Notes

[Research on the reputation as well as risks associated with monitor direct exposure in youngsters beneath several years involving age].
Three kinds of legacy brominated flame retardants (BFRs), including eight polybrominated diphenyl ether (PBDE) congeners, tetrabromobisphenol A (TBBPA), and three hexabromocyclododecane (HBCDD) isomers, were analyzed in 105 human milk samples collected in 2018 from Beijing, China. The tested BFRs all showed high detection frequencies, and HBCDD was the most abundant BFR, with a median level of 7.64 × 103 pg/g lipid, followed by BDE-153 (389 pg/g lipid), BDE-209 (283 pg/g lipid), and TBBPA (271 pg/g lipid). By comparing the results of the present study with those of our previous Beijing human milk surveys conducted in 2014 and 2011, the contamination of TBBPA and HBCDD increased steadily from 2011 to 2018, whereas that of PBDEs decreased sharply during this period. Our results suggested that the production and consumption of BFRs in China have shifted from PBDEs to other FRs. Education level and the consumption of animal-derived foods such as eggs and meat were identified as major influencing factors for some BFRs. For nursing infants, the median levels of lower bound BFR daily intake via human milk ingestion ranged from 4.62 × 10-2 ng/kg bw/day for BDE-154 to 30.6 ng/kg bw/day for HBCDD. The daily intake of most BFRs by breastfeeding is unlikely to pose significant health risks for Beijing nursing infants. However, the minimum margin of exposure (MOE) of HBCDD was below its threshold value, which indicated that its daily intake might raise health concerns for some breastfed infants.Metal exposures are ubiquitous around the world, while it is lack of prospective studies to evaluate the associations of exposure to multiple metal/metalloids with incident dyslipidemia. A total of 2947 participants without dyslipidemia at baseline were included in the analyses. We utilized inductively coupled plasma mass spectrometry to measure the baseline plasma metal concentrations. Unconditional logistic regression models were applied to estimate the relations between plasma metals and risk of incident dyslipidemia, and principal component analysis was performed to extract principal components of metals. During 5.01 ± 0.31 years of follow-up, 521 subjects were diagnosed with incident dyslipidemia. After multivariable adjustment, the odds ratios (ORs) of dyslipidemia comparing the highest quartiles to the lowest were 1.58 (95% CI 1.20, 2.08; Ptrend = 0.001) for aluminum, 1.34 (95% CI 1.03, 1.75; Ptrend = 0.03) for arsenic, 1.44 (1.09, 1.91; Ptrend = 0.03) for strontium, and 1.47 (95% CI 1.09, 2.00; Ptrend = 0.005) for vanadium. The four metals also showed significant associations with the subtypes of dyslipidemia, including low HDL-C and high LDL-C. The first principal component, which mainly represented aluminum, arsenic, barium, lead, vanadium, and zinc, was associated with increased risk of incident dyslipidemia, and the adjusted OR was 1.40 (95% CI 1.07, 1.84; Ptrend = 0.02) comparing extreme quartiles. The study indicated that elevated plasma aluminum, arsenic, strontium, and vanadium concentrations were associated with a higher incidence of dyslipidemia. These findings highlight the importance of controlling metal exposures for dyslipidemia prevention.Anode biofilm thickness is a key point for high and sustainable power generation in microbial fuel cells (MFCs). Over time, the formation of a thicker biofilm on anode electrode hinders the power generation performance of MFC by causing a longer electron transfer path and the accumulation of undesirable components in anode biofilm. To overcome these limitations, we used a novel strategy named quorum quenching (QQ) for the first time in order to control the biofilm thickness on the anode surface by inactivation of signal molecules among microorganisms. For this purpose, the isolated QQ bacteria (Rhodococcus sp. BH4) were immobilized into alginate beads (20, 40, and 80 mg/10 ml sodium alginate) and added to the anode chamber of MFCs. The MFC exhibited the best electrochemical activity (1924 mW m-2) with a biofilm thickness of 26 μm at 40 mg Rhodococcus sp. Etomoxir concentration BH4/10 ml sodium alginate. The inhibition of signal molecules in anode chamber reduced the production of extracellular polymeric substance (EPS) by preventing microbial communication amonganode microorganisms. Microscopic observations revealed that anode biofilm thickness and the abundance of dead bacteria significantly decreased with an increase in Rhodococcus sp. BH4 concentration in MFCs. Microbiome diversity showed an apparent difference among the microbial community structures of anode biofilms in MFCs containing vacant and Rhodococcus sp. BH4 beads. The data revealed that the QQ strategy is an efficient application for improving MFC performance and may shed light on future studies.The degradation of acetaminophen (ACM) was comparatively studied by UV/chlorine and UV/H2O2 systems. An apparent reduction in the removal rate was observed above the optimum pH levels of 7.0 and 3.0 in UV/chlorine and UV/H2O2 processes, respectively. The relative contribution of each oxidizing agent in ACM removal using the two advanced oxidation processes (AOPs) was evaluated. Even though hydroxyl radicals, with the contribution percentage of 90.1%, were determined as the primary oxidizing species in ACM removal using the UV/H2O2 process, reactive chlorine species (RCS), with 43.8% of contribution percentage, were also found to play a pivotal role in ACM removal using the UV/chlorine process. For instance, dichlorine radical (Cl2•-) showed an acceptable contribution percentage of 32.2% in the degradation of ACM by the UV/chlorine process. The rate of ACM degradation significantly rose to 99.9% and 75.6%, as higher amounts of oxidants were used in the UV/chlorine and UV/H2O2 processes, respectively, within 25 min. The introduction of HCO3- ions and humic acid remarkably decreased the rate of ACM degradation in both techniques used in this study. The presence of NO3- and Cl- ions did not considerably affect the removal rate in the UV/chlorine process. The acute toxicity analysis revealed that a more pronounced reduction in the ACM solution toxicity could be achieved by the UV/H2O2 process compared to the UV/chlorine process, which should be ascribed to the formation of chlorinated products in the UV/chlorine treatment. Eventually, plausible oxidation pathways were proposed for each process.
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