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-NO_x-VOC sensitivities. We found that the VOC-limited, VOC-NO_x-limited, and NO_x-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-NO_x-limited in the afternoon. Therefore, this study offers information on HCHO sources and corresponding O₃ production sensitivities to support strategic management decisions.

The strong radioactivity of iodine compounds derived from nuclear power plant wastes has motivated the development of highly efficient adsorbents. Porous aromatic frameworks (PAFs) have attracted much attention due to their low density and diverse structure. In this work, an azo group containing PAF solid, denoted as LNU-58, was prepared through Suzuki polymerization of tris-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl)-amine and 3,5-dibromoazobenzene building monomers. Based on the specific polarity properities of the azo groups, the electron-rich aromatic fragments in the hierarchical architecture efficiently capture iodine molecules with an adsorption capacity of 3533.11 mg g⁻¹ (353 wt%) for gaseous iodine and 903.6 mg g⁻¹ (90 wt%) for dissolved iodine. The iodine uptake per specific surface area up to 8.55 wt% m⁻² g⁻¹ achieves the highest level among all porous adsorbents. This work illustrates the successful preparation of a new type of porous adsorbent that is expected to be applied in the field of practical iodine adsorption.

Eating vegetables with pesticide residues over a long period of time causes serious adverse effects on the human body, such as acute poisoning, chronic poisoning, and endocrine system interference. To achieve the goal of a healthy society, it is an urgent issue to find a simple and effective method to detect organic pesticides. In this work, two fluorescent porous organic polymers, LNU-45 and LNU-47 (abbreviation for Liaoning University), were prepared using π-conjugated dibromopyrene monomer and boronic acid compounds as building units through a Suzuki coupling reaction. Due to the large π-electron delocalization effect, the resulting polymers revealed enhanced fluorescence performance. Significantly, in sharp contrast with the planar π-conjugated polymer framework (LNU-47), the distorted conjugated structure (LNU-45) shows a higher specific surface area and provides a broad interface for analyte interaction, which is helpful to achieve rapid response and detection sensitivity. LNU-45 exhibits strong fluorescence emission at 469 nm after excitation at 365 nm in THF solution, providing strong evidence for its suitability as a luminescent chemosensor for organic pesticides. The fluorescence quenching coefficients of LNU-45 for trifluralin and dicloran were 5710 and 12,000 (LNU-47 sample by ca. 1.98 and 3.38 times), respectively. Therefore, LNU-45 serves as an effective “real-time” sensor for the detection of trifluralin and dicloran with high sensitivity and selectivity.

Ultramicropores (size < 0.7 nm) are critically demanded to provide an efficient path for the penetration and transportation of electrolytes to achieve high-performance supercapacitors. Here, a self-sacrificial template approach is adopted, which introduces C8 alkyl chains with a kinetic diameter of 0.8–1 nm to occupy the cavity of a porous aromatic framework (PAF). During the heating process, the alkyl chains decompose from the dense architecture as the temperature increased from 500 to 600 °C, forming ∼1 nm micropores. The newly-obtained cavities provide sites for thermal-driven skeleton engineering (700–900 °C) to obtain ultramicropores. Based on the well-defined pore structure, the carbonized PAF solid revealed outstanding electrochemical performances, including high rate and long-term stability in a 6 M KOH electrolyte. Notably, the specific capacitance (294 F g⁻¹) derived from the self-sacrificial template method exceeds the capability of all the other methods for the construction of ultramicropores including self-template strategy, carbonization of nanoparticles, and template-assisted strategy. The synthesis of ultramicroporous carbons via the self-sacrificial template route opens up a promising gate to adjust the porous structure for high-performance applications in supercapacitors.