JPS60149664A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS60149664A
JPS60149664A JP476084A JP476084A JPS60149664A JP S60149664 A JPS60149664 A JP S60149664A JP 476084 A JP476084 A JP 476084A JP 476084 A JP476084 A JP 476084A JP S60149664 A JPS60149664 A JP S60149664A
Authority
JP
Japan
Prior art keywords
glass
filler
water
resin composition
glasses
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.)
Granted
Application number
JP476084A
Other languages
Japanese (ja)
Other versions
JPH0452302B2 (en
Inventor
Takashi Hashimoto
隆 橋本
Shinji Funayama
船山 真二
Hideo Okawa
秀夫 大川
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.)
Calp Kogyo KK
Original Assignee
Calp Kogyo KK
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 Calp Kogyo KK filed Critical Calp Kogyo KK
Priority to JP476084A priority Critical patent/JPS60149664A/en
Publication of JPS60149664A publication Critical patent/JPS60149664A/en
Publication of JPH0452302B2 publication Critical patent/JPH0452302B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To obtain a resin compsn. which has excellent impact and weld strengths and in which a filler is uniformly dispersed in a thermoplastic resin, by blending a filler having a surface treated with a water-soluble glass or a low- melting glass with a thermoplastic resin. CONSTITUTION:A resin compsn. is obtd. by blending a filler having a surface treated with a water-soluble glass and/or a low-melting glass. As the water-soluble glass, those contg. phosphorus pentoxide, boron oxide and alkali metal oxides are usually used. As the low-melting glass, those having a softening temp. of 500 deg.C or below are usually used. Examples of such glasses are silicate, phosphate and borate glasses. Examples of the fillers are calcium carbonate, talc, woodmeal and carbon black.

Description

【発明の詳細な説明】 本発明は樹脂組成物に関し、詳しくは充填材が熱可塑性
樹脂中に均一に分散しており、衝撃強度。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a resin composition, and more particularly, a filler is uniformly dispersed in a thermoplastic resin, and the composition has high impact strength.

ウェルド強さ等が優れている樹脂組成物に関する。The present invention relates to a resin composition having excellent weld strength and the like.

従来より、炭酸カルシウム、タルク、マイカなどの無機
充填材あるいは木粉、カーボンブラック等の有機充填材
などを合成樹脂に配合した樹脂組成物が知られており、
穏々の用途に巾広く利用されている。これら充填材は通
常、機械的物性等の改善のために加えられるものである
が、炭酸カルシウム、沈降性バリウム等の球状や不定形
のものは粒径が太きいと、樹脂組成物において外力の集
中点となりかえって機械的性質を低下させ、また粒径カ
ー小さすぎるものは、凝集を起こし易く、そのため粒径
の大きいものを用いた場合と同様の結果とな、す、粒径
に制限があった。また、タルク。
Conventionally, resin compositions have been known in which synthetic resins are blended with inorganic fillers such as calcium carbonate, talc, and mica, or organic fillers such as wood flour and carbon black.
It is widely used for mild purposes. These fillers are usually added to improve mechanical properties, etc. However, when spherical or irregularly shaped fillers such as calcium carbonate and precipitated barium have large particle sizes, they are difficult to resist external forces in resin compositions. If the particle size is too small, it will tend to agglomerate, resulting in the same result as using a large particle size. Ta. Also, talc.

マイカ等の扁平状のものは、その形状のため組成物の衝
撃強度、ウェルド強度の低下を招き、さらに混線時に形
状が破壊されやすく、不均質なものとなった。
Flat materials such as mica cause a decrease in the impact strength and weld strength of the composition due to their shape, and furthermore, the shape is easily destroyed when wires are crossed, resulting in non-uniformity.

そこで、本発明者らは熱可塑性樹脂に配合する充填拐の
粒径、形状などに制限なく、分散性が良好省あって、機
械的物性等が優れている樹脂組成物を開発すべく鋭意検
討した結果、特定のガラスにより充填材の表面処理をし
たものを含む樹脂組放物が、目的とする効果を達成でき
ることを見い出し、本発明を完成した。
Therefore, the present inventors have conducted intensive studies to develop a resin composition that has good dispersibility and excellent mechanical properties without any restrictions on the particle size or shape of the filler particles added to the thermoplastic resin. As a result, they discovered that a resin assembly containing a surface-treated filler using a specific glass can achieve the desired effect, and completed the present invention.

すなわち、本発明は水溶性ガラスおよび/また、、4よ
低融点ガラスにより表面処理した充填材を熱可塑性樹脂
に配合してなる樹脂組成物である。
That is, the present invention is a resin composition in which a thermoplastic resin is blended with a filler surface-treated with a water-soluble glass and/or a glass with a lower melting point than 4.

本発明に用いられる熱可塑性樹脂としては特に制限なく
、各種のものを使用できる。例えばポリエチレン、ホリ
フロピレン、アクリロニトリル−ブタジェン−スチレン
樹脂(ABS樹脂)、ナイロン−6やナイロン−6,6
などのポリアミド樹脂。
The thermoplastic resin used in the present invention is not particularly limited, and various types can be used. For example, polyethylene, holiflopyrene, acrylonitrile-butadiene-styrene resin (ABS resin), nylon-6 and nylon-6,6
Polyamide resin such as.

ポリスチレン、ポリエーテル、ポリエチレンテレフタレ
ートやポリブチレンテレフタレートなどのポリエステル
、ポリカーボネート、ポリ塩化ビニル、ポリエーテルス
ルホン、ポリメチルメタアクリレート、ポリオキシメチ
レン、ポリサル7オン。
Polystyrene, polyether, polyester such as polyethylene terephthalate and polybutylene terephthalate, polycarbonate, polyvinyl chloride, polyether sulfone, polymethyl methacrylate, polyoxymethylene, polysal 7one.

ポリ、フェニレンオキサイド、合成ゴム等が挙げられる
Examples include poly, phenylene oxide, synthetic rubber, and the like.

本発明の樹脂組成物は水溶性ガラスおよび/または低融
点ガラスにより表面処理した充填材を含有する。ここで
水溶性ガラスとしては特に制限はないが、通常五酸化リ
ン(PQO,) 、酸化ホウ素(BQ08)およびアル
カリ金属の酸化物(M2O、ここでMはアルカリ金属を
示す。)を含有するものが用いられる。特に各々のモル
比がP* 06 / B 208/M、0 = 40〜
55/6〜9/30〜60のものが好ましい。
The resin composition of the present invention contains a filler whose surface has been treated with water-soluble glass and/or low-melting glass. There are no particular restrictions on the water-soluble glass, but it usually contains phosphorus pentoxide (PQO), boron oxide (BQ08), and alkali metal oxide (M2O, where M represents an alkali metal). is used. In particular, each molar ratio is P*06/B208/M, 0 = 40~
55/6 to 9/30 to 60 is preferred.

次に、低融点ガラスとしては、通常軟化温度が500℃
以下のガラスが用いられる。このようなガラスとしては
例えばケイ酸塩ガラス、リン酸塩ガラス、ホウ酸塩ガラ
ス、ソーダ石灰ガラス、鉛ガラス、バリウムガラス、ゲ
ルマン酸塩ガラス。
Next, as a low melting point glass, the softening temperature is usually 500°C.
The following glasses are used: Such glasses include, for example, silicate glasses, phosphate glasses, borate glasses, soda lime glasses, lead glasses, barium glasses, germanate glasses.

アルミン酸塩ガラス、バナジン酸塩ガラス、亜砒酸塩ガ
ラス、タングステン酸塩ガラス、モリブデン酸塩ガラス
、硫酸塩ガラス、ノ・ロゲン化物ガラス、カルコゲナイ
ドガラスなどがあり、これらを単独で、あるいは組合せ
て用いることができる。
There are aluminate glasses, vanadate glasses, arsenite glasses, tungstate glasses, molybdate glasses, sulfate glasses, norogenide glasses, chalcogenide glasses, etc., and these can be used alone or in combination. I can do it.

また、充填材としては例えば炭酸カルシウム。Further, as a filler, for example, calcium carbonate is used.

タルク、マイカ、沈降性硫酸バリウム、ガラス繊維、シ
リカ、ガラスピーズ、金属粉などの無機充填材およびポ
プラ、モミ、モミジ、ナラなどの木粉やカーボンブラッ
ク等の有機充填材などが挙げられる。これらを単独ある
いは混合して用いることができる。これら充填材の粒径
は通常無機充填材0.5〜30μ、有機充填材325〜
60メツシュ程度である。
Examples include inorganic fillers such as talc, mica, precipitated barium sulfate, glass fiber, silica, glass peas, and metal powder, and organic fillers such as wood powder such as poplar, fir, maple, and oak, and carbon black. These can be used alone or in combination. The particle size of these fillers is usually 0.5 to 30μ for inorganic fillers and 325 to 30μ for organic fillers.
It is about 60 meters.

本発明において、上記充填材を水溶性ガラスおよび/ま
たは低融点ガラスにより、その表面を処理する方法とし
ては、種々の方法を適用することができるが、通常は充
填材と上記ガラスを混合して充填材の表面をガラスによ
りコーティングする方法が好ま【2い。コーティング方
法としては、例えば水溶性ガラスを用いる場合は、水溶
性ガラスの水溶液に充填材を添加し、加熱混合して水分
を蒸発することにより行うことができる。このときの処
理条件は、使用する水溶性ガラス、充填材などKより異
なるが、通常は120〜170℃の温度にて10〜20
分攪拌することにより行なう。
In the present invention, various methods can be applied to treat the surface of the filler with water-soluble glass and/or low-melting glass, but usually, the filler and the glass are mixed. A method in which the surface of the filler is coated with glass is preferred. For example, when using water-soluble glass, the coating method can be carried out by adding a filler to an aqueous solution of water-soluble glass, heating and mixing to evaporate water. The processing conditions at this time vary depending on the water-soluble glass, filler, etc. used, but usually the temperature is 120-170°C and the temperature is 10-20°C.
This is done by stirring for several minutes.

また、低融点ガラスを用いる場合は、充填材と混合して
低融点ガラスの軟化する温度まで加熱。
If low melting point glass is used, it is mixed with filler and heated to a temperature at which the low melting point glass softens.

混練することにより行なうことができる。なお、上記ガ
ラスは充填材に対して1〜20重量%、好ましくは2〜
15重量%の割合で加えればよい。
This can be done by kneading. In addition, the above-mentioned glass accounts for 1 to 20% by weight, preferably 2 to 20% by weight based on the filler.
It may be added at a rate of 15% by weight.

このようにして得られるガラスで表面を処理した充填材
は熱可塑性樹脂と混練した場合、充填材同志の凝集を防
ぎ、充填材の粒径、形状などにかかわらず均一な分散が
可能である。この水溶性ガラスおよび/または低融点ガ
ラスにより表面処理した充填材の配合量は特に制限なく
、樹脂組成物の使用目的などを考慮して決定すればよい
が、通常は10〜60重量%である。
When the filler whose surface has been treated with glass thus obtained is kneaded with a thermoplastic resin, it prevents the fillers from agglomerating together and enables uniform dispersion regardless of the particle size, shape, etc. of the filler. The amount of the filler surface-treated with water-soluble glass and/or low-melting glass is not particularly limited and may be determined by considering the intended use of the resin composition, but is usually 10 to 60% by weight. .

本発明の樹脂組成物には必要によりチタネート系カップ
リング剤を添加することができる。チクネート系カップ
リング剤を添加することによりガラス成分と充填材成分
との密着性が向上し、ガラスによる充填材の表面処理効
果が一層顕著となる。
A titanate coupling agent can be added to the resin composition of the present invention if necessary. By adding the thicnate coupling agent, the adhesion between the glass component and the filler component is improved, and the surface treatment effect of the filler by the glass becomes even more remarkable.

本発明において各成分の混練は通常行なわれている方法
、例えばバンバリーミキサ−1−軸押出機、二軸押出機
等の混練機を用いて行なわれる。
In the present invention, each component is kneaded by a conventional method, for example, using a kneading machine such as a Banbury mixer, a single-screw extruder, or a twin-screw extruder.

混練条件としては、例えば押出機を用いた場合、温度1
90〜230℃、バンバリーミキサ−な用いた場合、温
度190〜230℃で10〜20分間行なう。
For example, when using an extruder, the kneading conditions include a temperature of 1
If a Banbury mixer is used, the temperature is 190-230°C for 10-20 minutes.

次いで、このようにして得られた樹脂組成物をペレット
化し、さらにこのペレットを射出成形。
Next, the resin composition thus obtained is pelletized, and the pellets are then injection molded.

押出成形等の成形手段により適宜形状に成形して各種成
形品を製造することができる。
Various molded products can be manufactured by molding into appropriate shapes using molding means such as extrusion molding.

本発明の樹脂組成物は、ガラスで表面処理をした充填材
を用いているため、使用する充填材の粒径、形状等によ
る影響なしに充填材の凝集を防ぎ均一に分散l−ている
。したがって、この樹脂組成物を用いれば衝撃強度が極
めて優れた成形品が得られる。また、充填材の混純の際
の破壊が防止されるとともに形状による成形品の機械的
強度の低下、特にウェルド強度などの低下も防止される
Since the resin composition of the present invention uses a filler surface-treated with glass, the filler is prevented from agglomerating and is uniformly dispersed without being affected by the particle size, shape, etc. of the filler used. Therefore, by using this resin composition, a molded article with extremely excellent impact strength can be obtained. In addition, destruction during mixing of the filler is prevented, and a decrease in the mechanical strength of the molded product due to its shape, particularly in weld strength, is also prevented.

さらK、本発明の樹脂組成物は、上記のような特定の充
填拐を用いているため、ガラスに起因して剛性、硬さ、
耐熱性等が向上するほか、耐薬品性が非常に優れ、し、
かも成形に際し成形収縮率も小さい。
Furthermore, since the resin composition of the present invention uses the specific filling material as described above, it has low rigidity, hardness, and
In addition to improved heat resistance, it also has very good chemical resistance.
The molding shrinkage rate during molding is also small.

それ故、本発明の樹脂組成物は精密工業部制。Therefore, the resin composition of the present invention is manufactured under the precision industry system.

建材、オフィス機器ハウジング、音響部品2.自動車部
品などの素材として有効に利用することができる。
Building materials, office equipment housings, acoustic components 2. It can be effectively used as a material for automobile parts, etc.

次に、実施例により本発明の詳細な説明する。Next, the present invention will be explained in detail with reference to Examples.

実施例1 炭酸カルシウム30重量部を、水溶性ガラス(Pa5s
 41.2重fg %、N’a20 39.3重量%。
Example 1 30 parts by weight of calcium carbonate was added to water-soluble glass (Pa5s
41.2 fg%, N'a20 39.3% by weight.

Kso 12.5i!−□%、Tl20117.0重量
%)2頂に部の10ii%濃度水溶液に添加し、ヘンシ
ェルミキサーを用いて150℃で約10分間加熱混合し
て可及的に水分を蒸発させ、水溶性ガラスコーティング
炭酸カルシウムを得た。得られた水溶性ガラスコーティ
ング炭酸カルシウムにホモポリプロピレン(出光石油化
学(株)製、[、r−7ooG、J )70重量部を加
えてゲル化し、単軸押出機にて200℃で混練しペレッ
ト化した。次いで、ベレットを射出成形して得られたテ
ストピース(寸法:80X80X3.2mm)の耐薬品
性および機械的物性を評価した。結果は第1表および第
2表に示す。
Kso 12.5i! -□%, Tl20117.0% by weight) 2 to a 10ii% concentration aqueous solution of 20%, and heat-mixed at 150°C for about 10 minutes using a Henschel mixer to evaporate as much water as possible. A coated calcium carbonate was obtained. 70 parts by weight of homopolypropylene (manufactured by Idemitsu Petrochemical Co., Ltd., [, r-7ooG, J) was added to the obtained water-soluble glass-coated calcium carbonate to form a gel, and the mixture was kneaded at 200°C in a single-screw extruder to form pellets. It became. Next, the chemical resistance and mechanical properties of a test piece (dimensions: 80 x 80 x 3.2 mm) obtained by injection molding the pellet were evaluated. The results are shown in Tables 1 and 2.

なお、耐薬品性および物性は以下の如くして評価した。In addition, chemical resistance and physical properties were evaluated as follows.

評価方法 19 耐薬品性 テストピースを10%塩酸水溶液および5%酢酸水溶液
のそれぞれに浸漬し、70 ’Cで1時間沸騰した後、
溶出の有無を評価した。
Evaluation method 19 A chemical resistance test piece was immersed in a 10% hydrochloric acid aqueous solution and a 5% acetic acid aqueous solution, and after boiling at 70'C for 1 hour,
The presence or absence of elution was evaluated.

2、機械的物性 (1)引張強度 ASTM D−638K準拠 (2)曲げ弾性率 ASTM D−790に準拠 (3)アイゾツト衝撃強さ ASTM T)−256に準拠 (4)ロックウェル硬度 ASTM D−785に準拠 (5)熱変形温度 ASTM D−648に準拠 (6)ウェルド保持率 引張強度によるウェルドの有無の比較 (7)分散性 肉厚100μのフィルムをプレス成形し、光透過を目視
にて判断した。
2. Mechanical properties (1) Tensile strength ASTM D-638K compliant (2) Flexural modulus ASTM D-790 compliant (3) Izod impact strength ASTM T)-256 compliant (4) Rockwell hardness ASTM D- 785 (5) Heat distortion temperature ASTM D-648 (6) Weld retention rate Comparison of presence or absence of weld by tensile strength (7) Dispersibility Press-molding a film with a thickness of 100 μm and visually observing light transmission It was judged.

実施例2 実施例1において、水溶性ガラスの水分が80%蒸発し
た際にチタネート系カップリング剤0.3重量部を添加
したこと以外は実施例1と同様にしてテストピースを得
た。このテストピースについての物性測定結果を第2表
に示す。
Example 2 A test piece was obtained in the same manner as in Example 1, except that 0.3 parts by weight of a titanate coupling agent was added when 80% of the water in the water-soluble glass had evaporated. Table 2 shows the physical property measurement results for this test piece.

実施例3〜12および2゜比較例1〜11実施例1にお
いて、各成分の種類、配合量を第2表に示した割合とし
たこと以外は実施例1と同様にしてテストピースを得た
。このテストピースについての測定結果を第1表および
第2表に示す。
Examples 3 to 12 and 2° Comparative Examples 1 to 11 Test pieces were obtained in the same manner as in Example 1, except that the types and amounts of each component were set to the proportions shown in Table 2. . The measurement results for this test piece are shown in Tables 1 and 2.

実施例13 炭酸カルシウム30重量部に対して低融点ガラス3重量
部を添加し、加熱型インターミックスな用い380℃で
約10分間加熱混合し、ガラスフィラーコーティング炭
酸カルシウムを得た。得られたガラスフィラーコーティ
ング炭酸カルシウムにホモポリプロピレン70重量部を
添加し、バンバリーミキサ−を用いて150℃で約20
分間混練した。次に、ロール混練機およびシートペレタ
イザーを用いてペレットを得た。以下、実施例1と同様
にテストピースを得、機械的物性を評価した。結果を第
2表に示す3゜ 第1表 *l・・・添加剤としてチタネートカップリング剤(味
の素(株)製、[K几−TTSJ )をO−3重量%含
む。
Example 13 3 parts by weight of low-melting glass was added to 30 parts by weight of calcium carbonate, and the mixture was heated and mixed at 380° C. for about 10 minutes using a heated intermix to obtain glass filler-coated calcium carbonate. 70 parts by weight of homopolypropylene was added to the obtained glass filler-coated calcium carbonate, and the mixture was heated at 150°C using a Banbury mixer for about 20 parts by weight.
Kneaded for a minute. Next, pellets were obtained using a roll kneader and a sheet pelletizer. Hereinafter, test pieces were obtained in the same manner as in Example 1, and mechanical properties were evaluated. The results are shown in Table 2.3゜Table 1 *l: Contains O-3% by weight of a titanate coupling agent (manufactured by Ajinomoto Co., Ltd., [K-TTSJ)] as an additive.

牢2・・・PP:ホモポリプロピレン(出光石油化学(
株)製、−[J−700GJ ) PE:ポリエチレン(出光石油化学(株)製、[210
、yJ ) ABS:7り!Jロニトリルーブタジエンースチレン樹
脂(宇部ザイコン(株)製、1−BX−150J)*3
・・・QaOO+ ’炭酸カルシウム(金子鉱業(株)
製、[Ks−13ooJ ) タルク:浅田製粉(株)製、[5W−AJ沈降性BaS
O4:沈降性硫酸バリウム(バライト工業(株)製、 
「5TJ) マイカークラレ(株)製、「200KiJ木 粉:マル
イ(株)製、r 150MJガラスファイバー二旭フア
イバー(株)製、[03−MA−486AJ * 4 ・=荷重18.6kg/crrL2で測定した
Cell 2...PP: Homopolypropylene (Idemitsu Petrochemical (
Co., Ltd., -[J-700GJ) PE: Polyethylene (Idemitsu Petrochemical Co., Ltd., [210
,yJ) ABS:7ri! J lonitrile-butadiene-styrene resin (manufactured by Ube Zykon Co., Ltd., 1-BX-150J) *3
...QaOO+ 'Calcium carbonate (Kaneko Mining Co., Ltd.)
Talc: manufactured by Asada Seifun Co., Ltd., [5W-AJ sedimentary BaS
O4: Precipitated barium sulfate (manufactured by Barite Industries Co., Ltd.,
"5TJ) Manufactured by My Car Kuraray Co., Ltd., "200KiJ Wood Powder: Manufactured by Marui Co., Ltd., r 150MJ Glass Fiber Manufactured by Asahi Fiber Co., Ltd., [03-MA-486AJ * 4 = load 18.6kg/crrL2 It was measured.

Claims (1)

【特許請求の範囲】 l)水溶性ガラスおよび/または低融点ガラスにより表
面処理した充填材を熱可塑性樹脂に配合してなる樹脂組
成物。 2)水溶性jj ラスがPQO,、B、O,およびMQ
O(ただし、Mはアルカリ金属を示す。)をそれぞれ4
0〜55モル%、6〜9モル%および30〜60モル%
の割合で含むものである特許請求の範囲第1項記載の樹
脂組成物。 3)低融点ガラスが軟化温度5 ’OO’C以下のもの
である特許請求の範囲第1項記載の樹脂組成物。
[Claims] l) A resin composition comprising a thermoplastic resin and a filler surface-treated with water-soluble glass and/or low-melting glass. 2) Water-soluble jj ras are PQO, B, O, and MQ
4 each of O (where M represents an alkali metal)
0-55 mol%, 6-9 mol% and 30-60 mol%
2. The resin composition according to claim 1, wherein the resin composition comprises: 3) The resin composition according to claim 1, wherein the low melting point glass has a softening temperature of 5'OO'C or less.
JP476084A 1984-01-17 1984-01-17 Resin composition Granted JPS60149664A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP476084A JPS60149664A (en) 1984-01-17 1984-01-17 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP476084A JPS60149664A (en) 1984-01-17 1984-01-17 Resin composition

Publications (2)

Publication Number Publication Date
JPS60149664A true JPS60149664A (en) 1985-08-07
JPH0452302B2 JPH0452302B2 (en) 1992-08-21

Family

ID=11592842

Family Applications (1)

Application Number Title Priority Date Filing Date
JP476084A Granted JPS60149664A (en) 1984-01-17 1984-01-17 Resin composition

Country Status (1)

Country Link
JP (1) JPS60149664A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05177561A (en) * 1991-12-24 1993-07-20 Kaijirushi Hamono Kaihatsu Center:Kk Sharp-edged tool
US5298537A (en) * 1992-04-09 1994-03-29 E. I. Du Pont De Nemours And Company Polyoxymethylene compositions containing at least one encapsulated nucleant
CN102040791A (en) * 2010-10-22 2011-05-04 西安科技大学 Method for preparing organic polymer/silica sound-absorbing thermal insulation material
CN106221007A (en) * 2016-08-12 2016-12-14 苏州柯创电子材料有限公司 A kind of high intensity scraping-resistant polypropylene material of improvement
CN106867066A (en) * 2017-03-13 2017-06-20 阜阳市金木工艺品有限公司 A kind of Antistatic type wood rubber and plastic trielement composite material containing conductive black and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5311537A (en) * 1976-07-20 1978-02-02 Fujitsu Ltd Data processing system adopting virtual storing method
JPS54156048A (en) * 1978-05-31 1979-12-08 Matsushita Electric Works Ltd Synthetic resin molding compound
JPS55142032A (en) * 1979-04-24 1980-11-06 Furukawa Electric Co Ltd:The Aluminum hydroxide filler for rubber or plastic
JPS55157634A (en) * 1979-05-29 1980-12-08 Mitsubishi Petrochem Co Ltd Synthetic resin material having improved light transmission property and heat retaining property
JPS5736157A (en) * 1980-08-14 1982-02-26 Ishihara Sangyo Kaisha Ltd Pigment of titanium dioxide for polymer composition
JPS5752378A (en) * 1980-07-21 1982-03-27 Philips Nv Frequency converter
JPS5830250A (en) * 1981-08-17 1983-02-22 Oki Electric Ind Co Ltd Transmitting system

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5311537A (en) * 1976-07-20 1978-02-02 Fujitsu Ltd Data processing system adopting virtual storing method
JPS54156048A (en) * 1978-05-31 1979-12-08 Matsushita Electric Works Ltd Synthetic resin molding compound
JPS55142032A (en) * 1979-04-24 1980-11-06 Furukawa Electric Co Ltd:The Aluminum hydroxide filler for rubber or plastic
JPS55157634A (en) * 1979-05-29 1980-12-08 Mitsubishi Petrochem Co Ltd Synthetic resin material having improved light transmission property and heat retaining property
JPS5752378A (en) * 1980-07-21 1982-03-27 Philips Nv Frequency converter
JPS5736157A (en) * 1980-08-14 1982-02-26 Ishihara Sangyo Kaisha Ltd Pigment of titanium dioxide for polymer composition
JPS5830250A (en) * 1981-08-17 1983-02-22 Oki Electric Ind Co Ltd Transmitting system

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05177561A (en) * 1991-12-24 1993-07-20 Kaijirushi Hamono Kaihatsu Center:Kk Sharp-edged tool
US5298537A (en) * 1992-04-09 1994-03-29 E. I. Du Pont De Nemours And Company Polyoxymethylene compositions containing at least one encapsulated nucleant
CN102040791A (en) * 2010-10-22 2011-05-04 西安科技大学 Method for preparing organic polymer/silica sound-absorbing thermal insulation material
CN106221007A (en) * 2016-08-12 2016-12-14 苏州柯创电子材料有限公司 A kind of high intensity scraping-resistant polypropylene material of improvement
CN106867066A (en) * 2017-03-13 2017-06-20 阜阳市金木工艺品有限公司 A kind of Antistatic type wood rubber and plastic trielement composite material containing conductive black and preparation method thereof

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