Mixing state and influence factors controlling diurnal variation of particulate nitrophenol compounds at a suburban area in northern China.

Nitrophenols have received extensive attention due to their strong light-absorbing ability in the near-ultraviolet-visible region, which could be influenced by the atmospheric processes of nitrophenols. However, our knowledge and understanding of the formation and evolution of nitrophenols are still in the nascent stages. In the present study, the mixing states of four mononitrophenol particles (i.e., nitrophenol, methynitrophenol, nitrocatechol, and methoxynitrophenol), and one nitropolycyclic aromatic hydrocarbon particles (i.e., nitronaphthol (NN)) were investigated using a single-particle aerosol mass spectrometer (SPAMS) in November 2019 in Qingdao, China. The results showed, for the first time, that mononitrophenols and NN exhibit different mixing states and diurnal variations. Four mononitrophenols were internally mixed well with each other, and with organic acids, nitrates, potassium, and naphthalene. The diurnal variation in the number fraction of mononitrophenols presented two peaks at 07:00 to 09:00 and 18:00 to 20:00, and a valley at noon. Atmospheric environmental conditions, including NO2, O3, relative humidity, and temperature, can significantly influence the diurnal variation of mononitrophenols. Multiple linear regression and random forest regression models revealed that the main factors controlling the diurnal variation of mononitrophenols were photochemical reactions during the day and aqueous-phase reactions during the night. Unlike mononitrophenols, about 62-83% of NN were internally mixed with [NH4]+ and [H(NO3)2]-, but not with organic acids and potassium. The diurnal variation of NN was also different from that of mononitrophenols, generally increased from 17:00 to 10:00 and then rapidly decreaed from 11:00 to 16:00. These results imply that NN may have sources and atmospheric processes that are different from mononitrophenols. We speculate that this is mostly controlled by photochemical reactions and mixing with [NH4]+, which may influence the diurnal variation of NN in the ambient particles; however, this requires further confirmation. These findings extend our current understanding of the atmospheric formation and evolution of nitrophenols.

Origin of age softening in the refractory high-entropy alloys.

Refractory high-entropy alloys (RHEAs) are emerging materials with potential for use under extreme conditions. As a newly developed material system, a comprehensive understanding of their long-term stability under potential service temperatures remains to be established. This study examined a titanium-vanadium-niobium-tantalum alloy, a promising RHEA known for its superior high-temperature strength and room-temperature ductility. Using a combination of advanced analytical microscopies, Calculation of Phase Diagrams (CALPHAD) software, and nanoindentation, we investigated the evolution of its microstructure and mechanical properties upon aging at 700°C. Trace interstitials such as oxygen and nitrogen, initially contributing to solid solution strengthening, promote phase segregation during thermal aging. As a result of the depletion of solute interstitials within the metal matrix, a progressive softening is observed in the alloy as a function of aging time. This study, therefore, underscores the need for a better control of impurities in future development and application of RHEAs.

Influence of meteorological parameters and oxidizing capacity on characteristics of airborne particulate amines in an urban area of the Pearl River Delta, China.

Nine amine species in atmospheric particles during haze and low-pollution days with low and high relative humidity (RH) were analyzed in urban Guangzhou, China. The mean concentrations of total measured amines (Æ©amines) in fine particles were 208 ± 127, 63.7 ± 21.3, and 120 ± 20.1 ng m-3 during haze, low pollution-low RH (LP-LRH), and low pollution-high RH (LP-HRH) episodes, respectively. The dominant amine species were methylamine (MA), dimethylamine (DMA), diethylamine (DEA) and dibutylamine (DBA), which in total accounted for 82-91% of the Æ©amines during different pollution episodes. The contributions of Æ©amines-C to water-soluble organic carbon (WSOC) and Æ©amines-N to water-soluble organic nitrogen (WSON) were 1.52% and 2.49% during haze, 1.24% and 1.96% during LP-LRH, and 2.00 and 2.98% during LP-HRH days, respectively. The mass proportion of Æ©amines in fine particles was higher during LP-HRH periods (0.19%) than during haze and LP-LRH periods (0.16%). The mass proportion of DBA in Æ©amines increased from 7% during haze and LP-LRH episodes to 25% during LP-HRH episodes. Compared with other amines, DBA showed a stronger linear relationship with RH (r = 0.867, p < 0.01), which demonstrates its high sensitivity to high RH conditions. Meteorological parameters (including RH, the mixed layer depth, wind speed and temperature), the oxidizing capacity (ozone concentration), and gaseous pollutants (NOx and SO2) correlated with amines under different pollution conditions. Under high RH, acid-base reactions were the dominant pathway for the gas-to-particle distribution of amines in urban areas, while direct dissolution dominated in the background site. To our knowledge, this study is the first attempt to conduct in situ measurements of particulate amines during different pollution conditions in China, and further research is needed to in-depth understanding of the influence of amines on haze formation.

Study of nuclear modification factors of deuteron and anti-deuteron in Pb-Pb collisions at [Formula: see text].

The nuclear modification factors ([Formula: see text]) of d and [Formula: see text] have been studied using the parton and hadron cascade model plus the dynamically constrained phase space coalescence model in peripheral (40-60%) and central (0-5%) Pb-Pb collisions at [Formula: see text] with [Formula: see text]. It is found that the [Formula: see text] of [Formula: see text] is similar to that of hadrons ([Formula: see text]) and the [Formula: see text] of antiparticles is the same as that of particles. The suppression effect of d is more significant than that of baryons and mesons in the high-[Formula: see text] region. The suppression of [Formula: see text] at high-[Formula: see text] strongly depends on event centrality and mass of the particles, i.e., the central collision is more suppressed than the peripheral collision. Besides, the yield ratios and double ratios for different particle species, and the coalescence parameter [Formula: see text] for ([Formula: see text]) in pp and Pb-Pb collisions are discussed, respectively. It is observed that the yield ratios and double ratios of d to p and p to [Formula: see text] are similar to those of their anti-particles in three different collision systems, suggesting that the suppressions of matter ([Formula: see text]) and the corresponding antimatter ([Formula: see text]) are around the same level.

Controlled growth of single-crystalline metal nanowires via thermomigration across a nanoscale junction.

Mass transport driven by temperature gradient is commonly seen in fluids. However, here we demonstrate that when drawing a cold nano-tip off a hot solid substrate, thermomigration can be so rampant that it can be exploited for producing single-crystalline aluminum, copper, silver and tin nanowires. This demonstrates that in nanoscale objects, solids can mimic liquids in rapid morphological changes, by virtue of fast surface diffusion across short distances. During uniform growth, a thin neck-shaped ligament containing a grain boundary (GB) usually forms between the hot and the cold ends, sustaining an extremely high temperature gradient that should have driven even larger mass flux, if not counteracted by the relative sluggishness of plating into the GB and the resulting back stress. This GB-containing ligament is quite robust and can adapt to varying drawing directions and velocities, imparting good controllability to the nanowire growth in a manner akin to Czochralski crystal growth.

Long non-coding RNA ROR mitigates cobalt chloride-induced hypoxia injury through regulation of miR-145.

Obstructive sleep apnoea-hypopnoea syndrome (OSAHS) is a condition causing apnea and hypopnea. LncRNA-ROR revealed properties in regulating hypoxia response. Our study explored the roles of ROR in CoCl2-induced hypoxia injury in HK-2 cells. HK-2 cells were treated with CoCl2 to induce hypoxia injury. Cell viability, cell apoptosis and apoptotic proteins were detected using CCK-8, flow cytometry and western blot, respectively. The alter expression of ROR and miR-145 was achieved through transfection. Moreover, the expressions of HIF-α and ERK and MAPK related factors were examined using western blot. We found that CoCl2 decreased cell viability and increased apoptosis as well as increased the expression of ROR. ROR overexpression increased cell viability, decreased cell apoptosis. ROR overexpression upregulated anti-apoptotic proteins Bcl-2 and decreased p53, Bax and cleaved-Caspase-3. ROR overexpression also increased the expression of HIF-α. On the opposite, ROR silence led to the opposite results as relative to ROR overexpression. ROR overexpression decreased expression of miR-145. Co-transfection with ROR overexpression and miR-145 impaired the promoting effects of ROR in CoCl2 treated cells. ROR increased phosphorylation of ERK while decreased phosphorylation of MAPK. In conclusion, lncRNA ROR alleviated CoCl2-induced hypoxia injury through regulation of miR-145 as well as modulating ERK and MAPK signalling. Highlights CoCl2 induces ROR upregulation; Overexpression of ROR reduces CoCl2-induced HK-2 cell injury; Silence of ROR promotes CoCl2-induced HK-2 cell injury; Overexpression of ROR decreases miR-145 expression; ROR overexpression modulates ERK and MAPK signalling pathways through regulation of miR-145.

Upregulation of long noncoding RNA TUG1 contributes to the development of laryngocarcinoma by targeting miR-145-5p/ROCK1 axis.

Laryngocarcinoma is the most common head and neck cancer and has a high incidence and mortality, causing about 83 000 deaths per year worldwide. Our research aimed to investigate the possible role of long noncoding RNA (lncRNA) taurine upregulated gene 1 (TUG1) in laryngocarcinoma development. The messenger RNA (mRNA) levels of TUG1 in tumor tissues and control (plasma) samples of laryngocarcinoma patients as well as in laryngocarcinoma cells were detected. The influences of TUG1 suppression on cell biological processes (viability, apoptosis, migration, and invasion) and cytoskeleton rearrangement in laryngocarcinoma cells were tested. Moreover, we investigated the regulatory interaction between TUG1 and miR-145-5p, and identified the target gene of miR-145-5p. The association between TUG1 and the protein expressions of RhoA/rho associated coiled-coil containing protein kinase (ROCK)/matrix metalloproteinases (MMPs) pathway-associated factors were detected. TUG1 was found to be highly expressed in tumor tissues and plasma samples of laryngocarcinoma patients as well as in laryngocarcinoma cells. Suppression of TUG1 decreased laryngocarcinoma cell viability, increased apoptosis, and suppression migration, invasion, and cytoskeleton rearrangement. Moreover, TUG1 negatively regulated miR-145-5p. TUG1 regulated tumor growth (viability and apoptosis) and metastasis through miR-145-5p. Furthermore, ROCK1 was targeted by miR-145-5p, and miR-145-5p/ROCK1 partner was involved in the process of tumor growth and metastasis. Finally, we found that TUG1 functioned on laryngocarcinoma by activating RhoA/ROCK/MMPs pathway. Our study reveals that lncRNA TUG1 is upregulated in laryngocarcinoma and may be involved in the process of laryngocarcinoma through miR-145-5p downregulation and activating the RhoA/ROCK/MMPs signals.

Oxalate Formation Enhanced by Fe-Containing Particles and Environmental Implications.

We used a single particle mass spectrometry to online detect chemical compositions of individual particles over four seasons in Guangzhou. Number fractions (Nfs) of all the measured particles that contained oxalate were 1.9%, 5.2%, 25.1%, and 15.5%, whereas the Nfs of Fe-containing particles that were internally mixed with oxalate were 8.7%, 23.1%, 45.2%, and 31.2% from spring to winter, respectively. The results provided the first direct field measurements for the enhanced formation of oxalate associated with Fe-containing particles. Other oxidized organic compounds including formate, acetate, methylglyoxal, glyoxylate, purivate, malonate, and succinate were also detected in the Fe-containing particles. It is likely that reactive oxidant species (ROS) via Fenton reactions enhanced the formation of these organic compounds and their oxidation product oxalate. Gas-particle partitioning of oxalic acid followed by coordination with Fe might also partly contribute to the enhanced oxalate. Aerosol water content likely played an important role in the enhanced oxalate formation when the relative humidity is >60%. Interactions with Fe drove the diurnal variation of oxalate in the Fe-containing particles. The study could provide a reference for model simulation to improve understanding on the formation and fate of oxalate, and the evolution and climate impacts of particulate Fe.

[Pollution characteristics of organic and elemental carbon in PM2.5 in Taiyuan].

PM2.5 samples were collected at four sampling sites to study pollution characteristics of carbonaceous aerosols in Taiyuan during winter and summer. Organic carbon (OC) and elemental carbon (EC) in PM2.5 were analyzed by carbon analyzer, and the characteristics including pollution levels, temporal and spatial distributions of OC and EC, secondary organic carbon (SOC) and relationships of OC and EC were discussed in detail. The average concentrations of OC and EC in winter were 22.3 µg x m(-3) and 18.3 µg x m(-3), respectively, while in summer were 13.1 µg x m(-3) and 9.8 µg x m(-3), respectively. The concentrations of total carbon aerosol (TCA) accounted for 56.6% of PM2.5 in winter, and 36.5% in summer; the concentrations of OC and EC at four sites in winter were higher than those in summer, OC and EC levels showed a good uniformity in winter while in summer, the spatial distributions of OC and EC were obviously different; SOC levels were lighter than other cities; the correlation between OC and EC was stronger in winter than that in summer.

[Characteristics of organic carbon and elemental carbon in PM2.5 in Shuozhou City].

PM2.5 samples were collected at four sampling sites in Shuozhou during the heating and non-heating periods. Organic carbon (OC) and elemental carbon (EC) in PM2.5 were analyzed by Elementar Analysensysteme GmbH vario EL cube and the concentration, spatial and temporal distribution characteristics and main sources of OC and EC were studied. The results were as following: average concentrations of OC and EC in PM2.5 during non-heating period were (14.3 ± 2.7) µg x m(-3) and (10.3 ± 3.1) µg x m(-3) while (23.3 ± 5.9) µg xm(-3) and (20.0 ± 5.7) µg x m(-3) during heating period. The concentrations of OC and EC at four sites during the heating period were higher than those during the non-heating period. The concentrations of OC and EC at SW site during heating were the highest which were 28.5 µg x m(-3) and 28.1 µg x m(-3) while the concentrations at PS sites during non-heating period were the highest, which were 17.7 µg x m(-3) and 14.1 µg x m(-3). The ratios between OC and EC during the heating and non-heating period were all below 2 and the correlation between OC and EC was not good with R2 of 0. 66 during heating period and 0.52 during non-heating period which indicated that sources of carbon aerosols were complex. Carbonaceous aerosol pollution should be reduced by controlling the primary emissions such as coal combustion, vehicle exhaust and biomass burning, and by paying attention to secondary pollution at the same time to improve the air quality in Shuozhou City. The concentrations of SOC during heating and non-heating period were (6.44 ± 2.77) µg x m(-3) and (4.11 ± 1.92) µg x m(-3).

[Characterization of organic and elemental carbon in PM10 in Xinzhou City].

PM10 samples were collected at four sampling sites to study pollution characteristics of carbonaceous aerosols in Xinzhou during heating period (March) and non-heating period (July), 2011. Organic carbon (OC) and elemental carbon (EC) in PM10 were analyzed by Elementar Analysensysteme GmbH vario EL cube, and the characteristics including pollution levels, temporal and spatial distributions of OC and EC as well as OC/EC ratios were investigated in detail. The results were as following: OC and EC mass concentrations of PM10 in Xinzhou were (18.5 +/- 4.5) microg x m(-3) and (16.1 +/- 4.3) microg x m(-3), respectively. The concentrations of total carbon aerosol (TCA) accounted for 70.7% of PM10 during the heating period, and 43.8% during the non-heating period. The concentrations of OC at four sites during the heating period were higher than those during the non-heating period, and this trend was consistent with that of EC concentrations except for SQ site, which indicated coal combustion was a dominant source of OC and EC during the heating period. OC concentration at XT site and EC concentration at DC site were the highest, which were 24.1 microg x m(-3) and 22.0 microg x m(-3) respectively, while the concentrations of OC and EC at SQ site were both the lowest, which were 17.2 microg x m(-3) and 14.5 microg x m(-3), respectively, which indicated that the spatial distributions of OC and EC were obviously different. The average values of OC/EC ratios were all below 2, which indicated that the primary pollution was predominant. The correlation between OC and EC during the non-heating period was good with R2 of 0.55, indicating the emission sources were consistent and the vehicle exhaust played an important role, while the correlation was weak during the heating period (R2 = 0.13), which revealed that the emission sources of OC and EC were complicated. Carbonaceous aerosol pollution should be reduced by controlling the primary emissions such as coal combustion, vehicle exhaust, biomass burning and other industrial sources to improve the air quality in Xinzhou City.

[Characteristic of elements in PM2.5 and health risk assessment of heavy metals during heating season in Taiyuan].

The fine particulate matter (PM2.5) sampled during heating season in Taiyuan city and nineteen samples were used to investigate elemental concentrations and its source potential ecological risks of heavy metals, and to assess human exposure and health risk. The result indicated that main elements were Si, Ca, Al, Na, Mg, K, Fe in PM2.5. The main sources of elements in PM2.5 were divided into five categories including soil dust (43.46%), coal burning (15.69%), vehicle emission (13.41%), industrial dust (9.89%) and the construction cement dust (9.03%). Moreover, the order of potential ecological risk index of heavy metals in PM2.5 was Cd > Ni > Hg > Pb > Cu > Zn > As > Co > Cr > Mn, and the ecological hazards were high. The main exposure of heavy metals in atmosphere was respiratory inhalation . The exposure quantity for children was significantly higher than that for adult. The hazard index values suggested a potential non-carcinogenic risk in PM2.5.

Layered double hydroxides as efficient photocatalysts for visible-light degradation of Rhodamine B.

A series of Zn/M-NO3-LDHs (M=Al, Fe, Ti, and Fe/Ti) have been synthesized by two different methods, and their activities for visible-light photocatalytic degradation on Rhodamine B (RB) were tested. Solids were analyzed by XRD, FT-IR, and ICP characterization, confirming the formation of pure LDH phase with good crystal structure. It was observed that the band gap of these nitrate LDH materials was following this order: Zn/Fe-NO3-LDHs (2.55 eV)>Zn/Fe/Ti-NO3-LDHs (2.88 eV)>Zn/Ti-NO3-LDHs (3.0 3eV)>Zn/Al-NO3-LDHs (3.23 eV); however, the degradation performance of RB by four materials followed the order: Zn/Ti-NO3-LDHs (98%)>Zn/Al-NO3-LDHs (96%)>Zn/Fe/Ti-NO3-LDHs (88%)>Zn/Fe-NO3-LDHs (72%). In addition, a possible mechanism for photocatalytic degradation on RB has also been presumed. Moreover, after three regeneration cycles, the percentage of RB degradation rate was still close to 90%.

Facile synthesis of silver nano/micro-ribbons or saws assisted by polyoxomolybdate as mediator agent and vanadium(IV) as reducing agent.

Original and effective syntheses of crystalline silver wires and saw bundles, using reduced Keggin polyoxomolybdovanadate (POM) as mediator and reducing agent, were performed in acetonitrile at room temperature; several parameters influencing the final silver 1D-structures, with micrometric length and nanometric thickness, were varied: the nature of the POM, silver salts, vanadium(iv) source and the mild conditions.

[Ag6(PMo10V2O40](CH3COO).8H2O: A 3D macrocationic polyoxometallic Keggin complex.

Silver atoms and strongly interlinking Keggin units ensure the tridimensionnal macrocationic structure of [Ag(6)(PMo(10)V(2)O(40))](CH(3)COO).8H(2)O, which catalyzes O(2)-based oxidation of p-methoxytoluene in acetic acid by air.