Effect of H₂O and NH₃ on the synergistic oxidation reaction of SO₂ and NO₂ is investigated by theoretical calculation using the molecule system SO₂-2NO₂-nH₂O (n = 0, 1, 2, 3) and SO₂-2NO₂-nH₂O-mNH₃ (n = 0, 1, 2; m = 1, 2). Calculated results show that SO₂ is oxidized to SO₃ by N₂O₄ intermediate. The additional H₂O in the systems can reduce the energy barrier of oxidation step. The increasing number of H₂O molecules in the systems enhances the effect and promotes the production of HONO. When the proportion of H₂O to NH₃ is 1:1, with NH₃ included in the system, the energy barrier is lower than two pure H₂O molecules in the oxidation step. The present study indicates that the H₂O and NH₃ have thermodynamic effects on promoting the oxidation reaction of SO₂ and NO₂, and NH₃ has a more significant role in stabilizing product complexes. In these hydrolysis reactions, nethermost barrier energy (0.29 kcal/mol) can be found in the system SO₂-2NO₂-H₂O. It is obvious that the production of HONO is energetically favorable. A new reaction mechanism about SO₂ oxidation in the atmosphere is proposed, which can provide guidance for the further study of aerosol surface reactions.

Hydroxymethanesulfonate (HMS) is an important organosulfur compound in the atmosphere. In this work, we studied the formation mechanism of HMS via the reaction of formaldehyde with dissolved SO₂ using the quantum chemistry calculations. The results show that the barrier (9.7 kcal mol⁻¹) of the HCHO + HSO₃ ⁻ reaction is higher than that (1.6 kcal mol⁻¹) of the HCHO + SO₃ ²⁻ reaction, indicating that the HCHO + SO₃ ²⁻ reaction is easier to occur. For comparison, the reaction of acetaldehyde with dissolved SO₂ also was discussed. The barriers for the CH₃CHO + HSO₃ ⁻ reaction and CH₃CHO + SO₃ ²⁻ reaction are 16.6 kcal mol⁻¹, 2.5 kcal mol⁻¹, respectively. This result suggests that the reactivity of HCHO with dissolved SO₂ is higher than that of CH₃CHO. The further oxidation of CH₂(OH)SO₃ ⁻ and CH₃CH(OH)SO₃ ⁻ by an OH radical and O₂ shows that the SO₅˙⁻ radical can be produced.

This study synthesizes and comparatively investigates two squaric acid-based phthalocyanine-like dyes, SNF and its long-chain alkylated derivative LNF, to systematically elucidate the influence of peripheral hydrophobic groups on their third-order nonlinear optical (NLO) properties. The NLO characteristics were comprehensively characterized using femtosecond Z-scan and I-scan techniques at both 800 nm and 900 nm. Both dyes exhibited strong saturable absorption (SA), confirming their potential as saturable absorbers. Critically, the comparative analysis revealed that SNF exhibits a significantly greater nonlinear absorption coefficient (β) compared to LNF under identical conditions. For instance, at 800 nm, the β of SNF was approximately 3–5 times larger than that of LNF. This result conclusively demonstrates that the introduction of long hydrophobic alkyl chains attenuates the NLO response. Furthermore, I-scan measurements revealed excellent SA performance, with high modulation depths (e.g., LNF: 43.0% at 900 nm) and low saturation intensities. This work not only clarifies the structure–property relationship in these D-A-D dyes but also presents a clear strategy for modulating the NLO properties of organic chromophores for applications in near-infrared pulsed lasers.