JPS59164345A - Resin composition containing ultrafine silicic acid powder - Google Patents

Resin composition containing ultrafine silicic acid powder

Info

Publication number
JPS59164345A
JPS59164345A JP3862783A JP3862783A JPS59164345A JP S59164345 A JPS59164345 A JP S59164345A JP 3862783 A JP3862783 A JP 3862783A JP 3862783 A JP3862783 A JP 3862783A JP S59164345 A JPS59164345 A JP S59164345A
Authority
JP
Japan
Prior art keywords
silicic acid
acid powder
resin composition
composition containing
ultrafine silicic
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
JP3862783A
Other languages
Japanese (ja)
Other versions
JPH041016B2 (en
Inventor
Akira Yamamoto
晃 山本
Misao Miyamoto
操 宮本
Tomomitsu Kawasaki
川崎 智充
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP3862783A priority Critical patent/JPS59164345A/en
Publication of JPS59164345A publication Critical patent/JPS59164345A/en
Publication of JPH041016B2 publication Critical patent/JPH041016B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the titled compsn. having excellent light-diffusing ability and moldability, by incorporating a specified ultrafine silicic acid powder. CONSTITUTION:0.3-3.0phr of ultrafine silicic acid powder having an average particle size of 1-20mu, oil absorption of 30-70ml/100g and a sedimentation volume of 8-13ml/5g is blended with a thermoplastic resin such as PVC.

Description

【発明の詳細な説明】 本発明は熱可塑性プラスチックに対し、特殊な粉体特性
を有する超微粉末珪酸を併用する組成物に関するもので
あり、主な目的は、成形加工性の改良及び透明プラスチ
ックの場合は更に。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition in which ultrafine powdered silicic acid having special powder characteristics is used in combination with thermoplastics, and the main purpose is to improve moldability and to improve transparent plastics. Even more so in the case of .

光拡散性の付与である。従来、とうした目的には炭酸カ
ル7ウム(!特開昭57−155245号)や、炭酸カ
ルシウムと水酸化アルミニウムとの併用(特開昭j7−
162743号)等が公知の事実として知られている。
This is to impart light diffusivity. Conventionally, for this purpose, calcium carbonate (Japanese Patent Application Laid-Open No. 155245/1983) or a combination of calcium carbonate and aluminum hydroxide (Japanese Patent Application Laid-Open No. 1983-155245) have been used.
No. 162743) etc. are known facts.

然し、此等は単に、光拡散性を有しているのみに過ぎな
いが。
However, these materials merely have light diffusing properties.

本発明して於て使用する超微粉末珪酸は此等よシも光拡
散性がダれているのみならず、成形加工性の改良効果も
あり、経済性に於ても有利性が発揮されるので9本発明
を完成させるに至った。
The ultrafine powdered silicic acid used in the present invention not only has poor light diffusivity, but also has the effect of improving moldability, and is also economically advantageous. Therefore, the present invention was completed.

本発明に於て(併用する超微粉末珪酸Cj、コロイド状
シリカ〔スノーテックス(商品名);日産化学工業(件
)〕全乾乾、・■して製造したものでを)るが。
In the present invention, ultrafine powdered silicic acid Cj and colloidal silica (Snowtex (trade name); Nissan Chemical Industries, Ltd.) are completely dried and produced by (1).

更に他のプラスチック等で表面処理したものも。Furthermore, there are also those whose surface has been treated with other plastics, etc.

勿論、適用j〕J能である。此のN((微粉末珪酸の粉
体特性は、まず吸油針が、一般的な無機充填剤が200
d!7’100!7以上?示すのに対して、60〜7o
mL7+ o o yと小さく、更に、沈降容積が前者
の20〜80rnシ57に対して、8〜1リシ57と小
さい点が特徴である。此等の数値は微粉末珪酸の表面状
態及び形状を示すが、結論的には、ボイドの少ない比較
的球状に近い粉体であること全意味している。更に平均
粒径が1〜20μと粒度分布が非常にシャープな点も特
徴であり、此擲が相俟って神々の効果を発揮するものと
推定される。また、上述の平均粒径が1〜20μ、吸油
量力50−70 ”/ I 00 S’ 、沈I・l容
IN′1が8〜ヤ噂me、/ 5 Si’の条件のずれ
た物性をもつ)17シ粉末珪酸を用いた場合は、理由は
明確ではないが、光拡散性、散乱光誘過率、平行光線透
過率などの光学的Vt′J!6.に欠点が表われる。
Of course, it is applicable. This N
d! 7'100! More than 7? 60 to 7 o
It is characterized by a small sedimentation volume of 8 to 1 mL, 57, compared to the former's 20 to 80 mL, 57. These numerical values indicate the surface condition and shape of the fine powdered silicic acid, but in conclusion, they all mean that the powder is relatively spherical with few voids. Furthermore, it is characterized by a very sharp particle size distribution with an average particle diameter of 1 to 20 μm, and it is presumed that this combination of grinding produces a divine effect. In addition, the physical properties of the above-mentioned average particle size of 1 to 20μ, oil absorption power of 50-70"/I00S', sedimentation I.l volume IN'1 of 8 to 2000m, /5Si' When powdered silicic acid is used, for reasons that are not clear, defects appear in optical Vt'J!6. such as light diffusivity, scattered light permittivity, and parallel light transmittance.

此の超微動床珪酸の熱可塑性プラスチックに対する添加
量は0.3〜5.0 phrが好適である。その年が0
.5 phrより少量では成形加工性の改良効果及び光
拡散性のトj与効果が発ji1fされ稚く。
The amount of this ultrafinely agitated silicic acid added to the thermoplastic plastic is preferably 0.3 to 5.0 phr. The year is 0
.. If the amount is less than 5 phr, the effect of improving molding processability and the effect of imparting light diffusivity will be produced and will be poor.

一方、?+phrより多量になると1機械9勿性への悪
影響や透明性の完全喪失等欠点が強くなってしまう。
on the other hand,? If the amount exceeds +phr, disadvantages such as adverse effects on the quality of one machine and complete loss of transparency will become stronger.

本発明に於て9光拡散性を付与させる場合には。9 In the case of imparting light diffusivity in the present invention.

熱可塑性プラスチックの種類は透明性を有−するものに
限定されるが、こうした目的に曲用されるプラスチック
の1重類としては、ポリj篇化ビニル、ボリスヂレン、
ポリ(メタ)アクリル酸エステル、  −−1ポリカー
ボネート、ポリエステル、エボキ71等の単独重合体又
は他の成分との共重合樹脂が挙げられる。
The types of thermoplastic plastics are limited to those that have transparency, but the single class of plastics used for these purposes include polyvinyl vinyl, borisdylene,
Examples include homopolymers such as poly(meth)acrylic acid ester, --1 polycarbonate, polyester, and EBOKI 71, or copolymer resins with other components.

此の場合、成形品の形状は押出又はカレンダー成形に依
るフィルム、ソート類のみならず、射出成形、ブロー成
形、注入、カ1[下成形等に依り揮々の形状に適用する
ことが可能である。
In this case, the shape of the molded product can be applied not only to films and sorting by extrusion or calendar molding, but also to various shapes by injection molding, blow molding, injection, molding, etc. be.

以下、実施ρ(]に於て本発明の詳細な説明を行うが、
物性値の測定には下記の評価方法を用いた。
Hereinafter, the present invention will be explained in detail in the implementation ρ().
The following evaluation method was used to measure the physical property values.

(1)光、学的性質;ロール、プレス法で作成した肉j
9.2 mmの試料’lr−AEITM−D−1003
に準じて測定を行った。
(1) Optical and scientific properties: Meat made by roll and press methods
9.2 mm sample 'lr-AEITM-D-1003
Measurements were made according to.

■光拡散性;20wの螢光灯ランプ形状が見えなくなる
距#tで表わした。
(2) Light diffusivity: expressed as the distance #t at which the shape of a 20W fluorescent lamp becomes invisible.

(り溶融粘性;高(ヒ式フローデスク−を用い。(Melt viscosity; high (using a flow desk).

荷重;j50KF/、オリフィスは i mtnφx t []mm、/ 全1吏用して測定
した。
Load: j50KF/, orifice: i mtnφx t [] mm, / A total of 1 orifice was used for measurement.

■平均粒径;コールクーカウンター法 ■吸  油  量;  、TIS K5jOf■沈降容
積;試料52をメスシリンダー中に静かに滴下させて容
攬測定金行 う。
■Average particle size; Coal-coup counter method ■Oil absorption amount;

実施例−1及び比較例−1 塩fヒビニル樹脂11NVC(平均取合度fま700)
100部に対しテ、錫系安定剤(N−200(17)2
部、ステアリルアルコール(カルコール16)03部及
び各種充填剤ケ表−1に従って添加し。
Example-1 and Comparative Example-1 Salt f-hibinyl resin 11 NVC (average degree of absorption f 700)
Te, tin-based stabilizer (N-200(17)2) per 100 parts
1 part, 3 parts of stearyl alcohol (Calcol 16) and various fillers according to Table 1.

充分扛ソ拌混合した層表面温度160℃のロールで6分
間混舛して肉厚約o5゛このロール7−1・を作成した
The mixture was thoroughly stirred and mixed for 6 minutes on a roll with a surface temperature of 160°C to produce a roll 7-1 with a wall thickness of about 5 mm.

次いで、此のロール7−トを定寸法に切断して。Next, this roll 7-t was cut into a fixed size.

スペ−づ一内にれ゛を重ね、180℃にナツトされたプ
レスで6分間、加圧成形して、函厚2 mmのプレス板
を成形し7た。此所で成形したプレス板に就いて、光拡
散性及び光学的性質をjllJ定り、&0結果は表−1
に示すノ1ハりであるが9本発明ν咀成物は光拡散性を
有する上に、全光線透過率(Tt)の値が大きく、目+
’14とする効果を発揮している。
The sheets were stacked in a spacer and pressed for 6 minutes in a press set at 180°C to form a press plate with a box thickness of 2 mm. The light diffusivity and optical properties of the press plate molded here are determined by JLLJ, and the &0 results are shown in Table 1.
However, the ν chewy composition of the present invention not only has light diffusing properties but also has a large value of total light transmittance (Tt), and is good for the eyes.
'14 is proving effective.

一方、比較例で)1]いた充填剤は光拡散性を発(1(
し得なかρたり、全光線透過率(Tt)が7oチ以′ 
 下と小さな[直(〜か示し得ながった。
On the other hand, the filler with )1] in the comparative example exhibits light diffusing properties (1(
If the total light transmittance (Tt) is 7° or more,
Below and a small [direct (~ or could not be shown.

374 実ノイN<++−2及び比較例−2 ボリスヂレンP S (メルトフローレート;751i
//10分)100部に対し、各種充」1°へ剤全表−
2に従−)て添加し、実施例−1と同様に、100℃の
ロールで混練してシート金作成した。此のロールジート
ラ用いて180℃のプレスで7JO圧成形l〜て肉厚2
 mmのプレス板を作成、実施例−1と同様に光拡散性
及び、光学的性質を測定した。結果は表−2に示す通り
であるが9本発明組成物は全光線祷過率(Tt)の値が
大きい上に。
374 Real Noi N<++-2 and Comparative Example-2 Borisdylene P S (melt flow rate; 751i
// 10 minutes) For 100 parts, add various ingredients to 1 degree.
2) and kneaded with a roll at 100° C. in the same manner as in Example 1 to produce a sheet metal. Using this Roll Geetler, press at 180℃ to 7JO pressure molding l ~ wall thickness 2
A press plate of mm in diameter was prepared, and its light diffusivity and optical properties were measured in the same manner as in Example-1. The results are shown in Table 2.9 The composition of the present invention not only had a large value of total light penetration rate (Tt).

光拡散性がある。然し、比較例の組成物では此等の性能
を満足させるものは得られなかった。
Has light diffusing properties. However, the composition of the comparative example could not satisfy these performance requirements.

実施例−3及び比較例−3 PVO(Pm2O3)100部に対して、錫系安定剤(
N−2000K)2部、ステアリルアルコール(カルコ
ールs 6)0.3 FL 及U各種充填剤を表−6に
従って添加し、160℃のロールで3分間混線(〜た后
、粉砕して溶融粘度測定用の試料とした。溶融粘性は表
−6に示す通りで2本発明組成物は何れも充填剤を併用
しない系よりも溶1.411!粘度が低く、易加工性て
あった。
Example-3 and Comparative Example-3 To 100 parts of PVO (Pm2O3), tin-based stabilizer (
Add 2 parts of N-2000K), 0.3 FL of stearyl alcohol (Calcol S 6) and various fillers according to Table 6, mix with a roll at 160°C for 3 minutes, then crush and measure the melt viscosity. The melt viscosity was as shown in Table 6, and both of the two compositions of the present invention had a lower melt viscosity of 1.411! than the system without a filler, and were easier to process.

一方比較例は何れもその改良効果が本発明組成物のl/
ベルに至らなかった。
On the other hand, in all of the comparative examples, the improvement effect was that of the composition of the present invention.
It didn't reach the bell.

丁続補正書 昭和58年 11”Isg口 特許庁長官若杉和夫殿 1 事件の表示 昭和58年特許願第:38627号 2 発明の名称 超微粉末珪酸を含有する樹脂組成物 3  ?ili正をする者 4 補正の対象 明細書の発明の詳細な説明の欄 5 補正の内容 “ (190℃、’c、p、)Jに補正する。Letter of amendment 1981 11” Isg mouth Mr. Kazuo Wakasugi, Commissioner of the Patent Office 1 Display of incident 1981 Patent Application No.: 38627 2 Name of the invention Resin composition containing ultrafine powdered silicic acid 3? ili person who corrects 4 Target of correction Detailed description of the invention in the specification 5 Contents of amendment “ Corrected to (190°C, 'c, p,)J.

Claims (1)

【特許請求の範囲】[Claims] 平均粒径が1〜20μ、吸油針が30〜70“乏100
S’、沈降容積が8〜15屑り52の超()1文粉末珪
酸を03〜3. Ophr含有することk Q♀徴とす
る。熱可塑性プラスチック組成物。
Average particle size is 1~20μ, oil absorbing needle is 30~70"100"
S', sedimentation volume of 8-15 debris 52 super () 1 sentence powder silicic acid 03-3. Containing Ophr is a Q♀ symptom. Thermoplastic composition.
JP3862783A 1983-03-09 1983-03-09 Resin composition containing ultrafine silicic acid powder Granted JPS59164345A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3862783A JPS59164345A (en) 1983-03-09 1983-03-09 Resin composition containing ultrafine silicic acid powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3862783A JPS59164345A (en) 1983-03-09 1983-03-09 Resin composition containing ultrafine silicic acid powder

Publications (2)

Publication Number Publication Date
JPS59164345A true JPS59164345A (en) 1984-09-17
JPH041016B2 JPH041016B2 (en) 1992-01-09

Family

ID=12530473

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3862783A Granted JPS59164345A (en) 1983-03-09 1983-03-09 Resin composition containing ultrafine silicic acid powder

Country Status (1)

Country Link
JP (1) JPS59164345A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60139758A (en) * 1983-12-28 1985-07-24 Mitsubishi Rayon Co Ltd Light-diffusing plastic
JPS62243623A (en) * 1986-04-16 1987-10-24 Denki Kagaku Kogyo Kk Drawn sheet of styrene resin
US5089554A (en) * 1985-09-13 1992-02-18 Rhone-Poulenc Chimie De Base Silica reinforced elastomers
JP2005132983A (en) * 2003-10-31 2005-05-26 Denki Kagaku Kogyo Kk Styrene-based resin composition and molded product thereof
CN112724567A (en) * 2020-12-21 2021-04-30 常州顺唯尔材料科技有限公司 Heat-resistant light diffusion plate and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60139758A (en) * 1983-12-28 1985-07-24 Mitsubishi Rayon Co Ltd Light-diffusing plastic
US5089554A (en) * 1985-09-13 1992-02-18 Rhone-Poulenc Chimie De Base Silica reinforced elastomers
JPS62243623A (en) * 1986-04-16 1987-10-24 Denki Kagaku Kogyo Kk Drawn sheet of styrene resin
JPH06856B2 (en) * 1986-04-16 1994-01-05 電気化学工業株式会社 Styrenic resin stretch sheet
JP2005132983A (en) * 2003-10-31 2005-05-26 Denki Kagaku Kogyo Kk Styrene-based resin composition and molded product thereof
JP4610881B2 (en) * 2003-10-31 2011-01-12 電気化学工業株式会社 Styrenic resin composition and molded body thereof
CN112724567A (en) * 2020-12-21 2021-04-30 常州顺唯尔材料科技有限公司 Heat-resistant light diffusion plate and preparation method thereof

Also Published As

Publication number Publication date
JPH041016B2 (en) 1992-01-09

Similar Documents

Publication Publication Date Title
CN107163537B (en) A kind of clear scratch-resistant anti-electrostatic fire retardant polycarbonate composite material
JPH0790167A (en) Light-diffusing resin composition
JPS59164345A (en) Resin composition containing ultrafine silicic acid powder
GB2147001A (en) Filled thermoplastics
JPH08198976A (en) Light-diffusive methacrylic resin plate
WO2016158943A1 (en) Filler composition and polyolefin resin composition
JP6850559B2 (en) Thermoplastic resin composition
JP3613990B2 (en) Thermoplastic resin composition and molded body
JPS58189215A (en) Artificial marble having transparent feeling
JPH0632973A (en) Light-scattering polycarbonate resin composition
JP2013221084A (en) Film
JP2017078122A (en) Thermally conductive filler and transparent thermally conductive resin composition
JPH0258297B2 (en)
JP2009280693A (en) Glass-containing film and sheet
JPS61275344A (en) Light-diffusing vinylidene fluoride resin composition
JPS60186554A (en) Vinyl chloride resin composition
JP3447156B2 (en) Polycarbonate resin composition
JP2016125029A (en) Vinylidene fluoride resin composition and molded article of the same
JP3032730B2 (en) Polyester resin composition
JP3608392B2 (en) Polyester resin composition and molded article thereof
JPH07100985A (en) Photodiffusive laminated resin plate
JPS6357660A (en) Semitranslucent resin composition
JP3046412B2 (en) Resin composition
JP3940606B2 (en) Heat ray shielding daylight
JPH0931288A (en) Optodiffusive methacrylic resin composition and sheetlike product therefrom