JPS596220B2 - Injection molding machine cleaning method - Google Patents
Injection molding machine cleaning methodInfo
- Publication number
- JPS596220B2 JPS596220B2 JP201779A JP201779A JPS596220B2 JP S596220 B2 JPS596220 B2 JP S596220B2 JP 201779 A JP201779 A JP 201779A JP 201779 A JP201779 A JP 201779A JP S596220 B2 JPS596220 B2 JP S596220B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- injection molding
- molding machine
- temperature
- cleaning
- 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
- 238000001746 injection moulding Methods 0.000 title claims description 37
- 238000004140 cleaning Methods 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 15
- 229920005989 resin Polymers 0.000 claims description 48
- 239000011347 resin Substances 0.000 claims description 48
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 19
- 238000002844 melting Methods 0.000 claims description 18
- 230000008018 melting Effects 0.000 claims description 18
- 229920001225 polyester resin Polymers 0.000 claims description 16
- 239000004645 polyester resin Substances 0.000 claims description 16
- 229920001890 Novodur Polymers 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 238000000465 moulding Methods 0.000 description 13
- 229920000139 polyethylene terephthalate Polymers 0.000 description 11
- 239000005020 polyethylene terephthalate Substances 0.000 description 11
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- -1 α-monosubstituted styrene Chemical class 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000008188 pellet Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 229920001577 copolymer Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/17—Component parts, details or accessories; Auxiliary operations
- B29C45/1753—Cleaning or purging, e.g. of the injection unit
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】 本発明は、射出成形機洗浄方法に関するものである。[Detailed description of the invention] The present invention relates to a method for cleaning an injection molding machine.
さらに詳しくは、本発明は、スチレン系樹脂およびスチ
レン系樹脂の成形温度より高い融点を有する結晶性線状
ポリエステル樹脂の混合物を用いた射出成形機洗浄方法
に関するものである。More specifically, the present invention relates to a method for cleaning an injection molding machine using a mixture of a styrenic resin and a crystalline linear polyester resin having a melting point higher than the molding temperature of the styrenic resin.
一般に、成形樹脂の成形方法の一つとして射出成形がよ
く用いられている。Generally, injection molding is often used as one of the methods for molding molded resins.
射出成形機で成形樹脂を射出成形すると、射出成形を完
了した後、射出成形機内、すなわち、シリンダー内に樹
脂が滞留する。When a molded resin is injection molded using an injection molding machine, the resin remains inside the injection molding machine, that is, inside the cylinder after the injection molding is completed.
したがって、次に他の樹脂、あるいは他の色相の樹脂を
射出成形するにあたっては、射出成形機内に滞留する成
形樹脂を完全に除去することが必要である。Therefore, when injection molding another resin or a resin of a different color next time, it is necessary to completely remove the molding resin remaining in the injection molding machine.
この除去作業にあたっては、従来、多量の洗浄用の樹脂
が必要であり、とくに、黒色品を射出成形後に白色系の
淡色量を射出成形する場合などでは、きわめて多量の樹
脂量が必要で大きな損失を招いていた。Conventionally, this removal work requires a large amount of cleaning resin, and especially when injection molding a white or light color after injection molding a black product, an extremely large amount of resin is required and there is a large loss. was inviting.
一方、この洗浄作業による滞留した樹脂の除去が不完全
である状態のまま次の樹脂を射出成形した場合には、成
形品の表面に滞留した樹脂の色相を帯びたすぐが発生し
たり、互いに相溶性が乏しい場合には層状剥離を生じる
ために不良品となることがある。On the other hand, if the next resin is injection molded while the residual resin has not been completely removed by this cleaning process, stains may appear on the surface of the molded product with the hue of the residual resin, or they may overlap with each other. If the compatibility is poor, delamination may occur, resulting in a defective product.
これらの点から、とくに大型成形機を用いてスチレン系
樹脂を射出する場合などで、射出成形機内に滞留するス
チレン系樹脂を除去するにあたり、できるだけ少量の樹
脂を用いて、かつ完全に除去できる方法が必要となって
いる。From these points, when removing styrene resin that remains inside the injection molding machine, especially when styrene resin is injected using a large molding machine, we need a method that uses as little resin as possible and can completely remove it. is needed.
従来、これらの射出成形機内に滞留する成形樹脂の除去
方法として、各種の洗浄用樹脂を用いる方法が考案され
、一部では、洗浄用樹脂として市販されている。Conventionally, methods using various cleaning resins have been devised as methods for removing molding resin remaining in these injection molding machines, and some of them are commercially available as cleaning resins.
しかし、いずれも、洗浄効果が乏しい点、成形する樹脂
の物性低下を招く点、あるいは、きわめて高価であるた
め実用性がない点などから必ずしも満足すべきものでは
ない。However, none of these methods is necessarily satisfactory because they have poor cleaning effects, deteriorate the physical properties of the molded resin, or are extremely expensive and therefore impractical.
本発明者らは、上記の従来の問題点を解決した射出成形
機洗浄方法について鋭意検討した結果、本発明に到達し
た。The inventors of the present invention have arrived at the present invention as a result of intensive study on a method for cleaning an injection molding machine that solves the above-mentioned conventional problems.
すなわち、本発明の要旨とするところは、射出成形機内
に滞留するスチレン系樹脂を洗浄除去するにあたり、ス
チレン系樹脂および該スチレン系樹脂の溶融開始温度よ
り高い融点を有する結晶性線状ポリエステル樹脂の混合
物を第1段階目では、該スチレン系樹脂の溶融開始温度
以上で該結晶性線状ポリエステル樹脂の融点以下で、第
2段階目では該結晶性線状ポリエステル樹脂の融点以上
で、射出することを特徴とする射出成形機洗浄方法に関
する。That is, the gist of the present invention is that when cleaning and removing styrene resin remaining in an injection molding machine, a styrene resin and a crystalline linear polyester resin having a melting point higher than the melting start temperature of the styrenic resin are used. The mixture is injected in the first stage at a temperature higher than the melting start temperature of the styrenic resin and lower than the melting point of the crystalline linear polyester resin, and in the second stage at a temperature higher than the melting point of the crystalline linear polyester resin. The present invention relates to an injection molding machine cleaning method characterized by:
本発明によれば、射出成形機内に滞留する成形樹脂(ス
チレン系樹脂)を除去するにあたって、従来の方法に比
較して、きわめて少量の樹脂を用いて完全に除去するこ
とが可能である。According to the present invention, when removing molding resin (styrenic resin) that remains in an injection molding machine, it is possible to completely remove it using a much smaller amount of resin than in conventional methods.
本発明におけるスチレン系樹脂は、スチレン、α一置換
スチレン(例えばα−メチルスチレンなど)および核置
換スチレン(例えばクロロスチレンなど)などの重合体
、ならびにこれらの共重合体、さらにこれら単量体と共
重合可能なビニル化合物(例えばアクリロニトリル、メ
タクリロニトリル、アクリル酸、メタクリル酸、アクリ
ル酸エステル、メタクリル酸エステルなど)などより得
られる共重合体、およびこれらとゴム状重合体(例えば
ブタジェン系ゴム、アクリル系ゴム、エチレン−プロピ
レン系ゴムなど)などから得られる樹脂組成物などであ
る。The styrenic resin in the present invention includes polymers such as styrene, α-monosubstituted styrene (e.g., α-methylstyrene), and nuclear-substituted styrene (e.g., chlorostyrene), copolymers thereof, and monomers thereof. Copolymers obtained from copolymerizable vinyl compounds (for example, acrylonitrile, methacrylonitrile, acrylic acid, methacrylic acid, acrylic esters, methacrylic esters, etc.), and rubber-like polymers with these (for example, butadiene rubber, These include resin compositions obtained from acrylic rubber, ethylene-propylene rubber, etc.).
本発明において用いられるスチレン系樹脂の成形温度よ
り高い融点を有する結晶性線状ポリエステル樹脂は、例
えばテレフタル酸、イソフタル酸等の芳香族二塩基酸、
アジピン酸などの脂肪族二塩基酸またはこれらの低級ア
ルキルエステルとエチレングリコールなどの二価アルコ
ールから得られるポリエステル樹脂が用いられるが、特
にポリエチレンテレフタレート(PET)、ポリブチレ
ンテレフタレートなどが好ましい。The crystalline linear polyester resin having a melting point higher than the molding temperature of the styrene resin used in the present invention is, for example, an aromatic dibasic acid such as terephthalic acid or isophthalic acid,
A polyester resin obtained from an aliphatic dibasic acid such as adipic acid or a lower alkyl ester thereof and a dihydric alcohol such as ethylene glycol is used, and polyethylene terephthalate (PET), polybutylene terephthalate, etc. are particularly preferred.
また、これらのポリエステル樹脂はフィルムに大量に使
用されており、これらのフィルムから得られる安価なス
クラップ品などを使用することができる。Moreover, these polyester resins are used in large quantities for films, and inexpensive scrap products obtained from these films can be used.
本発明で用いられるスチレン系樹脂および結晶性線状ポ
リエステル樹脂の混合比率としては、スチレン系樹月¥
I)10〜70重量部に対して結晶性線状ポリエステル
樹脂(II)90〜30重量部とするのが好ましい。The mixing ratio of the styrene resin and the crystalline linear polyester resin used in the present invention is as follows:
It is preferable to use 90 to 30 parts by weight of the crystalline linear polyester resin (II) to 10 to 70 parts by weight of I).
(I)/(If)が重量比で10790未満では流動性
が低下し、70/30を越えると洗浄効果が低下する傾
向にある。When the weight ratio (I)/(If) is less than 10,790, fluidity tends to decrease, and when it exceeds 70/30, the cleaning effect tends to decrease.
本発明において、上記樹脂混合物を射出成形機内に充填
しながら系外へ射出する工程の温度としては、第1段階
ではスチレン系樹脂の成形温度以上で、かつ結晶性線状
ポリエステル樹脂の融点以下、第2段階では結晶性線状
ポリエステル樹脂の融点以上が好ましい。In the present invention, the temperature in the step of filling the resin mixture into the injection molding machine and injecting it out of the system is at least the molding temperature of the styrene resin and below the melting point of the crystalline linear polyester resin in the first step; In the second stage, the temperature is preferably higher than the melting point of the crystalline linear polyester resin.
それぞれの段階で滞留した樹脂の色相が消えるまで洗浄
するのが好ましい。It is preferable to wash until the hue of the resin remaining at each stage disappears.
例えば、AAS(アクリレート−アクリルゴム−スチレ
ン共重合体)およびPETの混合物を用いるに際しては
、第1段階では、190〜230℃、第2段階では24
0〜280℃の温度の範囲が望ましい。For example, when using a mixture of AAS (acrylate-acrylic rubber-styrene copolymer) and PET, the first stage is 190-230°C, and the second stage is 24°C.
A temperature range of 0 to 280°C is preferred.
この場合、第1段階で、190℃未満の場合、樹脂の流
動性が著しく低下するために成形が困難となり、また、
230℃を越える場合、滞留した樹脂の除去効果が低下
する傾向がある。In this case, if the temperature is lower than 190°C in the first stage, the fluidity of the resin will decrease significantly, making molding difficult;
If the temperature exceeds 230°C, the effect of removing the retained resin tends to decrease.
第2段階で、240℃未満の場合、PETが溶融せず、
280℃を越える場合、AASが一部、分解する可能性
がある。In the second stage, if the temperature is less than 240°C, PET will not melt,
If the temperature exceeds 280°C, there is a possibility that AAS will partially decompose.
本発明において、スチレン系樹脂と結晶性線状ポリエス
テル樹脂を混合する方法は、通常の方法でさしつかえな
い。In the present invention, the styrenic resin and the crystalline linear polyester resin may be mixed by any conventional method.
例えば、粉末あるいはペレット状の両者をブレンダーあ
るいはミキサーなどで容易に混合することができる。For example, both powder and pellet forms can be easily mixed using a blender or mixer.
ただし、結晶性線状ポリエステル樹脂の大きさは射出成
形機のノズル径より小さいことが好ましい。However, the size of the crystalline linear polyester resin is preferably smaller than the nozzle diameter of the injection molding machine.
ノズル径より著しく大きいとノズル等に結晶性ポリエス
テルが詰まって洗浄速度が低下することがある。If it is significantly larger than the nozzle diameter, the nozzle etc. may be clogged with crystalline polyester and the cleaning speed may be reduced.
次に、実施例によって更らに詳しく本発明について説明
するが、本発明は、これらによって限定されるものでは
ない。Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited thereto.
実施例 1
黒色に着色したAAS樹脂(日立化成工業■製のバイフ
ックスV6100A(溶融開始温度200℃)にカーボ
ンブラックを2%添加したペレット)を下記の成形条件
で60シヨツト射出成形した。Example 1 Sixty shots of a black colored AAS resin (pellets made by adding 2% carbon black to Byfux V6100A (melting start temperature 200°C) manufactured by Hitachi Chemical Co., Ltd.) were injection molded under the following molding conditions.
成形機:■日本製鋼新製のV36A−150型スクリユ
一式自動射出成形機
シリンダ一温度二〇1220℃
C2230°C
0230°C
ノズル2/30℃
射出圧カニ6ooKF!/crtt
スクリユ一回転数: 60 rpm
射出成形終了後、シリンダ一部を後退させて、AAS樹
脂パイタックスV6100A 40部、ポリエチレン
テレフタレート(PET融点250℃)60部を混合し
た後、シリンダ一温度をC1210°C1C2210℃
、03210℃、ノズル210℃に設定し、他の条件は
同一にして、シリンダー内に充填しながらノズルから系
外へ射出する作業を黒色が消えるまで続けた後、シリン
ダ一温度をC1240℃、02250℃、03250℃
、ノズル250℃に設定して、同様の作業をナチュラル
色に完全に変わるまで続けた。Molding machine: ■Nippon Steel's new V36A-150 type screw complete automatic injection molding machine Cylinder temperature 201220°C C2230°C 0230°C Nozzle 2/30°C Injection pressure crab 6ooKF! /crtt Screw rotation speed: 60 rpm After injection molding, a part of the cylinder is moved back, and 40 parts of AAS resin Pitax V6100A and 60 parts of polyethylene terephthalate (PET melting point 250°C) are mixed, and the cylinder temperature is set to C1210. °C1C2210℃
, 03210°C, nozzle 210°C, other conditions being the same, continue filling the cylinder and injecting it out of the system from the nozzle until the black color disappears, then set the cylinder temperature to 1240°C, 02250°C. °C, 03250 °C
, the nozzle was set at 250° C., and the same operation was continued until the color completely changed to a natural color.
滞留した黒色のAAS樹脂を完全に洗浄除去するのに要
した樹脂の量を測定した。The amount of resin required to completely wash away the retained black AAS resin was measured.
その結果を表1に示す。比較例 1
実施例1において、AAS樹脂を射出成形したのち、シ
リンダ一部を後退させて、ナチュラル色のAAS樹脂を
同一の射出成形条件で、シリンダー内に充填しながらノ
ズルから系外へ射出成形する作業を黒色のAAS樹脂を
完全に洗浄除去するまでくりかえした。The results are shown in Table 1. Comparative Example 1 In Example 1, after AAS resin was injection molded, a part of the cylinder was moved back and natural colored AAS resin was injected from the nozzle to the outside of the system while being filled into the cylinder under the same injection molding conditions. This process was repeated until the black AAS resin was completely washed away.
このときに要した樹脂量を測定し、表1に示した。The amount of resin required at this time was measured and shown in Table 1.
表1の結果から、AAS樹脂とPETの混合品を用いる
ことによって、シリンダー内に滞留したAAS樹脂を完
全に洗浄するのに要する樹脂の量が大幅に減少している
ことがみとめられる。From the results in Table 1, it can be seen that by using the mixture of AAS resin and PET, the amount of resin required to completely clean the AAS resin accumulated in the cylinder is significantly reduced.
実施例2〜4および比較例2
洗浄用混合物を次に示すとおりにし、シリンダ一温度を
表2に示すとおりにした以外は実施例1と同様に試験し
た。Examples 2 to 4 and Comparative Example 2 Tests were conducted in the same manner as in Example 1, except that the cleaning mixture was as shown below and the cylinder temperature was as shown in Table 2.
結果を表2に示す。0!Mf”′け=:5富:::=
○実施例3 (Ω命: (V6100A) :::
O実施例4[公合塁(V6100A) Ho:0比
較例2丁AAS(V6100A) 50部LPET
50部表2の結果からA
AS/PETの混合品を第1段階210℃、第2段階2
50°Cとシリンダ一温度を変化させて洗浄作業をおこ
なう方法はいずれも良好な結果が得られ、滞留したAA
S樹脂の除去には非常に効果があることがみとめられる
。The results are shown in Table 2. 0! Mf”’ke=:5 wealth:::= ○Example 3 (Ω life: (V6100A) :::
O Example 4 [Public base (V6100A) Ho: 0 Comparative example 2 AAS (V6100A) 50 copies LPET
A from the results of 50 parts table 2
The AS/PET mixture was heated at 210°C in the first stage, and at 210°C in the second stage.
All methods of cleaning by changing the cylinder temperature of 50°C yielded good results, and the accumulated AA was removed.
It is found that this method is very effective in removing S resin.
実施例5及び比較例3
実施例1に示した射出成形機を用いて同じ成形条件で三
菱モンサント■製のABS樹脂タフレックス210にカ
ーボンブラックを2%添加したペレットを60シヨツト
射出成形した。Example 5 and Comparative Example 3 Using the injection molding machine shown in Example 1, 60 shots of pellets prepared by adding 2% carbon black to ABS resin Tuflex 210 manufactured by Mitsubishi Monsanto ■ were injection molded under the same molding conditions.
射出成形後、ナチュラル品をシリンダー内に充填しなが
ら系外へ射出する作業をくり返して、射出成形機内を洗
浄した(ここまで比鯨例3)。After injection molding, the inside of the injection molding machine was cleaned by repeatedly filling the cylinder with a natural product and injecting it out of the system (so far, Example 3).
つぎに、黒色のタフレックス210のペレットを60シ
ヨツト射出成形後シリンダ一温度を01210℃、C2
10℃、C3210℃、ノズル210℃に設定して、タ
フレックス21040部、PET(融点250℃)60
部の混合物を用いて、射出成形機内を洗浄した。Next, after injection molding 60 shots of black Toughflex 210 pellets, the cylinder temperature was set to 01210°C, C2
Setting the temperature to 10℃, C3210℃, nozzle 210℃, Tuflex 21040 parts, PET (melting point 250℃) 60
The inside of the injection molding machine was cleaned using the mixture.
ついで、シリンダ一温度をC1240℃、C2250°
C1C3250℃、ノズル250℃に設定して(PET
成分は溶融させて)さらに洗浄した(ここまで実施例5
)。Next, the cylinder temperature was set to C1240℃ and C2250℃.
Set C1C3250℃, nozzle 250℃ (PET
The components were melted) and further washed (so far Example 5).
).
黒色からナチュラル品へ完全に変わるまで洗浄に要した
樹脂量をそれぞれ測定した。The amount of resin required for cleaning until the color completely changed from black to natural was measured.
その結果を表3に示した。The results are shown in Table 3.
実施例6〜8及び比較例4〜5
カーボンブラック2%で黒色に着色したAAS樹脂(パ
イタックスV6101AH)を下記の射出成形条件で3
0シヨツト射出成形した。Examples 6 to 8 and Comparative Examples 4 to 5 AAS resin (Pitax V6101AH) colored black with 2% carbon black was molded under the following injection molding conditions.
0 shot injection molding.
成形機:松山製作所の5I−50型インラインスクリユ
一式射出成形機
シリンダ一温度:C,230℃、C2230℃、ノズル
230°C
射出圧カニ 700Kp/ffl
スクリユ一回転数: 50 rpm
射出成形完了後、表4に示した上記AAS樹脂と同一の
AAS樹脂およびPET(融点250℃)の混合物を用
いて、表4に示したシリンダ一温度に設定して実施例1
と同様に黒色からナチュラル色に完全に変わるまで射出
成形機内を洗浄した。Molding machine: Matsuyama Seisakusho 5I-50 type inline screw complete injection molding machine Cylinder temperature: C, 230℃, C2230℃, nozzle 230℃ Injection pressure 700Kp/ffl Screw revolution speed: 50 rpm After injection molding is completed , using a mixture of the same AAS resin and PET (melting point 250° C.) as the above AAS resin shown in Table 4, and setting the cylinder temperature shown in Table 4 to Example 1.
In the same way, the inside of the injection molding machine was cleaned until the color completely changed from black to natural.
洗浄に要した樹脂量を測定したところ、表4に示した結
果を得た。When the amount of resin required for cleaning was measured, the results shown in Table 4 were obtained.
以上より明らかなように、本発明によれば、洗浄用樹脂
の使用量が少なくて、効果的に射出成形機の洗浄ができ
る。As is clear from the above, according to the present invention, an injection molding machine can be effectively cleaned with a small amount of cleaning resin used.
Claims (1)
するにあたり、スチレン系樹脂および該スチレン系樹脂
の溶融開始温度より高い融点を有する結晶性線状ポリエ
ステル樹脂の混合物を、第1段階目では、該スチレン系
樹脂の溶融開始温度以上で該結晶性線状ポリエステル樹
脂の融点以下で、第2段階目では該結晶性線状ポリエス
テル樹脂の融点以上で、射出することを特徴とする射出
成形機洗浄方法。1. In order to wash and remove the styrenic resin remaining in the injection molding machine, in the first step, a mixture of a styrenic resin and a crystalline linear polyester resin having a melting point higher than the melting start temperature of the styrenic resin is A method for cleaning an injection molding machine characterized by injecting at a temperature higher than the melting start temperature of the styrene resin and lower than the melting point of the crystalline linear polyester resin, and in a second step at a temperature higher than the melting point of the crystalline linear polyester resin. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP201779A JPS596220B2 (en) | 1979-01-10 | 1979-01-10 | Injection molding machine cleaning method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP201779A JPS596220B2 (en) | 1979-01-10 | 1979-01-10 | Injection molding machine cleaning method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5593436A JPS5593436A (en) | 1980-07-15 |
| JPS596220B2 true JPS596220B2 (en) | 1984-02-09 |
Family
ID=11517568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP201779A Expired JPS596220B2 (en) | 1979-01-10 | 1979-01-10 | Injection molding machine cleaning method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS596220B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6110798A (en) * | 1984-06-27 | 1986-01-18 | 日揮株式会社 | Method of washing volume reducer for solid waste |
| DE19858672A1 (en) * | 1998-12-18 | 2000-06-21 | Basf Ag | Composition for cleaning plastics processing equipment, especially injection molding machines comprises high melting thermoplastic particles in a lower-melting thermoplastic polymer |
-
1979
- 1979-01-10 JP JP201779A patent/JPS596220B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5593436A (en) | 1980-07-15 |
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