Enzymatic Synthesis of Polyaniline/Graphite Oxide Nanocomposites

2012 ◽  
Vol 1448 ◽  
Author(s):  
C. Guerrero-Bermea ◽  
S. Sepulveda-Guzman ◽  
R. Cruz-Silva
Keyword(s):  
Graphite Oxide ◽  
Enzymatic Synthesis ◽  
Colloidal Stability ◽  
Aqueous Dispersion ◽  
Enzymatic Polymerization ◽  
Polymerization Reaction ◽  
As Doping ◽  
Fourier Transformed Infrared Spectroscopy ◽  
Vis Spectroscopy ◽  
Horseradish Peroxide

ABSTRACTIn this work, we prepared graphite oxide (GO)/polyaniline nanocomposites by enzymatic polymerization of aniline in an aqueous dispersion of graphite oxide. Two GO dispersions with sheets having an average lateral size of 12.50 μm and 247 nm were used. The enzymatic polymerization was carried out in aqueous acidic medium using toluenesulfonic acid (TSA) as doping agent, horseradish peroxide (HRP) as catalyst, and hydrogen peroxide as oxidizer. The polymerization reaction was studied using 1.0, 2.5 and 5 wt % of GO and nGO dispersions. No changes were observed in the catalytic activity of the peroxidase during the enzymatic synthesis due to the additionof GO sheets. Scanning electron microscopy images show that PANI colloids were attached on GO sheets. The PANI-GO colloids were characterized by ultraviolet–visible spectroscopy and Fourier transformed infrared spectroscopy, whereas their colloidal stability was evaluated at different pHs. The UV-vis spectroscopy study revealed that GO affects the electronic conjugation of PANI modifying its absorption spectrum.

Seed-mediated synthesis and PEG coating of gold nanoparticles for controlling morphology and sizes

MRS Advances ◽  
2020 ◽  
Vol 5 (63) ◽  
pp. 3353-3360
Author(s):  
Susana Helena Arellano Ramírez ◽  
Perla García Casillas ◽  
Christian Chapa González
Keyword(s):  
Gold Nanoparticles ◽  
Polyethylene Glycol ◽  
Room Temperature ◽  
Colloidal Stability ◽  
Infrared Spectrometry ◽  
Ammonium Bromide ◽  
Chloroauric Acid ◽  
Vis Spectroscopy ◽  
Seed Mediated ◽  
Peg Coating

AbstractA significant area of research is biomedical applications of nanoparticles which involves efforts to control the physicochemical properties through simple and scalable processes. Gold nanoparticles have received considerable attention due to their unique properties that they exhibit based on their morphology. Gold nanospheres (AuNSs) and nanorods (AuNRs) were prepared with a seed-mediated method followed of polyethylene glycol (PEG)-coating. The seeds were prepared with 0.1 M cetyltrimethyl-ammonium bromide (CTAB), 0.005 M chloroauric acid (HAuCl4), and 0.01 M sodium borohydride (NaBH4) solution. Gold nanoparticles with spherical morphology was achieved by growth by aggregation at room temperature, while to achieve the rod morphology 0.1 M silver nitrate (AgNO3) and 0.1 M ascorbic acid solution were added. The gold nanoparticles obtained by the seed-mediated synthesis have spherical or rod shapes, depending on the experimental conditions, and a uniform particle size. Surface functionalization was developed using polyethylene glycol. Morphology, and size distribution of AuNPs were evaluated by Field Emission Scanning Electron Microscopy. The average size of AuNSs, and AuNRs was 7.85nm and 7.96 x 31.47nm respectively. Fourier transform infrared spectrometry was performed to corroborate the presence of PEG in the AuNPs surface. Additionally, suspensions of AuNSs and AuNRs were evaluated by UV-Vis spectroscopy. Gold nanoparticles were stored for several days at room temperature and it was observed that the colloidal stability increased once gold nanoparticles were coated with PEG due to the shield formed in the surface of the NPs and the increase in size which were 9.65±1.90 nm of diameter for AuNSs and for AuNRs were 29.03±5.88 and 8.39±1.02 nm for length and transverse axis, respectively.

Study on Dispersion and Characterization of Functionalized MWCNTs Prepared by Wet Oxidation

2014 ◽  
Vol 661 ◽  
pp. 8-13 ◽  
Author(s):  
Intan Syaffinazzilla Zaine ◽  
N.A.M. Napiah ◽  
Azmi Mohamad Yusof ◽  
A.N. Alias ◽  
A.M.M. Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Relative Intensity ◽  
Colloidal Stability ◽  
Structural Defects ◽  
Wet Oxidation ◽  
Defect Level ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Functionalized Mwcnts

The MWCNTs was functionalized by refluxing commercial MWCNTs (a-MWCNTs) in concentrated HNO3/H2SO4 (3:1 v/v) at 100°C for 6 hours. The dispersion of a-MWCNTs and functionalized MWCNTs (f-MWCNTs) were observed after 1 hour sonication in ethanol. Both samples were characterized by UV-vis spectroscopy for dispersion behavior. The dried f-MWCNTs and a-MWCNTs were characterized by Raman spectroscopy to estimate the defect level. The morphology of the samples were analyzed by Transmission Electron Microscopy (TEM). The f-MWCNTs was well dispersed in ethanol within 2 weeks of observations period. The colloidal stability of a-MWCNTs was low as it was easily sediment after 24 hours. The UV-vis spectra of f-MWCNTs show maximum absorbance at 250 nm meanwhile no absorbance was observed for a-MWCNTs. Analysis from Raman spectrum shows that the f-MWCNTs have relative intensity of 1.101 which is higher than a-MWCNTs that have relative intensity of 0.935. The image from TEM revealed that the f-MWCNTs have structural defects and the absence of amorphous carbon on sidewall meanwhile the a-MWCNTs indicate otherwise.

scholarly journals Synthesis of L-DOPA Based Melanins with Reproducible Physic-Chemical Properties

2018 ◽  
Author(s):  
Koen Vercruysse ◽  
Jayla Moore
Keyword(s):  
Ir Spectroscopy ◽  
Enzymatic Synthesis ◽  
Chemical Properties ◽  
Size Exclusion ◽  
Synthesis Methods ◽  
Ongoing Research ◽  
Vis Spectroscopy ◽  
Exclusion Chromatography ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

This report expands our ongoing research efforts into the non-enzymatic synthesis of melanins. We have explored four different methods for the synthesis of L-DOPA based melanins and evaluated the reproducibility of some of their physic-chemical properties. The melanins were synthesized through the addition of NaOH, tyrosinate or Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Two different approaches for the reactions involving Fe<sup>2+</sup> and H<sub>2</sub>O<sub>2</sub> were tested: a) addition of H<sub>2</sub>O<sub>2</sub> spread out over multiple days or b) addition of H<sub>2</sub>O<sub>2</sub> in one fraction at the start of the reaction. The physic-chemical properties of the melanins explored involved: 1) retention on size exclusion chromatography column, 2) FT-IR spectroscopy, 3) UV-Vis spectroscopy and 4) the capacity to reduce a redox dye, dichlorophenolindophenol. Overall the results obtained indicated that 1) the various synthesis methods lead to melanins with reproducible physic-chemical properties, 2) that the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> are distinctly different from the melanins synthesized in the presence of NaOH or tyrosinate and 3) that no distinctly different melanins were generated when comparing the two different synthesis approaches involving Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Only the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> appeared to possess the capacity to reduce dichlorophenolindophenol.

Ampicillin-augmented silver nanoparticles for synergistic antimicrobial response: A promising therapeutic approach

2021 ◽  
Vol 22 ◽  
Author(s):  
Kashan Khan ◽  
Mohd Aamir Qureshi ◽  
Ameer Azam ◽  
Moinuddin ◽  
Javed Musarrat ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Silver Nanoparticles ◽  
Zeta Potential ◽  
Bacterial Infections ◽  
Colloidal Stability ◽  
Resistant Bacteria ◽  
Antimicrobial Drugs ◽  
Vis Spectroscopy ◽  
Microbial Infections ◽  
Ft Ir

Aims: Globally Scientists are working to find more efficient antimicrobial drugs to treat microbial infections and kill drug-resistant bacteria. Background: Despite the availability of numerous antimicrobial drugs bacterial infections still poses a serious threat to global health. Due to a constant decline in the effectiveness of antibiotics owing to their repeated exposure as well as shortlasting antimicrobial activity, led to the demand for developing novel therapeutic agents capable of controlling microbial infections. Objective: In this study, we report antimicrobial activity of chemically synthesized silver nanoparticles (cAgNPs) augmented with ampicillin (amp) in order to increase antimicrobial response against Escherichia coli (gram –ve), Staphylococcus aureus (gram +ve) and Streptococcus mutans (gram +ve). Methods: Nanostructure, colloidal stability, morphology and size of cAgNPs before and after functionalization were explored by UV-vis spectroscopy, FT-IR, zeta potential and TEM. The formation and functionalization of cAgNPs was confirmed from UV-vis spectroscopy and FT-IR patterns. From TEM the average sizes of cAgNPs and cAgNP-amp were found to be 13 and 7.8 nm respectively, and change in colloidal stability after augmentation was confirmed from zeta potential values. The antimicrobial efficacies of cAgNP-amp and cAgNPs against E. coli S. aureus and S. mutans were studied by determining minimum inhibitory concentrations (MICs), zone of inhibition, assessment of viable and non-viable bacterial cells and quantitative assessment of biofilm. Results & Discussion: Our results revealed cAgNP-amp to be highly bactericidal compared to cAgNPs or amp alone. The nano-toxicity studies indicated cAgNP-amp to be less toxic compared to cAgNPs alone. Results: This study manifested that cAgNPs show synergistic antimicrobial effect when they get functionalized with amp suggesting their application in curing long-term bacterial infections.

Study on the Synthesis and Characterization of PANi/Nano-CeO2 Composites

2007 ◽  
Vol 124-126 ◽  
pp. 287-290 ◽  
Author(s):  
Fei Liu ◽  
Yong Jun He ◽  
Jeung Soo Huh
Keyword(s):  
In Situ Polymerization ◽  
Solid Phase ◽  
Polymerization Reaction ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Average Size

The nano-CeO2 was synthesized by two-step solid-phase reaction. The image of TEM showed that nano-CeO2 with an average size of about 70 nm. The series of polyaniline/nano-CeO2 composites with different PANi: CeO2 ratios were prepared by in-situ polymerization in the presence of hydrochloric acid (HCl) as dopant by adding nano-CeO2 into the polymerization reaction mixture of aniline. The composites obtained were characterized by FT-IR and UV-vis spectroscopy analysis. The FT-IR spectra of nanocomposites indicate different blue-shifts, attributed to C–N stretching mode for benzenoid unit. The UV-vis spectra of nanocomposites display einstein-shifts compared with PANi at 620nm. The conductivity properties of the composites are also changed compare to the pure PANi. These results suggest that the interactions between the polymer matrix and nanoparticles take place in polyaniline/nano- CeO2 composites.

Microwave-Assisted Synthesis of Cadmium Sulfide Nanoparticles: Effect of Hydroxide Ion Concentration

2013 ◽  
Vol 1617 ◽  
pp. 151-156 ◽  
Author(s):  
Israel López ◽  
Idalia Gómez
Keyword(s):  
Cadmium Sulfide ◽  
Aqueous Dispersion ◽  
Threshold Concentration ◽  
Ion Concentration ◽  
Microwave Assisted Synthesis ◽  
Cubic Phase ◽  
Hydroxide Ion ◽  
Microwave Assisted ◽  
Cadmium Sulfide Nanoparticles ◽  
Vis Spectroscopy

ABSTRACTCadmium sulfide nanoparticles were synthesized by a microwave-assisted route in aqueous dispersion. The cadmium sulfide nanoparticles showed an average diameter around 5 nm and a cubic phase corresponding to hawleyite. The aqueous dispersions of the nanoparticles were characterized by UV-Vis spectroscopy, luminescence analysis, transmission electron microscopy and X-ray diffraction. The addition of sodium hydroxide solutions at different concentrations causes a red-shift in the wavelength of the first excitonic absorption peak of the cadmium sulfide nanoparticles, indicating a reduction of the band gap energy. Besides, the intensity of the luminescence of the nanoparticle dispersions was increased. However, there is a threshold concentration of the hydroxide ion above which the precipitation of the cadmium sulfide nanoparticles occurs.

scholarly journals Polywave And Monowave Light-Curing Units Effects On Polymerization Efficiency Of Different Photoinitiators

2021 ◽  
Vol 24 (4) ◽  
Author(s):  
Peterson Oliveira Boeira ◽  
Mateus De Azevedo Kinalski ◽  
Mateus Bertolini Fernandes dos Santos ◽  
Rafael Ratto de Moraes ◽  
Giana Silveira Lima
Keyword(s):  
Phosphine Oxide ◽  
Second Generation ◽  
Degree Of Conversion ◽  
Polymerization Reaction ◽  
Third Generation ◽  
Test Results ◽  
Vis Spectroscopy ◽  
Light Curing ◽  
Post Hoc ◽  
High Degree

Objective: of this study was to characterize and correlate the absorption spectra of three photoinitiators [camphorquinone (CQ), diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide (TPO) and phenylbis (2,4,6-trimethylbenzoyl)-phosphine oxide (BAPO)], using second or third-generation light curing units (LCU), and to evaluate the degree of conversion and the physical properties of an experimental resin adhesive.  Material and methods: Second-generation (Radii-cal® and Emitter D®) and third-generation (Valo® Cordless and Bluephase N®) LCU were assessed regarding spectrum and irradiance rate of emitted light. Also, the photoinitiators (CQ, TPO and BAPO) were characterized by a light absorption spectrum assessed by UV-Vis spectroscopy, degree of conversion and yellowing effect. Statistical analyzes considered two-way ANOVA and post-hoc Tukey test.  Results: BAPO presented higher reactivity compared to TPO. Regarding degree of conversion of the photoinitiators activated by different light-curing units, the Emitter D® device promoted a high degree of conversion. BAPO presented the highest yellowing effect values. Conclusions: The emission and absorption characteristics of the photoinitiators were different. The polymerization reaction activated by the second-generation light-curing unit was reduced when using an experimental resin with photoinitiator TPO, and the third-generation light-curing unit showed a higher polymerization potential regardless of the photoinitiator. Keywords Light-curing of dental adhesives;  Photoinitiators dental; Curing lights dental.

scholarly journals Dispersion State Phase Diagram of Citrate-Coated Metallic Nanoparticles in Saline Solutions

2020 ◽  
Author(s):  
Sebastian Franco Ulloa ◽  
Giuseppina Tatulli ◽  
Sigbjørn Løland Bore ◽  
Mauro Moglianetti ◽  
Pier Paolo Pompa ◽  
...  
Keyword(s):  
Ionic Strength ◽  
Metallic Nanoparticles ◽  
Colloidal Stability ◽  
Particle Dispersion ◽  
Free Energy Calculations ◽  
Coarse Grained ◽  
Solvent Accessible Surface Area ◽  
Vis Spectroscopy ◽  
Dispersion State ◽  
Saline Solutions

The fundamental interactions underlying citrate-mediated chemical stability of metal nanoparticles (NPs), and their surface characteristics dictating particle dispersion/aggregation in aqueous solutions, are largely unclear. Here, we used a newly developed theoretical model to estimate the stoichiometry of citrate molecules chemisorbed onto spherical metallic NPs and define the uncovered solvent-accessible surface area of the NP. Then, we exploited two-body free energy calculations and extended coarse-grained molecular dynamics simulations of citrate-capped metallic NPs in saline solutions to explore an experimentally relevant range of NP charge, as well as the electrolytic medium’s ionic strength, a known trigger for aggregation. In this way, we define dispersion state phase diagrams of citrate-capped metal nanocolloids. UV-vis spectroscopy experiments validated our predictions and extended our results to NPs up to 35 nm. Altogether, our results disclose a complex interplay between the particle size, its surface charge density, and the ionic strength of the medium, which ultimately clarifies how these variables impact colloidal stability. <br>

scholarly journals Plasmonic Oligomers With Tunable Conductive Nanojunctions

2019 ◽  
Author(s):  
Xiaoyan Li ◽  
Jieli Lyu ◽  
Claire Goldmann ◽  
Mathieu Kociak ◽  
Doru Constantin ◽  
...  
Keyword(s):  
Colloidal Stability ◽  
Infrared Region ◽  
Original Method ◽  
Second Step ◽  
Nanometer Scale ◽  
Mid Infrared ◽  
Oligomer Formation ◽  
Colloidal Chemistry ◽  
Vis Spectroscopy ◽  
Electron Energy Loss

<p>Plasmonic particles can be welded together, but controlling the metallurgy of the hotspots is a challenge in colloidal chemistry. In this paper, we demonstrate an original method that connects gold particles to their neighbors by another metal of choice. To achieve this goal, we first assemble gold bipyramids in a tip-to-tip configuration, yielding short chains of variable length. The good colloidal stability and surface accessibility make the nanochains suitable seeds to grow metallic junctions in a second step. We follow the oligomer formation and the deposition of the second metal (i.e. silver or palladium) <i>via</i> UV/Vis spectroscopy and we map the plasmonic properties of the nanostructures at nanometer scale using electron energy loss spectroscopy. The formation of silver bridges leads to a huge redshift of the longitudinal plasmon modes into the mid-infrared region, while the addition of palladium results in a redshift accompanied by significant plasmon damping. </p>

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