2022
DOI: 10.1002/er.7697
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Novel urea‐based compounds as solid‐solid phase change materials: 1,3‐bisstearoylurea and 1,1,3,3‐tetrastearoylurea for thermal energy storage applications

Abstract: Summary 1,3‐Bisstearoylurea and 1,1,3,3‐tetrastearoylurea were produced as solid‐solid phase change materials (SS‐PCMs) for potential solar thermal energy storage (TES) applications via condensation of urea with the respective amount of carboxyl chloride (stearoyl chloride). Both 1,3‐bisstearoylurea and 1,1,3,3‐tetrastearoylurea were characterized by Fourier‐transform infrared (FT‐IR), 1H nuclear magnetic resonance, differential scanning calorimetry (DSC), and thermogravimetric (TG) analysis techniques. 1,3‐Bi… Show more

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Cited by 5 publications
(4 citation statements)
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“…Because of paraffin decomposition into CO 2 and H 2 O plus about 5% BC decomposition, IPW@HNTs@ PDA‐BC composite loses about 10% weight at 380–800 °C after 30 evaporation, which is the decomposition process of BC. [ 31,32 ]…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Because of paraffin decomposition into CO 2 and H 2 O plus about 5% BC decomposition, IPW@HNTs@ PDA‐BC composite loses about 10% weight at 380–800 °C after 30 evaporation, which is the decomposition process of BC. [ 31,32 ]…”
Section: Resultsmentioning
confidence: 99%
“…about 10% weight at 380-800 °C after 30 evaporation, which is the decomposition process of BC. [31,32] The TG spectra of pure IPW and IPW@HNTs@ PDA-BC composites in the evaporation rate test before and after 30 cycles are shown in Figure 5c. On the other hand, the IPW@HNTs@ PDA-BC composite results from a more substantial thermal degradation of the aerogel-coated IPW and a mild pyrolysis of the BC-based aerogel structure at high temperatures.…”
Section: Stability Of Ipw@hnts@ Pda-bc Compositesmentioning
confidence: 99%
“…corrosivity, sublimation tendencies) has demonstrated success in the literature previously. Examples of PCMs derived from fatty acids include fatty ureas, 25 esters, [26][27][28][29] thioureas, 30 carbonates 31 and amides. 17,18,32,33 These examples typically have melting temperatures below the intermediate temperature range (T m < 100 °C), with a notable exception being the fatty diamides and dicarbamates derived from stearic acid.…”
Section: Rsc Sustainability Accepted Manuscriptmentioning
confidence: 99%
“…[16] It is possible to modify organic PCMs to alter their functional properties. Studies of esters produced for this reason in the literature, [17][18][19][20] diesters, [21][22][23] alcohols, [24] dicarboxylic acid esters, [25] amides, [26][27][28] diamides, [29,30] sulfones, [31] and ureas [32] are increasing.…”
mentioning
confidence: 99%