In this work, new results concerning the potential of mixtures based on nitrogen doped titanium dioxide (TiO₂:N) and carbon nanotubes (CNTs) as possible catalyst candidates for the rhodamine B (RhB) UV photodegradation are reported. The RhB photodegradation was evaluated by UV–VIS absorption spectroscopy using samples of TiO₂:N and CNTs of the type of single-walled carbon nanotubes (SWNTs), double-wall carbon nanotubes (DWNTs), multi-wall carbon nanotubes (MWNTs), and single-walled carbon nanotubes functionalized with carboxyl groups (SWNT-COOH) having various concentrations of CNTs. The best photocatalytic performance was obtained for sample containing TiO₂:N and 2.5 wt.% SWNTs-COOH, when approx. 85% of dye removal was achieved after 300 min. of UV irradiation. The reaction kinetics of RhB aqueous solutions containing TiO₂:N/CNT mixtures followed a complex first-order kinetic model. The TiO₂:N/CNTs catalyst induced higher photodegradation efficiency of RhB than TiO₂:N due to the presence of CNTs, which act as adsorbent and dispersing agent and capture the photogenerated electrons of TiO₂:N hindering the electron–hole recombination.

In this work, new evidence for the photodegradation reactions of acetaminophen (AC) is reported by photoluminescence (PL), Raman scattering and FTIR spectroscopy. Under excitation wavelength of 320 nm, AC shows a PL band in the spectral range of 340–550 nm, whose intensity decreases by exposure to UV light. The chemical interaction of AC with the NaOH solutions, having the concentration ranging between 0.001 and 0.3 M, induces a gradual enhancement of the photoluminescence excitation (PLE) and PL spectra, when the exposure time of samples at the UV light increases until 140 min, as a result of the formation of p-aminophenol and sodium acetate. This behavior is not influenced by the excipients or other active compounds in pharmaceutical products as demonstrated by PLE and PL studies. Experimental arguments for the obtaining of p-aminophenol and sodium acetate, when AC has interacted with NaOH, are shown by Raman scattering and FTIR spectroscopy.

Nanocomposites based on Fe₃O₄ and carbonaceous nanoparticles (CNPs), including carbon nanotubes (CNTs) and graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)), such as Fe₃O₄@GO, Fe₃O₄@RGO, and Fe₃O₄@CNT, have demonstrated considerable potential in a number of health applications, including tissue regeneration and innovative cancer treatments such as hyperthermia (HT). This is due to their ability to transport drugs and generate localized heat under the influence of an alternating magnetic field on Fe₃O₄. Despite the promising potential of CNTs and graphene derivatives as drug delivery systems, their use in biological applications is hindered by challenges related to dispersion in physiological media and particle agglomeration. Hence, a solid foundation has been established for the integration of various synthesis techniques for these nanocomposites, with the wet co-precipitation method being the most prevalent. Moreover, the dimensions and morphology of the composite nanoparticles are directly correlated with the value of magnetic saturation, thus influencing the efficiency of the composite in drug delivery and other significant biomedical applications. The current demand for this type of material is related to the loading of a larger quantity of drugs within the hybrid structure of the carrier, with the objective of releasing this amount into the tumor cells. A second demand refers to the biocompatibility of the drug carrier and its capacity to permeate cell membranes, as well as the processes occurring within the drug carriers. The main objective of this paper is to review the synthesis methods used to prepare hybrids based on Fe₃O₄ and CNPs, such as GO, RGO, and CNTs, and to examinate their role in the formation of hybrid nanoparticles and the correlation between their morphology, the dimensions, and optical/magnetic properties.

In this work, the effect of the single-walled carbon nanotubes (SWNTs) as the mixtures of metallic and semiconducting tubes (M + S-SWNTs) as well as highly separated semiconducting (S-SWNTs) and metallic (M-SWNTs) tubes on the photoluminescence (PL) of poly(3-hexyl thiophene) (P3HT) was reported. Two methods were used to prepare such composites, that is, the chemical interaction of the two constituents and the electrochemical polymerization of the 3-hexyl thiophene onto the rough Au supports modified with carbon nanotubes (CNTs). The measurements of the anisotropic PL of these composites have highlighted a significant diminution of the angle of the binding of the P3HT films electrochemical synthetized onto Au electrodes covered with M + S-SWNTs. This change was attributed to metallic tubes, as was demonstrated using the anisotropic PL measurements carried out on the P3HT/M-SWNTs and P3HT/S-SWNTs composites. Small variations in the angle of the binding were reported in the case of the composites prepared by chemical interaction of the two constituents. The proposed mechanism to explain this behavior took into account the functionalization process of CNTs with P3HT. The experimental arguments of the functionalization process of CNTs with P3HT were shown by the UV-VIS-NIR and FTIR spectroscopy as well as surface-enhanced Raman scattering (SERS). A PL quenching process of P3HT induced both in the presence of S-SWNTs and M-SWNTs was reported, too. This process origins in the various de-excitation pathways which can be developed considering the energy levels diagram of the two constituents of each studied composite.

In this work, three methods for the synthesis of composites based on poly(ortho-toluidine) (POT) and WS₂ are reported: (a) the solid-state interaction (SSI) of POT with WS₂ nanoparticles (NPs); (b) the in situ chemical polymerization (ICP) of ortho-toluidine (OT); and (c) the electrochemical polymerization (ECP) of OT. The preparation of WS₂ sheets was performed by the ball milling of the WS₂ NPs followed by ultrasonication in the solvent N,N’-dimethyl formamide. During the synthesis of the POT/WS₂ composites by SSI and ICP, an additional exfoliation of the WS₂ NPs was reported. In this work, we demonstrated the following: (a) the ICP method leads to POT/WS₂ composites, which contain repeating units of POT in the leucoemeraldine salt (LS) state, while (b) the ECP method leads to POT/WS₂ composites, which contain repeating units of POT in the emeraldine salt (ES) state. Capacitances equal to 123.5, 465.76, and 751.6 mF cm⁻² in the cases of POT-ES/WS₂ composites, synthesized by SSI, ICP, and ECP, respectively, were reported.

Diamond traceability has been a major challenge for the gemological industry in recent decades. In this context, this paper presents new studies using UV-VIS-NIR spectroscopy to identify the traceability and geographical origin of diamonds. The aim of the work is to identify characteristic centers of fancy-color diamonds collected from Cullinan Mine, Democratic Republic of Congo (DRC), and the geographical regions with unknown origin. Depending on the origin of the diamonds, the UV-VIS-NIR spectra can be differentiated as follows: (i) the diamonds collected from Cullinan Mine show absorption bands assigned to N₁⁰, NV⁰, NV⁻, N₃V⁰, N₄V₂, and N₄V centers, which are accompanied by a vibronic structure localized between 415 and 394 nm (2.987–3.147 eV) and (ii) the diamonds from DRC show absorption bands attributed to N₁⁰, NV⁻, N₃V⁰, N₁⁺, and NVH centers. Using Raman spectroscopy, nitrogen concentration values of diamonds collected from the Cullinan mines and DRC between 41 and 185 ppm and 204–336 ppm, respectively, were reported. We prove that the simultaneous applicability of UV-VIS-NIR spectroscopy and Raman scattering as comparative tools for assessing diamond provenance can be a valuable strategy for an initial attribution of diamonds with unknown geographical origin, knowing the optical features of diamonds collected from Cullinan Mine and DRC.