JPH0739515B2 - Matte molding material composition - Google Patents

Matte molding material composition

Info

Publication number
JPH0739515B2
JPH0739515B2 JP61247618A JP24761886A JPH0739515B2 JP H0739515 B2 JPH0739515 B2 JP H0739515B2 JP 61247618 A JP61247618 A JP 61247618A JP 24761886 A JP24761886 A JP 24761886A JP H0739515 B2 JPH0739515 B2 JP H0739515B2
Authority
JP
Japan
Prior art keywords
calcium oxide
molding material
material composition
weight
test piece
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.)
Expired - Lifetime
Application number
JP61247618A
Other languages
Japanese (ja)
Other versions
JPS63101456A (en
Inventor
一郎 山元
正春 篠山
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.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Original Assignee
Dainichiseika Color and Chemicals Mfg 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 Dainichiseika Color and Chemicals Mfg Co Ltd filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Priority to JP61247618A priority Critical patent/JPH0739515B2/en
Publication of JPS63101456A publication Critical patent/JPS63101456A/en
Publication of JPH0739515B2 publication Critical patent/JPH0739515B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はポリエチレン、ポリプロピレンまたはポリスチ
レンからなる熱可塑性樹脂による成形物表面の艶消し効
果を有する艶消し成形材料組成物に係り、特に成形性あ
るいは成形物の物性等を損なわずに成形物表面の艶消し
効果を奏し得る艶消し成形材料組成物に関する。
TECHNICAL FIELD The present invention relates to a matte molding material composition having a matte effect on the surface of a molded article by a thermoplastic resin composed of polyethylene, polypropylene or polystyrene, and particularly to a moldability or The present invention relates to a matte molding material composition capable of producing a matte effect on the surface of a molded product without impairing the physical properties of the molded product.

〔従来の技術〕 熱可塑性樹脂を使用して射出成形、押出し成形等により
成形物を成形する際、成形物の質感を変えたり、重量感
あるいは高級感を出すために、例えばピアノ、エレクト
ーン等の鍵盤あるいはテレビ、OA機器等の成形物表面に
艶消し処理を施すことがある。
[Prior Art] When molding a molded product by injection molding, extrusion molding or the like using a thermoplastic resin, in order to change the texture of the molded product or to give a feeling of weight or luxury, for example, a piano, an electric tone, etc. Matte treatment may be applied to the surface of keyboards, molded products such as televisions and office automation equipment.

上述の艶消し処理として、従来、金型やカレンダーロー
ルの表面にエンボスを掛けて成形物表面に細かい模様を
付ける方法が採用されている。
As the above-mentioned delustering treatment, a method of embossing the surface of a mold or a calendar roll to form a fine pattern on the surface of the molded article has been conventionally used.

また、熱可塑性樹脂に炭酸カルシウム、タルク等の無機
質充填材を混入し、樹脂自体に艶消し効果をもたせる試
みもある。
There has also been an attempt to mix an inorganic filler such as calcium carbonate or talc into a thermoplastic resin so that the resin itself has a matting effect.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

しかし、前者の方法では金型、カレンダーロール等の表
面に模様を彫る費用が高く、また目地の細かい加工が難
しいという欠点がある。
However, the former method has the drawbacks that the cost of engraving a pattern on the surface of a mold, a calendar roll, etc. is high, and that it is difficult to make fine joints.

また、後者の方法では、前述無機質充填材の艶消し効果
が小さいためこの配合率が高くなり、このため、得られ
る成形物の物性、成形性等の低下を招いて実用性に乏し
い。
In the latter method, the matting effect of the above-mentioned inorganic filler is small, so that the blending ratio becomes high, which results in deterioration of the physical properties and moldability of the obtained molded product, resulting in poor practicability.

そこで、本発明者は前述の欠点を改良すべく鋭意研究を
行った結果、艶消し材として特定粒径の酸化カルシウム
粉末を選定することにより少量の配合量で卓越した艶消
し効果を奏し得、このため得られる成形物の物性、成形
性等の低下を招くことなく艶消し効果を達成し得ること
を見出し、本発明を完成するに至った。
Therefore, the present inventor has conducted extensive studies to improve the above-mentioned drawbacks, and by selecting a calcium oxide powder having a specific particle size as a matting material, it is possible to achieve an excellent matting effect with a small amount of compounding, Therefore, they have found that a matting effect can be achieved without deteriorating the physical properties and moldability of the obtained molded product, and completed the present invention.

本発明の目的は成形性あるいは成形物の物性等を損なわ
ずに成形物表面の艶消し効果を奏し得、前述の公知技術
に存する欠点を改良した艶消し成形材料組成物を提供す
ることにある。
An object of the present invention is to provide a matting molding material composition which can exert a matting effect on the surface of a molded product without impairing moldability or physical properties of the molded product, and which has improved the above-mentioned drawbacks in the known art. .

〔問題点を解決するための手段〕[Means for solving problems]

前述の目的を達成するため、本発明によれば、ポリエチ
レン、ポリプロピレンまたはポリスチレンからなる熱可
塑性樹脂に酸化カルシウム粉末を配合してなる艶消し成
形材料組成物において、前記酸化カルシウム粉末は粒径
が300μ以下であって、配合量が0.5〜30重量%であるこ
とを特徴とする。
In order to achieve the above-mentioned object, according to the present invention, in a matting molding material composition comprising a calcium oxide powder mixed with a thermoplastic resin composed of polyethylene, polypropylene or polystyrene, the calcium oxide powder has a particle size of 300μ. It is characterized in that the content is 0.5 to 30% by weight.

本発明に用いられる前述の熱可塑性樹脂はポリエチレ
ン、ポリプロピレンまたはポリスチレンである。
The thermoplastic resin used in the present invention is polyethylene, polypropylene or polystyrene.

また、酸化カルシウムは粒径が300μよりも大きいと粗
大粒子が目立ち、成形物表面が荒れて艶消し効果も小さ
くなり、また、配合量が0.5重量%以下では艶消し効果
が現れず、30重量%以上では得られる成形物の物性なら
びに成形性が低下し、したがって、本発明に適した酸化
カルシウムは粒径300μ以下、好ましくは100μ以下、配
合量0.5乃至30重量%、好ましくは1乃至10重量%であ
る。
When the particle size of calcium oxide is larger than 300μ, coarse particles are conspicuous and the surface of the molded product is roughened, and the matting effect is small, and when the compounding amount is 0.5% by weight or less, the matting effect does not appear and %, The physical properties and moldability of the obtained molded product are deteriorated. Therefore, the calcium oxide suitable for the present invention has a particle size of 300 μ or less, preferably 100 μ or less, and a compounding amount of 0.5 to 30% by weight, preferably 1 to 10% by weight. %.

なお、前述の酸化カルシウムは水との反応性が高いため
にその取り扱い上からシランカップリング剤、油剤、流
動パラフィン等で表面処理されたものが特に好ましい。
Since the above-mentioned calcium oxide has high reactivity with water, it is particularly preferable that the calcium oxide is surface-treated with a silane coupling agent, an oil agent, liquid paraffin or the like in view of its handling.

さらに本発明は前述の酸化カルシウムに加えて公知の着
色剤、安定剤、分散剤等を適当量配合することもでき
る。
Further, in the present invention, known colorants, stabilizers, dispersants and the like can be added in appropriate amounts in addition to the above-mentioned calcium oxide.

上述の本発明組成物は二本ロール等で混和されて射出成
形、押出成形等の成形材料として使用され、表面が艶消
しされた成形物を得る。
The above-mentioned composition of the present invention is mixed with a two-roll mill or the like and used as a molding material for injection molding, extrusion molding or the like to obtain a molded article having a matt surface.

〔作用〕[Action]

上述の本発明成形材料組成物は使用される酸化カルシウ
ムの粒径が300μ以下の小粒子であるため、成形物表面
の荒れを防止するとともに艶消し効果を増大させ、かつ
配合量が0.5乃至30重量%で少量であるため成形性もよ
く、かつ成形物の物性の低下を来たさない。
In the above-mentioned molding material composition of the present invention, since the particle size of calcium oxide used is small particles of 300 μ or less, the roughness of the surface of the molded product is prevented and the matting effect is increased, and the compounding amount is 0.5 to 30. Since it is a small amount by weight, the moldability is good, and the physical properties of the molded product are not deteriorated.

〔実施例〕〔Example〕

以下、本発明を実施例により詳述する。 Hereinafter, the present invention will be described in detail with reference to examples.

実施例−1 (1)高密度ポリエチレン(ハイゼックス2100J三井石
油化学工業株式会社製)に、粉砕され粒径74μ以下(20
0メッシュパス)に調整された酸化カルシウム30重量%
をロール温度180℃の二本ロール上で混和し、シート化
後、角ペレタイザーで角ペレット化した。
Example-1 (1) High-density polyethylene (Hi-Zex 2100J manufactured by Mitsui Petrochemical Industry Co., Ltd.) was crushed to a particle size of 74 μm or less (20
30 wt% calcium oxide adjusted to 0 mesh pass)
Was mixed on two rolls with a roll temperature of 180 ° C., formed into a sheet, and then pelletized into square pellets with a square pelletizer.

(2)つぎに、低密度ポリエチレン(ノバテックLF261
三菱化成株式会社製)にフアーネスブラック(三菱カー
ボン40B三菱化成株式会社製)30重量%を1.7テスト
バンバリーで混練分散し、二本ロールでシート化後角ペ
レタイザーで角ペレットにし、カーボンマスターバッチ
を得た。
(2) Next, low density polyethylene (Novatech LF261
30% by weight of Furness Black (Mitsubishi Carbon # 40B, manufactured by Mitsubishi Kasei Co., Ltd.) is mixed and dispersed in 1.7 test banbury to make a sheet with two rolls and then made into square pellets with a square pelletizer. Got

(3)(1)のペレットに(2)で作成したカーボンマ
スターバッチを2重量%ブレンドし、6.5cm×5cm×0.2c
mの試験片を射出成形により作成した。
(3) Blend 2% by weight of the carbon masterbatch prepared in (2) to the pellet of (1), and measure 6.5cm × 5cm × 0.2c
A test piece of m was prepared by injection molding.

実施例−2 実施例−1の成形用ペレットとして、ハイゼックス2100
Jに実施例−1(1)で得た酸化カルシウム30重量%を
含むペレットを33.33重量%、実施例−1(2)で作成
したカーボンマスターバッチを2重量%ブレンドしたも
のを使う以外は同様にして試験片を得た。
Example-2 As a molding pellet of Example-1, HiZex 2100
Same as J except that 33.33% by weight of pellets containing 30% by weight of calcium oxide obtained in Example-1 (1) and 2% by weight of the carbon masterbatch prepared in Example-1 (2) were blended in J A test piece was obtained.

実施例−3 実施例−2で酸化カルシウムとして、粉砕され、粒径が
300μ以下(50メッシュパス)の酸化カルシウムを使用
する以外は同様にして試験片を得た。
Example-3 In Example-2, as calcium oxide, it was crushed and the particle size was
A test piece was obtained in the same manner except that calcium oxide having a particle size of 300 μ or less (50 mesh pass) was used.

実施例−4 実施例−1、実施例−2のハイゼックス2100Jをポリプ
ロピレン(住友ノーブレンAH−561住友化学株式会社
製)に代えた以外は、実施例−2と同様にして試験片を
得た。
Example-4 A test piece was obtained in the same manner as in Example-2, except that polypropylene (Sumitomo Noblen AH-561 manufactured by Sumitomo Chemical Co., Ltd.) was used instead of Hi-Zex 2100J in Examples-1 and-2.

実施例−5 実施例−1、実施例−2のハイゼックス2100JをHIポリ
スチレン(ダイヤレックスHT−88三菱モンサント化成株
式会社製)に代えた以外は実施例−2と同様にして試験
片を得た。
Example-5 A test piece was obtained in the same manner as in Example-2, except that HI polystyrene (manufactured by Dialex HT-88 Mitsubishi Monsanto Kasei Co., Ltd.) was used instead of Hi-Zex 2100J in Example-1 and Example-2. .

実施例−6 実施例−2の実施例−1(1)で得たペレットを10重量
%にする以外は、同様にして試験片を得た。
Example-6 A test piece was obtained in the same manner as in Example-2 except that the pellet obtained in Example-1 (1) was changed to 10% by weight.

実施例−7 実施例−2の実施例−1(1)で得たペレットを2重量
%にする以外は、同様にして試験片を得た。
Example-7 A test piece was obtained in the same manner as in Example-2, except that the amount of the pellet obtained in Example-1 (1) was 2% by weight.

比較例−1 ハイゼックス2100Jに実施例−1(2)で作成したカー
ボンマスターバッチを2重量%ブレンドし、射出成形に
より試験片を得た。
Comparative Example-1 Hi-Zex 2100J was blended with 2% by weight of the carbon masterbatch prepared in Example-1 (2), and a test piece was obtained by injection molding.

比較例−2 比較例−1でハイゼックス2100Jを住友ノーブレンAH−5
61に代えた以外は同様にして試験片を得た。
Comparative Example-2 In Comparative Example-1, HiZex 2100J was added to Sumitomo Noblen AH-5.
A test piece was obtained in the same manner except that 61 was replaced.

比較例−3 比較例−1でハイゼックス2100JをダイヤレックスHT−8
8に代えた以外は同様にして試験片を得た。
Comparative Example-3 Hi-Zex 2100J was used in Comparative Example-1 and Dialex HT-8
A test piece was obtained in the same manner except that it was replaced with 8.

比較例−4 比較例−1でハイゼックス2100JをクララスチックSHFに
代えた以外は同様にして試験片を得た。
Comparative Example-4 A test piece was obtained in the same manner as in Comparative Example-1, except that Hi-Zex 2100J was replaced with Clarastic SHF.

比較例−5 実施例−2の実施例−1(1)で得たペレットを1%に
する以外は同様にして試験片を得た。
Comparative Example-5 A test piece was obtained in the same manner as in Example-2 except that the pellet obtained in Example-1 (1) was changed to 1%.

比較例−6 実施例−2で酸化カルシウムとして粉砕され粒径が300
μ以上(50メッシュオン)ある酸化カルシウムを使用す
る以外は同様にして試験片を得た。
Comparative Example-6 In Example-2, calcium oxide was pulverized to give a particle size of 300.
A test piece was obtained in the same manner except that calcium oxide having a size of μ or more (50 mesh on) was used.

比較例−7 実施例−2で酸化カルシウムの代わりに炭酸カルシウム
(ママカルソ日東粉化工業株式会社製)を使用する以外
は同様にして試験片を得た。
Comparative Example-7 A test piece was obtained in the same manner as in Example-2 except that calcium carbonate (Mamacarso Nitto Koka Kogyo Co., Ltd.) was used instead of calcium oxide.

比較例−8 実施例−2で酸化カルシウムの代わりにタルク(タルク
MS白石カルシウム工業株式会社製)を使用する以外は同
様にして試験片を得た。
Comparative Example-8 In Example-2, talc (talc) was used instead of calcium oxide.
A test piece was obtained in the same manner except that MS Shiraishi Calcium Industry Co., Ltd.) was used.

以上の試験片に対し、光源(螢光灯)の写り具合(写
像)および光沢の有無を目視で5段階に評価した。
With respect to the above test pieces, the appearance (image) of the light source (fluorescent lamp) and the presence / absence of gloss were visually evaluated in five levels.

結果を表−1に示す。The results are shown in Table-1.

表−1より酸化カルシウムが本発明の特定粒径以下であ
れば、成形物の外観を損なわず、低配合量で艶消し効果
を出す事がわかる。また、他のフィラーに比較しても卓
越しておりその特徴は明らかである。
It can be seen from Table 1 that if the calcium oxide has a specific particle size of the present invention or less, the appearance of the molded article is not impaired and a matting effect is obtained with a low compounding amount. It is also superior to other fillers and its characteristics are clear.

また、上述の実施例において、いずれも成形性がよく、
また得られた試料の物性低下はみられなかった。
In addition, in the above-mentioned examples, all have good moldability,
The physical properties of the obtained sample were not deteriorated.

〔効果〕〔effect〕

以上のとおり、本発明成形材料組成物は粒径300μ以下
の酸化カルシウム粉末を特定の少量使用したから、成形
性がよく、艶消し効果に優れ、かつ物性の低下を来さな
かった。
As described above, since the molding material composition of the present invention uses a specific small amount of calcium oxide powder having a particle size of 300 μ or less, the moldability is good, the matting effect is excellent, and the physical properties are not deteriorated.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】ポリエチレン、ポリプロピレンまたはポリ
スチレンからなる熱可塑性樹脂に酸化カルシウム粉末を
配合してなる艶消し成形材料組成物において、前記酸化
カルシウム粉末は粒径が300μ以下であって、配合量が
0.5〜30重量%であることを特徴とする艶消し成形材料
組成物。
1. A matting molding material composition comprising a thermoplastic resin made of polyethylene, polypropylene or polystyrene, and calcium oxide powder blended therein, wherein the calcium oxide powder has a particle size of 300 μm or less and a blending amount of
Matting molding material composition, characterized in that it is 0.5 to 30% by weight.
JP61247618A 1986-10-20 1986-10-20 Matte molding material composition Expired - Lifetime JPH0739515B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61247618A JPH0739515B2 (en) 1986-10-20 1986-10-20 Matte molding material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61247618A JPH0739515B2 (en) 1986-10-20 1986-10-20 Matte molding material composition

Publications (2)

Publication Number Publication Date
JPS63101456A JPS63101456A (en) 1988-05-06
JPH0739515B2 true JPH0739515B2 (en) 1995-05-01

Family

ID=17166187

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61247618A Expired - Lifetime JPH0739515B2 (en) 1986-10-20 1986-10-20 Matte molding material composition

Country Status (1)

Country Link
JP (1) JPH0739515B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2661184A1 (en) * 1990-04-19 1991-10-25 Borg Warner Chemical Europ Bv MOLDING COMPOSITIONS BASED ON AROMATIC POLYCARBONATE RESIN, ABS POLYMERIZATION AND SAN COPOLYMER HAVING MATERIAL SURFACE ASPECT.
NL193889C (en) * 1993-08-31 2001-01-03 Samsung Display Devices Co Ltd Image display device provided with far-infrared emitting material or medium.
JP5279184B2 (en) * 2006-12-19 2013-09-04 アイカ工業株式会社 Coating material composition

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5911627B2 (en) * 1976-04-01 1984-03-16 チッソ株式会社 Surface treated inorganic powder and its manufacturing method
JPS5331755A (en) * 1976-09-06 1978-03-25 Toray Ind Inc Delusterd polyester film
JPS60197713A (en) * 1984-01-23 1985-10-07 Japan Synthetic Rubber Co Ltd Thermoplastic resin composition

Also Published As

Publication number Publication date
JPS63101456A (en) 1988-05-06

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