2018
DOI: 10.1021/acs.energyfuels.7b03578
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Synthesis and Evaluation of Two Gas-Wetting Alteration Agents for a Shale Reservoir

Abstract: It is well-known that shale gas production is affected by the wettability of the reservoir. In this work, two gas-wetting alteration agents were synthesized and characterized by 1H NMR and FTIR. To evaluate the effect of the gas-wetting alteration agents on the shale wettability, the contact angle for droplets on the shale surface was detected, and the results showed that the contact angles of water and n-hexadecane increased from 36° and 0° to 119° and 88° after treatment with sodium [N-propyl-N-(perfluorooct… Show more

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Cited by 24 publications
(11 citation statements)
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“…Extensive efforts have been devoted to the synthesis and characterization of gas-wetting agents; fluorosurfactants and fluoropolymers dominate. Fluorosurfactants typically exhibit a more pronounced performance than fluoropolymers. However, the present fluorochemicals can only achieve intermediate gas-wetting due to the inability to fabricate a multiscale adsorption layer.…”
Section: Introductionmentioning
confidence: 99%
“…Extensive efforts have been devoted to the synthesis and characterization of gas-wetting agents; fluorosurfactants and fluoropolymers dominate. Fluorosurfactants typically exhibit a more pronounced performance than fluoropolymers. However, the present fluorochemicals can only achieve intermediate gas-wetting due to the inability to fabricate a multiscale adsorption layer.…”
Section: Introductionmentioning
confidence: 99%
“…Above 205 °C, the weight remains nearly unchanged. The Thermogravimetric result reveals that the decomposition of the novel fluorocarbon surfactant can proceed under relatively high-temperature 20 , 21 .
Figure 5 The thermal analysis curves of the novel fluorocarbon surfactant.
…”
Section: Resultsmentioning
confidence: 99%
“…Fifty milliliters of distilled water, 1.0 g of MMA (0.01 mol), and 0.1 g of OBS were added into the reaction vessel with condensation and stirring. Then, 4.0 g of F12 (0.01 mol) and 0.1 g of AIBN were dissolved in 50 mL of dimethylformamide (DMF) and added into the reaction vessel and stirred at 60 °C for 15 min under ultrasonic conditions. , Then, the reaction was heated to 80 °C and continued to react for 6 h. The emulsion with slight white fluorescence was prepared as a fluoropolymer microemulsion (Figure b). The reaction scheme is shown in Figure a.…”
Section: Methodsmentioning
confidence: 99%