JPS5991052A - High-frequency adhesive body - Google Patents

High-frequency adhesive body

Info

Publication number
JPS5991052A
JPS5991052A JP57201033A JP20103382A JPS5991052A JP S5991052 A JPS5991052 A JP S5991052A JP 57201033 A JP57201033 A JP 57201033A JP 20103382 A JP20103382 A JP 20103382A JP S5991052 A JPS5991052 A JP S5991052A
Authority
JP
Japan
Prior art keywords
frequency
adhesive
powder
resin
frequency adhesive
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
Application number
JP57201033A
Other languages
Japanese (ja)
Inventor
忠範 野村
杉本 権司
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP57201033A priority Critical patent/JPS5991052A/en
Publication of JPS5991052A publication Critical patent/JPS5991052A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/04Dielectric heating, e.g. high-frequency welding, i.e. radio frequency welding of plastic materials having dielectric properties, e.g. PVC
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/48Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/48Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
    • B29C65/486Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by their physical form being non-liquid, e.g. in the form of granules or powders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/02Preparation of the material, in the area to be joined, prior to joining or welding
    • B29C66/026Chemical pre-treatments
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/11Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
    • B29C66/112Single lapped joints
    • B29C66/1122Single lap to lap joints, i.e. overlap joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/20Particular design of joint configurations particular design of the joint lines, e.g. of the weld lines
    • B29C66/21Particular design of joint configurations particular design of the joint lines, e.g. of the weld lines said joint lines being formed by a single dot or dash or by several dots or dashes, i.e. spot joining or spot welding
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/43Joining a relatively small portion of the surface of said articles
    • B29C66/436Joining sheets for making articles comprising cushioning or padding materials, the weld being performed through the cushioning material, e.g. car seats
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/727General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being porous, e.g. foam
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/71General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/04Condition, form or state of moulded material or of the material to be shaped cellular or porous
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2009/00Layered products

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は高周波接着体に関するものである。更に詳しく
は、柔軟性、風会、伸び等に優れ、また、粉末接看剤を
用いるドライ法で製造でき、省エイ・ルギ−が達成され
、高周波接着により生殖性良好に製造し得る高周波接着
体に係るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a high frequency adhesive. More specifically, it is a high-frequency adhesive that has excellent flexibility, wind resistance, elongation, etc., can be manufactured by a dry method using a powder bonding agent, achieves energy saving and energy saving, and can be manufactured with good reproductive performance by high-frequency adhesive. It is related to the body.

従来は旨周波接看体として以下の構造体が公知である。Conventionally, the following structures are known as frequency contact bodies.

順次へへFボード等の基材層、高周波接着用フィルム層
、高周波接着性樹脂ラテックスがポリウレタンフォーム
骨格に一様に被膜を形成して々る高周波接看性りッショ
ン材盾、ρi周波接着用フィルム層、ファブリック等の
表装材層力)ら構成されている。
Sequentially: Base material layer such as F board, film layer for high frequency adhesive, high frequency adhesive resin latex forming a uniform coating on the polyurethane foam skeleton, high frequency contact material shield, for ρi frequency adhesive. It consists of a film layer, a covering material layer such as fabric, etc.

しかしながら従来の関周波接百体には以下に述べる不買
け・J欠点があった。
However, the conventional Kanshu wave concerto has the following drawbacks.

品賀的には、訓周波接着性樹脂ラテックスがポリウレタ
ン骨格に一様に被膜を形成するため、ポリウレタン本来
の柔軟性、風合、仲ひが形成されラテックス被膜により
阻害される欠点があった。
Shinaga had the disadvantage that because the frequency-tuning adhesive resin latex forms a uniform film on the polyurethane skeleton, the original flexibility, texture, and stiffness of polyurethane are formed and are inhibited by the latex film.

特に面周、クジ接右性を同上させようとする時、多錐の
ラテックスをポリウレタンフォームに含浸させなければ
ならず、−胸その被膜を埋くする結果となり柔軟性、風
合、伸びを低下させるという難点があった。
In particular, when trying to improve the face circumference and right angle, it is necessary to impregnate polyurethane foam with polypyramidal latex, which results in filling the breast film and reducing flexibility, texture, and elongation. There was a problem with letting it work.

ユ稈的0こは、ラテックスをポリウレタンに含浸する工
程はウェット法であり、多量の水分を蒸発させなければ
ならない欠点かぁ−)た。高周波接着体を組立てる工程
では、一部の商用波mW部の実用的接着力を得るため筒
周波接右用フィルムの挿入工程が必要であり、かつ高周
波接着体を組立てる際に余分の該フィルムの端切れが発
生するが、これは[11史用できずすてなければならな
い割一点があった。又高周波接着体を組立てる工程にお
ける基材層、フィルム層、クッション1−、フィルム層
、表装材層と5層全体の位置決めの鋪しさかあった。
Unfortunately, the process of impregnating latex into polyurethane is a wet method, which has the disadvantage that a large amount of water must be evaporated. In the process of assembling the high-frequency adhesive, it is necessary to insert a film for cylindrical frequency contact in order to obtain a practical adhesion force for part of the commercial wave mW part, and when assembling the high-frequency adhesive, an excess of the film must be inserted. There will be scraps, but this is due to [11]There was a portion that could not be used for historical purposes and had to be thrown away. Furthermore, in the process of assembling the high-frequency adhesive, it was difficult to position all five layers: the base material layer, the film layer, the cushion 1-, the film layer, and the facing material layer.

従来の1翼i周波接舌体の品賀上、工程上、組立上の欠
点・難点のない高周波f6 W体が要求せられていた0
本発明者らは以上の要求に対して、鋭意研究の結果尚周
波接着性樹脂粉末をポリウレタンフォーム骨格に、一様
に粒子状ζこ固着させた高周波接着性クッション材を用
いる事により、従来の高周波接着体のように商周波接着
用フィルムを使用することなく実用的な高周波接着され
た高周波接着体を提供す2ことが出来るに到った。しか
して、本発明は、駒次基材層、晶周波接貞性イ′ツショ
ン刊層、表装側層からなり、一部が冒周波接着されてな
ることを特徴とする高周波接着体である。
There was a demand for a high-frequency f6 W body that does not have the mechanical, process, and assembly drawbacks and difficulties of the conventional single-blade I-frequency tongue body.
In response to the above requirements, the present inventors have conducted extensive research and developed a high-frequency adhesive cushioning material in which high-frequency adhesive resin powder is uniformly adhered to a polyurethane foam skeleton in the form of particles. It has now become possible to provide a practical high-frequency bonded body without using a film for commercial frequency bonding unlike high-frequency bonded bodies. Accordingly, the present invention is a high-frequency bonded body comprising a piece base material layer, a crystal frequency contacting application layer, and a facing layer, some of which are bonded by high frequency bonding.

本発明の高周波接着体のクッション層にはウレタンフオ
ーム骨格茜周波接右性粉末を粒子状に一様に固着してい
る梅輩なので、ウレタンフオーム本来の柔軟性、風合、
伸びは全くそこなわれず、かつ、高周波接着性は実用的
である品質的利点の外、粉末を骨格に固着させるドライ
法であり−ラテツクスを含浸するウェット法に比べ、省
エイ・ルギーである工程上の利点もある。
The cushion layer of the high-frequency adhesive of the present invention has a urethane foam skeleton with madder frequency adhesion powder uniformly fixed in the form of particles, so the original flexibility and texture of the urethane foam is maintained.
In addition to the quality advantages of no loss of elongation and practical high-frequency adhesion, it is a dry method that fixes the powder to the skeleton - it is less expensive and less expensive than the wet method of impregnating latex. There are also process advantages.

又従来G′)高周波接着体に比べ、高周波接着性フィル
ムを使用しなくても良い利点の外、高周波接着体を組立
てる際の各側層の位を置ぎめの鋪しさを解消する工程上
の利点もと^る0 本発明の高周波接着体は順〆人基材層4、高周波接肯性
ノツショ/刊層3、表装側層2と高周彼憎循部1で一部
商周波接着された構造体である。
In addition to the advantage of not using a high-frequency adhesive film compared to the conventional G') high-frequency adhesive, there is also an advantage in the process of eliminating the difficulty in positioning each side layer when assembling the high-frequency adhesive. Advantages Based on 0 The high frequency adhesive body of the present invention is partially commercial frequency bonded with the base material layer 4, the high frequency positive layer 3, the facing side layer 2 and the high frequency negative circulation part 1. It is a struct.

本発明に用いられに基材層としては、繊維板、ハードボ
ード、ハニカム叡、樹脂板、合板、金属板等を1史用す
ることができる。ノ\−ドボード、台板、スチール板前
が安価であり好ましい。
As the base material layer used in the present invention, fiberboard, hardboard, honeycomb board, resin board, plywood, metal board, etc. can be used. Node boards, base plates, and steel plate fronts are inexpensive and preferable.

高周波接着性クッション材としては、高周波接石性樹脂
粉末がポリウレタンフォーム骨格に粒子状に一株に固着
してなる構造体が使用される0また天然パルプ集合体、
綿集合体、合成繊維集合体寺に本発明の1所周波接看性
粉末を含浸させ、繊維骨格に固着させた高周波接着性の
クッション刊は、特に表装祠がファブリックの場合であ
り、身体の衣服篤による静電気が発生する場合に都合が
良い。天然パルプ、綿、淋毒の天然繊維のスフ状のもの
は適当に吸湿性であり、表装制表面に発生する摩擦静′
岨気を少しづつクッション桐の方へ移動させる効果もあ
り好ましい。
As the high-frequency adhesive cushioning material, a structure in which high-frequency stone-contactable resin powder is adhered to a polyurethane foam skeleton in the form of particles is used.Also, a natural pulp aggregate,
A high-frequency adhesive cushion made by impregnating a cotton aggregate or a synthetic fiber aggregate with the frequency-adhesive powder of the present invention and fixing it to the fiber skeleton is particularly applicable when the covering is fabric, This is convenient when static electricity is generated due to clothing. Natural fibers such as natural pulp, cotton, and gonotoxic fibers are moderately hygroscopic and absorb the frictional static generated on the surface.
It also has the effect of moving the air little by little toward the cushion paulownia, which is preferable.

静電気拡散の簡便な評価方法として、例んばポリエステ
ル又はナイロンフィルムで表装材をYtNしタバコの灰
を表面に落し、牛ではらい洛しやすいものが静″嘔気拡
散が良好と判ボする方法がある。
A simple method for evaluating static electricity diffusion is, for example, by using polyester or nylon film as a covering material of YtN and dropping cigarette ash on the surface. be.

多孔体骨格にこれら粉末が粒子形態を残して固着した構
造について走査型電子顕微観観察及びそり写真に基づい
て述べる。
The structure in which these powders adhere to the porous body skeleton while leaving a particle shape will be described based on scanning electron microscopic observations and warpage photographs.

第5図は嵩舊贋16yitのポリウレタンフォーム原反
の電子顕微鏡写真である。第6図は塩化ビニリデン共恵
合体粉末をウレタンフオーム両路に粒子形態を残したま
まで固着させた高周波接着性クッション材層の電子顕微
鏡写真である。
FIG. 5 is an electron micrograph of a bulk polyurethane foam material of 16 yt. FIG. 6 is an electron micrograph of a high-frequency adhesive cushioning material layer in which vinylidene chloride co-merging powder is adhered to both sides of urethane foam while leaving its particle form intact.

第5図及び第6図から明らかなように骨格に高周波接層
性樹脂粉末が粒子形態を残して不連続に固着しているこ
とがわかる。この不連続に粒子形態を残して固着した構
造であることは、クッション材層の多孔体本来の風合な
どの特性を残すことにおいて重要な意味を有する。すな
わち、本発明の旨周波接石性りッション相層は、多孔体
の骨格の外力に対する自由度が残されたまま商周波接適
性が賦与された多孔体構造である。
As is clear from FIGS. 5 and 6, it can be seen that the high-frequency adhesion resin powder is discontinuously adhered to the skeleton, leaving a particle shape. This structure in which the particles remain discontinuously fixed has an important meaning in preserving the characteristics such as the original feel of the porous material of the cushioning material layer. That is, the frequency wave contactable friction phase layer of the present invention has a porous structure that is endowed with commercial frequency wave contactability while maintaining the degree of freedom of the porous body skeleton against external forces.

旨周波r&M性樹脂粉末として、塩化ビニリデン樹脂、
塩化ビニル樹脂、ポリアミド樹脂粉末のうち誘電体損失
が0.02B上のものが使用できる。
As frequency R&M resin powder, vinylidene chloride resin,
Among vinyl chloride resin and polyamide resin powder, those having a dielectric loss of 0.02B or more can be used.

好ましくは004以上が良く、史に(l(ましくは00
5が良い。誘゛市体損失が002未満であるとr所周波
誘電発熱が不充分であり、商周波接石する際加熱111
間が長くなったり、接石力が実用的でなくなるので好ま
しくない。
Preferably 004 or higher, historically (l (preferably 00
5 is good. If the dielectric loss is less than 0.02, the dielectric heat generation at the r frequency is insufficient, and the heating 111 occurs during commercial frequency stone contact.
This is undesirable because the gap becomes long and the stone contact force becomes impractical.

ウレタンフオーム骨格に固着する高周波接着性樹脂粉末
の量は、ウレタンフオームの嵩密度や必要な接貴力によ
り異るが、例えば199/lの嵩密度のウレタンフオー
ムを使用した場合、粉末固着量は5 Lj/を以上、1
809/を以下が良い。
The amount of high-frequency adhesive resin powder that adheres to the urethane foam skeleton varies depending on the bulk density of the urethane foam and the required adhesive force. For example, when using urethane foam with a bulk density of 199/l, the amount of powder adhered to 5 Lj/ or more, 1
809/ or less is better.

好ましくは1’oy/を以上、15θ9/を以下が良い
。更に好ましくは139/を以上、1009/4以Fが
良い。
Preferably, it is 1'oy/ or more and 15θ9/ or less. More preferably, it is 139/4 or more, and 1009/4 or more F.

粉末固f+f 景が597’を未ン岡であると、訓周波
接希力が実用的でなく、1809/’lを越えるとウレ
タンフオ ムの風合、仲ひが低トして好ましくない。
If the powder hardness f + f is less than 597', the frequency welding force will be impractical, and if it exceeds 1809/'l, the texture and strength of the urethane foam will deteriorate, which is undesirable.

1所周彼接肯性樹脂粉末の粒子径の範囲として、05μ
以上、1餌以下がウレタンフオームに固着させるのに良
い。好ましくは10μ以上、500μ以+、更に好まし
くは100μ以上、300μ以下である。
As the particle size range of the positive resin powder, 05μ
As mentioned above, one bait or less is good for making it stick to the urethane foam. Preferably it is 10μ or more and 500μ or more, more preferably 100μ or more and 300μ or less.

以上の粒子径の範囲をJIS標準フルイにて表示すると
それぞれ16メツシユパスであり、好ましくは32メツ
シユパスであり、更に好ましくは42メツシユパス、2
0oメツシユオンの範囲である。
When the above particle size range is expressed using a JIS standard sieve, it is 16 mesh passes, preferably 32 mesh passes, more preferably 42 mesh passes, 2 mesh passes, etc.
It is in the range of 0o mesh.

05μ未満の粒子では固着したrウレタンフオームの風
合、伸びを低下させたり、又1臥を越えると画周波接着
部に接着不拘−が起り(接着飛び)好ましくない。
If the particle size is less than 0.05 μm, the texture and elongation of the fixed R-urethane foam will be deteriorated, and if the particle size exceeds 1.0 μm, adhesion failure (adhesion skipping) will occur at the image frequency bonding area, which is not preferable.

高周波接右性粉末として好ましい塩化ビニリデン樹脂と
して、20モル%以上、93モル%以下の塩化ビニリデ
ン(A)成分と(A)と兵事台可能なモノマーから選ば
れた1種以上の7モル%以上、80モル%以゛トのモノ
マー(B)成分と(A)および/あるいは(B)と共■
合=1能な官能性七ツマ−から選はれた0モル%以上、
10モルCX以下のモノマ〜(C)成分からなる塩化ビ
ニリデン共重合体でありおよび/あるいは乳化型合法に
より重合した商分子鎖末端がラジカル開始剤分解生成物
の官能基である粉末が好ましい。
As the vinylidene chloride resin preferable as the high-frequency dextral powder, a vinylidene chloride (A) component of 20 mol % or more and 93 mol % or less and 7 mol % of one or more monomers selected from monomers that can be used with (A) Above, 80 mol% or more of the monomer (B) component and (A) and/or (B)
0 mol% or more selected from the seven functional sensual substances,
Preferably, the powder is a vinylidene chloride copolymer comprising 10 moles of CX or less of monomers to component (C) and/or is polymerized by an emulsion method and the molecular chain terminal thereof is a functional group of a decomposition product of a radical initiator.

(1B)として特に塩化ビニル、酢酸ビニル、アクリロ
ニトリル、メチルアクリレート、メチルメタクリレート
が工業的に量産され、兼価で良い。
In particular, vinyl chloride, vinyl acetate, acrylonitrile, methyl acrylate, and methyl methacrylate are industrially mass-produced as (1B), and may be used in combination.

(C)として特ζこアクリル酸、メタノリル酸、イタコ
ン酸、マレイン酸、無水マレイン酸、フマル酸、アクリ
ル酸アミド、メタクリル酸アミド、N−n−ブトキンア
クリル酸アミド、ヒドロキシエチルアクリレート、グリ
シジルアクリレート、グリシジルメタアクリレートが工
業的に生成されて、入手しやすく好ましい。
(C) Special acrylic acid, methanolic acid, itaconic acid, maleic acid, maleic anhydride, fumaric acid, acrylamide, methacrylic acid amide, N-n-butquine acrylamide, hydroxyethyl acrylate, glycidyl acrylate , glycidyl methacrylate is preferably produced industrially and easily available.

(A)成分が20モル%未満であると商用波誘電発熱量
が少なく、実用的篩周彼接着力が得られる程度に該粉末
が融解あるいは軟化あるいは架橋せず好ましくない。官
能性七ツマ−(C)を尋人することにより被接着剤との
濡れが該粉末の融解、軟化あるいは架橋するとき好まし
く作用すると考えりれるが、RMalは不明である。官
叱性七ツマ−(C、)のS入量0.(+5モル%以上に
おいて明確な画周波接着力の増大効果が認められる。又
、官能性七ツマ−CC)を用いない場合には乳化型合法
に、より車台させたら、ラジカル開始剤の分解生成物に
帰因すると考えられる高分子鎖末端に官能甚が尋人され
高周波接着力を同上させ好ましい。
If the content of component (A) is less than 20 mol %, the commercial wave dielectric heating value will be small, and the powder will not melt, soften, or crosslink to the extent that practical sieve circumferential adhesion can be obtained, which is undesirable. It is thought that the use of functionalized nitrate (C) works favorably when wetting with the adhesive melts, softens, or crosslinks the powder, but RMal is unknown. The amount of S in Kanjisei Nanatsuma (C,) is 0. (+5 mol% or more, a clear effect of increasing the image frequency adhesion force is observed.Also, when functional seven-termer-CC) is not used, the emulsion type method is used, and if it is made more compact, the decomposition of the radical initiator is generated. It is preferable that a functional group is added at the end of the polymer chain, which is considered to be due to a substance, to increase the high-frequency adhesive strength.

特に椅子、ペット、ソファ−寺の家具の様に構造的強度
を要求される場合には官能性モノマー成分および/また
は開始剤から生成してなる官能性共重合体末端がある方
が好ましい。
Particularly when structural strength is required, such as in furniture such as chairs, pets, sofas, etc., it is preferable to have a functional copolymer terminal formed from a functional monomer component and/or an initiator.

高周波接層性粉末として好ましい塩化ビニル樹脂として
、塩化ビニルを主成分とした共重合体が好ましく、更に
好ましくは官能性七ツマ−を導入してなる共重合体およ
び/あるいは乳化型合法によるラジカル開始剤分解生成
物の官能基を導入してなる共重合体が良い、・ 塩化ビニル成分として50モル%以上、92モルLX以
下、8モル%以上、50モル%以下のエチレン、プロピ
レン、酢酸ビニル、アクリル酸エステル、及びメタクリ
ル酸エステル、アクリロニトリルから選ばれたモノマー
成分の一押以上の組合せた成分からなる共重合体が工業
的に製造しゃすく好ましい。更に好ましくは官能基モノ
マー成分として、アクリル酸、メタクリル酸、マレイン
酸、無水マレイン酸、フマル酸、イタコン酸、アクリル
酸アミド、メタクリル酸アミド、N −u−ブトキンア
クリル酸アミド、ヒドロキシエチルアクリレート、グリ
シジルアクリレート、グリシジルメタアクリレートが工
業的に生産され、入手しゃすく好ましい。
As the vinyl chloride resin preferable as the high-frequency layering powder, a copolymer mainly composed of vinyl chloride is preferable, and more preferably a copolymer with a functional heptamer introduced therein and/or a radical initiation method using an emulsion type method. A copolymer formed by introducing a functional group of a chemical decomposition product is preferable. - As a vinyl chloride component, 50 mol% or more and 92 mol LX or less, 8 mol% or more and 50 mol% or less of ethylene, propylene, vinyl acetate, A copolymer comprising a combination of one or more monomer components selected from acrylic esters, methacrylic esters, and acrylonitrile is preferred because it can be manufactured industrially. More preferably, as the functional monomer component, acrylic acid, methacrylic acid, maleic acid, maleic anhydride, fumaric acid, itaconic acid, acrylamide, methacrylic acid amide, N-u-butquine acrylamide, hydroxyethyl acrylate, Glycidyl acrylate and glycidyl methacrylate are preferably industrially produced and readily available.

高周波接着性粉末として好ましいポリアミド樹脂として
は低融点のポリアミド樹脂が好ましい。
As the polyamide resin preferable as the high-frequency adhesive powder, a polyamide resin with a low melting point is preferable.

好ましい融点としては60゛C以上、200℃以下、更
に好まシ、<は70°C以上、180℃以下、最も好ま
しいのは80℃以上、150℃以下のポリアミド樹脂で
ある。一般にナイロン繊維に用いられるポリアミド樹脂
は融点が高く好ましくない。
A polyamide resin having a melting point of preferably 60°C or higher and 200°C or lower, more preferably 70°C or higher and 180°C or lower, most preferably 80°C or higher and 150°C or lower. Polyamide resins, which are generally used for nylon fibers, have a high melting point and are not preferred.

200Cを越える融点のポリアミド樹脂は西周波接1台
する時、高周波印加時間が長くなり、接着作業が遅くな
り好ましくない。60℃未満の融点のポリアミド樹脂は
高周波接着部の初期強度がでないので好ましくない。
A polyamide resin having a melting point exceeding 200C is not preferable because the high frequency application time becomes long and the bonding work becomes slow when one West Frequency wave is applied. A polyamide resin having a melting point of less than 60° C. is not preferred because the initial strength of the high-frequency bonded portion is low.

表装材層として、ファブリック、天然皮革、合成皮革か
ら選ばれた表装材が良い。ファブリックとしてナイロン
、ポリエステル、アクリル、ビニロン、ポリプロピレン
の合成繊維、アセテートの半会成繊維、レーヨン、キュ
プラの画成繊維、羊毛、綿、麻の天然繊維の中から選ば
れた繊維の単体での紡績または二押以上の混紡からなる
糸を用い、それらの糸を単体で編織または二押以上を父
編してなる編物、織物が使用できる。
As the facing material layer, a facing material selected from fabric, natural leather, and synthetic leather is preferable. Spinning single fibers as fabrics selected from synthetic fibers such as nylon, polyester, acrylic, vinylon, and polypropylene, semi-woven acetate fibers, defined fibers such as rayon and cupro, and natural fibers such as wool, cotton, and hemp. Alternatively, knitted or woven fabrics can be used by using yarns made of a blend of two or more yarns, knitting or weaving these yarns singly, or by father-knitting two or more yarns.

天然皮革として獣皮、例えば牛皮、羊皮、豚皮が一般的
に1す・用できる。合成皮革とし°Cポリウレタン皮革
、塩ビ皮φ゛、ポリアミド皮革が使用できる。
Animal skins such as cowskin, sheepskin, and pigskin can generally be used as natural leather. As synthetic leather, °C polyurethane leather, PVC leather, and polyamide leather can be used.

副周波(’l性桐脂粉末をポリウレタンフォーム中に含
浸する方法としては、 ■ パウダー含浚法:パウダー中にウレタンフオームを
通過させて含浸する方法 ■ 流動パウダー含浸θ;:パウダーを空気で流動化さ
せた中をフオームを通過させて含浸する方法 (■ エアーガン法:パウダーを空気中に分散させた〆
昆合物を吹き付けてパウダーを含浸する方法 ■ エアーサクション法:パウダーを空気中に分散又は
流動化させた中をフオームを通過させ、フオームの他面
を減圧にしてパウダーを含浸する方法 寺が採用される。
Methods for impregnating polyurethane foam with sub-frequency tung fat powder include: ■ Powder dredging method: A method in which the urethane foam is passed through the powder to impregnate it ■ Fluid powder impregnation θ: Fluidize the powder with air A method of impregnating the powder by passing it through a foam (■ Air gun method: A method of impregnating powder by spraying a powder mixture in which powder is dispersed in the air. ■ Air suction method: A method of dispersing powder in the air or impregnating it with powder. A method is adopted in which the powder is impregnated by passing the foam through the fluidized material and applying reduced pressure to the other side of the foam.

必要に応じてこれらの組合せた方法も採用できることは
いうまでもない。
It goes without saying that a combination of these methods can be employed as needed.

高周波接置性樹脂粉末をポリウレタンフォーム骨格に固
着する方法としては ■熱風焼結法:樹脂の軟化点又は融点以上に熱風にて加
熱して固着させる方法 ■赤外線焼結法:樹脂を赤外線にて加熱して固着させる
方法 ■高岡lジ焼結法:樹脂を高周波にて加熱して固着させ
る方法 青が採用される。
Methods for fixing high-frequency bondable resin powder to the polyurethane foam skeleton are: -Hot air sintering method: A method in which the resin is heated with hot air above its softening point or melting point to fix it. -Infrared sintering method: The resin is fixed using infrared rays. Method of fixing by heating ■Takaoka di-sintering method: A method of fixing resin by heating it with high frequency.

必要に応じてこれらの組合せた方法も採用できることは
いうまでもない1J 以下に本発明を詳4411に失弛例をもって説明するが
、この実施例のみに本発明は限足されない。
It goes without saying that a combination of these methods can be employed as required.The present invention will be explained in detail below using an example of laxation, but the present invention is not limited to this example.

なお、実施例中における評価方法は以下に記載する方法
によった。
In addition, the evaluation method in the examples was based on the method described below.

■高周波接着 パール高周波ウエルダ=(パールエff1(株))R−
203D (3K W 、 40MHz )を用い、表
装材層に4g巾、3 g cm長のシールバーに20 
Kg /en?加圧して当てて、同調ダイヤル80(’
200mA)にてシールした。シール時間は、表装材層
に合成皮革を用いた場合に15秒間、ファブリックを用
いた場合には30秒間jjりだ。冷却時間は加圧状態に
−Cシール時間と同じ時間放冷した。
■High-frequency adhesive pearl high-frequency welder = (Pearl FF1 Co., Ltd.) R-
203D (3KW, 40MHz) was used, and a seal bar with a width of 4g and a length of 3g cm was installed on the surface material layer.
Kg/en? Apply pressure and turn the tuning dial 80 ('
200 mA). The sealing time is 15 seconds when synthetic leather is used for the facing layer, and 30 seconds when fabric is used. The cooling time was the same as the -C sealing time in the pressurized state.

■接置強度 東洋ボールドウィン製TENSILON引張試験機UT
M−4Lを便用して引張速度50 tar 7分にて商
周仮接右面を180度の角度で剥離し、ノ・−ドボード
層と表装材層の剥離強度を測定した。なお試験片はIl
l 2.5 cmとした。
■Tensile strength Toyo Baldwin TENSILON tensile testing machine UT
Using M-4L, the right side of the temporary tangent of the quotient circumference was peeled off at an angle of 180 degrees at a tensile speed of 50 tar for 7 minutes, and the peel strength of the node board layer and the facing material layer was measured. The test piece is Il
l 2.5 cm.

実施例−1 表−1に示す塩化ビニリデン樹脂からなる42メツシユ
パス、170メツシユオンの置局’tFM 4’H層性
樹脂粉末を嵩密度t 6y7tの1すさ3 歎rbのポ
リウレタンフォームシート(第5図にウレタンフオーム
の電子顕微鏡写真を示す)に所定量含浸(嵩密度0.5
9 /ccの粉末を入れた含浸槽に・タレタンフオーム
シートを5m/凪n □)速度で浸漬通過させて粉末を
所定量含浸)させた後、40 MHzの高周波焼結炉に
て10秒間加熱し、ウレタンフオーム骨格に第6図に示
すように粉末を固着させた高周波接着性クッション材を
準備した。
Example 1 A polyurethane foam sheet with a bulk density of t 6y7t and a width of 3 rb (Fig. (shows an electron micrograph of urethane foam) is impregnated with a predetermined amount (bulk density 0.5
After impregnating a predetermined amount of powder by impregnating a Taretane foam sheet at a speed of 5 m/min □) into an impregnating bath containing 9/cc of powder, it was heated for 10 seconds in a 40 MHz high-frequency sintering furnace. Then, a high frequency adhesive cushioning material was prepared in which powder was adhered to the urethane foam skeleton as shown in FIG.

表装材層として、0.34m1!3’の塩化ビニル樹脂
レザー、糸材として5路厚のハードボード(日本ハード
ボード製)を用い、その間に筒周l皮接着性りッション
側層を市ね合せて、一部分を高周波接着し、訓周波接着
体を作成した。この部分的に筒周波接着させた部分の接
着力を測定した結果を表−1に示す。
As the facing material layer, 0.34 m1!3' of vinyl chloride resin leather was used, and as the thread material, 5-thickness hardboard (manufactured by Nippon Hardboard) was used, and in between, a cylindrical circumferential skin-adhesive cushion side layer was used. At the same time, a part was radio-frequency bonded to create a frequency-tuning bonded body. Table 1 shows the results of measuring the adhesive strength of this partially cylindrical frequency adhesive area.

表−1に示す如く、本発明の接着体の筒周波接百ノJは
実用的であり、風合の良いものであった。
As shown in Table 1, the cylindrical frequency wave resistance of the adhesive of the present invention was practical and had a good feel.

比較のため塩化ビニル70モル%、塩化ビニル30モル
に、アクリル酸1モル%よりなる固形分50Xの水分散
体をウレタンフオームに含浸させ、160℃5分乾燥さ
せ、高周波接着樹脂成分として389/を含有する高周
波接着性クッション材を実施例−1と同じ構成にて高周
波接着体とした。
For comparison, urethane foam was impregnated with an aqueous dispersion of 50X solid content consisting of 70 mol% vinyl chloride, 30 mols vinyl chloride, and 1 mol% acrylic acid, and dried at 160°C for 5 minutes to form a high-frequency adhesive resin component of 389/ A high frequency adhesive cushioning material containing the above was made into a high frequency adhesive body with the same structure as in Example-1.

この接着体の高周波接着力は粉末を用いたものと同程度
であるが風合がきわめて硬いものであった。
The high-frequency adhesive strength of this adhesive was comparable to that using powder, but the texture was extremely hard.

表−1実施例−1 ■DC塩化ビニリデン VC塩化ビニル 六入   アクリル酸 エマルジョン車台したものを塩析粉末にしたポリマー 実施例−2 実施例−1で用いた塩化ビニリデン成分70モル%、塩
化ビニル成分30モル%、アクリル酸成分1モル%から
なる共重合体粉末(42メツシユパス、200メツシユ
オン)を嵩密度t6p/zの厚さ10課のポリウレタン
フォームシートに389/を含浸させた後、1601G
の熱風焼結炉にて5分間加熱し、ウレタンフオームの骨
格に粉末を固着させた高周波接着性クッション材を2神
類準備した。
Table-1 Example-1 ■DC vinylidene chloride VC vinyl chloride 6 pieces Polymer obtained by salting out powder from acrylic acid emulsion chassis Example-2 Vinylidene chloride component used in Example-1 70 mol%, vinyl chloride component A polyurethane foam sheet having a bulk density of t6p/z and a thickness of 10 sections was impregnated with 389/ copolymer powder (42 mesh pass, 200 mesh pass) consisting of 30 mol% and 1 mol% of acrylic acid component, and then 1601G
Two types of high-frequency adhesive cushioning materials were prepared by heating in a hot-air sintering furnace for 5 minutes to adhere powder to a urethane foam skeleton.

1つはウレタンフオームシートの表面から深さ約2Mま
で粉末を骨格に固着させたもの、他の1つは10mbの
厚さ方向に一様に粉末を骨格に固着させたものである。
One is one in which the powder is fixed to the skeleton from the surface of the urethane foam sheet to a depth of approximately 2M, and the other is one in which the powder is fixed to the skeleton uniformly in the thickness direction of 10 mb.

基装材層としてポリエステルトリコット(目伺量s s
、o y /m )、基材層として埋さ5駄のハードボ
ードを重ね合せて、一部を高周波接着して高周波接着体
を作成した。この部分的な高周波接着部の接着力を測定
した結果を表−2に示す。表−2に示すごとく本発明の
接着体の高周波接着力は実用的であり又風合も良いもの
てあった。
Polyester tricot (texture amount s s
, o y /m ), 5 pieces of buried hardboard were superimposed as a base material layer, and a portion was bonded using high frequency to create a high frequency bonded body. Table 2 shows the results of measuring the adhesive strength of this partial high-frequency bonded area. As shown in Table 2, the high frequency adhesive strength of the adhesive of the present invention was practical and the texture was also good.

表−2実施例−2 ※高周波接着性樹脂粉末の固着していないポリウレタン
フォーム部分で破壊した。
Table 2 Example 2 *The polyurethane foam portion to which the high-frequency adhesive resin powder was not adhered was destroyed.

実施例−3 表−3に示す塩化ビニル樹脂からなる16メツシユパス
の高周波接着性樹脂粉末を嵩密度169/lの埋さ3欺
のポリウレタンフォームシートに389/を含浸させた
後、160℃の熱風焼結炉にて2分間加熱し、ウレタン
フオーム骨格に粉末を固着させた高周波接着性クッショ
ン材を準備した。
Example 3 After impregnating a polyurethane foam sheet with a bulk density of 169/l and a depth of 389/l with 16 mesh passes of high-frequency adhesive resin powder made of vinyl chloride resin shown in Table 3, hot air at 160°C was applied. A high-frequency adhesive cushioning material was prepared by heating in a sintering furnace for 2 minutes to adhere powder to a urethane foam skeleton.

表装相層としてポリエステルトリコット(目付量sso
g/m)、基材層として厚さ5肱のノ・−トポードを用
い、その間に高周波接着性クッション材を東ね合せて、
一部を〆i周波接着して、高周波接着体を作成した。こ
の部分的な高周波接着体の接着力を測定した結果を表−
3に示す。表−3に示す如く、本発明の接着体の高周波
接着力は実用的であり、風合の良いものであった。
Polyester tricot (basis weight sso
g/m), using a 5-elm thick notebook as the base material layer, and placing a high-frequency adhesive cushioning material between them,
A portion was subjected to i-frequency bonding to create a high-frequency bonded body. The results of measuring the adhesive strength of this partial high-frequency adhesive are shown below.
Shown in 3. As shown in Table 3, the high-frequency adhesive strength of the adhesive body of the present invention was practical and had a good texture.

比較のために、スミエリート1100(住友化学裂)の
塩化ビニル糸ラテックスをウレタンフオームに含浸させ
160℃5分乾燥させ、商周波接櫂成分として389/
を含有する高周波接着体クッション材を実施例−3と同
じ構成にして高周波接着体とした。この接着体の高周波
接着力は15に9/ 2. s cmであり、風合はき
わめて硬いものであった0 比較のため塩化ビニル単独重合体を固着させたものの高
周波接着力を測定した所、0.1 K9/ 2.5cm
であり実用的とは云い難い。
For comparison, urethane foam was impregnated with vinyl chloride yarn latex of Sumielite 1100 (Sumitomo Kagaku Kaisha), dried at 160°C for 5 minutes, and 389/
A high-frequency adhesive cushioning material containing the same composition as in Example-3 was used as a high-frequency adhesive. The high frequency adhesive strength of this adhesive is 15 to 9/2. s cm, and the texture was extremely hard.0 For comparison, we measured the high-frequency adhesive strength of a material to which vinyl chloride homopolymer was fixed, and found that it was 0.1 K9/2.5 cm.
Therefore, it is difficult to say that it is practical.

表−3(実施例−3) スミエリートは市販品を凍結乾燥し、微粉末状となして
ポリウレタンフォームに含浸させた。
Table 3 (Example 3) Sumielite was a commercially available product that was freeze-dried and made into a fine powder, which was then impregnated into polyurethane foam.

実施例−4 表−4に示すポリアミド樹脂からなる42メツシユパス
170メツシユオンの高周波接着性樹脂粉末を嵩密度1
69 / /−の埋さ3taのポリウレタンフォームシ
ートに38グ/を含浸させた後、1 s o ’cの高
周波焼結炉にて2分間加熱しウレタンフオーム骨格に粉
末を固着させた高周波接着性クッション材を準備した。
Example 4 A high-frequency adhesive resin powder of 42 mesh passes and 170 meshes made of the polyamide resin shown in Table 4 was prepared with a bulk density of 1.
High frequency adhesive property in which a 3 ta polyurethane foam sheet of 69//- was impregnated with 38 g/, and then heated for 2 minutes in a 1 s o 'c high frequency sintering furnace to fix the powder to the urethane foam skeleton. Prepared cushioning material.

実施例−2と同じ構成の高周波接着体として、部分的に
高周波接着した部分の接着力を測定した結果を表−4に
示す。表−4に示すごとく本発明の接着体の高周波(に
百方(・ま実用口′Jてあり、風合も良いものであった
Table 4 shows the results of measuring the adhesive strength of the partially high-frequency bonded portion of the high-frequency bonded body having the same configuration as Example-2. As shown in Table 4, the adhesive of the present invention was highly resistant to high frequencies and had a good texture.

比較例として、融点45℃のポリアミド樹脂(トーマイ
ド≠210)及び融点217’Cのナイロン6.9(旭
化成)を高周波接着性樹脂粉末として実施例−4と同一
条件で高周波接着体を作成した0 局部の高周波接着力を測定した所、ナイロン6.9のも
のは接着力はなく、融点45℃のポリアミド樹脂のもの
は融点が低すぎて骨格にうまく固着しなく風合も硬いも
のであった。
As a comparative example, a high-frequency bonded body was created under the same conditions as Example 4 using high-frequency adhesive resin powder of polyamide resin (Tomide≠210) with a melting point of 45°C and nylon 6.9 (Asahi Kasei) with a melting point of 217'C. When we measured local high-frequency adhesive strength, we found that the nylon 6.9 adhesive had no adhesive strength, and the polyamide resin adhesive with a melting point of 45°C had a melting point too low to adhere well to the skeleton and had a hard texture. .

表−4 実施例−5 実施例−1に用いたと同一の高周波接着性樹脂粉末を嵩
密度20W/Qの厚さ10Mの綿集合体(第7図)と嵩
密度2505/−/Qの厚さ5語の天然パルプ集合体(
第9図)にそれぞれ10g−/ρ、1305’/fi含
浸させた後、180oCの熱風式加熱炉にて2分間焼結
させ、綿繊維、天然パルプ繊維骨格に第8図、第10図
に示すように固着した高周波接着性クッション材を準備
した。
Table 4 Example 5 The same high-frequency adhesive resin powder used in Example 1 was mixed with a 10M thick cotton aggregate (Figure 7) with a bulk density of 20W/Q and a thickness of 2505/-/Q with a bulk density of 2505/-/Q. Natural pulp aggregate with five words (
Figure 9) was impregnated with 10g-/ρ and 1305'/fi, respectively, and sintered for 2 minutes in a hot air heating furnace at 180oC to form cotton fibers and natural pulp fiber skeletons as shown in Figures 8 and 10. A fixed high frequency adhesive cushioning material was prepared as shown.

表装材層として目付fit 350 f 7m2モケツ
トタイプのポリエステル7′アブリツク、基材として5
賜厚の合板を用い、その間に高周波接着性クッション材
層を重ね合わせて、一部分を高周波接着し、高周波接着
体を作成した。この部分的に高周波接着させた部分の接
着力を測定した結果を表−5に示す。
Fabric weight: fit 350 f 7 m2 moquette type polyester 7' abric as surface material layer, 5 as base material
A high-frequency bonded body was created by using thick plywood, overlapping a high-frequency adhesive cushioning material layer between them, and bonding a portion using high-frequency waves. Table 5 shows the results of measuring the adhesive strength of this partially high-frequency bonded portion.

表−5に示す如く、本発明の接着体の高周波接着力は実
用的であり、かつ適当な吸湿性があり、静電気の発生の
少ないものであった。
As shown in Table 5, the adhesive body of the present invention had a practical high-frequency adhesive strength, had appropriate hygroscopicity, and generated little static electricity.

表づ 以上まとめて本発明の利点を述べると ■ 低出力の高周波接着機にて、高速度で接着てき、A
い高周波接着力を有する接右体である。
In summary, the advantages of the present invention can be summarized as follows: ■ It can be bonded at high speed using a low-output high-frequency bonding machine, and A
It is a tangential body with strong high-frequency adhesive strength.

■ スパークしない高周波接着体である。■ It is a high frequency adhesive that does not cause sparks.

■ 高周波接着性フィルムが不用である。■ High frequency adhesive film is not required.

■ 部品数が少ないので、組立、接呑工程が合理化でき
る。
■ As the number of parts is small, assembly and assembling processes can be streamlined.

■ 部品数が少ないので、ロスの発生が少なくなり安価
な高周波接着体である。
■ Since there are fewer parts, there is less loss and it is an inexpensive high-frequency adhesive.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は塩ビレザーを表装材層に用いた高周波接着体の
一実施例を示す概略斜視図、第2図は第1図の接着体の
高周波接着部におけるA−A’断面図、第3図はファブ
リックを表装材層に用いた高周波接着体の一実施例を示
す斜視図、第4図は第6図の接着体の高周波接着体の高
周波接着部におけるB −B’断面図である。第5図は
高周波接着性クッション材の骨格部としてのウレタンフ
オームの骨格構造を示す電子顕微鏡写真、第6図はウレ
タンフオーム骨格に粉末接着剤が固着した高周波接着性
クッション材の構造を示す電子顕微鏡写真、第7図は編
集合体の微細構造を示す電子顕微鏡写真、第8図は綿集
合体骨格に粉末接着剤が固着した高周波接着性クッショ
ン材の微細構造を示す電子顕微鏡写真、第9図は天然ノ
くルプ繊維集合体の微細構造を示す電子顕微鏡写真、第
10図は天然パルプ繊維骨格に粉末接着剤が固着した高
周波接着性クッション材の微細構造を示す電子顕微鏡写
真である。 1・・・高周波接着部   2・・・表装材層6・・・
高周波接着性クッション材 4・・・基材層 出願人 旭化成工業株式会社 代理人 豊  1) 善 雄 第1図 1 第2図 第3図 ! 第4図 第5図 (ooP雀 第6図 100 F気 第7図 10(f= 第9図 ooPqn 第10図 100P荒 手  続  補  正  書 昭和57年12月23日 特許庁長官 若 杉 和 夫 殿 1 事件の表示 特願昭57−201033号 2 発明の名称 高周波接着体 3、補正をする者 事件との関係・特許出願人 大阪府大阪市北区堂島浜1丁目2番6号(003)旭化
成工業株式会社 代表取締役社長 宮 崎   輝 1代理人 東京都千代田区有楽町1丁目4番1号 三伯ビル 204号室電話501−21385、補正の
対象 6 補正の内容 (1)  明細書の特許請求の範囲を別紙の通り訂正す
る。 (2)  明細書第4貞15行目〜16行目の「ウレタ
ンフオーム骨格高周波接着性粉末を」を[ウレタンフオ
ーム骨格に高周波接着性粉末・を°]と訂正する。 (3)同第7頁・7行目〜8行目の「塩化ビニリデン樹
脂、塩化ビニル樹脂」を「塩化ビニリデン共重合体樹脂
、塩1ヒビニル共重合体樹脂」とn’J圧する。 (4)同第10頁19行目〜20行目の「塩化ビニル樹
脂として」を1塩化ビニル共重合体樹脂として」と訂正
する。 (5)同第12頁18行目〜19行目の[二押以上を交
編してなる」を「二種以上を交編または交織してなる」
と訂正する。 特許請求の範囲 (1)  高周波接合体において、順次基材層、高周波
接着性クッション材層、表装材層からなり、一部が1所
周波接着されてなることを特徴とする高周波接着体。 (2)  基材層がハードボード、樹脂板、合板、金属
板から選ばれた基材である特許請求の範囲第1項記載の
高周波接着体。 (3)  高周波接着性クッション材層がポリウレタン
フォーム骨格に高周波接着性樹脂粉末が粒子状に固着し
てなるクッション材である特許請求の範囲第1項記載の
高周波接着体。 (4)  表装材層がファブリック、天然皮革あるいは
合成皮革から選ばれた表装材である特許、i1求の範囲
第1項記載の高周波接着体。 (5)  高周波接着性樹脂粉末が塩化ビニリデン共重
■樹脂、塩化ビニル共重合体樹脂および/あるいはポリ
アシド樹脂から選ばれてなる粉末である特許請求の範囲
第3JJ記載の高周波接着体。 (6)該粉末が該フオーム骨格に59/を以上、180
グ/を以下固着してなるクッション材である特許請求の
範囲第1項、第2項または第3」↓1記載の高周波接着
体。
Fig. 1 is a schematic perspective view showing an embodiment of a high-frequency bonded body using PVC leather as the covering material layer; The figure is a perspective view showing an embodiment of a high-frequency bonded body using fabric as the covering material layer, and FIG. 4 is a sectional view taken along line BB' at the high-frequency bonded portion of the high-frequency bonded body of FIG. 6. Figure 5 is an electron micrograph showing the skeletal structure of urethane foam as the skeleton of a high-frequency adhesive cushioning material, and Figure 6 is an electron micrograph showing the structure of a high-frequency adhesive cushioning material in which powder adhesive is adhered to the urethane foam skeleton. Figure 7 is an electron micrograph showing the fine structure of edited coalescence, Figure 8 is an electron microscope photograph showing the fine structure of high-frequency adhesive cushioning material in which powder adhesive is adhered to the cotton aggregate skeleton, and Figure 9 is an electron microscope photograph showing the fine structure of the edited coalescence. FIG. 10 is an electron micrograph showing the microstructure of a natural pulp fiber aggregate. FIG. 10 is an electron micrograph showing the microstructure of a high-frequency adhesive cushioning material in which a powder adhesive is adhered to a natural pulp fiber skeleton. 1... High frequency adhesive part 2... Covering material layer 6...
High-frequency adhesive cushioning material 4...Base material layer Applicant: Asahi Kasei Corporation Agent Yutaka 1) Yoshio Figure 1 Figure 2 Figure 3! Figure 4 Figure 5 (ooP qn Figure 6 100 Fki Figure 7 10 (f = Figure 9 ooPqn Figure 10 100P Continued amendments Written by: December 23, 1981 Mr. Kazuo Wakasugi, Commissioner of the Patent Office) 1 Indication of the case Japanese Patent Application No. 57-201033 2 Name of the invention High-frequency adhesive 3. Person making the amendment Relationship to the case Patent applicant Asahi Kasei Kogyo 1-2-6 Dojimahama, Kita-ku, Osaka-shi, Osaka (003) Representative Director and President of Co., Ltd. Teru Miyazaki 1 Agent Room 204, Sanpaku Building, 1-4-1 Yurakucho, Chiyoda-ku, Tokyo Telephone: 501-21385 Subject of Amendment 6 Contents of Amendment (1) Scope of Claims in the Specification The correction is made as shown in the attached sheet. (2) "Urethane foam skeleton high-frequency adhesive powder" in lines 15 and 16 of No. 4 of the specification is corrected to "Urethane foam skeleton high-frequency adhesive powder." (3) Press "vinylidene chloride resin, vinyl chloride resin" on page 7, lines 7 to 8 with "vinylidene chloride copolymer resin, salt 1 vinyl copolymer resin" by n'J pressure. (4 ) On page 10, lines 19 to 20, "as vinyl chloride resin" is corrected to "as vinyl monochloride copolymer resin." (5) On page 12, lines 18 to 19, [2] "Made by inter-knitting or interweaving two or more types"
I am corrected. Claims (1) A high-frequency bonded body comprising a base material layer, a high-frequency adhesive cushioning material layer, and a facing material layer in this order, and a portion thereof is frequency-bonded at one location. (2) The high-frequency adhesive body according to claim 1, wherein the base material layer is a base material selected from hardboard, resin board, plywood, and metal plate. (3) The high-frequency adhesive body according to claim 1, wherein the high-frequency adhesive cushioning material layer is a cushioning material in which high-frequency adhesive resin powder is adhered in the form of particles to a polyurethane foam skeleton. (4) The high-frequency adhesive body according to item 1 of the patent application, wherein the facing material layer is a facing material selected from fabric, natural leather, or synthetic leather. (5) The high-frequency adhesive body according to claim 3JJ, wherein the high-frequency adhesive resin powder is a powder selected from vinylidene chloride copolymer resin, vinyl chloride copolymer resin, and/or polyacid resin. (6) the powder has a content of 59% or more to the foam skeleton, 180% or more;
1. The high-frequency adhesive according to claim 1, 2 or 3, which is a cushioning material formed by adhering adhesive.

Claims (1)

【特許請求の範囲】 (1)  高周波接合体において、順次基材層、高周波
接肴性クッション材層1表装材層からなり。 一部が筒周波接着されてなることを特徴とする高周波接
着体。 (2)基祠鳩がハードボード、樹脂板、合板、貧属根か
ら選ばれた基材である特許請求の範囲第1項記載の高周
波接着体。 (3:  高周波接着性クッション材層がポリウレタン
フォルム骨格に高周波接着性樹脂粉末が粒子状に同右し
てなるクッション材である特許請求の範囲第1項記載の
高周波接着体。 (4)  表装材層がファブリック、天然皮革あるいは
合成皮革から選ばれた表装材である特許請求の範囲第1
項記載の高周波接着体。 (5)高周波接着性樹脂粉末が塩化ビニリデン樹脂、塩
化ビニル兵事合体樹脂および/あるいはポリアミド樹脂
から選ばれてなる粉末である特許請求の41[!囲第3
項記載の高周波接着体。 (6)該粉末が該フオーム骨格番こ5fl/を以上、1
809/を以下lI!11gシてなるクッション材であ
る特許請求の範囲第1Jg、第2項または第3項記載の
高周波接着体。
[Scope of Claims] (1) A high-frequency bonded body comprising, in order, a base material layer, a high-frequency applicability cushioning material layer, and a surface material layer. A high-frequency bonded body characterized by being partially bonded by cylindrical frequency bonding. (2) The high-frequency adhesive body according to claim 1, wherein the base material is a base material selected from hardboard, resin board, plywood, and plywood. (3: The high-frequency adhesive body according to claim 1, wherein the high-frequency adhesive cushioning material layer is a cushioning material made of a polyurethane foam skeleton and high-frequency adhesive resin powder in the form of particles. (4) Facing material layer Claim 1 is a covering material selected from fabric, natural leather, or synthetic leather.
High frequency adhesive body as described in section. (5) The high-frequency adhesive resin powder is a powder selected from vinylidene chloride resin, vinyl chloride military composite resin, and/or polyamide resin, according to claim 41 [! Encircle 3
High frequency adhesive body as described in section. (6) The powder contains the foam skeleton 5 fl/ or more, 1
809/ below! The high-frequency adhesive according to claim 1, claim 2, or claim 3, which is a cushioning material made of 11g sheet.
JP57201033A 1982-11-18 1982-11-18 High-frequency adhesive body Pending JPS5991052A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57201033A JPS5991052A (en) 1982-11-18 1982-11-18 High-frequency adhesive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57201033A JPS5991052A (en) 1982-11-18 1982-11-18 High-frequency adhesive body

Publications (1)

Publication Number Publication Date
JPS5991052A true JPS5991052A (en) 1984-05-25

Family

ID=16434322

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57201033A Pending JPS5991052A (en) 1982-11-18 1982-11-18 High-frequency adhesive body

Country Status (1)

Country Link
JP (1) JPS5991052A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS617901A (en) * 1984-06-22 1986-01-14 Mitsubishi Electric Corp Digital control device
JPH0274254A (en) * 1988-09-08 1990-03-14 Uni Charm Corp Absorbing body for absorbable article and preparation thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5076181A (en) * 1973-10-09 1975-06-21
JPS5285274A (en) * 1976-01-08 1977-07-15 Toagosei Chem Ind Co Ltd Production of laminates for interior decoration

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5076181A (en) * 1973-10-09 1975-06-21
JPS5285274A (en) * 1976-01-08 1977-07-15 Toagosei Chem Ind Co Ltd Production of laminates for interior decoration

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS617901A (en) * 1984-06-22 1986-01-14 Mitsubishi Electric Corp Digital control device
JPH0274254A (en) * 1988-09-08 1990-03-14 Uni Charm Corp Absorbing body for absorbable article and preparation thereof
JPH0638814B2 (en) * 1988-09-08 1994-05-25 ユニ・チャーム株式会社 Absorbent body for absorbent article and manufacturing method thereof

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