This application claims the foreign priority benefit 35 U.S.C. § 119 of Japanese patent application No. 2018-220474 filed on Nov. 26, 2018, the disclosure of which is incorporated herein by reference.
The present invention relates to a core-sheath composite fiber and a method for producing a core-sheath composite fiber.
Core-sheath composite fibers are fibers that adopt a composite structure comprising a core member in the form of a filament and a sheath member wrapped around the core member like a sheath. The core-sheath composite fibers are designed to exert various effects that are hardly achievable by single-structured fibers by combining the core member and the sheath member that have different properties from each other. The core-sheath composite fibers have been utilized not only as materials of fabrics for filters and the like but also in a variety of fields including reinforcement materials for synthetic resin components and so forth.
Japanese Patent Publication No. 5198647 (Patent Document 1) discloses a ceiling material for an automobile comprising a composite fiber containing a high-density polyethylene as a sheath component and polyester as a core component, in which a melting temperature of the sheath component is in a range from 110° C. to 180° C. while a melting temperature of the core component is in a range from 240° C. to 270° C., and a three-dimensional porous network structure is formed by melting the sheath component by application of a high pressure at a high temperature so as to weld the sheath member to a reinforcement fiber.
A possible application of the above-described core-sheath composite fiber is for reinforcement to improve rigidity of a reinforcement target by: molding a cover by welding the core members of the core-sheath composite fibers; and welding the cover to an outer skin of the target. The cover formed from the core-sheath composite fibers includes numerous core members that penetrate the inside, and is therefore expected to have higher rigidity than that of a cover formed from a simple resin sheet. Nonetheless, an attempt to utilize the conventional core-sheath composite fibers for the aforementioned reinforcement application will cause the following problems.
If the melting points of the sheath member and the core member are close to each other, it is more likely to cause a failure in which the core member is also melted in melting the sheath member, and it is therefore difficult to press the core-sheath composite fibers into a composite material, a sheet, or the like. Although the invention according to Patent Document 1 discloses the respective ranges of the melting points of the sheath member and the core member, this invention does not disclose how many degrees Celsius the difference in melting point between the sheath member and the core member should be. While the difference in melting point calculated from the disclosed ranges of the melting points falls within a range from 60° C. to 160° C., the maximum difference of 160° C. is slightly insufficient for easily forming the composite material or the like.
An even more serious problem is deterioration in strength of the core-sheath composite fiber associated with a gap between the melting points of the core member and the sheath member.
The core member and the sheath member need to be attached firmly to each other in order to realize the core-sheath composite fiber that is high in strength and excellent as a reinforcement material. However, if the difference in melting point between the sheath member and the core member is increased in order to improve moldability into the composite material or the like, separation of the sheath member from the core member is more likely to occur on the other hand. The invention according to Patent Document 1 does not cope with this deterioration in strength resulted from the separation of the sheath from the core, and is thought to be deficient in strength for the reinforcement application.
Given the circumstances, it is an object of the present invention to provide a core-sheath composite fiber which is easily moldable into a composite material or the like and is also excellent in strength.
An aspect of the present invention provides a core-sheath composite fiber which includes a core member containing polyamide as a main component, and a sheath member containing modified polyethylene as a main component. Here, the core member has a melting point higher by at least 170° C. than a melting point of the sheath member.
According to the present invention, it is possible to provide a core-sheath composite fiber which is easily moldable into a composite material or the like and is also excellent in strength.
Next, a core-sheath structured filament according to an embodiment of the present invention will be described.
It is to be noted that the present invention is not limited only to the following embodiment.
The core-sheath composite fiber 10 of this embodiment includes a core member 11, and a sheath member 12 that is wrapped around the core member 11. The core-sheath composite fiber 10 is formed by extrusion. Each of the core member 11 and the sheath member 12 of this embodiment has an external shape with a round cross-section. Note that the external shape of the core member is not limited to such a round cross-section but may be an irregular cross-section provided with multiple projections, for instance.
A proportion between the core member 11 and the sheath member 12 in the transverse section taken in a direction perpendicular to a length direction as shown in
The core-sheath composite fiber 10 may adopt an eccentric structure. Nevertheless, the core member 11 is preferably arranged substantially at the center of the sheath member 12 as shown in
A possible application of the core-sheath composite fiber 10 is for reinforcement of a fuel tank of an automobile, for example. An outer skin of the fuel tank or the like frequently comprises polyethylene. Accordingly, a possible operation to improve a welding property of the core-sheath composite fiber 10 to the outer skin is to include polyethylene in the sheath member 12.
However, polyethylene is a substance which generally has a difficulty in establishing a bond with another substance, and it is hard to achieve firm adhesion between the core member 11 and the sheath member 12 that contains polyethylene. Accordingly, the use of polyethylene in the core member 11 may lead to deterioration in rigidity of the core-sheath composite fiber 10 due to separation of the sheath member 12 from the core member 11. In particular, in a case where the core-sheath composite fibers 10 is pressed into a composite material 100 (see
Given the situation, our researchers attempted to realize the core-sheath composite fiber 10 that has a large difference in melting point between the core member 11 and the sheath member 12 while having the high rigidity as well, by using modified polyethylene prepared by adding an unsaturated functional group to polyethylene so as to establish hydrogen bonding between the functional group and the sheath member 12.
The core-sheath composite fiber 10 prepared by adopting polyamide as the core member 11 and adopting maleic acid-modified polyethylene as the sheath member 12 is used as an example. Meanwhile, a core-sheath composite fiber prepared by adopting polyamide as the core member 11 and adopting polyethylene as the sheath member 12 is used as a comparative example.
Each of the two core-sheath composite fibers 10 is fixed onto two rollers 2 as shown in
As a result of the measurement, the displacement of the core-sheath composite fiber 10 of the comparative example was 2.140 mm. On the other hand, the displacement of the core-sheath composite fiber 10 of the example was 1.762 mm. The comparison of the two fibers reveals that the rigidity of the core-sheath composite fiber 10 of the example prepared by adopting maleic acid-modified polyethylene as the sheath member 12 is improved by 17% as compared to the core-sheath composite fiber 10 of the comparative example prepared by adopting unmodified polyethylene as the sheath member 12.
Based on the above-mentioned result, polyamide is used as a main component of the core member 11 of the core-sheath composite fiber 10 and modified polyethylene is used as a main component of the sheath member 12 thereof. Note that the main component of the core member 11 means a content in an amount of 40% by mass or more with respect to total components of the core member 11. The main component of the sheath member 12 means a content in an amount of 40% by mass or more with respect to total components of the sheath member 12.
A difference in melting point between the core member 11 and the sheath member 12 is equal to or above 170° C. or preferably equal to or above 180° C.
With the difference in melting point equal to or above 170° C., a failure of melting the core member 11 at the same time as melting the sheath member 12 is less likely to occur, and it is easier to press into the composite material 100 (see
Accordingly, an appropriate combination of polyamide as the main component of the core member 11 and modified polyethylene as the main component of the sheath member 12 of this embodiment are selected such that the difference in melting point between these components becomes equal to or above 170° C.
Now, details of respective components of the core member and the sheath member will be described below.
While polyamide constituting the main component of the core member 11 of this embodiment is not limited to a particular composition as long as the difference in melting point between polyamide and modified polyethylene serving as the main component of the sheath member 12 is equal to or above 170° C., this polyamide preferably has high rigidity in light of its intended use as the reinforcement member. Examples of available polyamide compositions include polyamide 6, polyamide 12, polyamide 66, and so forth.
Modified polyethylene constituting the main component of the sheath member 12 of this embodiment is not limited to a particular composition as long as such a composition can be melted in the course of blow molding into the fuel tank or the like being a target for the welding, and as far as the composition has a melting point that provides the difference in melting point from the polyamide composition being the main component of the core member 11, which is equal to or above 170° C., and the composition is also capable of establishing the hydrogen bonding with the polyamide composition.
An example of a method of obtaining such modified polyethylene is called graft modification. This is a method of attaching an unsaturated functional group to a carbon radical that is generated by cleaving the carbon-hydrogen bond in polyethylene. The carbon radical can be generated by electron beam irradiation or ionizing radiation irradiation, or by use of radical generators such as organic and inorganic peroxides.
The functional group to be used for the modification can be selected from a carboxyl group, an amino group, a hydroxyl group, a silanol group, and the like. Among these functional groups, the hydroxyl group is preferable and the carboxyl group is more preferable.
Examples of a structural unit having the functional group include structural units deriving from compounds such as unsaturated carboxylic acid or a derivative thereof, an ethylene-based unsaturated compound having a hydroxyl group, an ethylene-based unsaturated compound having an amino group, and an organic silicon compound having a vinyl group. Among these structural units, the ethylene-based unsaturated compound having the hydroxyl group is preferable and the unsaturated carboxylic acid or the derivative thereof is more preferable.
Examples of the unsaturated carboxylic acid or the derivative thereof include an unsaturated compound having one or more carboxylic groups, an ester of alkyl alcohol and a compound having a carboxylic group, an unsaturated compound having one or more carboxylic anhydride groups, etc.
Examples of the unsaturated carboxylic acid include acrylic acid, maleic acid, fumaric acid, tetrahydrophthalic acid, itaconic acid, citraconic acid, crotonic acid, isocrotonic acid, Nadic (registered trademark) acid (endo-cis-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid), etc.
Examples of the derivative of the unsaturated carboxylic acid include maleimide, maleic anhydride, citraconic anhydride, monomethyl maleate, dimethyl maleate, glycidyl maleate, etc.
These unsaturated carbonic acids and/or the derivatives thereof can be used alone or in combination of two or more of them. Among them, acrylic acid is preferable and maleic anhydride is more preferable in light of its high reactivity.
The multiple core-sheath composite fibers 10 are arranged into a bundle as shown in an upper part of
When the core-sheath composite fibers 10 are formed into the composite material 100 as described above, it is easier to form such composite materials 100 into a sheet 101 (see
The heating method is not limited to a particular method, and methods such as heating with an IR (infrared) heater, heating with hot-air, heating with a hot plate, and the like are conceivable. Among them, the IR heater or the hot-air heating is preferable from the viewpoints of low cost and simplicity.
While the methods involving the IR heater and the hot-air heating have the low-cost benefits on one hand, these methods face a difficulty in temperature control because a difference in temperature is prone to occur due to a difference in distance from a heat source. Nonetheless, according to the core-sheath composite fibers 10 of this embodiment, the difference in melting point between the core member 11 and the sheath member 12 is equal to or more than 170° C. Hence, the core members 11 are less likely to be melted even if the temperature of the sheath members 12 near the heat source may exceed the required temperature as a consequence of continuous heating until the melting of the sheath members 12 located away from the heat source. Thus, the core-sheath composite fibers 10 of the present invention can be formed into the composite material 100 easily at low costs without requiring precise temperature control as a consequence of using the inexpensive measures such as the IR heater and the hot-air heating.
The sheet 101 shown in
The above-described sheet 101 can be formed into a cover 102 more easily than forming the core-sheath composite fibers 10 directly into the cover 102 which is closely attached to the outer skin of the fuel tank or the like. The fuel tank or the like generally has a complicated shape, and a high level of workability is an important factor for forming the cover 102 that has an identical shape to the outside of the fuel tank or the like and is capable of being closely attached thereto.
The fuel tank includes a tank body T and two covers 102. Although the tank body T and the covers 102 are separated in
First, as shown in
Next, as shown in
When the parison P comes into contact with the covers 102, portions of the covers 102 in contact with the parison P are melted by the heat of the parison P. As a consequence, the tank body T (the parison P) and the covers 102 are welded. Here, the temperature of the parison P is set preferably in a range from 160° C. to 190° C. or more preferably in a range from 180° C. to 190° C.
It is understood that the foregoing description is that of the preferred embodiments of the invention and that various changes and modifications may be made thereto without departing from the spirit and scope of the invention as defined in the appended claims.
Number | Date | Country | Kind |
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2018-220474 | Nov 2018 | JP | national |