JPH07314520A - Extruded thick molded product and method for producing the same - Google Patents
Extruded thick molded product and method for producing the sameInfo
- Publication number
- JPH07314520A JPH07314520A JP7044754A JP4475495A JPH07314520A JP H07314520 A JPH07314520 A JP H07314520A JP 7044754 A JP7044754 A JP 7044754A JP 4475495 A JP4475495 A JP 4475495A JP H07314520 A JPH07314520 A JP H07314520A
- Authority
- JP
- Japan
- Prior art keywords
- wall thickness
- extruded
- molded product
- melt viscosity
- sec
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000004734 Polyphenylene sulfide Substances 0.000 claims abstract description 28
- 229920000069 polyphenylene sulfide Polymers 0.000 claims abstract description 28
- 239000000155 melt Substances 0.000 claims abstract description 16
- 238000002425 crystallisation Methods 0.000 claims abstract description 11
- 230000008025 crystallization Effects 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 238000002844 melting Methods 0.000 claims description 17
- 230000008018 melting Effects 0.000 claims description 17
- 238000000465 moulding Methods 0.000 claims description 10
- 238000005520 cutting process Methods 0.000 claims description 7
- 238000001125 extrusion Methods 0.000 abstract description 14
- 238000006116 polymerization reaction Methods 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 20
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 229910052979 sodium sulfide Inorganic materials 0.000 description 7
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 7
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000012299 nitrogen atmosphere Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 4
- 229910003475 inorganic filler Inorganic materials 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 235000012438 extruded product Nutrition 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ODPYDILFQYARBK-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-1,3,5-triene Chemical compound C1=CC=C2SC2=C1 ODPYDILFQYARBK-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 229920001283 Polyalkylene terephthalate Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- -1 polytetrafluoroethylene, tetrafluoroethylene copolymer Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
- B29C48/80—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the plasticising zone, e.g. by heating cylinders
- B29C48/83—Heating or cooling the cylinders
- B29C48/832—Heating
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
- B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
- B29C48/865—Heating
Landscapes
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
Abstract
(57)【要約】
【構成】 310℃、剪断速度200/秒での溶融粘度
の、310℃、剪断速度1200/秒での溶融粘度に対
する比が2.2〜3.0であり、310℃、剪断速度1
200/秒での溶融粘度が500〜2000Pa・s、
結晶化温度が160〜205℃であるポリフェニレンサ
ルファイド又はそれを主とする組成物よりなり、10m
m以上の肉厚を有する押出肉厚成形物。
【効果】 成形物の内部に亀裂やボイドが少なく、耐衝
撃性、強度特性等に優れるとともに溶融押出成形性に優
れ、肉厚の、丸棒や平板等に特に好適である。(57) [Summary] The ratio of the melt viscosity at 310 ° C and the shear rate of 200 / sec to the melt viscosity at 310 ° C and the shear rate of 1200 / sec is 2.2 to 3.0, and 310 ° C. , Shear rate 1
A melt viscosity at 200 / sec of 500 to 2000 Pa · s,
It is composed of polyphenylene sulfide having a crystallization temperature of 160 to 205 ° C. or a composition mainly containing it,
An extruded wall thickness molded product having a wall thickness of m or more. [Effect] There are few cracks and voids inside the molded product, and it is excellent in impact resistance, strength properties, and the like, and is also excellent in melt extrusion moldability, and is particularly suitable for thick round bars and flat plates.
Description
【0001】[0001]
【産業上の利用分野】本発明はポリフェニレンサルファ
イドよりなる押出肉厚成形物及びその製法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an extruded thick-walled molded product made of polyphenylene sulfide and a process for producing the same.
【0002】ポリフェニレンサルファイドは耐熱性、耐
薬品性、難燃性、剛性等に優れた高結晶性の熱可塑性樹
脂である。ポリフェニレンサルファイド成形品は射出成
形法や切削加工法等により製造されているが、このう
ち、射出成形法は射出成形条件が十分に検討された物品
並びに素材につき、それを大量生産する場合に適してい
る。これに対して切削加工法は少量生産する場合、射出
成形法では製造困難な特定構造若しくは特定寸法の精密
物品を生産する場合、或いは射出成形法による大量生産
の予備若しくは前段階で試験的に生産する場合等に適し
ており、切削加工用丸棒又は平板成形物は押出成形法に
より得ている。Polyphenylene sulfide is a highly crystalline thermoplastic resin excellent in heat resistance, chemical resistance, flame retardancy, rigidity and the like. Polyphenylene sulfide molded products are manufactured by injection molding method, cutting method, etc. Among them, the injection molding method is suitable for mass production of articles and materials for which injection molding conditions have been sufficiently examined. There is. On the other hand, when the cutting method is used for small-scale production, when manufacturing precision articles with a specific structure or specific dimensions that are difficult to manufacture by injection molding, or for trial production in the preliminary or previous stage of mass production by injection molding. For example, the round bar or flat plate molding for cutting is obtained by the extrusion molding method.
【0003】ところが10mm以上の肉厚を有する、丸
棒又は平板状の押出成形物を製造する場合、多くの丸棒
又は平板成形物の中心部に多数の微細な亀裂やボイドが
生じる問題がある。中心部にそのような欠陥があると、
この欠陥を含む切削加工品を製造する危険があり、また
中心部の微細な亀裂は、丸棒又は平板成形品の保管や運
搬中に徐々に丸棒又は平板成形品の表面に向かって進展
する場合がある等の問題がある。However, when a round bar or flat plate extruded product having a wall thickness of 10 mm or more is produced, there is a problem that many fine cracks and voids occur in the center of many round bar or flat plate molded products. . With such a defect in the center,
There is a risk of producing a machined product containing this defect, and minute cracks in the center gradually develop toward the surface of the round bar or flat plate molded product during storage or transportation of the round bar or flat plate molded product. There are problems such as cases.
【0004】そこで、このようなポリフェニレンサルフ
ァイドの押出成形性及び押出成形物の物性の欠点を克服
するために、種々の成形法の検討が試みられている。例
えば特開昭52ー11256号公報には、ダイの外部か
ら背圧を加えて押出成形を行なうことにより前記の問題
点を解決させることが提案されている。Therefore, in order to overcome the drawbacks of the extrusion moldability of polyphenylene sulfide and the physical properties of the extruded product, various molding methods have been studied. For example, Japanese Patent Application Laid-Open No. 52-11256 proposes to solve the above-mentioned problems by applying a back pressure from the outside of the die to perform extrusion molding.
【0005】また特開昭64ー8028号には押出機の
クロスヘッドに耐熱性材料のコアを供給し、当該コアの
上にポリフェニレンサルファイドを押出被覆し、冷却
後、当該コアを抜き取ることにより亀裂やボイドのない
中空のポリフェニレンサルファイドからなる切削加工品
が製造できることが開示されている。Further, in JP-A-64-8028, a core made of a heat-resistant material is supplied to a crosshead of an extruder, polyphenylene sulfide is extrusion-coated on the core, and after cooling, the core is extracted and cracked. It is disclosed that a machined product made of hollow polyphenylene sulfide having no voids can be produced.
【0006】しかしながら、これら公知の方法は、いず
れも成形作業が複雑で生産性に劣り、またポリフェニレ
ンサルファイド自体の溶融押出成形性や成形物の物性を
改善するものではない。However, none of these known methods is complicated in molding work and inferior in productivity, and does not improve melt extrusion moldability of polyphenylene sulfide itself or physical properties of a molded product.
【0007】[0007]
【発明が解決しようとする課題】本発明の目的は、成形
物の内部に亀裂やボイドが少なく、衝撃強度や曲げ強度
等の強度特性に優れるとともに溶融押出成形性に優れた
ポリフェニレンサルファイドからなる10mm以上の肉
厚を有する押出肉厚成形物及びその製造方法を提供する
ことにある。DISCLOSURE OF THE INVENTION The object of the present invention is to form a polyphenylene sulfide of 10 mm, which has few cracks and voids inside the molded article, has excellent strength characteristics such as impact strength and bending strength, and has excellent melt extrusion moldability. An object of the present invention is to provide an extruded wall thickness molded product having the above wall thickness and a method for producing the same.
【0008】[0008]
【課題を解決するための手段】本発明は従来技術の有す
る問題点を解決するべく鋭意研究した結果、溶融粘度の
剪断速度依存性と結晶化温度と溶融粘度を特定するポリ
フェニレンサルファイドを用いることにより10mm以
上の肉厚を有する肉厚押出成形物の成形加工性に優れ、
同時に成形物の内部に亀裂やボイドが少なく衝撃強度を
始めとする強度特性が向上した成形物が得られることを
見出したことに基づく。Means for Solving the Problems The present invention has been earnestly studied to solve the problems of the prior art, and as a result, by using polyphenylene sulfide which specifies shear rate dependence of melt viscosity, crystallization temperature and melt viscosity. Excellent in molding processability of thick-walled extrudates having a wall thickness of 10 mm or more,
At the same time, it is based on the finding that a molded product having few cracks and voids inside and improved strength characteristics such as impact strength can be obtained.
【0009】かくして本発明によれば、310℃、剪断
速度200/秒での溶融粘度の、310℃、剪断速度1
200/秒での溶融粘度に対する比(以下、この比を
「溶融粘度の剪断速度依存度」と呼ぶ)が2.2〜3.
0であり、310℃、剪断速度1200/秒での溶融粘
度が500〜2000Pa・s、結晶化温度が160〜
205℃であるポリフェニレンサルファイド又はその組
成物よりなり、10mm以上の肉厚を有する押出肉厚成
形物が提供される。Thus, according to the invention, a melt viscosity at 310 ° C. and a shear rate of 200 / sec of 310 ° C. and a shear rate of 1
The ratio to the melt viscosity at 200 / sec (hereinafter, this ratio is referred to as "shear rate dependence of melt viscosity") is 2.2 to 3.
0, 310 ° C., melt viscosity at shear rate of 1200 / sec of 500 to 2000 Pa · s, crystallization temperature of 160 to
An extruded thick-walled molded article having a wall thickness of 10 mm or more, which is made of polyphenylene sulfide at 205 ° C. or a composition thereof, is provided.
【0010】また、310℃、剪断速度200/秒での
溶融粘度の、310℃、剪断速度1200/秒での溶融
粘度に対する比が2.2〜3.0であり、310℃、剪
断速度1200/秒での溶融粘度が500〜2000P
a・s、結晶化温度が160〜205℃であるポリフェ
ニレンサルファイド又はその組成物を、一旦融点以上に
融解した後、ダイ内で融点未満にして後、押出成形し
て、10mm以上の肉厚とする押出肉厚成形物の製造方
法が提供される。以下、本発明を詳細に説明する。Further, the ratio of the melt viscosity at 310 ° C. and the shear rate of 200 / sec to the melt viscosity at 310 ° C. and the shear rate of 1200 / sec is 2.2 to 3.0, and 310 ° C. and the shear rate of 1200. / Sec melt viscosity is 500-2000P
a · s, polyphenylene sulfide having a crystallization temperature of 160 to 205 ° C. or a composition thereof is once melted to a melting point or higher, then lowered to below the melting point in a die, and then extrusion molded to obtain a wall thickness of 10 mm or more. A method for producing an extruded thick-walled molded article is provided. Hereinafter, the present invention will be described in detail.
【0011】本発明で用いるポリフェニレンサルファイ
ドは、ポリマーの主構成単位として、フェニレンサルフ
ァイドを繰返し単位中の50質量%以上、好ましくは7
0質量%以上含む、ホモポリマー或いはコポリマーであ
る。また、本発明で用いるポリフェニレンサルファイド
は、溶融粘度の剪断速度依存度が2.2〜3.0、好ま
しくは2.25〜2.9のものが用いられる。この溶融
粘度の剪断速度依存度が2.2未満では溶融押出成形時
に弾性が不足し、ダイスウェルも小さくなり、保形性が
劣り、成形加工性が悪いためである。他方、溶融粘度の
剪断速度依存度が3.0を越えると、溶融時の弾性が大
きくなりすぎ、ダイスウェルが大きくなって成形物の寸
法精度が低下し好ましくないためである。The polyphenylene sulfide used in the present invention contains phenylene sulfide as a main constitutional unit of a polymer in an amount of 50% by mass or more, preferably 7% by weight in a repeating unit.
It is a homopolymer or a copolymer containing 0% by mass or more. The polyphenylene sulfide used in the present invention has a shear viscosity dependence of melt viscosity of 2.2 to 3.0, preferably 2.25 to 2.9. If the melt viscosity has a shear rate dependency of less than 2.2, elasticity during melt extrusion is insufficient, die swell is reduced, shape retention is poor, and moldability is poor. On the other hand, if the shear viscosity dependence of the melt viscosity exceeds 3.0, the elasticity at the time of melting becomes too large, the die swell becomes large, and the dimensional accuracy of the molded product decreases, which is not preferable.
【0012】また、本発明で用いるポリフェニレンサル
ファイドは、結晶化温度が160〜205℃、好ましく
は165〜200℃のものが用いられる。ここで結晶化
温度とはポリフェニレンサルファイドを窒素気流下、3
20℃で2分間予熱した後、1分間加圧し、次いで急冷
して作製した無定形シート10mgを用い、差動走査熱
量計(DSC)(メトラー社製「DSC−30」を使
用)で窒素気流中340℃から10℃/分の降温速度で
冷却したときのチャート上に現れる発熱ピーク温度であ
る。結晶化温度が205℃を越えると溶融押出成形時
に、ダイから流出後の冷却過程での結晶化及び固化の速
度が大きくなりすぎて、肉厚が10mm以上の成形物の
内部に多数の微細な亀裂やボイドが生じ好ましくないた
めである。他方、結晶化温度が160℃未満では結晶性
の低下したものしか得られず、成形後の熱処理時に変形
して、外観の優れた成形物が得られなくなるためであ
る。The polyphenylene sulfide used in the present invention has a crystallization temperature of 160 to 205 ° C., preferably 165 to 200 ° C. Here, the crystallization temperature means that polyphenylene sulfide is used under a nitrogen stream for 3
Amorphous sheet 10 mg prepared by preheating at 20 ° C. for 2 minutes, pressurizing for 1 minute, and then rapidly cooling was used, and a differential scanning calorimeter (DSC) (using "DSC-30" manufactured by METTLER CORPORATION) was used for nitrogen flow. It is the exothermic peak temperature that appears on the chart when cooled at a cooling rate of 10 ° C / min from 340 ° C in the middle. If the crystallization temperature exceeds 205 ° C., the rate of crystallization and solidification in the cooling process after flowing out from the die becomes too high during melt extrusion molding, and a large number of fine particles are formed inside the molded product having a wall thickness of 10 mm or more. This is because cracks and voids are generated undesirably. On the other hand, if the crystallization temperature is lower than 160 ° C., only the crystallinity of which is lowered can be obtained, and the product is deformed during the heat treatment after molding, and a molded product having an excellent appearance cannot be obtained.
【0013】また、本発明で用いるポリフェニレンサル
ファイドは、310℃、剪断速度1200/秒で測定し
た溶融粘度が500〜2000Pa・s、好ましくは6
00〜1900Pa・s、より好ましくは700〜18
00Pa・sのものが用いられる。溶融粘度はキャピロ
グラフ(東洋精機社製)によりL/D=10mm/1m
mのノズルを用いて求めたものである。溶融粘度が50
0Pa・s未満では、成形物の十分な耐衝撃性及び強度
特性が得られないためである。他方、2000Pa・s
を越すと流動性が小さく、溶融成形性が低下し、好まし
くないためである。上記諸条件を満たすポリフェニレン
サルファイドは例えば特公昭57ー334号公報、1分
子当り3個以上のハロゲン置換基を有する少なくとも1
種のポリハロ芳香族化合物を用いた特公昭63ー337
75号公報等に記載の方法により製造することができ
る。The polyphenylene sulfide used in the present invention has a melt viscosity of 500 to 2000 Pa · s, preferably 6 when measured at 310 ° C. and a shear rate of 1200 / sec.
00 to 1900 Pa · s, more preferably 700 to 18
00 Pa · s is used. Melt viscosity is L / D = 10mm / 1m by Capirograph (manufactured by Toyo Seiki Co., Ltd.)
It is obtained using the m nozzle. Melt viscosity is 50
This is because if it is less than 0 Pa · s, sufficient impact resistance and strength characteristics of the molded product cannot be obtained. On the other hand, 2000 Pa · s
This is because if it exceeds the range, the fluidity is small and the melt moldability is deteriorated, which is not preferable. The polyphenylene sulfide satisfying the above-mentioned various conditions is disclosed in, for example, Japanese Patent Publication No. 57-334, and has at least 1 halogen-substituted group of 3 or more per molecule.
Japanese Patent Publication No. 63-337 using various polyhaloaromatic compounds
It can be produced by the method described in Japanese Patent Publication No. 75, etc.
【0014】本発明成形物にはポリフェニレンサルファ
イドの他に混合可能な各種任意成分を所望により含有さ
せても良い。その例としては無機充填材が挙げられる。
無機充填材としては例えば、シリカ、アルミナ、タル
ク、マイカ、カオリン、クレー、シリカアルミナ、酸化
チタン、炭酸カルシウム、ケイ酸カルシウム、リン酸カ
ルシウム、硫酸カルシウム、炭酸マグネシウム、酸化マ
グネシウム、リン酸マグネシウム、窒化珪素、ガラス、
ハイドロタルサイト、酸化ジルコニウム等の粒状、粉末
状或いは鱗片状のもの、又は、ガラス繊維、チタン酸カ
リウム繊維、炭素繊維、マイカセラミック繊維等の繊維
状のものを配合することができる。これらの無機充填材
は、それぞれ単独で、或いは2種以上組合わせて用いる
ことができる。また、これらの無機充填材は、シランカ
ップリング剤やチタネートカップリング剤で処理したも
のであっても良い。充填材の配合割合は、溶融加工性の
観点等から見て、通常、70質量%以下である。If desired, the molded product of the present invention may contain various optional components other than polyphenylene sulfide that can be mixed. An example thereof is an inorganic filler.
Examples of the inorganic filler include silica, alumina, talc, mica, kaolin, clay, silica-alumina, titanium oxide, calcium carbonate, calcium silicate, calcium phosphate, calcium sulfate, magnesium carbonate, magnesium oxide, magnesium phosphate, silicon nitride, Glass,
Granular, powdery or scaly ones such as hydrotalcite and zirconium oxide, or fibrous ones such as glass fibers, potassium titanate fibers, carbon fibers and mica ceramic fibers can be blended. These inorganic fillers can be used alone or in combination of two or more. Further, these inorganic fillers may be treated with a silane coupling agent or a titanate coupling agent. The mixing ratio of the filler is usually 70% by mass or less from the viewpoint of melt processability.
【0015】任意成分の別な例としてポリフェニレンサ
ルファイド以外の熱可塑性樹脂であって、ポリフェニレ
ンサルファイドの溶融成形温度領域、通常200〜38
0℃において熱分解等が生じがたいものが挙げられる。
例えば、ポリアミド、ポリエーテルエーテルケトン、ポ
リスルホン、ポリエーテルスルホン、ポリフェニレンエ
ーテル、ポリカーボネート、ポリアルキレンテレフタレ
ート、ポリオレフィン、ポリスチレン、ABS樹脂、ポ
リ弗化ビニリデン、ポリテトラフルオロエチレン、テト
ラフルオロエチレンコポリマー等を単独で、或いは2種
以上組合わせて配合することができる。これらの熱可塑
性樹脂の配合割合は、耐熱性、耐食性、耐薬品性、難燃
性などから見て、通常、40質量%以下の範囲である。Another example of the optional component is a thermoplastic resin other than polyphenylene sulfide, which has a melting temperature range of polyphenylene sulfide, usually 200 to 38.
Examples thereof include those that are unlikely to undergo thermal decomposition at 0 ° C.
For example, polyamide, polyetheretherketone, polysulfone, polyethersulfone, polyphenylene ether, polycarbonate, polyalkylene terephthalate, polyolefin, polystyrene, ABS resin, polyvinylidene fluoride, polytetrafluoroethylene, tetrafluoroethylene copolymer, etc. alone, Alternatively, two or more kinds can be combined and compounded. The blending ratio of these thermoplastic resins is usually 40% by mass or less in view of heat resistance, corrosion resistance, chemical resistance, flame retardancy and the like.
【0016】任意成分の更に別な例として、酸化防止
剤、熱安定剤、滑剤、離型剤、着色剤などの各種添加剤
が挙げられる。以上のような各成分を混合する方法は、
特に制限されるものではなく、一般に広く使用されてい
る方法、例えば、各成分をヘンシェルミキサー等の混合
機で混合するなどの方法を用いることができる。Further examples of the optional component include various additives such as an antioxidant, a heat stabilizer, a lubricant, a release agent and a coloring agent. The method of mixing the above components is
The method is not particularly limited, and a generally widely used method, for example, a method of mixing each component with a mixer such as a Henschel mixer can be used.
【0017】本発明の成形物を得るのにはポリフェニレ
ンサルファイド及び任意に包含される混合物よりなる粉
末をそのまま溶融押出成形機を用いて成形する方法或い
は粉末をペレット状に予め溶融成形してから、溶融押出
成形機にて成形する方法を用いることができる。本発明
に於いては溶融押出成形機で成形する際に、ダイ内で一
旦ポリフェニレンサルファイドの融点以上にしてポリフ
ェニレンサルファイドを融解した後、ダイ内でポリフェ
ニレンサルファイドの融点未満にして後、ダイより押出
して肉厚を10mm以上とする成形物にする方法が採用
される。このようにして押出肉厚成形物が得られ、肉厚
の、丸棒、平板等に好適に用いられる。In order to obtain the molded product of the present invention, a method of molding a powder of polyphenylene sulfide and a mixture optionally contained therein by using a melt extrusion molding machine as it is, or after melt-molding the powder into pellets in advance, A method of molding with a melt extruder can be used. In the present invention, when molding with a melt extrusion molding machine, after melting the polyphenylene sulfide once above the melting point of polyphenylene sulfide in the die, after lowering the melting point of polyphenylene sulfide in the die, then extruded from the die A method of forming a molded product having a wall thickness of 10 mm or more is adopted. In this way, an extruded thick-walled molded product is obtained, which is suitably used for thick-walled round bars, flat plates and the like.
【0018】尚、云うまでもないが、肉厚とは、例えば
丸棒であればその直径であり、楕円柱状の成形物であれ
ば短径であり、平板であればいわゆる厚さを指す。特に
肉厚を12mm以上、より好ましくは15mm以上とす
るものが従来技術に対して優位性をよりはっきりさせる
ことができる。成形物の肉厚の上限は押出成形可能であ
る限り、特に制限されるものではないが、通常は1m以
内、好ましくは50cm以内のものに適用される。Needless to say, the wall thickness means, for example, the diameter of a round bar, the short diameter of an elliptic cylinder shaped product, and the so-called thickness of a flat plate. In particular, the thickness of 12 mm or more, more preferably 15 mm or more can make the superiority to the prior art clearer. The upper limit of the wall thickness of the molded product is not particularly limited as long as it can be extruded, but it is usually within 1 m, preferably within 50 cm.
【0019】[0019]
【実施例】実施例及び比較例に於いて示す物性であって
前述していないものについての測定方法を以下に示す。 [融点]ポリフェニレンサルファイドを窒素気流下、3
20℃で2分間予熱した後、1分間加圧し、次いで急冷
して作製した無定形シート10mgを用い、差動走査熱
量計(DSC)(メトラー社製「DSC−30」を使
用)で窒素気流中10℃/分の昇温速度で昇温したとき
のチャート上に現れる融解に伴う吸熱ピーク温度であ
る。[Examples] The measurement methods for the physical properties shown in Examples and Comparative Examples and not mentioned above are shown below. [Melting point] Polyphenylene sulfide under nitrogen stream, 3
Amorphous sheet 10 mg prepared by preheating at 20 ° C. for 2 minutes, pressurizing for 1 minute, and then rapidly cooling was used, and a differential scanning calorimeter (DSC) (using "DSC-30" manufactured by METTLER CORPORATION) was used for nitrogen flow. It is the endothermic peak temperature associated with melting that appears on the chart when the temperature is raised at a heating rate of 10 ° C./min.
【0020】[衝撃強度]丸棒成形物の衝撃強度は丸棒
中心部より3.2mm×12.7mm×127mmの大
きさの試験片を切削加工により採取し、ASTM Dー
256に従い、ノッチなしで測定した。[Impact strength] The impact strength of the round bar molded product was measured by cutting a test piece measuring 3.2 mm x 12.7 mm x 127 mm from the center of the round bar, and according to ASTM D-256, there was no notch. It was measured at.
【0021】[曲げ強度]丸棒成形物の曲げ強度は、丸
棒中心部より3.2mm×12.7mm×127mmの
大きさの試験片を切削加工により採取し、ASTM D
ー790に従って測定した。[Bending Strength] The bending strength of the round bar molded product was measured according to ASTM D by cutting a test piece having a size of 3.2 mm × 12.7 mm × 127 mm from the center of the round bar.
-790.
【0022】[実施例1]含水硫化ナトリウム(水分5
3.79質量%)372kg及びN−メチルピロリドン
827kgを重合缶に仕込み、窒素雰囲気下で徐々に約
203℃まで昇温しながら、53.4モルの硫化水素と
共に水141.4kgを溜出させた。次にp−ジクロロ
ベンゼン322.5kg、1,2,4ートリクロロベン
ゼン0.799kgとNMP246kgを添加し、22
0℃で5時間重合を行なった。次いで水96.7kgを
添加し、255℃に昇温し5時間重合した後、更に24
5℃で5時間重合を継続した。Example 1 Hydrous sodium sulfide (water content 5)
372 kg of N-methylpyrrolidone and 827 kg of N-methylpyrrolidone were charged to a polymerization vessel, and 141.4 kg of water was distilled out together with 53.4 mol of hydrogen sulfide while gradually raising the temperature to about 203 ° C. under a nitrogen atmosphere. It was Next, 322.5 kg of p-dichlorobenzene, 0.799 kg of 1,2,4-trichlorobenzene and 246 kg of NMP were added.
Polymerization was carried out at 0 ° C. for 5 hours. Then, 96.7 kg of water was added, the temperature was raised to 255 ° C., polymerization was performed for 5 hours, and then 24 hours was further added.
Polymerization was continued at 5 ° C for 5 hours.
【0023】得られた反応混合液を目開き150μm
(100メッシュ)のスクリーンで篩分し、粒状ポリマ
ーを分離し、メタノール洗浄、水洗をそれぞれ3回行な
った後、脱水し、乾燥しポリマー(融点:284℃)を
得た。このポリマーを用いシリンダーの温度を300℃
とし、ダイの温度を250℃にして直径30mmの丸棒
成形物を押出成形した。丸棒の性能はポリマーの性状と
共に表1に示した。The reaction mixture obtained was opened to 150 μm.
After sieving with a (100 mesh) screen, the granular polymer was separated, washed with methanol three times and washed with water three times respectively, dehydrated and dried to obtain a polymer (melting point: 284 ° C.). Cylinder temperature is 300 ℃ using this polymer
Then, the die temperature was set to 250 ° C. and a round bar molded product having a diameter of 30 mm was extrusion molded. The performance of the round bar is shown in Table 1 together with the polymer properties.
【0024】[0024]
【表1】 [Table 1]
【0025】[実施例2]実施例1と同様にして、含水
硫化ナトリウム及びN−メチルピロリドンを重合缶に仕
込み、窒素雰囲気下で徐々に約203℃まで昇温しなが
ら、37.9モルの硫化水素と共に水140.4kgを
溜出させた。次にp−ジクロロベンゼン321.7k
g、1,2,4−トリクロロベンゼン0.797kgと
N−メチルピロリドン255kgの混合液を供給して2
20℃で5時間重合を行なった。次に水97.4kgを
添加し、255℃に昇温し5時間重合した後、さらに2
45℃で5時間重合を継続した。その後実施例1と同様
に後処理を行ないポリマー(融点:283℃)を得た。
このポリマーを用い、実施例1と同様に丸棒を成形し
た。その結果は表1に示す通りであった。[Example 2] In the same manner as in Example 1, water-containing sodium sulfide and N-methylpyrrolidone were charged into a polymerization vessel and gradually heated to about 203 ° C under a nitrogen atmosphere while 37.9 mol of 140.4 kg of water was distilled off together with hydrogen sulfide. Then p-dichlorobenzene 321.7k
g, 1,2,4-trichlorobenzene (0.797 kg) and N-methylpyrrolidone (255 kg) were mixed to supply 2
Polymerization was carried out at 20 ° C. for 5 hours. Next, 97.4 kg of water was added, the temperature was raised to 255 ° C., polymerization was performed for 5 hours, and then 2 more
The polymerization was continued at 45 ° C for 5 hours. Then, post-treatment was carried out in the same manner as in Example 1 to obtain a polymer (melting point: 283 ° C.).
Using this polymer, a round bar was molded in the same manner as in Example 1. The results are shown in Table 1.
【0026】[実施例3]実施例1と同様にして、含水
硫化ナトリウム及びN−メチルピロリドンを重合缶に仕
込み、窒素雰囲気下で徐々に約203℃まで昇温しなが
ら、55.6モルの硫化水素と共に水143.2kgを
溜出させた。次にp−ジクロロベンゼン319.0k
g、1,2,4−トリクロロベンゼン0.808kgと
N−メチルピロリドン243kgの混合液を供給して2
20℃で5時間重合を行なった。次に、水96.6kg
を添加し、255℃に昇温し5時間重合した後、さらに
245℃で5時間重合を継続した。その後実施例1と同
様に後処理を行ないポリマー(融点:283℃)を得
た。このポリマーを用い、実施例1と同様に丸棒を成形
した。その結果は表1に示す通りであった。[Example 3] In the same manner as in Example 1, water-containing sodium sulfide and N-methylpyrrolidone were charged into a polymerization vessel, and the temperature was gradually raised to about 203 ° C under nitrogen atmosphere. 143.2 kg of water was distilled off together with hydrogen sulfide. Then p-dichlorobenzene 319.0k
g, 1,2,4-trichlorobenzene (0.808 kg) and N-methylpyrrolidone (243 kg) are mixed to supply 2
Polymerization was carried out at 20 ° C. for 5 hours. Next, water 96.6kg
Was added, the temperature was raised to 255 ° C., polymerization was carried out for 5 hours, and then the polymerization was continued at 245 ° C. for 5 hours. Then, post-treatment was carried out in the same manner as in Example 1 to obtain a polymer (melting point: 283 ° C.). Using this polymer, a round bar was molded in the same manner as in Example 1. The results are shown in Table 1.
【0027】[比較例1]含水硫化ナトリウム(Na2
S・5H2O)20モル及びN−メチルピロリドン1
1.0kgを重合缶に仕込み、窒素雰囲気下で徐々に約
200℃まで昇温して、水1.27kg、N−メチルピ
ロリドン1.57kg及び0.46モルの硫化水素を溜
出させた。次にp−ジクロロベンゼン19.73モルと
N−メチルピロリドン3.2kgとを加えて210℃で
9時間重合した。次いで重合系の共存水が水/硫化ナト
リウムのモル比が4.7になるように重合系に水を添加
し、260℃で5時間重合した後、さらに245℃で3
時間重合した。その後、実施例1と同様に後処理を行な
い、ポリマー(融点:285℃)を得た。そのポリマー
の性状は表1に示す通りであった。このポリマーを用
い、実施例1と同様にして丸棒を成形した。得られた成
形物の性能は表1に示す通りであった。[Comparative Example 1] Hydrous sodium sulfide (Na 2
S.5H 2 O) 20 mol and N-methylpyrrolidone 1
1.0 kg was charged into a polymerization vessel and gradually heated to about 200 ° C. under a nitrogen atmosphere to distill 1.27 kg of water, 1.57 kg of N-methylpyrrolidone and 0.46 mol of hydrogen sulfide. Next, 19.73 mol of p-dichlorobenzene and 3.2 kg of N-methylpyrrolidone were added and polymerization was carried out at 210 ° C. for 9 hours. Next, water was added to the polymerization system so that the coexisting water of the polymerization system had a water / sodium sulfide molar ratio of 4.7, and polymerization was carried out at 260 ° C. for 5 hours, and then at 245 ° C. for 3 hours.
Polymerized for hours. Then, post-treatment was carried out in the same manner as in Example 1 to obtain a polymer (melting point: 285 ° C.). The properties of the polymer were as shown in Table 1. A round bar was molded using this polymer in the same manner as in Example 1. The performance of the obtained molded product was as shown in Table 1.
【0028】[比較例2]含水硫化ナトリウム(純度4
6.03%)373kg及びN−メチルピロリドン80
0kgを重合缶に仕込み、窒素雰囲気下で徐々に約20
3℃まで昇温しながら、水142kgを含むN−メチル
ピロリドン溶液を溜出させた。次にp−ジクロロベンゼ
ン318kgと1,2,4−トリクロロベンゼン0.3
93kgとN−メチルピロリドン255kgとの混合溶
液を供給して220℃で5時間重合した。次いで水94
kgを添加し、255℃に昇温して5時間重合した後、
さらに245℃で5.5時間重合を継続した。その後、
実施例1と同様に後処理を行ない、ポリマー(融点:2
84℃)を得た。そのポリマーの性状は表1に示す通り
であった。このポリマーを用い、実施例1と同様にして
丸棒を成形した。得られた成形物の性能は表1に示す通
りであった。[Comparative Example 2] Hydrous sodium sulfide (purity: 4
6.03%) 373 kg and N-methylpyrrolidone 80
Charge 0 kg into a polymerization can, and gradually increase it to about 20 in a nitrogen atmosphere.
An N-methylpyrrolidone solution containing 142 kg of water was distilled off while the temperature was raised to 3 ° C. Next, 318 kg of p-dichlorobenzene and 0.3 of 1,2,4-trichlorobenzene.
A mixed solution of 93 kg and 255 kg of N-methylpyrrolidone was supplied to carry out polymerization at 220 ° C. for 5 hours. Then water 94
After adding kg, heating to 255 ° C. and polymerizing for 5 hours,
Further, the polymerization was continued at 245 ° C. for 5.5 hours. afterwards,
Post-treatment was carried out in the same manner as in Example 1 to give a polymer (melting point: 2
84 ° C.) was obtained. The properties of the polymer were as shown in Table 1. A round bar was molded using this polymer in the same manner as in Example 1. The performance of the obtained molded product was as shown in Table 1.
【0029】[比較例3]含水硫化ナトリウム(純度4
6.4%)370kg及びN−メチルピロリドン800
kgを重合缶に仕込み、窒素雰囲気下で徐々に約203
℃まで昇温しながら、水144kgを含むN−メチルピ
ロリドン溶液を溜出させ、次いで水4kgを追加し、次
にp−ジクロロベンゼン320kgとN−メチルピロリ
ドン280kgとの混合溶液を供給して220℃で4時
間重合を行なった。さらに水110kgを添加し、26
0℃に昇温して5時間重合を継続した。得られた反応混
合液を目開き150μm(100メッシュ)のスクリー
ンで篩分し、粒状ポリマーを分離し、メタノール洗浄、
水洗を行なってポリマースラリーを得た。次に2質量%
のアンモニウムクロライド水溶液中に浸漬して、40℃
で30分間処理した後、水洗し、乾燥してポリマー(融
点:285℃)を得た。そのポリマーの性状は表1に示
す通りであった。このポリマーを用い、実施例1と同様
にして丸棒を成形した。得られた成形物の中心部には多
数の微細なボイドが生じており、衝撃強度、曲げ強度の
測定に供する試験片は得られなかった。[Comparative Example 3] Hydrous sodium sulfide (purity: 4
6.4%) 370 kg and N-methylpyrrolidone 800
After charging kg to a polymerization can, gradually increase it to about 203 in a nitrogen atmosphere.
While raising the temperature to 0 ° C., an N-methylpyrrolidone solution containing 144 kg of water was distilled off, 4 kg of water was then added, and then a mixed solution of 320 kg of p-dichlorobenzene and 280 kg of N-methylpyrrolidone was supplied to obtain 220 Polymerization was carried out at ℃ for 4 hours. Further add 110 kg of water, 26
The temperature was raised to 0 ° C. and the polymerization was continued for 5 hours. The obtained reaction mixture is sieved with a screen having an opening of 150 μm (100 mesh) to separate the granular polymer, washed with methanol,
It was washed with water to obtain a polymer slurry. Then 2% by mass
Dipping in ammonium chloride aqueous solution at 40 ℃
After being treated for 30 minutes with water, washed with water and dried to obtain a polymer (melting point: 285 ° C.). The properties of the polymer were as shown in Table 1. A round bar was molded using this polymer in the same manner as in Example 1. Many fine voids were formed in the center of the obtained molded product, and a test piece for measuring impact strength and bending strength could not be obtained.
【0030】[0030]
【発明の効果】10mm以上の肉厚を有する押出肉厚成
形物の内部に亀裂やボイドが少なく、耐衝撃性、強度特
性等に優れるとともに溶融押出成形性に優れ、肉厚の、
丸棒や平板等に特に好適である。The extruded thick-walled molded product having a wall thickness of 10 mm or more has few cracks and voids, is excellent in impact resistance, strength characteristics and the like, and is also excellent in melt extrusion moldability.
It is particularly suitable for round bars and flat plates.
Claims (10)
粘度の、310℃、剪断速度1200/秒での溶融粘度
に対する比が2.2〜3.0であり、310℃、剪断速
度1200/秒での溶融粘度が500〜2000Pa・
s、結晶化温度が160〜205℃であるポリフェニレ
ンサルファイド又はその組成物よりなり、10mm以上
の肉厚を有する押出肉厚成形物。1. The ratio of the melt viscosity at 310 ° C. and a shear rate of 200 / sec to the melt viscosity at 310 ° C. and a shear rate of 1200 / sec is 2.2 to 3.0, and at 310 ° C. and a shear rate of 1200. / Sec melt viscosity is 500-2000Pa
An extruded thick-walled molded product having a wall thickness of 10 mm or more, which is made of polyphenylene sulfide having a crystallization temperature of 160 to 205 ° C. or a composition thereof.
請求項1の押出肉厚成形物。2. The extruded wall thickness molded article according to claim 1, which is a round bar for cutting.
項1の押出肉厚成形物。3. The extruded wall thickness molded article according to claim 1, wherein the extruded wall thickness molded article is a flat plate molded article.
のいずれかの押出肉厚成形物。4. A wall thickness of 12 mm or more.
Extruded wall thickness molded product.
出肉厚成形物。5. The extruded wall thickness molding according to claim 4, which has a wall thickness of 15 mm or more.
粘度の、310℃、剪断速度1200/秒での溶融粘度
に対する比が2.2〜3.0であり、310℃、剪断速
度1200/秒での溶融粘度が500〜2000Pa・
s、結晶化温度が160〜205℃であるポリフェニレ
ンサルファイド又はその組成物を、一旦融点以上に融解
した後、ダイ内で融点未満にして後、押出成形して、1
0mm以上の肉厚とする押出肉厚成形物の製造方法。6. The ratio of melt viscosity at 310 ° C., shear rate 200 / sec to melt viscosity at 310 ° C., shear rate 1200 / sec is 2.2-3.0, 310 ° C., shear rate 1200. / Sec melt viscosity is 500-2000Pa
s, a polyphenylene sulfide having a crystallization temperature of 160 to 205 ° C. or a composition thereof is once melted to a melting point or higher, then brought to a temperature lower than the melting point in a die, and then extrusion-molded.
A method for producing an extruded thick molded product having a wall thickness of 0 mm or more.
請求項6の押出肉厚成形物の製造方法。7. The method for producing an extruded thick molded product according to claim 6, wherein the extruded thick molded product is a round bar for cutting.
項6の押出肉厚成形物の製造方法。8. The method for producing an extruded thick wall molded article according to claim 6, wherein the extruded thick wall molded article is a flat plate molded article.
のいずれかの押出肉厚成形物の製造方法。9. The wall thickness of 12 to 12 mm or more.
1. A method for producing an extruded wall thickness molded article.
押出肉厚成形物の製造方法。10. The method for producing an extruded wall thickness molded article according to claim 9, wherein the wall thickness is 15 mm or more.
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JP3547194 | 1994-02-08 | ||
JP6-83880 | 1994-03-30 | ||
JP6-35471 | 1994-03-30 | ||
JP8388094 | 1994-03-30 | ||
JP04475495A JP3652399B2 (en) | 1994-02-08 | 1995-02-08 | Extruded thick molded product and method for producing the same |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005078008A1 (en) * | 2004-02-16 | 2005-08-25 | Kureha Corporation | Stock shape for machining and production process thereof |
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1995
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005078008A1 (en) * | 2004-02-16 | 2005-08-25 | Kureha Corporation | Stock shape for machining and production process thereof |
US8158240B2 (en) | 2004-02-16 | 2012-04-17 | Kureha Corporation | Stock shape for machining |
US8158242B2 (en) | 2004-02-16 | 2012-04-17 | Kureha Corporation | Stock shape for machining and production process thereof |
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