Terephthalic acid synthesis at higher concentrations in high-temperature liquid water. 1. Effect of oxygen feed method

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Terephthalic Acid Synthesis at Higher Concentrations in High-Temperature Liquid Water. 1. Effect of Oxygen Feed Method

We conducted terephthalic acid (TPA) synthesis from p-xylene in high-temperature liquid water (HTW) at 3008C. The p-xylene concentration at the reaction condition was 0.2 mol L, which is the highest to date in research that achieved at least 80 mol % yields of TPA in HTW. Pure oxygen gas was the oxidant. Increasing the MnBr2 catalyst concentration increased the rate of TPA formation only slight...

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Terephthalic Acid Synthesis at Higher Concentrations in High-Temperature Liquid Water. 2. Eliminating Undesired Byproducts

We synthesized terephthalic acid (TPA) from p-xylene at an initial concentration above its solubility limit in high-temperature liquid water (HTW). The nominal p-xylene loading at the reaction conditions was 0.4 mol L , which is the highest reported to date for generation of high TPA yields ([70 mol %) in HTW. The presence of two liquid phases during the reaction did not appear to accelerate th...

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4,4′-Bipyridine–terephthalic acid (1/1)

The asymmetric unit of the title compound, C(10)H(8)N(2)·C(8)H(6)O(4), consists of one half-mol-ecule of each moiety, 4,4'-bipyridine (bpy) and terephthalic acid (bdc), both being located on crystallographic inversion centers. They are linked together via strong inter-molecular O-H⋯N hydrogen bonds, forming infinite chains propagating along [1-21]. The chains are further connected through C-H⋯O...

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Terephthalic acid–4,4′-bipyridine (2/1)

In the title compound, 2C(8)H(6)O(4)·C(10)H(8)N(2), the 4,4'-bipyridine mol-ecule is located on an inversion centre. In the crystal structure, strong inter-molecular O-H⋯N hydrogen bonds between the terephthalic acid and 4,4'-bipyridine mol-ecules lead to the formation of chains with graph-set motif C(2) (2)(8) along the diagonal of the bc plane.

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ژورنال

عنوان ژورنال: AIChE Journal

سال: 2009

ISSN: 0001-1541,1547-5905

DOI: 10.1002/aic.11718