Utilization Pathway Research Articles

A single-step crystallization process to remove potassium from sodium aluminate solution

The high concentration of potassium in sodium aluminate solution seriously threatens the seed precipitation process and reduces the quality of alumina products, but the separation of potassium is quite difficult due to the similar chemical properties between potassium and sodium ions. In this work, a novel single-step double salt crystallization (SDSC) process with low energy consumption was proposed to remove potassium from the concentrated sodium aluminate solution using sodium sulfate, and the corresponding removal performance, kinetics and mechanism were studied. The potassium concentration decreases with the increase of additive dosage and reaction temperature, while the high caustic alkali concentration hinders the potassium removal. At 70 °C, the SDSC process exhibits a rapid crystallization and reaches an equilibrium within 60 min because of the low activation energy and weak bonding of 3 K2SO4·Na2SO4·9H2O. Under the optimum conditions, the potassium removal efficiency can achieve 85.68 %, and the potassium concentration is reduced from 120 g∙L−1 to 24.54 g⋅L−1. Finally, a cyclic utilization pathway was obtained to economically and effectively remove potassium from the sodium aluminate solution.

The Thermodynamic Change Laws of CO2-Coupled Fractured Rock

Under the background of the “dual carbon” target, exploring the pathway of efficient geological storage and high energy utilization of CO2 is a hot issue in CO2 emission reduction research. Under the coupling effect of high geopathic stress in deep rock layers and thermal stress generated during the geological sequestration of CO2, CO2 infiltration into coal rock changes the ambient temperature around the rock, while thermal diffusion effects cause damage to the rock and influence fracture expansion. In the present study, CO2-water–rock coupling test system and characterization of fissure surface roughness were conducted to analyze the rock’s mechanical properties, damage, and fracture evolution. Modeling of the equivalent fissure was employed to reveal the heat transfer mechanism between the rock matrix and CO2. The results obtained illustrate that the rock samples coupled with CO2 exhibited remarkable changes in mechanical properties. These changes include an increase in the number of pores, enhanced inter-pore connectivity, and a planar type of surface roughness in the fissures, ultimately resulting in an increase in conductivity. Conversely, the remaining rock samples displayed poor mechanical properties and surface fracture connectivity. As pressure decreased, the heat transfer coefficient decreased from 86.9 W/m2·K to 57.5 W/m2·K, accompanied by a temperature drop from 33.6 °C to 30.6 °C, demonstrating a proportional relationship between pressure and the heat transfer coefficient. Furthermore, the flow rate gradually increased with the rise in CO2 pressure, indicating denser flow lines with faster flow rates. At 15 MPa, CO2 exhibits enhanced mobility.

Synthesis of large mesoporous silica for efficient CO2 adsorption using coal gasification fine slag

Coal gasification fine slag (CGFS), a byproduct of the coal gasification process, is currently being recognized as a resource with significant potential for value addition and sustainable applications, especially in synthesizing CO2 adsorbents. The overarching challenges in this domain include the attainment of high-efficiency, environmentally benign transformation of CGFS into useful products, and the development of cost-effective adsorbent materials featuring precisely engineered pore structures. In this study, a hierarchical porous nanostructured silica material is synthesized rapidly, efficiently, and cost-effectively through acid leaching and alkaline dissolution-assisted hydrothermal treatment, employing CGFS as the precursor. The mass ratios of sodium hydroxide (NaOH) to CGFS range from 0.4 to 1, resulting in varying morphologies and adsorption properties. Specifically, the sample with the NaOH to CGFS ratio of 0.6 (CGFS-0.6) shows the best adsorption performance. The adsorption capacities are 2.87 mmol/g and 8.49 mmol/g at 20 °C with 15 % and 45 % CO2 concentration, respectively. The material is characterized by a well-developed pore structure shaped like a bouquet of flowers, with a specific surface area of 457 m2/g and pore volume reaching 2.34 cm3/g. During the hydrothermal processing, silicate/aluminosilicate entities self-organized into a Si-O-Na/Al network structure, endowing the synthesized adsorbent with optimal internal porosity and silanol functionalities. The adsorption equilibrium is achieved rapidly within 10 min, and CO2 adsorption stability remains robust across 20 successive cycles. All isothermal models of the adsorbents conform to the Sips model. This study offers a promising pathway for the value-enhanced utilization of coal-derived solid wastes.

Molecular Photoelectrochemical Energy Storage Materials for Coupled Solar Batteries.

ConspectusSolar-to-electrochemical energy storage is one of the essential solar energy utilization pathways alongside solar-to-electricity and solar-to-chemical conversion. A coupled solar battery enables direct solar-to-electrochemical energy storage via photocoupled ion transfer using photoelectrochemical materials with light absorption/charge transfer and redox capabilities. Common photoelectrochemical materials face challenges due to insufficient solar spectrum utilization, which restricts their redox potential window and constrains energy conversion efficiency. In contrast, molecular photoelectrochemical energy storage materials are promising for their mechanism of exciton-involved redox reaction that allows for extra energy utilization from hot excitons generated by superbandgap excitation and localized heat after absorption of sub-bandgap photons. This enables more efficient redox reactions with a less restricted redox potentials window and, thus, better utilization of the full solar spectrum. Despite these advantages, practical application remains elusive due to the mismatch between the short lifetime of the charge separation state (<ns) and the slower redox reaction rate (>μs). This mismatch results in a significant portion of the photogenerated charges recombining before participating in desired electrochemical energy storage reactions, leading to diminished overall efficiency. It is therefore highly important to develop molecular materials with intrinsic prolonged charge separation state and extrinsic effective mass-electron transfer to enable efficient coupled solar batteries for practical applications.In this Account, we begin with an introduction of the general solar-to-electrochemical energy storage concept based on molecular photoelectrochemical energy storage materials, highlighting the advantages of periodic oxidative donor-reductive acceptor porous aggregate structures that have synergistic implications on charge separation state lifetime extension and mass-electron transfer. We then present our earliest trial on the design and application of molecular photoelectrochemical energy storage materials, which stimulated our subsequent studies on tuning electron donor and acceptor structures for enhanced charge separation and diverse photoelectrochemical redox reactions. Moreover, we introduce the best practices in the design and assembly of various coupled solar battery devices, along with our literature contributions and progresses in solar-to-electrochemical energy storage efficiency (ηSES) over nearly the past decade. Finally, we conclude by highlighting the universality of our strategies as essential design principles, spanning from regulating long-lived charge separation states and photocoupled ion transfer processes in molecular materials to the construction of efficient coupled solar batteries. We offer perspectives on the synergy between photovoltage and redox potentials and the practical significance of 3D printing, providing key evaluation indicators for large-scale application. This Account provides molecular level insights for the construction of high-efficiency photoelectrochemical energy storage materials and guidance for practical solar-to-electrochemical energy storage applications.

Neglected sludge solid phase in sludge pretreatment process: Physicochemical characterization and mechanism study of its role in anaerobic degradation

The low anaerobic digestion efficiency of the solid phase separated from pre-treated sludge indicates the need to explore other suitable resource utilization pathways for sludge solid phase. However, there is a lack of comprehensive and in-depth research on the physicochemical properties of sludge solid phase. This study comprehensively analyzes the characteristics of sludge solid phase and elucidates the mechanism of sludge solid phase in the anaerobic degradation of toxic wastewater. The results show that the surface free energy of sludge solid phase after different pre-treatments is mainly contributed by Lewis acid-base hydration free energy. The distribution of proteins on the surface of sludge solid phase plays a major role in the adhesion between sludge solid particles. Metal ions in the sludge solid phase are mainly present in the exchange state, followed by the carbonate state and the organics-bound state. The sludge solid phase obtained by sludge pH 12 + 150 °C treatment has the highest conductivity (1.36 mS/m) and capacitance (25.51 μF/g), mainly due to the presence of melanoidins in the sludge solid phase, which has similar semiquinone radicals to humic acids, thus increasing conductivity. The addition of sludge solid phase promotes an increase in cumulative methane production and rate of methane production. The sludge solid phase might play a role of an auxiliary carbon source acting as an adsorbent to buffer against toxicity inhibition and facilitate electron transfer. This study reveals the characteristics of sludge solid phase and its role in anaerobic digestion, providing theoretical guidance for finding suitable resource utilization pathways for sludge solid phase.

Graphitization transformation of aluminum electrolytic spent carbon cathode

Aluminum electrolysis spent cathode carbon (SCC), as typical solid hazardous waste, poses significant environmental risks. Harmless treatment of SCC and recycling of its carbon component are important research areas. In this study, SCC was subjected to microwave hydrothermal acid leaching to remove harmful components, followed by the production of high-quality graphite via iron-catalyzed graphitization. The effects of reaction temperature, heating time, and catalyst loading on the graphitization conversion of SCC were investigated. The catalytic graphitization process of SCC was optimized using the response surface method. The results show that when the reaction temperature is 1520 °C, the heating time is 85.24 min, and the catalyst loading is 46.15 wt%, the graphitization degree of the sample is 97.61 %. The samples prepared under the optimal conditions were characterized using XRD, Raman, SEM, and TEM. The results reveal that the catalytic graphitization process significantly influences the conversion of microcrystalline structures in SCC into graphite structures. The iron-catalyzed transformation of microcrystalline carbon was analyzed to elucidate the graphitization transformation mechanism. This study offers an effective pathway for the high-value utilization of SCC. It also serves as a technical reference for the catalytic graphitization conversion of carbon materials.

Beyond methane, new frontiers in anaerobic microbial hydrocarbon utilizing pathways.

Alkanes, single carbon methane to long-chain hydrocarbons (e.g. hexadecane and tetradecane), are important carbon sources to anaerobic microbial communities. In anoxic environments, archaea are known to utilize and produce methane via the methyl-coenzyme M reductase enzyme (MCR). Recent explorations of new environments, like deep sea sediments, that have coupled metagenomics and cultivation experiments revealed divergent MCRs, also referred to as alkyl-coenzyme M reductases (ACRs) in archaea, with similar mechanisms as the C1 utilizing canonical MCR mechanism. These ACR enzymes have been shown to activate other alkanes such as ethane, propane and butane for subsequent degradation. The reversibility of canonical MCRs suggests that these non-methane-activating homologues (ACRs) might have similar reversibility, perhaps mediated by undiscovered lineages that produce alkanes under certain conditions. The discovery of these alternative alkane utilization pathways holds significant promise for a breadth of potential biotechnological applications in bioremediation, energy production and climate change mitigation.

The valorisation of steel mill off-gas via chain elongation into higher value-added products: A prospective life cycle assessment

Nowadays, one of the greatest challenges for the steel industry is decarbonisation to decrease its pressure on the environment. For this purpose, deploying carbon capture and utilisation technologies such as syngas fermentation can be instrumental, as they allow carbon in steel mill off-gas to be converted into ethanol. However, as ethanol is of relative low value, technologies that can upgrade it towards higher-value chemicals are becoming attractive. One such a technology is chain elongation, as it can convert ethanol effluents from syngas fermentation into caproic acid, which can subsequently be used as a feedstock to produce chemicals such as plasticisers. As information regarding the environmental sustainability of chain elongation is limited, in this study, a prospective environmental hotspot analysis on chain elongation was performed, assessing climate change and resource footprint indicators, from a Life Cycle Assessment perspective, based on a theoretical scale-up. In addition, climate change impacts of a novel basic oxygen furnace gas (BOFG) to plasticiser value chain integrating the theoretically scaled-up chain elongation technology (PLAST) were assessed and compared with two other valorisation routes, considering a US and a European scenario: BOFG incineration with electricity production (ELEC) and syngas fermentation for the production of ethanol for use as a fuel (ETOH). The hotspot analysis showed that electricity and chemicals consumption, mainly K-acetate, were the largest contributors to both the climate change and resource consumption footprint. For the US scenario, the novel PLAST route showed similar climate change impacts to the ETOH route, while the impacts were 15% higher than those of the ELEC pathway. In the European scenario, with a greener electricity mix, the PLAST route showed similar impacts compared to both the ELEC and ETOH routes. Although uncertainties lie within the results, this study highlights the potential of chain elongation as a part of an alternative carbon capture and utilisation pathway for the steel industry. For this however, further technological advances are required, such as changes in process configurations and increases in caproic acid productivity, which should be the focus of future research.

Changes in Inhaled Nitric Oxide Use Across ICUs After Implementation of a Standard Pathway.

Inhaled nitric oxide (iNO) is a selective pulmonary vasodilator. It is expensive, frequently used, and not without risk. There is limited evidence supporting a standard approach to initiation and weaning. Our objective was to optimize the use of iNO in the cardiac ICU (CICU), PICU, and neonatal ICU (NICU) by establishing a standard approach to iNO utilization. A quality improvement study using a prospective cohort design with historical controls. Four hundred seven-bed free standing quaternary care academic children's hospital. All patients on iNO in the CICU, PICU, and NICU from January 1, 2017 to December 31, 2022. Unit-specific standard approaches to iNO initiation and weaning. Sixteen thousand eighty-seven patients were admitted to the CICU, PICU, and NICU with 9343 in the pre-iNO pathway era (January 1, 2017 to June 30, 2020) and 6744 in the postpathway era (July 1, 2020 to December 31, 2022). We found a decrease in the percentage of CICU patients initiated on iNO from 17.8% to 11.8% after implementation of the iNO utilization pathway. We did not observe a change in iNO utilization between the pre- and post-iNO pathway eras in either the PICU or NICU. Based on these data, we estimate 564 total days of iNO (-24%) were saved over 24 months in association with the standard pathway in the CICU, with associated cost savings. Implementation of a standard pathway for iNO use was associated with a statistically discernible reduction in total iNO usage in the CICU, but no change in iNO use in the NICU and PICU. These differential results likely occurred because of multiple contextual factors in each care setting.

Hydrothermally Assisted Conversion of Switchgrass into Hard Carbon as Anode Materials for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) are emerging as a viable alternative to lithium-ion batteries, reducing the reliance on scarce transition metals. Converting agricultural biomass into SIB anodes can remarkably enhance sustainability in both the agriculture and battery industries. However, the complex and costly synthesis and unsatisfactory electrochemical performance of biomass-derived hard carbon have hindered its further development. Herein, we employed a hydrothermally assisted carbonization process that converts switchgrass to battery-grade hard carbon capable of efficient Na-ion storage. The hydrothermal pretreatment effectively removed hemicellulose and impurities (e.g., lipids and ashes), creating thermally stable precursors suitable to produce hard carbon via carbonization. The elimination of hemicellulose and impurities contributes to a reduced surface area and lower oxygen content. With the modifications, the initial Coulombic efficiency (ICE) and cycling stability are improved concurrently. The optimized hard carbon showcased a high reversible specific capacity of 313.4 mAh g-1 at 100 mA g-1, a commendable ICE of 84.8%, and excellent cycling stability with a capacity retention of 308.4 mAh g-1 after 100 cycles. In short, this research introduces a cost-effective method for producing anode materials for SIBs and highlights a sustainable pathway for biomass utilization, underscoring mutual benefits for the energy and agricultural sectors.

Photothermal-responsive lignin-based polyurethane with mechanically robust, fast self-healing, solid-state plasticity and shape-memory performance

In light of the depletion of petrochemical resources and increase in environmental pollution, there has been a significant focus on utilizing natural biomass, specifically lignin, to develop sustainable and functional materials. This research presents the development of a lignin-based polyurethane (DLPU) with photothermal-responsiveness by incorporating lignin and oxime-carbamate bonds into polyurethane network. The abundant hydrogen bonds between lignin and the polyurethane matrix, along with its cross-linked structure, contribute to DLPU's excellent mechanical strength (30.2 MPa) and toughness (118.7 MJ·m−3). Moreover, the excellent photothermal conversion ability of DLPU (54.4 %) activates dynamic reversible behavior of oxime-carbamate bonds and hydrogen bonds, thereby endowing DLPU with exceptional self-healing performance. After 15 min of near-infrared irradiation, DLPU achieves self-healing efficiencies of 96.0 % for tensile strength and 96.3 % for elongation at break. Additionally, DLPU exhibits photocontrolled solid-state plasticity as well as an excellent phototriggered shape-memory effect (70 s), with shape fixity and recovery ratios reaching 98.8 % and 95.3 %, respectively. By exploiting the spatial controllability and photothermal-responsiveness of DLPU, we demonstrate multi-dimensional responsive materials with self-healing and shape-shifting properties. This work not only promotes the development of multi-functional polyurethanes but also provides a pathway for the high-value utilization of lignin.

Preparation of α-calcium sulfate hemihydrate with high mechanical strength from natural fibrous gypsum in KCl-mediated glycerol-water solution

Natural fibrous gypsum is a kind of high-quality gypsum resources, whose high-value added utilization pathway is to be transformed to α-calcium sulfate hemihydrate (α-HH), a cementitious material that can react with water to form pastes with mechanical strength. In this work, α-HH was prepared from natural fibrous gypsum in KCl mediated glycerol-water solution under mild condition. KCl played a simultaneous function on regulating the phase-transition kinetics, morphology and comprehensive strength of α-HH. Addition of low concentration of KCl prominently retarded the nucleation and growth rate of α-HH and decreased its aspect ratio due to the formation of syngenite on the side faces. While further increase of KCl concentration accelerated the nucleation and growth rate and decreased the crystal sizes. In the presence of 0.04 M KCl, the prepared α-HH presented a hexagonal prism shape with a length / width of 257.69–579.71 μm / 13.13–36.61 μm, and its dry comprehensive strength had reached 38.1 MPa that was comparable to those prepared in commercial, chloride and nitrate system. Altogether, the foreign ion-free glycerol-water solution contributed to transforming natural fibrous gypsum to α-HH with high purity and high mechanical strength.

Preparation of mesoporous biogas residue biochar via a self-template strategy for efficient removal of ciprofloxacin: Effect of pyrolysis temperature

Biochar preparation and application is an anticipated pathway for the resource utilization of biogas residue. In this study, biochars were prepared by the pyrolysis of biogas residue from food waste anaerobic digestion (named as BRBCs) under various pyrolysis temperatures (300, 500, 700, and 900 °C), and the effect of pyrolysis temperatures on the physicochemical characteristics of BRBCs was examined. The adsorption performance toward ciprofloxacin (CIP), a typical antibiotic in waterbodies, was also investigated. The results showed that pyrolysis temperature significantly changed the physicochemical properties of BRBCs. In addition, the minerals in the biogas residue, especially SiO2, were rearranged to form a mesoporous structure in biochar through a self-template strategy (without activator). BRBC prepared at 900 °C exhibited a high specific surface area and pore volume, well-developed mesopore structure, and more carbon structure defects, and exhibited the largest CIP adsorption capacity with 70.29 mg g−1, which was ascribed to the combined interaction of pore diffusion, π–π interactions, hydrogen bonding, complexation, and electrostatic forces. Furthermore, the adsorption of CIP by BRBC900 was well described by two-compartment kinetic and Langmuir isotherm models. BRBC900 showed good adsorption performance toward CIP at pH 7–9. The adsorption of CIP by BRBC is a spontaneous, exothermic, entropy-increasing process. Moreover, BRBC also presented a good recycling potential. Therefore, the preparation of mesoporous biochar based on a self-template strategy not only provides an option for the resource utilization of biogas residue but also offers a new option for the treatment of antibiotic wastewater.

Thermodynamic and exergy assessment of a biomass oxy-fuel combustion with supercritical carbon dioxide cycle under various recycle flue gas conditions

The ongoing development of second-generation oxy-fuel combustion system with higher oxygen concentration have presented a potential pathway for efficient biomass utilization. It also signified the meticulous role of recycled flue gas in altering the combustion behaviour in the combustor. Accordingly, investigation into different recirculation modes focusing on recycle ratio, wet/dry conditions, and excess oxygen ratio are conducted with an indirect supercritical power cycle integrated biomass oxy-fuel combustion system. Energy and exergy analyses, as well as composition of flue gas produced are presented. Energy and exergy efficiencies increased with reducing recycle ratio, with respective highest efficiency of 31.33% and 44.37% obtained at excess oxygen ratio of 1.01 and recycle ratio of 0.5 under wet condition. Investigation of CO2 and H2O concentration in produced flue gas depicted a separated stage profile under dry recycle condition, different from the slight diverging profile observed under wet condition when the recycle ratio varied. Concentration of NOx and SOx increased with decreasing recycle ratio and are generally higher under dry condition. Selective exergy analyses of the proposed power cycle presented highest exergy loss in the combustor, followed by the air separation unit, heat exchanger, CO2 compression and purification unit, and turbine generator. Based on the obtained result, wet recycle flue gas enhanced the combustion performance in the combustor but slightly impaired the convective heat transfer in the heat exchanger. The performance of proposed biomass power cycle is optimized at low recycle ratio of 0.5 under wet recycle condition.

Utilizing in situ construction of N-doped hierarchical porous carbon to achieve electronic control of highly dispersed Pd nanoparticles for efficient catalytic hydrogenation of CO2 to formic acid

Hydrogenation of CO2 to produce formic acid/formate is a significant pathway for future energy storage and utilization. The development of heterogeneous catalysts with high activity and stability for this process is still a challenge. In this work, the in-situ N-doped hierarchical porous carbon derived from distiller's grains was used as a support for Pd-based catalysts (Pd/NC) to convert CO2 into valuable chemicals while making high-value use of waste biomass. The optimum catalyst, Pd/NC-800, shown exceptional catalytic performance, achieving a turnover frequency (TOF) of 2060 h−1 at 100℃, 4 MPa in the catalytic CO2 hydrogenation to formate reaction. Comprehensive experimental results and density functional theory calculations indicate that the electronic effect between the pyridine N in the support and the Pd nanoparticles (NPs) can make the Pd surface reach the state of electron enrichment and enhance the metal-support interaction. Moreover, the synthesized material has hierarchical pore structure, which provides abundant Pd anchor location sites and improves mass transfer efficiency. The results not only provide a feasible strategy for the preparation of efficient CO2 hydrogenation catalysts, but also break a new and effective avenue for the resource utilization of distiller's grains.

Unraveling the adaptive strategies of Mycoplasma hominis through proteogenomic profiling of clinical isolates.

Mycoplasma hominis (M. hominis) belongs to the class Mollicutes, characterized by a very small genome size, reduction of metabolic pathways, including transcription factors, and the absence of a cell wall. Despite this, they adapt well not only to specific niches within the host organism but can also spread throughout the body, colonizing various organs and tissues. The adaptation mechanisms of M. hominis, as well as their regulatory pathways, are poorly understood. It is known that, when adapting to adverse conditions, Mycoplasmas can undergo phenotypic switches that may persist for several generations. To investigate the adaptive properties of M. hominis related to survival in the host, we conducted a comparative phenotypic and proteogenomic analysis of eight clinical isolates of M. hominis obtained from patients with urogenital infections and the laboratory strain H-34. We have shown that clinical isolates differ in phenotypic features from the laboratory strain, form biofilms more effectively and show resistance to ofloxacin. The comparative proteogenomic analysis revealed that, unlike the laboratory strain, the clinical isolates possess several features related to stress survival: they switch carbon metabolism, activating the energetically least advantageous pathway of nucleoside utilization, which allows slowing down cellular processes and transitioning to a starvation state; they reconfigure the repertoire of membrane proteins; they have integrative conjugative elements in their genomes, which are key mediators of horizontal gene transfer. The upregulation of the methylating subunit of the restriction-modification (RM) system type I and the additional components of RM systems found in clinical isolates suggest that DNA methylation may play a role in regulating the adaptation mechanisms of M. hominis in the host organism. It has been shown that based on the proteogenomic profile, namely the genome sequence, protein content, composition of the RM systems and additional subunits HsdM, HsdS and HsdR, composition and number of transposable elements, as well as the sequence of the main variable antigen Vaa, we can divide clinical isolates into two phenotypes: typical colonies (TC), which have a high growth rate, and atypical (aTC) mini-colonies, which have a slow growth rate and exhibit properties similar to persisters. We believe that the key mechanism of adaptation of M. hominis in the host is phenotypic restructuring, leading to a slowing down cellular processes and the formation of small atypical colonies. This is due to a switch in carbon metabolism and activation the pathway of nucleoside utilization. We hypothesize that DNA methylation may play a role in regulating this switch.

Treatment of waste marine clay by alkaline-activated ground granulated blast-furnace slag and municipal solid waste incineration bottom ash

The construction of coastal areas generates a substantial volume of waste marine clay (WMC), which poses environmental and safety challenges during the stockpiling process. The improved preparation of WMC as roadbed materials emerges as a crucial pathway for resource utilization. However, the engineering performance and durability of roadbed materials prepared from WMC have always been a concern for scholars and engineers. This study employs alkali-activated ground granulated blast-furnace slag (GGBFS) and municipal solid waste incineration bottom ash (MSWIBA) to solidify WMC for preparation of the roadbed materials. The results showed that the combined utilization of alkali-activated GGBFS and MSWIBA to improve WMC can meet the environmental and mechanical requirements of roadbed materials. The incorporation of 5-20% MSWIBA could improve the water stability coefficient and California bearing ratio to more than 85% and 80%, respectively. The durability of roadbed material was significantly improved by addition of MSWIBA. After 12 dry–wet cycles, the strength of the material without MSWIBA and with 5% MSWIBA was 0 and 2.87 MPa, respectively. Following analysis of engineering properties and durability, the optimal dosage of MSWIBA was determined to be 5%. The enhanced durability can be attributed to the optimization of material gradation and pore structure achieved through the incorporation of a small quantity of MSWIBA. The carbon emission and normalized global warming potentials of roadbed material treated by MSWIBA and GGBFS were much lower than that of cementitious binders such as ordinary Portland cement. These findings indicate that MSWIBA has the potential to substitute natural aggregates like sand and gravel, effectively improving the durability of roadbed materials and promoting the safe and efficient recycling of solid waste resources.

Activation of a silent lactose utilization pathway in an evolved Listeria monocytogenes F2365 outbreak isolate

Listeria monocytogenes, a widespread food-borne pathogen, utilizes diverse growth substrates including mono- and di-saccharides via PEP-phosphotransferase (PTS) systems. We evaluated a collection of L. monocytogenes isolates of different origins for their ability to utilize lactose, a disaccharide composed of galactose and glucose and the main carbon source in milk and dairy products. Notably, the dairy-associated outbreak strain F2365 could not utilize lactose efficiently, conceivably due to a frameshift mutation (lacR887del) resulting in a truncated LacR. Transcriptional activator LacR is involved in the expression of two PTS systems, encoded by the lpo operon lmo1718-1720 in combination with lmo2708 and the lmo2683-2685 operon, and linked to lactose and/or cellobiose metabolism in L. monocytogenes. Via experimental evolution of the ancestral strain F2365, an evolved isolate F2365 EV was obtained which showed enhanced growth and metabolism of lactose. Using the lactose-positive model strain L. monocytogenes EGDe as a control, HPLC experiments showed that EGDe and F2365 EV could consume lactose and utilize the glucose moiety, while the galactose moiety was exported from the cells. Genome sequencing of F2365 EV found the original lacR887del mutation was still present but an additional point mutation lmo2766C415T had occurred, resulting in an amino acid substitution in the putative regulator Lmo2766. The lmo2766 gene is located next to operon lmo2761-2765 with putative PTS genes in the genome. Notably, comparative RNAseq analysis confirmed that the lmo2761-2765 operon was strongly upregulated in F2365 EV in the presence of lactose but not in EGDe and F2365. Conversely, the LacR-regulated lpo operon, lmo2708, and lmo2683-2685 operon were only upregulated in EGDe. Additional growth and HPLC experiments, using mutants constructed in lactose-positive L. monocytogenes EGDe, showed reduced growth of the EGDe lacR887del mutant with no utilization of lactose, while the double mutant EGDe lacR887dellmo2766C415T showed enhanced growth and lactose utilization. Hence, these results demonstrate that an amino acid substitution in the Lmo2766 regulator activates a previously silent lactose utilization pathway encoded by PTS operon lmo2761-2765, facilitating the growth and metabolism of L. monocytogenes with lactose as a substrate. This finding enhances our understanding of the metabolic capabilities and adaptability of L. monocytogenes, offering a broader view of the lactose utilization capacity of this pathogen.

Analysis of current state, gaps, and opportunities for technologies in the Malaysian oil palm estates and palm oil mills towards net-zero emissions

Malaysia is the second largest producer and exporter of palm oil. Though several works have explored achieving emissions reduction in the palm oil sector, there existing gaps in analysing pathways for achieving net-zero emissions. Moreover, there are limited studies that evaluate the potential of palm oil biomass utilisation pathways based on emissions reduction capabilities, the cost of emissions reduction, and the technology readiness for implementation. Therefore, this study analysed decarbonisation pathways for the upstream and midstream segments of the palm oil sector in Malaysia, encompassing oil palm plantations and palm oil mills. Various sources of greenhouse gas emissions in oil palm plantations and palm oil mills were identified and estimates of emissions were determined as theoretical emissions. The current emissions were established based on the current best practice in the plantation and mill. Several biomass conversion technologies for the recovery of palm-based by-products and conversion into value-added products to decarbonise the palm oil sector and evaluated strategies to attain net-zero status are considered. In this work, the analysis considered both the existing technologies that are adopted by plantations and mills as well as the emerging technologies that have scope for implementation. With the proposed approach, the current emissions level for crude palm oil (CPO) production in Malaysia is estimated as 1121.49 kg CO2-eq/t CPO. In current industry practice, empty fruit bunch (EFB) is underutilised as mills are typically located at rural areas with lack of suitable transportation. Besides, the lack of accessibility to the grid also limits the potential of converting EFB into electricity as supply for national grid. This work examined various pathways for EFB utilisation under different scenarios evaluating their contribution potential towards net-zero target in an energy self-sustained CPO production. As shown in the results, converting EFB to briquettes and pellets are able to achieve the net-zero objective. Furthermore, EFB-biochar and EFB-syngas pathways also exhibit the potential to accomplish the net-zero target. Note that this work also assessed the technologies’ readiness levels, identified challenges in implementation, and proposed several recommendations.

Efficient adsorption of antibiotics in aqueous solution through ZnCl2-activated biochar derived from Spartina alterniflora

In recent years, Spartina alterniflora as an invasive species has seriously threatened the native coastal ecosystem of China. There is a lack of effective management and utilization methods towards Spartina alterniflora at present. To realize the ecological remediation and resource utilization of Spartina alterniflora, the functional biochar (BC) materials were successfully prepared using Spartina alterniflora as the substrates via the high temperature calcination method, which were utilized for efficient removal of antibiotics. The biochar was further activated by ZnCl2 (ZnBC) and optimized under different calcination temperatures and ZnCl2 dosages to improve the adsorption ability. Among these biochar materials, the ZnCl2-activated biochar obtained under the mass ratio of Spartina alterniflora to ZnCl2 of 1:5 and calcination temperature of 600 °C (ZnBC-600) exhibited the strongest adsorption performance towards sulfadiazine (SDZ) and ciprofloxacin (CIP), which can be attributed to the larger specific surface area, richer pore structure and more abundant surface oxygen-containing functional groups. Additionally, the adsorption kinetics and isotherms demonstrated that the adsorption of both SDZ and CIP onto ZnBC-600 (1:5) followed the pseudo-second-order kinetic model and Freundlich model. At the same time, the performances of Spartina alterniflora biochar derived from different biomass were compared under the condition of activation with ZnCl2, presenting the superior performance of ZnCl2 activated Spartina alterniflora biochar. Moreover, the adsorption mechanism of ZnBC-600 (1:5) was proposed, illustrating the crucial roles of effects of electrostatic attraction, pore filling, oxygen-containing groups complexation, π-π stacking and hydrogen bonding in the adsorption of antibiotics. Above all, this study not only provides a feasible strategy for the preparation of functional biochar derived from Spartina alterniflora for removing organic pollutants, but also opens up a new pathway for resource utilization of Spartina alterniflora.