Emission of phthalates from PVC and other materials

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Abstract
The main objective of this study was to generate quantitative and qualitative emission data on phthalates from different materials. To achieve this the existing (Chamber for Laboratory Investigations of Materials, Pollution and Air Quality) Climpaq-based procedure for simplified measurements of emissions of plasticizer from PVC and other plasticized materials was modified. It was applied to a range of products. Some of them were suspected of contributing to the indoor concentration of plasticizers. The emissions from PVC flooring, polyolefine flooring, a refrigerator list, two electric cables, PVC skirting and floor wax were studied in separate Climpaqs. The emission from the PVC flooring in the Climpaq was compared with results from the ultra-small chamber Field and Laboratory Emission Cell (FLEC). Sampling and analysis methods were optimized to measure plasticizers. Samples were taken in exhaust air from the chambers after 6, 35, 62, 105, and 150 days from the start of the experiment. PVC flooring was tested for an additional 100 days. Polyolefine covered with wax resulted in an air concentration of 22 microg/m3 of dibutylphthalate (DBP), which is two orders of magnitude larger than any other materials, but did not emit di(2-ethylhexyl)phthalate (DEHP). The other materials resulted in max concentration of approximately 1 microg/m3 of DEHP and low emissions of DBP. The concentration of DEHP in each chamber increased slowly to a rather stable level which was reached after 150 days. DBP concentrations in the chambers with PVC skirting, PVC flooring, polyolefine and floor wax reached their quasi-static equilibrium after 60 days. The modified method did not create sufficient data for the calculation of emission rates. Adsorption of emission on chamber surfaces made it impossible to use the first part of the experiment for emission rate calculation. When the concentration had stabilized, it was found to be almost identical and independent of chamber and ventilation rate. Emission rates were reduced at high concentrations probably because the concentration in the material was near equilibrium with the concentration in the chamber air.