Vertical distributions of wintertime atmospheric nitrogenous compounds and the corresponding OH radicals production in Leshan, southwest China.

Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) observations were operated from 02 to 21 December 2018 in Leshan, southwest China, to measure HONO, NO2 and aerosol extinction vertical distributions, and these were the first MAX-DOAS measurement results in Sichuan Basin. During the measurement period, characteristic ranges for surface concentration were found to be 0.26-4.58 km-1 and averaged at 0.93 km-1 for aerosol extinction, 0.49 to 35.2 ppb and averaged at 4.57 ppb for NO2 and 0.03 to 7.38 ppb and averaged at 1.05 ppb for HONO. Moreover, vertical profiles of aerosol, NO2 and HONO were retrieved from MAX-DOAS measurements using the Heidelberg Profile (HEIPRO) algorithm. By analysing the vertical gradients of pollutants and meteorological information, we found that aerosol and HONO are strongly localised, while NO2 is mainly transmitted from the north direction (city center direction). Nitrogen oxides such as HONO and NO2 are important for the production of hydroxyl radical (OH) and oxidative capacity in the troposphere. In this study, the averaged value of OH production rate from HONO is about 0.63 ppb/hr and maximum value of ratio between OH production from HONO and from (HONO+O3) is > 93% before12:00 in Leshan. In addition, combustion emission contributes to 26% for the source of HONO in Leshan, and we found that more NO2 being converted to HONO under the conditions with high aerosol extinction coefficient and high relative humidity is also a dominant factor for the secondary produce of HONO.

NOx-Reduction Performance Test for TiO2 Paint.

In South Korea, the gradual increase in particulate matter generation has received significant attention from central and local governments. Exhaust gas, which contains nitrogen oxides (NOx), is one of the main sources of particulate matter. In this study, the reduction of NOx using a coating material mixed with a titanium dioxide (TiO2) photocatalyst was demonstrated. The NOx reduction performance of the TiO2 photocatalyst-infused coating was evaluated by applying the ISO 22197-1: 2007 standard. Subsequently, the performance was evaluated by changing the NO gas concentration and ultraviolet (UV)-A irradiance under standard experimental conditions. It was determined that NOx reduction can be achieved even if the NO gas concentration and UV-A irradiance are lower than those under the standard conditions when the TiO2 photocatalyst-infused coating was used. This study revealed that NOx reduction can be realized through TiO2 photocatalyst-infused coating in winter or cloudy days with a low solar altitude. It was also confirmed that compared with the UV-A irradiance, the NO gas concentration has a greater effect on the NOx reduction performance of the TiO2 photocatalyst-infused coating. These findings can be used to evaluate a variety of construction materials with TiO2 photocatalysts in the future.

Bioleaching of metals from WEEE shredding dust.

A bioleaching process developed in two separate steps was investigated for the recovery of base metals, precious metals and rare earth elements from dusts generated by Waste Electrical and Electronic Equipment (WEEE) shredding. In the first step, base metals were almost completely leached from the dust in 8 days by Acidithiobacillus thiooxidans (DSM 9463) that lowered the pH of the leaching solution from 3.5 to 1.0. During this step, cerium, europium and neodymium were mobilized at high percentages (>99%), whereas lanthanum and yttrium reached an extraction yield of 80%. In the second step, the cyanide producing Pseudomonas putida WSC361 mobilized 48% of gold within 3 h from the A. thiooxidans leached shredding dust. This work demonstrated the potential application of biohydrometallurgy for resource recovery from WEEE shredding dust, destined to landfill disposal, and its effectiveness in the extraction of valuable substances, including elements at high supply risk as rare earths.

The power of the past: A roadmap for integrating nursing history into the curriculum.

The inclusion of nursing history within the undergraduate and graduate nursing curricula has waxed and waned over the years. The 2021 publication by the American Association of Colleges of Nursing, "The Essentials: Core Competencies for Professional Education," includes the expectation that nursing education curricula will include history content. This article aims to provide guidance to the nurse educator using a nursing history framework and a 5-step approach to integrate history into an already saturated curriculum. Through meaningful integration of nursing history at the course level with intentional alignment to existing course-level objectives, student learning will be enhanced. Student engagement with various historical sources will help students to achieve The Essentials' core competencies across the 10 Domains for Nursing. The various types of historical sources are explained and how to locate appropriate historical sources is included.

Spatiotemporal variations, surface inventory, and cross regional impact of current-use organoamine pesticides in Chinese Marginal Seas.

Current-use Organoamine Pesticides (CUOAPs) are a growing concern as emerging pesticide pollutants that were initially discovered on a large scale in Chinese Marginal Seas (CMSs). The highest level was detected in the East China Sea in the late spring and decreased in the following order: East China Sea (early spring) > the South China Sea > the Bohai Sea. The crucial role played by the Yangtze and Yellow rivers as significant terrestrial sources were established. The fluctuations in the land application and riverine input led to variations in the source, distribution, and seasonal patterns of CUOAPs. Terrestrial-exported CUOAPs were transported and redistributed spatially by the surface ocean currents, resulting in significant regional disparities. The results displayed a pronounced terrestrial source signature and a cross-regional impact. By the ocean current transport, CMSs will likely become a secondary source region for the surrounding seas.

Sedimentary records of persistent organic pollutants (OCPs and PCBs) in Ngoring Lake, the central Tibetan Plateau, China: Impacts of westerly atmospheric transport and cryospheric melting.

Lake sediments in remote alpine regions are used to infer information on persistent organic pollutants (POPs) delivery via long-range atmospheric transport (LRAT) with limited influences from local sources. When studying the deposition history of POPs on the Tibetan Plateau, regions influenced by westerly air mass flow have received insufficient attention compared with regions governed by the monsoon. Herein, we collected and dated two sediment cores from Ngoring Lake to reconstruct the depositional time trends of 24 organochlorine pesticides (OCPs) and 40 polychlorinated biphenyls (PCBs) and assess the response to emission reductions and climate change. DDTs, HCHs, hexachlorobenzene (HCB), and PCBs were all detected in the sediment core at low concentrations of 110-600, 4.3-400, 8.1-60, and 3.3-71 pg/g, respectively. The composition of PCBs, DDTs, and HCHs was dominated by congeners with 3 and 4 chlorines (avg. 70 %), p,p'-DDT (avg. 90 %), and ß-HCH (avg. 70 %), respectively, indicating the influence of LRAT and the contribution of technical DDT and technical HCH from potential source regions. Temporal trends of PCB concentrations normalized by total organic carbon echoed the peak of global emissions of PCBs around 1970. The rising trend of concentrations of ß-HCH and DDTs after the 1960s in sediments was mainly explained by the input of contaminants with melting ice and snow from a cryosphere shrinking under global warming. This study verifies that westerly air mass flow brings fewer contaminants to the lacustrine environment on the Tibetan Plateau than the monsoon and demonstrates the impacts of climate change on the secondary emission of POPs from the cryosphere to the sediments.

Identification of ozone sensitivity for NO2 and secondary HCHO based on MAX-DOAS measurements in northeast China.

In this study, tropospheric formaldehyde (HCHO) vertical column densities (VCDs) were measured using multi-axis differential optical absorption spectroscopy (MAX-DOAS) from January to November 2019 in Shenyang, Northeast China. The maximum HCHO VCD value appeared in the summer (1.74 × 1016 molec/cm2), due to increased photo-oxidation of volatile organic compounds (VOCs). HCHO concentrations increased from 08:00 and peaked near 13:00, which was mainly attributed to the increased release of isoprene from plants and enhanced photolysis at noon. The HCHO VCDs observed by MAX-DOAS and OMI have a good correlation coefficient (R) of 0.78, and the contributions from primary and secondary HCHO sources were distinguished by the multi-linear regression model. The anthropogenic emissions showed unobvious seasonal variations, and the primary HCHO was relatively stable in Shenyang. Secondary HCHO contributed 82.62%, 83.90%, 78.90%, and 41.53% to the total measured ambient HCHO during the winter, spring, summer, and autumn, respectively. We also found a good correlation (R = 0.78) between enhanced vegetation index (EVI) and HCHO VCDs, indicating that the oxidation of biogenic volatile organic compounds (BVOCs) was the main source of HCHO. The ratio of secondary HCHO to nitrogen dioxide (NO2) was used as the tracer to analyze O3-NOx-VOC sensitivities. We found that the VOC-limited, VOC-NOx-limited, and NOx-limited regimes made up 93.67%, 6.23%, 0.11% of the overall measurements, respectively. In addition, summertime ozone (O3) sensitivity changed from VOC-limited in the morning to VOC-NOx-limited in the afternoon. Therefore, this study offers information on HCHO sources and corresponding O3 production sensitivities to support strategic management decisions.

The characteristics and sources of roadside VOCs in Hong Kong: Effect of the LPG catalytic converter replacement programme.

In order to improve local air quality of Hong Kong, more than 99% taxies and public light buses were changed from diesel to liquefied petroleum gas (LPG) fuel type in the early 2000s. In addition to the catalytic converters wear and tear, it is necessary to control air pollutants emitted from LPG vehicles. Therefore, an LPG catalytic converter replacement programme (CCRP) was fulfilled from October 2013 to April 2014 by the Hong Kong government. Roadside volatile compounds (VOCs) were measured by on-line measurement techniques before and after the programme to evaluate the effectiveness of the LPG CCRP. The mixing ratios of total measured VOCs were found decreased from 69.3 ± 12.6 ppbv to 43.9 ± 6.5 ppbv after the LPG CCRP with the decreasing percentage of 36.7%. In addition, the total mixing ratio of LPG tracers, namely propane, i-butane, and n-butane, accounted for 49% of total measured VOCs before the LPG CCRP and the weighting percentage decreased to 34% after the programme. Moreover, the source apportionment of roadside VOCs also reflects the large decreasing trend of LPG vehicular emissions after the air pollution control measure. Due to the application of PTR-MS on measuring real-time VOCs and oxygenated volatile compounds (OVOCs) in this study, the emission ratios of individual OVOCs were investigated and being utilized to differentiate primary and secondary/biogenic sources of roadside OVOCs in Hong Kong. The findings demonstrate the effectiveness of the intervention programme, and are helpful to further implementation of air pollution control strategies in Hong Kong.

Comprehensive detection of nitrated aromatic compounds in fine particulate matter using gas chromatography and tandem mass spectrometry coupled with an electron capture negative ionization source.

Nitrated aromatic compounds (NACs) are toxic and allergenic airborne pollutants from both primary emissions and atmospheric reactions of aromatics with NO2. A comprehensive investigation of NACs is challenging given their low ambient levels. By applying gas chromatography and tandem mass spectrometry coupled with an electron capture negative ionization source, this study achieved a comprehensive high-throughput and standard-independent detection of nonpolar NACs in fine particulate matter (PM2.5) sampled over 2 years in Beijing, China. Overall, 1047 NACs were detected, among which, the elemental composition of 128 species were derived using time-of-flight mass spectrometry, and 25 species were confirmed using reference standards. In addition to mono-nitrated polycyclic aromatic hydrocarbons (NPAHs), di-nitrated PAHs and alkylated and oxygenated NPAHs were found. Cluster analysis suggested these compounds were derived from various sources particularly atmospheric reactions. We found that the annual levels of primary NPAHs decreased by 46.3-54.8% from 2012-2013 to 2016-2018, though the secondary species did not change significantly after normalization by PM2.5. These results were validated by diagnostic ratios, which indicated an increasing contribution from the secondary formation including nighttime reactions. This novel method for NACs detection may provide valuable insights into the formation mechanisms of NACs in the atmosphere.

Contaminant back-diffusion from low-permeability layers as affected by groundwater velocity: A laboratory investigation by box model and image analysis.

Low-permeability lenses represent potential sources of long-term release when filled from contaminant solute through direct contact with dissolved plumes. The redistribution of contaminant from low to high permeability aquifer zones (Back-Diffusion) was studied. Redistribution causes a long plume tail, commonly regarded as one of the main obstacles to effective groundwater remediation. Laboratory tests were performed to reproduce the redistribution process and to investigate the effect of pumping water on the remediation time of these contaminated low-permeability lenses. The test section used is representative of clay/silt lenses (k≈1∗10-10m/s/k≈1∗10-7m/s) in a sand aquifer (k≈1∗10-3m/s). Hence, an image analysis procedure was used to estimate the diffusive flux of contaminant released by these low-permeability zones. The proposed technique was validated performing a mass balance of a lens saturated by a known quantity of tracer. For each test, performed using a different groundwater velocity, the diffusive fluxes of contaminant released by lenses were compared and the remediation times of the low-permeability zones calculated. For each lens, the obtained remediation timeframes were used to define an analytical relation vs groundwater velocity and the coefficients of these relations were matched to grain size of the low-permeability lenses. Results show that an increase of the velocity field is not useful to diminish the total depletion times as the process mainly diffusive. This is significant when the remediation approach relies on pumping technology.

Comparative assessment of metallurgical recovery of metals from electronic waste with special emphasis on bioleaching.

Waste electrical and electronic equipment (WEEE) or electronic waste (e-waste) is one of the fastest growing waste streams in the urban environment worldwide. The core component of printed circuit board (PCB) in e-waste contains a complex array of metals in rich quantity, some of which are toxic to the environment and all of which are valuable resources. Therefore, the recycling of e-waste is an important aspect not only from the point of waste treatment but also from the recovery of metals for economic growth. Conventional approaches for recovery of metals from e-waste, viz. pyrometallurgical and hydrometallurgical techniques, are rapid and efficient, but cause secondary pollution and economically unviable. Limitations of the conventional techniques have led to a shift towards biometallurgical technique involving microbiological leaching of metals from e-waste in eco-friendly manner. However, optimization of certain biotic and abiotic factors such as microbial species, pH, temperature, nutrients, and aeration rate affect the bioleaching process and can lead to profitable recovery of metals from e-waste. The present review provides a comprehensive assessment on the metallurgical techniques for recovery of metals from e-waste with special emphasis on bioleaching process and the associated factors.

Polychlorinated biphenyls, polychlorinated dibenzo-p-dioxins and dibenzofurans in street dust of North Rhine-Westphalia, Germany.

In this study the occurrence of polychlorinated biphenyls (PCBs), polychlorinated dibenzodioxins and polychlorinated dibenzofurans (PCDDs/PCDFs) in street dust samples was investigated using pressurized liquid extraction and gas chromatography coupled to mass spectrometry. Street dust samples were taken from rural, urban, industrial and industrially influenced urban areas. PCB6 concentrations ranged from 5090±2200 µg/kg (average±standard error of mean) in dusts from industrial premises to 29±8.7 µg/kg in rural areas. Concentration ranges were for dioxin-like PCB toxicity equivalents (dl-PCB TEQ) from 362±164 ng/kg (industrial premises) to 6.5±1.8 ng/kg (rural areas), and for PCDD/PCDF TEQ from 503±448 ng/kg to 2.4±0.13 ng/kg, respectively. Area concentrations of PCB6 (0.040 µg/m2-22 µg/m2), dl-PCB TEQ (0.0038 ng/m2-2.6 ng/m2) and PCDD/PCDF TEQs (14 pg/m2-1980 pg/m2) were estimated. Furthermore, particle size related concentrations of PCBs and PCDD/PCDFs in street dusts were analysed showing throughout almost all samples a distinctive trend of increasing concentrations with decreasing particle sizes. Characterization of homologue patterns of PCBs and PCDDs/PCDFs in street dusts was performed showing a dependence of homologue patterns on different area types, especially for PCBs. It could be demonstrated that the analysis of concentrations in combination with specific homologue patterns of PCBs and PCDDs/PCDFs in street dust samples enables allocation of potential emission sources.

Release of contaminants from a heterogeneously fractured low permeability unit underlying a DNAPL source zone.

The invasion of DNAPL into fractured low permeability deposits results in the formation of secondary source zones that represent a long-term source of VOCs to adjacent aquifers. We present data from a site underlain by a fractured mudstone contaminated with TCE DNAPL that was poised for release following remediation of the overlying aquifer. Observations of contaminant distributions and fracture networks from the site and a nearby mudstone exposure respectively, enabled prediction of the imminent aquifer recontamination. The fractures, likely formed by gypsum dissolution, were characterised by fracture apertures and spacings that ranged from 0.01 to 49 mm and 0.047 to 3.37 m (10th and 90th percentile values) respectively. Numerical model results show that prediction of outward mass flux in the first year was highly variable (8 to 32 g/m²/d for an initial constant concentration with depth profile) and dependent on both the fracture spacing and aperture and the contaminant distribution. However after 1 year, assuming a heterogeneous distribution of fractures, mass flux was predictable within a narrow range of values (at 20 years; 0.04-0.08 g/m²/d). Similar results were obtained from more typical fracture networks with spacings of 0.1 to 0.5 m and apertures of 10 to 100 µm. These results suggest that when considering potential recontamination in a bounding aquifer, fracture characterisation may not be necessary and instead the focus should be on determining the surface area contributing contaminant mass to an aquifer, the contaminant concentration depth profiles, the hydraulic properties of the receiving aquifer and the elapsed time since aquifer remediation.