scholarly journals SOLVENT EFFECT ON ZERO-VALENT IRON NANOPARTICLES (nZVI) PREPARATION AND ITS THERMAL OXIDATION CHARACTERISTIC

2021 ◽  
Vol 10 (2) ◽  
Author(s):  
Patiparn Boonruam ◽  
Soipatta Soisuwan ◽  
Piyachat Wattanachai ◽  
Héctor Morillas ◽  
Settakorn Upasen
Keyword(s):  
Particle Size ◽  
Thermal Oxidation ◽  
Oxidation Reaction ◽  
Chemical Reduction ◽  
Chemical Properties ◽  
Spherical Shape ◽  
Zero Valent Iron ◽  
Synthesis Process ◽  
Cubic Phase ◽  
Chloride Hexahydrate

Zero-valent iron (ZVI) nanoparticle exists a nanoscale (1-100 nm) of the iron particle with zero oxidation number. It has acquired considerable attention for its potential to capture the free-electron moieties. The production and storage of ZVI material, however, is challenging because it is relatively unstable. In this research, we aim to study of solvent effects on ZVI preparation and its characterization. The nano-scaled ZVI was synthesized by a chemical reduction method. Iron (III) chloride hexahydrate (FeCl3·6H2O) was as a chemical precursor and sodium borohydride solution (NaBH4) as a reducing agent. Two parameters used in this study were: i) solvent types (ethanol, diethyl ether, and acetone) ii) proportion of solvent and deionized water (4:0, 4:1, and 4:2 by volume). We characterized the physical and chemical properties of the synthesized samples (e.g. particle size and distribution, morphology, and the chemical composition) using various techniques, for example, TEM, UV-Vis spectrophotometer, and XRD. Moreover, we performed a thermal oxidation reaction of synthesized powder samples using DSC and TGA tools. The results show that the nZVI particle formed a spherical shape with the smallest particle size of 39 nm. The solvent type was the key parameter protecting the oxidation reaction during the synthesis process. According to the spherical shape of the synthesized nZVI samples, an estimated specific surface area was also reported. The cubic structure of nZVI particles was estimated at 79-81 wt.%, and almost 20 wt.% was attributed to iron oxide (Fe2O3) cubic phase. The oxidation reaction occurred above 400oC. The minimum enthalpy of thermal oxidation was approximately 1600 J/g. Furthermore, the relation between thermal oxidation enthalpy and nZVI particle sizes were revealed and predicted by the Boltzmann equation.

scholarly journals Design, Preparation, and Characterization of Dioscin Nanosuspensions and Evaluation of Their Protective Effect against Carbon Tetrachloride-Induced Acute Liver Injury in Mice

2019 ◽  
Vol 2019 ◽  
pp. 1-16 ◽  
Author(s):  
Hong-Ye JU ◽  
Kun-Xia Hu ◽  
Guo-Wang Zhao ◽  
Zhi-Shu Tang ◽  
Xiao Song
Keyword(s):  
Particle Size ◽  
Protective Effect ◽  
Soybean Lecithin ◽  
Chemical Properties ◽  
Spherical Shape ◽  
Positive Control ◽  
The Body

The purpose of this study was to prepare a dioscin nanosuspension (Dio-NS) that has a better distance and high solubility for oral administration and to evaluate its hepatoprotective effects. Optimal primary manufacture parameters, including shear time, shear speed, emulation temperature, pressure, and cycles of homogenization, were determined by single-factor experiments. The concentrations of dioscin, SDS, and soybean lecithin were optimized using the central composite design-response surface method, and their effects on the mean particle size (MPS) and particle size distribution of Dio-NS were investigated. Characterization of the Dio-NS formulations included examinations of the surface morphology and physical status of dioscin in Dio-NS, the stability of Dio-NS at different temperatures, in vitro solubility, and liver protective effect in vivo. Under optimal conditions, Dio-NS had an MPS of 106.72 nm, polydispersity index of 0.221, and zeta potential of −34.27 mV. Furthermore, the proportion of dioscin in Dio-NS was approximately 21.26%. The observation of particles with a spherical shape and the disappearance of crystalline peaks indicated that the physical and chemical properties of Dio-NS were altered. Furthermore, we observed that the dissolution of Dio-NS was superior to that of a physical mixture and Dio-GZF. Moreover, Dio-NS was demonstrated to have a protective effect against CCl4-induced acute liver damage in mice that was equivalent to that of silymarin (a positive control drug) at the same dose. The good hepatoprotective effect of our Dio-NS preparation can provide a theoretical basis for investigating its absorption mechanisms in the body.

scholarly journals Synthesis of the platinum particle with the pH variation for the particle size control

2021 ◽  
Vol 2145 (1) ◽  
pp. 012038
Author(s):  
P Thongnopkun ◽  
W Kitprapot
Keyword(s):  
Particle Size ◽  
Chemical Reduction ◽  
Intrinsic Value ◽  
Size Control ◽  
Spherical Shape ◽  
Platinum Particle ◽  
Particle Sizes ◽  
Sem Images ◽  
Ph Variation ◽  
Reduction Methods

Abstract Platinum is a precious metal widely used in the jewelry industry due to its property and intrinsic value. The different particle sizes of platinum can be applied in various applications, especially for jewelry production. In the present article, submicron, and nano-sized platinum particle sizes were synthesized through simple chemical reduction methods and the effect of pH variation was revealed. The scanning electron microscope (SEM) images showed that the pH variations give rise to significant changes of the obtained particle size. The size of platinum particle was decreased from submicron to nanoscale while the pH was increased. The UV-Vis spectra indicated the maximum absorption at 220 nm confirming the spherical shape of the platinum particle. The FT-IR spectroscopy was used to analyze the residuals from the synthesis. The result showed that there is no indication of residual in the synthesized particle. Additionally, this synthesis can provide stability in terms of size and shape, as well as high production yield.

Yield Enhancement of Activated Carbon Palm Kernel Shells Based through Carbonization Solidification Process

2021 ◽  
Vol 1028 ◽  
pp. 313-318
Author(s):  
Tiara Amelia Valency ◽  
Azwar Manaf ◽  
Mas Ayu Elita Hafizah
Keyword(s):  
Particle Size ◽  
Activated Carbon ◽  
Palm Kernel ◽  
Chemical Properties ◽  
Solidification Process ◽  
Absorption Capacity ◽  
Yield Enhancement ◽  
Synthesis Process ◽  
Carbonization Process ◽  
Palm Kernel Shells

Utilization of palm oil waste in palm kernel shells as activated carbon, the activated carbon manufacturing goes through several processes, including dehydration, carbonization, and activation. Palm shell particle size was controlled during the activated carbon synthesis process through the temperature of the milling time and carbonization processes. The carbonization process was carried out using an electric furnace at carbonization temperatures 400, 600, and 800 °C, respectively. A carbonization time was 1 hour under vacuum condition to produce initial values of particle and grain sizes that had a neat structure and had absorption capacity. The particle size of formed activated carbon was measured by PSA (particle size analyzer) type Coulter LS 100Q micron scale. The particle size of active carbon was dependent on the carbonization temperature at 400, 600, and 800 °C was obtained particle size 19,90, 9,507, and 6,264 μm, respectively. Several characterizations are required to determine the properties of activated carbon was obtained. FTIR Spectrophotometer was used to observe activated carbon’s molecule structure before and after dehydration and carbonization process. It was found that the specific fingerprint at 2913,91 cm-1 and 2923,56 cm-1 for the carbon chain of activated carbon. Other physical and chemical properties were conducted to investigate moisture content, thermal property, yield enhancement, and formed product appearance.

An Overview of Optimization of Spherical Crystallisation Process

2013 ◽  
Vol 6 (4) ◽  
pp. 2203-2209
Author(s):  
N B Bhagat ◽  
A V Yadav ◽  
P R Mastud ◽  
R A Khutale
Keyword(s):  
Physical Phenomenon ◽  
Chemical Properties ◽  
Spherical Shape ◽  
Particle Engineering ◽  
Spherical Crystallization ◽  
Stirring Rate ◽  
Physico Chemical ◽  
Rate Selection ◽  
Pharmaceutical Agents ◽  
Spherical Crystals

In this article we describe the optimizing parameters in the process of spherical crystallisation. Particle engineering of active pharmaceutical agents is an innovative area of research in pharmaceutical industry because of several advantages. Spherical crystallization is one of the particle engineering technique in which drug directly gets crystallized and agglomerated into spherical shape. The spherical crystals can be obtained by different methods like solvent change, Quasi-emulsion droplet, ammonia diffusion and neutralisation. The optimization of process of spherical crystallization is important for obtaining the ideal spherical crystal agglomerates. It includes stirring rate, selection of solvent, pH, temperature etc. which affects on the physico-chemical properties of crystals. These optimizing parameters play its specific role in formation of spherical crystals. Stirring rate affects the shape as well as size of the final agglomerates and solvent selection helps in the formation of maximum amount of agglomerates in the system. The factors like pH and temperature should be maintained in case of drugs which show polymorphism. Apart from this, several others physical phenomenon or parameters like interfacial tension and rate of crystallisation are also important for thorough optimization of process.  

Application of Plakett-Burman Screening Design in Optimization of Process Parameters for Formulation of Canaglifozin Nanosuspension

2020 ◽  
Vol 13 (6) ◽  
pp. 5208-5216
Author(s):  
Nisha Patel ◽  
Hitesh A Patel
Keyword(s):  
Particle Size ◽  
Particle Diameter ◽  
Spherical Shape ◽  
Water Soluble ◽  
Pareto Chart ◽  
Independent Variables ◽  
Mean Particle Size ◽  
Screening Design ◽  
Stirring Time ◽  
Response Variables

In this study, we sought to improve the dissolution characteristics of a poorly water-soluble BCS class IV drug canaglifozin, by preparing nanosuspension using media milling method. A Plackett–Burman screening design was employed to screen the significant formulation and process variables. A total of 12 experiment were generated by design expert trial version 12 for screening 5 independent variables namely the amount of stabilizer in mg (X1), stirring time in hr (X2), amt of Zirconium oxide beads in gm (X3), amount of drug in mg (X4) and stirring speed in rpm (X5) while mean particle size in nm (Y1) and drug release in 10 min. were selected as the response variables. All the regression models yielded a good fit with high determination coefficient and F value. The Pareto chart depicted that all the independent variables except the amount of canaglifozin had a significant effect (p<0.001) on the response variables. The mathematical model for mean particle size generated from the regression analysis was given by mean particle size = +636.48889 -1.28267 amt of stabilizer(X1) -4.20417 stirring time (X2) -7.58333 amt of ZrO2 beads(X3) -0.105556 amt of drug(X4) -0.245167 stirring speed(X5) (R2=0.9484, F ratio=22.07, p<0.001). Prepared canaglifozin nanosuspension exemplified a significant improvement (p<0.05) in the release as compared to pure canaglifozin and marketed tablet with the optimum formulation releasing almost 80% drug within first 10min. Optimized nanosuspension showed spherical shape with surface oriented stabilizer molecules and a mean particle diameter of 120.5 nm. There was no change in crystalline nature after formulation and it was found to be chemically stable with high drug content.

Development and Ex-vivo Evaluation of Topiramate Mucoadhesive Nanoparticles for Intranasal Delivery

2020 ◽  
Vol 13 (6) ◽  
pp. 5250-5255
Author(s):  
Ashwin Kumar Tulasi ◽  
Anil Goud Kandhula ◽  
Ravi Krishna Velupula
Keyword(s):  
Particle Size ◽  
Nasal Mucosa ◽  
Intranasal Administration ◽  
Ex Vivo ◽  
Chemical Properties ◽  
Brain Targeting ◽  
Oral Tablet ◽  
Promising Alternative ◽  
Ex Vivo Permeation

Topiramate is a second-generation antiepileptic drug used in partial, generalized seizures as an oral tablet. Oral route of administration is most convenient but shows delayed absorption. Moreover, in emergency cases, parenteral administration is not possible as it requires medical assistance. Hence, the present study was aimed to develop topiramate mucoadhesive nanoparticles for intranasal administration using ionotropic gelation method. The developed nanoparticles were evaluated for physico-chemical properties like particle size, zeta potential, surface morphology, drug content, entrapment efficiency, in vitro drug release, mucoadhesive strength, and ex vivo permeation studies in excised porcine nasal mucosa. Optimized nanoparticle formulation (T9) was composed oil mucoadhesive agent (Chitosan 1% w/w), cross linking polymer (TPP) and topiramate 275mg, 100mg and 4% respectively. It showed particle size of 350nm, high encapsulation efficacy and strong mucoadhesive strength. In vitro drug diffusion of optimized formulation showed 95.12% release of drug after 180min. Ex-vivo permeation of drug across nasal mucosa was   88.05 % after 180min. Nasocilial toxicity studies showed optimized formulation did not damage the nasal mucosa. Thus, the intranasal administration of topiramate using chitosan can be a promising alternative for brain targeting and the treatment of epilepsy.

scholarly journals Facile Synthesis of Carboxymethyl Cellulose Coated Core/Shell SiO2@Cu Nanoparticles and Their Antifungal Activity against Phytophthora capsici

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 888
Author(s):  
Nguyen Thi Thanh Hai ◽  
Nguyen Duc Cuong ◽  
Nguyen Tran Quyen ◽  
Nguyen Quoc Hien ◽  
Tran Thi Dieu Hien ◽  
...  
Keyword(s):  
Antifungal Activity ◽  
Carboxymethyl Cellulose ◽  
Chemical Reduction ◽  
Low Cost ◽  
Phytophthora Capsici ◽  
Reduction Process ◽  
Spherical Shape ◽  
Core Shell ◽  
Cu Nanoparticles ◽  
Average Size

Cu nanoparticles are a potential material for creating novel alternative antimicrobial products due to their unique antibacterial/antifungal properties, stability, dispersion, low cost and abundance as well as being economical and ecofriendly. In this work, carboxymethyl cellulose coated core/shell SiO2@Cu nanoparticles (NPs) were synthesized by a simple and effective chemical reduction process. The initial SiO2 NPs, which were prepared from rice husk ash, were coated by a copper ultrathin film using hydrazine and carboxymethyl cellulose (CMC) as reducing agent and stable agent, respectively. The core/shell SiO2@Cu nanoparticles with an average size of ~19 nm were surrounded by CMC. The results indicated that the SiO2@Cu@CMC suspension was a homogenous morphology with a spherical shape, regular dispersion and good stability. Furthermore, the multicomponent SiO2@Cu@CMC NPs showed good antifungal activity against Phytophthora capsici (P. capsici). The novel Cu NPs-based multicomponent suspension is a key compound in the development of new fungicides for the control of the Phytophthora disease.

scholarly journals Composite Poly(vinyl alcohol)-Based Nanofibers Embedding Differently-Shaped Gold Nanoparticles: Preparation and Characterization

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1604
Author(s):  
Andrea Dodero ◽  
Maila Castellano ◽  
Paola Lova ◽  
Massimo Ottonelli ◽  
Elisabetta Brunengo ◽  
...  
Keyword(s):  
Vinyl Alcohol ◽  
Ad Hoc ◽  
Chemical Reduction ◽  
Chemical Properties ◽  
Single Step ◽  
Gold Nanostructures ◽  
Poly Vinyl Alcohol ◽  
Spherical Nanoparticles ◽  
Potential Applications ◽  
New Perspective

Poly(vinyl alcohol) nanofibrous mats containing ad hoc synthesized gold nanostructures were prepared via a single-step electrospinning procedure and investigated as a novel composite platform with several potential applications. Specifically, the effect of differently shaped and sized gold nanostructures on the resulting mat physical-chemical properties was investigated. In detail, nearly spherical nanoparticles and nanorods were first synthesized through a chemical reduction of gold precursors in water by using (hexadecyl)trimethylammonium bromide as the stabilizing agent. These nanostructures were then dispersed in poly(vinyl alcohol) aqueous solutions to prepare nanofibrous mats, which were then stabilized via a humble thermal treatment able to enhance their thermal stability and water resistance. Remarkably, the nanostructure type was proven to influence the mesh morphology, with the small spherical nanoparticles and the large nanorods leading to thinner well defined or bigger defect-rich nanofibers, respectively. Finally, the good mechanical properties shown by the prepared composite mats suggest their ease of handleability thereby opening new perspective applications.

Astaxanthin–garlic oil nanoemulsions preparation using spontaneous microemulsification technique: optimization and their physico–chemical properties

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Seyedalireza Mortazavi Tabrizi ◽  
Afshin Javadi ◽  
Navideh Anarjan ◽  
Seyyed Javid Mortazavi Tabrizi ◽  
Hamid Mirzaei
Keyword(s):  
Antioxidant Activity ◽  
Particle Size ◽  
Subcritical Water ◽  
Chemical Properties ◽  
Polydispersity Index ◽  
Garlic Oil ◽  
Physico Chemical ◽  
Minimum Particle Size ◽  
Oil In Water ◽  
Technique Optimization

AbstractGarlic oil in water nanoemulsion was resulted through subcritical water method (temperature of 120 °C and pressure of 1.5 bar, for 2 h), using aponin, as emulsifier. Based on the prepared garlic oil nanoemulsion, astaxanthin–garlic oil nanoemulsions were prepared using spontaneous microemulsification technique. Response surface methodology was employed to evaluate the effects of independent variables namely, amount of garlic oil nanoemulsion (1–9 mL) and amount of provided astaxanthin powder (1–9 g) on particle size and polydispersity index (PDI) of the resulted nanoemulsions. Results of optimization indicated that well dispersed and spherical nanodroplets were formed in the nanoemulsions with minimum particle size (76 nm) and polydispersity index (PDI, 0.358) and maximum zeta potential value (−8.01 mV), using garlic oil nanoemulsion amount of 8.27 mL and 4.15 g of astaxanthin powder. Strong antioxidant activity (>100%) of the prepared astaxanthin–garlic oil nanoemulsion, using obtained optimum amounts of the components, could be related to the highest antioxidant activity of the colloidal astaxanthin (>100%) as compared to that of the garlic oil nanoemulsion (16.4%). However, higher bactericidal activity of the resulted nanoemulsion against Escherichia coli and Staphylococcus aureus, were related to the main sulfur bioactive components of the garlic oil in which their main functional groups were detected by Fourier transform-infrared spectroscopy.

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