conversion of CO 2 hydrogenation to lower olefins via methanol as an intermediate is of great significance, but challenges still remain. Herein, we present a binary Mn 2 O 3 -ZnO oxide, which is responsible for catalytic hydrogenation of CO 2 to methanol. After combination of Mn 2 O 3 -ZnO and SAPO-34 molecular sieve, the catalytic reaction displays a markable increase. CO 2 adsorption by alkaline nature, followed by oxygen vacancy activation and synergistic hydrogenation over the binary Mn 2 O 3 -ZnO oxide are the prerequisites for the tandem reaction. However, the tandem spacing between oxide and molecular sieve plays a crucial role, because the suitable intimacy can induce enhanced methanol formation as intermediate via tandem dynamics effect, causing an apparent limitation for reverse water gas shift reaction at high temperature. The optimum mass ratio of 3:1 for two phases demonstrates that more components of binary oxide are needed to improve the rate of CO 2 hydrogenation to methanol, aiming to balance the two-step tandem reaction. Finally, under conditions of 380 ℃, 3 MPa and 3600 mL/g cat /h, 20%Mn 2 O 3 -ZnO/SAPO-34 tandem catalyst is obtained by physical ball milling after 15 min, with excellent stability, sulfur tolerance and catalytic performance with CO 2 conversion at almost 30%, lower olefins selectivity of 80.2% (propylene/ethylene = 5.6:1), and single-pass yield of 10.7%.

研究领域: 催化化学 · 能源化学 · 材料科学
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Reaction Chemistry & Engineering · 2024 · IF 3.4

Effect of the presence of CO2 on the stability of the methanol-to-olefins reaction catalyzed by Zn/SAPO-34 zeolite

Haobin Hu,Ke Ma,Zhenyu Cheng,Xinyu Qi,Haiyan Song,Zhijun Li,Yufeng Wang,Penghui Zhang,Chengyi Dai,Xiaoxun Ma

The methanol-to-olefins reaction is a viable and promising technological route to replace increasingly scarce petroleum resources. SAPO-34 zeolite is an ideal catalyst for the methanol-to-olefins reaction due to its suitable acidity and pore structure. However, a single zeolite catalyst has limited performance, and in this work, metal species were introduced on SAPO-34 molecular sieves to achieve higher low-carbon olefin selectivity through the modulation of acidity. However, since the introduction of metals promotes aromatic cycling, it allows the creation of carbonaceous precursors and reduces the catalyst lifetime. Therefore, the introduction of CO2 into the carrier gas inhibited the generation of carbonaceous precursors and thus prolonged the catalyst life. The presence of the metal species and their effects on SAPO-34's pores and structure were characterized by XPS, the change in acid amount was determined by NH3-TPD, and the adsorption strength of the catalyst for CO2 was determined by CO2-TPD, revealing the active sites of the catalyst. High low-carbon olefin selectivity and long catalyst life were also achieved, with low-carbon olefin selectivity of 88.0%.

CAS / MDL: 555-31-7
研究领域: 化学工程 · 催化科学
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Separations · 2022 ·Vol. 9 ·期 3 ·64 · IF 3.344

n-Octyltrichlorosilane Modified SAPO-34/PDMS Mixed Matrix Membranes for Propane/Nitrogen Mixture Separation

Weibin Cai,Jiangyu Xie,Jingyu Luo,Xiaohan Chen,Mingqian Wang,Yujun Wang,Jiding Li

In this study, zeolite molecular sieve SAPO-34/polydimethylsiloxane (PDMS) mixed matrix membranes (MMMs) were prepared to recover propane. n-Octyltrichlorosilane (OTCS) was introduced to improve compatibility between SAPO-34 and PDMS, and enhance the separation performance of the MMMs. Physicochemical properties of the MMMs were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and water contact angle (WCA). Results showed that, after modification, alkyl chains were successfully grafted onto SAPO-34 without changing its crystal structure, particles in the MMMs were evenly distributed in the base film, and the hydrophobicity of the MMMs was enhanced. Moreover, the effects of SAPO-34 filling content, operating pressure, and feed gas concentration on the separation performance was explored. This indicated that the modification with OTCS effectively enhanced the separation performance of SAPO-34/PDMS MMMs. When the filling content of modified SAPO-34 was 15%, the maximal separation factor of 22.1 was achieved, and the corresponding propane permeation rate was 101 GPU.Keywords:MMMs;SAPO-34;PDMS;OTCS;propane recovery

CAS / MDL: 142-82-5 5283-66-9
研究领域: 材料科学 · 化学工程
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CRYSTAL GROWTH & DESIGN · 2014 · IF 4.558

Hollow SAPO-34 Cubes with Hierarchically Organized Internal Structure

Jie Gong,Fei Tong,Xiaobo Ji,Changfeng Zeng,Chongqing Wang,Yinong Lv,Lixiong Zhang

We herein report novel hollow SAPO-34 cubes with a hierarchical internal structure. They are prepared from dry gels containing gelatin by a vapor-phase transport method. Microscopic characterization reveals that the cubes are constructed by symmetrically packed four two-top-point truncated octahedrons encapsulated by dense crystalline shells, exhibiting a structure-in-structure formation. The cubes show either +-shaped or the butterfly like X-shaped black spots on their faces under light. Investigation of the formation process of the hollow SAPO-34 cubes demonstrates a surface to core crystal growth route, which has not been found in vapor-phase transport synthesis of zeolites. A possible formation mechanism is proposed.

研究领域: 材料科学 · 化学工程
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Journal of the Taiwan Institute of Chemical Engineers · 2022 · IF 5.477

Seed-assisted synthesis of SAPO-34 zeolites: Genetic effect of seeds

Tao Zheng,Peng He,Rui Zhang,Xianghai Meng,Yuanyuan Yue,Hongtao Liu,Zhichang Liu,Chunming Xu,Haiyan Liu

Background In the past decades, seed-assisted synthesis of zeolites has become one of the research focuses. Understanding the effect of the seeds on their derived products, and thus tuning the physicochemical properties of those products by selecting suitable seeds is pivotal for synthesizing zeolites via seed-assisted method. Methods In this work, four kinds of SAPO-34 with different physicochemical properties were synthesized and used as seeds to prepare their corresponding products via the seed-assisted method. The physicochemical properties of the seeds and the corresponding products were characterized by XRD, SEM, N 2 adsorption-desorption, NH 3 -TPD, and 29 Si MAS NMR techniques. Significant Findings The results showed that the particle size, textural and acidity properties, and the silicon coordination of the seed-derived products are strongly correlated to their corresponding seeds, exhibiting genetic effects. By investigating the crystallization kinetics, we speculated that the genetic effects should be attributed to the incomplete dissolution of the seeds. During the crystallization process, the incompletely dissolved seed fragments are directly incorporated into the product and serve as models. These models then require the final zeolites to grow according to their patterns, retaining and inheriting their original characteristics.

CAS / MDL: 555-31-7 77-98-5 78-10-4
研究领域: 材料科学 · 化学工程
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 45 ·19220-19228 · IF 2.7

CO2 hydrogenation to light olefins over Zn–Zr/support-SAPO-34: comparison of different supports

Peng Lu,Qianwen Hu,Kui Wang,Shiyong Chen,Zongxiao Li,Xinjie Chen,Chuang Xing,Yanhong Wang,Ce Du

The efficient CO2 conversion to light olefins through hydrogenation is a feasible strategy to achieve carbon neutrality goals. Herein, a series of bimetallic Zn–Zr/supports are synthesized by a conventional impregnation method. We demonstrate that different supports endow catalysts with various specific surface areas, pore sizes, chemical adsorption performances, and acid densities. The effects of different support-loaded Zn–Zr coupled with SAPO-34 on CO2 hydrogenation to light olefins are investigated systematically. The CO2 conversion of Zn–Zr/Q10-SAPO-34, Zn–Zr/Q50-SAPO-34, Zn–Zr/γAl2O3-SAPO-34, Zn–Zr/MgO-SAPO-34 and Zn–Zr/S-1-SAPO-34 is 11.4%, 9.2%, 24.0%, 8.8%, and 16.2%, respectively, with corresponding light olefin selectivity of 39.0%, 28.1%, 30.4%, 4.8%, and 14.7%, respectively. Significantly, γAl2O3 is more conducive to CO2 conversion, while Q10 tends to produce light olefins. This work provides an effective reference for support selection in CO2 hydrogenation to light olefins.

CAS / MDL: 10196-18-6 4499-86-9
研究领域: 化学工程 · 环境科学
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JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY · 2021 ·Vol. 32 ·期 8 ·1598-1606 · IF 1.838

Preparation of SAPO-34-Based Catalyst for Conversion of Fructose to 5-Hydroxymethylfurfural

Zhang Yangyang,Shao Chuan,Qin Dongling,Yang Gang

Solid acid-catalyzed dehydration of fructose to produce 5-hydroxymethylfurfural (5-HMF) has been a hotspot in biomass conversion research in recent years. In this study, a novel SAPO-34-based catalyst was prepared by consecutive steps of titanium doping, sulfuric acid impregnation, and sulfonic acid functionalization. Characterization of the catalyst with X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), BrunauerEmmett-Teller (BET), inductively coupled plasma optical emission spectrometer (ICP-OES), and acid-base titration revealed different pore structures and more acid content compared to SAPO-34. The catalyst was applied to the preparation of 5-HMF by dehydration of fructose, and the maximum yield (74.0%) of 5-HMF was obtained by reacting in dimethyl sulfoxide (DMSO) at 170 °C for 50 min. In addition, the applicability of the catalytic system to other substrates and the stability of the catalyst after five cycles were investigated, which are valuable for further probing on the concerned aspects.

研究领域: 化学工程 · 生物质能转化
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

SAPO-34 crystals with nanosheet morphology synthesized by pyrophosphoric acid as new phosphorus source

Lei Zhao,Ge Yang,Haocheng Hu,Yuhao Sun,Zhuang Ma,Peng Peng,Eng-Poh Ng,Peng Tian,Hailing Guo,Mintova Svetlana

The nanosheet SAPO-34 zeolite crystals with a diameter of 300 nm and a thickness of 50 nm using a new phosphorus source (pyrophosphoric acid, H 4 P 2 O 7 ) were synthesized. The roles of the pyrophosphate (P 2 O 7 4− ) species in the crystallization of SAPO-34 were elucidated. The results suggested that one P atom from the P 2 O 7 4− species participated in the formation of the CHA framework structure while the other P atom served as a crystallization control agent, facilitating preferential crystal growth in [100] crystal plane. The SAPO-34 nanosheets have silica-rich shell and phosphorus-rich core leading to superior catalytic performance in methanol-to-olefin reaction (MTO). The catalytic lifetime of the SAPO-34 nanosheets was significantly improved due to the larger amount of medium-strong surface acidity and short diffusion pathway in comparison to the conventional SAPO-34 catalyst synthesized in the presence of the classical phosphorus source (H 3 PO 4 ).

CAS / MDL: 2466-09-3 77-98-5
研究领域: 材料科学 · 催化化学
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CATALYSIS LETTERS · 2021 ·Vol. 152 ·期 6 ·1651-1659 · IF 3.186

Efficient Methanol-to-Olefins Conversion Via Photothermal Effect Over TiN/SAPO-34 Catalyst

Tao Lei,Zhang Xueliang,Song Lizhu,Hu Huilin,Liu Lequan,Ye Jinhua,Wang Defa

As one of the most promising routes for production of low-carbon olefins (e.g., ethene and propene etc.), methanol-to-olefins (MTO) reaction is influenced largely by the temperature. Noble metal (e.g., Au, Ag, etc.) nanoparticles are known to exhibit the localized surface plasmon resonance (LSPR) effect, which has been applied in photothermal reactions. Owing to the increased light absorption ability in near-infrared region, titanium nitride (TiN) nanoparticles exhibit a superior LSPR effect over noble metals. Herein, we report on the MTO reaction via photothermal effect over a series of TiN(x)/SAPO-34 (x = 0.5, 0.75, 1, 2, 5, 10, 13 wt%) catalysts prepared by a simple mechanical grinding method. The MTO reaction over TiN(x)/SAPO-34 was carried out under a 300 W xenon lamp irradiation. The MTO reactivity of TiN(x)/SAPO-34 was influenced by both the photothermal temperature from the LSPR effect of TiN nanoparticles and the Brønsted acid sites on SAPO-34, both of which were dependent on the loading amount of TiN nanopartiles. The synergistic effect of high photothermal temperature, sufficient Brønsted acid sites and moderate BET surface area gave rise to the optimal catalytic performance of MTO reaction over TiN(10)/SAPO-34, which exhibited a methanol conversion of 73.1% and an ethene selectivity of 62.5%. Graphic Abstract

研究领域: 化学工程 · 材料科学
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Reaction Kinetics Mechanisms and Catalysis · 2019 ·Vol. 128 ·期 1 ·523-538 · IF 1.428

Sulfonic acid-functionalized hierarchical SAPO-34 for fructose dehydration to 5-hydroxymethylfurfural

Liu Zhonghai,Sun Zhenzhu,Qin Dongling,Yang Gang

Sulfonic acid-functionalized hierarchical SAPO-34 (S 1 -SAPO-34-SO 3 H) was prepared by post-grafting 3-mercaptopropyltriethoxysilane, and the sulfonic acid group was then oxidized by H 2 O 2 . The obtained catalysts were characterized by XRD, SEM, FTIR, TG, nitrogen adsorption, XRF, and acid–base titration. The acidity of the modified SAPO-34 increased, which confirmed the success of grafting. The catalytic properties during the dehydration of fructose to 5-hydroxymethylfurfural (5-HMF) were investigated. The yield of 5-HMF was up to 72%, and a 34% increase was found compared with the case of SAPO-34. The findings were discussed and attributed to the synergistic effects caused by both the acid groups and the mesopores. More basic investigations with regard to the conditions, including the reaction time, temperature, solvent, load and regeneration, are needed.

研究领域: 化学工程 · 催化材料
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EUROPEAN JOURNAL OF INORGANIC CHEMISTRY · 2020 ·Vol. 2020 ·期 22 ·2170-2176 · IF 2.529

Synthesis of SAPO-34 Zeolite from Laponite and Its Application in the MTO Reaction

Xueshuai Chen,Rongli Jiang,Zihan Zhou,Xingwen Wang

Graphical SAPO-34 zeolite was successfully synthesized from laponite as the single Si source. Laponite itself contains Li and Mg atoms, which were subsequently introduced into the structure of SAPO-34 via depolymerization-reorganization of laponite. Metal incorporation can reduce the amount of stronger acid sites and enhance the catalytic performance in the MTO reaction. In this work, SAPO-34 zeolite with high catalytic activity was successfully synthesized by hydrothermal method from laponite as the single Si source. Compared with the traditional method of synthesizing zeolites from clay, the laponite after swelling can be directly used in the synthesis process of zeolite. The crystallization behavior of SAPO-34 synthesized from laponite was investigated by XRD, FTIR, N 2 adsorption–desorption, SEM-EDX, ICP-MS, and DR-UV/Vis. The process can be summarized as follows: the Si and Mg elements were produced by the depolymerization of laponite, then the primary building units of SAPO-34 zeolite were formed under hydrothermal conditions; finally, the crystal nucleus began to form, and crystallization was triggered. Compared with the conventional SAPO-34 synthesized from TEOS, the SAPO-34 synthesized from laponite exhibited higher selectivity to light olefins and longer lifetime, which can be attributed to the suitable strength of acidity. This work points to a straightforward route to the synthesis of SAPO-34 from laponite.

CAS / MDL: 7664-38-2
研究领域: 材料科学 · 催化化学
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