JPH1143562A - Thermoplastic resin composition - Google Patents

Thermoplastic resin composition

Info

Publication number
JPH1143562A
JPH1143562A JP20452997A JP20452997A JPH1143562A JP H1143562 A JPH1143562 A JP H1143562A JP 20452997 A JP20452997 A JP 20452997A JP 20452997 A JP20452997 A JP 20452997A JP H1143562 A JPH1143562 A JP H1143562A
Authority
JP
Japan
Prior art keywords
polyethylene
weight
resin
intrinsic viscosity
molecular weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP20452997A
Other languages
Japanese (ja)
Inventor
Hidenori Kashiwa
英則 栢
Kunio Nishida
邦雄 西田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Chemicals Inc
Original Assignee
Mitsui Chemicals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsui Chemicals Inc filed Critical Mitsui Chemicals Inc
Priority to JP20452997A priority Critical patent/JPH1143562A/en
Publication of JPH1143562A publication Critical patent/JPH1143562A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the subject composition useful as e.g. a construction material with high mechanical strength by kneading a wood-based material with a polypropylene-based resin, a polyolefin resin modified with a polybasic acid anhydride, and the like. SOLUTION: This composition is obtained by including (A) 50-80 pts.wt. of a polypropylene-based resin 0.1-2 g/10 min in melt flow rate at 230 deg.C under a load of 2.16 kg, (B) a polyethylene-based resin 3.5-15 dL/g in intrinsic viscosity composed of an ultra-high-molecular polyethylene 10-40 dL/g in intrinsic viscosity determined in decalin solvent at 135 deg.C and 15-40 wt.% based on the ultra-high- molecular polyethylene, of a low- to high-molecular polyethylene, (D) 0.1-10 pts.wt. of a polyolefin-based resin modified with 0.1-20 wt.% of a polybasic acid anhydride, and (C) such an amount, based on a total of 100 pts.wt. of the components A and B, of a lignocelluslose-based material so as to be (90:10) to (30:70) in the weight ratio (A+B)/C.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、押し出し成形等の成形
加工において、任意の形状に容易に加工することがで
き、成型品として良好な機械強度を有する熱可塑性樹脂
組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermoplastic resin composition which can be easily formed into an arbitrary shape in molding such as extrusion molding and has good mechanical strength as a molded product.

【0002】[0002]

【従来の技術】ポリプロピレンに木質系材料を充填剤と
して使用する技術は特公昭59ー30176に開示され
ており、流動性の低下等で成形加工性に問題点があるこ
とが指摘されている。
2. Description of the Related Art The technique of using a wood-based material as a filler in polypropylene is disclosed in JP-B-59-30176, and it has been pointed out that there is a problem in moldability due to a decrease in fluidity and the like.

【0003】[0003]

【発明が解決しようとする課題】本発明は、熱可塑性樹
脂であるポリプロピレン系樹脂と木質系材料の木粉を混
練するに当たって、多塩基酸無水物変性で変性したポリ
プロピレン系樹脂およびポリエチレン系樹脂を添加する
ことで押し出し成形性が良好で、表面平滑性に優れ、エ
ッジのササクレの少ない成形加工ができ、かつ成形品と
しての良好な機械強度を有する熱可塑性樹脂組成物を提
供する。
DISCLOSURE OF THE INVENTION The present invention relates to a method of kneading a polypropylene resin which is a thermoplastic resin and wood powder of a woody material, by mixing a polypropylene resin and a polyethylene resin modified with a polybasic anhydride. Addition thereof provides a thermoplastic resin composition having good extrusion moldability, excellent surface smoothness, capable of forming with little edge swelling, and having good mechanical strength as a molded product.

【0004】[0004]

【課題を解決するための手段】本発明者等は、上記課題
を解決するために鋭意検討した結果、下記の組成物が樹
脂と木粉の界面接合性の改善された組成物を経済性を損
なわずに調整しうることを見いだし、本発明に到達し
た。すなわち、本発明は以下の化合物を提供する。 (A)230℃、2.16kg荷重におけるメルトフロ
ーレート(MFR;ASTM D1238−65T)が
0.1〜2g/10分であるポリプロピレン系樹脂50
〜80重量部、(B)135℃、デカリン溶媒中で測定
した極限粘度が10〜40dl/gである超高分子量ポ
リエチレン及び当該超高分子量ポリエチレンに対し、1
5〜40重量%の0.1〜5.0dl/gの低分子量な
いし高分子量ポリエチレンから実質的になる極限粘度
3.5〜15dl/gのポリエチレン系樹脂 (D)多塩基酸無水物変性量が0.1〜20wt%であ
る変性ポリオレフィン系樹脂0.1〜10重量部及び
(A)+(B)100重量部に対し、(C)リグノセル
ロース系およびセルロース系物質を、((A)+
(B))/(C)が90/10〜30/70の重量比で
添加することを特徴とする熱可塑性樹脂組成物。本発明
に用いられるポリプロピレン系樹脂(A)は、230
℃、2.16kg荷重におけるメルトフローレート(M
FR;ASTMD 1238−65T)が0.01〜2
g/10分、好ましくは0.05〜1g/10分である
ポリプロピレンおよび、プロピレンと20モル%以下の
エチレン及び/又はC3〜C20のαオレフィン共重合
体を意味する。好ましくはC3〜C8である。また、本
発明に用いるポリエチレン系樹脂(B)は、135℃、
デカリン溶媒中で測定した極限粘度が10〜40dl/
gである超高分子量ポリエチレン及び当該超高分子量ポ
リエチレンに対し、15〜40重量%の0.1〜5.0
dl/gの低分子量ないし高分子量ポリエチレンから実
質的になる極限粘度3.5〜15dl/gのポリエチレ
ン系樹脂であり、ポリエチレン及びエチレンと10モル
%以下のC3〜C20のαオレフィンとの共重合体を意
味する。好ましくはC3〜C8である。リグノセルロー
スおよびセルロース系物質(木質系材料)は木粉、木質
パルプ等であり原木や樹種はとくに制限はない。尿素等
での木酸の中和処理を行うことも可能である。リグノセ
ルロース系およびセルロース系物質(C)は、((A)
+(B))/(C)が90/10〜30/70の重量比
で添加することを特徴とする。多塩基酸変性オレフィン
系樹脂としては無水マレイン酸、マレイン酸ジメチル、
マレイン酸ジエチル、アクリル酸、メタクリル酸、テト
ラヒドロフタル酸、グリシジルメタクリレート、ヒドロ
キシメタクリレート等で変性されたポリプロピレン系樹
脂、ポリエチレン系樹脂、ポリブテン系樹脂、ポリー4
ーメチルペンテン系樹脂等が上げられる。多塩基酸無水
物の変性量としては、0.1〜20wt%であり、添加
量は1〜10重量部である。変性量、添加量は多い方が
好ましいが、経済性を考慮して効果とのかね合いで変性
ポリオレフィンの添加量を決める。混練方法は特に限定
されないが、ブレンダー、ニーダー、ミキシングロー
ル、バンバリーミキサー、1軸あるいは2軸の造粒機等
が挙げられる。例えば、2軸押し出し機で混練ゾーンの
設定温度を150℃〜200℃、好ましくは160℃〜
200℃、として混練組成物を得る方法が挙げられる。
温度が210℃以上では、木質材料の分解によるガスが
発生するため造粒温度を下げる必要がある。本発明にお
いては、無機系の充填剤、例えばタルク、炭酸カルシウ
ム等、あるいは有機系の充填剤、例えばポリエステル、
ポリアミド繊維等、そのほかに難燃剤、安定剤、紫外線
吸収剤、酸化防止剤、可塑剤、等の各種添加剤や顔染料
等の着色剤を添加することができる。また、橋かけ剤と
過酸化物の併用によりMT向上の方策も可能である。
Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, the following composition has been found to provide a composition having an improved interface bonding property between resin and wood flour. They have found that they can be adjusted without loss and arrived at the present invention. That is, the present invention provides the following compounds. (A) A polypropylene resin 50 having a melt flow rate (MFR; ASTM D1238-65T) of 0.1 to 2 g / 10 minutes at 230 ° C. and a load of 2.16 kg.
To 80 parts by weight, (B) an ultrahigh molecular weight polyethylene having an intrinsic viscosity of 10 to 40 dl / g measured in a decalin solvent at 135 ° C. and 1 to the ultrahigh molecular weight polyethylene
A polyethylene resin having an intrinsic viscosity of 3.5 to 15 dl / g substantially consisting of 5 to 40% by weight of 0.1 to 5.0 dl / g of low to high molecular weight polyethylene (D) polybasic anhydride modification amount Is 0.1 to 20% by weight, and 0.1 to 10 parts by weight of the modified polyolefin resin and 100 parts by weight of (A) + (B), the lignocellulosic and cellulosic substances are added to ((A) +
(B)) / (C) is added in a weight ratio of 90/10 to 30/70. The polypropylene resin (A) used in the present invention has 230
° C, melt flow rate at 2.16 kg load (M
FR; ASTM D1238-65T) 0.01 to 2
g / 10 minutes, preferably 0.05 to 1 g / 10 minutes, and polypropylene and 20 mol% or less of ethylene and / or a C3-C20 α-olefin copolymer. Preferably it is C3-C8. The polyethylene resin (B) used in the present invention has a temperature of 135 ° C.
The intrinsic viscosity measured in a decalin solvent is 10 to 40 dl /
g of ultrahigh molecular weight polyethylene and 15 to 40% by weight of 0.1 to 5.0% based on the ultrahigh molecular weight polyethylene.
A polyethylene resin having an intrinsic viscosity of 3.5 to 15 dl / g consisting essentially of low molecular weight to high molecular weight polyethylene of dl / g, and copolymerization of polyethylene and ethylene with 10 mol% or less of a C3-C20 α-olefin. Means coalescence. Preferably it is C3-C8. Lignocellulose and cellulosic substances (woody materials) are wood flour, woody pulp and the like, and the raw wood and tree species are not particularly limited. It is also possible to carry out a neutralization treatment of wood acid with urea or the like. Lignocellulosic and cellulosic substances (C) are ((A)
+ (B)) / (C) in a weight ratio of 90/10 to 30/70. Polybasic acid-modified olefin resins include maleic anhydride, dimethyl maleate,
Polypropylene resin, polyethylene resin, polybutene resin, poly-4 modified with diethyl maleate, acrylic acid, methacrylic acid, tetrahydrophthalic acid, glycidyl methacrylate, hydroxy methacrylate, etc.
-Methylpentene resin and the like. The modification amount of the polybasic acid anhydride is 0.1 to 20 wt%, and the addition amount is 1 to 10 parts by weight. It is preferable that the amount of modification and the amount of addition are large, but the amount of addition of the modified polyolefin is determined in consideration of the effect in consideration of economy. The method of kneading is not particularly limited, and examples thereof include a blender, a kneader, a mixing roll, a Banbury mixer, a single-shaft or twin-shaft granulator, and the like. For example, the set temperature of the kneading zone is set to 150 ° C. to 200 ° C., preferably 160 ° C.
A method of obtaining a kneaded composition at 200 ° C. can be mentioned.
When the temperature is 210 ° C. or higher, a gas is generated due to decomposition of the woody material, so that it is necessary to lower the granulation temperature. In the present invention, an inorganic filler such as talc, calcium carbonate or the like, or an organic filler such as polyester,
Various additives such as a flame retardant, a stabilizer, an ultraviolet absorber, an antioxidant, a plasticizer and the like, and a coloring agent such as a face dye can be added in addition to a polyamide fiber and the like. Also, a measure for improving MT can be achieved by using a crosslinking agent and a peroxide together.

【0005】[0005]

【発明の利用分野】本発明で用い得る成型品は、電気絶
縁材料、工業用部品材料、建築用材料等に多くの分野で
利用に好適である。特に、住宅部材、建築材料として
の、巾木、表面化粧板、ドア材、外壁材、洗面化粧台、
カウンター材、基礎受け板、窓枠、壁材、廻り縁木、手
すり、取っ手、構造材、土木角材、柱、床柱、飾り柱、
耐震材、壁紙建具天井材、下地材、畳、床、コンクリー
トパネル、足場材、遮蔽板、遮音板、家具の箱天井、
扉、前板裏板、棚板、袖板、幕板、甲板、背板、座板、
厨房部材、防水材、防かび材、防腐材、雨戸板、袖板、
腰板、側板、バスユニット、床パン、バス天井、バス
壁、バス、桶、衛陶機器、便座、便蓋、家電製品、ラジ
オテレビ受信機、キャビネット、ステレオキャビネッ
ト、アンプキャビネット、スピーカー、ピアノオルガン
の親板、大屋根、巻き屋根、上下巻物板、等に有用であ
る。さらに、本発明は木材工業における工業廃棄物とし
ての木質材や未利用の木質材等の有効利用が図れるとい
う利点を有しており工業的にきわめて有効である。
The molded articles which can be used in the present invention are suitable for use in many fields such as electric insulating materials, industrial parts materials and building materials. In particular, housing materials, building materials, skirting boards, surface decorative boards, door materials, outer wall materials, vanities,
Counter materials, foundation backing plates, window frames, wall materials, surrounding margins, handrails, handles, structural materials, civil engineering timber, pillars, floor pillars, decorative pillars,
Earthquake-resistant materials, wallpaper fitting ceiling materials, base materials, tatami mats, floors, concrete panels, scaffolding materials, shielding boards, sound insulation boards, furniture box ceilings,
Door, front board back board, shelf board, sleeve board, curtain board, deck, back board, seat board,
Kitchen parts, waterproofing materials, antifungal materials, preservatives, shutter boards, sleeve boards,
Hips, side plates, bath units, floor pans, bus ceilings, bath walls, baths, tubs, porcelain appliances, toilet seats, toilet lids, home appliances, radio TV receivers, cabinets, stereo cabinets, amplifier cabinets, speakers, piano organs Useful for parent boards, large roofs, rolled roofs, upper and lower scroll boards, etc. Further, the present invention has an advantage that wood materials and unused wood materials as industrial wastes in the wood industry can be effectively used, and is extremely industrially effective.

【0006】[0006]

【発明の実施の形態】次に本発明の実施例について説明
する。 《組成物の製造方法》 2軸押し出し機(日本製鋼所製 TEX30) バレル設定温度 160℃ スクリュー回転数 110rpmで樹脂温度が押し出し
機出口で180℃となるように設定した。 押し出し混練量:6kg/1時間 あらかじめ室温でヘンシェルミキサーを使って原料を均
一に混合してから造粒する。 《物性評価のためのプレスシート成形方法》 熱圧成形機を使用。 (株)神藤金属工業所製 70トンプレス成形機 加熱温度180℃ 予熱時間5分 プレス圧力 50kgf/cm2 加熱圧縮時間 5分 冷却時間 5分 50kgf/cm2 温度23℃ 成形品板厚 2mm 《物性評価のための測定方法》 MFR 190℃、2.16kg荷重 引張強度 ASTM D 638 曲げ強度 ASTM D 638 曲げ弾性率 ASTM D 638 アイゾット衝撃強度 ASTM D 256 成形性の評価 50mm押出機でL型の成形品を試作し、成形性と外観
を評価した。 成形温度190℃
Next, an embodiment of the present invention will be described. << Method of Manufacturing Composition >> Biaxial extruder (TEX30, manufactured by Nippon Steel Works Co., Ltd.) Barrel setting temperature: 160 ° C. At 110 rpm screw speed, the resin temperature was set to 180 ° C. at the extruder outlet. Extrusion kneading amount: 6 kg / 1 hour Raw materials are uniformly mixed in advance using a Henschel mixer at room temperature, and then granulated. << Press sheet molding method for evaluating physical properties >> A hot-press molding machine is used. 70-ton press molding machine manufactured by Shinto Metal Industry Co., Ltd. Heating temperature 180 ° C Preheating time 5 minutes Pressing pressure 50kgf / cm 2 Heating compression time 5 minutes Cooling time 5 minutes 50kgf / cm 2 Temperature 23 ° C Molded sheet thickness 2mm << Physical properties Measurement method for evaluation >> MFR 190 ° C., 2.16 kg load Tensile strength ASTM D 638 Flexural strength ASTM D 638 Flexural modulus ASTM D 638 Izod impact strength ASTM D 256 Evaluation of formability L-shaped molded product with 50 mm extruder Were prototyped, and the moldability and appearance were evaluated. Molding temperature 190 ° C

【0007】[0007]

【実施例1】ポリプロピレン(MFR 0.5g/10
分、ホモポリプロピレン、比重0.91)1.75k
g、135℃デカリン溶媒中の極限粘度が10dl/g
のポリエチレン(極限粘度1〜3dl/gのポリエチレ
ン系樹脂70重量%と極限粘度25〜35の超高分子量
ポリエチレン系樹脂30重量%からなる)0.75kg
と木粉2.5kg、変性ポリプロピレン(マレイン酸付
加量 3wt%)(135
Example 1 Polypropylene (MFR 0.5 g / 10
Min, homopolypropylene, specific gravity 0.91) 1.75k
g, intrinsic viscosity in decalin solvent at 135 ° C is 10 dl / g
0.75 kg of polyethylene (consisting of 70% by weight of a polyethylene resin having an intrinsic viscosity of 1 to 3 dl / g and 30% by weight of an ultrahigh molecular weight polyethylene resin having an intrinsic viscosity of 25 to 35)
And wood flour 2.5kg, modified polypropylene (maleic acid addition 3wt%) (135

【0008】℃、デカリン溶媒中℃, in decalin solvent

【η】=0.5dl/g)100gを室温でヘンシェル
ミキサーにより3分撹拌して配合した後、2軸押し出し
機PCM30(池貝工作所製)のバレル設定温度180
℃で6kg/1時間の押し出し量で混合組成物を得た。
このときのダイ出口の樹脂温度は190℃であった。上
記混合組成物をプレスシート成形方法で成形して、得ら
れた成形品の引張強度、曲げ強度、曲げ弾性率、衝撃強
度、を測定し結果を表1に示す。さらに、田辺製作所5
0mm押出機で成形温度190℃でL型成形品を成形
し。外観と成形性を評価した。
[Η] = 0.5 dl / g) 100 g of the mixture was stirred at room temperature with a Henschel mixer for 3 minutes and blended.
A mixed composition was obtained at an extrusion rate of 6 kg / hour at ℃.
The resin temperature at the die outlet at this time was 190 ° C. The above mixed composition was molded by a press sheet molding method, and the obtained molded article was measured for tensile strength, flexural strength, flexural modulus and impact strength, and the results are shown in Table 1. In addition, Tanabe Seisakusho 5
An L-shaped molded product was molded at a molding temperature of 190 ° C. using a 0 mm extruder. The appearance and moldability were evaluated.

【0009】[0009]

【実施例2】 (A)ポリプロピレン系樹脂1.25kg、(B)ポリ
エチレン系樹脂1.25kgとした以外は実施例1と同
様の操作を行った。結果を表1に示す。
Example 2 The same operation as in Example 1 was performed except that (A) 1.25 kg of a polypropylene resin and (B) 1.25 kg of a polyethylene resin. Table 1 shows the results.

【0010】[0010]

【実施例3】 (A)ポリプロピレン2.0kg、(B)ポリエチレン
系樹脂0.5kgとした以外は実施例1と同様の操作を
行った。結果を表1に示す。
Example 3 The same operation as in Example 1 was performed except that (A) 2.0 kg of polypropylene and (B) 0.5 kg of polyethylene resin. Table 1 shows the results.

【0011】[0011]

【比較例1】 (A)MFR(10g/10min)のポリプロピレン
および(B)MFR(5g/10min)のポリエチレ
ン系樹脂0.5kgとした以外は実施例1と同様の操作
を行った。その結果、押し出し成形における肌荒れやチ
ギレが顕著で満足な成形品は得られなかった。
Comparative Example 1 The same operation as in Example 1 was performed except that (A) polypropylene of MFR (10 g / 10 min) and (B) 0.5 kg of polyethylene resin of MFR (5 g / 10 min) were used. As a result, no satisfactory molded product was obtained in which the surface roughness and creaking in the extrusion molding were remarkable.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)230℃、2.16kg荷重におけ
るメルトフローレート(MFR;ASTM D1238
−65T)が0.1〜2g/10分であるポリプロピレ
ン系樹脂50〜80重量部、(B)135℃、デカリン
溶媒中で測定した極限粘度が10〜40dl/gである
超高分子量ポリエチレン及び当該超高分子量ポリエチレ
ンに対し、15〜40重量%の0.1〜5.0dl/g
の低分子量ないし高分子量ポリエチレンから実質的にな
る極限粘度3.5〜15dl/gのポリエチレン系樹脂 (D)多塩基酸無水物変性量が0.1〜20wt%であ
る変性ポリオレフィン系樹脂0.1〜10重量部及び
(A)+(B)100重量部に対し、(C)リグノセル
ロース系およびセルロース系物質を、((A)+
(B))/(C)が90/10〜30/70の重量比で
添加することを特徴とする熱可塑性樹脂組成物。
1. A melt flow rate (MFR; ASTM D1238) at 230 ° C. under a load of 2.16 kg.
(B) an ultrahigh molecular weight polyethylene having an intrinsic viscosity of 10 to 40 dl / g measured at 135 ° C. in a decalin solvent; 15 to 40% by weight of the ultra-high molecular weight polyethylene is 0.1 to 5.0 dl / g.
(D) a modified polyolefin resin having a polybasic anhydride modification amount of 0.1 to 20% by weight; a polyethylene resin having an intrinsic viscosity of 3.5 to 15 dl / g consisting essentially of a low molecular weight to high molecular weight polyethylene; With respect to 1 to 10 parts by weight and 100 parts by weight of (A) + (B), (C) a lignocellulose-based material and a cellulosic-based material were added to ((A) +
(B)) / (C) is added in a weight ratio of 90/10 to 30/70.
JP20452997A 1997-07-30 1997-07-30 Thermoplastic resin composition Pending JPH1143562A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20452997A JPH1143562A (en) 1997-07-30 1997-07-30 Thermoplastic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20452997A JPH1143562A (en) 1997-07-30 1997-07-30 Thermoplastic resin composition

Publications (1)

Publication Number Publication Date
JPH1143562A true JPH1143562A (en) 1999-02-16

Family

ID=16492056

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20452997A Pending JPH1143562A (en) 1997-07-30 1997-07-30 Thermoplastic resin composition

Country Status (1)

Country Link
JP (1) JPH1143562A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100389097B1 (en) * 1999-12-10 2003-06-25 이종선 A method manufacturing an artificial lumber and the composition
US7005464B2 (en) 2002-02-21 2006-02-28 Asahi Kasei Kabushiki Kaisha Woody synthetic resin compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100389097B1 (en) * 1999-12-10 2003-06-25 이종선 A method manufacturing an artificial lumber and the composition
US7005464B2 (en) 2002-02-21 2006-02-28 Asahi Kasei Kabushiki Kaisha Woody synthetic resin compositions

Similar Documents

Publication Publication Date Title
US7550404B2 (en) Wood-polymer-zeolite composites
CN108688281A (en) The cross-linked polyolefin foam of coextrusion with TPU coatings
TWI257403B (en) Woody synthetic resin compositions
CN108690345A (en) The method for preparing the cross-linked polyolefin of the coextrusion with TPU coatings
SK48598A3 (en) Co-extruded laminate comprising at least one propylene graft copolymer layer
JP3674150B2 (en) Polyolefin resin composition, composite material, and production method
JP3605946B2 (en) Polyolefin-based resin composition, composite material and manufacturing method
JP3066361B2 (en) Polyolefin resin composition for extrusion molding and method for producing the same
CN101565522B (en) Dynamically-vulcanization plastic-wood composite material and preparation method thereof
SK285636B6 (en) Plastics composition, process for their preparation and their use
JPH11217468A (en) Molding process for resin composition
CN110894329A (en) Sheet material, preparation method and use method
JPH1112401A (en) Thermoplastic resin composition
JP3605947B2 (en) Polyolefin-based resin composition, composite material and manufacturing method
JPH1143562A (en) Thermoplastic resin composition
JP4430202B2 (en) Method for producing polyolefin resin molded product having grain pattern
JP3651117B2 (en) Polyolefin resin composition, composite material, and production method
JP2005200614A (en) Polypropylene based resin composition and injection-molded product thereof
JPH10273538A (en) Production of polyolefin composition containing woody material
JP2001072817A (en) Resin composition, and molded product
JP2002348416A (en) Polyolefin resin composition for molding and its production method
JP2000263718A (en) Polyolefin resin molding and manufacture thereof
JPH11158294A (en) Production of molded article
JP2006002052A (en) Composite resin composition and molding of the same
CN101698723A (en) Ethylene propylene rubber grafted maleic anhydride modified polypropylene board and preparation method thereof