The in-depth knowledge on management and reducing annual acidic pollution is important for improving the sustainable livelihood of people living in areas with acid sulphate soils (ASS). This study involved a long-term (2001-2006), large-scale canal water quality monitoring network (87 locations) and a field experiment at nine sites to quantify the dynamic variability of acidic pollution and its source in a coastal area with ASS in the Mekong River Delta of Vietnam. Widespread acidic pollution (pH <5) of surface water occurred at the beginning of the rainy season, while pH of the canal water remained high (7-8) at the end of the rainy season and during the dry season. The study identified canal embankment deposits, made of ASS spoils from canal dredging/excavation, as the main source of acidic pollution in the surrounding canal network. The findings suggested that there was a linkage between the amount of acidic loads into canal networks and the age of the embankment deposits. The most acute pollution (pH ~ 3) occurred in canals with sluggish tidal water flow, at 1-2 years after the deposition of excavated spoils onto the embankments in ASS. The amount of acidic loads transferred to the canal networks could be quantified from environmental parameters, including cumulative rainfall, soil type and age of embankment deposits. The study implied that dredging/excavation of canals in ASS areas must be carried out judiciously as these activities may increase the source of acidic pollution to the surrounding water bodies.

Catalytic pyrolysis is a promising chemical recycling technology to supplement mechanical recycling since plastics can be broken down into monomers or converted to the required fuels and chemicals. In this study, a microwave (MW) -responsive SiC foam@zeoltie core-shell structured catalyst was proposed for the catalytic pyrolysis of polyolefins. Under microwave irradiation, the SiC foam core works as both microwave adsorber and catalyst support, thus concentrating the generated heat energy on the ZSM-5 zeolite shell, where the catalytic reaction takes place. SiC foam with an open cellular structure can also improve the global transport of mass and heat during plastics pyrolysis. In this work, the effects of the SiO₂/Al₂O₃ ratio and alkaline treatment of ZSM-5 zeolite coated SiC foam under MW irradiation on the variations in product distribution from low-density polyethylene (LDPE) pyrolysis were investigated at 450 °C. The results indicated that the appropriate acidity and pore structure were crucial to upgrading gas and liquid products. Particularly, the creation of a mesoporous structure in ZSM-5 zeolite via alkaline treatment could improve the diffusion of large molecules and products, thus significantly increasing the selectivity of high-valued light olefins and aromatics while inhibiting the formation of unwanted alkanes, which are expected in the chemical industry. Concretely, the concentration of olefins in gas increased to 51.0 vol% for ZSM-5(50)-0.25AT, and 65.6 vol% for ZSM-5 (50)-0.50AT, compared with 45.2 vol% for the parent ZSM-5(50). The relative concentration of aromatics in liquid decreased from 96.6% for ZSM-5(50) to 75.9% for ZSM-5(50)-0.25AT, and 71.1% for ZSM-5(50)-0.50AT. Given the respective yield of gas and liquid, the total selectivity of C2–C4 olefins and aromatics for mesoporous ZSM-5 zeolites could reach 58.6–64.9% during LDPE pyrolysis, which were higher than that for the parent ZSM-5 zeolite.

The influence of intercalated anions on the structure and composition of green rusts supplies a theoretical possibility for the investigation of the structural modification of Feᴵᴵ/Feᴵᴵᴵ (oxyhydr)oxide materials. β-Cyclodextrin was intercalated into the mixed-valent iron-based hydroxide layers to synthesize new green rust materials (β-CD GRs), pursuing high-capacity uraniumⱽᴵ (Uⱽᴵ) sorption. The molar ratios of Feᴵᴵ to Feᴵᴵᴵ and the molar ratios of β-CD GR to Feᴵᴵ + Feᴵᴵᴵ had a significant effect on the synthesis of β-CD GRs. The synthesis process was further optimized by the quadric predictor and desirability function in a central composite design in combination. Both strong acidity and alkalinity were harmful to the adsorption of β-CD GRs towards Uⱽᴵ. The pseudo-first-order kinetic model and Langmuir isotherm model were appropriate in fitting the whole adsorption process. The maximum monolayer adsorption capacity of β-CD GRs was 2548.61 mg/g. The presence of mimic groundwater constituents explicitly deteriorated the interaction between β-CD GR and Uⱽᴵ species. Nanoscale nodules and particles were formed on the β-CD GR after the adsorption experiments. The peaks at 1159 and 609 cm⁻¹ vanished with the band at 1103 cm⁻¹ being left-shifted to 1117 cm⁻¹ in the FTIR spectra of β-CD GR during the heterogeneous process. The intercalation of β-CD brought obvious enhancement of Uⱽᴵ species sorption to the GR material, which was combinedly driven by several reaction pathways and different from the unmodified GRs.

Acid deposition has been regarded as a serious factor in the deteriorative water environment and ecosystems. Despite the powerful acid emission control measures have been implemented by the Chinese government, many areas (especially Southeast China) are still suffering from acid deposition. The chemical and isotopic (δ³⁴S and ⁸⁷Sr/⁸⁶Sr) compositions of rainwater in Hangzhou, a typical megacity in Southeast China with serious acid rain problem, for one year were studied with the aim to better constrain potential sources and explore the causes of rainwater acidification. Most rainwater samples were acidic, with a VWM pH value of 4.65. SO₄²⁻ was the dominant anion and the main acid ion in rainwater. Sulfur isotope and the quantity equilibrium model revealed that sea salt, crustal, biogenic, and anthropogenic sulfur represented 2.3%, 0.1%, 16.7%, and 80.8% of the SO₄²⁻ source in rainwater, respectively. The back trajectory and strontium isotopes indicated that the base cations (BCs) in rainwater originated mainly from anthropogenic sources. The relatively low neutralizing capacity caused by limited BCs input and emission control measures undermines some efforts to reduce rainwater acidity. This case study demonstrated that a valuable tool to probe the source of acid rain and unravel the mechanism of rainwater acidification can be provided by multiple lines of evidence, including rainwater chemical compositions, stable sulfur isotopes, and stable strontium isotopes.

As energy use in the building sector is increasing worldwide, building materials with characteristics that save energy are becoming increasingly important; in addition, there is an emerging need for high-performance insulation materials with low thermal conductivity. However, thermal insulation should consider thermal conductivity, which is the main performance parameter, in addition to the water adsorption rate, acidity, and deformation and expansion due to drying conditions. This study evaluated the main performance of 21 insulation materials used at construction sites to objectively and clearly evaluate their overall performance, including their thermal conductivity. Thermal conductivity was measured by the heat flow meter method according to ASTM C518 and ISO 8301 standards; it was also evaluated according to the drying conditions. The water absorption rate was evaluated by ISO 2896 to ensure the sustainability and long-term thermal conductivity performance of the material. Acidity was evaluated with ASTM E861 to reduce the environmental load of the buildings and soil. The results of this study reviewed an appropriate method to measure the main performance according to the type of insulation.

Recycling of waste glycerol derived from biodiesel production to high value-added chemicals is essential for sustainable development of Bio-Circular-Green Economy. This work studied the conversion of glycerol to 1,3-propanediol over Pt/WOₓ/Al₂O₃ catalysts, pointing out the impacts of catalyst pore sizes and operating conditions for maximizing the yield of 1,3-propanediol. The results suggested that both pore confinement effect and number of available reactive metals as well as operating conditions determined the glycerol conversion and 1,3-propanediol selectivity. The small-pore 5Pt/WOₓ/S–Al₂O₃ catalyst (6.1 nm) gave a higher Pt dispersion (32.0%), a smaller Pt crystallite size (3.5 nm) and a higher number of acidity (0.47 mmol NH₃ g⁻¹) compared to those of the large-pore 5Pt/WOₓ/L-Al₂O₃ catalyst (40.3 nm). However, glycerol conversion and 1,3-propanediol yield over the small-pore 5Pt/WOₓ/S–Al₂O₃ catalyst were significantly lower than those of the large-pore Pt/WOₓ/L-Al₂O₃ catalyst, suggesting that the diffusional restriction within the small-pore catalyst suppressed transportation of molecules to expose catalytic active sites, favoring the excessive hydrogenolysis of 1,3-propanediol, giving rise to undesirable products. The best 1,3-propanediol yield of 32.8% at 78% glycerol conversion were achieved over the 5Pt/WOₓ/L-Al₂O₃ under optimal reaction condition of 220 °C, 6 MPa, 5 h reaction time and amount of catalyst to glycerol ratio of 0.25 g mL⁻¹. However, the 1,3-propanediol yield and glycerol conversion decreased to 19.6% and 51% after the 4th reaction-regeneration which were attributed to the carbonaceous deposition and the agglomeration of Pt particles.