Wilhelmseneliasen2536

001; OR 39.17; CI 4.81-319.23; NPV, 99.65 %), <32 weeks (OR 4.23; p 0.002) and <34 weeks of gestation (OR 2.66; p 0.01).

In our study, an UCA > 120 degrees allowed to identify those women with twin pregnancies at risk of sPTB and performed better than CL measurement.

120 degrees allowed to identify those women with twin pregnancies at risk of sPTB and performed better than CL measurement.Water-soluble vitamins are essential dietary components with a multitude of important functions that require quantification from food sources to characterise the nutritional status of food. In this study, we have developed a hydrophilic interaction chromatography (HILIC) based method coupled to single-quadrupole mass spectrometry (MS) for the analysis of selected water-soluble vitamins. Due to their involvement in energy release from macronutrients, the quantification of thiamine (B1), riboflavin (B2), nicotinamide (B3) and pyridoxine (B6) offers significant value in food analysis. A commercially available vegetable soup was selected as the food matrix for this study and utilised to develop an efficient extraction procedure for the vitamins of interest. Vitamins were extracted using meta-phosphoric acid coupled with a reducing agent, DL-dithiothreitol (DTT) to produce the parent compound. The extracted vitamins were then analysed using an LC-MS system with electrospray - atmospheric pressure ionization (ES-APngle quad MS method utilising SIM for the low-level quantification of four B vitamins in a vegetable soup matrix in under 20 min. This method has shown excellent linearity, intra- and inter-day reproducibility and is directly applicable to other plant-based food matrices.Heavy metal-containing wastewater can be treated by adsorption technology to obtain ultra-low concentration or high-quality treated effluent. Due to the constraints of the specific surface area, surface electrical structure and spatial effect of conventional adsorbents, it is often difficult to obtain adsorbents within high adsorption capacity. Graphene has characteristics of large specific surface area, small particle size, and high adsorption efficiency. It is considered as one of the research hotspots in recent years. However, despite graphene's unique properties, graphene-based adsorbents still have some drawbacks, i.e. graphene nanosheets are easier to be stacked with each other via π-π stacking and van der Waals interactions, which affect the site exposure, impede the rapid mass transport and limit its adsorption performance. Special strategy is needed to overcome its drawbacks. This work summarizes recent literatures on utilization of three strategies-surface functionalization regulation, morphology and structure control and material composite, to improve the adsorption properties of graphene-based adsorbent towards heavy metal removal. A brief summary, perspective on strategies to improving adsorption properties of graphene-based materials for heavy metal adsorption are also presented. Certainly, this review will be useful for designing and manufacturing of graphene-based nanomaterials for water treatment.The two-stage partial nitrification (PN)-Anammox process, during long term treatment of high-ammonia nitrogen leachate, faces challenges such as the adaptation of nitrite oxidation bacteria (NOB) and failure of real-time control of pH. Resultant instabilities including NH4+-N and NO3--N accumulation were overcome by culturing sludge fermentation liquid (SFL)-driven partial denitrification (PD) in situ in the Anammox process. Biodegradation of slowly biodegradable organics (SBO) in SFL created organics restriction condition, which limited the activity of denitrification bacteria and achieved its balance with Anammox bacteria. Produced NO3--N is reduced to NO2--N through PD, which further improved the removal of NH4+-N through Anammox. Adavivint purchase NO2--N was utilized timely by Anammox bacteria, which avoid further reduction of NO2--N to N2, and result in a high nitrate to nitrite transformation ratio (NTR) of 93.3%. Satisfactory nitrogen removal efficiency (NRE) and nitrogen removal rate (NRR) of 99.6% and 822.0 ± 9.0 g N/(m3∙d) were obtained, respectively. Key genera related to degradation of SBO, PD and Anammox were enriched. The value of narG/(nirK+nirS) increased from 0.05 on day 1-0.15 on day 250. Combining SFL-driven PD with two-stage Anammox process provided a novel insight for applying this process to realize advanced nitrogen removal in practical engineering.Formation of reactive oxygen species (ROS) via H2O2 activation is of vital importance in catalytic environmental chemistry, especially in degradation of organic pollutants. A new mixed niobium-cerium oxide (NbCeOx) was tailored for this purpose. A thorough structural and chemical characterization of NbCeOx along with CeO2 and Nb2O5 reference materials was carried out using TEM/STEM/EDS, SEM, XRD, XPS, EPR, UV-vis and N2 physisorption. The ability of the catalysts to activate H2O2 towards ROS formation was assessed on the basis of EPR and Raman measurements. Catalytic activity of the oxides was evaluated in degradation of methylene blue (MB) as a model pollutant. Very high activity of NbCeOx was attributed to the mixed redox-acidic nature of its surface, which originated from the synergy between Nb and Ce species. These two properties (redox activity and acidity) ensured convenient conditions for efficient activation of H2O2 and degradation of MB. The activity of NbCeOx in MB degradation was found 3 times higher than that of the commercial Nb2O5 CBMM catalyst and 240 times higher than that of CeO2. The mechanism of the degradation reaction was found to be an adsorption-triggered process initiated by hydroxyl radicals, generated on the surface via the transformation of O2-•/O22-.Mine-polluted wastewater with mercury (Hg) poses severe environmental pollution since Hg(II) can be converted to highly neurotoxic methylmercury (MeHg) under anaerobic conditions. Previous studies on Hg methylation have focused on aquatic sediments, but few have investigated the MeHg formation in water layers containing algae. In this study, we investigated the dynamic effect of algae on Hg methylation throughout the lifetime of algae. We found that Chlorella pyrenoidosa was a non-methylating alga and exhibited good tolerance to Hg stress (1-20 μg/L); thus Hg(II) could not inhibit the process of eutrophication. However, the presence of C. pyrenoidosa significantly enhanced the Hg methylation by Geobacter sulfurreducens PCA. Compared to the control sample without algae, the MeHg production rate of algae-bacteria samples remarkably exacerbated by 62.3-188.3% with the algal growth period at cell densities of 1.5 × 106-25 × 106 cells/mL. The increase of algal organic matter and thiols with the algal growth period resulted in the exacerbation of MeHg production. link2 The Hg methylation was also enhanced with the presence of dead algae, of which the enhancement was ~62.4% lower than that with the presence of live algae. Accordingly, the potential mechanism of Hg methylation in a freshwater algae-bacteria symbiotic system throughout the algal lifetime was proposed.We use molecular dynamic simulations to study the structural properties of deprotonated cyclohexanoic acid (DCHA) and heptanoic acid (DHA) immersed in water in pristine and hydroxylated carbon nanopores (PACNs and HACNs) in relation to NA removal by activated carbons (ACs). In PACNs, both NAs can aggregate on the pore surface by depleting water molecules, while water molecules accumulate in the area where there is no NA aggregation. The hydrophobic tails of NAs are generally in the interface water region (IWR), while the hydrophilic head groups prefer to be hydrated by water and form pairing with Na+ ions outside the IWR. The linear carbon tails of DHA tend to be parallel to the pore surface, while a slightly inclined configuration of the carbon ring in DCHA is observed. In HACNs, water forms a predominant interface layer by forming hydrogen bonding with -OH groups, while the hydrophobic tails of NAs are driven away from the surface. Both NAs have a more perpendicular orientation close to the pore surface with their hydrophilic head groups forming hydrogen bonding with -OH groups. The strong water film greatly reduces hydrophobic interactions as well as decreases the available adsorption sites for NAs.The ecological harm from methylsiloxanes has drawn worldwide attention. This study investigated three cyclic (D4-D6) and four linear siloxanes (L7-L10) in the eggs of free-range poultry collected near a rural industrial park in China and found total concentrations in the range of 19.2-1204 (median, 268) ng/g dry weight. Higher concentrations of methylsiloxanes were observed in chicken eggs than duck eggs. Cyclic siloxanes represented a median of 62.2% of the total methylsiloxane concentrations. A source assessment indicated that local soils and outdoor dust were more important sources of egg methylsiloxanes than poultry food. The partitioning of methylsiloxanes between egg yolk and egg albumen was investigated, and preferential distributions of the chemicals in the yolk were observed. This study confirmed that methylsiloxanes were highly prevalent in the study poultry eggs. The results suggested that the potential risks to some wild birds inhabiting this area should be of concern, as their physiologies and feeding ecologies are similar to those of the studied poultry, although available ecotoxicological data of the chemicals to birds remains scarce. Additional research is needed to characterize the accumulation of methylsiloxanes in different bird species and its associated adverse effects on their offspring.Many contaminated sites are acidic and the existing binders are mainly alkaline materials. Alkaline binders are used to treat contaminated sites in acidic environments and the solidification/stabilization (S/S) effect is affected by acid corrosion. Therefore, good application prospects exist in developing a binder suitable for the treatment of acidic contaminated sites. In this paper, a new acidic phosphoric-based geopolymer (named APG binder) was synthesized with fly ash as a raw material and aluminum dihydrogen phosphate as the reactant, and the APG binder was used for Pb2+ S/S for the first time. The pH of the APG binder with Pb2+ ranged from 2.56 to 4.09 during 7-28 days of curing, and its compressive strength with Pb2+ exceeded 10 MPa at 28 days. Moreover, Pb2+ had a significant impact on the APG binder compressive strength, and when the Pb2+ content was 0.6%, the APG binder yielded a maximum compressive strength of 6.5, 9.1 and 14.28 MPa at 7, 14, and 28 days, respectively. Furthermore, the compressive strength correlated well with pH and electrical conductivity. The proposed APG binder had a better S/S effect on Pb2+ than that of cement and alkali-activated geopolymers in acidic environments. link3 The stabilization mechanism of the APG binder for Pb2+ included chemical precipitation, physical adsorption and encapsulation.Toxic cyanobacterial blooms, often containing multiple toxins, are a serious public health issue. However, there are no known models that predict a cyanotoxin mixture (anatoxin-a, microcystin, saxitoxin). This paper presents two cyanotoxin mixture models (MIX) and compares them to two microcystin (MC) models from data collected in 2016-2017 from three recurring cyanobacterial bloom locations in Kabetogama Lake, Voyageurs National Park (Minnesota, USA). Models include those using near-real-time environmental variables (readily available) and those using additional comprehensive variables (based on laboratory analyses). Comprehensive models (R2 = 0.87 MC; R2 = 0.86 MIX) explained more variability than the environmental models (R2 = 0.58 MC; R2 = 0.57 MIX). Although neither MIX model was a better fit than the MC models, the MIX models produced no false negatives in the calibration dataset, indicating that all observations above regulatory guidelines were simulated by the MIX models. This is the first known use of Virtual Beach software for a cyanotoxin mixture model, and the methods used in this paper may be applicable to other lakes or beaches.