JPWO2016104634A1 - Thermoplastic resin composition and molded article thereof - Google Patents

Abstract

(A) A thermoplastic resin composition containing 99 to 50% by mass of a thermoplastic resin and (B) 50 to 1% by mass of lignin acetate, and a molded product thereof.

Description

  The present invention relates to a thermoplastic resin composition useful in electrical and electronic products, information communication equipment, OA equipment, machines, automobiles, industrial materials, building materials, and the like, and more particularly to a molded article thereof. The present invention relates to a thermoplastic resin composition suitably used as a material and a molded product thereof.

Plastics such as polyolefins must be flame retardant when used in electrical products, office automation equipment, and electrical and electronic products. Generally, there are many petroleum-derived compounds such as bromo flame retardants and phosphorus flame retardants. It is necessary to mix. Furthermore, with the recent increase in environmental awareness, materials with excellent durability and raw materials derived from biomass have been desired.
However, raw materials derived from biomass often use raw materials that compete with food, such as starch and sugar, as has become particularly prominent in the production of bioethanol, which leads to an increase in food prices and a decrease in food production. The problem was pointed out.
In view of this, a technology that is currently attracting a great deal of attention is a technology for producing raw materials from cellulosic biomass that does not compete with food.
Patent Document 1 discloses a technique of blending a thermoplastic resin with a lignin compound that is a raw material from cellulosic biomass. However, lignin is widely used and there is no description of flame retardancy by blending lignin. In addition, general lignin does not melt by heat, and when blended with a resin, it exists as an aggregate, which may reduce the mechanical properties and the appearance of the molded body. Patent Document 1 describes lignin acetate, but it is one of various general lignin compounds listed. In the examples, lignin acetate is not used, and effective acetic acid is used. Lignin is not specified.

Patent Document 2 discloses a lignin-containing resin composition comprising (a) 35 to 65% by weight of lignin and (b) 65 to 35% by weight of a thermoplastic resin, wherein wood chips are mixed with acetic acid and hydrochloric acid. It is described that "acetic acid digestion lignin" obtained by high-temperature steaming can be used. However, examples using kraft lignin and lignin sulfonic acid are described, but examples using lignin acetate soluble in ethyl acetate are not described.
Patent Document 3 describes a “lignin derivative having a reactive functional group introduced into a lignin derivative by chemical modification”, but does not describe lignin acetate. A resin composition blended with a thermoplastic resin is not described.
Patent Document 4 discloses a technique for improving the fluidity and flame retardancy of a resin by using a specific lignin. However, although this specific lignin also improves the dispersibility in the resin, the heat melting property may be insufficient, and the dispersibility in a resin having a low affinity with lignin such as polyolefin is poor. Since the dispersibility is poor, there is a risk of poor appearance or reduced tensile properties.

Japanese Patent Laid-Open No. 11-152410 JP 2001-261965 A JP 2010-163497 A JP 2014-15579 A

  An object of the present invention is to provide a thermoplastic resin composition having a reduced impact on the environment, high flame retardancy, excellent appearance, heat aging resistance, and weather resistance of the molded body, and a molded body thereof. .

As a result of intensive studies, the present inventors have found that the above-mentioned problems can be solved by using a thermoplastic resin composition containing a specific amount of a thermoplastic resin and a specific lignin and a molded product thereof. Reached.
That is, the present invention includes the following:
<1> a thermoplastic resin composition comprising (A) 99 to 50% by mass of a thermoplastic resin and (B) 50 to 1% by mass of lignin acetate;
<2> The thermoplastic resin composition according to the above <1>, wherein the (B) acetic acid lignin is an acetic acid lignin having heat melting property,
<3> The above (1) or <2>, wherein the (A) thermoplastic resin is at least one selected from the group consisting of an olefin resin, a polystyrene resin, a polyester resin, a polyamide resin, and a polycarbonate resin. A thermoplastic resin composition,
<4> The thermoplastic resin composition according to any one of the above <1> to <3>, comprising (A) 95 to 70% by mass of the thermoplastic resin and (B) 30 to 5% by mass of lignin acetate. And <5> a molded article of the thermoplastic resin composition according to any one of <1> to <4> above.

  Lignin acetate has extremely good dispersibility with respect to thermoplastic resins and has a high effect of improving flame retardancy. Therefore, the thermoplastic resin composition of the present invention is excellent in molding appearance, heat aging resistance, and weather resistance, and can be used for products that require good appearance such as a housing or outdoors. Further, since the dispersibility is good, it can be applied to a thin film. And since lignin which is derived from biomass and is a non-edible material is used, the thermoplastic resin composition of the present invention is a material having high environmental characteristics such as reduction of environmental load substances without competing with food.

Hereinafter, the present invention will be described in detail.
The thermoplastic resin composition of the present invention contains (A) 99 to 50% by mass of a thermoplastic resin and (B) 50 to 1% by mass of lignin acetate.
In the present specification, “(A) thermoplastic resin” is sometimes referred to as “component (A)”, and “(B) acetic acid lignin” is sometimes referred to as “component (B)”. Moreover, the prescription | regulation made preferable in this specification can be employ | adopted arbitrarily, and the combination of preferable things is more preferable.

<Component (A): Thermoplastic resin>
The thermoplastic resin is preferably at least one selected from the group consisting of an olefin resin, a polystyrene resin, a polyester resin, a polyamide resin, and a polycarbonate resin.

(1) Polyolefin resin Examples of the polyolefin resin mainly include the following.

(1-1) Polypropylene resin It can be composed of one or more selected from a propylene homopolymer, a copolymer containing propylene as a main component, and the like.

  Although there is no restriction | limiting in particular as a homopolymer of propylene, From a viewpoint of making it lightweight and excellent in a moldability, the melt mass flow rate (MFR) in 230 degreeC (2.16 kg) is 0.1-200 g / 10min. Propylene homopolymer is preferred. Furthermore, from the viewpoint of the rigidity and impact resistance of the resin composition, the melt mass flow rate at 230 ° C. (2.16 kg) is more preferably 0.2 to 60 g / 10 min.

The copolymer containing propylene as a main component is not particularly limited. For example, a copolymer of propylene and ethylene, or a random copolymer of one or more α-olefins other than propylene and propylene is used. And a block copolymer of propylene and one or more α-olefins other than propylene. Among the copolymers having propylene as a main component, the melt mass flow rate at 230 ° C. (2.16 kg) is 0.1 to 200 g / 10 min from the viewpoint of obtaining a light weight and excellent resin composition. Certain propylene copolymers are preferred. Furthermore, from the viewpoint of the rigidity and impact resistance of the resin composition, the melt mass flow rate at 230 ° C. (2.16 kg) is more preferably 0.2 to 60 g / 10 min.
Examples of α-olefins other than propylene include 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene and 1-hexadecene. , 1-octadecene, 1-eicosene and the like.

(1-2) Polyethylene resin It can be comprised by 1 type, or 2 or more types chosen from the homopolymer of ethylene, the copolymer which has ethylene as a main component, etc.

Examples of the ethylene homopolymer include low-density polyethylene, linear low-density polyethylene, and high-density polyethylene. From the viewpoint of light weight and excellent moldability, the density is 0.910 to 0.965 g / An ethylene homopolymer having a melt mass flow rate of 0.01 to 200 g / 10 min at cm ³ and 190 ° C. (2.16 kg) is preferred. If the melt mass flow rate at 190 ° C. (2.16 kg) is within the range, there is no possibility of causing problems in the fluidity of the resin composition and the surface appearance of the molded body, and it is 0.01 to 60 g / 10 minutes. Is more preferable.

Examples of the copolymer containing ethylene as a main component include a random copolymer of ethylene and an α-olefin other than ethylene, and a block copolymer of ethylene and an α-olefin other than ethylene. Among the copolymers having ethylene as a main component, from the viewpoint of obtaining a resin composition that is light and excellent in moldability, the melt mass flow rate at 190 ° C. (2.16 kg) is 0.01 to 200 g / 10 min. Certain ethylene copolymers are preferred. Moreover, if the melt mass flow rate at 190 ° C. (2.16 kg) is within the range, there is no possibility of causing problems in the fluidity of the resin composition and the surface appearance of the molded article, and 0.01 to 60 g / 10 min. More preferably.
Examples of α-olefins other than ethylene include propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1 -Hexadecene, 1-octadecene, 1-eicocene, etc. are mentioned.

  Examples of commercially available polyolefin resins include the series of polypropylene resins “Prime Polypro”, “Polyfine”, and “Prime TPO” manufactured by Prime Polymer Co., Ltd. (for example, product numbers: J-700GP, J-966HP), Prime Polyethylene resins “Hi-Zex”, “Neo-Zex”, “Ult-Zex”, “Moretec”, “Evolue” series (for example, high-density polyethylene resin, product number: 2200J) manufactured by Polymer Co., Ltd., and Tosoh Corporation Low-density polyethylene “Petrocene” series (for example, product number: Petrocene 190) and the like are available.

(2) Polystyrene resin Polystyrene resin is, for example, polystyrene, poly (p-methylstyrene), poly (m-methylstyrene), poly (p-tert-butylstyrene), poly (p-chlorostyrene), poly (polystyrene). (M-chlorostyrene), poly (p-fluorostyrene), hydrogenated polystyrene, and copolymers containing these structural units. These polystyrene resins may be used alone or in combination of two or more.
Examples of commercially available polystyrene resins include PS Japan Co., Ltd., “PSJ-polystyrene” series (for example, product number: H8672), Toyo Styrene Co., Ltd., “Toyostyrene” series, and the like.

(3) Polyester resin Polyol-polycarboxylic acid type polyester resin includes, for example, polyethylene terephthalate resin, polybutylene terephthalate resin, copolymer of terephthalic acid and 1,3-propanediol or 1,4-butanediol, polylactic acid Examples thereof include a resin and / or a copolymer resin containing polylactic acid. These polyester resins may be used alone or in combination of two or more.
A polylactic acid resin and / or a copolymer resin containing polylactic acid is obtained by subjecting lactic acid or lactic acid and other hydroxycarboxylic acid to heat dehydration polymerization to obtain low molecular weight polylactic acid or a copolymer thereof, which is further subjected to reduced pressure. Lactide, which is a cyclic dimer of lactic acid or a copolymer thereof, is obtained by thermal decomposition, and then lactide is polymerized in the presence of a catalyst such as a metal salt to copolymerize polylactic acid resin and / or polylactic acid. A resin is obtained.
Examples of commercially available polyol-polycarboxylic acid type polyester resins include “Mitsui PET ^™ ” series (for example, product number: Mitsui J125) manufactured by Mitsui Chemicals, Toyobo Co., Ltd., “Byron” series, and the like.
Examples of commercially available polylactic acid resins and / or copolymer resins containing polylactic acid include crystalline polylactic acid resin ("REVODE") manufactured by Zhejiang Hisun Biomaterials Co., Ltd. Series, L body / D body ratio = 100/0 to 85/5, for example, product number: Levoda 101) and “Lacea” which is a polylactic acid resin (manufactured by lactic acid fermentation of plant starch) manufactured by Mitsui Chemicals, Inc. Series etc. are mentioned.

(4) Polyamide resin Examples of the polyamide resin include a ring-opening polymer of lactam, a polycondensate of diamine and dibasic acid, and a polycondensate of ω-amino acid. These polyamide resins may be used alone or in combination of two or more.
Commercially available polyamide resins include nylon 6 and nylon 66 “Amilan” series (for example, product number: CM1017) manufactured by Toray Industries, Inc., “Leona” series polyamide 66 resin manufactured by Asahi Kasei Corporation, and Teijin ( "N-Nylon", "n, m-Nylon" series, and the like.

(5) Polycarbonate resin The polycarbonate resin as the component (A) may be an aromatic polycarbonate resin or an aliphatic polycarbonate resin, but from the viewpoint of affinity with the component (B), impact resistance and heat resistance. From the viewpoint of properties, it is more preferable to use an aromatic polycarbonate resin.
As the aromatic polycarbonate resin, an aromatic polycarbonate resin usually produced by a reaction between a dihydric phenol and a carbonate precursor can be used. The aromatic polycarbonate resin can be a main component of the resin composition because it has better heat resistance, flame retardancy, and impact resistance than other thermoplastic resins.
Further, when an aromatic polycarbonate-polyorganosiloxane copolymer or a resin containing an aromatic polycarbonate-polyorganosiloxane copolymer is used as the aromatic polycarbonate resin, flame retardancy and impact resistance at low temperatures are further improved. Can be improved. The polyorganosiloxane constituting the copolymer is more preferably polydimethylsiloxane from the viewpoint of flame retardancy.
Examples of commercially available aromatic polycarbonate resins include “Taflon” series manufactured by Idemitsu Kosan Co., Ltd. and “Panlite” series manufactured by Teijin Limited.

The thermoplastic resin of the component (A) may be used by appropriately mixing compatible ones. For example, if an appropriate amount of a polyester resin is mixed with an aromatic polycarbonate resin generally considered to have poor fluidity, the fluidity is improved.
In addition to the thermoplastic resins described in the above (1) to (5), other thermoplastic resins compatible with them, such as AS resin and (meth) acrylic acid ester (co) polymer, etc. An appropriate amount may be mixed.

<Component (B): Lignin acetate>
“Lignin acetate” refers to lignin in which a group derived from acetic acid is introduced (acetylated) into a part of the lignin skeleton.
Specifically, the method for producing lignin acetate is, for example, by digesting plant materials (for example, conifers, broadleaf trees, gramineous plants, etc.) that are raw materials of lignin using acetic acid, so that lignin acetate is obtained as pulp waste liquid. Can be obtained.

As a cooking method using acetic acid, for example, a plant material as a raw material for lignin is mixed with acetic acid and an inorganic acid (for example, hydrochloric acid, sulfuric acid, etc.) and reacted.
Acetic acid (100% conversion) is, for example, 500 parts by mass or more, preferably 900 parts by mass or more, for example, 30,000, with respect to 100 parts by mass of the plant material that is the raw material for lignin. It is 1 part by mass or less, preferably 15,000 parts by mass or less.
The blending ratio of the inorganic acid is, for example, 0.01 parts by mass or more, preferably 0.05 parts by mass or more with respect to 100 parts by mass of the plant material that is the raw material for lignin. For example, it is 10 parts by mass or less, preferably 5 parts by mass or less.
Moreover, as reaction conditions, reaction temperature is 30 degreeC or more, for example, Preferably, it is 50 degreeC or more, for example, 400 degrees C or less, Preferably, it is 250 degrees C or less. The reaction time is, for example, 0.5 hours or more, preferably 1 hour or more, for example, 20 hours or less, preferably 10 hours or less.

By such cooking, pulp is obtained and lignin acetate is obtained as a pulp waste liquid.
Next, in this method, the pulp is separated by a known separation method such as filtration, and the filtrate (pulp waste liquid) is collected, and the pulp waste liquid is concentrated by a known method using, for example, a rotary evaporator, vacuum distillation or the like. Thereafter, a large excess of ethyl acetate is added and stirred, and then the supernatant is collected. Solid acetate lignin [1] can be obtained from the obtained supernatant by removing (evaporating) ethyl acetate by a known method using, for example, a rotary evaporator, vacuum distillation or the like. The obtained lignin acetate [1] has heat melting properties. The term “thermal meltability” in the present invention refers to the property of softening and melting when heated to 100 ° C. or higher.
Further, a large excess of water is added to the remaining supernatant, and the mixture is stirred while being heated to about 90 ° C. After stirring, the mixture is allowed to stand and filtered to recover lignin acetate [2] as a solid content. The obtained lignin acetate [2] does not show hot meltability.

When the thermoplastic resin composition of the present invention comprises the thermoplastic resin of component (A) and the lignin acetate of component (B), the total amount of component (A) and component (B) is 100% by mass, The component (A) is contained in a proportion of 99 to 50% by mass and the component (B) in a proportion of 50 to 1% by mass.
The ratio of the component (A) to the component (B) is preferably 95 to 50% by mass of the component (A), 5 to 50% by mass of the component (B), and more preferably the component (A). 95-70 mass% and a component (B) are 5-30 mass%.
When the component (A) is less than 50% by mass, the weather resistance and heat aging resistance are not maintained in an appropriate state, and a good appearance cannot be obtained in the molded article. Moreover, if a component (B) is less than 1 mass%, the effect acquired by mix | blending a component (B) is not enough.
The total content of component (A) and component (B) in the thermoplastic resin composition of the present invention is preferably 95% by mass or more, more preferably 98% by mass or more, and still more preferably substantially 100% by mass. is there.

[Various additives]
If necessary, the thermoplastic resin composition of the present invention can contain various additives together with the component (A) and the component (B). Examples of such additives include ultraviolet absorbers, antioxidants, lubricants, crystal nucleating agents, softeners, antistatic agents, metal deactivators, antibacterial and antifungal agents, and pigments.
Examples of the ultraviolet absorber include benzophenone compounds, benzotriazole compounds, benzoate compounds, polyamide polyether block copolymers (providing permanent antistatic performance), and the like.
Although it does not specifically limit as antioxidant, A phenolic antioxidant, phosphorus antioxidant, thioether type antioxidant, etc. are mentioned. You may use these in combination of 1 or more type.
The lubricant is not particularly limited, and examples thereof include fatty acid amide lubricants, fatty acid ester lubricants, fatty acid lubricants, and fatty acid metal salt lubricants. You may use these in combination of 1 or more type.
The crystal nucleating agent is not particularly limited, and examples thereof include sorbitols, phosphorus nucleating agents, rosins, and petroleum resins.
The softening agent is not particularly limited, and examples thereof include liquid paraffin, mineral oil softener (process oil), and non-aromatic rubber mineral oil softener (process oil). These may be used individually by 1 type and may be used in combination of 2 or more type.

The antistatic agent is not particularly limited, and examples thereof include cationic antistatic agents, anionic antistatic agents, nonionic antistatic agents, amphoteric antistatic agents, and fatty acid partial esters such as glycerin fatty acid monoesters.
Although it does not specifically limit as a metal deactivator, A hydrazine type metal deactivator, a nitrogen compound type metal deactivator, a phosphite ester type metal deactivator, etc. are mentioned. You may use these in combination of 1 or more type.
Although it does not specifically limit as an antibacterial antifungal agent, An organic compound type antibacterial antifungal agent, a natural product organic antibacterial antifungal agent, an inorganic type antibacterial antifungal agent, etc. are mentioned.
Although it does not specifically limit as a pigment, An inorganic pigment, an organic pigment, etc. are mentioned. Examples of inorganic pigments include titanium oxide, calcium carbonate, and carbon black. Examples of organic pigments include azo pigments, acidic dye lakes, basic dye lakes, and condensed polycyclic pigments. These pigments may be used alone or in combination of two or more.
The compounding amount of the additive component is not particularly limited as long as the properties of the thermoplastic resin composition of the present invention are not impaired.

[Kneading and molding]
The thermoplastic resin composition of the present invention can be obtained by blending and kneading the components (A) and (B) in the above proportions and various additives added as necessary. At this time, the mixing and kneading are premixed by a commonly used equipment such as a ribbon blender, a drum tumbler, etc., and then a Henschel mixer, a Banbury mixer, a single screw extruder, a twin screw extruder, a multi screw extruder. This method can be performed by a method using a machine and a conider.
The heating temperature at the time of kneading is appropriately selected in the range of usually 160 to 350 ° C. depending on the kind of the thermoplastic resin. When a polyolefin resin is used as the thermoplastic resin, the temperature is in the range of 160 to 250 ° C. In the case of using a polyester resin, it is selected in the range of 170 to 280 ° C.
Moreover, when using a polyamide resin, it selects in the range of 240-290 degreeC, when using a polycarbonate resin, it is selected in the range of 270-350 degreeC, and when using a polylactic acid resin, it is selected in the range of 190-250 degreeC.

  The thermoplastic resin composition of the present invention is made from the pellets obtained by the above-mentioned melt-kneading and pelletizing as an injection molding method, injection compression molding method, extrusion molding method, blow molding method, press molding method, vacuum molding method. Various molded bodies can be produced by a foam molding method or the like. In particular, a pellet-shaped forming raw material is manufactured by the melt kneading method, and then the pellet is used suitably for manufacturing an injection-molded body by injection molding or injection compression molding and for manufacturing an extrusion-molded body by extrusion molding. be able to. Moreover, after forming into an extrusion sheet by extrusion molding, it is good also as a molded object by pressurizing and thermoforming.

  EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example, this invention is not restrict | limited at all by these Examples.

〔Measurement item〕
(1) Oxygen index The oxygen index (LOI, unit%) was measured in accordance with ASTM D2863.
(2) Weather resistance In the weather resistance test (black panel temperature 83 ° C, 300 hours), UV light was continuously irradiated for 300 hours using a sunshine weatherometer, and a cycle of rainfall (0.5 hours) between irradiations. Was repeated. About the test piece before and behind a test, the retention rate (%) of the elongation in the tensile test measured based on JISK7161 or JISK7113 was displayed on Tables 1-9 as a weather resistance parameter | index.
(3) Heat aging resistance In the heat aging resistance test (temperature 100 ° C.), the test piece was left in a constant temperature room for 100 hours, and the test piece before and after the test was subjected to a tensile test measured according to JIS K7161 or JIS K7113. The elongation retention (%) is shown in Tables 1 to 9 as an index of heat aging resistance.
(4) Molded body appearance The appearance of the test piece immediately after obtained by injection molding is visually observed as “A” (can be used) in which neither nudity nor silver is observed. In Tables 1 to 9, "B" (which can be used but performance is poor) was observed, and "C" (unusable) was observed for both.

[Example 1]
Each component was mix | blended in the ratio (mass part) shown in Table 1, and it supplied to the extruder (the Tanabe Plastic Machinery Co., Ltd. make, model name: VS40), and melt-kneaded at 210 degreeC and pelletized.
The obtained pellets were injection-molded under conditions of a cylinder temperature of 210 ° C. and a mold temperature of 50 ° C. using an injection molding machine (manufactured by Toshiba Machine Co., Ltd., model: IS100N) to obtain a molded body (test piece). The obtained molded body (length 127 mm × width 12.7 mm × thickness 3 mm) was measured for the following characteristics, and the results are shown in Table 1.

[Examples 2 to 14]
Each component was blended in the proportions (parts by mass) shown in Tables 1 to 9, and the melt kneading temperature, cylinder temperature, and mold temperature were changed as shown in Tables 1 to 9 in the same manner as in Example 1. The above properties were measured using the test pieces obtained by pelletization, and the results are shown in Tables 1-9.

[Comparative Examples 1 to 11]
As shown in Tables 1 to 9, in Comparative Examples 1 and 4 to 11, the component (A) is used alone, and in Comparative Examples 2 and 3, the component (A) and a large amount of the component (B) or the comparative component (C ) And pelletizing in the same manner as in Example 1 except that the melt kneading temperature, cylinder temperature, and mold temperature were changed as shown in Tables 1 to 9, and the above properties were obtained using the obtained test piece. The results are shown in Tables 1-9.

The materials used in each example are as follows.
(1) Component (A)
* Polypropylene 1
Made by Prime Polymer Co., Ltd., product number: J-700GP [Density = 0.905 g / cm ³ , MFR = 6.8 g / 10 min (230 ° C., 2.16 kg)]
* Polypropylene 2
Made by Prime Polymer Co., Ltd., product number: J-966HP [Density = 0.90 g / cm ³ , MFR = 23 g / 10 min (230 ° C., 2.16 kg)]
* High-density polyethylene, manufactured by Prime Polymer Co., Ltd., product number: 2200J [density = 0.95 g / cm ³ , MFR = 12 g / 10 min (190 ° C., 2.16 kg)]
* Low density polyethylene, manufactured by Tosoh Corporation, product number: Petrocene 190 [density = 0.92 g / cm ³ , MFR = 8 g / 10 min (190 ° C., 2.16 kg)]
* Aromatic polycarbonate Idemitsu Kosan Co., Ltd., product number: FN1900A (viscosity average molecular weight = 19,000, refractive index = 1.585)
* Polystyrene resin PS Japan Co., Ltd., product number: H8672 [MFR = 12 g / 10 min (220 ° C., 2.16 kg)]
* Polyester resin, manufactured by Mitsui Chemicals, product number: Mitsui J125 (polyethylene terephthalate)
* Polylactic acid resin Crystalline polylactic acid resin manufactured by Zhejiang Haisheng Biological Materials Co., Ltd. [Part No .: Levoda 101, L / D ratio = 98% or more]
* Polyamide Toray Co., Ltd. product number: CM1017 (polyamide 6)

(2) Component (B)
* Lignin acetate with heat melting * Lignin acetate without heat melting Corn stover is mixed with 950 g acetic acid (100% conversion) and 3 g sulfuric acid, reacted at 118 ° C. (under reflux) for 4 hours and digested to pulp. A reaction solution containing was obtained. The obtained reaction liquid was filtered to separate the pulp, the filtrate (pulp waste liquid) was collected, and the pulp waste liquid was concentrated using a rotary evaporator. Subsequently, 10 parts by mass of ethyl acetate was added to 1 part by mass of the pulp waste liquid and stirred, and then the supernatant was collected.
From the obtained supernatant, ethyl acetate was removed (distilled off) using a rotary evaporator to obtain 7.6 g of solid lignin acetate [1]. When the obtained lignin acetate [1] was heated at 150 ° C., it softened and melted. Therefore, lignin acetate [1] has a heat melting property.
On the other hand, 10 parts by mass of water was added to 1 part by mass of the remaining liquid from which the supernatant was collected, and the mixture was stirred while being heated to 95 ° C. After stirring, the mixture was left standing and filtered to obtain 8.1 g of lignin acetate [2] as a solid content. When the obtained lignin acetate [2] was heated at 200 ° C. or higher, it did not melt, and when 230 ° C. was exceeded, pyrolysis was started while producing smoke. Therefore, lignin acetate [2] does not exhibit hot meltability.

(3) Comparative component (C)
* Craft lignin Wako Pure Chemical Industries, Ltd.

The following can be understood from the results of Tables 1-9.
That is, as in the Examples, by blending an appropriate amount of “lignin acetate” into various thermoplastic resins, LOI increases and flame retardancy improves. Furthermore, weather resistance (tensile elongation retention rate) and heat aging resistance (tensile elongation retention rate) are superior to those with no additives and dispersibility is good, so the appearance of the molded article is excellent. .
On the other hand, as in Comparative Example 2, even when “Lignin Acetate” is blended, if the amount exceeds 50%, no further effect is seen, which adversely affects the appearance of the molded body.
Further, as in Comparative Example 3, even when an appropriate amount of lignin other than “acetic acid lignin” is blended, the effect on weatherability and heat aging resistance is small or almost ineffective, and the appearance of the molded product Adversely affect.

  The thermoplastic resin composition or molded product of the present invention is useful in the fields of electrical and electronic products, information communication equipment, OA equipment, machinery, automobiles, industrial materials, building materials, etc., and to the environment such as carbon dioxide emission reduction and fossil raw material reduction. It is suitably used as a material with a reduced influence.

Claims (5)

  (A) A thermoplastic resin composition containing 99 to 50% by mass of a thermoplastic resin and (B) 50 to 1% by mass of lignin acetate.   The thermoplastic resin composition according to claim 1, wherein the (B) acetic acid lignin is an accumulating lignin acetate.   The thermoplastic resin composition according to claim 1 or 2, wherein the (A) thermoplastic resin is at least one selected from the group consisting of an olefin resin, a polystyrene resin, a polyester resin, a polyamide resin, and a polycarbonate resin. .   The thermoplastic resin composition according to any one of claims 1 to 3, comprising (A) 95 to 70% by mass of the thermoplastic resin and (B) 30 to 5% by mass of lignin acetate.   The molded object of the thermoplastic resin composition as described in any one of Claims 1-4.