scholarly journals Digitization of Adsorption Isotherms from "The Thermodynamics and Hysteresis of Adsorption''

2021 ◽  
Vol 126 ◽  
Author(s):  
Daniel W. Siderius
Keyword(s):  
Carbon Dioxide ◽  
Sorption Isotherms ◽  
Domain Theory ◽  
Carbon Dioxide Adsorption ◽  
Laboratory Measurements ◽  
Practical Applications ◽  
Desorption Hysteresis ◽  
Desorption Isotherms ◽  
Adsorption Desorption ◽  
Independent Domain

Sorption isotherms collected from tables in the seminal dissertation, “The Thermodynamics and Hysteresis of Adsorption” by A. J. Brown, have been digitized and made publicly available, along with supporting software scripts that facilitates usage of the data. The isotherms include laboratory measurements of xenon, krypton, and carbon dioxide adsorption (and, when possible, desorption) isotherms on a single sample of Vycor glass1, at various temperatures including subcritical conditions for xenon and krypton. The highlight of this dataset is the collection of “scanning” isotherms for xenon on Vycor at 131 K. The scanning isotherms examine numerous trajectories through the adsorption-desorption hysteresis region, such as primary adsorption and desorption scanning isotherms that terminate at the hysteresis boundary, secondary scanning isotherms made by selective reversals that return to the boundary, and closed scanning loops. This dataset was originally used to test the independent domain theory of adsorption and continues to support successor theories of adsorption/desorption scanning hysteresis including more recent theories based on percolation models. Through digital preservation and release of the tables from Brown’s dissertation, these data are now more easily accessible and can continue to find use in developing models of adsorption for fundamental and practical applications.

scholarly journals Poly(ionic liquid)-Modified Metal Organic Framework for Carbon Dioxide Adsorption

Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 370 ◽  
Author(s):  
Guangyuan Yang ◽  
Jialin Yu ◽  
Sanwen Peng ◽  
Kuang Sheng ◽  
Haining Zhang
Keyword(s):  
Carbon Dioxide ◽  
Ionic Liquid ◽  
Composite Materials ◽  
Metal Organic Frameworks ◽  
Carbon Dioxide Partial Pressure ◽  
Carbon Dioxide Adsorption ◽  
Solid Sorbent ◽  
Practical Applications ◽  
Metal Organic ◽  
Poly Ionic Liquid

The design and synthesis of solid sorbents for effective carbon dioxide adsorption are essential for practical applications regarding carbon emissions. Herein, we report the synthesis of composite materials consisting of amine-functionalized imidazolium-type poly(ionic liquid) (PIL) and metal organic frameworks (MOFs) through complexation of amino groups and metal ions. The carbon dioxide adsorption behavior of the synthesized composite materials was evaluated using the temperature-programmed desorption (TPD) technique. Benefiting from the large surface area of metal organic frameworks and high carbon dioxide diffusivity in ionic liquid moieties, the carbon dioxide adsorption capacity of the synthesized composite material reached 19.5 cm3·g−1, which is much higher than that of pristine metal organic frameworks (3.1 cm3·g−1) under carbon dioxide partial pressure of 0.2 bar at 25 °C. The results demonstrate that the combination of functionalized poly(ionic liquid) with metal organic frameworks can be a promising solid sorbent for carbon dioxide adsorption.

scholarly journals STUDY OF CARBON DIOXIDE ADSORPTION ON CHROMOXIDE CATALYST ON NON-STATIONARY CONCENTRATIONS

2018 ◽  
Vol 61 (7) ◽  
pp. 37 ◽  
Author(s):  
Nikolay I. Kol'tsov ◽  
Vladislav Kh. Fedotov
Keyword(s):  
Experimental Data ◽  
Carbon Dioxide ◽  
Chemical Kinetics ◽  
Carbon Dioxide Adsorption ◽  
Dissociative Mechanism ◽  
Simple Method ◽  
Desorption Process ◽  
Adsorption And Desorption ◽  
Additional Information ◽  
Adsorption Desorption

Investigation of the regularities of chemical processes, not only near but also far from the stationary state, gives additional information on their mechanisms. In this paper, we present a new method for estimating rate constants of adsorption-desorption processes from the experimentally measured values of the nonstationary concentrations of an adsorbed substance, based on calculating the instantaneous rates of the adsorption (or desorption) process. This method allows to connect unknown kinetic parameters of adsorption (desorption) of a substance on the catalyst surface for various most probable assumed mechanisms with the calculated values of the instantaneous rates of adsorption-desorption processes. As a consequence, the method makes it possible to solve two types of inverse problems of chemical kinetics: calculate point and interval values of rates constants of adsorption and desorption; determine the most likely mechanism from several proposed mechanisms of implementation of these processes. Using this method, point and interval values of the rates constants of adsorption and desorption of carbon dioxide were determined on the base of nonstationary experimental data on adsorption on the assumption of carbon dioxide adsorption on a chromoxide catalyst to three proposed mechanisms: linear, bimolecular and dissociative. Based on the results of calculations, the corresponding non-stationary dependences of carbon dioxide adsorption were restored, which were compared with the experimental data. The obtained results confirm that the previously established dissociative mechanism of adsorption of carbon dioxide on the chromoside catalyst is the most probable. The developed simple method does not require the use of complex optimization calculations and can be used to solve the inverse problem of chemical kinetics associated with the determination of mechanisms and the estimation of the rates constants of adsorption and desorption of substances on various catalysts.Forcitation:Kol’tsov N.I., Fedotov V.Kh. Study of carbon dioxide adsorption on chromoxide catalyst on non-stationary concentrations. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 7. P. 37-42

scholarly journals Utilization of spent dregs for the production of activated carbon for CO2 adsorption

2017 ◽  
Vol 19 (2) ◽  
pp. 44-50 ◽  
Author(s):  
Jarosław Serafin
Keyword(s):  
Carbon Dioxide ◽  
Activated Carbon ◽  
Density Functional ◽  
Activated Carbons ◽  
Density Functional Theory Method ◽  
Textural Properties ◽  
Carbon Dioxide Adsorption ◽  
Functional Theory ◽  
Surface Areas ◽  
Adsorption Desorption

Abstract The objective of this work was preparation of activated carbon from spent dregs for carbon dioxide adsorption. A saturated solution of KOH was used as an activating agent. Samples were carbonized in the furnace at the temperature of 550°C. Textural properties of activated carbons were obtained based on the adsorption-desorption isotherms of nitrogen at −196°C and carbon dioxide at 0°C. The specific surface areas of activated carbons were calculated by the Brunauer – Emmett – Teller equation. The volumes of micropores were obtained by density functional theory method. The highest CO2 adsorption was 9.54 mmol/cm3 at 0°C – and 8.50 mmol/cm3 at 25°C.

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