Hybrid materials, with applications in fuchsine B color removal from wastewaters, were obtained by in situ incorporation of platinum nanoparticles and/or Pt-porphyrin derivatives into silica matrices. The inorganic silica matrices were synthesized by the sol-gel method, conducted in acid-base catalysis in two steps and further characterized by Nitrogen porosimetry, Small Angle Neutron Scattering (SANS), Scanning electron microscopy, Atomic force microscopy and UV-vis spectroscopy. All of the investigated silica hybrid materials were 100% efficient in removing fuchsine B if concentrations were lower than 1 × 10⁻⁵ M. For higher concentrations, the silica matrices containing platinum, either modified with Pt-metalloporphyrin or with platinum nanoparticles (PtNPs), are the most efficient materials for fuchsine B adsorption from wastewaters. It can be concluded that the presence of the platinum facilitates chemical interactions with the dye molecule through its amine functional groups. An excellent performance of 197.28 mg fuchsine B/g adsorbent material, in good agreement with the best values mentioned in literature, was achieved by PtNPs-silica material, capable of removing the dye from solutions of 5 × 10⁻⁴ M, even in still conditions.

Monitoring antibiotic retention in human body fluids after treatment and controlling heavy metal content in water are important requirements for a healthy society. Therefore, the approach proposed in this study is based on developing new optical sensors using porphyrin or its bifunctional hybrid materials made with AuNPs to accomplish the accurate detection of chloramphenicol and cobalt. To produce the new optical chloramphenicol sensors, 2,7,12,17-tetra-tert-butyl-5,10,15,20-tetraaza-21H,23H-porphine (TBAP) was used, both alone in an acid medium and as a hybrid material with AuNPs in a water–DMSO acidified environment. The same hybrid material in the unchanged water–DMSO medium was the sensing material used for Co²⁺ monitoring. The best results of the hybrid materials were explained by the synergistic effects between the TBAP azaporphyrin and AuNPs. Chloramphenicol was accurately detected in the range of concentrations between 3.58 × 10⁻⁶ M and 3.37 × 10⁻⁵ M, and the same hybrid material quantified Co²⁺ in the concentration range of 8.92 × 10⁻⁵ M–1.77 × 10⁻⁴ M. In addition, we proved that AuNPs can be used for the detection of azaporphyrin (from 2.66 × 10⁻⁵ M to 3.29 × 10⁻⁴ M), making them a useful tool to monitor porphyrin retention after cancer imaging procedures or in porphyria disease. In conclusion, we harnessed the multifunctionality of this azaporphyrin and of its newly obtained AuNP plasmonic hybrids to detect chloramphenicol and Co²⁺ quickly, simply, and with high precision.

A paramagnetic A₃B-type Mn(III)-porphyrin was synthesized and characterized by physical–chemical methods (UV-Vis, FT-IR, ¹H-NMR spectroscopy). The obtained compound was tested as a sensitive material for the spectrophotometric and potentiometric detection of iodine species. Using UV-Vis spectroscopy, the triiodide anions could be detected with high precision in the concentration interval of 1.02 × 10⁻⁵ to 2.3 × 10⁻⁵ M, with an LOD of 9.44 × 10⁻⁶ M. The PVC-based electrode using DOP as a plasticizer showed a sensitivity toward iodide in a wide concentration range of 1.0 × 10⁻⁵ to 1.0 × 10⁻¹ M, with an LOD of 8.0 × 10⁻⁶ M. Both methods are simple, low-cost, and efficient for the detection of iodine species in synthetic samples and pharmaceuticals.

Contamination of natural water sources with zinc ions poses serious ecological and health risks due to its toxicity and persistence. In this context, this study presents the preparation of new adsorbents based on acrylonitrile-divinylbenzene networks functionalized with aminophosphonate groups, selected for their strong chelating affinity towards Zn(II) ions. Both unmodified and functionalized materials were evaluated in adsorption experiments towards zinc ions. The adsorption capacity was evaluated as a function of the contact time and the initial zinc concentration. The functionalized adsorbents exhibited a significantly higher adsorption of zinc, attributed to the presence of aminophosphonate groups. In case of functionalisation with ethyl phosphonate group is achieved a maximum adsorption capacity of 101 mg/g. The equilibrium data followed the Langmuir isotherm, indicating monolayer adsorption, while the kinetic analysis followed the pseudo-second-order model, consistent with chemisorption. The optimal contact time was 60 min. Functionalized polymeric supports show strong potential for zinc ion removal, supporting their use in environmental remediation. Overall, the results demonstrate that aminophosphonate-functionalized polymers are highly effective adsorbents for the removal of zinc ions from contaminated waters.

The optical detection of thioacetamide was investigated using a metalated porphyrin, Mn(III)-5,10,15,20-tetrakis-(3,4-dimethoxyphenyl)-21H,23H-porphyrin chloride (Mn-3,4-diMeOPP), a gold colloid solution (AuNPs), and a complex formed between them (Mn-3,4-diMeOPP–AuNPs) in order to select the most sensitive material and to achieve complementarity between methods. Mn-3,4-diMeOPP, AuNPs, and their complex were synthesized and characterized by means of UV–Vis, FT-IR spectrometry, and AFM investigations. It could be concluded that Mn-3,4-diMeOPP could detect/quantify thioacetamide (TAA) in the range 3.13 × 10⁻⁸ M–7.67 × 10⁻⁷ M in a linear fashion, with a 99.85% confidence coefficient. The gold colloidal particles alone could detect TAA in an extremely narrow concentration domain of 2–9.8 × 10⁻⁷ M, slightly complementary with that of Mn-3,4-diMeOPP. The complex between Mn-3,4-diMeOPP and gold colloid proved to be able to quantify TAA in the trace domain with concentrations of 1.99 × 10⁻⁸ M–1.76 × 10⁻⁷ M in a polynomial fashion, with the method being more difficult. A potential mechanism for TAA detection based on Mn-3,4-diMeOPP is discussed based on computational modeling. The distorted porphyrin conformation and its electronic configuration favor the generation of a grid of electrostatic interactions between porphyrin and TAA.