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Tetradecyl oxalate and octadecyl oxalate as novel phase change materials for thermal energy storage

机译:草酸四烷基和草酸二烷基酯作为热能储存的新型相变材料

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This paper related to synthesis, structural characterization, thermal properties and thermal reliability of novel phase change materials (PCMs) running at different temperatures. Dicarboxylic acid esters were synthesized via the reaction of oxalic acid, 1-tetradecanol and 1-octadecanol without using any catalyst and under vacuum for the first time at high yield. Synthesized ditetradecyl oxalate (DTO) and dioctadecyl oxalate (DOO) were characterized structurally by Fourier transform infrared (FT-IR) spectroscopy with ATR accessory and H-1 Nuclear Magnetic Resonance (H-1 NMR) spectroscopy techniques. Thermophysical properties including melting and freezing temperature, phase change enthalpy, total enthalpy, and specific heat capacity were determined by a differential scanning calorimeter (DSC) as degradation temperatures were determined by a thermogravimetric analyzer (TGA). Phase change temperatures of DTO and DOO were 47 degrees C and 65 degrees C for melting and 44 degrees C and 63 degrees C for solidification respectively. Latent heat capacity of DTO and DOO ranged from 210.6 J/g to 244.9 J/g for heating period and from 208.3 J/g to 241.7 J/g for cooling period. TGA measurements indicated that degradation temperature of DTO and DOO started at 231 degrees C and 238 degrees C respectively, which are sufficiently above their potential working temperatures. Crystalline morphology of PCMs was examined by a polarized optic microscope (POM). Thermal conductivity of DTO and DOO were found slightly lower than the precursors. However it was proven that it could be gradually increased by graphite. DTO and DOO were confirmed in terms of structure and thermal reliability after 1000 times accelerated heating-cooling cycles. All results pointed out that synthesized dicarboxylic acid esters can be validated as solid-liquid PCMs for some solar energy storage applications.
机译:本文与在不同温度下运行的新型相变材料(PCMS)的合成,结构表征,热性能和热可靠性有关。通过草酸,1-四氯甲醇和1-十八烷醇的反应合成二羧酸酯,而不使用任何催化剂并在真空下以高产率在真空下合成。草酸二甲酯(DTO)和草酸二乙二烷基酯(DOO)在结构上通过傅里叶变换红外(FT-IR)光谱,具有ATR附件和H-1核磁共振(H-1 NMR)光谱技术。在包括熔融和冷冻温度,相变焓,总焓和特定热容量的热物理性质由差示扫描量热计(DSC)确定,因为通过热重分析仪(TGA)测定劣化温度。 DTO和DOO的相变温度分别为47℃和65℃,分别用于44℃和63℃。 DTO和DOO的潜热容量为加热期间的210.6J / g至244.9J / g,冷却期间为208.3J / g至241.7J / g。 TGA测量表明,DTO和DOO的降解温度分别在231摄氏度和238摄氏度下开始,其足够高于其潜在的工作温度。通过偏振光显微镜(POM)检查PCM的晶体形态。发现DTO和DOO的导热率略低于前体。然而,证明它可以通过石墨逐渐增加。在加速加热冷却循环1000倍后,在结构和热可靠性方面确认了DTO和DOO。所有结果指出,合成的二羧酸酯可以验证为用于一些太阳能储存应用的固液PCM。

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