Integrating In-Plane Thermoelectricity and Out-Plane Piezoresistivity for Fully Decoupled Temperature-Pressure Sensing.

A flexible sensor that simultaneously senses temperature and pressure is crucial in various fields, such as human-machine interaction, artificial intelligence, and biomedical applications. Previous research has mainly focused on single-function flexible sensors for e-skins or smart devices, and integrated bimodal sensing of temperature and pressure without complex crosstalk decoupling algorithms remains challenging. In this work, a flexible bimodal sensor is proposed that utilizes spatial orthogonality between in-plane thermoelectricity and out-plane piezoresistivity, which enables fully decoupled temperature-pressure sensing. The proposed bimodal sensor exhibits a high sensitivity of 281.46 µV K-1 for temperature sensing and 2.181 kPa-1 for pressure sensing. In the bimodal sensing mode, the sensor exhibits negligible mutual interference, providing a measurement error of ± 7% and ± 8% for temperature and pressure, respectively, within a 120 kPa pressure range and a 40 K temperature variation. Additionally, simultaneous spatial mapping of temperature and pressure with a bimodal sensor array enables contact shape identification with enhanced accuracy beyond the limit imposed by the number of sensing units. The proposed integrated bimodal sensing strategy does not require complex crosstalk decoupling algorithms, which represents a significant advancement in flexible sensors for applications that necessitate simultaneous sensing of temperature and pressure.

Life-Course Health Risk Assessment of PM2.5 Elements in China: Exposure Disparities by Species, Source, Age, Gender, and Location.

Key stages in people's lives have particular relevance for their health; the life-course approach stresses the importance of these stages. Here, we applied a life-course approach to analyze the health risks associated with PM2.5-bound elements, which were measured at three sites with varying environmental conditions in eastern China. Road traffic was found to be the primary source of PM2.5-bound elements at all three locations, but coal combustion was identified as the most important factor to induce both cancer risk (CR) and noncancer risk (NCR) across all age groups due to the higher toxicity of elements such as As and Pb associated with coal. Nearly half of NCR and over 90% of CR occurred in childhood (1-6 years) and adulthood (>18 years), respectively, and females have slightly higher NCR and lower CR than males. Rural population is found to be subject to the highest health risks. Synthesizing previous relevant studies and nationwide PM2.5 concentration measurements, we reveal ubiquitous and large urban-rural environmental exposure disparities over China.

Comparative analysis for the impacts of VOC subgroups and atmospheric oxidation capacity on O3 based on different observation-based methods at a suburban site in the North China Plain.

The persistent O3 pollution in the Beijing-Tianjin-Hebei (BTH) region remains unresolved, largely due to limited comprehension of O3-precursor relationship and photochemistry drivers. In this work, intraday O3 sensitivity evolution from VOC-limited (volatile organic compound) regime in the forenoon to transition regime in the late afternoon was inferred by relative incremental reactivity (RIR) in summer 2019 at Xianghe, a suburban site in BTH region, suggesting that VOC-focused control policy could combine with stringent afternoon NOx control. Then detailed impacts of VOC subgroups on O3 formation were further comprehensively quantified by parametric OH reactivity (KOH), O3 formation potential (OFP), as well as RIR weighted value and O3 formation path tracing (OFPT) approach based on photochemical box model. O3 episode days corresponded to stronger O3 formation, depicted by higher KOH (10.4 s-1), OFP (331.7 µg m-3), RIR weighted value (1.2), and F(O3)-OFPT (15.5 ppbv h-1). High proportions of isoprene and OVOCs (oxygenated VOCs) to the total KOH and the OFPT method were demonstrated whereas results of OFP and RIR-weighted presented extra great impacts of aromatics on O3 formation. The OFPT approach captured the process that has already happened and included final O3 response to the original VOC, thus reliable for replicating VOC impacts. The comparison results of the four methods showed similarities when utilizing KOH and OFPT methods, which reveals that the potential applicability of simple KOH for contingency VOC control and more complex OFPT method for detailed VOC- and source-oriented control during policy-making. To investigate propulsion of VOC-involved O3 photochemistry, atmospheric oxidation capacity (AOC) was quantified by two atmospheric oxidation indexes (AOI). Both AOIp_G (7.0 × 107 molec cm-3 s-1, potential AOC calculated by oxidation reaction rates) and AOIe_G (8.5 µmol m-3, estimated AOC given redox electron transfer for oxidation products) were stronger on O3 episode days, indicating that AOC promoted the radical cycling initiated from VOC oxidation and subsequent O3 production. Result-oriented AOIe_G reasonably characterized actual AOC inferred by good linear correlation between AOIe_G and O3 concentrations compared to process-oriented AOIp_G. Therefore, with continuous NOx abatement, AOIe_G should be considered to represent actual AOC, also O3-inducing ability.

Summertime Urban Ammonia Emissions May Be Substantially Underestimated in Beijing, China.

Ammonia (NH3) is critical to the nitrogen cycle and PM2.5 formation, yet a great deal of uncertainty exists in its urban emission quantifications. Model-underestimated NH3 concentrations have been reported for cities, yet few studies have provided an explanation. Here, we explore reasons for severe WRF-Chem model underestimations of NH3 concentrations in Beijing in August 2018, including simulated gas-particle partitioning, meteorology, regional transport, and emissions, using spatially refined (3 km resolution) NH3 emission estimates in the agricultural sector for Beijing-Tianjin-Hebei and in the traffic sector for Beijing. We find that simulated NH3 concentrations are significantly lower than ground-based and satellite observations during August in Beijing, while wintertime underestimations are much more moderate. Further analyses and sensitivity experiments show that such discrepancies cannot be attributed to factors other than biases in NH3 emissions. Using site measurements as constraints, we estimate that both agricultural and non-agricultural NH3 emission totals in Beijing shall increase by ∼5 times to match the observations. Future research should be performed to allocate underestimations to urban fertilizer, power, traffic, or residential sources. Dense and regular urban NH3 observations are necessary to constrain and validate bottom-up inventories and NHx simulation.

Syntheses and evaluation of acridone derivatives as anticancer agents targeting Kras promoter i-motif structure.

Two series of novel acridone derivatives were designed and synthesized, with their anticancer activity evaluated. Most of these compounds showed potent antiproliferative activity against cancer cell lines. Among them, compound C4 with dual 1,2,3-triazol moieties exhibited the most potent activity against Hep-G2 cells with IC50 value determined to be 6.29 ± 0.93 µM. Subsequent experiments showed that C4 could bind to and destabilize Kras gene promoter i-motif structure without significant interaction with its corresponding G-quadruplex. C4 could down-regulate Kras expression in Hep-G2 cells, possibly due to its interaction with the Kras i-motif. Further cellular studies indicated that C4 could induce apoptosis of Hep-G2 cells, possibly related to its effect on mitochondrial dysfunction. These results indicated that C4 could be further developed as a promising anticancer agent.

Analysis of VOC emissions and O3 control strategies in the Fenhe Plain cities, China.

Long-term continuous hourly measurements of ambient volatile organic compounds (VOCs) are scarce at the regional scale. In this study, a one-year hourly measurement campaign of VOCs was performed in Lvliang, Linfen, and Yuncheng in the heavily polluted Fenhe Plain region in China. The VOC average (±standard deviation, std) concentrations in Lvliang, Linfen, and Yuncheng were 44.4 ± 24.9, 45.7 ± 24.9, and 37.5 ± 25.0 ppbv, respectively. Compared to published data from the past two decades in China, the observed VOCs were at high concentration levels. VOCs in the Fenhe Plain cities were significantly impacted by industrial sources according to calculated emission ratios but were less affected by liquefied petroleum gas and natural gas (LPG/NG) and traffic emissions than those in megacities abroad. The emission inventories and observation data were combined for verification and identification of the key VOC species and sources controlling ozone (O3). Industrial emissions were the largest source of VOCs, accounting for 65%-79% of the total VOC emissions, while the coking industry accounted for 45.2%-66.0%. The emission inventories significantly underestimated oxygenated VOC (OVOC) emissions through the verification of VOC emission ratios. O3 control scenarios were analyzed by changing VOC/NOX reduction ratios through a photochemical box model. O3 control strategies were formulated considering local pollution control plans, emission inventories, and O3 formation regimes. The O3 reduction of reactivity-control measures was comparable with emission-control measures, ranging from 16% to 41%, which was contrary to the general perception that ozone formation potential (OFP)-based measures were more efficient for O3 reduction. Sources with high VOC emissions are accompanied by high OFP on the Fenhe Plain, indicating that the control of high-emission sources can effectively mitigate O3 pollution on this region.

Biological and Nonbiological Sources of Fluorescent Aerosol Particles in the Urban Atmosphere.

Online detection of bioaerosols based on the light-induced fluorescence (LIF) technique is still challenging due to the complexity of bioaerosols and the external/internal mixing with nonbiological fluorescent compositions. Although many lab studies have measured the fluorescence properties of the biological and nonbiological materials, there is still a scarcity of knowledge of the sources of fluorescent aerosol particles (FAP) in the ambient atmosphere. Here, we fill this gap by combining the online measurement of an LIF-based instrument (wideband integrated bioaerosol sensor, WIBS, 0.8-20 µm) with the measurements of typical biological matter and the compositions related to major nonbiological FAP from May to July in the megacity Beijing. We find that fungal spores and pollen are widely observed in all types of FAP using a WIBS. Bacteria are suggested to be associated with the fine mode FAP (excitation/emission: 280 nm/310-400 nm; 0.8-3 µm). The FL-B and -BC particles (emission in 420-650 nm) contributing the most to FAP are strongly associated with humic-like substances, dust, burning and combustion emissions, and secondary organic aerosols (SOA). This study provides a guide for interpreting individual FAP measured by LIF instruments and points to the applicability of online LIF instruments to characterize nonbiological compositions including SOA.

Effect of Different Combustion Processes on Atmospheric Nitrous Acid Formation Mechanisms: A Winter Comparative Observation in Urban, Suburban and Rural Areas of the North China Plain.

Atmospheric nitrous acid (HONO) is a dominant precursor of hydroxyl (OH) radicals, and its formation mechanisms are still controversial. Few studies have simultaneously explored effects of different combustion processes on HONO sources. Hereby, synchronous HONO measurement in urban (BJ), suburban (XH) and rural (DBT) areas with different combustion processes is performed in the North China Plain in winter. A box model is utilized to analyze HONO formation mechanisms. HONO concentration is the highest at the DBT site (2.51 ± 1.90 ppb), followed by the XH (2.18 ± 1.95 ppb) and BJ (1.17 ± 1.20 ppb) sites. Vehicle exhaust and coal combustion significantly contribute to nocturnal HONO at urban and rural sites, respectively. During a stagnant pollution period, the NO+OH reaction and combustion emissions are more crucial to HONO in urban and rural areas; meanwhile, the heterogeneous reaction of NO2 is more significant in suburban areas. Moreover, the production rate of OH from HONO photolysis is about 2 orders of magnitude higher than that from ozone photolysis. Consequently, vehicle exhaust and coal combustion can effectively emit HONO, further causing environmental pollution and health risks. It is necessary to expand the implementation of the clean energy transition policy in China, especially in areas with substantial coal combustion.

Significant reduction in atmospheric organic and elemental carbon in PM2.5 in 2+26 cities in northern China.

To better understand the change characteristics and reduction in organic carbon (OC) and elemental carbon (EC) in particulate matter (PM) with a diameter of ≤2.5 µm (PM2.5) driven by the most stringent clean air policies and pandemic-related lockdown measures in China, a comprehensive field campaign was performed to measure the carbonaceous components in PM2.5 on an hourly basis via harmonized analytical methods in the Beijing-Tianjin-Hebei and its surrounding region (including 2 + 26 cities) from January 1 to December 31, 2020. The results indicated that the annual average concentrations of OC and EC reached as low as 6.6 ± 5.7 and 1.8 ± 1.9 µg/m3, respectively, lower than those obtained in previous studies, which could be attributed to the effectiveness of the Clean Air Action Plan and the impact of the COVID-19-related lockdown measures implemented in China. Marked seasonal and diurnal variations in OC and EC were observed in the 2 + 26 cities. Significant correlations (p < 0.001) between OC and EC were found. The annual average secondary OC levels level ranged from 1.8-5.4 µg/m3, accounting for 37.7-73.0% of the OC concentration in the 2 + 26 cities estimated with the minimum R squared method. Based on Interagency Monitoring of Protected Visual Environments (IMPROVE) algorithms, the light extinction contribution of carbonaceous PM to the total amount reached 21.1% and 26.0% on average, suggesting that carbonaceous PM played a less important role in visibility impairment than did the other chemical components in PM2.5. This study is expected to provide an important real-time dataset and in-depth analysis of the significant reduction in OC and EC in PM2.5 driven by both the Clean Air Action Plan and COVID-19-related lockdown policies over the past few years, which could represent an insightful comparative case study for other developing countries/regions facing similar carbonaceous PM pollution.

Significant contribution of secondary particulate matter to recurrent air pollution: Evidence from in situ observation in the most polluted city of Fen-Wei Plain of China.

Particulate matter (PM) pollution in high emission regions will affect air quality, human health and climate change on both local and regional scales, and thus attract worldwide attention. In this study, a comprehensive study on PM2.5 and its chemical composition were performed in Yuncheng (the most polluted city of Fen-Wei Plain of China) from November 28, 2020 to January 24, 2021. The average concentration of PM2.5 was 87.8 ± 52.0 µg/m3, which were apparently lower than those observed during the same periods of past five years, attributable to the clean air action plan implemented in this region. NO3- and organic carbon (OC) were the dominant particulate components, which on average contributed 22.6% and 16.5% to PM2.5, respectively. The fractions of NO3-, NH4+, OC and trace metals increased while those of crustal materials and elemental carbon decreased with the degradation of PM2.5 pollution. Six types of PM2.5 sources were identified by the PMF model, including secondary inorganic aerosol (35.3%), coal combustion (28.7%), vehicular emission (20.7%), electroplating industry (8.6%), smelt industry (3.9%) and dust (2.8%). Locations of each identified source were pinpointed based on conditional probability function, potential source contribution function and concentration weighted trajectory, which showed that the geographical distribution of the sources of PM2.5 roughly agreed with the areas of high emission. Overall, this study provides valuable information on atmospheric pollution and deems beneficial for policymakers to take informed action to sustainably improve air quality in highly polluted region.

Characteristics and source attribution of PM2.5 during 2016 G20 Summit in Hangzhou: Efficacy of radical measures to reduce source emissions.

A field campaign was conducted to study the PM2.5 and atmospheric gases and aerosol's components to evaluate the efficacy of radical measures implemented by the Chinese government to improve air quality during the 2016 G20 Summit in Hangzhou China. The lower level of PM2.5 (32.48 ± 11.03 µg/m3) observed during the control period compared to pre-control and post-control periods showed that PM2.5 was alleviated by control policies. Based on the mass concentrations of particulate components, the emissions of PM2.5 from local sources including fossil fuel, coal combustion, industry and construction were effectively reduced, but non-exhaust emission was not reduced as effectively as expected. The accumulation of SNA (SO42-, NO3-, NH4+) was observed during the control period, due to the favourable synoptic weather conditions for photochemical reactions and heterogeneous hydrolysis. Because of transboundary transport during the control period, air masses from remote areas contributed significantly to local PM2.5. Although, secondary organic carbon (OCsec) exhibited more sensitivity than primary organic carbon (OCpri) to control measures, and the increased nitrogen oxidation ratio (NOR) implied the regional transport of aged secondary aerosols to the study area. Overall, the results from various approaches revealed that local pollution sources were kept under control, indicating that the implementation of mitigation measures were helpful in improving the air quality of Hangzhou during G20 summit. To reduce ambient levels of PM2.5 further in Hangzhou, regional control policies may have to be taken so as to reduce the impact of long-range transport of air masses from inland China.

Different HONO Sources for Three Layers at the Urban Area of Beijing.

Gaseous nitrous acid (HONO) is a crucial precursor of the hydroxyl (OH) radical, which is a "detergent" in the atmosphere. Nowadays, HONO formation mechanisms at polluted urban areas are controversial, which restricts the understanding of atmospheric oxidative capacity and radical cycling. Herein, multiday vertical observation of HONO and NOx was simultaneously performed at three heights at the urban area of Beijing for the first time. The vertical distribution of HONO was often unexpected, and it had the highest HONO concentration at 120 m, followed by those at 8 and 240 m. 0D box model simulations suggest that ground and aerosol surfaces might play similar roles in NO2 conversion at 8 m during the whole measurement. NO2 conversion on aerosol surfaces was the most important HONO source aloft during haze days. At daytime, a strong missing HONO source unexpectedly existed in the urban aloft, and it was relevant to solar radiation and consumed OH.

Seasonal variation and sources of derivatized phenols in atmospheric fine particulate matter in North China Plain.

Qualitative and quantitative analyses of derivatized phenols in Beijing and in Xinglong were performed from 2016 to 2017 using gas chromatography-mass spectrometry. The results showed substantially more severe pollution in Beijing. Of the 14 compounds detected, the total average concentration was 100 ng/m3 in Beijing, compared with 11.6 ng/m3 in Xinglong. More specifically, concentration of nitro-aromatic compounds (NACs) (81.9 ng/m3 in Beijing and 8.49 ng/m3 in Xinglong) was the highest, followed by aromatic acids (14.6 ng/m3 in Beijing and 2.42 ng/m3 in Xinglong) and aromatic aldehydes (3.62 ng/m3 in Beijing and 0.681 ng/m3 in Xinglong). In terms of seasonal variation, the highest concentrations were found for 4-nitrocatechol in winter in Beijing (79.1 ± 63.9 ng/m3) and 4-nitrophenol in winter in Xinglong (9.72 ± 8.94 ng/m3). The analysis also revealed diurnal variations across different seasons. Most compounds presented higher concentrations at night in winter because of the decreased boundary layer height and increased heating intensity. While some presented higher levels during the day, which attributed to the photo-oxidation process for summer and more biomass burning activities for autumn. Higher concentrations appeared in winter and autumn than in spring and summer, which resulted from more coal combustions and adverse meteorological conditions. The significant correlations among NACs indicated similar sources of pollution. Higher correlations presented within each subgroup than those between the subgroups. Good correlations between levoglucosan and nitrophenols, nitrocatechols, nitrosalicylic acids, with correlation coefficients (r) of 0.66, 0.69 and 0.69, respectively, indicating an important role of biomass burning among primary sources.

Meteorological mechanism for a large-scale persistent severe ozone pollution event over eastern China in 2017.

An intensive and persistent regional ozone pollution event occurred over eastern China from 25 June to 5 July 2017. 73 out of 96 selected cities, most located in the Beijing-Tianjin-Hebei and the surrounding area (BTHS), suffered severe ozone pollution. A north-south contrast ozone distribution, with higher ozone (199 ± 33 µg/m3) in the BTHS and lower ozone (118 ± 25 µg/m3) in the Yangtze River Delta (YRD), was found to be dominated by the position of the West Pacific Subtropical High (WPSH) and mid-high latitude wave activities. In the BTHS, the positive anomalies of geopotential height at 500 hPa and temperature at the surface indicated favorable meteorological conditions for local ozone formation. Prevailing northwesterly winds in the mid-high troposphere and warm advection induced by weak southerly winds in the low troposphere resulted in low-moderate relative humidity (RH), less total cloud cover (TCC), strong solar radiation and high temperatures. Moreover, southerly winds prevailing over the BTHS aggravated the pollution due to regional transportation of O3 and its precursors. On one hand, the deep sinking motion and inversion layer suppressed the dispersion of pollutants. On the other hand, O3-rich air in the upper layer was maintained at night due to temperature inversion, which facilitated O3 vertical transport to the surface in the next-day morning due to elevated convection. Generally, temperature, UV radiation, and RH showed good correlations with O3 in the BTHS, with rates of 8.51 (µg/m3)/°C (within the temperature range of 20-38°C), 59.54 (µg/m3)/(MJ/m2) and -1.93 (µg/m3)/%, respectively.

Fine Particle Constituents and Mortality: A Time-Series Study in Beijing, China.

There is a rising concern that fine particle (PM2.5) compositions may play an important role in explaining PM2.5-related mortality risks. However, PM2.5 constituents responsible for these risks have not yet been determined. To date, there are few PM2.5 constituent health studies in developing countries. We adopted a time-series approach, using generalized linear regression models to examine associations between short-term exposure to PM2.5 constituents and mortality. We analyzed data stratified by sex and by age groups (<65, 65-74, and >74) from 2013 to 2015 in Beijing, China. We also investigated seasonal patterns of such associations. For a 0 day lag, interquartile range increases in potassium, calcium, magnesium, and organic carbon were associated with 0.51% (95% CI: 0.17-0.85), 2.07% (95% CI: 0.71-3.44), 0.26% (95% CI: 0.08-0.44), and 2.65% (95% CI: 0.18-5.18) increases in respiratory mortality, and sulfate with a 1.57% (95% CI: 0.04-3.12) increase in cardiovascular mortality. In the season-stratified analysis, the association of some constituents (potassium, calcium, magnesium, nitrate, sulfate, and organic carbon) with respiratory mortality appeared to be stronger in cold seasons than in warm seasons. Older adults (65-74) may be susceptible to certain compositions. Our findings provide evidence that link PM2.5 constituents with mortality and suggest that adverse effects vary among constituents in different seasons.

Characterization of submicron particles during autumn in Beijing, China.

In this study, we performed a highly time-resolved chemical characterization of non-refractory submicron particles (NR-PM1) in Beijing by using an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). The results showed the average NR-PM1 mass concentration to be 56.4±58.0µg/m3, with a peak at 307.4µg/m3. Due to the high frequency of biomass burning in autumn, submicron particles significantly increased in organic content, which accounted for 51% of NR-PM1 on average. Secondary inorganic aerosols (sulfate+nitrate+ammonium) accounted for 46% of NR-PM1, of which sulfate, nitrate, and ammonium contributed 15%, 20%, and 11%, respectively. To determine the intrinsic relationships between the organic and inorganic species, we used the positive matrix factorization (PMF) model to merge the high-resolution mass spectra of the organic species and NO+ and NO2+ ions. The PMF analysis separated the mixed organic and nitrate (NO+ and NO2+) spectra into four organic factors, including hydrocarbon-like organic aerosol (HOA), oxygenated organic aerosol (OOA), cooking organic aerosol (COA), and biomass burning organic aerosol (BBOA), as well as one nitrate inorganic aerosol (NIA) factor. COA (33%) and OOA (30%) contributed the most to the total organic aerosol (OA) mass, followed by BBOA (20%) and HOA (17%). We successfully quantified the mass concentrations of the organic and inorganic nitrates by the NO+ and NO2+ ions signal in the organic and NIA factors. The organic nitrate mass varied from 0.01-6.8µg/m3, with an average of 1.0±1.1µg/m3, and organic nitrate components accounted for 10% of the total nitrate mass in this observation.

Characterizing ozone pollution in a petrochemical industrial area in Beijing, China: a case study using a chemical reaction model.

This study selected a petrochemical industrial complex in Beijing, China, to understand the characteristics of surface ozone (O3) in this industrial area through the on-site measurement campaign during the July-August of 2010 and 2011, and to reveal the response of local O3 to its precursors' emissions through the NCAR-Master Mechanism model (NCAR-MM) simulation. Measurement results showed that the O3 concentration in this industrial area was significantly higher, with the mean daily average of 124.6 µg/m(3) and mean daily maximum of 236.8 µg/m(3), which are, respectively, 90.9 and 50.6 % higher than those in Beijing urban area. Moreover, the diurnal O3 peak generally started up early in 11:00-12:00 and usually remained for 5-6 h, greatly different with the normal diurnal pattern of urban O3. Then, we used NCAR-MM to simulate the average diurnal variation of photochemical O3 in sunny days of August 2010 in both industrial and urban areas. A good agreement in O3 diurnal variation pattern and in O3 relative level was obtained for both areas. For example of O3 daily maximum, the calculated value in the industrial area was about 51 % higher than in the urban area, while measured value in the industrial area was approximately 60 % higher than in the urban area. Finally, the sensitivity analysis of photochemical O3 to its precursors was conducted based on a set of VOCs/NOx emissions cases. Simulation results implied that in the industrial area, the response of O3 to VOCs was negative and to NOx was positive under the current conditions, with the sensitivity coefficients of -0.16~-0.43 and +0.04~+0.06, respectively. By contrast, the urban area was within the VOCs-limitation regime, where ozone enhancement in response to increasing VOCs emissions and to decreasing NOx emission. So, we think that the VOCs emissions control for this petrochemical industrial complex will increase the potential risk of local ozone pollution aggravation, but will be helpful to inhibit the ozone formation in Beijing urban area through reducing the VOCs transport from the industrial area to the urban area.

Examining trends and variability of PM2.5-associated organic and elemental carbon in the megacity of Beijing, China: Insight from decadal continuous in-situ hourly observations.

Organic carbon (OC) and elemental carbon (EC) in fine particulate matter (PM2.5) play pivotal roles in impacting human health, air quality, and climate change dynamics. Long-term monitoring datasets of OC and EC in PM2.5 are indispensable for comprehending their temporal variations, spatial distribution, evolutionary patterns, and trends, as well as for assessing the effectiveness of clean air action plans. This study presents and scrutinizes a comprehensive 10-year hourly dataset of PM2.5-bound OC and EC in the megacity of Beijing, China, spanning from 2013 to 2022. Throughout the entire study period, the average concentrations of OC and EC were recorded at 8.8 ± 8.7 and 2.5 ± 3.0 µg/m3, respectively. Employing the seasonal and trend decomposition methodology, specifically the locally estimated scatter plot smoothing method combined with generalized least squares with the autoregressive moving average method, the study observed a significant decline in OC and EC concentrations, reducing by 5.8 % yr-1 and 9.9 % yr-1 at rates of 0.8 and 0.4 µg/m3 yr-1, respectively. These declining trends were consistently verified using Theil-Sen method. Notably, the winter months exhibited the most substantial declining trends, with rates of 9.3 % yr-1 for OC and 10.9 % yr-1 for EC, aligning with the positive impact of the implemented clean air action plan. Weekend spikes in OC and EC levels were attributed to factors such as traffic regulations and residential emissions. Diurnal variations showcased higher concentrations during nighttime and lower levels during daytime. Although meteorological factors demonstrated an overall positive impact with average reduction in OC and EC concentrations by 8.3 % and 8.7 %, clean air action plans including the Air Pollution Prevention and Control Action Plan (2013-2017) and the Three-Year Action Plan to Win the Blue Sky War (2018-2020) have more contributions in reducing the OC and EC concentrations with mass drop rates of 87.1 % and 89.2 % and 76.7 % and 96.7 %, respectively. Utilizing the non-parametric wind regression method, significant concentration hotspots were identified at wind speeds of ≤2 m/s, with diffuse signals recorded in the southwestern wind sectors at wind speeds of approximately 4-5 m/s. Interannual disparities in potential source regions of OC and EC were evident, with high potential source areas observed in the southern and northwestern provinces of Beijing from 2013 to 2018. In contrast, during 2019-2022, potential source areas with relatively high values of potential source contribution function were predominantly situated in the southern regions of Beijing. This analysis, grounded in observational data, provides insights into the decadal changes in the major atmospheric composition of PM2.5 and facilitates the evaluation of the efficacy of control policies, particularly relevant for developing countries.

Decyanative Heteroarylations of Glycine Derivatives.

Amino acids and aromatic nitrogen heterocycles are widely used in pharmaceuticals. Herein, we present an effective visible-light-driven thiobenzoic acid (TBA)-catalyzed decyanative C(sp3)-H heteroarylation of glycine derivatives. This process occurs under mild and straightforward conditions, affording a range of valuable yet challenging-to-obtain α-heteroaryl amino acid derivatives. Moreover, this organocatalytic C(sp3)-C(sp2) bond formation reaction is applicable to the late-stage modification of various short peptides.

Stereodivergent Synthesis of All Stereoisomers of 2,3-Disubstituted δ-Lactam Derivatives via Organocatalytic Cascade Reactions and Base-Induced Epimerization.

A protocol was developed to achieve stereodivergent synthesis of stereoisomers of δ-lactam bearing vicinal chiral centers. Organocatalytic cascade reactions were employed to produce the target products as the kinetic products, which exhibited remarkable enantioselectivities. In the presence of DBU, the kinetic product underwent epimerization to form a thermodynamically more stable diastereomer without loss in enantioselectivity. By simply switching the chiral organocatalyst and its enantiomer, we can efficiently obtain four stereoisomers with high enantioselectivities.