In recent years, the anti-corrosive properties of natural extracts as environmentally friendly inhibitors have gained considerable interest. This study evaluates the potential of Marjoram (Origanum majorana L.) essential oil (OML), collected from Salé, Morocco, as a corrosion inhibitor for mild steel in 1 M HCl medium. The protection performance of OML was assessed using various electrochemical techniques, including potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS), as well as the weight loss method. The influence of OML concentration and temperature on the inhibition performance were investigated. OML demonstrated pronounced inhibitory benefits via increasing the corrosion resistance of mild steel in the corrosive HCl solution, thus reducing the corrosion rate to 0.11 mg cm⁻² h⁻¹ and increasing the inhibition efficiency to 87.1% at an inhibitor concentration of 500 ppm. PDP confirmed that the inhibitor works as a mixed-type inhibitor with cathodic supremacy. EIS revealed that the charge transfer mechanism is the main controlling factor for the corrosion process. The thermodynamic parameters suggested a key role of OML physisorption in inhibition, following the Langmuir isotherm. Importantly, SEM and EDX analyses suggested the formation of a protective layer of the extract onto the steel surface, which shields the surface from corrosive species. This is owed to the functional group-rich phytochemicals of OML. Therefore, the development of bio-based corrosion inhibitors is not only a step towards more eco-friendly industrial practices, but also meets the growing demand for sustainable materials in a world with constrained resources.

Phytochemical-rich natural extracts have recently attracted intense attention as green corrosion inhibitors and costly benign coating components for the protection of metallic structures of immense commercial importance. Herein, various methods were applied to assess the corrosion protection efficiency of a methanolic extract of parsley (Petroselinum crispum) (PCE) on carbon steel C37 in 1 M HCl. Initially, the chemical profile of PCE was analyzed using gas chromatography/mass spectrometry (GC/MS), and myristicin and apiol were identified as the main components. The results from the weight loss, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP) techniques revealed a substantial reduction in the corrosion rate upon the use of PCE, with a maximum inhibition efficiency of 92% at 1 g L⁻¹ PCE. To optimize the performance, the corrosion behavior was investigated over a temperature range of 303–333 K and for concentrations of 0.1–1 g L⁻¹. The inhibition effectiveness increased at higher concentrations of PCE, whilst it decreased when the temperature was elevated. The query suggests that the adsorption process involves both physical and chemical mechanisms. The adsorption of PCE onto C37 was well described by the Langmuir adsorption isotherm. The data were used to determine the activation energy and thermodynamic parameters. The PCE coating acted as a mixed-type inhibitor, hampering both cathodic and anodic corrosion reactions. SEM further confirmed the formation of a protective coating film on the steel surface when exposed to PCE. UV-Vis and XRD were implemented to understand the inhibition mechanism and formed products at the microscopic and spectroscopic levels. Hence, the green PCE inhibitor may potentially be applied in corrosion mitigation due to its high corrosion protection efficacy and its environmentally benign nature.

This study investigates, in the first part, the synthesis and purification of a poorly crystalline hydroxyapatite (HAp) using natural Moroccan phosphate (Boucraa region) as a raw material. Despite its successful preparation, the obtained HAp was contaminated by several metallic cations (mostly Cd, Pb, Sn, Ti, Mn, Mg, Fe, and Al) migrated from the natural rocks during the digestion process, inhibiting HAp application in several sectors. To minimize the existence of these elements, the dissolution–precipitation technique (DP) was investigated as a non-selective purification process. Following the initial DP cycle conducted on the precipitated HAp, the removal efficiency was approximately 60% for Al, Fe, Mg, Mn, and Ti and 90% for Cd and Pb. After three consecutive DP cycles, notable improvement in the removal efficiency was observed, reaching 66% for Fe, 69% for Mg, 73% for Mn, and 74% for Al, while Cd, Pb, and Ti were totally removed. In the second part of this study, the purified HAp was digested using sulfuric acid to produce high-quality phosphoric acid (PA) and gypsum (GP). The elemental analysis of the PA indicates a removal efficiency of approximately 89% for Fe and over 94% for all the examined cations. In addition, the generated GP was dominated by SO₃ and CaO accompanied with minor impurities. Overall, this simple process proves to be practically useful, to reduce a broad spectrum of cationic impurities, and to be flexible to prepare valuable products such hydroxyapatite, phosphoric acid, and gypsum.

Cadmium (Cd) is a toxic heavy metal that disrupts spermatogenesis and steroidogenesis due to its long half-life. This study evaluated the impact of recovery alone or with zinc (Zn) supplementation on Cd-induced testicular toxicity. A total of 42 pubertal male Wistar rats were divided into seven groups of six rats each. The control group (1) received NaCl (0.9%). Groups 2, 3, and 4 were treated with Cd 10 μg/kg/d by intraperitoneal injection for 1, 2, and 3 months respectively. Group 5 received Cd for 3 months with a recovery period of 1 month; Group 6 was exposed to Cd for 3 months, followed by a 1-month recovery period combined with Zn supplementation. (0.5 mg/kg/d). The last group was treated with zinc at a dose of 0.5 mg/kg/day for one month. The results showed decreased body weight, testicular and epididymal weight, testicular dimensions, and sperm parameters, along with Cd accumulation in the testes. Cd caused testicular damage and reduced serum testosterone levels, with more pronounced effects in the 3-month treatment group. Recovery alone did not significantly reverse Cd’s toxic effects, whereas Zn supplementation mitigated most of the damage. Recovery combined with Zn supplementation was more effective in correcting Cd-induced testicular toxicity than recovery alone.