JPS5835533B2 - Expanded polystyrene treatment method - Google Patents

Expanded polystyrene treatment method

Info

Publication number
JPS5835533B2
JPS5835533B2 JP3639376A JP3639376A JPS5835533B2 JP S5835533 B2 JPS5835533 B2 JP S5835533B2 JP 3639376 A JP3639376 A JP 3639376A JP 3639376 A JP3639376 A JP 3639376A JP S5835533 B2 JPS5835533 B2 JP S5835533B2
Authority
JP
Japan
Prior art keywords
expanded polystyrene
dichlorobenzene
polystyrene
treatment method
tcd
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
Application number
JP3639376A
Other languages
Japanese (ja)
Other versions
JPS52117962A (en
Inventor
光晴 加藤
博美 河内
哲男 金安
悦三郎 工藤
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.)
Resonac Corp
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 JP3639376A priority Critical patent/JPS5835533B2/en
Publication of JPS52117962A publication Critical patent/JPS52117962A/en
Publication of JPS5835533B2 publication Critical patent/JPS5835533B2/en
Expired legal-status Critical Current

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  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Description

【発明の詳細な説明】 本発明は発泡ポリスチレンを昇華性物質である、p−ジ
クロルベンゼンおよび/またはトリシクロ(5,2,1
,0”・6)デカン(以下、JTCD、Jと略す。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides expanded polystyrene with p-dichlorobenzene and/or tricyclo(5,2,1
,0''・6) Decane (hereinafter abbreviated as JTCD, J).

)の蒸気を利用して発泡ポリスチレンの体積をそのまま
収縮させ処理することに関するものである。
) is used to shrink the volume of expanded polystyrene as it is.

従来、発泡ポリスチレンの廃棄物処理方法としては主に
焼却法が実施されているが省資源の立場から最近、廃棄
されたプラスチック類の再利用が重要視されるようにな
った。
Conventionally, incineration has been the main method for disposing of expanded polystyrene waste, but recently, from the standpoint of resource conservation, reuse of discarded plastics has become important.

そこで発泡ポリスチレンの再利用については、技術的に
は熱収縮、溶剤処理などが知られているにすぎない。
As for the reuse of expanded polystyrene, the only known techniques are heat shrinkage and solvent treatment.

しかし発泡ポリスチレンをはじめ廃棄された一般の可燃
性プラスチック類の焼却については燃焼熱が高いことか
ら焼却炉の破損および毒ガスなどの発生を伴うことが多
いことから問題とされている。
However, the incineration of general discarded combustible plastics, including foamed polystyrene, is problematic because the high heat of combustion often causes damage to the incinerator and the generation of poisonous gas.

また可燃性プラスチック類の熱処理についても防災上の
危険性を有すると共に経済的にも有利な方法とはいい難
い。
Furthermore, heat treatment of combustible plastics also poses a risk in terms of disaster prevention and is not an economically advantageous method.

一方溶剤処理についても溶剤回収などが困難なことから
実用的に好ましくない。
On the other hand, solvent treatment is also not preferred from a practical standpoint because it is difficult to recover the solvent.

そこで本発明はこのような従来の技術的な問題点を解決
したものである。
Therefore, the present invention solves these conventional technical problems.

すなわち本発明は発泡ポリスチレンをp−ジクロルベン
ゼン、TCDまたはこれらの混合物の蒸気と接触させ、
収縮させることを特徴とする、発泡ポリスチレンの処理
方法に関する。
That is, the present invention involves contacting expanded polystyrene with vapors of p-dichlorobenzene, TCD, or a mixture thereof;
The present invention relates to a method for treating expanded polystyrene, which is characterized by shrinking it.

発泡ポリスチレンとはポリスチレン又はスチレン共重合
体の発泡体成形物及び発泡体である。
Expanded polystyrene refers to foam moldings and foams of polystyrene or styrene copolymers.

本発明の方法は密閉された空間に任意の形状の発泡ポリ
スチレンを入れ、そこにp−ジクロルベンゼン、TCD
またはこれらの混合物を好ましくはその温度における飽
和蒸気圧に達するに十分な量を入れる。
The method of the present invention involves placing foamed polystyrene of any shape in a sealed space, p-dichlorobenzene, TCD
or a mixture thereof, preferably in an amount sufficient to reach the saturated vapor pressure at that temperature.

ただし飽和状態に至しめることを促進させる意味におい
て温度を常温から50℃の間で可変させてもよい。
However, the temperature may be varied between room temperature and 50° C. in order to promote reaching the saturated state.

それに伴い昇華物の蒸気と発泡ポリスチレンが接触しポ
リスチレンまたはスチレン共重合体を構成しているセル
を破壊し乾燥したままの状態で収縮させることができる
As a result, the vapor of the sublimate comes into contact with the foamed polystyrene, destroying the cells constituting the polystyrene or styrene copolymer and allowing the polystyrene to shrink in a dry state.

p−ジクロルベンゼンおよびTCDは、結晶状、粉末状
等、どのような形状でもよい。
p-dichlorobenzene and TCD may be in any form such as crystal or powder.

p−ジクロルベンゼンとTCDの混合液状物、またp−
ジクロルベンゼンまたはTCDと他の昇華性組成物、有
溶溶剤の混合物を使用してもよい。
A liquid mixture of p-dichlorobenzene and TCD, and p-
Mixtures of dichlorobenzene or TCD and other sublimable compositions and solvents may also be used.

上記密閉された空間とは、密閉容器でもよいし、昇華性
物質を通過させない材質例えばポリエステルフイルム、
アルミ箔等を使用することができる。
The above-mentioned sealed space may be an airtight container, or may be made of a material that does not allow sublimation substances to pass through, such as polyester film,
Aluminum foil etc. can be used.

次に本発明の実施例を示す。Next, examples of the present invention will be shown.

実施例 1 p−ジクロルベンゼン109を発泡ポリスチレン(長さ
30關の立方体)の入っている密閉容器(500CC)
の中に入れ室温で発泡ポリスチレンの体積の経口変化を
見たところ、実験開始後5日目に体積が1/1oに30
0日目は1/3oに減少した。
Example 1 P-dichlorobenzene 109 was placed in a sealed container (500CC) containing expanded polystyrene (30cm long cube).
When observing changes in the volume of polystyrene foam at room temperature, the volume decreased to 1/10 on the 5th day after the start of the experiment.
On day 0, it decreased to 1/3o.

実施例 2 脂環状炭化水素で昇華性を有する物質としてTCDを用
いて実施例1と同一条件でおこなった結果5日目に体積
が1/3に減少した。
Example 2 A test was carried out under the same conditions as in Example 1 using TCD as an alicyclic hydrocarbon having sublimation property. As a result, the volume decreased to 1/3 on the 5th day.

比較例 1 実施例1においてp−ジクロルベンゼンのかわりに障脳
を用い実施例1と同一条件でおこなった結果、発泡ポリ
スチレンの収縮はみられなかった。
Comparative Example 1 In Example 1, brain damage was used instead of p-dichlorobenzene and the test was carried out under the same conditions as in Example 1. As a result, no shrinkage of expanded polystyrene was observed.

比較例 2 実施例1においてp−ジクロルベンゼンのかわりにナフ
タリンを用い実施例1と同1条件でおこなった結果、発
泡ポリスチレンの収縮はみられなかった。
Comparative Example 2 In Example 1, naphthalene was used instead of p-dichlorobenzene under the same conditions as in Example 1. As a result, no shrinkage of the expanded polystyrene was observed.

比較例 3 実施例1においてp−ジクロルベンゼンのカワりに発泡
スチレンを溶解する溶剤として広く知られているアセト
ンを用い、実施例1と同一条件でおこなった結果、2日
目で発泡スチレンを溶解した。
Comparative Example 3 In Example 1, acetone, which is widely known as a solvent for dissolving styrene foam, was used in p-dichlorobenzene and the same conditions as in Example 1 were used. Dissolved.

以上より明らかなように、発泡ポリスチレンを、−ジク
ロルベンゼン、TcDを用い発泡ポリスチレンの体積を
収縮させ簡単に処理することができる。
As is clear from the above, expanded polystyrene can be easily treated by shrinking the volume of expanded polystyrene using -dichlorobenzene and TcD.

この方法は従来の熱処理、溶剤処理が、操作が煩雑であ
り、処理費用も高いのに対し、簡単な方法であり、発泡
ポリスチレンを再利用できやすくする。
Unlike conventional heat treatment and solvent treatment, which require complicated operations and high processing costs, this method is a simple method and allows expanded polystyrene to be easily reused.

また昇華性物質は粉末状または結晶状のままで用いるこ
とができるため回収および再利用が極めて簡単である。
Furthermore, since the sublimable substance can be used in powder or crystalline form, recovery and reuse are extremely easy.

これらの昇華物質は通常防臭剤、防虫剤として広く一般
的に使用されており、工業的にも安価に入手できる利点
がある。
These sublimated substances are generally widely used as deodorants and insect repellents, and have the advantage of being industrially available at low cost.

その他、収縮したポリスチレンは密度が増すことから容
易に粉砕しやすくなり、再利用も容易となる。
In addition, the increased density of shrunken polystyrene makes it easier to crush and recycle.

Claims (1)

【特許請求の範囲】[Claims] 1 発泡ポリスチレンをp−ジクロルベンゼン、トリシ
クロ(5,2,1,02・6)デカンまたはその混合物
の蒸気に接触させ、発泡ポリスチレンを収縮させること
を特徴とする発泡ポリスチレンの処理方法。
1. A method for treating foamed polystyrene, which comprises bringing the foamed polystyrene into contact with vapor of p-dichlorobenzene, tricyclo(5,2,1,02.6)decane, or a mixture thereof to shrink the foamed polystyrene.
JP3639376A 1976-03-31 1976-03-31 Expanded polystyrene treatment method Expired JPS5835533B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3639376A JPS5835533B2 (en) 1976-03-31 1976-03-31 Expanded polystyrene treatment method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3639376A JPS5835533B2 (en) 1976-03-31 1976-03-31 Expanded polystyrene treatment method

Publications (2)

Publication Number Publication Date
JPS52117962A JPS52117962A (en) 1977-10-03
JPS5835533B2 true JPS5835533B2 (en) 1983-08-03

Family

ID=12468601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3639376A Expired JPS5835533B2 (en) 1976-03-31 1976-03-31 Expanded polystyrene treatment method

Country Status (1)

Country Link
JP (1) JPS5835533B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09291170A (en) * 1996-03-01 1997-11-11 Japan Field Kk Method for shrinking foamed resin and apparatus therefor
JP4979946B2 (en) * 2005-12-27 2012-07-18 栗田工業株式会社 Method for producing biofilm-forming carrier and biofilm-forming carrier

Also Published As

Publication number Publication date
JPS52117962A (en) 1977-10-03

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