JPH05193053A - Rubber laminate for fuel - Google Patents
Rubber laminate for fuelInfo
- Publication number
- JPH05193053A JPH05193053A JP4027381A JP2738192A JPH05193053A JP H05193053 A JPH05193053 A JP H05193053A JP 4027381 A JP4027381 A JP 4027381A JP 2738192 A JP2738192 A JP 2738192A JP H05193053 A JPH05193053 A JP H05193053A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- layer
- nbr
- fuel
- trp
- 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
- 229920001971 elastomer Polymers 0.000 title claims abstract description 64
- 239000000446 fuel Substances 0.000 title claims abstract description 18
- 229920001973 fluoroelastomer Polymers 0.000 claims abstract description 21
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims abstract description 6
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 23
- 239000000126 substance Substances 0.000 claims description 11
- UEZWYKZHXASYJN-UHFFFAOYSA-N cyclohexylthiophthalimide Chemical compound O=C1C2=CC=CC=C2C(=O)N1SC1CCCCC1 UEZWYKZHXASYJN-UHFFFAOYSA-N 0.000 claims description 4
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 229920006027 ternary co-polymer Polymers 0.000 abstract description 2
- 125000005497 tetraalkylphosphonium group Chemical group 0.000 abstract 2
- 239000010410 layer Substances 0.000 description 47
- 238000004073 vulcanization Methods 0.000 description 15
- 239000003921 oil Substances 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000000295 fuel oil Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000011229 interlayer Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000012937 correction Methods 0.000 description 5
- 230000003014 reinforcing effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- ZZKZVYKAXYQGTK-UHFFFAOYSA-N 4-cyclohexylsulfanylisoindole-1,3-dione Chemical compound O=C1NC(=O)C2=C1C=CC=C2SC1CCCCC1 ZZKZVYKAXYQGTK-UHFFFAOYSA-N 0.000 description 2
- 241001441571 Hiodontidae Species 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000006229 carbon black Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000010060 peroxide vulcanization Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000010058 rubber compounding Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
Landscapes
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Rigid Pipes And Flexible Pipes (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、自動車の燃料油系統に
用いられる燃料用ゴムホースやダイヤフラムなど多層構
造のゴム積層体の改良に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in a rubber laminate having a multi-layer structure such as a rubber hose for fuel and a diaphragm used in a fuel oil system of an automobile.
【0002】[0002]
【従来の技術】自動車の燃料油系統には燃料用ゴムホー
スやダイヤフラムなど多層構造のゴム積層体が知られて
いる。この中で、エンジンルームの高温化や高圧循環に
伴う燃料油の酸化により、従来のNBRゴム最内層が硬
化劣化を生じるという問題や、SHED規制によるガソ
リン透過量の規制などのため、従来のNBR耐油層のガ
ソリンと接する表面にフッ素ゴムを積層して用いること
が行なわれている。2. Description of the Related Art In a fuel oil system of an automobile, a rubber laminate having a multi-layer structure such as a rubber hose for fuel and a diaphragm is known. Among them, the conventional NBR rubber innermost layer is hardened and deteriorated due to the oxidation of fuel oil due to the high temperature of the engine room and the high pressure circulation, and the conventional NBR rubber is regulated by the SHED regulation. It has been practiced to laminate and use fluororubber on the surface of the oil resistant layer that comes into contact with gasoline.
【0003】しかし、NBR層とフッ素ゴム層とは通常
は接着性に乏しく、実使用時の層間剥離やそれに伴う破
損が問題となっている。接着性を改良しようとする提案
も数多くなされているけれども、未だ完全とはいい難
い。例えば、特公昭55−16830号、特公昭55−16831号、
特公昭55−2336号、特開昭55−51554号、特開昭54−158
481号、特公昭57−49391号、特公昭59−35787号等の提
案は、いずれも成形プレスによる加圧加硫においても接
着状態は層間剥離であり、ホース製品では更に接着力が
低下するため、実用化が困難であった。However, the NBR layer and the fluororubber layer are usually poor in adhesiveness, and there has been a problem of delamination during actual use and damage associated therewith. Although many proposals have been made to improve the adhesiveness, it is still hard to say that it is perfect. For example, JP-B-55-16830, JP-B-55-16831,
JP-B-55-2336, JP-A-55-51554, JP-A-54-158
No. 481, Japanese Patent Publication No. 57-49391, Japanese Patent Publication No. 59-35787, etc. are all delaminated even in pressure vulcanization by a molding press, and the adhesive strength is further reduced in hose products. , Was difficult to put into practical use.
【0004】また、特開昭56−121762号、特開昭61−14
0692号、特開昭61−244545号、特開昭62−46641号、特
開昭62−46642号、特公昭61−16621号、特公昭61−1662
2号などの提案は、少なくともいずれか一方の層が過酸
化物加硫であり、たとえ層間接着力が充分であっても加
硫中の酸素や有機物の加硫阻害を避けるために、ホース
表面を鉛や樹脂で被覆するなどの特別の対策を必要と
し、結果的にコストアップにつながる難点を有してい
る。In addition, JP-A-56-121762 and JP-A-61-14
0692, JP 61-244545, JP 62-46641, JP 62-46642, JP 61-16621, JP 61-1662
Proposals such as No. 2 suggest that at least one of the layers is a peroxide vulcanizate, and even if the interlayer adhesion is sufficient, in order to avoid vulcanization inhibition of oxygen and organic substances during vulcanization, the hose surface It requires a special measure such as coating with lead or resin, and as a result, it has the drawback of increasing costs.
【0005】[0005]
【発明が解決しようとする課題】したがって、本発明は
このような難点がなく、内管ゴム層のフッ素系ゴム内側
層との接着性に極めて優れ、過酸化物加硫でもなく、更
に低コストで耐油性ホースとしての諸性能を満足させ得
る燃料用ゴム積層体を提供しようとするものである。Therefore, the present invention does not have such drawbacks, is extremely excellent in the adhesiveness of the inner tube rubber layer to the fluororubber inner layer, is not peroxide vulcanized, and has a low cost. Therefore, the present invention aims to provide a rubber laminate for fuel which can satisfy various performances as an oil resistant hose.
【0006】[0006]
【課題を解決するための手段】上記課題を検討した結
果、下記構造の燃料用ゴム積層体を開発した。すなわ
ち、フッ素系ゴム組成物からなる第1層と、アクリロニ
トリル含量が20〜60重量%のNBRあるいは水素化NB
Rをポリマー成分とするNBRゴム組成物からなる第1
層に接する第2層を有した積層体であって、前記NBR
ゴムに対して後記化2で示されるテトラアルキルホッソ
ニウムベンゾチアゾリウム(TRP-BTと略記)を添加
してなることを特徴とする燃料用ゴム積層体である。[Means for Solving the Problems] As a result of examining the above problems, a rubber laminate for fuel having the following structure was developed. That is, a first layer made of a fluororubber composition and NBR or hydrogenated NB having an acrylonitrile content of 20 to 60% by weight.
A first NBR rubber composition containing R as a polymer component
A laminate having a second layer in contact with a layer, said NBR
A rubber laminate for a fuel, characterized in that a tetraalkylphossonium benzothiazolium (abbreviated as TRP-BT) shown in Chemical Formula 2 below is added to the rubber.
【0007】ここにいう第1層の層状体に使用されるフ
ッ素系ゴム組成物とは、例えばフッ化ビニリデン、テト
ラフルオロエチレン、ヘキサフルオロプロピレンからな
る二元系又は三元系共重合体、具体的にはフッ化ビニリ
デン−六フッ化プロピレン共重合体やフッ化ビニリデン
−六フッ化プロピレン−四フッ化エチレン三元共重合体
などのポリマー成分を原料ゴムとし、これにカーボンブ
ラック、加硫系薬剤、金属酸化物等の副資材が適宜配合
されたものである。加硫系薬剤としてはハイドロキノン
やビスフェノールAなどのポリオール加硫系薬剤やジク
ミルパーオキサイド、ジアルキルパーオキサイドなどの
過酸化物系薬剤などが好ましい。The fluorine-based rubber composition used for the layered body of the first layer is, for example, a binary or ternary copolymer made of vinylidene fluoride, tetrafluoroethylene or hexafluoropropylene, specifically Specifically, polymer components such as vinylidene fluoride-hexafluoropropylene copolymer and vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene terpolymer are used as raw material rubber, carbon black, vulcanization system It is prepared by appropriately mixing auxiliary materials such as chemicals and metal oxides. Preferred vulcanizing agents are polyol vulcanizing agents such as hydroquinone and bisphenol A, and peroxide agents such as dicumyl peroxide and dialkyl peroxide.
【0008】一方、前記第1層のフッ素系ゴム組成物層
に接する第2層の層状体は、本発明に従うNBRゴム組
成物にて構成される。ここでNBRポリマーは、アクリ
ロニトリル含量が20〜60重量%のNBRあるいは水素化
NBRが使用される。On the other hand, the layered body of the second layer which is in contact with the fluorine-containing rubber composition layer of the first layer is composed of the NBR rubber composition according to the present invention. As the NBR polymer, NBR or hydrogenated NBR having an acrylonitrile content of 20 to 60% by weight is used.
【0009】アクリロニトリル含量が20重量%より少な
い場合には、燃料浸漬時による体積変化率(膨潤)が著し
く、耐燃料油性に問題が生じるからであり、アクリロニ
トリル含量が60重量%を越える場合には耐油性は向上す
るが耐寒性が悪化し、加工性にも問題が生じるからであ
る。したがって、これらの範囲を保持する率がフッ素系
ゴム層との有効な接着力及び全体の積層体の性能を得る
ために必要であり、これらの関係において20〜60重量%
の範囲とされることが望ましい。同様な観点から、水素
化NBRにもこれが適用されるのであり、かつNBRに
水素添加した水素化NBRにおいては、水素添加により
NBR主鎖に飽和結合を導入することにより、NBRの
耐油性に加えて耐熱性、耐オゾン性、耐薬品性、機械的
強度を付与することができ、本発明の構成にとって望ま
しいものである。This is because when the acrylonitrile content is less than 20% by weight, the volume change rate (swelling) due to fuel immersion is significant, which causes a problem in fuel oil resistance, and when the acrylonitrile content exceeds 60% by weight. This is because the oil resistance is improved, but the cold resistance is deteriorated and there is a problem in workability. Therefore, the rate of holding these ranges is necessary to obtain effective adhesive force with the fluororubber layer and the performance of the entire laminate, and in these relationships, 20 to 60% by weight.
It is desirable that the range is set to. From the same viewpoint, this is also applied to hydrogenated NBR, and in hydrogenated NBR obtained by hydrogenating NBR, by introducing a saturated bond into the NBR main chain by hydrogenation, it is possible to improve the oil resistance of NBR. Therefore, heat resistance, ozone resistance, chemical resistance and mechanical strength can be imparted, which is desirable for the constitution of the present invention.
【0010】このようなNBRポリマーに対して、従来
と同様に各種の配合剤、例えばカーボンブラック、フィ
ラーなどの充填剤、老化防止剤、加硫剤、加硫促進剤、
加硫助剤が配合される。更に必要に応じて軟化剤、可塑
剤、加工助剤、安定剤、着色剤などが適宜配合され得
る。ここで加硫剤、加硫促進剤は有機過酸化物系、ある
いは硫黄化合物やチアゾール系、スルフェンアミド系、
チウラム系、ジチオカルバメート系などの硫黄-促進剤
併用系、促進剤併用加硫系いずれも使用できるが、他の
積層体との適合性や加硫中の酸素や有機物の加硫阻害、
蒸気加硫による分解等を生じにくい点で、有機過酸化物
加硫よりも硫黄-促進剤併用加硫系及び促進剤併用加硫
系がより望ましい。Various compounding agents such as carbon black, fillers such as fillers, antioxidants, vulcanizing agents, vulcanization accelerators, etc. are added to the NBR polymer as in the conventional case.
A vulcanization aid is blended. Further, if necessary, a softening agent, a plasticizer, a processing aid, a stabilizer, a coloring agent and the like may be appropriately added. Here, the vulcanizing agent and the vulcanization accelerator are organic peroxides, or sulfur compounds, thiazoles, sulfenamides,
Sulfur-promoter combination system such as thiuram type, dithiocarbamate type, vulcanization system with accelerator can be used.
The sulfur-accelerator combination vulcanization system and the accelerator combination vulcanization system are more preferable than the organic peroxide vulcanization because they are less likely to be decomposed by steam vulcanization.
【0011】かかるNBRゴム組成物に対して、下記2
成分が必須成分、併用成分として添加されて、本発明の
NBRゴム組成物となるのである。まず、上記NBRゴ
ム配合に添加する必須成分としてのTRP-BTの添加
量は、NBRゴム100重量部に対して0.2〜8重量部、好
ましくは0.5〜5重量部である。TRP-BTの添加量が
0.2重量部以下であると接着性が充分でなく、添加に従
って接着性や引裂強度などは向上するが、同時にムーニ
ースコーチタイムが徐々に短くなり、引張強さ、耐寒
性、圧縮永久歪み等が悪化していく。添加量が8重量部
以上になると、スコーチが進行して、スコーチ焼けを生
じる。このTRP-BTは下記化2に示す構造である。With respect to such NBR rubber composition, the following 2
The component is added as an essential component or a combination component to form the NBR rubber composition of the present invention. First, the addition amount of TRP-BT as an essential component added to the above NBR rubber compounding is 0.2 to 8 parts by weight, preferably 0.5 to 5 parts by weight, based on 100 parts by weight of NBR rubber. The amount of TRP-BT added is
If the amount is less than 0.2 parts by weight, the adhesiveness will be insufficient, and the adhesiveness and tear strength will improve with the addition, but at the same time the Mooney scorch time will gradually decrease and the tensile strength, cold resistance, compression set, etc. will deteriorate. I will do it. If the addition amount is 8 parts by weight or more, scorch progresses and scorch burn occurs. This TRP-BT has the structure shown in Chemical Formula 2 below.
【化2】 [Chemical 2]
【0012】ここでRはアルキル基(CnH2n+1)で示さ
れる。中でもn=3〜6が本発明に好適に使用される。
n数が2より少ないとゴムのスコーチ焼けを促進し、n
数がそれより大きいと接着向上効果が低下していき、n
数が7以上になると実用上支障をきたすことがある。な
お、Rはそれぞれが異なるn数であってもよい。Here, R is represented by an alkyl group (CnH2n + 1). Especially, n = 3-6 is used suitably for this invention.
If the number of n is less than 2, scorching of rubber is promoted and n
If the number is larger than that, the effect of improving adhesion will decrease, and
If the number is 7 or more, there may be a practical problem. Note that each R may have a different number of n.
【0013】必要に応じて上記TRP-BTと共にN-
(シクロヘキシルチオ)フタルイミドが使用されるが、こ
のN-(シクロヘキシルチオ)フタルイミドは下記化3に
示す構造であって、その添加量はNBRゴム100重量部
に0〜8重量部、好ましくは0.5〜5重量部である。N-
(シクロヘキシルチオ)フタルイミドを添加しないと、熱
老化により接着力は低下しやすくなり、同時にムーニー
スコーチタイムも短くなり、加工上問題となる。N-(シ
クロヘキシルチオ)フタルイミドは添加に従って引張強
さ、圧縮永久歪みが若干低下するが、耐スコーチ性は向
上していく。そして積層体の初期接着力が著しく向上
し、熱老化後、温燃料浸漬後の層間剥離力も充分保持さ
れる。しかし、添加量が8重量部を越えると次第に加硫
度の低下が生じ、物性が悪化して、加工性も低下する。If necessary, N- along with the TRP-BT
(Cyclohexylthio) phthalimide is used, and this N- (cyclohexylthio) phthalimide has the structure shown in Chemical formula 3 below, and the amount of addition is 0 to 8 parts by weight, preferably 0.5 to 100 parts by weight of NBR rubber. 5 parts by weight. N-
If (cyclohexylthio) phthalimide is not added, the adhesive strength is likely to decrease due to heat aging, and at the same time the Mooney scorch time becomes short, which is a problem in processing. As N- (cyclohexylthio) phthalimide is added, the tensile strength and compression set are slightly lowered, but the scorch resistance is improved. Then, the initial adhesive strength of the laminate is remarkably improved, and after heat aging, the interlayer peeling strength after immersion in warm fuel is sufficiently maintained. However, when the amount added exceeds 8 parts by weight, the degree of vulcanization gradually decreases, the physical properties deteriorate, and the processability also decreases.
【化3】 [Chemical 3]
【0014】[0014]
【作用】第2層のNBRゴムにTRP-BTが添加され
たことにより、NBRゴム組成物からなる第2層とフッ
素系ゴム組成物からなる第1層との層間接着力が著しく
向上すると共に引裂強度が向上する。By adding TRP-BT to the NBR rubber of the second layer, the interlayer adhesion between the second layer of the NBR rubber composition and the first layer of the fluorine-based rubber composition is significantly improved. Tear strength is improved.
【0015】TRP-BTと共にN-(シクロヘキシルチ
オ)フタルイミドが併用されると、より層間接着力が完
全になると共に熱劣化に対する層間剥離強度が著しく向
上し、燃料油浸漬によっても層間剥離強度は充分に保持
されると共にスコーチタイムが適性に保持されるなどの
作用が得られる。When N- (cyclohexylthio) phthalimide is used in combination with TRP-BT, the interlayer adhesion becomes more complete and the interlaminar peel strength against heat deterioration is significantly improved, and the interlaminar peel strength is sufficient even when immersed in fuel oil. And the scorch time is properly maintained.
【0016】更に上記フッ素系ゴム組成物からなる第1
層と、上記成分を含むNBRゴム組成物からなる第2層
を積層して内管ゴム層とし、これに更に従来の補強糸
層、及び外管ゴム層からなる図1に例示したような燃料
用ゴム積層体は、耐油性ホースとしての耐候性、耐ガソ
リン性等の諸性能を満足させ得る作用が得られる。ま
た、他の積層体ダイヤフラムや、ライニングシートなど
においても充分な耐燃料油性が得られる。Further, the first of the above-mentioned fluororubber compositions is used.
1 and a second layer made of an NBR rubber composition containing the above-mentioned components are laminated to form an inner tube rubber layer, and a conventional reinforcing thread layer and an outer tube rubber layer are added to the fuel as illustrated in FIG. The rubber laminate for use has an effect of satisfying various properties such as weather resistance and gasoline resistance as an oil resistant hose. Further, sufficient fuel oil resistance can be obtained in other laminated body diaphragms, lining sheets and the like.
【0017】[0017]
【実施例】以下、本発明を実施例に基づいて詳細に説明
する。 実施例1〜9 比較例1,2 図1に示す構造の耐油性ゴムホースを以下に示す方法で
製造した。表2に示す配合からなるフッ素ゴム未加硫組
成物が第1層の内管ゴム内側層1、表1に示す配合から
なるNBRゴム組成物が第2層の内管ゴム外側層2とな
るように二重押出機により押出し成形をおこなった。こ
の内管ゴムホースの内径は7.5mm、肉厚は2.0mmでそのう
ち内側層の肉厚は約0.5mmであった。EXAMPLES The present invention will be described in detail below based on examples. Examples 1 to 9 Comparative Examples 1 and 2 An oil resistant rubber hose having the structure shown in FIG. 1 was manufactured by the method described below. The unvulcanized fluororubber composition having the composition shown in Table 2 is the inner layer rubber inner layer 1 of the first layer, and the NBR rubber composition having the composition shown in Table 1 is the inner layer rubber outer layer 2 of the second layer. Thus, extrusion molding was performed by a double extruder. The inner rubber hose had an inner diameter of 7.5 mm and a wall thickness of 2.0 mm, of which the inner layer had a wall thickness of about 0.5 mm.
【表1】 [Table 1]
【0018】 [0018]
【0019】この内管ゴムホースにポリエステル繊維か
らなる補強糸層3を、編み角52°でブレード編みにより
編み上げ、その外側にエピクロルヒドリンゴム組成物を
外管ゴム層4として押出し被覆した。この未加硫ゴムホ
ースに外径が7.5mmの金属製マンドレルを圧縮空気を使
って挿入した。挿入後の補強糸層3はほぼ静止角となっ
た。これを、直接蒸気加硫により8kgf/cm2で12分間加
硫した後、金属製マンドレルを引き抜いて、洗浄、加熱
処理して所望の耐油性ホースを得た。The inner tube rubber hose was braided with a reinforcing yarn layer 3 made of polyester fiber at a braiding angle of 52 °, and the epichlorohydrin rubber composition was extrusion-coated as an outer tube rubber layer 4 on the outer side thereof. A metal mandrel with an outer diameter of 7.5 mm was inserted into this unvulcanized rubber hose using compressed air. The reinforcing yarn layer 3 after the insertion had a substantially static angle. This was vulcanized by direct steam vulcanization at 8 kgf / cm 2 for 12 minutes, then the metal mandrel was pulled out, washed and heat treated to obtain a desired oil resistant hose.
【0020】製品剥離試験 上記製法によって得た補強ホース製品の試料を25mm長さ
に切り取り、軸線に沿って、フッ素ゴム内管内側層1を
露出させる半径方向の切目を入れ、このフッ素ゴム内管
内側層1と上記成分を含むNBRゴム組成物からなる第
2層の内管外側層2との間を90°程度剥離させて試験試
料を作成した。そして、この試験試料を図2に示すよう
な状態で製品剥離試験治具に取付け、25℃、50mm/minの
引張り速度で剥離試験を行なった。試験は未処理のも
の、燃料油C(イソオクタン/トルエン=50/50vol%)浸
漬40℃×48Hr後のもの、更に100℃、70時間及び120℃、
70時間の両方の加熱処理等について行ない、その結果を
表3に示した。Product Peeling Test A sample of the reinforcing hose product obtained by the above-mentioned manufacturing method is cut into a length of 25 mm, and a radial cut is made along the axis to expose the inner layer 1 of the fluororubber inner tube. A test sample was prepared by peeling about 90 ° between the inner layer 1 and the second outer layer 2 of the inner tube made of the NBR rubber composition containing the above components. Then, this test sample was attached to a product peeling test jig in the state shown in FIG. 2, and a peeling test was conducted at 25 ° C. and a pulling speed of 50 mm / min. The test is untreated, immersed in fuel oil C (isooctane / toluene = 50 / 50vol%) after 40 ℃ × 48Hr, 100 ℃, 70 hours and 120 ℃,
Both heat treatments were performed for 70 hours, and the results are shown in Table 3.
【0021】表3の結果より、本発明の構成による燃料
用ゴム積層体の層間接着による初期剥離強度、温燃料浸
漬による層間剥離強度の向上効果は明らかである。From the results shown in Table 3, the effect of improving the initial peel strength by the interlayer adhesion and the interlayer peel strength by the warm fuel immersion of the fuel rubber laminate according to the present invention is clear.
【表3】 [Table 3]
【0022】実施例10〜12 表1に示した実施例8のNBR配合において、TBP-
BTの前記化2に示すアルキル基のn数を、下記表4中
に示したものに変更した配合物を作成した。また、同様
に、フッ素ゴム配合物を表2に従って作成した。 Examples 10 to 12 In the NBR formulation of Example 8 shown in Table 1, TBP-
Formulations were prepared in which the n number of the alkyl groups shown in the chemical formula 2 of BT was changed to those shown in Table 4 below. Similarly, a fluororubber compound was prepared according to Table 2.
【0023】そして、上記配合のNBR組成物のシート
(厚さ2.0m/m)と前記フッ素ゴム配合物のシート(厚さ0.8
m/m)の未加硫ゴムを予め積層して、間隙2.0m/mのモール
ド成型金型(50トン,トランスファーモールド成形機)内
にセットして、160℃×15分加硫成形を行なった。この
加硫成形によりNBRシート肉厚1.5m/m、フッ素ゴムシ
ート肉厚0.5m/mが作成された。この積層シートを内部直
径D=50m/mで、周囲に約10m/mのフランジを有するアル
ミカップ14の形状に切り取り、フッ素ゴム層10を内側に
なるように塞いだ。そして内部に約20ccのガソリン12を
封入して、フランジ部と対応する環状パッキン13で挾ん
で、その間を周方向等分に設けたネジで締付けて、図3
のように、常にフッ素ゴム/NBR積層体とガソリンと
が接するように密閉した。このようにして形成した各実
施例のアルミカップを40℃の温風恒温機中に積層体が下
側となるように静置して、40℃×70Hr放置した。そし
て、フッ素ゴム層10とNBRゴム層11とからなる積層体
をアルミカップから取り外した外観の変化の状態を表5
にまとめた。A sheet of the NBR composition having the above composition
(Thickness 2.0 m / m) and a sheet of the fluororubber compound (thickness 0.8
(m / m) unvulcanized rubber is laminated in advance and set in a molding die (50 tons, transfer molding machine) with a gap of 2.0 m / m and vulcanized at 160 ° C for 15 minutes. It was By this vulcanization molding, a NBR sheet thickness of 1.5 m / m and a fluororubber sheet thickness of 0.5 m / m were prepared. This laminated sheet was cut into a shape of an aluminum cup 14 having an inner diameter D = 50 m / m and a flange of about 10 m / m on the periphery, and the fluororubber layer 10 was closed so as to be inside. Then, about 20 cc of gasoline 12 is filled inside, and it is sandwiched by the annular packing 13 corresponding to the flange portion, and the space between them is tightened with the screws equally divided in the circumferential direction.
As described above, the fluororubber / NBR laminate was constantly sealed so that the gasoline was in contact. The aluminum cup of each example thus formed was allowed to stand still in a warm air thermostat at 40 ° C. so that the laminate was on the lower side, and left at 40 ° C. × 70 hr. Then, the state of change in appearance when the laminated body including the fluororubber layer 10 and the NBR rubber layer 11 is removed from the aluminum cup is shown in Table 5.
Summarized in.
【0024】表5の結果より、テトラアルキルホッソニ
ウムベンゾチアゾリウム(TRP-BT)のアルキル基(C
nH2n+1)のn数が、n=3〜6内では、フッ素ゴムとN
BRゴムとの積層体の接着性、実使用性に問題がなく、
製品性能も良好であることがわかる。From the results shown in Table 5, the alkyl group (C of tetraalkylphossonium benzothiazolium (TRP-BT))
nH2n + 1) is within the range of n = 3-6, fluororubber and N
There is no problem in the adhesiveness of the laminate with BR rubber and the practical usability,
It can be seen that the product performance is also good.
【0025】 [0025]
【0026】[0026]
【発明の効果】本発明の構成により、本発明のフッ素ゴ
ムとNBRの積層体の接着は、前記耐油性ゴムホースの
製法で例示したように第1と第2の層状体を積層した未
加硫ゴム層を接着剤を用いることなく、加硫するだけで
優れた接着力を示す。フッ素ゴムとNBRの積層体の層
間接着による初期接着力が増し、燃料浸漬あるいは熟老
化後も接着力が低下せず、信頼性が向上し、安価で優れ
たゴム積層体となった。したがって、本発明による燃料
用ゴム積層体は、燃料用ゴムホース又はダイヤフラム、
燃料油保管用ライニングシート等の実使用状態にあって
も、その製品の品質信頼性が高いのであり、フッ素ゴム
層のさまざまな積層による製品への応用が可能であり、
性能面での向上効果がそれにより高められ、優れたコス
トパフォーマンスが実現できるのである。According to the constitution of the present invention, the adhesion of the laminated body of the fluororubber and the NBR of the present invention is carried out by unvulcanizing the first and second layered bodies laminated as exemplified in the manufacturing method of the oil resistant rubber hose. The rubber layer shows excellent adhesive strength only by vulcanization without using an adhesive. The initial adhesive strength due to the interlayer adhesion of the fluororubber / NBR laminate was increased, the adhesive strength did not decrease even after fuel immersion or aging, the reliability was improved, and an inexpensive rubber laminate was obtained. Therefore, the rubber laminate for fuel according to the present invention includes a rubber hose for fuel or a diaphragm,
Even when the lining sheet for fuel oil storage is in actual use, the quality of the product is highly reliable, and it can be applied to products by laminating various fluororubber layers.
As a result, the improvement effect in terms of performance is enhanced, and excellent cost performance can be realized.
【図1】耐油性ゴムホースの端部破断斜視図である。FIG. 1 is a cutaway perspective view of an oil resistant rubber hose.
【図2】製品剥離試験治具の斜視図である。FIG. 2 is a perspective view of a product peeling test jig.
【図3】耐ガソリン性試験の様子を示す断面図である。FIG. 3 is a cross-sectional view showing a state of a gasoline resistance test.
1 内管ゴム内側層 2 内管ゴム外側層 3 補強糸層 1 Inner tube rubber inner layer 2 Inner tube rubber outer layer 3 Reinforcing yarn layer
─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成4年2月27日[Submission date] February 27, 1992
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0004[Correction target item name] 0004
【補正方法】削除[Correction method] Delete
【手続補正2】[Procedure Amendment 2]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0005[Correction target item name] 0005
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【書類名】 明細書[Document name] Statement
【0005】[0005]
【発明が解決しようとする課題】そこで、本発明は更に
改良を加えて、内管ゴム層のフッ素系ゴム内側層との接
着性に極めて優れ、更に低コストで、耐油性ホースとし
ての諸性能を満足させ得る燃料用ゴム積層体を提供しよ
うとするものである。Therefore, the present invention has been further improved so that the adhesion of the inner tube rubber layer to the inner layer of the fluorocarbon rubber is extremely excellent, the cost is low, and various performances as an oil resistant hose are obtained. It is intended to provide a rubber laminate for fuel which can satisfy the above requirements.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // B29K 19:00 B29L 23:22 4F ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 5 Identification number Office reference number FI technical display location // B29K 19:00 B29L 23:22 4F
Claims (2)
アクリロニトリル含量が20〜60重量%のNBRあるいは
水素化NBRをポリマー成分とするNBRゴム組成物か
らなる第1層に接する第2層を有した積層体であって、
前記NBRゴムに対して下記化1で記されるテトラアル
キルホッソニウムベンゾチアゾリウム(TRP-BT)を
添加してなることを特徴とする燃料用ゴム積層体。 【化1】 1. A first layer comprising a fluororubber composition,
A laminate having a second layer in contact with a first layer comprising an NBR having an acrylonitrile content of 20 to 60% by weight or an NBR rubber composition containing hydrogenated NBR as a polymer component,
A rubber laminate for fuel, characterized in that tetraalkylphossonium benzothiazolium (TRP-BT) represented by the following chemical formula 1 is added to the NBR rubber. [Chemical 1]
チオ)フタルイミドを添加してなることを特徴とする請
求項1記載の燃料用ゴム積層体。2. The rubber laminate for fuel according to claim 1, wherein N- (cyclohexylthio) phthalimide is added together with TRP-BT.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4027381A JPH05193053A (en) | 1992-01-17 | 1992-01-17 | Rubber laminate for fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4027381A JPH05193053A (en) | 1992-01-17 | 1992-01-17 | Rubber laminate for fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05193053A true JPH05193053A (en) | 1993-08-03 |
Family
ID=12219475
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4027381A Pending JPH05193053A (en) | 1992-01-17 | 1992-01-17 | Rubber laminate for fuel |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05193053A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0759354A4 (en) * | 1994-01-24 | 1997-05-14 | Nippon Zeon Co | Laminate of vulcanizable rubber composition layers, process for producing rubber laminate, and rubber laminate |
WO2007129624A1 (en) * | 2006-05-01 | 2007-11-15 | Nippon Sheet Glass Company, Limited | Reinforcing cord, method for producing the same, and product using the reinforcing cord |
JP2010216495A (en) * | 2009-03-13 | 2010-09-30 | Bridgestone Corp | Rubber hose |
CN104262708A (en) * | 2014-10-22 | 2015-01-07 | 柳州市颖航汽配有限公司 | Preparation method of rubber part of automobile gas inlet pipe |
-
1992
- 1992-01-17 JP JP4027381A patent/JPH05193053A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0759354A4 (en) * | 1994-01-24 | 1997-05-14 | Nippon Zeon Co | Laminate of vulcanizable rubber composition layers, process for producing rubber laminate, and rubber laminate |
WO2007129624A1 (en) * | 2006-05-01 | 2007-11-15 | Nippon Sheet Glass Company, Limited | Reinforcing cord, method for producing the same, and product using the reinforcing cord |
JP2010216495A (en) * | 2009-03-13 | 2010-09-30 | Bridgestone Corp | Rubber hose |
CN104262708A (en) * | 2014-10-22 | 2015-01-07 | 柳州市颖航汽配有限公司 | Preparation method of rubber part of automobile gas inlet pipe |
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