Most bitumen in the Alberta oil sands (Canada) is extracted by thermal in-situ recovery. Despite the widespread use of in-situ bitumen extraction, little information is available on the release of petroleum hydrocarbons by this method to adjacent land and water. Here we analyzed the composition and abundance of parent and alkylated polycyclic aromatic compounds (PACs) in 11 radiometrically-dated lake sediment cores collected near in-situ operations at Cold Lake Alberta to assess potential petroleum contamination sources to surrounding lakes over the past century. Like open-pit mining areas, alkylated PACs in Cold Lake sediments were elevated compared to unsubstituted parent PACs and increased coeval with the onset of bitumen extraction in the area. Diagnostic ratios and pyrogenic indices showed that PAC sources to these lake sediments were dominantly pyrogenic, likely from historic forest fires, however they shifted to more petrogenic sources coeval with expanding oil sands extraction at Cold Lake. PACs in sediment from regional lakes are weakly correlated to their proximity to in-situ oil wells, once corrected for lake area. These results suggest that in-situ operations, via diesel-fueled vehicular emissions and the combustion of natural gas for steam generation, are a source of PACs to nearby lakes, but PACs did not exceed Canadian sediment quality guidelines for the protection of aquatic life.

The process improvement, a pilot remediation test and the decontamination mechanism of microwave-induced steam distillation (MISD) for petroleum hydrocarbons (PHs) removal were conducted. Processes of multistage steam distillation and carbon reinforcement were compared to determine the best remediation process. Pilot project was then carried out to explore the applicability of MISD in site-scale remediation. The remediation efficiency, procedures and influencing factors of site-scale MISD project were studied by monitoring variations of soil moisture, temperature and PHs concentrations. Furthermore, the decontamination mechanisms of PHs were clarified based on kinetic analysis. The results showed that the multistage steam distillation could improve 10%∼15% remediation efficiency, and the carbon reinforcement could shorten remediation duration of each steam distillation stage by 50%. Pilot MISD project adopted multistage steam distillation process and went through four (initial, rapid heating-up, gentle heating-up and quasi-equilibrium) remediation stages (overall temperature ≤100 °C). The final PHs removal rate was about 60%, which would get better with greater proportion of low boiling points components and stronger vapor extraction. Kinetic studies showed that PHs was removed by steam stripping and limited by intraparticle diffusion in the “steam distillation zone”, while local high temperature (＞100 °C) greatly improved PHs volatilization and provided activation energy for PHs desorbed and degraded in the “selective heating zone".

Uncoupling chemical looping gasification (CLG), the organic sulfur evolution was simulated and explored qualitatively and quantitatively using typical sulfur compounds on TG-MS and temperature-programmed fixed bed. The HS radical in the reductive atmosphere easier converted to H₂S and COS. H₂O activated the evolution of S which was stably bonded to carbon, and H₂ generated from gasification and oxidation of reductive Fe by H₂O contributed to the release of sulfur. The proportion of H₂S released from sulfur compounds was greater than 87% in steam gasification, and more than 60% during CLG. Oxygen carriers promoted the conversion of sulfur to SO₂ in the mid-temperature region (500 °C–700 °C), and H₂S in the high temperature region (700 °C–900 °C). Sulfur species played a pivotal role in sulfur evolution at low temperature of CLG. The organic sulfur in mercaptan and benzyl were more easily converted and escaped than in thiophene and phenyl. The thermal stability of sulfur species, the presence of steam and OC affected the initial temperature and peak concentration of gas sulfur release as well as sulfur distribution. Consequently, CLG strengthened the sulfur evolution, and made it possible to targeted restructure the distribution of sulfur by regulating process parameters, or blending fuel with different sulfur species for emission reduction, and selective conversion of sulfur.

During the COVID-19 pandemic, disposable surgical masks were generally disinfected and reused due to mask shortages. Herein, the role of disinfected masks as a source of microplastics (MPs) and nanoplastics (NPs) was investigated. The amount of MPs and NPs released from masks disinfected by UV ranged from 1054 ± 106 to 2472 ± 70 and from 2.55 ± 0.22 × 10⁹ to 6.72 ± 0.27 × 10⁹ particles/piece, respectively, comparable to that of the undisinfected masks, and the MPs were changed to small-sized particles. The amount of MPs and NPs released after alcohol and steam treatment were respectively lower and higher than those from undisinfected masks, and MPs were shifted to small-sized particles. The amount of MPs and NPs released in water after autoclaving was lower than for undisinfected masks. In all, the amount of fibers released after disinfection decreased greatly, and certain disinfection processes were found to increase the amount of small-sized NPs released from masks into aqueous environments.

Biofouling by marine organisms can result in a variety of negative environmental and economic consequences, with decontamination procedures remaining problematic, costly and labour-intensive. Here, we examined the efficacy of direct steam exposure to induce mortality of selected biofouling species: Mytilus edulis; Magallana gigas; Semibalanus balanoides; Fucus vesiculosus; and an Ulva sp. Total mortality occurred at 60-sec of steam exposure for M. edulis and juvenile M. gigas, at 30-sec for S. balanoides, while 300-sec was required for adult M. gigas. Application of steam reduced the biomass of F. vesiculosus and significantly reduced Ulva sp. biomass, with complete degradation being observed for Ulva sp. following 120-sec of exposure. Accordingly, it appears that steam exposure can cause mortality of biofouling organisms through thermal shock. Although preliminary, our novel and promising results suggest that steam applications could potentially be used to decontaminate niche areas and equipment.

The work aims to analyse an ejector refrigeration system powered with solar energy through serially connected collectors to lower greenhouse gases. The collectors chosen for the work are Scheffler and parabolic collectors with an area of 2.5 m² and 6 m², respectively. The steam generated by the collectors is stored temporarily in a 15-l storage tank. The thermic fluid transfers heat between the steam storage tank and refrigerant, and thus the generator temperature increases. This design was intended as an alternate for a traditional 3.5 kW room air conditioner with substantially lower energy consumption. This modified system consumed lesser energy input of about 20–30% than conventional air conditioners. Further, for the same specification, the ejector system has consumed less power of about 2.475 kW than the traditional refrigeration system.

In this study, we simulate the irrigation of tomato plants with arsenic (As)-contaminated water (from 0 to 3.2 mg L⁻¹) and investigate the effect of the application of silicon nanoparticle (Si NPs) in the form of silicon dioxide (0, 250, and 1000 mg L⁻¹) on As uptake and stress. Arsenic concentrations were determined in substrate and plant tissue at three different stratums. Phytotoxicity, As accumulation and translocation, photosynthetic pigments, and antioxidant activity of enzymatic and non-enzymatic compounds were also determined. Our results show that irrigation of tomato plants with As-contaminated water caused As substrate enrichment and As bioaccumulation (roots > leaves > steam), showing that the higher the concentration in irrigation water, the farther As translocated through the different tomato stratums. Additionally, phytotoxicity was observed at low concentrations of As, while tomato yield increased at high concentrations of As. We found that application of Si NPs decreased As translocation, tomato yield, and root biomass. Increased production of photosynthetic pigments and improved enzymatic activity (CAT and APX) suggested tomato plant adaptation at high As concentrations in the presence of Si NPs. Our results reveal likely impacts of As and nanoparticles on tomato production in places where As in groundwater is common and might represent a risk.

This study deals with the preparation of activated carbon (AC) from poly(ethylene terephthalate) (PET) waste and with the physicochemical characterization of AC and its use as adsorbent of bisphenol A (BPA) in aqueous solution. AC was prepared by chemical activation with KOH and by physical activation in steam. The activation with KOH was carried out by impregnation first of PET by wet and dry routes at the PET/KOH weight ratios of 1:1, 1:3, and 1:5 and by carbonization then of the resulting products at 850 °C for 2 h in N₂ atmosphere. The activation in steam was performed by heating at 900 °C for 1 h. The ACs were characterized by N₂ adsorption at − 196 °C, mercury porosity, mercury density measurements, FT-IR spectroscopy, and measurement of pH of the point of zero charge (pHₚzc). The activation yield is 58.4–49.4% with KOH in aqueous solution, 75.8–23.9% with solid KOH, and 5.9% with steam. Using solid KOH, greater developments of a more heterogeneous porosity with increasing impregnation PET/KOH ratio are achieved. For SK1:5, SBET is 1990 m² g⁻¹ and the pore volumes are 0.71 cm³ g⁻¹, micropores; 0.81 cm³ g⁻¹, mesopores; and 1.77 cm³ g⁻¹, macropores. The data of BPA adsorption fit better to the Ho and Mckay second order kinetic model than to the Lagergren first-order kinetic model and to the Langmuir equation than to the Freundlich equation. From the kinetic and thermodynamic standpoints, the adsorption process of BPA is more favorable for SK1:5.

The present study focused on the methodology for identification of the wastewater stream that presents the highest phenolic impact at a large oil refinery. As a case-study, the oil refinery, Petrogal S.A., in Sines, Portugal, was selected. Firstly, stripped sour water from the cracking complex was identified as the most relevant wastewater stream concerning phenolic emission. Secondly, multivariate data analysis was used, through projection to latent structures (PLS) regression, to find existing correlations between process parameters and phenols content in stripped sour water. The models developed allowed the prediction of phenols concentration with predictive errors down to 20.16 mg/L (corresponding to 8.2% average error), depending on the complexity of the correlation used, and R² values as high as 0.85. Models were based in input parameters related to fluid catalytic crackers (FCC) feedstock quality, crudemix and steam injected in the catalyst stripper. The studied data analysis approach showed to be useful as a tool to predict the phenolic content in stripped sour water. Such prediction would help improve the wastewater management system, especially the units responsible for phenol degradation. The methodology shown in this work can be used in other refineries containing catalytic cracking complexes, providing a tool which allows the online prediction of phenols in stripped sour water and the identification of the most relevant process parameters. An optimised system at any refinery leads to an improvement in the wastewater quality and costs associated with pollutant discharge; thus, the development of monitoring online tools, as proposed in this work, is essential.

Gold (Au) nanoparticles supported on certain platforms display highly efficient activity on nitroaromatics reduction. In this study, steam-activated carbon black (SCB) was used as a platform to fabricate Au/SCB composites via a green and simple method for 4-nitrophenol (4-NP) reduction. The obtained Au/SCB composites exhibit efficient catalytic performance in reduction of 4-NP (rate constant kₐₚₚ = 2.1925 min⁻¹). The effects of SCB activated under different steam temperature, Au loading amount, pH, and reaction temperature and NaBH₄ concentration were studied. The structural advantages of SCB as a platform were analyzed by various characterizations. Especially, the result of N₂ adsorption–desorption method showed that steam activating process could bring higher surface area (from 185.9689 to 249.0053 m²/g), larger pore volume (from 0.073268 to 0.165246 cm³/g), and more micropore for SCB when compared with initial CB, demonstrating the suitable of SCB for Au NP anchoring, thus promoting the catalytic activity. This work contributes to the fabrication of other supported metal nanoparticle catalysts for preparing different functional nanocomposites for different applications.