CN105916657A - Stretched film manufacturing method - Google Patents
Stretched film manufacturing method Download PDFInfo
- Publication number
- CN105916657A CN105916657A CN201580004847.XA CN201580004847A CN105916657A CN 105916657 A CN105916657 A CN 105916657A CN 201580004847 A CN201580004847 A CN 201580004847A CN 105916657 A CN105916657 A CN 105916657A
- Authority
- CN
- China
- Prior art keywords
- thermoplastic resin
- film
- composite film
- stretching
- stretched
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 31
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 213
- 230000009477 glass transition Effects 0.000 claims abstract description 64
- 229920005989 resin Polymers 0.000 claims abstract description 34
- 239000011347 resin Substances 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims description 60
- 238000001816 cooling Methods 0.000 claims description 14
- 239000004925 Acrylic resin Substances 0.000 claims description 11
- 229920000178 Acrylic resin Polymers 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 238000007493 shaping process Methods 0.000 claims 3
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 239000000155 melt Substances 0.000 claims 2
- 239000002131 composite material Substances 0.000 abstract description 178
- 238000010438 heat treatment Methods 0.000 abstract description 58
- 229920001169 thermoplastic Polymers 0.000 abstract 1
- 239000004416 thermosoftening plastic Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 273
- 239000005020 polyethylene terephthalate Substances 0.000 description 18
- 229920000139 polyethylene terephthalate Polymers 0.000 description 18
- -1 polyethylene terephthalate Polymers 0.000 description 13
- 239000002245 particle Substances 0.000 description 12
- 229920000515 polycarbonate Polymers 0.000 description 11
- 239000004417 polycarbonate Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 230000001360 synchronised effect Effects 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 238000004804 winding Methods 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000011112 polyethylene naphthalate Substances 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920006302 stretch film Polymers 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229920007019 PC/ABS Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 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
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/10—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial
- B29C55/12—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial
- B29C55/16—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial simultaneously
-
- 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
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0011—Combinations of extrusion moulding with other shaping operations combined with compression moulding
-
- 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
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
-
- 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
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0022—Combinations of extrusion moulding with other shaping operations combined with cutting
-
- 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
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- 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
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
- B29C48/19—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their edges
-
- 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
- B29C48/30—Extrusion nozzles or dies
-
- 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
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/91—Heating, e.g. for cross linking
-
- 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
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/914—Cooling drums
-
- 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
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/915—Cooling of flat articles, e.g. using specially adapted supporting means with means for improving the adhesion to the supporting means
- B29C48/9155—Pressure rollers
-
- 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
- B29C48/92—Measuring, controlling or regulating
-
- 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
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/10—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial
- B29C55/12—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial
- B29C55/14—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial successively
-
- 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
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C2049/787—Thickness
- B29C2049/78715—Thickness of the blown article thickness
-
- 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
- B29C48/30—Extrusion nozzles or dies
- B29C48/305—Extrusion nozzles or dies having a wide opening, e.g. for forming sheets
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Laminated Bodies (AREA)
Abstract
本发明提供一种拉伸薄膜的制造方法,该拉伸薄膜的制造方法包括:复合薄膜形成工序,在该复合薄膜形成工序中,通过在自成形用模(220)熔融共挤出第1热塑性树脂和与所述第1热塑性树脂不同的第2热塑性树脂之后对所述第1热塑性树脂和所述第2热塑性树脂进行冷却使其固化,从而形成包括由所述第1热塑性树脂构成的中央部、沿宽度方向形成于所述中央部的两端且由所述第2热塑性树脂构成的两端部的复合薄膜(100);以及拉伸工序,在该拉伸工序中,将所述复合薄膜(100)至少沿长度方向加热拉伸从而形成拉伸薄膜,该拉伸薄膜的制造方法的特征在于,作为所述第1热塑性树脂及所述第2热塑性树脂,使用玻璃化转变温度之差在10℃以下的热塑性树脂。
The present invention provides a method for producing a stretched film. The method for producing a stretched film comprises: a composite film forming step in which a first thermoplastic film is melted and coextruded through a self-forming die (220). The resin and the second thermoplastic resin different from the first thermoplastic resin are then cooled to solidify the first thermoplastic resin and the second thermoplastic resin, thereby forming a central portion including the first thermoplastic resin. , a composite film (100) formed at both ends of the central portion in the width direction and composed of the second thermoplastic resin at both ends; and a stretching step, in which the composite film is (100) Stretching by heating at least in the longitudinal direction to form a stretched film, the method for producing the stretched film is characterized in that as the first thermoplastic resin and the second thermoplastic resin, a difference in glass transition temperature between Thermoplastic resins below 10°C.
Description
技术领域technical field
本发明涉及一种拉伸薄膜的制造方法。The invention relates to a method for manufacturing a stretched film.
背景技术Background technique
在制造拉伸薄膜时,准备作为材料的薄膜,并使用将准备好的薄膜拉伸的方法,来将薄膜拉伸,作为拉伸薄膜的方法,公知有如下的同步双轴拉伸法等:一边利用夹具把持薄膜的两端部一边将薄膜输送至加热炉内,在加热炉内,利用把持着薄膜的两端部的夹具沿长度方向和宽度方向同时对薄膜进行加热拉伸。When manufacturing a stretched film, prepare a film as a material, and use the method of stretching the prepared film to stretch the film. As a method for stretching a film, the following synchronous biaxial stretching method, etc. are known: The film is conveyed into a heating furnace while holding both ends of the film with clips, and in the heating furnace, the film is simultaneously heated and stretched in the longitudinal direction and the width direction by the clips holding both ends of the film.
在这种同步双轴拉伸法中,通过在加热炉内,将薄膜沿长度方向和宽度方向拉伸从而将薄膜加热拉伸至所需要的拉伸倍率,但是,在拉伸薄膜时,由于对薄膜的、由夹具把持的部分即两端部施加较大的应力,因此两端部会产生裂缝,以此为契机,薄膜整体有可能断裂。因此已知下述技术:为了防止薄膜在加热拉伸时发生断裂,利用强度比构成本来欲得到的薄膜的树脂的强度大的树脂来对被夹具把持的两端部进行加强。In this synchronous biaxial stretching method, the film is heated and stretched to the required stretching ratio by stretching the film in the length direction and width direction in a heating furnace. However, when stretching the film, due to A large stress is applied to both ends of the film held by the jigs, so cracks are generated at both ends, and this may cause the entire film to break. Therefore, a technique is known in which both ends held by clips are reinforced with a resin stronger than the resin constituting the originally intended film in order to prevent the film from breaking when heated and stretched.
例如,专利文献1中公开了如下的技术:使用下述那样的加强薄膜,通过将该加强薄膜加热拉伸,从而制造拉伸薄膜,该加强薄膜是利用在加热拉伸时的拉伸应力值比构成薄膜的中央部的热塑性树脂在加热拉伸时的拉伸应力值大的热塑性树脂,在薄膜的宽度方向上的两端形成两端部而构成的。For example, Patent Document 1 discloses a technique of manufacturing a stretched film by heating and stretching the reinforced film using a reinforcing film using the tensile stress value at the time of heating and stretching. The thermoplastic resin having a larger tensile stress value when heated and stretched than the thermoplastic resin constituting the central portion of the film forms both end portions at both ends in the width direction of the film.
现有技术文献prior art literature
专利文献patent documents
专利文献1:日本特开2008-149511号公报Patent Document 1: Japanese Patent Laid-Open No. 2008-149511
发明内容Contents of the invention
发明要解决的问题The problem to be solved by the invention
然而,在该专利文献1的技术中,为了增大薄膜两端部的加热拉伸时的拉伸应力值,作为构成薄膜的两端部的热塑性树脂,使用了具有比构成薄膜的中央部的热塑性树脂的玻璃化转变温度高(例如,具有35℃以上较高的玻璃化转变温度)的玻璃化转变温度的热塑性树脂,因而存在如下的问题。However, in the technology of this patent document 1, in order to increase the tensile stress value at the time of heating and stretching at both ends of the film, as the thermoplastic resin constituting both ends of the film, a thermoplastic resin having a higher temperature than that constituting the central portion of the film is used. A thermoplastic resin having a high glass transition temperature (for example, having a high glass transition temperature of 35° C. or higher) has the following problems.
即,在专利文献1的技术中,在进行加热拉伸时,如果将加热炉内的加热温度设定为薄膜的中央部的玻璃化转变温度附近,则加热炉内的加热温度相对于薄膜的两端部的玻璃化转变温度而言过低,由此,还存在如下问题,即,两端部未充分地软化,在利用夹具把持着两端部进行拉伸时,会产生夹具的脱落、薄膜的断裂。另一方面,在专利文献1的技术中,如果将加热炉内的加热温度设定在薄膜的两端部的玻璃化转变温度附近,则加热炉内的加热温度相对于薄膜的中央部的玻璃化转变温度而言过高,因此,存在如下问题,即,中央部将会过度软化而无法对中央部适当地进行拉伸、中央部暴露于高温下而分子取向变得不均匀、得到的拉伸薄膜的强度降低。That is, in the technology of Patent Document 1, when heating and stretching, if the heating temperature in the heating furnace is set to be near the glass transition temperature of the central portion of the film, the heating temperature in the heating furnace will be higher than that of the film. The glass transition temperature of both ends is too low, so there is also a problem that both ends are not softened enough, and when the two ends are held by the clips and stretched, the clips will fall off, Breakage of the film. On the other hand, in the technology of Patent Document 1, if the heating temperature in the heating furnace is set near the glass transition temperature of both ends of the film, the heating temperature in the heating furnace will be lower than that of the glass in the center of the film. The transition temperature is too high, so there are problems that the center portion will be too softened to properly stretch the center portion, the molecular orientation of the center portion will become non-uniform when exposed to high temperature, and the resulting stretched The strength of the stretched film is reduced.
本发明是鉴于这样的实际情况而提出的,其目的在于,提供一种拉伸薄膜的制造方法,在该制造方法中,使用下述那样的复合薄膜,在加热拉伸这样的复合薄膜从而制造拉伸薄膜时,能够适当地进行加热拉伸,能够得到生产率和品质优异的拉伸薄膜。该复合薄膜是利用与构成薄膜的中央部的热塑性树脂不同的热塑性树脂在薄膜的宽度方向的两端形成两端部而构成的。The present invention has been made in view of such actual conditions, and its object is to provide a method for producing a stretched film. In this production method, the following composite film is used, and such a composite film is stretched under heating to produce When stretching a film, heating and stretching can be appropriately performed, and a stretched film excellent in productivity and quality can be obtained. This composite film is formed by forming both end portions at both ends in the width direction of the film using a thermoplastic resin different from the thermoplastic resin constituting the central portion of the film.
用于解决问题的方案solutions to problems
本发明的发明人发现,在制造拉伸薄膜时,作为构成加热拉伸前的薄膜的中央部的热塑性树脂和构成两端部的热塑性树脂,使用其玻璃化转变温度之差为10℃以下的树脂时会达到上述目的,由此完成了本发明。The inventors of the present invention found that when producing a stretched film, as the thermoplastic resin constituting the center portion of the film before heating stretching and the thermoplastic resin constituting both end portions, a glass transition temperature difference of 10° C. or less is used. Resin can achieve the above objects, thus completing the present invention.
即,根据本发明的拉伸薄膜的制造方法,该拉伸薄膜的制造方法包括:复合薄膜形成工序,在该复合薄膜形成工序中,通过在自成形用模熔融共挤出第1热塑性树脂和与所述第1热塑性树脂不同的第2热塑性树脂之后对所述第1热塑性树脂和所述第2热塑性树脂进行冷却使其固化,从而形成包括由所述第1热塑性树脂构成的中央部、沿宽度方向形成于所述中央部的两端且由所述第2热塑性树脂构成的两端部的复合薄膜;以及拉伸工序,在该拉伸工序中,将所述复合薄膜至少沿长度方向加热拉伸从而形成拉伸薄膜,该拉伸薄膜的制造方法的特征在于,作为所述第1热塑性树脂及所述第2热塑性树脂,使用玻璃化转变温度之差在10℃以下的热塑性树脂。That is, according to the method for producing a stretched film of the present invention, the method for producing a stretched film includes: a composite film forming step in which the first thermoplastic resin and the A second thermoplastic resin different from the first thermoplastic resin is then cooled to solidify the first thermoplastic resin and the second thermoplastic resin to form a central portion made of the first thermoplastic resin, along the a composite film formed at both ends of the central portion in the width direction and at both ends of the second thermoplastic resin; and a stretching step of heating the composite film at least in the longitudinal direction Stretching to form a stretched film. The method for producing the stretched film is characterized in that a thermoplastic resin having a difference in glass transition temperature of 10° C. or less is used as the first thermoplastic resin and the second thermoplastic resin.
在本发明的制造方法中,优选的是,加热拉伸前的所述复合薄膜中的、由所述第2热塑性树脂构成的所述两端部的常温下的断裂伸长率大于由所述第1热塑性树脂构成的所述中央部的常温下的断裂伸长率。In the production method of the present invention, it is preferable that the elongation at break at normal temperature of the both ends made of the second thermoplastic resin in the composite film before heating stretching is greater than that obtained by the composite film. Elongation at break at room temperature of the central portion made of the first thermoplastic resin.
在本发明的制造方法中,优选的是,由所述第2热塑性树脂构成的所述两端部的加热拉伸时的拉伸应力值为由所述第1热塑性树脂构成的所述中央部的加热拉伸时的拉伸应力值的4倍以内。In the production method of the present invention, it is preferable that the tensile stress value at the time of heated stretching of the both end portions made of the second thermoplastic resin be equal to that of the central portion made of the first thermoplastic resin. Within 4 times of the tensile stress value during heating and stretching.
在本发明的制造方法中,优选的是,所述第2热塑性树脂的从所述成形用模熔融共挤出时的粘度为所述第1热塑性树脂的从所述成形用模熔融共挤出时的粘度的0.5倍~2倍。In the production method of the present invention, it is preferable that the viscosity of the second thermoplastic resin when melted and coextruded from the molding die is equal to that of the first thermoplastic resin melted and coextruded from the molding die. 0.5 times to 2 times the viscosity at that time.
在本发明的制造方法中,优选的是,在所述拉伸工序中,利用不仅沿所述复合薄膜的长度方向进行拉伸、还沿所述复合薄膜的宽度方向进行拉伸的同步双轴拉伸法来对所述复合薄膜进行加热拉伸。In the production method of the present invention, preferably, in the stretching step, a synchronous biaxial stretching process that stretches not only the longitudinal direction of the composite film but also the width direction of the composite film is used. Stretching method is used to heat and stretch the composite film.
在本发明的制造方法中,优选的是,所述第1热塑性树脂为丙烯酸树脂。In the production method of the present invention, it is preferable that the first thermoplastic resin is an acrylic resin.
另外,在本发明的制造方法中,优选的是,所述第2热塑性树脂为在聚碳酸酯(PC)中混合具有比所述丙烯酸树脂的玻璃化转变温度低的玻璃化转变温度的热塑性树脂而成的混合树脂。In addition, in the production method of the present invention, it is preferable that the second thermoplastic resin is polycarbonate (PC) mixed with a thermoplastic resin having a glass transition temperature lower than that of the acrylic resin. made of mixed resin.
而且,在本发明的制造方法中,优选的是,在所述拉伸工序中对所述复合薄膜进行加热拉伸,使得所述复合薄膜的加热拉伸后的所述中央部的厚度在15μm~50μm的范围内。Furthermore, in the production method of the present invention, it is preferable that the composite film is heated and stretched in the stretching step so that the thickness of the central portion of the composite film after heating and stretching is 15 μm. ~50μm range.
发明的效果The effect of the invention
采用本发明,能够提供一种能够防止拉伸时的断裂、并且生产率及成品率优异的拉伸薄膜的制造方法。According to the present invention, it is possible to provide a method for producing a stretched film capable of preventing breakage during stretching and having excellent productivity and yield.
附图说明Description of drawings
图1是用于说明在复合薄膜形成工序中制作复合薄膜的方法的图。FIG. 1 is a diagram for explaining a method of producing a composite thin film in a composite thin film forming step.
图2是用于说明在拉伸工序中通过同步双轴拉伸法对复合薄膜进行拉伸的方法的图。Fig. 2 is a diagram for explaining a method of stretching a composite film by a simultaneous biaxial stretching method in a stretching step.
图3是表示在聚碳酸酯(PC)中混合聚对苯二甲酸乙二醇酯(PET)而得到的混合树脂的玻璃化转变温度的图表。Fig. 3 is a graph showing the glass transition temperature of a mixed resin obtained by mixing polycarbonate (PC) with polyethylene terephthalate (PET).
图4是表示对在实施例和比较例中使用的热塑性树脂在140℃的温度下进行加热拉伸时的与拉伸倍率相对应的拉伸应力值的图表。Fig. 4 is a graph showing tensile stress values corresponding to stretch ratios when thermoplastic resins used in Examples and Comparative Examples are stretched under heating at a temperature of 140°C.
具体实施方式detailed description
以下,基于附图说明本发明的实施方式。Hereinafter, embodiments of the present invention will be described based on the drawings.
本实施方式的拉伸薄膜的制造方法包括以下工序:复合薄膜形成工序,在该复合薄膜形成工序中,通过利用成形用的T型模将第1热塑性树脂和与第1热塑性树脂不同的第2热塑性树脂熔融共挤出来形成复合薄膜;以及拉伸工序,在该拉伸工序中,将该复合薄膜沿长度方向和宽度方向加热拉伸。The manufacturing method of the stretched film according to this embodiment includes the following steps: a composite film forming step in which the first thermoplastic resin and the second thermoplastic resin different from the first thermoplastic resin are formed by using a T-die for forming. thermoplastic resins are melted and co-extruded to form a composite film; and a stretching process of heating and stretching the composite film in a length direction and a width direction.
复合薄膜形成工序Composite film forming process
复合薄膜形成工序是通过自T型模熔融共挤出第1热塑性树脂和第2热塑性树脂来得到复合薄膜100的工序。在此,图1是用于说明复合薄膜形成工序的图。在本实施方式中,作为复合薄膜100,如图1所示,得到如下那样的薄膜:该薄膜包括中央部110、形成于中央部110的宽度方向上的两端的两端部120,其中,中央部110由第1热塑性树脂形成,两端部120由第2热塑性树脂形成。此外,复合薄膜100的中央部110是通过在后述的拉伸工序中被加热拉伸而成为拉伸薄膜的部分。另外,复合薄膜100的两端部120用于在对复合薄膜100进行加热拉伸时加强中央部110,在加热拉伸复合薄膜100之后,能够根据需要进行切割从而去除两端部120。在切割复合薄膜100时,期望通过对中央部110的两端的一部分进行切割来完全去除两端部120。在该情况下,中央部110的两端的一部分也被去除,但优选的是,将由后述的夹具310把持的部分全部去除。The composite film forming step is a step of obtaining the composite film 100 by melt-coextruding the first thermoplastic resin and the second thermoplastic resin from a T-die. Here, FIG. 1 is a diagram for explaining a composite thin film forming process. In this embodiment, as the composite film 100, as shown in FIG. The portion 110 is formed of a first thermoplastic resin, and the both end portions 120 are formed of a second thermoplastic resin. In addition, the central part 110 of the composite film 100 is a part which becomes a stretched film by heating and stretching in the stretching process mentioned later. In addition, the both ends 120 of the composite film 100 are used to reinforce the central portion 110 when the composite film 100 is heated and stretched. After the composite film 100 is heated and stretched, the both ends 120 can be removed by cutting as necessary. When cutting the composite film 100 , it is desirable to completely remove both end portions 120 by cutting a part of both end portions of the central portion 110 . In this case, a part of both ends of the central part 110 is also removed, but it is preferable to remove all the parts held by the jig 310 described later.
本实施方式中,作为构成复合薄膜100的中央部110的第1热塑性树脂、构成两端部120的第2热塑性树脂,分别采用了第1热塑性树脂的玻璃化转变温度Tg1和第2热塑性树脂的玻璃化转变温度Tg2之差(|Tg1-Tg2|)为10℃以下的热塑性树脂。由此,本实施方式中,如后述那样,在通过拉伸工序对复合薄膜100进行加热拉伸时,能够防止复合薄膜100的断裂等,能够提高拉伸薄膜的生产率。In this embodiment, as the first thermoplastic resin constituting the central portion 110 of the composite film 100 and the second thermoplastic resin constituting both end portions 120, the glass transition temperature Tg1 of the first thermoplastic resin and the second thermoplastic resin are respectively used. A thermoplastic resin whose glass transition temperature Tg 2 difference (|Tg 1 -Tg 2 |) is 10°C or less. Thus, in the present embodiment, when the composite film 100 is heated and stretched in the stretching step as described later, it is possible to prevent the composite film 100 from being broken, and to improve the productivity of the stretched film.
在复合薄膜形成工序中,首先,将第1热塑性树脂和第2热塑性树脂以加热熔融的状态经由供料头210供给至T型模220。In the composite film forming step, first, the first thermoplastic resin and the second thermoplastic resin are supplied to the T-die 220 through the supply block 210 in a heated and melted state.
在本实施方式中,在供料头210分别连结有用于熔融挤出第1热塑性树脂的第1熔融挤出机(未图示)和用于熔融挤出第2热塑性树脂的第2熔融挤出机(未图示)。作为这些熔融挤出机,其并不特别限定,能够使用单螺杆挤出机、双螺杆挤出机中的任意一者。并且,在本实施方式中,通过利用各熔融挤出机,在第1热塑性树脂的熔点(熔融)温度以上的温度下熔融挤出第1热塑性树脂,在第2热塑性树脂的熔点(熔融)温度以上的温度下熔融挤出第2热塑性树脂,从而将第1热塑性树脂和第2热塑性树脂供给至供料头210。In this embodiment, a first melt extruder (not shown) for melt extruding the first thermoplastic resin and a second melt extruder for melt extruding the second thermoplastic resin are connected to the supply head 210, respectively. machine (not shown). These melt extruders are not particularly limited, and any of a single-screw extruder and a twin-screw extruder can be used. Furthermore, in this embodiment, by using each melt extruder, the first thermoplastic resin is melt-extruded at a temperature equal to or higher than the melting point (melting) temperature of the first thermoplastic resin, and the melting point (melting) temperature of the second thermoplastic resin is The second thermoplastic resin is melt-extruded at the above temperature to supply the first thermoplastic resin and the second thermoplastic resin to the supply head 210 .
此外,在自供料头210向T型模220供给第1热塑性树脂和第2热塑性树脂时,以如下方式进行第1热塑性树脂和第2热塑性树脂的供给,即,如图1所示,利用T型模220得到的复合薄膜100构成为在由第1热塑性树脂形成的中央部110的两端分别形成有由第2热塑性树脂形成的两端部120。In addition, when the first thermoplastic resin and the second thermoplastic resin are supplied from the supply head 210 to the T-die 220, the supply of the first thermoplastic resin and the second thermoplastic resin is performed as follows, that is, as shown in FIG. The composite film 100 obtained by the mold 220 is configured such that both ends 120 made of the second thermoplastic resin are formed on both ends of the central part 110 made of the first thermoplastic resin.
具体而言,在供料头210上分别设有用于供给第1热塑性树脂的入口和相对于用于供给第1热塑性树脂的入口而言,用于向T型模220的扩宽方向(日文:拡幅方向)的两侧供给第2热塑性树脂的入口。并且,在本实施方式中,自供料头210的入口分别流入的第1热塑性树脂和第2热塑性树脂在供料头210内汇合,使第1热塑性树脂和第2热塑性树脂在供料头210的出口处以如下方式流出,即,以相对于T型模220的扩宽方向而言,第1热塑性树脂向中央部分流动且第2热塑性树脂向该第1热塑性树脂的两端部分流动这样的方式流出,并供给至T型模220。Specifically, the feed head 210 is provided with an inlet for supplying the first thermoplastic resin and, relative to the inlet for supplying the first thermoplastic resin, an inlet for widening the T-die 220 (Japanese: The inlets for the second thermoplastic resin are supplied on both sides in the horizontal direction). In addition, in this embodiment, the first thermoplastic resin and the second thermoplastic resin respectively flowed in from the inlet of the supply block 210 are merged in the supply block 210, and the first thermoplastic resin and the second thermoplastic resin flow in the supply block 210. The outlet flows out in such a manner that the first thermoplastic resin flows toward the central portion and the second thermoplastic resin flows toward both end portions of the first thermoplastic resin with respect to the widening direction of the T-die 220. , and supplied to the T-die 220.
并且,在T型模220中,利用设于T型模220内的歧管221使自供料头210供给过来的第1热塑性树脂和第2热塑性树脂沿宽度方向(第1热塑性树脂和第2热塑性树脂排列的方向)扩宽,由此,将第1热塑性树脂和第2热塑性树脂自模唇222呈片形状共挤出。And, in the T-die 220, the first thermoplastic resin and the second thermoplastic resin supplied from the supply head 210 are arranged in the width direction (the first thermoplastic resin and the second thermoplastic resin) by the manifold 221 provided in the T-die 220. The direction in which the resins are arranged) is widened, whereby the first thermoplastic resin and the second thermoplastic resin are co-extruded from the die lip 222 in a sheet shape.
接着,如图1所示,利用接触辊230和冷却辊240连续地牵引并夹压共挤出后的片状的第1热塑性树脂和第2热塑性树脂,使第1热塑性树脂和第2热塑性树脂冷却和固化,从而制作成包括由第1热塑性树脂形成的中央部110和形成于中央部110的两端且由第2热塑性树脂形成的两端部120的复合薄膜100。然后,利用复合薄膜卷绕辊(未图示)将制作好的复合薄膜100卷绕起来,由此能够连续地得到复合薄膜100。Next, as shown in FIG. 1 , the first thermoplastic resin and the second thermoplastic resin in the form of a co-extruded sheet are continuously drawn and pinched by the touch roll 230 and the cooling roll 240, so that the first thermoplastic resin and the second thermoplastic resin It is cooled and solidified to produce a composite film 100 including a central portion 110 formed of the first thermoplastic resin and both end portions 120 formed at both ends of the central portion 110 and formed of the second thermoplastic resin. Then, the prepared composite film 100 can be wound up with a composite film winding roll (not shown), whereby the composite film 100 can be continuously obtained.
拉伸工序stretching process
拉伸工序是将通过复合薄膜形成工序得到的复合薄膜100沿长度方向和宽度方向加热拉伸的工序。在此,图2是用于说明拉伸工序的图。在本实施方式的拉伸工序中,自所述复合薄膜卷绕辊送出复合薄膜100,如图2所示,通过一边利用夹具310把持复合薄膜100的两端部120一边将复合薄膜100沿长度方向和宽度方向同时拉伸的同步双轴拉伸法来对复合薄膜100进行加热拉伸。The stretching step is a step of heating and stretching the composite film 100 obtained in the composite film forming step in the longitudinal direction and the width direction. Here, FIG. 2 is a diagram for explaining the stretching step. In the stretching process of this embodiment, the composite film 100 is sent out from the composite film winding roll, and as shown in FIG. The composite film 100 is heated and stretched by a synchronous biaxial stretching method in which the composite film 100 is stretched simultaneously in the horizontal direction and the width direction.
具体而言,在拉伸工序中,自复合薄膜卷绕辊连续地送出复合薄膜100,使用多个夹具隔开恒定间隔地分别把持复合薄膜100的两端部120,利用各夹具310将复合薄膜100输送至拉伸炉320内,在拉伸炉320内,利用各夹具310将复合薄膜100沿长度方向和宽度方向拉伸从而使其延展。此时,复合薄膜100在被夹具310把持着的状态下被输送从而通过拉伸炉320内,在拉伸炉320内的预热带中,复合薄膜100被预加热至比构成复合薄膜100的两端部120中的第2热塑性树脂的玻璃化转变温度高10℃~30℃左右的温度之后,在拉伸炉320内的拉伸带中,在保持复合薄膜100的温度的状态下利用夹具310沿长度方向和宽度方向拉伸复合薄膜100从而使其沿长度方向和宽度方向延展。并且,接着,通过使拉伸后的薄膜在冷却热固化带中被冷却及固化,从而能够得到拉伸薄膜。然后,通过打开夹具310,并利用辊进行卷绕,从而能够连续得到拉伸薄膜。Specifically, in the stretching process, the composite film 100 is continuously sent out from the composite film winding roll, and the both ends 120 of the composite film 100 are held at constant intervals using a plurality of clamps, and the composite film is stretched by each clamp 310. The composite film 100 is transported to the stretching furnace 320 , and in the stretching furnace 320 , the composite film 100 is stretched in the longitudinal direction and the width direction by the respective clips 310 to be stretched. At this time, the composite film 100 is conveyed while being held by the clamps 310 and passes through the stretching furnace 320 . After the glass transition temperature of the second thermoplastic resin in both ends 120 is higher by about 10°C to 30°C, in the stretching belt in the stretching furnace 320, the composite film 100 is kept at the temperature by using a clip. 310 stretches the composite film 100 lengthwise and widthwise so that it expands lengthwise and widthwise. Then, the stretched film can be obtained by cooling and solidifying the stretched film in a cooling thermosetting belt. Then, the stretched film can be obtained continuously by opening the clamp 310 and winding it up with a roll.
另外,在本实施方式中,为了使复合薄膜100通过拉伸炉320内而设有供夹具310移动的一对导轨。一对导轨分别设置于图2所示的对复合薄膜100的两端部120的上侧进行把持的夹具310的位置和对两端部120的下侧进行把持的夹具310的位置,在拉伸炉320内的预热带中,一对导轨互相平行,在拉伸带中,该一对导轨互相沿复合薄膜100的宽度方向分开,在冷却热固化带中,该一对导轨又互相平行。或者,也可以是,考虑到在拉伸带中被加热拉伸后的拉伸薄膜在冷却热固化带中固化时的收缩量,在冷却热固化带内,使一对导轨彼此之间的距离以拉伸薄膜位于拉伸带的输出侧时的宽度为基准在宽度方向上彼此靠近百分之几左右。在本实施方式中,通过使把持着复合薄膜100的两端部120的夹具310沿着这样的导轨移动,能够输送和拉伸复合薄膜100。In addition, in the present embodiment, a pair of guide rails for moving the clips 310 is provided to allow the composite film 100 to pass through the stretching furnace 320 . A pair of guide rails are respectively arranged on the positions of the clamps 310 that hold the upper side of the two ends 120 of the composite film 100 shown in FIG. In the preheating zone in the furnace 320, a pair of guide rails are parallel to each other. In the stretching zone, the pair of guide rails are separated from each other along the width direction of the composite film 100. In the cooling heat curing zone, the pair of guide rails are parallel to each other. Alternatively, it is also possible to set the distance between a pair of guide rails in the cooling thermosetting belt in consideration of the shrinkage of the stretched film after being heated and stretched in the stretching belt when it is solidified in the cooling thermosetting belt. Based on the width when the stretched film is positioned on the output side of the stretching belt, they are close to each other by about several percent in the width direction. In the present embodiment, the composite film 100 can be conveyed and stretched by moving the grippers 310 holding both ends 120 of the composite film 100 along such guide rails.
在本实施方式中,使用沿着这样的导轨移动的夹具310在拉伸炉320内的拉伸带中拉伸复合薄膜100。即,在拉伸炉320内的拉伸带中,通过进行使把持着复合薄膜100的两端部120的夹具310以沿着导轨在宽度方向上远离的方式移动并同时使夹具310彼此之间的间隔扩大的控制,从而将复合薄膜100的两端部120如图2所示的箭头那样沿长度方向和宽度方向拉伸。由此,将复合薄膜100的中央部110和两端部120分别沿长度方向和宽度方向加热拉伸至需要的拉伸倍率。然后,加热拉伸后的复合薄膜100在拉伸炉320内的冷却热固化带中被冷却和固化,并利用设于拉伸炉320之外的辊进行卷绕,由此能够连续地得到拉伸薄膜。In the present embodiment, the composite film 100 is stretched in a stretching belt in a stretching furnace 320 using a gripper 310 moving along such rails. That is, in the stretching belt in the stretching furnace 320, the grippers 310 that hold the both ends 120 of the composite film 100 are moved so as to be apart in the width direction along the guide rails, and at the same time, the grippers 310 are separated from each other. Controlling the expansion of the gap, the both ends 120 of the composite film 100 are stretched in the longitudinal direction and the width direction as shown by the arrows in FIG. 2 . Thus, the central portion 110 and both end portions 120 of the composite film 100 are heated and stretched in the longitudinal direction and the width direction respectively to a required stretching ratio. Then, the heated and stretched composite film 100 is cooled and solidified in the cooling thermosetting belt in the stretching furnace 320, and is wound up with a roll provided outside the stretching furnace 320, thereby continuously obtaining a stretched film 100. Stretch film.
如上所述,在本实施方式中,通过利用复合薄膜形成工序来形成包括由第1热塑性树脂形成的中央部110和由第2热塑性树脂形成的两端部120的复合薄膜100,并利用拉伸工序将复合薄膜100的中央部110和两端部120加热拉伸,能够得到拉伸薄膜。As described above, in the present embodiment, the composite film 100 including the central portion 110 formed of the first thermoplastic resin and the both end portions 120 formed of the second thermoplastic resin is formed by using the composite film forming process, and the composite film 100 is formed by stretching. Step The central part 110 and both end parts 120 of the composite film 100 are heated and stretched to obtain a stretched film.
此外,在本实施方式中,也可以是,通过将拉伸工序和复合薄膜形成工序设为连贯的连续生产线来得到拉伸薄膜。In addition, in the present embodiment, the stretched film may be obtained by making the stretching step and the composite film forming step a continuous continuous line.
另外,本实施方式中,对于以这种方式得到的拉伸薄膜,可以根据需要对两端部120这部分进行切割。由此,可以使拉伸薄膜成为仅由中央部110所构成的薄膜。In addition, in this embodiment, with respect to the stretched film obtained in this way, the part of both ends 120 can be cut as needed. Thereby, the stretched film can be made into the film which consists of the center part 110 only.
另外,在本实施方式中,加热拉伸后的复合薄膜100的中央部110的厚度优选为15μm~50μm,更优选为20μm~40μm。通过将加热拉伸后的复合薄膜100的中央部110的厚度控制在上述范围内,能够防止在加热拉伸中发生复合薄膜100的断裂,能够适当地进行复合薄膜100的加热拉伸。In addition, in this embodiment, the thickness of the central portion 110 of the composite film 100 after heating and stretching is preferably 15 μm to 50 μm, and more preferably 20 μm to 40 μm. By controlling the thickness of the central portion 110 of the composite film 100 after heating and stretching within the above range, it is possible to prevent the composite film 100 from being broken during the heating and stretching, and to perform heating and stretching of the composite film 100 appropriately.
在此,在本实施方式中,作为构成复合薄膜100的中央部110的第1热塑性树脂及构成两端部120的第2热塑性树脂,采用第1热塑性树脂的玻璃化转变温度Tg1和第2热塑性树脂的玻璃化转变温度Tg2之间的差(|Tg1-Tg2|)为10℃以下的热塑性树脂。由此,采用本实施方式,在加热拉伸复合薄膜100时,能够防止把持着复合薄膜100的夹具310的脱离及复合薄膜100的断裂,能够提高拉伸薄膜的生产率。Here, in this embodiment, as the first thermoplastic resin constituting the central portion 110 of the composite film 100 and the second thermoplastic resin constituting both end portions 120, the glass transition temperature Tg1 of the first thermoplastic resin and the second thermoplastic resin are used. A thermoplastic resin in which the difference (|Tg 1 −Tg 2 |) between the glass transition temperatures Tg 2 of the thermoplastic resin is 10° C. or less. Thus, according to the present embodiment, when the composite film 100 is heated and stretched, it is possible to prevent the jigs 310 holding the composite film 100 from detaching and the composite film 100 from breaking, and the productivity of the stretched film can be improved.
即,在复合薄膜100中,如果两端部120的玻璃化转变温度Tg2与中央部110的玻璃化转变温度Tg1相比过高,则在加热拉伸时拉伸炉320内的加热温度不会达到两端部120的玻璃化转变温度Tg2,两端部120的软化变得不够充分(拉伸两端部120所需的拉伸应力值较高的状态),因此,在如图2所示那样利用夹具310把持并拉伸两端部120时,存在夹具310有可能脱离的问题。而且,此时,是拉伸两端部120所需的拉伸应力值较高的状态,因此,在如图2所示那样利用夹具310拉伸两端部120时,还存在如下问题,即,两端部120没有被拉伸而是断裂,或者,在中央部110和两端部120之间的边界部分产生裂缝,由此导致复合薄膜100断裂的问题。对此也可以考虑如下方法:在拉伸炉320内加热复合薄膜100时,加热复合薄膜100整体的同时,只对两端部120进一步局部地以高温进行加热从而使其软化,由此使两端部120的拉伸变得容易,但是,如图2所示,在拉伸炉320内,两端部120的位置随着复合薄膜100的输送及拉伸而逐渐变化,因此,还存在如下问题,即,为了只对两端部120以高温进行加热而使拉伸炉320内的温度的控制变得繁锁。That is, in the composite film 100, if the glass transition temperature Tg 2 of both end portions 120 is too high compared with the glass transition temperature Tg 1 of the central portion 110, the heating temperature in the stretching furnace 320 will The glass transition temperature Tg 2 of the both ends 120 is not reached, and the softening of the both ends 120 becomes insufficient (a state where the tensile stress value required to stretch the both ends 120 is high), therefore, in the 2, there is a problem that the clips 310 may come off when both ends 120 are gripped and stretched by the clips 310. Moreover, at this time, the tensile stress value required to stretch the both ends 120 is high, therefore, when the both ends 120 are stretched by the jig 310 as shown in FIG. , the both end portions 120 are not stretched but are broken, or a crack occurs at the boundary portion between the central portion 110 and the both end portions 120, thereby causing a problem that the composite film 100 is broken. In this regard, when heating the composite film 100 in the stretching furnace 320, while heating the composite film 100 as a whole, only the both ends 120 are further locally heated at a high temperature to soften them, thereby making both ends 120 soft. The stretching of the end portion 120 becomes easy, but, as shown in FIG. 2, in the stretching furnace 320, the positions of the both ends 120 gradually change along with the conveyance and stretching of the composite film 100. Therefore, there are also the following: The problem is that the control of the temperature in the drawing furnace 320 is cumbersome in order to heat only the both ends 120 at a high temperature.
另一方面,在复合薄膜100中的两端部120的玻璃化转变温度Tg2与中央部110的玻璃化转变温度Tg1相比过低的情况下,在加热拉伸时,拉伸炉320内的加热温度超过两端部120的玻璃化转变温度Tg2,两端部120将会过度软化,因此,在如图2所示那样利用夹具310将复合薄膜100的两端部120沿宽度方向拉伸时,存在两端部120优先被拉伸,利用夹具310拉伸的力无法传递到中央部110,导致中央部110的拉伸不够充分的问题。而且,由于加热拉伸时两端部120过度软化,导致两端部120热粘接于夹具310,或者加热拉伸后两端部120发生收缩,由此,也存在拉伸薄膜的生产率和成品率降低的问题。On the other hand, when the glass transition temperature Tg 2 of both end portions 120 of the composite film 100 is too low compared with the glass transition temperature Tg 1 of the central portion 110, the stretching furnace 320 If the heating temperature inside exceeds the glass transition temperature Tg 2 of the two ends 120, the two ends 120 will be excessively softened. Therefore, as shown in FIG. During stretching, both ends 120 are preferentially stretched, and the force of stretching by the jig 310 cannot be transmitted to the central portion 110 , resulting in insufficient stretching of the central portion 110 . Moreover, due to the excessive softening of both ends 120 during heating and stretching, the two ends 120 are thermally bonded to the jig 310, or the two ends 120 shrink after heating and stretching, thus, there are also problems in the productivity and finished product of the stretched film. rate reduction problem.
对此,采用本实施方式,在复合薄膜100中,通过使形成中央部110的第1热塑性树脂的玻璃化转变温度Tg1和形成两端部120的第2热塑性树脂的玻璃化转变温度Tg2之间的差(|Tg1-Tg2|)在上述范围,能够防止在加热拉伸复合薄膜100时发生夹具310的脱离及复合薄膜100的断裂等不良情况,能够适当地对复合薄膜100进行加热拉伸,因此能够提高拉伸薄膜的生产率和成品率。In this regard, according to the present embodiment, in the composite film 100, the glass transition temperature Tg 1 of the first thermoplastic resin forming the central portion 110 and the glass transition temperature Tg 2 of the second thermoplastic resin forming the end portions 120 If the difference (|Tg 1 -Tg 2 |) is in the above range, it is possible to prevent the detachment of the clip 310 and the breakage of the composite film 100 when the composite film 100 is heated and stretched, and the composite film 100 can be properly processed. Stretching by heating can improve the productivity and yield of the stretched film.
此外,在本实施方式中,作为第1热塑性树脂及第2热塑性树脂,可以采用上述那样玻璃化转变温度差(|Tg1-Tg2|)在10℃以下的热塑性树脂,然而玻璃化转变温度差(|Tg1-Tg2|)优选在5℃以下,更优选在3℃以下。In addition, in this embodiment, as the first thermoplastic resin and the second thermoplastic resin, thermoplastic resins having a glass transition temperature difference (|Tg 1 −Tg 2 |) as described above can be used at 10° C. or less, but the glass transition temperature The difference (|Tg 1 −Tg 2 |) is preferably 5°C or lower, more preferably 3°C or lower.
另外,一直以来,为了防止在利用夹具310将复合薄膜100加热拉伸时的夹具310的脱离、复合薄膜100的断裂,公知的方法是:在复合薄膜100的两端部120添加橡胶弹性颗粒从而使两端部120软化的(提高常温下的断裂伸长率)方法。然而,在该方法中,由于两端部120中的橡胶弹性颗粒容易因热而劣化,因此存在如下的问题。即,在从T型模220熔融共挤出复合薄膜100时,因热而劣化的橡胶弹性颗粒会析出于T型模220的模唇222之上而形成堆积物,有可能因该堆积物而使复合薄膜100产生压痕,或者,有可能导致堆积物混入拉伸薄膜的产品卷而使拉伸薄膜的品质降低。而且,若形成有这样的橡胶弹性颗粒的堆积物,则在如图2所示那样利用夹具310对复合薄膜100进行加热拉伸时,堆积物有可能进入到复合薄膜100和夹具310之间,由此,还有可能导致复合薄膜100容易断裂。In addition, in order to prevent the detachment of the clip 310 and the breakage of the composite film 100 when the composite film 100 is heated and stretched by the clip 310, a known method is to add rubber elastic particles to the both ends 120 of the composite film 100 to A method of softening both ends 120 (increasing the elongation at break at room temperature). However, in this method, since the rubber elastic particles in both end portions 120 are easily deteriorated by heat, there is a problem as follows. That is, when the composite film 100 is melted and co-extruded from the T-die 220, rubber elastic particles degraded by heat are precipitated on the lip 222 of the T-die 220 to form deposits, which may cause damage to the film due to the deposits. There is a possibility that the composite film 100 will be indented, or deposits may be mixed into the product roll of the stretched film, thereby deteriorating the quality of the stretched film. Moreover, if such deposits of rubber elastic particles are formed, the deposits may enter between the composite film 100 and the clips 310 when the composite film 100 is heated and stretched by the clips 310 as shown in FIG. As a result, the composite film 100 may be easily broken.
与此相对,采用本实施方式,则无需在复合薄膜100的两端部120添加这样的橡胶弹性颗粒,或者,能够使向两端部120添加的橡胶弹性颗粒的量较少,因此,能够抑制熔融共挤出复合薄膜100时析出橡胶弹性颗粒,从而能够使得到的拉伸薄膜的品质优异。On the other hand, according to this embodiment, it is not necessary to add such rubber elastic particles to the both ends 120 of the composite film 100, or the amount of rubber elastic particles added to the both ends 120 can be reduced, therefore, it is possible to suppress When the composite film 100 is melt-coextruded, rubber elastic particles are precipitated, so that the quality of the obtained stretched film can be excellent.
此外,在本实施方式中,作为用于形成中央部110的第1热塑性树脂,只要根据所需的拉伸薄膜的用途等进行选择即可,能够使用例如丙烯酸树脂(PMMA)、环状烯烃共聚物(COC)等。In addition, in this embodiment, as the first thermoplastic resin for forming the central portion 110, it is only necessary to select according to the application of the desired stretched film, for example, acrylic resin (PMMA), cyclic olefin copolymerized resin, etc., can be used. substance (COC), etc.
另外,作为用于形成两端部120的第2热塑性树脂,选择与上述的第1热塑性树脂的玻璃化转变温度的差(|Tg1-Tg2|)在上述范围的热塑性树脂即可。In addition, as the second thermoplastic resin for forming both ends 120 , a thermoplastic resin whose glass transition temperature difference (|Tg 1 −Tg 2 |) from the above-mentioned first thermoplastic resin is in the above-mentioned range may be selected.
另外,作为用于形成两端部120的第2热塑性树脂,除了选择与第1热塑性树脂的玻璃化转变温度差(|Tg1-Tg2|)在上述范围的热塑性树脂之外,还可以从以下观点出发来进行选择。In addition, as the second thermoplastic resin for forming the both end portions 120, in addition to selecting a thermoplastic resin having a glass transition temperature difference (|Tg 1 −Tg 2 |) from the first thermoplastic resin within the above-mentioned range, it can also be selected from Choose from the following points of view.
例如,作为第2热塑性树脂,优选采用从T型模220熔融共挤出时的粘度为第1热塑性树脂的粘度的0.5倍~2倍的热塑性树脂。在此,粘度的测定可以以例如将JIS K7199作为基准通过流变仪(日文:キャピログラフ)测定而得到。由此,能够减小熔融共挤出时的第1热塑性树脂和第2热塑性树脂的粘度差,在从T型模220熔融共挤出的复合薄膜100中,能够防止构成中央部110及两端部120的树脂之间互相掺杂的现象。For example, as the second thermoplastic resin, it is preferable to use a thermoplastic resin whose viscosity when melted and co-extruded from the T-die 220 is 0.5 to 2 times the viscosity of the first thermoplastic resin. Here, the viscosity can be measured, for example, with a rheometer (Japanese: Capirograph) based on JIS K7199. Thus, the difference in viscosity between the first thermoplastic resin and the second thermoplastic resin during melt coextrusion can be reduced, and in the composite film 100 melt coextruded from the T-die 220, it is possible to prevent the central portion 110 and both ends from being formed. The phenomenon that the resins of the part 120 are doped with each other.
即,进行熔融共挤出时,如果第2热塑性树脂的粘度与第1热塑性树脂的粘度相比过高,则在熔融共挤出的复合薄膜100中,由粘度较高的第2热塑性树脂构成的两端部120将会向中央部110的表面流动,覆盖中央部110的一部分,导致树脂之间互相掺杂。另一方面,如果第2热塑性树脂的粘度与第1热塑性树脂的粘度相比过低,则在熔融共挤出的复合薄膜100中,由粘度较高的第1热塑性树脂构成的中央部110会覆盖两端部120的一部分,导致树脂之间互相掺杂。That is, when performing melt co-extrusion, if the viscosity of the second thermoplastic resin is too high compared with the viscosity of the first thermoplastic resin, the composite film 100 formed by melt co-extrusion will be composed of the second thermoplastic resin with higher viscosity. The two end portions 120 will flow toward the surface of the central portion 110 and cover a part of the central portion 110 , resulting in mutual doping between the resins. On the other hand, if the viscosity of the second thermoplastic resin is too low compared with the viscosity of the first thermoplastic resin, in the melt-coextruded composite film 100, the central portion 110 made of the higher-viscosity first thermoplastic resin will Covering a part of both ends 120 results in doping between the resins.
因此,在本实施方式中,通过将熔融共挤出时的第1热塑性树脂和第2热塑性树脂的粘度差减小到上述范围,能够防止加热拉伸后的复合薄膜100中发生构成中央部110的树脂与构成两端部120的树脂互相混合,由此,在得到拉伸薄膜时,在如上述那样切割两端部120时能够减少切割的部分,能够提高拉伸薄膜的成品率。Therefore, in the present embodiment, by reducing the difference in viscosity between the first thermoplastic resin and the second thermoplastic resin during melt coextrusion to the above-mentioned range, it is possible to prevent the central portion 110 from forming in the composite film 100 after thermal stretching. The resin and the resin constituting the both ends 120 are mixed with each other, thereby reducing the number of cut parts when cutting the ends 120 as described above when obtaining a stretched film, and improving the yield of the stretched film.
另外,作为第2热塑性树脂,优选采用这样的热塑性树脂,对于通过该热塑性树脂得到的复合薄膜100而言,能够使加热拉伸时的中央部110的拉伸应力值和加热拉伸时的两端部120的拉伸应力值的差在规定的范围。具体而言,作为第2热塑性树脂,优选采用这样的热塑性树脂,通过该热塑性树脂形成的两端部120的加热拉伸时的拉伸应力值为中央部110的加热拉伸时的拉伸应力值的4倍以内。此外,拉伸应力值是表示在将复合薄膜100拉伸到需要的拉伸倍率时拉伸中央部110、两端部120所需要的拉伸负荷的值。由此,在加热拉伸复合薄膜100时,中央部110和两端部120的相对于拉伸应力的变形量彼此相近,能够更有效防止加热拉伸时的拉伸薄膜的断裂及夹具脱离,能够进一步提高拉伸薄膜的生产率。In addition, as the second thermoplastic resin, it is preferable to use a thermoplastic resin that can make the tensile stress value of the central portion 110 during thermal stretching and the two The difference in the tensile stress value of the end portion 120 is within a predetermined range. Specifically, as the second thermoplastic resin, it is preferable to use a thermoplastic resin whose tensile stress value during heated stretching of both end portions 120 formed of this thermoplastic resin is the tensile stress value of the central portion 110 during heated stretching. within 4 times of the value. In addition, the tensile stress value is a value indicating the tensile load required to stretch the central portion 110 and both end portions 120 when the composite film 100 is stretched to a desired stretching ratio. Thus, when the composite film 100 is heated and stretched, the deformation amounts of the central portion 110 and both end portions 120 relative to the tensile stress are similar to each other, and the fracture of the stretched film and the detachment of the clips during the heating and stretching can be more effectively prevented. The productivity of the stretched film can be further improved.
进一步优选使用如下热塑性树脂作为第2热塑性树脂,该热塑性树脂能够使得得到的加热拉伸前的复合薄膜100中的、两端部120的常温下的断裂伸长率高于中央部110的常温下的断裂伸长率。此外,常温的断裂伸长率为表示在10℃~30℃左右的常温环境下将中央部110、两端部120拉伸至断裂时的尺寸相对于拉伸前的尺寸的伸长率的值。由此,在加热拉伸复合薄膜100时,与中央部110相比两端部120不易断裂,并且能够防止两端部120产生裂缝,从而能够防止整个复合薄膜100的断裂。It is further preferable to use, as the second thermoplastic resin, a thermoplastic resin capable of making the elongation at break at the normal temperature of both end parts 120 higher than that of the central part 110 in the obtained composite film 100 before heating and stretching. elongation at break. In addition, the elongation at break at normal temperature is a value indicating the elongation of the dimension when the central portion 110 and both end portions 120 are stretched to break in a normal temperature environment of about 10° C. to 30° C. with respect to the dimension before stretching. . Thus, when the composite film 100 is heated and stretched, the both ends 120 are less likely to be broken than the central portion 110 , and cracks can be prevented from occurring at the both ends 120 , thereby preventing the entire composite film 100 from being broken.
此外,作为第2热塑性树脂,基于上述观点,具体而言,能够采用如下的热塑性树脂。例如,在使用丙烯酸树脂作为第1热塑性树脂时,作为第2热塑性树脂,能够单独使用聚萘二甲酸乙二醇酯(PEN)、环烯烃聚合物(COP)等中的一种材料,或者能够使用将两种以上的上述材料混合后而得的混合树脂。Moreover, as a 2nd thermoplastic resin, the following thermoplastic resin can be specifically used from the said viewpoint. For example, when an acrylic resin is used as the first thermoplastic resin, as the second thermoplastic resin, one of polyethylene naphthalate (PEN), cycloolefin polymer (COP) and the like can be used alone, or can be A mixed resin obtained by mixing two or more of the aforementioned materials is used.
另外,作为第2热塑性树脂,也可以使用在不妨碍拉伸薄膜的生产率的范围内,向所述第1热塑性树脂添加了少量的橡胶弹性颗粒而得到的树脂。In addition, as the second thermoplastic resin, a resin obtained by adding a small amount of rubber elastic particles to the first thermoplastic resin within a range that does not hinder the productivity of the stretched film may be used.
或者,作为第2热塑性树脂,能够使用向比第1热塑性树脂的玻璃化转变温度高且与第1热塑性树脂的玻璃化转变温度之差超过10℃的热塑性树脂(耐热性的热塑性树脂)中混合比第1热塑性树脂的玻璃化转变温度低的热塑性树脂(低温熔融性的热塑性树脂)而得到的混合树脂。此时,通过对上述的耐热性的热塑性树脂和低温熔融性的热塑性树脂之间的混合比率进行调整来对得到的混合树脂的玻璃化转变温度进行调整,使得第1热塑性树脂的玻璃化转变温度与第2热塑性树脂的玻璃化转变温度之差(|Tg1-Tg2|)在所述范围内。Alternatively, as the second thermoplastic resin, a thermoplastic resin (heat-resistant thermoplastic resin) having a glass transition temperature higher than that of the first thermoplastic resin and having a difference of more than 10° C. from the glass transition temperature of the first thermoplastic resin can be used. A mixed resin obtained by mixing a thermoplastic resin (low-temperature meltable thermoplastic resin) that has a lower glass transition temperature than the first thermoplastic resin. At this time, by adjusting the mixing ratio between the above-mentioned heat-resistant thermoplastic resin and the low-temperature melting thermoplastic resin, the glass transition temperature of the obtained mixed resin is adjusted so that the glass transition temperature of the first thermoplastic resin The difference between the temperature and the glass transition temperature of the second thermoplastic resin (|Tg 1 −Tg 2 |) is within the above range.
在此,在使用玻璃化转变温度Tg1为120℃左右的丙烯酸树脂作为第1热塑性树脂的情况下,作为第2热塑性树脂,能够使用例如通过向玻璃化转变温度为较高的150℃左右的聚碳酸酯(PC)中混合玻璃化转变温度为较低的70℃左右的聚对苯二甲酸乙二醇酯(PET)从而将玻璃化转变温度调整为与上述玻璃化转变温度Tg1相同程度的120℃附近而得到的混合树脂。Here, when an acrylic resin having a glass transition temperature Tg1 of about 120°C is used as the first thermoplastic resin, as the second thermoplastic resin, for example, an acrylic resin having a higher glass transition temperature of about 150°C can be used. Polyethylene terephthalate (PET), which has a relatively low glass transition temperature of around 70°C, is mixed with polycarbonate (PC) to adjust the glass transition temperature to the same level as the above-mentioned glass transition temperature Tg 1 A mixed resin obtained near 120°C.
此外,在使用这样的混合树脂作为第2热塑性树脂的情况下,作为耐热性的热塑性树脂,能够使用聚碳酸酯(PC)、环烯烃聚合物(COP)等。另外,作为低温熔融性的热塑性树脂,能够使用聚对苯二甲酸乙二醇酯(PET)和聚萘二甲酸乙二醇酯(PEN)等聚酯、丙烯腈-丁二烯-苯乙烯(ABS)、聚乙烯(PE)、聚酯(PES)、聚对苯二甲酸丁二酯(PBT)等。在本实施方式中,在这些材料之中,从易于调整得到的混合树脂的玻璃化转变温度这样的观点考虑,作为耐热性的热塑性树脂,优选使用聚碳酸酯(PC),作为低温熔融性的热塑性树脂,优选使用聚对苯二甲酸乙二醇酯(PET)。In addition, when such a mixed resin is used as the second thermoplastic resin, polycarbonate (PC), cycloolefin polymer (COP), or the like can be used as the heat-resistant thermoplastic resin. In addition, polyesters such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), acrylonitrile-butadiene-styrene ( ABS), polyethylene (PE), polyester (PES), polybutylene terephthalate (PBT), etc. In the present embodiment, among these materials, polycarbonate (PC) is preferably used as the heat-resistant thermoplastic resin from the viewpoint of easy adjustment of the glass transition temperature of the mixed resin obtained, and polycarbonate (PC) is preferably used as the low-temperature melting resin. As the thermoplastic resin, polyethylene terephthalate (PET) is preferably used.
在此,图3是表示向聚碳酸酯(PC)混合聚对苯二甲酸乙二醇酯(PET)后得到的混合树脂的玻璃化转变温度的测量结果的图表。此外,图3中示出,利用示差扫描量热法(DSC)对聚对苯二甲酸乙二醇酯(PET)相对于聚碳酸酯(PC)的含有比例分别为0%、25%、50%、75%、100%的树脂的玻璃化转变温度进行测量后的结果。在此,在示差扫描量热法(DSC)的测量中,无论聚对苯二甲酸乙二醇酯(PET)的含有比例为哪一个值,混合树脂的玻璃化转变温度均没有变大,而是大致固定在一点。Here, FIG. 3 is a graph showing the measurement results of the glass transition temperature of a mixed resin obtained by mixing polyethylene terephthalate (PET) with polycarbonate (PC). In addition, as shown in FIG. 3, the content ratios of polyethylene terephthalate (PET) to polycarbonate (PC) by differential scanning calorimetry (DSC) were 0%, 25%, and 50%, respectively. %, 75%, 100% of the glass transition temperature of the resin to measure the results. Here, in the differential scanning calorimetry (DSC) measurement, regardless of the content ratio of polyethylene terephthalate (PET), the glass transition temperature of the mixed resin did not increase, while is roughly fixed at one point.
如图3所示,对于向聚对苯二甲酸乙二醇酯(PET)混合聚碳酸酯(PC)而得到的混合树脂,能够根据聚对苯二甲酸乙二醇酯(PET)的含有比例而相应地使玻璃化转变温度变化。由此,在本实施方式中,在使用这样的混合树脂作为第2热塑性树脂的情况下,能够易于对第2热塑性树脂的玻璃化转变温度Tg2进行调整,能够将第1热塑性树脂的玻璃化转变温度Tg1与第2热塑性树脂的玻璃化转变温度Tg2之差(|Tg1-Tg2|)控制在上述范围内。As shown in FIG. 3, for a mixed resin obtained by mixing polycarbonate (PC) with polyethylene terephthalate (PET), it is possible to The glass transition temperature changes accordingly. Therefore, in the present embodiment, when such a mixed resin is used as the second thermoplastic resin, the glass transition temperature Tg 2 of the second thermoplastic resin can be easily adjusted, and the glass transition temperature of the first thermoplastic resin can be adjusted. The difference (|Tg 1 −Tg 2 |) between the transition temperature Tg 1 and the glass transition temperature Tg 2 of the second thermoplastic resin is controlled within the above range.
此外,作为对于通过这样的第1热塑性树脂及第2热塑性树脂得到的复合薄膜100进行加热拉伸的方法,如图2所示,在上述的例子中示出了采用将复合薄膜100沿长度方向和宽度方向这两个方向加热拉伸的同步双轴拉伸法的例子,但在本实施方式中,也可以使用将复合薄膜100仅沿长度方向上单轴拉伸的方法。In addition, as a method of heating and stretching the composite film 100 obtained by such a first thermoplastic resin and a second thermoplastic resin, as shown in FIG. Although this is an example of a simultaneous biaxial stretching method that heats and stretches in two directions, the width direction and the width direction, in this embodiment, a method of uniaxially stretching the composite film 100 only in the longitudinal direction may also be used.
此时,能够与图2所示的同步双轴拉伸法同样地进行复合薄膜100的沿长度方向的加热拉伸。即,能够使用如下方法:一边利用夹具310把持复合薄膜100的两端部120一边将复合薄膜100输送至拉伸炉320内,之后,在拉伸炉320内,不使把持着复合薄膜100的两端部120的各夹具310沿宽度方向移动,而是通过使夹具310彼此之间的间隔扩大来仅沿长度方向进行加热拉伸。At this time, heating and stretching of the composite film 100 in the longitudinal direction can be performed in the same manner as the simultaneous biaxial stretching method shown in FIG. 2 . That is, a method of transporting the composite film 100 into the stretching furnace 320 while holding both ends 120 of the composite film 100 with the jigs 310, and then, in the stretching furnace 320, the person holding the composite film 100 can be used. Each clip 310 of both end parts 120 is moved in the width direction, but heat-stretching is performed only in the longitudinal direction by increasing the distance between the clips 310 .
在本实施方式中,不管是在沿长度方向和宽度方向进行同步双轴拉伸的情况下还是在仅沿长度方向进行单轴拉伸的情况下,通过如图2所示那样一边利用夹具310把持复合薄膜100的两端部120一边进行拉伸,与以往使用的逐次双轴拉伸法相比,均能够提高拉伸薄膜的生产率,并能够使得到的拉伸薄膜的品质优异。In this embodiment, regardless of whether simultaneous biaxial stretching is performed in the longitudinal direction and the width direction or in the case of uniaxial stretching only in the longitudinal direction, by using the jig 310 as shown in FIG. Stretching while holding the both ends 120 of the composite film 100 can improve the productivity of the stretched film and improve the quality of the stretched film obtained compared with the conventional sequential biaxial stretching method.
此外,以往的逐次双轴拉伸法是将利用图1所示的方法制作成的复合薄膜100首先沿长度方向加热拉伸、之后沿宽度方向进行加热拉伸的方法。在逐次双轴拉伸法中,在利用多个辊输送复合薄膜100从而将复合薄膜100沿长度方向加热拉伸之后,如图2所示那样,一边利用夹具310把持复合薄膜100的两端部120一边将复合薄膜100沿宽度方向加热拉伸。In addition, the conventional sequential biaxial stretching method is a method of heating and stretching the composite film 100 produced by the method shown in FIG. 1 first in the longitudinal direction and then heating and stretching in the width direction. In the sequential biaxial stretching method, after the composite film 100 is heated and stretched in the longitudinal direction by conveying the composite film 100 with a plurality of rollers, as shown in FIG. 120 while heating and stretching the composite film 100 in the width direction.
在此,在逐次双轴拉伸法中,具体而言,以如下方式将复合薄膜100沿长度方向拉伸。即,采用逐次双轴拉伸法,利用被预先加热后的多个预热辊一边输送复合薄膜100一边将复合薄膜100预加热至两端部120的玻璃化转变温度左右,然后一边利用红外线加热器等将预加热后的复合薄膜100进一步加热至比两端部120的玻璃化转变温度高10℃~30℃左右的温度一边利用冷却辊连续地输送复合薄膜100。此时,通过使冷却辊的输送速度快于预热带辊的输送速度,从而使预热带辊与冷却辊之间产生张力,利用该张力将复合薄膜100沿长度方向拉伸至需要的拉伸倍率。Here, in the sequential biaxial stretching method, specifically, the composite film 100 is stretched in the longitudinal direction as follows. That is, the sequential biaxial stretching method is adopted, and the composite film 100 is preheated to about the glass transition temperature of both ends 120 while conveying the composite film 100 by a plurality of preheated preheating rolls, and then heated by infrared rays. The preheated composite film 100 is further heated to a temperature about 10° C. to 30° C. higher than the glass transition temperature of both ends 120 by using a device or the like, and the composite film 100 is continuously conveyed by cooling rolls. At this time, by making the conveying speed of the cooling roller faster than the conveying speed of the preheating roller, tension is generated between the preheating roller and the cooling roller, and the composite film 100 is stretched in the longitudinal direction to the required tension by using the tension. Magnification.
在此,在逐次双轴拉伸法中,在将复合薄膜100沿长度方向拉伸时,由于复合薄膜100的表面接触于预热辊和冷却辊,因此有可能使复合薄膜100的表面产生擦伤而使得到的拉伸薄膜的外观品质降低。另外,在逐次双轴拉伸法中,在将复合薄膜100沿长度方向加热拉伸时,由于复合薄膜100的两端部120的宽度方向的位置没有被固定,因此,复合薄膜100有可能因热而沿宽度方向收缩,从而使拉伸薄膜的生产率降低。Here, in the sequential biaxial stretching method, when the composite film 100 is stretched in the longitudinal direction, since the surface of the composite film 100 is in contact with the preheating roll and the cooling roll, the surface of the composite film 100 may be rubbed. The appearance quality of the obtained stretched film deteriorates due to scratches. In addition, in the sequential biaxial stretching method, when the composite film 100 is heated and stretched in the longitudinal direction, since the positions of the two ends 120 of the composite film 100 in the width direction are not fixed, the composite film 100 may be damaged due to Heat shrinks in the width direction, thereby reducing the productivity of the stretched film.
与此相对,采用本实施方式,通过使用所述同步双轴拉伸法或所述仅沿长度方向单轴拉伸的方法(即,如图2所示,通过使用一边利用夹具310把持复合薄膜100的两端部120一边将复合薄膜100沿长度方向拉伸的方法)来进行复合薄膜100的沿长度方向的拉伸,能够避免复合薄膜100与辊之间的接触,因此能够减少加热拉伸后的复合薄膜100的表面的擦伤。由此,对于对加热拉伸后的复合薄膜100的两端部120进行切割而得到的拉伸薄膜,能够提高其外观品质,尤其是,能够较佳地应用于外观品质要求严格的光学薄膜等。并且,采用本实施方式,由于在将复合薄膜100沿长度方向拉伸时利用夹具310把持复合薄膜100的两端部120,因此能够防止复合薄膜100因热而沿宽度方向收缩,从而能够提高拉伸薄膜的生产率。In contrast, in this embodiment, by using the simultaneous biaxial stretching method or the method of uniaxial stretching only in the longitudinal direction (that is, as shown in FIG. The two ends 120 of 100 stretch the composite film 100 along the longitudinal direction) to carry out the stretching of the composite film 100 along the longitudinal direction, which can avoid the contact between the composite film 100 and the roller, so the heating and stretching can be reduced. After the surface of the composite film 100 is scratched. Thus, for the stretched film obtained by cutting the both ends 120 of the heated and stretched composite film 100, the appearance quality can be improved, and in particular, it can be preferably applied to optical films and the like that require strict appearance quality. . And, according to this embodiment, since the both ends 120 of the composite film 100 are held by the clips 310 when the composite film 100 is stretched in the longitudinal direction, it is possible to prevent the composite film 100 from shrinking in the width direction due to heat, thereby improving the tensile strength. stretch film productivity.
实施例Example
以下,列举实施例更具体地说明本发明,但本发明并不限定于这些实施例。Hereinafter, although an Example is given and this invention is demonstrated more concretely, this invention is not limited to these Examples.
实施例1Example 1
作为用于形成复合薄膜100的中央部110的第1热塑性树脂,准备了丙烯酸树脂(玻璃化转变温度Tg1:123℃,常温下的断裂伸长率:5%),作为用于形成复合薄膜100的两端部120的第2热塑性树脂,准备了添加有少量的橡胶弹性颗粒的丙烯酸树脂(玻璃化转变温度Tg2:125℃,常温下的断裂伸长率:18%)。As the first thermoplastic resin for forming the central portion 110 of the composite film 100, an acrylic resin (glass transition temperature Tg 1 : 123° C., elongation at break at room temperature: 5%) was prepared as the first thermoplastic resin for forming the composite film 100. As the second thermoplastic resin at both ends 120 of 100, an acrylic resin (glass transition temperature Tg 2 : 125° C., elongation at break at room temperature: 18%) added with a small amount of rubber elastic particles was prepared.
在此,对于第1热塑性树脂和第2热塑性树脂,利用示差扫描量热法(DSC)测量出两者的玻璃化转变温度,利用拉伸试验机(ORIENTECCORPORATION制造,型号:RTC-1210A)来测量出两者的常温下的断裂伸长率。以下的实施例2~实施例5和比较例1也是同样的。Here, for the first thermoplastic resin and the second thermoplastic resin, the glass transition temperatures of both were measured by differential scanning calorimetry (DSC), and measured by a tensile tester (manufactured by ORIENTEC CORPORATION, model: RTC-1210A) The elongation at break at room temperature for both. The same applies to the following Examples 2 to 5 and Comparative Example 1.
另外,对于第1热塑性树脂和第2热塑性树脂,在将两者分别制作成厚度100μm的单体薄膜之后,对在将单体薄膜加热到140℃的状态下逐渐拉伸时的拉伸应力进行了测量。将结果表示在图4的(A)中。在此,在图4的(A)中,示出了相对于拉伸倍率(表示以拉伸前的单体薄膜的尺寸为基准向任意一个方向拉伸了拉伸前的尺寸的百分之几的量的值)而言,拉伸至该拉伸倍率所需要的拉伸应力值。另外,在图4的(A)中,将第1热塑性树脂的测量结果作为中央部110,将第2热塑性树脂的测量结果作为两端部120。In addition, for the first thermoplastic resin and the second thermoplastic resin, the tensile stress when the monomer film was gradually stretched in a state heated to 140° C. measured. The results are shown in (A) of FIG. 4 . Here, in (A) of FIG. 4 , it shows the percentage of stretching the size before stretching in any one direction with respect to the stretching ratio (representing the size of the monomer film before stretching). In terms of the value of the amount of a few), the stretching stress value required for stretching to the stretching ratio. In addition, in (A) of FIG. 4 , the measurement result of the first thermoplastic resin is taken as the central portion 110 , and the measurement result of the second thermoplastic resin is taken as both ends 120 .
接着,利用准备好的第1热塑性树脂及第2热塑性树脂,通过图1表示的方法,在以下的条件下制作出复合薄膜100。在此,制作出的复合薄膜100的整体宽度约为315mm,其中从两端的端部起的各约50mm宽度的区域为两端部120,剩余的中央的区域为中央部110。此外,在本实施例中,作为第2热塑性树脂使用了添加有橡胶弹性颗粒的丙烯酸树脂,但是,由于添加的橡胶弹性颗粒的量较少,因而能够抑制熔融共挤出复合薄膜100时的橡胶弹性颗粒的析出。Next, using the prepared first thermoplastic resin and second thermoplastic resin, the composite film 100 was produced under the following conditions by the method shown in FIG. 1 . Here, the overall width of the produced composite film 100 is about 315 mm, wherein the regions with a width of about 50 mm from both ends are the two ends 120 , and the remaining central regions are the center 110 . In addition, in this embodiment, the acrylic resin added with rubber elastic particles was used as the second thermoplastic resin, but since the amount of rubber elastic particles added is small, it is possible to suppress the occurrence of the rubber when the composite film 100 is melted and co-extruded. The precipitation of elastic particles.
T型模220出口宽度:380mmT-die 220 outlet width: 380mm
冷却辊240的牵引速度:6mpmTraction speed of chill roll 240: 6mpm
向供料头210供给的第1热塑性树脂的供给量:15kg/hrSupply amount of the first thermoplastic resin supplied to the supply head 210: 15kg/hr
向供料头210供给的第2热塑性树脂的供给量:5kg/hrSupply amount of the second thermoplastic resin supplied to the supply head 210: 5kg/hr
在此,对于得到的复合薄膜100,通过观察能够明确地确认中央部110和两端部120之间的边界,确认到在复合薄膜100中树脂之间没有发生混合。Here, in the obtained composite film 100 , the boundary between the central portion 110 and both end portions 120 was clearly confirmed by observation, and it was confirmed that the resins in the composite film 100 were not mixed.
接着,如图2所示,对于得到的复合薄膜100,利用夹具310把持两端部120,通过同步双轴拉伸法,并且在以下条件下沿长度方向和宽度方向进行了加热拉伸。此外,对于加热拉伸后的复合薄膜100,在加热拉伸后的中央部110中的中央部分的宽度400mm的区域测量出厚度及断裂强度时,厚度及断裂强度(在常温下拉伸至断裂时的拉伸强度)的分布在±5%以内。Next, as shown in FIG. 2 , both ends 120 of the obtained composite film 100 were grasped by clamps 310 , and heated and stretched in the longitudinal direction and the width direction under the following conditions by simultaneous biaxial stretching. In addition, for the composite film 100 after heating and stretching, when the thickness and breaking strength were measured in the region of the width 400 mm of the central part 110 after heating and stretching, the thickness and breaking strength (stretched to break at room temperature When the tensile strength) distribution within ± 5%.
进行加热拉伸前的输入侧速度:1mpmInput side speed before heating and stretching: 1mpm
进行加热拉伸后的输出侧速度:2mpmOutput side speed after heating and stretching: 2mpm
拉伸倍率:长度方向100%×宽度方向100%(长度方向两倍×宽度方向两倍)Stretch ratio: 100% in the length direction x 100% in the width direction (twice in the length direction x twice in the width direction)
夹具310把持位置:自复合薄膜100的端部起的15mm的位置Gripping position of the jig 310: 15 mm from the end of the composite film 100
预热带温度、距离:140℃、350mmPreheating temperature, distance: 140°C, 350mm
拉伸带温度、距离:140℃、500mmStretch belt temperature, distance: 140°C, 500mm
冷却热固化温度、距离:90℃、700mmCooling heat curing temperature, distance: 90 ℃, 700mm
此外,本实施例中,在对复合薄膜100进行加热拉伸的期间,没有发生夹具310脱离及复合薄膜100的断裂,能够连续地制造出品质优异的拉伸薄膜。In addition, in the present example, during heating and stretching of the composite film 100 , no detachment of the clips 310 and no breakage of the composite film 100 occurred, and a stretched film of excellent quality could be continuously produced.
实施例2Example 2
作为用于形成复合薄膜100的两端部120的第2热塑性树脂,使用了相对于75重量%的聚碳酸酯(PC)混合25重量%的聚对苯二甲酸乙二醇酯(PET)而得到的混合树脂(玻璃化转变温度Tg2:125℃,常温下的断裂伸长率:20%),除此以外,以与实施例1相同的方式得到拉伸薄膜,并且同样地测量出两端部120(第2热塑性树脂)的单体薄膜的拉伸应力。将结果示于图4的(A)。As the second thermoplastic resin for forming both ends 120 of the composite film 100, 25% by weight of polyethylene terephthalate (PET) was mixed with 75% by weight of polycarbonate (PC). Except for the obtained mixed resin (glass transition temperature Tg 2 : 125° C., elongation at break at normal temperature: 20%), a stretched film was obtained in the same manner as in Example 1, and both were measured in the same manner. Tensile stress of the monomer film at the end portion 120 (second thermoplastic resin). The results are shown in (A) of FIG. 4 .
此外,在实施例2中,也与实施例1同样地,对于利用熔融共挤出得到的复合薄膜100,能够通过观察明确地确认到中央部110和两端部120之间的边界,确认到在复合薄膜100中树脂之间没有发生混合。而且,在对复合薄膜100进行加热拉伸期间,没有发生夹具310的脱离及复合薄膜100的断裂,能够连续地制造出品质优异的拉伸薄膜。In addition, in Example 2, as in Example 1, for the composite film 100 obtained by melt coextrusion, the boundary between the central part 110 and both end parts 120 can be clearly confirmed by observation, and it is confirmed that No intermingling of resins occurs in the composite film 100 . In addition, during stretching of the composite film 100 by heating, the separation of the clips 310 and the breakage of the composite film 100 do not occur, and a stretched film of excellent quality can be continuously produced.
实施例3Example 3
作为用于形成复合薄膜100的两端部120的第2热塑性树脂,使用了在聚碳酸酯(PC)中混合丙烯酸树脂(PMMA)而成的混合树脂(玻璃化转变温度Tg2:122℃,常温下的断裂伸长率:25%),除此之外,以与实施例1相同的方式得到拉伸薄膜,并且同样地测量出两端部120(第2热塑性树脂)的单体薄膜的拉伸应力。将结果示于图4的(A)。As the second thermoplastic resin for forming both ends 120 of the composite film 100, a mixed resin (glass transition temperature Tg 2 : 122°C, Elongation at break at room temperature: 25%), except that, a stretched film was obtained in the same manner as in Example 1, and the elongation of the monomer film at both ends 120 (the second thermoplastic resin) was measured in the same manner. tensile stress. The results are shown in (A) of FIG. 4 .
此外,在实施例3,也与实施例1同样地,对于利用熔融共挤出得到的复合薄膜100,能够通过观察明确地确认到中央部110和两端部120之间的边界,确认到在复合薄膜100中树脂之间没有发生混合。并且,在对复合薄膜100进行加热拉伸的期间,没有发生夹具310的脱离及复合薄膜100的断裂,能够连续地制造出品质优异的拉伸薄膜。In addition, in Example 3, as in Example 1, for the composite film 100 obtained by melt coextrusion, the boundary between the central part 110 and both end parts 120 can be clearly confirmed by observation, and it is confirmed that No mixing between the resins in the composite film 100 occurs. In addition, during heating and stretching of the composite film 100 , detachment of the clips 310 and breakage of the composite film 100 do not occur, and a stretched film of excellent quality can be continuously produced.
实施例4Example 4
作为用于形成复合薄膜100的两端部120的第2热塑性树脂,使用了将聚碳酸酯(PC)和丙烯腈-丁二烯-苯乙烯(ABS)混合而制成的PC/ABS合金(玻璃化转变温度Tg2:120℃,常温下的断裂伸长率:180%),除此之外,以与实施例1相同的方式得到了拉伸薄膜,并且同样地测量出两端部120(第2热塑性树脂)的单体薄膜的拉伸应力。将结果示于图4的(B)。此外,与图4的(A)同样地,图4的(B)是表示使用第1热塑性树脂及第2热塑性树脂制作成的单体薄膜的拉伸应力的测量结果的图表,图4的(B)的纵轴的刻度与图4的(A)不同。As the second thermoplastic resin for forming both ends 120 of the composite film 100, a PC/ABS alloy ( Glass transition temperature Tg 2 : 120°C, elongation at break at normal temperature: 180%), except that, a stretched film was obtained in the same manner as in Example 1, and 120° at both ends were measured in the same manner. Tensile stress of the monomer film of (the second thermoplastic resin). The results are shown in (B) of FIG. 4 . In addition, like FIG. 4(A), FIG. 4(B) is a graph showing the measurement results of the tensile stress of the monomer film made of the first thermoplastic resin and the second thermoplastic resin, and FIG. 4( The scale of the vertical axis of B) is different from that of (A) of FIG. 4 .
在此,在实施例4中,与实施例1同样地,对于利用熔融共挤出得到的复合薄膜100,能够通过观察明确地确认到中央部110和两端部120之间的边界,确认到在复合薄膜100中树脂之间没有发生混合。Here, in Example 4, as in Example 1, for the composite film 100 obtained by melt coextrusion, the boundary between the central part 110 and both end parts 120 can be clearly confirmed by observation, and it is confirmed that No intermingling of resins occurs in the composite film 100 .
另一方面,在实施例4中,由于当拉伸倍率为100%时,两端部120的拉伸应力相对于中央部110的拉伸应力而言较高,约为中央部110的拉伸应力的7.7倍,因此,在进行复合薄膜100的加热拉伸时,难以对两端部120进行拉伸,偶尔会发生夹具310的脱离。但是,在实施例4中,夹具310脱离的发生频率较低,因而能够连续地制造品质优异的拉伸薄膜。On the other hand, in Example 4, since the tensile stress of both end portions 120 is higher than that of the central portion 110 when the stretching ratio is 100%, the tensile stress of the central portion 110 is about 100%. 7.7 times the stress. Therefore, when heating and stretching the composite film 100, it is difficult to stretch the both ends 120, and the clip 310 may occasionally come off. However, in Example 4, the occurrence frequency of detachment of the clips 310 was low, and thus a stretched film of excellent quality could be continuously produced.
实施例5Example 5
作为用于形成复合薄膜100的两端部120的第2热塑性树脂,使用了聚萘二甲酸乙二醇酯(PEN)(玻璃化转变温度Tg2:120℃,常温下的断裂伸长率:300%),除此之外,以与实施例1相同的方式得到了拉伸薄膜,并且同样地测量出两端部120(第2热塑性树脂)的单体薄膜的拉伸应力。将结果示于图4的(A)。As the second thermoplastic resin for forming both ends 120 of the composite film 100, polyethylene naphthalate (PEN) (glass transition temperature Tg 2 : 120°C, elongation at break at room temperature: 300%), except that a stretched film was obtained in the same manner as in Example 1, and the tensile stress of the monomer film at both ends 120 (second thermoplastic resin) was measured in the same manner. The results are shown in (A) of FIG. 4 .
在此,在实施例5中,在熔融共挤出第1热塑性树脂及第2热塑性树脂时,得到的复合薄膜100中的中央部110和两端部120之间的边界变得略为不明显。考虑其原因在于,第1热塑性树脂及第2热塑性树脂的熔融共挤出时的粘度差较大,因此,中央部110及两端部120微量混合在一起。但是,在实施例5中,得到的拉伸薄膜中不存在品质问题。Here, in Example 5, when the first thermoplastic resin and the second thermoplastic resin were melt-coextruded, the boundary between the central portion 110 and both end portions 120 in the obtained composite film 100 became slightly inconspicuous. The reason for this is considered to be that the central portion 110 and both end portions 120 are slightly mixed together because the viscosity difference between the first thermoplastic resin and the second thermoplastic resin is large during melt coextrusion. However, in Example 5, there was no quality problem in the obtained stretched film.
另外,在实施例5中,与实施例1同样地,在进行复合薄膜100的加热拉伸期间,没有发生夹具310脱离及复合薄膜100的断裂,能够连续地制造品质优异的拉伸薄膜。In addition, in Example 5, as in Example 1, during heating and stretching of the composite film 100 , no detachment of the clips 310 and no breakage of the composite film 100 occurred, and a stretched film of excellent quality could be continuously produced.
比较例1Comparative example 1
作为用于形成复合薄膜100的两端部120的第2热塑性树脂,使用了聚碳酸酯(PC)(玻璃化转变温度Tg2:143℃,常温下的断裂伸长率:170%),除此之外,以与实施例1同样的方式得到拉伸薄膜,并且同样地测量出两端部120(第2热塑性树脂)的单体薄膜的拉伸应力。将结果示于图4的(B)。As the second thermoplastic resin for forming both ends 120 of the composite film 100, polycarbonate (PC) (glass transition temperature Tg 2 : 143°C, elongation at break at room temperature: 170%) was used, except Otherwise, a stretched film was obtained in the same manner as in Example 1, and the tensile stress of the single film at both ends 120 (second thermoplastic resin) was measured in the same manner. The results are shown in (B) of FIG. 4 .
此外,与实施例1同样地,对于比较例1的利用熔融共挤出得到的复合薄膜100,也能够通过观察明确确认到中央部110和两端部120之间的边界,并且确认到在复合薄膜100中树脂之间没有发生混合。In addition, as in Example 1, for the composite film 100 obtained by melt coextrusion in Comparative Example 1, the boundary between the central part 110 and both end parts 120 can also be clearly confirmed by observation, and it is confirmed that the composite film 100 in the composite No mixing between the resins in the film 100 occurs.
然而,在比较例1中,在加热拉伸复合薄膜100时,预热带及拉伸带的温度(140℃)没有达到构成两端部120的第2热塑性树脂的玻璃化转变温度Tg2(143℃),因此,两端部120并没有充分软化,由此,经常发生夹具310的脱离,无法得到拉伸薄膜。对此,在比较例1中,将通过同步双轴拉伸法进行加热拉伸时的预热带及拉伸带的温度从140℃变更为160℃,由此,能够使两端部120软化从而进行加热拉伸,但是,由于得到的拉伸薄膜暴露于高温下,因而分子取向不均匀化导致强度降低,进而使得膜厚也变得不均匀,品质差。However, in Comparative Example 1, when heating and stretching the composite film 100, the temperature (140° C.) of the preheating zone and the stretching zone did not reach the glass transition temperature Tg 2 ( 143° C.), therefore, both ends 120 are not sufficiently softened, and thus, detachment of the clips 310 often occurs, and a stretched film cannot be obtained. On the other hand, in Comparative Example 1, the temperature of the preheating belt and the stretching belt when heating and stretching by the simultaneous biaxial stretching method was changed from 140°C to 160°C, thereby softening the both ends 120 Thus, heating and stretching is performed, but since the obtained stretched film is exposed to high temperature, the molecular orientation becomes non-uniform and the strength decreases, and the film thickness also becomes non-uniform, resulting in poor quality.
如上所述,在第1热塑性树脂的玻璃化转变温度Tg1和第2热塑性树脂的玻璃化转变温度Tg2的差(|Tg1-Tg2|)在10℃以下的实施例1~5中,在进行复合薄膜100的加热拉伸时,由于能够抑制合薄膜100的断裂及夹具310的脱离,因而能够得到品质优异的拉伸薄膜,并能够提高拉伸薄膜的生产率。As described above, in Examples 1 to 5 in which the difference between the glass transition temperature Tg 1 of the first thermoplastic resin and the glass transition temperature Tg 2 of the second thermoplastic resin (|Tg 1 −Tg 2 |) was 10°C or less Therefore, when the composite film 100 is heated and stretched, since the fracture of the composite film 100 and the detachment of the clips 310 can be suppressed, a stretched film with excellent quality can be obtained, and the productivity of the stretched film can be improved.
另一方面,就上述那样的第1热塑性树脂的玻璃化转变温度Tg1和第2热塑性树脂的玻璃化转变温度Tg2的差(|Tg1-Tg2|)超过10℃的比较例1而言,在进行复合薄膜100的加热拉伸时,经常发生夹具310的脱离,无法得到拉伸薄膜,拉伸薄膜的生产率较差。On the other hand, in Comparative Example 1 in which the difference (|Tg 1 −Tg 2 |) between the glass transition temperature Tg 1 of the first thermoplastic resin and the glass transition temperature Tg 2 of the second thermoplastic resin exceeded 10°C, In other words, when the composite film 100 is heated and stretched, the clips 310 often detach, the stretched film cannot be obtained, and the productivity of the stretched film is poor.
附图标记说明Explanation of reference signs
100…复合薄膜100…Composite film
110…中央部110…Central part
120…两端部120...both ends
210…供料头210…feed head
220…T型模220…T type die
230…接触辊230…contact roller
240…冷却辊240...cooling roll
310…夹具310...Clamp
320…拉伸炉320…drawing furnace
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010234916.9A CN111331805B (en) | 2014-01-17 | 2015-01-13 | Method for producing stretched film |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014-006467 | 2014-01-17 | ||
JP2014006467A JP6338864B2 (en) | 2014-01-17 | 2014-01-17 | Method for producing stretched film |
PCT/JP2015/050667 WO2015108034A1 (en) | 2014-01-17 | 2015-01-13 | Stretched film manufacturing method |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010234916.9A Division CN111331805B (en) | 2014-01-17 | 2015-01-13 | Method for producing stretched film |
Publications (1)
Publication Number | Publication Date |
---|---|
CN105916657A true CN105916657A (en) | 2016-08-31 |
Family
ID=53542923
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201580004847.XA Pending CN105916657A (en) | 2014-01-17 | 2015-01-13 | Stretched film manufacturing method |
CN202010234916.9A Active CN111331805B (en) | 2014-01-17 | 2015-01-13 | Method for producing stretched film |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010234916.9A Active CN111331805B (en) | 2014-01-17 | 2015-01-13 | Method for producing stretched film |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP6338864B2 (en) |
KR (1) | KR102209119B1 (en) |
CN (2) | CN105916657A (en) |
WO (1) | WO2015108034A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112238589A (en) * | 2019-07-18 | 2021-01-19 | 布鲁克纳机械有限责任两合公司 | Method and device for producing melt films and/or plastic films |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0707938A2 (en) * | 1994-10-19 | 1996-04-24 | Hoechst Diafoil GmbH | Process for producing thermoplastic film by lateral coextrusion |
JP2008149511A (en) * | 2006-12-15 | 2008-07-03 | Toyo Kohan Co Ltd | Method for producing stretched film |
WO2008146696A1 (en) * | 2007-05-25 | 2008-12-04 | Fujifilm Corporation | Method for production of bi-axially oriented thermoplastic resin film, and base film for optical film |
CN102245363A (en) * | 2008-12-10 | 2011-11-16 | 特里奥凡德国有限公司及两合公司 | Method for producing polypropylene films |
JP2012086433A (en) * | 2010-10-19 | 2012-05-10 | Konica Minolta Opto Inc | Method of manufacturing optical film |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08207119A (en) * | 1994-10-19 | 1996-08-13 | Diafoil Co Ltd | Production of thermoplastic resin sheet or film |
JP4331846B2 (en) * | 2000-01-19 | 2009-09-16 | 積水化学工業株式会社 | Laminated glass interlayer film and laminated glass |
US6900147B2 (en) * | 2001-11-28 | 2005-05-31 | Kimberly-Clark Worldwide, Inc. | Nonwoven webs having improved necking uniformity |
JP4089511B2 (en) | 2003-05-22 | 2008-05-28 | 松下電工株式会社 | Resin sheet rolling equipment |
JP5123654B2 (en) * | 2007-12-11 | 2013-01-23 | 住友化学株式会社 | Method for producing extruded resin plate |
GB0915425D0 (en) * | 2009-09-04 | 2009-10-07 | Megaplast Sa | Reinforced thin film for flexible packaging |
JP5499983B2 (en) * | 2010-08-04 | 2014-05-21 | 日本ゼオン株式会社 | Method for producing stretched optical film |
JP2014069438A (en) * | 2012-09-28 | 2014-04-21 | Nippon Shokubai Co Ltd | Production method of stretched film |
-
2014
- 2014-01-17 JP JP2014006467A patent/JP6338864B2/en active Active
-
2015
- 2015-01-13 WO PCT/JP2015/050667 patent/WO2015108034A1/en active Application Filing
- 2015-01-13 KR KR1020167021802A patent/KR102209119B1/en active Active
- 2015-01-13 CN CN201580004847.XA patent/CN105916657A/en active Pending
- 2015-01-13 CN CN202010234916.9A patent/CN111331805B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0707938A2 (en) * | 1994-10-19 | 1996-04-24 | Hoechst Diafoil GmbH | Process for producing thermoplastic film by lateral coextrusion |
JP2008149511A (en) * | 2006-12-15 | 2008-07-03 | Toyo Kohan Co Ltd | Method for producing stretched film |
WO2008146696A1 (en) * | 2007-05-25 | 2008-12-04 | Fujifilm Corporation | Method for production of bi-axially oriented thermoplastic resin film, and base film for optical film |
CN102245363A (en) * | 2008-12-10 | 2011-11-16 | 特里奥凡德国有限公司及两合公司 | Method for producing polypropylene films |
JP2012086433A (en) * | 2010-10-19 | 2012-05-10 | Konica Minolta Opto Inc | Method of manufacturing optical film |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112238589A (en) * | 2019-07-18 | 2021-01-19 | 布鲁克纳机械有限责任两合公司 | Method and device for producing melt films and/or plastic films |
CN112238589B (en) * | 2019-07-18 | 2022-11-29 | 布鲁克纳机械有限责任两合公司 | Method and apparatus for producing a melt film and/or a plastic film |
US11712832B2 (en) | 2019-07-18 | 2023-08-01 | Brückner Maschinenbau GmbH | Method and device for producing a melt and/or plastic film |
US11951668B2 (en) | 2019-07-18 | 2024-04-09 | Bruckner Maschinenbau Gmbh | Method and device for producing a melt and/or plastic film |
Also Published As
Publication number | Publication date |
---|---|
KR102209119B1 (en) | 2021-01-27 |
KR20160108444A (en) | 2016-09-19 |
CN111331805A (en) | 2020-06-26 |
JP2015134450A (en) | 2015-07-27 |
JP6338864B2 (en) | 2018-06-06 |
CN111331805B (en) | 2022-05-10 |
WO2015108034A1 (en) | 2015-07-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105916655B (en) | Stretch film manufacturing method | |
TWI423877B (en) | Production method of stretched film and stretch film | |
WO2002096622A1 (en) | Processes and apparatus for making transversely drawn films with substantially uniaxial orientation | |
CN106476309B (en) | Manufacturing method and manufacturing apparatus of slitting stretched film | |
CN105916654B (en) | The manufacture method of oriented film | |
CN105916656B (en) | The manufacturing method of oriented film | |
CN104494177A (en) | System for producing back sealing strips | |
CN111331805B (en) | Method for producing stretched film | |
JP6338865B2 (en) | Method for producing stretched film | |
JP6354237B2 (en) | Fragile film manufacturing method and apparatus | |
JP4097823B2 (en) | Method for producing biaxially stretched polyamide film | |
JP6377355B2 (en) | Method for producing stretched film | |
JP2936688B2 (en) | Method for producing thermoplastic resin film | |
JP2013129169A (en) | Method of manufacturing biaxially oriented nylon film | |
TW201334947A (en) | Holder and heat treatment method | |
JP2841816B2 (en) | Method for producing thermoplastic resin film | |
JP2002067141A (en) | Method for manufacturing sequentially biaxially stretched film | |
CN118973797A (en) | Method for producing a thermoformed plastic part made of polyethylene terephthalate | |
JPS61158424A (en) | Double-layer orientation method | |
JPH07108598A (en) | Production of polyamide film |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160831 |