Investigation on the Thermal Stability of Deep Eutectic Solvents

注册 English

Investigation on the Thermal Stability of Deep Eutectic Solvents

Wenjun CHEN , Zhimin XUE , Jinfang WANG , Jingyun JIANG , Xinhui ZHAO , Tiancheng MU

Citation: CHEN Wenjun, XUE Zhimin, WANG Jinfang, JIANG Jingyun, ZHAO Xinhui, MU Tiancheng. Investigation on the Thermal Stability of Deep Eutectic Solvents[J]. Acta Physico-Chimica Sinica, 2018, 34(8): 904-911. doi: 10.3866/PKU.WHXB201712281 shu

shu

低共熔溶剂的热稳定性研究

陈文君 ^1, ,
薛智敏 ^{2,
,} ,
王晋芳 ^1, ,
蒋静云 ^1, ,
赵新辉 ^1, ,
牟天成 ^{1,
,}

1.
中国人民大学化学系，北京 100872
2.
北京林业大学材料科学与技术学院，北京 100083

通讯作者: 薛智敏, zmxue@bjfu.edu.cn
牟天成, tcmu@ruc.edu.cn

基金项目:
国家自然科学基金 21503016

国家自然科学基金 21773307

国家自然科学基金(21773307, 21503016)资助项目

摘要: 近年来，低共熔溶剂(DESs)引起了人们的广泛关注，在诸多领域得到应用。DESs一般由氢键供体(HBDs)和氢键受体(HBAs)通过氢键作用形成，其热稳定性研究对于其高温应用具有重要意义。本文利用热重分析法(TG)对40种DESs的热稳定性进行了系统研究，并得到了所研究DESs的开始分解温度(T_onset)。值得注意的是，DESs受热后的变化情况与离子液体不同，呈现出分阶段失重的现象。通常形成DESs的氢键在升温后首先被破坏，从而导致DESs分解成组成其的HBDs和HBAs。然后热稳定性较差(或者沸点较低)的HBDs首先分解(或挥发)，而HBAs则在更高温度下分解(或挥发)。例如常见的HBA氯化胆碱(ChCl)在250 ℃附近开始分解。氢键强度对DESs受热后的表现起着重要的作用，DESs中的氢键会阻碍分子“逃脱”，使得T_onset向高温方向移动。此外，我们考察了阴离子、氢键供体、摩尔比对DESs热稳定性的影响，发现HBDs自身的挥发或分解对DESs的热稳定性起着决定性作用。由于用T_onset值会高估DESs的热稳定性，长期热稳定性的考察对其工业应用具有重要价值。本研究能帮助人们理解DESs的热分解行为，为制备具有适当热稳定性的DESs提供依据。

关键词:

English

Investigation on the Thermal Stability of Deep Eutectic Solvents

1.
Department of Chemistry, Renmin University of China, Beijing 100872, P. R. China
2.
College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, P. R. China

Corresponding author: XUE Zhimin, zmxue@bjfu.edu.cn MU Tiancheng, tcmu@ruc.edu.cn

Received Date: 12 December 2017
Accepted Date: 26 December 2017
Revised Date: 26 December 2017
Available Online: 15 August 2018
Fund Project:

The project was supported by the National Natural Science Foundation of China (21773307, 21503016)

Abstract: In recent years, deep eutectic solvents (DESs) have attracted considerable attention. They have been applied in many fields such as dissolution and separation, electrochemistry, materials preparation, reaction, and catalysis. The DESs are generally formed by the hydrogen bonding interactions between hydrogen-bond donors (HBDs) and acceptors (HBAs). Knowledge of the thermal stability of DESs is very important for their application at high temperatures. However, there have been relatively few studies on the thermal stability of DESs. Herein, a systematic investigation on the thermal stability of 40 DESs was carried out using thermal gravimetric analysis (TGA), and the onset decomposition temperatures (T_onset) of these solvents were obtained. The most important conclusion drawn from this work is that the thermal behavior of DESs is quite different from that of ionic liquids. The anions or cations of ionic liquids decompose first, followed by the decomposition of the opposite ion at elevated temperatures. On the other hand, the DESs generally first decompose to HBDs and HBAs at high temperatures through the weakening of the hydrogen bond interactions. Subsequently, the HBDs with relatively low boiling points or poor stabilities undergo volatilization or decomposition; the HBAs also undergo volatilization or decomposition but at a higher temperature. For example, the most commonly used HBA choline chloride (ChCl) begins to decompose at around 250 ℃. The hydrogen bond plays an important role in the thermal stability of DESs. It hinders the "escape" of molecules and requires greater energy to break than pure HBAs and HBDs, which causes the T_onset of DESs to shift to higher temperatures. Note that the thermal stability of HBDs has a crucial effect on the T_onset of DESs. The HBDs would decompose or volatilize first during TGA because of their relatively poor thermal stability or lower boiling points. The more stable the HBDs are, the greater would be the T_onset values of the corresponding DESs. Further, the effects of anions on HBAs, molar ratio of HBAs to HBDs, and heating rate in fast scan TGA have been discussed. As the heating rate increased, the TGA curves of DESs shifted to higher temperatures gradually, and the temperature hysteretic effect became prominent when the rate reached 10 ℃?min?1. From an industrial application point of view, there is an overestimation of the onset decomposition temperatures of DESs by T_onset, so the long-term stability of DESs was investigated at the end of the study. This study could help understand the thermal behavior of DESs (progressive decomposition) and provide guidance for designing DESs with appropriate thermal stability for practical applications.

Key words:

1. [1]
  Zhang, Z.; Song, J.; Han, B. Chem. Rev. 2017, 117, 6834. doi: 10.1021/acs.chemrev.6b00457
2. [2]
  Xue, Z.; Zhang, Z.; Han, J.; Chen, Y.; Mu, T. Int. J. Greenhouse Gas Control 2011, 5, 628. doi: 10.1016/j.ijggc.2011.05.014
3. [3]
  Zhao, W.; Xue, Z.; Wang, J.; Jiang, J.; Zhao, X.; Mu, T. ACS Appl. Mater. Interfaces 2015, 7, 27608. doi: 10.1021/acsami.5b10734
4. [4]
  Cao, Y.; Chen, Y.; Sun, X.; Zhang, Z.; Mu, T. Phys. Chem. Chem. Phys. 2012, 14, 12252. doi: 10.1039/C2CP41798G
5. [5]
  王晓静, 牟天成.科学通报, 2015, 60, 2516.doi: 10.1360/N972015-00266Wang, X. J.; Mu, T. Chin. Sci. Bull. 2015, 60, 2516. doi: 10.1360/N972015-00266
6. [6]
  Tang, B.; Row, K. H. Monatsh. Chem. 2013, 144, 1427. doi: 10.1007/s00706-013-1050-3
7. [7]
  Smith, E. L.; Abbott, A. P.; Ryder, K. S. Chem. Rev. 2014, 114, 11060. doi: 10.1021/cr300162p
8. [8]
  Maugeri, Z.; de Maria, P. D. RSC Adv. 2012, 2, 421. doi: 10.1039/C1RA00630D
9. [9]
  Zhang, Q.; De Oliveira Vigier, K.; Royer, S.; Jerome, F. Chem. Soc. Rev. 2012, 41, 7108. doi: 10.1039/C2CS35178A
10. [10]
  Jhong, H. R.; Wong, D. S. H.; Wan, C. C.; Wang, Y. Y.; Wei, T. C. Electrochem. Commun. 2009, 11, 209. doi: 10.1016/j.elecom.2008.11.001
11. [11]
  Liu, P.; Hao, J. W.; Mo, L. P.; Zhang, Z. H. RSC Adv. 2015, 5, 48675. doi: 10.1039/C5RA05746A
12. [12]
  Nkuku, C. A.; LeSuer, R. J. Phys. Chem. B 2007, 111, 13271. doi: 10.1021/jp075794j
13. [13]
  Jiang, J.; Yan, C.; Zhao, X.; Luo, H.; Xue, Z.; Mu, T. Green Chem. 2017, 19, 3023. doi: 10.1039/C7GC01012E
14. [14]
  Jiang, J.; Zhao, W.; Xue, Z.; Li, Q.; Yan, C.; Mu, T. ACS Sustainable Chem. Eng. 2016, 4, 5814. doi: 10.1021/acssuschemeng.6b01860
15. [15]
  Li, G.; Yan, C.; Cao, B.; Jiang, J.; Zhao, W.; Wang, J.; Mu, T. Green Chem. 2016, 18, 2522. doi: 10.1039/C5GC02691A
16. [16]
  Chen, Y.; Cao, Y.; Shi, Y.; Xue, Z.; Mu, T. Ind. Eng. Chem. Res. 2012, 51, 7418. doi: 10.1021/ie300247v
17. [17]
  Cao, Y.; Mu, T. Ind. Eng. Chem. Res.2014, 53, 8651. doi: 10.1021/ie5009597
18. [18]
  Xue, Z.; Zhang, Y.; Zhou, X. -Q.; Cao, Y.; Mu, T. Thermochim. Acta 2014, 578, 59. doi: 10.1016/j.tca.2013.12.005
19. [19]
  Liu, S.; Chen, Y.; Shi, Y.; Sun, H.; Zhou, Z.; Mu, T. J. Mol. Liq. 2015, 206, 95. doi: 10.1016/j.molliq.2015.02.022
20. [20]
  Sun, X.; Liu, S.; Khan, A.; Zhao, C.; Yan, C.; Mu, T. New J. Chem. 2014, 38, 3449. doi: 10.1039/C4NJ00384E
21. [21]
  Li, Q.; Jiang, J.; Li, G.; Zhao, W.; Zhao, X.; Mu, T. Sci. China Chem. 2016, 59, 571. doi: 10.1007/s11426-016-5566-3
22. [22]
  Wang, B.; Qin, L.; Mu, T.; Xue, Z.; Gao, G. Chem. Rev. 2017, 117, 7113. doi: 10.1021/acs.chemrev.6b00594.
23. [23]
  Morrison, H. G.; Sun, C. C.; Neervannan, S. Int. J. Pharm. 2009, 378, 136. doi: 10.1016/j.ijpharm.2009.05.039
24. [24]
  Abbott, A. P.; Boothby, D.; Capper, G.; Davies, D. L.; Rasheed, R. K. J. Am. Chem. Soc. 2004, 126, 9142. doi: 10.1021/ja048266j
25. [25]
  Lynam, J. G.; Kumar, N.; Wong, M. J. Bioresour. Technol. 2017, 238, 684. doi: 10.1016/j.biortech.2017.04.079
26. [26]
  Abbott, A. P.; Capper, G.; Davies, D. L.; Rasheed, R. K.; Tambyrajah, V. Chem. Commun. 2003, 70. doi: 10.1039/B210714G
27. [27]
  Abbott, A. P.; Capper, G.; Davies, D. L.; Munro, H. L.; Rasheed, R. K.; Tambyrajah, V. Chem. Commun. 2001, 2010. doi: 10.1039/B106357J
28. [28]
  Hayyan, A.; Mjalli, F. S.; AlNashef, I. M.; Al-Wahaibi, Y. M.; Al-Wahaibi, T.; Hashim, M. A. J. Mol. Liq. 2013, 178, 137. doi: 10.1016/j.molliq.2012.11.025
29. [29]
  Ilgen, F.; Ott, D.; Kralisch, D.; Reil, C.; Palmberger, A.; Konig, B. Green Chem.2009, 11, 1948. doi: 10.1039/B917548M
30. [30]
  Sun, S.; Niu, Y.; Xu, Q.; Sun, Z.; Wei, X. Ind. Eng. Chem. Res.2015, 54, 8019. doi: 10.1021/acs.iecr.5b01789
31. [31]
  Abbott, A. R.; Capper, G.; Gray, S. ChemPhysChem 2006, 7, 803. doi: 10.1002/cphc.200500489
32. [32]
  Amarasekara, A. S.; Owereh, O. S. J. Therm. Anal. Calorim.2011, 103, 1027. doi: 10.1007/s10973-010-1101-5
33. [33]
  Jagadeeswara Rao, C.; Venkata Krishnan, R.; Venkatesan, K. A.; Nagarajan, K.; Srinivasan, T. G. J. Therm. Anal. Calorim. 2009, 97, 937. doi: 10.1007/s10973-009-0193-2
34. [34]
  Ngo, H. L.; LeCompte, K.; Hargens, L.; McEwen, A. B. Thermochim. Acta 2000, 357–358, 97. doi: 10.1016/S0040-6031[00]00373-7
35. [35]
  Yue, D.; Jing, Y.; Ma, J.; Yao, Y.; Jia, Y. J. Therm. Anal. Calorim. 2012, 110, 773. doi: 10.1007/s10973-011-1960-4
36. [36]
  Heym, F.; Etzold, B. J. M.; Kern, C.; Jess, A. Phys. Chem. Chem. Phys. 2010, 12, 12089. doi: 10.1039/C0CP00097C
37. [37]
  Seeberger, A.; Andresen, A. -K.; Jess, A. Phys. Chem. Chem. Phys. 2009, 11, 9375. doi: 10.1039/B909624H
38. [38]
  Wooster, T. J.; Johanson, K. M.; Fraser, K. J.; MacFarlane, D. R.; Scott, J. L. Green Chem.2006, 8, 691. doi: 10.1039/B606395K
39. [39]
  Del Sesto, R. E.; McCleskey, T. M.; Macomber, C.; Ott, K. C.; Koppisch, A. T.; Baker, G. A.; Burrell, A. K. Thermochim. Acta 2009, 491, 118. doi: 10.1016/j.tca.2009.02.023
40. [40]
  Crosthwaite, J. M.; Muldoon, M. J.; Dixon, J. K.; Anderson, J. L.; Brennecke, J. F. J. Chem. Thermodyn. 2005, 37, 559. doi: 10.1016/j.jct.2005.03.013

WeChat

扫一扫看文章

计量

PDF下载量: 140
文章访问数: 2006
HTML全文浏览量: 336

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

/

下载: 全尺寸图片幻灯片

分享

用微信扫码二维码

分享至好友和朋友圈