JPS60223836A - Recovery of starting material from scrap film having fine solid particle layer on surface - Google Patents
Recovery of starting material from scrap film having fine solid particle layer on surfaceInfo
- Publication number
- JPS60223836A JPS60223836A JP59081569A JP8156984A JPS60223836A JP S60223836 A JPS60223836 A JP S60223836A JP 59081569 A JP59081569 A JP 59081569A JP 8156984 A JP8156984 A JP 8156984A JP S60223836 A JPS60223836 A JP S60223836A
- Authority
- JP
- Japan
- Prior art keywords
- fine solid
- film
- raw materials
- waste
- base film
- 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
- 239000007787 solid Substances 0.000 title claims description 21
- 239000002245 particle Substances 0.000 title claims description 6
- 238000011084 recovery Methods 0.000 title description 3
- 239000007858 starting material Substances 0.000 title 1
- 238000000034 method Methods 0.000 claims description 21
- 239000006247 magnetic powder Substances 0.000 claims description 20
- 239000002699 waste material Substances 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 17
- 239000004094 surface-active agent Substances 0.000 claims description 15
- 239000002994 raw material Substances 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 8
- -1 polyethylene terephthalate Polymers 0.000 claims description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 229920003002 synthetic resin Polymers 0.000 claims 1
- 239000000057 synthetic resin Substances 0.000 claims 1
- 239000002585 base Substances 0.000 description 23
- 239000011230 binding agent Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000696 magnetic material Substances 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000009775 high-speed stirring Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000531 Co alloy Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010169 landfilling Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 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
- 238000003672 processing method Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B17/00—Recovery of plastics or other constituents of waste material containing plastics
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B17/00—Recovery of plastics or other constituents of waste material containing plastics
- B29B17/02—Separating plastics from other materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B17/00—Recovery of plastics or other constituents of waste material containing plastics
- B29B17/02—Separating plastics from other materials
- B29B2017/0213—Specific separating techniques
- B29B2017/0217—Mechanical separating techniques; devices therefor
- B29B2017/0231—Centrifugating, cyclones
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B17/00—Recovery of plastics or other constituents of waste material containing plastics
- B29B17/02—Separating plastics from other materials
- B29B2017/0213—Specific separating techniques
- B29B2017/0217—Mechanical separating techniques; devices therefor
- B29B2017/0237—Mechanical separating techniques; devices therefor using density difference
- B29B2017/0244—Mechanical separating techniques; devices therefor using density difference in liquids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2705/00—Use of metals, their alloys or their compounds, for preformed parts, e.g. for inserts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2705/00—Use of metals, their alloys or their compounds, for preformed parts, e.g. for inserts
- B29K2705/08—Transition metals
- B29K2705/12—Iron
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2009/00—Layered products
- B29L2009/005—Layered products coated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2017/00—Carriers for sound or information
- B29L2017/008—Tapes
-
- 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
- Y02W30/52—Mechanical processing of waste for the recovery of materials, e.g. crushing, shredding, separation or disassembly
-
- 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
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Mechanical Engineering (AREA)
- Compounds Of Iron (AREA)
- Processing Of Solid Wastes (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[発明の技術分野]
本発明は、表面に微粒固形物層の形成されたフィルム屑
からの原料回収方法に係わり、特に廃品の磁気記録材、
料のフィルムからベースフィルムおよび磁性体粉末等を
純品としC容易に回収し得る方法に関する。[Detailed Description of the Invention] [Technical Field of the Invention] The present invention relates to a method for recovering raw materials from film scraps having a fine solid layer formed on the surface thereof, and in particular to scrap magnetic recording materials,
This invention relates to a method for easily recovering pure base films, magnetic powders, etc. from raw materials.
[発明の技術的背景とその問題点]
近年、情報産業の急速な進展により、オーディブ等の磁
気記録テープ、磁気カード、フロッピーディスク等の微
粒固形物が大量に使用されるようになつCきている。[Technical background of the invention and its problems] In recent years, with the rapid development of the information industry, fine solid particles such as magnetic recording tapes such as audio recording tapes, magnetic cards, and floppy disks have come to be used in large quantities. There is.
その結果、この磁気記録材料の廃品が、製造工程上の不
合格品や一般消費者段階での使用済み品としC各所に大
量に発生しているが、現状においては埋め立て、焼却等
の方法によって廃棄されており、資源の再利用という見
地からの有効利用が望まれている。As a result, a large amount of scrap magnetic recording materials are being generated in various places as rejected products in the manufacturing process or used products at the general consumer stage, but currently they are being disposed of by methods such as landfilling and incineration. It has been discarded, and it is hoped that it will be used effectively from the perspective of resource reuse.
従来、廃品の磁気記録材料から磁性粉末を回収する方法
については、2.3検討がなされCいるが、未だ実用化
するまでには至っていない。Conventionally, 2.3 studies have been conducted on methods for recovering magnetic powder from waste magnetic recording materials, but they have not yet been put to practical use.
ずなわら、磁気記録材料には多くの種類があり、磁性体
の種類および含有量、有機バインダの種類および含有量
、可塑剤、安定剤、潤滑剤、その他の添加剤の種類およ
び含有量、さらにコーティング方式、積層組成等によつ
Cベースフィルムからの磁性体粉末の剥離のし易さは千
差万別であり、全てに適用可能な回収方法は、未だ知ら
れていない。There are many types of magnetic recording materials, and the types and contents of magnetic materials, types and contents of organic binders, types and contents of plasticizers, stabilizers, lubricants, and other additives, Furthermore, the ease with which the magnetic powder can be peeled off from the C base film varies depending on the coating method, laminated composition, etc., and a recovery method that can be applied to all of them is not yet known.
しかして廃品の磁気記録材料には、これらが混在してお
り、したがって廃品の磁気記録材料からベースフィルム
および磁性粉末を回収するには、いずれの種類の廃品に
も適用し得る処理方法でなければ実用的とはいえない。However, waste magnetic recording materials contain a mixture of these materials, and therefore, in order to recover the base film and magnetic powder from waste magnetic recording materials, a processing method that can be applied to any type of waste is required. It's not practical.
特に、近年においては、耐摩耗性向上等の性能の高度化
が要求されるため、容易に磁性体粉末層が剥離しない磁
気記録材料が多く出現し、ベースフィルムおよび磁性体
粉末の回収が困難となっている。In particular, in recent years, due to the demand for more advanced performance such as improved wear resistance, many magnetic recording materials have appeared whose magnetic powder layers do not peel off easily, making it difficult to recover the base film and magnetic powder. It has become.
例えば、従来技術として、磁気記録材料の廃品を強アル
カリ水溶液に浸漬し、ベースフィルムと磁性体粉末とに
分離する方法が知られているが、単に廃品をアルカリ水
溶液に浸漬するだけでは付着物が膨潤す、るにとどまり
、これをベースから完全に剥離して、ベースフィルムお
よび磁性体粉末を純粋に回収することは不可能であり、
また劇薬である強アルカリを使用するため作業上注意を
要すし、さらに設備にも防食を施さなければならないと
いう問題もあった。For example, as a conventional technique, a method is known in which waste magnetic recording material is immersed in a strong alkaline aqueous solution to separate it into a base film and magnetic powder. It only swells, and it is impossible to completely peel it off from the base and collect the base film and magnetic powder purely.
Furthermore, since a strong alkali, which is a powerful chemical, is used, caution is required during work, and there is also the problem that corrosion protection must be applied to the equipment.
また、この方法で分離した磁性体粉末中には、多量の有
機バインダが混入しているため、その分離に多くの手数
を要するという難点もあった。Furthermore, since a large amount of organic binder is mixed in the magnetic powder separated by this method, there is also the drawback that separation thereof requires a lot of effort.
このため磁気記録材料からベースフィルムおよび磁性体
粉末を回収できたとしても、回収物に不純物が残存しや
すく、これをそのまま成型材料や磁性材料等の本来の用
途に用いることができず、それらの利用価値を低減させ
ることになっていた。For this reason, even if base films and magnetic powders can be recovered from magnetic recording materials, impurities tend to remain in the recovered materials, and they cannot be used as they are for their original purpose such as molding materials or magnetic materials. It was supposed to reduce its utility value.
また一般に廃品としてだされるフィルムは、厚さが薄く
、しかも重なったり折れ曲がっl〔りしているため、通
常の洗浄方法により水中で撹拌しただけCは、重なった
フィルム屑面間の微粒固形物を完全に分離することが困
難であった。In addition, films that are generally disposed of as waste are thin, and are often overlapping or bent. Therefore, when agitated in water using a normal cleaning method, fine solid particles can be collected between the overlapping film scraps. It was difficult to completely separate the
[発明の目的]
本発明はかかる従来の事情に対処してなされたもので、
あらゆる種類の微粒固形物層を有するフィルム屑に適用
することができ、それらの廃品よりベースフィルムおよ
び微粒固形物を利用価値の高い純品として分離回収する
ことができ、しかも強アルカリを使用しない回収方法を
提供することを目的とする。[Object of the invention] The present invention has been made in response to such conventional circumstances,
It can be applied to all kinds of film waste with a layer of fine solid matter, and the base film and fine solid matter can be separated and recovered from these waste products as pure products with high utility value, and the recovery method does not require the use of strong alkalis. The purpose is to provide a method.
[発明の概要]
すなわち本発明の表面に微粒固形物層が形成されたフィ
ルム屑から原料回収方法は、ベースフィルム上に微粒固
形物層の形成されたフィルム屑から原料を回収するにあ
たり、前記フィルム屑を、0.01〜5重量%の界面活
性剤を含む水溶液に浸漬し、高速回転翼を備えた撹拌機
を用いて攪拌することを特徴としている。[Summary of the Invention] In other words, the method for recovering raw materials from film scraps having a fine solid layer formed on the surface of the present invention includes a method for recovering raw materials from film scraps having a fine solid layer formed on a base film. It is characterized in that the scraps are immersed in an aqueous solution containing 0.01 to 5% by weight of a surfactant and stirred using a stirrer equipped with high-speed rotary blades.
本発明の適用可能なフィルム屑には、オーディA録音テ
ープ、コンピュータテープ、ビデオテープ等の磁気記録
テープ、磁気カード、フロッピーディスク等の事実1全
ての磁気記録材料の屑の他、写真フィルム、マスクフィ
ルム、導電フィルムの屑等が包含さ塾る。Film scraps to which the present invention can be applied include scraps of all magnetic recording materials such as audio A recording tapes, computer tapes, video tapes, magnetic cards, floppy disks, etc., as well as photographic films and masks. Film, conductive film scraps, etc. are included.
この種のフィルム屑は、支持体となるベースフィルムと
、このベースフィルム上に形成された微粒固形物と、こ
れらのベースフィルムと微粒固形物とを結合するための
有機バインダ、可塑剤、安定剤、膨潤剤、その他の添加
剤等から構成されるいるが、その種類や含有量、また]
−ティング方式や積層組成等は何ら限定されるものでは
ない。This type of film waste consists of a base film that serves as a support, a fine solid material formed on this base film, an organic binder, a plasticizer, and a stabilizer for bonding the base film and the fine solid material. , swelling agents, other additives, etc., but their types and contents, and]
There are no limitations on the coating method, laminated composition, etc.
このようなフィルム屑のベースフィルムとしては、ポリ
エチレンテレフタレート等のポリエステル、ポリプロピ
レン、ポリエチレン、ポリ塩化ビニル等が例示される。Examples of the base film of such film waste include polyester such as polyethylene terephthalate, polypropylene, polyethylene, polyvinyl chloride, and the like.
また微粒固形物としては、酸化鉄、純鉄、フェライト、
コバルト合金、酸化クロム等の磁性体粉末の他、銀(写
真フィルム)、カーボン(マスクフィルム)等が例示さ
れる。In addition, fine solids include iron oxide, pure iron, ferrite,
Examples include magnetic powder such as cobalt alloy and chromium oxide, as well as silver (photographic film), carbon (mask film), and the like.
さらに有機バインダとしては、ユリア樹脂、メラミン樹
脂、グアナミン等のアミン系樹脂、ポリエステル系樹脂
、エポキシ系樹脂、アクリル系樹脂、メラミン系樹脂、
ポリウレタン系樹脂、芳香族炭化水素系樹脂、シリコー
ン系樹脂、塩化ビニル−酢酸ビニル共重合体等の熱硬化
性樹脂や熱可塑性樹脂等をベースとした有機バインダが
あげられる。Furthermore, organic binders include urea resin, melamine resin, amine resin such as guanamine, polyester resin, epoxy resin, acrylic resin, melamine resin,
Examples include organic binders based on thermosetting resins and thermoplastic resins such as polyurethane resins, aromatic hydrocarbon resins, silicone resins, and vinyl chloride-vinyl acetate copolymers.
本発明に使用される水溶液に用いられる界面活性剤とし
ては、陰イオン性、陽イオン性、非イオン性、両性イオ
ン性のいずれでもよく、α−オレフィン系、高級アルコ
ール系、脂肪酸系、スルフォン酸系等の汎用の界面活性
剤を用いることができる。The surfactant used in the aqueous solution used in the present invention may be anionic, cationic, nonionic, or zwitterionic, and may be α-olefin, higher alcohol, fatty acid, or sulfonic acid. A general-purpose surfactant such as a surfactant such as a surfactant can be used.
これらの界面活性剤は、1種もしくは2種以上混合して
使用される。These surfactants may be used alone or in combination of two or more.
混合溶液中の界面活性剤の濃度は、0.01〜5重量%
が好ましく、特に0.05〜3重量%の範囲が適してい
る。界面活性剤の配合量が0.01重量%未満の場合に
は剥離速度が小さくなつ゛C実用上不利であり、逆に5
重量%を越えると、泡立ちが激しくなって回収すべきベ
ースフィルムおよび磁性体粉末の取組への移行が大きく
なるため好ましくない。The concentration of surfactant in the mixed solution is 0.01 to 5% by weight.
is preferred, and a range of 0.05 to 3% by weight is particularly suitable. If the blending amount of the surfactant is less than 0.01% by weight, the peeling speed will be low, which is disadvantageous in practice;
If it exceeds % by weight, it is not preferable because foaming becomes intense and the transfer of the base film and magnetic powder to be collected becomes large.
使用づる混合溶液の使用温度は5〜100℃が好ましい
。5℃未満では剥離の速度が小さくなり、逆に100℃
を越えると、ベースフィルムおよび磁性体粉末の熱劣化
が生じるようになり、さらに作業上危険を伴うようにな
るので好ましくない。The working temperature of the mixed solution used is preferably 5 to 100°C. Below 5°C, the rate of peeling decreases; on the other hand, below 100°C
Exceeding this is not preferable because the base film and the magnetic powder will be thermally degraded and the work will be dangerous.
フィルム屑は、予め細片状に裁断され、上記のような界
面活性剤を含む混合溶液に浸漬され高速撹拌翼を備えた
撹拌機で攪拌処理されるが、界面活性剤との相互作用に
加えC高速撹拌翼のせん断力および遠心力により、短時
間のうちに微粒固形物層がベース材料から剥離され、か
つ微粒化される。また、その他の固着剤、可塑剤等は、
処理溶液上部の取組へ移行し容易に分離される。撹拌機
の回転翼の回転数および大きさは、周速で20〜40I
ll/秒、そのとき発生する遠心力が150〜300k
g−1/82程度のものが適している。Film scraps are cut into strips in advance, immersed in a mixed solution containing a surfactant as described above, and stirred using a stirrer equipped with high-speed stirring blades. C. Due to the shear force and centrifugal force of the high-speed stirring blades, the fine solid layer is peeled off from the base material and atomized in a short time. In addition, other fixing agents, plasticizers, etc.
The treatment solution moves to the upper part of the solution and is easily separated. The rotation speed and size of the rotary blade of the stirrer are 20 to 40I in circumferential speed.
ll/sec, the centrifugal force generated at that time is 150-300k
A material of about g-1/82 is suitable.
このような高速回転翼を備えた撹拌機としCは、例えば
ヘンシェルミキサ(三井三池化工機(株)商品名)があ
げられる。ヘンシェルミキサの回転翼の回転数は可変と
され”〔いるが、通常この回転翼は2011/秒、40
11/秒(いずれも周速)の2段階に切り換え゛て使用
される。An example of an agitator C equipped with such a high-speed rotary blade is a Henschel mixer (trade name, manufactured by Mitsui Miike Kakoki Co., Ltd.). The rotation speed of the Henschel mixer rotor is said to be variable, but normally this rotor is 2011/sec, 40
It is used by switching between two stages of 11/sec (both peripheral speeds).
本発明においては、撹拌過程で剥離された微粒固形物が
遠心力により沈降する一方、有機バインダが界面活性剤
の形成する泡に吸着されて表面に浮上して分離される。In the present invention, while the particulate solids exfoliated during the stirring process settle due to centrifugal force, the organic binder is adsorbed by the bubbles formed by the surfactant and floats to the surface and is separated.
フィルム屑に対する水溶液の量は伺ら限定されるもので
はなく、水溶液が処理材料に対し攪拌し易い轍Cあれば
よい。The amount of the aqueous solution relative to the film scraps is not limited, as long as there is a rut C that allows the aqueous solution to be easily stirred into the material to be treated.
撹拌時間は磁気記録材料の種類、形状、界面活性剤濃度
、処理温度によって自由に変えられるが、剥離を有効に
行なわせ、ベースの分子量低下を最小限に抑制する時間
とすることが肝要である。The stirring time can be freely changed depending on the type and shape of the magnetic recording material, surfactant concentration, and processing temperature, but it is important to select a time that allows for effective peeling and minimizes the decrease in the molecular weight of the base. .
攪拌処理終了後、固着剤その他の添加剤が移行した処理
溶液上部の取組を分離除去する。取組が除去された残存
液は濾過法、比重差による分離法等により処理されてベ
ースフィルムと微粒固形物とに分離される。ここで分離
されたベースフィルムおよび磁性体粉末は、それぞれ洗
浄、乾燥して再度同一または任意の用途に使用される。After the stirring process is completed, the upper portion of the processing solution to which the fixing agent and other additives have migrated is separated and removed. The remaining liquid from which the particles have been removed is treated by a filtration method, a separation method based on a difference in specific gravity, etc., and is separated into a base film and fine solid particles. The base film and magnetic powder separated here are washed, dried, and used again for the same or any desired purpose.
[発明の実施例] 以下本発明の実施例について説明する。[Embodiments of the invention] Examples of the present invention will be described below.
実施例
ベースがポリエチレンテレフタレート、磁性体がフェラ
イトからなり、これらの重儀比が44゜9:55.1で
ある市販のビデオテープの屑を、約5C11程度の長さ
のテープ片に裁断して試料とした。この試料2 kgを
、2重量%の界面活性剤(例えばオレイン酸ソーダ、ド
デシルベンゼンスルフォン酸 1:1配合)を含む80
℃の混合水溶液201とともにヘンシエルミキザに入れ
、ytJ半機を用い−C10分間攪拌したく回転数24
5Or・p−m、遠心力150kg ”III /s2
)。Example A commercially available videotape waste whose base was made of polyethylene terephthalate and whose magnetic material was made of ferrite and whose weight ratio was 44°9:55.1 was cut into pieces of tape with a length of about 5C11. It was used as a sample. 2 kg of this sample was mixed with 80% by weight of a surfactant containing 2% by weight of a surfactant (for example, a 1:1 combination of sodium oleate and dodecylbenzenesulfonic acid).
Place the mixed aqueous solution at 201 °C in a Henschel mixer and stir for 10 minutes using a YTJ half-machine at a rotation speed of 24.
5Or・pm, centrifugal force 150kg ”III/s2
).
撹拌と同時に液面に泡が形成され、撹拌時間経過ととも
に、剥離した有機バインダが泡層に捕捉された。Bubbles were formed on the liquid surface simultaneously with stirring, and as the stirring time elapsed, the peeled organic binder was captured in the foam layer.
その後、泡層を分離し、テープ片を処理液中から取出し
3回水洗し乾燥させたところ、磁性体粉末の他の付着物
のないポリエチレンテレフタレート4.04aが採取さ
れた。また残りの液を重力沈降させ、沈降した磁性体粉
末を3回水洗した後乾燥させたところ、純度99.9%
以上のフエライ1〜粉末4.96uが採取された。Thereafter, the foam layer was separated, and the tape piece was taken out from the treatment solution, washed with water three times, and dried. Polyethylene terephthalate 4.04a was collected without any other adhesion of magnetic powder. The remaining liquid was allowed to settle by gravity, and the settled magnetic powder was washed with water three times and dried, resulting in a purity of 99.9%.
4.96 u of the above powder was collected.
これとは別に比較例としC1界面活性剤を使用しなかっ
た点を除い−C実施例1と同一の条f1でビデオテープ
の屑を処理してポリエチレンテレフタレートとフェライ
トとに分離した。この比較例では10分間の撹拌によっ
てもベースフィルムへの残留付着物が多量に残存し、さ
らに30分間撹拌を続けてもベースフィルムへの残留付
着物の存在が認められた。Separately, as a comparative example, videotape waste was treated with the same strip f1 as in Example 1 except that the C1 surfactant was not used to separate it into polyethylene terephthalate and ferrite. In this comparative example, a large amount of residual deposits remained on the base film even after stirring for 10 minutes, and the presence of residual deposits on the base film was observed even after stirring for an additional 30 minutes.
また3回の水洗により分離された磁性体粉末中には有機
バインダの混入物が多く認められ、5回の水洗によって
も有機バインダを完全に除くことはできなかった。In addition, a large amount of organic binder was found in the magnetic powder separated by washing with water three times, and the organic binder could not be completely removed even after washing with water five times.
[発明の効果]
以上説明したように本発明方法によれば、いかなる種類
の表面に微粒固形物層の形成されたフィルム屑からも、
容易かつ効率的にベースフィルムおよび磁性体粉末を純
粋な状態で回収することができる。従って、回収された
ベースフィルムおよび磁性体粉末は、それらの本来の付
加価値の高い用途に原料として使用することができる。[Effects of the Invention] As explained above, according to the method of the present invention, any type of film waste with a fine solid layer formed on its surface can be removed.
The base film and magnetic powder can be easily and efficiently recovered in a pure state. Therefore, the recovered base film and magnetic powder can be used as raw materials for their original high value-added applications.
さらに本発明においては、強アルカリを使用しないので
作業上安全であり、かつ設備に特別な防食を施す必要が
ない利点もある。Furthermore, the present invention has the advantage that it is safe to work with since no strong alkali is used, and there is no need to provide special anti-corrosion protection to the equipment.
Claims (6)
ィルム屑から原料を回収するにあたり、前記フィルム屑
を、0.01〜5重量%の界面活性剤を含む水溶液に浸
漬し、高速回転翼を備えた撹拌機を用いて攪拌すること
を特徴とする表面に微粒固形物層の形成されたフィルム
屑から原料を回収ブる方法。(1) When recovering raw materials from film waste with a fine solid layer formed on the base film, the film waste is immersed in an aqueous solution containing 0.01 to 5% by weight of a surfactant, and A method for recovering raw materials from film waste having a layer of fine solid matter formed on its surface, characterized by stirring using a stirrer equipped with.
囲第1項記載の表面に微粒固形物層の形成されたフィル
ム屑から原料を回収する方法。(2) A method for recovering raw materials from film waste having a fine solid layer formed on the surface thereof according to claim 1, wherein the temperature of the aqueous solution is 5 to 100°C.
範囲第3項記載の表面に微粒固形物層の形成されたフィ
ルム屑から原料を回収する方法。(3) A method for recovering raw materials from film scraps having a fine solid layer formed on the surface thereof according to claim 3, wherein the base film is a synthetic resin material.
物層の形成されたフィルム屑から原料を回収する方法。(4) A method of recovering raw materials from film waste in which the base film has a layer of solid polyethylene terephthalate particles.
1項記載の表面に微粒固形物層の形成されたフィルム屑
から原料を回収する方法。(5) A method for recovering raw materials from film waste having a layer of fine solid matter formed on its surface as claimed in claim 1, wherein the fine solid matter is a magnetic powder.
であり、かつこれによって形成される遠心力が150〜
300kg−m/S2である特許請求の範囲第1項記載
の表面に微粒固形物層の形成されたフィルム屑から原料
を回収する方法。(6) The rotation speed of the high-speed rotor blade is 20 to 40 m/s (circumferential speed)
and the centrifugal force formed by this is 150~
300 kg-m/S2. A method for recovering raw materials from film waste having a fine solid layer formed on its surface as claimed in claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59081569A JPS60223836A (en) | 1984-04-23 | 1984-04-23 | Recovery of starting material from scrap film having fine solid particle layer on surface |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59081569A JPS60223836A (en) | 1984-04-23 | 1984-04-23 | Recovery of starting material from scrap film having fine solid particle layer on surface |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60223836A true JPS60223836A (en) | 1985-11-08 |
Family
ID=13749925
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59081569A Pending JPS60223836A (en) | 1984-04-23 | 1984-04-23 | Recovery of starting material from scrap film having fine solid particle layer on surface |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60223836A (en) |
-
1984
- 1984-04-23 JP JP59081569A patent/JPS60223836A/en active Pending
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