JPH04152133A - Preparation of damping material - Google Patents
Preparation of damping materialInfo
- Publication number
- JPH04152133A JPH04152133A JP2278667A JP27866790A JPH04152133A JP H04152133 A JPH04152133 A JP H04152133A JP 2278667 A JP2278667 A JP 2278667A JP 27866790 A JP27866790 A JP 27866790A JP H04152133 A JPH04152133 A JP H04152133A
- Authority
- JP
- Japan
- Prior art keywords
- vibration
- induction heating
- thermoplastic resin
- electromagnetic induction
- ultrasonic
- 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
- 239000000463 material Substances 0.000 title claims abstract description 36
- 238000013016 damping Methods 0.000 title claims abstract description 23
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 22
- 238000010438 heat treatment Methods 0.000 claims abstract description 20
- 230000005674 electromagnetic induction Effects 0.000 claims abstract description 14
- 238000000576 coating method Methods 0.000 claims description 40
- 239000011248 coating agent Substances 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 31
- 230000005540 biological transmission Effects 0.000 claims description 8
- 238000005304 joining Methods 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 3
- 229920005989 resin Polymers 0.000 abstract description 17
- 239000011347 resin Substances 0.000 abstract description 17
- 230000000694 effects Effects 0.000 abstract description 10
- 238000003466 welding Methods 0.000 abstract description 2
- 239000003973 paint Substances 0.000 description 32
- 230000004927 fusion Effects 0.000 description 10
- -1 polyethylene Polymers 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000004049 embossing Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 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 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000007500 overflow downdraw method Methods 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 238000007611 bar coating method Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000010960 cold rolled steel Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 125000005461 organic phosphorous group Chemical group 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000009774 resonance method Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000001743 silencing effect Effects 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、良好な制振性・消音性と高い接着性さらに高
加工性を備えた複合拘束型制振材料を、簡便かつ効率的
な方法で製造する方法に関する。Detailed Description of the Invention (Field of Industrial Application) The present invention provides a simple and efficient composite restraint type vibration damping material that has good vibration damping and noise damping properties, high adhesive properties, and high processability. The present invention relates to a method for manufacturing the method.
(従来の技術)
自動車、家電、産業機械、建材等から発生する騒音・振
動が、社会的に影響を与えており、防音対策や振動対策
として各種検討が行われている。(Prior Art) Noise and vibration generated from automobiles, home appliances, industrial machinery, building materials, etc. have an impact on society, and various studies are being conducted as soundproofing and vibration countermeasures.
高分子材料と金属を組み合せ、高分子の振動減衰性能が
高い点を応用した複合型の割振材料、さらに高分子材料
をサンドイッチした拘束型の割振材料が試みられている
。Attempts are being made to create a composite type of allocation material that combines a polymer material and a metal, taking advantage of the high vibration damping performance of polymers, as well as a constrained type of allocation material that uses a sandwich of polymer materials.
例えば、特開昭59−57743号公報及び特開昭60
、−82349号公報には、中心層に振動減衰性能を有
する合成樹脂層、熱可塑性樹脂(プレス)加工用制振複
合鋼板が、開示されている。For example, JP-A-59-57743 and JP-A-60
, No. 82349 discloses a vibration-damping composite steel plate for thermoplastic resin (press) processing, which has a synthetic resin layer having vibration damping performance in the center layer.
(発明が解決しようとする課題)
しかしながら、特開昭59−57743号公報には接合
方法の具体的記載がなく、特開昭60−82349号公
報では制振層がフィルムであり、鋼板の間にフィルムを
置き、加熱圧着する方法であり、製造ラインが大がかり
であり、さらに加工度の大きなものに適用できず、制振
効果も満足の得られるレベルにはなっていない等の問題
点がある。(Problems to be Solved by the Invention) However, JP-A No. 59-57743 does not specifically describe the joining method, and in JP-A No. 60-82349, the damping layer is a film, and the damping layer is formed between steel plates. This method requires a large-scale production line, and cannot be applied to highly processed items, and the vibration damping effect is not at a satisfactory level. .
(課題を解決するための手段)
本発明者は、超音波振動又は電磁誘導加熱を用いて部分
的に接合融着することにより、良好な割振性、高い接着
性さらに高加工性を備えた制振材料の製造方法を見出し
たものである。(Means for Solving the Problems) The present inventor has achieved a control system with good vibration distribution properties, high adhesion properties, and high workability by partially bonding and fusing using ultrasonic vibration or electromagnetic induction heating. We have discovered a method for manufacturing wafer materials.
本発明は、下記の工程を経る制振材料の製造方法である
。The present invention is a method for producing a vibration damping material that involves the following steps.
FA+素材の重ね合せ面に熱可塑性樹脂塗膜を形成する
工程
(B)該熱可塑性樹脂塗膜面に凹凸部を形成する工程
fc)接合面が下記 (ア)または(イ)からなる組み
合せで接合する工程
f7) fA)工程塗膜面と (B)工程塗膜面[1f
B)工程塗膜面と fB)工程塗膜面(D+接合面を、
(伺非平滑面からなる超音波伝達ホーンを具備した超音
波発生装置により、または (帽電磁誘導加熱装置によ
り、加圧しながら超音波振動または電磁誘導加熱により
接合融着面を部分的に形成する工程
以下、本発明の詳細な説明する。Step of forming a thermoplastic resin coating on the overlapping surface of the FA+ material (B) Step of forming uneven parts on the surface of the thermoplastic resin coating fc) The bonding surface is a combination of the following (a) or (b). Joining process f7) fA) Process coating surface and (B) Process coating surface [1f
B) Process coating surface and fB) Process coating surface (D+ bonding surface,
(By an ultrasonic generator equipped with an ultrasonic transmission horn consisting of a non-smooth surface, or (by an electromagnetic induction heating device, the bonding surface is partially formed by ultrasonic vibration or electromagnetic induction heating while applying pressure.) The present invention will be described in detail below.
本発明で用いる素材としては、冷延鋼板、亜鉛(合金)
めっき鋼板、アルミニウム(合金)板鋼(めっき)板、
真鍮板、ステンレス板等の金属材料、FRP、ポリエチ
レン、ポリプロピレン。Materials used in the present invention include cold rolled steel plate, zinc (alloy)
Plated steel sheet, aluminum (alloy) sheet steel (plated) sheet,
Metal materials such as brass plates and stainless steel plates, FRP, polyethylene, and polypropylene.
エチレン−酢酸ビニル共重合体、ポリアミド、ポリアク
リル、ポリエステル1エチレン−ポリビニルアルコール
共重合体、塩化ビニル樹脂、塩化ビニリデン樹脂、ポリ
カーボネート、ポリウレタン等のプラスチック材料、ガ
ラス、紙、木、布、M戸物、タイル等の陶器、セメント
、コンクリート等の無機質材料等を用いることができる
。素材が金属の場合には化成処理されていてもよく、ま
た脱脂の状態であってもよく、さらに表面を機械的処理
したものでもよい。非金属の場合、化成処理は不要だが
、脱脂や機械的さらに放電処理等の方法を行ってもよい
。Plastic materials such as ethylene-vinyl acetate copolymer, polyamide, polyacrylic, polyester 1-ethylene-polyvinyl alcohol copolymer, vinyl chloride resin, vinylidene chloride resin, polycarbonate, polyurethane, glass, paper, wood, cloth, M door items , ceramics such as tiles, inorganic materials such as cement, concrete, etc. can be used. When the material is metal, it may be chemically treated, degreased, or the surface may be mechanically treated. In the case of nonmetals, chemical conversion treatment is not necessary, but methods such as degreasing, mechanical treatment, and discharge treatment may be performed.
なお、接合融着する方法が電磁誘導加熱の場合には、素
材が導電体でなければならず、非導電体の素材は、導電
性塗料の塗布等の導電性処理を行ってから融着させる。Note that if the joining and fusing method is electromagnetic induction heating, the material must be a conductor, and non-conductive materials must be treated to become conductive, such as by applying conductive paint, before being fused. .
本発明の工程(A+は、素材に熱可塑性樹脂塗膜を形成
する工程である。通常は、熱可塑性樹脂塗膜を形成後、
−時保管しておくが、前記塗膜形成工程と融着工程が連
続した連続工程であってもよい。The process of the present invention (A+ is the process of forming a thermoplastic resin coating on the material. Usually, after forming the thermoplastic resin coating,
However, the coating film forming step and the fusing step may be a continuous step.
本発明で素材に形成する熱可塑性樹脂塗料は、重ね合せ
面に用いる。用いることができる熱可塑性樹脂塗料の樹
脂としては、塗料分野で通常用いることのできる塩素化
ポリエチレン、塩素化ポリプロピレン等の塩素化オレフ
ィン系樹脂、塩化ビニル樹脂、酢酸ビニル、塩化ビニリ
デン及びこれらを共重合したビニル樹脂、セルロース系
樹脂。The thermoplastic resin coating formed on the material according to the present invention is used on the overlapping surfaces. Resins for thermoplastic resin paints that can be used include chlorinated olefin resins such as chlorinated polyethylene and chlorinated polypropylene, which are commonly used in the paint field, vinyl chloride resins, vinyl acetate, vinylidene chloride, and copolymers of these. vinyl resin, cellulose resin.
アセタール樹脂、アルキド樹脂、塩化ゴム系樹脂等を挙
げることができる。乾燥膜厚は、重ね合せる相互の側で
膜厚は 1/1〜1/6の比率で、片側で50〜300
μmが好ましい。Examples include acetal resin, alkyd resin, and chlorinated rubber resin. The dry film thickness is 1/1 to 1/6 on the mutually overlapping sides, and 50 to 300 on one side.
μm is preferred.
さらに本発明では、塩化ビニル樹脂のプラスチゾル、オ
ルガノゾルであるディスバージョンも好都合に用いられ
るが、かかる塩化ビニル樹脂ディスバージョンとしては
ペースト用塩化ビニル樹脂(平均重合度P=800〜3
000) /ブレンド用塩化ビニル樹脂(平均重合度P
=400〜1500) = 10010〜50/ 5
0重量比を主成分として、この主成分100重量部に対
して、可塑剤としてフタル酸エステル系、直鎖二塩基酸
エステル系、トリメリット酸エステル系、高分子ポリエ
ステル系、エポキシ化大豆油類系を20〜90重量部配
合し、さらに安定剤として鉛塩系、金属石けん系、エポ
キシ系、有機スズ系、有機亜リン酸化合物等を、単独あ
るいは組み合せて2〜10重量部配合したものが挙げら
れる。塗膜中の塩化ビニル樹脂は55重量%以上とする
。Furthermore, in the present invention, plastisols and organosols of vinyl chloride resin dispersions are also conveniently used.
000) / Vinyl chloride resin for blending (average degree of polymerization P
=400~1500) =10010~50/5
0 weight ratio as the main component, and 100 parts by weight of this main component as plasticizers such as phthalate esters, linear dibasic acid esters, trimellitate esters, high molecular polyesters, and epoxidized soybean oils. 20 to 90 parts by weight of a stabilizer, and 2 to 10 parts by weight of a lead salt type, metal soap type, epoxy type, organic tin type, organic phosphorous acid compound, etc. alone or in combination as a stabilizer. Can be mentioned. The amount of vinyl chloride resin in the coating film is 55% by weight or more.
本発明の重ね合せ面を形成する塗膜に用いる塗料は、ク
リヤー塗料としてもまた着色塗料としても用いられるの
で顔料は任意であるが、使用する場合、かかる顔料は塗
料用として常用のものでよく、酸化チタン、カーボンブ
ラック、黄色酸化鉄 弁柄などの無機顔料、及びフタロ
シャニンブルー フタ口シャニングリーン、キナクリド
ンレッドなどの有機顔料が使用できる。The paint used for the coating film forming the overlapping surfaces of the present invention can be used as both a clear paint and a colored paint, so any pigment may be used, but if used, the pigment may be one commonly used for paints. Inorganic pigments such as , titanium oxide, carbon black, yellow iron oxide Bengara, and organic pigments such as phthalosyanine blue, phthaloshanine green, and quinacridone red can be used.
本発明で割振材料の外側になる面の塗膜を形成するため
に用いる塗料は、重ね合せ面に用いる塗料と同じ熱可塑
性樹脂を用いてもよく、またプレコート用塗料として用
いる熱硬化性樹脂塗料を用いてもよい。乾燥膜厚ば8〜
200μm、好ましくは10〜100μmの範囲とする
。素材がプレコート鋼板の場合は10〜20μm、ボス
トコート鋼板で20〜50μm、プラスチック材で20
〜50μm、紙では10〜20μmとすることが望まし
い。In the present invention, the paint used to form the coating film on the outer surface of the distributed material may be the same thermoplastic resin as the paint used on the overlapping surface, or the thermosetting resin paint used as the pre-coat paint. may also be used. Dry film thickness: 8~
The thickness is 200 μm, preferably in the range of 10 to 100 μm. 10 to 20 μm if the material is pre-coated steel plate, 20 to 50 μm if the material is post-coated steel plate, and 20 μm if the material is plastic material.
~50 μm, preferably 10 to 20 μm for paper.
このような塗料に用いられる熱硬化性樹脂としては、例
えば、アクリル樹脂、ポリエステル樹脂、アルキド樹脂
、インシアネート硬化型アクリル樹脂等の塗膜形成性樹
脂を挙げることができ、これらは必要に応じて、アミノ
樹脂やブロックイソシアネート等の架橋剤と一緒に用い
られる。Examples of thermosetting resins used in such paints include film-forming resins such as acrylic resins, polyester resins, alkyd resins, and incyanate-curing acrylic resins, which may be used as needed. , used together with crosslinking agents such as amino resins and blocked isocyanates.
該樹脂には、必要に応じて油脂又は脂肪酸を30重量%
程度まで加えて、柔軟性を付与したアルキド樹脂として
用いることもできる。The resin may contain 30% by weight of oil or fatty acid as necessary.
In addition, it can also be used as an alkyd resin with added flexibility.
本発明では、有機溶剤可溶の樹脂だけでなく、水溶性、
水分散性、乳化された樹脂の水系塗料を用いることがで
きる。In the present invention, not only organic solvent-soluble resins but also water-soluble,
Water-based paints made of water-dispersible or emulsified resins can be used.
外側になる面の塗膜を形成するために用いられる塗料は
、割振材料として外側の目に触れる側(非重ね合せ面の
おもて側)は、耐食性、意匠性の点で、単独又は複数の
着色塗料又は着色塗料の上にクリヤー塗料を塗り重ねる
方法を用いる。非重ね合せ面の裏側に当たる面はおもて
面と同一でもよく、意匠性は特に必要としない点から、
耐食性を具備したプライマーだけでもよい。外側になる
面の塗膜の形成は、本発明の工程の中で任意に選択する
ことができる。前記塗料には、各種添加剤を配合するこ
とができ、配合することのできる各種添加剤としては、
ドデシルベンゼンスルホン酸等の硬化触媒、ベンゾフェ
ノール系等の紫外線吸収剤、フェノール系、スルフォイ
ド系等の酸化防止剤、シリコーンや有機高分子等の表面
調整剤、タレ止め剤、増粘剤等の添加剤を挙げることが
でき、これらは塗料中に5重量部以下の量で配合して、
塗料性能や塗膜性能を改善することができる。The paint used to form the paint film on the outer surface is a distribution material, and the outer visible side (the front side of the non-overlapping surface) can be used singly or in combination in terms of corrosion resistance and design. A method is used in which colored paint or clear paint is applied over colored paint. The surface on the back side of the non-overlapping surface may be the same as the front surface, and there is no particular need for design.
A primer with corrosion resistance may be sufficient. Formation of the coating film on the outer surface can be arbitrarily selected in the process of the present invention. Various additives can be blended into the paint, and the various additives that can be blended include:
Addition of curing catalysts such as dodecylbenzenesulfonic acid, ultraviolet absorbers such as benzophenol, antioxidants such as phenol and sulfide, surface conditioners such as silicone and organic polymers, anti-sagging agents, thickeners, etc. These agents can be included in the paint in an amount of 5 parts by weight or less,
Paint performance and film performance can be improved.
但し、これらの配合量が多くなりすぎると、塗膜形成時
にハジキが生じたり、層間付着性が悪くなったりするお
それがあるので好ましくない。However, if the amount of these compounds is too large, repellency may occur during coating film formation or interlayer adhesion may deteriorate, which is not preferable.
重ね合せ面及び非重ね合せ面の塗膜を形成するために用
いる塗料ともに、各成分の混合には、塗料製造に慣用さ
れているペイントシエイカーディゾルバー、ボールミル
、サンドグラインドミル、ニーダ−等の装置を用いる。For mixing each component of both the paints used to form coatings on the overlapping and non-overlapping surfaces, equipment such as paint shaker dissolvers, ball mills, sand grind mills, kneaders, etc. that are commonly used in paint manufacturing are used. Use.
これらの塗料の塗装方法は、特に限定されずエアスプレ
ー塗装、エアレス塗装、静1i塗装などの通常の塗装方
法、また特に、塗布厚の精度、塗布表面の平滑性等に優
れたグラビアコーティング方法、ロールコーティング方
法、カーテンコーティング方法、バーコーティング方法
、オフセットグラビアコーティング方法等も採用される
。The coating methods for these paints are not particularly limited, and include ordinary coating methods such as air spray coating, airless coating, static 1i coating, and in particular, gravure coating methods that are excellent in coating thickness accuracy, coating surface smoothness, etc. Roll coating methods, curtain coating methods, bar coating methods, offset gravure coating methods, etc. are also adopted.
本発明の工程FB)では、工程(Al によって重ね合
せ面にすでに形成されている熱可塑性樹脂塗膜面に凹凸
部を形成するが、材料の重ね合せ面を接合して超音波振
動または電磁誘導加熱により融着させるときに、接合面
の熱可塑性樹脂塗膜面が平滑であると接合融着が不充分
で割振・消音効果が発揮されないため、少なくとも接合
面の片側の熱可塑性樹脂塗膜面に凹凸部を形成させる。In step FB) of the present invention, irregularities are formed on the thermoplastic resin coating surface that has already been formed on the overlapping surfaces using Al. When fusing by heating, if the thermoplastic resin coating surface on the joint surface is smooth, the bonding will be insufficient and the vibration distribution/silencing effect will not be achieved. to form uneven parts.
凹凸部を形成させる方法としては、エンボスロールによ
る転写方法、骨材を散布させる方法等を用いる。好まし
い方法としては、エンボスロールによる転写方法である
。工程+B)での凹凸付与をしないで工程(Alでの塗
料組成的にちぢみ塗料や骨材入り塗料により、予め塗膜
にちぢみを発生させておいても、また、骨材により非平
滑面を形成してもよい。凹凸部は高さが1OLLra以
上、熱可塑性樹脂塗膜の乾燥膜厚の半分以下が好ましく
、できるだけ均一に付与することが望ましい。As a method for forming the uneven portions, a transfer method using an embossing roll, a method of dispersing aggregate, etc. are used. A preferred method is a transfer method using an embossing roll. Even if the paint film is made to wrinkle in advance by using a paint with a shrinking composition or a paint containing aggregate, it is possible to create uneven surfaces without adding unevenness in step + B). The uneven portions preferably have a height of 1 OLLra or more, less than half the dry film thickness of the thermoplastic resin coating, and are desirably applied as uniformly as possible.
本発明の工程(C1は重ね合せ面の接合工程であり、素
材が2枚の時には、下記 (ア)または(伺の組み合せ
で接合し、素材が3枚以上の時には、各接合面が (ア
)及び/または(利の組み合せで接合する。接合は、次
工程FD+の超音波振動または電磁誘導加熱するために
接合面を重ね合せる。The process of the present invention (C1 is the joining process of the overlapping surfaces. When there are two materials, they are joined using the following combinations of (A) or (A). When there are three or more materials, each joining surface is (A). ) and/or (bonding is performed by a combination of advantages. For bonding, the bonding surfaces are overlapped for ultrasonic vibration or electromagnetic induction heating in the next step FD+.
本発明の工程(D)では、FC+工程での組み合せによ
る接合面を融着する。熱可塑性樹脂塗膜面を以下の (
イ)または(ロ)の2方法により融合する方法がとられ
る。In the step (D) of the present invention, the joint surfaces formed by the combination in the FC+ step are fused. The thermoplastic resin coating surface is shown below (
There are two methods of fusion: a) or b).
接合融着する温度は、熱可塑性樹脂塗膜が融着するのに
必要な温度以上であればよく、例えば150〜300℃
の範囲が好ましい。The temperature for bonding and fusing may be at least the temperature necessary for fusing the thermoplastic resin coating, for example, 150 to 300°C.
A range of is preferred.
(イ)超音波発生装置の先端に具備されている超音波伝
達ホーンを加圧しながら、超音波振動を加える。超音波
振動によって発生する摩擦発熱作用により、相互の熱可
塑性樹脂塗膜を融着させることができる。(b) Apply ultrasonic vibration while pressurizing the ultrasonic transmission horn provided at the tip of the ultrasonic generator. The thermoplastic resin coatings can be fused together by the frictional heat generation effect generated by the ultrasonic vibrations.
本発明での超音波振動による融着方法は、(1)超音波
伝達ホーンの塗膜接触面が非平滑であること、(2)融
着面が部分的である。In the fusion method using ultrasonic vibration in the present invention, (1) the coating contact surface of the ultrasonic transmission horn is non-smooth, and (2) the fusion surface is partial.
伝達ホーンの形状は丸状、角状等であり、寸法は丸状で
直径5〜20mm、角状で幅2〜20m、長さ2〜20
mm、接触面は格子型、ストライブ型、同心円型の構成
でギザギザにして粗度は 100〜1000μmが好ま
しい。非平滑にすることにより接触面が増え、接着強度
が高くなる。The shape of the transmission horn is round, square, etc., and the dimensions are round with a diameter of 5 to 20 mm, square with a width of 2 to 20 m, and a length of 2 to 20 mm.
mm, and the contact surface preferably has a lattice-type, striped-type, or concentric-circular configuration with jagged edges and a roughness of 100 to 1000 μm. By making it non-smooth, the contact surface increases and the adhesive strength increases.
融着面を全面でなく部分的にすることで、割振効果を一
段と高めることができる。The distribution effect can be further enhanced by making the fusion surface partial rather than the entire surface.
部分的とは、前記超音波伝達ホーンが接触し融着した融
着間隔を5〜100mmにするのが好ましい。By "partially", it is preferable that the distance between the fused parts where the ultrasonic transmission horn contacts and fused the parts is 5 to 100 mm.
部分的とは、非全面であれば前記間隔にとられれずに効
果が発揮できる。Partially means that the effect can be exerted without the above-mentioned spacing as long as it is not the entire surface.
本発明での超音波振動は、5〜50K HZ 、振動時
間0.2〜60秒が好ましく、加圧することにより融合
効果を高めるが、加圧条件は 1〜5 kg/ 0m2
で行う。The ultrasonic vibration in the present invention is preferably 5-50 KHz and vibration time 0.2-60 seconds, and pressurization increases the fusion effect, but the pressurization conditions are 1-5 kg/0 m2
Do it with
(ロ)電磁誘導加熱方法は、高周波磁場内に導電体を置
くと、ヒステリシス損とうす電流によるジュール熱によ
って極めて短時間に発熱することを利用して、導電体材
料を加熱し、重ね合せ面に形成された熱可塑性樹脂塗膜
を融着させることができる。(b) The electromagnetic induction heating method uses the fact that when a conductor is placed in a high-frequency magnetic field, it generates heat in an extremely short time due to Joule heat caused by hysteresis loss and a decaying current. Thermoplastic resin coatings formed on can be fused.
本発明での電磁誘導加熱による融着方法は、flj高周
波発振器、(2)加圧プレス、(3)加熱コイル、(4
)発熱体及び、ベークライト、シリコーン等の非金属材
料からなる架台とで構成される。The fusion method using electromagnetic induction heating in the present invention includes a flj high-frequency oscillator, (2) a pressure press, (3) a heating coil, and (4)
) Consists of a heating element and a pedestal made of non-metallic material such as Bakelite or silicone.
高周波発振器としては、出力2〜50KW、周波数50
KH2〜3MH2,発振時間2〜60秒が好ましい。As a high frequency oscillator, output 2~50KW, frequency 50
KH2 to 3MH2 and oscillation time 2 to 60 seconds are preferable.
本発明の割振材料が折曲げやプレス等の加工を要する場
合には、本発明の制振材料の製造工程の前でも後でもよ
い。経済性・効率性の点からは、後加工の方が好ましい
。超音波振動の場合と同じ<、電磁誘導加熱の場合にも
、融着面は全面でなく、部分的にすることが必要である
。If the damping material of the present invention requires processing such as bending or pressing, it may be processed before or after the manufacturing process of the vibration damping material of the present invention. From the point of view of economy and efficiency, post-processing is preferable. As in the case of ultrasonic vibration, also in the case of electromagnetic induction heating, it is necessary that the fusion surface is not all over, but only partially.
(作用)
本発明では、熱可塑性樹脂塗膜を素材の重ね合せ面に塗
膜形成することにより、超音波振動またはtga誘導加
熱により接合面が融着し、素材の間に樹脂層を形成する
ことができ、振動が緩衝されることにより制振・消音効
果が得られる。さらに融着面を部分的に形成することに
より、融着面に対して非融着面が振動や音に対する緩衝
作用により、相乗的に一段と割振・消音効果が得られる
。(Function) In the present invention, by forming a thermoplastic resin coating film on the overlapping surfaces of materials, the joining surfaces are fused by ultrasonic vibration or TGA induction heating, and a resin layer is formed between the materials. By damping vibrations, vibration damping and noise damping effects can be obtained. Furthermore, by partially forming the fused surface, the non-fused surface has a buffering effect against vibration and sound relative to the fused surface, so that synergistically further vibration distribution and noise reduction effects can be obtained.
(実施例)
以下、本発明を実施例に基づいて、さらに具体的に説明
するが、本発明の技術的範囲をこれらの実施例に限定す
るものでないことはいうまでもない。(Examples) Hereinafter, the present invention will be explained in more detail based on Examples, but it goes without saying that the technical scope of the present invention is not limited to these Examples.
裏11引↓
両面を表面調整(NPコンディショナー200/日本ペ
イント■製)後、クロメート化成処理(サーフコートN
RC300/日本ペイント■製)し、合せ面に表1の内
面用塗料を乾燥膜厚(以下膜厚という)が各々 loo
umで塗装し乾燥させた 2枚の溶融亜鉛めっき鋼板を
#備し、外面になる両面に塗料T−1を塗装した。2枚
の重ね合せ面をそれぞれエンボスロールにて、エンボス
深さが約50μmの凸部を形成した。超音波融着装置(
SONOPET1200B /精電舎電子工業■製)を
用いて、周波数19・15KH2,時間07秒、加圧1
.5kg/c+n2の条件で融着した。Back side 11 pull ↓ After surface conditioning on both sides (NP conditioner 200/manufactured by Nippon Paint), chromate conversion treatment (Surf coat N
RC300/manufactured by Nippon Paint ■), and applied the inner surface paint shown in Table 1 to the mating surfaces with a dry film thickness (hereinafter referred to as film thickness) of loo.
Two hot-dip galvanized steel plates were coated with um and dried, and both outer surfaces were coated with paint T-1. A convex portion having an embossing depth of approximately 50 μm was formed on each of the overlapping surfaces of the two sheets using an embossing roll. Ultrasonic fusion device (
Using SONOPET1200B / Seidensha Electronics Industry ■), frequency 19.15KH2, time 07 seconds, pressurization 1
.. Fusion was carried out under the condition of 5 kg/c+n2.
この時の超音波伝達ホーンの先端形状は、直径10mm
の丸状で、接触面は粗度700μmの格子型のものを用
いた。融着面の間隔は、最も狭いところで100mmの
部分的融着を行った。その後、割振性。The tip shape of the ultrasonic transmission horn at this time is 10 mm in diameter.
A lattice-shaped contact surface with a round shape and a roughness of 700 μm was used. Partial fusion was performed with a spacing between the fusion surfaces of 100 mm at the narrowest point. Then allocability.
消音性、接着性を評価し、さらに深絞り加工を行い、加
工性を評価した。結果を表2に示した。Sound deadening properties and adhesion properties were evaluated, and further deep drawing was performed to evaluate workability. The results are shown in Table 2.
L1髭呈ニュユ
実施例工に基づき表2の組み合せで実施し、結果を表2
に示した。なお、tM3誘導加熱は、′r4磁誘導ウエ
つダー(VH−10に/精電舎電子工業■製)を用いた
。The combinations shown in Table 2 were carried out based on the L1 beard presentation example, and the results are shown in Table 2.
It was shown to. For the tM3 induction heating, a 'r4 magnetic induction wafer (VH-10/manufactured by Seidensha Electronics Co., Ltd.) was used.
願を五土ニュ
実施例1の、重ね合せ面に凸部を形成しない例(比較例
1)、接合融着を加熱ロールにより全面融着させた例(
比較例2)、超音波伝達ホーンの接触面を平滑にした例
〔比較例3)を、他の条件は実施例1と同様に行い、結
果を表2に示した。An example in which no convex portions were formed on the overlapping surfaces of Gotonu Example 1 (Comparative Example 1), and an example in which the entire surface was fused using a heating roll (
Comparative Example 2) and an example in which the contact surface of the ultrasonic transmission horn was made smooth [Comparative Example 3] were conducted under the same conditions as in Example 1, and the results are shown in Table 2.
FT
乾燥膜厚
評価方法及び評価基準
1.制振性
共振法により、FFTアナライザー装置(型式2032
/P & K社製)を用いて、幅20mm。FT dry film thickness evaluation method and evaluation criteria 1. Using the damped resonance method, the FFT analyzer device (model 2032
/manufactured by P & K Co., Ltd.), width 20 mm.
長さ200mm 、短冊状試験片を40℃で周波数を変
えて共振点を求めて、ピークから3db下がった点(半
値点)における帯域幅=f xflと、その共振周波数
fnの比から損失係数ηを求めた。Find the resonance point of a strip-shaped test piece with a length of 200 mm at 40°C by changing the frequency, and calculate the loss coefficient η from the ratio of the bandwidth = f xfl and the resonance frequency fn at a point 3 db lower than the peak (half-value point). I asked for
η” (f−−f+ )/fn 2 。η” (f--f+)/fn 2.
消音性
融着後300mmX 3QOmmの板を切り出し、上部
2か所を糸で吊り下げて、プラスチックハンマーで試験
片を強打して、音の残響を下記の評価基準で評価した。After sound-dampening welding, a 300mm x 3QOmm board was cut out, the upper two parts were suspended by threads, the test piece was hit with a plastic hammer, and the sound reverberation was evaluated using the following evaluation criteria.
○・・・残響なし △・・・多少残響あり X・・・残響が多い 3 。○...No reverberation △・・・There is some reverberation X: Lots of reverberation 3.
接着性
テンシロン(型式5S−207D−UA/東洋ボールド
ウィン製)を用いて、20mm/分、20°Cで引張り
強度を測定し、材料の熱可塑性樹脂塗膜が剥がれた時の
強度を測定した。The tensile strength was measured using adhesive Tensilon (Model 5S-207D-UA/manufactured by Toyo Baldwin) at 20 mm/min and 20°C, and the strength when the thermoplastic resin coating of the material was peeled off was measured.
(単位:kg/cff12)
4、加工性
融着後の試験片を、深絞り加工では円筒深絞り試験器(
Bl−142型/工リクセン社製)を用いて、しわ押え
圧3トン、ポンチ径50mmφ、ダイス径52.4mm
φ、絞り深さ40mm、ブランク径95mmで加工し、
折曲げ(L型)加工ではエキセンプレス(OEP−15
に/盛光板金社製)を用いてL型に折り曲げて5それぞ
れ塗膜の剥離、ズレ、ユガミ等を調べた。(Unit: kg/cff12) 4. Workability The test piece after fusion is deep drawn using a cylindrical deep drawing tester (
Bl-142 type/manufactured by Koriksen Co., Ltd.) with a wrinkle presser pressure of 3 tons, punch diameter of 50 mmφ, and die diameter of 52.4 mm.
φ, drawing depth 40mm, blank diameter 95mm,
For bending (L-shape) processing, an eccentric press (OEP-15) is used.
(manufactured by Seiko Sheet Metal Co., Ltd.) into an L shape, and the peeling, misalignment, discoloration, etc. of the coating film were examined.
○・・・異常なし
△・・・ズレ、ユガミあり
×・・・剥離あり
(発明の効果)
本発明の割振材料は、板状のもの、前加工されているも
のの区別な(、部分接合融着が簡単にでき、良好な制振
性・消音性・高い接着性、さらに高加工性を備えた制振
材料を製造することが可能となった。○... No abnormalities △... Misalignment, distortion ×... Peeling (effects of the invention) The distributed material of the present invention does not distinguish between plate-shaped and pre-processed materials (partially bonded and fused). It has become possible to produce a vibration damping material that is easy to apply, has good vibration damping properties, sound deadening properties, high adhesion properties, and high processability.
このような特徴を有する本発明の割振材料は、家電製品
、自動車、産業機械、建材等の振動・騒音対策の必要な
分野で好適に利用することができる。The distribution material of the present invention having such characteristics can be suitably used in fields where vibration and noise countermeasures are required, such as home appliances, automobiles, industrial machinery, and building materials.
特許出題人 日本ペイント株式会社Patent questioner: Nippon Paint Co., Ltd.
Claims (1)
方法 (A)素材の重ね合せ面に熱可塑性樹脂塗膜を形成する
工程 (B)該熱可塑性樹脂塗膜面に凹凸部を形成する工程 (C)接合面が下記(ア)または(イ)からなる組み合
せで接合する工程 (ア)(A)工程塗膜面と(B)工程塗膜面(イ)(B
)工程塗膜面と(B)工程塗膜面(D)接合面を、(イ
)非平滑面からなる超音波伝達ホーンを具備した超音波
発生装置により、または(ロ)電磁誘導加熱装置により
、加圧しながら超音波振動または電磁誘導加熱により接
合融着面を部分的に形成する工程[Claims] 1. A method for producing a vibration damping material characterized by passing through the following steps (A) Step of forming a thermoplastic resin coating on the overlapping surfaces of the materials (B) Step of forming the thermoplastic resin coating Step (C) of forming irregularities on the film surface (C) Step of joining the joint surfaces in a combination of (A) or (B) below (A) Process coating surface and (B) Process coating surface (I) )(B
) process coating surface and (B) process coating surface (D) bonding surface by (a) an ultrasonic generator equipped with an ultrasonic transmission horn consisting of a non-smooth surface, or (b) an electromagnetic induction heating device. , a process of partially forming the bonding surface by ultrasonic vibration or electromagnetic induction heating while applying pressure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2278667A JPH04152133A (en) | 1990-10-16 | 1990-10-16 | Preparation of damping material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2278667A JPH04152133A (en) | 1990-10-16 | 1990-10-16 | Preparation of damping material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04152133A true JPH04152133A (en) | 1992-05-26 |
Family
ID=17600485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2278667A Pending JPH04152133A (en) | 1990-10-16 | 1990-10-16 | Preparation of damping material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04152133A (en) |
-
1990
- 1990-10-16 JP JP2278667A patent/JPH04152133A/en active Pending
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