JPH0791409B2 - Expandable styrene resin particle composition - Google Patents

Expandable styrene resin particle composition

Info

Publication number
JPH0791409B2
JPH0791409B2 JP3556688A JP3556688A JPH0791409B2 JP H0791409 B2 JPH0791409 B2 JP H0791409B2 JP 3556688 A JP3556688 A JP 3556688A JP 3556688 A JP3556688 A JP 3556688A JP H0791409 B2 JPH0791409 B2 JP H0791409B2
Authority
JP
Japan
Prior art keywords
particle composition
expandable
resin particles
resin particle
styrene resin
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
JP3556688A
Other languages
Japanese (ja)
Other versions
JPH01210435A (en
Inventor
哲也 加藤
光生 舘石
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.)
Showa Denko Materials Co Ltd
Original Assignee
Hitachi 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP3556688A priority Critical patent/JPH0791409B2/en
Publication of JPH01210435A publication Critical patent/JPH01210435A/en
Publication of JPH0791409B2 publication Critical patent/JPH0791409B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は発泡性スチレン系樹脂粒子組成物に関し,詳述
すれば,該粒子を発泡成形することにより得られる成形
品を容器として使用するのに好適な発泡性スチレン系樹
脂粒子組成物に関する。
TECHNICAL FIELD The present invention relates to a foamable styrene resin particle composition, and more specifically, a molded article obtained by foam molding the particles is used as a container. And a suitable expandable styrene resin particle composition.

(従来の技術) 発泡性スチレン系樹脂粒子は,スチーム等によつて加熱
され,一次発泡された後,小孔を有する金型に充填さ
れ,加熱され,二次発泡し,成形される。成形品は経済
性,断熱性,軽量性,衛生性等に優れているため,梱包
材料,断熱材,容器等として多くの分野で使用されてい
る。
(Prior Art) The expandable styrenic resin particles are heated by steam or the like to be primary foamed, then filled in a mold having small holes, heated, secondary foamed and molded. Molded products are used in many fields as packing materials, heat insulating materials, containers, etc., because they are economical, heat insulating, lightweight, hygienic and the like.

発泡性スチレン系樹脂粒子は,一般に,常温で気体若し
くは液状の脂肪族炭化水素,例えばプロパン,ブタン,
ペンタン,ヘキサン等をポリスチレンビーズと共に水性
媒体中に分散し,加熱される方法によつて製造される。
こうして得られた発泡性スチレン系樹脂粒子は前述の工
程を経て成形されるが,得られた成形品は発泡性スチレ
ン系樹脂粒子を石垣状に詰み重ねて成り,発泡圧と熱に
よつて融着されているため,それぞれの該粒子は一体化
されておらず,その結果,容器として使用すると,その
内容物が容器外壁に浸透し易いものとなる。浸透を防止
するには,該粒子の融着性を強くし,浸透しうる空隙を
少なくすること,又は該粒子表面の性質を内容物と相溶
しない性質を持たせる方法がある。
Expandable styrenic resin particles are generally aliphatic hydrocarbons that are gaseous or liquid at room temperature, such as propane, butane,
It is manufactured by a method in which pentane, hexane and the like are dispersed together with polystyrene beads in an aqueous medium and heated.
The expandable styrenic resin particles obtained in this way are molded through the above-mentioned process, but the obtained molded product is made by stacking the expandable styrenic resin particles in the shape of a stone wall and melting them by foaming pressure and heat. Since they are deposited, the particles are not integrated so that when used as a container, their contents tend to penetrate the outer wall of the container. In order to prevent permeation, there is a method in which the fusibility of the particles is strengthened, the permeable voids are reduced, or the surface properties of the particles are made incompatible with the contents.

前者の方法として一般に行われているのは,成形時の加
熱を強くすることであり,より欠陥の少ない成形品を得
るためには,成形温度は低めに設定し,長時間加熱の必
要がある。
Generally, the former method is to increase the heating during molding. In order to obtain a molded product with fewer defects, it is necessary to set the molding temperature to a low temperature and to heat it for a long time. .

後者の方法としては,一次発泡における該粒子の集塊化
を防止するため一般に使用されている金属石けんを通常
より多量に用いることが行われているが,成形におい
て,粒子の融着が阻害されるため前述の方法と同様に成
形時間が長くなり,いずれにしても成形サイクルが長
く,工業的に有用な方法とは言い難い。
As the latter method, generally used metal soap is used in a larger amount than usual in order to prevent agglomeration of the particles in the primary foaming, but fusion of particles is inhibited in molding. Therefore, the molding time becomes long as in the above-mentioned method, and in any case, the molding cycle is long, and it is hard to say that this method is industrially useful.

そこで,より短い成形時間で内容物の浸透の少ない発泡
性スチレン系樹脂粒子が過去提案されている。例えば特
公昭56−34172号公報では蔗糖エステルで発泡性スチレ
ン系樹脂粒子表面の被覆,特公昭56−51178号公報では
ポリエーテル又はポリオール及びポリリン酸塩での発泡
性スチレン系樹脂粒子表面の被覆,特開昭59−24731号
公報ではポリアルキレングリコールの脂肪酸エステルで
の発泡性スチレン系樹脂粒子表面の被覆,特開昭59−41
339号公報ではパーフルオロアルキル基含有リン酸エス
テルでの発泡性スチレン系樹脂粒子表面の被覆が提案さ
れている。
Therefore, expandable styrenic resin particles have been proposed in the past with a shorter molding time and less penetration of the contents. For example, in JP-B-56-34172, the surface of expandable styrene-based resin particles is coated with sucrose ester, and in JP-B-56-51178, the surface of expandable styrene-based resin particles is coated with polyether or polyol and polyphosphate. In JP-A-59-24731, coating of the surface of expandable styrenic resin particles with fatty acid ester of polyalkylene glycol, JP-A-59-41
Japanese Patent No. 339 proposes coating the surface of expandable styrene resin particles with a perfluoroalkyl group-containing phosphate ester.

(発明が解決しようとする課題) 前述の公報のうち特開昭59−41339号公報以外は,成形
された容器が使用される目的とする収納される内容物を
浸透するのを防止したものであり,収納されるものが異
なると,また,異なる結果を示していた。一方,特開昭
59−41339号公報はパーフルオロアルキル基含有リン酸
エステルを発泡性スチレン系樹脂表面に0.01〜0.2重量
%被覆することを特徴としているが,これは繊維や紙の
撥水,撥油剤として既に一般に使用されており,本発明
のいかなる収納物もはじき,浸透を防止するうえで有効
である。
(Problems to be Solved by the Invention) Of the above-mentioned publications, except for JP-A-59-41339, it is intended to prevent a molded container from penetrating the intended contents to be stored. Yes, and different things were stored and showed different results. On the other hand,
Japanese Patent No. 59-41339 is characterized in that a perfluoroalkyl group-containing phosphate ester is coated on the surface of a foamable styrenic resin in an amount of 0.01 to 0.2% by weight, which is generally used as a water and oil repellent agent for fibers and paper. It has been used and is effective in repelling and preventing penetration of any of the items of the invention.

しかしながら,パーフルオロアルキル基含有リン酸エス
テルは該発泡粒子を熱融着を阻害する働きも併せもち,
結果として,成形時の加熱必要時間が長くなり,初期の
目的を達成しえないものであつた。
However, the perfluoroalkyl group-containing phosphate ester also has the function of inhibiting the heat fusion of the expanded particles,
As a result, the time required for heating at the time of molding became long and the initial purpose could not be achieved.

本発明は,発泡性スチレン系樹脂粒子組成物であつて,
これを容器として使用したとき,収納される内容物が容
器外壁へ浸透せず,しかも短い成形時間で成形可能な発
泡性スチレン系樹脂粒子組成物を提供することを目的と
する。
The present invention provides an expandable styrenic resin particle composition,
It is an object of the present invention to provide an expandable styrene resin particle composition in which the content stored does not penetrate into the outer wall of the container when it is used as a container and can be molded in a short molding time.

(課題を解決するための手段) 本発明は,発泡性スチレン系樹脂粒子の表面に,一般式
(I); (但し,lは4〜10の整数,mは1又は2,nは2〜10の整数
であり,R1はH,炭素数1〜18のアルキル基又は炭素数1
〜18の水酸基含有アルキル基である)で表わされる化合
物を必須成分とする被覆層を有することを特徴とする発
泡性スチレン系樹脂粒子組成物に関する。
(Means for Solving the Problems) The present invention provides a compound of the general formula (I); (However, l is an integer of 4 to 10, m is 1 or 2, n is an integer of 2 to 10, R 1 is H, an alkyl group having 1 to 18 carbons, or 1 carbon
To 18 hydroxyl group-containing alkyl groups) to a foamable styrenic resin particle composition having a coating layer as an essential component.

本発明における発泡性スチレン系樹脂粒子としては,従
来公知のものが使用でき,スチレンのホモポリマー若し
くはスチレンとアクリロニトリル,メタクリル酸メチ
ル,メタクリル酸ブチル等のメタクリル酸エステル,ア
クリル酸メチル,アクリル酸エチル,アクリル酸ブチル
等のアクリル酸エステル,α−メチルスチレン,クロル
スチレン,ビニルトルエン等のスチレン誘導体などの1
種又は2種以上のコポリマーを基材樹脂とし,該樹脂に
プロパン,イソブタン,n−ブタン,イソペンタン,n−ペ
ンタン等の脂肪族炭化水素,又はフレオン11,フレオン1
2等のフロン化合物などの常温で液体状又は気体状の発
泡剤が,好ましくは1〜10重量%含浸されたものなどで
ある。これらの発泡性スチレン系樹脂粒子は,公知の方
法によつて製造することができる。
As the expandable styrenic resin particles in the present invention, conventionally known ones can be used, and homopolymers of styrene or styrene and acrylonitrile, methyl methacrylate, methacrylic acid esters such as butyl methacrylate, methyl acrylate, ethyl acrylate, Acrylic esters such as butyl acrylate, styrene derivatives such as α-methylstyrene, chlorostyrene, vinyltoluene, etc. 1
As a base resin of one kind or a copolymer of two or more kinds, and an aliphatic hydrocarbon such as propane, isobutane, n-butane, isopentane, and n-pentane, or Freon 11, Freon 1
It is preferably such that a foaming agent which is liquid or gaseous at room temperature, such as a CFC compound such as 2, is impregnated at 1 to 10% by weight. These expandable styrene resin particles can be produced by a known method.

発泡性スチレン系樹脂粒子の被覆に使用される前記一般
式(I)で表される化合物は,パーフルオロアルキルス
ルホンアミドのリン酸アンモニウムであり,公知の化合
物である。
The compound represented by the general formula (I) used for coating the expandable styrenic resin particles is a perfluoroalkylsulfonamide ammonium phosphate, which is a known compound.

一般式(I)で表わされる化合物の具体例を以下に示
す。
Specific examples of the compound represented by formula (I) are shown below.

一般式(I)で表わされる化合物の使用量は,発泡性ス
チレン系樹脂粒子に対して,0.0001〜0.05重量%が好ま
しく,特に0.001〜0.02重量%が好ましい。この化合物
の使用量が少なすぎると十分な撥水撥油効果を得ること
が困難となり,また,多すぎると,効果がそれほど向上
しないばかりでなく,成形工程において樹脂粒子間の熱
融着を阻害してしまう。
The amount of the compound represented by the general formula (I) used is preferably 0.0001 to 0.05% by weight, more preferably 0.001 to 0.02% by weight, based on the expandable styrenic resin particles. If the amount of this compound used is too small, it becomes difficult to obtain a sufficient water / oil repellency effect, and if it is too large, not only does the effect not improve so much, but also heat fusion between resin particles is hindered in the molding process. Resulting in.

発泡性スチレン系樹脂粒子を被覆において,前記一般式
(I)で表わされる化合物の他に,従来公知の被覆剤成
分を併用することができる。例えば,一時発泡における
集塊化防止のために使用されるステアリン酸亜鉛,ステ
アリン酸カルシウムなどの金属石けん,エチレンビスア
ミド,ステアリン酸アミドのような脂肪酸アミド類であ
る。これらの集塊化防止剤は,発泡性スチレン系樹脂粒
子に対して0.05〜0.5重量%使用するのが好ましい。ま
た,一時発泡樹脂粒子の静電気防止剤として使用される
グリセリン,ソルビツト,ポリエチレングリコール,ポ
リプロピレングリコール等の多価アルコール,ソルビタ
ンエステル,高級脂肪族のエチレンオキシド付加物等の
ノニオン系界面活性剤等の併用も可能である。これらの
静電気防止剤は,発泡性スチレン系樹脂粒子に対して0.
005〜0.2重量%使用されるのが好ましい。
In coating the expandable styrenic resin particles, in addition to the compound represented by the general formula (I), conventionally known coating agent components can be used in combination. Examples thereof include metal soaps such as zinc stearate and calcium stearate used for preventing agglomeration in temporary foaming, and fatty acid amides such as ethylene bisamide and stearic acid amide. These agglomeration inhibitors are preferably used in an amount of 0.05 to 0.5% by weight based on the expandable styrenic resin particles. In addition, glycerin, sorbit, polyhydric alcohols such as polyethylene glycol and polypropylene glycol, which are used as antistatic agents for expanded resin particles, sorbitan esters, and nonionic surfactants such as higher aliphatic ethylene oxide adducts can be used in combination. It is possible. These antistatic agents are added to expandable styrenic resin particles at 0.
It is preferably used from 005 to 0.2% by weight.

本発明において,発泡性スチレン系樹脂粒子表面への被
覆層の形成は,従来既知の手段で行うことができる。例
えば,リボンブレンダー,Vブレンダー,ヘンシエルミキ
サー,レデイゲミキサー等の混合器で,発泡性スチレン
系樹脂粒子及び上記各被覆剤成分を混合することによつ
て行うことができる。
In the present invention, the formation of the coating layer on the surface of the expandable styrenic resin particles can be performed by a conventionally known means. For example, it can be carried out by mixing the expandable styrenic resin particles and the above-mentioned respective coating agent components in a mixer such as a ribbon blender, a V blender, a Hensiel mixer, and a Redige mixer.

こうして得られた発泡性スチレン系樹脂粒子組成物を使
用すると,短い成形加熱でも,粒子同士の融着の良い,
かつその粒子界面が撥水,撥油の性質を持つ成型品が得
られる。例えば,従来の成形品では大豆油に対する接触
角が40゜付近にあるのに対し,50〜60゜と濡れにくくな
る。
By using the expandable styrenic resin particle composition thus obtained, the particles are well fused even with a short molding heating.
In addition, a molded product having water-repellent and oil-repellent properties at its particle interface can be obtained. For example, the contact angle of soybean oil in the conventional molded product is around 40 °, whereas it becomes difficult to wet at 50-60 °.

従つて本発明の組成物はドーナツ,ハンバーガー,フラ
イドチキン,即席麺,カレールウ,ラード,マヨネーズ
等の油性若しくは脂肪性の食品を直接包装しても,壁を
通しての容器外への浸透を防止出来る容器を作る材料と
なる。
Therefore, the composition of the present invention is a container which can prevent the penetration of the oily or fatty food such as donut, hamburger, fried chicken, instant noodles, curry roux, lard and mayonnaise through the wall to the outside of the container. It becomes the material for making.

(実施例) 実施例1〜2 発泡剤として5.5重量%のペンタン(i−ペンタン/n−
ペンタン=1/9)を含有する直径0.35〜0.59mmの発泡性
ポリスチレン粒子(日立化成工業(株)製5SG)1000gを
ヘンシエルミキサーに入れ,ここに,アンモニウムビス
(Nエチル−2−パーフルオロオクチルスルホンアミド
エチル)ホスフエート を表1に示す量(固形分換算)の,ステアリン酸亜鉛1.
5g及びグリセリン0.5gを順次添加混合して被覆し,発泡
性ポリスチレン樹脂粒子組成物を得た。これをバツチ式
一次発泡装置で熱風とスチームの混合気を熱媒として加
熱し,嵩密度0.1g/mlになる様発泡し,一次発泡粒子を
得た。これを常温,常圧下で16時間熟成したのち,内容
積500cc,肉厚2.0mmのカツプ状成形品を得るための金型
に充填し,表1に示す時間加熱したのち4時間冷却し,
発泡スチロール製カツプを得た。
Examples Examples 1-2 5.5% by weight of pentane (i-pentane / n-as a blowing agent)
1000 g of expandable polystyrene particles (5SG manufactured by Hitachi Chemical Co., Ltd.) containing 0.35 to 0.59 mm in diameter containing pentane = 1/9) were placed in a Hensiel mixer, and ammonium bis (N-ethyl-2-perfluoro) was added thereto. Octylsulfonamidoethyl) phosphate Table 1 shows the amount (in terms of solid content) of zinc stearate 1.
5 g and 0.5 g of glycerin were sequentially added and mixed for coating to obtain a foamable polystyrene resin particle composition. This was heated in a batch type primary foaming device using a mixture of hot air and steam as a heating medium, and foamed to a bulk density of 0.1 g / ml to obtain primary expanded particles. After aging this for 16 hours at room temperature and normal pressure, it was filled in a mold for obtaining a cup-shaped molded product with an internal volume of 500cc and a wall thickness of 2.0mm, heated for the time shown in Table 1, and then cooled for 4 hours,
A foam polystyrene cup was obtained.

得られたカツプにサラダ油350ccを入れ浸透性テストを
行ない,にじみ出す迄の時間を表1に示した。また,得
られたカツプを割つて,粒子間の界面で剥離をせず,粒
子自身が割れるものの割合を調べ,融着度として表1に
示した。
350 cc of salad oil was put in the obtained cup and a permeability test was conducted, and the time until oozing is shown in Table 1. Further, the obtained cup was broken and the ratio of the particles that did not separate at the interface between the particles and cracked themselves was examined, and the fusion degree is shown in Table 1.

比較例1〜2 実施例1においてアンモニウムビス(Nエチル−2−パ
ーフルオロオクチルスルホンアミドエチル)ホスフエー
トを使用しない以外は同様にして発泡スチロールカツプ
を得,テストを行なつた。その結果を表1に示す。
Comparative Examples 1-2 A foamed styrene cup was obtained and tested in the same manner as in Example 1 except that ammonium bis (N-ethyl-2-perfluorooctylsulfonamidoethyl) phosphate was not used. The results are shown in Table 1.

比較例3〜4 実施例2において,アンモニウムビス(Nエチル−2−
パーフルオロオクチルスルホンアミドエチル)ホスフエ
ートの代りに,パーフルオロアルキルリン酸アンモニウ
ム(旭硝子(株)製,サーフロンS−112)使用した他
は,同様にして発泡スチロールカツプを得,テストを行
なつた。その結果を表1に示す。
Comparative Examples 3 to 4 In Example 2, ammonium bis (N ethyl-2-
Instead of using perfluorooctylsulfonamidoethyl) phosphate, ammonium perfluoroalkyl phosphate (Surflon S-112, manufactured by Asahi Glass Co., Ltd.) was used, and a styrofoam cup was obtained and tested in the same manner. The results are shown in Table 1.

(発明の効果) 本発明の発泡性スチレン系樹脂粒子組成物は,短い成形
時間で成形することができ,かつ,容器として形成した
とき,収納される内容物が容器の壁から浸透しにくい。
(Effects of the Invention) The expandable styrenic resin particle composition of the present invention can be molded in a short molding time, and when formed as a container, the stored contents are less likely to penetrate the wall of the container.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】発泡性スチレン系樹脂粒子の表面に,一般
式(I); (但し,lは4〜10の整数,mは1又は2,nは2〜10の整数
であり,R1はH,炭素数1〜18のアルキル基又は炭素数1
〜18の水酸基含有アルキル基である)で表わされる化合
物を必須成分とする被覆層を有することを特徴とする発
泡性スチレン系樹脂粒子組成物。
1. The surface of the expandable styrenic resin particles has the general formula (I); (However, l is an integer of 4 to 10, m is 1 or 2, n is an integer of 2 to 10, R 1 is H, an alkyl group having 1 to 18 carbons, or 1 carbon
To 18 is a hydroxyl group-containing alkyl group), and an expandable styrene resin particle composition having a coating layer containing a compound represented by the formula (1) as an essential component.
【請求項2】一般式(I)で表わされる化合物の量が,
発泡性スチレン系樹脂粒子に対して0.0001〜0.05重量%
である請求項第1項記載の発泡性スチレン系樹脂粒子組
成物。
2. The amount of the compound represented by the general formula (I) is
0.0001 to 0.05% by weight based on expandable styrene resin particles
The expandable styrene resin particle composition according to claim 1.
JP3556688A 1988-02-18 1988-02-18 Expandable styrene resin particle composition Expired - Lifetime JPH0791409B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3556688A JPH0791409B2 (en) 1988-02-18 1988-02-18 Expandable styrene resin particle composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3556688A JPH0791409B2 (en) 1988-02-18 1988-02-18 Expandable styrene resin particle composition

Publications (2)

Publication Number Publication Date
JPH01210435A JPH01210435A (en) 1989-08-24
JPH0791409B2 true JPH0791409B2 (en) 1995-10-04

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JP5303906B2 (en) * 2007-11-07 2013-10-02 株式会社カネカ Expandable styrenic resin particles and foamed molded article

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