...
首页> 外文期刊>Journal of Chemical and Engineering Data: the ACS Journal for Data >Thermodynamic Properties and Crystal Structures of the Adductive 2,6-Naphthalenedicarboxylic Acid Crystallization with N,N-Dimethyl Acetamide and N-Methyl Pyrrolidone
【24h】

Thermodynamic Properties and Crystal Structures of the Adductive 2,6-Naphthalenedicarboxylic Acid Crystallization with N,N-Dimethyl Acetamide and N-Methyl Pyrrolidone

机译:N,N-二甲基乙酰胺和N-甲基吡咯烷酮对2,6-萘二甲酸加合物结晶的热力学性质和晶体结构

获取原文
获取原文并翻译 | 示例
           

摘要

The crystal structures and thermodynamic properties of NDA-DMAC and NDA-NMP adduct crystals, the solubilities of 2,6-naphthalenedicarboxylic acid (NDA) in N,iV-dimethyl acetamide (DMAC) and N-methyl pyrrolidone (NMP) over a temperature range from (293.2 to 373.2) K were studied in this paper. The results show that: (1) The asymmetric units of NDA-DMAC and NDA-NMP adduct crystals both contain one half molecule of NDA and one molecule of the solvent which are linked mainly by hydrogen bonds. (2) The thermal stabilities of the two adducts are both poor, and the initial dissociation temperature of NDA-DMAC and NDA-NMP adducts are about 306.29 K and 322.75 K, respectively. (3) The solubilities of NDA in DMAC and NMP solvents at (293.2 to 373.2) K both increase with the rise of experimental temperature. Below the dissociation temperature, the equilibrium solid phase is the adduct crystal with the adduct solvent. Otherwise, the equilibrium solid phase is the pure NDA solid with the adduct crystal dissociating. The solubility data are correlated by the Buchowski equation or the nonrandom two-liquid (NRTL) activity coefficient model.
机译:NDA-DMAC和NDA-NMP加合物晶体的晶体结构和热力学性质,2,6-萘二甲酸(NDA)在N,iV-二甲基乙酰胺(DMAC)和N-甲基吡咯烷酮(NMP)中的溶解度本文研究的范围是(293.2至373.2)K。结果表明:(1)NDA-DMAC和NDA-NMP加合物晶体的不对称单元均含有一个半分子的NDA和一分子的溶剂,它们主要通过氢键连接。 (2)两种加合物的热稳定性均较差,NDA-DMAC和NDA-NMP加合物的初始解离温度分别为约306.29K和322.75K。 (3)NDA在DMAC和NMP溶剂中(293.2至373.2)K的溶解度均随实验温度的升高而增加。在解离温度以下,平衡固相为具有加合物溶剂的加合物晶体。否则,平衡固相是加合物晶体解离的纯NDA固体。溶解度数据通过Buchowski方程或非随机两液(NRTL)活性系数模型进行关联。

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