Syntheses, Characterization, and Antibacterial Evaluation of P. grandiflora Extracts Conjugated with Gold Nanoparticles

Background. With the recent increase in antibiotic resistance to conventional antibiotics, gold nanoparticles, and medicinal plants, extracts present an interesting alternative. Objectives. This study aimed to synthesize, characterize, and evaluate Pyrenacantha grandiflora Baill extracts and gold nanoparticle conjugates against pathogenic bacteria. Methods. We synthesized gold nanoparticles by chemical and biological methods. The nanoparticles were characterized by the use of UV-visible spectrophotometry, followed by transmission electron microscopy (TEM) and energy-dispersive X-ray analysis (EDX). Gold nanoparticles were conjugated to plant extracts and analyzed with a Fourier-transform infrared spectroscope (FTIR). We determined the antimicrobial activity of the conjugates using well diffusion and the microdilution assays. Results. The UV–visible spectra of gold nanoparticles showed a synthesis peak at 530 nm. FTIR analysis indicated functional biomolecules that were associated with plant extract conjugated gold nanoparticles; the formation of C–H group and carbonyl (C=O) groups, –OH carbonyl, and C≡C groups were also observed. Biologically synthesized nanoparticles were star-shaped when observed by TEM with an average size of 11 nm. Gold nanoparticles synthesized with P. grandiflora water extracts showed the largest zone of inhibition (22 mm). When the gold nanoparticles synthesized by the biological method were conjugated with acetone extracts of P. grandiflora, MIC as low as 0.0063 mg/mL was observed against beta-lactamase producing K. pneumonia. The activity of acetone extracts was improved with chemically synthesized gold nanoparticles particularly when beta-lactamase producing E. coli and MRSA were used as test organisms. A synergistic effect was observed against all tested bacteria, except for MRSA when gold nanoparticles were conjugated with acetone extract. Conclusion. Overall, P. grandiflora tuber extracts conjugated with gold nanoparticles showed a very good antibacterial activity that improved both plant extract and gold nanoparticle’s individual activity.

Synthesis of Cobalt-Nickel Nanoparticles via a Liquid-Phase Reduction Process

Cobalt-nickel nanoparticles (Co-Ni-NPs) show promising electrochemical performance in oxygen and hydrogen evolution reactions (OER and HER) due to their physicochemical properties such as electronic configuration and great electrochemical stability. Therefore, developing new economically and environmentally friendly methods of synthesizing Co-Ni-NPs has become a practical requirement. Co-Ni-NPs were produced by employing the liquid-phase reduction method. Nickel and cobalt sulfate solutions in hydrazine monohydrate with various mixing ratios were used as raw materials. Nickel plays an important role in the nucleation process via increasing the reduction reaction rate throughout the formation of Co-Ni-NPs. Furthermore, the acceleration of the Co-Ni-NPs formation process may be attributed to the partial dissolution of Ni(OH)2 in the presence of N2H4 and/or citrate-anions and the formation of the Ni-N2H4 or Ni-Cit complexes in contrast to Co(OH)2.

Optimization, Characterization, and Antibacterial Activity of Copper Nanoparticles Synthesized Using Senna didymobotrya Root Extract

The economic burden and high mortality associated with multidrug-resistant bacteria is a major public health concern. Biosynthesized copper nanoparticles (CuNPs) could be a potential alternative to combat bacterial resistance to conventional medicine. This study for the first time aimed at optimizing the synthesis conditions (concentration of copper ions, temperature, and pH) to obtain the smallest size of CuNPs, characterizing and testing the antibacterial efficacy of CuNPs prepared from Senna didymobotrya (S. didymobotrya) roots. Extraction was done by the Soxhlet method using methanol as the solvent. Gas chromatography-mass spectrometry (GC-MS) analysis was performed to identify compounds in S. didymobotrya root extracts. Box–Behnken design was used to obtain optimal synthesis conditions as determined using a particle analyzer. Characterization was done using ultraviolet-visible (UV-Vis), particle size analyzer, X-ray diffraction, zeta potentiometer, and Fourier transform infrared (FT-IR). Bioassay was conducted using the Kirby–Bauer disk diffusion susceptibility test. The major compounds identified by GC-MS in reference to the NIST library were benzoic acid, thymol, N-benzyl-2-phenethylamine, benzaldehyde, vanillin, phenylacetic acid, and benzothiazole. UV-Vis spectrum showed a characteristic peak at 570 nm indicating the formation of CuNPs. The optimum synthesis conditions were temperature of 80°C, pH 3.0, and copper ion concentration of 0.0125 M. The FT-IR spectrum showed absorptions in the range 3500–3400 cm−1 (N-H stretch), 3400–2400 cm−1 (O-H stretch), and 988–830 cm−1 (C-H bend) and peak at 1612 cm−1 (C=C stretch), and 1271 cm−1 (C-O bend). Cu nanoparticle sizes were 5.55–63.60 nm. The zeta potential value was −69.4 mV indicating that they were stable. The biosynthesized nanoparticles exhibited significant antimicrobial activity on Escherichia coli and Staphylococcus aureus with the zone of inhibition diameters of 26.00 ± 0.58 mm and 30.00 ± 0.58 mm compared to amoxicillin clavulanate (standard) with inhibition diameters of 20 ± 0.58 mm and 28.00 ± 0.58 mm, respectively.

Green Synthesis, Characterization, and Evaluation of the Antimicrobial Activity of Camellia sinensis Silver Nanoparticles

An extremely worrying and alarming increase in the level of multiple drug resistance is reported in Sudan, in which bacterial strains are becoming resistant to many commonly available antibiotics. Eventually, it is becoming extremely difficult to treat debilitating infections. In search of promising solutions to this arising crisis, Camellia sinensis silver nanoparticles were synthesized using the green synthesis method. The synthesis of the Camellia sinensis silver nanoparticles is confirmed using analytical methods as ultraviolet-visible spectroscopy, X-ray diffractometer, and scanning electron microscopy. Using the ultraviolet-visible spectroscopy, an absorption band of 412 nm was observed. Furthermore, scanning electron microscopy revealed the presence of silver nanoparticles which fell within the range of 1–100 nm, and X-ray diffractometer analysis showed three intense peaks with a maximum intense peak at 24.3 theta. Nanoparticles distribution between 12 nm and 64 nm was observed with an average diameter of 18.115 nm. It also revealed orthorhombic-shaped nanoparticles. The synthesized nanoparticles showed antimicrobial activity against Staphylococcus aureus with a zone of inhibition of 7 mm, but none was detected against Escherichia coli. The obtained physicochemical properties were correlated with the antibacterial activity of the silver nanoparticles.

Multipeak Emissions and Electrical Properties of ZnO/Si Heterojunctions Based on ZnO Nanoflakes by Spin Coating Technique

ZnO/Si heterojunctions have been fabricated by spinning ZnO nanoflakes on the p-type single crystal silicon by using the spin coating technique. Photoluminescence spectra of as-grown and annealed ZnO/Si heterojunctions have been recorded under the excitation of 336 nm. Multipeaks between ∼360 nm and ∼430 nm from annealed ZnO/Si heterojunctions have been analyzed, the origins of which have been ascribed to the effects of one or multiple LO phonons. The rectifying effects can be observed from the prototypical devices based on ZnO/Si heterojunctions. Although the parameters obtained by analyzing the current density-voltage characteristics are away from those from the ideal device, it is believed that ZnO/Si heterojunctions in the present work will be a potential candidate in the optoelectronic field through modulating and optimizing the fabrication conditions.

Synthesis of Gold Nanoparticles Using Tannin-Rich Extract and Coating onto Cotton Textiles for Catalytic Degradation of Congo Red

Gold nanoparticles (AuNPs) were synthesized under ambient conditions from chloroauric acid in aqueous solution at pH 4. Tannin-rich extract from Xylocarpus granatum bark was used as both reducing and capping agent, rapidly converting Au (I) salt to AuNPs. Transmission electron microscopy showed the as-prepared AuNPs to be predominantly spherical, with an average diameter of 17 nm. The AuNPs were tested for catalytic reduction of Congo red (CR), a carcinogenic azo dye, in aqueous sodium borohydride solution. Cotton samples were coated with the AuNPs, taking on a reddish-purple color. The samples showed significantly reduced tearing strength after coating, though tensile strength was unaffected. UV-visible spectroscopy was used to determine the dye concentration in the water. CR degradation was observed only when AuNPs were present, and the efficiency of degradation was strongly linked to the AuNP loading. The AuNP-coated fabrics left only a 4.7% CR concentration in the solution after 24 h and therefore promise as a heterogeneous catalyst for degradation of CR in aqueous solution.

Adsorptive Removal of Cd(II) Ions from Wastewater Using Maleic Anhydride Nanocellulose

In this study, both pristine cellulose nanocrystalline (CNC) and maleic anhydride functionalized cellulose nanocrystalline (MA-CNC) were prepared from the stems of Eichhornia crassipes weed by the sulfuric acid hydrolysis method. The as-prepared adsorbents were characterized by using X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and Brunauer–Emmett–Teller (BET) instruments. These materials were applied for the removal of Cd(II) ions from WW. The uptake mechanism was fixed to both Langmuir and Freundlich adsorption isotherms with a maximum Cd(II) ion uptake capability (qmax) of 75.76 and 215.52 mg g−1 by CNC and MA-CNC adsorbents, respectively. Pseudo-second-order (PSO) kinetic model was well fitted to the uptake process. The adsorbent regeneration study was done after desorption of Cd(II) ions from the adsorbent by HCl washing. Results exhibited that the adsorbent was reused for the removal of Cd(II) ions from real WW after successive 13th cycle.

Low-Temperature Synthesis of Vanadium Dioxide Thin Films by Sol-Gel Dip Coating Method

The vanadium dioxide (VO2) thin films were synthesized by sol-gel dipping on a glass slide substrate at low temperature of 500°C in a vacuum tube furnace at a pressure of 2 × 10−3 mbar by 2-step calcination without an intermediate gas purging. Synthesis conditions, including temperature, vacuum pressure, and calcination steps in the vacuum tube furnace, were investigated to find the optimum condition that promoted the formation of VO2 phase. It was found that the 2nd calcination step was very important in realizing the monoclinic vanadium dioxide (VO2 (M)). The results of the valence electron analysis revealed the outstanding phase of VO2 and a small amount of V2O5 and V2O3 phases. The small crystallites of the VO2 were homogeneously distributed on the surface, and the grain was of an irregular shape of ∼220−380 nm in size. The film’s thickness was in a range of 69−74 nm. The film exhibited a metal-to-insulator transformation temperature of ∼68oC and good thermochromic property. Visible optical transmittance remained at ∼40−50% when the sample’s temperature changed from 25 to 80°C for a near infrared (NIR) region.

Green Synthesis of Silver Nanoparticles Using Catharanthus roseus Flower Extracts and the Determination of Their Antioxidant, Antimicrobial, and Photocatalytic Activity

The present study describes the antioxidant, antimicrobial, and photocatalytic activity of silver nanoparticles (AGNPs) synthesized using six varieties of Catharanthus roseus flower extracts for the first time. Initially, the synthesized AgNPs were visually confirmed by color change. Further, the formation, size, and shape of the synthesized AgNPs were characterized by UV-Vis spectroscopy and scanning electron microscopy (SEM). The SEM image of purple flower AgNPs and the calculated bandgap energies of the synthesized AgNPs showed that the synthesized AgNPs were in the range of 0–30 nm. Qualitative phytochemical analysis revealed the presence of the phytocompounds that were responsible for the capping, formation, bioreduction, and stabilization of AgNPs. The antioxidant ability of the AgNPs and their respective flower extracts were analyzed using TFC, TPC, TAC, DPPH, FRAP, and IC50 assays. The results of the antioxidant assays indicated that the AgNPs showed higher antioxidant activity compared to their respective flower extracts. The synthesized AgNPs showed significant antimicrobial activity against Gram-negative Escherichia coli compared to Gram-positive Staphylococcus aureus assayed using the agar well diffusion method. Furthermore, the photocatalytic activity of the synthesized purple flower AgNPs at two different concentrations 5000 ppm and 333 ppm was analyzed by the removal of methyl orange dye from an aqueous solution under sunlight irradiation in the presence of NaBH4 catalyst. Results indicated that 333 ppm purple flower AgNPs exhibited an efficient photocatalytic activity in the degradation of methyl orange compared to 5000 ppm purple flower AgNPs in 20 minutes. Thus, the results obtained indicated that Catharanthus roseus is an ecofriendly source for the green synthesis of AgNPs which can be used as a novel antioxidant, antimicrobial, and photocatalytic agent; thereby, it can be used in a variety of applications to improve the quality of human life.

Factors Determining the Removal Efficiency of Procion MX in Waters Using Titanate Nanotubes Catalyzed by UV Irradiation

The treatment of wastewater from the textile industry containing organic dyes faces many challenges since these compounds resist the biodegradation process in conventional treatment units. Among the physicochemical processes, photocatalysis is considered a facile, cheap, and environmental-friendly technology for treating persistent organic pollutants in waters at low concentrations. This study investigated several physicochemical factors determining the photocatalytic activity of titanate nanotubes (TNTs) to remove Procion MX 032 (PMX), an azo dye, in waters. Degradation of PMX by photocatalytic oxidation process at room temperature (30°C) was set up with the UV irradiation in the presence of different types of photocatalyst such as ST-01 (100% anatase), industrial TiO2, TNTs calcined at 120°C and 500°C. Effect of reaction time, catalyst amount, pH, light wavelength and intensity, and oxidants was investigated. Consequently, TNTs calcined at 500°C provided the highest removal efficiency. The photocatalytic oxidation of PMX by TNT calcined at 500°C was affected by pH variation, getting the highest removal at pH of 8, and inhibited with the presence of H2O2 and O2. Particularly, the PMX degradation using titanate nanotubes was optimized under the UV-A intensity of 100 W/m2. The dye was degraded by more than 95% at the TNTs concentration of 75 mg/L and pH 8.0 after 90 min. The results suggest that photocatalysis using TNTs can be a simple but efficient treatment method to remove PMX and potentially be applied for the treatment of wastewaters containing dyes.