Gestational
exposure to environmental chemicals and subsequent
permeation through the placental barrier represents potential health
risks to both pregnant women and their fetuses. In the present study,
we explored prenatal exposure to a suite of 46 emerging plasticizers
and synthetic antioxidants (including five transformation products
of 2,6-di-tert-butyl-4-hydroxytoluene, BHT) and their
potency to cross human placenta based on a total of 109 maternal and
cord serum pairs. Most of these chemicals have rarely or never been
investigated for prenatal exposure and associated health risks. Eleven
of them exhibited detection frequency greater than 50% in maternal
blood, including dibutyl fumarate (DBF), 2,6-di-tert-butylphenol (2,4-DtBP), 1,3-diphenylguanidine (DPG),
methyl-2-(benzoyl)benzoate (MBB), triethyl citrate (TEC), BHT, and
its five metabolites, with a median concentration from 0.05 to 3.1
ng/mL. The transplacental transfer efficiency (TTE) was determined
for selected chemicals with valid measurements in more than 10 maternal/cord
blood pairs, and the mean TTEs exhibited a large variation (i.e.,
0.29–2.14) between chemicals. The determined TTEs for some
of the target chemicals were comparable to the predicted values by
our previously proposed models developed from molecular descriptors,
indicating that their transplacental transfer potency could be largely
affected by physicochemical properties and molecular structures. However,
additional biological and physiological factors may influence the
potency of environmental chemicals to cross human placenta. Overall,
our study findings raise concern on human exposure to an increasing
list of plastic additives during critical life stages (e.g., pregnancy)
and potential health risks.
Compared with V 2 O 5 −WO 3 /TiO 2 , the ceria catalyst supported on sulfated zirconia (referred to as CeSZ) shows a superior alkali resistance for selective catalytic reduction of NO in flue gases. It reveals an unexpected result that a moderate amount of potassium (normally considered as SCR poisons) could even enhance the activity of CeSZ catalyst. To investigate this exceptional phenomenon, we studied the surface acid−base properties of CeSZ catalysts with different amounts of K and their influences on SCR performances. Although K resulted in a sharp decrease in Brønsted acid sites, the total acidity, especially strong acidity, barely changed when K/Ce was less than 0.4. It was proposed that a small amount of potassium could initially alter some Brønsted acid sites to Lewis ones, therefore retaining the majority of total acidity. Moreover, increased surface basicity due to K depositing led to an enhancement in NO chemisorption and oxidation, which is beneficial to the SCR process via the reaction of NO 2 and NO x ad-species with adsorbed NH 3 species. This explains why the SCR catalytic activity was improved at lower temperature for CeSZ catalysts after K depositing. Therefore, the catalytic activity and reaction temperature window of CeSZ catalyst could be controlled by simply tuning the surface acid/base sites, which may give some inspiration to improve the catalytic activity and poisoning tolerance.
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