Industrial Process for Production of an Aromatic Carbonate

Active Publication Date: 2007-11-15
ASAHI KASEI KOGYO KK
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0077] It has been discovered that according to the present invention, taking an alkyl aryl carbonate as a starting material, which is obtainable from a dialkyl carbonate and an aromatic monohydroxy compound, a diaryl carbonate can be produced on an industrial scale of not less than 1 ton per hour, preferably not less than 2 tons per hour, more preferably not less than 3 tons per hour, with a high selectivity of not less than 95%, preferably not less than 97%, more preferably not less than 99%, stably for a prolonged period of time of not less than 2000 hours, preferably not less than 3000 hours, more preferably not less than 5000 hours. A diaryl carbonate obtained by subjecting the aromatic carbonates containing the diaryl carbonate as a main component obtained through the present invention to separation/purification through distillation or the like is of high purity, and is useful as a raw material of a transesterification method polycarbonate or polyester carbonate or the like, or as a raw material of a non-phosgene method isocyanate or urethane or the like. Moreover, according to the present invention, because a starting material and catalyst not containing a halogen are generally used, the diaryl carbonate obtained has a halogen content of not more than 0.1 ppm, preferably not more than 10 ppb, more preferably not more than 1 ppb.

Problems solved by technology

However, these have all been on a small scale and short operating time laboratory level, and there have been no disclosures whatsoever on a specific process or apparatus enabling mass production on an industrial scale.

Method used

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  • Industrial Process for Production of an Aromatic Carbonate
  • Industrial Process for Production of an Aromatic Carbonate

Examples

Experimental program
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Effect test

Example

Example 1

[0134] A continuous multi-stage distillation column as shown in FIG. 1 having L=3100 cm, D=500 cm, L / D=6.2, n=30, D / d1=3.85, and D / d2=11.1 was used. In this example, as the internal, two sets of Mellapak (total theoretical number of stages 11) were installed in the upper portion, and the sieve tray having the cross-sectional area per hole of approximately 1.3 cm2 and a number of holes of approximately 250 / m2 was used in the lower portion.

[0135] A mixture containing 18% by weight of methyl phenyl carbonate that had been obtained by subjecting a mixture containing dimethyl carbonate and phenol in a weight ratio of dimethyl carbonate / phenol=1.3 to a transesterification reaction was used as a starting material. This starting material contained 26% by weight of dimethyl carbonate, 6% by weight of anisole, 48% by weight of phenol, and 1% by weight of diphenyl carbonate, and further contained approximately 100 ppm of Pb(OPh)2 as a catalyst. The starting material substanti

Example

Example 2

[0138] Reactive distillation was carried out under the following conditions using the same continuous multi-stage distillation column as in Example 1.

[0139] A mixture containing 21% by weight of methyl phenyl carbonate that had been obtained by subjecting a mixture containing dimethyl carbonate and phenol in a weight ratio of dimethyl carbonate / phenol=1.9 to a transesterification reaction was used as a starting material. This starting material contained 32% by weight of dimethyl carbonate, 5% by weight of anisole, 41% by weight of phenol, and 1% by weight of diphenyl carbonate, and further contained approximately 250 ppm of Pb(OPh)2 as a catalyst. The starting material substantially did not contain halogens (outside the detection limit for the ion chromatography, i.e. 1 ppb or less).

[0140] The starting material was introduced into the continuous multi-stage distillation column at a flow rate of 80 ton / hr from a starting material inlet installed between the Mellapak and

Example

Example 3

[0142] Reactive distillation was carried out under the following conditions using the same continuous multi-stage distillation column as in Example 1, except that the cross-sectional area per hole of the sieve tray was made to be approximately 1.8 cm2.

[0143] A mixture containing 16% by weight of methyl phenyl carbonate that had been obtained by subjecting a mixture containing dimethyl carbonate and phenol in a weight ratio of dimethyl carbonate / phenol=1.4 to a transesterification reaction was used as a starting material. This starting material contained 27% by weight of dimethyl carbonate, 7% by weight of anisole, 49% by weight of phenol, and 0.5% by weight of diphenyl carbonate, and further contained approximately 200 ppm of Pb(OPh)2 as a catalyst. The starting material substantially did not contain halogens (outside the detection limit for the ion chromatography, i.e. 1 ppb or less).

[0144] The starting material was introduced into the continuous multi-stage distillation

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Abstract

It is an object of the present invention to provide, for the case of continuously producing aromatic carbonates containing a diaryl carbonate as a main product by taking an alkyl aryl carbonate as a starting material, which is obtainable through a transesterification reaction between a dialkyl carbonate and an aromatic monohydroxy compound, using a continuous multi-stage distillation column in which a catalyst is present, and continuously feeding the starting material into the continuous multi-stage distillation column, a specific process that enables the diaryl carbonate to be produced with high selectivity and high productivity stably for a prolonged period of time on an industrial scale of not less than 1 ton per hour. Although there have been various proposals regarding processes for the production of aromatic carbonates by means of a reactive distillation method, these have all been on a small scale and short operating time laboratory level, and there have been no disclosures whatsoever on a specific process or apparatus enabling mass production on an industrial scale. According to the present invention, there is provided a specified continuous multi-stage distillation column, and there is also provided a specific process that enables a diaryl carbonate to be produced with high selectivity and high productivity stably for a prolonged period of time on an industrial scale of not less than 1 ton per hour from an alkyl aryl carbonate.

Description

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Claims

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Application Information

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Owner ASAHI KASEI KOGYO KK
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