US20030118761A1

Movatterモバイル変換

Info

Publication number: US20030118761A1
Application number: US10/036,743
Authority: US
Inventors: Thomas Triebes; Mary Kister; Kermit Littleton
Original assignee: Kimberly Clark Worldwide Inc
Current assignee: Kimberly Clark Worldwide Inc
Priority date: 2001-12-21
Filing date: 2001-12-21
Publication date: 2003-06-26
Also published as: AU2002348411A1; CA2470405A1; US7329442B2; WO2003056955A1; JP2005514529A; MXPA04005972A; US20030118837A1; EP1455611A1

Abstract

An elastomeric article (e.g., glove, condom, etc.) that includes a chemical protection layer that will not substantially dissolve when applied with certain chemicals or solvents, such as methyl methyacrylate, is provided. The chemical protection layer contains at least one crosslinked, modified silicone elastomer. For example, in one embodiment, the modified silicone chemical protection layer covers the outer surface of a styrene-ethylene-butylene-styrene (S-EB-S) block copolymer substrate body to impart relative chemical resistance to the resulting elastomeric article.

Description

BACKGROUND OF THE INVENTION

Elastomeric articles, such as gloves, are often formed from synthetic polymers. Unfortunately, one problem sometimes associated with the formation of elastomeric articles from some types of synthetic polymers is that they tend to dissolve when contacted with certain chemicals or solvents. The dissolution of the elastomeric polymer may be especially problematic when used in certain fields, such as in the medical or automotive field. For example, a surgeon often wears elastomeric gloves during a procedure to protect the patient and surgeon from the possible spread of infection or disease. During the procedure, the surgeon may be required to utilize various chemicals or solvents, such as bone cement, that may undesirably dissolve the elastomeric polymer forming the glove, thereby exposing the surgeon's skin.[0001]

As such, a need currently exists for an improved elastomeric article that is relatively resistant to various types of chemicals or solvents.[0002]

SUMMARY OF THE INVENTION

In accordance with one embodiment of the present invention, an elastomeric article (e.g., glove, condom, etc.) is disclosed that comprises a substrate body including a layer made of an elastomeric material and a chemical protection layer covering the outside surface of the substrate body. The chemical protection layer includes at least one modified silicone elastomer that has been crosslinked. For example, in one embodiment, the modified silicone elastomer is selected from the group consisting of phenyl-modified silicones, vinyl-modified silicones, methyl-modified silicones, fluoro-modified silicones, alkyl-modified silicones, alkoxy-modified silicones, alkylamino-modified silicones, and combinations thereof.[0003]

The substrate body, as indicated above, contains an elastomeric material. In some instances, the elastomeric material of the substrate body is selected from the group consisting of styrene-ethylene-butylene-styrene block copolymers, styrene-isoprene-styrene block copolymers, styrene-polybutadiene-styrene block copolymers, styrene-isoprene block copolymers, styrene-butadiene block copolymers, natural rubber latex, nitrile rubbers, isoprene rubbers, chloroprene rubbers, polyvinyl chlorides, silicone rubbers, and combinations thereof. For example, in one embodiment, the elastomeric material of the substrate body contains at least one styrene-ethylene-butylene-styrene triblock copolymer.[0004]

Besides the layers mentioned above, the elastomeric article may also contains other layers. In one embodiment, for instance, the elastomeric article can contain a donning layer overlying the inside surface of the substrate body. If desired, a lubricant layer may also overlay the inside surface of the donning layer.[0005]

In accordance with another embodiment of the present invention, a method for forming an elastomeric article (e.g., glove, condom, etc.) is disclosed. In particular, the method includes furnishing a liquid solution comprising a modified silicone elastomer and a solvent. A former having the shape of the elastomeric article is dipped into the liquid solution and withdrawn therefrom. The solvent is then evaporated from the liquid solution present on the former so that a modified silicone elastomer film is formed thereon. To induce crosslinking in the modified silicone elastomer, it is heated, such as to a temperature of from about 200° F. to about 400° F., and in some embodiments, from about 200° F. to about 350° F.[0006]

Various properties of the chemical protection layer may be varied to achieve an elastomeric article having certain characteristics. For example, the solids content of the uncrosslinked modified silicone elastomer can be from about 5% to about 40%, and in some embodiments, from about 10% to about 35%. Furthermore, the uncrosslinked modified silicone elastomer can have a viscosity of from about 300 centipoise to about 7000 centipoise, and in some embodiments, from about 600 centipoise to about 4000 centipoise. Moreover, the modified silicone elastomer film can have a thickness of from about 0.001 millimeters to about 0.4 millimeters, in some embodiments, from about 0.01 millimeters to about 0.30 millimeters, and in some embodiments, from about 0.01 millimeters to about 0.20 millimeters.[0007]

The method can also include dipping the crosslinked, modified silicone-coated former into a liquid solution of an elastomeric material (e.g., styrene-ethylene-butylene-styrene) to form the substrate body. In some embodiments, the former is further dipped into a liquid solution to apply a donning layer on the inside surface of the substrate body.[0008]

Other features and aspects of the present invention are discussed in greater detail below.[0009]

BRIEF DESCRIPTION OF THE DRAWINGS

A full and enabling disclosure of the present invention, including the best mode thereof, directed to one of ordinary skill in the art, is set forth in the specification, which makes reference to the appended drawings, in which:[0010]

FIG. 1 is a perspective view of one embodiment of an elastomeric glove made according to the invention;[0011]

FIG. 2 is a cross-sectional view of the glove illustrated in FIG. 1 taken along a line[0012]2-2; and

FIG. 3 is a block flow diagram illustrating one embodiment of a method for forming an elastomeric article of the present invention.[0013]

Repeat use of reference characters in the present specification and drawings is intended to represent the same or analogous features or elements of the invention.[0014]

DETAILED DESCRIPTION OF REPRESENTATIVE EMBODIMENTS

Reference now will be made in detail to various embodiments of the invention, one or more examples of which are set forth below. Each example is provided by way of explanation, not limitation of the invention. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. For instance, features illustrated or described as part of one embodiment, can be used on another embodiment to yield a still further embodiment. Thus, it is intended that the present invention cover such modifications and variations.[0015]

In general, the present invention is directed to an elastomeric article that includes a chemical protection layer that will not substantially dissolve when contacted with certain chemicals or solvents, such as bone cement. The chemical protection layer contains at least one crosslinked, modified silicone elastomer. For example, in one embodiment, the modified silicone chemical protection layer covers the outer surface of a styrene-ethylene-butylene-styrene (S-EB-S) block copolymer substrate body to impart relative chemical resistance to the resulting elastomeric article.[0016]

Any of a variety of elastomeric articles can be provided with improved chemical resistance properties in accordance with the present invention. For example, gloves and condoms, as well as medical devices, such as dilatation balloons, inflatable cuffs, external catheters, catheter balloons, instrument covers, and the like, can be formed according to the present invention. In addition, it should also be understood that other types of elastomeric articles may also be formed according to the present invention. For example, elastomeric materials often used in automotive applications, such as flexible rubber hoses, can also be formed with the crosslinked modified silicone elastomer in accordance with the present invention.[0017]

Referring to FIGS.[0018]1-2, for example, one embodiment of anelastomeric glove20 is illustrated that can be placed on the hand of a user22. Theglove20 includes asubstrate body24 having the basic shape of the glove. Thesubstrate body24 can generally be formed from any of a variety of natural and/or synthetic elastomeric materials known in the art. For instance, some examples of suitable elastomeric materials include, but are not limited to, S-EB-S (styrene-ethylene-butylene-styrene) block copolymers, S-I-S (styrene-isoprene-styrene) block copolymers, S-B-S (styrene-butadiene-styrene) block copolymers, S-I (styrene-isoprene) block copolymers, S-B (styrene-butadiene) block copolymers, natural rubber latex, nitrile rubbers, isoprene rubbers, chloroprene rubbers, polyvinyl chlorides, silicone rubbers, and combinations thereof. Other suitable elastomeric materials that can be used to form thesubstrate body24 may be described in U.S. Pat. No. 6,306,514 to Weikel, et al., which is incorporated herein in its entirety by reference thereto for all purposes.

In one particular embodiment, the[0019]

substrate body

24 contains at least one elastomeric block copolymer. Some S-EB-S block copolymers and methods for forming solutions thereof are described in U.S. Pat. Nos. 5,112,900 to Buddenhagen, et al.; 5,407,715 to Buddenhagen, et al.; 5,900,452 to Plamthottam; and 6,288,159 to Plamthottam, which are incorporated herein in their entirety by reference thereto for all purposes.

The polystyrene end blocks of S-EB-S block copolymers utilized in the present invention typically have a weight average molecular weight of at least about 15,000 Daltons, and in some embodiments, from about 18,000 to about 20,000 Daltons. Moreover, the polystyrene end blocks of the block copolymers typically constitute from about 25% to about 35% by weight of the total weight of the S-EB-S polymer, which is generally from about 50,000 to about 300,000 Daltons. When utilizing such a weight average molecular weight of the polystyrene end blocks, the resulting elastomeric films can exhibit superior strength properties and have limited crack formation during drying and fusion.[0020]

If desired, mixtures of two or more S-EB-S copolymers may be utilized. In some instances, for example, two S-EB-S copolymers are utilized in which each block copolymer constitutes from about 40% to about 60% by weight of the mixture. In one embodiment, the first S-EB-S block copolymer has a solution viscosity of about 6500 cps at 25% by weight of copolymer in toluene (at 77° F.) and the second S-EB-S block copolymer has a solution viscosity of about 2000 cps at 10% by weight of copolymer in toluene (at 77° F.).[0021]

The use of S-EB-S block copolymer(s) in the[0022]

substrate body

24 can generally provide a number of benefits. For example, elastomers based upon the S-EB-S block elastomeric block copolymers are substantially resistant to attack by ozone or by other oxidative conditions. Moreover, the mechanical properties of the S-EB-S block copolymers may be selected to provide the desirable combination of tensile strength, elasticity, and tactility utilized in some applications. The structure, properties, and some applications of some S-EB-S elastomers are disclosed in U.S. Pat. Nos. 3,485,787; 3,830,767; 4,006,116; 4,039,629; 4,041,103; 4,386,179; 4,481,323; 4,511,354; and 4,613,640, which are incorporated herein in their entirety by reference thereto for all purposes.

Some commercially available examples of S-EB-S block copolymers, such as described above, include, but are not limited to, Kraton® G1650, Kraton® G1651, Kraton® G1652, which are available from Kraton Polymers of Houston, Tex. Kraton® G1650 is an S-EB-S block copolymer having a styrene/central block ratio of 28/72 and a Brookfield Viscosity in toluene solution (20% concentration by weight) at 77° F. of 1500 centipoise. Kraton® G1651 is an S-EB-S block copolymer having a styrene/central block ratio of 33/67 and a Brookfield Viscosity in toluene solution (20% concentration by weight) at 77° F. of 2000 centipoise. Kraton® G1652 is an S-EB-S block copolymer having a styrene/central block ratio of 29/71 and a Brookfield Viscosity in toluene solution (20% concentration by weight) at 77° F. of 550 centipoise.[0023]

The S-EB-S block copolymer(s) may optionally have end-block compatible resins added to the polystyrene end blocks. The added end-block compatible resin increases the glass transition temperature (T[0024]_g) of the S-EB-S block copolymer. The increased T_gallows the final products to be used at higher temperatures. For instance, one suitable example of such an end-block compatible resin is poly alpha methyl styrene.

A plasticizer (e.g., an oil) can also be mixed with the S-EB-S block copolymer(s) to enhance the resulting properties of the elastomeric article. For example, in one embodiment, the plasticizer can include a mineral oil, such as a refined petroleum paraffinic hydrocarbon oil, which is described in Entries 6971 and 6972 of the Merck Index, Eighth Edition. The plasticizer can generally be mixed with the S-EB-S block copolymers in any desired amount. For example, in some embodiments, the plasticizer comprises between about 30 to about 80 parts by weight of the total mass of the S-EB-S block copolymer(s).[0025]

Besides containing a plasticizer, the S-EB-S block copolymer(s) can also be mixed with a solvent. In particular, S-EB-S block copolymers are often provided as a solid. In such instances, a solvent can be utilized to enhance the ability of the copolymers to be used in a dipping process, as described in more detail below. Any solvent capable of dissolving one or more S-EB-S block copolymers can generally be used in the present invention. For example, some suitable solvents that can be used include toluene and cyclohexane. Once mixed with the copolymer(s), the ingredients can be mixed for a sufficient time to reach a homogeneous solution and then filtered to remove any undesired particulate matter.[0026]

Regardless of the particular material used to form the[0027]

substrate body

24 theglove20 also includes achemical protection layer36 that covers the outer surface of thesubstrate body24 during use. Thus, for example, thechemical protection layer36 can form an environment-exposedsurface21 of the glove, or can be positioned between thesubstrate body24 and an additional layer that forms the environment-exposedsurface21. Thechemical protection layer36 contains a modified silicone elastomer that is crosslinked to impart chemical resistance to theglove20. As used herein, the term “modified silicone” generally refers to a broad family of synthetic polymers that have a repeating silicon-oxygen backbone with organic groups attached to the backbone (pendant and/or terminating). For instance, some suitable silicones that can be used in the present invention include, but are not limited to, phenyl-modified silicones, vinyl-modified silicones, methyl-modified silicones, fluoro-modified silicones, alkyl-modified silicones, alkoxy-modified silicones, alkylamino-modified silicones, and combinations thereof.

Some suitable phenyl-modified silicones include, but are not limited to, dimethyldiphenylpolysiloxane copolymers; dimethyl, methylphenylpolysiloxane copolymers; polymethylphenylsiloxane; and methylphenyl, dimethylsiloxane copolymers. Phenyl modified silicones that have a relatively low phenyl content (less than about 50 mole %) may be particularly effective in the present invention. For example, the phenyl-modified silicone can be a diphenyl-modified silicone, such as a diphenylsiloxane-modified dimethylpolysiloxane.[0028]

For most applications, the phenyl-modified silicones contain phenyl units in an amount from about 0.5 mole % to about 50 mole %, in some embodiments in an amount less than about 25 mole %, and in some embodiments, in an amount less than about 15 mole %. In one particular embodiment, a diphenylsiloxane-modified dimethylpolysiloxane can be used that contains diphenylsiloxane units in an amount less than about 5 mole %, and particularly in an amount less than about 2 mole %. The diphenylsiloxane-modified dimethylpolysiloxane can be synthesized by reacting diphenylsiloxane with dimethylsiloxane.[0029]

As indicated above, fluoro-modified silicones can also be used in the present invention. For instance, one suitable fluoro-modified silicone that can be used is a trifluoropropyl modified polysiloxane, such as a trifluoropropylsiloxane modified dimethylpolysiloxane. A trifluoropropylsiloxane modified dimethylpolysiloxane can be synthesized by reacting methyl, 3,3,3 trifluoropropylsiloxane with dimethylsiloxane. The fluoro-modified silicones can contain from about 5 mole % to about 95 mole %, and in some embodiments, from about 40 mole % to about 60 mole % of fluoro groups, such as trifluoropropylsiloxane units. In one embodiment, a trifluoropropylsiloxane-modified dimethylpolysiloxane is used that contains 50 mole % trifluoropropylsiloxane units.[0030]

Besides the above-mentioned modified silicone elastomers, other modified silicone elastomers may also be utilized in the present invention. For instance, some suitable vinyl-modified silicones include, but are not limited to, vinyldimethyl terminated polydimethylsiloxanes; vinylmethyl, dimethylpolysiloxane copolymers; vinyldimethyl terminated vinylmethyl, dimethylpolysiloxane copolymers; divinylmethyl terminated polydimethylsiloxanes; polydimethylsiloxane, mono vinyl, mono n-butyldimethyl terminated; and vinylphenylmethyl terminated polydimethylsiloxanes. Further, some methyl-modified silicones that can be used include, but are not limited to, dimethylhydro terminated polydimethylsiloxanes; methylhydro, dimethylpolysiloxane copolymers; methylhydro terminated methyloctyl siloxane copolymers; and methylhydro, phenylmethyl siloxane copolymers.[0031]

The particular elastomers described above are meant to include hetero- or co-polymers formed from polymerization or copolymerization of dimethylsiloxane cyclics and diphenylsiloxane cyclics or trifluoropropylsiloxane cyclics with appropriate endcapping units. Thus, for example, the terms “diphenyl modified dimethylpolysiloxanes” and “copoloymers of diphenylpolysiloxane and dimethylpolysiloxane” may be used interchangeably.[0032]

If desired, the[0033]

chemical protection layer

36 can be formed from two or more separate components. When utilized, the separate components may contain the same or different types of modified silicone elastomers. For example, in one embodiment, thechemical protection layer36 contains two components, designated herein as part “A” and “B”. In one embodiment, part A contains a polydimethylsiloxane that is vinyl and methyl terminated. A platinum catalyst is also included that contains a complex of platinum with vinyl-containing oligosiloxanes (complex of platinum and divinyltetramethyldisiloxane with typical levels of active platinum of 5 to 50 parts per million). Part B is essentially identical to part A, except that it also includes a crosslinker and crosslinking inhibitor. The crosslinker can be, for example, polydimethylsiloxane with hydrogen on the siloxane chain, commonly called methyl hydrogen. The crosslinker concentration can vary from about 0.3 to about 4 parts per hundred parts of the mass of polydimethylsiloxane. The crosslinking inhibitor can, for example, contain an oligosiloxane with high concentration of vinyl-containing substituents of any of the class of compounds known as acetylinic alcohols. For example, one suitable crosslinking inhibitor is tetravinyl tetramethyl cyclotetrasiloxane. The inhibitor may be used in concentrations as low as 0.02 parts per hundred parts to as high as 0.5 parts per hundred parts. In forming theouter layer 36, parts A and B are mixed together prior to dipping in a 1:1 ratio by weight.

Some commercially available diphenyl modified dimethylsilicones, such as described above, can be obtained from NuSil Technologies under various trade names including MED 6400, MED 10-6400, MED 6600, MED 10-6600, MED 6640, and MED 10-6640. For example, the following Table provides some physical properties for MED 6400, MED 6600, and MED 6640.[0034]



MED 6400*	MED 6600*	MED 6640*

Viscosity, cP	600	300	7000
Solvent	Xylene	Xylene	Xylene
Solids Content	35	35	25
Cure System	Platinum-based	Platinum-based	Platinum-based

Other suitable modified silicone elastomers that can be used in the present invention are believed to be described in U.S. Pat. Nos. 4,309,557 to Compton, et al.; 6,136,039 to Kristonsson, et al.; 6,160,151 to Compton, et al.; 6,243,938 to Lubrecht; and WO 01/41700, which are incorporated herein in their entirety by reference thereto for all purposes. Moreover, the modified silicone elastomers used in the present invention may also contain fillers, such as reinforcing silica; processing aids; additives; pigments; and the like, as is conventional in the art.[0035]

The solids content and/or viscosity of the[0036]

chemical protection layer

36 can generally be varied to achieve the desired chemical resistance. For example, the modified silicone elastomer(s) used to form thechemical protection layer36 can have a solids content of between about 5% to about 40%, and in some embodiments, between about 10% to about 35%. To lower the solids content of a commercially available modified silicone elastomer, for example, additional amounts of solvent can be utilized. Further, the viscosity of the modified silicone elastomer(s) used to form thechemical protection layer36 can range from about 300 centipoise to about 7000 centipoise, and in some embodiments, from about 600 to about 4000 centipoise. By varying the solids content and/or viscosity of thechemical protection layer36, the presence of the modified silicone elastomer in the glove can be controlled. For example, to form a glove with a higher level of chemical resistance, the modified silicone elastomer used in such layer can have a relatively high solids content and viscosity so that a greater percentage of the silicone is incorporated into the layer during the forming process. The thickness of thechemical protection layer36 can also vary. For example, the thickness can range from about 0.001 millimeters to about 0.4 millimeters, in some embodiments, from about 0.01 millimeters to about 0.30 millimeters, and in some embodiments, from about 0.01 millimeters to about 0.20 millimeters.

Besides the[0037]

chemical protection layer

36 and thesubstrate body24 theglove20 can also contain other layers. For example, as shown in FIG. 2, theglove20 can contain acoating26 that contacts the body of the user22 during use. In this embodiment, thecoating26 includes a donninglayer30 overlying and contacting thesubstrate body24 and asurfactant layer32 overlying and contacting the donninglayer30.

The donning[0038]

layer

30 can contain any of a variety of different elastomeric polymers that are capable of facilitating donning of the glove. Some examples of suitable materials for the donninglayer30 include, but are not limited to, polybutadienes (e.g., syndiotactic 1,2 polybutadiene), polyurethanes, halogenated copolymers, and the like. For instance, in one embodiment, an unsaturated styrene-isoprene (SIS) having tri- or radial-blocks can be utilized. In some embodiments, the SIS block copolymer has a polystyrene end block content of from about 10% to about 20% by weight, and particularly from about 15% to about 18% by weight, of the total weight of the SIS block copolymer. Moreover, the molecular weight of the polystyrene end blocks is typically at least about 5,000 grams per mole. Some examples of suitable mid-block unsaturated SIS block copolymers include, but are not limited to, Kraton® D1107 available from Kraton Polymers and Vector® 511 and Vector® 4111 available from Dexco Polymers of Houston, Tex.

Another suitable donning material is 1,2 polybutadiene (e.g., syndiotactic 1,2 polybutadiene). In one embodiment, for example, the donning[0039]

layer

30 is formed from a solution that contains from about 2% to about 7% by weight, and particularly from about 3% to about 4% by weight of 1,2 polybutadiene in a solvent (e.g., toluene). For instance, one suitable example of a polybutadiene material that can be dissolved in toluene to form a coating solution is “COMPATIBAG”, which is available from Presto Products of Appleton, Wis. and contains syndiotactic 1,2 polybutadiene. The 1,2 polybutadiene can also be formed as an emulsion to be applied as the donninglayer30. In some embodiments, for example, the emulsion contains from about 5% to about 14% by weight, and particularly about 9% by weight of 1,2 polybutadiene in a surfactant mixture. In one embodiment, the surfactant mixture is sodium dioctyl sulfosuccinate in an amount from about 10 phr (parts per hundred rubber) to about 100 phr, and particularly 40 phr in water. Pre-dispersion can be achieved by dispersing the surfactant mixture and 1,2 polybutadiene solution using a mixer, such as a high shear mixture. In one embodiment, the pre-dispersion is then mixed for about 5 minutes in a rotor/stator (such as a Ross X Series) mixer to generate an average particle size of less than about 1 micrometer. The resulting emulsion can then be filtered and the solvent can be removed by vacuum distillation.

In addition, polyurethanes may also be utilized as a donning material. For example, in one embodiment, Hyslip 20022 (available from Noveon, Inc.) can be utilized. Hyslip 20022 contains 1-methyl-2-pyrrolidone and waterborne polyurethane. Other examples of donning materials that can be utilized in the donning[0040]

layer

30 may be described in U.S. Pat. No. 5,792,531 to Littleton, et al., which is incorporated herein in its entirety by reference thereto for all purposes.

A[0041]

lubricant layer

32 can also overly the donninglayer30 to aid in donning the article when the user's body is either wet or dry. Thelubricant layer32, for example, can include a cationic (e.g., cetyl pyridinium chloride), an anionic (e.g., sodium lauryl sulfate), or a nonionic surfactant. For instance, in one embodiment, thelubricant layer32 contains a quaternary ammonium compound, such as Verisoft BTMS (available from Goldschmidt Chemical Corp. of Dublin, Ohio) and a silicone emulsion (AF-60) obtained from General Electric Silicone. Verisoft BTMS contains behnyl trimethyl sulfate and cetyl alcohol, while AF-60 contains polydimethylsiloxane, acetylaldehyde, and small percentages of emulsifiers. In another embodiment, thelubricant layer32 contains a medical-grade silicone such as Dow Corning 365 silicone, which is believed to contain water, polydimethylsiloxane, octylphenoxy polyethoxy ethanol, propylene glycol, and polyethylene glycol sorbitan monolaurate.

Further, besides the above-mentioned layers, the[0042]

glove

20 can also contain additional layers if desired. For example, in one embodiment, theglove20 contains alayer37 that defines an environment-exposedsurface21 of theglove20. Although optional, thelayer37 can be utilized to inhibit blocking between the layers and to facilitate stripping of theglove20 from a former. For example, in one embodiment, thelayer37 can contain styrene-polybutadiene-styrene (S-B-S) or a polyurethane material. It should also be understood, however, that thechemical protection layer36 can define the environment-exposedsurface21 of theglove20. In such instances, thelayer37 may or may not be positioned between thechemical protection layer36 and thesubstrate body24.

An elastomeric article made in accordance with the present invention can generally be formed using a variety of processes known in the art. In fact, any process capable of making an elastomeric article can be utilized in the present invention. For example, elastomeric article formation techniques can utilize dipping, spraying, chlorination, drying, curing, as well as any other technique known in the art. In this regard, referring to FIG. 3, one embodiment of a method of dip forming a glove will now be described in more detail. Although a batch process is described and shown herein, it should be understood that semi-batch and continuous processes may also be utilized in the present invention.[0043]

Initially, any well-known former, such as formers made from metals, ceramics, or plastics, is provided. Although glove-shaped formers are described herein, it should also be understood that formers having any other shape (e.g., condom-shaped) can be used in accordance with the present invention to form articles having different shapes. The former is dipped into a dip tank containing the modified silicone elastomer and solvent, such as xylene, water, etc. (illustrated as numeral[0044]62). A high shear mixer is utilized for a sufficient time to reach a homogeneous solution prior to dipping. After dipping, the former is removed slowly from the dip tank, leaving a thin, uniform layer of the liquid silicone elastomer solution deposited onto the former. Once removed from the dip tank, the modified silicone-coated former is then dried to remove the solvent from the coating (illustrated as numeral64). For example, in some embodiments, the modified silicone-coated former can be air dried at a temperature of from about 100° F. to about 240° F.

Once dried, the former is then transferred to a curing station (e.g., oven) where the modified silicone is cured (illustrated as numeral[0045]66). The curing station heats the modified silicone-coated former to a temperature sufficient to achieve the desired level of crosslinking. For example, in some embodiments, the curing station heats the modified silicone-coated former to a temperature ranging from about 200° F. to about 400° F., and in some embodiments, from about 200° F. to about 350° F. It should be understood that the curing station may also be used to remove solvent from thechemical protection layer36. In such instances, the modified silicone-coated former may not be dried before being transferred to the curing station. For example, the oven may be divided into two different zones with a former being conveyed through the zones of increasing temperature. One example is an oven having two zones with the first zone being dedicated primarily to drying and the second zone being dedicated primarily to curing. For example, the first zone can heat the former to about 220° F. and the second zone can heat the former to about 350° F. When heated, the catalyst and crosslinking agent contained in the modified silicone coating of the former are used to crosslink the silicone by forming a bridge between silicone chains.

The dipping procedure is repeated as necessary so that the[0046]

chemical protection layer

36 has the desired thickness. By way of example, thechemical protection layer36 of a glove produced by dip forming can have a thickness of from about 0.01 millimeters to about 0.20 millimeters.

After the[0047]

chemical protection layer

36 is formed, the entire former is then dipped into a dip tank containing the elastomeric polymer(s) used to form the substrate body24 (illustrated as numeral68). In one embodiment, for example, the former is dipped into a dip tank that contains at least one styrene-ethylene-butylene-styrene (S-EB-S) block copolymer, mineral oil, and a mutual solvent (e.g., toluene). The former is dipped into a liquid solution of the elastomer a sufficient number of times to build up the desired thickness on the form. By way of example, thesubstrate body24 can have a thickness of from about 0.004 to about 0.012 inches. The glove is then allowed to dry. Methods for dip-forming S-EB-S layers are described in more detail in U.S. Pat. Nos. 5,112,900 to Buddenhagen, et al. and 5,407,715 to Buddenhagen, et al.

The glove former is then dipped into a solution to form the donning[0048]

layer

30 of the glove (illustrated as numeral70). In one embodiment, for example, the glove former is dipped into a solution of 1,2 syndiotactic polybutadiene and toluene. The glove is then dried. Once the body of the glove is formed, such as described above, a bead roll station (not shown) can, in some embodiments, be utilized to impart a cuff to the glove. For instance, the bead roll station can contain one or more bead rolls such that the former is indexed therethrough to be provided with cuffs. The formers may then be transferred to a stripping station (not shown). The stripping station can involve automatic or manual removal of the gloves from the formers. For example, in one embodiment, the gloves are manually removed from each former by turning each glove inside-out as it is stripped from its corresponding former.

After being stripped, the gloves can then be chlorinated, if desired, using any known chlorination technique, such as described in U.S. Pat. No. 5,792,531 to Littleton, et al. (illustrated as numeral[0049]72). Upon chlorination, a lubricant can also be applied to the donning surface of the glove (illustrated as numeral74). Specifically, the lubricant is applied to the donning surface of the glove using a sponge during a tumbling process. The glove is then dried in a hot air dryer.

Although various constructions and techniques for forming elastomeric articles have been described above, it should be understood that the present invention is not limited to any particular construction or technique for forming the article. For example, the layers described above may not be utilized in all instances. Additionally, other layers not specifically referred to above may be utilized in the present invention. Furthermore, the present invention is also not limited to any particular type of elastomeric article. For instance, condoms, flexible automotive hoses, and the like, may all be formed in accordance with the present invention with improved chemical resistance.[0050]

The present invention may be better understood with reference to the following example.[0051]

EXAMPLE

The ability of an elastomeric article to be imparted with chemical resistance in accordance with the present invention was demonstrated. Initially, a glove-shaped former was dipped into a tank containing MED 10-6640, a modified silicone elastomer available from NuSil Technologies. After dipping, the former was removed from the silicone dip tank and allowed to dry in air at a temperature of 220° F. to remove the solvent therefrom. Once dried, the modified silicone-coated former was then transferred to an oven, where it was crosslinked at a temperature of 350° F. The resulting modified silicone layer had a thickness of about 0.10 millimeters.[0052]

Upon forming the modified silicone layer, the former was then dipped into a dip tank that contained an S-EB-S composition. Specifically, the S-EB-S composition contained 50% by weight Kraton® 1650 and 50% by weight Kraton® 1651. The S-EB-S composition was combined with mineral oil (67 parts per hundred rubber) and then dissolved in toluene so that the resulting solids content was about 20%. After dipping, the former was removed from the S-EB-S composition and dried in air at a temperature of 220° F. The thickness of the resulting glove was 0.27 millimeters.[0053]

Various glove samples formed in the manner described above were then tested to determine the chemical resistance of the glove. The solvents utilized to test the samples are set forth below in Table 1.[0054]

TABLE 1


Solvents Tested

Type	Trade Name	Manufacturer

Bone Cement	PALACOS R RADIOPAQUE¹	Biomet Orthopedics
		(Washaw, Indiana)
	PALACOS R RADIOPAQUE²	Biomet Orthopedics
		(Washaw, Indiana)
Glue	SUPER GLUE	Elmer's Products
		(Columbus, Ohio)
	KRAZY GLUE	Elmer's Products
		(Columbus, Ohio)
	SUREHOLD PLASTIC	Surehold, Inc.
	SURGERY	(Chicago, Illinois)
Tissue Adhesive	GLUSTITCH	Glustitch, Inc.
		(Delta, British
		Columbia, Canada)
	DERMABOND³	Ethicon, Inc.
		(Somerville,
		New Jersey)

For each solvent tested, a glove was first donned on one hand. The solvent was placed between the thumb, index, and middle finger, and a sweeping motion was then made for about 5 minutes (for bone cement) and about 10 minutes (for glue and tissue adhesive) with the thumb over the fingers. During the test period, the glove was visually inspected for irregularities, such as evidence of granular rubber particles, splits, cracks, dissolved rubber, increase in tackiness, discoloration, and the like. In addition to the above-mentioned test, an additional test was also conducted for the samples applied with glue and tissue adhesive. Specifically, a drop of the respective solvent was placed on each sample. The glove was then stretched in the location where the solvent was applied. After[0055]24 hours, the glove was again stretched in the same location.

Upon inspection, no irregularities were visually observed in any of the glove samples tested.[0056]

While the invention has been described in detail with respect to the specific embodiments thereof, it will be appreciated that those skilled in the art, upon attaining an understanding of the foregoing, may readily conceive of alterations to, variations of, and equivalents to these embodiments. Accordingly, the scope of the present invention should be assessed as that of the appended claims and any equivalents thereto.[0057]