C08G63/88

HEAT-SHRINKABLE POLYESTER FILM AND PRODUCTION METHOD THEREOF
20230039563 · 2023-02-09 ·

A heat-shrinkable polyester film includes at least one polyester material made of at least one polyester forming composition which includes a dibasic carboxylic mixture and a diol mixture. The heat-shrinkable polyester film has a heat shrinkage rate of not lower than 25% in a shrinkage direction, which is measured by immersing the heat-shrinkable polyester film in hot water at 65° C. for 10 seconds. A method for producing the heat-shrinkable polyester film is also disclosed.

Methods and compositions for preparing particle boards

An amorphous polylactic acid polymer having a weight average molecular weight in the range of about 35,000 to 180,000 is described. The polylactic acid polymer composition can be hammer milled without cryogenics result in the form of particles wherein 90% of the particles have particle size of about 250 μm or less and the material has a glass transition temperature of between about 55° C. to about 58° C. and a relative viscosity of about 1.45 to about 1.95 centipoise. The polymer composition can be used to form an aqueous suspension. The material is ideally suited for use in preparing particleboard. A method is disclosed for preparing such polylactic acid polymers. The method involves obtaining an amorphous polylactic acid polymer having a weight average molecular weight of between about 115,000 to about 180,000. Treating the polylactic acid polymer to reduce the molecular weight to between about 35,000 to 45,000 such that it has a glass transition temperature of between about 55° C. and 58° C. and a relative viscosity of about 1.45 to about 1.95. Material can be formed into particles in a commercial hammer mill with bypass such that 90% of the initial mass results in the particles which can pass thru a sieve having a pore size of about 250 μm. During particle board formation the temperature of around 140-140 C being reached to optimally activate the adhesive; Bond strengths and throughput rates of resulting particle boards can be controlled thereafter, with variable combination of particle sizes, adhesive loading and initial moisture content.

Methods and compositions for preparing particle boards

An amorphous polylactic acid polymer having a weight average molecular weight in the range of about 35,000 to 180,000 is described. The polylactic acid polymer composition can be hammer milled without cryogenics result in the form of particles wherein 90% of the particles have particle size of about 250 μm or less and the material has a glass transition temperature of between about 55° C. to about 58° C. and a relative viscosity of about 1.45 to about 1.95 centipoise. The polymer composition can be used to form an aqueous suspension. The material is ideally suited for use in preparing particleboard. A method is disclosed for preparing such polylactic acid polymers. The method involves obtaining an amorphous polylactic acid polymer having a weight average molecular weight of between about 115,000 to about 180,000. Treating the polylactic acid polymer to reduce the molecular weight to between about 35,000 to 45,000 such that it has a glass transition temperature of between about 55° C. and 58° C. and a relative viscosity of about 1.45 to about 1.95. Material can be formed into particles in a commercial hammer mill with bypass such that 90% of the initial mass results in the particles which can pass thru a sieve having a pore size of about 250 μm. During particle board formation the temperature of around 140-140 C being reached to optimally activate the adhesive; Bond strengths and throughput rates of resulting particle boards can be controlled thereafter, with variable combination of particle sizes, adhesive loading and initial moisture content.

Process and apparatus for direct crystallization of polycondensates
11566104 · 2023-01-31 · ·

The present invention relates to a process for continuous production of partly crystalline polycondensate pellet material, comprising the steps of forming a polycondensate melt into pellet material; separating the liquid cooling medium from the pellet material in a first treatment space, wherein the pellets after exit from the first treatment space exhibit a temperature T.sub.GR, and crystallizing the pellet material in a second treatment space, wherein in the second treatment space fluidized bed conditions exist, and in the second treatment space the pellets are heated by supply of energy from the exterior by means of a process gas.

Process and apparatus for direct crystallization of polycondensates
11566104 · 2023-01-31 · ·

The present invention relates to a process for continuous production of partly crystalline polycondensate pellet material, comprising the steps of forming a polycondensate melt into pellet material; separating the liquid cooling medium from the pellet material in a first treatment space, wherein the pellets after exit from the first treatment space exhibit a temperature T.sub.GR, and crystallizing the pellet material in a second treatment space, wherein in the second treatment space fluidized bed conditions exist, and in the second treatment space the pellets are heated by supply of energy from the exterior by means of a process gas.

Polymer composition for selective sintering
11560451 · 2023-01-24 · ·

A polymer composition for the production of shaped objects via selective sintering includes ≥70.0 wt % of poly(ethylene terephthalate), wherein ≥25.0 wt % and ≤90.0 wt % of the poly(ethylene terephthalate has resulted from a selective sintering process as unsintered material. The polymer composition is a powder having a D.sub.10 of ≥10 and ≤40 μm, a D.sub.50 of ≥75 and ≤100 μm, and a D.sub.90 of ≥160 and ≤200 μm. The polymer composition allows for the production of an article having a continuous use temperature of ≥100° C., and results in a low change of molecular weight during exposure to selective sintering powder processing temperatures. Further, the polymer composition allows for a significant reduction of the waste material generated during selective sintering as the unsintered material does not have to be disposed of as waste but may be used again.

Polymer composition for selective sintering
11560451 · 2023-01-24 · ·

A polymer composition for the production of shaped objects via selective sintering includes ≥70.0 wt % of poly(ethylene terephthalate), wherein ≥25.0 wt % and ≤90.0 wt % of the poly(ethylene terephthalate has resulted from a selective sintering process as unsintered material. The polymer composition is a powder having a D.sub.10 of ≥10 and ≤40 μm, a D.sub.50 of ≥75 and ≤100 μm, and a D.sub.90 of ≥160 and ≤200 μm. The polymer composition allows for the production of an article having a continuous use temperature of ≥100° C., and results in a low change of molecular weight during exposure to selective sintering powder processing temperatures. Further, the polymer composition allows for a significant reduction of the waste material generated during selective sintering as the unsintered material does not have to be disposed of as waste but may be used again.

Method for producing sterilized oxygen-absorbing multilayer body

A method for producing a sterilized oxygen-absorbing multilayer body is provided. The method may include: irradiating with radiation an oxygen-absorbing multilayer body comprising at least an oxygen-absorbing layer containing a transition metal catalyst and a thermoplastic resin (a) having a tetralin ring as a structural unit and a layer containing a thermoplastic resin (b); and heating the oxygen-absorbing multilayer body which has been irradiated with radiation in the sterilizing step at a temperature of the glass transition temperature of the thermoplastic resin (a) minus 20° C. or more and lower than the glass transition temperature of the thermoplastic resin (a) for 50 hours or more.

Method for producing sterilized oxygen-absorbing multilayer body

A method for producing a sterilized oxygen-absorbing multilayer body is provided. The method may include: irradiating with radiation an oxygen-absorbing multilayer body comprising at least an oxygen-absorbing layer containing a transition metal catalyst and a thermoplastic resin (a) having a tetralin ring as a structural unit and a layer containing a thermoplastic resin (b); and heating the oxygen-absorbing multilayer body which has been irradiated with radiation in the sterilizing step at a temperature of the glass transition temperature of the thermoplastic resin (a) minus 20° C. or more and lower than the glass transition temperature of the thermoplastic resin (a) for 50 hours or more.

Toughened polyester composites containing polyester matrix and droplets of high boiling liquid therein

A toughened polyester composite comprising: (i) a polyester matrix and (ii) droplets of a high boiling point liquid having a boiling point of at least 140° C. dispersed in said polyester matrix, wherein the high boiling point liquid is present in an amount of 0.1-10 wt % by weight of the toughened polyester composite, and wherein the composite may further include: (iii) a modifier selected from polycarboxylic, polyol, and polyamine compounds, wherein the modifier is present in an amount of 0.1-10 wt % by weight of the toughened polyester composite. Methods for producing the polyester composite are also described.