JPH05209082A - Production of reclaimed cushioning body - Google Patents
Production of reclaimed cushioning bodyInfo
- Publication number
- JPH05209082A JPH05209082A JP4038594A JP3859492A JPH05209082A JP H05209082 A JPH05209082 A JP H05209082A JP 4038594 A JP4038594 A JP 4038594A JP 3859492 A JP3859492 A JP 3859492A JP H05209082 A JPH05209082 A JP H05209082A
- Authority
- JP
- Japan
- Prior art keywords
- buffer
- container
- foam
- closed container
- strips
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 239000006260 foam Substances 0.000 claims abstract description 44
- 239000000463 material Substances 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 21
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 239000011347 resin Substances 0.000 claims abstract description 20
- 239000012943 hotmelt Substances 0.000 claims abstract description 15
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 13
- 239000000057 synthetic resin Substances 0.000 claims abstract description 13
- 229920001971 elastomer Polymers 0.000 claims abstract description 10
- 239000000872 buffer Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 15
- 238000002485 combustion reaction Methods 0.000 claims description 13
- 239000002360 explosive Substances 0.000 claims description 13
- 239000012557 regeneration buffer Substances 0.000 claims description 7
- 239000002699 waste material Substances 0.000 abstract description 13
- 239000000853 adhesive Substances 0.000 abstract description 7
- 230000001070 adhesive effect Effects 0.000 abstract description 7
- 239000007789 gas Substances 0.000 description 38
- 229920005992 thermoplastic resin Polymers 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 230000001172 regenerating effect Effects 0.000 description 8
- 239000007800 oxidant agent Substances 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 238000003466 welding Methods 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920005830 Polyurethane Foam Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/141—Feedstock
- Y02P20/143—Feedstock the feedstock being recycled material, e.g. plastics
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Buffer Packaging (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】この発明は、合成樹脂発泡体の廃
棄物から再生緩衝体を製造する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a regenerated buffer from waste synthetic resin foam.
【0002】[0002]
【従来の技術】ポリウレタン発泡体あるいはポリエチレ
ン発泡体などの合成樹脂発泡体は、軽量で、断熱性、衝
撃緩衝性に優れるため、緩衝体や梱包体あるいは断熱
材、保温材などにおいて幅広く用いられている。2. Description of the Related Art Since synthetic resin foams such as polyurethane foams and polyethylene foams are lightweight and have excellent heat insulating properties and shock absorbing properties, they are widely used as cushioning materials, packaging materials, heat insulating materials, heat insulating materials, etc. There is.
【0003】しかしながら、近年において発泡体の大量
使用により廃棄物として出される発泡体の量も膨大にな
り、その処理が問題になっていた。特に、最近になって
地球環境のことが大きな社会問題となり、廃棄物の減
少、資源の有効活用が叫ばれるようになり、発泡体の再
生利用が要求されるようになった。However, in recent years, due to the large amount of foam used, the amount of foam discharged as a waste also becomes enormous, and its treatment has become a problem. In particular, recently, the global environment has become a major social issue, and the reduction of waste and the effective use of resources have been called for, and the recycling of foam has been required.
【0004】発泡体廃棄物の処理方法としては次のもの
が提案されている。その一つは、廃棄物としての軟質ポ
リウレタンフォームなどを細かく粉砕し、その発泡体細
片と接着剤とを混合してその混合物を加圧加熱すること
により、発泡体細片を接着して再生緩衝体を製造する方
法である。また、他のものは、廃棄物としての熱可塑性
樹脂発泡体を細かく粉砕し、その発泡体細片を発泡体の
発火点以下の温度に加熱したヒーターに押し付けて溶融
処理する方法である。(特開昭62−205138号公
報に記載)The following methods have been proposed for treating foam waste. One of them is to pulverize soft polyurethane foam etc. as waste into small pieces, mix the foam strips with an adhesive and heat the mixture under pressure to bond the foam strips and regenerate them. It is a method of manufacturing a buffer. The other method is a method in which a thermoplastic resin foam as waste is finely crushed and the foam pieces are pressed against a heater heated to a temperature below the ignition point of the foam to perform a melting treatment. (Described in JP-A-62-205138)
【0005】しかるに、前者の接着剤を用いる方法にあ
っては、熱可塑性樹脂発泡体、特にはポリエチレン発泡
体あるいはポリプロピレン発泡体などのポリオレフィン
系発泡体廃棄物から再生緩衝体を製造しようとすると、
それらの発泡体が接着性に劣るために、得られる再生緩
衝体が元の発泡体細片に分離しやすく、実用性のある再
生緩衝体を得難いという問題があった。However, in the former method using an adhesive, when a regenerated buffer is produced from a thermoplastic resin foam, particularly a polyolefin foam waste such as polyethylene foam or polypropylene foam,
Since these foams are poor in adhesiveness, the regenerated buffer obtained is easy to separate into the original foam pieces, and there is a problem that it is difficult to obtain a practical regenerated buffer.
【0006】また、後者の方法にあっては、発泡体細片
をヒーターに強く押し付けながら溶融させねばならない
ため、発泡体細片の気孔が潰れやすく均一な再生緩衝体
が得られないばかりか、その溶融などの処理に時間がか
かるという問題があった。さらに、発泡体細片を、ヒー
ターに押し付けながら溶融炉から押し出さねばならない
ため装置が複雑になる問題があった。Further, in the latter method, since the foam strip must be pressed against the heater to melt it, the pores of the foam strip are easily crushed and a uniform regenerating buffer cannot be obtained. There is a problem that the processing such as the melting takes time. Further, the foam strip must be pushed out of the melting furnace while being pressed against the heater, which causes a problem that the device becomes complicated.
【0007】本発明者らは、先に、熱可塑性樹脂発泡体
細片を容器に密に収容し、その容器内に可燃性気体を充
填し爆発燃焼させることにより、熱可塑性樹脂発泡細片
の表面を互いに溶着させて一つの発泡体とする再生発泡
体の製造方法を提供した。(特願平3−29584号)The inventors of the present invention previously stored the thermoplastic resin foam strips in a container tightly, filled the container with a combustible gas, and explosively burned the thermoplastic resin foam strips. Provided is a method for producing a regenerated foam by fusing the surfaces together to form a single foam. (Japanese Patent Application No. 3-29584)
【0008】この方法によれば、熱可塑性樹脂発泡体の
廃棄物から実用性のある再生発泡体を簡便に得ることが
できる。According to this method, a practical recycled foam can be easily obtained from the waste of the thermoplastic resin foam.
【0009】ところが、この方法では、熱可塑性樹脂発
泡体が前述したポリオレフィン系の発泡体である場合に
は、細片間の接着力が乏しく、得られた再生発泡体の形
が崩れたりすることがあった。また、ゴムチップなどの
非発泡体や熱可塑性樹脂以外の樹脂には適用できなかっ
た。However, in this method, when the thermoplastic resin foam is the above-mentioned polyolefin-based foam, the adhesive strength between the strips is poor, and the shape of the regenerated foam obtained may be lost. was there. In addition, it cannot be applied to non-foamed materials such as rubber chips and resins other than thermoplastic resins.
【0010】[0010]
【発明が解決しようとする課題】この発明は、上記した
問題点を悉く解決するために提案されたものであって、
ゴムチップなどの非発泡体やポリオレフィン系の比較的
接着力が乏しい合成樹脂の廃棄物から、実用性のある再
生緩衝体を短時間にしかも簡便に得ることのできる再生
緩衝体の製造方法を提供しようとするものである。SUMMARY OF THE INVENTION The present invention has been proposed in order to solve the above problems,
A method for manufacturing a regenerating buffer, which can easily obtain a practical regenerating buffer in a short time from waste of non-foam such as rubber chips or polyolefin-based synthetic resin with relatively poor adhesive strength It is what
【0011】[0011]
【課題を解決するための手段】すなわち、この発明は、
合成樹脂発泡体または合成樹脂発泡体とゴム等の異材質
よりなる緩衝材を約2〜30mmの大きさの細片に破砕
し、前記細片とホットメルト樹脂とを混合するととも
に、前記混合物を密閉容器内に密に収容し、次いで前記
密閉容器内に可燃性気体を充満し、該可燃性気体を爆発
燃焼させて、前記緩衝材細片を一体に接合して緩衝体を
得ることを特徴とする再生緩衝体の製造方法に係る。That is, the present invention is
The synthetic resin foam or the synthetic resin foam and a cushioning material made of a different material such as rubber are crushed into small pieces having a size of about 2 to 30 mm, and the small pieces and the hot melt resin are mixed, and the mixture is mixed. Characterized by tightly accommodating in a hermetic container, then filling the combustible gas in the hermetic container, explosively burning the combustible gas, and joining the buffer material strips integrally to obtain a buffer body The present invention relates to a method for manufacturing a regeneration buffer.
【0012】[0012]
【作用】容器に収容された緩衝材細片とホットメルト樹
脂との混合物は、容器に充満された可燃性気体の爆発燃
焼熱によって該ホットメルト樹脂および緩衝材中の熱可
塑性樹脂発泡体表面が溶融し、接着されにくいオレフィ
ン系樹脂やゴムなどであっても、隣接細片を接合一体化
して一つの再生緩衝体となす。その際、前記混合物が圧
縮状態で密に容器に収容されていれば、隣接した細片が
復元力によって互いに強く押し合いながら溶着するた
め、溶着が確実かつ強いものになる。しかも、接着に比
べて溶着の方が結合力が大であるため、得られた緩衝体
の形状が崩れるおそれがない。また、可燃性気体の爆発
燃焼は一瞬に起こり、その発生圧力は容器内の細片に均
一に加わるため、再生緩衝体の製造に要する時間が極め
て短くて済むばかりか得られる再生緩衝体の気孔も均一
である。The mixture of the buffer strips and the hot-melt resin contained in the container causes the surface of the thermoplastic resin foam in the hot-melt resin and the buffer due to the explosive combustion heat of the combustible gas filled in the container. Even if it is an olefin-based resin or rubber that melts and is difficult to adhere, adjacent strips are joined and integrated into one regenerative buffer. At that time, if the mixture is densely housed in a container in a compressed state, adjacent strips are pressed against each other by the restoring force and are welded to each other, so that the welding is sure and strong. Moreover, since the bonding force is larger in welding than in bonding, there is no fear that the shape of the obtained cushioning body will collapse. In addition, the explosive combustion of flammable gas occurs instantly, and the generated pressure is evenly applied to the strip inside the container.Therefore, the time required to manufacture the regenerative buffer is extremely short, and the pores of the regenerative buffer are obtained. Is also uniform.
【0013】[0013]
【実施例】以下添付の図面に従ってこの発明を詳細に説
明する。図1はこの発明の再生緩衝体の製造方法の一実
施例における緩衝材混合物収容時の容器の断面図、図2
はこの発明製法に用いられる密閉容器の一例を示す斜視
図、図3は網状籠の一例を示す斜視図、図4はこの発明
製法の他の例を示す断面図、図5はプレスした状態を示
す断面図、図6はプレス解除時を示す断面図、図7は再
生緩衝体取出し時を示す斜視図である。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described in detail below with reference to the accompanying drawings. FIG. 1 is a cross-sectional view of a container at the time of containing a cushioning material mixture in an embodiment of a method for manufacturing a regenerated cushioning body of the present invention, FIG.
Is a perspective view showing an example of a closed container used in the production method of the present invention, FIG. 3 is a perspective view showing an example of a mesh basket, FIG. 4 is a sectional view showing another example of the production method of the present invention, and FIG. 5 shows a pressed state. 6 is a cross-sectional view showing when the press is released, and FIG. 7 is a perspective view showing when the regeneration buffer is taken out.
【0014】まず、合成樹脂発泡体などからなる緩衝材
を、あらかじめ粉砕機によって細かくし、緩衝材細片1
0を得る。この実施例において、前記緩衝材にはポリエ
チレン発泡体廃棄物を用いている。First, a buffer material made of synthetic resin foam or the like is finely crushed in advance by a crusher to form a buffer material strip 1.
Get 0. In this embodiment, polyethylene foam waste is used as the cushioning material.
【0015】この発明に用いられる緩衝材としては、ポ
リエチレン、ポリプロピレン、ポリ塩化ビニル、ポリス
チレンなどの熱可塑性樹脂発泡体、ポリウレタンなどの
熱硬化性樹脂発泡体などの一種または二種以上が混合し
て用いられる。前記緩衝材には、ブチルゴムやSBR、
NBRなどの異材質を混合することも可能である。As the cushioning material used in the present invention, one kind or two or more kinds of thermoplastic resin foams such as polyethylene, polypropylene, polyvinyl chloride and polystyrene and thermosetting resin foams such as polyurethane are mixed. Used. Butyl rubber, SBR,
It is also possible to mix different materials such as NBR.
【0016】前記緩衝材細片10の大きさは約2〜30
mmが適当である。この細片の大きさが2mmより小さ
い場合には、爆発燃焼によって細片が溶失するおそれが
ある。また、30mmより大きい場合には、細片間の隙
間が大きくなり接着が不完全になるだけでなく、細片を
接着するためのホットメルト樹脂量が増しコスト高とな
るおそれがある。なお、前記細片10の大きさはすべて
均一にする必要はなく、むしろ容器内に密に収容するこ
とができるように、細片を不揃いに形成する方が好まし
い。The size of the buffer material strip 10 is about 2 to 30.
mm is suitable. If the size of the strip is smaller than 2 mm, the strip may be melted and lost due to explosive combustion. On the other hand, if it is larger than 30 mm, not only the gap between the strips becomes large and the adhesion becomes incomplete, but also the amount of the hot melt resin for adhering the strips increases and the cost may increase. The size of the strips 10 does not have to be uniform, but rather the strips are preferably formed in a non-uniform manner so that they can be densely housed in a container.
【0017】この緩衝材細片10にホットメルト樹脂1
1を混合し緩衝材混合物を得る。前記ホットメルト樹脂
11としては、ペレットあるいはフレーク状または粉末
状の公知の低融点ホットメルト接着材が用いられる。こ
の実施例において、前記緩衝材細片10とホットメルト
樹脂11との混合比は7:3(容積比)である。なお、
このホットメルト樹脂11の混合量は、接合される緩衝
材細片の種類や量によって適宜に設定され、前記緩衝材
細片が熱硬化性樹脂やゴムチップなどの場合は増量し
て、実用的な接着力を付与することが好ましい。その
際、緩衝材細片10に静電気を起こすことによって、ホ
ットメルト樹脂11を前記緩衝材細片10に効果的に付
着させることができる。Hot-melt resin 1 is added to the cushioning material strip 10.
1 to mix to obtain a buffer mixture. As the hot melt resin 11, a known low melting point hot melt adhesive in the form of pellets, flakes or powder is used. In this embodiment, the mixing ratio of the buffer strip 10 and the hot melt resin 11 is 7: 3 (volume ratio). In addition,
The mixing amount of the hot melt resin 11 is appropriately set according to the type and amount of the cushioning material strip to be joined, and when the cushioning material strip is a thermosetting resin or a rubber chip, the amount is increased to a practical level. It is preferable to impart an adhesive force. At this time, the hot melt resin 11 can be effectively attached to the buffer material strip 10 by generating static electricity in the buffer material strip 10.
【0018】得られた混合物1.5立方メートルを、図
1のように、内寸法1005×2005×505mmで
内容積が約1.0立方メートルからなる厚さ20mmの
鉄板製密閉容器12内に収容し密封する。The resulting mixture of 1.5 cubic meters is housed in an iron plate hermetic container 12 having a thickness of 20 mm and having an internal size of 1005 × 2005 × 505 mm and an internal volume of about 1.0 cubic meter as shown in FIG. Seal it.
【0019】密閉容器12の一例を図2に示す。この密
閉容器12は、鉄など可燃性気体の爆発燃焼に充分耐え
うる強度を有し、一方に蓋13が開閉可能に形成されて
いるとともに、一端が真空ポンプ(図示せず)に連結さ
れた吸引パイプ14と気体充填用パイプ15と図示しな
い電源に接続された点火プラグ16と圧力計(図示せ
ず)が設けられている。なお、前記点火プラグ16は自
動車用のものを用いている。An example of the closed container 12 is shown in FIG. The closed container 12 has a strength sufficient to withstand explosive combustion of combustible gas such as iron, has a lid 13 formed on one side so as to be openable and closable, and has one end connected to a vacuum pump (not shown). A suction pipe 14, a gas filling pipe 15, an ignition plug 16 connected to a power source (not shown), and a pressure gauge (not shown) are provided. The spark plug 16 used is for an automobile.
【0020】また、前記緩衝材混合物は、あらかじめ、
図3に示されるような網状籠17に密に詰めておき、こ
の網状籠17が前記密閉容器12内に収められる。前記
網状籠17上部は開閉可能な蓋18になっている。ま
た、前記網状籠17の網目は緩衝材細片が飛び出さない
大きさに形成されている。それによって、緩衝材混合物
が密閉容器12内に収容しやすくなるとともに、爆発燃
焼の際に再生緩衝体が前記密閉容器12壁面にくっつい
てしまうということがない。The cushioning material mixture may be prepared in advance by
The net cage 17 as shown in FIG. 3 is packed tightly, and the net cage 17 is housed in the closed container 12. An upper portion of the net cage 17 is a lid 18 that can be opened and closed. Further, the mesh of the mesh cage 17 is formed in a size such that the cushioning material strip does not protrude. As a result, the cushioning material mixture is easily accommodated in the closed container 12, and the regenerated cushioning body does not stick to the wall surface of the closed container 12 during explosive combustion.
【0021】次に、真空ポンプの作動により、吸引パイ
プ14を介して密閉容器12内の空気を吸い出し、内部
の圧力が20mmHgになった時点で真空ポンプの作動
を止め、吸引パイプ14途中に設けられたバルブ(図示
せず)を閉じる。密閉容器12内の空気を外部に吸引す
る理由は、前記密閉容器12内に空気が多量に存在する
と、後述する可燃性気体の充填が困難になるだけでな
く、可燃性気体の爆発燃焼力が低下するためである。Next, the vacuum pump is actuated to suck out the air in the closed container 12 through the suction pipe 14, and when the internal pressure reaches 20 mmHg, the operation of the vacuum pump is stopped and the suction pipe 14 is provided. Close the valve (not shown) provided. The reason for sucking the air in the airtight container 12 to the outside is that if a large amount of air is present in the airtight container 12, not only is it difficult to fill the flammable gas described below, but the explosive combustion power of the flammable gas is This is because it will decrease.
【0022】そして、水素と酸素を容積比において2:
1.1に混合した可燃性気体20を、気体充填用パイプ
15を介して0.5立方メートル/分の速度で密閉容器
12内に充填する。密閉容器12内の圧力が760mm
Hgになった時点で、前記気体充填用パイプ15のバル
ブ(図示せず)を閉じる。可燃性気体の充填時間は約2
分であった。なお、前記可燃性気体は加圧して(たとえ
ば2kg/cm2 の圧力で)密閉容器12内に充填する
ことにより、爆発燃焼時のエネルギーを大にでき一層効
率よく溶着することができる。Then, the volume ratio of hydrogen to oxygen is 2:
The flammable gas 20 mixed with 1.1 is filled into the closed container 12 through the gas filling pipe 15 at a rate of 0.5 cubic meters / minute. The pressure in the closed container 12 is 760 mm
At the time of reaching Hg, the valve (not shown) of the gas filling pipe 15 is closed. Filling time for flammable gas is about 2
It was a minute. The flammable gas is pressurized (for example, at a pressure of 2 kg / cm 2 ) to be filled in the closed container 12, so that energy at the time of explosive combustion can be increased and welding can be performed more efficiently.
【0023】この発明製法における可燃性気体20とし
ては、種々の可酸化剤と酸化剤との混合物が用いられ
る。可酸化剤としては、水素が最適であるがその他メタ
ン、エタン、プロパン、エチレン、プロピレン、アセチ
レンなども使用することができる。一方、酸化剤として
は、酸素が最適であるが、その他、空気、オゾンなども
使用することができる。可酸化剤と酸化剤との最適混合
比は、可酸化剤および酸化剤の種類あるいは用いられる
合成樹脂発泡体の材質などによっても異なるが、例とし
て、水素と酸素では体積比で2:1、あるいはアセチレ
ンと酸素では体積比で2:5である。なお、可燃性気体
の爆発燃焼は、密閉容器内で前記可燃性気体20に点火
プラグ16によって点火されてなされる。As the combustible gas 20 in the method of the present invention, a mixture of various oxidants and oxidants is used. Hydrogen is most suitable as the oxidizable agent, but methane, ethane, propane, ethylene, propylene, acetylene and the like can also be used. On the other hand, oxygen is most suitable as the oxidant, but air, ozone, etc. can also be used. The optimum mixing ratio of the oxidizer and the oxidizer varies depending on the kind of the oxidizer and the oxidizer or the material of the synthetic resin foam used, but for example, hydrogen and oxygen are 2: 1 in volume ratio, Alternatively, the volume ratio of acetylene and oxygen is 2: 5. The explosive combustion of the combustible gas is performed by igniting the combustible gas 20 by the ignition plug 16 in the closed container.
【0024】気体充填用パイプ15のバルブを閉じたま
ま1分間放置して、可燃性気体が密閉容器12内および
緩衝材細片10間にまんべんなく行き渡るようにする。
その後、点火プラグ16に点火し、密閉容器12内の可
燃性気体を爆発燃焼する。そして、その直後に前記気体
充填用パイプ15を用いて、密閉容器内の圧力が760
mmHgに戻るまで二酸化炭素を前記密閉容器12内に
導入する。それによって、可燃性気体20の爆発燃焼を
瞬時に終わらせて、緩衝材細片10全体が溶け出すのを
防止するためである。The valve of the gas filling pipe 15 is left for 1 minute with the valve closed so that the combustible gas is evenly distributed in the closed container 12 and between the buffer material strips 10.
After that, the ignition plug 16 is ignited, and the combustible gas in the closed container 12 is exploded and burned. Immediately after that, the pressure in the closed container is adjusted to 760 by using the gas filling pipe 15.
Carbon dioxide is introduced into the closed container 12 until it returns to mmHg. This is because the explosive combustion of the combustible gas 20 is ended in an instant, and the buffer material strips 10 are prevented from entirely melting.
【0025】また、前記可燃性気体の爆発燃焼によって
減圧となった密閉容器内の圧力を、大気圧760mmH
gに戻すのは、その後の再生緩衝体取出し時に密閉容器
の蓋13を開けやすくするためである。The pressure in the closed container, which has been reduced by the explosive combustion of the combustible gas, is set to the atmospheric pressure of 760 mmH.
The reason for returning to g is to make it easier to open the lid 13 of the closed container when the regeneration buffer is subsequently taken out.
【0026】二酸化炭素を密閉容器12内に導入して1
分経過後に、密閉容器12の蓋13を開けて網状籠17
を取り出し、さらにその網状籠17から500×100
0×2000mmの直方体からなる一つの再生緩衝体を
取り出した。得られた再生緩衝体は、混合されたホット
メルト樹脂が溶融して隣接する緩衝材細片を互いに結合
し、強固に一体化したもので、気孔がほとんど潰れてい
ない均一なものであった。1 was introduced by introducing carbon dioxide into the closed container 12.
After a lapse of minutes, the lid 13 of the closed container 12 is opened to open the net cage 17
Take out and then 500 × 100 from the mesh basket 17
One regeneration buffer consisting of a 0 × 2000 mm rectangular parallelepiped was taken out. The regenerated buffer body obtained was one in which the mixed hot-melt resin was melted and the adjacent buffer material strips were bonded to each other to be firmly integrated, and the pores were hardly collapsed and were uniform.
【0027】図4ないし図7はこの発明の他の実施例を
示したものである。まず、図4に図示したように、先の
実施例において用いられた緩衝材混合物1.47立方メ
ートルを内寸法が1000×2000×700mm、内
容積が1.4立方メートルからなる鉄製網状籠41に収
容した。図中の符号で図1と同一の符号は同一の部材を
示す。前記緩衝材混合物の収容量は、その細片が容器内
で過度に密とならず後述する可燃性気体との接触面積が
充分となるように決定した。また、前記網状籠41は、
上部が開口し、かつ側面の一部が蓋48によって開閉可
能に形成されているとともに、その網目は収容される緩
衝材混合物が飛び出さない大きさよりなる。4 to 7 show another embodiment of the present invention. First, as shown in FIG. 4, 1.47 cubic meters of the cushioning material mixture used in the previous example is accommodated in an iron net cage 41 having an internal size of 1000 × 2000 × 700 mm and an internal volume of 1.4 cubic meters. did. The same reference numerals as those in FIG. 1 denote the same members in the drawings. The amount of the cushioning material mixture accommodated was determined such that the strips were not excessively dense in the container and the contact area with the flammable gas described below was sufficient. In addition, the net cage 41 is
The upper part is opened, and a part of the side surface is formed so as to be openable and closable by the lid 48, and the mesh has a size that does not cause the buffer material mixture to be contained to pop out.
【0028】そして、その網状籠41を密閉容器42に
収容した。この密閉容器42は厚み70mmの鉄板製
で、内法が1050×2050×780mmの大きさに
形成され、蓋43によって開閉可能に構成される。な
お、図中の符号44は一端が真空ポンプ(図示せず)に
連結された吸引パイプ、45は気体充填用パイプ、49
は図示しない電源に接続された点火プラグである。Then, the mesh basket 41 was housed in a closed container 42. The closed container 42 is made of an iron plate having a thickness of 70 mm, has an inner size of 1050 × 2050 × 780 mm, and can be opened / closed by a lid 43. In the figure, reference numeral 44 is a suction pipe whose one end is connected to a vacuum pump (not shown), 45 is a gas filling pipe, and 49
Is a spark plug connected to a power source (not shown).
【0029】この密閉容器42には、その上部に外部の
油圧シリンダ47と連結したプレス板46が密閉容器4
2および網状籠41内を上下動可能に配置されている。
該プレス板46は、下面にシリコン離型剤が塗布され
て、後述する可燃性気体の爆発燃焼時まで密閉容器42
上部に配される。前記プレス板46の大きさは980×
1980×20mmである。A press plate 46 connected to an external hydraulic cylinder 47 is provided on the top of the closed container 42.
2 and the net cage 41 are arranged so as to be vertically movable.
A silicon mold release agent is applied to the lower surface of the press plate 46, and the hermetically sealed container 42 is used until the explosive combustion of combustible gas described later.
It is arranged at the top. The press plate 46 has a size of 980 ×
It is 1980 x 20 mm.
【0030】次いで、真空ポンプの作動により、前記吸
引パイプ44を介して密閉容器42内の空気を吸い出
し、内部の圧力が20mmHgになった時点で真空ポン
プの作動を止め、吸引パイプ44途中に設けられたバル
ブ(図示せず)を閉じる。Then, by operating the vacuum pump, the air in the closed container 42 is sucked out through the suction pipe 44, and when the internal pressure reaches 20 mmHg, the operation of the vacuum pump is stopped and the suction pipe 44 is provided on the way. Close the valve (not shown) provided.
【0031】そして、先の実施例で用いられた、水素と
酸素の容積比が2:1.1に調整された可燃性気体20
を、気体充填用パイプ45を介して0.5立方メートル
/分の速度で密閉容器42内に充填する。密閉容器42
内の圧力が760mmHgになった時点で、前記気体充
填用パイプ45のバルブ(図示せず)を閉じる。可燃性
気体の充填時間は約2分であった。Then, the combustible gas 20 used in the previous embodiment, in which the volume ratio of hydrogen and oxygen was adjusted to 2: 1.1.
Is filled into the closed container 42 through the gas filling pipe 45 at a rate of 0.5 cubic meters / minute. Closed container 42
When the internal pressure reaches 760 mmHg, the valve (not shown) of the gas filling pipe 45 is closed. The filling time of the flammable gas was about 2 minutes.
【0032】前記気体充填用パイプ45のバルブを閉じ
たまま1分間放置して、可燃性気体が密閉容器42内お
よび緩衝材細片10間にまんべんなく行き渡るようにす
る。その後、点火プラグ49に点火し、密閉容器42内
の可燃性気体を爆発燃焼させる。The valve of the gas filling pipe 45 is left closed for 1 minute so that the combustible gas is evenly distributed in the closed container 42 and between the buffer material strips 10. After that, the ignition plug 49 is ignited, and the flammable gas in the closed container 42 is exploded and burned.
【0033】前記可燃性気体の爆発燃焼直後、図5に示
されるように、油圧シリンダ47を作動させてプレス板
46を下降させ、緩衝体を高さ40mmになるまでプレ
スする。プレスに要する時間は約20秒であった。Immediately after the explosive combustion of the combustible gas, as shown in FIG. 5, the hydraulic cylinder 47 is operated to lower the press plate 46, and the buffer body is pressed to a height of 40 mm. The time required for pressing was about 20 seconds.
【0034】前記プレス板46によって前記緩衝材混合
物がプレスされた状態を3分30秒続けた後、プレス状
態を維持したままで、前記気体充填用パイプ45を介し
て、容器内の圧力が760mmHgに戻るまで二酸化炭
素を前記密閉容器42内に導入し、図6に示されるよう
に、油圧シリンダ47を作動させ、前記プレス板46を
密閉容器42上部に戻してプレスを解除する。After the buffer material mixture has been pressed by the press plate 46 for 3 minutes and 30 seconds, the pressure inside the container is 760 mmHg through the gas filling pipe 45 while maintaining the pressed state. The carbon dioxide is introduced into the closed container 42 until the process returns to step 1, the hydraulic cylinder 47 is operated, and the press plate 46 is returned to the upper part of the closed container 42 to release the press, as shown in FIG.
【0035】そして、図7に示したように、密閉容器4
2の蓋43を開けて網状籠41を取り出し、蓋48を開
けて一つの再生緩衝体50を取り出した。得られた緩衝
体50の大きさは1000×2000×400mmの直
方体で、隣接する緩衝材細片は混合されたホットメルト
樹脂によって互いに接合され、プレスによって強固に一
体化されたものであり、気孔がほとんど潰れていない均
一なものであった。Then, as shown in FIG. 7, the closed container 4
The lid 43 of No. 2 was opened, the net-like basket 41 was taken out, the lid 48 was opened, and one regeneration buffer 50 was taken out. The size of the obtained cushioning body 50 is a rectangular parallelepiped of 1000 × 2000 × 400 mm, and the neighboring cushioning material strips are joined together by a mixed hot melt resin and are firmly integrated by pressing. It was a uniform one with almost no collapse.
【0036】[0036]
【発明の効果】以上図示し説明したように、この発明の
再生緩衝体の製造方法によれば、合成樹脂発泡体または
合成樹脂発泡体とゴム等の異材質よりなる緩衝材を約2
〜30mmの大きさの細片に破砕し、前記細片とホット
メルト樹脂とを混合するとともに、前記混合物を密閉容
器内に密に収容し、次いで前記密閉容器内に可燃性気体
を充満し、該可燃性気体を爆発燃焼させて、前記緩衝材
細片を一体に接合して緩衝体を得るので、ゴムチップな
どの非発泡体やポリオレフィン系の比較的接着力が乏し
い合成樹脂の廃棄物であっても、実用性のある再生緩衝
体を短時間にしかも簡便に得ることができ、産業廃棄物
の減少、資源の有効活用の点で大きな利点を有するもの
である。As shown and described above, according to the method for manufacturing a regenerative cushioning body of the present invention, a synthetic resin foam or a synthetic resin foam and a cushioning material made of a different material such as rubber are used in an amount of about 2 or less.
Crush into small pieces having a size of ˜30 mm, mix the small pieces and the hot-melt resin, tightly store the mixture in a closed container, and then fill the closed container with a flammable gas, Since the flammable gas is explosively burned and the cushioning material strips are integrally joined to obtain a cushioning body, it is a waste product of a non-foamed material such as a rubber chip or a polyolefin-based synthetic resin having a relatively poor adhesive strength. However, it is possible to easily obtain a practical regeneration buffer in a short time, and it has great advantages in terms of reduction of industrial waste and effective use of resources.
【図1】この発明の再生緩衝体の製造方法の一実施例に
おける緩衝材混合物収容時の容器の断面図である。FIG. 1 is a cross-sectional view of a container at the time of containing a cushioning material mixture in an embodiment of a method for manufacturing a regenerative cushioning body of the present invention.
【図2】この発明製法に用いられる容器の一例を示す斜
視図である。FIG. 2 is a perspective view showing an example of a container used in the manufacturing method of the present invention.
【図3】網状籠の一例を示す斜視図である。FIG. 3 is a perspective view showing an example of a net cage.
【図4】この発明製法の他の例を示す断面図である。FIG. 4 is a sectional view showing another example of the manufacturing method of the present invention.
【図5】プレスした状態を示す断面図である。FIG. 5 is a cross-sectional view showing a pressed state.
【図6】プレス解除時を示す断面図である。FIG. 6 is a cross-sectional view showing when the press is released.
【図7】再生緩衝体取出し時を示す斜視図である。FIG. 7 is a perspective view showing the time when the reproduction buffer is taken out.
【符号の説明】 10 緩衝材細片 11 ホットメルト樹脂 12 密閉容器 17 網状籠 20 可燃性気体[Explanation of symbols] 10 buffer material strips 11 hot melt resin 12 closed container 17 reticulated basket 20 flammable gas
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B29K 105:26 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display B29K 105: 26
Claims (2)
ゴム等の異材質よりなる緩衝材を約2〜30mmの大き
さの細片に破砕し、前記細片とホットメルト樹脂とを混
合するとともに、前記混合物を密閉容器内に密に収容
し、次いで前記密閉容器内に可燃性気体を充満し、該可
燃性気体を爆発燃焼させて、前記緩衝材細片を一体に接
合して緩衝体を得ることを特徴とする再生緩衝体の製造
方法。1. A synthetic resin foam or a cushioning material made of a different material such as synthetic resin foam and rubber is crushed into strips having a size of about 2 to 30 mm, and the strips and the hot melt resin are mixed. Together, the mixture is tightly housed in a closed container, then the closed container is filled with a flammable gas, and the flammable gas is explosively burned to integrally join the buffer material strips to a buffer body. A method for producing a regeneration buffer, which comprises:
焼後、容器内の緩衝材細片をプレスすることを特徴とす
る再生緩衝体の製造方法。2. The method for manufacturing a regenerated buffer body according to claim 1, wherein after the explosive combustion of the combustible gas, the buffer material strip in the container is pressed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4038594A JPH05209082A (en) | 1992-01-29 | 1992-01-29 | Production of reclaimed cushioning body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4038594A JPH05209082A (en) | 1992-01-29 | 1992-01-29 | Production of reclaimed cushioning body |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05209082A true JPH05209082A (en) | 1993-08-20 |
Family
ID=12529626
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4038594A Pending JPH05209082A (en) | 1992-01-29 | 1992-01-29 | Production of reclaimed cushioning body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH05209082A (en) |
-
1992
- 1992-01-29 JP JP4038594A patent/JPH05209082A/en active Pending
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