scholarly journals Experimental study on the adverse effect of gel fracturing fluid on gas sorption behavior for Illinois coal

2021 ◽  
Author(s):  
Qiming Huang ◽  
Jun Li ◽  
Shimin Liu ◽  
Gang Wang
Keyword(s):  
Sorption Capacity ◽  
Sorption Behavior ◽  
Gas Sorption ◽  
Fracturing Fluid ◽  
Reservoir Stimulation ◽  
Adsorption Sites ◽  
Pore Blockage ◽  
Desorption Hysteresis ◽  
Coal Reservoir ◽  
The Impact

AbstractHydraulic fracturing is an effective technology for coal reservoir stimulation. After fracturing operation and flowback, a fraction of fracturing fluid will be essentially remained in the formation which ultimately damages the flowability of the formation. In this study, we quantified the gel-based fracturing fluid induced damages on gas sorption for Illinois coal in US. We conducted the high-pressure methane and CO2 sorption experiments to investigate the sorption damage due to the gel residue. The infrared spectroscopy tests were used to analyze the evolution of the functional group of the coal during fracturing fluid treatment. The results show that there is no significant chemical reaction between the fracturing fluid and coal, and the damage of sorption is attributed to the physical blockage and interactions. As the concentration of fracturing fluid increases, the density of residues on the coal surface increases and the adhesion film becomes progressively denser. The adhesion film on coal can apparently reduce the number of adsorption sites for gas and lead to a decrease of gas sorption capacity. In addition, the gel residue can decrease the interconnectivity of pore structure of coal which can also limit the sorption capacity by isolating the gas from the potential sorption sites. For the low concentration of fracturing fluid, the Langmuir volume was reduced to less than one-half of that of raw coal. After the fracturing fluid invades, the desorption hysteresis of methane and CO2 in coal was found to be amplified. The impact on the methane desorption hysteresis is significantly higher than CO2 does. The reason for the increasing of hysteresis may be that the adsorption swelling caused by the residue adhered on the pore edge, or the pore blockage caused by the residue invasion under high gas pressure. The results of this study quantitatively confirm the fracturing fluid induced gas sorption damage on coal and provide a baseline assessment for coal fracturing fluid formulation and technology.

scholarly journals Kerogen nanoscale structure and CO2 adsorption in shale micropores

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Aleksandra Gonciaruk ◽  
Matthew R. Hall ◽  
Michael W. Fay ◽  
Christopher D. J. Parmenter ◽  
Christopher H. Vane ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Chemical Composition ◽  
Focused Ion Beam ◽  
Gas Adsorption ◽  
Ion Beam ◽  
Molecular Size ◽  
Gas Sorption ◽  
Nanoscale Structures ◽  
Adsorption Sites ◽  
Nanoscale Structure

AbstractGas storage and recovery processes in shales critically depend on nano-scale porosity and chemical composition, but information about the nanoscale pore geometry and connectivity of kerogen, insoluble organic shale matter, is largely unavailable. Using adsorption microcalorimetry, we show that once strong adsorption sites within nanoscale network are taken, gas adsorption even at very low pressure is governed by pore width rather than chemical composition. A combination of focused ion beam with scanning electron microscopy and transmission electron microscopy reveal the nanoscale structure of kerogen includes not only the ubiquitous amorphous phase but also highly graphitized sheets, fiber- and onion-like structures creating nanoscale voids accessible for gas sorption. Nanoscale structures bridge the current gap between molecular size and macropore scale in existing models for kerogen, thus allowing accurate prediction of gas sorption, storage and diffusion properties in shales.

scholarly journals Effect of moisture condensation on vapour transmission through porous membranes

2021 ◽  
pp. 152808372110142
Author(s):  
Ariana Khakpour ◽  
Michael Gibbons ◽  
Sanjeev Chandra
Keyword(s):  
Water Vapour ◽  
Moisture Diffusion ◽  
Porous Membrane ◽  
Water Evaporation ◽  
Porous Membranes ◽  
Water Vapour Concentration ◽  
Vapour Concentration ◽  
Vapour Diffusion ◽  
Pore Blockage ◽  
The Impact

Porous membranes find natural application in various fields and industries. Water condensation on membranes can block pores, reduce vapour transmissibility, and diminish the porous membranes' performance. This research investigates the rate of water vapour transmission through microporous nylon and nanofibrous Gore-Tex membranes. Testing consisted of placing the membrane at the intersection of two chambers with varied initial humidity conditions. One compartment is initially set to a high ([Formula: see text]water vapour concentration and the other low ([Formula: see text], with changes in humidity recorded as a function of time. The impact of pore blockage was explored by pre-wetting the membranes with water or interposing glycerine onto the membrane pores before testing. Pore blockage was measured using image analysis for the nylon membrane. The mass flow rate of water vapour ( ṁv) diffusing through a porous membrane is proportional to both its area (A) and the difference in vapour concentration across its two faces ([Formula: see text], such that [Formula: see text] where K is defined as the moisture diffusion coefficient. Correlations are presented for the variation of K as a function of [Formula: see text]. Liquid contamination on the porous membrane has been shown to reduce the moisture diffusion rate through the membrane due to pore blockage and the subsequent reduced open area available for vapour diffusion. Water evaporation from the membrane's surface was observed to add to the mass of vapour diffusing through the membrane. A model was developed to predict the effect of membrane wetting on vapour diffusion and showed good agreement with experimental data.

Ionic π-Conjugated Polymer Networks by Catalyst-Free Polymerization, Photoluminescence and Gas Sorption Behavior

2016 ◽  
Vol 217 (17) ◽  
pp. 1886-1898 ◽  
Author(s):  
Tomáš Faukner ◽  
Arnošt Zukal ◽  
Jiří Brus ◽  
Jiří Zedník ◽  
Jan Sedláček
Keyword(s):  
Conjugated Polymer ◽  
Polymer Networks ◽  
Sorption Behavior ◽  
Gas Sorption ◽  
Catalyst Free

scholarly journals The binary gas sorption in the bituminous coal of the Huaibei Coalfield in China

2018 ◽  
Vol 36 (9-10) ◽  
pp. 1612-1628 ◽  
Author(s):  
Lei Zhang ◽  
Zhiwei Ye ◽  
Mingxue Li ◽  
Cun Zhang ◽  
Qingsheng Bai ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Sorption Capacity ◽  
Bituminous Coal ◽  
Gas Adsorption ◽  
Langmuir Equation ◽  
Separation Coefficient ◽  
Gas Sorption ◽  
Langmuir Adsorption ◽  
Gas Molecules ◽  
Huaibei Coalfield

Knowledge of the gas sorption characteristics of a coal not only helps to explain the mechanism of enhanced coalbed methane recovery but also provides an important basis for simultaneous coal and gas extraction. In consequence, the pure and binary gas excess sorption capacity of methane, carbon dioxide, and nitrogen of bituminous coal samples derived from the Xutuan Coal Mine in Huaibei coalfield, in Anhui Province in China, was measured using the volumetric method. The fitting analysis of the pure gas Langmuir adsorption model was carried out. The binary gas excess sorption measurement showed that the final sorption capacity of bituminous samples was the same no matter what the gas adsorption order of competitive adsorption and displacement adsorption. Hence, coal gas adsorption is physical adsorption, i.e. the different adsorption and desorption process of gas molecules does not affect the final adsorption amount of coal to each component of gas. Using the fitting parameters obtained by the Langmuir equation, the extended Langmuir equation was used to predict the adsorption capacity for each component of the binary gas. The comparison between predicted adsorption capacity and measured adsorption capacity showed that the extended Langmuir equation can better describe the trend of the adsorption isotherm curves of a binary gas under different pressures. The separation coefficient and displacement coefficient were defined from Langmuir adsorption theory. The separation coefficient involves the proportion of each component in the free phase and the proportion of each component in the adsorption phase. The displacement coefficient involves the displacement ability of gas molecules at adsorption sites by free gas molecules.

The impact of variable carbonation and decarbonation conditions on the CO2 sorption capacity of CaO-based sorbents

2019 ◽  
Vol 73 (12) ◽  
pp. 3031-3042
Author(s):  
Marek Staf ◽  
Barbora Miklová ◽  
Veronika Kyselová
Keyword(s):  
Sorption Capacity ◽  
Co2 Sorption ◽  
The Impact

scholarly journals The Effect of Adhesive Additives on Silica Gel Water Sorption Properties

Entropy ◽  
2020 ◽  
Vol 22 (3) ◽  
pp. 327
Author(s):  
Karol Sztekler ◽  
Wojciech Kalawa ◽  
Agata Mlonka-Medrala ◽  
Wojciech Nowak ◽  
Łukasz Mika ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Silica Gel ◽  
Water Sorption ◽  
High Reliability ◽  
Electricity Consumption ◽  
Hydroxyethyl Cellulose ◽  
Poly Vinyl Alcohol ◽  
Dynamic Adsorption ◽  
Metal Plates ◽  
The Impact

Adsorption chillers are characterized by low electricity consumption, lack of moving parts, and high reliability. The disadvantage of these chillers is their large weight due to low adsorbent sorption capacity. Therefore, the attention is turned to finding a sorbent with a high water sorption capacity and enhanced thermal conductivity to increase chiller efficiency. The article discusses the impact of selected adhesives used for the production of an adsorption bed in order to improve heat exchange on its surface. Experiments with silica gel with three commercial types of glue on metal plates representing heat exchanger were performed. The structure of samples was observed under a microscope to determine the coverage of adsorbent by glue. To determine the kinetics of the free adsorption, the amounts of moisture adsorbed and the desorption dynamics the prepared samples of coated bed on metal plates were moisturized and dried in a moisture analyzer. Samples made of silica gel mixed with the adhesive 2-hydroxyethyl cellulose, show high adsorption capacity, low dynamic adsorption, and medium dynamic desorption. Samples containing adhesive poly(vinyl alcohol) adsorb less moisture, but free adsorption and desorption were more dynamic. Samples containing the adhesive hydroxyethyl cellulose show lower moisture capacity, relatively dynamic adsorption, and lower dynamic desorption.

Gas sorption and diffusion damages by guar-based fracturing fluid for CBM reservoirs

Fuel ◽  
2019 ◽  
Vol 251 ◽  
pp. 30-44 ◽  
Author(s):  
Qiming Huang ◽  
Shimin Liu ◽  
Gang Wang ◽  
Bing Wu ◽  
Yun Yang ◽  
...  
Keyword(s):  
Gas Sorption ◽  
Fracturing Fluid ◽  
And Diffusion

scholarly journals An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

2020 ◽  
Vol 11 ◽  
pp. 310-322
Author(s):  
Felix M Badaczewski ◽  
Marc O Loeh ◽  
Torben Pfaff ◽  
Dirk Wallacher ◽  
Daniel Clemens ◽  
...  
Keyword(s):  
Neutron Scattering ◽  
Carbon Materials ◽  
Pore Space ◽  
Atomic Scale ◽  
Sorption Behavior ◽  
Wide Angle ◽  
Large Organic Molecule ◽  
Nanoscale Pore ◽  
Nanopore Structure ◽  
The Impact

This study is dedicated to link the nanoscale pore space of carbon materials, prepared by hard-templating of meso-macroporous SiO2 monoliths, to the corresponding nanoscale polyaromatic microstructure using two different carbon precursors wthat generally exhibit markedly different carbonization properties, i.e., a graphitizable pitch and a non-graphitizable resin. The micro- and mesoporosity of these monolithic carbon materials was studied by the sorption behavior of a relatively large organic molecule (p-xylene) in comparison to typical gas adsorbates (Ar). In addition, to obtain a detailed view on the nanopore space small-angle neutron scattering (SANS) combined with in situ physisorption was applied, using deuterated p-xylene (DPX) as a contrast-matching agent in the neutron scattering process. The impact of the carbon precursor on the structural order on an atomic scale in terms of size and disorder of the carbon microstructure, on the nanopore structure, and on the template process is analyzed by special evaluation approaches for SANS and wide-angle X-ray scattering (WAXS). The WAXS analysis shows that the pitch-based monolithic material exhibits a more ordered microstructure consisting of larger graphene stacks and similar graphene layer sizes compared to the monolithic resin. Another major finding is the discrepancy in the accessible micro/mesoporosity between Ar and deuterated p-xylene that found for the two different carbon precursors, pitch and resin, which can be regarded as representative carbon precursors in general. These differences essentially indicate that physisorption using probe gases such as Ar or N2 can provide misleading parameters if to be used to appraise the accessibility of the nanoscale pore space.

Sorption Behavior of Neptunium on Bentonite-Effect of Calcium Ion on the Sorption -

1994 ◽  
Vol 353 ◽  
Author(s):  
Naofumi Kozai ◽  
Toshihiko Ohnuki ◽  
Susumu Muraoka
Keyword(s):  
Distribution Coefficient ◽  
Sorption Capacity ◽  
Calcium Ion ◽  
Strong Acid ◽  
Sorption Behavior ◽  
Exchangeable Cation ◽  
Batch Type ◽  
Ph Range

AbstractThe sorption behavior of neptunium on bentonite was studied with batch type sorption and desorption experiments over a pH range of 2 to 8. A series of parallel studies using Na-smectite, Ca-smectite and admixtures of Na-smectite and calcite quantified the capacity of Ca2+ (which occurs in bentonite as an exchangeable cation of smectite and as a component of calcite) to inhibit the sorption of neptunium. The distribution coefficient (Kd) of neptunium for bentonite was constant from pH 2 to 7, while for pure Na-smectite Kd increased below pH 5 due to “specific sorption” of neptunium on Na-smectite. Specific sorption was defined as occurring when neptunium could be desorbed by a strong acid (1 M HCl) but was stable in the presence of 1 M KCl. It was found that the quantity of neptunium sorbed on Na-smectite was inversely proportional to the concentration of Ca2+ in solution, an effect most pronounced at pH <5. These results show that Ca2+ limits the specific sorption capacity of Na-smectite for neptunium. Similarly, in the mixture of Na-smectite and calcite, sufficient Ca2+ was solubilized to depress neptunium sorption. This investigation demonstrates that Ca2+ contained in bentonite as exchangeable cation and released from calcite reduces the specific sorption of neptunium.

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