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JPS5817135A - Modification of low-density polyethylene resin - Google Patents

Modification of low-density polyethylene resin

Info

Publication number
JPS5817135A
JPS5817135A JP11627481A JP11627481A JPS5817135A JP S5817135 A JPS5817135 A JP S5817135A JP 11627481 A JP11627481 A JP 11627481A JP 11627481 A JP11627481 A JP 11627481A JP S5817135 A JPS5817135 A JP S5817135A
Authority
JP
Japan
Prior art keywords
low
density polyethylene
polyethylene resin
nucleating agent
sorbitol
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
JP11627481A
Other languages
Japanese (ja)
Other versions
JPS616091B2 (en
Inventor
Toshiaki Kobayashi
稔明 小林
Masafumi Yoshimura
雅史 吉村
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.)
New Japan Chemical Co Ltd
Original Assignee
New Japan Chemical 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 New Japan Chemical Co Ltd filed Critical New Japan Chemical Co Ltd
Priority to JP11627481A priority Critical patent/JPS5817135A/en
Publication of JPS5817135A publication Critical patent/JPS5817135A/en
Publication of JPS616091B2 publication Critical patent/JPS616091B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To improve transparency, surface gloss, molding speed, etc. of moldings without causing faults such as bleedout, etc., by blending a specified sorbitol derivative as a nucleating agent with a low-density polyethylene resin. CONSTITUTION:0.03-3wt% compd. of the formula (wherein X is halogen, 1- 3C lower alkyl; n is 1-3 when X is halogen and n is 2-5 when X is lower alkyl; p is 0-1) as a nucleating agent is blended with (linear) low-density polyethylene to modify the same. The compd. of the formula can be obtd. by condensing sorbitol or xylitol with a substd. benzaldehyde. Examples of the compd. of the formula are di(2,4-dimethylbenzylidene) sorbitol and di(p-chlorobenzylidene)sorbitol.

Description

【発明の詳細な説明】 本発IjlFl低密度ポリエチレン系樹脂、詳しくは鐘
状低密度ポリエチレシもしくは低書度ポリエチレシに核
剤を配合して、2等樹脂成形物O透明性、表両光沢、成
形スピード等を改善する方法に関する。       
 ・ 従来よ)低書度ポリエチレン系樹脂の透明性部の改善に
、核剤例えばジペンジリダンソルピトール又はメチル置
換ジベンジリデシソルピトールO添加が有効であること
は知られている(41公昭45−22008%、021
1023190号)。
Detailed Description of the Invention: A nucleating agent is blended with the IjlFl low-density polyethylene resin of the present invention, specifically, a bell-shaped low-density polyethylene resin or a low-texture polyethylene resin, to obtain a second grade resin molded product with transparency, gloss on both surfaces, and molding. Concerning how to improve speed etc.
・It is known that addition of a nucleating agent such as dipendylidan solpitol or methyl-substituted dibenzylidesi solpitol O is effective for improving the transparency of low-visibility polyethylene resins (41 Kosho 45-22008%, 021
No. 1023190).

しかしながら従来全知の核剤における透明性改善効果を
初めとする各種効果はi改善される余地がある。ま九メ
チル置換ジベシジ゛リヅンソルピトール社、優れえ改善
効果を奏す箒が、低密度ポリエチレン系樹脂への配合に
当シブリードアウトしゃすい欠点が娶る。
However, there is room for improvement in the various effects of conventional nucleating agents, including the effect of improving transparency. Although nine methyl-substituted dibecidiliden salts have excellent improvement effects, they are incorporated into low-density polyethylene resins and suffer from the drawbacks of sibly lead-out.

本発明者らは、上記公知の核剤に比し一層有効な改質効
果を奏し得しかもブリードアウト等の欠点を解消する新
しい核剤につき種々研究を重ねえ。
The present inventors have conducted various studies on a new nucleating agent that can exhibit a more effective modification effect than the above-mentioned known nucleating agent and eliminate drawbacks such as bleed-out.

その結果下記一般式(DK示す化合物が低密度ポリエチ
レンに対して核剤として極めて優れ九作用を発揮すると
共に、この作用は線状低密度ポリエチレンに対しても同
様に発揮されることを見い出し、ζζに本発明を完成す
るに至った。
As a result, we discovered that a compound represented by the following general formula (DK) exhibits an extremely excellent nucleating effect on low-density polyethylene, and that this effect is also exhibited in the same way on linear low-density polyethylene. The present invention was finally completed.

即ち本発明は、線状低密度ポリエチレシもしく紘低書−
ポリエチレンに、一般式 〔式中Xはへ〇ゲン原子又は辰素数1−io低級アル中
ル基・を示し、亀はXがハロゲシ原子の場合t−Sの整
数を、またXが低級アル中ル基の場合2−5の整数を示
す。2社0又#iiを示す。〕で表わされる化合物を配
合することを特徴とする低密度ポリエチレン系樹脂の改
質方法に係る。
That is, the present invention is directed to linear low-density polyethylene resin or
For polyethylene, the general formula [wherein X represents a hexagen atom or a 1-io lower alkyl group], when X is a halogen atom, the tortoise represents an integer of t-S, and X represents a lower alkyl group indicates an integer between 2 and 5. 2 companies 0 and #ii are shown. The present invention relates to a method for modifying a low-density polyethylene resin, which comprises blending a compound represented by the following.

本実′@によれば低密度ポリIチレシ系樹脂成形物O製
造に蟲り、従来用いられ先例(1%/−h上記一般式C
I)で表わされる特定の化金物を配合するととに基づい
て、該化合物が、線状低密度ポリエチレンもしくは低密
度ポリエチレ2/に対し核剤として機能し、原着な透明
性、表面光沢等の改善効果、成形速度の短縮効果等を発
揮すると共に、ブリードアウト等O欠点を生じることな
く、かくして極めで優れえ緒特性を具備する樹脂が収得
される。
According to Honji'@, the manufacturing process of low-density poly-I resin molded products O is based on the conventionally used precedent (1%/-h of the above general formula C).
Based on the fact that the specific metal compound represented by I) is blended, the compound functions as a nucleating agent for linear low density polyethylene or low density polyethylene 2/, and improves the original transparency, surface gloss, etc. In this way, a resin is obtained which exhibits an improvement effect, an effect of shortening the molding speed, etc., and has extremely excellent elastic properties without causing defects such as bleed-out.

本発明に用いる上記一般式(I)で表わされる化合物中
、Xで定義されるへ〇ゲン原子としては、塩素、臭素、
沃素又社弗素原子を、炭素数1−50低級アル中ル基と
してはメチル、エチル、プロビル又はイソプロビル基が
夫々包含される。α)。
In the compound represented by the above general formula (I) used in the present invention, the hegen atom defined by X includes chlorine, bromine,
Examples of the iodine or fluorine atom and lower alkyl groups having 1 to 5 carbon atoms include methyl, ethyl, propyl, and isopropyl groups, respectively. α).

で示される好ましい置換基としては例えばジエチル、ジ
エチル、トリメチル、ペンタメチル、トラエチル、り0
0、ジグ00.プot、フル1ロ基吟を例示できる。上
記一般式(I)の化合物状、ツルじトール又は中シリト
ールと上記置換基を有する置換ベンズアルダしド類とを
常法に従い縮合反応させるととによ〉容易Kll造でき
る。
Preferred substituents represented by are, for example, diethyl, diethyl, trimethyl, pentamethyl, traethyl,
0, jig 00. Examples include ``Pot'' and ``Full 1 Rokigin''. It can be easily prepared by condensing the compound of general formula (I), turditol or medium silitol, with a substituted benzaldoxide having the above substituent group in accordance with a conventional method.

上記化合物を配合して本発明所期の効果を奏し得る・低
密度ポリエチレシ系樹脂に社、1度が約0−94t/−
以下のエチレンコポリマー又はエチレシ含量5011以
上のエチレンコポリマーが包含される。上記コポリマー
を構成し得るコ亡ツマー社エチレシと共重合し得る各種
のものをいずれも使用できる。代表的コポリマーとして
はx9しン/酢酸ビニi、エチレン/メタクリレート、
エチレン/アクリレート、1予しン/−−オレフイン(
ラテン、プロピレン、へ十セシ、オクチル等)を例示で
きる。また本発明の上記ポリエチレシ系樹脂は、線状低
密度ポリIチレシをも包含する・上記低密度ポリエチレ
ン系樹脂に対する一般式(I)で表わされる化合物の配
合量は、特に限定されないが通常約0.03〜3重量%
、好ましくは約0.05〜2重量−とするのがよく、ζ
0[1M内の配合により、充分に本発明所期の効果は発
揮される。
The desired effects of the present invention can be achieved by blending the above compounds into low-density polyethylene resin;
The following ethylene copolymers or ethylene copolymers having an ethylene content of 5011 or more are included. Any of the various materials that can be copolymerized with Kotsumar Echireshi, which can constitute the above-mentioned copolymer, can be used. Typical copolymers include x9shin/vinyl acetate, ethylene/methacrylate,
Ethylene/acrylate, ethylene/--olefin (
(Latin, propylene, hexose, octyl, etc.) can be exemplified. The polyethylene resin of the present invention also includes linear low-density polyethylene resin. The amount of the compound represented by the general formula (I) in the low-density polyethylene resin is not particularly limited, but is usually about 0. .03-3% by weight
, preferably about 0.05 to 2 weight, and ζ
The intended effects of the present invention can be sufficiently exhibited by blending within 0[1M.

本発明方法は、低密度ポリエチレシ系樹脂に核剤として
上記一般式(I)の化合物を配合する以外は、常法Ki
tい実施され、上記化合物の配合方法も亦、全知の核剤
の配合と同様にして行ない得る。
The method of the present invention employs conventional Ki
The method of compounding the above-mentioned compounds can also be carried out in the same manner as the compounding of known nucleating agents.

七O配杏は例えば粉末樹脂ペレットに直接ブレンドして
もよく、予め樹脂に配合してこれをベレット化してもよ
い。これらの配合に当、つては、通常のバシバリーミ中
1サー、エクストル−ター、〇−5−1110fls合
機を用い得ることも常法と変らない。
For example, the 7O apricot may be directly blended into powdered resin pellets, or may be blended with the resin in advance and made into pellets. In blending these, it is no different from the conventional method that a conventional vacuum cleaner, extruder, and 0-5-1110fls combiner can be used.

配合後の成形操作は、通常の方法に従い、樹脂が溶融さ
れる温度条件下に加熱して行ない得る。
The molding operation after compounding can be carried out by heating under temperature conditions that melt the resin, according to a conventional method.

を九上記樹脂の成形に当っては、通常慣用される安定剤
、滑剤、酸化防止剤、帯電防止剤、増量剤、分散剤、顔
料、発泡剤等の添加使用や高書度ポリエチレン、ボリプ
0ピレン、ポリブテン、ボ 、リプタジエン等O添加も
何ら差支えない・以下本発明実施例及び比較例を挙げ説
明する。
When molding the above resin, commonly used stabilizers, lubricants, antioxidants, antistatic agents, fillers, dispersants, pigments, foaming agents, etc., and the addition of high-density polyethylene, polypropylene, etc. There is no problem with the addition of O such as pyrene, polybutene, polybutene, liptadiene, etc. Examples and comparative examples of the present invention will be described below.

尚各側中部又は−は重量基準による。Note that the middle part or - on each side is based on weight.

実施例・ ! 酸化防止剤としてBHTo、1−を含む線状低密度ポリ
エチレシ系樹脂・(米liI  タウケ!カル・ズ社製
、Iチレシ含量約9511IIのエチレンごプテシコボ
リマー、1度0.955f/d)の70部又は80部に
、ジー(2,4−ジメチルベンシリダシ)ツルe)−L
ol*?25−バッチ(LDPK 99 phr及びジ
(2,4−ジメチルベンシリダシ)ツルピトーhtph
r融解−金物)の30部又は20部を加え、220℃で
溶融混合し、とれをインフレーション成形機を用いて空
冷法により成形して、フィルム厚み50μ襲のインフレ
ーションフィルムを作成した。
Example· ! 70 parts of a linear low-density polyethylene resin containing BHTo and 1- as an antioxidant (manufactured by U.S. LiI Tauke! Cal's, ethylene plastic polymer with a content of about 9511 II, 0.955 f/d per degree) or to 80 parts, di(2,4-dimethylbensyridasi)tsurue)-L
ol*? 25-batch (LDPK 99 phr and di(2,4-dimethylbensyridasi) tulpitoh tph
30 or 20 parts of molten hardware) were added, melted and mixed at 220°C, and the resulting mixture was molded by an air cooling method using an inflation molding machine to create a blown film with a film thickness of 50 μm.

実施例 2〜7 上記実施例tVcおいて核剤として用いたジメチル置換
ジベシザールソルビットに代え、下記各化合物を用い同
様にしてフィルムを作成した。
Examples 2 to 7 Films were prepared in the same manner using the following compounds in place of the dimethyl-substituted dibecizal sorbitol used as the nucleating agent in Example tVc above.

実施例ム     使用核剤 比較例 1 実施例IKThいて核剤とする化合物を配合する′こと
電く同様にしてフィルムを作成した。
Example Comparative example of nucleating agent used 1 A film was prepared in the same manner as in Example IKTh, in which a compound to be used as a nucleating agent was blended.

比較例 2 核剤としてジー(P−メチルベシジリデン)ソルビトー
ルの同量を用い実施例1と同様にした。
Comparative Example 2 The same procedure as in Example 1 was carried out using the same amount of di(P-methylbesidylidene) sorbitol as a nucleating agent.

上記6例で得九フィルムの曇)度をASTM D−10
03−52に従い測定し友。結果を下記第1!IK示す
The haze of the nine films obtained in the above six examples was determined by ASTM D-10.
Measured according to 03-52. The results are below! Show IK.

第  1  表 尚第1表中比較例2における膏印は、づリードが認めら
れ九ことを示す。
Table 1 The blank mark in Comparative Example 2 in Table 1 indicates that lead was observed.

実施例 8〜14 酸化防止剤としてBHlo、1−を含む低密度ポリエチ
レン(日本ユニカ社I1.d−0,923、MI=3.
2>を用い、これに核剤として実施例1〜7で用いたと
同じ化合物の夫々所定量を配会し、同11Kして厚さ5
0μ凰のインフレーションフィルムを作成しえ。
Examples 8 to 14 Low density polyethylene containing BHlo, 1- as an antioxidant (Nippon Unica I1.d-0,923, MI=3.
2>, a predetermined amount of each of the same compounds used in Examples 1 to 7 as a nucleating agent was added thereto, and heated at 11K to a thickness of 5.
Create a blown film of 0μ凰.

比較例 3 上記実施例8〜14において、核剤を用いることなく、
同様にしてフィルムを作成−しえ。
Comparative Example 3 In Examples 8 to 14 above, without using a nucleating agent,
A film was made in the same way.

得られた各フィルムにつき、前記と同様にして曇)度を
測定した結果を下記第21Ik示す。
The haze degree of each film obtained was measured in the same manner as described above, and the results are shown in Section 21 Ik below.

第  2  表 実施例 15〜19 実施例1と同一の線状低密度ポリエチレシ系樹脂に、下
記第3表に示す各化合物を核剤として夫々所定量添加し
、これらを夫々220℃で二軸ミルを用いて溶融混合し
、50Kt/ai、5分、170℃でプレス成形後室温
に冷却して1調厚さのシートを、作成しえ。
Table 2 Examples 15 to 19 Predetermined amounts of each of the compounds shown in Table 3 below were added as a nucleating agent to the same linear low-density polyethylene resin as in Example 1, and each compound was milled in a twin-screw mill at 220°C. The mixture was melt-mixed and press-formed at 170°C for 5 minutes at 50Kt/ai, then cooled to room temperature to produce a sheet of one thickness.

比較例 4及び5 上記各実施例において核剤を添加することなく(比較例
4)又は、核剤として1.−、(F−メチルベシジリデ
シ)ツルじトールO所定量を用い、夫々同様にしてシー
トを作成し良。
Comparative Examples 4 and 5 In each of the above Examples, either no nucleating agent was added (Comparative Example 4) or 1. Sheets were prepared in the same manner using the prescribed amounts of - and (F-methylbesidylidecyl)turjitol O.

得られた各シートの曇)度を同様にして測定し九結果な
下配第3表に示す。
The degree of haze of each sheet obtained was measured in the same manner and the results are shown in Table 3 below.

第  3  表 上記第1表乃至第3宍よシ本発明によれば、無添加に比
し、優れ九透明性を有する樹脂製品が得られ、しかもブ
リードの発生するおそれも全くまいことが判る。これに
対し公知のジー(P−メチルベンジリヅシ)ソルビトー
ルの使用線比較例2及び5に示すように、曇り度の改善
効果が尚不充分であるか又はブリード発生があシ好まし
くないことが判る・ (以 上)
Table 3 From Tables 1 to 3 above, it can be seen that according to the present invention, a resin product having superior transparency compared to the case without additives can be obtained, and there is no possibility of bleeding occurring. On the other hand, as shown in Comparative Examples 2 and 5 using the known di-(P-methylbenzyridushi)sorbitol, the haze improvement effect is still insufficient or bleeding occurs, which is undesirable. I understand (more than that)

Claims (1)

【特許請求の範囲】 ■ 鐘状低書度ポリエチレシもしくは低書度ポリエチレ
シに、一般式 〔式中X社へOfン原子又は炭素数1〜5の低級アル中
ル基を示し、襲はXがへ〇ゲシ原子O場合1〜30整数
を、を友Xが低級アル中ル基O場合2〜50整数を示す
。Pは0又はlを示す。〕 で表わされる化合物を配合することを特徴とする低冑度
ポリエチレシ系樹脂の改質方法。
[Scope of Claims] ■ A bell-shaped low-texture polyethylene resin or a low-texture polyethylene resin having a general formula [wherein X represents an Of atom or a lower alkyl group having 1 to 5 carbon atoms, and 〇When the atom atom O is an integer of 1 to 30, and when the atom X is a lower alkyl group O, an integer of 2 to 50 is shown. P represents 0 or l. ] A method for modifying a low-strength polyethylene resin, which comprises blending a compound represented by the following.
JP11627481A 1981-07-23 1981-07-23 Modification of low-density polyethylene resin Granted JPS5817135A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11627481A JPS5817135A (en) 1981-07-23 1981-07-23 Modification of low-density polyethylene resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11627481A JPS5817135A (en) 1981-07-23 1981-07-23 Modification of low-density polyethylene resin

Publications (2)

Publication Number Publication Date
JPS5817135A true JPS5817135A (en) 1983-02-01
JPS616091B2 JPS616091B2 (en) 1986-02-24

Family

ID=14683014

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11627481A Granted JPS5817135A (en) 1981-07-23 1981-07-23 Modification of low-density polyethylene resin

Country Status (1)

Country Link
JP (1) JPS5817135A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58185632A (en) * 1982-04-23 1983-10-29 Iic Kagaku Kogyo Kk Polyolefin resin composition
WO2009139350A1 (en) 2008-05-16 2009-11-19 株式会社Adeka Polyolefin resin composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58185632A (en) * 1982-04-23 1983-10-29 Iic Kagaku Kogyo Kk Polyolefin resin composition
JPH0424375B2 (en) * 1982-04-23 1992-04-24 Iishii Kagaku Kogyo Kk
WO2009139350A1 (en) 2008-05-16 2009-11-19 株式会社Adeka Polyolefin resin composition
US8546473B2 (en) 2008-05-16 2013-10-01 Adeka Corporation Polyolefin resin composition
EP2837654A1 (en) 2008-05-16 2015-02-18 Adeka Corporation Polyolefin resin composition

Also Published As

Publication number Publication date
JPS616091B2 (en) 1986-02-24

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