PRINTER FRIENDLY VERSION

Hydrogenated Nitrile.

ASTM D1418 Designation: HNBR

ASTM D 2000, SAE J200 Type / Class: DH

RELATIVE COST: High

GENERAL TEMPERATURE RANGE: -25° to +300° F

 

Though the double bonds within nitrile’s butadiene segments are needed for cross-linking, they are also the predominant attack sites for heat, chemicals, and oxidation. As part of an ongoing effort to engineer more resistant compounds, a different class of nitrile was developed in the 1980s. Initially known as highly saturated nitrile (HSN), this class is now more commonly called hydrogenated nitrile butadiene rubber (HNBR), or just hydrogenated nitrile (see Figure 36).

Hydrogenated nitrile results from the hydrogenation of standard nitrile. Hydrogenation is the process of adding hydrogen atoms to the butadiene segments. Adding hydrogen greatly reduces the number of carbon-to-carbon double bonds that would otherwise be weak links in the polymer chain. Why are double bonds weak? It stems from valence, or the ability of an atom to form one or more energy bonds with neighboring atoms. A carbon atom can form four distinct covalent bonds. Because carbon has this valence of four, it is most “satisfied” when it has actually formed four single bonds (a state known as saturation) rather than two single bonds and a double bond. A satisfied, saturated atom is more stable, so a compound composed largely of saturated carbons is less reactive and more resistant to chemical attack.

As shown in Figure 36, HNBR’s main chain is primarily composed of highly saturated hydrocarbons and acrylonitrile (ACN). Thanks to their saturation, the hydrocarbon segments impart heat, chemical, and ozone resistance. On the down side, increased hydrogenation also leads to decreased low temperature elasticity. As with standard nitrile, the ACN content of HNBR imparts toughness, as well as fuel and oil resistance. This ACN content can be modified for specific uses. There are also a few remaining unsaturated butadiene segments (typically well under 10%) to facilitate peroxide curing or, in some instances, sulfur vulcanization. Peroxide-cured HNBR has improved thermal properties and will not continue to vulcanize like sulfur-cured nitriles.

HNBR is used in automotive air conditioning systems where R134a refrigerant gas has replaced the chlorofluorocarbon (CFC)-containing R12 refrigerant. HNBR is used in fuel parts due to its increased resistance to sour gasoline and ozone. It is used in engine applications because of its resistance to elevated temperatures and oil additives.

HNBR has excellent abrasion resistance, making it a viable alternative to fluoroelastomers (FKM). HNBR also has better low temperature properties and tear resistance than FKM.

HNBR PERFORMS WELL IN:
Petroleum oils & fuels
Silicone oils & greases
Water & steam (up to 300° F/149° C)
Ozone

HNBR DOES NOT PERFORM WELL IN:
Chlorinated hydrocarbons
Polar solvents (esters & ketones)
Strong acids

 

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“As part of an ongoing effort to engineer more resistant compounds, a different class of nitrile was developed in the 1980s.”

 


Figure 36