2020
DOI: 10.1039/d0ta03442h
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Tunable LiCl@UiO-66 composites for water sorption-based heat transformation applications

Abstract:

No deliquescence, cycle stability, increased water uptake over a neat MOF and LiCl at low humidity, and high coefficient of performance.

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Cited by 74 publications
(41 citation statements)
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“…It is worth noting that although composite sorbents with solution leakage may shows very high water uptake at high RH, they are not the true composite sorbent as result of irreversible salt losses and agglomeration of salts once they are applied in large-scale SAWH systems. 50 Therefore, it is highly valuable to develop porous matrix with ultrahigh pore volume to load a high content of salts and store a large amount of adsorbed water for preventing the risk of liquid leakage.…”
Section: Introductionmentioning
confidence: 99%
“…It is worth noting that although composite sorbents with solution leakage may shows very high water uptake at high RH, they are not the true composite sorbent as result of irreversible salt losses and agglomeration of salts once they are applied in large-scale SAWH systems. 50 Therefore, it is highly valuable to develop porous matrix with ultrahigh pore volume to load a high content of salts and store a large amount of adsorbed water for preventing the risk of liquid leakage.…”
Section: Introductionmentioning
confidence: 99%
“…The water uptake at 0.4 relative pressure of the composite ES-47-CaCl 2 , which has uniform mesopores with an average pore size of 10.2 nm and a total pore volume (0.207 cm 3 /g), was 1.7% lower than the water uptake of the composite W-46-CaCl 2 with a smaller pore diameter (8.3 nm) and a larger total pore volume (0.252 cm 3 /g). The water uptake curve of the composite with W-46-γ-Al 2 O 3 and 15 wt% LiCl showed a plateau at 0.038 p/p o due to the formation of lithium chloride hydrate [44], while this plateau was not observed for the composites with lower salt content.…”
Section: Water Sorption Propertiesmentioning
confidence: 89%
“…Energy capacity increased gradually from 998 ± 20 kJ kg -1 (AF-Ca 1 ) to 1840 ± 20 kJ kg -1 (AF-Ca ). As an increase in the amount of CaCl 2 in the composite enhanced the water sorption capacity and consequently, energy storage capacity in kJ kg -1 [37,39,76]. Besides, the aluminium fumarate composites with higher amounts of salt (AF-Ca 2 and AF-Ca 3 ) show experimental dehydration heats higher than expected by simple addition of the two contributions of the salt and the support (as derived from the experiments performed on CaCl 2 .2H 2 O and AF separately, Table 3).…”
Section: Heat Storage Performance and Water Sorption Propertiesmentioning
confidence: 99%