WO2017159583A1 - エアバッグ用コーティング基布およびその製造方法 - Google Patents
エアバッグ用コーティング基布およびその製造方法 Download PDFInfo
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- WO2017159583A1 WO2017159583A1 PCT/JP2017/009865 JP2017009865W WO2017159583A1 WO 2017159583 A1 WO2017159583 A1 WO 2017159583A1 JP 2017009865 W JP2017009865 W JP 2017009865W WO 2017159583 A1 WO2017159583 A1 WO 2017159583A1
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- base fabric
- knife
- fabric
- coating
- resin
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/23—Inflatable members
- B60R21/235—Inflatable members characterised by their material
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
- D06N3/0006—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using woven fabrics
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0086—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique
- D06N3/0088—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique by directly applying the resin
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/128—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with silicon polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/23—Inflatable members
- B60R21/235—Inflatable members characterised by their material
- B60R2021/23504—Inflatable members characterised by their material characterised by material
- B60R2021/23509—Fabric
- B60R2021/23514—Fabric coated fabric
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2209/00—Properties of the materials
- D06N2209/10—Properties of the materials having mechanical properties
- D06N2209/103—Resistant to mechanical forces, e.g. shock, impact, puncture, flexion, shear, compression, tear
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2211/00—Specially adapted uses
- D06N2211/12—Decorative or sun protection articles
- D06N2211/26—Vehicles, transportation
- D06N2211/268—Airbags
Definitions
- the present invention relates to a coating base fabric used for an automobile airbag, and more specifically, an excellent quality coating base fabric for an airbag and a coating base for an airbag with less physical property variation in the width direction of the base fabric and less adhesive ball defects. It is related with the manufacturing method of cloth.
- airbags which have been rapidly installed as one of the safety parts of automobiles, detect high-pressure, high-pressure gas from the inflator when a car crash occurs. It is used for the purpose of preventing and protecting the body of a driver or passenger, particularly the head, from colliding with a handle, a windshield, a door glass or the like by rapidly deploying an airbag.
- automobile airbags are not only used for driver seats and passenger seats, but also practically used for knee airbags, side airbags, curtain airbags, etc., and it is common to install a plurality of airbags. ing.
- a knife-on-air method also called a floating knife coating method
- the resin surrounding the knife accumulates, and it may fall on the base fabric, resulting in a paste ball defect in which a ball-shaped resin adheres.
- a paste ball defect As a matter of quality.
- Patent Document 1 As a coating base fabric for an airbag, the contact pressure between the knife and the fabric was applied within a range of 1 to 15 N / cm, and the base fabric tension was applied within a range of 500 to 3000 N / m.
- Patent Document 1 An example is disclosed (Patent Document 1). The purpose is to make the resin coating width on the base fabric appropriate by adjusting the contact pressure between the knife blade and the fabric and the tension of the fabric within the specified range. No consideration is given to the drawbacks or tear strength, which has a large impact on the burst when the airbag is deployed.
- Patent Document 2 discloses a technique for applying a higher tension to the ear portion (the end region of the base fabric) than the central portion in the width direction of the base base fabric.
- a method for applying a high tension to the ear it is disclosed to install an equipment called a third support.
- a third support it is considered possible to apply a constant tension in the width direction by this method, since it is applied in a state in which the cloth is bent, not only the coated stripe at the bent portion is likely to occur, but also the bending is included. A tension difference in the width direction was generated, and there was a risk of variations in tear strength in the width direction.
- the object of the present invention is to provide a coating base fabric for an air bag, which is not solved by the prior art and has little difference in physical properties between the elimination of glue ball defects and the tear strength in the width direction of the base fabric.
- the coating base fabric for an airbag of the present invention that can solve the above-described problems has the following configuration. That is, the present invention 1.
- the coating base fabric for an air bag as described in 1 above, wherein the coating amount of the elastomer resin is 15 to 50 g / m 2 . 3. 3.
- the coated base fabric for airbags of the present invention can provide a coated base fabric for airbags with few glue ball defects and a small difference in physical properties of tear strength in the width direction of the base fabric.
- even a curtain airbag that requires particularly high internal pressure retention performance and a wide base fabric area can provide a coating base fabric for an airbag that is excellent in reliability of deployment performance, quality, and cost.
- the woven fabric composed of synthetic fiber filaments means a woven fabric woven using synthetic fiber filament yarns.
- the woven fabric is excellent in that it is excellent in mechanical strength and can be reduced in thickness.
- plain weave, twill weave, satin weave, and these changed weaves, multiaxial weaves, etc. can be applied, and plain fabrics that are superior in mechanical strength are particularly preferable.
- Examples of synthetic fibers include aliphatic polyamide fibers such as nylon 66, nylon 6, nylon 46, and nylon 12, aromatic polyamide fibers such as aramid fibers, and polyester fibers such as polyethylene terephthalate, polytrimethylene terephthalate, and polybutylene terephthalate. used.
- Other examples include wholly aromatic polyester fibers, polyparaphenine / benzobis / oxazole fibers (PBO fibers), ultrahigh molecular weight polyethylene fibers, polyphenylene sulfide fibers, and polyether ketone fibers.
- polyester fiber and polyamide fiber are preferable, and polyamide 66 is particularly preferable. Further, these fibers may be obtained from raw materials that are partially or wholly reused.
- these synthetic fibers may contain various additives in order to improve process passability in the raw yarn manufacturing process and the post-processing process.
- the additive include an antioxidant, a heat stabilizer, a smoothing agent, an antistatic agent, a thickener, a flame retardant, and the like.
- the synthetic fiber may be an original yarn or dyed after yarn production. Further, the cross section of the single yarn may be an irregular cross section in addition to a normal round cross section. As the synthetic fiber, it is preferable to use a multifilament yarn having 72 filaments or more from the viewpoint of flexibility and smoothness of the coating surface.
- the base water used has a boiling water shrinkage of 5 to 10% because a high-quality base fabric with less wrinkles can be obtained.
- the boiling water shrinkage of the raw yarn is less than 5%, even if the raw yarn shrinks during processing after weaving, the voids of the fabric before coating (hereinafter referred to as the base base fabric) are not filled, resulting in air permeability. As a result, the base fabric is likely to cause a rise in yarn and misalignment of yarns.
- the shrinkage rate exceeds 10%, the voids are filled more in the post-processing, but the yarn forming property becomes extremely difficult. More preferably, it is 5.5 to 9.5%.
- Existing looms such as water jet loom, air jet loom, rapier loom, etc. can be applied to the loom used when weaving the base base fabric, and known devices such as jacquard can be used as the opening machine.
- the woven base fabric may be subjected to scouring and washing to remove glue, excess oil component and dirt, but may be finished into a woven fabric without scouring.
- the woven fabric may be passed through a hot water bath at 70 to 98 ° C. for a period of 1 second to 10 minutes for the purpose of shrinking.
- a hot water bath at 70 to 98 ° C. for a period of 1 second to 10 minutes for the purpose of shrinking.
- it is preferable to apply a traveling tension only in the traveling direction and not expand in the weft direction, but contract the weft. Thereafter, it can be dried to a predetermined moisture content in the drying step.
- a base base fabric for a coating base fabric can be obtained.
- the coating resin applied to the base fabric is preferably an elastomer resin having heat resistance, cold resistance and flame retardancy, and most preferably a silicone resin.
- silicone resins include addition polymerization type silicone rubber.
- dimethyl silicone rubber, methyl vinyl silicone rubber, methyl phenyl silicone rubber, trimethyl silicone rubber, fluoro silicone rubber, methyl silicone resin, methyl phenyl silicone resin, methyl vinyl silicone resin, epoxy modified silicone resin, acrylic modified silicone resin, polyester modified A silicone resin etc. are mentioned.
- methyl vinyl silicone rubber is preferable because it has rubber elasticity after curing, is excellent in strength and elongation, and is advantageous in terms of cost.
- the resin viscosity of the silicone resin used is preferably 5000 to 40000 mPa ⁇ sec, more preferably 7000 to 38000 mPa ⁇ sec.
- the resin viscosity exceeds 40,000 mPa ⁇ sec, it is necessary to apply a tension in the warp direction more than necessary to achieve a coating amount of 50 g / m 2 or less, which is not preferable because it damages the base fabric.
- the viscosity is less than 5000 mPa ⁇ sec, the resin penetrates into the base base fabric, and a desired air permeability cannot be achieved.
- Any solvent-based or solvent-free system may be used as long as the viscosity can be adjusted within the above range, but a solvent-free system is preferable in consideration of the influence on the environment.
- the viscosity of the resin composition containing additives other than the resin that is, the viscosity of the resin actually applied to the base base fabric is referred to as “resin viscosity”.
- the alkenyl group-containing polysiloxane constituting the resin layer of the coating base fabric of the present invention has two alkenyl groups bonded to silicon atoms in one molecule in order to form a silicone resin film having rubber elasticity after the resin is cured. It is necessary to contain above.
- Examples of the position of the silicon atom to which the alkenyl group is bonded in the alkenyl group-containing polysiloxane skeleton include the terminal of the molecular chain and / or the middle of the molecular chain (non-terminal of the molecular chain). A straight chain containing a group is preferred.
- the viscosity of the alkenyl group-containing polysiloxane component at 25 ° C. is preferably 10 to 50 Pa ⁇ sec, and preferably 15 to 45 Pa from the viewpoint of physical properties such as adhesion of the cured product to fibers, rubber strength, blocking resistance, and workability. -Sec is more preferable.
- the organohydrogenpolysiloxane constituting the silicone-based resin reacts with the alkenyl group-containing polysiloxane through a hydrosilylation addition reaction to act as a crosslinking agent.
- the molecular structure of the organohydrogenpolysiloxane may be, for example, a linear, cyclic, branched, or three-dimensional network structure.
- Organohydrogenpolysiloxane has at least two (usually about 2 to 300) or more hydrogen atoms bonded to silicon atoms in one molecule.
- the hydrogen atoms bonded to these silicon atoms are located only at either the molecular chain end or in the middle of the molecular chain (ie, the molecular chain non-terminal). Or both.
- the organohydrogenpolysiloxane (B) preferably has a viscosity at 25 ° C. of 0.1 to 1,000 mPa ⁇ sec, and more preferably 0.1 to 500 mPa ⁇ sec.
- the compounding amount of the organohydrogenpolysiloxane (B) is usually 1 to 1 hydrogen atoms bonded to the silicon atoms in the component (B) with respect to one alkenyl group bonded to the silicon atoms in the component (A).
- the amount is in the range of 20, preferably 1 to 10, more preferably 1 to 5.
- a reaction curing agent When a silicone resin is used, a reaction curing agent may be used, and a typical example is platinum or a platinum compound catalyst (platinum catalyst).
- platinum catalyst platinum catalyst
- Known materials can be used, and specific examples include platinum black, chloroplatinic acid, alcohol-modified products of chloroplatinic acid, complexes of chloroplatinic acid and olefins, aldehydes, vinyl siloxanes or acetylene alcohols.
- platinum compound catalyst the more the platinum compound catalyst is mixed, the more the hydrosilylation reaction is promoted. In general, however, 100 to 2000 ppm of platinum metal is generally added to the composition.
- the silicone resin contains an adhesion assistant.
- the adhesion assistant for example, at least selected from the group consisting of an amino silane coupling agent, an epoxy-modified silane coupling agent, a vinyl silane coupling agent, a chloro silane coupling agent, and a mercapto silane coupling agent Although 1 or more types are mentioned, it is not limited to these.
- reinforcing inorganic fillers such as fumed silica and dry silica, cross-linkable silicone (silicone resin) with adjusted end groups, non-reinforcing inorganic such as calcium carbonate, calcium silicate, and titanium dioxide Fillers can be added.
- the amount of these inorganic fillers used is preferably 0.1 to 200 parts by weight, more preferably 0.1 to 100 parts by weight of the alkenyl group-containing polysiloxane component.
- an inorganic pigment or an organic pigment may be added as a colorant.
- the inorganic pigment include carbon black, titanium oxide, red bengara, black bengara, titanium yellow, and cobalt blue.
- Series yellow, red
- isoindolinone yellow, orange
- quinacridone red, purple
- diketopyrrolopyrrole Orange, red, purple
- anthraquinone yellow, red, blue
- Dioxazine purple
- benzimidazolone Orange
- copper phthalocyanine blue
- allylamide yellow
- the traveling angle of the base fabric through the knife used during coating and the support immediately after the knife is used. Is very important.
- a method for applying the resin a conventionally known method is used, but knife coating is preferable from the viewpoint of ease of adjustment of the coating amount and influence when foreign matters (projections) are mixed, and a coating method using a knife-on-air method Is more preferable.
- the knife to be used may be either an integral doctor knife or a blade knife, but the blade knife is more preferable in consideration of the maintainability of the knife.
- the resin can easily penetrate into the inside of the fabric, but it becomes difficult for the resin to be present on the surface of the fabric on the coating surface, particularly on the top, and the airflow suppression originally required for the coating base fabric cannot be achieved.
- the knife blade at the time of coating has a role of blocking the resin to be coated and spreading it in the width direction to apply a uniform coating amount.
- As the tip shape of the knife blade used for this knife coating a semicircular shape, a square shape, and the like have been used, but this was mainly for the purpose of adjusting the amount of resin applied.
- the inventor has found that the use of knives having different shapes at the front and rear of the tip of the blade achieves both reduction of damage to the base fabric and elimination of the adhesive ball defect.
- a semicircular shape in which the knife blade is in contact with the cloth that is, the blade tip shape has a range of 160 degrees or more has been preferably used.
- Paste balls are also observed when coated in a semicircular shape. This is because the resin to be applied is compressed along the knife blade and applied to the base fabric, and then a small amount of resin not used for application passes through the knife blade and is released from the pressure applied by the knife blade. This is presumed to be due to the phenomenon of wrapping around the back side along the knife blade. It is considered that a small amount of resin accumulates to a level that can be visually observed at the production level, and finally falls on the base fabric, resulting in a paste ball defect.
- a preferable knife shape one having a quarter circle shape at the front and a square shape (right angle type) at the rear portion (FIG. 3) is used.
- Various combinations are possible, such as a 1/4 circle shape at the front and a partially rounded shape at the rear (Fig. 4), but the front is 1/4 circle (round type) and the rear is square (right angle type) ) Is most preferable.
- the radius of the quarter circle at the front is preferably 0.2 mm to 1.5 mm.
- the blade thickness at the portion where the circular shape starts is preferably in the range of 0.4 mm to 3.0 mm. If it is this range, the application quantity of resin will not increase too much, and the damage to a base fabric can be suppressed to the minimum. It is preferable that the blade thickness from the knife durability surface to the base of the blade not in contact with the base cloth is constant.
- the running angle of the base fabric is preferably 3 to 15 °. More preferably, the angle is 4 to 10 °. If the running angle is less than 3 °, it is not preferable because the resin ball cannot be prevented from entering the back side of the blade even if the shape of the knife blade is changed, and the adhesive ball defect tends to increase. On the other hand, if the running angle is larger than 15 °, the adhesive ball defect can be suppressed, but as a result, the cloth is pushed in with an excessive force, not only the amount of resin applied becomes excessive, but also the width direction of the base cloth. It is difficult to make the physical properties uniform.
- the above-mentioned running angle of the base fabric is based on the line connecting the base fabric supports positioned before and after the knife, and the reference line and the actual base fabric formed by being pushed by the knife blade during coating are as follows.
- the support may have a flat surface called a bed, or the base fabric may be sent out by a roller. In the case of a bed, a flat surface may be arranged along the running direction of the base fabric (in parallel to the ground).
- the base fabric may be smoothed.
- the knife bed itself may be inclined and installed. If the tilt angle is too large, the base fabric is damaged, which is not preferable.
- the reference line may be a line connecting the position where the roller and the cloth are in contact with each other, or the position where the coated base cloth is first in contact with the roller.
- the angle between the reference line and the base fabric is measured at two points before and after the knife blade passes, but a method with a small angle may be adopted.
- the angle after coating is often smaller than that before the coating blade, and the angle after coating is often adopted.
- the temperature and tension for heating are not particularly limited as long as the density of the base fabric does not change, but is preferably 80 to 130 ° C, more preferably 90 to 120 ° C. If it is less than 80 degreeC, the smoothing effect of a base base fabric will not appear easily.
- the base fabric having a large ear tab is different in the way of applying heat at the center and the end of the ear, resulting in a problem that the fabric is not smoothed.
- this heating device known methods such as a method of passing a heating roll and a method of passing through a heating oven can be used. Further, the lower limit of the running tension that does not cause wrinkles, and the upper limit of the range in which the density does not change.
- the coated base fabric of the present invention is characterized by small variations in tear strength in the width direction.
- the tear strength in the width direction is equally divided into 12 in the width direction of the coating base fabric, and the tear strength is measured at the center 10 points.
- An average value and variance are obtained from the measured values, and the value (coefficient of variation) expressed by dividing the variance by the average value and expressed in 100 minutes is 5% or less in both the longitudinal direction and the weft direction. Preferably it is 4.5% or less, More preferably, it is 4.0% or less.
- the coated base fabric of the present invention has a paste ball defect number of 2.0 points / 100 m or less.
- the target of glue ball defects is that when the long part is 2 mm or more, the amount of glue ball defects generated is inspected 2000 m from the obtained coating base fabric, and the generated amount of glue ball defects is 2.0 points / 100 m or less. Preferably it is 1.0 point / 100 m or less. If the adhesive ball defect is 2.0 points / 100 m or less, there is an advantage that the deployment behavior of the airbag can be obtained. This glue ball defect can be found by visual inspection.
- a general heating method such as hot air, infrared light, microwave, or the like can be used.
- the heating temperature and time it suffices if the temperature reaches a temperature sufficient for the elastomer resin to cure.
- the heating temperature is 150 to 220 ° C., and the heating time is 0.2 to 5 minutes.
- the total fineness of the filament yarn constituting the woven fabric (base fabric) is preferably 200 to 1000 dtex.
- the total fineness exceeds 1000 dtex, the thickness of the woven fabric (base fabric) increases, and the storage property of the airbag tends to deteriorate.
- the total fineness is less than 200 dtex, the mechanical properties during the operation of the airbag, such as the tearing mechanical properties of the coating base fabric, are likely to deteriorate.
- the cover factor of the woven fabric (base fabric) is preferably 1,700 to 2,500, more preferably 1,900 to 2,450. If the cover factor is less than 1,700, physical characteristics (such as tensile strength) necessary for an airbag are lowered. On the other hand, when the cover factor exceeds 2,500, there are limits due to weaving and storage properties.
- Coating amount The coated base fabric after curing the elastomer resin is sampled at a 5 cm square, and the mass is measured. After immersing in a solvent that dissolves only the base fabric fibers (hexafluoroisopropanol in the case of polyamide 66) to dissolve the base fabric, only the insoluble elastomer resin layer is recovered and washed with acetone. After vacuum drying, the sample was weighed. Incidentally, the coating amount, expressed in mass per 1m 2 (g / m 2) .
- Example 1 A polyamide 66 multifilament yarn having an original yarn strength of 8.4 cN / dtex, a total fineness of 470 dtex, and 72 filaments was woven in a water jet loom as a plain weave. Subsequently, after shrinking with boiling water at 95 ° C., drying finish was performed at 130 ° C. to obtain a woven fabric having a warp density of 46 / 2.54 cm, a weft density of 46 / 2.54 cm, and a cover factor of 1,994. .
- the knife had a tip thickness of 1.0 mm, and used a front round type and a right rear type (FIG. 3).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 14000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Thereafter, curing treatment was performed at 200 ° C. for 1 minute to obtain a coated base fabric having an application amount of 25 g / m 2 .
- the heating roller used before coating at this time was set to 110 ° C., and the running angle of the knife and the base fabric of the support immediately after was 8 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 2 A polyamide 66 multifilament yarn having an original yarn strength of 8.3 cN / dtex and a total fineness of 470 dtex and 144 filaments was woven in a water jet loom as a plain weave. Subsequently, after shrinking with boiling water at 95 ° C., drying finish was performed at 130 ° C. to obtain a woven fabric having a warp density of 46 / 2.54 cm, a weft density of 46 / 2.54 cm, and a cover factor of 1,994. .
- Example 2 Using this woven fabric (base fabric), coating was performed in the same manner as in Example 1.
- the knife used at this time had a front end thickness of 0.45 mm, and used a front round type and a rear right angle type (FIG. 3).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 18000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Thereafter, a curing treatment was performed at 200 ° C. for 1 minute to obtain a coated base fabric having an application amount of 20 g / m 2 .
- the heating roller used before coating at this time was set at 110 ° C., and the running angle of the knife and the base fabric of the support immediately after was 5 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 3 Using the woven fabric (base fabric) of Example 2, coating was performed in the same manner as in Example 1.
- the knife used at this time had a tip portion thickness of 0.60 mm, and was cut into a front round shape and a rear partial square shape (FIG. 4).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 37000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Thereafter, curing treatment was performed at 200 ° C. for 1 minute to obtain a coated base fabric having an application amount of 25 g / m 2 .
- the heating roller used before coating was set at 115 ° C., and the running angle of the knife and the base fabric of the support immediately after was 4 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 4 A polyamide 66 multifilament yarn having an original yarn strength of 8.4 cN / dtex, a total fineness of 350 dtex, and 108 filaments was woven in a water jet loom as a plain weave. Next, after shrinking with 95 ° C. boiling water, drying finish was performed at 130 ° C. to obtain a woven fabric having a warp density of 55 / 2.54 cm, a weft density of 55 / 2.54 cm, and a cover factor of 2,208. .
- Example 2 Using this woven fabric (base fabric), coating was performed in the same manner as in Example 1.
- the knife used at this time had a front end thickness of 0.35 mm, and used a front round type and a right rear type (FIG. 3).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 17000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Then cured for 1 minute at 200 ° C., the amount of coating to obtain a coated base fabric is 20 g / m 2.
- the heating roller used before coating at this time was set to 120 ° C., and the running angle of the knife and the base fabric of the support immediately after was 5 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 5 A polyamide 66 multifilament yarn having an original yarn strength of 8.5 cN / dtex, a total fineness of 235 dtex, and 72 filaments was woven in a water jet loom as a plain weave. Next, after shrinking with boiling water at 95 ° C., drying finish was performed at 130 ° C. to obtain a woven fabric having a warp density of 73 / 2.54 cm, a weft density of 73 / 2.54 cm, and a cover factor of 2,238. .
- Example 2 Using this woven fabric (base fabric), coating was performed in the same manner as in Example 1.
- the knife used at this time had a tip thickness of 0.50 mm, and used a front round type and a rear right angle type (FIG. 3).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 14000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Thereafter, curing treatment was performed at 200 ° C. for 1 minute to obtain a coated base fabric having an application amount of 17 g / m 2 .
- the heating roller used before coating at this time was set at 110 ° C., and the running angle of the knife and the base fabric of the support immediately after was 7 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 6 A polyamide 66 multifilament yarn having an original yarn strength of 8.4 cN / dtex and a total fineness of 940 dtex and 144 filaments was woven in a water jet loom as a plain weave. Next, after shrinking with 95 ° C. boiling water, drying finish was performed at 130 ° C. to obtain a woven fabric having a warp density of 37 / 2.54 cm, a weft density of 37 / 2.54 cm, and a cover factor of 2.269. .
- Example 1 Using this woven fabric (base fabric), coating was performed in the same manner as in Example 1.
- the knife used at this time had a tip thickness of 2.50 mm, and used a front round type and a right rear type (FIG. 3).
- An addition polymerization type solventless vinylmethylsilicone resin having a resin viscosity of 8000 mPa ⁇ sec was applied to one side of the woven fabric (base base fabric) by a knife-on-air method. Thereafter, curing treatment was performed at 200 ° C. for 1 minute to obtain a coated base fabric having an application amount of 45 g / m 2 .
- the heating roller used before coating at this time was set to 110 ° C., and the running angle of the knife and the base fabric of the support immediately after was 8 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 1.
- the obtained coated base fabric had a low coefficient of variation in tear strength in the width direction, and was excellent in quality against glue ball defects.
- Example 1 The same base fabric as in Example 2 was used, and the tip shape of the knife did not change between the front part and the rear part, and the same resin and coating method were used as in Example 2 except that a round type (FIG. 6) was used. .
- the properties of the resulting coated base fabric were evaluated and are shown in Table 2. Although the obtained coated base fabric had a variation coefficient of tear strength in the width direction, it could not be said that the quality was excellent due to the large number of glue ball defects.
- Example 2 The same base fabric as in Example 3 was used, the tip shape of the knife did not change at the front part and the rear part, and the same resin and coating method as in Example 3 were used, except that a square one (FIG. 5) was used. .
- the properties of the resulting coated base fabric were evaluated and are shown in Table 2.
- the resulting coated base fabric was excellent in terms of the quality of glue ball defects, but the coefficient of variation in tear strength in the width direction was high in both the warp direction and the weft direction.
- Example 3 Coating was carried out in the same manner as in Example 4 except that a base base fabric similar to that in Example 4 was used and the running angle of the base fabric of the support immediately after the knife was set to 18 °.
- the properties of the resulting coated base fabric were evaluated and are shown in Table 2.
- the resulting coated base fabric was excellent in quality against the glue ball defects, but because the amount of indentation by the knife blade was too much, the knife fabric was damaged significantly and the coefficient of variation in tear strength in the width direction was large. The results were high in both the longitude and latitude directions.
- Example 4 Coating was carried out in the same manner as in Example 4 except that a base base fabric similar to that in Example 4 was used and the running angle of the base fabric of the support immediately after the knife was set to 2 °. The properties of the resulting coated base fabric were evaluated and are shown in Table 2. The obtained coated base fabric had a larger amount of resin adhesion than Example 4. Moreover, it cannot be said that the quality is excellent due to the large number of occurrences of paste ball defects.
- the coated base fabric for airbag of the present invention has few defects of glue balls and maintains uniform tear strength properties in the width direction of the base fabric. Therefore, even if the airbag is required to have particularly high internal pressure retention performance, -The industrial contribution is large because it has the advantages of excellent reliability, low loss during cutting, and excellent cost performance.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Mechanical Engineering (AREA)
- Air Bags (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Woven Fabrics (AREA)
Abstract
Description
すなわち、本発明は、
1.合成繊維フィラメントから構成された織物の片面に、エラストマー樹脂が塗布されてなるエアバッグ用コーティング基布であって、コーティング基布の幅方向の引裂強力の変動係数(CV%)が経方向、緯方向共に5%以下であり、かつ糊玉欠点の発生数が2.0点/100m以下であることを特徴とするエアバッグ用コーティング基布。
2.エラストマー樹脂の塗布量が15~50g/m2である上記1に記載のエアバッグ用コーティング基布。
3.織物を構成するフィラメントの総繊度が、200~1000dtexである上記1または2に記載のエアバッグ用コーティング基布。
4.織物のカバーファクターが、1,700~2,500である上記1~3のいずれかに記載のエアバッグ用コーティング基布。
5.エラストマー樹脂が付加重合型の無溶剤シリコーンである上記1~4のいずれかに記載のエアバッグ用コーティング基布。
6.エラストマー樹脂の粘度が、5000~40000mPa・sである上記1~5のいずれかに記載のエアバッグ用コーティング基布。
7.樹脂の塗布方法がナイフオンエアー方式であり、前後で異なる形状をしたナイフを用いることを特徴とする上記1~6のいずれかに記載のエアバッグ用コーティング基布の製造方法。
8.ナイフを押し込む際の基布の走行角度が3~15°である上記1~7のいずれかに記載のエアバッグ用コーティング基布の製造方法。
本発明において、合成繊維フィラメントから構成された織物とは、合成繊維フィラメント糸条を用いて製織される織物を意味する。織物は、機械的強度に優れ、厚さを薄くできるという点で優れている。織物の組織は、例えば、平織、綾織、朱子織およびこれらの変化織、多軸織などが適用でき、なかでも機械的強度により優れる平織物が特に好ましい。
本発明者は、刃の先端を前面と後面で異なる形状をしたナイフを用いることで基布へのダメージ軽減と糊玉欠点の解消を両立することを見出したものである。
ナイフの耐久性の面から基布に接するナイフ先端から接しない刃の根元までの刃厚を一定にすることが好ましい。
JIS L-1095 9.4.1記載の方法で測定する。
フィラメント糸条の断面写真よりフィラメント数を数える。
JIS L-1096 8.6.1記載の方法で測定する。
CF=√(経糸の総繊度)×経糸密度+√(緯糸の総繊度)×緯糸密度
なお、総繊度の単位はdtex、織密度の単位は本/2.54cmである。
エラストマー樹脂を硬化させた後のコーティング基布を5cm角で採取し、質量を測定する。ベース基布である繊維のみを溶かす溶剤(ポリアミド66の場合は、ヘキサフルオロイソプロパノール)に浸漬してベース基布を溶解させた後、不溶物であるエラストマー樹脂層のみを回収してアセトン洗浄を行い、真空乾燥後、試料の秤量を行った。なお、塗布量は、1m2あたりの質量(g/m2)で表した。
ISO13937-2記載の方法で測定する。ただしサンプリングの方法は、コーティング基布を幅方向に均等に12分割した後、両端の2区画は採用せず、中央の10区画で測定を行う。経方向は中央で10分割した各区画の出来るだけ中央でサンプリングを行う。緯方向はNz側の5点はNz方向から引き裂かれるように、反Nz側の5点は反Nz方向から引き裂かれるように、分割した領域の端からサンプリングを行う。
コーティング後の基布2000mに対して、最も長い部分で2mm以上の糊玉欠点数を目視によりカウントし、100m当たりの発生数を計算した。
原糸強度が8.4cN/dtexで総繊度が470dtex、72フィラメントのポリアミド66マルチフィラメント糸を、平織りにてウォータージェットルームにて製織した。次いで、95℃の沸水にて収縮加工した後、130℃で乾燥仕上げをし、経密度46本/2.54cm、緯密度46本/2.54cm、カバーファクターが1,994の織物を得た。
この織物(ベース基布)の片面に、樹脂粘度が14000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が25g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは110℃に設定し、ナイフと直後の支持体の基布の走行角度は8°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
原糸強度が8.3cN/dtexで総繊度が470dtex、144フィラメントのポリアミド66マルチフィラメント糸を、平織りにてウォータージェットルームにて製織した。次いで、95℃の沸水にて収縮加工した後、130℃で乾燥仕上げをし、経密度46本/2.54cm、緯密度46本/2.54cm、カバーファクターが1,994の織物を得た。
この織物(ベース基布)の片面に、樹脂粘度が18000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が20g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは110℃に設定し、ナイフと直後の支持体の基布の走行角度は5°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
実施例2の織物(ベース基布)を用い、実施例1と同様の方法でコーティングを行った。この時使用したナイフは先端部厚みが0.60mmで、前部ラウンド型、後部一部角型に削った形状(図4)のものを用いた。
この織物(ベース基布)の片面に、樹脂粘度が37000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が25g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは115℃に設定し、ナイフと直後の支持体の基布の走行角度は4°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
原糸強度が8.4cN/dtexで総繊度が350dtex、108フィラメントのポリアミド66マルチフィラメント糸を、平織りにてウォータージェットルームにて製織した。次いで、95℃の沸水にて収縮加工した後、130℃で乾燥仕上げをし、経密度55本/2.54cm、緯密度55本/2.54cm、カバーファクターが2,208の織物を得た。
この織物(ベース基布)の片面に、樹脂粘度が17000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が20g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは120℃に設定し、ナイフと直後の支持体の基布の走行角度は5°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
原糸強度が8.5cN/dtexで総繊度が235dtex、72フィラメントのポリアミド66マルチフィラメント糸を、平織りにてウォータージェットルームにて製織した。次いで、95℃の沸水にて収縮加工した後、130℃で乾燥仕上げをし、経密度73本/2.54cm、緯密度73本/2.54cm、カバーファクターが2,238の織物を得た。
この織物(ベース基布)の片面に、樹脂粘度が14000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が17g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは110℃に設定し、ナイフと直後の支持体の基布の走行角度は7°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
原糸強度が8.4cN/dtexで総繊度が940dtex、144フィラメントのポリアミド66マルチフィラメント糸を、平織りにてウォータージェットルームにて製織した。次いで、95℃の沸水にて収縮加工した後、130℃で乾燥仕上げをし、経密度37本/2.54cm、緯密度37本/2.54cm、カバーファクターが2.269の織物を得た。
この織物(ベース基布)の片面に、樹脂粘度が8000mPa・secである付加重合型の無溶剤ビニルメチルシリコーン樹脂をナイフオンエアー方式にて塗布した。その後、200℃で1分間硬化処理し、塗布量が45g/m2であるコーティング基布を得た。この時塗布する前に使用した加熱ローラは110℃に設定し、ナイフと直後の支持体の基布の走行角度は8°であった。
得られたコーティング基布の特性を評価し、表1に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数が低く、糊玉欠点に対する品位は優れていた。
実施例2と同様のベース基布を用い、ナイフの先端形状が前部、後部で変化無く、ラウンド型のもの(図6)を用いる以外は実施例2と同様の樹脂、コーティング方法で実施した。
得られたコーティング基布の特性を評価し、表2に示した。得られたコーティング基布は、幅方向の引裂強力の変動係数は範囲内であるが、糊玉欠点の発生数が多いために品位が優れているとは言えなかった。
実施例3と同様のベース基布を用い、ナイフの先端形状が前部、後部で変化無く、角型のもの(図5)を用いる以外は実施例3と同様の樹脂、コーティング方法で実施した。
得られたコーティング基布の特性を評価し、表2に示した。得られたコーティング基布は、糊玉欠点に対する品位は優れていたが、幅方向の引裂強力の変動係数が経方向、緯方向共に高かった。
実施例4と同様のベース基布を用い、ナイフと直後の支持体の基布の走行角度を18°に設定する以外は実施例4と同様の方法でコーティングを実施した。
得られたコーティング基布の特性を評価し、表2に示した。得られたコーティング基布は、糊玉欠点に対する品位は優れていたが、ナイフ刃による押し込み量が多すぎるために、ナイフ刃による基布へのダメージが大きく、幅方向の引裂強力の変動係数が経方向、緯方向共に高い結果であった。
実施例4と同様のベース基布を用い、ナイフと直後の支持体の基布の走行角度を2°に設定する以外は実施例4と同様の方法でコーティングを実施した。
得られたコーティング基布の特性を評価し、表2に示した。得られたコーティング基布は、実施例4に比較し、樹脂の付着量が多くなった。また、糊玉欠点の発生数が多いために品位が優れているとは言えなかった。
2 樹脂塗布工程のナイフの前にある支持体
3 樹脂塗布工程のナイフの後にある支持体
4 ナイフ
5 基布
6 基布の進行方向
7 基準線
8 基準線と布が形成する走行角度
10 本発明に使用するナイフ先端形状の例 (前部:半円状、後部:角型)
11 本発明に使用するナイフ先端形状の例 (前部:半円状、後部:角型に削った形状)
12 本発明に使用するナイフ先端形状の例 (前部:角型、後部:角型)
13 本発明に使用するナイフ先端形状の例 (前部:丸型、後部:丸型)
Claims (8)
- 合成繊維フィラメントから構成された織物の片面に、エラストマー樹脂が塗布されてなるエアバッグ用コーティング基布であって、幅方向の引裂強力の変動係数(CV%)が経方向、緯方向共に5%以下であり、かつ糊玉欠点の発生数が2.0点/100m以下であることを特徴とするエアバッグ用コーティング基布。
- エラストマー樹脂の塗布量が15~50g/m2である請求項1に記載のエアバッグ用コーティング基布。
- 織物を構成するフィラメントの総繊度が、200~1000dtexである請求項1または2に記載のエアバッグ用コーティング基布。
- 織物のカバーファクターが、1,700~2,500である請求項1~3のいずれかに記載のエアバッグ用コーティング基布。
- エラストマー樹脂が付加重合型の無溶剤シリコーンである請求項1~4のいずれかに記載のエアバッグ用コーティング基布。
- エラストマー樹脂の粘度が、5000~40000mPa・sである請求項1~5のいずれかに記載のエアバッグ用コーティング基布。
- 樹脂の塗布方法がナイフオンエアー方式であり、前後で異なる形状をしたナイフを用いることを特徴とする請求項1~6のいずれかに記載のエアバッグ用コーティング基布の製造方法。
- ナイフを押し込む際の基布の走行角度が3~15°である請求項1~7のいずれかに記載のエアバッグ用コーティング基布の製造方法。
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WO2019146286A1 (ja) * | 2018-01-26 | 2019-08-01 | 東レ株式会社 | 基布、ジェットルームおよび基布の製造方法 |
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JPWO2019146286A1 (ja) * | 2018-01-26 | 2020-11-19 | 東レ株式会社 | 基布、ジェットルームおよび基布の製造方法 |
EP3744887A4 (en) * | 2018-01-26 | 2021-10-13 | Toray Industries, Inc. | BASE FABRIC, JET WEAVING AND BASIC FABRIC PRODUCTION PROCESS |
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JP7388191B2 (ja) | 2018-01-26 | 2023-11-29 | 東レ株式会社 | 基布、ジェットルームおよび基布の製造方法 |
Also Published As
Publication number | Publication date |
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EP3431653A4 (en) | 2019-09-04 |
CN108699763A (zh) | 2018-10-23 |
JP6973373B2 (ja) | 2021-11-24 |
JPWO2017159583A1 (ja) | 2019-01-24 |
CN108699763B (zh) | 2021-09-14 |
EP3431653A1 (en) | 2019-01-23 |
US20190071048A1 (en) | 2019-03-07 |
MX2018011247A (es) | 2019-03-28 |
US10940825B2 (en) | 2021-03-09 |
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