Today’s cleanroom environments in the pharmaceutical and semiconductor markets require the highest level of material performance across a broad spectrum of requirements. New, sophisticated medicines are made using advanced manufacturing technologies and materials. High technology cleanroom environments often contain polymeric sheets, coatings, wall coverings, and polymeric foam for insulation. These are used to create lightweight structures, walls, partitions, ceilings, and pipe and ducting insulation.

In general, fluoropolymers and, in particular, films, coatings, and insulating foams made from polyvinylidene fluoride (PVDF) do not support the growth of mold. Covering exposed surfaces with PVDF polymer provides a high-purity “inert” surface which does not support the growth of microorganisms and provides the resistance needed to withstand the harsh chemicals used for cleaning and sterilization. Fluoropolymer-based paints and solution coatings offer another option for cleanroom designers because these coatings resist fungal growth as well.

Fungal and microbial growth resistance is very important in cleanroom environments, but also important are fire resistance and low smoke generation, low moisture absorption, insulating properties, abrasion resistance, and non-shedding properties to prevent the introduction of contaminants into the manufacturing process.

ANTIFUNGAL PROPERTIES
Low surface energy makes it difficult for mold to grow on the surface of foam insulation. Tested according to ASTM G21-96 (2002), Standard Practice for Determining Resistance of Synthetic Polymeric Materials to Fungi, such foams showed no observed growth after the required 28-day exposure. This resultwas also confirmed by microscopic examination.

Pure synthetic polymers are usually fungus-resistant because they offer no carbon source for the growth of fungi. Unfortunately, polymer additives such as plasticizers, cellulosics, lubricants, stabilizers, and colorants often permit fungal attack of plastic materials. PVDF contains no plasticizers or other process additives, is inherently very pure, hydrophobic, and resists microbial attack, even under conditions favorable for such attack, namely, temperatures from 2–38 °C (35–100 °F)and relative humidity from 60 to 100%.

Table 1 shows the organisms that were used for the testing.

FIRE RESISTANCE
Today’s pharmaceutical companies have large investments in development, testing, FDA approval, and production of drugs. Even slight delays in production can result in financial losses. The financial impact of fire or smoke damageto a manufacturing facility can be very significant.

In order to limit the risk due to fire and smoke, Factory Mutual (FM), Underwriters Laboratories (UL), ASTM, and other testing agencies have developed fire-testing methods to characterize the fire performance of materials. For cleanroom materials, FM has established a fire and smoke standard called FM 4910 (Cleanroom Materials Flammability Test Protocol). This standard was developed to reduce the risk of fire and the resultant financial impact should one occur.

Many polymeric materials will readily burn, provide fuel to a fire, and produce large amounts of smoke. However, PVDF is inherently flame retardant without additives.