Achieving Carbon Mitigation with Economic Benefits through High-Resolution Analysis of Renewable Resource Integration in Global Coastal Cities.

Coastal regions, home to more than half of the global population and contributing over 50% to the global economy, possess vast renewable resources, such as seawater and solar energy. The effective utilization of these resources, through the seawater-cooled district cooling system (SWDCS), seawater toilet flushing (SWTF), and rooftop solar photovoltaic system (RTPV), has the potential to significantly reduce carbon emissions. However, implementing these technologies in different geographic contexts to achieve the desired carbon and economic outcomes at the city level lacks a clear roadmap. To address this challenge, we comprehensively analyzed 12 coastal megacities worldwide by integrating geospatial building data. Our study evaluated the potential energy savings, carbon mitigation, and levelized carbon abatement costs (LCACs) from a life cycle perspective. The results revealed that using seawater and solar energy within urban boundaries can reduce electricity consumption from 1 to 24% across these cities. The spatial distribution of the LCAC for seawater-based systems exhibited more variation compared to the RTPV. By applying specific LCAC thresholds ranging from 0 to 225 USD/tCO2e, all cities could achieve both carbon reductions and economic benefits. These thresholds resulted in up to 80 million tonnes of carbon emission reductions and 5 billion USD of economic benefits, respectively. Our study provides valuable insights into integrating renewable resource systems, enabling coastal cities to achieve carbon and economic advantages at the city scale simultaneously.

Evaluating UV254 absorbance reductions in landfill leachate for municipal sewage co-treatment through timed UV/electrooxidation.

Landfill leachate contains dissolved organic matter (DOM) exhibiting high ultraviolet absorbance at 254 nm (UVA254). The UVA254 limits leachate co-treatment with municipal sewage by hindering the downstream UV disinfection efficiency at wastewater treatment plants. Here, we alleviated the UVA254 by timing the radiation in a UV/electrooxidation (UV/EO) process to accelerate reactive species formation. At 200 A·m-2, the UV radiation was delayed by 10 min to accumulate 21 mg·L-1 as Cl2, which enhanced the initial radical formation rate by 5.25 times compared with a simultaneous UV/EO. The timed operation increased the steady-state concentrations of ClO• by 700 times to 4.11 × 10-14 M and reduced the leachate UVA254 by 78.2% after 60 min. We identified that aromatic formulas with low oxygen content were susceptible to UV/EO from Fourier-transform ion cyclotron resonance mass spectrometry analysis. The toxicity of the treated leachate and generated byproducts was assessed through specific oxygen uptake rates (SOUR) and developmental assays with Platynereis dumerilii. After quenching the residual chlorine, leachate co-treatment at 3.5% v/v presented minimal toxicological risk. Our findings provide operational insights for applying UV/EO in high UVA254 matrices such as landfill leachate.

Flushing Toilets and Cooling Spaces with Seawater Improve Water-Energy Securities and Achieve Carbon Mitigations in Coastal Cities.

Exploring alternative water sources and improving the efficiency of energy uses are crucial approaches to strengthening the water-energy securities and achieving carbon mitigations in sub(tropical) coastal cities. Seawater use for toilet flushing and district cooling systems is reportedly practical for achieving multiaspect benefits in Hong Kong. However, the currently followed practices are yet to be systematically evaluated for scale expansions and system adaptation in other coastal cities. The significance of using seawater to enhance local water-energy securities and carbon mitigations in urban areas remains unknown. Herein, we developed a high-resolution scheme to quantify the effects of the large-scale urban use of seawater on a city's reliance on non-local and non-natural water and energy supplies and its carbon mitigation goals. We applied the developed scheme in Hong Kong, Jeddah, and Miami to assess diverse climates and urban characteristics. The annual water and energy saving potentials were found to be 16-28% and 3-11% of the annual freshwater and electricity consumption, respectively. Life cycle carbon mitigations were accomplished in the compact cities of Hong Kong and Miami (2.3 and 4.6% of the cities' mitigation goals, respectively) but not in a sprawled city like Jeddah. Moreover, our results suggest that district-level decisions could result in optimal outcomes supporting seawater use in urban areas.

Coupling methane and bioactive polysaccharide recovery from wasted activated sludge: A sustainable strategy for sludge treatment.

Bioactive polysaccharides (PSs) are valuable resources that can be extracted from waste activated sludge (WAS). The PS extraction process causes cell lysis that may enhance hydrolytic processes during anaerobic digestion (AD) and thus increase the methane production. Thus, coupling PSs and methane recovery from WAS could be an efficient and sustainable sludge treatment. In present study, we comprehensively evaluated this novel process from the efficiencies of different coupling strategies, properties of the extracted PSs, and environmental impacts. The results showed that when the PS extraction was before AD, it produced 76.03 ± 2.00 mL of methane per gram of volatile solids (VS) and afforded a PS yield of 6.3 ± 0.09% (w:w), with a PS sulfate content of 13.15% ± 0.06%. In contrast, when PS extraction was after AD, the methane production decreased to 58.14 ± 0.99 mL of methane per gram of VS and afforded a PS yield of 5.67% ± 0.18% (w:w) in VS, with a PS sulfate content of 2.60% ± 0.04%. When there were two PS extractions before and after AD, the methane production, PS yield and sulfate content were 76.03 ± 2.00 mL of methane per gram of VS, 11.54 ± 0.62% and 8.35 ± 0.12%, respectively. Then, the bioactivity of the extracted PSs was assessed by one anti-inflammation assay and three anti-oxidation assays, and statistical analysis revealed that these four bioactivities of PSs were influenced by their sulfate content, protein content and monosaccharide composition, especially the ratios of arabinose and rhamnose. Furthermore, the environmental impact analysis shows that S1 was the best in five environmental indicators compared with other three non-coupled processes. These findings suggest that the coupling PSs and methane recovery process should be further explored to determine its potential for large-scale sludge treatment.

Reusable self-floating carriers recover heavy metals from industrial wastewater through heterogeneous nucleation for resource reuse.

Coagulation-flocculation in industrial wastewater treatment drives environmental pollution from landfilling heavy metal-laden sludge. Efficient separation of the sludge is crucial for cost-effective metal recovery. This study explored a new separation method of Cu2+, Ni2+, Zn2+ and Cr3+ via self-floating metal hydroxides assisted by hollow glass microsphere (HGM) carriers. The amount of OH- was stoichiometric to the positive charges of metal ions, mixed with 1 mg mL-1 HGM, causing metal hydroxides to attach to HGM surface via heterogeneous nucleation. The self-floating system removed 37.5% and 14.0% more metals than sedimentation at 50 and 200 mg L-1 metal concentrations. HGM additions increased the particle size of metal hydroxides by up to 12.5 times to that of HGM at 18.8 ± 1.1 µm, benefiting their solid-liquid separation. By pumping the wastewater downward in column reactor at velocities equal to or less than the self-floating sludge, 96.4% metals were removed in continuous flow. The recovery rates of HGM and metals reached 92.0 ± 2.2% and 92.7 ± 3.2%, and the concentration of the recovered metal reached 19,339 ± 394 mg L-1 for potential reutilization in industrial electroplating. This research investigated a new separation strategy based on solid self-flotation for sustainable treatment of metal-laden wastewater.

Superfast degradation of micropollutants in water by reactive species generated from the reaction between chlorine dioxide and sulfite.

Chlorine dioxide (ClO2) is used as an oxidant or disinfectant in (waste)water treatment, whereas sulfite is a prevalent reducing agent to quench the excess ClO2. This study demonstrated that seven micropollutants with structural diversity could be rapidly degraded in the reaction between ClO2 and sulfite under environmentally relevant conditions in synthetic and real drinking water. For example, carbamazepine, which is recalcitrant to standalone ClO2 or sulfite, was degraded by 55%-80% in 10 s in the ClO2/sulfite process at 30-µM ClO2 and 30-µM sulfite concentrations within a pH range of 6.0-11.0. Results from experiments and a kinetic model supported that chlorine monoxide (ClO·) and sulfate radicals (SO4·-) were generated in the ClO2/sulfite process, while hydroxyl radical generation was insignificant. Apart from radicals, dichlorine trioxide (Cl2O3) was generated and largely contributed to micropollutant degradation, supported by experimental results using stopped-flow spectrometry and quantum chemical calculations. The impacts of pH, sulfite dosage, and water matrix components (chloride, bicarbonate, and natural organic matter) on micropollutant abatement in the ClO2/sulfite process were evaluated and discussed. When treating the real potable water, the concentrations of organic (five regulated disinfection byproducts) and inorganic byproducts (chlorite and chlorate) formed in the ClO2/sulfite process were all below the drinking water standards. This study disclosed fundamental knowledge advancements relevant to the reaction mechanisms between ClO2 and sulfite, and highlighed a novel process to abate micropollutants in water and wastewater.

Importance of Combined Electrochemical Process Sequence and Electrode Arrangements: A Lab-scale Trial of Real Reverse Osmosis Landfill Leachate Concentrate.

Reverse osmosis (RO) is a widely applied technique for wastewater effluent reuse and landfill leachate treatment. The latter generates a refractory RO leachate concentrate (ROLC), for which cost-effective treatment is required. This study focuses on a two-step electrochemical method consisting of aluminum-based electrocoagulation (EC), and simultaneous electrooxidation-electrocoagulation with a titanium-based lead dioxide (Ti/ß-PbO2) anode and aluminum cathode (EOEC) assembly. The sequence and electrode arrangements of the combined electrochemical process were investigated to determine the organic transformation, Ti/ß-PbO2 anode viability, and energy consumption. Series-based EC-EOEC decreased the total chemical oxygen demand (COD) from 8750 mg L-1 to 380 mg L-1, a 96% removal efficiency, in 3.5 hours at 141 A m-2. Under a low energy consumption of 28.7 kWh kgCOD-1, the ROLC biodegradability (BOD5/COD) significantly increased from 0.015 to 0.530, which was ascribed to aromatic removal (e.g., -C=C) and an increase in -COOH functional groups. Furthermore, the rapid removal of natural organic matter and increase in pH elevation from EC suppressed the dissolution of Pb from the Ti/ß-PbO2 anode during the subsequent EOEC, thereby leaving 0.061 mg L-1 in the ROLC after treatment. The treatment cost was 3.86 USD kgCOD-1, which was approximately 34% lower than that of previously reported electrochemical processes for ROLC treatment. These findings obtained with a real RO concentrate provide a foundation for scaling up this new electrochemical treatment approach.

Magnetic resonance lymphography of sentinel lymph nodes in patients with breast cancer using superparamagnetic iron oxide: a feasibility study.

BACKGROUND: The sentinel lymph node (SLN) biopsy technique using superparamagnetic iron oxide (SPIO) as a tracer instead of radioisotopes has been described. To further advance this technique, we evaluated preoperative SPIO-MR sentinel lymphography to facilitate the accurate identification of the lymphatic pathways and primary SLN. METHODS: A prospective study was performed in ten patients with breast cancer and clinically negative axillary lymph nodes. None of the patients received preoperative chemotherapy. After 1.6 ml of SPIO (ferucarbotran) was injected in the subareolar breast tissue, sentinel axillary lymph nodes were detected by MRI in T2*-weighted gradient echo images and resected using the serial SPIO-SLN biopsy procedure with a handheld magnetometer. RESULTS: In one patient, gadolinium-enhanced MR imaging was performed at the same time as SPIO-MR lymphography, and this patient was excluded from further analysis. In all patients (9/9) SLNs were detected by SPIO-MR sentinel lymphography and successfully identified at surgery. The number of SLNs detected by lymphography (mean 2.7) significantly correlated with SLNs identified at surgery (mean 2.2). One patient had nodal metastases. In one patient, skin color changed to brown at the injection site and resolved spontaneously. There were no severe reactions to the procedure or complications in any patient. CONCLUSIONS: This is the first study to evaluate SPIO both as a contrast material in MR sentinel lymphography and as a tracer in SLN biopsy using an integrated method. The acquired three-dimensional imaging demonstrated excellent image quality and usefulness to identify SLN in conjunction with SLN biopsy.