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Building age-stratified red-colored body mobile or portable fatty acid reference point runs utilizing model-based clustering as well as repetitive application of the actual harris-boyd technique.
25 mg/kg NP-OVA co-exposure synergistically decreased nuclear factor-κB (NF-κB) mRNA expression in the lung tissues of pups; Exposure to 50 mg/kg NP combined with OVA antagonized the increased expression of high mobility group box 1 (HMGB1) mRNA in the lung tissue. The combined exposure to 50 mg/kg NP and OVA synergistically increased HMGB1 protein expression in the lung tissues. 25 mg/kg NP-OVA co-exposure antagonized the increased nuclear factor-κB (NF-κB) protein expression in the lung tissues. There was a positive correlation between NP content and HMGB1 protein expression in the lung tissue of asthmatic pups (r = 0.602, P less then 0.001). In conclusion, gestational and lactational exposure to 100 mg/kg NP in maternal rats exacerbated airway inflammation in OVA-induced asthmatic pups, and there is an interactive effect between NP and OVA. When the perinatal rats were exposed to 100 mg/kg NP, the levels of HMGB1 and NF-κB in the lung tissues of OVA-induced asthmatic pups were increased. Air quality in large cities has worsened in recent years as a consequence people's health is directly affected. Among the toxic compounds released to environmental air are polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs (nitro-PAHs), and oxygenated PAHs (oxy-PAHs). Performant methods to analyze these compounds is necessary to enable adequate monitoring of air quality. Thus, this manuscript presents the development of a highly sensitive method to analyze PAHs, nitro-PAHs, and oxy-PAHs collected from ambient air (PM2.5) and the gas phase for a period of one year in the urban area of Belo Horizonte, Brazil. PAHs and their derivatives were extracted by cold fiber solid phase microextraction (CF-SPME) and analyzed by gas chromatography coupled to mass spectrometry (GC/MS). The proposed method allows simultaneous analysis of 16 PAHs, nitro-PAHs and oxy-PAHs, presenting very good limits of detection and quantification, as well as appropriate precision and recovery. The results obtained for the period of one year allowed different studies. The compounds collected simultaneously from gas and particulate phase showed that total concentration of 16 PAHs were higher in the gas phase than in the particulate. On the other hand, nitro-PAHs and oxy-PAHs presented similar concentration in gas and particulate phases. The potential carcinogenicity of PAHs relative to benzo[a]pyrene showed benzo[a]pyrene equivalents of 0.49 ng m-3. The estimated risk of lifetime lung cancer was 5 × 10-5. Principal component analysis and diagnostic ratio was applied for source distribution indicating that burning of gasoline, diesel and biomass accounted for the PAHs profile in ambient air samples. Cryptomelane-type octahedral molecular sieve (OMS-2) is one of the most promising catalysts for VOCs oxidation, and introduction of metal ions in OMS-2 tunnel is widely used for tailoring its catalytic activity. Here, different types of alkali earth metal ions with the same X/Mn atomic ratio of approximately 0.012 (X represents Mg2+, Ca2+, and Sr2+) were successfully introduced into OMS-2 tunnel by a one-step redox reaction. The catalytic test showed that introducing alkali earth metal ions into tunnels had a considerable effect on the catalytic performance of OMS-2 for benzene oxidation. The Sr2+ doped OMS-2 catalyst exhibited the better catalytic activity compared with those of Mg-OMS-2 and Ca-OMS-2 samples, and was also superior to a commercial 0.5% Pt/Al2O3 catalyst, as evidenced by its low reaction temperatures of T50 = 200 °C and T90 = 223 °C (corresponding to benzene conversions at 50% and 90%, respectively). The origin of the considerable effect of alkali earth metal doping on the catalytic activity of OMS-2 catalysts was experimentally and theoretically investigated by an 18O2 isotopic labeling experiment, CO temperature-programmed reduction, O2 temperature-programmed oxidation, and density functional theory calculations. The greatest catalytic activity of Sr-OMS-2 compared with those of Mg-OMS-2 and Ca-OMS-2 samples was attributed to its highest lattice oxygen activity as well as its largest surface area. By introducing alkali earth metal ions into the OMS-2 tunnel, we developed a low-cost and highly efficient catalyst that could be used as alternative to noble metal catalysts. To address the challenge of trichloroethene (TCE) remediation in low permeability zone, an inexpensive Cu-Ni bimetallic cathode was proposed in electrokinetic (EK) remediation system to couple electrokinetic migration with in situ electrochemical hydrodechlorination. Aqueous phase TCE was originally added into the anolyte so that breakthrough curves through the low permeability porous soil compartment could be obtained to better understand TCE migration driven by electroosmosis flow using different cathodes. The Cu-Ni cathode resulted in more TCE migration of 7.64 mg compared to that of 5.99 mg with Ni and 4.22 mg with mixed metal oxide (MMO) cathode, suggesting that the Cu-Ni cathode was capable of driving more TCE flux out of the contaminated soil. With the Cu-Ni cathode, 98.4% of TCE flux that reached the cathode was electrochemically reduced on the cathode, which was much higher than that with MMO cathode (77.9%) or Ni cathode (59.6%). Avelumab datasheet TCE mass that was transported by electroosmosis flow increased from 2.04 to 6.68 mg when the voltage gradient increased from 1 to 4 V cm-1, with the normalized energy consumption increasing from 0.06 to 0.16 kWh kg-1 per unit water movement, and from 0.54 to 2.55 kWh g-1 per unit TCE transport. For TCE that did reach the cathode compartment, > 98% degradation maintained at the Cu-Ni cathode with various voltage gradients. The coupled electrokinetic and electrochemical hydrodechlorination technology appears to be a promising strategy for the remediation of low permeability porous media. Emerging pollutants represent a new global problem for water quality. As these compounds get into the environment, they cause severe threats to aquatic environments and human health and are typically resistant to conventional wastewater treatments. In this work, TiO2 nanoparticles surface was functionalized with silver (Ag) nanoparticles, and solvent cast and electrospun membranes of poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were prepared with different concentrations of TiO2 and Ag-TiO2 to produce a multifunctional material. The photocatalytic activity of the nanocomposites was evaluated through the degradation of norfloxacin under ultraviolet (UV) and visible radiation. It is shown that nanocomposites with Ag-TiO2 show the highest degradation efficiencies 64.2% under UV and 80.7% under visible radiation, for 90 and 300 min, respectively. Furthermore, the recyclability of the membranes has also been demonstrated. Finally, it is shown the antimicrobial activity of the nanocomposite membranes, demonstrating the suitability of the Ag-TiO2/PVDF-HFP nanocomposites as multifunctional photocatalytic and antimicrobial membranes for water remediation applications.
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