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JPS5910902B2 - Elastomeric cushion devices for products and objects - Google Patents

Elastomeric cushion devices for products and objects

Info

Publication number
JPS5910902B2
JPS5910902B2 JP53127795A JP12779578A JPS5910902B2 JP S5910902 B2 JPS5910902 B2 JP S5910902B2 JP 53127795 A JP53127795 A JP 53127795A JP 12779578 A JP12779578 A JP 12779578A JP S5910902 B2 JPS5910902 B2 JP S5910902B2
Authority
JP
Japan
Prior art keywords
chamber
elastomeric
objects
rubber
articles
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.)
Expired
Application number
JP53127795A
Other languages
Japanese (ja)
Other versions
JPS54116063A (en
Inventor
マリオン・エフ・ルデイ
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of JPS54116063A publication Critical patent/JPS54116063A/en
Publication of JPS5910902B2 publication Critical patent/JPS5910902B2/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D22/00Producing hollow articles
    • B29D22/02Inflatable articles
    • 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
    • B29C66/40General 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
    • B29C66/439Joining sheets for making inflated articles without using a mould
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/02Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents specially adapted to protect contents from mechanical damage
    • B65D81/03Wrappers or envelopes with shock-absorbing properties, e.g. bubble films
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D2400/00Functions or special features of garments
    • A41D2400/10Heat retention or warming
    • A41D2400/14Heat retention or warming inflatable
    • 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
    • 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
    • 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
    • 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
    • B29K2007/00Use of natural rubber as moulding material
    • 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
    • B29K2009/00Use of rubber derived from conjugated dienes, as moulding material
    • 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
    • B29K2009/00Use of rubber derived from conjugated dienes, as moulding material
    • B29K2009/06SB polymers, i.e. butadiene-styrene polymers
    • 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
    • B29K2011/00Use of rubber derived from chloroprene as moulding material
    • 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
    • B29K2019/00Use of rubber not provided for in a single one of main groups B29K2007/00 - B29K2011/00, as moulding material
    • 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
    • B29K2021/00Use of unspecified rubbers as moulding material
    • 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • B29K2023/0608PE, i.e. polyethylene characterised by its density
    • B29K2023/0633LDPE, i.e. low density polyethylene
    • 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene
    • 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/18Polymers of hydrocarbons having four or more carbon atoms, e.g. polymers of butylene, e.g. PB, i.e. polybutylene
    • B29K2023/22Copolymers of isobutene, e.g. butyl rubber
    • 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
    • B29K2027/00Use of polyvinylhalogenides or derivatives thereof as moulding material
    • 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
    • B29K2027/00Use of polyvinylhalogenides or derivatives thereof as moulding material
    • B29K2027/06PVC, i.e. polyvinylchloride
    • 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
    • B29K2027/00Use of polyvinylhalogenides or derivatives thereof as moulding material
    • B29K2027/12Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
    • B29K2027/14PVF, i.e. polyvinyl fluoride
    • 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
    • B29K2031/00Use of polyvinylesters or derivatives thereof as moulding material
    • B29K2031/04Polymers of vinyl acetate, e.g. PVAc, i.e. polyvinyl acetate
    • 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
    • B29K2033/00Use of polymers of unsaturated acids or derivatives thereof as moulding material
    • B29K2033/18Polymers of nitriles
    • B29K2033/20PAN, i.e. polyacrylonitrile
    • 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
    • B29K2067/00Use of polyesters or derivatives thereof, as moulding material
    • 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
    • B29K2075/00Use of PU, i.e. polyureas or polyurethanes or derivatives thereof, as moulding material
    • 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
    • B29K2081/00Use of polymers having sulfur, with or without nitrogen, oxygen or carbon only, in the main chain, as moulding material
    • 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
    • B29K2081/00Use of polymers having sulfur, with or without nitrogen, oxygen or carbon only, in the main chain, as moulding material
    • B29K2081/04Polysulfides, e.g. PPS, i.e. polyphenylene sulfide or derivatives thereof
    • 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
    • B29K2083/00Use of polymers having silicon, with or without sulfur, nitrogen, oxygen, or carbon only, in the main chain, as moulding material
    • 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
    • B29K2105/0085Copolymers
    • 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
    • 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0046Elastic
    • 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0065Permeability to gases
    • 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0065Permeability to gases
    • B29K2995/0067Permeability to gases non-permeable
    • 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
    • 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
    • B29L2022/00Hollow articles
    • B29L2022/02Inflatable articles
    • 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
    • B29L2031/00Other particular articles
    • B29L2031/712Containers; Packaging elements or accessories, Packages
    • B29L2031/7138Shock absorbing

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Buffer Packaging (AREA)
  • Vibration Dampers (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Description

【発明の詳細な説明】 本発明は、製品または物体を保護するデバイスに関し、
さらに詳述すれば、ガス媒質で充填された柔軟性チヤン
バを有しかつ物体や製品を損傷しないように保護するク
ツシヨン デバイスに係るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a device for protecting products or objects;
More particularly, the invention relates to a cushion device having a flexible chamber filled with a gaseous medium and protecting objects or products from damage.

従来、包装用材料は取扱いおよび出荷中製品にクツシヨ
ン保護を与えるためにプラスチツクシート間に空気含有
チャンバを熱封入することによつて作られてきた。
Traditionally, packaging materials have been made by heat-sealing air-containing chambers between sheets of plastic to provide cushioning protection to the product during handling and shipping.

チャンバは分離され、通常円筒形または球形であり、大
気圧の空気を含有する。シートは通常非エラストマ性で
あり、数個のフイルム層のラミネーシヨンから構成され
、1つ以上の層がバリヤ材料(たとえばPVDCサラン
)であり、1つ以上の他の層が熱封着性である。薄い単
一層(積層しないもの)のエラストマフィルムは、多く
のガスに対して比較的高いガス拡散率を持つため、クツ
シヨン材料として実用的でないことが判明している。ガ
ス充填チヤンバは、チャンバ内のガスと周囲大気間に圧
力差が存在する場合には、非常に短い時間で平坦になる
。たとえば、チヤンバがフイルムを弾性的に膨張させて
形成された場合には、チヤンバは原体積の約50%を製
造時から1〜4週間で失ない、約6ケ月で本質的に平坦
になる。積層フイルムは端縁部のみが熱封着可能であり
、きわめて高価なフイルム以外は、比較的悪い物理的性
質を有する。多くのガスに対して低い拡散率を有するバ
リヤ フイルムは、外部荷重が長時間にわたつてかかる
ときまたは材料が高温にさらされるとき、チャンバから
空気が絞り出されないようにするために使用される。現
在の製品においては、チャンバは予成形され、ついで部
分的に膨張させられ、それにより内蔵ガスの膨張・収縮
を可能にする幾分しわのよつた非加圧チヤンバを形成し
、クツシヨン製品が過膨張や破裂を起こすことなく航空
機で輸送できるようにする。既知クツシヨン デバイス
の一タイプは米国特許第3589037号に開示されて
いる。薄い積層バリヤ形材料が現在のクツシヨン デバ
イスに使用されているから、各チヤンバ内の圧力が約3
〜4psig以上になるとクツシヨン材料は破裂する。
積層バリヤ材料は熱封着が困難であるから、シートを相
互に接合する溶接部が弱く、時効または温度により劣化
する。したがつて、従来のクツシヨン デバイスはその
支える定常状態の荷重が制限される。たとえば、1平方
フィート当り150ポンドの荷重が最高値としてしばし
ば規定される。さらに、従来のクツシヨン デバイスは
破裂や空気の損失を起こすことなく耐えうる動荷重(衝
撃荷重)が非常に制限される。その結果として、クツシ
ヨン デバイスの使用は計器、電子部品などのような軽
量製品のみの保護に通常限定される。包装分野以外の分
野、たとえば、弾性、衝撃吸収性の靴の中底、靴の発泡
バツドの代用としてのクツシヨン材料、競技用道具のパ
ツドなどに、従来のクツシヨン デバイスを使用する試
みが行なわれた。
The chamber is separate, usually cylindrical or spherical, and contains air at atmospheric pressure. The sheet is usually non-elastomeric and consists of a laminate of several film layers, one or more of which is a barrier material (e.g. PVDC saran) and one or more other layers which are heat sealable. be. Thin, single layer (non-laminated) elastomeric films have been found to be impractical as cushioning materials due to their relatively high gas diffusivities for many gases. A gas-filled chamber flattens out in a very short time if a pressure difference exists between the gas in the chamber and the surrounding atmosphere. For example, if the chamber is formed by elastically expanding a film, the chamber will lose approximately 50% of its original volume within one to four weeks from the time of manufacture and become essentially flat in approximately six months. Laminated films can be heat sealed only at the edges and have relatively poor physical properties in all but the most expensive films. Barrier films with low diffusivities for many gases are used to prevent air from being squeezed out of the chamber when external loads are applied over long periods of time or when the material is exposed to high temperatures. In current products, the chamber is preformed and then partially inflated, thereby forming a somewhat wrinkled, non-pressurized chamber that allows the gas contained therein to expand and contract, causing the cushion product to overheat. Enables transportation by aircraft without swelling or rupturing. One type of known cushion device is disclosed in US Pat. No. 3,589,037. Because thin, laminated barrier-type materials are used in current cushion devices, the pressure in each chamber is approximately 3
Above ~4 psig, the cushion material will burst.
Laminated barrier materials are difficult to heat seal, so the welds that join the sheets together are weak and degrade with age or temperature. Therefore, conventional cushion devices are limited in the steady state loads they can support. For example, a load of 150 pounds per square foot is often specified as a maximum. Furthermore, conventional cushioning devices are very limited in the dynamic loads (shock loads) they can withstand without rupture or loss of air. As a result, the use of cushioning devices is typically limited to protecting only lightweight products such as instruments, electronic components, and the like. Attempts have been made to use conventional cushioning devices in fields other than the packaging field, such as elastic, shock-absorbing shoe insoles, cushioning materials as a substitute for foam butts in shoes, padding for athletic equipment, etc. .

しかしながら、材料が脆弱であり、溶接部の強度が弱く
、かつ高度の変化によつて起こる大きな体積変化の基本
的問題のために、これらの試みは成功しなかつた。本発
明の一目的は、高強度、耐疲労性エラストマ材料から作
られ、高い構造強度および高い定常状態荷重ならびに大
きい衝撃荷重に耐える能力を有し、かつきびしいたわみ
と組合せられた極端なサイクル荷重の反復印加に対する
非常に良好な抵抗を有するところの、改良された、永久
的に膨張したクツシヨン デバイスを提供することであ
る。
However, these attempts were unsuccessful due to the fundamental problems of brittle materials, weak welds, and large volume changes caused by changes in altitude. It is an object of the present invention to be made from high strength, fatigue resistant elastomeric materials, have high structural strength and the ability to withstand high steady state loads as well as large impact loads, and withstand extreme cyclic loads combined with severe deflection. An object of the present invention is to provide an improved permanently inflated cushion device that has very good resistance to repeated applications.

本発明の別の目的は、ガスで膨張させられた複数の分離
チヤンバを有し、大気圧および温度の変化が、チャンバ
内のガス圧力を増加し、それらの体積の小変化を起こし
ても、各チャンバまたはセルを破裂させることがなく、
耐久性および信頼性が高くかつ長い耐用寿命を有すると
ころの、エラストマ クツシヨン デバイスを提供する
ことである。一般的面において、本発明に係るクツシヨ
ンデバイスは、連通または分離チヤンバを形成するため
に所望間隔で封着された一対のエラストマ性、透過性シ
ートを含み、チヤンバはガスまたはガス混合物で大気圧
または大気圧以上の圧力でありうる所定圧力まで部分的
または完全に充填または膨張される。
Another object of the invention is to have a plurality of separation chambers inflated with gas so that changes in atmospheric pressure and temperature can increase the gas pressure in the chambers and cause small changes in their volume. without rupturing each chamber or cell,
An object of the present invention is to provide an elastomeric friction device that is highly durable, reliable, and has a long service life. In general terms, the cushion device of the present invention includes a pair of elastomeric, permeable sheets sealed at a desired distance to form a communicating or separating chamber, the chamber being filled with a gas or gas mixture at atmospheric pressure. or partially or completely filled or inflated to a predetermined pressure, which may be greater than atmospheric pressure.

選択ガスまたはガス混合物はチヤンバの外部への透過性
シート中の拡散率が非常に低く、周囲空気はチャンバ内
部へのシート中の拡散率が比較的高く、チヤンバ内の空
気の分圧とガスまたはガス混合物の分圧の和から得られ
る、チャンバ内の全圧が増加する。チャンバ内に最初に
置かれたガスまたはガス混合物の圧力は、エラストマシ
ート中のこのようなガスまたはガス混合物の拡散により
、非常に緩慢な率で低下するが、周囲空気はより容易に
シートを通つてチャンバ内へ拡散し、その結果としてチ
ヤンバ内の全圧力がガスまたはガス混合物の初期膨張圧
力より高くなる。チヤンバ内のこの全圧力は長期間にわ
たつて減小しうるが、長時間ガスの初期膨張圧力より依
然として高く、その後の時間にわたつて圧力を非常にゆ
つくり失ない、この間クツシヨン デバイスはそのクツ
シヨンまたは衝撃吸収機能を依然として遂行する。クツ
シヨン デバイスはクツシヨン分野以外の用途を有する
The selected gas or gas mixture has a very low diffusivity through the permeable sheet to the outside of the chamber, and the ambient air has a relatively high diffusivity through the sheet to the inside of the chamber, so that the partial pressure of the air inside the chamber and the gas or The total pressure in the chamber, resulting from the sum of the partial pressures of the gas mixture, increases. The pressure of the gas or gas mixture initially placed in the chamber decreases at a very slow rate due to diffusion of such gas or gas mixture through the elastomer sheet, but the ambient air is more easily forced through the sheet. and diffuse into the chamber, resulting in a total pressure within the chamber greater than the initial expansion pressure of the gas or gas mixture. Although this total pressure within the chamber may decrease over time, it is still higher than the initial expansion pressure of the gas for an extended period of time and does not lose pressure very slowly over the following time, during which time the cushion device or still perform the shock absorption function. Cushion devices have applications outside of the cushion field.

このデバイスは競技用床マツトとして形成し、救命具、
振動工具用ハンドルグリツプ、および2個の剛性部材間
に配置される出荷用パレツトとして機能するように成形
することができる。本発明に係る他のデバイスは、永久
的に膨張した枕類および家具類の詰め物である発泡パツ
ドの代りに使用する永久膨張クツシヨンのような、間欠
的に荷重のかかるものである。
This device is configured as a competition floor mat and can be used as a life preserver,
It can be shaped to function as a handle grip for a vibrating tool and as a shipping pallet placed between two rigid members. Other devices according to the invention are those that are subject to intermittent loading, such as permanently expanded cushions for use in place of permanently expanded foam padding in pillows and furniture.

人がこのようなデバイス上にすわりまたにねると、チヤ
ンバ内の空気の一部はチヤンバから外方へ拡散するが、
荷重が除去されると、空気はチヤンバ内へ拡散して戻り
、チャンバを自動的に再膨張させて次の荷重サイクルを
適切に受ける状態に置く。クツシヨンデバイスの他の用
途については明細書の後部で説明する。本発明は、その
原理を具体化したいくつかの形態の考察からさらに明ら
かになる他の利点および目的を有する。
When a person sits or sleeps on such a device, some of the air within the chamber diffuses outward from the chamber;
When the load is removed, air diffuses back into the chamber, automatically re-inflating the chamber and positioning it to properly receive the next load cycle. Other uses of the cushion device are discussed later in the specification. The invention has other advantages and objects that become more apparent from a consideration of some embodiments of its principles.

これらの形態は本明細書および添付図面において図示記
載される。しかしながら、これらの形態は、本発明の一
般的原理の例示を目的としたものであり、制限的意味に
とられるべきでないことを理解すべきである。第1,2
図に示す本発明の形態においては、エラストマ材料の2
つのシート11,12から形成されたクツシヨン デバ
イス10のセグメントが示され、分離した球形チヤンバ
14を形成するために円形溶接部13を備え(たとえば
高周波熱封着技術により形成されたもの)、チャンバは
エラストマ シート材料を通る拡散率の低いガスで部分
的にまたは完全に膨張させられている。
These forms are illustrated and described herein and in the accompanying drawings. It should be understood, however, that these forms are intended to be illustrative of the general principles of the invention and are not to be taken in a limiting sense. 1st, 2nd
In the form of the invention shown in the figures, two parts of the elastomeric material are
A segment of the cushioning device 10 is shown formed from two sheets 11, 12 with circular welds 13 to form separate spherical chambers 14 (e.g. formed by high frequency heat sealing techniques), the chambers being Elastomeric sheet material that is partially or fully expanded with a gas that has a low diffusion rate through the material.

第2図に示す球形チヤンバはエラストマ材料の薄いシー
トを設け、比較的高い圧力に膨張させることによつて得
られる。第3図に示すものでは、より厚い、より高いモ
ジユラスのシートが使用され、第2図に示すチャンバと
実質的に同一の圧力に膨張させられると、楕円体形チヤ
ンバ14aを形成する。これらのチヤンバが第2図のチ
ヤンバに使用した圧力より低い圧力に膨張させられるな
らば、第2図のシートの場合にも楕円体形チヤンバが形
成されるであろう。第4,5図に示すように、エラスト
マ材料の2つのシート11a,12aは、チヤンバを相
互に離間しかつ各チヤンバを包囲する円形位置13aに
おいて溶接されている。
The spherical chamber shown in FIG. 2 is obtained by providing a thin sheet of elastomeric material and inflating it to a relatively high pressure. In the one shown in FIG. 3, a thicker, higher modulus sheet is used which, when inflated to substantially the same pressure as the chamber shown in FIG. 2, forms an ellipsoidal shaped chamber 14a. If these chambers were inflated to a pressure lower than that used for the FIG. 2 chamber, ellipsoidal shaped chambers would also be formed in the case of the FIG. 2 sheet. As shown in FIGS. 4 and 5, two sheets of elastomeric material 11a, 12a are welded at circular locations 13a that space the chambers from each other and surround each chamber.

第4,5図の製品を作る一方法においては、上部シート
11aが溶接前に最初に真空成形されてドーム端付円筒
形チヤンバ14bを形成する。真空がなお印加されてい
る間に、上部シートと下部シートが円形パターン13a
において溶接される。ついで所望ガスがチャンバに導入
されて第5図に示す円筒形チヤンバ14bを形成する。
第6,7図に示すクツシヨン デバイスにおいては、上
部シート11bと下部シート12bが正方形パターン1
3bにおいて溶接され、楕円体形チャンバ14cを形成
している。
In one method of making the product of Figures 4 and 5, the top sheet 11a is first vacuum formed to form a dome-ended cylindrical chamber 14b before welding. While the vacuum is still applied, the top and bottom sheets are shaped in a circular pattern 13a.
Welded at A desired gas is then introduced into the chamber to form the cylindrical chamber 14b shown in FIG.
In the cushion device shown in FIGS. 6 and 7, the upper sheet 11b and the lower sheet 12b are arranged in a square pattern 1.
3b to form an ellipsoidal chamber 14c.

溶接領域におけるこの正方形パターンは第1,2図の円
形パターンより小さい総合溶接区域を有し、より完全か
つ均一な空気支持表面を与える。第8,9,10図に示
すクツシヨン デバイスにおいては、溶接区域13cは
長方形パターンにおいて設けられている(第8図)。
This square pattern in the weld area has a smaller overall weld area than the circular pattern of FIGS. 1 and 2, providing a more complete and uniform air bearing surface. In the cushion devices shown in Figures 8, 9 and 10, the weld areas 13c are provided in a rectangular pattern (Figure 8).

加圧されると、各チヤンバ14dは細長くなり(第9図
)、円形断面を有する(第10図)。クツシヨン デバ
イスの形成に使用しうるエラストマ材料はある特性を持
つべきである。
When pressurized, each chamber 14d becomes elongated (Figure 9) and has a circular cross section (Figure 10). Elastomeric materials that can be used to form cushion devices should have certain properties.

第一の特性は種々の手段特に誘導加熱封着技術の使用に
よるすぐれた熱封着性である。これにより、シートを相
互に固着する高強度の完全な溶接区域が得られ、高い、
定常状態応力に耐えることができるとともに、きびしい
動荷重状態の下で起こる、長時間の周期的応力変動およ
び応力逆転にも耐えることができる。第二の特性は引張
強度、弾性係数、クリーブ等の適切な物理的性質に関す
るものである。第三の特性は選択された膨張ガス/蒸気
(以後「スーパガス」と称することもある)に対する非
常に低い透過性および空気(N2O2)に対するかなり
高い透過性である。クツシヨン デバイスにおける別の
重要な要因はシートまたはフイルムの膨張に使用される
特殊ガス/蒸気のグループである。
The first property is excellent heat sealability by various means, particularly the use of induction heat sealing techniques. This results in a high-strength, complete weld area that secures the sheets to each other, with high,
It is capable of withstanding steady-state stresses as well as long-term cyclic stress fluctuations and stress reversals that occur under severe dynamic loading conditions. The second property concerns appropriate physical properties such as tensile strength, modulus of elasticity, cleave, etc. The third property is a very low permeability to selected inflation gases/steams (hereinafter sometimes referred to as "supergases") and a fairly high permeability to air (N2O2). Another important factor in cushioning devices is the group of special gases/steams used to expand the sheet or film.

これらのガス/蒸気は、非常に大きい分子および非常に
低い溶解度係数を持つものであるから、特殊エラストマ
材料中のきわめて低い拡散率を示すクラスに属するもの
である。ガスは不活性であり、非極性であり、均等/対
称の、球形、楕円体形(扁平(0b1ate)または扁
長(PrOlate))の分子形状または対称分岐分子
形状を持つものである。これらのガスは無毒性であり、
非可燃性であり、金属に対して非腐食性である。それら
はすぐれた誘電性ガスおよび液体であり、高レベルの電
子付着および捕獲能力を有し、すべてのポリマ、エラス
トマおよびプラスチツク(ソリツド フイルム)中の著
しく低減した拡散率を示す。これらの特殊エラストマ材
料から作られたチヤンバを膨張させるために特殊ガスが
使用されるときには、クツシヨン デバイスは非常に長
い時間にわたつて初期膨張圧力を維持することができ、
圧力損はほとんど起こらない。
These gases/vapors are of a class that exhibits very low diffusivity in special elastomeric materials because they have very large molecules and very low solubility coefficients. The gas is inert, non-polar, and has a uniform/symmetrical, spherical, ellipsoidal (oblate or prolate) molecular shape or symmetrical branched molecular shape. These gases are non-toxic and
Non-flammable and non-corrosive to metals. They are excellent dielectric gases and liquids, have high levels of electron attachment and capture ability, and exhibit significantly reduced diffusivity in all polymers, elastomers and plastics (solid films). When special gases are used to inflate chambers made from these special elastomeric materials, the cushion device can maintain the initial inflation pressure for a very long time;
Almost no pressure loss occurs.

これは「永久」膨張と称される。永久膨張は2つの重要
な要因の組合せ、すなわち、(1)スーパガスのきわめ
て低い透過性と、(2圧自己加圧」現象との組合せの結
果である。多くのテストが5年間にわたつて行なわれ、
これにより典型的なエラストマ フイルム中のスーパガ
スの拡散率はきわめて低いことが確認された。
This is called "permanent" expansion. Permanent expansion is the result of a combination of two important factors: (1) the extremely low permeability of the supergas and the phenomenon of "two-pressure self-pressurization." Many tests were carried out over a five-year period. Re,
This confirmed that the diffusion rate of supergas in typical elastomer films is extremely low.

テストしたスーパガスの大部分は次の物質からなるグル
ープからのガス/蒸気であつた。すなわち、ヘキサフル
オルエタン、六フツ化硫黄、ペルフルォルプロパン、ペ
ルフルオルブタン ペルフルオルペンタン、ペルフルオ
ルヘキサン、ペルフルオルヘプタン、オクタフルオルシ
クロブタン、ペルフルオルシクロブタン、ヘキサフルオ
ルプロピレン、テトラフルオルメタン、モノクロロペン
タフルオルエタン、1・2−ジクロロテトラフルオルエ
タン、1・1・2−トリクロロ−1・2・2一トリフル
オルエタン、クロロトリフルオルエチレン、ブロモトリ
フルオルメタン、モノクロロトリフルオルメタン、モノ
クロロジフルオルメタン。好適なガス/蒸気はヘキサフ
ルオルエタンおよび六フツ化硫黄である。テストした典
型的なシートまたはフイルムの大部分は次の材料からな
るグループからのものであつた。
Most of the supergases tested were gases/vapors from the group consisting of: Namely, hexafluoroethane, sulfur hexafluoride, perfluoropropane, perfluorobutane, perfluoropentane, perfluorohexane, perfluoroheptane, octafluorocyclobutane, perfluorocyclobutane, hexafluoropropylene. , tetrafluoromethane, monochloropentafluoroethane, 1,2-dichlorotetrafluoroethane, 1,1,2-trichloro-1,2,2-trifluoroethane, chlorotrifluoroethylene, bromotrifluoromethane, Monochlorotrifluoromethane, monochlorodifluoromethane. Preferred gases/vapors are hexafluoroethane and sulfur hexafluoride. Most of the typical sheets or films tested were from the following group of materials:

すなわち、ポリウレタン、ポリエステルエラストマ、フ
ルオル エラストマ、塩素化ポリエチレン、ポリ塩化ビ
ニル、クロロスルホン化ポリエチレン、ポリエチレン/
酢酸エチレンビニルコポリマ、ネオプレン、ブタジエン
アクリロニトリル ゴム、ブタジエン スチレン ゴ
ム、エチレン プロピレン ポリマ、天然ゴム、高カシ
ノリコーン ゴム、低密度ポリエチレン、アダクトゴム
、サルフアイド ゴム、メチル ゴム、ブチル ゴム、
熱可塑性ゴム。
Namely, polyurethane, polyester elastomer, fluoroelastomer, chlorinated polyethylene, polyvinyl chloride, chlorosulfonated polyethylene, polyethylene/
Ethylene Vinyl Acetate Copolymer, Neoprene, Butadiene Acrylonitrile Rubber, Butadiene Styrene Rubber, Ethylene Propylene Polymer, Natural Rubber, High Cassinoricone Rubber, Low Density Polyethylene, Adduct Rubber, Sulfide Rubber, Methyl Rubber, Butyl Rubber,
thermoplastic rubber.

ポリウレタンは好適な材料である。大部分のテストはス
ーパガスの拡散速度を加速してテストを保存性にするた
めに比較的高い圧力(20psig)で行なわれた。
Polyurethane is a preferred material. Most tests were conducted at relatively high pressure (20 psig) to accelerate the diffusion rate of the supergas and make the test preservative.

多くのテストにおいて、2年のテスト後、チャンバ内の
圧力はなお初期膨張圧力を超えた。すべてのテストにお
いて、圧力降下はきわめて緩慢であつた。1平方インチ
当り数オンスから数ポンドまでの比較的低い膨張圧力に
おいては、この時間は少なくとも5倍延長された(2年
から10年へ)。
In many tests, after two years of testing, the pressure within the chamber still exceeded the initial inflation pressure. In all tests the pressure drop was very slow. At relatively low expansion pressures, from a few ounces to a few pounds per square inch, this time was extended at least five times (from two years to ten years).

さらに、すべてのテストにおいて、圧力は最初の2〜4
ケ月テスト中初期膨張圧力より実際にかなり上昇した。
「自己加圧」と称されるのはこの圧力上昇現象である。
自己加圧は、スーパガスの圧力に対する抵抗に関する特
殊フイルムまたはシートの透過性が低いことと、空気の
通過に対する特殊フイルムまたはシートの透過性がはる
かに高いこととが結合された結果である。膨張チャンバ
を包囲する大気環境中の空気は、チヤンバ内部の空気の
分圧がチヤンバ外部の分圧(すなわち14.7psia
)に等しくなるまでチャンバ内へ拡散する。各チヤンバ
内の全圧力は空気の分圧とスーパガスの分圧の和である
。空気が流入しつつある間スーパガスは流出しないから
、エラストマ材料の1つから作られた定積チヤンバ内に
約14.7psiの圧力上昇が可能である。第11図は
本発明のパツケージまたはクツシヨン デバイスの典型
的なエラストマ チヤンバ内の圧力上昇を示すグラフで
あつて、チヤンバは最初にフレオン116のようなスー
パガスの1種で1.0psigまで加圧された。図示の
ように、圧力は6週間後1.0psigから6.5p8
1gまで上昇した(曲線1)。テスト中チヤンバが伸張
し、その体積が約40%増加したけれども、これは65
0%の圧力上昇である。体積が一定に維持されたならば
、この特定スーパガスの場合には、曲線2に示すように
、全圧力は15.2psigまで上昇したであろう。
Furthermore, in all tests the pressure was
During the month test, the initial inflation pressure actually increased considerably.
It is this pressure increase phenomenon that is referred to as "self-pressurization."
Self-pressurization is the result of the combination of the lower permeability of the special film or sheet with respect to resistance to the pressure of the supergas and the much higher permeability of the special film or sheet with respect to the passage of air. The air in the atmospheric environment surrounding the expansion chamber is such that the partial pressure of the air inside the chamber is equal to the partial pressure outside the chamber (i.e., 14.7 psia).
) into the chamber. The total pressure in each chamber is the sum of the air partial pressure and the supergas partial pressure. Since supergas does not exit while air is flowing in, a pressure rise of approximately 14.7 psi is possible within the constant volume chamber made from one of the elastomeric materials. FIG. 11 is a graph showing the pressure build-up within a typical elastomeric chamber of a packaging or cushioning device of the present invention, where the chamber was initially pressurized to 1.0 psig with one of the supergases, such as Freon 116. . As shown, pressures range from 1.0 psig to 6.5 p8 after 6 weeks.
It increased to 1g (curve 1). Although the chamber was stretched during the test and its volume increased by approximately 40%, this was only 65
0% pressure increase. If the volume remained constant, the total pressure would have increased to 15.2 psig for this particular supergas, as shown in curve 2.

クツシヨン デバイスがパツケージ材料として使用され
るときには、各加圧チヤンバは低圧、通常は2.0ps
ig以下で作用するように膨張させられる。したがつて
、自己加圧に起因する圧力増加を緩和することが必要で
ある。これは空気とスーパガスの混合物でチヤンバを膨
張させることによつて行なわれる。第12図の曲線1が
示すように、エラストマ チヤンバ内の25%スーパガ
スと75%空気の混合物は1.0から2.2゜への圧力
土昇を起こすにすぎない。25〜75%、50〜50%
および100〜0%のスーパガス一空気混合物を有する
定積チャンバ内の圧力上昇もまた第12図に示されてい
る。
When the cushion device is used as a packaging material, each pressurized chamber has a low pressure, typically 2.0 ps.
It is inflated to act below ig. Therefore, it is necessary to alleviate the pressure increase caused by self-pressurization. This is done by inflating the chamber with a mixture of air and supergas. As shown by curve 1 in FIG. 12, a mixture of 25% supergas and 75% air in the elastomer chamber causes only a pressure rise of 1.0 to 2.2 degrees. 25-75%, 50-50%
The pressure rise in a constant volume chamber with a 100-0% supergas-air mixture is also shown in FIG.

圧カチャンバが初期膨張において完全な体積まで膨張さ
せられておらず、膨張直後しわのよつた状態にある場合
には、圧力上昇がさらに低減される。
The pressure rise is further reduced if the pressure chamber is not expanded to its full volume during the initial expansion and is in a wrinkled state immediately after expansion.

自己加圧圧力上昇が起こると、チャンバの体積が拡張し
、スーパガスの圧力が降下する。このアプローチへのか
ぎはチャンバが完全に膨張した時点においてスーパガス
分圧が設計圧力に達するようにすることである。周囲空
気はエラストマフイルムを通過してチャンバに入り、そ
の内部の圧力を増加する。すなわち、空気の分圧がスー
パガスの分圧に加えられ、ゼロPsigより高い全圧を
生ずる。しかしながら、チャンバは最初にしわのよつた
状態にあるため、チャンバの体積は拡張し、この拡張は
チャンバの最終体積に達するまで自己加圧によつて続行
する。安定状態に達して内部圧力がたとえば1/2ps
igになるのには数週間を要する。安定状態に達するた
めの周囲空気の内方拡散は「エージング」と称される。
エージングが終ると、チャンバ内の圧力ぱ空気の大気圧
(14.7psia)とスーパガスの分圧の和になる。
When the self-pressurizing pressure rise occurs, the chamber volume expands and the supergas pressure drops. The key to this approach is to ensure that the supergas partial pressure reaches the design pressure when the chamber is fully expanded. Ambient air passes through the elastomeric film and enters the chamber, increasing the pressure inside it. That is, the partial pressure of air is added to the partial pressure of supergas to produce a total pressure greater than zero Psig. However, since the chamber is initially in a wrinkled state, the volume of the chamber expands and this expansion continues due to self-pressurization until the final volume of the chamber is reached. When a stable state is reached and the internal pressure is, for example, 1/2 ps
It takes several weeks to become ig. The inward diffusion of ambient air to reach a steady state is referred to as "aging."
After aging, the pressure in the chamber becomes the sum of the atmospheric pressure of the air (14.7 psia) and the partial pressure of the supergas.

チャンバ内のゲージ圧力を上昇させて0以上に維持する
のはスーパガスの分圧である。チヤンバ内にスーパガス
が存在しない場合には、チヤンバは100%の空気を含
み、デバイスは適正に機能しないであろう。使用中に荷
重がかかると、空気はチヤンバから絞り出され、他のパ
ッケージ材料の場合のようにバリヤ材料が使用されてい
ないから、クツシヨン デバイスは平坦になる。したが
つて、デバイスにその永久膨張特性を与えるものはスー
パガスであり、デバイスはその耐用寿命を通じて適正に
機能するために十分な量のスーパガスをガス混合物中に
含有しなければならない。したがつて、デバイス内の圧
力は大気圧より少なくともやや高くなければならず、特
定圧力は設計荷重条件に依存する。製造上の観点からは
、チヤンバを大気圧のガスで充填することが望ましい。
自己加圧現象があるので、これはなされうる。製造完了
後、自己加圧はエージング過程中圧力を大気圧より高い
レベルに自動的に上昇させる。前述したように、デバイ
スにその永久膨張特性を与えかつ圧力損をほとんど起こ
すことなくきわめて長い時間にわたつて重荷重下でデバ
イスを使用できるようにするのはデバイス内の比較的小
量のスーパガスである。最小量のスーパガスと最大量の
空気を使用することによりクツシヨン デバイスのコス
トが低減される。スーパガスの最適量はサイクルに依存
する。重荷重はより高い濃度のスーパガスを必要とする
。上述のことは、荷重がかかると、クツシヨンデバイス
が幾分圧縮され、スーパガスと空気の圧力が荷重を支え
るに十分な程度に上昇するという事実によつて説明でき
る。
It is the partial pressure of the supergas that raises the gauge pressure in the chamber and maintains it above zero. If there is no supergas in the chamber, the chamber will contain 100% air and the device will not function properly. When loaded during use, air is squeezed out of the chamber and the cushion device flattens because no barrier material is used as with other packaging materials. Therefore, it is the supergas that gives the device its permanent expansion properties, and the device must contain a sufficient amount of supergas in the gas mixture to function properly throughout its useful life. Therefore, the pressure within the device must be at least slightly higher than atmospheric pressure, with the specific pressure depending on the design loading conditions. From a manufacturing standpoint, it is desirable to fill the chamber with gas at atmospheric pressure.
This can be done because there is a self-pressurization phenomenon. After manufacturing is complete, self-pressurization automatically increases the pressure to a level above atmospheric pressure during the aging process. As previously mentioned, it is the relatively small amount of supergas within the device that gives the device its permanent expansion properties and allows it to be used under heavy loads for very long periods of time with little pressure loss. be. The cost of the cushion device is reduced by using a minimum amount of supergas and a maximum amount of air. The optimum amount of supergas is cycle dependent. Heavy loads require higher concentrations of supergas. The above can be explained by the fact that when a load is applied, the cushion device compresses somewhat and the pressure of the supergas and air increases enough to support the load.

空気の圧力は大気圧以上になつているから、空気は荷重
下でチャンバから徐々に拡散して出る。スーパガスは拡
散して出ない。荷重がかかつている限り、空気はチヤン
バから緩慢に拡散し続け、チヤンバは緩慢に圧縮さ,れ
て体積が小さくなり、それによりスーパガスの圧力が上
昇する。空気の分圧とスーパガスの分圧の和は荷重を支
えるに常に十分であり、空気圧が降下しかつスーパガス
圧が上昇するのである。荷重が連続的に長時間かかる場
合には(たとえば、通常の荷重で3〜4ケ月)、空気の
分圧が最低値すなわち14.7psia(大気圧)に低
減された最終状態に到達する。このときスーパガス圧は
その最高値にある。拡散過程は安定化しており、ガスは
もはや拡散しない。荷重が除去されると、自己加圧現象
が再び起こつて空気が内方へ拡散し、チヤンバ内の圧力
はもとの無荷重状態に戻る。
Since the air pressure is above atmospheric pressure, the air gradually diffuses out of the chamber under load. Supergas does not diffuse out. As long as the load is applied, air continues to slowly diffuse out of the chamber, slowly compressing the chamber and reducing its volume, thereby increasing the pressure of the supergas. The sum of the air partial pressure and the supergas partial pressure is always sufficient to support the load, causing the air pressure to drop and the supergas pressure to rise. If the load is applied continuously for an extended period of time (e.g., 3-4 months at normal load), a final state is reached in which the partial pressure of the air is reduced to a minimum value, i.e., 14.7 psia (atmospheric pressure). At this time the supergas pressure is at its highest value. The diffusion process has stabilized and the gas no longer diffuses. When the load is removed, the self-pressurization phenomenon occurs again and the air diffuses inward, returning the pressure in the chamber to its original unloaded state.

したがつて、クツシヨンデバイスは自己補償および自己
回復特性を有する。通常の使用においては、荷重は上述
した最終状態に近ずくほど長くはかからない。しかしな
がら、[底をつく(BOttOming−0ut)」よ
うな最悪条件の下でもデバイスが適正に機能し続けるこ
とが好ましい。チヤンバが底をつかないようにするため
、チヤンバは無荷重状態で十分な量のスーパガスを含み
、最悪状態(空気量が最低限度まで減少したとき)でも
チヤンバがなお適当な量のガスを含むようにすべきであ
る。クツシヨン デバイスの自己回復または自己再膨張
特性は、家具類の詰め物としての発泡パツドの代りに使
用される永久的に膨張した枕類およびクツシヨンのよう
な、間欠的に荷重のかかるデバイスに適用できる。
Therefore, the cushion device has self-compensating and self-healing properties. In normal use, the load will not last long enough to approach the final state described above. However, it is preferable that the device continue to function properly even under worst-case conditions, such as "BOttOming-0ut". In order to prevent the chamber from bottoming out, the chamber must contain a sufficient amount of supergas in the unloaded state, so that even in the worst case conditions (when the air volume is reduced to a minimum) the chamber still contains a suitable amount of gas. should be. The self-healing or self-reinflating properties of cushion devices are applicable to intermittent loaded devices such as permanently expanded pillows and cushions used in place of foam padding as upholstery in furniture.

荷重を支えるためには比較的小量のスーパガスがチャン
バ内の空気−スーパガス混合物に要求される。人がクツ
シヨンまたは膨張家具上にすわつている間=部の空気が
外方へ拡散するが、荷重が除去されたとき(特に夜中)
空気は枕またはクツシヨン内へ拡散して戻り、クツシヨ
ン類は自動的に再膨張して次の荷重サイクルに対する準
備ができる。高度の変化はエラストマ クツシヨン デ
バイスに影響を及ぼす。
A relatively small amount of supergas is required in the air-supergas mixture within the chamber to support the load. Air diffuses outward while a person is sitting on a cushion or inflatable furniture, but when the load is removed (especially at night)
The air diffuses back into the pillow or cushion and the cushion automatically reinflates and is ready for the next load cycle. Changes in altitude affect elastomeric devices.

高高度においては、周囲圧力が低く、チャンバ内の圧力
とその外部の圧力との差が海水面におけるよりはるかに
大きい。先行技術のバリヤ材料形製品の場合には、ギア
ピンが通常約5000〜8000フイート高度の圧力に
なる航空機に取付けられると、空気チヤンバは大幅に膨
張して破裂する可能性がある。本発明に係るエラストマ
製品の場合には、物理的特性がすぐれておりかつ溶接部
が完全であるため、圧力増加は性能に悪影響を及ぼさな
い。
At high altitudes, the ambient pressure is low and the difference between the pressure inside the chamber and the pressure outside it is much greater than at sea level. In the case of prior art barrier material shaped products, when the gear pin is installed in an aircraft where the pressure is typically around 5,000 to 8,000 feet altitude, the air chamber can expand significantly and rupture. In the case of the elastomeric product according to the invention, increased pressure does not adversely affect performance due to the excellent physical properties and integrity of the weld.

コロラド州デンバ一で起こるように、高高度に放置され
た場合、チャンバ内の空気はすぐに外方へ拡散し、製品
はその初期膨張状態に向つて復帰するであろう。これに
対応して、クツシヨン デバイスが低高度または海水面
まで降下すると、周囲空気がチヤンバ内へ拡散するであ
ろう。工業的包装分野以外のクツシヨン デバイスの用
途は、スキー靴ならびにホツケ一 スケートおよびロー
ラ スケートのような靴形スケートのような、靴類用の
軽量で、耐久性の強いクツシヨン部材である。
If left at high altitude, as occurs in Denver, Colorado, the air within the chamber will quickly diffuse outward and the product will return to its initial expanded state. Correspondingly, as the cushion device descends to low altitude or sea level, ambient air will diffuse into the chamber. Applications for cushioning devices outside of the industrial packaging field are lightweight, durable cushioning members for footwear, such as ski boots and shoe-shaped skates such as shoe skates and roller skates.

永久的に膨張した製品を足と下脚部を包囲するに適した
形状にし、靴類の発泡パッドに代えて改良クツシヨン部
材として使用する。クツシヨン デバイスの別の用途は
足の甲上に嵌合する永久膨張タンクである。永久的に膨
張したクツシヨン デバイスは靴の中底またはライナと
して使用でき、従来製品の欠点を克服し、より良好な弾
性、衝撃吸収性および寒冷に対するより大きな絶縁性を
与える。
The permanently expanded product is shaped to enclose the foot and lower leg and is used as an improved cushioning member to replace foam padding in footwear. Another use for cushion devices is as a permanent inflation tank that fits over the top of the foot. Permanently inflated cushion devices can be used as shoe insoles or liners, overcoming the drawbacks of conventional products and providing better elasticity, shock absorption and greater cold insulation.

本発明のクツシヨン デバイスの別の用途はドア シー
ルおよび窓シールであり、先行技術の押出加工ゴムまた
は発泡プラスチツク ストリツプの代りに使用できる。
Another use for the cushion device of the present invention is in door and window seals, where it can be used in place of prior art extruded rubber or foam plastic strips.

ある期間使用すると、発泡体はその形状および弾性を失
なつて機能しなくなる。本発明に係るシールは第8〜1
0図に示した細長い、長方形チヤンバから作られ、特定
のシール用途に適した幅と長さに切断され継がれる。本
発明のエラストマ クツシヨン デバイスはまたヘルメ
ツトのシエルと着用者の頭との間の永久膨張ライナとし
て使用することもできる。衝撃吸収特性はフツトボール
、モータサイクリング等の活動に使用されるヘルメツト
においてきわめて有利である。これらのヘルメツトが永
久膨張ライナと共に使用される剛性(しかし軽量)外部
シエルを持つように設計されるならば、1500G以上
のきわめてきびしい衝撃荷重を125G以下に減衰する
ことができる。U.S.DepartmentOfTr
anspOrtatiOnの手順に従つてモータサイク
ルヘルメツトのテストが行なわれた。これらのテストに
おいて、模擬頭を有するヘルメツトが約8フイートの高
さから鋼製半球形アンビルの上へ落される。Depar
tmentOfTranspOrtatiOn規格は最
高衝撃が2ミリ秒間800Gを超えないことを要求する
。本発明に係るクツシヨン ライナはこの規格を満たし
かつかなりの余裕がある。知られている限り、他のヘル
メツトは本発明に係るものほど該規格を満足していない
。同様に、クツシヨン デバイスはフツト ボール用シ
ヨルダ パツド、キドニイ パツド、レツグ パツドの
ような、競技用道具のパツド、およびホツケ一、ベース
ボールなどのような、他のスポーツ用のパツドとして製
作使用することができる。
After a period of use, the foam loses its shape and elasticity and ceases to function. The seal according to the present invention is No. 8 to 1.
It is constructed from an elongated, rectangular chamber as shown in Figure 0, cut and pieced to the appropriate width and length for the particular sealing application. The elastomeric device of the present invention can also be used as a permanent expansion liner between the helmet shell and the wearer's head. Shock absorption properties are extremely advantageous in helmets used for activities such as football and motorcycling. If these helmets are designed with a rigid (but lightweight) outer shell used with a permanent expansion liner, extremely severe impact loads of 1500 G or more can be attenuated to 125 G or less. U. S. DepartmentOfTr
Motorcycle helmets were tested according to the anspOrtatiOn procedure. In these tests, a helmet with a simulated head is dropped from a height of approximately 8 feet onto a steel hemispherical anvil. Depar
The tmentOfTranspOrtatiOn standard requires that the maximum impact not exceed 800G for 2 milliseconds. The cushion liner according to the present invention meets this standard and has considerable margin. As far as is known, other helmets do not meet this standard as well as the one according to the invention. Similarly, cushion devices can be constructed and used as pads for athletic equipment, such as shoulder pads, kidney pads, and leg pads for football, and pads for other sports, such as shoulder pads, baseball, etc. can.

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

第1図は本発明に係るクツシヨンまたは衝撃吸収デバイ
スの一部分の平面図である。 第2図は第1図の2〜2線断面図である。第3図は第2
図のものより厚いエラストマ材料から作られたクツシヨ
ン デバイスの第2図に相当する図である。第4図はク
ツシヨンまたは衝撃吸収デバイスの別の実施態様0平面
図である。第5図は第4図の5〜5線断面図である。第
6図はクツシヨンまたは衝撃吸収デバイスのさらに別の
実施態様の平面図である。第7図は第6図の7〜7線断
面図である。第8図はクツシヨンまたは衝撃吸収デバイ
スのさらに別の実施態様の平面図である。第9図は第8
図の9〜9線断面図である。第10図は第8図の10〜
10線断面図である。第11図はチャンバ内への空気の
逆拡散によるエラストマ チャンバの自己加圧を示すグ
ラフである。第12図は最初にチヤンバ内にある空気と
他のガスの異なる混合物によるエラストマ チヤンバの
自己加圧に起因する圧力上昇を示すグラフである。10
・・・・・・クツシヨン デバイス、11,12・・・
・・・エラストマ シート、13・・・・・・溶接区域
、14・・・・・・チヤンバ。
FIG. 1 is a plan view of a portion of a cushion or shock absorbing device according to the present invention. FIG. 2 is a sectional view taken along line 2-2 in FIG. 1. Figure 3 is the second
Figure 2 corresponds to Figure 2 of a cushion device made from a thicker elastomeric material than that shown; FIG. 4 is a plan view of another embodiment of a cushion or shock absorbing device. FIG. 5 is a sectional view taken along line 5-5 in FIG. 4. FIG. 6 is a plan view of yet another embodiment of a cushion or shock absorbing device. FIG. 7 is a sectional view taken along line 7-7 in FIG. 6. FIG. 8 is a plan view of yet another embodiment of a cushion or shock absorbing device. Figure 9 is the 8th
It is a sectional view taken along line 9-9 in the figure. Figure 10 is from 10 in Figure 8.
10 is a sectional view taken along line 10. FIG. 11 is a graph illustrating the self-pressurization of an elastomeric chamber due to back-diffusion of air into the chamber. FIG. 12 is a graph showing the pressure increase due to self-pressurization of the elastomer chamber by different mixtures of air and other gases initially present in the chamber. 10
...Cushion device, 11, 12...
... Elastomer sheet, 13 ... Welding area, 14 ... Chamber.

Claims (1)

【特許請求の範囲】 1 積層エラストマーシート材にそれぞれ独立に設けた
チャンバー内にガスを封入してなるクッションデバイス
において、前記シート材を封入ガスに対しては透過性が
低く、各チャンバーを取りまく周囲の空気に対しては透
過性の高い素坂で構成し、前記封入ガスとして不活性、
無極性、且つ大分子のガスを用い、その封入ガス圧で各
チャンバーに最小限の容積を確保させ、外部要因によつ
て生ずるチャンバーの膨張、収縮によりチャンバー内へ
の空気の流出入を可能にしたことを特徴とする製品およ
び物体用エラストマクッションデバイス。 2 前記ガスが、ヘキサフルオルエタン、六フッ化硫黄
、ペルフルオルプロパン、ベルフルオルブタン、ペルフ
ルオルペンタン、ペルフルオルヘキサン、ペルフルオル
ヘプタン、オクタフルオルシクロブタン、ペルフルオル
シクロブタン、ヘキサフルオルプロピレン、テトラフル
オルメタン、モノクロロペンタフルオルエタン、1・2
−ジクロロテトラフルオルエタン、1・1・2−トリク
ロロ−1・2・2トリフルオルエタン、クロロトリフル
オルエチレン、ブロモトリフルオルメタン、およびモノ
クロロトリフルオルメタンからなるグループから選択さ
れている特許請求の範囲第1項記載の製品および物体用
エラストマクッションデバイス。 3 前記エラストマシート材が、ポリウレタン、ポリエ
ステルエラストマブチルゴム、フルオルエラストマ、塩
素化ポリエチレン、ポリ塩化ビニル、クロロスルホン化
ポリエチレン、ポリエチレン/酢酸エチレンビニルコポ
リマ、ネオプレン、ブタジエンアクリロニトリルゴムブ
タジエンスチレンゴム、エチレンプロピレンポリマ天然
ゴム、高力シリコーンゴム、低密度ポリエチレン、アダ
クトゴム、サルファイドゴム、メチルゴム、および熱可
塑性ゴムからなる材料のグループから選択されている特
許請求の範囲第1項記載の製品および物体用エラストマ
クッションデバイス。 4 前記エラストマシート材が、ポリウレタン、ポリエ
ステルエラストマ、ブチルゴム、フルオルエラストマ、
塩素化ポリエチレン、ポリ塩化ビニル、クロロスルホン
化ポリエチレン、ポリエチレン/酢酸エチレンビニルコ
ポリマ、ネオプレン、ブタジエンアクリロニトリルゴム
、ブタジエンスチレンゴム、エチレンプロピレンポリマ
、天然ゴム、高力シリコーン、ゴム、低密度ポリエチレ
ン、アダクトゴム、サルファイドゴム、メチルゴム、お
よび熱可塑性ゴムからなる材料のグループから選択され
ている特許請求の範囲第1項記載の製品および物体用エ
ラストマクッションデバイス。 5 前記チャンバが球形である特許請求の範囲第1項記
載の製品および物体用エラストマクッションデバイス。 6 前記チャンバが楕円体形である特許請求の範囲第1
項記載の製品および物体用エラストマクッションデバイ
ス。 7 前記チャンバが一般に円筒形である特許請求の範囲
第1項記載の製品および物体用エラストマクッションデ
バイス。 8 前記各チャンバが実質的に正方形の部分を有する特
許請求の範囲第1項記載の製品および物体用エラストマ
クッションデバイス。 9 前記各チャンバが長方形の部分を有する特許請求の
範囲第1項記載の製品および物体用エラストマクッショ
ンデバイス。 10 前記各チャンバが長方形の部分を有し、前記チャ
ンバ同士が配列位置をずらした格子状配列関係にある特
許請求の範囲第1項記載の製品および物体用エラストマ
クッションデバイス。 11 前記エラストマシート材がエーテル系ポリウレタ
ンである特許請求の範囲第1項記載の製品および物体用
エラストマクッションデバイス。 12 前記チャンバーが、前記ガスで前記初期値まで膨
張させられたとき部分的につぶれている特許請求の範囲
第1項記載の製品および物体用エラストマクッションデ
バイス。 13 前記チャンバが、前記ガスで前記初期値まで膨張
させられたとき部分的につぶれている特許請求の範囲第
7項記載の製品および物体用エラストマクッションデバ
イス。 14 前記積層エラストマシート材、前記チャンバの膨
張にさいして球形チャンバを形成するために離間した円
形溶接区域において相互に封着されている特許請求の範
囲第1項記載の製品および物体用エラストマクッション
デバイス。 15 前記エラストマシート材が、前記チャンバーの膨
張にさいして楕円体形チャンバーを形成するために離間
した円形溶接区域において相互に封着されている特許請
求の範囲第1項記載の製品および物体用エラストマクッ
ションデバイス。 16 前記エラストマシート材が、前記チャンバーの膨
張にさいして一般に円筒形チャンバーを形成するために
離間した円形溶接区域において相互に封着されている特
許請求の範囲第1項記載の製品および物体用エラストマ
クッションデバイス。 17 前記エラストマシート材が、一般にドーム形のチ
ャンバーを形成するために離間した溶接区域において相
互に封着され、各チャンバーが溶接区域に実質的に正方
形の部分を有する特許請求の範囲第1項記載の製品およ
び物体用エラストマクッションデバイス。 18 前記エラストマシート材が、一般にアーチ形のチ
ャンバーを形成するために離間した溶接区域において相
互に封着され、各チャンバーが溶接区域に実質的に長方
形の部分を有する特許請求の範囲第1項記載の製品およ
び物体用エラストマクッションデバイス。 19 前記チャンバーが、前記ガスで前記初期値まで膨
張させられたとき部分的につぶれている特許請求の範囲
第14項記載の製品および物体用エラストマクッション
デバイス。 20 前記チャンバーが、前記ガスで前記初期値まで膨
張させられたとき部分的につぶれている特許請求の範囲
第15項記載の製品および物体用エラストマクッション
デバイス。 21 前記チャンバーが、前記ガスで前記初期値まで膨
張させられたとき部分的につぶれている特許請求の範囲
第16項記載の製品および物体用エラストマクッション
デバイス。 22 所定初期値まで膨張する加圧ガスが、大気圧以上
の圧力を有する初期チャンバー膨張混合物を形成するた
めに空気で希釈されている特許請求の範囲第1項記載の
製品および物体用エラストマクッションデバイス。 23 前記周囲空気が、前記封着部材を通つて前記チャ
ンバー内へ拡散し、前記チャンバー内の圧力を前記初期
値以上に増加している特許請求の範囲第1項記載の製品
および物体用エラストマクッションデバイス。
[Claims] 1. A cushion device in which a gas is sealed in chambers provided independently in a laminated elastomer sheet material, wherein the sheet material has low permeability to the sealed gas and the surrounding area surrounding each chamber is low. It is composed of a plain material that is highly permeable to the air, and the filled gas is inert,
Using a non-polar, large molecular gas, the pressure of the filled gas ensures a minimum volume in each chamber, and air can flow in and out of the chamber by expanding and contracting the chamber caused by external factors. An elastomeric cushion device for products and objects characterized by: 2 The gas is hexafluoroethane, sulfur hexafluoride, perfluoropropane, perfluorobutane, perfluoropentane, perfluorohexane, perfluoroheptane, octafluorocyclobutane, perfluorocyclobutane, hexafluorocyclobutane, Fluoropropylene, tetrafluoromethane, monochloropentafluoroethane, 1/2
- dichlorotetrafluoroethane, 1,1,2-trichloro-1,2,2trifluoroethane, chlorotrifluoroethylene, bromotrifluoromethane, and monochlorotrifluoromethane; Elastomeric cushion devices for products and objects according to scope 1. 3. The elastomer sheet material is polyurethane, polyester elastobutyl rubber, fluoroelastomer, chlorinated polyethylene, polyvinyl chloride, chlorosulfonated polyethylene, polyethylene/ethylene vinyl acetate copolymer, neoprene, butadiene acrylonitrile rubber, butadiene styrene rubber, ethylene propylene polymer natural The elastomeric cushioning device for products and objects of claim 1 selected from the group of materials consisting of rubber, high strength silicone rubber, low density polyethylene, adduct rubber, sulfide rubber, methyl rubber, and thermoplastic rubber. 4 The elastomer sheet material is polyurethane, polyester elastomer, butyl rubber, fluoroelastomer,
Chlorinated polyethylene, polyvinyl chloride, chlorosulfonated polyethylene, polyethylene/ethylene vinyl acetate copolymer, neoprene, butadiene acrylonitrile rubber, butadiene styrene rubber, ethylene propylene polymer, natural rubber, high strength silicone, rubber, low density polyethylene, adduct rubber, sulfide Elastomeric cushioning device for products and objects according to claim 1, selected from the group of materials consisting of rubber, methyl rubber and thermoplastic rubber. 5. The elastomeric cushioning device for articles and objects of claim 1, wherein said chamber is spherical. 6. Claim 1, wherein the chamber is ellipsoidal.
Elastomeric Cushion Devices for Products and Objects Listed in Section. 7. The elastomeric cushioning device for articles and objects of claim 1, wherein said chamber is generally cylindrical. 8. The elastomeric cushioning device for articles and objects of claim 1, wherein each said chamber has a substantially square section. 9. The elastomeric cushioning device for articles and objects of claim 1, wherein each chamber has a rectangular portion. 10. The elastomeric cushion device for products and objects according to claim 1, wherein each of the chambers has a rectangular portion, and the chambers are arranged in a grid-like arrangement with shifted positions. 11. The elastomeric cushion device for products and objects according to claim 1, wherein the elastomeric sheet material is an ether polyurethane. 12. The elastomeric cushioning device for articles and objects of claim 1, wherein said chamber is partially collapsed when inflated to said initial value with said gas. 13. The elastomeric cushioning device for articles and objects of claim 7, wherein said chamber is partially collapsed when inflated to said initial value with said gas. 14. An elastomeric cushioning device for articles and objects according to claim 1, wherein the laminated elastomeric sheet material is sealed to each other at spaced apart circular welded areas to form a spherical chamber upon expansion of the chamber. . 15. The elastomeric cushion for articles and objects of claim 1, wherein said elastomeric sheet material is sealed to each other at spaced apart circular welded areas to form an ellipsoidal shaped chamber upon expansion of said chamber. device. 16. The elastomer for articles and objects of claim 1, wherein said elastomeric sheet material is sealed to one another at spaced apart circular welded areas to form a generally cylindrical chamber upon expansion of said chamber. cushion device. 17. The elastomeric sheet material is sealed to each other at spaced apart weld areas to form generally dome-shaped chambers, each chamber having a substantially square portion in the weld area. Elastomeric cushion devices for products and objects. 18. The elastomeric sheet material is sealed to each other at spaced apart welded areas to form generally arcuate chambers, each chamber having a substantially rectangular portion in the welded area. Elastomeric cushion devices for products and objects. 19. The elastomeric cushioning device for articles and objects of claim 14, wherein said chamber is partially collapsed when inflated to said initial value with said gas. 20. The elastomeric cushioning device for articles and objects of claim 15, wherein said chamber is partially collapsed when inflated with said gas to said initial value. 21. The elastomeric cushioning device for articles and objects of claim 16, wherein said chamber is partially collapsed when inflated with said gas to said initial value. 22. Elastomeric cushioning device for articles and objects according to claim 1, wherein the pressurized gas expanding to a predetermined initial value is diluted with air to form an initial chamber expansion mixture having a pressure above atmospheric pressure. . 23. The elastomeric cushion for articles and objects of claim 1, wherein the ambient air diffuses into the chamber through the sealing member and increases the pressure within the chamber above the initial value. device.
JP53127795A 1977-10-20 1978-10-17 Elastomeric cushion devices for products and objects Expired JPS5910902B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84408077A 1977-10-20 1977-10-20
US000000844080 1977-10-20

Publications (2)

Publication Number Publication Date
JPS54116063A JPS54116063A (en) 1979-09-10
JPS5910902B2 true JPS5910902B2 (en) 1984-03-12

Family

ID=25291755

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53127795A Expired JPS5910902B2 (en) 1977-10-20 1978-10-17 Elastomeric cushion devices for products and objects

Country Status (5)

Country Link
JP (1) JPS5910902B2 (en)
CA (1) CA1087644A (en)
DE (1) DE2845798C2 (en)
FR (1) FR2406520A2 (en)
GB (1) GB2010085B (en)

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JPS5531482A (en) * 1978-05-05 1980-03-05 Rudy Marion F Selffexpansion device
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US5042176A (en) * 1989-01-19 1991-08-27 Robert C. Bogert Load carrying cushioning device with improved barrier material for control of diffusion pumping
FR2757236B1 (en) * 1996-12-12 2001-01-19 Grizot Gerard PROCESS FOR PRODUCING AN AIR CUSHION ON A RECEIVING STRUCTURE AND AIR CUSHION OBTAINED BY THE PROCESS
JP5312915B2 (en) * 2008-11-18 2013-10-09 川上産業株式会社 Air bubble sheet for corrugated cardboard
CN102049517A (en) * 2010-10-15 2011-05-11 任首旺 Powder sintering type bulb triangular surface frame material
CN104118645B (en) * 2014-07-25 2017-12-05 厦门艾美森新材料科技股份有限公司 Pack air cushion
CN106516428A (en) * 2016-12-26 2017-03-22 深圳市华星光电技术有限公司 Unequal-thickness bubble pad and making method and packaging structure thereof
CN219221140U (en) * 2023-01-19 2023-06-20 图达通智能科技(宁波)有限公司 Vibration damping member, sensor, and carrier system

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GB964742A (en) * 1962-03-26 1964-07-22 Talley Surgical Instr Ltd Improvements in or relating to pressure point pads
GB1057874A (en) * 1962-07-10 1967-02-08 Technopol Lab Ltd Improvements in or relating to pneumatic cushions
DE1195473B (en) * 1962-10-03 1965-06-24 Danfoss As Gas cushion
FR1484626A (en) * 1963-08-16 1967-06-16 Du Pont Improvements to ultramicrocellular structures and method of preparing such structures
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DE2148401B2 (en) * 1971-09-28 1980-03-27 Metzeler Kautschuk Ag, 8000 Muenchen Flexible hollow body that can be filled with a flowable medium
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US4183156A (en) * 1977-01-14 1980-01-15 Robert C. Bogert Insole construction for articles of footwear

Also Published As

Publication number Publication date
DE2845798C2 (en) 1987-03-12
CA1087644A (en) 1980-10-14
FR2406520A2 (en) 1979-05-18
DE2845798A1 (en) 1979-04-26
GB2010085A (en) 1979-06-27
JPS54116063A (en) 1979-09-10
FR2406520B2 (en) 1985-01-04
GB2010085B (en) 1982-03-03

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