In this review, a 5-year overview on environmentally friendly approaches for the extraction of the most relevant organic pollutants in soil, sediment, particulate matter, and sewage sludge coupled with chromatographic analysis is reported. Organic contaminants encompass various compounds derived from personal care products, industrial chemicals, microplastics, organic matter combustion, agricultural practices, and plasticizer material. The principles of green analytical chemistry (GAC) and green sample preparation (GSP) serve as a guideline for the development of more environmentally sustainable analytical protocols. This study focuses attention on microwave-assisted extraction (MAE), ultrasound-assisted extraction (UAE), matrix solid-phase dispersion (MSPD), and microextraction techniques, such as solid-phase microextraction (SPME), stir bar sorptive extraction (SBSE), hollow-fiber liquid-phase microextraction (HF-LPME), spray-assisted droplet formation-based liquid-phase microextraction (SADF-LPME), and dispersive liquid–liquid extraction (DLLME). These approaches represent the most relevant eco-friendly sample preparation for the advanced extraction of target analytes from environmental solid samples.

The recovery of lithium from extracts obtained from a black mass of spent lithium-ion batteries treated with a ternary solvent system at acidic pH was investigated using flat-sheet nanofiltration (NF) membranes operated according to a dead-end configuration. Specifically, four samples obtained at different pH values (2.5 and 5) and extraction times (48, 96 and 168 h) were treated in selected operating conditions by using two commercial polymeric membranes (denoted DK and HL, with an approximate molecular weight cut-off of 150–300 Da) up to a volume reduction factor (VRF) of 4. Membrane performance was assessed in terms of productivity and selectivity towards specific ions, including lithium. For most treated samples, the HL membrane exhibited higher permeate fluxes in comparison to the DK membrane. However, the DK membrane performed better in terms of lithium rejection than the HL membrane, with a negative rejection at VRF 4 observed for all treated samples. More than 90% of multivalent ions were rejected by both membranes independently of the VRF. The membrane ability to retain multivalent ions led to their progressive concentration in the retentate as the VRF increased. The extraction time did not impact the NF performance of both membranes in terms of ion rejection. For the DK membrane conditions of extraction of 96 h and pH 5 represented the best trade-off between flux, ion rejection, and total lithium recovery.

Cosmetic products contain numerous metals used as pigments, UV filters, preservatives, antiperspirants and antimicrobial agents, which are responsible for allergic skin reactions, with the most common being nickel. To reduce skin penetration of Ni, innovative pharmaceutical formulations such as lipogels with chelating action against the metal ions themselves can be used. Chelation therapy allows a chelating agent to combine with metal ions to form a stable ring structure called a chelate. The chelate structure is more soluble in water than the toxic metal, which facilitates removal of the toxic metal from the tissue and its excretion by the kidneys. The aim of the following work was to evaluate the chelating properties against nickel ions of different types of lipogels containing flavonoids such as resveratrol and epigallocatechin gallate with chelating activities largely dependent on the number and position of their hydroxyl groups. The results obtained showed that lipogels based on epigallocatechin gallate show high chelating action against nickel, especially at low concentrations. In addition, rheological studies showed an ideal profile to ensure viscoelasticity and swelling of the lipogel within 48 h, confirming reports of 75% epigallocatechin release from the lipogel after 48 h. Tests have shown that lipogels based on epigallocatechin gallate have high chelating action against nickel, especially at low concentrations.