Background: Herbicides are chemical agents that promote plant and crop growth by killing weeds and other pests. However, unconsumed and excessively used herbicides may enter groundwater and agricultural areas, damaging water, air, and soil resources. Mesotrione (MT) is an extensively used herbicide to cultivate corn, sugarcane, and vegetables. Excessive consumption of MT residues pollutes the soil, water, and environmental systems. Methods: Henceforth, the potential electrocatalyst of the tungsten trioxide nanorods on the carbon microsphere (WO3/C) composite was synthesized for nanomolar electrocatalytic detection of MT. The electrocatalysts of WO3/C were synthesized hydrothermally, and the WO3/C composite was in-situ constructed by using the reflux method. Significant findings: Remarkably, the as-prepared WO3/C composite displayed a fantastic sensing platform for MT, characterized by an astonishingly nanomolar detection limit (10 nm), notable sensitivity (1.284 mu A mu M-1 cm-2), exceptional selectivity, and amazing stability. The actual sample test was carried out using MT added in food and environmental samples of corn, sugar cane, sewage water, and river water. The minimum MT response recovery in vegetable and water samples was determined to be approximately 97 % and 99 %, respectively. The results indicate that the WO3/C composite is an effective electrode material for real-time MT measurement in portable devices.

(3-Hexachlorocyclohexane ((3-HCH) is a persistent organochlorine pesticide that poses a significant threat to the ecological environment, necessitating the urgent development of effective degradation methods. Microbial degradation has demonstrated substantial potential among various bioremediation techniques due to its environmentally friendly and economical characteristics. This study evaluates the degradation capability of Enterobacter sp. CS01 on (3-HCH, its physiological responses, and its potential application in soil remediation. Under optimal conditions (pH 7, 30 degrees C), 51 % of (3-HCH was effectively removed. Metabolomics and antioxidant enzyme activity analyses revealed that CS01 defends against oxidative damage by modulating the activities of superoxide dismutase (SOD) and catalase (CAT), involving butyrate, alanine, aspartate, and glutamate metabolism, as well as the pentose phosphate pathway. CS01 converts (3-HCH into less toxic intermediates through dichloride elimination, dehalogenation of hydrogen, and hydrolysis reactions. Soil experiments indicated that soil enzyme activities (S-POD, S-DHA, S-PPO) are closely related to the degradation of (3-HCH, with the order of carbon source utilization being esters, amino acids, and sugars. This study provides new insights into the microbial degradation mechanisms of organochlorine pesticides and aids in the development of more efficient and environmentally friendly degradation technologies.

An Integrated Process Intensification (IPI) technology-based roadmap is proposed for the utilization of renewables (water, air and biomass/unavoidable waste) in the small-scale distributed production of the following primary products: electricity, H-2, NH3, HNO3 and symbiotic advanced (SX) fertilizers with CO2 mineralization capacity to achieve negative CO2 emission. Such a production platform is an integrated intensified biorefinery (IIBR), used as an alternative to large-scale centralized production which relies on green electricity and CCUS. Hence, the capacity and availability of the renewable biomass and unavoidable waste were examined. The critical elements of the IIBR include gasification/syngas production; syngas cleaning; electricity generation; and the conversion of clean syngas (which contains H-2, CO, CH4, CO2 and N-2) to the primary products using nonthermal plasma catalytic reactors with in situ NH3 sequestration for SA fertilizers. The status of these critical elements is critically reviewed with regard to their techno-economics and suitability for industrial applications. Using novel gasifiers powered by a combination of CO2, H2O and O-2-enhanced air as the oxidant, it is possible to obtain syngas with high H-2 concentration suitable for NH3 synthesis. Gasifier performances for syngas generation and cleaning, electricity production and emissions are evaluated and compared with gasifiers at 50 kWe and 1-2 MWe scales. The catalyst and plasma catalytic reactor systems for NH3 production with or without in situ reactive sequestration are considered in detail. The performance of the catalysts in different plasma reactions is widely different. The high intensity power (HIP) processing of perovskite (barium titanate) and unary/binary spinel oxide catalysts (or their combination) performs best in several syntheses, including NH3 production, NOx from air and fertigation fertilizers from plasma-activated water. These catalysts can be represented as BaTi1-vO3-x{#}(y)N-z (black, piezoelectric barium titanate, bp-{BTO}) and (M3-jMkO4-m)-M-(1)-O-(2){#}(n)N-r/SiO2 (unary (k = 0) or a binary (k > 0) silane-coated SiO2-supported spinel oxide catalyst, denoted as M/Si = X) where {#} infers oxygen vacancy. HIP processing in air causes oxygen vacancies, nitrogen substitution, the acquisition of piezoelectric state and porosity and chemical/morphological heterogeneity, all of which make the catalysts highly active. Their morphological evaluation indicates the generation of dust particles (leading to porogenesis), 2D-nano/micro plates and structured ribbons, leading to quantum effects under plasma catalytic synthesis, including the acquisition of high-energy particles from the plasma space to prevent product dissociation as a result of electron impact. M/Si = X (X > 1/2) and bp-{BTO} catalysts generate plasma under microwave irradiation (including pulsed microwave) and hence can be used in a packed bed mode in microwave plasma reactors with plasma on and within the pores of the catalyst. Such reactors are suitable for electric-powered small-scale industrial operations. When combined with the in situ reactive separation of NH3 in the so-called Multi-Reaction Zone Reactor using NH3 sequestration agents to create SA fertilizers, the techno-economics of the plasma catalytic synthesis of fertilizers become favorable due to the elimination of product separation costs and the quality of the SA fertilizers which act as an artificial root system. The SA fertilizers provide soil fertility, biodiversity, high yield, efficient water and nutrient use and carbon sequestration through mineralization. They can prevent environmental damage and help plants and crops to adapt to the emerging harsh environmental and climate conditions through the formation of artificial rhizosphere and rhizosheath. The functions of the SA fertilizers should be taken into account when comparing the techno-economics of SA fertilizers with current fertilizers.

This review paper explores the use of red mud as a sustainable alternative for construction materials and soil stabilisation due to its unique chemical and mineral composition, a waste produced during the extraction of aluminium from bauxite ore. The disposal of red mud is a major environmental issue worldwide due to its high alkalinity and large production volume. Although this material has already been utilised as construction material (e.g., bricks, cement, concrete), it can also be incorporated for waste water treatment and lead to waste reduction. In soil stabilisation, red mud's alkaline nature, pozzolanic properties, and fine particle size improve soil structure and strength, offering a cost-effective solution. Utilising red mud as a filling material for low-lying areas addresses the disposal problem while contributing to infrastructure development projects. This study highlights construction materials' mechanical properties and durability by incorporating bauxite tailings and also incorporating valorisation of red mud as a precursor for alkali-activated binder. This paper comprises recent research findings and practical applications associated with the use of this waste. Also, it discusses the benefits and challenges associated with the large-scale use of red mud. It gives an idea about how the strength and durability of construction materials can be improved considering overall environmental impact. Future perspectives on policy, technology, and environmental impact are also discussed to provide a comprehensive understanding of red mud's potential for sustainable development. Red mud enhances the properties of materials like strength, durability, and thermal resistance of construction materials like bricks, ceramic, and cement.Red mud increases soil load-bearing capacity, reduces plasticity, and enhances erosion resistance, making it ideal for foundations and road construction.Using red mud reduces dependency on traditional raw materials, conserving natural resources and lowering environmental impacts.Red mud in construction and soil stabilisation contributes to durable, eco-friendly structures and supports sustainable land use.

Oxalate esters and isosorbide serve as intriguing polymer building blocks, as they can be sourced from renewable resources, such as CO2 and glucose, and the resulting polyesters offer outstanding material properties. However, the low reactivity of the secondary hydroxyl groups makes it difficult to generate high-molecular-weight polymers from isosorbide. Combining diaryl oxalates with isosorbide appears to be a promising approach to produce high-molecular-weight isosorbide-based polyoxalates (PISOX). This strategy seems to be scalable, has a short polymerization time (<5 h), and uniquely, there is no need for a catalyst. PISOX demonstrates outstanding thermal, mechanical, and barrier properties; its barrier to oxygen is 35 times better than PLA, it possesses mechanical properties comparable to high-performance thermoplastics, and the glass transition temperature of 167 degrees C can be modified by comonomer incorporation. What makes this high-performance material truly exceptional is that it decomposes into CO2 and biomass in just a few months in soil under home-composting conditions and it hydrolyzes without enzymes present in less than a year in 20 degrees C water. This unique combination of properties has the potential to be utilized in a range of applications, such as biomedical uses, water-resistant coatings, compostable plastic bags for gardening and agriculture, and packaging plastics with diminished environmental impact.

This study evaluates the substitution of calcined clay for a waste from the petrochemical industry, spent fluid catalytic cracking catalyst (FCC), as a source of reactive aluminosilicates in Limestone Calcined Clay Cements (LC3) systems. Three carbonate types were used to make cement-type LC3: a high-purity calcium carbonate, waste from the marble industry, and another from a dolomite soil source. LC3 blends were prepared by mixing 50 wt% OPC, 5 wt% calcium sulfate dihydrate, 30 wt% FCC and 15 wt% from each carbonate source. A mixture than substituting the carbonate source for a siliceous source was prepared to analyse the influence of carbonate phases in LC3 systems. The hydration process of the LC3 blends was studied by X-ray diffraction, thermogravimetric analyses, isothermal calorimetry and FESEM. Mechanical properties were studied by measuring compressive strength at 7, 28 and 90 days. The obtained results corroborated that the mortars prepared with LC3 cements using the FCC obtained higher compressive strength than the control mortar prepared with ordinary Portland cement (OPC) at 28 and 90 curing days. It has been demonstrated that FCC is a by-product that can substitute calcined clay, and the different sources of carbonates such as high purity, waste or contaminated with magnesium do not interfere with the performance of this type of cement.

Asphalt or oil spills containing asphaltene can contaminate soil, water bodies, and ecosystems. Natural balances are disrupted by this contamination. Asphaltene contaminates water sources such as rivers, lakes, and aquifers, making them unfit for human consumption. Aquatic habitats are damaged, and aquatic organisms cannot reproduce, grow, or maintain health. Air pollutants, including sulfur dioxide, nitrogen oxides, volatile organic compounds, and particulate matter, are released when asphaltene-containing materials are burned. Here, we have developed a new method for the degradation of asphaltene that is fast, clean, and cost-effective. The asphaltene was degraded using NixMnyO piezo catalyst in this study. By using NixMnyO under mechanical force, the result showed that asphaltene was degraded to the extent of 94.7 %. Piezo based on NixMnyO has shown promising reusability when compared to conventional catalysts. Despite being used for 11 runs, it maintained 94% of its activity for 11 consecutive cycles. As well as analyzing the kinetics and thermodynamics of piezo asphaltene degradation, a mechanism pathway was developed for piezo degradation of asphaltene. Radical scavenger experiments showed that superoxide radicals, holes, and hydroxyl radicals are involved in the degradation of asphaltene by NixMnyO piezo catalysts. However, hydroxyl radicals and holes are responsible for the majority of asphaltene degradation.

Soil and water pollution are current global environmental and agricultural challenges, adversely affected by ineffective industrial waste treatment before discharging into the environment combined with inefficient long-term inputs of fertilizers. The development of targeted fertilizers delivery vehicles, sufficient soil/water remediation, and contamination detection systems using eco-friendly technologies become critically important. Due to their high specific surface area, biocompatibility, easiness of operation, and high performance, nanomaterials-based controllable soil fertility promoters, adsorbents, sensors, and photocatalysts are promising tools for soil/water pollution prevention, remediation, and monitoring. Altogether, crystallinity, hydrophilic-tunable surface chemistry, and 3D forming ability of nanocellulose (NC), in addition to biodegradability, regeneration ability, and mechanical properties of NC nanocomposite hydrogels (NCHs), lead to advancing promising soil/water nanohydrogels-based targeted fertilizers delivery vehicles, adsorbents, co-adsorbents/co-sensors, and co-adsorbents/co-photocatalysts. In these systems, NCHs introduce 3D rigid porous scaffolds for homogenous dispersing/fixing of functional groups, fertilizers, fluorescence sources, and photocatalysts. Also, they present stimuli-responsive networks for fertilizer regulation in soil, and matrixes with extra active sites enabling contaminates immobilization/degradation. This review outlines an update of the most recent potential utilization of functionalized NCHs-based soil/water adsorbents, photocatalysts, sensors, and slow/targeted fertilizers release vehicles. An in-depth discussion of surface pretreatments-modifications used to improve their performance, fabrication methods, application properties, and working mechanisms was discussed. The potential limitations and future perspectives on using NCHs in fertilizer/water management, soil/water remediation, and detection are highlighted.

Environmental context Mitigating the environmental fallout of industrial accidents is crucial. In a recent study, researchers conducted tests on model substrates to explore the effectiveness of bioremediation in treating complex refinery contaminants resulting from both accidental and deliberate facility damage. The research reveals that bioremediation can be a promising, eco-friendly solution for cleaning up such pollutants, aligning with broader efforts to combat environmental harm resulting from industrial incidents.Rationale Bioremediation harnesses microorganisms' diverse metabolic abilities to detoxify and eliminate pollutants, particularly hydrocarbon-based ones such as oil. This natural biodegradation process performed by microorganisms is a cost-effective method for environmental cleanup compared to other remediation technologies.Methodology In this study, we examined the fate of heavy metals, cobalt and molybdenum, by the analysis of the basic chemical parameters of other sample components, such as n-hexane extractable substances and total petroleum hydrocarbons. The metal content was determined using inductively coupled plasma-optical emission spectrometry (ICP-OES). Exchangeable (loosely bound to the surface of particles and due to its high mobility and availability is crucial for understanding the potential immediate impact of metal contamination) and more stable fractions of the metal and the metal forms were determined using a sequential extraction method. The phase composition of the samples was determined by X-ray diffraction.Results In our microbiological analysis, we isolated various cultures from a consortium of microorganisms. Basic chemical analysis indicators, such as n-hexane extractable substances, total petroleum hydrocarbons and humic acids, reflected robust microbiological activity. During the study, metals in exchangeable form decreased and those in more stable forms increased.Discussion The sequential extraction of cobalt and molybdenum revealed shifts in various metal fractions within the bioaugmented substrate post-bioremediation, differing from the initial substrate. These alterations in metal fractions are likely attributable to microbial actions, leading to the formation of more stable metal fractions throughout the bioremediation process.