Increasing the particle size of polymers

Details Increasing the particle size of polymers Increasing the particle size of polymers

1995-01-24

1998-08-25

Acquah, Samuel A.

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Treating polymer containing material or treating a solid...

528361, 528499, 528500, 528501, 528502, 528503, 435135, 435136, C08F 618, C12P 764

Patent

active

057984409

DESCRIPTION:

BRIEF SUMMARY
THIS INVENTION relates to increasing the particle size of polymers.
In the production of polyester polymers especially those which are microbially produced the particle sizes of the polymers may be too small for convenient handling; for example in the course of production processes it may be necessary to separate such particles from aqueous liquid media. Such separations are more difficult if the particles are small than if they are large.
Surprisingly we have found that polyesters, especially those which are microbially produced, for example polymers and copolymers of hydroxyalkanoic acids especially polymers and copolymers of hydroxybutyric acid are capable of surprisingly rapid agglomeration at temperatures substantially below their peak melting points when in suspension in a liquid medium producing particles well suited to solid liquid separation with little molecular weight loss.
This invention comprises a process in which polyester particles, in suspension in a liquid medium in which if such medium comprises matter derived from microbial cells the said matter other than polyester has been at least partly chemically degraded, are agglomerated by maintaining the suspension at a temperature in excess of 80.degree. C. and preferably in excess of 90.degree. C. for example in excess of 100.degree. C. and preferably 30.degree. to 80.degree. C. and more preferably 40.degree. to 70.degree. C. below the peak melting point of the polyester as determined by differential scanning calorimetry for a time sufficient to cause substantial agglomeration.
Suitable temperatures in the case of polymers of hydroxybutyric acid, for example copolymers of hydroxybutyric and hydroxyvaleric acid containing up to 25%, for example 5 to 20% of hydroxyvaleric acid residues, the balance being substantially all hydroxybutyric acid residues, are in the range 120.degree. to 160.degree. C. In general a considerable amount of agglomeration can be achieved with such materials in about 1 minute at 130.degree. C. The large particles formed are agglomerates of the fine particles of the original suspension. The fine particles, in the case of microbially produced polymers, are usually <1 .mu.m in diameter (as assessed by the diameter of a sphere of equivalent volume). The process in this case, especially in the case of polymers of hydroxybutyric acid and copolymers thereof with hydroxyvaleric acid, enables the production of a fused network of polymer strands resulting in a highly porous, mechanically strong agglomerate with excellent filtration and washing characteristics. Suitably, the agglomerates produced have a weight average diameter of at least 50 .mu.m and preferably 100 to 1000 .mu.m, for example 200 to 500 .mu.m. They suitably have a high porosity for example 0.7 to 0.8 and preferably at least 0.6. Relative to non-agglomerated particles the filtration rate (based on the specific cake resistance) is increased by 100 to 10,000 times. Agglomeration may be achieved with minimal influence on molecular weight. At 30 minutes residence time at 130.degree. C. <30% reduction is obtained, and at 1 minute the loss is undetectable.
It will be appreciated that it is necessary where the particles are derived from microbially produced polyester that the residual microbial material surrounding the particles should be at least sufficiently degraded to permit the polyester particles to come into contact with one another in the liquid medium.
We have surprisingly found that an increase in particle sizes may still be obtained despite the presence of soluble microbial components and degradation products. It may be desirable, especially if the particles initially recovered are contaminated with microbial matter or degradation products thereof to resuspend them in a second liquid medium and/or further treat them for example with a second liquid medium in which further processing for example chemical treatment (which may be treatment with a bleach for example hydrogen peroxide) may take place and to recover the particles from the new liquid medium. The

REFERENCES:
patent: 5213976 (1993-05-01), Blauhut et al.

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