JP2023083053A - Resin material for molding - Google Patents

Abstract

To provide a resin material for molding which is formed by uniformly mixing a woody biomass roasted material or a woody biomass carbide, and a thermoplastic resin, has such high viscosity as to prevent breakage and cracking during injection molding, and facilitates molding.SOLUTION: A resin material for molding contains 10-90 mass% of a woody biomass roasted material or a woody biomass carbide having an average particle diameter of 100 μm or less, and further contains a polyamide-based resin.SELECTED DRAWING: None

Description

TECHNICAL FIELD The present invention relates to a molding resin material containing a roasted woody biomass or a carbonized woody biomass and a polyamide resin.

Biomass materials are attracting attention as industrial resources. Biomass materials mean materials derived from organisms such as plants. Since biomass materials are organic substances, carbon dioxide is emitted when they are burned. However, the carbon contained in this is derived from the carbon dioxide absorbed from the atmosphere by photosynthesis during the biomass growth process, so the use of biomass materials does not increase the amount of carbon dioxide in the atmosphere as a whole. It is said that it is good to think. This property is called carbon neutral.

Against the backdrop of global environmental issues such as global warming, there is an urgent need to promote resource conservation, material recycling aimed at converting waste into raw materials, and environmental recycling cycles represented by biodegradable plastics. However, the revised Recycling Law and the Green Purchasing Law have been established, and the need for products that comply with these laws is increasing.

Under these circumstances, blending biomass materials into resin molded products, which are widely used from materials for automobile parts to daily necessities, promotes the practice of the concept of carbon neutrality. For example, Patent Document 1 describes a polyamide resin composition containing a surface modifier such as cellulose, a polyamide resin, or an oligomer of a thermoplastic resin. Patent Document 2 describes a resin composition containing cellulose, polyamide resin and elastomer.

Japanese Patent Application Laid-Open No. 2021-120468 Japanese Patent Application Laid-Open No. 2020-29488

However, when "woody biomass" and "polyamide resin" are simply mixed and heated and melted to form a mold, the woody biomass is hydrophilic and cannot be uniformly mixed with the polyamide resin. There are problems such as that the resin body is cut into small pieces at the exit of the device for injecting the mixture of the system biomass and the polyamide resin, and that the surface of the resulting molded article is not smooth.

For example, in Patent Document 1, it is necessary to add a surface modifier such as an oligomer of a thermoplastic resin, which increases the cost. In Patent Document 2, it is necessary to add an elastomer, which similarly increases the cost.

Therefore, an object of the present invention is to provide a resin material for molding mixed with woody biomass, in which woody biomass and polyamide resin are uniformly mixed, and there is little cutting or cracking during molding such as injection. The present invention relates to providing a resin material at low cost.

The present inventors have found that a molding resin material with excellent moldability can be obtained by mixing and heating and kneading a pulverized woody biomass roasted material or a woody biomass carbonized material and a polyamide resin. The present invention has been completed.

The present invention includes, but is not limited to, the following.
(1) A molding resin material containing 10 to 90% by mass of roasted woody biomass or pulverized woody biomass carbonized material having an average particle size of 100 μm or less, and further containing a polyamide resin.
(2) The molding resin material according to (1), wherein the thermoplastic elastomer includes any one of a styrene/butadiene block copolymer, an ethylene/octene copolymer, and a propylene/ethylene copolymer.
(3) The molding resin material according to any one of (1) to (2), further comprising a biodegradable resin.

According to the present invention, it is possible to stably produce a highly sticky molding resin material containing roasted woody biomass or pulverized woody biomass carbonized material that does not cause cuts, cracks, etc. during injection molding. In addition, by increasing the blending ratio of the roasted woody biomass, it is possible to obtain a resin material for molding that is excellent in carbon neutrality.

The roasted woody biomass of the present invention is obtained by heating woody biomass under conditions of an oxygen concentration of 10% or less and a substance temperature of 240 to 350°C.

The woody biomass charcoal of the present invention is obtained by heating woody biomass under conditions of an oxygen concentration of 10% or less and a substance temperature of 400 to 700°C.

In the present invention, both broad-leaved trees and coniferous trees can be used as raw materials for woody biomass. Specifically, but not limited to, broad-leaved trees include eucalyptus, Hevea brasiliensis, beech, China, white birch, poplar, acacia, oak, maple, senoki, elm, paulownia, magnolia, willow, sen, and Quercus phillyraeoides. , Quercus serrata, Sawtooth oak, Horse chestnut, Japanese zelkova, Mizume, Dogwood, Aodamo, etc. Conifers include Japanese cedar, Ezo spruce, Japanese larch, Japanese black pine, Sakhalin fir, Himekomatsu, Yew, Nezuko, Japanese spruce fir, Japanese fir, Dogwood, Fir, Spanish mackerel, Togasawara , Asunaro, Japanese cypress, Japanese hemlock, Japanese hemlock, cypress, yew, dogwood, spruce, yellow cedar, Lawson cypress, Douglas fir, Sitka spruce, Radiata pine, Eastern spruce, Eastern white pine , western larch, western fur, western hemlock, tamarack and the like.

Among these, eucalyptus wood and Hevea brasiliensis are preferred. Eucalyptus includes Eucalyptus (hereinafter abbreviated as E.) calophylla, E. citriodora, E. diversicolor, E. globulus, E. grandis, E. urograndis, E. gummifera, E. marginata, E. nesophila, E. nitens, E. amygdalina, E. camaldulensis, E. delegatensis, E. gigantea, E. muelleriana, E. obliqua, E. regnans, E. sieberiana, E. viminalis, E. marginata, and the like.

In the present invention, the form of woody biomass used as a raw material is not limited, and for example, wood chips, bark, sawdust, and sawdust can be preferably used. In a preferred embodiment, woody biomass with a size of 50 mm or less can be used as a raw material. For example, the woody biomass can be pulverized to a size of 50 mm or less, and pulverized to a size of 1 mm or more and 50 mm or less. It is preferable to use woody biomass as a raw material. In the present invention, the size of the pulverized woody biomass is the size of the circular hole of the sifter. When pulverizing woody biomass, it is preferable to pulverize with, for example, a hammer mill or a knife-cutting biomass fuel chipper.

In the present invention, roasted woody biomass is used. Torrefaction generally refers to a process of heating in a low-oxygen atmosphere at a lower temperature than the so-called carbonization process. The temperature for carbonization treatment of wood is usually 400 to 700°C, but in the present invention, the roasting is performed at 240 to 350°C. Roasting yields a solid fuel that has a higher energy density than its starting material.

The processing conditions for roasting in the present invention are an oxygen concentration of 10% or less and a substance temperature of 240 to 350°C. Here, the substance temperature in roasting is the temperature of the woody biomass near the exit of the roasting treatment apparatus. In the present invention, the roasting is performed under the condition that the oxygen concentration is 10% or less, but if the oxygen concentration exceeds 10%, the material yield and heat yield may decrease. Also, if the substance temperature is less than 240°C, it is difficult to pulverize the roasted product to a small particle size, and if it exceeds 350°C, the substance yield and heat yield decrease. The material temperature is preferably 240-330°C, more preferably 250-320°C. Thermal decomposition of hemicellulose becomes significant at around 270°C, whereas thermal decomposition of cellulose becomes significant at around 355°C, and lignin at around 365°C. Therefore, it is presumed that it becomes possible to preferentially thermally decompose hemicellulose and produce a molding resin material that can achieve both material yield and pulverizability.

In the present invention, the apparatus for roasting treatment is not particularly limited, but a rotary kiln and/or a vertical furnace are preferred. In order to adjust the oxygen concentration to 10% or less, it is preferable to replace the inside of the apparatus with an inert gas such as nitrogen. The treatment time of the roasting treatment is not particularly limited, but is preferably 1 to 180 minutes, more preferably 5 to 120 minutes, and even more preferably 10 to 60 minutes. When using a continuous apparatus, the residence time in the roasting apparatus should be controlled.

In the present invention, an external heat roasting device may be used as the roasting device. For example, an externally heated rotary kiln has a structure in which part or all of the kiln inner cylinder is covered with a kiln outer cylinder, and woody biomass is roasted in the inner cylinder and fuel is burned in the outer cylinder. to indirectly heat the woody biomass inside the inner cylinder. The temperature in the kiln outer cylinder can be 400-800°C, preferably 450-750°C. If the temperature in the kiln outer cylinder is less than 400° C., the woody biomass in the kiln inner cylinder will be insufficiently pyrolyzed, and the pulverizability of the resulting solid fuel will be reduced. On the other hand, if the temperature exceeds 800° C., the temperature of the woody biomass inside the kiln inner cylinder rises excessively, and the material yield and heat yield of the obtained solid fuel decrease.

The roasted product used in the present invention preferably has a substance yield of 60 to 90% and a heat yield of 70 to 95% relative to the woody biomass as a raw material. The hard glove crushability index (HGI) specified in JIS M 8801:2004, which is an index of crushability, is preferably 25 or more, more preferably 30 or more. A higher HGI indicates easier pulverization. When the HGI is in the range of 25 to 70, it becomes easy to mix with a thermoplastic resin and perform molding.

The roasted product or carbonized product used in the present invention may be molded. That is, a pulverized starting material (roasted product) of woody biomass is molded into briquettes or pellets. Molding facilitates handling and increases the density, thereby reducing transportation costs. The bulk density of the molded product after the densification treatment is preferably 500 kg/m3 or more, more preferably 600 kg/m3 or more. The bulk density can be measured according to JIS K 2151, 6 "Bulk Density Test Method".

In the present invention, the device for molding the roasted product is not particularly limited. ) etc. are desirable.

In the present invention, when the roasted product or charcoalized product is molded, the moisture content of the roasted product is preferably 8 to 50%, more preferably 10 to 30%. If the water content is less than 8%, clogging occurs inside the briquette or pelletizer, making it impossible to stably produce moldings. If the moisture content exceeds 50%, it is difficult to mold and is discharged in the form of powder or paste.

In the present invention, a binder may be added to the roasted product or charcoal. Although the binder is not particularly limited, for example, organic polymers such as starch and lignin, inorganic polymers such as acrylic acid amide, and agricultural residues such as wheat bran (residues generated during wheat flour production) can be preferably used. From the viewpoint of efficiently and effectively utilizing woody biomass, the number of parts added to the binder is preferably as small as possible. However, even if 50 parts by mass or more is added, it is not impossible to increase the density.

In the present invention, it is preferable to pulverize the roasted product or charcoal before kneading with the thermoplastic resin. The average particle size of the pulverized material or carbide must be 100 μm or less, and more preferably 50 μm or less. If the average particle size of the pulverized product of the roasted product or carbide is larger than 100 μm, uniform mixing with the resin becomes difficult, and the resin body is cut into small pieces at the outlet of the device for injecting the mixture of the pulverized product and the resin. Problems such as difficulty in carrying out to the apparatus may occur. In addition, the average particle size is a volume 50% average particle size (D50) measured by a laser light scattering method (laser diffraction method), and a laser diffraction/scattering particle size distribution analyzer (Malvern Co., Ltd., device name : Mastersizer 2000) or the like.

The pulverizer used for pulverizing the roasted product may be any device capable of pulverizing organic matter, for example, but not limited to, ball mill, rod mill, bead mill, conical mill, disc mill, edge mill, hammer mill, mortar, and pellet mill. , VSI mill, Willy mill, roller mill, jet mill, masscolloider, etc. can be used.

The molding resin material of the present invention can be obtained by heating and kneading the roasted product, the thermoplastic resin, and the acid-modified polyolefin. In order to achieve a high level of carbon neutrality, it is preferable that the roasted product content in the resin material for molding is high. It must be 90 mass % or less, preferably 20 mass % or more and 90 mass % or less, more preferably 40 mass % or more and 80 mass % or less.

Polyamide resins used in the present invention include polyamide 6 (nylon 6, PA6), polyamide 66 (nylon 66, PA66), polyamide 610 (PA610), polyamide 612 (PA612), polyamide 11 (PA11), polyamide 12 (PA12 ), polyamide 46, polyamide XD10 (PAXD10), polyamide MXD6 (PAMXD6) and the like can be preferably used.

In the present invention, thermoplastic resins other than polyamide-based resins may be used. Examples of thermoplastic resins include polyethylene and polypropylene, but are not limited to these, and any resin that can be plasticized and molded by heat can be used. Among them, polyethylene such as LDPE (low density polyethylene) and polypropylene are preferable from the viewpoint of moldability.

In the present invention, a biodegradable resin may be used as the thermoplastic resin other than the polyamide resin. Examples of thermoplastic biodegradable resins include, but are not limited to, polylactic acid (PLA), polybutylene succinate, polyethylene succinate, polyglycol, polycaprolactone, and polyvinyl alcohol. Also, two or more thermoplastic resins can be used at the same time.

In the present invention, by adding a thermoplastic elastomer, a resin material for molding with high stickiness that does not cause cuts or cracks during injection molding can be stably produced even if pulverized woody biomass roasted products are blended. can do.

As the thermoplastic elastomer used in the present invention, a styrene-based thermoplastic elastomer can be mentioned. More specifically, styrene-butadiene-styrene (SBS) copolymer, styrene-isoprene-styrene (SIS) copolymer, styrene-ethylene-butylene-styrene (SEBS) copolymer, styrene-ethylene-propylene- Block copolymers such as styrene (SEPS) copolymers and styrene-butadiene-butylene-styrene (SBBS) copolymers can be mentioned. These may be used individually by 1 type, and may be used in mixture of 2 or more types.

Moreover, a polyolefin-based elastomer can be mentioned as the thermoplastic elastomer used in the present invention. More specifically, ethylene-butene copolymer, EPR (ethylene-propylene copolymer), modified ethylene-butene copolymer, EEA (ethylene-ethyl acrylate copolymer), modified EEA, modified EPR, modified EPDM (ethylene-propylene-diene terpolymer), ionomer, α-olefin copolymer, modified IR (isoprene rubber), modified SEBS (styrene-ethylene-butylene-styrene copolymer), halogenated isobutylene-paramethyl Examples include styrene copolymers, ethylene-acrylic acid modified products, ethylene-vinyl acetate copolymers, acid modified products thereof, and mixtures containing them as main components. These may be used individually by 1 type, and may be used in mixture of 2 or more types.

Preferred thermoplastic elastomers for use in the present invention include styrene/butadiene block copolymers, ethylene/octene copolymers, propylene/ethylene copolymers, and the like. A styrene/butadiene block copolymer is particularly preferred. Further, the thermoplastic elastomer may be modified with maleic anhydride, fumaric anhydride, or the like. The styrene/butadiene block copolymer preferably has a styrene content of 15 to 30% by mass.

The blending ratio of the thermoplastic elastomer is preferably 1 to 20% by mass, more preferably 3 to 10% by mass.

A molded article can be obtained by heat-treating the resin material for molding of the present invention. The temperature at which the resin material for molding of the present invention is heat-treated (heated, melted, kneaded, etc.) is usually about 100 to 300°C, preferably about 110 to 250°C, and particularly preferably about 120 to 220°C. be. The molded article obtained by the heat treatment can be molded into a desired shape using a conventionally known resin molded article.

In the method for producing the resin material for molding of the present invention, an apparatus commonly used for resin molding can be used for heating and kneading the roasted product and the acid-modified polyolefin. For example, a general extruder or twin-screw kneading extruder can be used. As the twin-screw kneading extruder, TEX series manufactured by Japan Steel Works, Ltd. can be used.

Various molded articles can be produced using the molding resin material of the present invention. Molding can be carried out by conventional methods used for molding thermoplastic resins, such as, but not limited to, injection molding, extrusion molding, blow molding, mold molding, blow molding, foam molding, and the like. be able to.

The resin material for molding of the present invention or a molded article obtained by molding it may contain an organic substance and/or an inorganic substance other than the thermoplastic resin and the roasted product. Other components include, for example, alkalis such as sodium hydroxide, potassium hydroxide, magnesium hydroxide, and calcium hydroxide; inorganic fillers such as clay, talc, calcium carbonate, maiko, titanium dioxide, and zinc oxide; carbon black. , graphite, glass flakes and other organic fillers; red iron oxide, azo pigments, phthalocyanine and other dyes or pigments; dispersants, lubricants, plasticizers, mold release agents, flame retardants, antioxidants (phenolic antioxidants, agent, sulfur-based antioxidant), antistatic agent, light stabilizer, ultraviolet absorber, metal deactivator, crystallization accelerator (nucleating agent), foaming agent, cross-linking agent, antibacterial agent, etc. agents and the like.

The molding resin material of the present invention can be molded for various purposes and can be used as a substitute for plastic products. Molded articles obtained from the molding resin material of the present invention include, for example, trays and the like, automobile parts, interiors such as dashboards of automobiles, baggage compartments for airplanes, structural members of transportation equipment, and housings for home electric appliances. ), electrical appliance parts, cards, various containers such as toner containers, building materials, seedling pots, agricultural sheets, writing instruments, wooden products, household appliances, straws, cups, toys, sporting goods, harbor parts, building parts, power generation It can be widely applied to machine parts, tools, fishing gear, packaging materials, 3D printer models, pallets, food containers, tableware, cutlery (spoon, fork, etc.), chopsticks, various sheets, and the like. When these products are no longer needed, they will be disposed of. can be treated as not increasing the amount of carbon dioxide in

Hereinafter, the present invention will be described in more detail with reference to experimental examples of the present invention, but the present invention is not limited to these experimental examples. Unless otherwise specified, parts and % indicate parts by mass and % by mass, and numerical ranges are described as including their endpoints.

[Example 1]
Wood chips of Eucalyptus Eurograndis were pulverized with a disc chipper. After pulverization, the pulverized chips with a size of 1 to 50 mm were dried using a conveyor dryer (manufactured by Alvan Blanch Co., Ltd.) at a hot air temperature of 70° C. for 3 hours to adjust the water content to 10%.
Subsequently, using a large rotary kiln type carbonization furnace, the oxygen concentration is 1% or less, the material temperature of the crushed chips in the carbonization furnace is 260 ° C., and the roasting is performed for a residence time of 12 minutes to produce woody biomass. of the roasted product was obtained. After cooling the obtained roasted product, it was pulverized with a turbo mill (manufactured by Freund Turbo Co., Ltd.) to an average particle size of 34 μm.
Next, the pulverized roasted product and a polyamide resin (polyamide 6 (PA6), trade name: 1013B, manufactured by Ube Industries) were mixed at a compounding ratio of 25:75, and DSM Xplore Compounder 15 (manufactured by Leo Labo) was used. Kneading at 190° C. for 6 minutes, heating cylinder at 190° C., molding (9 bar, 2 s-11 bar, 0.5 s-11 bar, 24 s), and mold at 40° C. After making a dumbbell of the resin material for molding, physical properties were measured.
The average particle size of the pulverized roasted product was measured with a laser diffraction particle size analyzer (Mastersizer 3000, manufactured by Malvern), and the 50% particle size on a volume basis was taken as the average particle size.

[Example 2]
A molding resin material was produced in the same manner as in Example 1, except that the blending ratio of the pulverized roasted product and the polyamide resin was 51:49.

[Example 3]
Hardwood charcoal (National Carbon Technology) was pulverized with a turbo mill (Freund Turbo Co., Ltd.) to an average particle size of 7.5 μm.
A molding resin material was produced in the same manner as in Example 1, except that the compounding ratio of the pulverized carbide and the polyamide resin was 25:75.
The average particle size of the pulverized carbide was measured with a laser diffraction particle size analyzer (Mastersizer 3000, manufactured by Malvern), and the 50% particle size on a volume basis was defined as the average particle size.

[Comparative Example 1]
A molding resin material was produced in the same manner as in Example 1 using only the polyamide-based resin without adding the pulverized roasted product or the pulverized carbonized product.

The resin materials for molding produced in Examples 1 to 3 and Comparative Example 1 were subjected to tensile tests by the following method, and the results are shown in Table 1.
[Tensile test]:
A JIS K 6251 dumbbell was prepared using DSM Xplore Compounder 15 (manufactured by Leo Labo Co., Ltd.) and measured at a tensile speed of 1 mm/min according to JIS K 7161: Plastics - Tensile property test method.

As shown in Table 1, the molding resin materials of Examples 1 to 3 exhibited the same elastic modulus and maximum stress as the molding resin material of Comparative Example 1. In particular, Example 2, in which the blending ratio of the pulverized roasted product was 51% by mass, exhibited a high elastic modulus.

Claims (3)

A molding resin material containing 10 to 90% by mass of roasted woody biomass or pulverized woody biomass carbonized material having an average particle size of 100 μm or less, and further containing a polyamide resin. 2. The molding resin material according to claim 1, wherein the thermoplastic elastomer includes any one of a styrene/butadiene block copolymer, an ethylene/octene copolymer, and a propylene/ethylene copolymer. 3. The molding resin material according to claim 1, further comprising a biodegradable resin.