Ongwandee Maneerat, Morrison Glenn C
Missouri University of Science & Technology, MO, USA.
Environ Sci Technol. 2008 Aug 1;42(15):5415-20. doi: 10.1021/es071935j.
Sorptive interactions with indoor surfaces strongly influence indoor exposure to organic pollutants. Adsorption itself may be influenced by indoor levels of common indoor gases such as CO2, NH3, and H2O. We quantified sorption characteristics of trimethylamine (TMA) on carpet and painted wallboard, while challenging the surface with gas-phase CO2, NH3 and H2O. We show that the capacity of the carpet to sorb TMA, doubles when the CO2 mixing ratio is increased from 0 to 1000 ppm CO2 at 90% relative humidity. In contrast, NH3 decreases the surface capacity of both carpet and latex paint. Sorption of TMA to these indoor materials is primarily caused by interactions at one or more interfaces. Dissolution of TMA and aqueous acid-base chemistry appear to also contribute to the overall sorptive capacity of carpet at high relative humidity. The reduction in the distribution coefficient, k(e), in the presence of NH3 is explained by competition between TMA and NH3 molecules for sites on the substrates at low-to-medium relative humidity conditions.
与室内表面的吸附相互作用强烈影响室内对有机污染物的暴露。吸附本身可能受到常见室内气体如二氧化碳、氨气和水的室内浓度的影响。我们量化了三甲胺(TMA)在地毯和涂漆墙板上的吸附特性,同时用气相二氧化碳、氨气和水对表面进行挑战。我们表明,在90%相对湿度下,当二氧化碳混合比从0增加到1000 ppm时,地毯吸附TMA的能力会加倍。相比之下,氨气会降低地毯和乳胶漆的表面吸附能力。TMA对这些室内材料的吸附主要是由一个或多个界面处的相互作用引起的。在高相对湿度下,TMA的溶解和酸碱水相化学似乎也对地毯的整体吸附能力有贡献。在低至中等相对湿度条件下,TMA和氨气分子在底物上争夺位点,这解释了在氨气存在下分配系数k(e)的降低。