JPH11217476A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

Info

Publication number
JPH11217476A
JPH11217476A JP3551298A JP3551298A JPH11217476A JP H11217476 A JPH11217476 A JP H11217476A JP 3551298 A JP3551298 A JP 3551298A JP 3551298 A JP3551298 A JP 3551298A JP H11217476 A JPH11217476 A JP H11217476A
Authority
JP
Japan
Prior art keywords
weight
vinyl chloride
chloride resin
parts
component
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
JP3551298A
Other languages
Japanese (ja)
Inventor
Atsushi Tsukamoto
淳 塚本
Toshio Nagase
敏夫 永瀬
Toshiya Kobayashi
俊哉 小林
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.)
Zeon Corp
Zeon Kasei Co Ltd
Original Assignee
Zeon Kasei Co Ltd
Nippon Zeon Co Ltd
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 Zeon Kasei Co Ltd, Nippon Zeon Co Ltd filed Critical Zeon Kasei Co Ltd
Priority to JP3551298A priority Critical patent/JPH11217476A/en
Publication of JPH11217476A publication Critical patent/JPH11217476A/en
Pending legal-status Critical Current

Links

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  • Dry Formation Of Fiberboard And The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a vinyl chloride resin composition which can give a rigid molding having high woody appearance and improved impact strength and suited for construction materials such as sashes and furniture. SOLUTION: There is provided with a vinyl chloride resin composition comprising (A) 100 pts.wt. vinyl chloride resin, (B) 5-150 pts.wt. wood flour having a mean particle diameter of 50-500 μm, (C) 2-50 wt.%, based on component B, polyvinyl alcohol having a degree of saponification of 70 mol.% or above at 20 deg.C and having a viscosity of 25-95 cP as measured in a 4 wt.% aqueous solution, and (D) 5-20 pts.wt. impact-resistant impact modifier.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は木粉を多量に配合し
た塩化ビニル系樹脂組成物に関する。詳しくは、木質感
に富んだ、建材に適する、機械的強度の改良された成形
品を与えることができる硬質塩化ビニル系樹脂組成物に
関する。
The present invention relates to a vinyl chloride resin composition containing a large amount of wood flour. More specifically, the present invention relates to a hard vinyl chloride-based resin composition capable of providing a molded article rich in woody feel, suitable for building materials, and having improved mechanical strength.

【0002】[0002]

【従来の技術】近来、木材に似た外観や触感を現出する
目的で、塩化ビニル系樹脂に木粉を配合する方法が行わ
れている。しかし、木粉を相当量配合した塩化ビニル系
樹脂成形品は、引張り強度や耐衝撃強度等の機械的強度
が十分とはいえない問題を有している。
2. Description of the Related Art In recent years, a method of blending wood powder with a vinyl chloride resin has been used for the purpose of producing an appearance and feel similar to wood. However, a vinyl chloride resin molded product containing a considerable amount of wood powder has a problem that the mechanical strength such as tensile strength and impact strength is not sufficient.

【0003】木目の明瞭化や加工のし易さを改善するた
め、木粉に加えて尿素樹脂を添加した塩化ビニル系樹脂
組成物が提案されている(特開昭60−42007号公
報、特開昭60−73807号公報、特開昭60−73
808号公報)。また、木粉の他にマイカなどの無機充
填剤と、ポリエチレン、エチレン−酢酸ビニル共重合体
またはABS樹脂を添加した塩化ビニル系樹脂組成物
は、線膨張率が小さく、耐衝撃性および成形性に優れる
ことが開示された(特開昭60−192746号公報、
特開昭60−192747号公報)。しかし、これらに
よっても木粉の均一混合性に欠け、かつ、成形品の木質
感の現出が不十分である。無機粉末やプラスチック粉末
を付着させた木粉をプラスチック加工時に配合すること
によって木粉の均一分散性は大幅に改善されるが(特開
平5−177610号、特開平5−261708号)、
単にこのような木粉を塩化ビニル系樹脂に配合するのみ
では、木質感に富んだ成形品を、殊に耐衝撃強度の満足
できる成形品を押出成形することは困難であった。即
ち、特に木粉の配合量が多い硬質配合の場合、耐衝撃強
化剤を配合しても、木粉が往々にして樹脂連続層から遊
離してしまい、応力がかかるとき木粉界面に亀裂面を生
じやすいのであった。そのため、木粉高部数配合であっ
て、耐衝撃強度の改良された硬質成形品を与えることの
できる硬質塩化ビニル系樹脂組成物の出現が待たれるよ
うになった。
[0003] In order to improve the clarity and ease of processing of wood grain, a vinyl chloride resin composition in which a urea resin is added in addition to wood flour has been proposed (Japanese Patent Application Laid-Open No. Sho 60-42007, JP-A-60-73807, JP-A-60-73
808). In addition, a vinyl chloride resin composition obtained by adding an inorganic filler such as mica in addition to wood flour and polyethylene, ethylene-vinyl acetate copolymer or ABS resin has a low coefficient of linear expansion, impact resistance and moldability. (JP-A-60-192746,
JP-A-60-192747). However, these also lack the uniform mixing property of wood flour and the appearance of the woody texture of the molded product is insufficient. By blending wood powder to which inorganic powder or plastic powder is attached at the time of plastic processing, the uniform dispersibility of wood powder is greatly improved (JP-A-5-177610, JP-A-5-261708).
Simply blending such wood flour into a vinyl chloride-based resin has made it difficult to extrude a molded product rich in wood texture, especially a molded product having satisfactory impact resistance. That is, especially in the case of a hard compound having a large amount of wood powder, even when an impact-resistant reinforcing agent is added, the wood powder is often released from the continuous resin layer, and when stress is applied, a crack surface is formed at the wood powder interface. Easily occurred. Therefore, the appearance of a hard vinyl chloride-based resin composition which can provide a hard molded product having a high content of wood flour and improved impact strength has been awaited.

【0004】[0004]

【発明が解決しようとする課題】上記の状況に鑑み、本
発明の目的は、窓枠などの建材や家具材に適する、木質
感に富んだ、耐衝撃強度の改良された硬質成形品を与え
ることができる塩化ビニル系樹脂組成物を提供すること
にある。
SUMMARY OF THE INVENTION In view of the above situation, an object of the present invention is to provide a hard molded product which is suitable for building materials such as window frames and furniture, and which is rich in woodiness and has improved impact strength. To provide a vinyl chloride-based resin composition that can be used.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記の課
題に対し、塩化ビニル系樹脂に、木粉とともに、特定の
ポリビニルアルコールと耐衝撃強化剤とを配合すること
により上記目的が達成されることを見出し、この知見に
基づいて本発明を完成するに至った。すなわち、本発明
は、(1)(A)塩化ビニル系樹脂100重量部、
(B)平均粒径50〜500μmの木粉5〜150重量
部、(C)けん化度70モル%以上で温度20℃におけ
る4重量%水溶液の粘度が25〜95cpsであるポリ
ビニルアルコールを(B)成分の重量の2〜50%量お
よび(D)耐衝撃強化剤5〜20重量部を含有してなる
塩化ビニル系樹脂組成物、および、(2)(A)塩化ビ
ニル系樹脂100重量部、(B)平均粒径50〜500
μmの木粉5〜150重量部、(C)けん化度70モル
%以上で温度20℃における4重量%水溶液の粘度が2
5〜95cpsであるポリビニルアルコールを(B)成
分の重量の2〜50%量および(D)耐衝撃強化剤5〜
20重量部を含有してなる塩化ビニル系樹脂押出成形
品、を提供するものである。
Means for Solving the Problems The present inventors have solved the above-mentioned problems by attaining the above object by blending a specific polyvinyl alcohol and an impact-resistant reinforcing agent together with wood powder in a vinyl chloride resin. The present invention was completed based on this finding. That is, the present invention provides (1) (A) 100 parts by weight of a vinyl chloride resin,
(B) 5 to 150 parts by weight of wood powder having an average particle size of 50 to 500 μm, and (C) polyvinyl alcohol having a saponification degree of 70 mol% or more and a 4% by weight aqueous solution at a temperature of 20 ° C. having a viscosity of 25 to 95 cps. (2) (A) 100 parts by weight of a vinyl chloride-based resin, which comprises 2 to 50% by weight of the components and (D) 5 to 20 parts by weight of an impact-resistant reinforcing agent; (B) Average particle size 50 to 500
5-150 parts by weight of wood powder of (μm), (C) viscosity of a 4% by weight aqueous solution at a temperature of 20 ° C. with a saponification degree of 70 mol% or more is 2
5 to 95 cps of polyvinyl alcohol in an amount of 2 to 50% of the weight of the component (B) and (D)
A vinyl chloride resin extruded product containing 20 parts by weight.

【0006】[0006]

【発明の実施の形態】以下、本発明につき詳細に説明す
る。本発明の組成物において(A)成分として使用され
る塩化ビニル系樹脂は、塩化ビニルの単独重合体の他、
塩化ビニル単位を50重量%以上、好ましくは70重量
%以上含有する共重合体を含む。塩化ビニル共重合体の
場合の共単量体としては、例えば、エチレン、プロピレ
ンなどのオレフィン類;塩化アリル、塩化ビニリデン、
フッ化ビニル、三フッ化塩化エチレンなどのハロゲン化
オレフィン類;酢酸ビニル、プロピオン酸ビニルなどの
カルボン酸ビニルエステル類;イソブチルビニルエーテ
ル、セチルビニルエーテルなどのビニルエーテル類;ア
リル−3−クロロ−2−オキシプロピルエーテル、アリ
ルグリシジルエーテルなどのアリルエーテル類;アクリ
ル酸、マレイン酸、イタコン酸、アクリル酸−2−ヒド
ロキシエチル、メチルメタクリレート、マレイン酸モノ
メチル、マレイン酸ジエチル、無水マレイン酸などの不
飽和カルボン酸、そのエステルまたはその酸無水物類;
アクリロニトリル、メタクリロニトリルなどの不飽和ニ
トリル類;アクリルアミド、N−メチロールアクリルア
ミド、アクリルアミド−2−メチルプロパンスルホン
酸、(メタ)アクリルアミドプロピルトリメチルアンモ
ニウムクロライドなどのアクリルアミド類;アリルアミ
ン安息香酸塩、ジアリルジメチルアンモニウムクロライ
ドなどのアリルアミンおよびその誘導体類などを挙げる
ことができる。以上に例示した単量体は、共重合可能な
単量体の一部に過ぎず、近畿化学協会ビニル部会編「ポ
リ塩化ビニル」日刊工業新聞社(1988年)75〜1
04ページに例示されている各種単量体が使用可能であ
る。また、エチレン−酢酸ビニル共重合体、エチレン−
メチルメタクリレート共重合体、エチレン−アクリル酸
エチル共重合体、塩素化ポリエチレンなどの樹脂に、塩
化ビニルまたは塩化ビニルと前記した共重合可能な単量
体とをグラフト重合したような樹脂も含まれる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. The vinyl chloride resin used as the component (A) in the composition of the present invention includes, in addition to a vinyl chloride homopolymer,
Copolymers containing 50% by weight or more, preferably 70% by weight or more of vinyl chloride units are included. Examples of the comonomer in the case of the vinyl chloride copolymer include olefins such as ethylene and propylene; allyl chloride, vinylidene chloride,
Halogenated olefins such as vinyl fluoride and ethylene trifluoride chloride; carboxylic acid vinyl esters such as vinyl acetate and vinyl propionate; vinyl ethers such as isobutyl vinyl ether and cetyl vinyl ether; allyl-3-chloro-2-oxypropyl Ethers, allyl ethers such as allyl glycidyl ether; unsaturated carboxylic acids such as acrylic acid, maleic acid, itaconic acid, 2-hydroxyethyl acrylate, methyl methacrylate, monomethyl maleate, diethyl maleate, and maleic anhydride; Esters or acid anhydrides thereof;
Unsaturated nitriles such as acrylonitrile and methacrylonitrile; acrylamides such as acrylamide, N-methylolacrylamide, acrylamide-2-methylpropanesulfonic acid, (meth) acrylamidopropyltrimethylammonium chloride; allylamine benzoate and diallyldimethylammonium chloride And derivatives thereof. The monomers exemplified above are only a part of the copolymerizable monomers, and are described in "Polyvinyl Chloride" edited by Kinki Chemical Society Vinyl Subcommittee, Nikkan Kogyo Shimbun (1988) 75-1.
Various monomers exemplified on page 04 can be used. Also, ethylene-vinyl acetate copolymer, ethylene-
Resins such as methyl methacrylate copolymer, ethylene-ethyl acrylate copolymer, chlorinated polyethylene, and the like, also include resins obtained by graft-polymerizing vinyl chloride or the above-mentioned copolymerizable monomer with vinyl chloride.

【0007】これらの塩化ビニル系樹脂は、懸濁重合、
乳化重合、溶液重合、塊状重合など、従来から知られて
いるいずれの製造法によって作られてもよい。塩化ビニ
ル系樹脂の平均重合度はJIS K 6721規定の測
定法で400〜1,500が好ましく、より好ましくは
600〜1,100の範囲にあるものを好適に使用する
ことができる。塩化ビニル系樹脂の平均重合度が400
より小さいと、発泡倍率が上がりにくい傾向があり、逆
に1,500より大きいと発泡セルに粗大なものが多く
混在するおそれがある。
[0007] These vinyl chloride resins are prepared by suspension polymerization,
It may be produced by any conventionally known production method such as emulsion polymerization, solution polymerization and bulk polymerization. The average degree of polymerization of the vinyl chloride resin is preferably from 400 to 1,500, more preferably from 600 to 1,100, as determined by the measurement method specified in JIS K 6721. Average degree of polymerization of vinyl chloride resin is 400
If it is smaller, the foaming ratio tends to be hardly increased. Conversely, if it is larger than 1,500, many coarse cells may be mixed in the foam cells.

【0008】本発明において、(B)成分として、平均
粒径50〜500μmの木粉が、塩化ビニル系樹脂
(A)100重量部あたり5〜150重量部、好ましく
は35〜120重量部、更に好ましくは40〜100重
量部用いられる。該木粉の配合量が5重量部より少ない
と成形品に木質感を発現しにくく、また、150重量部
を越えると成形品が脆弱なものとなる。本発明に用いら
れる木粉の樹種は特に限定されず、杉、ツガ、ラワンな
どの針葉樹や広葉樹の木材片、鉋屑、鋸屑などの木材を
用い得る。これら木材から本発明の(B)成分を得るに
は、例えば、該木材を粉砕機により平均粒径が500μ
m以下の木粉とするのが好ましい。本発明に用いられる
木粉は、特開平5−177610号公報および特開平5
−261708号公報に開示されているような硬い小粒
子を表面に付着させた木粉であってもよい。硬い小粒子
としては、硬度が木粉より大きく、平均粒径が木粉の平
均粒径より小さい粒子が用いられる。具体的には、例え
ば、金属、金属酸化物および金属塩、無機化合物ならび
にプラスチック粒子などが挙げられる。好ましい小粒子
は酸化チタン、ニッケル、炭酸カルシウム、シリカ、マ
イカなどの無機系または金属系粒子である。硬い小粒子
が木粉表面に付着する態様は、木粉への硬い小粒子の喰
い込みを含む抱き込み結合、喰い込み結合された複数の
硬い小粒子の相互による挟み込み結合などの、硬い小粒
子の木粉表面部に対する押しつけ外力による付着であっ
てもよいし、あるいは木粉に接着剤により硬い小粒子を
付着させてもよい。この場合は例えば上記の木粉を硬い
小粒子1〜50重量%と共にボールミルなどに仕込み、
窒素雰囲気下など粉塵爆発が防止された条件下に処理す
る方法が行い得る。
In the present invention, as the component (B), wood powder having an average particle size of 50 to 500 μm is contained in an amount of 5 to 150 parts by weight, preferably 35 to 120 parts by weight, per 100 parts by weight of the vinyl chloride resin (A). Preferably, it is used in an amount of 40 to 100 parts by weight. If the amount of the wood flour is less than 5 parts by weight, it is difficult for the molded article to exhibit a woody feeling, and if it exceeds 150 parts by weight, the molded article becomes brittle. The tree species of the wood flour used in the present invention is not particularly limited, and coniferous or hardwood wood pieces such as cedar, hemlock and lauan, and wood such as planing and sawdust can be used. In order to obtain the component (B) of the present invention from these woods, for example, the woods are milled with a pulverizer to have an average particle size of 500 μm.
m or less wood flour is preferred. Wood flour used in the present invention is disclosed in JP-A-5-177610 and JP-A-5-177610.
Wood powder having hard small particles adhered to the surface as disclosed in JP-A-261708 may be used. As the hard small particles, particles having a hardness higher than that of wood flour and an average particle size smaller than the average particle size of wood flour are used. Specific examples include metals, metal oxides and metal salts, inorganic compounds, and plastic particles. Preferred small particles are inorganic or metallic particles such as titanium oxide, nickel, calcium carbonate, silica, and mica. The mode in which the hard small particles adhere to the surface of the wood flour includes hard small particles such as an entanglement bond including biting of the hard small particles into the wood flour, and a pinch bond between a plurality of hard small particles that have been bitten bonded. Adhesion by pressing against the surface of the wood powder may be applied, or hard small particles may be attached to the wood powder by an adhesive. In this case, for example, the wood flour is charged into a ball mill together with 1 to 50% by weight of hard small particles,
A method of treating under a condition in which dust explosion is prevented, such as under a nitrogen atmosphere, can be performed.

【0009】本発明に用いられる(B)成分の平均粒径
は50〜500μm、好ましくは30〜100μmであ
る。ここに平均粒径とは、粉末を篩分析して目開きに対
する累積重量%曲線を得、その50重量%に該当する目
開きの値の読みをいう。(B)成分の平均粒径が50μ
mより小さいと嵩比重が小さくなって組成物調製のため
の混合操作性が悪くなり、また500μmより大きいと
成形品表面が荒れ、かつボイドが発生しやすくなる。
(B)成分中の水分は10重量%以下であることが好ま
しく、より好ましくは5重量%以下である。本発明組成
物では、(C)成分としてポリビニルアルコールを用い
る。ポリビニルアルコールは、(B)成分の木粉に吸着
して木粉をマトリックスの塩化ビニル系樹脂になじみや
すくする作用を有する。(C)成分としてのポリビニル
アルコールは、通常、ポリ酢酸ビニルをけん化して得ら
れるものであり、けん化度は70モル%以上であること
が必要で、好ましくは75〜100モル%である。けん
化度が70モル%より小さいと木粉に吸着しにくくなり
耐衝撃強度が低下する虞がある。
The average particle size of the component (B) used in the present invention is 50 to 500 μm, preferably 30 to 100 μm. Here, the average particle diameter means a reading of the value of the mesh corresponding to 50% by weight of a curve obtained by analyzing the powder by sieve analysis to obtain a cumulative weight% curve with respect to the mesh. Component (B) has an average particle size of 50 μm.
If it is less than m, the bulk specific gravity becomes small and the mixing operability for preparing the composition becomes poor, and if it is more than 500 μm, the surface of the molded article becomes rough and voids are liable to occur.
The water content of the component (B) is preferably at most 10% by weight, more preferably at most 5% by weight. In the composition of the present invention, polyvinyl alcohol is used as the component (C). Polyvinyl alcohol has an effect of adsorbing to the wood powder of the component (B) to make the wood powder easily compatible with the vinyl chloride resin of the matrix. The polyvinyl alcohol as the component (C) is usually obtained by saponifying polyvinyl acetate, and the saponification degree needs to be 70 mol% or more, and preferably 75 to 100 mol%. If the saponification degree is smaller than 70 mol%, it is difficult to adsorb to wood powder, and the impact strength may be reduced.

【0010】(C)成分のポリビニルアルコールの平均
重合度の指標となる4重量%水溶液の粘度は、温度20
℃において25〜95cpsであることが必要で、好ま
しくは30〜85cpsである。ポリビニルアルコール
の4重量%水溶液の粘度が25cpsより小さいと、即
ち分子量が小さすぎると耐衝撃強化剤との相互作用が生
じにくくなり、また、95cpsより大きいと、即ち分
子量が大きすぎると成形品の表面が滑らかさを欠く虞が
ある。また、本発明組成物の(C)成分として、上記の
けん化度および水溶液粘度の範囲にあるポリビニルアル
コールをカルボキシル変性、カチオン変性またはアセト
アセチル変性したもの等であっても同様に使用すること
ができる。(C)成分の配合量は(B)成分の木粉の使
用重量の2〜50%量であることが好ましく、5〜30
%量であることが更に好ましい。(C)成分の量が
(B)成分の重量の2%量より少ないと、耐衝撃強化剤
との相互作用が発現しにくくなるので耐衝撃強度が改善
されない危険がある。また、(C)成分の量が(B)成
分の重量の50%量より多いと、組成物が吸水性を帯び
るようになり、成型品に気泡が生ずる虞がある。
The viscosity of a 4% by weight aqueous solution, which is an index of the average degree of polymerization of the polyvinyl alcohol of the component (C), is 20 ° C.
It is necessary that the temperature be 25 to 95 cps at C, and preferably 30 to 85 cps. If the viscosity of the 4% by weight aqueous solution of polyvinyl alcohol is less than 25 cps, that is, if the molecular weight is too small, interaction with the impact-resistant reinforcing agent is difficult to occur. The surface may lack smoothness. Further, as the component (C) of the composition of the present invention, polyvinyl alcohol having the above-mentioned saponification degree and aqueous solution viscosity in the range of carboxyl modification, cation modification or acetoacetyl modification can be used in the same manner. . The compounding amount of the component (C) is preferably 2 to 50% of the weight of the wood flour of the component (B), and is 5 to 30%.
% Is more preferable. When the amount of the component (C) is less than 2% of the weight of the component (B), the interaction with the impact-resistant reinforcing agent becomes difficult to develop, and there is a risk that the impact strength is not improved. On the other hand, when the amount of the component (C) is more than 50% of the weight of the component (B), the composition becomes water-absorbing, and there is a possibility that bubbles may be generated in a molded product.

【0011】(C)成分のポリビニルアルコールの使用
方法としては、予め(B)成分の木粉に吸着させてから
(A)成分の塩化ビニル系樹脂に配合する方法を採るこ
とが好ましい。ポリビニルアルコールを木粉に吸着させ
るには、例えば、木粉をヘンシェルミキサーに入れて高
速攪拌しつつジャケットにスチームを通して加熱し、内
温が70℃程度に上がったとき、所定量のポリビニルア
ルコールの2〜10重量%の水溶液を少量づつ添加し、
引き続き昇温しつつ水蒸気を揮散させ、130℃程度に
なったら冷却する方法が挙げられる。この方法によれば
水分を木粉の含水量として1重量%程度にまで低減でき
る。
As a method for using the polyvinyl alcohol as the component (C), it is preferable to adopt a method in which the polyvinyl alcohol is previously adsorbed to the wood powder of the component (B) and then mixed with the vinyl chloride resin as the component (A). To adsorb polyvinyl alcohol to wood flour, for example, wood flour is put into a Henschel mixer and heated with steam through a jacket while stirring at high speed. When the internal temperature rises to about 70 ° C., a predetermined amount of polyvinyl alcohol 2 -10 wt% aqueous solution is added little by little,
There is a method of vaporizing water vapor while continuously raising the temperature, and cooling when the temperature reaches about 130 ° C. According to this method, the water content can be reduced to about 1% by weight as the water content of the wood flour.

【0012】本発明組成物には、(D)成分として成型
品の耐衝撃強度を向上させるため、耐衝撃強化剤が使用
される。かかる耐衝撃強化剤としては、アクリロニトリ
ル−ブタジエン−スチレン共重合体(ABS)、メチル
メタクリレート−ブタジエン−スチレン共重合体(MB
S)、アクリル樹脂系耐衝撃強化剤、塩素化ポリエチレ
ン等の塩化ビニル系樹脂用の耐衝撃強化剤として公知の
ものが用いられる。(D)成分の耐衝撃強化剤は、木粉
が配合された塩化ビニル系樹脂組成物にあっては添加さ
れればそれなりに耐衝撃性を改善する作用を有するが、
本発明においては、(C)成分のポリビニルアルコール
の添加と相俟って特段に耐衝撃性が改善されるのであ
る。かかる(D)成分の使用量としては、(A)成分の
塩化ビニル系樹脂100重量部当たり5〜20重量部が
好ましく、7〜15重量部であると更に好ましい。
(D)成分の使用量が5重量部より少ないと成型品の耐
衝撃強度を改善することが難しく、一方、20重量部よ
り多く用いても耐衝撃強度の向上がそれに伴わない上に
引張り強度が大きく低下する虞がある。
In the composition of the present invention, an impact modifier is used as a component (D) in order to improve the impact resistance of the molded article. Examples of such impact modifiers include acrylonitrile-butadiene-styrene copolymer (ABS) and methyl methacrylate-butadiene-styrene copolymer (MB).
S), an acrylic resin-based impact modifier, and a known impact modifier for vinyl chloride resins such as chlorinated polyethylene are used. The impact resistance enhancer of the component (D) has an effect of improving the impact resistance by itself when added to a vinyl chloride resin composition containing wood flour.
In the present invention, the impact resistance is particularly improved in combination with the addition of the polyvinyl alcohol as the component (C). The amount of the component (D) is preferably 5 to 20 parts by weight, more preferably 7 to 15 parts by weight, per 100 parts by weight of the vinyl chloride resin of the component (A).
If the amount of the component (D) is less than 5 parts by weight, it is difficult to improve the impact strength of the molded product. On the other hand, if the amount is more than 20 parts by weight, the impact strength is not improved and the tensile strength is not increased. May be greatly reduced.

【0013】本発明組成物には、上記の各成分に加え
て、通常の塩化ビニル系樹脂の加工時に用いられる熱安
定剤のほか、滑剤、加工助剤、相溶化剤、紫外線吸収
剤、顔料、充填剤、発泡剤、帯電防止剤、可塑剤などを
適宜添加することができる。滑剤としては、ステアリン
酸リチウム、ステアリン酸マグネシウム、ステアリン酸
アルミニウム、ステアリン酸カルシウム、ステアリン酸
ストロンチウム、ステアリン酸バリウム、ラウリン酸カ
ルシウム、ラウリン酸バリウム、2−エチルヘキソイン
酸バリウム、リシノール酸バリウム、ステアリン酸亜
鉛、ナフテン酸亜鉛、ラウリン酸カドミウム、ステアリ
ン酸鉛、二塩基性フタル酸鉛などの金属せっけん類;n
−ブチルステアレート、メチルヒドロキシステアレー
ト、多価アルコール脂肪酸エステル、エステル系ワック
スなどの脂肪酸エステル類;ステアリン酸、ヒドロキシ
ステアリン酸などの脂肪酸類;ステアロアミド、オキシ
ステアロアミド、オレイルアミド、ベヘンアミド、メチ
レンビスステアロアミド、エチレンビスステアロアミ
ド、N,N′−ジステアリルコハク酸アミドなどのアミ
ド化合物;三塩基性硫酸塩、塩基性亜硫酸鉛、二塩基性
亜リン酸鉛などの無機酸鉛類、ポリエチレンワックスな
どの中から選択された1種または2種以上が使用され
る。使用量は、通常、(A)成分の塩化ビニル系樹脂1
00重量部当たり0.2〜10重量部である。
The composition of the present invention contains, in addition to the above-mentioned components, a heat stabilizer used in the processing of an ordinary vinyl chloride resin, a lubricant, a processing aid, a compatibilizer, an ultraviolet absorber, and a pigment. , A filler, a foaming agent, an antistatic agent, a plasticizer, and the like can be appropriately added. Lubricants include lithium stearate, magnesium stearate, aluminum stearate, calcium stearate, strontium stearate, barium stearate, calcium laurate, barium laurate, barium 2-ethylhexoate, barium ricinoleate, zinc stearate, naphthenic acid Metal soaps such as zinc, cadmium laurate, lead stearate, dibasic lead phthalate; n
-Fatty acid esters such as butyl stearate, methylhydroxystearate, polyhydric alcohol fatty acid esters, ester waxes; fatty acids such as stearic acid and hydroxystearic acid; stearamide, oxystearamide, oleylamide, behenamide, methylenebis Amide compounds such as stearoamide, ethylenebisstearamide, N, N'-distearylsuccinamide; inorganic acid salts such as tribasic sulfate, basic lead sulfite, and dibasic lead phosphite; One or more selected from polyethylene wax and the like are used. The amount used is usually the vinyl chloride resin 1 of the component (A).
0.2 to 10 parts by weight per 100 parts by weight.

【0014】加工助剤としては、公知のメチルメタクリ
レート系重合体が好適に使用できる。かかるメチルメタ
クリレート系加工助剤は、メチルメタクリレート単位を
60重量%以上、好ましくは65〜90重量%含有する
共重合体である。また、該メチルメタクリレート樹脂系
加工助剤の分子量の指標となる比粘度、即ち、その0.
2grを溶解したクロロホルム溶液100mlの25℃
における比粘度は、0.3〜1.0であることが好まし
い。このようなメチルメタクリレート樹脂系加工助剤の
市販品の例としては、日本セオン(株)製ハイブレンB
401、三菱レイヨン(株)製P−551,鐘淵化学
(株)製カネエースPA−11、呉羽化学工業(株)製
クレハHIA−15等が挙げられる。加工助剤の添加量
は、通常、(A)成分の塩化ビニル系樹脂100重量部
当たり0.2〜5重量部である。塩化ビニル系樹脂と木
粉の系における相溶化剤としては、エポキシ基含有塩化
ビニル樹脂、エポキシ基含有メチルメタクリレート樹
脂、エポキシ基含有アセトニトリル−メチルメタクリレ
ート共重合体、オキサゾリン基含有塩化ビニル系樹脂、
オキサゾリン基含有メチルメタクリレート樹脂、オキサ
ゾリン基含有アセトニトリル−メチルメタクリレート共
重合体等が好適である。
As the processing aid, a known methyl methacrylate polymer can be preferably used. Such a methyl methacrylate processing aid is a copolymer containing 60% by weight or more, preferably 65 to 90% by weight of a methyl methacrylate unit. Further, the specific viscosity which is an index of the molecular weight of the methyl methacrylate resin-based processing aid, that is, the specific viscosity is 0.1%.
25 ml of chloroform solution 100 ml dissolved 2 gr
Is preferably 0.3 to 1.0. Examples of commercial products of such a methyl methacrylate resin-based processing aid include Hybrene B manufactured by Nippon Seon Co., Ltd.
401, P-551 manufactured by Mitsubishi Rayon Co., Ltd., Kaneace PA-11 manufactured by Kanegafuchi Chemical Co., Ltd., Kureha HIA-15 manufactured by Kureha Chemical Industry Co., Ltd., and the like. The amount of the processing aid is usually 0.2 to 5 parts by weight per 100 parts by weight of the vinyl chloride resin as the component (A). As the compatibilizer in the vinyl chloride resin and wood flour system, epoxy group-containing vinyl chloride resin, epoxy group-containing methyl methacrylate resin, epoxy group-containing acetonitrile-methyl methacrylate copolymer, oxazoline group-containing vinyl chloride resin,
Oxazoline group-containing methyl methacrylate resin, oxazoline group-containing acetonitrile-methyl methacrylate copolymer and the like are preferred.

【0015】本発明組成物を調製するには、通常、先
ず、前記のように(C)成分のポリビニルアルコールを
水溶液として(B)成分の木粉に予め吸着処理をして乾
燥させておき、これを(A)、(D)成分などと共にヘ
ンシェルミキサーなどの混合機に投入する。混合機に投
入された混合成分を、激しく攪拌しつつ120〜160
℃に昇温する。この混合の過程で木粉に吸収されている
水分を揮散させる。上記温度に到達したら混合物をクー
リングミキサーに移して冷却する。取出された粉末状の
混合物をそのまま成形用のコンパウンドとすることがで
きるが、ペレット化しても良い。ペレット作成の好まし
い方法としては、二軸押出機を用い、150〜170℃
にて、かつベント孔から木粉中の残留水分を排出しつつ
ペレットを製造する方法が挙げられる。
In order to prepare the composition of the present invention, first, as described above, the polyvinyl alcohol of the component (C) is converted into an aqueous solution, and the wood powder of the component (B) is adsorbed in advance and dried. This is put into a mixer such as a Henschel mixer together with the components (A) and (D). The mixed components put in the mixer are stirred vigorously for 120-160.
Heat to ° C. In this mixing process, the moisture absorbed in the wood flour is volatilized. When the above temperature is reached, the mixture is transferred to a cooling mixer and cooled. The extracted powdery mixture can be used as a molding compound as it is, but may be pelletized. As a preferable method for producing pellets, a twin-screw extruder is used,
And a method of producing pellets while discharging residual moisture in wood flour from a vent hole.

【0016】本発明組成物を用いて、天然木材に似た硬
質の塩化ビニル系樹脂成形品を得るための成形方法とし
ては、特に制限はないが上記の粉末状コンパウンドまた
はペレットを通常押出機にかけて成形する。押出成形の
条件としては、一般の硬質の塩化ビニル系樹脂の押出成
形と同様な条件が採られる。かくして得られる押出成形
品は、塩化ビニル系樹脂の連続層が木粉に馴染んでいる
ので十分に大きな機械的強度を有する。押出成形品の形
態は、建材や家具材などの用途に応じたものとすればよ
く、一般に板状、シート状、角柱状、円柱状、異形など
が挙げられる。
The molding method for obtaining a hard vinyl chloride resin molded article similar to natural wood using the composition of the present invention is not particularly limited, but the above powdery compound or pellet is usually subjected to an extruder. Molding. As the conditions for the extrusion molding, the same conditions as in the extrusion molding of a general hard vinyl chloride resin are employed. The extruded product thus obtained has a sufficiently large mechanical strength because the continuous layer of the vinyl chloride resin is adapted to the wood flour. The form of the extruded product may be in accordance with the use such as a building material or a furniture material, and generally includes a plate shape, a sheet shape, a prism shape, a column shape, and a deformed shape.

【0017】次に本発明の塩化ビニル系樹脂組成物の発
明の種々の態様を示す。 (1)(A)塩化ビニル系樹脂100重量部、(B)平
均粒径50〜500μmの木粉5〜150重量部、
(C)けん化度70モル%以上で温度20℃における4
重量%水溶液の粘度が25〜95cpsであるポリビニ
ルアルコールを(B)成分の重量の2〜50%量および
(D)耐衝撃強化剤5〜20重量部を含有してなる塩化
ビニル系樹脂組成物。 (2)塩化ビニル系樹脂(A)の平均重合度が400〜
1,500である上記(1)記載の塩化ビニル系樹脂組
成物。
Next, various embodiments of the invention of the vinyl chloride resin composition of the present invention will be described. (1) (A) 100 parts by weight of a vinyl chloride resin, (B) 5-150 parts by weight of wood powder having an average particle size of 50 to 500 μm,
(C) 4 at a temperature of 20 ° C. with a degree of saponification of 70 mol% or more.
A vinyl chloride resin composition comprising polyvinyl alcohol having a viscosity of 25 to 95 cps by weight of an aqueous solution containing 2 to 50% by weight of the component (B) and 5 to 20 parts by weight of an impact-resistant reinforcing agent (D). . (2) The average degree of polymerization of the vinyl chloride resin (A) is 400 to
The vinyl chloride resin composition according to the above (1), which is 1,500.

【0018】(3)(C)成分ポリビニルアルコールの
けん化度が75〜100モル%である上記(1)または
(2)に記載の塩化ビニル系樹脂組成物。 (4)平均粒径50〜500μmの木粉(B)の含有量
が25〜120重量部である上記(1)〜(3)のいず
れかに記載の塩化ビニル系樹脂組成物。 (5)(C)成分の配合量が、(B)成分の重量の5〜
30%量である上記(1)〜(4)のれかに記載の塩化
ビニル系樹脂組成物。 (6)(A)、(B)、(C)および(D)成分の他
に、さらに、化ビニル系樹脂(A)100重量部あたり
(E)滑剤0.2〜10重量部および(F)加工助剤
0.2〜5重量部を含有する上記(1)〜(5)のいず
れかに記載の塩化ビニル系樹脂組成物。 (7)(A)塩化ビニル系樹脂100重量部、(B)平
均粒径50〜500μmの木粉5〜150重量部、
(C)けん化度70モル%以上で温度20℃における4
重量%水溶液の粘度が25〜95cpsであるポリビニ
ルアルコールを(B)成分の重量の2〜50%量および
(D)耐衝撃強化剤5〜20重量部を含有してなる塩化
ビニル系樹脂押出成形品。
(3) Component (C) The vinyl chloride resin composition according to the above (1) or (2), wherein the polyvinyl alcohol has a saponification degree of 75 to 100 mol%. (4) The vinyl chloride resin composition according to any one of the above (1) to (3), wherein the content of the wood powder (B) having an average particle size of 50 to 500 μm is 25 to 120 parts by weight. (5) The amount of the component (C) is 5 to 5 times the weight of the component (B).
The vinyl chloride resin composition according to any one of the above (1) to (4), wherein the amount is 30%. (6) In addition to the components (A), (B), (C), and (D), 0.2 to 10 parts by weight of the lubricant (E) and (F) per 100 parts by weight of the vinyl resin (A). (5) The vinyl chloride resin composition according to any one of the above (1) to (5), comprising 0.2 to 5 parts by weight of a processing aid. (7) (A) 100 parts by weight of vinyl chloride resin, (B) 5-150 parts by weight of wood powder having an average particle size of 50 to 500 μm,
(C) 4 at a temperature of 20 ° C. with a degree of saponification of 70 mol% or more.
Extrusion molding of polyvinyl chloride resin containing polyvinyl alcohol having a viscosity of 25 to 95 cps by weight of an aqueous solution containing 2 to 50% of the weight of component (B) and 5 to 20 parts by weight of (D) impact modifier. Goods.

【0019】[0019]

【実施例】次に実施例および比較例を挙げて、本発明の
塩化ビニル系樹脂組成物について具体的に説明するが、
本発明はこれら実施例に限定されるものではない。な
お、部数および%は特記しない限り重量基準である。特
性評価は下記の方法により行った。 (1)耐衝撃強度 JIS K 7111 に則り、5号試験片を用いてシ
ャルピー耐衝撃強度を測定した。 (2)引張り強度 JIS K 7113 に則り、1号試験片を用いて引
張り速度10mm/分にて測定した。 (3)成形品表面性状 成形品の表面から目視および指触し、下記の4等級で評
価する。 A:滑らか B:鮫肌状 C:粒状突起が多い
EXAMPLES The vinyl chloride resin composition of the present invention will be specifically described below with reference to Examples and Comparative Examples.
The present invention is not limited to these examples. Parts and percentages are by weight unless otherwise specified. The characteristic evaluation was performed by the following method. (1) Impact Strength The Charpy impact strength was measured using a No. 5 test piece in accordance with JIS K 7111. (2) Tensile strength In accordance with JIS K 7113, the tensile strength was measured using a No. 1 test piece at a tensile speed of 10 mm / min. (3) Surface Properties of Molded Product The surface of the molded product is visually observed and touched, and evaluated according to the following four grades. A: Smooth B: Shark skin C: Many granular protrusions

【0020】実施例1〜4、比較例1〜5 比較例1および比較例5を除く各例における表1に示す
量のポリビニルアルコールを用いた濃度5重量%の水溶
液(ただし比較例4は水とエタノールの等重量混合溶
液)を予め調製しておく。先ず、所定量の木粉をヘンシ
ェルミキサーに入れ(ただし比較例1および比較例5を
除く)、激しく攪拌しつつジャケットにスチームを通し
て昇温する。内温が65℃になった時点で、先に調製し
ておいたポリビニルアルコールの水溶液を小刻みに分け
て添加しつつ引き続き昇温し、130℃になった時点で
冷却してポリビニルアルコールを吸着した木粉(含水率
0.8〜1.1重量%)を得た。ついで、表1に示す種
類と量の各成分をヘンシェルミキサーにて次の要領でブ
レンドした。
Examples 1 to 4 and Comparative Examples 1 to 5 In each of Examples except Comparative Examples 1 and 5, an aqueous solution having a concentration of 5% by weight using the amount of polyvinyl alcohol shown in Table 1 (however, Comparative Example 4 is water And an equal weight solution of ethanol and ethanol) are prepared in advance. First, a predetermined amount of wood flour is put into a Henschel mixer (however, except for Comparative Examples 1 and 5), and steam is passed through a jacket with vigorous stirring to raise the temperature. When the internal temperature reached 65 ° C., the temperature was continuously increased while the previously prepared aqueous solution of polyvinyl alcohol was added in small increments, and when the temperature reached 130 ° C., the polyvinyl alcohol was adsorbed by cooling. Wood flour (moisture content 0.8-1.1% by weight) was obtained. Then, each kind of component and amount shown in Table 1 were blended by a Henschel mixer in the following manner.

【0021】塩化ビニル樹脂、ポリビニルアルコールを
吸着した木粉(ただし、比較例1および比較例5では木
粉のみ)、耐衝撃強化剤、熱安定剤お、滑剤、および加
工助剤を仕込んで混合しつつ木粉に残留していた水分
(比較例4では水分とメタノール)を揮発させた。温度
が上昇して140℃になったら混合物をクーリングミキ
サーに移して室温まで温度を下げた。得られた粉末状の
混合物は、シリンダー径65mmの一軸押出機を用いて
下記条件にてペレットにした。 スクリュウ:L/D=24、圧縮比2.5、回転数30rpm 設定温度 :C1 =140℃、C2 =150℃、C3 =160℃ C4 =170℃、ヘッド170℃、ダイス170℃ ダイス :3mmφペレット×12孔 ランド長さ:10mm
A vinyl chloride resin, wood flour adsorbing polyvinyl alcohol (only wood flour in Comparative Examples 1 and 5), an impact resistance enhancer, a heat stabilizer, a lubricant, and a processing aid are charged and mixed. The water remaining in the wood flour (water and methanol in Comparative Example 4) was volatilized. When the temperature rose to 140 ° C., the mixture was transferred to a cooling mixer and cooled to room temperature. The obtained powdery mixture was formed into pellets under the following conditions using a single screw extruder having a cylinder diameter of 65 mm. Screw: L / D = 24, compression ratio 2.5, rotation speed 30 rpm Set temperature: C1 = 140 ° C., C2 = 150 ° C., C3 = 160 ° C. C4 = 170 ° C., head 170 ° C., die 170 ° C. dice: 3 mmφ pellet × 12 holes Land length: 10mm

【0022】こうして得られたペレットを、シリンダー
径65mmの一軸押出機により下記条件にて押出成形し
た。成形品の特性を表1に示す。 スクリュウ:L/D=24、圧縮比2.5、回転数30rpm 設定温度 :C1 =160℃、C2 =170℃、C3 =175℃ C4 =180℃、ヘッド180℃、D1 =180℃ D2 =180℃ ダイス :厚み4mm幅×50mmベルト ランド長さ:10mm
The pellets thus obtained were extruded by a single screw extruder having a cylinder diameter of 65 mm under the following conditions. Table 1 shows the characteristics of the molded product. Screw: L / D = 24, compression ratio 2.5, rotation speed 30 rpm Set temperature: C1 = 160 ° C., C2 = 170 ° C., C3 = 175 ° C. C4 = 180 ° C., head 180 ° C., D1 = 180 ° C. D2 = 180 ℃ Dice: 4mm thick x 50mm belt Land length: 10mm

【0023】[0023]

【表1】 [Table 1]

【0024】注 *1 ZEST700L、新第一塩ビ(株)製、塩化ビ
ニル樹脂、平均重合度680。 *2 セルユント、(株)シマダ商会製、木粉、平均粒
径80μm、水分5重量%。 *3 ゴーセノールKH−20、日本合成化学工業
(株)製、けん化度78.5〜81.5モル%、4重量
%水溶液の粘度78.5〜81.5cps。 *4 ゴーセノールNH−20、日本合成化学工業
(株)製、けん化度98.5〜99.4モル%、4重量
%水溶液の粘度35〜43cps。 *5 ゴーセノールKP−08、日本合成化学工業
(株)製、けん化度71.0〜75.0モル%、4重量
%水溶液の粘度6〜9cps。 *6 ゴーセファイマーL−7514、日本合成化学工
業(株)製、けん化度30〜40モル%、水に不溶で4
重量%水溶液の粘度測定できず。 *7 カネエースFM−20、鐘淵化学工業(株)製、
アクリル樹脂系耐衝撃強化剤。 *8 カネエースB−56、鐘淵化学工業(株)製、M
BS系耐衝撃強化剤。 *9 エラスレン301A、昭和電工(株)製、非結晶
性塩素化ポリエチレン、 塩素含有量30%、ムーニ
ー粘度70(MS1+4 100℃)。 *10 ハイブレンB401、日本ゼオン(株)製、メ
チルメタクリレート樹脂系加工助剤。 *11 プラスチック用添加剤KS−4C、共同薬品
(株)製、錫系熱安定剤。 *12 リケルターSL02,理研ビタミン(株)製、
脂肪酸エステル系滑剤。 *13 LOXIOL G60、ヘンケルジャパン
(株)製、脂肪酸(二塩基酸)エステル系滑剤。 *14 LOXIOL G21、ヘンケルジャパン
(株)製、高級脂肪酸系滑剤。 *15 カーボンブラック〔TPH0012、東洋イン
キ製造(株)製〕/縮合アゾレッド(TXH4360、
同社製)/ビスアゾイエロー(TXH2110、同社
製)複合顔料
Note * 1 ZEST 700L, manufactured by Shin Daiichi Vinyl Co., Ltd., vinyl chloride resin, average degree of polymerization 680. * 2 Celluunt, manufactured by Shimada Shokai Co., Ltd., wood flour, average particle size 80 μm, moisture 5% by weight. * 3 Gohsenol KH-20, manufactured by Nippon Synthetic Chemical Industry Co., Ltd., having a saponification degree of 78.5 to 81.5 mol% and a viscosity of a 4% by weight aqueous solution of 78.5 to 81.5 cps. * 4 Gohsenol NH-20, manufactured by Nippon Synthetic Chemical Industry Co., Ltd., having a saponification degree of 98.5 to 99.4 mol% and a viscosity of a 4% by weight aqueous solution of 35 to 43 cps. * 5 Gohsenol KP-08, manufactured by Nippon Synthetic Chemical Industry Co., Ltd., having a saponification degree of 71.0 to 75.0 mol% and a viscosity of a 4% by weight aqueous solution of 6 to 9 cps. * 6 Gosefimer L-7514, manufactured by Nippon Synthetic Chemical Industry Co., Ltd., having a saponification degree of 30 to 40 mol% and being insoluble in water, 4
Unable to measure viscosity of weight% aqueous solution * 7 Kane Ace FM-20, manufactured by Kanegafuchi Chemical Industry Co., Ltd.
Acrylic resin impact modifier. * 8 Kane Ace B-56, manufactured by Kanegafuchi Chemical Industry Co., Ltd., M
BS-based impact modifier. * 9 Elaslen 301A, manufactured by Showa Denko KK, amorphous chlorinated polyethylene, chlorine content 30%, Mooney viscosity 70 (MS 1 + 4 100 ° C). * 10 Hybrene B401, manufactured by Zeon Corporation, methyl methacrylate resin-based processing aid. * 11 Plastic additive KS-4C, manufactured by Kyodo Yakuhin, tin-based heat stabilizer. * 12 Riquelter SL02, manufactured by Riken Vitamin Co., Ltd.
Fatty acid ester lubricant. * 13 LOXIOL G60, manufactured by Henkel Japan KK, fatty acid (dibasic acid) ester lubricant. * 14 LOXIOL G21, a higher fatty acid lubricant manufactured by Henkel Japan Co., Ltd. * 15 Carbon black [TPH0012, manufactured by Toyo Ink Mfg. Co., Ltd.] / Condensed azo red (TXH4360,
Company pigment) / Bisazo Yellow (TXH2110, Company) composite pigment

【0025】各種配合の組成物を用いて、厚み4mm、
幅50mmの硬質の平板を押出成形して比較評価した。
全てにおいて木質感に富んだ外観の成形品が得られた。
ただし、比較例4の場合のみ表面に鮫肌状の小さな起伏
が見られた。本発明の要件を備えた組成物を用いて成形
した実施例1〜4では、(C)成分のポリビニルアルコ
ールが添加されていない比較例1に比較して、いずれも
耐衝撃強度が2倍以上大きく、引張り強度は心持ち低下
するもなお十分大きな値を示し、そして表面性状の良好
な成形品が得られた。しかし、本発明の要件を満足しな
い組成物を用いて成形した各比較例は、いずれも耐衝撃
強度の小さな成形品を与えた。耐衝撃強化剤を配合しな
い比較例2や、耐衝撃強化剤を配合してもポリビニルア
ルコール本発明の規定外のものを用いた比較例30およ
び4は、比較例1に対し全く耐衝撃強度を改善しなかっ
た。また、耐衝撃強化剤を配合しても、ポリビニルアル
コールを添加しなかった比較例5は、わずかに向上した
耐衝撃強度の値を示した。
Using the compositions of various formulations, a thickness of 4 mm,
A hard flat plate having a width of 50 mm was extruded and comparatively evaluated.
In all cases, molded articles having a woody appearance were obtained.
However, only in the case of Comparative Example 4, small shank-like undulations were observed on the surface. In each of Examples 1 to 4 molded using the composition having the requirements of the present invention, the impact strength was twice or more as compared with Comparative Example 1 in which the polyvinyl alcohol as the component (C) was not added. Although it was large, the tensile strength showed a sufficiently large value although the durability was lowered, and a molded product having good surface properties was obtained. However, each comparative example molded using a composition that did not satisfy the requirements of the present invention gave a molded article having low impact strength. Comparative Example 2 in which no impact modifier was added, and Comparative Examples 30 and 4 in which polyvinyl alcohol was used outside of the scope of the present invention even when an impact modifier was added, had a completely higher impact strength than Comparative Example 1. Did not improve. In addition, Comparative Example 5 in which polyvinyl alcohol was not added even when the impact resistance enhancer was blended showed a slightly improved impact resistance value.

【0026】[0026]

【発明の効果】本発明組成物を用いることにより、木質
感に富んだ、建材に適する、耐衝撃強度の大幅に改良さ
れた硬質塩化ビニル系樹脂成形品を得ることができる。
By using the composition of the present invention, it is possible to obtain a hard vinyl chloride resin molded article which is rich in woodiness, is suitable for building materials, and has greatly improved impact strength.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 55:00) (72)発明者 小林 俊哉 神奈川県川崎市川崎区夜光一丁目2番1号 ゼオン化成株式会社川崎研究所内──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C08L 55:00) (72) Inventor Toshiya Kobayashi 1-1-2, Yakko, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture Zeon Chemical Co., Ltd. Kawasaki Laboratory

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (A)塩化ビニル系樹脂100重量部、
(B)平均粒径50〜500μmの木粉5〜150重量
部、(C)けん化度70モル%以上で温度20℃におけ
る4重量%水溶液の粘度が25〜95cpsであるポリ
ビニルアルコールを(B)成分の重量の2〜50%量お
よび(D)耐衝撃強化剤5〜20重量部を含有してなる
塩化ビニル系樹脂組成物。
(A) 100 parts by weight of a vinyl chloride resin,
(B) 5 to 150 parts by weight of wood powder having an average particle size of 50 to 500 μm, and (C) polyvinyl alcohol having a saponification degree of 70 mol% or more and a 4% by weight aqueous solution at a temperature of 20 ° C. having a viscosity of 25 to 95 cps. A vinyl chloride resin composition comprising 2 to 50% by weight of the components and (D) 5 to 20 parts by weight of an impact modifier.
【請求項2】 (A)塩化ビニル系樹脂100重量部、
(B)平均粒径50〜500μmの木粉5〜150重量
部、(C)けん化度70モル%以上で温度20℃におけ
る4重量%水溶液の粘度が25〜95cpsであるポリ
ビニルアルコールを(B)成分の重量の2〜50%量お
よび(D)耐衝撃強化剤5〜20重量部を含有してなる
塩化ビニル系樹脂押出成形品。
(A) 100 parts by weight of a vinyl chloride resin,
(B) 5 to 150 parts by weight of wood powder having an average particle size of 50 to 500 μm, and (C) polyvinyl alcohol having a saponification degree of 70 mol% or more and a 4% by weight aqueous solution at a temperature of 20 ° C. having a viscosity of 25 to 95 cps. An extruded vinyl chloride resin comprising 2 to 50% by weight of the components and (D) 5 to 20 parts by weight of an impact modifier.
JP3551298A 1998-02-02 1998-02-02 Vinyl chloride resin composition Pending JPH11217476A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3551298A JPH11217476A (en) 1998-02-02 1998-02-02 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3551298A JPH11217476A (en) 1998-02-02 1998-02-02 Vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH11217476A true JPH11217476A (en) 1999-08-10

Family

ID=12443816

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3551298A Pending JPH11217476A (en) 1998-02-02 1998-02-02 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH11217476A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009001735A (en) * 2007-06-25 2009-01-08 Taiyo Vinyl Corp Polyvinyl chloride-based polymer composition recycled from vinyl chloride wallpaper, and flooring sheet made from the composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009001735A (en) * 2007-06-25 2009-01-08 Taiyo Vinyl Corp Polyvinyl chloride-based polymer composition recycled from vinyl chloride wallpaper, and flooring sheet made from the composition

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