Risk assessment of broflanilide for human and non-target terrestrial organisms in cauliflower production.

Broflanilide is a newly-developed meta-diamide insecticide, proposed for the control of a wide variety of chewing pests on many crops. In view of the proposed use of broflanilide and its environmental fate, it may be exposed to consumers and non-target organisms, which adversely affect human and the environment. In this paper, a rapid, sensitive and valid UPLC-MS/MS method was established for simultaneous analysis of broflanilide and its two major metabolites, DM-8007 and S (PFP-OH)-8007, in cauliflower. Then, the dissipation behaviors and final residues of broflanilide and its two major metabolites in cauliflower from eight sites with different climatic conditions in China were studied via the described analytical method. In addition, the acute toxicity test of 9.5 % suspension concentrate of broflanilide, broflanilide standard, DM-8007 and S (PFP-OH)-8007 were conducted to non-target terrestrial organisms. Risk assessment for human and non-target terrestrial organisms in cauliflower production was evaluated based on the maximum annual application rates and intervals. The results showed that the highest residue of broflanilide detected in cauliflower samples was all lower than the corresponding MRLs (2 mg/kg) in Japan. Chronic food dietary risk estimates for broflanilide do not exceed 50 % for all the Chinese population groups. Moreover, broflanilide is of low acute toxicity to birds and earthworm, while broflanilide and its metabolites is classified as highly toxic to adult honeybees. Acute risks of broflanilide to birds and earthworms were deemed to be acceptable in a realistic worst-case scenario, while its risk to adult honeybees and ladybug was unacceptable. A protection statement for honeybees and ladybug is required to recognize the high toxicity of broflanilide on related product labels. The study will be conducive to provide guidance for the rational application of broflanilide in cauliflower production.

Dissipation and dietary exposure risk assessment of spinosad, thiocyclam, and its metabolite nereistoxin in cucumber and groundwater for different population groups.

A QuEChERS (quick, easy, cheap, effective, rugged, and safe) technique using ultrahigh-performance liquid chromatography with tandem mass spectrometry for the analysis of spinosad (spinosyn A + spinosyn D), thiocyclam, and nereistoxin in cucumber was developed with mean recoveries of 93-104%, relative standard deviations of ≤9%, and limits of quantification of 0.01 mg/kg. Field trials of spinosad and thiocyclam were performed in 12 representative cultivating areas in China. Field trial results indicate that spinosyn A and spinosyn D easily dissipated in cucumber with half-lives of 2.48-6.24 and <3 days, respectively. Nereistoxin was produced after thiocyclam application and was more persistent than its parent. The terminal residues of spinosad were all below the maximum residue limits (0.2 mg/kg) in China, whereas the terminal concentration of nereistoxin (calculated as the stoichiometric equivalent of thiocyclam), which was much higher than that of thiocyclam, was far beyond the maximum residue limits of thiocyclam in cucumber (0.01 mg/kg) established by the European Union. The predicted no-effect concentrations of spinosyn A, spinosyn D, thiocyclam, and nereistoxin leaching into groundwater were estimated using China-PEARL (Pesticide Emission Assessment at Regional and Local scales) models after application. However, the dietary (food and water) exposure risk quotient for different populations was below 1 with a preharvest interval set at 5 days after the last application, indicating that the application of spinosad and thiocyclam in cucumber was unlikely to pose unacceptable risk for human health. This study provides data for the safe use of spinosad and thiocyclam in cucumber ecosystem.

Discovery of significant atmospheric emission of halogenated polycyclic aromatic hydrocarbons from secondary zinc smelting.

Chlorinated and brominated polycyclic aromatic hydrocarbons (Cl/Br-PAHs) are emerging persistent organic pollutants. Current knowledge on the emissions of Cl/Br- PAHs is far insufficient for source control, much less on their formation mechanisms. In this field study, Cl/Br-PAHs formation mechanisms were proposed from the macro perspective of practical secondary metal smelting industries. We found secondary zinc smelting as a significant source of Cl/Br-PAHs (9553 ng/m3 in stack gas), exceeding concentrations from other metal smelting sources by 1-2 orders of magnitude. Cl/Br-PAH emission characteristics differed between various secondary metal smelting processes, indicating dominance of different formation mechanisms. Cl/Br-PAHs with fewer rings were dominant from secondary zinc smelting and secondary copper smelting. Differently, emissions from secondary aluminum smelting were dominated by congeners with more rings. The differences in congener profiles were attributable to the catalytic effects of metal compounds during smelting activities. Zinc oxide and copper oxide dominantly catalyzed dehydrogenation reactions, contributing to the formation of intermediate radicals and subsequent dimerization to Cl/Br-PAHs with fewer rings. Differently, aluminum oxide induced alkylation reactions and accelerated ring growth, resulting in the formation of Cl-PAHs with more rings. The newly proposed mechanisms can successfully explain the emission characteristics of Cl/Br-PAHs during smelting activities, which should be important implication for Cl/Br-PAHs targeted source control.

Characterizing the emissions of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) from electric arc furnaces during steel-making.

The amount of steel produced using electric arc furnaces (EAFs) has been increasing in recent years. In this study, stack gases from EAFs in steelmaking plants were analyzed to determine if they are also dominant sources of polybrominated dibenzo-p-dioxin and dibenzofuran (PBDD/F) emissions in China. Isotope dilution high-resolution gas chromatography high-resolution mass spectrometry for qualitative and quantitative analysis of PBDD/F congeners revealed that the mean PBDD/F mass concentrations were 271.1-9467.8 pg Nm-3 for the preheating stages (PS) of three EAF plants and that the corresponding toxic equivalents (TEQs) were 10.8-971.2 pg TEQ Nm-3. The PBDD/F mass concentration from the smelting stage (SS) at plant E3 was 261.9 pg Nm-3 (4.5 pg TEQ Nm-3). The PBDD/F emission factors (EF) during the preheating stage for the three plants were 0.0356-1.51 µg TEQ t-1, and the EF was 0.0359 µg TEQ t-1 during the E3 smelting stage. PBDD/Fs were found to contribute 2.39-67.85% to the total mass and 2.84-57.68% to the total dioxin TEQ. These wide fluctuations were caused by differences in the composition of feeding materials and the working temperature of bag filters. Overall, the results indicate that PBDD/F emissions from EAF steelmaking should receive increased attention. The PBDD/F congener patterns among the three EAF plants were variable, possibly because of differences in raw materials. The results presented herein will facilitate assessment of the contribution of EAFs to total PBDD/F emissions in China and investigations of PBDD/F emissions at different stages of steelmaking processes using EAFs.

Inventory of Polychlorinated Naphthalene Emissions from Waste Incineration and Metallurgical Sources in China.

Polychlorinated naphthalenes (PCNs) are highly toxic persistent organic pollutants (POPs) that are a relatively new addition to the Stockholm Convention as of 2015. The levels of unintentional emissions of PCNs from important industrial thermal sources on national scales are unclear but are important for understanding potential human exposure. In this study, an inventory was compiled of PCN emissions from priority industrial sources of unintentional POPs in China. Estimated emissions from four typical POP sources in the reference year (2014) in China were 511.6 kg by mass and 7650.8 mg of toxic equivalent. Waste incineration, secondary nonferrous smelting, electric arc furnace steelmaking, and iron ore sintering plants contributed 38.8, 15.4, 29.2, and 16.6%, respectively, to the total emissions. The Eastern Seaboard of China and the Hebei region in North China, which have intensive industrial activity and high population densities, were dominant contributors of PCNs. Only 18.6% of the counties where waste incineration plants were located emitted PCNs at a level higher than 1.00 × 10-1 mg of toxic equivalent, whereas 80% of the counties where metallurgical plants were located emitted PCNs at this level. These results indicate effective implementation of POP control in the waste incineration industry in China. This study clarifies the unintentionally emission levels of PCNs in China and provides important information for strategy development to control source emissions.

Levels and characteristics of polychlorinated biphenyls in surface sediments of the Chaobai river, a source of drinking water for Beijing, China.

We collected surface sediments from the Chaobai river, the dominant source of drinking water for Beijing, China, to assess the status of contamination by polychlorinated biphenyls and evaluate their sources. Total concentrations of polychlorinated biphenyls in the sediments ranged from 0.125 to 70.6 ng/g dry weight and correlated with the locations relating to painting operation such as printing factories and construction material markets. Dioxin-like polychlorinated biphenyls were present and corresponded with constituents of commercial polychlorinated biphenyl mixtures. Principal component analysis indicated two dominant sources of polychlorinated biphenyls in the sediments-deposition from airborne emissions and point-source pollution from factories. An ecological risk assessment concluded that there was only slight polychlorinated biphenyl pollution in the sediments of the Chaobai river, which was not likely to induce adverse biological effects. Our findings provide information for polychlorinated biphenyl risk assessment and recognition of the dominant sources of these compounds in drinking water in China.

Risk evaluation of environmentally persistent free radicals in airborne particulate matter and influence of atmospheric factors.

Environmentally persistent free radicals (EPFRs) was considered unrecognized composition of air pollutants and might help explain the long-standing medical mystery of why non-smokers develop tobacco-related diseases like lung cancer. EPFRs in airborne fine particulate matter (PM2.5) can induce oxidative and DNA damage when inhaled. We assessed the inhalation risk of EPFRs in PM2.5 and factors influencing this risk in Beijing as a large city with frequent haze events. The average concentration of EPFRs in PM2.5 was 6.00 × 1017 spins/m3 in spring, autumn, and winter; lower concentrations were recorded in the summer. To estimate the daily inhalation risk of EPFRs in PM2.5, we used the equivalent EPFRs in cigarette tar. The average daily inhalation exposure of EPFRs in PM2.5 was estimated to be the equivalent of 33.1 cigarette tar EPFRs per day (range: 0.53-226.9) during both haze and non-haze days. The major factors influencing EPFR concentrations in the atmosphere were precipitation and humidity, which reduced airborne concentrations. Levels of PM2.5 and carbon monoxide were positively correlated with EPFR concentrations. The health risks of inhaling airborne EPFRs could be significant and should be recognized and quantified.

Hepatitis B virus core protein promotes hepatocarcinogenesis by enhancing Src expression and activating the Src/PI3K/Akt pathway.

Hepatitis B virus core protein (HBc) is expressed preferentially in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC). HBc can function as an oncogene arising from its gene regulatory properties, but how it contributes functionally to hepatocarcinogenesis remains unclear. In this study, we determined the molecular and functional roles of HBc during HBV-associated hepatocellular tumorigenesis. HBc increased tumor formation of hepatoma cells. Moreover, expression of HBc specifically promoted proliferation of hepatoma cells in vitro. Mechanistic investigations revealed that these effects were caused by activation of the Src/PI3K/Akt pathway through proximal switch from inactive Src to the active form of the kinase by HBc. HBc-mediated sarcoma (Src) kinase activation was associated with down-regulation of C-terminal Src kinase (Csk). In addition, HBc enhances Src expression by activation of alternative Src 1A promoter in an Sp1 transcription factor-dependent manner. Proliferation induced by stable HBc expression was associated with increased G1-S cell cycle progression mediated by Src kinase activation. HBc-induced cellular proliferation and tumor formation were reversed by administration of the Src inhibitor saracatinib. Together, our findings suggest that HBc promotes tumorigenesis of hepatoma cells by enhancing the expression of total Src and the active form of the kinase and subsequently activates Src/PI3K/Akt signaling pathway, revealing novel insights into the underlying mechanisms of HBV-associated hepatocarcinogenesis.-Liu, W., Guo, T.-F., Jing, Z.-T., Yang, Z., Liu, L., Yang, Y.-P., Lin, X., Tong, Q.-Y. Hepatitis B virus core protein promotes hepatocarcinogenesis by enhancing Src expression and activating the Src/PI3K/Akt pathway.

Polychlorinated naphthalene (PCN) emissions and characteristics during different secondary copper smelting stages.

The amounts and characteristics of polychlorinated naphthalenes (PCNs) emitted by a secondary copper smelter were investigated. Differences in the amounts and characteristics of PCNs emitted during different smelting stages were investigated, and the main stage during which PCNs were emitted was identified. PCN concentrations in stack gases emitted during secondary copper smelting were 477.0-762.5 ng/m3 (4.4-8.3 pg toxic equivalents/m3). The contributions of the different stages to total PCN emissions decreased in the order feeding-fusion stage (65% of total PCN emissions) > oxidation stage (27%) > deoxidation stage (8%). The main contributor to PCN emissions during secondary copper smelting was the feeding-fusion stage. PCN concentrations and profiles in stack gas, fly ash, and deposit ash collected during different smelting stages were determined. PCNs in stack gases were mainly less-chlorinated homologs, and fly ash and deposit ash were dominated by highly-chlorinated homologs. These results will help improve strategies for decreasing and eliminating PCN emissions during secondary copper production.

Unintentional persistent organic pollutants in cement kilns co-processing solid wastes.

Co-processing solid waste in cement kilns has become increasingly widespread in recent years. Persistent organic pollutants (POPs) can be unintentionally produced and emitted from cement kilns, especially kilns in which solid waste is co-processed. Unintentionally produced POP formation and emission by cement kilns co-processing solid waste therefore need to be studied in detail to allow the potential risks posed by cement kiln co-processing techniques to be assessed. Many field studies and laboratory simulation experiments have been performed to investigate the formation and release of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). However, the formations, characteristics and emission factors of various emerging unintentionally produced POPs have not been comprehensively reviewed. Here, emissions of well-known unintentionally produced POPs (PCDD/Fs and polychlorinated biphenyls) and emerging unintentionally produced dioxin-like POPs (polybrominated dibenzo-p-dioxins and dibenzofurans, polychlorinated naphthalenes, and chlorinated and brominated polycyclic aromatic hydrocarbons) in cement kilns co-processing solid waste are reviewed, focusing on formations and influencing factors of those unintentional POPs. Data from field studies indicated that the main stages in which POPs are unintentionally produced in cement kilns co-processing solid waste are the cyclone preheater outlet, suspension preheater boiler, humidifier tower, and back-end bag filter. The raw material composition, chlorine and bromine contents, and temperature are the most important factors affecting POP formation. The homolog distributions and congener profiles of POPs formed unintentionally in cement kilns were compared, and it was found that larger amounts of less-chlorinated homologs than more-chlorinated homologs are emitted. Emission factors for various unintentionally produced POPs for cement kilns co-processing solid waste were summarized, and could be useful for compiling global emission inventories for pollutants covered by the Stockholm Convention. This comprehensive review improves our understanding of unintentional production and emissions of POPs by cement kilns co-processing solid waste.

Brominated dioxins and furans in a cement kiln co-processing municipal solid waste.

A field study and theoretical calculations were performed to clarify the levels, profiles, and distributions of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) in a cement kiln co-processing solid waste, with a focus on the PBDF formation mechanism. The raw materials contributed greatly to input of PBDD/Fs into the cement kiln. The PBDD/F concentrations in the raw materials were much higher than those in particle samples from different process stages in the cement kiln. The PBDD/F concentrations in the clinkers were 1.40% of the concentrations in the raw materials, which indicated that the high destruction efficiencies for PBDD/Fs by cement kiln. PBDD/F distribution patterns in particle samples collected from different process stages indicated the cement kiln backend was a major site for PBDD/F formation. PBDFs with high levels of halogenation, such as heptabrominated furans (HpBDF), were the dominant contributors to the total PBDD/F concentrations and accounted for 42%-73% of the total PBDD/F concentrations in the particle samples. Our results showed that co-processing of municipal solid waste in a cement kiln may influence the congener profile of PBDD/Fs, especially for the higher halogenated PBDD fraction. In addition, there were significant correlations between the decabromodiphenyl ether and heptabrominated furan concentrations, which is an indicator of transformation from polybrominated diphenyl ethers to PBDD/Fs. Theoretical calculations were performed and demonstrated that elimination of HBr and Br2 from polybrominated diphenyl ethers were the dominant formation pathways for PBDD/Fs. These pathways differed from that for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs).

Real-world evidence of combined treatment of biologics and exclusive enteral nutrition in patients with ileum-dominant Crohn's disease: A multicenter study.

BACKGROUND & AIMS: Although biologics were prescribed to achieve and maintain clinical remission of active Crohn's disease (CD), almost half of patients experienced a loss of response or intolerance. Here, we investigated the efficacy of combined treatment of biologics and 16-weeks exclusive enteral nutrition (EEN) in moderate-to-severe CD patients with small intestine lesions. METHODS: This was a real-world, multicenter retrospective study, from October 2016 to March 2023, medical records of patients registered at three IBD centers were reviewed for patients with ileal or ileocolonic CD in moderate-to-severe activity. All patients received treatment of biologics with concomitant 16-week EEN (BioEEN) or biologics alone (Bio). The clinical outcomes and endoscopic outcomes were assessed at week 16 and 52. RESULTS: There was no statistically significant difference between Bio (97 patients) and BioEEN group (100 patients) at baseline for demographic and clinical characteristics. Compared to treatment with biologics alone, patients with BioEEN treatment achieved higher rates of clinical response (95.0% vs. 66.0%), clinical remission (87.0% vs. 52.6%), endoscopic response (91.4% vs. 47.4%) including mucosal healing (85.7% vs. 23.7%) at week 16. The superiority of BioEEN sustained in maintenance, with 84.7% (vs. 49.1%) clinical response, 77.8% (vs. 38.6%) clinical remission, 69.2% (vs. 32.6%) endoscopic response and 51.9% (vs. 18.6%) mucosal healing at week 52. CONCLUSIONS: Combined treatment of biologics and 16-week EEN was an efficient therapeutic strategy with affirmative effectiveness for small intestine diseases of active CD.

Impact of oral care modalities on the incidence of ventilator-associated pneumonia in the intensive care unit: A meta-analysis.

BACKGROUND: At present, evidence of the role of oral hygiene in ICU-related pneumonia is rare. The study aimed to evaluate the effectiveness of toothbrush-based oral care in preventing ventilator-associated pneumonia (VAP) in patients with mechanical ventilation in the ICU. METHODS: Ten databases were searched for randomized controlled trials (RCTs) evaluating toothbrush-based oral care for preventing VAP in patients with mechanical ventilation in ICU. Quality assessment and data extraction were independently performed by 2 researchers. The meta-analysis was performed using RevMan 5.3 software. RESULTS: Thirteen RCTs with 657 patients were included. Tooth brushing + 0.2%/0.12% chlorhexidine was associated with reduced incidence of VAP compared to chlorhexidine (OR = 0.63, 95% confidence interval [CI]: 0.43-0.91, P = .01) or tooth brushing + placebo (OR = 0.47, 95% CI: 0.25-0.86, P = .02) in patients with mechanical ventilation in ICU, but was similar to cotton wipe with 0.2% or 0.12% chlorhexidine (OR = 1.33, 95% CI: 0.77-2.29, P = .31). CONCLUSIONS: Tooth brushing combined with chlorhexidine mouthwash can prevent VAP in patients with mechanical ventilation in ICU. There is no advantage of tooth brushing combined with chlorhexidine mouthwash over cotton wipe with chlorhexidine mouthwash for preventing VAP in these patients.

Efficacy of Ustekinumab Optimization by 2 Initial Intravenous Doses in Adult Patients With Severe Crohn's Disease.

BACKGROUND: Although increasing studies have reported that dose escalation can improve treatment response to ustekinumab in patients with Crohn's disease (CD), their strategies mainly focus on maintenance regimen. Evidence of ustekinumab dose escalation in induction regimen, particularly in severe CD, remains limited. This study evaluated the efficacy and safety of intravenous ustekinumab with 2 initial doses in patients with severely active CD. METHODS: A retrospective observational study of 99 adult patients with severe CD treated with ustekinumab from 3 IBD centers included 48 patients with standard and 51 with optimized induction treatment. Clinical outcomes, inflammatory biomarkers including fecal calprotectin (FC) normalization, and endoscopic outcomes were evaluated at weeks 16 and 48. Adverse events and treatment decisions after initial induction were also collected. RESULTS: Compared with the standard group, 2 initial intravenous injections of ustekinumab achieved higher clinical response (92.2%, 47 of 51, P = .656), clinical remission (88.2%, 45 of 51, P = .221), endoscopic response (75.8%, 25 of 33, P = .125), and FC normalization (70.6%, 36 of 51, P = .138) at week 16. The mucosal healing rate at week 16 (63.6%, P = .022) was statistically higher in the optimization group. At week 48, patients with optimized treatment achieved higher clinical response (80.4%, 41 of 51, P = .003), clinical remission (70.6%, 36 of 51, P = .007), FC normalization (66.7%, 34 of 51, P = .031), endoscopic response (72.7%, 24 of 33, P = .006), and mucosal healing (57.6%, 19 of 33, P = .004). At the last follow-up, 82.4% of optimally treated patients adhered to continued treatment with ustekinumab (P < .001). CONCLUSIONS: Optimization of ustekinumab by 2 initial intravenous inductions is more effective than standard therapy for adult patients with severe CD.

This study used an optimization strategy in severe adult Crohn's disease with 2 initial intravenous doses of ustekinumab. This new strategy proved to be effective and safe.

High expression of centromere protein A and its molecular mechanism and clinical significance in prostate cancer: A study based on data mining and immunohistochemistry.

The progression of prostate cancer (PCa) leads to poor prognosis. However, the molecular mechanism of PCa is still not completely clear. This study aimed to elucidate the important role of centromere protein A (CENPA) in PCa. Large numbers of bulk RNA sequencing (RNA-seq) data and in-house immunohistochemistry data were used in analysing the expression level of CENPA in PCa and metastatic PCa (MPCa). Single-cell RNA-seq data was used to explore the expression status of CENPA in different prostate subpopulations. Enrichment analysis was employed to detect the function of CENPA in PCa. Clinicopathological parameters analysis was utilised in analysing the clinical value of CENPA. The results showed that CENPA was upregulated in PCa (standardised mean difference [SMD] = 0.83, p = 0.001) and MPCa (SMD = 0.61, p = 0.029). CENPA was overexpressed in prostate cancer stem cells (CSCs) with androgen receptor (AR) negative compared to epithelial cells with AR positive. CENPA may influence the development of PCa through affecting cell cycle. Patients with nodal metastasis had higher expression level of CENPA. And patients with high CENPA expression had poor disease-free survival. Taken together, Overexpression of CENPA may influence the development of PCa by regulating cell cycle and promoting metastasis.

Skeletal muscle-secreted DLPC orchestrates systemic energy homeostasis by enhancing adipose browning.

MyoD is a skeletal muscle-specifically expressed transcription factor and plays a critical role in regulating myogenesis during muscle development and regeneration. However, whether myofibers-expressed MyoD exerts its metabolic function in regulating whole body energy homeostasis in vivo remains largely unknown. Here, we report that genetic deletion of Myod in male mice enhances the oxidative metabolism of muscle and, intriguingly, renders the male mice resistant to high fat diet-induced obesity. By performing lipidomic analysis in muscle-conditioned medium and serum, we identify 1,2-dilinoleoyl-sn-glycero-3-phosphocholine (DLPC) as a muscle-released lipid that is responsible for MyoD-orchestrated body energy homeostasis in male Myod KO mice. Functionally, the administration of DLPC significantly ameliorates HFD-induced obesity in male mice. Mechanistically, DLPC is found to induce white adipose browning via lipid peroxidation-mediated p38 signaling in male mice. Collectively, our findings not only uncover a novel function of MyoD in controlling systemic energy homeostasis through the muscle-derived lipokine DLPC but also suggest that the DLPC might have clinical potential for treating obesity in humans.

Congener profiles and process distributions of polychlorinated biphenyls, polychlorinated naphthalenes and chlorinated polycyclic aromatic hydrocarbons from secondary copper smelting.

Secondary copper smelting is an important industrial source of unintentionally produced persistent organic pollutants (UPOPs) emissions. Herein, field study on industrial-scale plants was conducted to clarify the levels and profiles of polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs) and chlorinated polycyclic aromatic hydrocarbons (> 3 rings, Cl-PAHs) from secondary copper smelting plants. The three UPOPs emission levels from the oxygen-enriched smelting furnace were higher than that from the anode furnace, which was attributed to the low-grade raw materials used. The toxic equivalent quantity concentrations of Cl-PAHs were 1.3-4.4 and 4.6-18.9 times higher than that of PCBs and PCNs, respectively. Thus, the emission control of Cl-PAHs in the secondary copper industry should be of concern. The chlorination degree of PCBs and PCNs was ~4 after the gas-cooling stage but was reduced to 1-2 in the stack outlet. This result indicated that the PCBs and PCNs congeners that were generated during the cooling stage were mainly higher-chlorinated. After purification by air pollution control devices (APCDs), the high-chlorinated congeners were removed simultaneously with the fly ash, whereas the low-chlorinated congeners may be regenerated and transferred into the stack gas due to possible memory effect within the APCDs.

Recognition of the molecular characterization and mechanisms of heterogeneously formed organic pollutants from metallurgical industries by FT-ICR-MS and GC/Q-TOF-MS.

Emissions of numerous targeted and non-targeted organic pollutants from industrial activities are one of the major contributors to the global air pollution. However, comprehensive recognition of their molecular characterization and real industrial scale mechanisms have never been achieved. Herein, by using high resolution mass spectrometry, we firstly give an insight into the molecular characterization and mechanisms of organic pollutants formed on fly ashes from secondary smelting of Al, Cu, Pb, and Zn and electric arc furnace steel-making. We found that lipid-like, unsaturated hydrocarbon and carboxyl-rich alicyclic molecule-like structures were the major chemical classes. Methylation- and oxidation-related reactions were suggested to be the major formation mechanisms. The predominance of carboxyl-rich structures in the fly ash further proved the contribution of metallurgical industrial emissions to air pollution. Findings in this study could be significant for further understanding the contribution of industrial emissions to air pollutions and conducting their source emission control.

One-Step Covalent Surface Modification to Achieve Oil-Water Separation Performance of a Non-Fluorinated Durable Superhydrophobic Fabric.

In this work, a durable superhydrophobic fabric was fabricated by a facile covalent surface modification strategy, in which the anchoring of 10-undecenoyl chloride (UC) onto the fabric through the esterification reaction and covalent grafting of n-dodecyl-thiol (DT) via thiol-ene click chemistry were integrated into one step. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM) measurement results demonstrated that UC and DT were covalently grafted onto the fabric surface. The formed gully-like rough structure by the grafted UC and DT on the fabric surface together with the inherent microfiber structure, combined with the grafted low-surface-energy materials of UC and DT, gave the resultant modified DT-UC@fabric superhydrophobic performance. The superhydrophobic DT-UC@fabric was used for separation of oil-water mixtures; it exhibited high separation efficiency of more than 98%. In addition, it presented excellent durability against mechanical damage; even after 100 cyclic tape-peeling and abrasion tests, the DT-UC@fabric could preserve superhydrophobic performance, which was ascribed to the formed covalent interactions between the fabric surface and the grafted UC and DT. Therefore, this work provided a facile, efficient strategy for fabricating superhydrophobic composites with excellent durability, which exhibited a promising prospect in the application of self-cleaning and oil-water separation.

Profiles, spatial distributions and inventory of brominated dioxin and furan emissions from secondary nonferrous smelting industries in China.

Nonferrous metallurgical processes are important sources of carcinogenic polybrominated dibenzo-p-dioxin and dibenzofuran (PBDD/Fs) that transport globally. Studies on the profiles, spatial distributions and inventory of PBDD/F emissions into the atmosphere from nonferrous metallurgical plants are needed for better source control. In this study, field investigations on PBDD/F emissions from typical nonferrous metallurgical plants were conducted to characterize the PBDD/F profiles and derive their emission factors. Based on the PBDD/F profiles, diagnostic ratios of PBDD/Fs for secondary copper, zinc and lead smelting were proposed for identifying the potential sources of PBDD/Fs in environment. The PBDD/F emission factors for the secondary copper, lead, and zinc smelting plants were 0.71, 1.65, and 1.54 µg toxic equivalents/t, respectively. The estimated annual input of PBDD/Fs into atmosphere by secondary nonferrous metallurgical plants in China was 212.4 g by mass and 3511.3 mg by toxic equivalents, which is of significance for further evolving a global inventory. The spatial distribution of PBDD/F emissions from nonferrous metallurgical plants in China was mapped. Larger amounts of PBDD/Fs were emitted in the southeastern coastal region and northern China than elsewhere in China.