JPS6121141B2 - - Google Patents
Info
- Publication number
- JPS6121141B2 JPS6121141B2 JP56037525A JP3752581A JPS6121141B2 JP S6121141 B2 JPS6121141 B2 JP S6121141B2 JP 56037525 A JP56037525 A JP 56037525A JP 3752581 A JP3752581 A JP 3752581A JP S6121141 B2 JPS6121141 B2 JP S6121141B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- sheet
- weight
- reinforcing
- reinforcing material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920005989 resin Polymers 0.000 claims description 70
- 239000011347 resin Substances 0.000 claims description 70
- 239000000463 material Substances 0.000 claims description 39
- 239000012779 reinforcing material Substances 0.000 claims description 29
- 238000010438 heat treatment Methods 0.000 claims description 20
- 229920001187 thermosetting polymer Polymers 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 18
- 239000011324 bead Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000010425 asbestos Substances 0.000 claims description 8
- 229910052895 riebeckite Inorganic materials 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 7
- 239000004744 fabric Substances 0.000 claims description 6
- 239000003365 glass fiber Substances 0.000 claims description 5
- 235000011187 glycerol Nutrition 0.000 claims description 5
- 239000011342 resin composition Substances 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 239000000155 melt Substances 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 4
- 230000008018 melting Effects 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 3
- 230000003014 reinforcing effect Effects 0.000 description 31
- 239000003822 epoxy resin Substances 0.000 description 20
- 229920000647 polyepoxide Polymers 0.000 description 20
- 238000007665 sagging Methods 0.000 description 14
- 229910000831 Steel Inorganic materials 0.000 description 13
- 238000001723 curing Methods 0.000 description 13
- 239000010959 steel Substances 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- 239000006260 foam Substances 0.000 description 7
- 238000005187 foaming Methods 0.000 description 7
- -1 glycidyl ester type Chemical compound 0.000 description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 230000002787 reinforcement Effects 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
- YTWBFUCJVWKCCK-UHFFFAOYSA-N 2-heptadecyl-1h-imidazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC=CN1 YTWBFUCJVWKCCK-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- UTTHLMXOSUFZCQ-UHFFFAOYSA-N benzene-1,3-dicarbohydrazide Chemical compound NNC(=O)C1=CC=CC(C(=O)NN)=C1 UTTHLMXOSUFZCQ-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000001177 diphosphate Substances 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000005007 epoxy-phenolic resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011900 installation process Methods 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000011387 rubberized asphalt concrete Substances 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Body Structure For Vehicles (AREA)
Description
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è£åŒ·æã«é¢ãããDETAILED DESCRIPTION OF THE INVENTION The present invention relates to a reinforcing material that contributes to weight reduction as reinforcement for plate materials.
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ãè€éåãããªã©ã®æ¬ ç¹ãæããŠããã Conventionally, in automobiles, various types of reinforcement have been applied to car body steel plates. For example, for roofs, fenders, hoods, trunks, quarter panels, and doors that have relatively wide and flat shapes but are thin, it is necessary to provide appropriate structural rigidity against external forces. Since then, a method has been adopted in which an inner plate made of a metal reinforcing member is attached to an outer plate by spot welding or adhesive. However, this method has drawbacks such as the heavy weight of the metal reinforcing members, which goes against the trend of thinner outer panels designed to reduce the weight of car bodies, increases weight and costs, and complicates the installation process. It had
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ãŠããã In addition, as shown in Japanese Utility Model Application Publication No. 55-101659, for example, for the purpose of vibration isolation and reinforcement of the outer panel of the vehicle body,
A method is also known in which a polymeric material such as asphalt rubber, epoxy resin, acrylic resin, phenolic resin, or unsaturated polyester resin is coated or pasted on the back side of the outer panel to a considerable thickness and over a considerable area. In this method, the rigidity is said to be proportional to the cube of the thickness, so increasing the thickness can increase the rigidity, but the increased amount of resin increases weight and costs. It has the same drawbacks as the metal reinforcing member.
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匷æããã®æ§æãšãããã®ã§ããã This invention was made in view of the conventional situation, and aims to provide a reinforcing material that is lightweight, inexpensive, and significantly improves the rigidity of an object to be attached. An uncured or semi-cured thermosetting reinforced resin sheet (hereinafter referred to as "non-sagging property imparting substance") containing a substance for imparting a melt viscosity that can prevent drooping during heating and melting (hereinafter referred to as "non-sagging property imparting material"). A bead-forming material that is made narrower than this sheet and forms a bead-shaped bulge on the sheet before the sheet is cured is attached to one side of the reinforced resin sheet (simply referred to as a reinforced resin sheet), and The reinforcing material is constructed such that the wide hem portion of the sheet on the side of the bead forming material forms a mounting surface for the object to be mounted.
以äžããã®çºæãå³é¢ã«åºã¥ããŠèª¬æããã The present invention will be explained below based on the drawings.
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ããŠããã FIG. 1 and FIG. 2 show an embodiment of the reinforcing material according to the present invention, in which the reinforcing material 1 is a fiber base material 2.
A reinforcing resin sheet 3 of thermosetting resin, such as an epoxy resin, prepared in an uncured or semi-cured and flexible prepreg state and containing a non-sagging property imparting substance; It consists of a bead forming material 4 made of a foamed resin sheet attached to one side, and this bead forming material 4 is formed narrower than the reinforcing resin sheet 3. The hem portions 3a, 3a of the reinforcing resin sheet on the side of the bead forming material 4, which protrude beyond the width of the bead forming material 4, constitute a mounting surface to be attached to an object to be mounted, such as a back surface 5a of a door outer panel 5 of an automobile.
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ãšãªãã The reinforcing material 1 is attached to the mounting surface 3 as shown in FIG.
a, 3a are attached to the back surface 5a of the door outer panel 5, and by heating after attachment, the viscosity of the reinforcing resin sheet 3 temporarily decreases, and the reinforcing resin sheet 3 is attached to the attached surface 3 on the door outer panel 5.
While a and 3a are brought into closer contact with each other, the bead forming material 4 is foamed and its cross section becomes larger, and the reinforcing resin sheet 3 is pushed up from the roots 3c and 3c of the mounting surface 3a, and the bead-shaped swollen portion 3b is formed before it hardens. As the reinforcing resin sheet 3 is formed and further heated over time, it hardens and becomes the state shown in FIG. 3.
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ãŠããïŒã In the present invention, the fiber base material in the reinforced resin sheet can be positioned, for example, outside the intermediate portion of the layers of the sheet. FIG. 2 shows this example, in which the fiber base material is unevenly distributed on the outside (that is, the bead forming material is attached to the non-uniformly distributed side of the fiber base material).
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ããšã«ããã€ããããšãã§ããã Next, the fiber base material 2, reinforcing resin sheet 3, and bead forming material 4 in the reinforcing material 1 will be explained in more detail. First, the reinforcing resin sheet 3 is a thermosetting resin made by blending a thermosetting resin with a heat-activated curing agent and a non-sagging property imparting substance that becomes non-sagging property when the resin is molten. It can be produced by molding the composition into a sheet in an uncured or semi-cured state according to a conventional method, and then fusion-bonding it to a fiber base material at the same time as this sheet molding or each time the sheet is molded.
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éšããšãã«å¥œé©ã«ã¯0.7ã2.5éééšã§ããã A typical non-sagging material that is an important component in the above-mentioned thermosetting resin composition is asbestos powder. The proportion is preferably 2 to 20 parts by weight, particularly preferably 4 to 15 parts by weight, based on 100 parts by weight of the total amount of the curable resin and the thermoplastic resin and rubber component used in combination. Another typical example is a mixed system of finely powdered silica and glycerin, in which the ratio of finely powdered silica used is 4 to 10 parts by weight per 100 parts by weight of the polymer component in the thermosetting resin composition. Parts by weight, particularly preferably from 2 to 7 parts by weight, and for glycerin from 0.5 to 3 parts by weight, particularly preferably from 0.7 to 2.5 parts by weight.
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ãã®ãšããŠéžã°ãããã®ã§ããã If an excessive amount of these non-sagging imparting substances is used, the initial adhesion to the door outer panel 5 or the like becomes insufficient, and temporary adhesion to the door outer panel 5 or the like becomes difficult, which tends to impair workability. Furthermore, the adhesion force to the door outer panel 5 and the like after heating and curing decreases, and there is a risk that the fiber-reinforced resin layer may peel off from the door outer panel surface during handling such as bending. In addition, these anti-sagging property imparting substances are effective in imparting non-sagging properties to thermosetting resins, and also provide good results in terms of the strength of the fiber-reinforced resin layer. It is the chosen one.
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ã§ããã The thermosetting resin in which such a non-sagging property imparting substance is to be blended has fixed shape at room temperature, and as long as this condition is met, it may be a mixture of a solid resin and a liquid resin at room temperature. , or may be semi-hardened. Specific examples of such thermosetting resins include glycidyl ether type,
Various epoxy resins such as glycidyl ester type, glycidyl amine type, linear aliphatic epoxide type, and alicyclic epoxide type are preferable from the viewpoint of adhesion to metal plates. However, other thermosetting resins such as melamine, polyester, phenol, urea, etc. can also be used.
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éšã«å¯ŸããŠéåžžïŒã15éééšã®å²åã§ããã The heat-activated curing agent to be added to this thermosetting resin may be any ordinary curing agent that exhibits curing action when heated, and generally it is sufficient if it is active in the temperature range of 80 to 200°C, for example, for curing epoxy resins. Examples of the agent include dicyandiamide, 4,4'-diaminodiphenylsulfone, imidazole derivatives such as 2-n-heptadecyl imidazole, isophthalic acid dihydrazide, N·N-dialkyl urea derivatives, N·N-dialkylthiourea derivatives, etc. is used. The amount used may be generally 1 to 15 parts by weight per 100 parts by weight of the epoxy resin.
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ãã In addition to the above components, the thermosetting resin composition also contains
Various additives are blended as necessary for the purpose of imparting cohesive force to the composition to the extent that it can be formed into a sheet, and improving wettability to a metal plate.
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ãã For example, in order to improve sheet forming ability,
Thermoplastic resins such as polyvinyl butyral, polyamide, polyamide derivatives, polyesters, polysulfones, polyketones, high molecular weight epoxy resins derived from bisphenol A and epichlordrine, and rubbers such as butadiene-acrylonitrile copolymers or derivatives thereof. You can mix ingredients etc. The amount used is preferably about 5 to 100 parts by weight per 100 parts by weight of the thermosetting resin.
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ããŠãããã In addition, for the purpose of improving the wettability of door outer panels, etc., reactive diluents such as butyl glycidyl ether and monoglycidyl ether of long-chain alcohols, phthalic acid plasticizers such as dioctyl phthalate, and triclean diphosphate are used. Phosphoric acid plasticizers and the like can be added. The amount of these components is preferably about 5 to 30 parts by weight per 100 parts by weight of the thermosetting resin. Other general fillers, such as calcium carbonate, silicic acids, carbon black, etc., which have some function of imparting anti-sagging properties, may be blended within a range that does not impair adhesive strength or other properties.
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代衚çãªãã®ãã¬ã©ã¹ç¹ç¶åžã§ããã Furthermore, as the fiber base material in the reinforced resin sheet, sheets such as inorganic fiber cloth such as glass fiber or asbestos fiber, organic fiber cloth such as linen, cotton, nylon, polyester, or polypropylene, or nonwoven fabric made of polyester fiber, polypropylene fiber, etc. There are fiber base materials. Among these, particularly preferred are inorganic fiber cloths, a typical example of which is glass fiber cloth.
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ïŒã§ç€ºãããå€ãæå³ããã When a woven fabric is used as the fiber base material in the present invention, its porosity is preferably 70% or less. The porosity means a value expressed by a-b/aÃ100 (%), where a is the planar area of the woven fabric and b is the planar area of the fibers occupying this planar area.
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ãã The thickness of the reinforced resin sheet of this invention varies depending on the reinforced location and purpose of reinforcement, but is generally 0.1
~40mm, preferably 0.3~20mm. Further, it is desirable that this reinforcing resin sheet has adhesiveness at room temperature for temporary adhesion to the door outer panel 5 and the like.
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ãã®ã§ããã Next, the foamable resin sheet as the bead forming material 4 has the property of foaming when heated above the decomposition temperature of the foaming agent contained therein, and the above-mentioned reinforcing resin provided on this sheet so that the sheet 3 can be in close contact with the door outer panel 5 on at least both sides in the width direction of the bead forming material 4;
It is formed into a narrower width than the reinforced resin sheet 3 described above.
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ãšãã§ããã Such foamable resin sheets are made by, for example, adding various thermosetting or thermoplastic polymers to a blowing agent and, if necessary, a foaming auxiliary agent, a curing agent, a curing accelerator, a crosslinking agent, a crosslinking auxiliary agent, a filler, and a coloring agent. After mixing the foaming agent, stabilizer, etc. with a mixing roll, etc., the foaming agent is mixed under temperature conditions that do not decompose (slight decomposition is fine).
It can be made by sheet molding according to conventional methods.
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ãžããç³»ååç©ãªã©ãããã Thermosetting or thermoplastic polymers used above include thermosetting resins such as epoxy resins, phenolic resins, and polyester resins, polyethylene, ethylene-vinyl acetate copolymers, adhesive polyolefins, etc. The agent may be any agent that foams when the reinforcing resin sheet is heated and cured and does not foam during sheet molding, such as azo compounds, nitroso compounds, hydrazide compounds, and the like.
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ããã®ã§ããããšãæãŸããã The thickness of the above foamable resin sheet is usually 0.2~
5 mm, preferably about 0.5 to 2 mm,
Further, it is desirable that the foaming ratio during heating is practically 2 to 30 times.
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ãããšã奜ãŸããã Next, to explain the curing process of the reinforcing material 1 in more detail, the reinforcing material 1 is brought into close contact with the door outer panel 5 as shown in FIG. The elastic resin sheet is foamed, and the curing of the sheet 3 is completed each time the foaming is completed. As a result, as shown in FIG. 3, a fiber-reinforced resin layer having bead-shaped bulges 3b is formed by the expansion force caused by foaming. At this time, it is preferable to take care that the gelation time of the reinforcing resin sheet at a certain temperature is about 1 to 20 minutes longer than the foaming completion time of the foamable resin sheet at the same temperature.
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åæã«å ç±ããããšãå¯èœã§ããã As the heating means, a conventional heating method such as a hot air circulation heating furnace, an infrared heating furnace, a high frequency induction heating furnace, etc. can be adopted. It is also possible to heat the paint at the same time as the paint baking process for car bodies in the car manufacturing line.
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æ ¹ïŒïœè¿åã®æš¹èåãåäžããããšããã By the way, in such heating and foaming curing, if the reinforcing resin sheet 3 causes a rapid viscosity drop when melted, the resin component that softened and flowed at the initial stage of heating may become hardened by the fiber base material 2. There is a risk that the resin will drip down, especially the resin near the base 3c of the bulging portion 3b.
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ããã However, the above-mentioned reinforced resin sheet 3 of the present invention
Since the composition contains a non-sagging additive substance and is given the property that it does not easily sag in a molten and fluid state, the above-mentioned sagging phenomenon hardly occurs. However, before it begins to sag, it begins to gel, its viscosity rapidly increases, and it hardens.
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æ§ãåŸãããã Therefore, the fiber-reinforced resin layer that is finally hardened and formed exhibits its original strength without thinning or resin loss at the bases 3c and 3c, and also suppresses overall thinning or resin loss. Due to the functions of the fiber reinforced resin layer, the foam layer and the bulging portion 3b, the effect of reinforcing the door outer panel 5, etc. is increased, and further improved strength or rigidity can be obtained.
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ããããšãã§ããã As detailed above, according to the method of the present invention, when constructing a reinforcing material using a reinforcing resin sheet and a bead forming material, the reinforcing resin sheet blended with a non-sagging property imparting substance is used as the reinforcing resin sheet. Therefore, it is possible to provide a highly reliable reinforcing material that can better exhibit its original reinforcing effect when reinforcing this reinforcing material by closely adhering it to a door outer panel or the like and heat-curing it.
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çšããããšãã§ããã The reinforcing material of the present invention is not limited to steel plates such as the outer panels of automobiles mentioned above, but can be applied to a wide variety of thin metal plates, such as cases of various vehicles and home appliances such as electric refrigerators and washing machines. Can be applied.
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çã«èª¬æããããªãã以äžã«ãããŠéšãšããã¯é
ééšãæå³ãããã®ãšããã EXAMPLES Below, examples of the present invention will be described in more detail. In addition, in the following, parts shall mean parts by weight.
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æŽçŽ¡ç€Ÿè£œã®ããªãšã¹ãã«æš¹èïŒ30éšãããŠã¢ãŸãŒ
ã«2MZâAZINEïŒååœåæç€Ÿè£œã®ãšããã·æš¹è
çšæœåšç¡¬åå€ïŒïŒéšããžã·ã¢ã³ãžã¢ããïŒæ¥æ¬ã«
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æš¹èçµæç©ããéåžžã®ããã·ã³ã°ããŒã«ã«ãŠæ··ç·Ž
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äžäœåããŠåã1.2mmã®è£åŒ·ãšããã·æš¹èã·ãŒã
ãåŸããExample 1 55 parts of Epicote #828 (bisphenol A type liquid epoxy resin manufactured by Yuka Shell Co., Ltd.), 15 parts of Epicote #1004 (bisphenol A type solid epoxy resin manufactured by Yuka Shell Co., Ltd.), Vylon #500 (30 parts of polyester resin manufactured by Toyobo Co., Ltd.), 3 parts of Kyuazol 2MZ-AZINE (latent curing agent for epoxy resin manufactured by Shikoku Kasei Co., Ltd.), 5 parts of dicyandiamide (latent curing agent for epoxy resin manufactured by Nippon Carbide Co., Ltd.),
An epoxy resin composition consisting of 30 parts of talc and 7 parts of asbestos powder was kneaded using an ordinary mixing roll, and then formed into a sheet with a predetermined thickness using a hot press. Next, a glass fiber cloth (3020A manufactured by Nitto Boseki Co., Ltd.) was fused and integrated on one side of this sheet by heat pressing to obtain a reinforced epoxy resin sheet with a thickness of 1.2 mm.
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¢é
žããã«å
±éåäœïŒäžäºã
ãªã±ãã«ã«ç€Ÿè£œã®ãšããã¬ãã¯ã¹ïŒ°â2807ïŒ100
éšãçºæ³¡å€ïŒæ°žååæç€Ÿè£œã®FEâïŒïŒïŒéšãã
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ã¶ãŒã«ãŠãã¬ããåããã®ã¡ãæŒåºæåœ¢æ©ã«ãŠæŒ
åºæž©åºŠ120âã®æ¡ä»¶ã§åãïŒmmã®çºæ³¡æ§æš¹èã·ãŒ
ãïŒããŒã圢ææïŒãåŸãã Separately, ethylene-vinyl acetate copolymer (Evaflex P-2807 manufactured by Mitsui Polychemical Co., Ltd.) 100
1 part, 6 parts of a blowing agent (FE-9 manufactured by Eiwa Kasei Co., Ltd.),
After uniformly kneading with a mixing roll and pelletizing with a pelletizer, a foamable resin sheet (bead forming material) with a thickness of 1 mm was obtained using an extrusion molding machine at an extrusion temperature of 120°C.
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å·Ÿã«åæããåºæãšå察åŽã®é¢ã«ãïŒcmå·Ÿã«åæ
ããäžèšã®çºæ³¡æ§æš¹èã·ãŒãã貌ãã€ããŠè£åŒ·æ
ãšããããã®è£åŒ·æãã0.7mmåã®éŒæ¿ã«ãçºæ³¡
æ§æš¹èã·ãŒããå
åŽãšãªãããã«è²Œãã€ã150â
é°å²æ°äžã§60åéå ç±ããŠéŒæ¿é¢ã«åŒ·åã«åºçã
ããã Next, add the reinforced epoxy resin sheet to 5 cm.
It was cut into widths, and the foamed resin sheet cut into 1 cm width was pasted on the opposite side from the base material to serve as a reinforcing material. This reinforcing material was pasted on a 0.7mm thick steel plate with the foamed resin sheet on the inside and heated to 150°C.
It was heated in an atmosphere for 60 minutes to strongly adhere to the steel plate surface.
ãã®å ç±äžãè£åŒ·ãšããã·æš¹èã·ãŒãã®æš¹èå
ã®åºæããé¢è±åäžããããšã¯ãªããæå®ã®çºæ³¡
åçã«ãããçºæ³¡å±€ãšãã®çºæ³¡å±€ã«ãã€ãŠããŒã
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èå±€ãšãããªãè£åŒ·å±€ãåŸãããããã®è£åŒ·å±€ã¯
å€èгãè¯å¥œã§ãã€ãã During this heating, the resin component of the reinforced epoxy resin sheet does not separate from the base material and sag, and the foam layer has a predetermined expansion ratio and a bead-shaped bulge is formed by this foam layer. A reinforcing layer consisting of a good fiber-reinforced resin layer was obtained. This reinforcing layer also had a good appearance.
ãã®ããã«è£åŒ·ããéŒæ¿ã詊éšçãšããŠãäžèš
ã®åŠã匷床詊éšãè¡ãªã€ãã The following strength tests were conducted using the thus reinforced steel plates as test pieces.
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å
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æ²çååŸïŒmmã®éååæé¢ãåããïŒæã®åçŽ
å¹³æ¿ïŒå·Ÿ50mmïŒãæããæ¯æå°ã§ãå·Ÿ50mmã«ãã
ã詊éšçãæ°Žå¹³ã«æ¯æãããã®äžå€®éšã«äžéšãã
æ²çååŸ10mmã®ïŒµååæé¢ãåããåçŽå¹³æ¿ïŒå·Ÿ
50mmïŒã§è·éãå ãããšãã®æå€§æ²ãå¿åïŒKgïŒ
50mmå·ŸïŒã§æž¬å®ããã<Strength test> A test with a width of 50 mm on a support stand having two vertical flat plates (width 50 mm) whose tips exhibit an inverted U-shaped cross section with a radius of curvature of 5 mm, arranged in parallel with a distance of 10 mm between the tips. The piece is supported horizontally, and a vertical flat plate (width
Maximum bending stress (Kg/
50mm width).
äžèšã®è©Šéšçµæã¯ã45KgïŒ50mmå·Ÿãšãªããè£åŒ·
æªçœ®ããªããæœãããŠããªãéŒæ¿åç¬ã®æå€§æ²ã
å¿åãïŒKgïŒ50mmå·Ÿã§ãã€ãã®ã«å¯Ÿããéåžžã«ã
ãããè£åŒ·å¹æãåŸãããŠããããšãå€ã€ãã The above test results showed that the steel plate was 45Kg/50mm width, and the maximum bending stress of the steel plate alone without any reinforcement measures was 8Kg/50mm width, but an extremely excellent reinforcing effect was obtained. I found out.
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åŸãããã®è£åŒ·æãçšããŠå®æœäŸïŒãšåæ§ã®æäœ
ã§éŒæ¿ã®è£åŒ·ã詊ã¿ãããå ç±äžã«ãè£åŒ·ãšãã
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ããComparative Example A reinforcing material was obtained in the same manner as in Example 1, except that asbestos powder was not blended into the epoxy resin composition. An attempt was made to reinforce a steel plate using this reinforcing material in the same manner as in Example 1, but during heating, the resin content of the reinforcing epoxy resin sheet dripped, resulting in a poor appearance and making it impossible to obtain the desired reinforcing effect. I couldn't do it.
宿œäŸ ïŒ
ãšãã³ãŒãïŒ828ïŒååºïŒ10éšããšãã³ãŒã«
ïŒ1004ïŒååºïŒ55éšããã€ã«ãŒCTBN1300ÃïŒ
ïŒB.Fã°ãããªãã瀟補ã®ã«ã«ããã·ã«åºå«ææ¶²
ç¶ãããªã«ãŽã ïŒ35éšãD.PããŒãããŒïŒäžžåã
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ã«ã¬ã©ã¹ç¹ç¶åžïŒæ¥æ±çŽ¡ç©ç€Ÿè£œã®WE21D104ïŒã
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ãšããã·æš¹èã·ãŒããåŸããExample 2 Epicor #828 (above) 10 copies, Epicor #1004 (above) 55 copies, Hiker CTBN1300 x 8
An epoxy resin composition consisting of 35 parts of carboxyl group-containing liquid nitrile rubber (manufactured by BF Gutudoritsu), 4 parts of DP hardener (hardening agent manufactured by Maruwa Biochemical Co., Ltd.), 5 parts of dicyandiamide, 30 parts of talc, and 10 parts of asbestos powder. After kneading with a normal mixing roll, the mixture was formed into a sheet with a predetermined thickness using a hot press. Next, glass fiber cloth (WE21D104 manufactured by Nitto Boseki Co., Ltd.) was fused and integrated on one side of this sheet by heat pressing to obtain a reinforced epoxy resin sheet with a thickness of 1.0 mm.
ã€ãã«ãäžèšã®ã·ãŒããïŒcmå·Ÿã«åæããåºæ
ãšå察åŽã®é¢ã«ãïŒcmå·Ÿã«åæãã宿œäŸïŒã§åŸ
ãçºæ³¡æ§æš¹èã·ãŒãã貌ãã€ããŠè£åŒ·æãšããã
ãã®è£åŒ·æããå°é¢ãšå¹³è¡ã«çœ®ããã0.7mmåã®
éŒæ¿ã®äžåŽã«ãçºæ³¡æ§æš¹èã·ãŒããå
åŽãšãªãã
ãã«è²Œãã€ããã€ãã§150âé°å²æ°äžã§60åéå
ç±ããŠéŒæ¿é¢ã«åŒ·åã«åºçãããã Next, the above-mentioned sheet was cut into a 5 cm width, and the foamed resin sheet obtained in Example 1 cut into a 1 cm width was attached to the surface opposite to the base material to serve as a reinforcing material.
This reinforcing material is pasted on the underside of a 0.7mm thick steel plate placed parallel to the ground, with the foamed resin sheet on the inside, and then heated in an atmosphere of 150â for 60 minutes to strengthen the steel plate surface. It was fixed to.
äžèšã®å ç±äžãè£åŒ·ãšããã·æš¹èã·ãŒãã®æš¹è
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çºæ³¡åçã«ãããçºæ³¡å±€ãšãã®çºæ³¡å±€ã«ãã€ãŠã
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å±€ã¯å€èгãè¯å¥œã§ãã€ãããŸããã®ããã«è£åŒ·ã
ããéŒæ¿ã®æå€§æ²ãå¿åã¯42KgïŒ50mmå·Ÿã§ãã€
ãã During the above heating, there was no phenomenon in which the resin component of the reinforced epoxy resin sheet dripped from the base material, and a bead-shaped bulge was formed by the foam layer with a predetermined expansion ratio and this foam layer. A reinforcing layer consisting of a fiber-reinforced resin layer with good strength was obtained. This reinforcing layer also had a good appearance. The maximum bending stress of the steel plate reinforced in this way was 42 kg/50 mm width.
宿œäŸ ïŒ
ãšããã·æš¹èçµæç©äžã®ã¢ã¹ãã¹ãç²ïŒéšã®ä»£
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åŸãããã®è£åŒ·æãçšããŠå®æœäŸïŒãšåæ§ã®æäœ
ã§éŒæ¿ãè£åŒ·ãããšãããå ç±äžã®æš¹èã®ããèœ
ã¡ããããããšãªã宿œäŸïŒãšåæ§ã®è£åŒ·å±€ã圢
æã§ããããã®ããã«è£åŒ·ããéŒæ¿ã®æå€§æ²ãå¿
åã¯43KgïŒ50mmå·Ÿã§ãã€ããExample 3 A reinforcing material was obtained in the same manner as in Example 1, except that 6 parts of finely powdered silica and 1 part of glycerin were used instead of 7 parts of asbestos powder in the epoxy resin composition. When a steel plate was reinforced using this reinforcing material in the same manner as in Example 1, a reinforcing layer similar to that in Example 1 could be formed without dripping of the resin during heating. The maximum bending stress of the steel plate reinforced in this way was 43 kg/50 mm width.
第ïŒå³ã¯ãã®çºæã®è£åŒ·æã®äžå®æœäŸã瀺ãæ
èŠå³ã第ïŒå³ã¯è£åŒ·æã®å ç±åã®è£
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çé¢ãïŒïœâŠâŠããŒãç¶èš
åºéšãïŒâŠâŠããŒã圢ææã
FIG. 1 is a perspective view showing one embodiment of the reinforcing material of the present invention, FIG. 2 is a sectional view showing the reinforcing material in a state in which it is installed before heating, and FIG. 3 is a sectional view showing the state after heating. DESCRIPTION OF SYMBOLS 1... Reinforcement material, 2... Fibrous base material, 3... Reinforced resin sheet, 3a... Mounting surface, 3b... Bead-shaped swelling part, 4... Bead forming material.
Claims (1)
鲿¢ããããããªæº¶èç²åºŠãéäžããããã®ç©è³ª
ãé åããæªç¡¬åãªããå硬åç¶ã®ç±ç¡¬åæ§è£åŒ·
æš¹èã·ãŒãã®äžé¢ã«ããã®ã·ãŒããã现巟ã«ãã
ãã€åèšã·ãŒãã硬åããåã«ã·ãŒãã«ããŒãç¶
èšåºéšã圢æããããŒã圢ææãæ·»çãããåèš
ããŒã圢ææã®å·Ÿããåºã匵ãåºããåèšã·ãŒã
ã®ããŒã圢ææåŽã®è£Ÿéšãè£ çé¢ã圢æããããš
ãç¹åŸŽãšããè£åŒ·æã ïŒ å ç±æº¶èæã®åäžã鲿¢ããããããªæº¶èç²
床ãéäžããããã®ç©è³ªãã¢ã¹ãã¹ãç²ãããª
ãããã®ã¢ã¹ãã¹ãç²ãç±ç¡¬åæ§æš¹èçµæç©äžã®
ããªããŒæå100éééšã«å¯ŸããŠïŒã20éééšé
åããç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®è£åŒ·æã ïŒ å ç±æº¶èæã®åäžã鲿¢ããããããªæº¶èç²
床ãéäžããããã®ç©è³ªãåŸ®ç²æ«ã·ãªã«ãšã°ãªã»
ãªã³ãšã®æ··åç³»ãããªããããããç±ç¡¬åæ§æš¹è
çµæç©äžã®ããªããŒæå100éééšã«å¯ŸããŠåŸ®ç²
æ«ã·ãªã«ã§ïŒã10éééšãã°ãªã»ãªã³ã§0.5ãïŒ
éééšé åããç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®è£åŒ·
æã ïŒ ç¹ç¶åºæãã¬ã©ã¹ç¹ç¶åžã§ããç¹èš±è«æ±ã®ç¯
å²ç¬¬ïŒé ãªãã第ïŒé ã®ããããã«èšèŒã®è£åŒ·
æã[Scope of Claims] 1. An uncured or semi-cured thermosetting reinforced resin sheet containing a fiber base material and containing a substance to impart a melt viscosity that can prevent drooping during heating and melting. A bead forming material having a width narrower than that of the sheet and forming a bead-shaped bulge on the sheet before the sheet is cured is attached to one side, and a bead of the sheet protrudes wider than the width of the bead forming material. A reinforcing material characterized in that a hem on the side of the forming material forms a mounting surface. 2. The substance for imparting a melt viscosity that can prevent drooping during heating and melting is composed of asbestos powder, and this asbestos powder is added in an amount of 2 to 20 parts by weight per 100 parts by weight of the polymer component in the thermosetting resin composition. The reinforcing material according to claim 1, in which the reinforcing material is blended in parts by weight. 3 The substance for imparting a melt viscosity that can prevent drooping during heating and melting is a mixture of finely powdered silica and glycerin, which is added to 100 parts by weight of the polymer component in the thermosetting resin composition. 4 to 10 parts by weight of finely powdered silica and 0.5 to 3 parts by weight of glycerin
The reinforcing material according to claim 1, in which the reinforcing material is blended in parts by weight. 4. The reinforcing material according to any one of claims 1 to 3, wherein the fiber base material is a glass fiber cloth.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56037525A JPS57151352A (en) | 1981-03-16 | 1981-03-16 | Reinforcing material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56037525A JPS57151352A (en) | 1981-03-16 | 1981-03-16 | Reinforcing material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57151352A JPS57151352A (en) | 1982-09-18 |
| JPS6121141B2 true JPS6121141B2 (en) | 1986-05-26 |
Family
ID=12499952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56037525A Granted JPS57151352A (en) | 1981-03-16 | 1981-03-16 | Reinforcing material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57151352A (en) |
-
1981
- 1981-03-16 JP JP56037525A patent/JPS57151352A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57151352A (en) | 1982-09-18 |
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