Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
  • C08J5/045—Reinforcing macromolecular compounds with loose or coherent fibrous material with vegetable or animal fibrous material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y70/00—Materials specially adapted for additive manufacturing
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J11/00—Recovery or working-up of waste materials
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/005—Processes for mixing polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
  • C08J5/047—Reinforcing macromolecular compounds with loose or coherent fibrous material with mixed fibrous material
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
  • C08K3/20—Oxides; Hydroxides
  • C08K3/22—Oxides; Hydroxides of metals
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L101/00—Compositions of unspecified macromolecular compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
  • C08L3/04—Starch derivatives, e.g. crosslinked derivatives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
  • C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
  • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
  • C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L97/00—Compositions of lignin-containing materials
  • C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
  • B29C64/10—Processes of additive manufacturing
  • B29C64/106—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
  • B29C64/10—Processes of additive manufacturing
  • B29C64/106—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
  • B29C64/118—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING 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
  • B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
  • B29K2023/10—Polymers of propylene
  • B29K2023/12—PP, i.e. polypropylene
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING 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
  • B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
  • B29K2067/04—Polyesters derived from hydroxycarboxylic acids
  • B29K2067/046—PLA, i.e. polylactic acid or polylactide
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING 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
  • B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
  • B29K2105/06—Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
  • B29K2105/16—Fillers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING 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
  • B29K2511/00—Use of natural products or their composites, not provided for in groups B29K2401/00 - B29K2509/00, as filler
  • B29K2511/10—Natural fibres, e.g. wool or cotton
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2300/00—Characterised by the use of unspecified polymers
  • C08J2300/22—Thermoplastic resins
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
  • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
  • C08J2323/10—Homopolymers or copolymers of propene
  • C08J2323/12—Polypropene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2367/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2397/00—Characterised by the use of lignin-containing materials
  • C08J2397/02—Lignocellulosic material, e.g. wood, straw or bagasse
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
  • C08K3/20—Oxides; Hydroxides
  • C08K3/22—Oxides; Hydroxides of metals
  • C08K2003/2206—Oxides; Hydroxides of metals of calcium, strontium or barium
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape

Definitions

• the present invention relates to a composite material comprising at least one thermoplastic resin and granular shive from hemp and/or flax.
• the invention further relates to a method for preparing the above-mentioned composite material and the use of the latter in the 3D printing technologies, namely the manufacture of three-dimensional objects by additive manufacturing, starting from a digital 3D model .
• the composite materials are obtained thanks to the combination of two or more materials different from each other and they are widely used thanks to their enhanced physical-mechanical properties, among which higher resistance and long-duration with respect to those of the single starting materials.
• thermoplastic resins comprising matrices of thermoplastic resins and components of natural origin, in particular natural fibers derived from Kenaf, hemp, flax, jute, henequen, leafs of pineapple, sisal, wood and sawdust are currently known.
• natural fibers derived from Kenaf, hemp, flax, jute, henequen, leafs of pineapple, sisal, wood and sawdust.
• the possibility to recycle the processing scraps of such components of natural origin raises particular interest.
• the products obtained from the processing of the hemp or flax plant are the long fibers (used in the textile industry), the bast fibers or bast (from which the cellulose is obtained) and the ligneous stems or shive .
• the Applicant considered how to provide a composite material having enhanced physical-mechanical properties and more lightness, starting from waste material from hemp or flax processing and which, at the same time, has an enhanced workability and is cheaper.
• the Applicant was able to obtain such results by using, into a composite material, a component having a fine particle size derived from waste of hemp or flax processing, to date used as fertilizer, as fuel pellet, in the field of green-building, together with lime and as animal litter.
• the Applicant found that the above- mentioned problem is solved through a composite material comprising a thermoplastic resin and shive from hemp and/or flax with fine particle size, wherein resin and shive are present in a certain ratio by weight.
• the present invention relates to a composite material comprising at least one thermoplastic resin and from 5 to 180 parts by weight of granular shive from hemp and/or flax, with respect to 100 parts by weight of the thermoplastic resin, with particles having an average particle size lower than 0.2 mm, preferably lower than 0.1 mm.
• the composite material according to the present invention has an enhanced workability, as the granular shive from hemp and/or flax with particle size lower than 0.2 mm, preferably 0.1 mm, disperses in a more homogenous manner with the thermoplastic resin, both with respect to other components derived from hemp with a higher particle size, and with respect to other materials with a particle size lower than 0.2 mm, for example sawdust.
• Another advantage related to the particle size characterizing the shive according to the invention is to allow the use of high amounts of shive with respect to the amount of resin, determining both a higher lightness of the resultant material and an economical advantage, as it allows to decrease the amount of resin used in the composite material, without adversely affecting the thermoplastic properties of the composite material obtained.
• the shive used in the present invention represents a waste material of the hemp and/or flax processing, and therefore its reuse does not involve additional costs, indeed it represents a manner for using such waste product.
• shive according to the present invention allows to obtain a composite material with enhanced processability in the molten state with respect to, for example, the addition of short hemp fibers, which tend to increase the viscosity of the melted and to create obstructions when the material is processed by the passage through nozzles with a very small particle size, for example lower than 2 mm or also lower than 0.4 mm. That makes the material according to the invention particularly suitable for the manufacture of three-dimensional objects by 3D printing, which requires the use of nozzles of those sizes .
• the wording "granular shive from hemp and/or flax with particles having an average particle size lower than 0.2 mm, preferably lower than 0.1 mm” means a fine powder obtained from the processing of the large shive, for example by grinding.
• the fine shive can also derive from the suction of powders which disperse during the processing of hemp straws.
• the term “large shive” (which generally has a particle size of 1-2 cm) means the shive obtained by separation (for example by scutching) of the shive itself (also known as “woody stem”) from the bast fiber (also called “bast”) .
• the granular shive from hemp and/or flax in general has substantially spherically-shaped particles, which is not to be confused with the so called short hemp fibers which are characterized by a fibrillary structure.
• Such structural difference can be appreciated, for example, by optical microscope observation or, preferably, by scanning electron microscope (SEM) observation.
• the particles of shive have an average particle size from 5 ⁇ to 300 ⁇ , more preferably from 10 ⁇ to 100 ⁇ .
• the average particle size can be determined according to the known techniques. Particularly, for average sizes such as those indicated above, the laser diffraction technique, according to the standard ISO 13320-1 (1999), is generally used. As for higher sizes (up to 0.2 mm) techniques based on the analysis of images obtained by microscope can be used.
• a parameter which can be used for characterizing particles of shive is the aspect ratio, namely the ratio between the higher diameter and the smaller diameter, perpendicular to the higher diameter, determined on a projection onto the plane of each particle (Feret diameter) .
• Such parameter can be determined through the analysis of images obtained by the microscope, as described in the standard ISO 9276-6 (2008) .
• the shive has an aspect ratio from 0.5 to 2.0, preferably from 0.8 to 1.2, even more preferably from 0.9 to 1.1.
• the composite material according to the present invention further comprises from 0.1 to 60 parts by weight of bast fibers (bast) from hemp and/or flax having a length from 0.5 cm to 4 cm, preferably from 0.6 cm to 2 cm.
• the used thermoplastic resin can be of natural or synthetic origin.
• the thermoplastic resin is of synthetic origin, it is preferably selected from polyethylene terephthalate (PET) , polypropylene (PP) , polyethylene (PE) , acrylonitrile-butadiene-styrene (ABS) copolymer, polypropylene/polyethylene terephthalate copolymer, ethylene-propylene copolymer.
• thermoplastic resin When the thermoplastic resin is of natural origin, it is preferably selected from polylactic acid (PLA) , polyhydroxyalkanoates (PHA) , modified starches (such as, for example, those known under the commercial name “Mater B”) or polyethylene from bioethanol (known under the commercial name “BIO PET 30”) , more preferably PLA, which are characterized by high biodegradability.
• PLA polylactic acid
• PHA polyhydroxyalkanoates
• modified starches such as, for example, those known under the commercial name "Mater B”
• polyethylene from bioethanol known under the commercial name "BIO PET 30”
• PLA polylactic acid
• PHA polyhydroxyalkanoates
• BIO PET 30 polyethylene from bioethanol
• the composite material according to the invention further comprises a particle-shaped component having an average particle size lower than 0.2 mm, preferably lower than 0.1 mm, for example a component derived from coconut shell, namely the hard shell of coconut (brownish covering) , to which the meat (pulp) adheres and which needs to be broken in order to reach the meat itself.
• a component derived from coconut shell namely the hard shell of coconut (brownish covering)
• Such component is preferably obtained by breaking operations of the hard shell of coconut, which are carried out in order to take the pulp.
• such component can derive by grinding coconut shell residues.
• the composite material further comprises a binding agent, which allows to improve the mechanical properties of the material itself. It is believed that such binding effect is obtained thanks to the capability of the binding agent of binding the silicates present in the shive .
• the binding agent is selected from selected from alkali metal oxides and/or alkaline-earth metal oxides, preferably calcium oxide.
• the present invention relates to a method for the manufacture of the composite material as defined above comprising the steps of:
• the present invention relates to the use of the composite material as defined above for the manufacture of three-dimensional objects by 3D printing.
• the 3D printing is an additive manufacturing of three-dimensional objects, starting from a digital 3D model.
• FDM fused deposition modeling
• One of the most widespread techniques is the so-called "fused deposition modeling” (FDM), which provide the overlapping of thin layers of thermoplastic material in the molten state obtained starting from filaments which are directed to an application head where the filament is melted and placed on a platform by nozzles, thus forming subsequent layers according to the 3D model provided.
• FDM fused deposition modeling
• the composite material according to the invention is in the filament form, for example filament coils or rolls, which are directed to the application head of the 3D printer.
• the use of the composite material according to the invention in the field of the 3D printing advantageously allows to avoid the formation of obstructions in the application nozzles, which instead are often formed when composite materials containing a fibrous component are used, for example hemp fibers, which have a marked tendency to adhere to the nozzles walls, thus impeding the material deposition .
• figure 1 shows the results of the tensile tests carried out on the composite material according to the invention
• figure 2 shows the SEM image related to the composite material according to the invention
• figures 3 and 4 show the SEM images related to the composite material containing hemp fibers in place of granular shive .
• the composite material according to the invention was prepared by placing into a vessel made of aluminum about 2g of PLA (equal to about twenty granules of PLA) and then heated on a plate to a temperature of 300 °C in order to obtain the PLA melting. Then, about 1 g of shive constituted by particles having an average particle size lower than 0.1 mm was added, namely equal to about 40% by weight with respect to the total weight of the composite material obtained and then the whole was homogenized by mixing for at least 5 minutes, decreasing the plate temperature.
• the composite material obtained had good workability and it was placed on an aluminum foil and a sample in the plate- form having a thickness equal to about 3 mm was obtained by pressing, which was left to cool up to hardening.
• the sample was subjected to several tests in order to test the physical-mechanical properties of the sample itself. The results showed that the material tested is rigid, hard and it has properties of flexural, tensile and impact strength, equal to or higher than the thermoplastic resin alone. Furthermore, once hardened, the sample was subjected to conditions of water washout mechanical stress keeping intact its properties, without undergoing degradation.
• thermoplastic resin already produced with shive so as to reuse it without causing the separation between the phases.
• the sample obtained in the preceding example was melted into a 100 ml beaker on a heating plate, at a temperature of 300°C (mixture 1) .
• the material was subjected to stirring.
• 2g of PLA were melted on a heating plate into a 100 ml beaker, and then shive 1 g was gradually added.
• the whole was mixed.
• mixture 2 was combined with mixture 1 and the whole was mixed, maintaining the plate temperature at 300°C.
• the obtained composite material had good workability and it was placed on an aluminum foil and a sample in the plate-form having a thickness of 2-3 mm was obtained by pressing, which was left to cool up to hardening.
• the sample was subjected to several tests in order to test the physical-mechanical properties of the sample itself. The results showed that the material tested has surprising hardness, tensile, flexural mechanical properties and it has good properties of resilience in addition to a low weight.
• thermoplastic resin A test, in which polypropylene (PP) was used as thermoplastic resin, was carried out. 2 g of PP were placed into a 100 ml beaker and melted on a heating plate at 300 °C. Simultaneously, about 1 g of shive, with an average particle size lower than 0.1 mm, was weighted in a crucible. After having achieved the temperature of 100°C, namely when PP was almost completely melted, the shive was gradually added. The sample was subjected to several tests in order to test the physical-mechanical properties of the sample itself, particularly the obtained material was subjected to water flow (for 10 min) , showing a great resistance to water. Furthermore, such material showed an excellent tensile strength.
• PP polypropylene
• EXAMPLE 4 (comparison) The examples 1-3 were repeated using sawdust in place of shive, wherein said sawdust had a particle size comparable to the particle size of the shive used in examples 1-3, namely a particle size lower than 0.1 mm, wherein the sawdust was present in an amount of 50% by weight of the total composition with respect to the resin.
• the obtained material was subjected to several tests in order to test the physical-mechanical properties thereof. The results showed that the tested material has worse workability than the materials obtained in the examples 1-3.
• Mixtures of PLA and shive were made in several ratios from each other, in particular 5, 10, 15, 20 and 25 parts by weight of shive respectively, with respect to 100 parts by weight of PLA, wherein the shive has an average particle size of about 50 ⁇ .
• a Brabender Plastograph mixer was used at a temperature of 170°C for 10 minutes. Samples of material thus obtained were fractured and analyzed by scanning electron microscope SEM. As showed in figure 2, the microscope analysis highlighted as the samples containing shive have cavities attributable to the granular particles of shive which were extracted from the matrix after the fracture .
• the example 5 was repeated using, in the place of shive, hemp fibers having an average length of 2 mm and the scanning electron microscope (SEM) analysis highlighted (see Figures 3 and 4) the presence of fibrillar structures only and the absence of cavities in the samples of material obtained. Furthermore, the fibrillar structures have poor adhesion with respect to the matrix of thermoplastic resin.

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• 2016
  • 2016-04-01 JP JP2018502843A patent/JP2018513906A/ja active Pending
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