A flexible and robust model for low temperature catalytic desorption of CO 2 from CO 2 -loaded amines over solid acid catalysts

2017 ◽  
Vol 170 ◽  
pp. 518-529 ◽  
Author(s):  
Benjamin Decardi-Nelson ◽  
Ananda Akachuku ◽  
Priscilla Osei ◽  
Wayuta Srisang ◽  
Fatima Pouryousefi ◽  
...  
Keyword(s):  
Low Temperature ◽  
Solid Acid ◽  
Solid Acid Catalysts ◽  
Acid Catalysts ◽  
Robust Model

scholarly journals Preparation of Carbon-Based Solid Acid Catalysts Using Rice Straw Biomass and Their Application in Hydration of α-Pinene

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 213 ◽  
Author(s):  
Zhaozhou Wei ◽  
Deyuan Xiong ◽  
Pengzhi Duan ◽  
Shilei Ding ◽  
Yuanlin Li ◽  
...  
Keyword(s):  
Low Temperature ◽  
Rice Straw ◽  
Photoelectron Spectroscopy ◽  
Solid Acid ◽  
Solid Acid Catalysts ◽  
Side Reactions ◽  
Acid Catalysts ◽  
High Porosity ◽  
Ft Ir ◽  
Carbon Based

Carbon-based solid acid catalysts were prepared using rice straw (RS) waste, and the effects of carbonization temperature and sulfonation temperature on the catalytic activity were investigated. The properties of the catalysts were characterized using thermo gravimetric (TG), scanning electron microscope (SEM), Brunauer–Emmet–Teller (BET), Fourier transform infrared spectroscopy (FT-IR), temperature-programmed desorption (TPD), and X-ray photoelectron spectroscopy (XPS), and their activities were investigated through the hydration of α-pinene. The conversion of α-pinene and the selectivity of α-terpineol reached 67.60% and 57.07% at 80 °C and atmospheric pressure in 24 h, respectively. The high catalytic capacity of the catalyst is attributed to the high acid site density and high porosity of the catalyst. TPD analysis and FT-IR spectroscopy showed that the catalyst produced by low-temperature carbonization at 300 °C followed by low-temperature sulfonation at 80 °C had abundant strong acid sites (0.82 mmol/g), which can effectively inhibit the side reactions of hydrated α-pinene. The total acidity reached 2.87 mmol/g. N2-physisorption analysis clearly indicated that the obtained catalysts were mesopore-predominant materials, and the SBET and VTotal of catalysts reached 420.9 m2/g and 4.048 cm3/g, respectively. Preparation of the catalyst involves low energy consumption, and its cheap raw materials make the whole process simple, economical, and environmentally friendly.

scholarly journals Spectroscopic investigation into the design of solid–acid catalysts for the low temperature dehydration of ethanol

2016 ◽  
Vol 18 (26) ◽  
pp. 17303-17310 ◽  
Author(s):  
Matthew E. Potter ◽  
Sivan V. Aswegen ◽  
Emma K. Gibson ◽  
Ian P. Silverwood ◽  
Robert Raja
Keyword(s):  
Low Temperature ◽  
Neutron Scattering ◽  
Vibrational Spectroscopy ◽  
Spectroscopic Investigation ◽  
Solid Acid ◽  
Solid Acid Catalysts ◽  
Acid Catalysts ◽  
Ethanol Dehydration ◽  
Spectroscopy Studies

Combining in situ neutron scattering and vibrational spectroscopy studies to elucidate the mechanism of ethanol dehydration in SAPO-34 catalysts.

Preparation of Strong Acid Catalysts by Sulfate Treatment of Calcined Boehmite

1992 ◽  
Vol 57 (11) ◽  
pp. 2241-2247 ◽  
Author(s):  
Tomáš Hochmann ◽  
Karel Setínek
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Aluminum Sulfate ◽  
Solid Acid ◽  
Strong Acid ◽  
Acid Strength ◽  
Solid Acid Catalysts ◽  
Acid Catalysts ◽  
Preparation Methods ◽  
Indicator Method

Solid acid catalysts with acid strength of -14.52 < H0 < -8.2 were prepared by sulfate treatment of the samples of boehmite calcined at 105-800 °C. Two preparation methods were used: impregnation of the calcined boehmite with 3.5 M H2SO4 or mixing of the boehmite samples with anhydrous aluminum sulfate, in both cases followed by calcination in nitrogen at 650 °C. The catalysts were characterized by measurements of surface area, adsorption of pyridine and benzene, acid strength measurements by the indicator method and by catalytic activity tests in the isomerization of cyclohexene, p-xylene and n-hexane. Properties of the catalysts prepared by both methods were comparable.

scholarly journals Metal–Organic Framework-Based Solid Acid Materials for Biomass Upgrade

2021 ◽  
Author(s):  
Yutian Qin ◽  
Jun Guo ◽  
Meiting Zhao
Keyword(s):  
High Efficiency ◽  
Solid Acid ◽  
Metal Organic Framework ◽  
Acid Sites ◽  
Solid Acid Catalysts ◽  
Future Research ◽  
Acid Catalysts ◽  
Metal Organic ◽  
Biomass Transformation ◽  
Organic Framework

AbstractBiomass is a green and producible source of energy and chemicals. Hence, developing high-efficiency catalysts for biomass utilization and transformation is urgently demanded. Metal–organic framework (MOF)-based solid acid materials have been considered as promising catalysts in biomass transformation. In this review, we first introduce the genre of Lewis acid and Brønsted acid sites commonly generated in MOFs or MOF-based composites. Then, the methods for the generation and adjustment of corresponding acid sites are overviewed. Next, the catalytic applications of MOF-based solid acid materials in various biomass transformation reactions are summarized and discussed. Furthermore, based on our personal insights, the challenges and outlook on the future development of MOF-based solid acid catalysts are provided. We hope that this review will provide an instructive roadmap for future research on MOFs and MOF-based composites for biomass transformation.

scholarly journals Nonthermal Plasma Induced Fabrication of Solid Acid Catalysts for Glycerol Dehydration to Acrolein

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 391
Author(s):  
Lu Liu ◽  
Xiaofei Philip Ye
Keyword(s):  
Solid Acid ◽  
Nonthermal Plasma ◽  
Temperature Programmed Desorption ◽  
Argon Atmosphere ◽  
Solid Acid Catalysts ◽  
Acid Catalysts ◽  
Pyridine Adsorption ◽  
X Ray ◽  
Glycerol Dehydration ◽  
Temperature Programmed

The feasibility of fabricating better solid acid catalysts using nonthermal plasma (NTP) technology for biobased acrolein production is demonstrated. NTP discharge exposure was integrated in catalyst fabrication in air or argon atmosphere. The fabricated catalysts were characterized by Brunauer–Emmett–Teller surface area analysis, temperature-programmed desorption of ammonia, X-ray powder diffraction and Fourier-transform infrared spectroscopy of pyridine adsorption, in comparison to regularly prepared catalysts as a control. Further, kinetic results collected via glycerol dehydration experiments were compared, and improvement in acrolein selectivity was displayed when the catalyst was fabricated in the argon NTP, but not in the air NTP. Possible mechanisms for the improvement were also discussed.

S-Acylation of aliphatic and aromatic thiols with carboxylic acids and their esters over solid acid catalysts in the gas phase at temperatures above 200°C

2013 ◽  
Vol 464-465 ◽  
pp. 332-338 ◽  
Author(s):  
Sayoko Nagashima ◽  
Hitomi Yamazaki ◽  
Kentaro Kudo ◽  
Satoshi Kamiguchi ◽  
Teiji Chihara
Keyword(s):  
Gas Phase ◽  
Carboxylic Acids ◽  
Solid Acid ◽  
Solid Acid Catalysts ◽  
Acid Catalysts ◽  
Aromatic Thiols
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