scholarly journals pH Induced Fabrication of Kaolinite-Chitosan Biocomposite

2016 ◽  
Vol 68 ◽  
pp. 1-9 ◽  
Author(s):  
Shaikat Chandra Dey ◽  
Mohammad Al-Amin ◽  
Taslim Ur Rashid ◽  
Md Ashaduzzaman ◽  
Sayed Md Shamsuddin
Keyword(s):  
Environmental Science ◽  
Average Particle Size ◽  
Chitosan Solution ◽  
Aqueous System ◽  
Vital Role ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Morphological Studies ◽  
Functionalized Materials

Functionalization of indigenous materials improves inherent physicochemical properties that depend mainly on their fabrication techniques. Here, pH triggered biocomposites using different proportions of kaolinite and chitosan were fabricated. It was revealed that the biocomposites were formed in 1M acetic acid and stabilized after dropwise addition of the mixture of kaolinite and chitosan solution in 3M NaOH. Binding of kaolinite and chitosan at their interface through functional groups was studied using Fourier transform infrared (FT-IR) spectroscopy and dynamic light scattering (DLS). The average particle size of the biocomposite in aqueous system having 80% w/w kaolinite and 20% w/w chitosan was determined to be 400.8 nm. Crystallinity disappearance of chitosan in the biocomposite, as shown in x-ray diffraction (XRD) spectrum, supports the wrapping of kaolinite with soft and flexible chitosan. Differential scanning calorimetry (DSC) showed the thermal stability of the biocomposites and it was found that the biocomposite fabricated from 50% w/w kaolinite and 50% w/w chitosan was stabled up to 318°C. Morphological studies were carried out using scanning electron microscopy (SEM), where a progressive tendency towards granular morphology was evidenced with increase in kaolinite content. These functionalized materials in bionanocomposite structure would play a vital role in advanced research in analytical and environmental science.

A Calcination Technology for Ultrafine La3NbO7 Powder Prepared by Sol-Gel Process

2011 ◽  
Vol 412 ◽  
pp. 271-274
Author(s):  
Ying Li ◽  
Qiang Xu ◽  
Ling Dai
Keyword(s):  
Single Phase ◽  
Sol Gel ◽  
Average Particle Size ◽  
Complex Method ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Acid Complex ◽  
Calcination Process ◽  
Sol Gel Process

In order to prepare ultrafine La3NbO7 powder, a potential material for thermal barrier coatings, the calcination process of La3NbO7 was studied in this paper.The precursor of La3NbO7 was synthesized by using a citric acid complex method. A calcination process had been systematically investigated. The reaction temperature was determined by differential scanning calorimetry (DSC). The phase composition of powders was characterized by X-ray diffraction (XRD), and the morphology was obtained by scanning electron microscope (SEM). The results revealed that the single-phase La3NbO7 powder could be successfully prepared while the calcination temperature exceeded 800°C and a better morphology could be maintained at 800°C for 4 hours. Considering all above, an optimum calcination scheme was adopted at 800°C for 4 hours. The as-prepared La3NbO7 powders had a grain size of about 50nm and an average particle size of about 300nm.

scholarly journals PCL/PHBV Microparticles as Innovative Carriers for Oral Controlled Release of Manidipine Dihydrochloride

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Fernanda Malaquias Barboza ◽  
Willian Moreira Machado ◽  
Luiz Renato Olchanheski Junior ◽  
Josiane Padilha de Paula ◽  
Sônia Faria Zawadzki ◽  
...  
Keyword(s):  
Controlled Release ◽  
Animal Studies ◽  
Average Particle Size ◽  
Spherical Shape ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Chemically Modified ◽  
Diffraction Patterns

Microparticles of poly(ε-caprolactone) (PCL) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing manidipine dihydrochloride (MAN) were successfully prepared by the simple emulsion/solvent evaporation method. All formulations showed loading efficiency rates greater than 80% and average particle size less than 8 μm. Formulations had spherical shape with smooth and porous surface for PCL and PHBV, respectively. According to Fourier-transform infrared spectroscopy, initial components were not chemically modified during microencapsulation. X-ray diffraction patterns and differential scanning calorimetry demonstrated that this process led to drug amorphization.In vitrodissolution studies showed that all microparticles prolonged MAN release, mainly which one obtained using PCL that contained 5% of drug loaded (PCL-M5). Animal studies demonstrated that formulationPCL-M5was able to keep the variation of mean arterial pressure after phenylephrine administration up to 24 hours. These data confirmed the sustained antihypertensive effect of the investigated microparticles. Results provided an experimental basis for using formulationPCL-M5as a feasible carrier for oral controlled release of MAN intended for treating high blood pressure.

scholarly journals Effects of Hydrothermal and Microwave Dual Treatment and Zein on the Enzymolysis of High Amylose Corn Starch

Gels ◽  
2022 ◽  
Vol 8 (1) ◽  
pp. 29
Author(s):  
Jie Liu ◽  
Qiuye Yang ◽  
Tiantian Yuan ◽  
Yawei Liu ◽  
Guihong Fang
Keyword(s):  
Moisture Content ◽  
Corn Starch ◽  
Average Particle Size ◽  
Microwave Treatment ◽  
Decomposition Temperature ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
High Amylose

Resistant starch (RS) type 2-high-amylose corn starch (HACS) was subjected to simultaneous hydrothermal (25% moisture content, 90 °C for 12 h) and microwave (35% moisture content, 40 W/g microwaving for 4 min) treatment and zein (at a zein to treated starch ratio of 1:5, 50 °C for 1 h) to improve its resistance to enzymolysis. Scanning electron microscopy (SEM) highlighted the aggregation and adhesion of the composite. The average particle size of the composite (27.65 μm) was exceeded that of both the HACS (12.52 μm) and the hydrothermal and microwave treated HACS (hydro-micro-HACS) (12.68 μm). The X-ray diffraction results revealed that the hydro-micro-HACS and composite remained B-type, while their crystallinity significantly decreased to 16.98% and 12.11%, respectively. The viscosity of the hydro-micro-HACS and composite at 50 °C was 25.41% and 35.36% lower than that of HACS. The differential scanning calorimetry (DSC) results demonstrated that the composite displayed a new endothermic peak at 95.79 °C, while the weight loss rate and decomposition temperature were 7.61% and 2.39% lower than HACS, respectively. The RS content in HACS, the hydro-micro-HACS, and composite was 47.12%, 57.28%, and 62.74%, respectively. In conclusion, hydrothermal and microwave treatment combined with zein provide an efficient physical strategy to enhance the RS type 2-HACS.

Sol–gel-based chemical synthesis of NdFeB hard magnetic nanoparticles

2018 ◽  
Vol 32 (34n36) ◽  
pp. 1840070 ◽  
Author(s):  
Jinshan Zhang ◽  
Wei Wu ◽  
Fangshi Meng ◽  
Hao Ding ◽  
Jiling Dong
Keyword(s):  
Saturation Magnetization ◽  
Sol Gel ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Oxide Powders ◽  
Intermediate Phases ◽  
Washing Process ◽  
Oxide Phases

NdFeB nanoparticles were synthesized by a sol–gel method. Firstly, NdFeB gel was prepared by using citric acid and glycol as the gel, and the corresponding salts of Nd, Fe and boric acid. The gel was subsequently annealed under a high temperature condition to obtain NdFeB-oxide phases. Then NdFeB nanoparticles were yielded by reductive annealing of precursors. Microstructure, phase composition and magnetic properties were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and vibrating sample magnetometer (VSM), and also differential scanning calorimetry (DSC) analysis was performed to determine the annealing temperature. At 400[Formula: see text]C, intermediate phases of Fe3BO5 and NdBO3 were formed and stable up to 600[Formula: see text]C; while at 800[Formula: see text]C, they would reacted in presence of oxygen to form NdFeO3 and B2O3. Nd2O3 and Fe2O3 were also formed at this temperature. SEM micrographs of reduced powders after washing process showed an average particle size below 100 nm in all the samples. VSM results showed the oxide powder formed at 800[Formula: see text]C had a coercivity of 1.55 kOe and a saturation magnetization of 1.08 emu/g. The powder synthesized by reduction of oxide powders at 800[Formula: see text]C had a coercivity of 1.02 kOe and a saturation magnetization of 14.17 emu/g.

Role of gadolinium(III) complex in improving thermal stability of polythiophene composite

2015 ◽  
Vol 69 (10) ◽  
Author(s):  
Ferooze Ahmad Rafiqi ◽  
Kowsar Majid
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Average Particle Size ◽  
Degree Of Crystallinity ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Thermal Stability Of

AbstractThis paper involves the preparation of polythiophene (PTP) and its composite by the oxidative polymerisation method by using ferric chloride as an oxidant and thiophene monomer. The gadolinium( III) complex obtained by the refluxing technique was used as dopant in the PTP matrix. On the basis of the spectroscopic characterisation, seven-coordinate geometry is proposed for the complex. Conductance measurement confirms the non-selectrolyte nature of complex. The PTP and its composite were subjected to FTIR, X-ray diffraction and scanning electron microscope techniques. The powder X-ray diffraction pattern showed the high crystalline nature of the complex which in turn developed a good degree of crystallinity in the PTP composite. The average particle size was calculated as 4.655 ˚A and 3.737 ˚A for the dopant and PTP composite, respectively, by using Debye Scherrer’s equation. Thermal analysis was performed by thermogravimetric (TG) analysis, differential thermal analysis (DTA) and differential scanning calorimetry (DSC) techniques. The TG, DTA and DSC results were well-correlated. The thermal analysis revealed the high thermal stability of the dopant which in turn improved the thermal stability of the PTP composite, revealing the potential of the composite for high temperature applications.

scholarly journals Thermal, Structural, and Physical Properties of Freeze Dried Tropical Fruit Powder

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
K. A. Athmaselvi ◽  
C. Kumar ◽  
M. Balasubramanian ◽  
Ishita Roy
Keyword(s):  
Particle Size ◽  
Physical Properties ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Tropical Fruit ◽  
X Ray ◽  
Freeze Dried ◽  
Fruit Powder ◽  
Lcr Meter

This study evaluates the physical properties of freeze dried tropical (guava, sapota, and papaya) fruit powders. Thermal stability and weight loss were evaluated using TGA-DSC and IR, which showed pectin as the main solid constituent. LCR meter measured electrical conductivity, dielectric constant, and dielectric loss factor. Functional groups assessed by FTIR showed presence of chlorides, and O–H and N–H bonds in guava, chloride and C–H bond in papaya, and chlorides, and C=O and C–H bonds in sapota. Particle size and type of starch were evaluated by X-ray diffraction and microstructure through scanning electronic microscopy. A semicrystalline profile and average particle size of the fruit powders were evidenced by X-ray diffraction and lamellar/spherical morphologies by SEM. Presence of A-type starch was observed in all three fruits. Dependence of electric and dielectric properties on frequency and temperature was observed.

scholarly journals Synthesis of MgO Nanoparticles by Solvent Mixed Spray Pyrolysis Technique for Optical Investigation

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
K. R. Nemade ◽  
S. A. Waghuley
Keyword(s):  
Particle Size ◽  
Spray Pyrolysis ◽  
Spray Pyrolysis Technique ◽  
Average Particle Size ◽  
Band Gap Energy ◽  
Average Particle ◽  
Optical Investigation ◽  
X Ray Diffraction ◽  
Mgo Nanoparticles ◽  
Electron Microscope Analysis

Solvent mixed spray pyrolysis technique has attracted a global interest in the synthesis of nanomaterials since reactions can be run in liquid state without further heating. Magnesium oxide (MgO) is a category of the practical semiconductor metal oxides, which is extensively used as catalyst and optical material. In the present study, MgO nanoparticles were successfully synthesized using a solvent mixed spray pyrolysis. The X-ray diffraction pattern confirmed the formation of MgO phase with an excellent crystalline structure. Debye-Scherrer equation is used for the determination of particle size, which was found to be 9.2 nm. Tunneling electron microscope analysis indicated that the as-synthesized particles are nanoparticles with an average particle size of 9 nm. Meanwhile, the ultraviolet-visible spectroscopy of the resulting product was evaluated to study its optical property via measurement of the band gap energy value.

Samanea saman: A Novel Mucoadhesive Gum

2021 ◽  
pp. 57-62
Author(s):  
Nayana S. Baste ◽  
Ganesh. D. Basarkar
Keyword(s):  
Stress Measurement ◽  
Average Particle Size ◽  
Physicochemical Characterization ◽  
Qualitative Evaluation ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Natural Polymers ◽  
Chemical Evaluation ◽  
Research Article ◽  
Samanea Saman

Natural polymers are the most accepted pharmaceutical excipients of formulator’s choice. The reasons for this are their cost effectiveness, biocompatibility and availability. In this research article natural gum was extracted from the seeds of Samanea saman by using ethanol as a solvent. The physicochemical characterization like Loss on drying, Total ash and Acid insoluble ash, Swelling Index, Viscosity and qualitative evaluation of purified gum was done. The percent yield of gum was found to 6% w/w and the swelling index was found to be 18.5. Total ash value (7.5% w/w) and Acid insoluble ash value (1.4%w/w) shows purity of gum whereas 3.2% w/w loss on drying suggest low moisture content of gum. Chemical evaluation shows presence of carbohydrate. X ray diffraction graph of gum shows crystalline nature. The gum has average particle size 45.0±0.32 to 50±0.18μm, and the surface texture of the particles was found to be rough and irregular by scanning Electron Microscopy. Mucoadhesive property of gum was evaluated by Swelling index, Mucoadhesive force, Shear stress measurement. For this study polymeric tablet of gum with concentrations like 10%, 30%, 50%, 70% and 90 %w/w were formulated and the results shows best mucoadhesive and swelling property. From the above result the gum may be used in the formulation of mucoadhesive dosage form.

Synthesis of Emulsion for Water-Based Pigment Ink Jet

2011 ◽  
Vol 380 ◽  
pp. 81-84
Author(s):  
Li Ming Zhang ◽  
Xiu Lan Xin ◽  
Wei Jiang
Keyword(s):  
Particle Size ◽  
Water Resistance ◽  
Average Particle Size ◽  
Average Particle ◽  
Scanning Calorimetry ◽  
Reactive Surfactant ◽  
Potential Value ◽  
Ink Jet ◽  
Water Based ◽  
Pigment Ink

The water-based pigment ink jet emulsion whose particle size was less than 100nm was synthesized by the polymerization of methyl methacrylate, butyl acrylate and ethylhexyl acrylate, and anionic reactive surfactant and nonionic surfactant were used as the emulsifiers. The effects of particle size and water resistance were studied. The glass transition temperature was tested by differential scanning calorimetry. The average particle size of emulsion was range from 60nm to70nm, zeta potential value was less than -60mv; viscosity was 3.5mps; water absorption was 5.9%.

scholarly journals Hydrothermal synthesis of tetragonal barium titanate nanopowders under moderate conditions

2021 ◽  
Vol 15 (2) ◽  
pp. 179-183
Author(s):  
Huaxing Meng ◽  
Zhiwu Chen ◽  
Zhenya Lu ◽  
Xin Wang ◽  
Xiaoyi Fu
Keyword(s):  
Barium Titanate ◽  
Average Particle Size ◽  
Ammonia Solution ◽  
Average Particle ◽  
Titanium Hydroxide ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
Uniform Size ◽  
Dominant Structure ◽  
Hydrolysis Of

Monodispersed tetragonal barium titanate (BaTiO3) nanopowders were synthesized by a convenient hydrothermal route at a low temperature of 200?C in only 24 h. The key point of this method is to promote the generation of ultrafine titanium hydroxide precipitation precursors with the help of absolute ethyl alcohol and ammonia solution during the hydrolysis of Ti(OC4H9)4. The results of X-ray diffraction and Raman spectra show that the as-prepared BaTiO3 nanopowders possess tetragonal-dominant structure. The synthesized tetragonal BaTiO3 nanopowders exhibit relatively uniform size and good dispersity, with the average particle size of 96.1 nm and a tetragonality of 1.0073, which enable broad application prospects in the field of multilayer ceramic capacitors.

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