JPH01295078A - Manufacture for gasket compound material - Google Patents
Manufacture for gasket compound materialInfo
- Publication number
- JPH01295078A JPH01295078A JP12070688A JP12070688A JPH01295078A JP H01295078 A JPH01295078 A JP H01295078A JP 12070688 A JP12070688 A JP 12070688A JP 12070688 A JP12070688 A JP 12070688A JP H01295078 A JPH01295078 A JP H01295078A
- Authority
- JP
- Japan
- Prior art keywords
- gasket
- resin
- mold
- liquid resin
- molding groove
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 239000000463 material Substances 0.000 title abstract description 5
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 229920005989 resin Polymers 0.000 claims abstract description 48
- 239000011347 resin Substances 0.000 claims abstract description 48
- 238000000465 moulding Methods 0.000 claims abstract description 24
- 239000007788 liquid Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 24
- 239000002131 composite material Substances 0.000 claims description 18
- 238000002347 injection Methods 0.000 claims description 4
- 239000007924 injection Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 abstract description 7
- 238000000576 coating method Methods 0.000 abstract description 7
- 239000007789 gas Substances 0.000 description 17
- 238000010438 heat treatment Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 239000003094 microcapsule Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 238000010107 reaction injection moulding Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- BKWAVXQSZLEURV-UHFFFAOYSA-N 2-chloro-1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)C(Cl)C(F)(F)F BKWAVXQSZLEURV-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004944 Liquid Silicone Rubber Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229960004065 perflutren Drugs 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- PCHQDTOLHOFHHK-UHFFFAOYSA-L zinc;hydrogen carbonate Chemical compound [Zn+2].OC([O-])=O.OC([O-])=O PCHQDTOLHOFHHK-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はシリンダーヘッド、オイルパン等の車輌部品、
モータハウジング等の電機部品等、ガスケットを介して
他部品との接合を必要とされる各種被着部品にガスケッ
トを接着し、ガスゲットと被着部品の一体化されたガス
ケット複合体を製造する方法に係り、特に、ガスケット
の寸法精度が良り、パリやボイドがないガスケット複合
体の製造方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention is applicable to vehicle parts such as cylinder heads and oil pans;
A method of bonding gaskets to various adherend parts that require connection to other parts via gaskets, such as electrical parts such as motor housings, and manufacturing gasket composites in which the gas get and adherend parts are integrated. In particular, the present invention relates to a method of manufacturing a gasket composite having good dimensional accuracy and no voids or voids.
各種車輌部品、例えばシリンダーヘッド、オイルパン、
計器カバー、インテークマニホールド、ニゲシーストマ
ニホールド等、あるいはまた、各種電機部品、例えばフ
ロッピーディスク、モータハウジング等、各種部品はガ
スケットを介して他部品との接合を必要とされ、このた
め、前記各種部品(以下、被着部品という)にあらかし
めガスケット層の被着されたガスケット複合体が開発さ
れている。Various vehicle parts, such as cylinder heads, oil pans,
Various parts such as instrument covers, intake manifolds, exhaust manifolds, etc., or various electrical parts such as floppy disks and motor housings need to be connected to other parts via gaskets. Gasket composites have been developed in which a roughened gasket layer is adhered to the adhered part (hereinafter referred to as the adhered part).
この種のガスケット複合体の製造方法として、従来、ガ
スケットの被着すべき被着部品に液状ガスケット材料を
スクリーン印刷により印刷して、被着部品にガスゲット
を形成する方法が知られている。(特公昭43−472
7号公報参照)。As a method for manufacturing this type of gasket composite, a method is conventionally known in which a liquid gasket material is printed on a part to which a gasket is to be attached by screen printing to form a gas get on the part. (Tokuko Sho 43-472
(See Publication No. 7).
また、被着部品のフランジ面に液状シール材をロボ7)
等により塗布した後、接着硬化する方法も知られている
。In addition, apply liquid sealant to the flange surface of the adhered parts.
There is also known a method in which the adhesive is cured after being applied by a method such as the following.
さらに、射出成形により被着部品にガスケット層を形成
する方法も知られている。Furthermore, a method of forming a gasket layer on an adhered part by injection molding is also known.
さらにまた、被成形部品に液状樹脂を塗りつけ、これを
かぶせ型で覆って硬化させる方法も提唱されている。(
特開昭60−237267号公轄参照)。Furthermore, a method has been proposed in which a liquid resin is applied to the part to be molded, and the resin is covered with a mold and cured. (
(Refer to Japanese Patent Application Publication No. 60-237267).
しかし、前述第1番目の方法はガスケット層の厚みが多
くとれず、かつ被着部品のガスケット被着面が平面でな
ければならない等の制限を有している。However, the first method described above has limitations such as the inability to provide a large thickness of the gasket layer and the need for the gasket-adhering surface of the adhered part to be flat.
また、第2番目の方法は塗布ビードの合わせ部の精度や
、ビードの寸法精度にも問題がある。Furthermore, the second method has problems with the accuracy of the joining portion of the coating beads and the dimensional accuracy of the beads.
さらに第3番目の方法は寸法精度や量産性に優れている
ものの、金型コストが高く、少量多種生産に向いておら
ず、かつ型締め力が強いため、弱い被着部品や、傷のつ
きやすい部品の成形には向いていない。さらに、この方
法は金型との離型の問題があり、接着によりガスケット
と被着体部品を一体化することがむづかしいという問題
もある。Furthermore, although the third method has excellent dimensional accuracy and mass production, the mold cost is high, it is not suitable for low-volume, high-mix production, and the mold clamping force is strong, so it is difficult to use with weak adherent parts or damage. It is not suitable for molding easy parts. Furthermore, this method has the problem of release from the mold, and there is also the problem that it is difficult to integrate the gasket and the adherend component by adhesion.
次に、第4番目の方法はかぶせ型をかふせる際、キャビ
ティ内に空気だまりができやすかったり、さらには液状
樹脂がはみ出してパリが出来やすいという欠点を有して
いる。Next, the fourth method has the disadvantage that air pockets are likely to be formed in the cavity when the covering mold is covered, and furthermore, the liquid resin is likely to overflow and cause cracks.
そこで、本発明の目的はガスケットの寸法精度が良く、
かつパリやボイドがなく、前述の公知技術に存する欠点
を改良したガスケット複合体の製造方法を提供すること
にある。Therefore, the purpose of the present invention is to improve the dimensional accuracy of the gasket.
Another object of the present invention is to provide a method for producing a gasket composite which is free from voids and voids and which improves the drawbacks of the above-mentioned known techniques.
前述の目的を達成するため、本発明によれば、ガスゲッ
ト成形型に形成されたガスゲット成形溝に硬化膨脹性液
状樹脂を注入し、その上にガスケットの被着すべき被着
部品を覆いかぶせて圧着の後、前記樹脂を硬化膨張させ
て前記被着部品に接着し、ガスケットと被着部品の一体
化されたガスケント複合体を得ることを特(衣とする。In order to achieve the above-mentioned object, according to the present invention, a cured expandable liquid resin is injected into a gas get molding groove formed in a gas get mold, and a part to be covered with a gasket is covered thereon. After covering and crimping, the resin is cured and expanded and adhered to the adhered part to obtain a gasket composite in which the gasket and the adhered part are integrated.
以下、本発明を添付図面を用いて詳述する。Hereinafter, the present invention will be explained in detail using the accompanying drawings.
第1図、第2図および第3図はそれぞれ本発明方法の一
工程を表した工程図であって、第1図に示されるように
ガスケット成形型lの中空部2の底面3にはガスケット
成形溝4が刻設され、このガスケット成形/J[4には
硬化膨脹性液状樹脂5が吐出ノズル6を通してハンドリ
ングにより、あるいはロボット等の自動操作により注入
される。ガスケット成形型lは少なくとも前記樹脂5と
接触する部分が該樹脂5と離型性を有する材質、例えば
テフロンやシリコーン樹脂等で形成されるが、あるいは
テフロン、シリコーン、チノ化ホウ素、ジルコニア等の
離型剤を塗布することにより離型処理して形成される。1, 2, and 3 are process diagrams showing one step of the method of the present invention, and as shown in FIG. 1, the bottom surface 3 of the hollow part 2 of the gasket mold l has a gasket A forming groove 4 is cut into the gasket forming groove 4, and a cured expandable liquid resin 5 is injected into the gasket forming groove 4 through a discharge nozzle 6 by handling or by automatic operation using a robot or the like. At least the part of the gasket mold 1 that comes into contact with the resin 5 is made of a material that has release properties from the resin 5, such as Teflon or silicone resin. It is formed by applying a molding agent and performing a mold release process.
また、面記樹脂5のガスケット成形溝4への注入量はガ
スケット成形溝4の深さよりも少ない量であって、かつ
硬化膨脹後ガスケット成形溝4の深さよりも高くなるよ
うな量である。Further, the amount of surface resin 5 injected into the gasket forming groove 4 is an amount smaller than the depth of the gasket forming groove 4 and higher than the depth of the gasket forming groove 4 after curing and expansion.
これを具体的に示せば、液状樹脂5の硬化膨脹後の容積
を■1とし、ガスケット成形/1%4の容積をvoとす
ると、V + / V o ” 1 、05〜5 、0
)範。To express this concretely, if the volume of the liquid resin 5 after curing and expansion is 1, and the volume of gasket molding/1% 4 is vo, then V + /V o ” 1,05~5,0
) Range.
内であることが好ましい。これが1.05よりも小さい
と、硬化膨脹後に硬化物が被着部品に到達しなかったり
、エアベントが充分に行われず、ボイドが発生するおそ
れがある。また、5.0よりも大きくなると、豚腸内圧
が高くなって、必要以上に破着物品の圧着力を上げる必
要が生じ、さらに液状樹脂がはみ出してパリが発生しや
すくなる。It is preferable that it be within. If this is smaller than 1.05, the cured product may not reach the adhered part after curing and expansion, or air venting may not be performed sufficiently, leading to the possibility that voids may occur. On the other hand, if it is larger than 5.0, the pressure in the pig's intestine will increase, making it necessary to increase the pressing force of the torn article more than necessary, and furthermore, the liquid resin will spill out and flakes are likely to occur.
次いで、本発明は前述のようにして硬化膨脹性液状樹脂
5の注入されたガスゲット成形溝4上に、第2図ならび
に第3図に示されるようにガスケットの被着すべき被着
部品7を覆いかぶせ、プレス板8を介して加圧ラム9に
より圧着しながら硬化膨張性液状樹脂5を硬化膨脹させ
る。このときの圧着力は数kg f /数百kgfであ
る。また、この樹脂5の硬化に際して、加熱加圧を必要
とする場合には、ヒータ10の内蔵されたプレス板8を
用いて加熱加圧するが、一方、第3図示のように内部に
ヒータ10の内蔵された成形型lを用いてガスケット成
形型1の側から樹脂5を加熱してもかまわず、あるいは
また、誘導、誘電、超音波加熱等で加熱してもよく、さ
らには全体を加熱炉に入れて加熱してもよい。Next, in the present invention, as shown in FIGS. 2 and 3, a part 7 to be covered with a gasket is placed on the gas get molding groove 4 into which the cured expandable liquid resin 5 has been injected as described above. is covered, and the cured expandable liquid resin 5 is cured and expanded while being pressed by a pressurizing ram 9 via a press plate 8. The pressing force at this time is several kgf/several hundred kgf. In addition, when heat and pressure are required to cure the resin 5, the heat and pressure is applied using a press plate 8 having a built-in heater 10. The resin 5 may be heated from the side of the gasket mold 1 using the built-in mold 1, or it may be heated by induction, dielectric, ultrasonic heating, etc., or the entire resin 5 may be heated in a heating furnace. You can also heat it by putting it in.
このとき、樹脂5は当初第4図(a)に示されるように
、ガスケット成形溝4の深さhlよりも少ない量、例え
ばh2の高さの量であるが、第4図(b)に示されるよ
うにガスケット成形/lI4の上に被着部品7を覆いか
ぶせるとともにこの上からヒータ10の内蔵されたブレ
2手反8を当て力くって矢印方向に加熱圧着すると、や
がて樹脂5は硬化し始め、ガスケット成形溝4内のエア
を追い出しながら矢印方向に膨脹し、最終的には第4図
(C)に示されるようにガスケット成形溝4の深さhl
よりも高いところまで硬化膨脹して被着部品7に当接し
て接着する。このとき、樹脂5はガスゲット成形溝4の
面とは接着せず、被着部品7のみと選択的に接着し、脱
型の後第5図示のように、ガスケノ)5aと被着部品7
の一体化されたガスケット複合体Aを形成する。At this time, as shown in FIG. 4(a), the amount of resin 5 is initially smaller than the depth hl of the gasket molding groove 4, for example, the height h2, but as shown in FIG. 4(b). As shown, the adhered part 7 is placed over the gasket molding/lI4, and the part 7 is heated and pressed in the direction of the arrow by applying pressure from above with the built-in blur 2 of the heater 10, and then the resin 5 is hardened. It expands in the direction of the arrow while expelling the air in the gasket forming groove 4, and finally the depth hl of the gasket forming groove 4 increases as shown in FIG. 4(C).
It hardens and expands to a height higher than that, contacts the adherend part 7, and adheres. At this time, the resin 5 does not adhere to the surface of the gas get molding groove 4, but selectively adheres only to the adhered part 7, and after demolding, as shown in the fifth figure, the resin 5 is bonded to the adhered part 7.
forming an integrated gasket composite A.
なお、第4図(d)に示されるように、被着部品7の樹
脂5との当接個所は凹形状であってもよく、この場合、
樹脂5は前述と同様、エアを追い出しながら膨脹し、や
がて凹部の底面7aに当接して接着する。In addition, as shown in FIG. 4(d), the contact portion of the adhered part 7 with the resin 5 may have a concave shape; in this case,
As described above, the resin 5 expands while expelling air, and eventually comes into contact with and adheres to the bottom surface 7a of the recess.
また、第5間のガスケット複合体Aにおいて、ガスケッ
ト5aと被着部材7の接着部11からパリ、はみ出しの
発生を防止するために、第6図に示されるように、境界
部11にガスケット成形型1の底面3から突起12を形
成し、成型の際に突起12を被着部品7にくい込ませて
行うようにし、あるいは第7図示のように、境界部11
に、テフロン、シリコーン等、離型性を有する軟質材料
からなる軟質パツキン13を挟着して成型し、さらには
第8図に示されるように、テフロン、シリコーン等、離
型性を有する軟質材料からなり、高さがガスケット成形
溝4の深さよりもやや高い断面コ字型の溝状型材4をガ
スケット成形溝4に嵌め込み、先端部15を底面3から
やや突出させた状態で成型してもよい。In addition, in the gasket composite A between the fifth gap and the gasket 5a, in order to prevent the adhesive portion 11 between the gasket 5a and the adhered member 7 from popping out, a gasket is formed on the boundary portion 11 as shown in FIG. A protrusion 12 is formed from the bottom surface 3 of the mold 1, and the protrusion 12 is inserted into the adherend part 7 during molding, or as shown in FIG.
A soft packing 13 made of a soft material with mold releasability such as Teflon or silicone is sandwiched and molded, and as shown in FIG. Even if a grooved material 4 having a U-shaped cross section with a height slightly higher than the depth of the gasket molding groove 4 is fitted into the gasket molding groove 4 and molded with the tip 15 slightly protruding from the bottom surface 3. good.
上述のようにして得られる本発明ガスケット複合体Aは
ガスケット成形溝4の形状を任意に選定することにより
任意の形状に成型でき、例えば、第9図(a)、(b)
、(c)、(d)に示されるような断面形状に成型され
る。The gasket composite A of the present invention obtained as described above can be molded into any shape by arbitrarily selecting the shape of the gasket molding groove 4, for example, as shown in FIGS. 9(a) and (b).
, (c), and (d).
また、本発明に用いられる硬化膨張性液状樹脂5はガス
ケット成形溝4への圧入時には液状を呈し、硬化時に膨
脹して体積が増えるものであって、液状樹脂そのものと
しては例えば、縮合、付加、過酸化物架橋反応による液
状シリコーンゴム、ウレタン樹脂、エポキシ樹脂、ナイ
ロン、フェノール樹脂、ポリブタジェン等のRIM(反
応射出成形)用樹脂、樹脂粉末と可ヅ剤を混合し、液状
としたプラスチゾル、その他ポリサルファイド、ポリア
クリルウレタン、ポリアクリロニトリルブタジエンコボ
リマー等の反応性液状ゴム、硬化性樹脂等が挙げられ、
硬化に体積を膨脹させる手段としては例えば、発泡剤の
添加、溶剤マイクロカプセルの添加、反応生成物として
ガスを発生させる方法、ガスや溶剤を混合し、加熱によ
り膨脹させる方法等が挙げられる。Further, the cured expandable liquid resin 5 used in the present invention is in a liquid state when press-fitted into the gasket molding groove 4, and expands during curing to increase its volume. Liquid silicone rubber produced by peroxide crosslinking reaction, urethane resin, epoxy resin, nylon, phenol resin, resin for RIM (reaction injection molding) such as polybutadiene, plastisol made into a liquid by mixing resin powder and a softening agent, and other polysulfides. , reactive liquid rubbers such as polyacrylic urethane, polyacrylonitrile butadiene copolymer, curable resins, etc.
Examples of means for expanding the volume during curing include adding a foaming agent, adding solvent microcapsules, generating gas as a reaction product, mixing gas and solvent, and expanding by heating.
ここで、発泡剤としては重炭酸ナトリウム、重炭酸亜鉛
等の無機系発泡剤、N、N’−ジニトロソペンタンメチ
レンテトラミン、アゾカルボンアミド等の有機系発泡剤
等が挙げられ、この配合量は液状樹脂100重量部に対
して0.1〜40重量部であり、0.1重量部より少な
いと充分な膨張効果が得られず、また、40重量部より
多いと硬化物の物性を著しく損なうおそれがある。また
、溶剤マイクロカプセルとしてはアルコール系の低沸点
溶剤等を塩化ビニリデン等の殻壁で包んだ粒径数ミクロ
ン−数100ミクロンのものが挙げられ、具体的には松
本油脂製薬(株)製「マツモトマイクロスフェア−F−
30、F−50J等である。この添加量は前記発泡剤と
同様である。Examples of the blowing agent include inorganic blowing agents such as sodium bicarbonate and zinc bicarbonate, and organic blowing agents such as N,N'-dinitrosopentane methylenetetramine and azocarbonamide. The amount is 0.1 to 40 parts by weight per 100 parts by weight of the liquid resin; if it is less than 0.1 part by weight, a sufficient expansion effect cannot be obtained, and if it is more than 40 parts by weight, the physical properties of the cured product will be significantly impaired. There is a risk. In addition, examples of solvent microcapsules include those with a particle size of several microns to several hundred microns, in which a low-boiling point solvent such as alcohol is wrapped in a shell wall such as vinylidene chloride. Matsumoto Microsphere-F-
30, F-50J, etc. The amount added is the same as that of the foaming agent.
反応生成物としてガスを発生させる方法としては、例え
ばシリコーン樹脂の場合、水素基をもったシロキサンと
シラノール店を有するシロキサンを酸、アルカリ土類金
属化合物、白金系等の触媒の存在下で脱水素縮合反応さ
せ、発生する水素ガスを利用し、また、ウレタン樹脂の
場合、イソシアネート基と水を反応させて発生する炭酸
ガスを利用する。For example, in the case of silicone resin, a method for generating gas as a reaction product is to dehydrogenate siloxane with hydrogen groups and siloxane with silanol stores in the presence of an acid, an alkaline earth metal compound, a platinum-based catalyst, etc. A condensation reaction is carried out, and the generated hydrogen gas is used. In the case of urethane resin, an isocyanate group and water are reacted, and carbon dioxide gas generated is used.
ガスや溶剤を混合して加熱により膨張させる方法として
は、例えばフッ素化炭化水素(パーフルオロシクロブタ
ン、パーフルオロプロパン、クロロヘキサフルオロプロ
パン等)、プロパン、ブタン、ペンタン、ヘキサン等の
炭化水素類、アルコール類、エステル類、エーテル類、
ケトン類、ハロゲン化炭化水素、N2.0!、co2等
のガス類を単独で、あるいは複数種の混合物として、液
状樹脂中に溶かし込み、あるいは強制的に攪拌混合し、
次いでこのガスの混合された液状樹脂を加熱することに
よりガスを発生させ、液状樹脂を膨張する。Examples of methods of mixing gases and solvents and expanding them by heating include fluorinated hydrocarbons (perfluorocyclobutane, perfluoropropane, chlorohexafluoropropane, etc.), hydrocarbons such as propane, butane, pentane, hexane, and alcohol. esters, ethers,
Ketones, halogenated hydrocarbons, N2.0! , CO2 and other gases alone or as a mixture of multiple types are dissolved in a liquid resin, or by forcibly stirring and mixing.
Next, by heating the liquid resin mixed with this gas, gas is generated and the liquid resin is expanded.
このときのガスの添加量は前記発泡剤と同様である。The amount of gas added at this time is the same as that of the foaming agent.
本発明にかかるガスケット複合体のシール性は被着部品
の圧着圧力との相関によって得られるものであるが、従
来の射出成形、RIM成形、LIM成形の型締力に比べ
て極端に低い圧力で充分に達成される。すなわち、通常
の射出成形の型締力は、
型締力(k+rf)−投影面積〔−〕×有効射出圧力(
kgf/c111)
によって求められ、小さな部品をつくるのにも数10を
以上の型締力を必要とする。The sealing performance of the gasket composite according to the present invention is achieved through a correlation with the pressure of the adhered parts, which is extremely low compared to the mold clamping force of conventional injection molding, RIM molding, and LIM molding. fully achieved. In other words, the mold clamping force for normal injection molding is: mold clamping force (k+rf) - projected area [-] x effective injection pressure (
kgf/c111), and even making small parts requires a mold clamping force of several 10 or more.
これに対して、本発明では、
圧着力(kgf)=投影面積〔d〕×
液状樹脂の豚腸圧(kgf/all)
でよく、液状樹脂の初期の充填量および膨張率を調整す
ることで数kg (〜数百kg (という1端に低い圧
着力で成形可能となる。In contrast, in the present invention, the following formula is sufficient: crimping force (kgf) = projected area [d] x pig intestinal pressure of liquid resin (kgf/all), and by adjusting the initial filling amount and expansion rate of liquid resin. It is possible to mold with a low pressure force of several kg (~several hundred kg) at one end.
また、本発明に用いられる成形型は構造が簡単で、精度
および強度的にも通常の射出成型にくらべてそれほど高
いものが要求されず、このため多品種少量生産に向いて
いる。Furthermore, the mold used in the present invention has a simple structure and does not require much higher accuracy and strength than ordinary injection molding, and is therefore suitable for high-mix, low-volume production.
さらに、本発明では従来のスクリーン印刷では不可能で
あった一部に突起のある立体的な被着部品に対しても成
形可能である。Furthermore, according to the present invention, it is possible to form three-dimensional adherend parts having some protrusions, which was impossible with conventional screen printing.
以下、本発明を実施例により詳述する。 Hereinafter, the present invention will be explained in detail with reference to Examples.
爽迎典上二土エル悦匠上二1
第1図に示す形状のガスケット成形型として、硬度D7
5、伸び400%、引張強度43Qkg f / cd
(Dふっ素樹脂製成形型であって、ガスケット成形溝
が溝断面2×2龍のものを用い、この成形溝に表−1に
示す液状樹脂(U−1,U−2)を1,2m−ノズル径
の吐出ノズルからロボットにより注入し注入後、直ちに
J I S G3141冷間圧延口板(40X90×2
tm)の鉄板を第2図示のように上から覆いかぶせ、加
熱、加圧を行い、成形溝の液状樹脂を膨張硬化させた。As a gasket mold having the shape shown in Figure 1, the hardness is D7.
5. Elongation 400%, tensile strength 43Qkg f/cd
(Use a D fluororesin mold with a gasket molding groove of 2 x 2 groove cross section, and apply 1.2 m of liquid resin (U-1, U-2) shown in Table 1 to this molding groove. - Inject by robot from the discharge nozzle of the nozzle diameter. Immediately after injection, JIS G3141 cold rolling mouth plate (40
tm) iron plate was covered from above as shown in the second figure, and heating and pressure were applied to expand and harden the liquid resin in the molding groove.
このときの各種条件ならびに試験結果を表−2に示す。Table 2 shows various conditions and test results at this time.
・/ ・ / /′ / / /′ / 表−11量g。・/ ・ / /′ / / /′ / Table-11 Quantity g.
表−2において、耐圧性試験は得られた複合体にアクリ
ル板をかぶせ、M8のボルト4本で4ずみを締めつけた
後、水柱30ONの圧力をかけて5分間保持し、もれが
はっきり生じるかどうかを目視にて観察することにより
行った。また、接着性試験については、ガスゲット層を
指先でつまみ、軽く引張ったときにはがれるかどうかを
観察することにより行った。In Table 2, the pressure resistance test was carried out by covering the obtained composite with an acrylic plate, tightening it four times with four M8 bolts, applying a pressure of 30 ON water column and holding it for 5 minutes, and leakage clearly occurred. This was determined by visual observation. The adhesion test was conducted by pinching the gas get layer with fingertips and observing whether it would peel off when pulled lightly.
表−2から、本発明にかかる実施例1〜4はいずれの試
験でも良好な結果を示したが、注入容積割合が4.0%
と低い比較例1では接着性に劣ってもれが発生するとと
もにボイドが発生し、また、圧着力の小さい比較例2で
はパリの発生が著しいことがわかった。From Table 2, Examples 1 to 4 according to the present invention showed good results in all tests, but the injection volume ratio was 4.0%.
It was found that Comparative Example 1, which had a low adhesive strength, had poor adhesion and leakage and voids occurred, and Comparative Example 2, which had a low pressure bonding force, had a significant occurrence of flaking.
プμm生り二1
表−1の液状樹脂の代わりに表−3の樹脂を用いたこと
を除いて実施例1〜4と同様にして行い、条件ならびに
試験結果を表−4に示した。Tests were conducted in the same manner as in Examples 1 to 4, except that the resin shown in Table 3 was used instead of the liquid resin shown in Table 1, and the conditions and test results are shown in Table 4.
なお、表−3において、rKE1830Jは信越化学工
業(株)製−液加熱硬化型自己接着タイプのシリコーン
エラストマーであり、「F 30jならびにrF−5
0Jは松本油脂製薬(株)製の溶剤マイクロカプセルで
ある。In Table 3, rKE1830J is a self-adhesive silicone elastomer manufactured by Shin-Etsu Chemical Co., Ltd.
0J is a solvent microcapsule manufactured by Matsumoto Yushi Pharmaceutical Co., Ltd.
表−3
表−4
表−4から、本発明にかかる実施例5〜9はいずれも各
種試験において良好な結果を示すことがわかる。Table 3 Table 4 Table 4 shows that Examples 5 to 9 according to the present invention all showed good results in various tests.
以上のとおり、本発明方法によれば、簡単な成形型を用
いて、かつ極めて低い圧着力で、ボイドもパリも発生せ
ず、しかも接着は良好なガスケット複合体を容易に、確
実に成形加工することができる。As described above, according to the method of the present invention, it is possible to easily and reliably mold a gasket composite that does not generate voids or flakes and has good adhesion using a simple mold and with extremely low pressure bonding force. can do.
第1図は本発明にかかるガスヶ、/)成形型の一具体例
の斜視図ならびに本発明の一工程を表した説明図であり
、第2図ならびに第3図はそれぞれ本発明方法を説明す
るための断面図であり、第4図(a)、(b)、(c)
、(d)は本発明にかかる液状樹脂の硬化膨脹状態を表
した断面図であり、第5図は本発明方法によって得られ
たガスケット複合体の一具体例の斜視図であり、第6図
、第7図および第8図はそれぞれパリ、はみ出し等を防
止するだめの好ましい具体例を表した断面図であり、第
9図(a)、(b)、(c)、(d)はそれぞれガスケ
ット層の形状を表した断面図である。
1・・・ガスケット成形型、
4・・・ガスケット成形溝、
5・・・硬化膨張性液状樹脂、 7・・・被着部品、A
・・・ガスケット複合体。
特許出願人 株式会社スリーボンド
代理人 弁理士 染谷 仁、□
各7目
(d)
リ ダ
箋5圏
箋9目
(、Q)FIG. 1 is a perspective view of a specific example of a gas mold and a mold according to the present invention, and an explanatory diagram showing one step of the present invention, and FIGS. 2 and 3 each illustrate the method of the present invention. 4(a), (b), (c).
, (d) are cross-sectional views showing the cured and expanded state of the liquid resin according to the present invention, FIG. 5 is a perspective view of a specific example of a gasket composite obtained by the method of the present invention, and FIG. , FIG. 7, and FIG. 8 are sectional views showing preferred specific examples of the stopper for preventing cracks, extrusion, etc., respectively, and FIGS. 9(a), (b), (c), and (d) are respectively FIG. 3 is a cross-sectional view showing the shape of a gasket layer. DESCRIPTION OF SYMBOLS 1... Gasket mold, 4... Gasket forming groove, 5... Cured expandable liquid resin, 7... Adhered parts, A
...Gasket complex. Patent applicant ThreeBond Co., Ltd. Agent Patent attorney Hitoshi Someya, □ 7th each (d) Reader 5th circle 9th (, Q)
Claims (4)
に硬化膨脹性液状樹脂を注入し、その上にガスケットの
被着すべき被着部品を覆いかぶせて圧着の後、前記樹脂
を硬化膨脹させて前記被着部品に接着し、ガスケットと
被着部品の一体化されたガスケット複合体を得ることを
特徴とするガスケット複合体の製造方法。(1) Inject a cured expandable liquid resin into the gasket molding groove formed in the gasket mold, cover the part to be covered with the gasket and press it, and then harden and expand the resin. A method for producing a gasket composite, which comprises adhering to the adhered part to obtain a gasket composite in which the gasket and the adhered part are integrated.
脹性液状樹脂の注入量がガスケット成形溝の深さよりも
少ない量であって、硬化膨張後ガスケット成形溝の深さ
よりも高くなるような量であるガスケット複合体の製造
方法。(2) In the method according to claim 1, the amount of the cured expandable liquid resin injected is smaller than the depth of the gasket forming groove, and is higher than the depth of the gasket forming groove after curing and expansion. A method of manufacturing a gasket composite in a quantity of
脹性液状樹脂の注入量が前記液状樹脂の硬化膨脹後の容
積をV_1、とし、前記ガスケット成形溝の容積をV_
0とした場合、V_1/V_0=1.05〜5.0の範
囲内であるガスケット複合体の製造方法。(3) In the method according to claim 2, the injection amount of the cured expandable liquid resin is such that the volume of the liquid resin after cure and expansion is V_1, and the volume of the gasket forming groove is V_1.
A method for manufacturing a gasket composite in which V_1/V_0 is within the range of 1.05 to 5.0 when V_1/V_0 is 0.
は数kgf〜数百kgfの範囲内であるガスケット複合
体の製造方法。(4) The method of manufacturing a gasket composite according to claim 1, wherein the pressure force is within a range of several kgf to several hundred kgf.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12070688A JPH01295078A (en) | 1988-05-19 | 1988-05-19 | Manufacture for gasket compound material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12070688A JPH01295078A (en) | 1988-05-19 | 1988-05-19 | Manufacture for gasket compound material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01295078A true JPH01295078A (en) | 1989-11-28 |
Family
ID=14792975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12070688A Pending JPH01295078A (en) | 1988-05-19 | 1988-05-19 | Manufacture for gasket compound material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01295078A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0408317A2 (en) * | 1989-07-11 | 1991-01-16 | LOCTITE (IRELAND) Ltd. | Method of forming gaskets by injection and compositions for use therein |
EP0671575A2 (en) * | 1993-11-17 | 1995-09-13 | Toyota Jidosha Kabushiki Kaisha | Process of forming gasket directly on workpiece, apparatus and mold suitable for the process |
DE19818475A1 (en) * | 1998-04-24 | 1999-11-18 | Siemens Ag | Joint seal between two moving parts one in relation to other, used e.g. in IC engine fuel injection systems, vehicle braking systems or hydraulic jacks |
GB2543370A (en) * | 2016-03-17 | 2017-04-19 | Galvgard (U K ) Ltd | A gasket arrangement |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6016255A (en) * | 1983-07-06 | 1985-01-28 | Shinwa Boeki Kk | Packing sealing material for filter |
JPS6282010A (en) * | 1985-10-04 | 1987-04-15 | Mitsuboshi Belting Ltd | Manufacture of foamed molded article |
-
1988
- 1988-05-19 JP JP12070688A patent/JPH01295078A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6016255A (en) * | 1983-07-06 | 1985-01-28 | Shinwa Boeki Kk | Packing sealing material for filter |
JPS6282010A (en) * | 1985-10-04 | 1987-04-15 | Mitsuboshi Belting Ltd | Manufacture of foamed molded article |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0408317A2 (en) * | 1989-07-11 | 1991-01-16 | LOCTITE (IRELAND) Ltd. | Method of forming gaskets by injection and compositions for use therein |
US5116558A (en) * | 1989-07-11 | 1992-05-26 | Loctite (Ireland) Limited | Method of forming gaskets by injection and compositions for use therein |
EP0671575A2 (en) * | 1993-11-17 | 1995-09-13 | Toyota Jidosha Kabushiki Kaisha | Process of forming gasket directly on workpiece, apparatus and mold suitable for the process |
EP0671575A3 (en) * | 1993-11-17 | 1995-10-25 | Toyota Motor Co Ltd | |
US5686032A (en) * | 1993-11-17 | 1997-11-11 | Toyota Jidosha Kabushiki Kaisha | Process of forming a gasket directly on workpiece, using a mold clamped to the workpiece |
DE19818475A1 (en) * | 1998-04-24 | 1999-11-18 | Siemens Ag | Joint seal between two moving parts one in relation to other, used e.g. in IC engine fuel injection systems, vehicle braking systems or hydraulic jacks |
DE19818475C2 (en) * | 1998-04-24 | 2001-05-31 | Siemens Ag | Fluid seal assembly and method of sealing |
GB2543370A (en) * | 2016-03-17 | 2017-04-19 | Galvgard (U K ) Ltd | A gasket arrangement |
GB2543370B (en) * | 2016-03-17 | 2019-04-10 | Galvgard U K Ltd | A gasket arrangement |
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