首页> 外文会议>International symposium on heat transfer and energy conservation >Pairs SrCl2-NH4Cl-NH3 and CaCl2-BaCl2-NH3 for a Two-stage Adsorption Freezing Cycle Driven by Low-temperature Heat Source
【24h】

Pairs SrCl2-NH4Cl-NH3 and CaCl2-BaCl2-NH3 for a Two-stage Adsorption Freezing Cycle Driven by Low-temperature Heat Source

机译:用于由低温热源驱动的两级吸附冷冻循环的对SrCl2-NH4Cl-NH3和CaCl2-BaCl2-NH3

获取原文

摘要

As an environmental benign and energy saving refrigeration technology, adsorption refrigeration has a great potential for the utilization of a low-grade energy, such as solar energy and industrial waste heat below 100oC. A two-stage adsorption refrigeration cycle was proposed based on adsorption refrigeration process and resorption process. Refrigeration performances of the working pairs were tested at different evaporation and condensation temperature. The results show that the present two-stage adsorption refrigeration cycle could obtain cooling output with -25°C when the temperature of heat resource was 70°C.The adsorption quantity of SrCl2 and CaCl2 are both more than 94% of theoretical adsorption quantity. Compared with SrCl2-NH4Cl-NH3 and CaCl2-BaCl2-NH3, generally the working pair of CaCl2-BaCl2-NH3 has optimal data of COP while the working pair of SrCl2-NH4Cl-NH3 has the optimal data of SCP. The maximum COP and SCP of the cycle were 0.25 and 0.25, 230.6W/kg and 278.7W/kg, respectively, for the working pairs of SrCl2-NH4Cl-NH3 and CaCl2-BaCl2-NH3, when the temperature of the cooling water was 25°C.
机译:作为一种环境良性和节能制冷技术,吸附制冷具有利用低级能源的巨大潜力,例如低于100℃的太阳能和工业废物。基于吸附制冷方法和吸收过程提出了一种两级吸附制冷循环。在不同的蒸发和冷凝温度下测试工作对的制冷性能。结果表明,当热资源温度为70℃时,目前的两级吸附制冷循环可以获得-25℃的冷却输出。SrCl2和CaCl2的吸附量均超过理论吸附量的94%。与SrCl2-NH4Cl-NH3和CaCl2-BaCl2-NH3相比,通常工作对CaCl2-Bacl2-NH3具有COP的最佳数据,而MRCl2-NH4Cl-NH3的工作对具有SCP的最佳数据。当冷却水的温度是时,循环的最大COP和SCP分别为0.25和0.25,230.6W / kg和278.7w / kg,用于SRCl2-NH4Cl-NH3和CaCl2-BaCl2-NH3的工作对25°C。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号