JPH08252823A - Manufacture of nonflammable biodegradable plastic - Google Patents

Manufacture of nonflammable biodegradable plastic

Info

Publication number
JPH08252823A
JPH08252823A JP5864995A JP5864995A JPH08252823A JP H08252823 A JPH08252823 A JP H08252823A JP 5864995 A JP5864995 A JP 5864995A JP 5864995 A JP5864995 A JP 5864995A JP H08252823 A JPH08252823 A JP H08252823A
Authority
JP
Japan
Prior art keywords
plastic
nonflammability
powder
molding
biodegradability
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.)
Pending
Application number
JP5864995A
Other languages
Japanese (ja)
Inventor
Takafumi Hataya
隆文 端谷
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.)
Fujitsu Ltd
Original Assignee
Fujitsu 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 Fujitsu Ltd filed Critical Fujitsu Ltd
Priority to JP5864995A priority Critical patent/JPH08252823A/en
Publication of JPH08252823A publication Critical patent/JPH08252823A/en
Pending legal-status Critical Current

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  • Injection Moulding Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Biological Depolymerization Polymers (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)

Abstract

PURPOSE: To realize the giving of nonflammability to a plastic by a method wherein molding is carried out under the condition that at least either one of an aluminum hydroxide powder and a magnesium hydroxide powder is added to pellets made of a biodegradable plastic stock. CONSTITUTION: As a means for making a plastic nonflammable, Al(OH)3 or Mg(OH)2 is mixed with stock so as to absorb the heat developing at the burning of the plastic, resulting in resolving and, at the same time, generating water and showing nonflammability due to its heat absorbing action and the generation of water. However, since nonflammability, biodegradability, mechanical properties and the like have mutually contradictory relationships and added hydroxide molecules are coordinated so as to surround the spherulitic structures of the biodegradable plastic, the biodegradability lowers. As a result, by carrying out the molding of the plastic under the condition that the mixing percentage of at least either one of an Al(OH)3 powder and a Mg(OH)2 powder is set to be 30-50wt.%, the physical properties and nonflammability necessary for the plastic can be maintained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は難燃性を付与した生分解
性プラスチックスの製造方法に関する。プラスチックス
は土中に埋めても腐らず、焼くと高熱や有害なガスを発
生することから、この処理は地球環境の維持の面から大
きな問題となっている。そして、この打開策として生分
解性プラスチックスが着目され、今まで日用雑貨品、衛
生用品、遊戯用品など主として使い捨て用品に対して実
用化が進められている。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a biodegradable plastic having flame retardancy. Since plastics do not rot when buried in the soil and generate high heat and harmful gas when burned, this treatment is a major problem in terms of maintaining the global environment. Biodegradable plastics have been paid attention to as a breakthrough measure, and have been put into practical use until now mainly for disposable items such as daily sundries, hygiene products, play products.

【0002】一方、電機製品についても筐体などを生分
解性プラスチックスで形成し、回収後の処理を容易にし
たいと云う希望はあるものゝ、電機製品として使用する
場合には日本工業規格(JIS)やUL(Under-writer
Laboratory)規格に決められている難燃性規格を満たす
必要があり、現在の生分解性プラスチックスでは対応で
きない。
On the other hand, regarding electrical products, there is a desire to make the casing and the like of biodegradable plastics to facilitate the treatment after collection. When used as electrical products, Japanese Industrial Standards ( JIS) and UL (Under-writer)
It is necessary to meet the flame-retardant standard set in the Laboratory standard, and current biodegradable plastics cannot support it.

【0003】[0003]

【従来の技術】生分解性プラスチックスは自然界におい
て微生物が関与して低分子化合物に分解されるプラスチ
ックスと定義されており、現在において実用化されてい
る生分解性プラスチックスは次の3種類に大別すること
ができる。 微生物産生ポリエステル 化学合成高分子化合物 天然高分子利用物 こゝで、は微生物が合成するポリエステル、例えば、
3-ヒドロキシブチレート( 略称3HB)や3-ヒドロキシ
バリレート( 略称3HV)などからなるポリエステルを
用いるもので、両者のランダム共重合体〔P(3HB−
3HV)〕からなるポリエステルは既に商用化されてい
る。
2. Description of the Related Art Biodegradable plastics are defined in the natural world as plastics that are decomposed into low molecular weight compounds by the involvement of microorganisms. The biodegradable plastics currently in practical use are the following three types. Can be roughly divided into Microorganism-produced polyester Chemically-synthesized polymer compound This is a natural polymer utilization product. This is polyester synthesized by microorganisms, for example,
A polyester composed of 3-hydroxybutyrate (abbreviation 3HB) or 3-hydroxyvalerate (abbreviation 3HV) is used, and a random copolymer of both [P (3HB-
3HV)] has already been commercialized.

【0004】また、はポリエステルとポリ乳酸とに二
分することができ、前者はジカルボン酸と二価アルコー
ルとを縮合してできるポリエステルを使用するものであ
り、後者はグルコースを乳酸醗酵させて乳酸を、次に、
乳酸を環化反応させてラクチドを、次に、ラクチドを開
環重合させてポリ乳酸として製品化したものである。
Further, is capable of being divided into polyester and polylactic acid, the former uses polyester obtained by condensing dicarboxylic acid and dihydric alcohol, and the latter uses lactic acid fermentation of glucose to produce lactic acid. ,next,
Lactide is cyclized to give lactide, and then lactide is subjected to ring-opening polymerization to produce polylactic acid.

【0005】また、は澱粉や変性ポリビニルアルコー
ルなどの天然高分子を原料とし、植物油などを可塑剤と
して樹脂化して使用するものである。そして、これらの
プラスチックスは土壌中に埋没しておくと、土壌中に生
息する放線菌やアルカリゲネス族などの微生物の作用に
より低分子量の化合物に分解され、最終的には炭酸ガス
(CO2 )、アンモニア(NH3 )および水(H2 O)
になって植物の肥料となる。
In addition, a natural polymer such as starch or modified polyvinyl alcohol is used as a raw material, and vegetable oil or the like is used as a plasticizer and made into a resin. When these plastics are buried in soil, they are decomposed into low molecular weight compounds by the action of microorganisms such as actinomycetes and Alcaligenes that inhabit the soil, and eventually carbon dioxide (CO 2 ) , Ammonia (NH 3 ) and water (H 2 O)
Becomes a fertilizer for plants.

【0006】然しながら、現在、実用化されているかゝ
る生分解性プラスチックスは何れも難燃性を備えていな
い。
However, none of the biodegradable plastics that have been put into practical use at present are flame retardant.

【0007】[0007]

【発明が解決しようとする課題】現在、実用化されてい
る生分解性プラスチックスは難燃性を備えていない。そ
こで難燃性を付与して用途を電機製品にまで拡大させる
ことが課題である。
The biodegradable plastics currently in practical use do not have flame retardancy. Therefore, it is an issue to impart flame retardancy and expand its application to electrical products.

【0008】[0008]

【課題を解決するための手段】上記の課題は生分解性プ
ラスチックス原料よりなるペレットに水酸化アルミニウ
ム〔Al(OH)3〕粉末または水酸化マグネシウム〔Mg
(OH)2〕粉末の少なくとも一方を添加し成形すること
により解決することができる。
[Means for Solving the Problems] The above-mentioned problems are solved by forming pellets made of a biodegradable plastics raw material into aluminum hydroxide [Al (OH) 3 ] powder or magnesium hydroxide [Mg
This can be solved by adding at least one of (OH) 2 ] powder and molding.

【0009】[0009]

【作用】プラスチックスを難燃性にする手段として、一
般にハロゲン原子を有する難燃剤、例えば、ハロゲン化
無水フタール酸,臭素化ポリオールなどを原料中に加え
ておき、プラスチックスが燃焼する際に発生する熱によ
り難燃剤が分解し、その際に生ずるハロゲンガスが酸素
(O2 )の供給を遮断する方法がとられている。然し、
ハロゲンガスは人体に有害なことから好ましい方法とは
言えない。
[Function] As a means for making plastics flame-retardant, a flame-retardant agent having a halogen atom, for example, halogenated phthalic anhydride, brominated polyol, etc. is generally added to the raw material to generate when the plastics burn. The flame retardant is decomposed by the heat generated, and the halogen gas generated at that time interrupts the supply of oxygen (O 2 ). However,
Halogen gas is not a preferable method because it is harmful to the human body.

【0010】発明者はプラスチックスを難燃性にする手
段としてAl(OH)3やMg(OH)2を原料中に配合してお
く方法に着目した。(例えば、特開昭63-183960 、特開
昭63-198212 ) この方法は、プラスチックスが燃焼する際に発生する熱
をこれらの材料が吸熱して分解すると共に水(H2 O)
を生じ、吸熱作用と水の発生により難燃性を示すもので
ある。
The inventor has paid attention to a method of incorporating Al (OH) 3 or Mg (OH) 2 into the raw material as a means for making plastics flame-retardant. (For example, JP-A-63-183960 and JP-A-63-198212) In this method, the heat generated when the plastics are burned is absorbed by these materials and decomposed, and water (H 2 O) is generated.
And shows flame retardancy due to the endothermic action and the generation of water.

【0011】 2Al(OH)3 → Al23 + 3H2 O − 73 kcal ・・・(1) 然し、このような難燃剤を添加する場合の問題点は、添
加量に比例して難燃性は顕著になるものゝ、生分解性や
機械的性質などの物性が低下し、相反の関係にあること
である。
2Al (OH) 3 → Al 2 O 3 + 3H 2 O − 73 kcal (1) However, the problem in adding such a flame retardant is that the flame retardant is proportional to the amount added. The properties are conspicuous, and the physical properties such as biodegradability and mechanical properties are deteriorated and there is a contradictory relationship.

【0012】すなわち、添加した水酸化物分子は生分解
性プラスチックスの球晶構造を取り巻くように配位する
結果、生分解性を低下させると思われる。そこで、本発
明はAl(OH)3粉末またはMg(OH)2粉末の少なくとも
一方をプラスチックスが必要とする物性と難燃性を維持
する範囲に添加して成形するもので、実験の結果は混合
率を30%程度とすることにより好結果を得ることができ
た。
That is, it is considered that the added hydroxide molecules are coordinated so as to surround the spherulite structure of the biodegradable plastics, resulting in a decrease in biodegradability. Therefore, in the present invention, at least one of Al (OH) 3 powder and Mg (OH) 2 powder is added in a range that maintains the physical properties and flame retardancy required by plastics, and molding is performed. Good results could be obtained by setting the mixing ratio to about 30%.

【0013】次に、樹脂の成形には射出成形法(Injecti
on-mold)が使われることが多いが、生分解性プラスチッ
クスは一般に融点が低く、分解し易いことから生分解性
を損なわないためにはプラスチックスの融点近傍の温度
でなるべく短時間で処理を行うのが好ましく、実験によ
れば、混練機でのシリンダ内の滞留時間を3秒以内と
し、射出成形機のシリンダ内の滞留時間を7秒以内と
し、溶融温度をプラスチックスの溶融温度より+30℃以
内に保つことにより好結果を得ることができた。
Next, an injection molding method (Injecti
On-mold) is often used, but biodegradable plastics generally have a low melting point and are easily decomposed, so in order not to impair biodegradability, treat them at a temperature near the melting point of the plastics in the shortest possible time. According to the experiment, the residence time in the cylinder of the kneading machine is 3 seconds or less, the residence time in the cylinder of the injection molding machine is 7 seconds or less, and the melting temperature is higher than the melting temperature of the plastics. Good results could be obtained by keeping the temperature within + 30 ° C.

【0014】[0014]

【実施例】【Example】

実施例1:生分解性プラスチックスとして化学合成高分
子化合物に属する脂肪族ポリエステル(品名ビオノー
レ,品番#1020, 昭和高分子) のペレットを用い、ま
た、Al(OH)3としては純度99.8%で粒径が5〜10μm
のものを使用し、両者の混合率としては90:10〜50:50
の5段階に変えた。
Example 1 As the biodegradable plastics, pellets of an aliphatic polyester (product name Bionore, product number # 1020, Showa High Polymer) belonging to a chemically synthesized polymer compound were used, and as Al (OH) 3 , the purity was 99.8%. Particle size 5 ~ 10μm
The mixing ratio of the two is 90:10 to 50:50.
It changed into 5 steps.

【0015】また、混練条件としては、混練機としてラ
ボプラストミル(東洋精機)を使用し、ノズル温度を11
5 〜120 ℃, トルクを4〜6kg,滞留時間を3秒以内と
し、射出条件としては、成形機として射出成形機(品名
JC-25SS,日本製鋼所) を使用し、射出温度を134 〜144
℃, 射出時間7秒,冷却温度20〜40℃, 冷却時間15〜20
秒, 射出圧力300 〜450 kgf/cm2 の条件で行い、60×20
×2 mm の試験片を作った。
As the kneading conditions, a Labo Plastomill (Toyo Seiki) is used as the kneading machine, and the nozzle temperature is 11
5 to 120 ° C, torque 4 to 6 kg, residence time within 3 seconds, and injection conditions are injection molding machine (product name).
(JC-25SS, Japan Steel Works) using an injection temperature of 134-144.
℃, injection time 7 seconds, cooling temperature 20-40 ℃, cooling time 15-20
Sec, performed under conditions of injection pressure 300 ~450 kgf / cm 2, 60 × 20
A test piece of × 2 mm was prepared.

【0016】そして、試験片を使用して機械的性質と難
燃性(JIS A1321準拠)を測定した。その方法は、試験片
を垂直に保持すると共に試験片の下側305 mm の位置に
ガーゼを置き、試験片の下端をカスバーナで10秒間加熱
して着火せしめ、その後に燃焼を続けるか、また、燃焼
して溶けた滴下物がガーゼに落ちた後にガーゼが燃える
か否かを調べるものである。 1.機械的な物性 Al(OH)3の含有率 引張り降伏応力(kgf/mm2) 規定曲げ強さ(kgf/mm2) 0 % 2.9 2.1 10 % 2.8 2.2 20 % 2.5 2.3 30 % 2.4 2.8 40 % 2.2 3.0 50 % 2.2 2.8 この結果から、難燃剤の含有率が増すに従って引張り降
伏応力は次第に下がり、また曲げ強さは次第に増して飽
和するのが判る。 2.難燃性試験 Al(OH)3の含有率 炎分離後の状況 ガーゼへの着火の状況 0 % 燃え続ける 着火する 10 % 燃え続ける 着火する 20 % 燃え続ける 着火する 30 % 消える 着火しない 40 % 消える 着火しない 50 % 消える 着火しない この結果から難燃性を持たせるにはAl(OH)3を少なく
とも30 %含有させる必要があることが判る。 3.混練温度と射出成形温度の生分解性に及ぼす影響 上記の脂肪族ポリエステル(品名ビオノーレ,品番#10
20, 昭和高分子) にAl(OH)3を30 %含有させ、混練
温度と射出成形温度を変えて試験片を作り、この試験片
を土壌中に100 日間に亙って埋没して生分解性を測定し
た。なお、ビオノーレ#1020の溶融温度は114 ℃であ
る。 処理温度が低い条件(混練温度115 〜120 ℃, 射出温度134 〜144 ℃) ・・・・・・・・・・・・・・・・・・・・重量10%減少 処理温度が高い条件(混練温度125 〜140 ℃, 射出温度160 〜170 ℃) ・・・・・・・・・・・・・・・・・・・・重量2%減少 この結果から、生分解性を損なわないためには成形温度
をなるべく低く保つ必要があることが判る。
Then, the test piece was used to measure the mechanical properties and flame retardancy (according to JIS A1321). The method is to hold the test piece vertically and place the gauze on the lower side of the test piece 305 mm, heat the lower end of the test piece with a casverner for 10 seconds to ignite, and then continue burning, or The purpose of this test is to investigate whether or not the gauze burns after the burned and melted drops fall onto the gauze. 1. Mechanical Properties Al (OH) 3 Content Tensile Yield Stress (kgf / mm 2 ) Specified Bending Strength (kgf / mm 2 ) 0% 2.9 2.1 10% 2.8 2.2 20% 2.5 2.3 30% 2.4 2.8 40% 2.2 3.0 50% 2.2 2.8 From these results, it can be seen that the tensile yield stress gradually decreases and the flexural strength gradually increases and saturates as the content of the flame retardant increases. 2. Flame-retardant test Content of Al (OH) 3 Situation after separation of flame Situation of ignition on gauze 0% Continue to burn 10% Continue to burn 20% Continue to burn 30% Continue to burn 30% Do not burn 40% Do not burn No 50% extinguished No ignition This result shows that at least 30% of Al (OH) 3 must be contained to have flame retardancy. 3. Effect of kneading temperature and injection molding temperature on biodegradability The above-mentioned aliphatic polyester (Product name: Bionore, Product number: # 10)
(20, Showa High Polymer) containing 30% of Al (OH) 3 and changing the kneading temperature and injection molding temperature to make a test piece, which was buried in soil for 100 days and biodegraded. The sex was measured. The melting temperature of Bionore # 1020 is 114 ° C. Conditions with low processing temperature (kneading temperature 115-120 ℃, injection temperature 134-144 ℃) ・ ・ ・ ・ ・ ・ ・ 10% reduction in weight High-processing condition ( Kneading temperature 125-140 ℃, injection temperature 160-170 ℃) ・ ・ ・ ・ ・ ・ 2% reduction in weight From these results, in order not to impair biodegradability It is understood that the molding temperature should be kept as low as possible.

【0017】[0017]

【発明の効果】本発明の実施により生分解性プラスチッ
クスに難燃性を付与することができるが、そのためには
Al(OH)3粉末またはMg(OH)2粉末を30重量%程度加
える必要があり、また、成形はプラスチックスの溶融温
度になるべく近い温度で行うことが必要である。
EFFECTS OF THE INVENTION By implementing the present invention, it is possible to impart flame retardancy to biodegradable plastics. For that purpose, it is necessary to add about 30% by weight of Al (OH) 3 powder or Mg (OH) 2 powder. In addition, molding must be performed at a temperature as close as possible to the melting temperature of plastics.

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08K 3/20 KJR C08K 3/20 KJR 3/26 KAD 3/26 KAD // C08L 67/04 LPM C08L 67/04 LPM Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI Technical display location C08K 3/20 KJR C08K 3/20 KJR 3/26 KAD 3/26 KAD // C08L 67/04 LPM C08L 67 / 04 LPM

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 生分解性プラスチックス原料よりなるペ
レットに水酸化アルミニウム粉末または水酸化マグネシ
ウム粉末の少なくとも一方を添加し成形することを特徴
とする難燃性生分解プラスチックスの製造方法。
1. A method for producing a flame-retardant biodegradable plastics, which comprises adding at least one of aluminum hydroxide powder and magnesium hydroxide powder to a pellet made of a raw material of biodegradable plastics, and molding.
【請求項2】 前記水酸化アルミニウム粉末または水酸
化マグネシウム粉末の含有量が30〜50重量%であること
を特徴とする請求項1記載の難燃性生分解プラスチック
スの製造方法。
2. The method for producing a flame-retardant biodegradable plastics according to claim 1, wherein the content of the aluminum hydroxide powder or the magnesium hydroxide powder is 30 to 50% by weight.
JP5864995A 1995-03-17 1995-03-17 Manufacture of nonflammable biodegradable plastic Pending JPH08252823A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5864995A JPH08252823A (en) 1995-03-17 1995-03-17 Manufacture of nonflammable biodegradable plastic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5864995A JPH08252823A (en) 1995-03-17 1995-03-17 Manufacture of nonflammable biodegradable plastic

Publications (1)

Publication Number Publication Date
JPH08252823A true JPH08252823A (en) 1996-10-01

Family

ID=13090438

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5864995A Pending JPH08252823A (en) 1995-03-17 1995-03-17 Manufacture of nonflammable biodegradable plastic

Country Status (1)

Country Link
JP (1) JPH08252823A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0913426A1 (en) * 1997-10-31 1999-05-06 Ticona GmbH Thermoplastic flame retardant molding compositions containing aluminium hydroxide
EP1609820A4 (en) * 2003-04-02 2006-04-12 Mitsubishi Plastics Inc Injection-molded object
WO2006051640A1 (en) 2004-11-15 2006-05-18 Unitika Ltd. Flame-retardant biodegradable polyester resin composition, process for producing the same, and molded object obtained therefrom
US7439283B2 (en) 2002-09-06 2008-10-21 Mitsubishi Plastics, Inc. Flame retardant resin composition and flame-retardant injection-molding
WO2009153934A1 (en) 2008-06-16 2009-12-23 株式会社Adeka Non-halogen flame-retardant synthetic resin composition
WO2010004799A1 (en) * 2008-07-10 2010-01-14 日本電気株式会社 Polylactic acid resin composition and polylactic acid resin molded body

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0913426A1 (en) * 1997-10-31 1999-05-06 Ticona GmbH Thermoplastic flame retardant molding compositions containing aluminium hydroxide
KR100954924B1 (en) * 2002-09-06 2010-04-27 미쓰비시 쥬시 가부시끼가이샤 Flame-retardant resin composition and flame-retardant injection molding
US7439283B2 (en) 2002-09-06 2008-10-21 Mitsubishi Plastics, Inc. Flame retardant resin composition and flame-retardant injection-molding
EP1609820A4 (en) * 2003-04-02 2006-04-12 Mitsubishi Plastics Inc Injection-molded object
US8349935B2 (en) 2003-04-02 2013-01-08 Mitsubishi Plastics, Inc. Polylactic acid resin article comprising grains of metal-hydroxide particles
KR101156384B1 (en) * 2003-04-02 2012-06-13 소니 가부시끼가이샤 Injection-molded object
JP5036318B2 (en) * 2004-11-15 2012-09-26 ユニチカ株式会社 Flame retardant polylactic acid resin composition, method for producing the same, and molded product obtained therefrom
JPWO2006051640A1 (en) * 2004-11-15 2008-05-29 ユニチカ株式会社 Flame retardant biodegradable polyester resin composition, method for producing the same, and molded product obtained therefrom
WO2006051640A1 (en) 2004-11-15 2006-05-18 Unitika Ltd. Flame-retardant biodegradable polyester resin composition, process for producing the same, and molded object obtained therefrom
WO2009153934A1 (en) 2008-06-16 2009-12-23 株式会社Adeka Non-halogen flame-retardant synthetic resin composition
WO2010004799A1 (en) * 2008-07-10 2010-01-14 日本電気株式会社 Polylactic acid resin composition and polylactic acid resin molded body
JP5747503B2 (en) * 2008-07-10 2015-07-15 日本電気株式会社 Polylactic acid resin composition and polylactic acid resin molded article
US9550876B2 (en) 2008-07-10 2017-01-24 Nec Corporation Polylactic acid resin composition and polylactic acid resin molded body

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