Novel styryl colorants based on anchoring methoxy with anthracene as a donor linked with various active methylene acceptor groups to derive a conjugated π-system along with push-pull geometry were synthesized and well characterized. Photophysical properties were studied in different polarity solvents. The impact of solvent polarizability is delivered in redshifts in absorption and emission spectra, in addition to enhancing the quantum yield. The benzoxazole and benzimidazole moieties in 4c and 4d demonstrated heat stability of more than 300 °C. Fluorescent intensity is directly proportional to the viscosity and 4a demonstrates a notable viscosity sensor through 1.36 fold increase in intensity. In comparison to other styryl dyes, 4c and 4d were shown to have higher values in DMSO for polarizability (53.3496 × 10-24 esu and 53.7459 × 10-24 esu) and first-order hyperpolarizability (86.3467 × 10-30 esu and 89.1941 × 10-30 esu) as well as second-order hyperpolarizability (1768.9121 × 10-36 esu and 1740.6940 × 10-36 esu) due to presence of heterocyclic character. NLO properties of all the styryl dyes 4a-4e are within the fundamental boundary limits. The 4d (benzoxazole) dye exhibited a small HOMO-LUMO energy gap of 2.8825 eV, whereas the 4b and 4e dyes had a larger band gap due to the presence of a carbonyl group.

Organic luminescence materials makes the molecule more enthusiastic in wide  variety of  applications. The luminescent organic materials are in a attraction of the researchers, and the  Aggregation-Induced Emission (AIE) is attributed to the occurrence that particular chromophores (typically fluorophores) display very low or nearly no emission in the monomolecular soluble state but become highly emissive when forming aggregates in solution or in solid state.  This phenomenon is relatively abnormal when compared with many other traditional fluorophores. AIE research suppresses aggregation-caused quenching (ACQ). Nevertheless, the carbon dots (CDs) and quantum dots have shown to have tyical florescence properties, therefore, recent years many researchers have also attracted for their developments.  The CDs, luminescent, and AIE materials are not only used in biomedical applications and organic light-emitting diodes but also in sensing, self-assembly, and other areas. One should introduce promising material to a designed framework that exhibits AIE characteristics to ensure moral results in AIE. Amongest, AIE-active tetraphenylethylene (TPE) is attractive fluorophores due to its easy synthesis strategy. This review article discusses the synthesis properties of TPE, CDs, and luminescent materials with a broad range of applications. We have outlined linear, branched-shaped supramolecular, and hybrid macromolecules due to its potential in the future.

This paper analyses the intertwined impacts of the 2018 US sanctions on Iran and the COVID-19 pandemic (as examples of unplanned international conflicts and global crises) on the source and extent of air pollution in Tehran, the capital of Iran. The impacts are parametrized using the levels of criteria air pollutants (CAP) for 5 years (2015-2020), which were previously deweathered using the promising machine learning technique of Random Forest (RF). The absolute principal component scores-multiple linear regression (APCS-MLR) method and the bivariate polar plot (BPP) technique are used here to analyze the source apportionment profile of the city for the business as usual (BAU; 2015 to 2018), sanctions (2019), and COVID-19 and sanctions (2020) intervals. The results show the severe impact of the 2018 US sanctions on Tehran\'s air quality (AQ); O3, NO2, CO, PM2.5, and PM10 levels increased by 117%, 55%, 20%, 35%, and 10%, respectively, while SO2 levels decreased by 30%. The sanctions also triggered a number of events, such as the disruption of the high-grade fuel supply chain and the Mazut crisis, which directly or indirectly accelerated the photochemical production of local tropospheric ozone to some extent. Sanctions also disrupted Tehran\'s AQ response to the pandemic, with CAP levels decreasing by only 2-7% during the pandemic. The ozone and PM10 BPPs show that the source apportionment profile of the city is dominated by local anthropogenic emission sources, especially urban transport, after the sanctions and the pandemic. Results also show that the impact of soft wars, such as the US sanctions against Iran, on urban air quality degradation is much stronger than that of hard wars, such as the Russia-Ukraine war.

Organophosphate esters (OPEs) serve as significant flame retardants and plasticizers in various petrochemical downstream products. The petrochemical industry could be a potential source of atmospheric OPEs, but their emissions from this industry are poorly understood. The present study revealed the spatial variation, emission, and atmospheric transport of traditional and novel OPEs (TOPEs and NOPEs, respectively) in atmospheric particulate matter (PM) across Hainan and Guangdong petrochemical complexes (HNPC and GDPC, respectively) in southern China. The total concentrations of TOPEs ranged from 232 to 46,002 pg/m3 and from 200 to 20,347 pg/m3 in the HNPC and GDPC, respectively, which were substantially higher than those of NOPEs (HNPC: 23.5-147 pg/m3, GDPC: 13.9-465 pg/m3). Enterprises involved in the production of downstream petrochemical products presented relatively high concentrations of OPEs, indicating evident emissions of these pollutants in the petrochemical industry. The correlations of PM-bound OPEs in the atmosphere are determined mainly by their coaddition to industrial products or their coexistence in technical mixtures. The annual emissions of TOPEs and NOPEs in the HNPC were 42.6 kg and 0.34 kg, respectively, and those in the GDPC were 116 kg and 1.85 kg, respectively. OPEs from the HNPC can reach Vietnam, Cambodia, and Guangxi Province, China, and those from the GDPC can reach Guangxi Province and Hunan Province via atmospheric transmission after 24 h of emission. The OPE concentrations reaching the receptor regions were generally less than 3.20 pg/m3. Risk assessment revealed that OPE inhalation exposure on two petrochemical complexes likely poses minor risks for people living in the study areas, but the risk resulting from two chlorinated OPEs should be noted since they are close to the threshold values. This study has implications for enhancing control measures for OPE emissions to reduce health risks related to the petrochemical industry.

An excellent agreement for simulated and measured absorption and emission spectra is found for four donor-acceptor aromatic molecules (tetraphenylpyrazine, tetraphenylethene, distirylanthracene and hexaphenylsilole) whose derivatives serve as solid state photosensitizers. After comparing several hybrid TDDFT functionals, EOM-CCSD, and experiments, the best agreement was found with TD-B3LYP and double zeta basis sets (6-31G** and def2-SVP) for one molecule in gas phase. A full characterisation of twelve to twenty electronic excited states was performed in every system. Symmetry-forbidden bands are found in the absorption spectra by sampling a hundred vibrationally geometries from a Wigner distribution. The density of states in the region 2-6 eV was also analysed, showing a very packed region of excited states and suggesting that dark electronic states may play a role in the dynamics of some of the photoexcited systems. Further calculations were done with QM/xTB at geometries extracted from previously published X-ray data to evaluate the influence of the environment on the excitations of the four aggregated molecular crystals.

The CO2 emission activity of xylotrophic fungi responding to an increase in temperature in the range of 10-30 °C with pure dikaryotic cultures of Fomes fomentarius s. str., F. inzengae, Fomitopsis betulina, F. pinicola, and Phellinus igniarius was analyzed. Emission activity was assessed by the difference in CO2 concentration in 0.5 L exposure chambers with Petri dishes with mycelium growing on agar at the beginning of exposure and an hour later using a Gasmet DX-4030 FTIR spectrometer (Gasmet Technologies Oy, Finland), error measurements ±50 ppm. Specific (μg CO2/cm2/h) and total (μg CO2/h) emission activity and its relationship with temperature and size (area) of the mycelium were assessed. It is shown that in the range of 10-30 °C, the specific and total CO2 emission activity of the mycelium is closely and positively related to temperature. Specific emission, which is an indicator of the respiratory activity of the mycelium, does not depend on its size; its only driver is temperature, the relationship with which is linear: an increase in temperature by 10 °C causes an increase in the specific emission activity of the mycelium by 1.7 times. The total CO2 emission activity, which is an indicator of the total amount of CO2 emitted, is directly proportional to the specific emission activity and the size of the mycelium. In the range of 10-30 °C, an increase in temperature causes an almost equal increase in both the specific emission activity of the mycelium (Q10 1.7) and its growth (Q10 1.5) and causes an exponential increase in the total emission of CO2. This must be taken into account when predicting CO2 emissions from woody debris under climate change, as it could potentially contribute to accelerating climate change.

: In this contribution we report on a novel approach towards luminescent light-responsive ligands. To this end, cyanostilbene- guanidiniocarbonyl-pyrrole hybrids were designed and investigated. Merging of a luminophore with a supramolecular bioactive ligand bears numerous advantages by overcoming the typical drawbacks of drug-labelling, influencing the overall performance of the active species by attachment of a large luminophore. Here we were able to establish a simple and easily accessible synthesis route to different cyanostyryl-guanidininiocarbonyl-pyrrole (CGCP) derivatives. These compounds were investigated regarding their light-responsive double bond isomerisation, their molecular structures in single crystals by means of X-ray diffractometry, their emission properties by state of the art photophysical characterisation as well as bioimaging and assessment of cell toxicity.

The rising of municipal solid waste incineration (MSWI), constituting 5 % of NOx emissions in Beijing, poses a significant challenge to improving air quality. This study establishes a comprehensive historical inventory of air pollutants (APs) emitted from MSWI plants between 2004 and 2023. The inventory was developed using both the continuous emissions monitoring systems (CEMS)-based method and the EF (emission factors) -based method, incorporating detailed plant-level activity data and localized EF derived from field measurements. These include data from CEMS and manual monitoring. Analysis of CEMS data reveals high compliance rates with emission limits for MSW in Beijing, with 99.9 %, 99.5 %, 99.8 %, 98.7 %, and 99.5 % of units meeting standards for PM, SO2, NOx, CO and HCl, respectively. This suggests effective implementation of emission standards in Beijing, although further strengthening of policies, particularly for CO emissions, is warranted. Overall, total AP emissions have increased annually largely attributed to measures implemented for DeSOx, DeNOx, and DePM since 1998. Most MSWI facilities are located in suburban areas rather than urban cores. Emissions of SO2, HCl, CO, Hg, Cd + Ti, other metals, dioxins, VOCs, and NH3 exhibit a spatially homogeneous distribution at the district level, while PM and NOx emissions demonstrate heterogeneity. Scenario analysis underscores the importance of continuous improvement and upgrading of advanced air pollution control devices. This study contributes a methodological framework for estimating emissions, reducing uncertainties, and informing policy-making to mitigate APs emissions in megacities. It serves as a valuable reference for similar cities grappling with air quality challenges.

This study examines catalytic ability of various zeolite materials in converting discarded tire pyrolyzed oil by employing a moderate sized pyrolysis plant of a 10 L working volume. The study revealed that the yield of liquid fractions using γ-Al2O3 was greater than that of HZSM-5 and HY, while the yield of condensates were limited in the absence of catalyst. The tire waste pyrolysis oil catalytcially enhanced by alumina catalyst analyzed using Fourier transform infrared spectroscopy exhibited the stretching bands corresponding to aromatic and non-aromatic compounds. The GC MS analysis revealed that the cyclic unsaturated fragment percentages in liquids were decreased by the catalysts to 53.9% with HY, 59.0% with γ-Al2O3, and 62.2% with HZSM-5, which in turn was converted into aromatic chemicals. Nitrogen adsorption desorption analysis revealed that γ-Al2O3 has an enhanced surface area of 635 m2/g which improved its catalytic performance. The cracked liquid oil had viscosity (10.36 cSt), values of pour and flash temperatures of -2.2 °C and 41 °C respectively, analogous to petroleum diesel. The upgraded pyrolysis oil (10%) is blended with gasoline (90%), and emission analysis was performed. Moreover, liquid oil needs post treatment (refining) for its use as energy source in transportation application. The novelty of this research is in its comparative analysis of multiple catalysts under controlled conditions using a small pilot-scale pyrolysis reactor, which provides insights into optimizing the pyrolysis process for industrial applications.