مورد إلكتروني

Setting up In2O3-ZrO2/SAPO-34 Catalyst for Improving Olefin Production via Hydrogenation of CO2/CO Mixtures

التفاصيل البيبلوغرافية
العنوان: Setting up In2O3-ZrO2/SAPO-34 Catalyst for Improving Olefin Production via Hydrogenation of CO2/CO Mixtures
بيانات النشر: MDPI 2023-07-14
تفاصيل مُضافة: Ingeniería química
Ingeniaritza kimikoa
Portillo Bazaco, Ander
Parra Ipiña, Onintze
Aguayo Urquijo, Andrés Tomás
Ereña Loizaga, Javier
Bilbao Elorriaga, Javier
Ateka Bilbao, Ainara
نوع الوثيقة: Electronic Resource
مستخلص: The adequate configuration and the effect of the reduction was studied for the In2O3-ZrO2/SAPO-34 catalyst with the aim of improving its performance (activity and selectivity in the pseudo-steady state) for the hydrogenation of CO, CO2 and CO2/CO (COx) mixtures into olefins. The experiments were carried out in a packed bed reactor at 400 °C; 30 bar; a H2/COx ratio of 3; CO2/COx ratios of 0, 0.5 and 1; a space time (referred to as In2O3-ZrO2 catalyst mass) of 3.35 gInZr h molC−1; and a time on stream up to 24 h. The mixture of individual catalyst particles, with an SAPO-34 to In2O3-ZrO2 mass ratio of 1/2, led to a better performance than hybrid catalysts prepared via pelletizing and better than the arrangement of individual catalysts in a dual bed. The deactivation of the catalyst using coke deposition and the remnant activity in the pseudo-steady state of the catalyst were dependent on the CO2 content in the feed since the synergy of the capabilities of the SAPO-34 catalyst to form coke and of the In2O3-ZrO2 catalyst to hydrogenate its precursors were affected. The partial reduction of the In2O3-ZrO2/SAPO-34 catalyst (corresponding to a superficial In0/In2O3 ratio of 0.04) improved its performance over the untreated and fully reduced catalyst in the hydrogenation of CO to olefins, but barely affected CO2/CO mixtures’ hydrogenation.
مصطلحات الفهرس: CO2, In2O3 catalyst, SAPO-34 catalyst, methanol synthesis, olefin synthesis, coke deactivation, info:eu-repo/semantics/article
URL: http://hdl.handle.net/10810/62092
https://www.mdpi.com/2073-4344/13/7/1101
2073-4344
https://www.mdpi.com/2073-4344/13/7/1101
info:eu-repo/grantAgreement/EC/H2020/823745
info:eu-repo/grantAgreement/MICINN/PID2019-108448RB-100
info:eu-repo/grantAgreement/MINECO/BES2017-081135
الإتاحة: Open access content. Open access content
ملاحظة: This work was carried out with the financial support of the Ministry of Science, Innovation and Universities of the Spanish Government (PID2019-108448RB-100), the Basque Government (Project IT1645-22), the European Regional Development Funds (ERDF) and the European Commission (HORIZON H2020-MSCA RISE-2018. Contract No. 823745). A. Portillo is grateful for the Ph.D. grant from the Ministry of Science, Innovation and Universities of the Spanish Government (BES2017-081135) and O. Parra is grateful for the Ph.D. grant from the Basque Government (PRE_2021_1_0014). The authors are thankful for the technical and human support provided by SGIker (UPV/EHU).
English
أرقام أخرى: ESUPV oai:addi.ehu.eus:10810/62092
1405406223
المصدر المساهم: REPOSITORIO DE LA UNIVERSIDAD DEL PAIS
From OAIster®, provided by the OCLC Cooperative.
رقم الأكسشن: edsoai.on1405406223
قاعدة البيانات: OAIster