Microplastic/nanoplastic toxicity in plants: an imminent concern.

The toxic impact of microplastics/nanoplastics (MPs/NPs) in plants and the food chain has recently become a top priority. Several research articles highlighted the impact of MPs/NPs on the aquatic food chain; however, very little has been done in the terrestrial ecosystem. A number of studies revealed that MPs/NPs uptake and subsequent translocation in plants alter plant morphological, physiological, biochemical, and genetic properties to varying degrees. However, there is a research gap regarding MPs/NPs entry into plants, associated factors influencing phytotoxicity levels, and potential remediation plans in terms of food safety and security. To address these issues, all sources of MPs/NPs intrusion in agroecosystems should be revised to avoid these hazardous materials with special consideration as preventive measures. Furthermore, this review focuses on the routes of accumulation and transmission of MPs/NPs into plant tissues, related aspects influencing the intensity of plant stress, and potential solutions to improve food quality and quantity. This paper also concludes by providing an outlook approach of applying exogenous melatonin and introducing engineered plants that would enhance stress tolerance against MPs/NPs. In addition, an overview of inoculation of beneficial microorganisms and encapsulated enzymes in soil has been addressed, which would make the degradation of MPs/NPs faster.

Highly Sensitive Potentiometric pH Sensor Based on Polyaniline Modified Carbon Fiber Cloth for Food and Pharmaceutical Applications.

This study introduces a potentiometric pH sensor that is extremely sensitive and specifically designed for food and pharmaceutical applications. The sensor utilizes a pH-sensitive interface fabricated by electropolymerizing polyaniline (PANI) on carbon fiber cloth (CFC). Structural and morphological analyses of PANI-CFC and CFC have been conducted by using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and X-ray photoelectron spectroscopy (XPS). The investigation of the functional groups was conducted by using Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. The electrochemical characteristics were assessed by utilization of cyclic voltammetry (CV) and open-circuit potential (OCP) measurements in a three-electrode configuration. The sensor exhibited a sensitivity of 60.9 mV/pH, while retaining consistent performance within the pH range of 4 to 12. The repeatability and robustness of the sensors were verified. The accuracy of the PANI-CFC sensor was confirmed by validation using real samples, demonstrating its compatibility with commercially available pH sensors. The application of density functional theory (DFT) calculations revealed an interaction energy of -173.2886 kcal/mol, indicating a strong affinity of H+ ions towards PANI-CFC electrode. Further investigation was conducted to examine the chemical reactivity of PANI, revealing a HOMO-LUMO energy gap of -0.98 eV. This study highlights the PANI-CFC sensor as a reliable and efficient pH-sensing platform for food and pharmaceuticals applications, performing robustly in both laboratory and real-world settings.

Removal of microplastics from aqueous media using activated jute stick charcoal.

Microplastics (MPs), which are repositories of various pollutants, have significant effects on the people and the environment. Therefore, there is an urgent need for efficient and eco-friendly techniques to eliminate microplastics from water-based environments. This study introduces a new method for producing jute stick-activated charcoal (JSAC) by placing jute sticks on high-temperature pyrolysis without oxygen, followed by chemical activation with HCl. This process greatly enhances the adsorption capacity of JSAC for polyvinylchloride-based microplastics (PVC-MPs). JSAC was characterized using UV-Vis, FT-IR, XRD, and SEM studies both before and after adsorption. The study investigated the influence of pH, adsorbent quantity, and contact time on the optimization of the JSAC process. The PVC-MPs exhibited a maximum adsorption capacity of 94.12 % for the target MPs (5 g L-1) within 120 min when 10 g L-1 of JSAC was added at pH 7. This work also examined adsorption rate and various isotherm models. Adsorption kinetics analysis reveals electrostatic, hydrogen bond, π-π, and hydrophobic interactions are the combined forces responsible for MPs adsorption onto JSAC. However, the decrease in hydrophobicity in acidic or basic media led to a decrease in adsorption. The isotherm analysis was conducted using the Langmuir isotherm model, and predicted the maximum adsorption capacity of PVC-MPs to be 4.4668 mg/g. Furthermore, by employing density functional theory, the interaction energy after PVC-MP adsorption was calculated to be -269 kcal/mol, demonstrating robust adsorption and agreement with the experimental findings. Due to its large surface area and porous structure containing many functional groups, JSAC can potentially be used to treat MP contamination in water.

Post-pandemic micro/nanoplastic pollution: Toward a sustainable management.

The global health crisis caused by the COVID-19 pandemic has resulted in massive plastic pollution from the use of personal protection equipment (PPE), with polypropylene (PP) being a major component. Owing to the weathering of exposed PPEs, such contamination causes microplastic (MP) and nanoplastic (NP) pollution and is extremely likely to act as a vector for the transportation of COVID-19 from one area to another. Thus, a post-pandemic scenario can forecast with certainty that a significant amount of plastic garbage combined with MP/NP formation has an adverse effect on the ecosystem. Therefore, updating traditional waste management practices, such as landfilling and incineration, is essential for making plastic waste management sustainable to avert this looming catastrophe. This study investigates the post-pandemic scenario of MP/NP pollution and provides an outlook on an integrated approach to the recycling of PP-based plastic wastes. The recovery of crude oil, solid char, hydrocarbon gases, and construction materials by approximately 75, 33, 55, and 2 %, respectively, could be achieved in an environmentally friendly and cost-effective manner. Furthermore, the development of biodegradable and self-sanitizing smart PPEs has been identified as a promising alternative for drastically reducing plastic pollution.

Progress in biohythane production from microalgae-wastewater sludge co-digestion: An integrated biorefinery approach.

Recent advances in microalgae to biohythane (bio-H2 and bio-CH4) conversion have achieved growing attention due to their eco-friendly and energy-efficient nature. Although microalgae are considered a potential 3rd - 4th generation biomass, their low C/N ratio and cell-wall biopolymers are challenging for biohythane production. This study emphasizes the solutions to mitigate the adverse effects of microalgae-based biohythane production using co-digestion with wastewater sludge. Wastewater sludge, an emerging environmental concern, is reviewed to be an effective co-substrate with microalgae to establish a biorefinery approach. The future trends and prospects of this biorefinery approach is critically reviewed to attain a profitable process. This study also reviewed the advantages of microalgae-wastewater co-cultivation and the application of activated sludge for bio-flocculation as a cost-effective solution for microalgae cultivation and harvesting. Microalgae-wastewater co-cultivation is also recommended to be effective for biohythane purification. The liquid digestate is suggested to be used as a culture media to enhance microalgal growth; whereas, the solid digestate could be transformed into resources through hydrothermal processes as a solution of digestate management. A practical biorefinery approach combining the synergistic benefits of microalgae-wastewater sludge and its biological conversion to biohythane would be an adjoining link to the beginning of a sustainable future.

Detection and removal of microplastics in wastewater: evolution and impact.

The pervasiveness of microplastics in aquatic ecosystems has become a major environmental issue in recent years. The gradual dumping of plastic wastes, inadequate standard detection methods with specific removal techniques, and slow disposal rate of microplastics make it ubiquitous in the environment. Evidence shows that microplastics act as a potential vector by adsorbing different heavy metals, pathogens, and other chemical additives widely used in different raw plastic production. Microplastics are ingested by aquatic creatures such as fish and different crustaceans, and finally, people ingest them at the tertiary level of the food chain. This phenomenon is responsible for blocking the digestion tracts, disturbing the digestive behavior, finally decreasing the reproductive growth of entire living organisms. Because of these consequences, microplastics have become an increasing concern as a newly emerging potential threat, and therefore, the control of microplastics in aquatic media is required. This paper provides a critical analysis of existing and newly developed methods for detecting and separating microplastics from discharged wastewater, which are the ultimate challenges in the microplastic treatment systems. A critical study on the effect of microplastics on aquatic organisms and human health is also discussed. Thus, this analysis provides a complete understanding of entire strategies for detecting and removing microplastics and their associated issues to ensure a waste discharge standard to minimize the ultimate potential impact in aquatic environments.

Pencil graphite as electrode platform for free chlorine sensors and energy storage devices.

Multifunctional and low-cost electrode materials are desirable for the next-generation sensors and energy storage applications. This paper reports the use of pencil graphite as an electrode for dual applications that include the detection of free residual chlorine using electro-oxidation process and as an electrochemical energy storage cathode. The pencil graphite is transferred to cellulose paper by drawing ten times and applied for the detection of free residual chlorine, which shows a sensitivity of 27 µA mM-1 cm-2 with a limit of detection of 88.9 µM and linearity up to 7 mM. The sample matrix effect study for the commonly interfering ions such as NO3-, SO42-, CO32-, Cl-, HCO3- shows minimal impact on free residual chlorine detection. Pencil graphite then used after cyclic voltammogram treatment as a cathode in the aqueous Zn/Al-ion battery, showing an average discharge potential plateau of ~1.1 V, with a specific cathode capacity of ~54.1 mAh g-1 at a current of 55 mA g-1. It maintains ~95.8% of its initial efficiency after 100 cycles. Results obtained from the density functional theory calculation is consistent with the electro-oxidation process involved in the detection of free residual chlorine, as well as intercalation and de-intercalation behavior of Al3+ into the graphite layers of Zn/Al-ion battery. Therefore, pencil graphite due to its excellent electro-oxidation and conducting properties, can be successfully implemented as low cost, disposable and green material for both sensor and energy-storage applications.

Development of Tungsten Oxide Nanoparticle Modified Carbon Fibre Cloth as Flexible pH Sensor.

A reagent-less pH sensor based on disposable and low cost carbon fibre cloth (CFC) is demonstrated for the first time, where tungsten oxide nanoparticles were grown directly onto the CFC substrate. For comparison purpose, tungsten oxide nanoparticle modified glassy carbon electrode (GCE) was also fabricated as a pH sensor, where hydrothermally synthesized tungsten oxide nanoparticles were drop casted onto the GCE surface. The corresponding equilibrium potential using tungsten oxide/CFC as a pH sensor was measured using open circuit potential (OCP), and was found to be linear over the pH range of 3-10, with a sensitivity of 41.38 mVpH-1, and response time of 150 s. In the case of tungsten oxide/GCE as a pH sensor, square wave voltammetry (SWV) was used to measure the shifts in peak potential and was found to be linear with a pH range of 3-11, and a sensitivity of 60 mVpH-1 with a potential drift of 2.4-5.0% after 3 hour of continuous use. The advantages of tungsten oxide/CFC and tungsten oxide/GCE as pH sensing electrode have been directly compared with the commercial glass probe based electrode, and validated in real un-buffered samples. Thereby, tungsten oxide nanoparticles with good sensitivity and long term stability could be potentially implemented as a low cost and robust pH sensor in numerous applications for the Internet of Things (IoT).

Disposable sensor based on enzyme-free Ni nanowire array electrode to detect glutamate.

Enzyme free electrochemical sensor platform based on a vertically aligned nickel nanowire array (NiNAE) and Pt coated nickel nanowire array (Pt/NiNAE) have been developed to detect glutamate. Morphological characterisation of Ni electrodes was carried out using scanning and transmission electron microscopy combined with energy dispersive X-ray (SEM-EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM). Cyclic voltammetry (CV) and amperometry were used to evaluate the catalytic activity of the NiNAE and the Pt/NiNAE for glutamate. It has been found that both NiNAE and Pt/NiNAE electrodes showed remarkably enhanced electrocatalytic activity towards glutamate compared to planar Ni electrodes, and showed higher catalytic activity when compared to other metallic nanostructure electrodes such as gold nanowire array electrodes (AuNAE) and Pt coated gold nanowire array electrode (Pt/AuNAE). The sensitivity of NiNAE and Pt/NiNAE has been found to be 65 and 96 µA mM(-1) cm(-2), respectively, which is approximately 6 to 9 times higher than the state of the art glutamate sensor. Under optimal detection conditions, the as prepared sensors exhibited linear behaviour for glutamate detection in the concentration up to 8mM for both NiNAE and Pt/NiNAE with a limit of detection of 68 and 83 µM, respectively. Experimental results show that the vertically aligned ordered nickel nanowire array electrode (NiNAE) has significant promise for fabricating cost effective, enzyme-less, sensitive, stable and selective sensor platform.

Disposable biosensor based on immobilisation of glutamate oxidase on Pt nanoparticles modified Au nanowire array electrode.

Novel electrochemical platform based on Pt nanoparticle modified ordered three-dimensional gold nanowire arrays (PtNP/NAEs) for the amperometric sensing of H(2)O(2) and glutamate is developed. Pt nanoparticle (PtNP) is fabricated by electrodeposition onto the 3D nanowires and characterised using scanning electron microscopy (SEM) and cyclic voltammetry. The deposited nanoparticles have an average size of 20 nm. The PtNP/NAE shows a linear response of up to 20 mM for H(2)O(2) detection with a sensitivity of 194.60 µA mM(-1) cm(-2) at 20°C. It can detect 1 µM (S/N=3) of H(2)O(2) at normal condition without using any enzyme or mediator. Analytical performance of this electrode is tested by immobilising glutamate oxidase (GlutOx) through cross-linking in the matrix of bovine serum albumin (BSA), Nafion and glutaraldehyde. At physiological pH, the biosensor showed the sensitivity of 10.76 µA mM(-1) cm(-2), with a linear range of up to 0.8 mM.

A stable and selective electrochemical biosensor for the liver enzyme alanine aminotransferase (ALT).

An electrochemical method to determine alanine aminotransferase (ALT) activity over its normal and elevated physiological range was developed based upon detection of L-glutamate at a glutamate oxidase-modified platinum electrode. Measurements were carried out in the presence of ALT co-substrates L-alanine and alpha-ketoglutarate and current response from either the oxidation of hydrogen peroxide or the re-oxidation of the mediator ferrocene carboxylic acid was employed. The enzyme electrode was tested over a 6-month period and found to retain 79% of its original activity towards ALT detection with >200 measurements performed over this time. Signals associated with interfering electroactive species (ascorbic acid and uric acid) were eliminated using background subtraction at a denatured glutamate oxidase enzyme electrode. The sensitivity of the device was found to be 0.845 nA U(-1) L ALT with t(90)=180 s, linear range 10-1000 U L(-1) and LOD of 3.29 U L(-1) using amperometry at E(app)=0.4 V vs. Ag/AgCl at 308 K (35 degrees C).