Womblegrace0859

This combination of measurements and theoretical predictions demonstrates a useful tool for evaluating degradation efficiencies and/or mechanisms of organic contaminants and may promote new and improved applications of isotope analysis in laboratory and field investigations.The active substances coumaphos, tau-fluvalinate and amitraz are among the most commonly employed synthetic miticides to control varroa infestations in apiculture. These compounds can persist inside the beehive matrices and can be detected long time after their application. The present study describes the application of a new passive sampling methodology to assess the dissipation of these miticides as well as the cross-contamination in neighboring beehives. The APIStrips are a recently developed sampling device based on the sorbent Tenax, which shows a remarkable versatility for the sorption of molecules onto its surface. This avoids the need of actively sampling apicultural matrices such as living bees, wax or reserves (honey and pollen), therefore allowing to obtain representative information of the contamination in the beehive environment in one single matrix. ACH-CFDIS The results show that the amitraz-based treatments have the fastest dissipation rate (half-life of 11-14 days), whereas tau-fluvalinate and coumaphos remain inside the beehive environment for longer time periods, with a half-life up to 39 days. In the present study, tau-fluvalinate originated an intense cross-contamination, as opposed to coumaphos and amitraz. This study also demonstrates the contribution of drifting forager bees in the pesticide cross-contamination phenomena. Moreover, the sampling of adult living bees has been compared to the APIStrip-based sampling, and the experimental results show that the latter is more effective and consistent than traditional active sampling strategies. The active substances included in this study do not migrate to the honey from the treated colonies in significant amounts.A sea urchin-shaped, single-layer, and hollow NiO-NiS photocatalyst with a large surface area was designed for carbon dioxide (CO2) conversion in this study. A d-glucose polymeric hollow frame was fabricated using a d-glucose monomer, and NiO particles were stably grown on it using the hydrothermal method to form a hollow NiO surface. The d-glucose frame was removed by heat treatment to create hollowed NiO; hollowed NiO-NiS (h-NiO-NiS) was subsequently obtained through ion exchange between the O ions in NiO and S ions in the sulfur powder. Additionally, we attempted to determine the correlation among the surface area of the h-NiO-NiS catalyst, CO2 gas adsorption capacity, and catalyst performance. The surface area of the h-NiO-NiS catalyst was ten times larger than that of the nanometer-sized NiO-NiS (n-NiO-NiS, 21.2 m2 g-1) catalyst. The CO2 photocatalytic conversion performance of the hollowed catalyst was approximately seven times larger than that of the nanosized catalyst. As the amount of ion-exchanged S increased, methane selectivity increased, and optimal methane production was obtained when the weight ratio of NiO and sulfur powder was 1 4. Using temperature-programmed desorption (TPD) analyses of CO2 and H2O, the adsorption of water molecules on the Ni-S surface and that of CO2 gas on the Ni-O surface during CO2 conversion reaction were confirmed. The h-NiO-NiS catalyst facilitated an effective charge separation through a well-developed interfacial transition between the linked NiS and NiO, and resulted in increased CO2 photoreduction performance under sunlight.Phosphate functionalized graphene oxide (PGO) was successfully prepared by Arbuzov reaction and employed for adsorption of resorcinol from an aqueous phase. The phosphate functional groups were successfully incorporated onto the PGO surface by the formation of P-C bonds as identified by the analysis of FTIR and XPS spectra. The evaluation of adsorption capacity of resorcinol onto PGO exhibited significant improvement of resorcinol removal, achieving an adsorption capacity of 50.25 mg/g in the pH range of 4-7 which was 15 times higher than pristine graphene oxide. The addition of 2.4 M and 5 M NaCl in the adsorption system significantly increased the adsorption capacity towards resorcinol from 50.25 mg/g to 82.10 mg/g and 128.10 mg/g, respectively. Based on kinetics and adsorption isotherm studies, Pseudo-First-Order and Langmuir model are the best model to describe the adsorption process indicating that the adsorption is dominantly controlled by physisorption. The thermodynamic analysis suggested that the adsorption process was the favorable, spontaneous, and endothermic process. Besides, the interplay of hydrogen bonding and π-π interactions is proposed to be the governing physisorption mechanism. The outstanding reusability and better adsorption performance make PGO a promising adsorbent for environmental remediation of resorcinol.Dissolved organic matter (DOM) is ubiquitous in aquatic environments, whose behaviors and fate are highly related to the chemical compositions and size distribution. In this study, the UV-induced photodegradation properties of DOMs with different origins (i.e., macrophyte- and algae-derived) were investigated using absorption and fluorescence spectroscopy as well as flow field-flow fractionation (FlFFF). Results showed that, irrespective of DOM origins, the chromophoric components could be more effectively photo-degraded than the non-chromophoric ones. Though the two DOMs were characterized with similar fluorophores, the photodegradation properties showed obvious heterogeneities in DOM origins and molecular weights (MWs). Compared to macrophyte-derived DOM (MDOM), the algae-derived DOM (ADOM) exhibited a higher degradation rate and efficiency due to the abundance of labile components like newborn protein-like substances. The FlFFF results revealed a high photo-preferability of 100 kDa-0.45 μm protein-like MDOM and same photo-sensitivity of the size-fractionated humic-like moieties, testifying the reduction of molecular sizes during the photodegradation. However, the increase in relative percentage for 100 kDa-0.45 μm protein-like components and 5-15 kDa humic-like moieties implied a possible enhancement of molecular sizes for ADOM during the early period (i.e., the first hour) of photodegradation. This study provides new insights into the origin-related heterogeneities in compositions and size distribution for DOM transformation.