Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From carboxylic acid or derivative thereof
Reexamination Certificate
2001-08-30
2003-07-08
Boykin, Terressa M. (Department: 1711)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From carboxylic acid or derivative thereof
C528S271000
Reexamination Certificate
active
06590060
ABSTRACT:
The present invention refers to the manufacturing of polyester-type polymers and refers particularly to the solid phase post-condensation steps.
The manufacture of polyesters is generally carried out in several steps. The first step is a step of esterification or transesterification of a carboxylic diacid or a diacid diester with a diol. This step is followed by a melt phase polymerization step. As the reaction advances, the product becomes more and more viscous. Above a certain viscosity the technology used nowadays does not permit the continuation of the reaction. The viscosity limit attained in melt phase is generally around 85 ml/g (viscosity index). If higher molecular weight compounds are to be obtained, it is necessary to proceed with the reaction in solid phase. This step is called a solid phase post-condensation step. It consists in proceeding with the condensation through heating in a gaseous medium or under vacuum, the polymer being in the form of solid elements. This step is very slow and constitutes a limiting step in the process of manufacturing a polyester.
It is known that a limiting factor in solid phase post-condensation is the diffusion of condensation by-products within the polymeric mass. To speed up the solid phase post-condensation, U.S. Pat. No. 5,391,694 discloses a process which permits the increase of the exchange surface between the solid particles and the gaseous medium surrounding them by providing them with particular shapes during solidification. U.S. Pat. No. 4,755,587 teaches manufacturing porous tablets by compacting crystalline very light granulometry polymer powders. U.S. Pat. 5,532,335 teaches the improvement in heat transfer within a solid phase post-condensation medium by effecting the same in a liquid eventually pressurized medium and by increasing the post-condensation temperature.
Notwithstanding the progress reached, efforts are always being made to obtain an improved performance solid phase post-condensation step. The object of the present invention is to accelerate condensation kinetics by improving the diffusion of the condensation by-products outwards from within the particles. To attain this object, the present invention employs a step preceding post-condensation, consisting in dipping the solidified polymer in a swelling medium.
Therefor, the invention proposes a process for manufacturing polyester comprising at least the following steps:
a) esterifying or transesterifying a carboxylic diacid or a diester of a carboxylic diacid with a diol,
b) polymerizing in melt phase the esterification or transesterification product,
c) solidifying and granulating,
d) placing in contact the granules with a liquid swelling medium,
e) post-condensing the granules in solid phase.
These steps constitute the essential operations necessary to carry out the process. The process may comprise others. Each of these steps may eventually be subdivided in elementary operations within several installations.
Polymerization step b) is in fact widely applied by industry. It consists in a condensation in the molten state of the reaction product of step a). It is in general catalyzed by a metal compound, for example, antimonium trioxide. During the advancement of the reaction, the product becomes more and more viscous.
Beyond a certain viscosity, the type of technology presently employed does not permit the reaction to proceed. The limit in viscosity attained in the molten phase is generally around 85 ml/g. If higher molecular weight compounds are desired, it is necessary to proceed with a solid phase condensation.
By viscosity it is to be understood the viscosity index (VI) in ml/g measured at 25° C. with the help of a Ubbelohde type viscosimeter for a 0.005 g/ml solution of polymer dissolved at 115° C. in a mixture comprising 50% by weight of phenol and 50% by weight of 1,2-dichlorobenzene.
During step c) the molten polymer coming from step b) is made into the form of a granular solid, for example by extrusion and cooling. It is then essentially amorphous. The granules exitting this step can be used either as they are, eventually after crystallization, or can be submitted to solid phase post-condensation for applications requiring higher molecular weight polymers.
The solid phase post-condensation carried out during step e) consists in heating the granules coming from step c) to temperatures comprised between the glass transition temperature of the polymer and the melt temperature thereof. This condensation is accompanied by the separation of reaction products, especially of diol.
In order to speed up the post-condensation kinetics, the present invention comprises a step d) of preparing the granules coming from step c). This step consists in placing in contact said granules with with a liquid swelling medium. The operation makes the granules become porous, thereby reducing the diffusional path, and thus increasing their specific exchange surface.
The diffusion of the diol coming from post-condensation is thus facilitated. Such a property permits speeding up the subsequent solid phase condensation step. The placing in contact may be effected by any means, for example by immersion. The step may be effected either continuously or discontinuously.
As examples of liquid swelling media, the following compounds can be mentioned: methylene chloride, dioxane, nitromethane, acetone, benzene, dimethylformamide, dimehtylacetamide, methanol, ethanol, chloroform, trichloroethylene, tetrachloroethylene, carbon tetrachloride, toluene, benzyl alcohol, methyl-vinyl-ketone. Acetone particularly provides very good results.
The above-described steps are necessary for the realization of the invention, but the process can include others, either upstream, downstream or intermediately. The process according to the invention may particularly include a step of crystallizing the granules between the placing in contact and the solid phase condensation steps.
The swelling liquid medium may be used at room temperature or maximum at a temperature lower than the boiling temperature of the liquid and the melt temperature of the treated polymer.
The placing in contact with the swelling medium may be applied to polymers having molecular weights advantageously higher than a molecular weight corresponding to a viscosity index around 30 ml/g. The process may be applied to polymers having higher viscosity indexes, especially until viscosity indexes around 90 ml/g. It may alternatively be applied to very high viscosity index polymers, for example up to 130 ml/g, in order to manufacture very high molecular weight compounds.
The carrying out of the step of placing in contact with the swelling medium provides substantial technological improvements to the process. It can thus permit reducing the number of polymerization reactors. It can permit simplifying or eliminating the crystallization procedures usually carried out. For example, since the classic process for preparing polymers after solidification and before post-condensation consists in a passage through three units for pre-crystallization, crystallization and crystallization-conditioning the invention can reduce the number of operations so that not more than two placing in contact steps are employed, for example through immersion, and crvstallization/conditioning.
The process according to the present invention can be used to prepare polyester-type polymers. It can be applied to polyesters obtained from the following diacids: terephthalic acid, isophthalic acid, naphthalenedioic acid, and mixtures thereof, and the following diols: ethylene glycol, propylene glycol, butane diol, neopentyl glycol, diethylene glycol, bisphenol and mixtures thereof. It can be applied particularly to the manufacture of poy(ethylene terephthalate).
Other details and advantages of the invention will become apparent from the examples given hereunder for illustrative purposes only.
REFERENCES:
patent: 3390134 (1968-06-01), Kibler
patent: 4080317 (1978-03-01), Morawetz et al.
patent: 4613664 (1986-09-01), Tate et al.
patent: 4755587 (1988-07-01), Rinehart
patent: 516447
Boykin Terressa M.
Darby & Darby
Rhodia Ster S.A.
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