JPH01192950A - Resin composition and building materials - Google Patents

Resin composition and building materials

Info

Publication number
JPH01192950A
JPH01192950A JP1979588A JP1979588A JPH01192950A JP H01192950 A JPH01192950 A JP H01192950A JP 1979588 A JP1979588 A JP 1979588A JP 1979588 A JP1979588 A JP 1979588A JP H01192950 A JPH01192950 A JP H01192950A
Authority
JP
Japan
Prior art keywords
resin composition
vinyl alcohol
building materials
resin
humidity
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
JP1979588A
Other languages
Japanese (ja)
Inventor
Shoichi Yoshitani
吉谷 昭一
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.)
NOF Corp
Original Assignee
Nippon Oil and Fats 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 Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP1979588A priority Critical patent/JPH01192950A/en
Publication of JPH01192950A publication Critical patent/JPH01192950A/en
Pending legal-status Critical Current

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Landscapes

  • Finishing Walls (AREA)
  • Floor Finish (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Building Environments (AREA)

Abstract

PURPOSE:To obtain such building materials that can keep the humidity in a room about constant by mixing a specific weight percentage of mineral system filler provided with fine holes having an absorption action into olefin vinyl alcohol copolymerization resin. CONSTITUTION:5-200weight% of mineral system filler provided with fine holes having an absorption action is mixed into 100weight% of olefin vinyl alcohol copolymerization resin to form resin composition. The resin composition has high mechanical strength and moisture absorption - and discharge efficiency. Accordingly, when it is used as building materials, water content is discharged in case indoor humidity is low, water content is absorbed in case indoor humidity is high, and a room temperature is kept about constant to improve living environment.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は釘打ち性、耐衝撃性、調湿性に優れた樹脂組成
物とその応用品である建築材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a resin composition with excellent nailing properties, impact resistance, and humidity control properties, and a building material that is an application thereof.

〔従来の技術〕[Conventional technology]

建築材料の素材には木材や合成樹脂をはじめとする様々
な素材が使用される。最近では装飾性や個性を有するも
のの需要が高い、このためプリント合板や合成樹脂製壁
紙のような、表面に合成樹脂を塗布または塗装したもの
が多用されている。
Various materials are used for building materials, including wood and synthetic resin. Recently, there is a high demand for decorative and unique materials, and for this reason, materials whose surfaces are coated or painted with synthetic resin, such as printed plywood and synthetic resin wallpaper, are often used.

また合成vA脂製の建築材料は生産性が高く、複雑 。In addition, building materials made of synthetic vA resin are highly productive and complex.

な形状も賦形可能な他、軽量化が達成出来るため木質素
材の代替材料としても用いられるようになった。
In addition to being able to be formed into various shapes, it is also lightweight, so it has come to be used as an alternative to wood materials.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

内装材として木材を使用した家屋に比べ1合成樹脂を用
いた家屋は住み心地が良くないと言われる。木材は水分
を吸収、放出するので室内の湿度を略一定に保つことが
出来るが1合成樹脂には木材のような吸放湿性がないか
らである。太材の表面に合成樹脂を塗装した建築材料も
同様である。
It is said that houses made of synthetic resin are less comfortable to live in than houses made of wood as interior materials. This is because wood absorbs and releases moisture, so it is possible to keep indoor humidity at a nearly constant level, but synthetic resin does not have the moisture absorption and release properties that wood does. The same applies to building materials made of thick wood coated with synthetic resin.

また合成樹脂製の建築材料は、室内の水分が壁面等に付
着する結露現象が生じ易い、壁面等に結露が生じると他
の構成材料を腐敗させる原因となリ、家屋の耐用年数を
著しく低下させてしまう。
In addition, synthetic resin building materials are prone to condensation, where indoor moisture adheres to walls, etc. If dew condenses on walls, etc., it can cause other constituent materials to rot, significantly reducing the service life of the house. I'll let you.

さらに内装材に用いる合成樹脂は剛性が高く、釘打ちの
際に割れ易く、釘の保持力も小さいという問題がある。
Furthermore, the synthetic resin used for the interior material has a high rigidity, which causes it to break easily when nailed, and has a low nail holding power.

本発明は上記の課題を解決するためになされたもので、
木質材料同様の機械的強度および吸放湿性を有する樹脂
組成物とその応用品である建築材料を提供することを目
的とする。
The present invention was made to solve the above problems,
The object of the present invention is to provide a resin composition that has mechanical strength and moisture absorption and desorption properties similar to those of wood materials, and a building material that is an applied product thereof.

〔課題を解決するための手段〕[Means to solve the problem]

上記の各問題点を解決するための本発明を説り1する。 The present invention for solving each of the above-mentioned problems will be explained.

第1の発明である樹脂組成物は、オレフィン−ビニルア
ルコール共重合樹脂100重量部に対して、吸着作用を
示す細孔を有する鉱物系充填材5〜200重量部を配合
したことを特徴としている。
The resin composition of the first invention is characterized in that 5 to 200 parts by weight of a mineral filler having pores exhibiting an adsorption effect is blended with 100 parts by weight of the olefin-vinyl alcohol copolymer resin. .

第2の発明である樹脂組成物は、第1の発明の鉱物系充
填材の平均粒径が0.5〜200μmであることを特徴
としている。
The resin composition of the second invention is characterized in that the mineral filler of the first invention has an average particle size of 0.5 to 200 μm.

第3の発明である建築材料は、第1の発明の樹脂組成物
からなることを特徴としている。
A building material according to the third invention is characterized by comprising the resin composition according to the first invention.

第4の発明である建築材料は、第2の発明の樹脂組成物
からなることを特徴としている。
A building material according to a fourth invention is characterized by comprising the resin composition according to the second invention.

前記した発明の樹脂組成物および建築材料の樹脂成分で
あるオレフィン−ビニルアルコール共重合樹脂は、オレ
フィンとビニルアルコールが共重合した構造のものを使
用出来る。特にエチレン−ビニルアルコール共重合体が
機械的強度、成形性の点で良好である。
As the olefin-vinyl alcohol copolymer resin which is the resin component of the resin composition and building material of the invention described above, those having a structure in which olefin and vinyl alcohol are copolymerized can be used. In particular, ethylene-vinyl alcohol copolymers are good in terms of mechanical strength and moldability.

これらの発明の樹脂組成物や建築材料に用いる鉱物系充
填材にはガス吸着性を有する材料を使用する。特にゼオ
ライト、セピオライトが好適である。鉱物系充填材の配
合量は、オレフィン−ビニルアルコール共重合樹脂10
0重量部に対して5〜200重量部配合することが好ま
しい、5重量部未満の場合は好適な吸放湿性が得られず
、200重量部より多い場合には物理的強度が低下する
。また鉱物系充填材の平均粒径は0.5〜200pmで
あることが望ましい、0.5μ−未満の場合は成形性が
劣り、200#L脂より大きい場合は樹脂組成物および
建築材料の表面性が低下する。
A material having gas adsorption properties is used as the mineral filler used in the resin compositions and building materials of these inventions. Zeolite and sepiolite are particularly suitable. The blending amount of the mineral filler is 10% of the olefin-vinyl alcohol copolymer resin.
It is preferable to mix 5 to 200 parts by weight with respect to 0 parts by weight. If it is less than 5 parts by weight, suitable moisture absorption and desorption properties cannot be obtained, and if it is more than 200 parts by weight, physical strength will decrease. In addition, it is desirable that the average particle size of the mineral filler is 0.5 to 200 pm.If it is less than 0.5μ, the moldability will be poor, and if it is larger than 200#L, it will be difficult to form the surface of the resin composition and building materials. Sexuality decreases.

オレフィン−ビニルアルコール共重合樹脂と鉱物系充填
材の混合方法は、一般的に合成樹脂と充填材の混合に用
いる方法で良いが、特に押出し機、ニーダ、バンバリー
ミキサを用いて混合する方法が望ましい。
The method for mixing the olefin-vinyl alcohol copolymer resin and the mineral filler may be the method generally used for mixing synthetic resins and fillers, but it is particularly desirable to mix using an extruder, kneader, or Banbury mixer. .

これらの樹脂組成物や建築材料を成形するには、押出し
成形法、射出成形法、加圧成形法等の−・般の熱可塑性
樹脂の成形に使用する成形法で成形することが出来る。
These resin compositions and building materials can be molded by molding methods used for molding general thermoplastic resins, such as extrusion molding, injection molding, and pressure molding.

生産性の点からは押出し成形法が好ましい。From the viewpoint of productivity, extrusion molding is preferred.

なおこれらの樹脂組成物や建築材料には、充填材として
例えば炭酸カルシウムや木粉、各種添加剤として、例え
ば滑剤、酸化防止剤、帯電防止剤、難燃剤、防かび剤、
発泡剤、ねずみ忌避剤、防蟻剤、紫外線吸収剤1着色剤
を配合しても良い。
These resin compositions and building materials contain fillers such as calcium carbonate and wood flour, and various additives such as lubricants, antioxidants, antistatic agents, flame retardants, fungicides,
A foaming agent, a mouse repellent, an anti-termite agent, an ultraviolet absorber, and a coloring agent may be added.

〔作用〕[Effect]

本発明の樹脂組成物や建築材料は、高湿度環境下では水
分を吸収し、低湿度環境化では含有する水分を放出する
。また、釘等が打ち込まれても、ひび割れが発生するこ
とはなく、°釘を確実に保持する。
The resin composition and building material of the present invention absorb moisture in a high humidity environment, and release the contained moisture in a low humidity environment. Furthermore, even if a nail or the like is driven into it, no cracks will occur, and the nail will be held securely.

〔実施例〕〔Example〕

以下、本発明の実施例を詳細に説明する。なお比較例は
本発明を適用外の例である。
Examples of the present invention will be described in detail below. Note that the comparative example is an example to which the present invention is not applicable.

実施例1 オレフィン−ビニルアルコール共重合体樹脂として、エ
チレン−ビニルアルコール共重合体樹脂(日本合成化学
工業社製、ソアノールD、エチレン含有軟29mo1%
)70重量部と、鉱物系充填材として5分級により平均
粒径を35μmとしたセビオライト(近江鉱業株式会社
製、ミラクレーG4/8)30重量部を、同方向二軸押
出し混線41!(栗本鉄工所株式会社製、 KRCニー
ダS−1型)を用いて220″Cで溶融混練し、樹脂組
成物を得た。得られた樹脂組成物を成形温度200・〜
220℃でプレス成形し、5X15QX150mmの試
料板を作製した。
Example 1 As an olefin-vinyl alcohol copolymer resin, an ethylene-vinyl alcohol copolymer resin (manufactured by Nippon Gosei Kagaku Kogyo Co., Ltd., Soarnol D, ethylene-containing soft 29 mo1%)
) and 30 parts by weight of Seviolite (manufactured by Omi Mining Co., Ltd., Miraclay G4/8) with an average particle size of 35 μm after 5 classification as a mineral filler were extruded in the same direction with 41! (manufactured by Kurimoto Iron Works Co., Ltd., model KRC kneader S-1) was melt-kneaded at 220"C to obtain a resin composition.
Press molding was performed at 220° C. to produce a sample plate measuring 5×15Q×150 mm.

実施例2 オレフィン−ビニルアルコール共重合体樹脂と鉱物系充
填材の量を夫々50重量部とする他は、実施例1と同様
にして試料板を作製した。
Example 2 A sample plate was prepared in the same manner as in Example 1, except that the amounts of the olefin-vinyl alcohol copolymer resin and the mineral filler were each 50 parts by weight.

実施例3 オレフィン−ビニルアルコール共重合体樹脂として、エ
チレン−ビニルアルコール共重合体樹脂(日本合成化学
工業社製、ソアノールD、エチレン含有量29mo1%
)を用いる他は、実施例1と同様にして試料板を作製し
た。
Example 3 As the olefin-vinyl alcohol copolymer resin, ethylene-vinyl alcohol copolymer resin (manufactured by Nippon Gosei Kagaku Kogyo Co., Ltd., Soarnol D, ethylene content 29 mo1%) was used.
) A sample plate was prepared in the same manner as in Example 1, except that the sample plate was used.

実施例4 鉱物系充填材として4A型ゼオライト(日本化学T業株
式会社製、ゼオスターNA−110P、平均粒径3μ層
)を用いる他は、実施例1と同様にして試料板を作製し
た。
Example 4 A sample plate was prepared in the same manner as in Example 1, except that 4A type zeolite (manufactured by Nippon Kagaku T Gyo Co., Ltd., Zeostar NA-110P, layer with average particle size of 3 μm) was used as the mineral filler.

比較例1 オレフィン−ビニルアルコール共重合体樹脂の量を97
瓜量部と、鉱物系充填材の量を3重量部とする他は、実
施例1と同様にして試料板を作製した。
Comparative Example 1 The amount of olefin-vinyl alcohol copolymer resin was 97%.
A sample plate was prepared in the same manner as in Example 1, except that the amount of melon and mineral filler was changed to 3 parts by weight.

比較例2 オレフィン−ビニルアルコール共重合体11脂の量を3
0東量部と、鉱物系充填材の量を70重量部とする他は
、実施例1と同様にして溶融混練したが、混練性が悪く
樹脂組成物を得られなかった。
Comparative Example 2 Olefin-vinyl alcohol copolymer 11 The amount of fat was 3
Melt-kneading was carried out in the same manner as in Example 1 except that the amount of the mineral filler was 70 parts by weight, but the kneading properties were poor and a resin composition could not be obtained.

比較例3 オレフィン−ビニルアルコール共用合体樹脂単独を、断
面が5X150mmのダイを取付けた押出し成形機に投
入し、成形温度180〜220℃で押出し成形する。そ
の成形品を切断して5X150X15haの試料板を得
た。
Comparative Example 3 The olefin-vinyl alcohol copolymer resin alone was put into an extrusion molding machine equipped with a die having a cross section of 5 x 150 mm, and extrusion molded at a molding temperature of 180 to 220°C. The molded product was cut to obtain a sample plate of 5×150×15 ha.

比較例4 オレフィン−ビニルアルコール共重合体樹脂の代わりに
、ポリプロピレン樹脂(三井東圧化学社製、ノーブレン
JH)I−791)を用いる他は、実2施例1と同様に
して試料板を得た。
Comparative Example 4 A sample plate was obtained in the same manner as Example 2 and Example 1, except that polypropylene resin (Mitsui Toatsu Chemical Co., Ltd., Noblen JH I-791) was used instead of the olefin-vinyl alcohol copolymer resin. Ta.

比較例5 鉱物系充填材として1分級により平均粒径を0.3μm
にしたセピオライト(近江鉱業株式会社製、ミラクレー
〇478)を用いる他は、実施例1と同様にして混線溶
融したが、混練性が悪く樹脂組成物を得られなかった。
Comparative Example 5 As a mineral filler, the average particle size was 0.3 μm by 1 classification.
Cross-wire melting was carried out in the same manner as in Example 1, except that sepiolite (manufactured by Ohmi Mining Co., Ltd., Miraclay 0478) was used, but the kneading properties were poor and a resin composition could not be obtained.

比較例6 鉱物系充填材として5分級により平均粒径な250IA
a+にしたセピオライト(近江鉱業株式会社製、ミラク
レー04/8)を用いる他は、実施例1と同様にして試
料板を得た。得られた試料板は表面の凹凸が激しいもの
であった。
Comparative Example 6 As a mineral filler, the average particle size was 250IA by 5 classification.
A sample plate was obtained in the same manner as in Example 1, except that a+ sepiolite (manufactured by Ohmi Mining Co., Ltd., Miraclay 04/8) was used. The obtained sample plate had a severely uneven surface.

比較例7 鉱物系充填材としてマイカ((株)クラレ製、スジライ
トマイカ325HK)を用いる他は、実施例1と同様に
して試料板を得た。
Comparative Example 7 A sample plate was obtained in the same manner as in Example 1, except that mica (Sujirite Mica 325HK, manufactured by Kuraray Co., Ltd.) was used as the mineral filler.

なお、これらの試料板はそのまま建築材料として使用す
ることが可能である。
Note that these sample plates can be used as construction materials as they are.

夫々の実施例および比較例で得られた試料板は以下の方
法で評価する。
The sample plates obtained in each Example and Comparative Example were evaluated by the following method.

・機械的強度(釘打ちに対する割れにくさ)5℃、50
%R,H,の環境下で、直径3+s層、長さ85mmの
鉄製釘を試料板中央に金錫で打ち込み、試料板の割れ具
合を目視で観察した。
・Mechanical strength (resistance to nailing) 5℃, 50
%R, H, an iron nail with a diameter of 3+s layer and a length of 85 mm was driven into the center of the sample plate with gold tin, and the degree of cracking of the sample plate was visually observed.

・調湿性(吸湿性および放湿性) 真空デシケータ(内容jA8.7見)に試料板を入れて
内部を十分に脱気した後、23°C1相対湿度20%R
,H,以下の乾燥空気を封入する。封入直後と3時間経
過後の湿度を測定し、その湿度変化から放湿性を評価す
る0次に+If度デシケータ内部を脱気し、23℃、相
対湿度80%R,H,以上の湿潤空気を封入する。封入
直後と3詩間経過後の湿度をJlll定し、同様にして
吸湿性を評価する。
- Humidity control (hygroscopicity and moisture release) After placing the sample plate in a vacuum desiccator (see Contents JA8.7) and thoroughly deaerating the inside, heat at 23°C1 relative humidity 20%R.
, H, the following dry air is enclosed. Measure the humidity immediately after sealing and after 3 hours, and evaluate the moisture release performance from the humidity change. Degas the inside of the desiccator at 0th + If degree, and humid air at 23 ° C and relative humidity of 80% R, H or more. Encapsulate. The humidity was determined immediately after enclosing and after three passages, and the hygroscopicity was evaluated in the same manner.

機械的強度試験では、釘を打込んでもひび割れが発生し
ないものをOlひび割れが発生したものを×とする。調
湿性試験では、3時間経過後のデシケータ内の湿度が2
0%R,H,以上変化したものを0.20%R,)1.
未満のものを×とする。総合評価としては、全ての項目
が良好なものを○、それ以外のものを×とする。
In the mechanical strength test, those with no cracks even after driving a nail are given a mark of "×" and those with Ol cracks. In the humidity control test, the humidity inside the desiccator after 3 hours was 2.
0%R,H, those that have changed more than 0.20%R,) 1.
If it is less than that, mark it as ×. As for the overall evaluation, if all items are good, ○ is given, and otherwise, × is given.

これらの結果を次表に示す。These results are shown in the table below.

(以下余白) 第  1  表 〔発明の効果〕 以上詳細に説明したように、本発明の樹脂組成物は機械
的強度に優れ、吸放湿性を有している。
(The following is a blank space) Table 1 [Effects of the Invention] As explained in detail above, the resin composition of the present invention has excellent mechanical strength and moisture absorbing and releasing properties.

この樹脂組成物を用いた建築材料は、木材を加■した建
築材料よりも生産性に優れており、軽量で複雑な形状の
ものも生産可使である。施工時には木材同様に釘を打つ
ことが出来る。また木材同様の調湿性を有している。家
屋の材料に使用すると家屋内が低湿度の時は水分を放出
し、高湿度の時には水分を吸収して室内の湿度を略一定
に保つため、快適な生活を送ることが出来る。
Building materials using this resin composition have better productivity than building materials made from wood, and can be produced and used even in lightweight and complex shapes. During construction, nails can be driven in just like wood. It also has moisture control properties similar to wood. When used as a building material, it releases moisture when the humidity inside the house is low, and absorbs moisture when the humidity is high, keeping the indoor humidity almost constant, making it possible to live a comfortable life.

特許出願人  日本油脂株式会社Patent applicant: NOF Corporation

Claims (1)

【特許請求の範囲】 1、オレフィン−ビニルアルコール共重合樹脂100重
量部に対して、吸着作用を示す細孔を有する鉱物系充填
材5〜200重量部を配合したことを特徴とする樹脂組
成物。 2、前記鉱物系充填材の平均粒径が0.5〜200μm
であることを特徴とする特許請求の範囲第1項記載の樹
脂組成物。 3、特許請求の範囲第1項記載の樹脂組成物からなる建
築材料。 4、特許請求の範囲第2項記載の樹脂組成物からなる建
築材料。
[Claims] 1. A resin composition characterized in that 5 to 200 parts by weight of a mineral filler having pores exhibiting an adsorption effect is blended with 100 parts by weight of an olefin-vinyl alcohol copolymer resin. . 2. The average particle size of the mineral filler is 0.5 to 200 μm
The resin composition according to claim 1, characterized in that: 3. A building material comprising the resin composition according to claim 1. 4. A building material comprising the resin composition according to claim 2.
JP1979588A 1988-01-29 1988-01-29 Resin composition and building materials Pending JPH01192950A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1979588A JPH01192950A (en) 1988-01-29 1988-01-29 Resin composition and building materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1979588A JPH01192950A (en) 1988-01-29 1988-01-29 Resin composition and building materials

Publications (1)

Publication Number Publication Date
JPH01192950A true JPH01192950A (en) 1989-08-03

Family

ID=12009281

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1979588A Pending JPH01192950A (en) 1988-01-29 1988-01-29 Resin composition and building materials

Country Status (1)

Country Link
JP (1) JPH01192950A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018025951A1 (en) * 2016-08-04 2018-02-08 株式会社Tbm Molded resin object

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018025951A1 (en) * 2016-08-04 2018-02-08 株式会社Tbm Molded resin object
JPWO2018025951A1 (en) * 2016-08-04 2018-12-20 株式会社Tbm Resin molded body

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