US20160208070A1 - Foamable resin composition for foam sheet, foam sheet, process for preparing particulate polylactic acid and process for preparing foam sheet - Google Patents

Foamable resin composition for foam sheet, foam sheet, process for preparing particulate polylactic acid and process for preparing foam sheet Download PDF

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Publication number
US20160208070A1
US20160208070A1 US14/913,994 US201414913994A US2016208070A1 US 20160208070 A1 US20160208070 A1 US 20160208070A1 US 201414913994 A US201414913994 A US 201414913994A US 2016208070 A1 US2016208070 A1 US 2016208070A1
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United States
Prior art keywords
polylactic acid
foam sheet
acid resin
spray
spray nozzle
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Abandoned
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US14/913,994
Inventor
Jun-Beom Shin
Sung-Yong Kang
Min-Hee Lee
Hea-Won KWON
Kyoung-Min KANG
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LX Hausys Ltd
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LG Hausys Ltd
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Assigned to LG HAUSYS, LTD. reassignment LG HAUSYS, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KANG, KYOUNG-MIN, KANG, SUNG-YONG, KWON, Hea-Won, LEE, MIN-HEE, SHIN, Jun-Beom
Publication of US20160208070A1 publication Critical patent/US20160208070A1/en
Priority to US15/874,632 priority Critical patent/US10508176B2/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/28Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/04Particle-shaped
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    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • B01J2/02Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
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    • B29B9/10Making granules by moulding the material, i.e. treating it in the molten state
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/12Making granules characterised by structure or composition
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
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    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/46Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
    • B29C44/50Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying
    • B29C44/505Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying extruding the compound through a flat die
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0012Combinations of extrusion moulding with other shaping operations combined with shaping by internal pressure generated in the material, e.g. foaming
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0021Combinations of extrusion moulding with other shaping operations combined with joining, lining or laminating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D7/00Producing flat articles, e.g. films or sheets
    • B29D7/01Films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • C08J3/122Pulverisation by spraying
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0004Use of compounding ingredients, the chemical constitution of which is unknown, broadly defined, or irrelevant
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05BSPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B5/00Electrostatic spraying apparatus; Spraying apparatus with means for charging the spray electrically; Apparatus for spraying liquids or other fluent materials by other electric means
    • B05B5/001Electrostatic spraying apparatus; Spraying apparatus with means for charging the spray electrically; Apparatus for spraying liquids or other fluent materials by other electric means incorporating means for heating or cooling, e.g. the material to be sprayed
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/30Extrusion nozzles or dies
    • B29C48/305Extrusion nozzles or dies having a wide opening, e.g. for forming sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2035/00Use of polymers of unsaturated polycarboxylic acids or derivatives thereof as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2067/00Use of polyesters or derivatives thereof, as moulding material
    • B29K2067/04Polyesters derived from hydroxycarboxylic acids
    • B29K2067/046PLA, i.e. polylactic acid or polylactide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/25Solid
    • B29K2105/251Particles, powder or granules
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2201/00Foams characterised by the foaming process
    • C08J2201/04Foams characterised by the foaming process characterised by the elimination of a liquid or solid component, e.g. precipitation, leaching out, evaporation
    • C08J2201/05Elimination by evaporation or heat degradation of a liquid phase
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2300/00Characterised by the use of unspecified polymers
    • C08J2300/16Biodegradable polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/04Polyesters derived from hydroxy carboxylic acids, e.g. lactones
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/06Biodegradable
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    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/16Applications used for films

Definitions

  • the present disclosure relates to a foamable resin composition for a foam sheet, a foam sheet, a process for preparing a particulate polylactic acid resin, and a process for preparing a foam sheet.
  • Products in which a polylactic acid is used are produced through multiple heat processes. It has been reported that a polylactic acid is sensitive to heat, and, therefore, a hydrolysis proceeds at a high temperature. Due to the property of the polylactic acid, a hydrolysis caused by heat during a process for preparing a polylactic acid product leads to a change of a molecular weight, which affects the state of the end product produced.
  • One embodiment of the present disclosure provides a foamable resin composition for a foam sheet, which can produce a foam sheet including a polylactic acid resin and having an improved shelf-life.
  • Another embodiment of the present disclosure provides a process for preparing a polylactic acid resin of microparticles, included in the foamable resin composition.
  • Still another embodiment of the present disclosure provides a process for preparing a foam sheet, using the foamable resin composition for a foam sheet.
  • a foamable resin composition for a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 ⁇ m to about 100 ⁇ m, is provided.
  • a foam sheet prepared by molding the composition may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • the composition may be a suspension in which the polylactic acid resin particles are dispersed in a liquid solvent.
  • a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 ⁇ m to 100 ⁇ m, is provided.
  • the foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • a process for preparing a particulate polylactic acid resin comprises: introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and spraying the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid.
  • the polylactic acid resin may be introduced into an extruder, and then transferred to an spray nozzle and heated in the spray nozzle to form the molten polylactic acid spray solution.
  • the polylactic acid resin n the form of pellet or powder may be introduced into the extruder.
  • the molten polylactic acid spray solution may be introduced into the spray nozzle together with an air and then discharged.
  • a temperature of the air that is introduced into the spray nozzle may be of about 300° C. to about 500° C.
  • a pressure of the air that is injected into the spray nozzle may be of about 100 psi to about 1,000 psi
  • an injection speed of the air that is injected into the spray nozzle may be of about 10 m/s to about 50 m/s.
  • a temperature of the spray nozzle may be of about 200° C. to about 400° C.
  • a pressure of the spray nozzle may be of about 10 psi to about 1,000 psi.
  • a diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm.
  • the molten polylactic acid spray solution may comprise at least one additive selected from the group consisting of a lubricant, a plasticizer, and a combination thereof.
  • the molten polylactic acid spray solution may have a viscosity of about 1,500 cps to about 2,000 cps at 250° C.
  • a voltage of about 2,000 V to about 50,000 V may be applied to the spray nozzle to carry out a melt electrostatic spray deposition.
  • the particulate polylactic acid resin may have an average particle size of about 1 ⁇ m to about 100 ⁇ m.
  • a process for preparing a foam sheet comprising a polylactic acid foam layer comprising: mixing a particulate polylactic acid resin having an average particle size of 1 ⁇ m to 100 ⁇ m, a foam resin, and an additive to form a foamable resin composition, and then applying the foamable resin composition to form a layer; and allowing the resultant layer to foam and consequently forming a foam layer is provided.
  • the particulate polylactic acid resin is obtained by a melt spray method.
  • the foam sheet prepared by the process may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • a foam sheet prepared by using the microparticulate polylactic acid resin has excellent durability and surface property and improved shelf-life.
  • FIG. 1 schematically shows a process flow diagram of a process for preparing a foam sheet according to one embodiment of the present disclosure
  • FIG. 2 schematically shows a process flow diagram of a process for preparing a foam sheet.
  • polylactic acid resin particles having an average particle size of about 1 ⁇ m to about 100 ⁇ m are provided.
  • the polylactic acid resin particles having the particle size range may be prepared by a melt spray method. Further, more uniform polylactic acid particles may be obtained by introducing an air having a high temperature and a high pressure together to an spray nozzle during performing the melt spray method.
  • the melt spray method may be carried out by a melt electrostatic spray deposition (melt ESD) applying a voltage during performing the melt spray method.
  • a process according to another embodiment of the present disclosure for preparing polylactic acid resin particles having an average particle size of about 1 ⁇ m to about 100 ⁇ m comprises: introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and spraying the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid.
  • the process for preparing a particulate polylactic acid resin has advantages to easily control the size of the polylactic acid resin particles formed by applying the melt spray method and to make a distribution of the particle size uniform.
  • ploylactic acid resin particles having an average particle size of about 1 ⁇ m to about 100 ⁇ m may be prepared by the process for preparing a particulate polylactic acid resin.
  • a polylactic acid in the form of pellet or powder is introduced into an extruder equipped with an spray nozzle, and then the polylactic acid is melted in the high temperature spray nozzle to form a molten polylactic acid spray solution.
  • molten polylactic acid spray solution is sprayed in the form of a liquid droplet in micrometers.
  • spraying is performed in a cooling chamber, allowing the liquid droplet to be cooled to form microparticles of the polylactic acid resin.
  • the melt spray method is optionally carried out by a melt electrostatic spray deposition applying a voltage to the spray nozzle.
  • the molten polylactic acid spray solution is introduced into the spray nozzle together with an air and then discharged.
  • the size and shape of a liquid droplet of the molten polylactic acid spray solution discharged may be controlled, whereby the particle size of a polylactic acid resin to be finally obtained may be controlled.
  • a temperature of the air that is introduced into the spray nozzle may be of about 300° C. to about 500° C.
  • a pressure of the air may be of about 10 psi to about 1,000 psi
  • an injection speed of the air may be of about 10 m/s to about 50 m/s.
  • a viscosity of the melted polylactic acid may be controlled to be sprayed as a liquid droplet in micrometers.
  • To control the viscosity of the melted polylactic acid resin may be achieved by a method, such as adjusting the temperature of the spray nozzle, adding an additive, such as a lubricant, a plasticizer, or the like, together with the polylactic acid resin, to the extruder to be compounded, or introducing a gas such as CO 2 to the polylactic acid resin in the form of pellet, and the like.
  • a method such as adjusting the temperature of the spray nozzle, adding an additive, such as a lubricant, a plasticizer, or the like, together with the polylactic acid resin, to the extruder to be compounded, or introducing a gas such as CO 2 to the polylactic acid resin in the form of pellet, and the like.
  • a diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm.
  • a viscosity of the molten polylactic acid spray solution may be of about 1,500 cps to about 2,000 cps at about 250° C.
  • a coating solution having the above viscosity range a microparticulate polylactic acid resin may be formed.
  • Process conditions of the melt spray method are not particularly limited, and the known process conditions, for example, a pressure of the spray nozzle of about 100 psi to about 1,000 psi may be applied.
  • melt spray method should be carried out at a temperature range in which the polylactic acid melts.
  • a temperature of the spray nozzle may be of about 200° C. to about 400° C.
  • a diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm in order to form the microparticulate polylactic acid resin as described above.
  • the melt spray method may be carried out, for example, by a melt electrostatic spray deposition applying a voltage of about 2,000 V to about 50,000 V to the spray nozzle.
  • microparticulate polylactic acid resin which may be prepared by the process can be advantageously applied to a preparation of a foam sheet.
  • a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 ⁇ m to about 100 ⁇ m.
  • the foam sheet may be prepared by using the polylactic acid resin particles having a small particle size in micrometers, in accordance with a process for preparing a foam sheet as mentioned below, and the thus prepared foam sheet minimizes the number of heat processes to minimize the degradation of the polylactic acid resin, allowing the maintenance of higher molecular weight.
  • the foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • FIG. 2 shows a process flow diagram of an exemplary process for preparing a foam sheet.
  • a foam sheet applied with a polylactic acid resin has been produced through a variety of processes. More specifically, a lubricant, an additive, a stabilizer, or the like is firstly added to a polylactic acid resin in the form of powder or pellet, followed by blending, kneading and T-die extrusion, and then lamination with paper and foaming process. In general, until a foam sheet is prepared by the processes, approximately at least three or four heat processes are performed.
  • a polylactic acid resin is known to be sensitive to heat treatment since it is hydrolyzed at a high temperature. Due to the property of the polylactic acid resin, the hydrolysis of the foam sheet, applied with the polylactic acid resin, by heat during a process affects the molecular weight of the polylactic acid resin to result in the degradation of a product.
  • a process for preparing a foam sheet capable of reducing the number of heat processes by using a microparticulate polylactic acid resin, is provided.
  • a process for preparing a foam sheet comprising a polylactic acid foam layer comprising: mixing a particulate polylactic acid resin having an average particle size of about 1 ⁇ m to about 100 ⁇ m, a foam resin, and an additive to form a foamable resin composition, and then applying the foamable resin composition to form a layer; and allowing the resultant layer to foam and consequently forming a foam layer is provided.
  • the foamable resin composition allows the polylactic acid resin to be mixed in a microparticle size to form a suspension.
  • the foamable resin composition in the form of sol-gel may foams to form a polylactic acid foam layer.
  • FIG. 1 shows a process flow diagram of a process for preparing a foam sheet according to one embodiment of the present disclosure.
  • a powder of polylactic acid particles having a micro size is firstly prepared by applying a melt spray method ( FIG. 1 , MELT ESD step); a suspension is prepared by mixing a foamable resin composition comprising the powder of polylactic acid particles having a micro size ( FIG. 1 , MIXING (PREPARING SOL) step); a coating layer is formed by coating the suspension on a substrate ( FIG. 1 , SOL COATING step); and, subsequently, the coating layer foams ( FIG. 1 , FOAMING step) to form a foam layer, whereby a foam sheet may be prepared.
  • a melt spray method FIG. 1 , MELT ESD step
  • MIXING PREPARING SOL
  • a foam sheet comprising a polylactic acid foam layer comprising the above polylactic acid resin particles having an average particle size of about 1 ⁇ m to about 100 ⁇ m may be prepared.
  • the foam resin may be a material used in preparing a foam layer of a foam sheet, such as PVC, polyurethane, and the like, without being limited thereto.
  • the microparticles of the polylactic acid resin are evenly dispersed. Since the polylactic acid resin is evenly dispersed, the surface property of the product, the foam sheet finally produced, may be improved, whereby the durability of the foam sheet is enhanced.
  • the process for preparing a foam sheet may reduce the number of heat processes, compared with the well-known processes for preparing a foam sheet, the damage resulting from a hydrolysis of a polylactic acid resin may be remarkably lowered, whereby the loss of the molecular weight by the hydrolysis of the polylactic acid resin may be inhibited. Therefore, the foam sheet prepared by the above process unexpectedly improves the product degradation by heat processes to result in an extended shelf-life.
  • the molecular weight of the microparticulate polylactic acid resin may be maintained without a remarkable loss resulting from a hydrolysis.
  • the foam sheet produced by the above process for preparing a foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • the foam sheet produced by the above process for preparing a foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 or more.
  • particles having an average particle size of 50 ⁇ m were prepared by a melt electrostatic spray deposition.
  • a temperature of an spray nozzle was 250° C.
  • a pressure of the spray nozzle was 500 psi
  • a diameter of the spray nozzle was 1 mm
  • a voltage of 20,000 V was applied to the spray nozzle
  • a viscosity of a molten polylactic acid spray solution was 2,000 cps at 250° C.
  • the resulting polylactic acid particles, and additives including a plasticizer, a stabilizer, a lubricant and the like were added and blended to prepare a polylactic acid resin-containing sol.
  • the resulting polylactic acid resin-containing sol was subjected to a sol-gel coating on a substrate, followed by drying (foaming) to obtain a foam sheet sample having a thickness of about 0.5 mm.
  • Additive including a plasticizer, a stabilizer, a lubricant and the like was added to a polylactic acid resin in the form of pellet as in Example 1 and mixed to prepare a polylactic acid resin-containing mixture composition.
  • the polylactic acid resin-containing mixture composition was kneaded at 150° C. with a Banbury mixer, and the first and the second mixing were conducted with two roll mill at 150° C.
  • the thus prepared mixing materials were subjected to calendering process and foaming process to obtain a foam sheet having a thickness of about 0.5 mm.
  • Example 1 With respect to the foam sheet samples prepared in Example 1 and Comparative Example 1, the weight average molecular weights thereof were determined with the GPC (gel permeation chromatography) (e2695, Waters), and shown in Table 1.
  • GPC gel permeation chromatography
  • Example 1 Each of the foam sheets prepared in Example 1 and Comparative Example 1 was determined for its impact resistance according to the ASTM D256 method, and results are shown in Table 1.
  • Example 1 The surface property of each of the foam sheets prepared in Example 1 and Comparative Example 1 were visually determined, and shown in Table 1.
  • the evaluation criteria are visual assessment and the surface property was scored from 5 (excellent) to 1 (NG) using a 5-point scale.

Abstract

Disclosed herein is a foamable resin composition for a foam sheet including polylactic acid resin particles, each of the particles having a particle size of about 1 μm to about 100 μm. A process for preparing a particulate polylactic acid resin includes: introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and injecting the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid. In addition, disclosed herein is a process for preparing a foam sheet using the foamable resin composition for a foam sheet including a polylactic acid resin.

Description

    TECHNICAL FIELD
  • The present disclosure relates to a foamable resin composition for a foam sheet, a foam sheet, a process for preparing a particulate polylactic acid resin, and a process for preparing a foam sheet.
  • BACKGROUND ART
  • Products in which a polylactic acid is used are produced through multiple heat processes. It has been reported that a polylactic acid is sensitive to heat, and, therefore, a hydrolysis proceeds at a high temperature. Due to the property of the polylactic acid, a hydrolysis caused by heat during a process for preparing a polylactic acid product leads to a change of a molecular weight, which affects the state of the end product produced.
  • DISCLOSURE Technical Problem
  • One embodiment of the present disclosure provides a foamable resin composition for a foam sheet, which can produce a foam sheet including a polylactic acid resin and having an improved shelf-life.
  • Another embodiment of the present disclosure provides a process for preparing a polylactic acid resin of microparticles, included in the foamable resin composition.
  • Still another embodiment of the present disclosure provides a process for preparing a foam sheet, using the foamable resin composition for a foam sheet.
  • Technical Solution
  • In one embodiment of the present disclosure, a foamable resin composition for a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 μm to about 100 μm, is provided.
  • A foam sheet prepared by molding the composition may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • The composition may be a suspension in which the polylactic acid resin particles are dispersed in a liquid solvent.
  • In another embodiment of the present disclosure, a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 μm to 100 μm, is provided.
  • The foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • In still another embodiment of the present disclosure, a process for preparing a particulate polylactic acid resin comprises: introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and spraying the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid.
  • The polylactic acid resin may be introduced into an extruder, and then transferred to an spray nozzle and heated in the spray nozzle to form the molten polylactic acid spray solution.
  • The polylactic acid resin n the form of pellet or powder may be introduced into the extruder.
  • The molten polylactic acid spray solution may be introduced into the spray nozzle together with an air and then discharged.
  • A temperature of the air that is introduced into the spray nozzle may be of about 300° C. to about 500° C., a pressure of the air that is injected into the spray nozzle may be of about 100 psi to about 1,000 psi, an injection speed of the air that is injected into the spray nozzle may be of about 10 m/s to about 50 m/s.
  • A temperature of the spray nozzle may be of about 200° C. to about 400° C.
  • A pressure of the spray nozzle may be of about 10 psi to about 1,000 psi.
  • A diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm.
  • The molten polylactic acid spray solution may comprise at least one additive selected from the group consisting of a lubricant, a plasticizer, and a combination thereof.
  • The molten polylactic acid spray solution may have a viscosity of about 1,500 cps to about 2,000 cps at 250° C.
  • A voltage of about 2,000 V to about 50,000 V may be applied to the spray nozzle to carry out a melt electrostatic spray deposition.
  • The particulate polylactic acid resin may have an average particle size of about 1 μm to about 100 μm.
  • In still another embodiment of the present disclosure, a process for preparing a foam sheet comprising a polylactic acid foam layer, comprising: mixing a particulate polylactic acid resin having an average particle size of 1 μm to 100 μm, a foam resin, and an additive to form a foamable resin composition, and then applying the foamable resin composition to form a layer; and allowing the resultant layer to foam and consequently forming a foam layer is provided.
  • The particulate polylactic acid resin is obtained by a melt spray method.
  • The foam sheet prepared by the process may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • Advantageous Effects
  • A foam sheet prepared by using the microparticulate polylactic acid resin has excellent durability and surface property and improved shelf-life.
  • DESCRIPTION OF DRAWINGS
  • FIG. 1 schematically shows a process flow diagram of a process for preparing a foam sheet according to one embodiment of the present disclosure; and
  • FIG. 2 schematically shows a process flow diagram of a process for preparing a foam sheet.
  • BEST MODE
  • Hereinafter, exemplary embodiments of the present disclosure will be described in detail. It should be understood, however, that the drawings and detailed description thereto are not intended to limit the present disclosure to the particular form disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the present disclosure as defined by the appended claims.
  • In one embodiment of the present disclosure, polylactic acid resin particles having an average particle size of about 1 μm to about 100 μm are provided.
  • The polylactic acid resin particles having the particle size range may be prepared by a melt spray method. Further, more uniform polylactic acid particles may be obtained by introducing an air having a high temperature and a high pressure together to an spray nozzle during performing the melt spray method. The melt spray method may be carried out by a melt electrostatic spray deposition (melt ESD) applying a voltage during performing the melt spray method.
  • A process according to another embodiment of the present disclosure for preparing polylactic acid resin particles having an average particle size of about 1 μm to about 100 μm, comprises: introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and spraying the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid.
  • The process for preparing a particulate polylactic acid resin has advantages to easily control the size of the polylactic acid resin particles formed by applying the melt spray method and to make a distribution of the particle size uniform. For example, ploylactic acid resin particles having an average particle size of about 1 μm to about 100 μm may be prepared by the process for preparing a particulate polylactic acid resin.
  • To perform the melt spray method, firstly, a polylactic acid in the form of pellet or powder is introduced into an extruder equipped with an spray nozzle, and then the polylactic acid is melted in the high temperature spray nozzle to form a molten polylactic acid spray solution. Such molten polylactic acid spray solution is sprayed in the form of a liquid droplet in micrometers. In addition, such spraying is performed in a cooling chamber, allowing the liquid droplet to be cooled to form microparticles of the polylactic acid resin.
  • The melt spray method is optionally carried out by a melt electrostatic spray deposition applying a voltage to the spray nozzle.
  • The molten polylactic acid spray solution is introduced into the spray nozzle together with an air and then discharged.
  • By controlling the temperature, pressure and velocity of the air that is introduced into the spray nozzle, the size and shape of a liquid droplet of the molten polylactic acid spray solution discharged may be controlled, whereby the particle size of a polylactic acid resin to be finally obtained may be controlled.
  • For example, a temperature of the air that is introduced into the spray nozzle may be of about 300° C. to about 500° C., a pressure of the air may be of about 10 psi to about 1,000 psi, and an injection speed of the air may be of about 10 m/s to about 50 m/s.
  • In the melt spray method, a viscosity of the melted polylactic acid may be controlled to be sprayed as a liquid droplet in micrometers.
  • To control the viscosity of the melted polylactic acid resin may be achieved by a method, such as adjusting the temperature of the spray nozzle, adding an additive, such as a lubricant, a plasticizer, or the like, together with the polylactic acid resin, to the extruder to be compounded, or introducing a gas such as CO2 to the polylactic acid resin in the form of pellet, and the like.
  • For example, a diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm.
  • In particular, a viscosity of the molten polylactic acid spray solution may be of about 1,500 cps to about 2,000 cps at about 250° C. With forming a coating solution having the above viscosity range, a microparticulate polylactic acid resin may be formed.
  • Process conditions of the melt spray method are not particularly limited, and the known process conditions, for example, a pressure of the spray nozzle of about 100 psi to about 1,000 psi may be applied.
  • However, the melt spray method should be carried out at a temperature range in which the polylactic acid melts. For example, a temperature of the spray nozzle may be of about 200° C. to about 400° C.
  • In addition, a diameter of the spray nozzle may be of about 0.5 mm to about 3.0 mm in order to form the microparticulate polylactic acid resin as described above.
  • The melt spray method may be carried out, for example, by a melt electrostatic spray deposition applying a voltage of about 2,000 V to about 50,000 V to the spray nozzle.
  • The microparticulate polylactic acid resin which may be prepared by the process can be advantageously applied to a preparation of a foam sheet.
  • In another embodiment of the present disclosure, a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of about 1 μm to about 100 μm, is provided. The foam sheet may be prepared by using the polylactic acid resin particles having a small particle size in micrometers, in accordance with a process for preparing a foam sheet as mentioned below, and the thus prepared foam sheet minimizes the number of heat processes to minimize the degradation of the polylactic acid resin, allowing the maintenance of higher molecular weight. In particular, the foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • FIG. 2 shows a process flow diagram of an exemplary process for preparing a foam sheet. Generally, a foam sheet applied with a polylactic acid resin has been produced through a variety of processes. More specifically, a lubricant, an additive, a stabilizer, or the like is firstly added to a polylactic acid resin in the form of powder or pellet, followed by blending, kneading and T-die extrusion, and then lamination with paper and foaming process. In general, until a foam sheet is prepared by the processes, approximately at least three or four heat processes are performed.
  • However, a polylactic acid resin is known to be sensitive to heat treatment since it is hydrolyzed at a high temperature. Due to the property of the polylactic acid resin, the hydrolysis of the foam sheet, applied with the polylactic acid resin, by heat during a process affects the molecular weight of the polylactic acid resin to result in the degradation of a product.
  • In still another embodiment of the present disclosure, a process for preparing a foam sheet, capable of reducing the number of heat processes by using a microparticulate polylactic acid resin, is provided.
  • In one embodiment, a process for preparing a foam sheet comprising a polylactic acid foam layer, comprising: mixing a particulate polylactic acid resin having an average particle size of about 1 μm to about 100 μm, a foam resin, and an additive to form a foamable resin composition, and then applying the foamable resin composition to form a layer; and allowing the resultant layer to foam and consequently forming a foam layer is provided.
  • The foamable resin composition allows the polylactic acid resin to be mixed in a microparticle size to form a suspension. Specifically, the foamable resin composition in the form of sol-gel may foams to form a polylactic acid foam layer.
  • FIG. 1 shows a process flow diagram of a process for preparing a foam sheet according to one embodiment of the present disclosure. A powder of polylactic acid particles having a micro size is firstly prepared by applying a melt spray method (FIG. 1, MELT ESD step); a suspension is prepared by mixing a foamable resin composition comprising the powder of polylactic acid particles having a micro size (FIG. 1, MIXING (PREPARING SOL) step); a coating layer is formed by coating the suspension on a substrate (FIG. 1, SOL COATING step); and, subsequently, the coating layer foams (FIG. 1, FOAMING step) to form a foam layer, whereby a foam sheet may be prepared.
  • By the process for preparing a foam sheet, a foam sheet comprising a polylactic acid foam layer comprising the above polylactic acid resin particles having an average particle size of about 1 μm to about 100 μm may be prepared.
  • The foam resin may be a material used in preparing a foam layer of a foam sheet, such as PVC, polyurethane, and the like, without being limited thereto.
  • In the foam layer formed as described above, the microparticles of the polylactic acid resin are evenly dispersed. Since the polylactic acid resin is evenly dispersed, the surface property of the product, the foam sheet finally produced, may be improved, whereby the durability of the foam sheet is enhanced.
  • Since the process for preparing a foam sheet may reduce the number of heat processes, compared with the well-known processes for preparing a foam sheet, the damage resulting from a hydrolysis of a polylactic acid resin may be remarkably lowered, whereby the loss of the molecular weight by the hydrolysis of the polylactic acid resin may be inhibited. Therefore, the foam sheet prepared by the above process unexpectedly improves the product degradation by heat processes to result in an extended shelf-life.
  • In the foam sheet produced by the above process for preparing a foam sheet, the molecular weight of the microparticulate polylactic acid resin may be maintained without a remarkable loss resulting from a hydrolysis. For example, the foam sheet produced by the above process for preparing a foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 to about 200,000.
  • Particularly, the foam sheet produced by the above process for preparing a foam sheet may comprise a polylactic acid resin having a weight average molecular weight of about 100,000 or more.
  • Hereinafter, the present disclosure will be explained in more detail with reference to an example and a comparative example. However, it should be understood that these examples are provided for illustration only and are not to be in any way construed as limiting the present disclosure.
  • EXAMPLES Example 1
  • Using a polylactic acid resin in the form of pellet, particles having an average particle size of 50 μm were prepared by a melt electrostatic spray deposition. On performing the melt electrostatic spray deposition, a temperature of an spray nozzle was 250° C., a pressure of the spray nozzle was 500 psi, and a diameter of the spray nozzle was 1 mm, a voltage of 20,000 V was applied to the spray nozzle, and a viscosity of a molten polylactic acid spray solution was 2,000 cps at 250° C.
  • The resulting polylactic acid particles, and additives including a plasticizer, a stabilizer, a lubricant and the like were added and blended to prepare a polylactic acid resin-containing sol. The resulting polylactic acid resin-containing sol was subjected to a sol-gel coating on a substrate, followed by drying (foaming) to obtain a foam sheet sample having a thickness of about 0.5 mm.
  • Comparative Example 1
  • Additive including a plasticizer, a stabilizer, a lubricant and the like was added to a polylactic acid resin in the form of pellet as in Example 1 and mixed to prepare a polylactic acid resin-containing mixture composition. The polylactic acid resin-containing mixture composition was kneaded at 150° C. with a Banbury mixer, and the first and the second mixing were conducted with two roll mill at 150° C. The thus prepared mixing materials were subjected to calendering process and foaming process to obtain a foam sheet having a thickness of about 0.5 mm.
  • EVALUATION Experiment 1: Polylactic Acid Molecular Weight Determination
  • With respect to the foam sheet samples prepared in Example 1 and Comparative Example 1, the weight average molecular weights thereof were determined with the GPC (gel permeation chromatography) (e2695, Waters), and shown in Table 1.
  • Experiment 2: Durability Evaluation
  • Each of the foam sheets prepared in Example 1 and Comparative Example 1 was determined for its impact resistance according to the ASTM D256 method, and results are shown in Table 1.
  • Experiment 3: Surface Property Evaluation
  • The surface property of each of the foam sheets prepared in Example 1 and Comparative Example 1 were visually determined, and shown in Table 1. The evaluation criteria are visual assessment and the surface property was scored from 5 (excellent) to 1 (NG) using a 5-point scale.
  • TABLE 1
    Polylactic acid
    particles before Polylactic acid
    preparation of Polylactic acid in foam sheet of
    foam sheet of in foam sheet Comparative
    Items Example 1 of Example 1 Example 1
    Weight average 150,000 120,000 80,000
    molecular weight
    Impact resistance 20 30
    [kgf · cm/cm]
    Surface Property Blocking: 5 Blocking: 4
    Blushing: 4 Blushing: 3

Claims (20)

1. A foamable resin composition for a foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of 1 μm to 100 μm.
2. The foamable resin composition according to claim 1, wherein a foam sheet prepared by molding the composition comprises a polylactic acid resin having a weight average molecular weight of 100,000 to 200,000.
3. The foamable resin composition according to claim 1, wherein the composition is a suspension in which the polylactic acid resin particles are dispersed in a liquid solvent.
4. A foam sheet comprising polylactic acid resin particles, each of the particles having a particle size of 1 μm to 100 μm.
5. The foam sheet according to claim 4, wherein the foam sheet comprises a polylactic acid resin having a weight average molecular weight of 100,000 to 200,000.
6. A process for preparing a particulate polylactic acid resin comprising:
introducing a polylactic acid resin and then forming a molten polylactic acid spray solution; and
spraying the molten polylactic acid spray solution by a melt spray method and simultaneously cooling the molten polylactic acid spray solution to obtain a particulate polylactic acid.
7. The process according to claim 6, wherein the polylactic acid resin is introduced into an extruder, and then transferred to an spray nozzle and heated in the spray nozzle to form the molten polylactic acid spray solution.
8. The process according to claim 7, wherein the polylactic acid resin in the form of pellet or powder is introduced into the extruder.
9. The process according to claim 8, wherein the molten polylactic acid spray solution is introduced into the spray nozzle together with an air and then discharged.
10. The process according to claim 9, wherein a temperature of the air that is injected into the spray nozzle is of 300° C. to 500° C., a pressure of the air that is injected into the spray nozzle is of 100 psi to 1,000 psi, and an injection speed of the air that is injected into the spray nozzle is of 10 m/s to 50 m/s.
11. The process according to claim 7, wherein a temperature of the spray nozzle is of 200° C. to 400° C.
12. The process according to claim 7, wherein a pressure of the spray nozzle is of 10 psi to 1,000 psi.
13. The process according to claim 7, wherein a diameter of the spray nozzle is of 0.5 mm to 3.0 mm.
14. The process according to claim 6, wherein the molten polylactic acid spray solution comprises at least one additive selected from the group consisting of a lubricant, a plasticizer, and a combination thereof.
15. The process according to claim 6, wherein the molten polylactic acid spray solution has a viscosity of 1,500 cps to 2,000 cps at 250° C.
16. The process according to claim 7, wherein a voltage of 2,000 V to 50,000 V is applied to the spray nozzle to carry out a melt electrostatic spray deposition.
17. The process according to claim 6, wherein the particulate polylactic acid resin has an average particle size of 1 μm to 100 μm.
18. (canceled)
19. (canceled)
20. (canceled)
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US11001677B2 (en) 2017-03-09 2021-05-11 Lg Hausys, Ltd. Thermoplastic polymer particles having low impurity content
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CN105492529B (en) 2018-07-03
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US10508176B2 (en) 2019-12-17
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