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The overall persistence, Pov, has been suggested as an indicator that integrates single media half-lives and phase partitioning. However, the application of this indicator is hindered by the fact that there are different definitions of Pov and that the most common measure of Pov, the residence time at steady state, depends heavily on the release pattern. Here, different measures are compared that can be used to compute Pov from the mass of a chemical in the environment as a function of time in a dynamic multimedia model. These measures include the equivalence width, which corresponds to the residence time at steady state, the mean value of the function of mass vs time ("mean time"), and the clearance time. The temporal remote state is defined as the state of the model system long after the stop of emissions; it is independent of the release pattern of a chemical. The mean time in the temporal remote state reflects the long-term removal rate of a chemical and is used as a persistence benchmark. Correlations of the three measures of Pov to the persistence benchmark are analyzed. The maximum equivalence width, which is obtained with release to one of the media air, water, or soil, is a good approximation of the mean time in the temporal remote state. Because the maximum equivalence width is identical to the maximum residence time at steady state, the mean time in the temporal remote state can be estimated with existing steady-state models.  相似文献   
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We propose a multimedia model-based methodology to evaluate whether a chemical substance qualifies as POP-like based on overall persistence (Pov) and potential for long-range transport (LRTP). It relies upon screening chemicals against the Pov and LRTP characteristics of selected reference chemicals with well-established environmental fates. Results indicate that chemicals of high and low concern in terms of persistence and long-range transport can be consistently identified by eight contemporary multimedia models using the proposed methodology. Model results for three hypothetical chemicals illustrate that the model-based classification of chemicals according to Pov and LRTP is not always consistent with the single-media half-life approach proposed by the UNEP Stockholm Convention and thatthe models provide additional insight into the likely long-term hazards associated with chemicals in the environment. We suggest this model-based classification method be adopted as a complement to screening against defined half-life criteria at the initial stages of tiered assessments designed to identify POP-like chemicals and to prioritize further environmental fate studies for new and existing chemicals.  相似文献   
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Simultaneous Hall and conductivity measurements have been performed on sputtered polycrystalline thin films and on bulk ceramic specimens of nearly stoichiometric CeO2 in the temperature range between 900° and 1040°C. The measurements have been performed in air using low-frequency alternating current. In the case of the bulk ceramic specimens, an upper limit for the carrier mobility of ≤0.2 cm2/(V·s) has been obtained, which is in accordance with data from the literature for bulk samples. The conductivity of the thin films (l/1Ω·m) at 1000°C) is in accordance with data from the literature for bulk ceramics. The carrier density derived from the Hall measurements (3 × 1016/cm3 at 1000°C) increases with increasing temperature, whereas the Hall mobility (4 cm2(V·s) at 1000°C) decreases with increasing temperature. These values differ from literature data for bulk ceramic specimens. The difference may be duelo the small grain diameters (∼200 nm) in the 1-μm-thick thin films.  相似文献   
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Simultaneous Hall and conductivity measurements were performed in situ between 650° and 1050°C on n-type semiconducting BaSnO3ceramics. The variation of the Hall mobility and the Hall carrier density as a function of oxygen partial pressure between 102 and 105 Pa and of temperature was investigated. At temperatures below 900°C the conductivity exhibits a dependence on temperature and oxygen partial pressure which is mainly determined by variations of the Hall mobility. Above 900°C most of the significant dependence is due to a variation in carrier density. Furthermore, a simple defect model assuming doubly ionized oxygen vacancies and acceptor impurities is discussed for BaSnO3.  相似文献   
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