The mechanisms of soot’s photochemistry are still unclear, especially, how the microstructure and composition of soot influence its photoactivity. In the current study, we started with the exploration of the microstructure of soot particles and gained new insights. The elemental-carbon fraction of soot (E-soot), considered the core component of soot and can reflect the intrinsic characteristics of soot, was extracted by organic solvents and characterized in terms of structure and chemical reactivity. The intrinsic structure of E-soot was found to be more analogous to reduced graphene oxide than to graphene, in terms of containing similar levels of defective sites such as oxygen-containing functional groups and environmentally persistent free radicals, as well as exhibiting similar optoelectronic performance. The generation of reactive oxygen species via an electron transfer pathway under visible light suggests that reduced graphene oxide-like E-soot can serve as a potential carbo-photocatalyst, which facilitates elucidating the mechanism of E-soot’s role during soot’s photochemical aging. Our study reveals the intrinsic structure of soot and its role in photo-triggered reactive oxygen species production, which is vital for atmospheric and health effects.

Swift degradation of the coral reef ecosystems urges the need to identify the reef decline drivers. Due to their widespread use, bioaccumulative and toxic characteristics, chlorinated organic compounds, such as chlorinated paraffins (CPs), are regarded as specific pollutants of concern. Yet little is known about the occurrence of CPs in the coral reef ecosystems. This study focuses on the short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs). Their distribution and congener pattern were investigated in the water-SPM-sediment system and in the corals of the Larak coral reef for the first time. Chlorinated paraffins were detected in all the coral species. Their total loadings ranged from 42.1 to 178 ng g⁻¹ dw in coral tissue, from 6.0 to 144 ng g⁻¹dw in the skeleton, and from 55.0 to 240 ng g⁻¹dw in zooxanthellae. Soft corals were found to accumulate more CPs than Scleractinian corals. Zooxanthellae and mucus accumulated more CPs than tissue and skeleton. In most cases, congener group patterns were dominated by C₁₃ (for SCCPs) and C₁₇ (MCCPs) groups, respectively. The congener patterns of CPs altered to some extent between mucus and the remaining coral compartments. High loadings of CPs were detected in the skeleton of the bleached corals. Moreover, a significant negative correlation between the levels of CPs and the symbiodinium density was observed.

Bisphenol A (BPA) is a widely concerned endocrine disrupting chemical and hard to be removed through conventional wastewater treatment processes. In this study, we developed a TiO2 decorated titanate nanotubes composite (TiO2/TNTs) and used for photocatalytic degradation of BPA. TEM and XRD analysis show that the TiO2/TNTs is a nano-composite of anatase and titanate, with anatase acting as the primary photocatalytic site and titanate as the skeleton. TiO2/TNTs exhibited excellent photocatalytic reactivity and its easy-settling property leaded to good reusability. After 5 reuse cycles, TiO2/TNTs also could photo-degrade 91.2% of BPA with a high rate constant (k1) of 0.039 min⁻¹, which was much better than TiO2 and TNTs. Higher pH facilitated photocatalysis due to more reactive oxygen species produced and less material aggregation. The presence of NaCl and CaCl2 showed negligible effects on BPA degradation, but NaHCO3 caused an inhibition effect resulting from consumption of ·OH. Humic acid inhibited degradation mainly due to blockage of the active sites of TiO2/TNTs. Degradation pathway was well interpreted through theoretical calculation. Hydroxyl radical played the dominate role in BPA photodegradation, and the atoms of BPA with high Fukui index based on density-functional theory (DFT) calculation are the radical easy-attacking (f⁰) sites. Considering the good photocatalytic reactivity, reusability, stability and settle property, TiO2/TNTs promises to be an efficient alternative for removal of organic compounds from wastewaters.

In this study, coral soft tissue, skeleton and zooxanthellae, as well as their ambient sediment and seawater were analyzed for polycyclic aromatic hydrocarbons (PAHs) with a special focus on perylene. Samples were collected from two different environments: the Kharg Island, which is affected by numerous anthropogenic stressors and Larak Island, which is mainly used for recreational and fishing activities and is characterized by dense vegetation. The heaviest loadings of PAHs were observed on Kharg Island, yet higher concentrations of perylene were detected on Larak Island and it was identified as the prevailing compound in this area. Pyrogenic perylene sources were prevailing on Kharg Island, whereas the perylene on Larak Island was determined to be of natural origin. After analyzing the biological samples, higher perylene concentrations were observed in zooxanthellae than in tissue and skeleton. The lowest and the highest perylene loadings were found in the tissue and skeleton of Platygyra daedalea and Porites lutea, respectively. This applies to both reefs. We found that perylene distribution in the corals and their ambient environment follows an irregular pattern, demonstrating remarkable effects from the local inputs. The lipid content in the coral tissue and the location of the coral colony were deduced to be the main factors affecting perylene distribution in corals. On Larak Island, a significant correlation between perylene loadings in sediment and corals was observed. On Kharg Island, a strong interaction between the water column and the corals was detected. The symbiotic relationship between the corals and zooxanthellae might play the most significant role in bioconcentration and bioaccumulation of perylene. Due to the insolubility of PAHs, they could be transferred through a food chain to zooxanthellae and eventually deposited in the coral bodies.

Sludge is an inevitable by-product of municipal wastewater treatment processes, and its high moisture content poses a major challenge for its subsequent treatment and disposal. Previous studies have explored the effects of applying modified corn-core powder (MCCP) on dewatering sludge. Here, we characterized the effects of applying both MCCP and sludge-based biochar (SBB) on dewatering sludge. Analysis of the anti-shear ability of SBB revealed that SBB was a skeleton builder with high compressive strength, demonstrating that SBB could maintain the permeability of sludge under high-pressure filtration processes and facilitate the flow of bound water. Dissipative particle dynamics (DPD) was used to simulated the sludge flocculating process and verify the feasibility of the experiment. As the simulation progressed, the reaction in the sludge network reached equilibrium and the simulated structure of the sludge became loose. The dewatering performance and physicochemical properties of the treated sludge were studied to further characterize the effect of this combined technology. Compared with MCCP-sludge, MCCP&SBB-sludge, which was treated by 20% DS (mass of dry solids in sludge) of SBB and 20% DS of MCCP, achieved superior dewaterability. This combined method reduced the specific resistance of filtration by 76% and enlarged the net sludge solids yield by 138%. Further study of the properties of MCCP&SBB-sludge revealed a loose structure that resembled the structure recovered by the simulation, suggesting that the DPD simulation method simulated the sludge flocculating process successfully. Therefore, the combined application of MCCP and SBB was superior for sludge dewatering because of the synergistic effects of MCCP and SBB.

Inspired by the adhesion of marine mussels, a kind of superhydrophobic oil sorbent was successfully fabricated by robustly immobilizing the micro/nanostructure layer onto the sponge skeleton. The as-prepared sponges possess excellent hydrophobicity with the water contact angle of 154°, which enables the sponge to selectively absorb various oils floating on water surface. The oil sorption capacities of as-prepared sponge for a series of oils can reach 18.3–46.8g/g. The absorbed oil can be recovered by mechanical squeezing and the resulting sponge can be recycled more than 70 cycles while still keeping high oil sorption capability. More importantly, the obtained sponge has excellent affinity to the high viscosity oils. Therefore, the as-prepared sponge might find practical applications in the large-scale removal of oils especially high viscosity oils from water surface.

The present study was carried out on the Porites coral growth bands (1979 to 2014) to measure the metal accumulation for assessing the environmental pollution status. The concentrations of studied metals are compared with similar global studies, which indicate that the metals are probably derived from natural sources. The identical peaks of Fe and Mn are perfectly matched with Cu, Cr and Ni concentrations. However, the metal profile trend is slightly depressed from a regular trend in Zn, Cd and Pb peaks. The metal accumulation affinity of the reef skeleton is ranked in the following order Cr>Cd>Pb>Fe>Mn>Cu>Ni>Zn. The distribution of metal constituents in coral growth bands is primarily controlled by Fe and Mn in the reef skeleton. Other reef associated metals such as Pb and Cd are derived from other sources like coastal developments and anthropogenic sources.

Measurements of coral structural strength are coupled with a fluid dynamics-structural analysis to investigate the resilience of coral to wave loading under sea level rise and a typical Great Barrier Reef lagoon wave climate. The measured structural properties were used to determine the wave conditions and flow velocities that lead to structural failure. Hydrodynamic modelling was subsequently used to investigate the type of the bathymetry where coral is most vulnerable to breakage under cyclonic wave conditions, and how sea level rise (SLR) changes this vulnerability. Massive corals are determined not to be vulnerable to wave induced structural damage, whereas branching corals are susceptible at wave induced orbital velocities exceeding 0.5m/s. Model results from a large suite of idealised bathymetry suggest that SLR of 1m or a loss of skeleton strength of order 25% significantly increases the area of reef flat where branching corals are exposed to damaging wave induced flows.