Preparation and characterization of hybrid polypyrrole nanoparticles as a conducting polymer with controllable size.

Hybrid polypyrrole (PPy) nanoparticles were prepared using a low-temperature oxidative polymerization process in an acidic solution with polyethyleneimine (PEI) as a template and amine source. The results showed that the nanoparticles have an amorphous structure in the X-ray diffractogram and exhibited good dispersibility in water, uniform size, and a specific conductivity ranging from 0.1 to 6.9 S/cm. The particle size could be tuned from 85 to 300 nm by varying the reactant concentration. Undoping the samples with sodium hydroxide (NaOH) solution altered the optical absorption properties and surface roughness of the particles. However, it did not affect the particle size. The nanoparticles also exhibited optical sensing properties based on their UV-vis absorption changes with the pH. Moreover, nanoparticles could have potential applications in gene delivery and bio-adsorption for contaminant removal. This work demonstrates a simple and effective method for preparing hybrid polypyrrole nanoparticles with controllable size, dispersibility, and conductivity for various nanotechnology, biotechnology, and environmental engineering purposes.

UV-shielding properties of a cost-effective hybrid PMMA-based thin film coatings using TiO2 and ZnO nanoparticles: a comprehensive evaluation.

This study aimed to assess the UV-shielding features of the PMMA-based thin film coatings with the addition of TiO2 and ZnO nanoparticles as nanofillers considering different contents. Furthermore, the effect of TiO2/ZnO nanohybrids at different ratios and concentrations was examined. The XRD, FTIR, SEM, and EDX analyses characterized the prepared films' functional groups, structure, and morphology. Meanwhile, the coatings' optical properties and UV-protecting capability were investigated by ultraviolet-visible (UV-Vis) spectroscopy. The UV-Vis spectroscopic study revealed that as the concentration of nanoparticles increased in the hybrid-coated PMMA, the absorption in the UVA region increased. Overall, it can be concluded that the optimal coatings for PMMA were 0.1 wt% TiO2, 0.1 wt% ZnO, and 0.025:0.025 wt% TiO2: ZnO nanohybrid. Considering the acquired FT-IR of PMMA with different content of nanoparticles before and after exposure to the UV irradiation, for some films, it was confirmed that the polymer-based thin films degraded after 720 h, with either decreasing or increasing intensity of the degraded polymer, peak shifting, and band broadening. Notably, the FTIR results were in good agreement with UV-Vis outcomes. In addition, XRD diffraction peaks demonstrated that the pure PMMA matrix and PMMA coating films did not show any characteristic peaks indicating the presence of nanoparticles. All diffraction patterns were similar with and without any nanoparticles. Therefore, it depicted the amorphous nature of polymer thin film.

The catalytic performance of CuFe2O4@CQD nanocomposite as a high-perform heterogeneous nanocatalyst in nitroaniline group reduction.

In this study, we fabricated an economical, non-toxic, and convenient magnetic nanocomposite of CuFe2O4 nanoparticles (NPs)/carbon quantum dots (CQDs) of citric acid via the co-precipitation method. Afterward, obtained magnetic nanocomposite was used as a nanocatalyst to reduce the ortho-nitroaniline (o-NA) and para-nitroaniline (p-NA) using a reducer agent of sodium borohydride (NaBH4). To investigate the functional groups, crystallite, structure, morphology, and nanoparticle size of the prepared nanocomposite, FT-IR, XRD, TEM, BET, and SEM were employed. The catalytic performance of the nanocatalyst was experimentally evaluated based on the ultraviolet-visible absorbance to assess the reduction of o-NA and p-NA. The acquired outcomes illustrated that the prepared heterogeneous catalyst significantly enhanced the reduction of o-NA and p-NA substrates. The analysis of the absorption showed a remarkable decrease for ortho-NA and para-NA at λmax = 415 nm in 27 s and λmax = 380 nm in 8 s, respectively. The constant rate (kapp) of ortho-NA and para-NA at the stated λmax was 8.39 × 10-2 s-1 and 5.48 × 10-1 s-1. The most highlighted result of this work was that the CuFe2O4@CQD nanocomposite fabricated from citric acid performed better than absolute CuFe2O4 NPs, since nanocomposite containing CQDs had a more significant impact than copper ferrite NPs.

The Catalytic Reduction of Nitroanilines Using Synthesized CuFe2 O4 Nanoparticles in an Aqueous Medium.

The primary objective of this research is to investigate the reduction of 4-nitroaniline (4-NA) and 2-nitroaniline (2-NA) using synthesized copper ferrite nanoparticles (NPs) via facile one-step hydrothermal method as a heterogeneous nano-catalyst. Nitroanilines were reduced in the presence and without the catalyst with a constant amount (100 mg) of reducing agent of sodium borohydride (NaBH4 ) at room temperature in water to amino compounds. To characterize the functional groups, size, structure, and morphology of as-prepared magnetic NPs, FTIR, XRD, SEM, and TEM were employed. The UV-Vis spectrum was utilized to explore the catalytic effect of CuFe2 O4 . The outcomes revealed that the synthesized CuFe2 O4 as a heterogeneous magnetic nano-catalyst catalyzed the reduction of 4-NA and 2-NA significantly faster than other candidate catalysts. The outcomes demonstrated that the catalyst catalyzed 4-nitroaniline to para-phenylenediamine (p-PDA) and 2-nitroaniline to ortho-phenylenediamine (o-PDA) with a constant rate of 7.49×10-2  s-1 and 3.19×10-2  s-1 , and conversion percentage of 96.5 and 95.6, in 40 s and 90 s, sequentially. Furthermore, the nanoparticles could be recovered by a magnetic separation method and reused for six consecutive cycles without remarkable loss of catalytic ability.