Synthetic dyes are commonly used in food products like soft drinks, vegetable sauces, jellies, etc. Most artificial dyes can cause cancer, therefore it is very important to develop sensors to detect them in food samples. Voltammetric methods with carbon paste electrodes (CPEs) are promising for this purpose. However, modification of CPEs is necessary to detect the commercial dyes in food samples in the presence of interferents. In the current review, we have discussed the different previous research in which detection of dyes is performed in real samples with good detection limits. The current review will be helpful for readers who are interested in developing low-cost electrodes for the effective determination of dyes in commercial products like soft drinks and vegetable sauces.

The environmental impact of synthetic dyes presents a significant challenge due to their toxicity and persistence in ecosystems. Recent advancements in surfactant-modified adsorbent materials offer a promising solution for effective dye removal. Surfactants, recognized for their nontoxic and eco-friendly properties, enhance the performance of adsorbents by improving their dye-capturing capabilities. This review explores the innovative integration of surfactants into various adsorbent matrices for the removal of common dyes, such as methylene blue, malachite green, rhodamine B, congo red, and methyl orange. By focusing on the interactions between surfactant-modified adsorbents and dye molecules, we provide insights into the mechanisms that enhance the adsorption efficiency. We also address the influence of competing ions and salts typically found in wastewater, emphasizing their role in shaping adsorption dynamics. Furthermore, we discuss critical factors affecting the regeneration and reusability of these materials, highlighting their potential for industrial applications. Unlike previous reviews that primarily focused on either adsorbent-dye or surfactant–dye interactions, this Review emphasizes the synergistic integration of surfactants within adsorbent matrices. By exploring the interactions of surfactant-assisted modified adsorbents and dye molecules, this review aims to provide valuable insights into the development of advanced and cost-effective materials for enhanced dye removal.

Ionic liquids (ILs) have proven to be a potential medium for the extraction and separation of essential oils (EOs) from the most varied sources. This review presents a summary of the primary outcomes obtained through the application of ionic liquid-based processes for the extraction and separation of different constituents of EOs (such as terpenes, ketones, phenols, oxides, esters, aldehydes, and alcohols). ILs have been examined as solvents, co-solvents, adjuvants, electrolytes, and cosurfactants, and they have been utilized in the synthesis of IL-supported materials for separation. In addition, the application of hybrid solvents, including deep eutectic solvents (DESs), further broadens the applicability of ILs to particular EO components. A key feature of ILs is their adaptable selectivity at the molecular level. Interactions such as hydrogen bonding, e.g., imidazolium-based ILs with hydroxyl groups of phenolic compounds, π–π stacking between aromatic cations and terpene backbones, and electrostatic or hydrophobic effects that control the solubilization and dissociation of esters and aldehydes enable ILs to achieve better resolution than conventional solvents. These interactions provide a higher extraction efficiency and better purity of the target compounds. Herein, IL-based solid–liquid green extraction techniques are reviewed and compared in terms of their extraction and separation capabilities. Modern trends, including computational methods, machine learning (ML) optimization, and advanced algorithms for process optimization techniques, are used to improve results, which are often used for single-parameter modifications, such as optimizing solvent ratios or extraction conditions. These examples show that ML can help improve IL-based extraction in practice, but complete end-to-end design systems are still in the future. Combining ML with multi-scale modeling and robotic testing for automated, iterative optimization is probably necessary to realize such dramatic potential. The environmental impact of ILs is also reviewed in terms of toxicity and biodegradability, along with reuse, recovery, and purification processes. The major achievements and future challenges in this discipline are addressed, with a specific focus on the primary loopholes encountered within the IL community devoted to the separation processes, and some measures are proposed to overcome the existing limitations.

In the agricultural field, pesticides are used tremendously to shield our crops from insects, weeds, and diseases. Only a small percentage of pesticides employed reach their intended target, and the remainder passes through the soil, contaminating ground and surface-water supplies, damaging the crop fields, and ultimately harming the crop, including humans and other creatures. Alternative approaches for pesticide measurement have recently received a lot of attention, thanks to the growing interest in the on-site detection of analytes using electrochemical techniques that can replace standard chromatographic procedures. Among all organochlorine pesticides such as gamma-lindane are hazardous, toxic, and omnipresent contaminants in the environment. Here, in this review, we summarize the different ways of the gamma-lindane detection, performing the electrochemical techniques viz cyclic, differential, square wave voltammetry, and amperometry using various bare and surface-modified glassy carbon and pencil carbon electrodes. The analytical performances are reported as the limit of detection 18.8 nM (GCE–AONP–PANI–SWCNT), 37,000 nM (GCE), 38.1 nM (Bare HBPE), 21.3 nM (Nyl-MHBPE); percentage recovery is 103%.

Neurotransmitters (NTs) with hydroxyl groups can now be identified electrochemically, utilizing a variety of electrodes and voltammetric techniques. In particular, in monoamine, the position of the hydroxyl groups might alter the sensing properties of a certain neurotransmitter. Numerous research studies using electrodes modified on their surfaces to better detect specific neurotransmitters when other interfering factors are present are reviewed to improve the precision of these measures. An investigation of the monoamine neurotransmitters at nanoscale using electrochemical methods is the primary goal of this review article. It will be used to determine which sort of electrode is ideal for this purpose. The use of carbon materials, such as graphite carbon fiber, carbon fiber micro-electrodes, glassy carbon, and 3D printed electrodes are only some of the electrodes with surface modifications that can be utilized for this purpose. Electrochemical methods for real-time detection and quantification of monoamine neurotransmitters in real samples at the nanomolar level are summarized in this paper.