JPH07109375A - Sintered porous polyacetal resin article - Google Patents
Sintered porous polyacetal resin articleInfo
- Publication number
- JPH07109375A JPH07109375A JP5253998A JP25399893A JPH07109375A JP H07109375 A JPH07109375 A JP H07109375A JP 5253998 A JP5253998 A JP 5253998A JP 25399893 A JP25399893 A JP 25399893A JP H07109375 A JPH07109375 A JP H07109375A
- Authority
- JP
- Japan
- Prior art keywords
- polyacetal resin
- polyacetal
- melting point
- component
- sintering
- 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
Links
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ポリアセタール樹脂焼
結多孔体に関するものである。更に詳しくは、融点の異
なる2種以上のポリアセタール樹脂を併用して焼結成形
してなる、耐薬品性、寸法安定性に優れたポリアセター
ル樹脂焼結多孔体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyacetal resin sintered porous body. More specifically, the present invention relates to a sintered polyacetal resin porous body having excellent chemical resistance and dimensional stability, which is formed by sintering two or more kinds of polyacetal resins having different melting points together.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】周知の
如く、ポリアセタール樹脂は、機械的性質、電機的性質
などの物理的特性、耐薬品性、耐熱性などの化学的特性
の優れたエンジニアリング樹脂として、近年極めて広汎
な分野において利用されている。特に、ポリアセタール
樹脂が優れた耐薬品性を有する事により、ガソリン、灯
油等に直接接する部品、サインペンのキャップ等に使用
されている。又、これら用途の周辺には、フィルター作
用や、細孔への他物質の含浸性を要求される部品があ
り、主にポリオレフィン、フッ素樹脂、ナイロン樹脂等
を用い焼結成形によって高分子多孔体を得て、部品を製
造している。ポリアセタール樹脂はその耐薬品性、耐熱
性等から、これら部品への適用が試みられてきたが、焼
結成形において成形条件幅が狭く、又、結晶性樹脂であ
るために結晶化前後の体積変化が大きく、寸法精度が出
にくいという欠点があるため、上述の利点があるにもか
かかわらず、焼結多孔体には従来使用されていないのが
実状である。これらの要求に応えるため、従来より、ガ
ラスビーズ、タルク、炭酸カルシウム等の無機フィラー
を添加する方法が知られている。しかし、これらの方法
では、ポリアセタール樹脂と無機フィラー間の界面強度
が得られず、充分な機械強度が出ない。又、無機フィラ
ーの形状が限定されるため、所望の孔径が得られないと
いう欠点を有している。そこで、機械的強度に優れ、か
つ、焼結成形が容易に行え、寸法精度に優れる、ポリア
セタール樹脂材料および焼結多孔体の開発が望まれてい
た。BACKGROUND OF THE INVENTION As is well known, polyacetal resins are engineering resins having excellent physical properties such as mechanical properties and electrical properties, and chemical properties such as chemical resistance and heat resistance. In recent years, it has been used in a very wide range of fields. In particular, since polyacetal resin has excellent chemical resistance, it is used for parts that come into direct contact with gasoline, kerosene, etc., caps for felt-tip pens, and the like. In the vicinity of these applications, there are parts that are required to have a filter function and the ability to impregnate pores with other substances. Polymeric porous materials are mainly formed by sintering using polyolefin, fluororesin, nylon resin, etc. To get the parts manufactured. Polyacetal resin has been tried to be applied to these parts due to its chemical resistance, heat resistance, etc., but the range of molding conditions in sintering molding is narrow, and since it is a crystalline resin, the volume change before and after crystallization is changed. However, in spite of the above-mentioned advantages, they have not been used in the past for sintered porous bodies. In order to meet these demands, conventionally known is a method of adding an inorganic filler such as glass beads, talc, calcium carbonate or the like. However, in these methods, the interfacial strength between the polyacetal resin and the inorganic filler cannot be obtained, and sufficient mechanical strength cannot be obtained. Further, since the shape of the inorganic filler is limited, there is a drawback that a desired pore size cannot be obtained. Therefore, it has been desired to develop a polyacetal resin material and a sintered porous body that have excellent mechanical strength, can be easily sintered and molded, and have excellent dimensional accuracy.
【0003】[0003]
【課題を解決するための手段】本発明者らは、ポリアセ
タール樹脂本来の特性を犠牲にする事なく、焼結成形性
に優れ、得られた高分子多孔体成形品の寸法精度が高い
ポリアセタール樹脂の開発をすべく鋭意研究を重ねた結
果、融点が異なる2種以上のポリアセタール樹脂を併用
するのが有効である事を見出し、本発明を完成するに至
った。即ち本発明は、融点が5℃以上異なる2種以上の
ポリアセタール樹脂から構成された焼結多孔体、並びに
(A) ポリアセタール樹脂、95〜5重量%と、(B) (A) の
ポリアセタール樹脂に対して5℃以上融点が異なる他の
ポリアセタール樹脂1種以上、5〜95重量%とを用い、
(A) 、(B) の粉末を混合、あるいは(A) と(B) を混練し
た後で粉末とし、焼結することを特徴とするポリアセタ
ール樹脂焼結多孔体の製造方法に関する。DISCLOSURE OF THE INVENTION The present inventors have found that the polyacetal resin having excellent sinter moldability and high dimensional accuracy of the obtained polymer porous molded article without sacrificing the original properties of the polyacetal resin. As a result of intensive studies to develop the above, it was found that it is effective to use two or more kinds of polyacetal resins having different melting points together, and the present invention has been completed. That is, the present invention relates to a sintered porous body composed of two or more kinds of polyacetal resins having melting points different by 5 ° C. or more, and
(A) polyacetal resin, 95 to 5% by weight, and (B) one or more other polyacetal resin having a melting point different from that of the polyacetal resin of (A) by 5 ° C. or more, 5 to 95% by weight,
The present invention relates to a method for producing a sintered polyacetal resin porous body, which comprises mixing the powders of (A) and (B) or kneading (A) and (B) into powder and sintering the mixture.
【0004】以下、本発明を詳しく説明する。本発明に
おいて用いられる(A) 、(B) 成分のポリアセタール樹脂
は、オキシメチレン基(-CH2O-)を主たる構成単位とす
る高分子化合物で、ポリオキシメチレンホモポリマー、
オキシメチレン基以外に他の構成単位を少量有するコポ
リマー、ターポリマー、ブロックポリマーのいずれもが
含まれる。又、その重合度に関しても特に制限はない。
(A) 成分、(B) 成分のポリアセタール樹脂の違いは融点
(ここで意味する融点とは、ピークトップとする)であ
る。即ち、本発明においては、(A) 、(B) 成分として、
融点の差が5℃以上、好ましくは10℃以上のポリアセタ
ール樹脂を併用することを特徴とする。ここで、両成分
の融点の差が5℃未満の場合、焼結成形における成形条
件が狭く、得られた焼結成形品の強度が小さくてもろく
なるか、寸法精度の低いものしか得られない。尚、(B)
成分として2種以上を用いる場合、夫々の(A) 成分に対
する融点の差が5℃以上であれば良く、(B) 成分同士の
融点差は特に問題とされない。このような融点に差のあ
るポリアセタール樹脂は、共重合成分の有無やその比率
等により適宜調製できる。The present invention will be described in detail below. The polyacetal resin of the components (A) and (B) used in the present invention is a polymer compound having an oxymethylene group (—CH 2 O—) as a main constituent unit, and a polyoxymethylene homopolymer,
It includes any of copolymers, terpolymers and block polymers having a small amount of other constitutional units in addition to the oxymethylene group. Also, there is no particular limitation on the degree of polymerization.
The difference between the polyacetal resin of the component (A) and the polyacetal resin of the component (B) is the melting point (the melting point here means the peak top). That is, in the present invention, as the components (A) and (B),
It is characterized in that a polyacetal resin having a difference in melting point of 5 ° C. or higher, preferably 10 ° C. or higher is used in combination. Here, when the difference in melting point between the two components is less than 5 ° C., the molding conditions in the sintering molding are narrow, and the strength of the obtained sintered molded product becomes weak and fragile, or only dimensional accuracy is low. . Incidentally, (B)
When two or more components are used, the difference in melting point between the respective components (A) is 5 ° C. or more, and the difference in melting points between the components (B) is not a particular problem. Such a polyacetal resin having a different melting point can be appropriately prepared depending on the presence or absence of the copolymerization component and the ratio thereof.
【0005】ここで用いられる、(A) 、(B) のポリアセ
タール樹脂の配合比率は、重量で(A) /(B) が95/5〜
5/95の範囲が好ましい。この範囲外の場合、焼結成形
において成形条件が狭く、得られた焼結成形品の強度が
小さくてもろくなるか、寸法精度の低いものしか得られ
ない上に、得られた製品にクラックが発生することもあ
る。又、本発明の構成成分であるポリアセタール樹脂に
は、更に公知の各種安定剤を添加して熱安定性、耐候安
定性等を補強することが望ましい。この目的のために公
知の酸化防止剤や、窒素含有化合物、アルカリまたはア
ルカリ土類金属化合物等を1種または2種以上合わせて
使用する事が望ましい。又、本発明の組成物は各種カー
ボンブラック、その他各種の染顔量を適宜添加し、任意
に着色することもできる。更にその目的に応じ、所望の
特性を付与するために、従来公知の添加剤、核剤、離型
剤、帯電防止剤、その他界面活性剤、あるいはポリアセ
タール樹脂以外の有機高分子材料、無機、有機強化剤等
を1種または2種以上添加含有させることが可能であ
る。The mixing ratio of the polyacetal resins (A) and (B) used here is such that (A) / (B) is 95/5 to 5 by weight.
A range of 5/95 is preferred. If the content is out of this range, the molding conditions in the sintering molding are narrow, the strength of the obtained sintered molded product is small and it becomes brittle, or only the one with low dimensional accuracy is obtained, and the cracked product is obtained. It may occur. Further, it is desirable to add various known stabilizers to the polyacetal resin which is a constituent of the present invention to reinforce the thermal stability, weather stability and the like. For this purpose, it is desirable to use one or more known antioxidants, nitrogen-containing compounds, alkali or alkaline earth metal compounds and the like in combination. Further, the composition of the present invention can be optionally colored by appropriately adding various carbon blacks and other various face dyeing amounts. Further, according to the purpose, in order to impart desired properties, conventionally known additives, nucleating agents, releasing agents, antistatic agents, other surfactants, or organic polymer materials other than polyacetal resin, inorganic, organic It is possible to add one or more reinforcing agents and the like.
【0006】本発明の構成成分であるポリアセタール樹
脂は、一般に合成樹脂組成物の調製法として公知の設備
と方法により調製することができる。即ち、必要な成分
を混合し、1軸または2軸の押出機を使用して混練し、
押し出した後、ペレットを粉砕してもよく、また、融点
の異なるポリアセタール樹脂を、各々別々に粉砕した
後、混合しても良い。また、前記安定剤、添加剤等の配
合物は、任意のいかなる段階で加えてもよい。The polyacetal resin which is a constituent of the present invention can be prepared by the equipment and method generally known as a method for preparing a synthetic resin composition. That is, the necessary components are mixed and kneaded using a single-screw or twin-screw extruder,
After extrusion, the pellets may be crushed, or polyacetal resins having different melting points may be crushed separately and then mixed. In addition, the compounds such as the stabilizer and the additives may be added at any arbitrary stage.
【0007】本発明の焼結多孔体は、例えば(A) 、(B)
夫々の粉末を用意し、それらを混合するか、あるいは
(A) と(B) を溶融混練した後で粉末とし、次いで、常法
により所定の温度で焼結成形することにより製造でき
る。焼結温度は、一般に、(A) 、(B) 成分の融点の高い
方の融点以下である。又、本発明は後記実施例からも明
らかなように、比較的低い温度でも焼結が可能であり、
焼結成形における成形条件幅が広いという利点がある。The sintered porous body of the present invention is, for example, (A), (B)
Prepare each powder and mix them, or
It can be produced by melt-kneading (A) and (B) into a powder, and then sinter-molding at a predetermined temperature by an ordinary method. The sintering temperature is generally lower than or equal to the higher melting point of the components (A) and (B). Further, as is apparent from the examples described below, the present invention enables sintering even at a relatively low temperature,
There is an advantage that the range of molding conditions in the sintering molding is wide.
【0008】又、本発明の焼結多孔体において下記の式
により多孔率を求めた場合、多孔率が20〜80%のものは
特に優れた性質を所持しており、ろ過材や液浸材、油浸
軸受の基材に用いた場合、液浸性、ろ過性が良好であっ
て望ましい多孔体である。多孔率が20%より低い場合は
液浸性、ろ過性が不足して実用上問題があり、多孔率が
80%より高い場合は機械的強度が不足して問題がでる。 Φ(多孔率)={1−W/(V×ρ)}×100 (%) W:成形品重量(g) V:成形品体積(cm3) ρ:ポリアセタール真比重(1.41g/cm3)Further, when the porosity of the sintered porous body of the present invention is calculated by the following formula, those having a porosity of 20 to 80% have particularly excellent properties. When used as a base material for oil-impregnated bearings, it is a desirable porous body because it has good liquid immersion and filterability. When the porosity is lower than 20%, the liquid immersion property and the filterability are insufficient and there is a problem in practical use.
If it is higher than 80%, the mechanical strength is insufficient and problems occur. Φ (porosity) = {1-W / (V × ρ)} × 100 (%) W: Weight of molded product (g) V: Volume of molded product (cm 3 ) ρ: Polyacetal true specific gravity (1.41 g / cm 3) )
【0009】[0009]
【実施例】以下、本発明を実施例に更に詳しく説明する
が、本発明はこれらに限定されるものではない。尚、比
較例、実施例において、特性値の評価に用いた方法は以
下の通りである。 (1) 焼結成形 表1に記載した所定量のポリアセタール樹脂粉末(100
〜200 メッシュパス品)を内寸法100 L×30W×20H
(mm)の上部が開口した、長方形のメス金型に入れ、そ
の上方開口部からオス金型を挿入し、 150kg/cm2 で10
0 L×30W×10mm厚まで加圧圧縮し、これを窒素気流
中、所定温度の加熱炉に入れて20分焼結した。 (2) 成形収縮率 (1) で得られた、焼結成形体の成形品寸法(L)を測定
し、以下の式より成形収縮率を求めた。 MS(成形収縮率)=(L0 −L)/L0 L :成形品寸法 L0 :金型寸法 (3) 成形品強度 (1) で得られた成形品を用いて、曲げ強度を測定した。
試験方法はASTM D 790に準拠して行った。EXAMPLES The present invention will be described in more detail with reference to examples below, but the present invention is not limited thereto. In the comparative examples and examples, the methods used for evaluating the characteristic values are as follows. (1) Sintering molding Predetermined amount of polyacetal resin powder (100
~ 200 mesh pass product) inside dimensions 100 L x 30 W x 20 H
(Mm) is placed in a rectangular female mold with an opening at the top, and the male mold is inserted through the upper opening, and 10 kg at 150 kg / cm 2
It was pressed and compressed to a thickness of 0 L × 30 W × 10 mm, placed in a heating furnace at a predetermined temperature in a nitrogen stream, and sintered for 20 minutes. (2) Molding shrinkage ratio The molded product dimension (L) of the sintered compact obtained in (1) was measured, and the molding shrinkage ratio was calculated from the following formula. MS (molding shrinkage rate) = (L 0 −L) / L 0 L: Molded product size L 0 : Mold size (3) Molded product strength (1) Measured flexural strength using the molded product did.
The test method was according to ASTM D 790.
【0010】比較例1、2 融点175 ℃のポリアセタール樹脂A(旭化成(株)製、
テナック5010、ホモポリマー)及び融点165 ℃のポ
リアセタール樹脂B(ポリプラスチックス(株)製、ジ
ュラコンM90−44、コポリマー)を別々に粉砕し、
所望の粒度の粉体を得た。以下、夫々を単独で用いて、
前記の方法によって焼結成形を行った。結果を表1に示
す。 実施例1〜5 比較例1、2で使用した各々のポリマー粉体を、室温で
表1に示す割合で混合した後、表1に示す成形温度で焼
結成形を行った。結果を表1に示す。 実施例6 比較例1、2で使用した各々のポリマー粉体を、室温で
表1に示す割合で混合した後、2軸押出機を用いて混練
したのち、粉砕を行い、所望の粒度の粉体を得た。以
下、表1に示す成形温度で焼結成形を行った。結果を表
1に示す。Comparative Examples 1 and 2 Polyacetal resin A having a melting point of 175 ° C. (manufactured by Asahi Kasei Corp.,
Tenac 5010, a homopolymer) and a polyacetal resin B having a melting point of 165 ° C. (manufactured by Polyplastics Co., Ltd., DURACON M90-44, copolymer) are ground separately.
A powder of the desired particle size was obtained. In the following, using each individually,
Sintering was performed by the above method. The results are shown in Table 1. Examples 1 to 5 The polymer powders used in Comparative Examples 1 and 2 were mixed at room temperature in the proportions shown in Table 1, and then sintered and molded at the molding temperature shown in Table 1. The results are shown in Table 1. Example 6 The respective polymer powders used in Comparative Examples 1 and 2 were mixed at room temperature in the proportions shown in Table 1, and then kneaded using a twin-screw extruder, and then pulverized to obtain a powder having a desired particle size. Got the body Hereinafter, sintering molding was performed at the molding temperature shown in Table 1. The results are shown in Table 1.
【0011】実施例7 融点170 ℃のポリアセタール樹脂C(試作コポリマー)
と融点165 ℃のポリアセタール樹脂Bを別々に粉砕し、
所望の粒度の粉体を得た。以下、実施例1〜5と同じ方
法で焼結成形を行った。結果を表1に示す。Example 7 Polyacetal resin C (prototype copolymer) having a melting point of 170 ° C.
And polyacetal resin B having a melting point of 165 ° C. are pulverized separately,
A powder of the desired particle size was obtained. Hereinafter, sinter molding was performed by the same method as in Examples 1 to 5. The results are shown in Table 1.
【0012】[0012]
【表1】 [Table 1]
【0013】[0013]
【発明の効果】以上の説明および実施例から明らかなよ
うに、融点が異なる二種以上のポリアセタール樹脂を配
合する事により、実用的な成形条件幅を有する焼結成形
ができる様になった。得られた焼結成形品は寸法精度、
機械強度が良好で、なおかつ耐薬品性に優れた実用的な
焼結多孔体となった。As is apparent from the above description and the examples, by mixing two or more kinds of polyacetal resins having different melting points, it becomes possible to carry out sintering molding having a practical molding condition range. The obtained sintered molded product has dimensional accuracy,
It became a practical sintered porous body with good mechanical strength and excellent chemical resistance.
Claims (3)
セタール樹脂から構成された焼結多孔体。1. A sintered porous body composed of two or more kinds of polyacetal resins having melting points different by 5 ° C. or more.
リアセタール樹脂焼結多孔体。2. The polyacetal resin sintered porous body according to claim 1, which has a porosity of 20 to 80%.
と、(B) (A) のポリアセタール樹脂に対して5℃以上融
点が異なる他のポリアセタール樹脂1種以上、5〜95重
量%とを用い、(A) 、(B) の粉末を混合、あるいは(A)
と(B) を溶融混練した後で粉末とし、焼結成形すること
を特徴とするポリアセタール樹脂焼結多孔体の製造方
法。3. A polyacetal resin (A), 95 to 5% by weight
And (B) one or more other polyacetal resins having different melting points of 5 ° C. or more with respect to the polyacetal resin of (A), 5 to 95% by weight, and mixing the powders of (A) and (B), or (A)
A method for producing a sintered polyacetal resin porous body, which comprises melt-kneading (B) and (B), converting the powder into powder, and sintering the powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5253998A JPH07109375A (en) | 1993-10-12 | 1993-10-12 | Sintered porous polyacetal resin article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5253998A JPH07109375A (en) | 1993-10-12 | 1993-10-12 | Sintered porous polyacetal resin article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07109375A true JPH07109375A (en) | 1995-04-25 |
Family
ID=17258846
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5253998A Pending JPH07109375A (en) | 1993-10-12 | 1993-10-12 | Sintered porous polyacetal resin article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07109375A (en) |
-
1993
- 1993-10-12 JP JP5253998A patent/JPH07109375A/en active Pending
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