WO2015155861A1 - スライドファスナー用ポリアミド樹脂組成物、スライドファスナー用部品及びそれを備えたスライドファスナー - Google Patents
スライドファスナー用ポリアミド樹脂組成物、スライドファスナー用部品及びそれを備えたスライドファスナー Download PDFInfo
- Publication number
- WO2015155861A1 WO2015155861A1 PCT/JP2014/060348 JP2014060348W WO2015155861A1 WO 2015155861 A1 WO2015155861 A1 WO 2015155861A1 JP 2014060348 W JP2014060348 W JP 2014060348W WO 2015155861 A1 WO2015155861 A1 WO 2015155861A1
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- Prior art keywords
- polyamide resin
- polyamide
- mass
- resin composition
- slide fastener
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A44—HABERDASHERY; JEWELLERY
- A44B—BUTTONS, PINS, BUCKLES, SLIDE FASTENERS, OR THE LIKE
- A44B19/00—Slide fasteners
- A44B19/24—Details
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- A—HUMAN NECESSITIES
- A44—HABERDASHERY; JEWELLERY
- A44B—BUTTONS, PINS, BUCKLES, SLIDE FASTENERS, OR THE LIKE
- A44B19/00—Slide fasteners
- A44B19/24—Details
- A44B19/26—Sliders
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- A—HUMAN NECESSITIES
- A44—HABERDASHERY; JEWELLERY
- A44B—BUTTONS, PINS, BUCKLES, SLIDE FASTENERS, OR THE LIKE
- A44B19/00—Slide fasteners
- A44B19/24—Details
- A44B19/26—Sliders
- A44B19/262—Pull members; Ornamental attachments for sliders
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- A—HUMAN NECESSITIES
- A44—HABERDASHERY; JEWELLERY
- A44B—BUTTONS, PINS, BUCKLES, SLIDE FASTENERS, OR THE LIKE
- A44B19/00—Slide fasteners
- A44B19/24—Details
- A44B19/36—Means for permanently uniting the stringers at the end; Means for stopping movement of slider at the end
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- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D2500/00—Materials for garments
- A41D2500/50—Synthetic resins or rubbers
Definitions
- the present invention relates to a resin composition for slide fasteners.
- the present invention also relates to a slide fastener part made from the resin composition. Furthermore, this invention relates to the slide fastener provided with the said component.
- the slide fastener is an opening / closing tool for articles that are used not only for daily necessities such as clothing, bags, shoes and sundries, but also for industrial items such as water tanks, fishing nets and space suits.
- FIG. 1 shows a configuration example of a slide fastener.
- the slide fastener 10 controls the opening and closing of a fastener by engaging and separating a pair of long tapes 11, a number of elements 12 that are meshing portions of fasteners attached along one side edge of each tape, and the elements 12.
- the slider 13 is mainly composed of three parts. Further, in order to prevent the slider 13 from falling off, an upper stopper 14 and an opening tool 15 can be provided. On the surface of the slider 13, in addition to the handle 16, a handle cover 17 that is a part for fixing the handle 16 to the slider. Can also be attached.
- the components of the slide fastener are molded parts that can be manufactured by injection molding, and can be manufactured using polyamide as a material.
- Patent Document 1 is reinforced with glass fiber for the purpose of improving the durability of a slider used for a slide fastener for bedding, the durability against washing and the iron, and the sliding resistance of the slider.
- a method for injection molding a slider using a polyamide as a material is described (claim 1). It is described that the glass fiber has a length of 4 to 8 mm and a content of 25% by weight or more (claim 1). It is described that the slider is subjected to a recrystallization process after forming (claim 1). Further, it is described that polyamides 6 and 6 are used as the polyamide (claim 6). It is also described that a polyamide containing no lubricant or gliding agent is used and the glass fiber content is about 40% by weight (Claim 5).
- Patent Document 2 also describes that a polyamide resin can be used as a component for a slide fastener.
- polyamide 6, polyamide 66, polyamide MXD6, polyamide 6T, polyamide 11 and polyamide 12 are listed as polyamide resins. Particularly, it is described that a polyamide resin having 80% by mole or more of a capramide repeating unit and / or a polyamide resin having 80% by mole or more of a hexamethylene adipamide repeating unit is preferable.
- Patent Document 3 discloses a polyamide resin composition containing 30 to 50% by mass of polyamide, 50 to 70% by mass of reinforcing fibers, and 50% by mass or more of the polyamide is an aliphatic polyamide. Yes. And it is described from the viewpoint of improving the plating property that the aliphatic polyamide in the polyamide is preferably 80% by mass or more.
- the pull cover, pull handle, top stop, bottom stop and element are particularly small, and are directly related to the overall mechanical strength of the slide fastener, the overall strength of the slider and the lateral pulling strength of the chain. It is.
- dyeing is usually performed from the viewpoint of aesthetics.
- the main component is an aliphatic polyamide such as polyamide 6 or 6 or a reinforcing fiber is mixed to exert strength.
- the slider body when a slider body is produced by combining aliphatic polyamide and reinforcing fibers, the slider body can exhibit excellent strength even after dyeing.
- small parts such as the above-mentioned handle cover, handle, top stopper, bottom stopper and element are made of a material combining aliphatic polyamide and reinforcing fiber, the strength reduction after dyeing is remarkable. I understood that.
- the inventor examined the cause of the above problem and inferred as follows. Small parts such as the handle cover, handle, top stopper, bottom stopper and element are smaller than the slider body. Therefore, the orientation of the reinforcing fibers dispersed in the polyamide resin matrix is not uniform, and the strength improving effect by the reinforcing fibers cannot be fully enjoyed. In addition, the aliphatic polyamide has a great decrease in strength after water absorption. From these facts, when a small part made of a material combining an aliphatic polyamide and a reinforcing fiber is dyed, the strength of the aliphatic polyamide itself, which has been reduced by water absorption, is reflected in the fastener part.
- the present inventor has sought a polyamide resin material that is less likely to decrease in strength after water absorption and that can be easily injection-molded for small parts, and that an aromatic polyamide having a low melting point is advantageous. I found. The present invention has been completed based on this knowledge.
- the present invention is a polyamide resin composition for a slide fastener containing a polyamide resin and reinforcing fibers, wherein the total mass of the polyamide resin and reinforcing fibers accounts for 90% by mass or more of the composition, and the polyamide resin
- the ratio of the aromatic polyamide having a melting point of 200 to 250 ° C. exceeds 70% by mass, and the content of the reinforcing fiber in the total mass of the polyamide resin and the reinforcing fiber is 45 to 70% by mass.
- It is a polyamide resin composition for slide fasteners.
- the ratio of the aromatic polyamide having a melting point of 200 to 250 ° C. in the polyamide resin exceeds 80% by mass.
- the polyamide resin further contains an aliphatic polyamide having a water absorption smaller than that of the aromatic polyamide and a melting point of 200 to 250 ° C. .
- the ratio of polyamide MXD6 having a melting point of 200 to 250 ° C. in the polyamide resin exceeds 70 mass%.
- a ratio of polyamide MXD6 having a melting point of 200 to 250 ° C. in the polyamide resin is 80 to 95% by mass, and the polyamide resin
- the proportion of the aliphatic polyamide having a water absorption rate smaller than that of the aromatic polyamide and having a melting point of 200 to 250 ° C. is 5 to 20% by mass.
- the polyamide resin composition for slide fastener according to the present invention, has a melt flow rate of 10 to 50 g / 10 min.
- the present invention is a slide fastener part made from the polyamide resin composition for slide fastener according to the present invention.
- the slide fastener part according to the present invention is a handle, a handle cover, an upper stopper, a lower stopper or an element.
- the slide fastener component according to the present invention is an element in another embodiment.
- the slide fastener part according to the present invention is dyed.
- FIG. 1 Another aspect of the present invention is a fastener stringer in which a plurality of elements according to the present invention are attached to a side edge of a fastener tape to form an element row.
- the present invention is a slide fastener including the slide fastener part or fastener stringer according to the present invention.
- the slide fastener according to the present invention is at least one selected from the group consisting of a pull handle, a pull cover, an upper stopper, a lower stopper, and an element row made of the polyamide resin composition for slide fastener according to the present invention.
- the parts are provided.
- the slide fastener according to the present invention is a polyamide resin composition containing a polyamide resin and a reinforcing fiber, and the total mass of the polyamide resin and the reinforcing fiber accounts for 90% by mass or more in the composition.
- the ratio of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is 60% by mass or more, and the content of the reinforcing fiber in the total mass of the polyamide resin and the reinforcing fiber is 45 to 70% by mass.
- the slide fastener according to the present invention includes a handle and a handle cover made of the polyamide resin composition for a slide fastener according to the present invention, and further includes a polyamide resin and a reinforced fiber.
- the total mass of the polyamide resin and the reinforcing fiber accounts for 90% by mass or more in the composition, and the proportion of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is 60% by mass or more.
- a slider body made of a polyamide resin composition in which the content of the reinforcing fiber in the total mass of the polyamide resin and the reinforcing fiber is 45 to 70% by mass.
- the slide fastener according to the present invention includes an element array made of the polyamide resin composition for slide fastener according to the present invention, and further includes a polyamide resin and a reinforced fiber.
- the total mass of the polyamide resin and the reinforcing fiber accounts for 90% by mass or more in the composition, and the proportion of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is 60% by mass or more,
- a slider body made of a polyamide resin composition having a content of the reinforcing fibers in the total mass of the polyamide resin and the reinforcing fibers of 45 to 70% by mass is provided.
- a slide fastener having excellent strength after dyeing can be obtained.
- the slider body is made mainly of aliphatic polyamide
- these small parts are made mainly of aromatic polyamide, and by adding reinforcing fibers to both, it is excellent in both strength and open / close durability. Slide fastener is obtained.
- FIG. 1 It is a front view which shows the example of 1 structure of the slide fastener which concerns on this invention. It is a disassembled perspective view of one Embodiment of the slider which concerns on this invention. It is a perspective view of the slider comprised by assembling each component shown in FIG.
- Aromatic polyamide (1. Polyamide resin composition suitable for small parts) ⁇ 1-1 Aromatic polyamide>
- one of the features is that an aromatic polyamide having a melting point of 200 to 250 ° C. is used.
- the melting point of the aromatic polyamide By setting the melting point of the aromatic polyamide to 250 ° C. or less, it is possible to provide fluidity advantageous to injection molding even for small parts such as a pull handle, a pull cover, an upper stopper, a lower stopper and an element.
- the element is a small part, and fluidity during injection molding is important, and if the temperature at the time of injection molding is too high, the problem arises that the fastener tape will burn, so the aromatic polyamide used It is advantageous to keep the melting point of ⁇ 250 ° C.
- the melting point of the aromatic polyamide is preferably 245 ° C. or lower, more preferably 240 ° C. or lower.
- the low melting point polyamide resin has a reduced number of amide bonds per unit molecular structure and becomes a flexible chain, so that the strength and rigidity tend to decrease. Therefore, it is preferable to use an aromatic polyamide having a melting point of 200 ° C. or higher, more preferably an aromatic polyamide having a melting point of 210 ° C. or higher, and further to use an aromatic polyamide having a melting point of 220 ° C. or higher. Is more preferable.
- the melting point of the aromatic polyamide is the temperature at the top of the endothermic peak when the endothermic amount is measured by DSC (differential scanning calorimeter).
- DSC differential scanning calorimeter
- the endothermic peak top temperature on the highest temperature side is defined as the melting point. Therefore, when a plurality of aromatic polyamides are used, the melting point is measured based on the aromatic polyamide having the highest melting point. However, even when a plurality of aromatic polyamides are used, it is preferable that the melting points of the respective polyamide resins are all within the above-described range.
- the ratio of the aromatic polyamide having a melting point of 200 to 250 ° C. in the polyamide resin is more than 70% by mass. It can be mentioned as one.
- polyamide resin mainly composed of aliphatic polyamide is used in small parts such as handle, handle cover, top stopper, bottom stopper and element, the effect of improving strength by reinforcing fibers is difficult to be exhibited. If moisture is absorbed, fastener parts having sufficient strength cannot be obtained.
- a polyamide resin containing aromatic polyamide as a main component, it is possible to suppress a decrease in strength after water absorption in small parts such as a handle, a handle cover, a top stopper, a bottom stopper, and an element.
- the ratio of the aromatic polyamide having a melting point of 200 to 250 ° C. in the polyamide resin is preferably 75% by mass or more, more preferably 80% by mass or more, and still more preferably 85% by mass or more. preferable.
- the ratio of the aromatic polyamide having a melting point of 200 to 250 ° C. in the polyamide resin may be 100% by mass, but as will be described later, an aliphatic polyamide having a predetermined melting point and water absorption is blended in a small amount in the polyamide resin. Thus, the strength of the fastener part can be improved. Therefore, the proportion of the aromatic polyamide having a melting point of 200 to 250 ° C. in the polyamide resin is preferably 95% by mass or less, and more preferably 90% by mass or less.
- Aromatic polyamide refers to a polyamide having at least one aromatic ring in the molecule, generally synthesized using aromatic diamine and aromatic dicarboxylic acid as raw materials, and synthesized using aromatic diamine and aliphatic dicarboxylic acid as raw materials. Or those synthesized using aliphatic diamine and aromatic dicarboxylic acid as raw materials.
- aromatic diamines include metaxylylenediamine, paraxylylenediamine, metaphenylenediamine, and paraphenylenediamine.
- aliphatic diamine examples include linear or branched chains such as ethylenediamine, propylenediamine, butylenediamine, hexamethylenediamine, 2-methylpropanediamine, 3-methylpropanediamine, octamethylenediamine, decanediamine, and dodecanediamine. Of aliphatic diamines.
- Aromatic dicarboxylic acids include phthalic acid, terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid, 2-chloroterephthalic acid, 2-methylterephthalic acid, 5-methylisophthalic acid, and 5-sodium sulfoisophthalic acid and 1,5- And naphthalenedicarboxylic acid.
- aliphatic dicarboxylic acid examples include succinic acid, propanedioic acid, butanedioic acid, pentanedioic acid, adipic acid, heptanedioic acid, octanedioic acid, nonanedioic acid, decanedioic acid, dodecanedioic acid, and undecanedioic acid.
- linear or branched aliphatic dicarboxylic acids such as dimer acid and hydrogenated dimer acid.
- aromatic polyamide examples include polyhexamethylene isophthalamide (polyamide 6I), polyhexamethylene terephthalamide (polyamide 6T), polymetaxylylene adipamide (polyamide MXD6), polyparaxylylene adipamide (Polyamide PXD6), polybis (3-methyl-4-aminohexyl) methane terephthalamide (polyamide PACMT), polybis (3-methyl-4-aminohexyl) methane isophthalamide (polyamide PACMI), polytetramethylene terephthalamide (polyamide 4T) ), Polypentamethylene terephthalamide (polyamide 5T), poly-2-methylpentamethylene terephthalamide (polyamide M-5T), polyhexamethylene hexaterephthalamide (polyamide 6T), Rihexamethylene hexahydroterephthalamide (polyamide 6T (H)), poly-2-methyl-octamethylene terephthalamide
- Polyamide resin has different melting points depending on the molecular structure and molecular weight. In addition, even if the molecular structure is the same, the melting point changes if the molecular weight is different. Therefore, the melting point of these aromatic polyamides can be adjusted by controlling the molecular weight. By increasing the molecular weight, the melting point can be raised, and conversely, by lowering the molecular weight, the melting point can be lowered.
- polyamide MXD6 is preferable because it provides excellent strength even after water absorption and a commercial product having a melting point in the above-described range is easily available. Therefore, in the aromatic polyamide component used in the polyamide resin according to the present invention, 90% by mass or more is preferably composed of polyamide MXD6, more preferably 95% by mass or more is composed of polyamide MXD6, 99 It is even more preferable that the mass% or more is composed of polyamide MXD6, and it is even more preferable that 100 mass% is composed of polyamide MXD6.
- one feature is that an aliphatic polyamide having a water absorption smaller than that of the aromatic polyamide described above and having a melting point of 200 to 250 ° C. is blended.
- the polyamide resin used in the present invention is mainly characterized by the aromatic polyamide as a main component.
- a predetermined aliphatic polyamide as a minor component
- the present inventor can stabilize the fastener part having high strength after dyeing by blending an aliphatic polyamide having a lower water absorption than the aromatic polyamide used (for example, MXD6 has a water absorption of 5% or more). And found that it can be obtained.
- the water absorption of the aliphatic polyamide used is preferably less than 5%, more preferably 4% or less, even more preferably 3.5% or less, and even more preferably 3% or less.
- the water absorption rate means a saturated water absorption rate measured on a flat plate injected by injection molding according to JIS K7209: 2000.
- the merit of setting the melting point of the aliphatic polyamide to 200 to 250 ° C. is as described in the explanation of the aromatic polyamide, but a preferable embodiment will be described just in case.
- the melting point of the aliphatic polyamide is preferably 245 ° C. or lower, more preferably 240 ° C. or lower.
- the melting point of the aliphatic polyamide is preferably 210 ° C. or higher, more preferably 220 ° C. or higher.
- the melting point of the aliphatic polyamide is the endothermic peak top temperature when the endotherm is measured by DSC (differential scanning calorimeter).
- DSC differential scanning calorimeter
- the melting point is measured based on the aliphatic polyamide having the highest melting point.
- the melting points of the respective polyamide resins are all within the above-described range.
- the blending ratio in the polyamide resin of the aliphatic polyamide having the predetermined melting point and water absorption described above has a suitable range in which the effect of improving the strength after water absorption can be obtained.
- the strength improving effect is significantly exhibited when the blending ratio of the aliphatic polyamide in the polyamide resin is 5% by mass or more, and preferably 10% by mass or more.
- an excessive blending ratio of the aliphatic polyamide causes a decrease in strength. Therefore, the blending ratio of the aliphatic polyamide is preferably 40% by mass or less in the polyamide resin, and 30% by mass. More preferably, it is more preferably 20% by mass or less.
- Aliphatic polyamide refers to a polyamide composed of an aliphatic skeleton, generally synthesized from aliphatic amines and aliphatic dicarboxylic acids as raw materials, or synthesized from aliphatic ⁇ -amino acids or their lactams as raw materials. Can be classified as polyamide.
- aliphatic diamine examples include linear or branched chains such as ethylenediamine, propylenediamine, butylenediamine, hexamethylenediamine, 2-methylpropanediamine, 3-methylpropanediamine, octamethylenediamine, decanediamine, and dodecanediamine. And aliphatic diamines.
- aliphatic dicarboxylic acid examples include succinic acid, propanedioic acid, butanedioic acid, pentanedioic acid, adipic acid, heptanedioic acid, octanedioic acid, nonanedioic acid, decanedioic acid, dodecanedioic acid, and undecanedioic acid.
- linear or branched aliphatic dicarboxylic acids such as dimer acid and hydrogenated dimer acid.
- Examples of the aliphatic ⁇ -amino acid include 6-aminohexanoic acid, 11-aminoundecanoic acid, 12-aminododecanoic acid and the like.
- Examples of the lactam include ⁇ -caprolactam, undecane lactam, and lauryl lactam.
- the specific structure of the aliphatic polyamide is not limited, but the following formula: —NHR 1 NHC ( ⁇ O) R 2 C ( ⁇ O) — or —NHR 1 C ( ⁇ O) — (wherein R 1 and R 2 are the same or different groups, and are alkylene groups having at least 2 carbon atoms, preferably alkylene groups having 2 to 12, more preferably 6 to 10 carbon atoms.
- R 1 and R 2 are the same or different groups, and are alkylene groups having at least 2 carbon atoms, preferably alkylene groups having 2 to 12, more preferably 6 to 10 carbon atoms.
- a typical example is a polyamide having repeating monomer units represented by.) Or a combination thereof.
- aliphatic polyamide examples include polytetramethylene adipamide (polyamide 46), polyhexamethylene adipamide (polyamide 66), polyhexamethylene azelainamide (polyamide 69), polyhexamethylene sebacinamide (polyamide 610).
- Polyhexamethylene dodecandiamide (polyamide 612), polyheptamethylene pimelinamide (polyamide 77), polyoctamethylene suberamide (polyamide 88), polynonamethylene azelite amide (polyamide 99), and polydecamethylene azelainamide (
- polyamide 109 poly(4-aminobutyric acid) (polyamide 4), poly (6-aminohexanoic acid) Polyamide 6), poly (7-aminoheptanoic acid) (polyamide 7), poly (8-aminooctanoic acid) (polyamide 8), poly (9-aminononanoic acid) (polyamide 9), poly (10-aminodecanoic acid) ( Fat synthesized by polycondensation reaction of ⁇ -amino acids such as polyamide 109), poly (4-aminobutyric acid) (polyamide 4), poly (6-aminohexanoic acid) Polyamide 6), poly (7-a
- a copolymer obtained by an arbitrary combination of repeating units of aliphatic polyamide can also be used.
- aliphatic polyamide copolymers include caprolactam / hexamethylene adipamide copolymer (nylon 6/6, 6), hexamethylene adipamide / caprolactam copolymer (nylon 6, 6). / 6), hexamethylene adipamide / hexamethylene-azelainamide copolymer (nylon 6, 6/6, 9) and the like.
- the melting point of these aliphatic polyamides can be adjusted by controlling the molecular weight, as with aromatic polyamides. By increasing the molecular weight, the melting point can be raised, and conversely, by lowering the molecular weight, the melting point can be lowered.
- aliphatic polyamides one selected from the group consisting of polyamide 66, polyamide 610 and polyamide 612 from the viewpoint of giving excellent strength even after water absorption and from the viewpoint of easy availability of commercial products having a melting point in the above-mentioned range.
- the above is preferable, and polyamide 612 is more preferable. Therefore, in the aliphatic polyamide component according to the present invention, 90% by mass or more is preferably composed of these three types, more preferably 95% by mass or more is composed of these three types, and 99% by mass. It is even more preferable that the above is composed of these three types, and it is even more preferable that 100% by mass is composed of these three types.
- 90% by mass or more is preferably composed of polyamide 612, more preferably 95% by mass or more is composed of polyamide 612, and 99% by mass or more is polyamide. It is even more preferable that it is composed of 612, and it is even more preferable that 100% by mass is composed of polyamide 612.
- the concentration of the reinforcing fiber is preferably 45% by mass or more, and more preferably 50% by mass or more. However, if the concentration of the reinforcing fiber is too high, the moldability deteriorates and the strength also decreases. Therefore, the concentration of the reinforcing fiber in the total mass of the polyamide resin and the reinforcing fiber is preferably 70% by mass or less, More preferably, it is 60% by mass or less.
- the reinforcing fiber used in the present invention is not limited.
- organic fibers such as carbon fiber and aramid fiber
- glass fiber e.g, glass fiber, acicular wollastonite, whisker (eg, calcium titanate whisker, calcium carbonate).
- whisker eg, calcium titanate whisker, calcium carbonate
- Inorganic fibers such as whiskers and aluminum borate whiskers
- the average fiber diameter before compounding with the resin is preferably about 3 to 20 ⁇ m, more preferably about 5 to 12 ⁇ m.
- the average fiber length before compounding with the resin is preferably about 1 mm to 10 mm, and more preferably about 3 mm to 6 mm.
- the fiber diameter refers to the diameter when the cross-sectional area of the reinforcing fiber is obtained and the cross-sectional area is calculated as a perfect circle.
- the average fiber length of the reinforcing fibers is generally 1/10 to 1/20, for example, 0.1 to 1 mm, typically 0.1 to 0.5 mm.
- the total content of the polyamide resin and the reinforcing fibers in the polyamide resin composition is preferably 90% by mass or more, more preferably 95% by mass or more from the viewpoint of achieving a desired strength.
- Polyamide resins are susceptible to yellowing and thus have low color reproducibility, but color reproducibility can be enhanced by adding pigments.
- the content of the pigment in the polyamide resin composition is preferably 0.5% by mass or more with respect to the total mass of the polyamide resin and the reinforcing fiber, and is 1.0% by mass or more. Is more preferable.
- the content of the pigment in the polyamide resin composition is preferably less than 5.0% by mass with respect to the total mass of the polyamide resin and the reinforcing fibers, and is 4.5% by mass or less, from the viewpoint of dark dyeability. More preferably. If there are too many pigments, white will be too strong, for example, red will become pink, and it will be difficult to express dark colors.
- the pigment include, but are not limited to, zinc sulfide, antimony oxide, titanium oxide, and zinc oxide. Zinc sulfide is preferable from the viewpoint of safety.
- common additives such as a heat resistance stabilizer, a weather resistance, a hydrolysis resistance, and an antioxidant are, for example, 10.0% by mass or less in total, typically 5% by mass or less, and more. Typically, you may add so that it may become 2 mass% or less.
- a metal salt of a fatty acid having 20 to 40 carbon atoms preferably a metal salt of montanic acid
- the metal montanate include calcium montanate, sodium montanate, zinc montanate, lithium montanate, magnesium montanate, and aluminum montanate.
- the content of the fatty acid salt is preferably 0.1 to 2.0 parts by mass with respect to 100 parts by mass in total of the polyamide resin and the reinforcing fibers.
- the content of the fatty acid salt is more preferably 0.3 to 1.0 part by mass with respect to 100 parts by mass in total of the polyamide resin and the reinforcing fiber.
- melt flow rate varies depending on the molecular weight of the polyamide and the content of reinforcing fibers.
- MFR melt flow rate
- the MFR is excessively low, the flow rate is deteriorated, so that the filling rate when the fastener part is injection-molded is deteriorated, resulting in problems such as a decrease in yield and a prolonged molding cycle.
- a preferred MFR is 5 to 40 g / 10 min, a more preferred MFR is 8 to 30 g / 10 min, and an even more preferred MFR is 10 to 25 g / 10 min.
- MFR is measured at 280 ° C. and a measurement load of 2.16 kg according to JIS K7210 (Method A).
- polyamide resin composition suitable for slider body Among the fastener parts, it is preferable to use the above-mentioned polyamide resin mainly composed of aromatic polyamide for small parts such as a pull handle, a pull cover, an upper stopper, a lower stopper and an element.
- the slider body has a strong demand for not only strength but also reciprocating opening / closing durability.
- the slider body is a relatively large part among the fastener parts, and since the difficulty at the time of injection molding is small, a material having a relatively high melting point can also be used. By using a material having a high melting point, an improvement in strength can be expected. And since it is a comparatively big component, the strength improvement effect by a reinforced fiber is easy to be exhibited, and it is not necessary to worry about the strength fall by the water absorption at the time of dyeing.
- the polyamide resin composition suitable for the slider body according to the present invention contains a polyamide resin and reinforcing fibers, and the total mass of the polyamide resin and reinforcing fibers accounts for 90% by mass or more of the composition,
- the ratio of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is 60% by mass or more, and the content of the reinforcing fiber in the total mass of the polyamide resin and the reinforcing fiber is 45 to 70% by mass. is there.
- an aliphatic polyamide having a melting point of 220 to 310 ° C. can be used. Since the slider body is a relatively large part, it can be injection-molded even at a high melting point. However, if an aliphatic polyamide having an excessively high melting point is used, the molding temperature becomes high and yellowing tends to occur.
- An aliphatic polyamide having a melting point of 305 ° C. or lower is more preferably used, and an aliphatic polyamide having a melting point of 300 ° C. or lower is still more preferable.
- low melting point polyamide resin has fewer amide bonds per unit molecular structure and tends to be lower in strength and rigidity due to its flexible chain, so use aliphatic polyamide with melting point of 220 ° C or higher. It is preferable to use an aliphatic polyamide having a melting point of 240 ° C. or higher, and it is even more preferable to use an aliphatic polyamide having a melting point of 250 ° C. or higher.
- the proportion of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is 60% by mass or more.
- the reciprocating open / close durability can be improved by increasing the blending ratio of the aliphatic polyamide.
- the slider body is the part that receives friction most frequently due to sliding with the element, and it is important to improve the reciprocating durability. From the viewpoint of enhancing the reciprocating durability, the proportion of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is preferably 65% by mass or more.
- the strength of the fastener part can be improved by blending an aromatic polyamide having a predetermined melting point. Therefore, the proportion of the aliphatic polyamide having a melting point of 220 to 310 ° C. in the polyamide resin is preferably 90% by mass or less, more preferably 80% by mass or less, and even more preferably 75% by mass or less.
- the melting point of the aliphatic polyamide is the endothermic peak top temperature when the endotherm is measured by DSC (differential scanning calorimeter).
- DSC differential scanning calorimeter
- the melting point is measured based on the aliphatic polyamide having the highest melting point.
- the melting points of the respective polyamide resins are all within the above-described range.
- Aromatic polyamide In one embodiment of the polyamide resin composition suitable for the slider body according to the present invention, an aromatic polyamide having a melting point of 230 to 310 ° C. can be blended. The strength improvement effect can be expected by blending the aromatic polyamide.
- the slider body Since the slider body is a relatively large part, it can be injection-molded even at a high melting point. However, if an aromatic polyamide having an excessively high melting point is used, the molding temperature becomes high and yellowing tends to occur.
- An aromatic polyamide having a melting point of 305 ° C. or lower is more preferable, and an aromatic polyamide having a melting point of 300 ° C. or lower is even more preferable.
- polyamide resins with a low melting point have fewer amide bonds per unit molecular structure and tend to be flexible chains, which tend to reduce strength and rigidity.
- Use aromatic polyamides with a melting point of 230 ° C or higher It is preferable to use an aromatic polyamide having a melting point of 240 ° C. or higher, and it is even more preferable to use an aromatic polyamide having a melting point of 250 ° C. or higher.
- the ratio of the aromatic polyamide having a melting point of 230 to 310 ° C. in the polyamide resin is 10% by mass or more.
- the ratio of the aromatic polyamide having a melting point of 230 to 310 ° C. in the polyamide resin is preferably 20% by mass or more, and more preferably 25% by mass or more.
- the ratio of the aromatic polyamide having a melting point of 230 to 310 ° C. in the polyamide resin is 40% by mass. The following is preferable, and 35 mass% or less is more preferable.
- the melting point of the aromatic polyamide is the temperature at the top of the endothermic peak when the endothermic amount is measured by DSC (differential scanning calorimeter).
- DSC differential scanning calorimeter
- the endothermic peak top temperature on the highest temperature side is defined as the melting point. Therefore, when a plurality of aromatic polyamides are used, the melting point is measured based on the aromatic polyamide having the highest melting point. However, even when a plurality of aromatic polyamides are used, it is preferable that the melting points of the respective polyamide resins are all within the above-described range.
- the strength of the slider body can be enhanced.
- the description regarding the specific aspect and content of a reinforced fiber is as having mentioned above in the paragraph of "1.
- the polyamide resin composition suitable for a small component is preferably 90% by mass or more, more preferably 95% by mass or more from the viewpoint of achieving a desired strength. is there.
- Polyamide resins are susceptible to yellowing and thus have low color reproducibility, but color reproducibility can be enhanced by adding pigments.
- the content of the pigment in the polyamide resin composition is preferably 0.5% by mass or more with respect to the total mass of the polyamide resin and the reinforcing fiber, and is 1.0% by mass or more. Is more preferable.
- the content of the pigment in the polyamide resin composition is preferably less than 5.0% by mass with respect to the total mass of the polyamide resin and the reinforcing fibers, and is 4.5% by mass or less, from the viewpoint of dark dyeability. More preferably. If there are too many pigments, white will be too strong, for example, red will become pink, and it will be difficult to express dark colors.
- the pigment include, but are not limited to, zinc sulfide, antimony oxide, titanium oxide, and zinc oxide. Zinc sulfide is preferable from the viewpoint of safety.
- common additives such as a heat resistance stabilizer, a weather resistance, a hydrolysis resistance, and an antioxidant are, for example, 10.0% by mass or less in total, typically 5% by mass or less, and more. Typically, you may add so that it may become 2 mass% or less.
- slide fastener Various slide fastener parts can be produced using the polyamide resin composition according to the present invention as a material, and these can be assembled into a slide fastener.
- Polyamide resin composition suitable for small parts is used as a material, and small parts such as a handle, a handle cover, a top stopper, a bottom stopper, and an element are formed by injection molding. Parts can be made.
- a fastener stringer in which a plurality of elements are attached to the side edge of the fastener tape to form an element row can also be produced.
- the slider body can be manufactured by injection molding using the polyamide resin composition described in the paragraph of “2.
- Polyamide resin composition suitable for slider body as a material.
- the slide fastener includes a handle and a handle cover made of the polyamide resin composition described in the paragraph of “1.
- Polyamide resin composition suitable for small parts A slider having a slider body made of the polyamide resin composition described in the paragraph “A polyamide resin composition suitable for a slider body” can be produced.
- a slide fastener including the slider can be manufactured.
- the slider is advantageous with respect to the slider overall strength and the torsional strength after dyeing, and is excellent in reciprocating open / close durability.
- the slider 20 is connected to the slider body 21 and the upper wing plate 21a side of the slider body 21, and a handle 23 that is clamped by the user when the slider 20 is slidably displaced to engage or separate the element row.
- a handle cover 24 for sandwiching the one end 22 of the handle 23 between the upper wing plate 21a and rotatably holding the handle 2 at the one end 22 on the outer surface of the upper wing plate 21a.
- a metallic elastic plate member 25 is sandwiched between the upper blade 21a and the handle cover 24 to provide an automatic stop function.
- the upper wing plate 21a and the handle cover 24 are connected to each other by a pair of claw portions 26a, 26b protruding from the outer surface of the upper wing plate 21a, a pair of claw portions 27a formed at the front and rear portions of the handle cover 24, This is done by engaging with 27b.
- thermoplastic polyether resins such as polyoxymethylene (POM), thermoplastic polyester resins such as polybutylene terephthalate (PBT), thermoplastic polyolefin resins such as polypropylene, polyvinyl chloride (PVC)
- a slide fastener can be constructed in combination with elements made of various materials such as thermoplastic polyvinyl resins such as thermoplastic fluororesins such as ethylene tetrafluoroethylene.
- polyamide resin composition suitable for small parts as a material, an element having high strength after dyeing can be provided.
- the material of the slider body to be combined with the element is preferably the polyamide resin composition described in the paragraph “2.
- thermoplastic polyether resin such as polyoxymethylene (POM), thermoplastic polyester resin such as polybutylene terephthalate (PBT), thermoplastic polyolefin resin such as polypropylene, thermoplastic polyvinyl resin such as polyvinyl chloride (PVC)
- POM polyoxymethylene
- PBT polybutylene terephthalate
- PVC polyvinyl resin
- Building slide fasteners in combination with resin sliders made of various materials such as thermoplastic fluororesins such as ethylenetetrafluoroethylene, metal sliders such as stainless steel, zinc, copper, iron, aluminum, and alloys using these Can do.
- polyamide and reinforcing fibers which are components of the resin composition, are sufficiently kneaded so that the components are not biased.
- a single screw extruder, a twin screw extruder, a kneader or the like can be used.
- the resin composition after kneading is injection-molded using a mold having a predetermined fastener part shape, a non-dyed slide fastener part is completed.
- Dyeing can be applied to unstained parts for slide fasteners.
- the dyeing method There is no particular limitation on the dyeing method, but dip dyeing and printing are typical.
- the dye is not limited, but a metal-containing dye, an acid dye, a selenium dye, and a disperse dye are suitable.
- an acid dye can be particularly suitably used because of good dyeability and fastness.
- Dyeing can be performed simultaneously with other components of the slide fastener or can be performed separately.
- metal plating can be applied to the fastener part according to the present invention.
- the metal plating include, but are not limited to, chromium plating, nickel plating, copper plating, gold plating, brass plating, and other alloy plating.
- the method of metal plating There is no particular limitation on the method of metal plating.
- electroplating preferably electroless plating is performed before electroplating
- dry plating such as vacuum deposition, sputtering, or ion plating is appropriately performed. Just do it. You may combine these methods.
- an electroplating method capable of firmly covering even the inside of a small and complex shaped part is preferable, and it is more preferable to perform electroplating after preliminarily performing electroless plating.
- handle, handle cover and element The following were prepared as a polyamide resin for a handle, a handle cover and an element.
- MXD6 melting point: 235 ° C., water absorption: 5.5% (catalog value)
- PA610 melting point: 225 ° C., water absorption: 4.0% (catalog value)
- PA612 melting point: 212 ° C, water absorption: 3.0% (catalog value)
- PA6T (melting point: 295 ° C., water absorption: 6.2% (catalog value))
- PA6 (melting point: 225 ° C, water absorption: 10.7% (catalog value))
- Glass fibers (average fiber diameter: 11 ⁇ m, average fiber length before molding: 3 mm, average fiber length after molding: 0.25 mm) were used as reinforcing fibers.
- the polyamide resin and glass fiber are kneaded using a twin-screw extruder so as to have each blending ratio (mass basis) shown in Table 1, and then the molten resin is extruded into a strand shape and solidified in a cooling water bath. Then, pellets of each resin composition were prepared by cutting the strands with a pelletizer. The pellets were injection-molded to produce a fastener stringer in which the element rows of the form shown in FIG. 1 (registered trademark: screwlon) (M class size defined in JIS S3015: 2007) were attached to the side edges of the fastener tape. . Similarly, the handle cover and the handle having the shape shown in FIG. 2 were produced from the pellets by injection molding. Thereafter, these parts were immersed in water at 23 ° C. for 72 hours.
- a slider having the shape shown in FIG. 3 was assembled using the handle after absorbing water, the handle cover, and the slider body. Also, the fastener chain was assembled by meshing the element rows of a pair of fastener stringers.
- Example 1 since the blending of the polyamide resin composition was appropriate, the slider overall strength after water absorption was 169 N or more, the slider pulling torsion strength after water absorption was 58 N or more, and the chain lateral pulling strength after water absorption was 741 N or more. And had high mechanical strength.
- Example 3 and Example 4 to which a small amount of aliphatic polyamide was added were excellent in that the slider overall strength after water absorption protruded.
- the transverse pulling strength is about 750 N, it can be said that the element made of the polyamide resin composition according to the present invention exhibits extremely excellent strength.
- Comparative Example 1 since the ratio of the glass fiber was too small, sufficient slider overall strength and chain lateral pulling strength were not obtained after water absorption.
- Comparative Example 2 the ratio of MXD6, which is an aromatic polyamide, was too small, and after absorbing water, the slider overall strength, the pulling torsional strength, and the chain lateral pulling strength were not all satisfactory.
- Comparative Example 3 the use of an aromatic polyamide having a high melting point deteriorated the fluidity, and it was not possible to injection mold an element row which is a particularly small part. Since Comparative Example 4 used PA6 which is an aliphatic polyamide, the slider overall strength, the pulling torsional strength, and the chain lateral pulling strength were not all satisfactory.
- the reciprocating endurance (JIS S3015: 2007) of the slider in Examples 1 to 5 was 1500 times or more.
- MXD6 was blended in the slider body instead of PA66 and the reciprocating endurance of the slider.
- the abnormality was found in every 100 reciprocations.
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Slide Fasteners (AREA)
Abstract
Description
<1-1 芳香族ポリアミド>
本発明に係るスライドファスナー用ポリアミド樹脂組成物の一実施形態においては、200~250℃の融点をもつ芳香族ポリアミドを使用する点を特徴の一つとして挙げることができる。
本発明に係るスライドファスナー用ポリアミド樹脂組成物の一実施形態においては、吸水率が前述した芳香族ポリアミドよりも小さく、融点が200~250℃である脂肪族ポリアミドを配合することを特徴の一つとして挙げることができる。本発明で使用するポリアミド樹脂においては、芳香族ポリアミドを主成分とすることが特徴の一つであることは先述した通りであるが、所定の脂肪族ポリアミドを副成分として配合することにより、芳香族ポリアミド単独で用いた場合よりも染色後の強度が向上するという利点が得られる。
ポリアミド樹脂組成物中に強化繊維を含有させることで、ファスナー部品の強度を強化することができる。ポリアミドはシランカップリング剤、チタネート系カップリング剤又はアルミネート系カップリング剤などで表面処理することにより、ポリエステルに比べて強化繊維へ親和性向上が見込めるため、強化繊維を多量に添加しても強度を損なうこと無く高剛性化することが可能である。具体的には、ポリアミド樹脂と強化繊維の合計質量中、強化繊維の濃度を45質量%以上とすることが好ましく、50質量%以上とすることがより好ましい。但し、強化繊維の濃度が高すぎると成形性が悪化し、また、強度も低下することから、ポリアミド樹脂と強化繊維の合計質量中の強化繊維の濃度は70質量%以下とするのが好ましく、60%質量以下とするのがより好ましい。
ポリアミド樹脂は黄変しやすいため色再現性が低いが、顔料を添加することで色再現性を高めることができる。一方で、顔料の添加量が多くなると強度が低下したり、白すぎることにより染色時に高濃度色がでない問題があるため高濃度での添加は好ましくない。ポリアミド樹脂組成物中の顔料の含有量は色再現性の観点から、ポリアミド樹脂及び強化繊維の合計質量に対して0.5質量%以上とすることが好ましく、1.0質量%以上とすることがより好ましい。また、ポリアミド樹脂組成物中の顔料の含有量は濃色染色性の観点から、ポリアミド樹脂及び強化繊維の合計質量に対して5.0質量%未満とすることが好ましく、4.5質量%以下とすることがより好ましい。顔料が多すぎると、白色が強すぎるので、例えば赤色がピンク色になってしまい、濃色が表出しにくくなる。顔料の例としては、限定的ではないが、硫化亜鉛、酸化アンチモン、酸化チタン、酸化亜鉛が挙げられ、安全性の観点から硫化亜鉛が好ましい。
本発明においては、使用するポリアミド樹脂組成物のメルトフローレート(MFR)を制御することが好ましい。MFRはポリアミドの分子量や強化繊維の含有量などに影響を受けて変化する。MFRが過度に低くなると流れ性の悪化によりファスナー部品を射出成形する際の充填率が悪くなり、歩留まり低下や成形サイクルの長期化などの問題が生じる。一方、MFRが過剰に高くなると、強度が低下するのみならず、分子量分布の広がりにより流れムラが発生して外観不良となったり、ポリマー成分由来の吸水率の影響により夏場環境の寸法安定性が悪くなったりするなどの問題が発生する。好ましいMFRは5~40g/10分であり、より好ましいMFRは8~30g/10分であり、更により好ましいMFRは10~25g/10分である。本発明においては、MFRはJIS K7210(A法)に準拠して280℃、測定荷重2.16kgで測定する。MFRがこの範囲にある樹脂組成物を用いることにより、成形性及び品質安定性に優れたスライドファスナー用成形部品を高い生産効率で製造することが可能である。
ファスナー部品の中でも、引手、引手カバー、上止め、下止め及びエレメントのような小型部品については、上述した芳香族ポリアミド主体のポリアミド樹脂を使用することが好ましい。しかしながら、スライダー胴体は強度のみならず往復開閉耐久性に対する要請が強い。また、スライダー胴体はファスナー部品の中では比較的大きい部品であり、射出成形時の困難性は小さいことから、比較的融点の高い材料も使用できる。融点の高い材料を使用することで強度の向上が期待できる。そして、比較的大きな部品なので、強化繊維による強度向上効果が発揮されやすく、染色時の吸水による強度の低下も心配する必要はない。
本発明に係るスライダー胴体に好適な脂肪族ポリアミドの一実施形態においては、融点が220~310℃である脂肪族ポリアミドを使用することができる。スライダー胴体は比較的大きな部品のため、高い融点でも射出成形可能であるが、過度に高い融点をもつ脂肪族ポリアミドを使用すると、成形温度が高くなり、黄変しやすくなることから、融点が310℃以下の脂肪族ポリアミドを使用することが好ましく、融点が305℃以下の脂肪族ポリアミドを使用することがより好ましく、融点が300℃以下の脂肪族ポリアミドを使用することが更により好ましい。また、低融点のポリアミド樹脂は単位分子構造当たりのアミド結合の数が少なくなり、フレキシブルな鎖状となるため強度及び剛性が低下する傾向にあるため、融点が220℃以上の脂肪族ポリアミドを使用することが好ましく、融点が240℃以上の脂肪族ポリアミドを使用することがより好ましく、融点が250℃以上の脂肪族ポリアミドを使用することが更により好ましい。
本発明に係るスライダー胴体に好適なポリアミド樹脂組成物の一実施形態においては、融点が230~310℃である芳香族ポリアミドを配合することができる。芳香族ポリアミドを配合することで強度向上効果が期待できる。
ポリアミド樹脂組成物中に強化繊維を含有させることで、スライダー胴体の強度を強化することができる。強化繊維の具体的な態様や含有量に関する説明は「1.小型部品に好適なポリアミド樹脂組成物」の段落で先述した通りである。そして、スライダー胴体においても、ポリアミド樹脂組成物中のポリアミド樹脂と強化繊維の合計含有量は、所望の強度を達成する観点から90質量%以上であることが好ましく、より好ましくは95質量%以上である。
ポリアミド樹脂は黄変しやすいため色再現性が低いが、顔料を添加することで色再現性を高めることができる。一方で、顔料の添加量が多くなると強度が低下したり、白すぎることにより染色時に高濃度色がでない問題があるため高濃度での添加は好ましくない。ポリアミド樹脂組成物中の顔料の含有量は色再現性の観点から、ポリアミド樹脂及び強化繊維の合計質量に対して0.5質量%以上とすることが好ましく、1.0質量%以上とすることがより好ましい。また、ポリアミド樹脂組成物中の顔料の含有量は濃色染色性の観点から、ポリアミド樹脂及び強化繊維の合計質量に対して5.0質量%未満とすることが好ましく、4.5質量%以下とすることがより好ましい。顔料が多すぎると、白色が強すぎるので、例えば赤色がピンク色になってしまい、濃色が表出しにくくなる。顔料の例としては、限定的ではないが、硫化亜鉛、酸化アンチモン、酸化チタン、酸化亜鉛が挙げられ、安全性の観点から硫化亜鉛が好ましい。
本発明に係るポリアミド樹脂組成物を材料として各種のスライドファスナー用部品を作製し、これらを組み立ててスライドファスナーとすることができる。具体的には、「1.小型部品に好適なポリアミド樹脂組成物」の段落で記載したポリアミド樹脂組成物を材料とし、射出成形により、引手、引手カバー、上止め、下止め及びエレメント等の小型部品を作製することができる。ファスナーテープの側縁にエレメントが複数取着されてエレメント列が形成されているファスナーストリンガーを作製することもできる。また、「2.スライダー胴体に好適なポリアミド樹脂組成物」の段落で記載したポリアミド樹脂組成物を材料とし、射出成形により、スライダー胴体を作製することができる。
引手、引手カバー及びエレメント用のポリアミド樹脂として以下を用意した。
・MXD6(融点:235℃、吸水率:5.5%(カタログ値))
・PA610(融点:225℃、吸水率:4.0%(カタログ値))
・PA612(融点:212℃、吸水率:3.0%(カタログ値))
・PA6T(融点:295℃、吸水率:6.2%(カタログ値))
・PA6(融点:225℃、吸水率:10.7%(カタログ値))
PA66(融点:265℃、吸水率:8.8%(カタログ値))とガラス繊維(平均繊維径:11μm、成形前の平均繊維長:3mm、成形後の平均繊維長:0.25mm)をPA66:ガラス繊維=40:60の配合割合(質量基準)となるように、二軸押出機を用いて混練し、その後、溶融樹脂をストランド状に押出し、冷却水槽にて固化させた後、ストランドをペレタイザーでカットすることで、ポリアミド樹脂組成物のペレットを調製した。これを射出成形して、JIS S3015:2007に規定されるM級(チェーン幅が5.5mm以上7.0mm未満)のスライドファスナー用のスライダー胴体を作製した。当該スライダー胴体を72時間23℃の水に浸漬した。
上記で作製した吸水後の引手、引手カバー及びスライダー胴体を用いて、図3に示す形状のスライダーを組み立てた。また、一対のファスナーストリンガーのエレメント列を噛み合わせてファスナーチェーンを組み立てた。
(融点)
各ポリアミド樹脂の融点はDSC(セイコーインスツルメント社製:EXTAR6000)を用いて、先述した定義に基づき、以下の条件で測定した。
・サンプル量:5~10mg
・雰囲気:窒素ガス
・昇温スピード:10℃/min
・測定温度範囲:0~350℃
・リファレンスパン:空
(スライダー及びチェーンの強度)
作製したスライダーに対してはスライダー総合強度、スライダー引手ねじり強度を、作製したスライドファスナーチェーンに対してはチェーン横引き強度試験をそれぞれJIS S3015:2007に準拠して行った。
(MFR)
引手、引手カバー及びエレメント用のポリアミド樹脂組成物について、先述した測定条件によりMFRを測定した。
比較例2は芳香族ポリアミドであるMXD6の割合が少なすぎたことで、吸水後、スライダー総合強度、引手ねじり強度及びチェーン横引き強度が何れも満足行くものとはならなかった。
比較例3は融点の高い芳香族ポリアミドを使用したことで流動性が悪化し、特に小さな部品であるエレメント列を射出成形できなかった。
比較例4は脂肪族ポリアミドであるPA6を用いたことで、スライダー総合強度、引手ねじり強度及びチェーン横引き強度が何れも満足行くものとはならなかった。
11 長尺テープ
12 エレメント
13 スライダー
14 上止め
15 開き具
16 引き手
17 引手カバー
20 スライダー
21 スライダー胴体
21a 上翼板
22 引手の一端部
23 引手
24 引手カバー
25 弾性板状部材
26a、26b スライダー胴体の爪部
27a、27b 引手カバーの爪部
Claims (16)
- ポリアミド樹脂及び強化繊維を含有するスライドファスナー用ポリアミド樹脂組成物であって、ポリアミド樹脂及び強化繊維の合計質量が前記組成物中の90質量%以上を占め、前記ポリアミド樹脂中の融点が200~250℃である芳香族ポリアミドの割合が70質量%を超えており、前記ポリアミド樹脂及び前記強化繊維の合計質量中の前記強化繊維の含有量が45~70質量%であるスライドファスナー用ポリアミド樹脂組成物。
- 前記ポリアミド樹脂中の融点が200~250℃である芳香族ポリアミドの割合が80質量%を超える請求項1に記載のポリアミド樹脂組成物。
- 前記ポリアミド樹脂は吸水率が前記芳香族ポリアミドよりも小さく、融点が200~250℃である脂肪族ポリアミドを更に含有する請求項1又は2に記載のポリアミド樹脂組成物。
- 前記ポリアミド樹脂中の融点が200~250℃であるポリアミドMXD6の割合が70質量%を超える請求項1~3の何れか一項に記載のポリアミド樹脂組成物。
- 前記ポリアミド樹脂中の融点が200~250℃であるポリアミドMXD6の割合が80~95質量%であり、前記ポリアミド樹脂中の吸水率が前記芳香族ポリアミドよりも小さく、融点が200~250℃である脂肪族ポリアミドの割合が5~20質量%である請求項1~4の何れか一項に記載のポリアミド樹脂組成物。
- 前記ポリアミド樹脂組成物のメルトフローレートが10~50g/10分である請求項1~5の何れか一項に記載のポリアミド樹脂組成物。
- 請求項1~6の何れか一項に記載のスライドファスナー用ポリアミド樹脂組成物を材料としたスライドファスナー用部品。
- 引手、引手カバー、上止め、下止め又はエレメントである請求項7に記載のスライドファスナー用部品。
- エレメントである請求項7に記載のスライドファスナー用部品。
- 染色されている請求項7~9の何れか一項に記載のスライドファスナー用部品。
- ファスナーテープの側縁に請求項9に記載のエレメントが複数取着されてエレメント列が形成されているファスナーストリンガー。
- 請求項7~9の何れか一項に記載のスライドファスナー用部品又は請求項11に記載のファスナーストリンガーを備えたスライドファスナー。
- 請求項1~6の何れか一項に記載のスライドファスナー用ポリアミド樹脂組成物を材料とした引手、引手カバー、上止め、下止め及びエレメント列よりなる群から選択される少なくとも1種の部品を備えたスライドファスナー。
- ポリアミド樹脂及び強化繊維を含有するポリアミド樹脂組成物であって、ポリアミド樹脂及び強化繊維の合計質量が前記組成物中の90質量%以上を占め、前記ポリアミド樹脂中の融点が220~310℃である脂肪族ポリアミドの割合が60質量%以上であり、前記ポリアミド樹脂及び前記強化繊維の合計質量中の前記強化繊維の含有量が45~70質量%であるポリアミド樹脂組成物を材料としたスライダー胴体を更に備えた請求項12又は13に記載のスライドファスナー。
- 請求項1~6の何れか一項に記載のスライドファスナー用ポリアミド樹脂組成物を材料とした引手及び引手カバーを備え、更に、ポリアミド樹脂及び強化繊維を含有するポリアミド樹脂組成物であって、ポリアミド樹脂及び強化繊維の合計質量が前記組成物中の90質量%以上を占め、前記ポリアミド樹脂中の融点が220~310℃である脂肪族ポリアミドの割合が60質量%以上であり、前記ポリアミド樹脂及び前記強化繊維の合計質量中の前記強化繊維の含有量が45~70質量%であるポリアミド樹脂組成物を材料としたスライダー胴体を備えた請求項13に記載のスライドファスナー。
- 請求項1~6の何れか一項に記載のスライドファスナー用ポリアミド樹脂組成物を材料としたエレメント列を備え、更に、ポリアミド樹脂及び強化繊維を含有するポリアミド樹脂組成物であって、ポリアミド樹脂及び強化繊維の合計質量が前記組成物中の90質量%以上を占め、前記ポリアミド樹脂中の融点が220~310℃である脂肪族ポリアミドの割合が60質量%以上であり、前記ポリアミド樹脂及び前記強化繊維の合計質量中の前記強化繊維の含有量が45~70質量%であるポリアミド樹脂組成物を材料としたスライダー胴体を備えた請求項13に記載のスライドファスナー。
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US15/123,521 US10064454B2 (en) | 2014-04-09 | 2014-04-09 | Polyamide resin composition for slide fasteners, slide fastener component, and slide fastener provided with same |
CN201480076752.4A CN106061311B (zh) | 2014-04-09 | 2014-04-09 | 拉链用聚酰胺树脂组合物、拉链用部件及具备该部件的拉链 |
JP2016512535A JP6266094B2 (ja) | 2014-04-09 | 2014-04-09 | スライドファスナー用ポリアミド樹脂組成物、スライドファスナー用部品及びそれを備えたスライドファスナー |
PCT/JP2014/060348 WO2015155861A1 (ja) | 2014-04-09 | 2014-04-09 | スライドファスナー用ポリアミド樹脂組成物、スライドファスナー用部品及びそれを備えたスライドファスナー |
TW104111479A TWI558768B (zh) | 2014-04-09 | 2015-04-09 | A polyamide resin composition for a zipper, a zipper member, and a zipper having the same |
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USD818394S1 (en) * | 2016-06-30 | 2018-05-22 | Ideal Fastener (Guangdong) Industries Ltd. | Zipper tooth |
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