Kinetics of the Mono-esterification Between Terephthalic Acid and 1,4-Butanediol

田文玉; 曾作祥; 薛为岚; 李应宾; 章添钰

doi:10.1016/S1004-9541(10)60236-4

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Kinetics of the Mono-esterification Between Terephthalic Acid and 1,4-Butanediol

Updated：2026-01-06

- Kinetics of the Mono-esterification Between Terephthalic Acid and 1,4-Butanediol
- Chinese Journal of Chemical Engineering Vol. 18, Issue 3, Pages: 391-396(2010)
- Affiliations：
  
  1. Department of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology,Shijiazhuang,China,050018
  2. Institute of Chemical Engineering, East China University of Science and Technology,Shanghai,China,200237
- Author bio：
- Funds：
- DOI：10.1016/S1004-9541(10)60236-4
  CLC：
- Published：2010
- Accepted：
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TIAN Wenyu, ZENG Zuoxiang, XUE Weilan, LI Yingbin, ZHANG Tianyu. Kinetics of the Mono-esterification Between Terephthalic Acid and 1,4-Butanediol[J]. , 2010, 18(3): 391-396.
DOI：

TIAN Wenyu, ZENG Zuoxiang, XUE Weilan, LI Yingbin, ZHANG Tianyu. Kinetics of the Mono-esterification Between Terephthalic Acid and 1,4-Butanediol[J]. , 2010, 18(3): 391-396. DOI： 10.1016/S1004-9541(10)60236-4.

摘要

Abstract

The chemical kinetics of the monoesterification between terephthalic acid(TPA)and 1

4-butanediol (BDO)catalyzed by a metallo-organic compound was studied using the initial rate method.The experiments were carried out in the temperature range of 463-483 K

and butylhydroxyoxo-stannane(BuSnOOH)and tetrabutyl titanate[Ti(OBu)

]

were used as catalyst respectively.The initial rates of the reaction catalyzed by BuSnOOH or Ti(OBu)

were measured at a series of initial concentrations of BDO(or TPA) with the concentration of TPA(or BDO)kept constant.The reaction orders of reagents were determined by the initial rate method.The results indicate that the reaction order for TPA is related with the species of catalyst and it is 2 and 0.7 for BuSnOOH and Ti(OBu)

respectively.However

the order for BDO is the same 0.9 for the two catalysts.Furthermore

the effects of temperature and catalyst concentration are investigated

and the activation energies and the reaction rate constants for the two catalysts were determined.

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