EP1983854A2 - Handschuh mit hoher chemischer widerstandsfähigkeit - Google Patents

Handschuh mit hoher chemischer widerstandsfähigkeit

Info

Publication number
EP1983854A2
EP1983854A2 EP07730881A EP07730881A EP1983854A2 EP 1983854 A2 EP1983854 A2 EP 1983854A2 EP 07730881 A EP07730881 A EP 07730881A EP 07730881 A EP07730881 A EP 07730881A EP 1983854 A2 EP1983854 A2 EP 1983854A2
Authority
EP
European Patent Office
Prior art keywords
layer
article according
latex
mold
dipping
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP07730881A
Other languages
English (en)
French (fr)
Other versions
EP1983854B1 (de
Inventor
Jean Curtet
Olivier Pillard
Christine David
Sandrine Pinchon
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.)
Hutchinson SA
Original Assignee
Hutchinson SA
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 Hutchinson SA filed Critical Hutchinson SA
Publication of EP1983854A2 publication Critical patent/EP1983854A2/de
Application granted granted Critical
Publication of EP1983854B1 publication Critical patent/EP1983854B1/de
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D19/00Gloves
    • A41D19/0055Plastic or rubber gloves
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D31/00Materials specially adapted for outerwear
    • A41D31/04Materials specially adapted for outerwear characterised by special function or use
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/263Coating layer not in excess of 5 mils thick or equivalent
    • Y10T428/264Up to 3 mils
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/269Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension including synthetic resin or polymer layer or component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/3154Of fluorinated addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31826Of natural rubber
    • Y10T428/31833Next to aldehyde or ketone condensation product or addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers

Definitions

  • the present invention relates to a protective article to protect the user from the risks associated with the handling of chemicals.
  • multilayer materials are usually used which comprise at least one layer of a material impervious to said chemicals, i.e. a barrier material.
  • a barrier material i.e. a material impervious to said chemicals.
  • the effectiveness of the barrier effect of a material is determined by its resistance to permeation, which is measured by the time it takes for a given chemical to pass through the material.
  • Materials used to make personal protective equipment must also have sufficient mechanical strength and puncture resistance for common use, such as in a laboratory or workshop.
  • a protective garment such as a glove which has a three-dimensional structure, which is devoid of seams or external welds and which is flexible is preferred. so that you can marry the user's movements. Finally, we also expect such a glove that it is resistant to water.
  • a barrier material provides protection against a limited number of chemicals.
  • a common solution is to superimpose resistant gloves to each of these families in order to provide additional protection. This solution, resulting in a superimposition not very ergonomic, has the disadvantage of hindering handling.
  • the inner layer which is in contact with the skin of the user, is made of polyvinyl alcohol while the outer layer is made of rubber.
  • the outer layer of rubber which is resistant to water, is very easily degraded in contact with certain solvents organic. Therefore these gloves are not suitable for handling these chemicals.
  • Protective articles having a multilayer structure based on polyolefin and on EVOH are also known: US Pat. No. 5,491,022, US 5,059,447, US Pat. No. 4,855,178, US 5,162,148. protection have the disadvantage of providing a low level of chemical protection vis-à-vis amines (methylamine, ethylamine, ..) and to have a low mechanical and thermal protection and low elasticity. On the other hand, these materials, when assembled to produce a glove, have at the welds extra thickness relative to the rest of the material, which is not the case for articles obtained by dipping.
  • Chemical protection has two complementary aspects: On the one hand, it is evaluated for a certain number of chemicals the duration during which a barrier material resists permeation by each of these products taken individually. On the other hand it is considered, for a desired duration of resistance, how many families of different chemicals such a material barrier.
  • the object of the invention was to provide a barrier material for as many chemicals as possible for as long as possible.
  • Such a result has been obtained according to the present invention by the superposition of a layer of natural or synthetic latex, a partially hydrolyzed polyvinyl alcohol layer, a layer of a synthetic latex and optionally a silica-based topcoat and a dispersion of a cationic fluoropolymer.
  • US-5,438,709 discloses an elastomeric glove covered with a layer of polyvinyl alcohol and a thickening agent.
  • the polyvinyl alcohol used is of a fully hydrolysed quality.
  • the gloves described in this document are more particularly intended to be used as a base for forming an orthopedic bandage, because of their slippery character in the presence of water.
  • JP 56-078930 discloses a textile glove which is dipped in a polyvinyl alcohol solution and then dried and dipped in a dispersion of a polyvinyl chloride (PVC) resin, before being demolded. This process gives a textile glove that is pleasant and flexible contact.
  • PVC polyvinyl chloride
  • the subject of the invention is a protective article, preferably a glove, offering improved protection against penetration by chemicals, this article comprising:
  • the protection article further comprises:
  • the materials of the invention make it possible to increase the duration of passage of said material by the solvents and to constitute a barrier against a wider range of chemicals.
  • this material and the articles obtained from this material are of remarkable elasticity with respect to multi-layer materials of the prior art and are water resistant.
  • the articles of the invention preferably comprise a support layer consisting of a textile. It may be a fabric or a knit, based on a natural fiber such as cotton, wool, linen, viscose, or synthetic fiber such as polyester, polyamide, of polyethylene, in particular high modulus and high tenacity polyethylene, aramid or para-aramid, or a mixture of several types of fibers.
  • a support layer consisting of a textile. It may be a fabric or a knit, based on a natural fiber such as cotton, wool, linen, viscose, or synthetic fiber such as polyester, polyamide, of polyethylene, in particular high modulus and high tenacity polyethylene, aramid or para-aramid, or a mixture of several types of fibers.
  • the textile support is cotton.
  • the textile support layer which is in contact with the skin of the user, is intended both to promote the mechanical strength of the article of the invention and to offer a pleasant contact to the user during long use. .
  • the latex layer (i) is chosen for its chemical barrier properties. It is chosen from natural latices and synthetic latices.
  • a natural latex layer has the advantage of giving greater flexibility to the protective articles and, at equal thickness, of being less expensive than a layer of synthetic latex.
  • the latex layer may constitute the first or the second thickness of the protective article from the skin of the user and towards the outer face of the article. protection.
  • the latex layer (i) may consist of a polychloroprene latex, but also a nitrile or butyl rubber, a polyvinyl chloride, a fluoroelastomer, a polyurethane, a chlorosulfonylpolyethylene, a chlorinated polyethylene, an ethylene acrylic, a polyacrylate or a combination of these materials.
  • provision may be made for using a layer of natural latex to which a layer of synthetic latex is superimposed.
  • the synthetic latex may constitute the support layer or the second or third layer of the protection article of the invention.
  • the last layer of latex is covered with an adhesion layer intended to promote better adhesion of the polyvinyl alcohol layer to the latex.
  • This intermediate adhesion layer may consist of any material known to those skilled in the art and capable of performing this function. It may be in particular a mixture of latex, identical to that used in (i) and PVA used in (ii). Preferably, a mixture of an acrylic latex and PVA used in (ii) is chosen.
  • the adhesion layer improves the mechanical strength of the protective article, particularly its peel strength, and contributes to the flexibility of the article.
  • the application of the adhesion layer may be replaced by the application of a coagulant of the polyvinyl alcohol.
  • a layer (ii) of polyvinyl alcohol (PVA) is then provided, either directly on the latex, or on the intermediate adhesion layer, or on the PVA coagulant.
  • This layer (ii) consists of partially hydrolyzed polyvinyl alcohol having a degree of hydrolysis of between 70 and 95%, preferably between 85 and 90%.
  • the layer (iii) of synthetic latex may consist of any synthetic latex as already described above for layer (i).
  • the layer (iii) of synthetic latex is chosen from acrylic latices, styrene-butadiene latices and self-crosslinking nitrile latices.
  • the layer (iii) of synthetic latex also comprises polyvinyl alcohol.
  • the polyvinyl alcohol used in layer (iii) has any degree of hydrolysis. Preferably, it has a degree of hydrolysis of between 70 and 95%.
  • the polyvinyl alcohol of layer (iii) is the same as that of layer (ii).
  • the proportion of latex and polyvinyl alcohol in the mixture of the layer (iii) is between 3 and 10%, preferably 4 to 8% of polyvinyl alcohol, by weight of active material relative to the weight of synthetic latex.
  • the outer layer (iv) is advantageously constituted by a mixture of silica in aqueous dispersion and a cationic fluorinated resin.
  • the silica is a precipitated silica or a fumed silica.
  • the silica is a fumed silica of colloidal nature.
  • the latex of the layer (i) or the PVA of the layer (ii), the latex of the layer (iii) and optionally the mixture of the layer (iv) can be applied repeatedly with a drying step intermediate between two applications.
  • the protective article of the invention comprises a layer thickness (i) of natural or synthetic latex ranging from 100 to 400 microns.
  • the protective article of the invention comprises a layer of polyvinyl alcohol (ii) with a thickness of between 30 and 200 ⁇ m.
  • the protective article of the invention comprises a layer thickness (ii) of PVA, with a hydrolysis rate ranging from 70 to 95%, from 60 to 150 ⁇ m and a thickness of synthetic latex layer (iii). with a thickness of 10 to 20 ⁇ m.
  • the protective article of the invention comprises a layer of mixture (iv) of silica and fluororesin with a thickness ranging from 1 to 5 microns.
  • the thickness of the adhesion layer is between 5 and 50 microns.
  • the resistance to penetration by solvents of the protective articles of the invention is greater than the sum of the strengths of each of the constituent materials of these articles.
  • Polychloroprene and partially hydrolyzed PVAs are known for their resistance to permeation by chemicals.
  • the materials of the invention when present in the same protection article and in the order indicated above, make it possible to obtain a protection much higher than the sum of the protections conferred by each of the individual materials.
  • the protective articles of the invention have good water resistance and are of satisfactory flexibility.
  • Another object of the invention is a method of producing a protective article for protecting the manipulator from the risks associated with the use of chemicals.
  • Such a method comprises the following steps: a) optionally, dressing a mold with a textile layer; b) optionally dipping the mold or the mold / textile assembly resulting from step a) in a coagulating solution; c) dipping the mold or the mold / textile assembly from step a) or step b) into one or more aqueous dispersions of natural or synthetic latex (i); d) optionally dipping the coated mold from step c) in water to allow removal of the coagulant solution; e) drying and optionally vulcanization of the coated mold from step c) or step d); f) optionally dipping the coated mold obtained at the end of step c), d) or e) in one or more adhesion layers; g) dipping the coated mold obtained at the end of step c) or step d) or e) or f) in one or more aqueous solutions of partially hydrolyzed PVA of hydrolysis rate of between 70 and 95; %.
  • step g) dipping the coated mold obtained at the end of step g) in one or more aqueous dispersions of self-crosslinking synthetic latex, preferably chosen from acrylic latices, styrene-butadiene latices or nitrile latices; i) non-obligatorily, but preferably, dipping of the coated mold obtained at the end of step h) in one or more aqueous dispersions of a cationic fluorinated resin comprising silica; and in the final step: j) removal of the glove by sliding on the mold.
  • aqueous dispersions of self-crosslinking synthetic latex preferably chosen from acrylic latices, styrene-butadiene latices or nitrile latices
  • the textile support, or the mold is coated with natural or synthetic latex by a quenching operation known to those skilled in the art.
  • Each quenching step is optionally followed by drying and a step of vulcanization or gelling in an oven.
  • the invention provides for dipping the optionally coated mold in a solution for coagulating the latex, then drying, then optionally soaking in one or more synthetic elastomer baths, each quenching being followed by drying until complete coagulation of the elastomer and then rinsing in water or in any solvent allowing the removal of the coagulant solution.
  • each dipping step f) to i) is followed by drying for a period of 5 minutes to about 1 hour, at a temperature of 30 to 90 ° C.
  • the dipping technique is particularly suitable for the manufacture of protective equipment such as gloves, overboots, and more generally, all items having a three-dimensional structure
  • a protection article according to the invention by using other technologies known to those skilled in the art such as coating, since the succession of the layers of materials described above is reconstituted in the order indicated.
  • the invention further relates to the protective articles described above and characterized in that they are in the form of a glove, an overboot, a combination, a hood, a tarpaulin , pants, jacket.
  • aqueous solutions of polyvinyl alcohol being generally very dilute, it is preferably carried out several successive dipping in step g).
  • Manufacture of a glove a- One dresses a shape using a cotton textile. b- The dressed form is soaked for 10 seconds in a coagulating solution. c- The dressed shape is soaked for 120 seconds in a natural latex bath. The form is then quenched for 20 seconds in a polychloroprene latex bath. This operation is repeated so as to form a second layer of polychloroprene latex. The shape is then soaked in water to allow the removal of the coagulating solution. After drying and vulcanization of the preceding layers, the form is soaked for 5 seconds in a bath consisting of:
  • the percentages are given by weight of dry matter in the composition.
  • the composition is in the form of an aqueous dispersion at 30% solids content. After drying for 15 minutes at 75 ° C., the form is soaked for 5 seconds in a bath consisting of:
  • the percentages are given by weight of dry matter in the composition.
  • the composition is in the form of an aqueous dispersion containing 12% solids. Operation g- is repeated a second time. After drying for 30 minutes at 75 ° C., the form is soaked for 5 seconds in a bath consisting of:
  • composition 1.5% by weight of an acid catalyst (diammonium chloride). The percentages are given by weight of dry matter in the composition.
  • the composition is in the form of an aqueous dispersion containing 28% solids. After drying for 30 minutes at 85 ° C., the form is soaked for 2 seconds in a bath consisting of: 71% by weight of water
  • colloidal silica (Bindzil marketed by the company Eka Chemicals)
  • the percentages are given by weight of dry matter in the composition.
  • the composition is in the form of an aqueous dispersion containing 18% solids.
  • the glove is crosslinked by heating at 120 ° C. for 30 minutes and it is demolded.
  • Example 1 The process of Example 1 is repeated by eliminating step (i-) and using in step (h-) a dispersion consisting of:
  • the percentages are given by weight of active ingredient in the composition.
  • the composition is in the form of an aqueous dispersion containing 40% solids.
  • Example 1 The process of Example 1 is repeated by eliminating step (i-) and using in step (h-) a dispersion consisting of:
  • composition is in the form of an aqueous dispersion at 45% solids content.
  • pellets are then fixed in each of the absorption cells, the external face being placed towards the side containing the demineralized water.
  • This method determines the water swelling of the outside of a glove.
  • the principle is based on the ability of a film to swell in contact with water.
  • the glove of the invention (Example 1) has a mass swelling evaluated by its variation index of 8.7% by weight after 90 minutes without visual degradation.
  • the good water resistance of the glove of the invention can be illustrated by the test below.
  • the multilayer glove of Example 1 has peel strengths between layers (ii) and (i) of a minimum value of 4.5 N / cm according to the standard ISO 36.
  • this glove has the following mechanical properties according to EN 374-3.
  • Abrasion Level 3 Cleavage: Level 1 Tearing: Level 4 Perforation: Level 1.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Gloves (AREA)
  • Laminated Bodies (AREA)
  • Professional, Industrial, Or Sporting Protective Garments (AREA)
EP07730881A 2006-02-02 2007-01-29 Handschuh mit hoher chemischer widerstandsfähigkeit Not-in-force EP1983854B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0600947A FR2896667B1 (fr) 2006-02-02 2006-02-02 Gant a haute resistance chimique
PCT/FR2007/000163 WO2007088265A2 (fr) 2006-02-02 2007-01-29 Gant a haute resistance chimique

Publications (2)

Publication Number Publication Date
EP1983854A2 true EP1983854A2 (de) 2008-10-29
EP1983854B1 EP1983854B1 (de) 2009-07-01

Family

ID=37398764

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07730881A Not-in-force EP1983854B1 (de) 2006-02-02 2007-01-29 Handschuh mit hoher chemischer widerstandsfähigkeit

Country Status (7)

Country Link
US (1) US20090068443A1 (de)
EP (1) EP1983854B1 (de)
JP (1) JP2009525411A (de)
AT (1) ATE434949T1 (de)
DE (1) DE602007001448D1 (de)
FR (1) FR2896667B1 (de)
WO (1) WO2007088265A2 (de)

Cited By (1)

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WO2023152176A1 (de) 2022-02-11 2023-08-17 Uvex Safety Gloves Gmbh & Co. Kg Verfahren zur herstellung von chemieschutzkleidung sowie eine solche

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CN102387911B (zh) 2009-02-05 2015-03-04 狄特科技私人有限公司 弹性体膜的制备方法
US20120047626A1 (en) * 2010-08-24 2012-03-01 Honeywell International Inc. Seamless Chemical Resistant Glove
DE102011101800A1 (de) * 2011-05-17 2012-11-22 Mattias Finzelberg Schutzhandschuh
DE102011107443A1 (de) * 2011-07-08 2013-01-10 Mattias Finzelberg Schutzhandschuh mit textilem Innenfutter
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US9538952B2 (en) 2012-10-30 2017-01-10 Medicametrix, Inc. Controller for measuring prostate volume
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US20140165263A1 (en) * 2012-12-18 2014-06-19 Ansell Limited Fluid repellent elastomeric barrier
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KR102658786B1 (ko) 2015-10-18 2024-04-19 얼리젼스 코포레이션 수계 히드로겔 블렌드 코팅 및 엘라스토머 물품에의 적용 방법
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023152176A1 (de) 2022-02-11 2023-08-17 Uvex Safety Gloves Gmbh & Co. Kg Verfahren zur herstellung von chemieschutzkleidung sowie eine solche
DE102022103308A1 (de) 2022-02-11 2023-08-17 Uvex Safety Gloves Gmbh & Co. Kg Verfahren zur Herstellung von Chemieschutzkleidung sowie eine solche

Also Published As

Publication number Publication date
FR2896667A1 (fr) 2007-08-03
EP1983854B1 (de) 2009-07-01
FR2896667B1 (fr) 2008-04-11
JP2009525411A (ja) 2009-07-09
DE602007001448D1 (de) 2009-08-13
WO2007088265A3 (fr) 2007-09-20
WO2007088265A2 (fr) 2007-08-09
ATE434949T1 (de) 2009-07-15
US20090068443A1 (en) 2009-03-12

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