DuPont™ Neoprene W, WM1, WHV 100, WHV - RT Vanderbilt ...

DuPont™ Neoprene W, WM1, WHV 100, WHV - RT Vanderbilt ... DuPont™ Neoprene W, WM1, WHV 100, WHV - RT Vanderbilt ...

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Processing and Performance Features* Resists Mechanical Breakdown The molecular weight of DuPont Neoprene W, W M1, WHV 100, and WHV does not decrease under mechanical shear or with chemical peptization. However, some reduction in viscosity may occur under high shear conditions. The degree of softening is greater for Neoprene WHV and WHV 100 which are higher molecular weight polymers. Compounds of Neoprene W, W M1, WHV 100 and WHV mix faster, have better mill release, and yield extrudates that are more resistant to distortion than do compounds of Neoprene GNA or GRT. Broad Compounding Latitude The wide range of viscosity available with these four polymers makes it possible to accommodate virtually any desired loading of fillers and plasticizers while still maintaining workable compound viscosity. Because cure accelerators must be used with these types to achieve practical cure rates, processing safety and cure rate can be varied to suit processing requirements. Optimum Heat and Compression Set Resistance Neoprene W, W M1, WHV 100 and WHV can be compounded to provide the best resistance to heat aging and lowest compression set of any Neoprene grades. *For information on general characteristics of the Neoprene W family and the relationship of Neoprene W, W M1, WHV 100 and WHV to other types of Neoprene, see bulletins “The Neoprene W Family,” “Selection Guide for Neoprene,” and “Types of Neoprene.” Handling Precautions DuPont is not aware of any unusual health hazards associated with Neoprene W, W M1, WHV 100, or WHV. However, routine industrial hygiene practices are recommended to avoid such conditions as dust buildup or static charges. For additional information, read DuPont reference “Guide for Safety and Handling and FDA Status of Neoprene Solid Polymers” and observe the precautions noted therein. The compounding ingredients used with Neoprene W, W M1, WHV 100, or WHV to prepare finished products may present hazards in handling and use. Before proceeding with any compounding work, consult and follow label directions and handling precautions from suppliers of all ingredients. Information on European Union Dangerous Preparations Directive 1999/45/EC related to Colophony Skin Sensitization Colophony is classified as a skin contact sensitizer under European Union Dangerous Preparations Directive 1999/45/EC effective July 30, 2002. This Directive requires labeling of products that contain colophony at levels equal to or greater than 0.1% (refer to the Directives for specific details). Solid (dry type) Neoprene adhesive grade products manufactured by DuPont contain about 4% colophony (CAS No. 8050-09-7). Toxicological tests have demonstrated that dry Neoprene is not a skin sensitizer. Because of this testing, dry Neoprene polymer is not subject to mandatory labeling under the above Directive despite the presence of the colophony. However, when these Neoprene adhesive grade products are dissolved in organic solvents, the colophony may still be present at concentrations up to 0.8% depending on the solids content of the solutions. In the absence of data showing the adhesive is not a skin sensitizer, the adhesive could be subject to the above EU regulation. It is recommended that manufacturers and marketers of adhesive solutions containing DuPont (dry type) adhesive grade products determine whether the colophony level is above 0.1%. If the manufactured preparation has a colophony content of less than 0.1% it will not be subject to mandatory labeling (provided no other constituents necessitate mandatory labeling). Manufactured preparations that contain higher colophony contents will require the labeling and/or container notices described in the Directive.

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Processing and Performance Features*<br />

Resists Mechanical Breakdown<br />

The molecular weight of DuPont <strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong>, and <strong>WHV</strong> does not decrease under<br />

mechanical shear or with chemical peptization. However, some reduction in viscosity may occur under<br />

high shear conditions. The degree of softening is greater for <strong>Neoprene</strong> <strong>WHV</strong> and <strong>WHV</strong> <strong>100</strong> which are<br />

higher molecular weight polymers.<br />

Compounds of <strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong> and <strong>WHV</strong> mix faster, have better mill release, and yield<br />

extrudates that are more resistant to distortion than do compounds of <strong>Neoprene</strong> GNA or G<strong>RT</strong>.<br />

Broad Compounding Latitude<br />

The wide range of viscosity available with these four polymers makes it possible to accommodate virtually<br />

any desired loading of fillers and plasticizers while still maintaining workable compound viscosity.<br />

Because cure accelerators must be used with these types to achieve practical cure rates, processing<br />

safety and cure rate can be varied to suit processing requirements.<br />

Optimum Heat and Compression Set Resistance<br />

<strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong> and <strong>WHV</strong> can be compounded to provide the best resistance to heat<br />

aging and lowest compression set of any <strong>Neoprene</strong> grades.<br />

*For information on general characteristics of the <strong>Neoprene</strong> W family and the relationship of <strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong> and <strong>WHV</strong> to other types of<br />

<strong>Neoprene</strong>, see bulletins “The <strong>Neoprene</strong> W Family,” “Selection Guide for <strong>Neoprene</strong>,” and “Types of <strong>Neoprene</strong>.”<br />

Handling Precautions<br />

DuPont is not aware of any unusual health hazards associated with <strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong>, or<br />

<strong>WHV</strong>. However, routine industrial hygiene practices are recommended to avoid such conditions as dust<br />

buildup or static charges. For additional information, read DuPont reference “Guide for Safety and<br />

Handling and FDA Status of <strong>Neoprene</strong> Solid Polymers” and observe the precautions noted therein.<br />

The compounding ingredients used with <strong>Neoprene</strong> W, W M1, <strong>WHV</strong> <strong>100</strong>, or <strong>WHV</strong> to prepare finished<br />

products may present hazards in handling and use. Before proceeding with any compounding work,<br />

consult and follow label directions and handling precautions from suppliers of all ingredients.<br />

Information on European Union Dangerous Preparations Directive 1999/45/EC related to<br />

Colophony Skin Sensitization<br />

Colophony is classified as a skin contact sensitizer under European Union Dangerous Preparations<br />

Directive 1999/45/EC effective July 30, 2002. This Directive requires labeling of products that contain<br />

colophony at levels equal to or greater than 0.1% (refer to the Directives for specific details). Solid<br />

(dry type) <strong>Neoprene</strong> adhesive grade products manufactured by DuPont contain about 4% colophony<br />

(CAS No. 8050-09-7). Toxicological tests have demonstrated that dry <strong>Neoprene</strong> is not a skin sensitizer.<br />

Because of this testing, dry <strong>Neoprene</strong> polymer is not subject to mandatory labeling under the above<br />

Directive despite the presence of the colophony. However, when these <strong>Neoprene</strong> adhesive grade<br />

products are dissolved in organic solvents, the colophony may still be present at concentrations up to<br />

0.8% depending on the solids content of the solutions. In the absence of data showing the adhesive is not<br />

a skin sensitizer, the adhesive could be subject to the above EU regulation.<br />

It is recommended that manufacturers and marketers of adhesive solutions containing DuPont (dry type)<br />

adhesive grade products determine whether the colophony level is above 0.1%. If the manufactured<br />

preparation has a colophony content of less than 0.1% it will not be subject to mandatory labeling<br />

(provided no other constituents necessitate mandatory labeling). Manufactured preparations that contain<br />

higher colophony contents will require the labeling and/or container notices described in the Directive.

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