JPH03107300A - Multilayer speaker diaphragm - Google Patents
Multilayer speaker diaphragmInfo
- Publication number
- JPH03107300A JPH03107300A JP24607889A JP24607889A JPH03107300A JP H03107300 A JPH03107300 A JP H03107300A JP 24607889 A JP24607889 A JP 24607889A JP 24607889 A JP24607889 A JP 24607889A JP H03107300 A JPH03107300 A JP H03107300A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- parts
- polyester
- polyethylene terephthalate
- speaker diaphragm
- 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.)
- Granted
Links
- -1 polyethylene terephthalate Polymers 0.000 claims abstract description 19
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 18
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 15
- 229920000098 polyolefin Polymers 0.000 claims abstract description 13
- 229920000139 polyethylene terephthalate Polymers 0.000 claims abstract description 11
- 239000005020 polyethylene terephthalate Substances 0.000 claims abstract description 11
- 239000011342 resin composition Substances 0.000 claims abstract description 9
- 229920001225 polyester resin Polymers 0.000 claims abstract description 7
- 239000004645 polyester resin Substances 0.000 claims abstract description 7
- 229920006346 thermoplastic polyester elastomer Polymers 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims description 14
- 229920000728 polyester Polymers 0.000 abstract description 14
- 230000002349 favourable effect Effects 0.000 abstract 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 239000010410 layer Substances 0.000 description 6
- 229920001971 elastomer Polymers 0.000 description 5
- 239000000806 elastomer Substances 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001230 polyarylate Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000010456 wollastonite Substances 0.000 description 3
- 229910052882 wollastonite Inorganic materials 0.000 description 3
- 229920000106 Liquid crystal polymer Polymers 0.000 description 2
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000002249 anxiolytic agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- JJOJFIHJIRWASH-UHFFFAOYSA-N icosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCC(O)=O JJOJFIHJIRWASH-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- MFJDFPRQTMQVHI-UHFFFAOYSA-N 3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound O=C1OCOC(=O)C2=CC=C1C=C2 MFJDFPRQTMQVHI-UHFFFAOYSA-N 0.000 description 1
- QLIQIXIBZLTPGQ-UHFFFAOYSA-N 4-(2-hydroxyethoxy)benzoic acid Chemical compound OCCOC1=CC=C(C(O)=O)C=C1 QLIQIXIBZLTPGQ-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- WPDNUCQHNPMNEO-UHFFFAOYSA-N 7-ethyloctadecanedioic acid Chemical compound OC(=O)CCCCCC(CC)CCCCCCCCCCC(O)=O WPDNUCQHNPMNEO-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- BNJOQKFENDDGSC-UHFFFAOYSA-N octadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCC(O)=O BNJOQKFENDDGSC-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Diaphragms For Electromechanical Transducers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はスピーカーコーン等に代表されるスピーカー振
動板に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a speaker diaphragm represented by a speaker cone or the like.
従来よりスピーカーコーンの材料としては、紙またはポ
リオレフィン系重合体フィルム及びそれらに無機材料を
混入させた材料が多く使用され、また最近では特開昭5
7−154994号公報、特開昭62−205127号
公報、特開昭62−149296号公報、特開昭62−
101281号公報等に見られるように、液晶フィルム
も使用され始めている。Conventionally, paper or polyolefin polymer films and materials mixed with inorganic materials have often been used as materials for speaker cones.
7-154994, JP-A-62-205127, JP-A-62-149296, JP-A-62-
Liquid crystal films are also beginning to be used, as seen in Japanese Patent No. 101281 and the like.
しかし、紙あるいはポリオレフィン系重合体フィルムを
使用したスピーカーコーンは、内部損失tanδが高く
、価格が安いという利点はあるが、紙及びポリオレフィ
ンは比弾性率E/ρ(Eは弾性率、ρは密度)が低いた
めに、スピーカーコーンとしての性能のバランスが不十
分である。このため紙及びポリオレフィンに無機材料、
特にマイカ、炭素繊維を混入させ、比弾性率を上昇させ
る方法が行われているが、無機材料の混入量にも限界が
あり、充分満足のいく比弾性率に到っていないのが現状
である。また、ポリオレフィンは耐熱性の点で不利であ
り、カーステレオや大出力用スピーカーには向かない。However, speaker cones using paper or polyolefin polymer film have the advantage of high internal loss tan δ and low price; ), the performance as a speaker cone is insufficiently balanced. For this reason, inorganic materials are used in paper and polyolefin.
In particular, methods have been used to increase the specific elastic modulus by mixing mica and carbon fiber, but there is a limit to the amount of inorganic materials that can be mixed, and the current situation is that a fully satisfactory specific elastic modulus has not been achieved. be. Additionally, polyolefin is disadvantageous in terms of heat resistance, making it unsuitable for car stereos and high-output speakers.
また、液晶ポリマーを使用したスピーカー振動板の場合
は、高い比弾性率、内部損失、耐熱性は得られるものの
、液晶ポリマーは価格が高く、また異方性が高く不均質
な構造を有するため、充分満足のいくスピーカーコーン
が得られない。In addition, in the case of speaker diaphragms using liquid crystal polymers, although high specific elastic modulus, internal loss, and heat resistance can be obtained, liquid crystal polymers are expensive, have high anisotropy, and have a non-uniform structure. A fully satisfactory speaker cone cannot be obtained.
本発明は、かかる問題点を解決するためになされたもの
で、高い耐熱性と適度な比弾性率、内部損失及び経済性
を合わせもつスピーカー振動板を得ることを目的とする
ものである。The present invention has been made to solve these problems, and aims to provide a speaker diaphragm that has high heat resistance, appropriate specific modulus, internal loss, and economical efficiency.
すなわち、本発明は、ポリエチレンテレフタレート10
0重量部に対して、(イ)平均粒径50μ以下の無機化
合物5〜50重量部、(ロ)平均粒径lOμ以下の無機
化合物もしくはポリオレフィン0.5〜10重量部を配
合した樹脂組成物の層と、熱可塑性ポリエステル系エラ
ストマーの層との中間層にポリエチレンテレフタレート
以外のポリエステル樹脂の層を配置したシートにより構
成した多層スピーカー振動板である。That is, the present invention provides polyethylene terephthalate 10
A resin composition containing (a) 5 to 50 parts by weight of an inorganic compound with an average particle size of 50 μ or less, and (b) 0.5 to 10 parts by weight of an inorganic compound or polyolefin with an average particle size of 10 μ or less per 0 parts by weight. This is a multilayer speaker diaphragm made of a sheet in which a layer of a polyester resin other than polyethylene terephthalate is arranged as an intermediate layer between a layer of a polyester resin and a layer of a thermoplastic polyester elastomer.
本発明で使用するポリエチレンテレフタレートとしては
出発原料がテレフタル酸またはテレフタル酸のアルキル
エステル誘導体およびエチレングリコールの他に、共重
合成分としてイソフタル酸、ナフタレンジカルボン酸、
ジフェニルエーテルジカルボン酸、ジフェニルメタジカ
ルボン酸、ジフェニルスルホンジカルボン酸、p−(2
−ヒドロキシエトキシ)安息香酸、5−ナトリウムスル
ホイソフタル酸、アジピン酸、アゼライン酸、セバシン
酸、ドデカン−1,12−ジカルボン酸、テトラデカン
−1,14−ジカルボン酸、ヘキサデカン−1,16−
ジカルボン酸、オクタデカン−1,18−ジカルボン酸
、6−エチル−ヘキサデカン−1,16−ジカルボン酸
等のジカルボン酸成分、プロピレングリコール、ジエチ
レングリコール、ブチレングリコール、ペンチルグリコ
ール、ネオペンチルグリコール、ヘキサメチレングリコ
ール、ポリエチレングリコール、ポリテトラメチレング
リコール等のポリアルキレングリコール等のグリコール
成分を含有してもよく、これを構成する繰り返し単位の
80モル%以上がエチレンテレフタレートからなるもの
である。The polyethylene terephthalate used in the present invention includes starting materials such as terephthalic acid or an alkyl ester derivative of terephthalic acid, and ethylene glycol, as well as isophthalic acid, naphthalene dicarboxylic acid,
diphenyl ether dicarboxylic acid, diphenyl metadicarboxylic acid, diphenyl sulfone dicarboxylic acid, p-(2
-hydroxyethoxy)benzoic acid, 5-sodium sulfoisophthalic acid, adipic acid, azelaic acid, sebacic acid, dodecane-1,12-dicarboxylic acid, tetradecane-1,14-dicarboxylic acid, hexadecane-1,16-
Dicarboxylic acid, dicarboxylic acid components such as octadecane-1,18-dicarboxylic acid, 6-ethyl-hexadecane-1,16-dicarboxylic acid, propylene glycol, diethylene glycol, butylene glycol, pentyl glycol, neopentyl glycol, hexamethylene glycol, polyethylene It may contain a glycol component such as polyalkylene glycol such as glycol or polytetramethylene glycol, and 80 mol% or more of the repeating units constituting this are composed of ethylene terephthalate.
本発明の(イ)成分として使用される無機化合物は、そ
の粒径、形状によってシート表面の平滑剤、強化材、機
械的性質の異方性の緩和剤、結晶核剤としての効果が異
なる。平均粒径が約50μを越えると、その効果が小さ
くなるので、通例は平均粒径50μ以下の無機化合物が
有用である。The inorganic compound used as component (a) of the present invention has different effects as a smoothing agent for the sheet surface, a reinforcing material, an anisotropic relaxant of mechanical properties, and a crystal nucleating agent depending on its particle size and shape. Generally, inorganic compounds with an average particle size of 50 microns or less are useful, since the effect diminishes when the average particle size exceeds about 50 microns.
平均粒径50μ以下の無機化合物の具体例としてはカー
ボンブラック、シリカ、炭酸カルシウム、合成ケイ酸及
びケイ酸塩、亜鉛華、ハロサイトクレー、カオリン、塩
基性炭酸マグネシウム、マイカ、タルク、石英粉、ウオ
ラストナイト、ドロマイト粉、酸化チタン、硫酸バリウ
ム、硫酸カルシウム、アルミナ等を挙げることができ、
これらの無機化合物の一種またはそれ以上を使用するこ
とができる。なかでもタルク、マイカ、ウオラストナイ
トが本発明において効果が大きい。Specific examples of inorganic compounds with an average particle size of 50μ or less include carbon black, silica, calcium carbonate, synthetic silicic acid and silicate, zinc white, hallosite clay, kaolin, basic magnesium carbonate, mica, talc, quartz powder, Examples include wollastonite, dolomite powder, titanium oxide, barium sulfate, calcium sulfate, alumina, etc.
One or more of these inorganic compounds can be used. Among them, talc, mica, and wollastonite are particularly effective in the present invention.
本発明の(0)成分として使用される平均粒径lOμ以
下の無機化合物としては、タルク、炭酸カルシウム、ウ
オラストナイト等を挙げることができるが、特にタルク
が本発明において効果が大きい。Examples of the inorganic compound having an average particle diameter of 1Oμ or less used as component (0) of the present invention include talc, calcium carbonate, and wollastonite, but talc is particularly effective in the present invention.
(0)成分としては、上記の代わりに、ポリオレフィン
も非常に有効であり、結晶化を促進させるだけでなく、
耐衝撃性が向上するという利点がある。As component (0), polyolefin is also very effective instead of the above, and it not only promotes crystallization but also
This has the advantage of improved impact resistance.
ポリオレフィンとしては、低密度ポリエチレン(LDP
E)、高密度ポリエチレン(HDPH)、直鎖状低密度
ポリエチレン(LLDPE)等のポリエチレン、ポリプ
ロピレン(pp)およびそれらの無水マレイン酸グラフ
ト変性等の変性ポリオレフィンが使用できる。As polyolefin, low density polyethylene (LDP
E), polyethylenes such as high-density polyethylene (HDPH) and linear low-density polyethylene (LLDPE), polypropylene (PP), and modified polyolefins such as maleic anhydride graft modification thereof can be used.
また、平均粒径lOμ以下の無機化合物とポリオレフィ
ンとを併用することも可能である。It is also possible to use an inorganic compound with an average particle diameter of 10μ or less and a polyolefin in combination.
本発明の樹脂組成中の各成分の配合比については、(イ
)成分、すなわち平均粒径50μ以下の無機化合物はポ
リエステル成分100重量部に対して5重量部より少な
いと、シートの表面平滑剤、機械的性質の異方性緩和剤
、強化材としての効果が不十分であり、また逆に50重
量部より多く配合すると機械的性質が著しく劣化する。Regarding the blending ratio of each component in the resin composition of the present invention, component (a), that is, an inorganic compound with an average particle size of 50 μm or less, is less than 5 parts by weight per 100 parts by weight of the polyester component, and is used as a surface smoothing agent for the sheet. However, it is insufficiently effective as an anisotropic relaxant and reinforcing agent for mechanical properties, and conversely, if it is added in an amount exceeding 50 parts by weight, mechanical properties are significantly deteriorated.
したがって、(イ)成分の配合量はポリエステル成分1
00重量部に対して5〜50重量部であり、好ましくは
10〜30重量部である。Therefore, the blending amount of component (a) is 1 polyester component.
The amount is 5 to 50 parts by weight, preferably 10 to 30 parts by weight.
また(0)成分、すなわち熱可塑性ポリエステル100
重量部に対して配合する平均粒径lOμ以下の無機化合
物またはポリオレフィンの量としては、0.5重量部に
至らない場合は、結晶化度の上昇が遅(、成形加工の経
済性の問題がおこる。一方、10重量部を越えて配合し
ても結晶化度上昇の速度は飽和しており、かつ機械的性
質が低下し始めるので、熱可塑性ポリエステル100重
量部に対して配合する平均粒径10μ以下の無機化合物
またはポリオレフィンの量は0.5〜10重量部、好ま
しくは1〜5重量部である。In addition, component (0), that is, thermoplastic polyester 100
If the amount of inorganic compound or polyolefin with an average particle size of 10μ or less is less than 0.5 parts by weight, the increase in crystallinity will be slow (and the economical problem of molding). On the other hand, even if the amount exceeds 10 parts by weight, the rate of increase in crystallinity is saturated and the mechanical properties begin to deteriorate. The amount of the inorganic compound or polyolefin with a size of 10 microns or less is 0.5 to 10 parts by weight, preferably 1 to 5 parts by weight.
尚、本発明における樹脂組成物は必要に応じてさらに熱
安定材、酸化安定剤、光安定剤、滑剤、顔料、難燃剤、
可塑剤等の添加剤を配合してもよい。In addition, the resin composition in the present invention may further contain a heat stabilizer, an oxidation stabilizer, a light stabilizer, a lubricant, a pigment, a flame retardant,
Additives such as plasticizers may be added.
本発明で使用する熱可塑性ポリエステル系エラストマー
としては、ハードセグメントが芳香族ポリエステル、ソ
フトセグメントが脂肪族ポリエーテルよりなるポリエス
テル−ポリエステル型エラストマーおよびハードセグメ
ントが芳香族ポリエステル、ソフトセグメントが脂肪族
ポリエステルよりなるポリエステル−ポリエステル型エ
ラストマーを使用することができる。The thermoplastic polyester elastomer used in the present invention includes a polyester-polyester type elastomer in which the hard segment is an aromatic polyester and the soft segment is an aliphatic polyether, and the hard segment is an aromatic polyester and the soft segment is an aliphatic polyester. Polyester-polyester type elastomers can be used.
本発明で使用するポリエステル樹脂としては、ポリブチ
レンテレフタレート、1.4−シクロヘキサンメチレン
テレフタレート、ビスフェールAを主原料とするボリア
リレートおよびポリカーボネート、バラヒドロキシ安息
香酸や2,6ナフタレンジカルボン酸等を主原料とする
全芳香族および半芳香族液晶ポリエステル等およびそれ
らを40%以上含む共重合樹脂組成物を使用することが
できる。The polyester resins used in the present invention include polybutylene terephthalate, 1,4-cyclohexane methylene terephthalate, polyarylates and polycarbonates whose main raw materials are bisphael A, and polyhydroxybenzoic acid, 2,6 naphthalene dicarboxylic acid, etc., whose main raw materials are polyester resins. It is possible to use fully aromatic and semi-aromatic liquid crystalline polyesters, etc., and copolymer resin compositions containing 40% or more thereof.
また、本発明におけるポリエチレンテレフタレート樹脂
と熱可塑性ポリエステル系エラストマーおよびポリエス
テル樹脂との重量比率は40〜94:3〜30: 3〜
30、好ましくは60〜90: 5〜20:5〜20で
ある。さらに本発明における多層シートの製造方法とし
ては、多層ダイを用いる成分を共押出し、製膜する方法
が製造コスト面等より有利であるが、押出しラミネート
等の方法により製造することもできる。Further, the weight ratio of the polyethylene terephthalate resin to the thermoplastic polyester elastomer and the polyester resin in the present invention is 40 to 94:3 to 30:3 to
30, preferably 60-90:5-20:5-20. Furthermore, as a method for manufacturing the multilayer sheet in the present invention, a method of coextruding components using a multilayer die to form a film is more advantageous in terms of manufacturing cost, but it can also be manufactured by methods such as extrusion lamination.
次に、本発明を実施例によって具体的に説明する。以下
の実施例において、部は重量部を示す。Next, the present invention will be specifically explained using examples. In the following examples, parts indicate parts by weight.
実施例1
固有粘度1.0のポリエチレンテレフタレート樹脂10
0部に平均粒径40μのマイカ30部およびLLDPE
(三菱油化■LX529 ) 3部を2軸押比機で溶融
混練して作成したペレットと、ポリエステル系熱可塑性
エラストマー(東し・デュポン■ハイトレル4047)
および液晶ポリエステル(ユニチカ■ロッドランLC−
5000)をそれぞれ専用の押出機3台を用いて多層ダ
イから押出し、PIET樹脂組成物(125μ)/液晶
ポリエステル(10μ)/エラストマー(30μ)/液
晶ポリエステル(10μ)/PET樹脂組成物(125
μ)の5層構成の厚さ300μのシートを製造した。得
られたシートを真空・圧空(プラグアシスト)成形機(
浅野研究所■、FLPD−1414−H−20で、14
0℃にシートを予熱し、金属温度170℃、6秒/回の
サイクルタイムでスピーカー振動板を成形したところ、
表2に示すように成形性は良好で耐熱性も高く、比弾性
率、内部損失も適当で良好をスピーカー振動板が得られ
た。Example 1 Polyethylene terephthalate resin 10 with an intrinsic viscosity of 1.0
0 parts, 30 parts of mica with an average particle size of 40μ, and LLDPE
(Mitsubishi Yuka LX529) Pellets made by melt-kneading 3 parts using a twin-screw presser and polyester thermoplastic elastomer (Toshi/DuPont Hytrel 4047)
and liquid crystal polyester (Unitika Rodran LC-
5000) was extruded from a multilayer die using three dedicated extruders, respectively, to obtain PIET resin composition (125μ)/liquid crystal polyester (10μ)/elastomer (30μ)/liquid crystal polyester (10μ)/PET resin composition (125μ).
A 300μ thick sheet of 5 layers was produced. The obtained sheet is passed through a vacuum/pressure (plug assist) molding machine (
Asano Laboratory ■, FLPD-1414-H-20, 14
When the sheet was preheated to 0°C and a speaker diaphragm was formed at a metal temperature of 170°C and a cycle time of 6 seconds/time,
As shown in Table 2, a speaker diaphragm with good moldability, high heat resistance, appropriate specific modulus of elasticity, and appropriate internal loss was obtained.
実施例2
PIiT樹脂100部に平均粒径40μのマイカ30部
および無水マレイン酸グラフト変性LLDPIE(三菱
油化■モデイックト200F) 3部を2軸押比機で溶
融、混練して作成したペレットと、ポリエステル系エラ
ストマー(東し・デュポン■ハイトレル6377)およ
びボリアリレート(ユニチカ■U−6000)をそれぞ
れ専用の押出機3台を用いて多層ダイから押出し、PE
T樹脂組成物(250μ)/ボリアリレート(20μ)
/エラストマー(30μ)の3層構成のシートを製造し
、実施例1と同様の方法でスピーカー振動板を成形した
ところ、表2に示すように成形性も良好で耐熱性も高く
、比弾性率、内部損失も適当で良好なスピーカー振動板
が得られた。Example 2 Pellets were prepared by melting and kneading 100 parts of PIiT resin, 30 parts of mica with an average particle size of 40 μm, and 3 parts of maleic anhydride graft modified LLDPIE (Mitsubishi Yuka Modified 200F) using a twin-screw presser; Polyester elastomer (Toshi DuPont Hytrel 6377) and polyarylate (Unitika U-6000) were extruded through a multilayer die using three dedicated extruders, and PE
T resin composition (250μ) / polyarylate (20μ)
A sheet with a three-layer structure of /elastomer (30μ) was manufactured and a speaker diaphragm was molded in the same manner as in Example 1. As shown in Table 2, it had good moldability, high heat resistance, and a specific modulus of elasticity. A good speaker diaphragm with appropriate internal loss was obtained.
比較例1〜4
実施例と同様の方法で表1の如く単層シートにてスピー
カー振動板を作成した。スピーカー振動板の物性等を表
2に示した。Comparative Examples 1 to 4 Speaker diaphragms were made from single-layer sheets as shown in Table 1 in the same manner as in the examples. Table 2 shows the physical properties of the speaker diaphragm.
本発明の多層スピーカー振動板は、ポリプロピレン、ポ
リエチレン、ナイロン6、ポリスチレン等のポリマーと
比較して耐熱性、寸法安定性の点で優れており、多層化
する事により従来の単層シートで得られない優れた比弾
性率および内部損失を兼備えており、しかも共押出し成
形法によりシートを作成する大量生産の製造方法をとる
ことが可能となった。また、真空圧空成形等により、短
時間のサイクルタイムでの成形が可能となり、その経済
効果も大である。The multilayer speaker diaphragm of the present invention has superior heat resistance and dimensional stability compared to polymers such as polypropylene, polyethylene, nylon 6, and polystyrene. It has excellent specific elastic modulus and internal loss, and it has become possible to mass-produce sheets by coextrusion molding. In addition, vacuum-pressure molding and the like enable molding in a short cycle time, which has great economic effects.
Claims (1)
イ)平均粒径50μ以下の無機化合物5〜50重量部、
(ロ)平均粒径10μ以下の無機化合物もしくはポリオ
レフィン0.5〜10重量部を配合した樹脂組成物の層
と、熱可塑性ポリエステル系エラストマーの層との中間
層にポリエチレンテレフタレート以外のポリエステル樹
脂の層を配置したシートにより構成したことを特徴とす
る多層スピーカー振動板。For 100 parts by weight of polyethylene terephthalate, (
b) 5 to 50 parts by weight of an inorganic compound with an average particle size of 50 μm or less,
(b) A layer of polyester resin other than polyethylene terephthalate in the intermediate layer between a layer of a resin composition containing 0.5 to 10 parts by weight of an inorganic compound or polyolefin with an average particle size of 10 μ or less and a layer of thermoplastic polyester elastomer. A multilayer speaker diaphragm characterized in that it is composed of sheets arranged with.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24607889A JP2731260B2 (en) | 1989-09-20 | 1989-09-20 | Multilayer speaker diaphragm |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24607889A JP2731260B2 (en) | 1989-09-20 | 1989-09-20 | Multilayer speaker diaphragm |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03107300A true JPH03107300A (en) | 1991-05-07 |
| JP2731260B2 JP2731260B2 (en) | 1998-03-25 |
Family
ID=17143151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24607889A Expired - Lifetime JP2731260B2 (en) | 1989-09-20 | 1989-09-20 | Multilayer speaker diaphragm |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2731260B2 (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7708111B2 (en) * | 2005-07-21 | 2010-05-04 | Sony Corporation | Acoustic diaphragm and method for manufacturing an acoustic diaphragm |
| CN108551642A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108551640A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108551643A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108668205A (en) * | 2018-06-15 | 2018-10-16 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108966088A (en) * | 2018-06-15 | 2018-12-07 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loudspeaker |
| CN109005487A (en) * | 2018-06-15 | 2018-12-14 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loudspeaker |
| JP2021526770A (en) * | 2018-06-15 | 2021-10-07 | ゴルテック インコーポレイテッド | speaker |
| JP2021527991A (en) * | 2018-06-15 | 2021-10-14 | ゴルテック インコーポレイテッド | speaker |
| WO2022113990A1 (en) * | 2020-11-27 | 2022-06-02 | デンカ株式会社 | Multilayer film for speaker diaphragms and method for producing same |
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1989
- 1989-09-20 JP JP24607889A patent/JP2731260B2/en not_active Expired - Lifetime
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7708111B2 (en) * | 2005-07-21 | 2010-05-04 | Sony Corporation | Acoustic diaphragm and method for manufacturing an acoustic diaphragm |
| CN108551642A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108551640A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108551643A (en) * | 2018-06-15 | 2018-09-18 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108668205A (en) * | 2018-06-15 | 2018-10-16 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loud speaker |
| CN108966088A (en) * | 2018-06-15 | 2018-12-07 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loudspeaker |
| CN109005487A (en) * | 2018-06-15 | 2018-12-14 | 歌尔股份有限公司 | The diaphragm of loudspeaker and loudspeaker |
| CN109005487B (en) * | 2018-06-15 | 2020-03-24 | 歌尔股份有限公司 | Loudspeaker diaphragm and loudspeaker |
| CN108551640B (en) * | 2018-06-15 | 2020-09-18 | 歌尔股份有限公司 | Loudspeaker diaphragm and loudspeaker |
| CN108551642B (en) * | 2018-06-15 | 2020-09-22 | 歌尔股份有限公司 | Loudspeaker diaphragm and loudspeaker |
| CN108668205B (en) * | 2018-06-15 | 2020-09-22 | 歌尔股份有限公司 | Loudspeaker diaphragm and loudspeaker |
| CN108966088B (en) * | 2018-06-15 | 2020-09-22 | 歌尔股份有限公司 | Loudspeaker diaphragm and loudspeaker |
| JP2021526770A (en) * | 2018-06-15 | 2021-10-07 | ゴルテック インコーポレイテッド | speaker |
| JP2021526769A (en) * | 2018-06-15 | 2021-10-07 | ゴルテック インコーポレイテッド | Speaker vibrating membrane and speaker |
| JP2021527995A (en) * | 2018-06-15 | 2021-10-14 | ゴルテック インコーポレイテッド | Speaker vibrating membrane and speaker |
| JP2021527991A (en) * | 2018-06-15 | 2021-10-14 | ゴルテック インコーポレイテッド | speaker |
| WO2022113990A1 (en) * | 2020-11-27 | 2022-06-02 | デンカ株式会社 | Multilayer film for speaker diaphragms and method for producing same |
| TWI871497B (en) * | 2020-11-27 | 2025-02-01 | 日商電化股份有限公司 | Laminated film for speaker vibration plate and manufacturing method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2731260B2 (en) | 1998-03-25 |
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