On thermal stability of polydiphenylenesulfophthalide lithium salt

被引:1
|
作者
Shishlov, N. M. [1 ]
Akhmetzyanov, Sh. S. [1 ]
Khursan, S. L. [1 ]
机构
[1] Russian Acad Sci, Ufa Inst Chem, 71 Prosp Oktyabrya, Ufa 450075, Russia
关键词
polytriarylcarbinol; polydiphenylenesulfophthalide; thermolysis; radicals; dissociation energies; IR spectra; electronic spectra; DFT calculations; NAFION; DEGRADATION; HYDRATION; WATER;
D O I
10.1007/s11172-016-1603-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thermolysis of polytriarylcarbinol (PTAC-Li) (lithium salt of polydiphenylenesulfophthalide (PDSP)) was studied in the temperature range from 100 to 500 A degrees D<inverted exclamation> by thermogravimetric analysis (TG) and IR and electronic spectroscopy to check the available data on the higher thermal stability of PDSP salts over the initial polymer. The mass losses detected by the TG method in the polymer salt at 80-150 and 240-350 A degrees D are mainly caused by the desorption of weakly and strongly bound water. According to the calculations in the B3LYP/6-311+G(d,p) approximation, the D-DDe and C-SO (3) (-) Li+ bonds are weakest in the carbinol model for PTAC-Li (D(C-O) = D(C-S) = 72 kcal mol(-1)). The thermolysis of PDSP is accompanied by SO2 evolution, whereas hydroxy and sulfo groups detached from PTAC-Li macromolecules remain in the thermolyzate. Phenol fragments and an inorganic phase, the final form of which is lithium sulfate, are formed in this process. An analysis of the IR and UV spectra of the thermolyzates of PTAC-Li and PDSP confirmed that fluorenyl fragments are predominantly formed upon the thermolysis of these polymers. The data obtained do not confirm a higher stability of PTAC-Li compared to that of PDSP.
引用
收藏
页码:2437 / 2443
页数:7
相关论文
共 50 条
  • [1] On thermal stability of polydiphenylenesulfophthalide lithium salt
    N. M. Shishlov
    Sh. S. Akhmetzyanov
    S. L. Khursan
    Russian Chemical Bulletin, 2016, 65 : 2437 - 2443
  • [2] Ionic conductivity and thermal stability of lithium salt/potassium bifluoride electrolytes for thermal batteries
    Yazdani, Aliakbar
    Sanghadasa, Mohan
    Botte, Gerardine G.
    JOURNAL OF POWER SOURCES, 2020, 453
  • [3] Radical products of thermal decomposition of polydiphenylenesulfophthalide
    Shishlov, N. M.
    Akhmetzyanov, Sh. S.
    Khursan, S. L.
    RUSSIAN CHEMICAL BULLETIN, 2013, 62 (07) : 1614 - 1624
  • [4] Radical products of thermal decomposition of polydiphenylenesulfophthalide
    N. M. Shishlov
    Sh. S. Akhmetzyanov
    S. L. Khursan
    Russian Chemical Bulletin, 2013, 62 : 1614 - 1624
  • [5] The influence of lithium salt on the interfacial reactions controlling the thermal stability of graphite anodes
    Andersson, AM
    Herstedt, M
    Bishop, AG
    Edström, K
    ELECTROCHIMICA ACTA, 2002, 47 (12) : 1885 - 1898
  • [6] Oxidative stability and thermal performance of ester based lube oil with lithium salt additives
    Yeh, Feng-Min
    Volli, Vikranth
    Bin Laiwang
    Tung, Pei-Hsuan
    Shu, Chi-Min
    APPLIED THERMAL ENGINEERING, 2019, 150 : 1328 - 1336
  • [7] Effects of solvents and salt on the thermal stability of lithiated graphite used in lithium ion battery
    Wang, Qingsong
    Sun, Jinhua
    Chen, Chunhua
    JOURNAL OF HAZARDOUS MATERIALS, 2009, 167 (1-3) : 1209 - 1214
  • [8] Polycarbonate-Based Lithium Salt-Containing Electrolytes: New Insights into Thermal Stability
    Buchheit, Annika
    Gruenebaum, Mariano
    Tessmer, Britta
    Winter, Martin
    Wiemhoefer, Hans-Dieter
    JOURNAL OF PHYSICAL CHEMISTRY C, 2021, 125 (08): : 4371 - 4378
  • [9] Influence of salt, solvents, and additives on the thermal stability of delithiated cathodes in lithium-ion batteries
    Lee, Yongho
    Kim, Sang-Ok
    Mun, Junyoung
    Park, Min-Sik
    Kim, Ki Jae
    Lee, Kwan Young
    Choi, Wonchang
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2017, 807 : 174 - 180
  • [10] The Thermal Stability of Lithium Solid Electrolytes with Metallic Lithium
    Chen, Rusong
    Nolan, Adelaide M.
    Lu, Jiaze
    Wang, Junyang
    Yu, Xiqian
    Mo, Yifei
    Chen, Liquan
    Huang, Xuejie
    Li, Hong
    JOULE, 2020, 4 (04) : 812 - 821