35 results about "PLLA polymer" patented technology

A thermoplastic resin composition comprising a polylactic acid polymer (A), an acrylic polymer (B) containing units of methyl methacrylate monomer, and a graft copolymer (C) obtained by graft-polymerizing a vinyl monomer onto a rubbery polymer, wherein the refractive index, Rc, of the graft copolymer (C) and the total refractive index, Rab, of the polylactic acid polymer (A) and the acrylic polymer (B) satisfy the following formula (1)−0.004≦Rc−Rab≦+0.008  (1).

A resin composition contains poly(lactic acid) and a cellulosic ester, a resin composition excellent in transparency, mechanical properties, and thermostability; a biaxially drawn film containing poly(lactic acid) and at least one compound selected from cellulosic esters, poly(meth)acrylates, and polyvinyl compounds having a glass transition temperature of 60° C. or higher; and a biaxially drawn film excellent in transparency, mechanical properties, and thermostability. The resin composition is obtained by melt-kneading a poly(lactic acid) polymer with a weight average molecular weight of 50,000 or higher and a cellulosic ester; a resin composition excellent in transparency and having luminous transmittance of 40% or higher for visible light with 400 nm; a molded article and a film made of the resin composition; a poly(lactic acid) biaxially drawn film containing a poly(lactic acid) polymer with a weight average molecular weight of 50,000 or higher and at least one compound selected from cellulosic esters, poly(meth)acrylates, and polyvinyl compounds having a glass transition temperature of 60° C. or higher; a poly(lactic acid) biaxially drawn film excellent in transparency and having film haze of 10% or lower.

The present invention relates to a composition comprising a poly-D- lactic acid (PDLA) polymer and a poly-L-lactic acid (PLLA) polymer. The present invention also relates to a method for the production of a moulded part comprising the steps of heating a mould, and supplying to the mould a composition comprising a poly-D-lactic acid (PDLA) polymer and a poly-L-lactic acid (PDLA) polymer. The present invention relates to a composition comprising a poly-D-lactic acid (PDLA) polymer and a poly-L-lactic acid (PLLA) polymer for use in injection-moulding, thermoforming and / or film blowing. The present invention also relates to a composition that can be obtained by heating a composition comprising a poly-D- lactic acid (PDLA) polymer and a poly-L-lactic acid (PDLA) polymer.

The invention relates to a mixture of biodegradable polyesters comprising: (A) a polyhydroxy acid of the poly-ε-caprolactone type and its copolymers, (B) aliphatic polyester, and (C) a polymer of polylactic acid, in which the concentration of (A) varies with respect to (A+B) in the range between 40 and 70% by weight, and the concentration of (C) with respects to (A+B+C) lies between 2 and 30%.

The present invention is directed to a blended composition comprising one or more polycarbonates wherein at least one of the polycarbonates is a polyesterpolycarbonate having at least one unit derived from a soft block ester unit, e.g., sebacic acid, and at least one unit derived from bisphenol A, and a polylactic polymer wherein the composition has an overall biocontent of at least 10% according to ASTMD6866.

The invention discloses a polylactic acid elastic non-woven material beneficial to tissue regeneration and a preparation method thereof. The nano-micron polylactic acid elastic non-woven material is an integrated structure composed of polylactic acid nano-micron fibers as the main body and polyolefin elastic filaments as the skeleton. Its preparation method is as follows: the modified polylactic acid polymer and the polyolefin elastic skeleton are subjected to in-situ injection molding to obtain a laminated fiber web, and then the laminated fiber web is subjected to water jet composite processing to form an integrated structure, and then the integrated structure A fiber web is ironed on one side to obtain a nano-micron elastic lightweight patch and a preparation method thereof. The non-woven material prepared by this method has an integrated structure, no delamination and good anti-adhesion effect. At the same time, the non-woven material also has excellent elasticity and flexibility, and can be used for hernia patch, medical dressing, medical bandage, etc. multiple fields. The preparation method of the non-woven patch has the characteristics of short process flow, high production speed and low cost, and is suitable for large-scale industrial production.

A hydroxyapatite ceramic hybrid material includes a hydroxyapatite ceramic structure having pores therein and a biodegradable polymer included in the pores in the hydroxyapatite ceramic structure. The biodegradable polymer can be a poly L-lactic acid polymer. A method for preparing a hydroxyapatite ceramic-biodegradable polymer hybrid material includes preparing a porous hydroxyapatite ceramic containing pores having an average pore diameter of 10 μm or larger; and forming a biodegradable polymer in the pores of the porous hydroxyapatite ceramic. The porous hydroxyapatite ceramic may be prepared by: preparing a slurry comprising hydroxyapatite fibers and heat-degradable particles in a selected solvent; filtering the slurry to obtain a paste; preparing a molded body using the paste; compacting the molded body to produce a green compact; and firing the green compact at a temperature at least 1000° C. to produce a porous hydroxyapatite ceramic structure.

The invention belongs to an oral matrix membrane and a preparation method thereof in the field of preparation methods of medical biodegradable filling materials. The base material of the oral matrix membrane is composed of polylactic acid polymer (PDLLA), acetyl tributyl citrate (ATBC) and Polylactic acid (PLLA) is mixed, of which polylactic acid polymer is 75~89.5%, acetyl tributyl citrate is 10.5~13%, and L-polylactic acid is 0~12%. The oral matrix membrane has a three-layer structure, that is, an upper layer (1), a middle layer (2) and a bottom layer (3), and each layer is provided with through holes (4). The invention overcomes the lack of biodegradable matrix materials in the existing periodontal disease treatment technology and cannot ensure the success of bone grafting treatment. The oral matrix membrane and its preparation method provided for people have good tissue adhesion and can promote cell Reproduction, and can be completely biodegradable within a certain period of time.

The present invention provides a germ-repellent elastomer comprising: a base polymer selected from latex, synthetic rubber, thermoplastic elastomers, or copolymers or mixtures thereof; and at least one germ-repelling modifier selected from one or more polyethoxylated non-ionic surfactants such that a highly hydrophilic moiety is imparted from the at least one germ-repelling modifier to the base polymer either by physical or reaction extrusion.

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.