scholarly journals Catalytic Performance of Phosphorus Incorporated HZSM-5 in Coupling Transformation of Methanol with 1-butene to Propylene

2021 ◽  
Vol 72 (3) ◽  
pp. 33-44
Author(s):  
Haifeng Tian ◽  
Yongyong Nan ◽  
Jinlong Lv ◽  
Fei Zha ◽  
Xiaohua Tang ◽  
...  

Directly incorporated phosphorus species into the framework of HZSM-5 zeolite (H[P, Al]-ZSM-5) was successfully synthesized by the facile hydrothermal method. It was characterized by employing XRD, ICP-OES, SEM, FT-IR, N2 adsorption-desorption, NH3-TPD, XPS and TG-DTA, respectively. The effects of the phosphorus species content, temperature, WHSV, and the molar ratio of methanol/1-butene in coupling transformation of methanol with 1-butene to propylene catalyzed by H[P, Al]-ZSM-5 in a fixed bed reactor were studied systematically. Tests have suggested the acid content and specific surface area of H[P, Al]-ZSM-5 are reduced. Under the condition of reaction temperature at 550�Z, molar ratio of methanol/1-butene to 1.0, reaction pressure at 0.1 MPa and WHSV= 3.53 h-1, the P-modified HZSM-5 zeolite (with the P2O5 molar composition of 0.4 )the selectivity and yield of propylene are 35.6% and 32.5%, respectively.

2019 ◽  
Vol 15 (1) ◽  
pp. 112-118
Author(s):  
Nastaran Parsafard ◽  
Mohammad Hasan Peyrovi ◽  
Zahra Mohammadian ◽  
Niloofar Atashi

CoMo-supported mesoporous catalysts were synthesized by 50 wt% of HZSM-5 and 50 wt% of FSM-16, KIT-6, and MCM-48. These catalysts were prepared by the wet-impregnation method and pre-sulfided with CS2. The catalytic performance was evaluated for HDS reaction of dibenzothiophene over a temperature range of 250-400 °C in a micro fixed-bed reactor under atmospheric pressure. The supported CoMo bimetallic catalysts were characterized by XRD, XRF, FT-IR, N2 adsorption-desorption, and SEM. The CoMo/KIT-6/HZSM-5 indicate higher activity than other catalysts at 400 °C for dibenzothiophene hydrodesulphurization. Also, the best selectivity to cyclohexylbenzene (CHB) is related to CoMo/FSM-16/HZSM-5. The activation energy was also calculated for all prepared catalysts for the conversions of less than 10%; according to which, the activation energy for CoMo/KIT-6/HZSM-5 is less than other catalysts (~21 kJ/mol) which can be related to the appropriate pore size and high surface area of the support. Copyright © 2020 BCREC Group. All rights reserved 


Author(s):  
Radwa A. El-Salamony ◽  
Sara A. El-Sharaky ◽  
Seham A. Al-Temtamy ◽  
Ahmed M. Al-Sabagh ◽  
Hamada M. Killa

Abstract Recently, because of the increasing demand for natural gas and the reduction of greenhouse gases, interests have focused on producing synthetic natural gas (SNG), which is suggested as an important future energy carrier. Hydrogenation of CO2, the so-called methanation reaction, is a suitable technique for the fixation of CO2. Nickel supported on yttrium oxide and promoted with cobalt were prepared by the wet-impregnation method respectively and characterized using SBET, XRD, FTIR, XPS, TPR, and HRTEM/EDX. CO2 hydrogenation over the Ni/Y2O3 catalyst was examined and compared with Co–Ni/Y2O3 catalysts, Co% = 10 and 15 wt/wt. The catalytic test was conducted with the use of a fixed-bed reactor under atmospheric pressure. The catalytic performance temperature was 350 °C with a supply of H2:CO2 molar ratio of 4 and a total flow rate of 200 mL/min. The CH4 yield was reached 67%, and CO2 conversion extended 48.5% with CO traces over 10Co–Ni/Y2O3 catalyst. This encourages the direct methanation reaction mechanism. However, the reaction mechanism over Ni/Y2O3 catalyst shows different behaviors rather than that over bi-metal catalysts, whereas the steam reforming of methane reaction was arisen associated with methane consumption besides increase in H2 and CO formation; at the same temperature reaction.


2017 ◽  
Vol 751 ◽  
pp. 512-517 ◽  
Author(s):  
Supranee Lao-Ubol ◽  
Phunthinee Somwongsa ◽  
Pracha Laoauyporn ◽  
Pasinee Panith ◽  
Siriporn Larpkiattaworn ◽  
...  

Five different types of silica catalyst (SBA-15, SBA-15-PO3H2, and three different Si/Al ratio of commercial zeolites (30, 80 and 280) were used to study the transformation of methanol to hydrocarbon (MTH). The aim of this study was to investigate the effect of pore diameter and acidity in the structure of silica catalysts on the process performances in terms of methanol conversion and hydrocarbon selectivity. The mesoporous silica catalysts were prepared by co-condensation method. The catalysts samples were characterized by GC-MS, XRD, BET, and NH3-TPD techniques. The catalytic performance of synthesized and commercial catalysts for MTH process was evaluated using a homemade fixed bed reactor at temperature (300°C). It was found that the liquid hydrocarbon product provided by zeolite catalysts is aromatic hydrocarbons-rich. High Si/Al zeolites with larger pore size lead to higher selectivity and yield to paraffins (C1-C7). In contrast to commercial zeolite catalyst, SBA-15 and its modification with phosphorus species showed no conversion under studied condition. These results indicate that both pore diameter and acidity influence the product distribution in methanol to hydrocarbon process.


2011 ◽  
Vol 236-238 ◽  
pp. 1067-1072
Author(s):  
Li Ping Liu ◽  
Xiao Jian Ma ◽  
Peng Zhang ◽  
Ya Nan Liu

Hydrogen production by ethanol steam reforming over Ni-Cu/ZnO catalyst in the temperatures range of 250-550°C was studied on a fixed bed reactor. The effects of reaction temperature and water/ethanol molar ratio on hydrogen production were investigated. The structure and surface characteristics of the catalyst were measured by scanning electron microscopy (SEM), X-ray diffraction (XRD) and differential thermal analyzer (TG-DSC). The results show that the Ni-Cu/ZnO catalyst has good catalytic performance with higher hydrogen yield of 4.87molH2/molEtOH reacted. A comparison of hydrogen production from ethanol steam reforming over Ni-Cu/ZnO catalyst with over a commercial catalyst was made in this paper.


2009 ◽  
Vol 16 (03) ◽  
pp. 343-349 ◽  
Author(s):  
YUZHOU YING ◽  
KANKA FENG ◽  
ZHIGUO LV ◽  
ZHENMEI GUO ◽  
JINSHENG GAO

Nano copper-based catalysts were prepared by co-precipitation method and the performance of catalytic hydrogenation for methyl 3-hydroxypropionate (MHP) to 1, 3-propanediol (1, 3-PDO) on the nano catalysts were studied under a high-pressure microcontinuum fixed-bed reactor. The effects of structure, texture, and composition of the catalysts on the catalytic performance were investigated by characterizing the catalysts with XRD, TG–DTG, SEM, and N 2 adsorption/desorption analysis technique. The results showed that addition of promoters enhanced the activity and selectivity of copper-based catalysts, which promoted the dispersion of the active components effectively and stabilized the active center of the catalysts. Especially, the copper-based catalyst of loaded P could restrain side-reaction effectively and improve selectivity obviously, the conversion of MHP and the selectivity of 1, 3-PDO could be 91.30% and reach 90.15%, respectively.


2014 ◽  
Vol 962-965 ◽  
pp. 751-754 ◽  
Author(s):  
Wang Feng ◽  
Bai Ting ◽  
Duan Chao ◽  
Wen Ting Qu ◽  
Xi Ling Liu ◽  
...  

The catalytic performance on HZSM-5/SAPO-34 catalyst in ethanol to propylene was tested in continuous-flow fixed-bed reactor. Coke on HZSM-5/SAPO-34 catalyst for ethanol to propylene was studied by O2-TPO, N2isothermal adsorption–desorption and NH3-TPD.The result showed that the strong and medium acid sites were the active centers of coke deposition; Coke mainly deposited in mesoporous and some coke blocked microporous orifice; In the initial stage of reaction, the high yield of propylene may be benefited from coke deposition, which adjusted the acidity and structure of HZSM-5/SAPO-34.


2014 ◽  
Vol 12 (1) ◽  
pp. 355-362 ◽  
Author(s):  
Saeid Abbasian ◽  
Majid Taghizadeh

Abstract H-ZSM-5 nanozeolite was hydrothermally synthesized under static conditions. Evaluation of hydrothermal synthesis of ZSM-5 was performed by treating the synthesis mixture using different aging processes, consist of ultrasonic, stirring, and microwave-assisted aging, prior to the conventional hydrothermal treatment. The catalytic performances of selected catalysts were studied for the dehydration of methanol to dimethyl ether (DME) in a fixed-bed reactor under the same operating conditions (T = 300°C, P = 1 atm, and WHSV = 26 h−1). The prepared samples were characterized by XRD, SEM, BET, NH3-TPD and FT-IR techniques. The results showed that ultrasonic and microwave-assisted aging shortened the crystallization time and reduced crystal size of the obtained products without having any considerable effects on their catalytic activities.


2010 ◽  
Vol 132 ◽  
pp. 228-235 ◽  
Author(s):  
Xu Li ◽  
Guan Zhong Lu ◽  
Yang Long Guo ◽  
Yun Guo ◽  
Yan Qin Wang

A novel solid superbase catalyst of La2O3-ZnO/ZrO2 was prepared, and its H– value (Hammett function) of surface basic strength reaches 26.5. The catalytic activity of La2O3-ZnO/ZrO2 was evaluated for the transesterification of soybean oil (SBO) with methanol to biodiesel in a fixed bed reactor under atmospheric pressure. The results show that the chemical composition of the La2O3-ZnO/ZrO2 catalyst influences both its H– value and catalytic performance, the appropriate content of ZrO2 is 60 wt.% and the La2O3/ZnO molar ratio is 4~5/1. La2O3-ZnO/ZrO2 is an effective catalyst for the transesterification of SBO, and the SBO conversion reaches 71.3% at 70°C for 12h.


2012 ◽  
Vol 535-537 ◽  
pp. 2139-2142
Author(s):  
Ming Yu Zhang ◽  
Hua Wang ◽  
Wen Gui Gao

A series of CuO-ZnO-CeO2-ZrO2/HZSM-5 catalysts were prepared and characterized by XRD, H2-TPR. CO2hydrogenation to DME was carried out in a fixed bed reactor to test the catalytic performance of Ce-modified CuO-ZnO-ZrO2/HZSM-5 catalyst under the condition of GHSV=1800 h-1, p=3.0 MPa and T=250°C. The results indicate that the added CeO2improved the performance of the bifunctional catalysts, the CO2conversion and DME selectivity were obviously improved. CuO-ZnO-CeO2-ZrO2/HZSM-5 catalyst with Ce to Zr molar ratio of 1/1 showed the highest activity for DME synthesis from CO2hydrogenation.


2022 ◽  
Vol 16 ◽  
Author(s):  
Mustapha Dib ◽  
Marieme Kacem ◽  
Soumaya Talbi ◽  
Hajiba Ouchetto ◽  
Khadija Ouchetto ◽  
...  

Background: Pyran is an heterocyclic oxygen-containing compound that displays a wide range of therapeutic activities. Additionally, pyran is also one of the important structural subunits widely found in pharmaceuticals products. This makes it a recent focus for researchers from the industry and academic institutions. Herein, we reported an efficient and environmentally friendly one-pot strategy for the synthesis of bioactive 4H-pyran compounds via a multicomponent reaction of ethyl acetoacetate, malononitrile and substituted aromatic aldehydes in the presence of the heterogeneous spinel catalyst ( MgAl2O4 ) under mild conditions (room temperature and green solvents). The MgAl2O4 nanocatalyst was prepared from Mg/Al-LDH with a molar ratio 3 of Mg2+/Al3+ by heat treatment at 800°C. The samples were studied by a various characterization techniques such as XRD, TG-dTG, FT-IR and N2 adsorption-desorption. Good to excellent yields and facile separation of the catalyst from the reaction mixture are two of the most appealing features of this approach. Thus, bioactive molecules with pyran units may have fascinating biological properties. An efficient and green strategy for the one-pot synthesis of bioactive 4H-pyran compounds has been described. The pyrans heterocycles were produced by multicomponent reaction of ethyl acetoacetate, malononirile and substituted aromatic aldehydes in the presence of MgAl2O4 spinel nanocatalyst under mild conditions (room temperature and green solvents). MgAl2O4 nanocatalytst was prepared from Mg/Al-LDH with a molar ratio 3 of Mg2+/Al3+ by thermal treatment at 800°C. The samples were investigated by various characterization techniques such as XRD, TG-dTG, FT-IR and N2 adsorption-desorption. The following are the appealing qualities of this unique strategy including good to exceptional yields, and ease of separation of catalyst from the reaction mixture. Thus, the obtained bioactive compounds containing pyrans motif can be exhibiting interested biological activities. Methods: The substituted 4H-pyran compounds were carried out by condensation reaction of substituted aromatic aldehydes, ethyl ethyl acetoacetate and malononirile by using MgAl2O4 nanocatalyst under sustainable conditions. Objective: To develop an efficient methodology for synthesis of 4H-pyran heterocyclic molecules may have interesting applications in biology using a heterogeneous and easily synthesized catalyst. Results: This procedure outlines the synthesis of bioactive compounds in good yields and with ease of catalyst extraction from the reaction mixture under sustainable reaction conditions. Conclusion: In conclusion, it is important to reiterate that a spinel nanostucture has been successfully prepared and fully characterized using different physicochemical analysis methods. The catalytic activity of this heterogeneous catalyst was examined through the one-pot condensation of aryl benzaldehyde, malononitrile and ethyl acetoacetate. Therefore, we have developed a green method for the preparation of 4H-pyrans derivatives using MgAl2O4 as an efficient heterogeneous catalyst. The reactions were performed under green conditions, which have many benefits such as undergoing a simple procedure, good to excellent yields and easy to separate the catalyst.


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