JPS6148405B2 - - Google Patents
Info
- Publication number
- JPS6148405B2 JPS6148405B2 JP5798779A JP5798779A JPS6148405B2 JP S6148405 B2 JPS6148405 B2 JP S6148405B2 JP 5798779 A JP5798779 A JP 5798779A JP 5798779 A JP5798779 A JP 5798779A JP S6148405 B2 JPS6148405 B2 JP S6148405B2
- Authority
- JP
- Japan
- Prior art keywords
- thermoplastic polymer
- dryer
- additive
- chips
- additives
- 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
- 239000000654 additive Substances 0.000 claims description 51
- 230000000996 additive effect Effects 0.000 claims description 27
- 229920001169 thermoplastic Polymers 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 6
- 239000007790 solid phase Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 description 25
- -1 polyethylene terephthalate Polymers 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000010186 staining Methods 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
Landscapes
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Moulding By Coating Moulds (AREA)
Description
本発明は熱可塑性重合体成形物の製造方法、特
に添加剤を均一に混合した熱可塑性重合体成形物
を経済的に製造する方法に関する。
熱可塑性重合体、例えばポリエチレンテレフタ
レートやポリブチレンテレフタレートで代表され
るポリエステル、6―ナイロンや66―ナイロンで
代表されるポリアミド、ポリエチレンやポリプロ
ピレンで代表されるポリオレフイン等は多くの優
れた特性を有しているため繊維、フイルム、その
他の成形物等に広く利用されており、これらは一
般に乾燥した後溶融成形されている。しかしなが
ら、これらの用途を更に拡大するため、その特性
の改善又は欠点の解消等を目的として種々の添加
剤を混合することが計られている。
従来、添加剤特に固相の添加剤を混合した重合
体成形物を製造するには、重合体の合成時に添加
剤を添加混合する方法、重合体チツプと添加剤と
を混合機を用いて混合してから乾燥、成形に供す
る方法が主として採用されている。しかしなが
ら、前者の方法では合成工程が繁雑になつたり、
合成装置を汚染したり、更には添加剤の種類によ
つては合成条件下で分解変質する等の欠点があ
り、後者の方法では混合機が余分に必要になり、
更には連続的に乾燥、溶融成形する場合に適用す
ると添加剤を均一に混合し難くなる等の欠点があ
る。
本発明者は、上記欠点を解消せんとして、連続
的に運転する乾燥機中に重合体チツプと添加剤と
を別々に一定量宛供給して乾燥機中において両者
を混合することを試みた。しかしながら、かかる
方法では得られた成形物中の添加剤は均一に混合
されず、不均一な製品しか得られなかつた。更に
この方法について鋭意検討を重ねた結果、添加剤
の計量器の出口近傍に圧抜口を設け、且つ重合体
チツプと添加剤とを乾燥機前の配管中で合流させ
れば、添加剤が均一に混合された成形物が得られ
ることを知り、本発明に到達した。
即ち、本発明は熱可塑性重合体チツプと固相の
添加剤とを連続的に別々に計量し、乾燥機に供給
して乾燥し、次いで溶融成形して熱可塑性重合体
成形物を製造するに際し、少なくとも添加剤の計
量器と乾燥機との間に圧抜口を設け且つ熱可塑性
重合体チツプと添加剤とを乾燥機前の配管中で合
流せしめることを特徴とする熱可塑性重合体成形
物の製造方法である。
本発明を図を用いて説明する。図は本発明の一
実施態様例を示す簡略図であり、図中1は添加剤
用ホツパー、2は添加剤用計量器、3は圧抜口、
4はロータリーフイーダ、5は添加剤供給管、6
は重合体チツプ用ホツパー、7は重合体チツプ計
量用ロータリーフイーダ、8は重合体チツプ供給
管、9は添加剤供給管5と重合体チツプ供給管8
との合流点、10は乾燥機である。
添加剤用計量器2と乾燥機10の間には圧抜口
3を設ける必要がある。こうすることによつて添
加剤の計量及び流れを精確に且つ円滑にすること
ができる。圧抜口3の位置は添加剤用計量器2と
乾燥機10との間であれば、どこでもよいが、乾
燥機内の熱風ロスを防ぐ点から、乾燥機10より
可及的に遠くすること換言すれば計量器2の出口
近傍に設けるのが好ましく、更に圧抜口3と乾燥
機10との間に図に示す如くロータリーフイーダ
ーを設ければ乾燥機内の熱風ロスをより防止でき
る点で好ましい。また、重合体チツプ用計量器と
乾燥機との間にも、圧抜口を設けても差支えな
い。
また、重合体チツプと添加剤とは、乾燥機10
に入る前に予め配管中で合流させるべきである。
図における9が両者の合流点である。この合流点
は特に制限する必要はなく、乾燥機入口の近傍で
あつてもよいが、通常0.3m以上乾燥機より離れ
た点が好ましい。両者を配管中で合流させるに
は、重合体チツプの流れ中に添加剤を供給するよ
うにしてもよいが、特に図に示すように添加剤供
給管5に直線状に延びる直管部を設け、この直管
部にここから枝状に分岐する枝管として重合体チ
ツプ供給管を接続し、添加剤の流れ中に重合体チ
ツプを供給すると、得られる成形物中の添加剤の
分布がより均一になるので好ましい。なお、重合
体チツプと添加剤とを別々に乾燥機に供給したの
では、得られる成形物における添加剤の分布が不
均一になる。
ここで使用する乾燥機は、連続式のものであれ
ば特別の形式にする必要はなく、例えば回転式乾
燥機、流動層式乾燥機、撹拌式乾燥機等は好まし
く使用される。また、乾燥に次いで行なう溶融成
形にも、特別の方法を採用する必要はなく、例え
ばエクストルーダー方式、溶融格子方式等任意に
採用することができる。
本発明で言う熱可塑性重合体とは、溶融成形可
能な熱可塑性重合体であれば任意でよく、特にポ
リエチレンテレフタレートやポリブチレンテレフ
タレートの如きポリエステル、6―ナイロンや66
―ナイロンの如きポリアミド、ポリエチレンやポ
リプロピレンの如きポリオレフイン等が好まし
い。また、その形状は粒状、円柱状、角柱状、サ
イコロ状、平板状、フレークス状の如く粉末以外
の任意の形状でよく、本発明においてはこれらを
チツプと略称する。
また、本発明で言う添加剤は上記重合体の乾燥
条件下で固相状態を保持する添加剤であれば任意
でよく、例えば帯電防止剤、防炎剤、着色剤、螢
光増白剤、滑剤、安定剤、易染剤等をあげること
ができる。また、その形状は粉粒状等任意でよ
く、特に混合すべき上記重合体チツプと同一乃至
類似の形状にしたものが好ましい。なかでも、上
記重合体に添加剤を高濃度に含有させてチツプ化
した所謂マスターチツプにして使用すれば、乾燥
機中で生じ易い重合体チツプと添加剤との分級を
充分に防止することができるので好ましい。添加
剤の重合体チツプに対する使用割合は極めて広い
範囲、例えば数分の1から数百分の1にわたる広
い範囲で問題なく行なわれる。
本発明によれば、特別な混合機を使用すること
なく、また重合体の合成装置を汚染することな
く、長期間連続して添加剤を均一に混合した成形
物を極めて経済的に製造することができる。
以下に実施例をあげて更に本発明を説明する。
なお、添加剤の混合斑は、得られたフイラメント
を編立て染色し、染色斑の程度によつて混合斑の
尺度にした。染色斑は5段階法によつて行ない、
5級が最も良好、1級が最も悪いものであり、3
級以上を合格とした。
実施例1〜3及び比較例1,2
図に示す装置を使用し、添加剤用計量器として
東邦エレジニアリング社製アクリソン101―BC
型連続計量器を用い、添加剤供給管の直管部を内
径80mmとし、重合体チツプ供給管を内径100mmの
枝管とし、両者の供給管の合流部から乾燥機まで
の距離を10mとし、乾燥機として回転型熱風乾燥
機を用いた。
重合体チツプ用ホツパー6よりロータリーフイ
ーダ7によつて固有粘度(25℃、オルソクロロフ
エノール溶媒中)0.60のポリエチレンテレフタレ
ートチツプ(チツプ形状4×4×2(mm)の平板
状)を毎時335Kgの割合で連続的に計量供給し、
同時に添加剤用ホツパー1より計量器2によつ
て、第1表に示す種々の形状の固有粘度0.60のポ
リエチレンテレフタレートに平均分子量20000の
ポリオキシエチレングリコールを5重量%混合し
たマスターチツプを毎時110Kgの割合で連続的に
計量供給した。乾燥機内の温度は140℃に保持
し、乾燥機内のチツプ滞留時間は3時間にした。
乾燥後混合チツプを紡糸機の直前に設置したタン
クに一旦貯蔵してから紡糸機に供給し、溶融温度
280℃でエクストルーダにより溶融吐出し、
1100m/分の速度で捲取り、単糸繊度7デニール
の未延伸糸を得た。この未延伸糸を75℃で3倍に
延伸し、120℃で熱固定した。添加剤の混合斑を
示す染色斑は第1表に示す通りである。
比較のため、図に示す圧抜口3を閉じ、圧抜作
用をなくす以外は上記実施例と同様に行ない、結
果を比較例1として第1表に示した。
更に比較のため、ポリエチレンテレフタレート
チツプ供給管を直接乾燥機に接続し、ポリエチレ
ンテレフタレートチツプとマスターチツプを別々
に乾燥機に供給する以外は上記実施例と同様に行
ない、結果を比較例2として第1表に示した。
The present invention relates to a method for producing thermoplastic polymer moldings, and more particularly to a method for economically producing thermoplastic polymer moldings in which additives are uniformly mixed. Thermoplastic polymers, such as polyesters such as polyethylene terephthalate and polybutylene terephthalate, polyamides such as 6-nylon and 66-nylon, and polyolefins such as polyethylene and polypropylene, have many excellent properties. Because of this, it is widely used in fibers, films, and other molded products, which are generally melt-molded after drying. However, in order to further expand these uses, attempts are being made to mix various additives with the aim of improving their properties or eliminating their drawbacks. Conventionally, in order to manufacture polymer molded articles mixed with additives, especially solid-phase additives, there have been two methods: adding and mixing the additives during polymer synthesis, and mixing polymer chips and additives using a mixer. The most commonly used method is to dry and then mold the material. However, in the former method, the synthesis process becomes complicated,
There are disadvantages such as contaminating the synthesis equipment and furthermore, depending on the type of additive, it may decompose and deteriorate under the synthesis conditions, and the latter method requires an extra mixer.
Furthermore, when applied to continuous drying and melt molding, there are drawbacks such as difficulty in uniformly mixing additives. In an attempt to overcome the above-mentioned drawbacks, the present inventor attempted to feed polymer chips and additives in fixed amounts separately into a continuously operating dryer and then mix the two in the dryer. However, in this method, the additives in the molded product obtained are not mixed uniformly, and only a non-uniform product is obtained. Furthermore, as a result of extensive research into this method, we found that if a pressure release port is provided near the outlet of the additive meter and the polymer chips and additives are combined in the pipe in front of the dryer, the additives can be removed. The present invention was developed based on the knowledge that a uniformly mixed molded product can be obtained. That is, the present invention involves continuously and separately weighing thermoplastic polymer chips and solid-phase additives, supplying them to a dryer to dry them, and then melt-molding them to produce a thermoplastic polymer molded product. A thermoplastic polymer molded article, characterized in that a pressure release port is provided between at least an additive meter and a dryer, and the thermoplastic polymer chips and additives are combined in a pipe in front of the dryer. This is a manufacturing method. The present invention will be explained using figures. The figure is a simplified diagram showing an embodiment of the present invention, in which 1 is an additive hopper, 2 is an additive meter, 3 is a pressure outlet,
4 is a rotary feeder, 5 is an additive supply pipe, 6
7 is a hopper for polymer chips, 7 is a rotary feeder for weighing polymer chips, 8 is a polymer chip supply pipe, 9 is an additive supply pipe 5 and a polymer chip supply pipe 8
10 is a dryer. It is necessary to provide a pressure release port 3 between the additive measuring device 2 and the dryer 10. By doing so, it is possible to accurately and smoothly measure and flow the additive. The pressure release port 3 may be located anywhere between the additive measuring device 2 and the dryer 10, but it should be located as far away from the dryer 10 as possible in order to prevent loss of hot air inside the dryer. If so, it is preferable to install it near the outlet of the meter 2, and it is also preferable to install a rotary feeder between the pressure release port 3 and the dryer 10 as shown in the figure, since hot air loss inside the dryer can be further prevented. . Further, a pressure release port may be provided between the polymer chip measuring device and the dryer. In addition, the polymer chips and additives are dried in a dryer.
They should be merged in the piping before entering.
9 in the figure is the meeting point of both. This merging point does not need to be particularly limited and may be near the dryer inlet, but it is usually preferably at least 0.3 m away from the dryer. In order to merge the two in a pipe, the additive may be supplied during the flow of polymer chips, but in particular, as shown in the figure, a straight pipe section extending in a straight line is provided in the additive supply pipe 5. If a polymer chip supply pipe is connected to this straight pipe as a branch pipe branching from here and the polymer chips are fed into the flow of the additive, the distribution of the additive in the resulting molded product will be improved. This is preferable because it becomes uniform. Note that if the polymer chips and additives are fed separately to the dryer, the distribution of the additives in the resulting molded product will be uneven. The dryer used here does not need to be of a special type as long as it is a continuous type, and for example, a rotary dryer, a fluidized bed dryer, an agitation dryer, etc. are preferably used. Further, there is no need to adopt a special method for melt molding performed after drying, and any method such as an extruder method or a melt lattice method can be employed. The thermoplastic polymer referred to in the present invention may be any thermoplastic polymer that can be melt-molded, particularly polyester such as polyethylene terephthalate and polybutylene terephthalate, 6-nylon, 66
- Polyamides such as nylon, polyolefins such as polyethylene and polypropylene, etc. are preferred. Further, the shape thereof may be any shape other than powder, such as granules, cylinders, prisms, dice, flat plates, and flakes, and in the present invention, these are abbreviated as chips. Further, the additive referred to in the present invention may be any additive as long as it maintains a solid phase state under drying conditions of the above polymer, such as an antistatic agent, a flame retardant, a coloring agent, a fluorescent whitening agent, etc. Examples include lubricants, stabilizers, dyeing agents, etc. Further, the shape thereof may be arbitrary such as powder or granule, and it is particularly preferable to have the same or similar shape to the above-mentioned polymer chips to be mixed. In particular, if the above-mentioned polymer is used in the form of chips containing a high concentration of additives, so-called master chips, it is possible to sufficiently prevent the classification of polymer chips and additives that is likely to occur in a dryer. This is preferable because it can be done. The ratio of the additive to the polymer chip can be varied over a very wide range, for example from a fraction of a fraction to a fraction of a hundredth, without any problem. According to the present invention, it is possible to extremely economically produce molded articles in which additives are uniformly mixed continuously over a long period of time without using a special mixer or without contaminating the polymer synthesis equipment. I can do it. The present invention will be further explained below with reference to Examples.
Incidentally, the mixed mottling of the additives was measured by knitting and dyeing the obtained filament and measuring the degree of the dyeing mottling. Staining spots are performed using a five-step method,
Grade 5 is the best, grade 1 is the worst, and grade 3 is the best.
A grade above grade was considered a passing grade. Examples 1 to 3 and Comparative Examples 1 and 2 The apparatus shown in the figure was used, and Acrison 101-BC manufactured by Toho Elesineering Co., Ltd. was used as an additive measuring device.
Using a type continuous meter, the straight part of the additive supply pipe was made to have an inner diameter of 80 mm, the polymer chip supply pipe was made into a branch pipe with an inner diameter of 100 mm, and the distance from the confluence of both supply pipes to the dryer was 10 m. A rotary hot air dryer was used as the dryer. Polyethylene terephthalate chips (chip shape: 4 x 4 x 2 (mm) flat plate) with an intrinsic viscosity (25°C, in orthochlorophenol solvent) of 0.60 are fed from a polymer chip hopper 6 to a rotary feeder 7 at a rate of 335 kg per hour. Continuously metered and supplied in proportions,
At the same time, from the additive hopper 1, using the measuring device 2, master chips prepared by mixing 5% by weight of polyoxyethylene glycol with an average molecular weight of 20,000 with polyethylene terephthalate having an intrinsic viscosity of 0.60 in various shapes shown in Table 1 were added at a rate of 110 kg per hour. Continuously metered in proportions. The temperature inside the dryer was maintained at 140°C, and the residence time of the chips in the dryer was 3 hours.
After drying, the mixed chips are temporarily stored in a tank installed just before the spinning machine, then supplied to the spinning machine, and the melting temperature is
Melt and discharge with an extruder at 280℃,
It was wound at a speed of 1100 m/min to obtain an undrawn yarn with a single yarn fineness of 7 denier. This undrawn yarn was drawn three times at 75°C and heat-set at 120°C. The staining spots indicating additive mixing spots are shown in Table 1. For comparison, the same procedure as in the above Example was carried out except that the pressure relief port 3 shown in the figure was closed to eliminate the pressure relief effect, and the results are shown in Table 1 as Comparative Example 1. Furthermore, for comparison, the same procedure as in the above example was carried out except that the polyethylene terephthalate chips supply pipe was directly connected to the dryer and the polyethylene terephthalate chips and master chips were separately supplied to the dryer, and the results were used as Comparative Example 2. Shown in the table.
【表】
実施例 4
実施例1におけるポリエチレンテレフタレート
チツプ供給管とマスターチツプ供給管とを逆に取
付けて、即ちポリエチレンテレフタレートチツプ
供給管の直管部にマスターチツプ供給管を枝管と
して取付けた以外は実施例1と同様に行なつたと
ころ、染色斑は3〜3.5級であつた。
実施例 5
実施例1と同一の装置を使用し、重合体チツプ
用ホツパー6よりロータリーフイダー7によつて
固有粘度(25℃、m―クレゾール溶媒中)1.3の
6―ナイロンチツプ(チツプ形状は2mmφ×2mm
の円柱状)を毎時360Kgの割合で連続的に計量供
給し、同時に添加剤用ホツパー1より計量器2に
よつて固有粘度1.3の6―ナイロンに平均分子量
10000のポリオキシエチレングリコールを7重量
%混合したマスターチツプを毎時90Kgの割合で連
続的に計量供給した。乾燥機内の乾燥媒体として
は窒素を使用し、130℃に保持し、乾燥機内のチ
ツプ滞留時間は4時間にした。乾燥後のチツプは
空気と遮断し、連続的にエクストルーダーに供給
して溶融温度260℃、吐出速度30m/分でフイル
ム状に押出し、長さ方向に4倍、巾方向に2倍に
延伸して厚さ20μの二軸延伸フイルムを得、この
フイルムを染色し、染色斑を実施例1と同様に5
段階で示し、ポリオキシエチレングリコールの混
合斑の尺度としたところ、染着斑は3.5〜4級で
あつた。[Table] Example 4 Except that the polyethylene terephthalate chip supply pipe and master chip supply pipe in Example 1 were installed in reverse, that is, the master chip supply pipe was installed as a branch pipe on the straight pipe part of the polyethylene terephthalate chip supply pipe. When the same procedure as in Example 1 was carried out, the staining spots were grade 3 to 3.5. Example 5 Using the same equipment as in Example 1, 6-nylon chips (chip shape: 2mmφ×2mm
(cylindrical shape) at a rate of 360 kg per hour, and at the same time, from the additive hopper 1, the average molecular weight
Master chips containing 7% by weight of 10,000 polyoxyethylene glycol were continuously metered in at a rate of 90 kg/hour. Nitrogen was used as the drying medium in the dryer, maintained at 130°C, and the residence time of the chips in the dryer was 4 hours. After drying, the chips are isolated from air and continuously fed into an extruder, extruded into a film at a melting temperature of 260°C and a discharge speed of 30 m/min, and stretched 4 times in the length direction and 2 times in the width direction. A biaxially stretched film with a thickness of 20 μm was obtained, and this film was dyed, and the dyed spots were 5
When expressed in stages and used as a scale for polyoxyethylene glycol mixed spots, the staining spots were grade 3.5 to grade 4.
図は本発明の一実施態様例を示す簡略図であ
る。
図中2は添加剤用計量器、3は圧抜口、7は重
合体チツプ用計量器、9は添加剤と重合体チツプ
との合流点、10は乾燥機である。
The figure is a simplified diagram showing an example of an embodiment of the present invention. In the figure, 2 is a measuring device for additives, 3 is a pressure outlet, 7 is a measuring device for polymer chips, 9 is a confluence point of additives and polymer chips, and 10 is a dryer.
Claims (1)
続的に別々に計量し、乾燥機に供給して乾燥し、
次いで溶融成形して熱可塑性重合体成形物を製造
するに際し、少なくとも添加剤の計量器と乾燥機
との間に圧抜口を設け且つ熱加塑性重合体チツプ
と添加剤とを乾燥機前の配管中で合流せしめるこ
とを特徴とする熱可塑性重合体成形物の製造方
法。 2 熱可塑性重合体チツプと添加剤との合流が添
加剤供給配管の直管部に接続した熱可塑性重合体
供給枝管により添加剤の流れ中に熱可塑性重合体
チツプを供給することにより行なわれる特許請求
の範囲第1項記載の熱可塑性重合体成形物の製造
方法。 3 添加剤が、熱可塑性重合体チツプと同一乃至
類似の形状、大きさである特許請求の範囲第1項
又は第2項記載の熱可塑性重合体成形物の製造方
法。[Claims] 1. Thermoplastic polymer chips and solid phase additives are continuously and separately weighed, fed to a dryer and dried,
Next, when producing a thermoplastic polymer molded article by melt molding, a pressure release port is provided at least between the additive meter and the dryer, and the thermoplastic polymer chips and additives are removed before the dryer. A method for producing a thermoplastic polymer molded article, characterized by merging it in a pipe. 2. The joining of the thermoplastic polymer chips and the additive is carried out by feeding the thermoplastic polymer chips into the flow of the additive through a thermoplastic polymer supply branch pipe connected to the straight pipe section of the additive supply pipe. A method for producing a thermoplastic polymer molded article according to claim 1. 3. The method for producing a thermoplastic polymer molded article according to claim 1 or 2, wherein the additive has the same or similar shape and size as the thermoplastic polymer chips.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5798779A JPS55150317A (en) | 1979-05-14 | 1979-05-14 | Process for producing thermoplastic rolymer molded article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5798779A JPS55150317A (en) | 1979-05-14 | 1979-05-14 | Process for producing thermoplastic rolymer molded article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55150317A JPS55150317A (en) | 1980-11-22 |
| JPS6148405B2 true JPS6148405B2 (en) | 1986-10-24 |
Family
ID=13071353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5798779A Granted JPS55150317A (en) | 1979-05-14 | 1979-05-14 | Process for producing thermoplastic rolymer molded article |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS55150317A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0328516U (en) * | 1989-07-28 | 1991-03-22 | ||
| JPH0328515U (en) * | 1989-07-28 | 1991-03-22 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57185345A (en) * | 1981-05-08 | 1982-11-15 | Diafoil Co Ltd | Production of polyester film |
| JP5889668B2 (en) * | 2012-02-21 | 2016-03-22 | 株式会社ニフコ | Resin pellet material supply device and resin molding system |
-
1979
- 1979-05-14 JP JP5798779A patent/JPS55150317A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0328516U (en) * | 1989-07-28 | 1991-03-22 | ||
| JPH0328515U (en) * | 1989-07-28 | 1991-03-22 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS55150317A (en) | 1980-11-22 |
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