Method for manufacturing polyol esters
A technology of polyol esters and polyols, which is applied in the field of preparing polyol esters, and can solve problems such as acid quality damage
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Embodiment 1
[0059] Preparation of triethylene glycol di-2-ethylhexanoate (3G8 ester); esterified with fresh in the presence of activated carbon
[0060] The esterification of triethylene glycol and 2-ethylhexanoic acid was carried out in a heatable 1-liter four-necked flask equipped with a stirrer, internal thermometer and water separator.
[0061] The flask was initially charged with 250 grams (1.66 moles) of triethylene glycol and 680 grams (4.72 moles) of fresh 2-ethylhexanoic acid and 0.4% by weight of activated carbon based on the total reaction mixture. While stirring and applying a slight reduced pressure of 900 hPa, the mixture was heated to 225°C. When this temperature is reached, the pressure is gradually reduced to 400 hPa, and the formed reaction water is removed on the water separator while allowing 2-ethylhexanoic acid to flow back to the reaction vessel. The progress of the reaction was monitored by continuously weighing the water discharged through the water separator and by t...
Embodiment 2
[0067] Preparation of triethylene glycol di-2-ethylhexanoate (3G8 ester); esterification in the presence of activated carbon and reuse of the intermediate fraction from the previous esterification batch
[0068] Example 2 was performed similarly to Example 1, with the only difference being that instead of fresh 2-ethylhexanoic acid, an intermediate fraction of 2-ethylhexanoic acid collected from the previous esterification batch was used.
Embodiment 3
[0069] Example 3 (comparative example):
[0070] Preparation of triethylene glycol di-2-ethylhexanoate (3G8 ester); esterification in the presence of activated carbon and reuse of all recovered acids from previous esterification batches
[0071] Example 3 was performed similarly to Example 2, except that instead of the 2-ethylhexanoic acid intermediate fraction, all the 2-ethylhexanoic acid recovered from the previous esterification batch was used.
[0072] The color numbers of the post-treatment triethylene glycol di-2-ethylhexanoate obtained according to Examples 1 to 3 are listed in Table 1 below. The ester content measured by gas chromatography is consistent with other indexes, such as residual acid content or water content.
[0073] Table 1: Color numbers of triethylene glycol di-2-ethylhexanoate prepared according to Examples 1, 2 and 3
[0074]
[0075] The method of the present invention to partially recycle the aliphatic monocarboxylic acid recovered in the esterification i...
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Abstract
Description
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