JPS5813162B2 - Shoe sole molding method that reuses waste material from polyurethane cast soles - Google Patents
Shoe sole molding method that reuses waste material from polyurethane cast solesInfo
- Publication number
- JPS5813162B2 JPS5813162B2 JP54138940A JP13894079A JPS5813162B2 JP S5813162 B2 JPS5813162 B2 JP S5813162B2 JP 54138940 A JP54138940 A JP 54138940A JP 13894079 A JP13894079 A JP 13894079A JP S5813162 B2 JPS5813162 B2 JP S5813162B2
- Authority
- JP
- Japan
- Prior art keywords
- polyurethane
- soles
- cast
- shoe sole
- mixed
- 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
Links
- 229920002635 polyurethane Polymers 0.000 title claims description 19
- 239000004814 polyurethane Substances 0.000 title claims description 19
- 238000000465 moulding Methods 0.000 title claims description 9
- 238000000034 method Methods 0.000 title claims description 6
- 239000002699 waste material Substances 0.000 title claims 6
- 239000000203 mixture Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- 238000010298 pulverizing process Methods 0.000 claims description 4
- 238000001746 injection moulding Methods 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 claims 4
- 239000005038 ethylene vinyl acetate Substances 0.000 claims 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims 4
- 238000000227 grinding Methods 0.000 claims 1
- 239000008188 pellet Substances 0.000 claims 1
- 239000002002 slurry Substances 0.000 claims 1
- 230000000704 physical effect Effects 0.000 description 9
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 8
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 3
- 229920005749 polyurethane resin Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004636 vulcanized rubber Substances 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
- 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)
- Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
注型ポリウレタン底は周知の通りインシアネート基の高
い反応性を利用して数10秒単位で反応を完結して成形
品とするため、比較的不良率が高く、又橋かけ構造を含
むため他の熱可塑性樹脂に比べても再生利用しにくいの
でこれまでこのようなウレタン底スクラップはすべて廃
棄処分されてきている。DETAILED DESCRIPTION OF THE INVENTION As is well known, cast polyurethane soles utilize the high reactivity of incyanate groups to complete the reaction in several tens of seconds to form a molded product, resulting in a relatively high defect rate. Because it contains a bridging structure, it is difficult to recycle compared to other thermoplastic resins, so all such urethane bottom scraps have been disposed of until now.
しかし最近は靴の生産量の増加と共にウレタン底の生産
量も増し、それに伴って発生するスクラップの廃棄対策
は環境規制の強化も手伝って一層切実な問題となってい
る。However, recently, with the increase in the production of shoes, the production of urethane soles has also increased, and measures to dispose of the resulting scrap have become an even more pressing issue due to the tightening of environmental regulations.
本願の発明者は以上の様な現状を考慮してウレタン樹脂
と良相溶性を示すPVCとのブレンド底としての再利用
の検討を行った。Taking the above-mentioned current situation into consideration, the inventor of the present application has investigated the reuse of urethane resin and PVC, which exhibits good compatibility, as a blend bottom.
(1)PVC底材及びポリウレタンスクラップとして実
験に供する注型ポリウレタンは表1に示すものを用いた
。(1) The cast polyurethanes shown in Table 1 were used as PVC bottom materials and polyurethane scraps in the experiments.
ポリウレタンについては再生利用するに際して注型時の
反応条件であるイソシアネートサイドとポリエールサイ
ドの混合比、すなわちNCO/OH比とかポリウレタン
自身の種類の相違がPVCへの分散の良し悪しに影響す
ると考えられるので、ここではまずウレタン底の主流と
なっているポリエステル系に限定して異なるNCO/O
H比および樹脂を選定して実験用資料とした。When recycling polyurethane, it is thought that the mixing ratio of isocyanate side and polyale side, which is the reaction condition during casting, that is, the NCO/OH ratio, and the difference in the type of polyurethane itself will affect the quality of dispersion into PVC. Therefore, we will first focus on polyester, which is the mainstream of urethane soles, and introduce different NCO/O
The H ratio and resin were selected and used as experimental materials.
(2)注型ポリウレタン底は発泡体であるためにPVC
のブレンドに際しては粉砕又は適当な大きさに裁断して
PVCとの均一混合性を高める前処理が必要であり、粉
砕については冷凍粉砕を、また裁断機又はハサミによっ
て行った。(2) Since the cast polyurethane bottom is a foam, PVC
When blending, it is necessary to perform pre-treatment to improve homogeneous mixing with PVC by pulverizing or cutting into appropriate sizes, and the pulverizing was carried out by freeze-pulverizing, using a cutter or scissors.
(3)靴底用PVCコンパウンドの混合は特許請求の範
囲に記載した4通りの方法に拠った。(3) The PVC compound for shoe soles was mixed according to the four methods described in the claims.
尚、物性詳験用テストピースはプレス成形で0.04〜
3mm厚のシートを作成し測定試料としたこの加工また
は成形条件を表2に示す。In addition, the test piece for physical property details is press-molded to 0.04~
Table 2 shows the processing or molding conditions for producing a 3 mm thick sheet and using it as a measurement sample.
(4) 底材としての基本的な性能評価として、摩耗試
験、引張り、引裂き強さ、伸び及び硬さの測定を行った
。(4) As a basic performance evaluation as a bottom material, an abrasion test, tensile strength, tear strength, elongation, and hardness were measured.
用いた装置はそれぞれテーパ一式摩耗試験機、ショツパ
ー型引張り試験機及びDurometer Aである。The devices used were a taper set abrasion tester, a Schopper type tensile tester, and a Durometer A, respectively.
注型ウレタン成形機には20,18,12面どりなどの
金型がありこの数字は原料を金型に注入してから反応を
完結して製品を取り出すまでの1サイクルの長さを示す
指標となるものである。Cast urethane molding machines have molds with 20, 18, and 12 sides, and this number is an indicator of the length of one cycle from injecting the raw material into the mold to completing the reaction and taking out the product. This is the result.
すなわち、ウレタン底材のメーカーは使用する機種に依
って(西ドイツデスマス社製を基準にした)1サイクル
で反応を完結するポリウレタン樹脂を選定せねばならず
底材の硬さの調整は金型への注入量とかOH/NCOの
当量比を変えることによって所望のものとすることがで
きる。In other words, the manufacturer of urethane bottom material must select a polyurethane resin that completes the reaction in one cycle (based on the model made by Desmas in West Germany), depending on the model used, and the hardness of the bottom material must be adjusted by the mold. A desired value can be obtained by changing the amount of injection and the equivalence ratio of OH/NCO.
このような各種の条件より発生するスクラップがPVC
と均一混合して物性の良好なブレンド物が得られるかど
うかが問題となる。Scrap generated from these various conditions is PVC.
The question is whether or not a blend with good physical properties can be obtained by uniformly mixing the materials.
そこで上述のような条件の相違に依るブレンド部性への
影響を検討した。Therefore, we investigated the effects of the above-mentioned differences on blend properties.
まず、第1図は各種の割合でポリウレタンAを底用PV
Cコンパウンドに添加したブレンド物の物性を示したも
のである。First, Figure 1 shows how polyurethane A is applied to the bottom PV in various proportions.
This figure shows the physical properties of the blend added to Compound C.
一般的傾向として10%程度のスクラップ添加で最も良
好な物性を示し摩耗特性を考慮した実用的な添加範囲と
しては約20%以内又は60%以上の範囲で興味ある性
質を有するブレンド底が期待出来る。As a general trend, the best physical properties are obtained when scrap is added at around 10%, and a blend bottom with interesting properties can be expected within approximately 20% or over 60% as a practical addition range considering wear characteristics. .
またウレタン添加量が100%の場合、すなわちウレタ
ン単独では通常の加硫ゴムに優るとも劣らぬ物性を持つ
特に極めてすぐれた耐摩耗性を示す熱可塑性ゴムが得ら
れ、これなどは単に底材のみに止まらずその特性を生か
した他の用途が期待される。In addition, when the amount of urethane added is 100%, that is, when using urethane alone, a thermoplastic rubber is obtained that exhibits extremely excellent abrasion resistance and physical properties that are comparable to those of ordinary vulcanized rubber. In addition to this, other uses that take advantage of its properties are expected.
次に第1図で明らかなとおりPVCrichの場合は1
0%前後で興味ある特性を示したが、種類の異なるウレ
タン樹脂についてもPVCrich領域で同様の傾向を
示すか否かを調べた。Next, as shown in Figure 1, in the case of PVCrich, 1
Interesting characteristics were shown at around 0%, but we investigated whether different types of urethane resins would show similar trends in the PVC rich region.
普通普通靴底材の性能評価をするにあたっては摩耗特性
が重要な試験項目として挙げられる。When evaluating the performance of ordinary shoe sole materials, wear characteristics are usually cited as an important test item.
これは1000回あたりの摩耗減量、mg数をもって表
示される。This is expressed as a wear loss per 1000 cycles, in mg.
第3図は使用するスクラップの違いによりブレンド物性
に大きな差があるかどうかを摩耗特性から調べたもので
ある。Figure 3 shows whether there is a large difference in blend physical properties depending on the scrap used, from the viewpoint of wear characteristics.
図で明らかな通り良好な摩耗特性を保持するだめの添加
限界に多少の差を認める程度で、10phr以上の添加
では同傾向を示し、物性が低下する、この傾向は引張り
、引き裂き特性についても全く同様であった。As is clear from the figure, there is a slight difference in the additive limit that maintains good wear properties, and when the addition amount exceeds 10 phr, the same tendency is shown, and the physical properties deteriorate.This tendency also applies to tensile and tear properties. It was similar.
図4はPVCとウレタンの均一混合性、すなわちブレン
ド物性に大きな影響を持つと考えられるOH/NCOの
混合比の違いがブレンド物性にどのように影響を及ぼす
かを同様に摩耗特性より調べたものである。Figure 4 shows the homogeneous mixability of PVC and urethane, that is, how the difference in the mixing ratio of OH/NCO, which is thought to have a large effect on the blend properties, affects the blend properties from the wear characteristics. It is.
ウレタン樹脂の配合比100/107に比べ硬質配合は
5 phr以上添加すると著しく低下が見られる。Compared to the urethane resin blending ratio of 100/107, the hard blend shows a significant decrease when 5 phr or more is added.
これは架橋密度が増して溶融温度が高くなったために相
溶性が握くなったものと考えられる。This is thought to be due to the increased crosslinking density and higher melting temperature, which resulted in poor compatibility.
したがって、再生利用の立場より必要以上は硬質配合は
樹脂の選定を含めてできる限りさけることが望ましいと
考えられる。Therefore, from the standpoint of recycling, it is considered desirable to avoid hard compounding as much as possible, including in the selection of resins.
すなわち硬質配合を必要とする場合にも必要以上の架橋
密度、あるいは溶融温度のものにならぬような樹脂の選
定、配合が望まれる。That is, even when a hard compound is required, it is desirable to select and compound a resin that does not have a crosslinking density or melting temperature higher than necessary.
尚、スクラップは発泡体であり、一度ロールを通過させ
た方がPVCの分散が早い。Note that the scrap is a foam, and the PVC is dispersed more quickly once it passes through the rolls.
従って混合機としては加熱型エーダー・ブレンドフィー
ダーが適当であり、又ポリウレタン樹脂に関して最適条
件で注型したスクラップについてはPVCとすぐれだ相
溶性を示し、特に、5〜10hr程度で最も優れた物性
を示す。Therefore, a heating type eder blend feeder is suitable as a mixer, and scrap cast under the optimum conditions for polyurethane resin shows excellent compatibility with PVC, and in particular, the best physical properties are obtained after about 5 to 10 hours. show.
また添加量が60Nc%以上では次第にゴム様を呈する
が、60Nc%添加量のものについては射出成形による
実用性のある底材が予備実験で得られた。Further, when the amount added is 60 Nc% or more, it gradually becomes rubber-like, but with an amount added of 60 Nc%, a practical bottom material was obtained by injection molding in preliminary experiments.
尚、表1は実験用試料として供するポリウレタン樹脂及
び塩化ビニル樹脂を示し、表2は加工成形の条件を示す
ものである。Note that Table 1 shows the polyurethane resin and vinyl chloride resin used as experimental samples, and Table 2 shows the processing and molding conditions.
図は本発明の実施例を示すものであって、第1図は靴底
用軟質PVCにポリウレタンスクラップを各種の割合で
添加したブレンド物の物性を示す図、第2図はポリウレ
タン樹脂の違いによる各種ブレンド物の摩耗特性に及ぼ
す影響を示す図、第3図はOH/NCO反応比の異なる
ポリウレタンスクラップの添加量が摩耗特性に及ぼす影
響を示す図である。The figures show examples of the present invention. Figure 1 shows the physical properties of a blend made by adding various proportions of polyurethane scrap to soft PVC for shoe soles, and Figure 2 shows the properties of a blend made by adding polyurethane scrap in various proportions to soft PVC for shoe soles. FIG. 3 is a diagram showing the influence of various blends on the wear characteristics, and FIG. 3 is a diagram showing the influence of the added amount of polyurethane scrap having different OH/NCO reaction ratios on the wear characteristics.
Claims (1)
140℃〜165℃に加熱しつつ約2分間ロール練りを
施してクレープ状のシート状物を得たのちこれを約6〜
7mm角のペレット状に細断し、この細断粒に塩化ビニ
ール若しくはエチレン−酢酸ビニール共重合体等のコン
パウンドを混入して約165℃に加熱しつつ約5分間ロ
ール混合を施しこれ等のブレンドシートを構成し、然る
のちこのブレンドシートを約165℃に加熱しつつプレ
ス成形を施すことを特徴とするポリウレタン製の注型靴
底の廃材を再利用する靴底の成形法。 2 ポリウレタン製の注型靴底の廃材のスリラップを約
140℃〜165℃に加熱しつつ約3分間ロールを以て
混練した後に塩化ビニール若しくはエチレン−酢酸ビニ
ール共重合体等のコンパウンドを混入して約165℃に
加熱しつつ約5分間ロール混合を施しこれ等のブレンド
シートを構成し、然るのちこのブレンドシ一トを約16
5℃に加熱しつつプレス成形を指すことを特徴とするポ
リウレタン製の注型靴底の廃材を再利用する靴底の成形
法。 3 ポリウレタン製の注型靴底の廃材のスクラップをパ
ンバリーで混練した後にこれに塩化ビニル若しくはエチ
レン−酢酸ビニール共重合体等のコンパウンドを混入し
て約165℃に加熱しつつロール混合を施し、然るのち
これを165℃に加熱しつつプレス加工を施すか若しく
はヘッド180℃、ノズル180℃、シリンダー160
℃、射出圧1000kg/cm2の射出成形を施すこと
を特徴とするポリウレタン製の注型靴底の廃材を再利用
する靴底の成形法。 4 ポリウレタン製の注型靴底の廃材のスクラップを冷
凍粉砕等の手段によって粉砕し、これを塩化ビニル若し
くはエチレン−酢酸ビニール共重体等のコンパウンドと
ドライブレンドし、然る後にこれに射出成形を施すこと
を特徴とするポリウレタン製の注型靴底の廃材を再利用
する靴底の成形法。[Claims] 1 Scraps of cast-molded shoe soles made of polyurethane are heated to about 140°C to 165°C and roll-kneaded for about 2 minutes to obtain a crepe-like sheet. 6~
Shredded into 7 mm square pellets, mixed with a compound such as vinyl chloride or ethylene-vinyl acetate copolymer, and mixed with a roll for about 5 minutes while heating to about 165 ° C. A method for forming a shoe sole by reusing waste materials from cast shoe soles made of polyurethane, which comprises forming a sheet and then press-molding the blended sheet while heating it to about 165°C. 2 Sliprap of scrap material from polyurethane cast shoe soles is heated to approximately 140°C to 165°C and kneaded with a roll for approximately 3 minutes, and then a compound such as vinyl chloride or ethylene-vinyl acetate copolymer is mixed in to form a slurry of approximately 165°C. These blend sheets were formed by roll mixing for about 5 minutes while heating to
A shoe sole molding method that reuses waste material from polyurethane cast soles, which is characterized by press molding while heating to 5°C. 3 Scraps of cast-molded polyurethane shoe soles are kneaded in a panbury, then mixed with a compound such as vinyl chloride or ethylene-vinyl acetate copolymer, heated to approximately 165°C, and mixed with a roll. After that, press it while heating it to 165℃, or press it with a head of 180℃, a nozzle of 180℃, and a cylinder of 160℃.
A shoe sole molding method that reuses waste materials from polyurethane cast soles, which is characterized by injection molding at a temperature of 1,000 kg/cm2 at an injection pressure of 1,000 kg/cm2. 4. Grinding scraps of waste material from polyurethane cast shoe soles by means such as cryo-pulverization, dry-blending this with a compound such as vinyl chloride or ethylene-vinyl acetate copolymer, and then subjecting it to injection molding. A shoe sole molding method that reuses waste material from polyurethane cast soles.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54138940A JPS5813162B2 (en) | 1979-10-27 | 1979-10-27 | Shoe sole molding method that reuses waste material from polyurethane cast soles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54138940A JPS5813162B2 (en) | 1979-10-27 | 1979-10-27 | Shoe sole molding method that reuses waste material from polyurethane cast soles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5663301A JPS5663301A (en) | 1981-05-29 |
| JPS5813162B2 true JPS5813162B2 (en) | 1983-03-12 |
Family
ID=15233695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54138940A Expired JPS5813162B2 (en) | 1979-10-27 | 1979-10-27 | Shoe sole molding method that reuses waste material from polyurethane cast soles |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5813162B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4880129B2 (en) * | 2001-04-03 | 2012-02-22 | アキレス株式会社 | Injection molding boots recycling method |
-
1979
- 1979-10-27 JP JP54138940A patent/JPS5813162B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5663301A (en) | 1981-05-29 |
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