scholarly journals Synthesis and Physicochemical Characteristics of Chitosan Extracted from Pinna deltoides

2021 ◽  
Vol 11 (4) ◽  
pp. 4061-4070
Keyword(s):  
Physicochemical Characteristics ◽  
Common Species ◽  
Ftir Analysis ◽  
Aliphatic Compound ◽  
X Ray ◽  
Micro Raman Spectroscopy ◽  
Wide Range ◽  
Pen Shell ◽  
Crystalline Nature ◽  
By Catch

Chitosan, a naturally produced polysaccharide that has a wide range of uses in biological, pharmacological, industrial, and commercial settings. The pen shell Pinna deltoides is a common species found along the coast of Thondi, and it is often collected as by-catch by fishermen. These species contain a high amount of chitin, which may be converted into chitosan. The goal of this research is to extract chitosan from P. deltoides and characterize it utilizing techniques like Fourier Transform Infrared Spectroscopy (FTIR), Micro Raman Spectroscopy, X-ray Powder Diffractometry (XRD), Thermogravimetric Analysis (TGA), and Scanning Electron Microscopy (SEM). The existence of C-O-C glycosidic connection (1156 cm-1), NHCO group (1216 cm-1), aliphatic compound, -CH2 bend (1418 cm-1), and asymmetric CH2 stretching were verified by FTIR analysis (1204 cm-1). Chitosan extract exhibited a greater degree of deacetylation of 55.17%, which is consistent with prior studies. The highest peaks in the Micro Raman Spectra were 2937 cm-1, 1106 cm-1, and 1376 cm-1. The crystallinity of the chitosan at 2θ was anticipated using X-ray Powder Diffractometry (XRD) data at about 20°-25°. SEM micrograms verified the crystalline nature of the chitosan by revealing its soft and crystal-like arrangement of the chitosan. TGA was used to assess the sample's thermal constancy, and the chitosan's stability was found to be consistent with that of prior research.

A Particular Structure of B-doped μc-Si/a-Si:H Layers on Insulator

1992 ◽  
Vol 283 ◽  
Author(s):  
M. Le Berre ◽  
M. Lemiti ◽  
P. Pinard ◽  
E. Bustarret ◽  
W. Grieshaber ◽  
...  
Keyword(s):  
Cross Section ◽  
Microcrystalline Structure ◽  
X Ray Diffraction ◽  
Relative Thickness ◽  
X Ray ◽  
Preparation Conditions ◽  
Wide Range ◽  
Local Measurements ◽  
Crystalline Nature ◽  
Optimized Conditions

ABSTRACTMicrocrystalline films of thicknesses ranging from 0.3 to 1.1 μm have been deposited on oxidized silicon wafers by PECVD in a 50KHz capacitive discharge reactor at 450°C. Two series of films have been elaborated over a wide range of boron concentrations at the same H2:SiH4 ratio of 9:1. Cross section TEM micrographs showed the films to consist of two sublayers of distinct crystalline nature, whose relative thickness depends on the preparation conditions. With a strongly <220> textured microcrystalline structure, the overlayer snowed a columnar morphology, while the amorphous underlayer reached thicknesses of 350nm. Two additional striking features were observed by TEM: - The grains took two symmetrical orientations relative to the preferential [220] growth axis;- The interface between the amorphous and crystalline regions had a sawtooth pattern with a period around 300nm. In contrast to these microstructural results, the B-profile as measured by SIMS was found to be fiat accross the whole thickness. These local measurements are compared to the results of grazing X ray diffraction and Raman measurements. We observe and discuss a discrepancy between the X ray coherence length and the dimensions of the columns as observed by TEM. While optimized conditions lead to a vanishing amorphous sublayer, the more original features described above are tentatively interpreted taking into account the high compressive strains in the layers deposited at low plasma frequencies.

scholarly journals Can Inorganic Bovine Bone Grafts Present Distinct Properties?

2014 ◽  
Vol 25 (4) ◽  
pp. 282-288 ◽  
Author(s):  
Fernanda de Paula do Desterro ◽  
Márcia Soares Sader ◽  
Glória Dulce de Almeida Soares ◽  
Guaracilei Maciel Vidigal Jr
Keyword(s):  
Surface Area ◽  
Calcium Release ◽  
Physicochemical Characteristics ◽  
Molar Ratio ◽  
Nanoporous Structure ◽  
Bovine Bone ◽  
Ftir Analysis ◽  
X Ray Diffraction ◽  
Absorption Bands ◽  
X Ray

The aim of this study was to evaluate the physicochemical characteristics of 3 mineralized bovine inorganic biomaterials and correlate them with the dissolution rate. Bio-Oss(r), GenoxInorgânico(r), and Bonefill(r) were examined using field emission gun scanning electron microscopy (FEG-SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), specific surface area (BET), calcium/phosphorous molar ratio and a dissolution assay. Bio-Oss(r) showed a micro- and nanoporous structure consisting of 15-nm hydroxyapatite (HA) crystallites; Genox(r), a microporous structure composed of 39-nm HA crystallites; and Bonefill(r), micro- and nanoporous structure of indeterminable crystallite size. FTIR analysis showed that Bio-Oss(r) and Genox(r) were composed of calcium phosphate. The absorption bands of phosphate were poorly defined in Bonefill(r). By XRD, Bio-Oss(r) was shown to contain peaks related to the carbonated HA, whereas Genox(r) only contained peaks corresponding to HA. The broad bands in Bonefill(r) indicated low crystallinity. Bio-Oss(r) showed a greater surface area and calcium release rate than that of Genox(r). Although all biomaterials were of bovine origin, the different manufacturing processes result in materials with different physicochemical properties and may influence the biological and clinical response.

Counterfeit Parts Recognition and Detection for Failure Analysts

2010 ◽  
Author(s):  
Katherine V. Whittington
Keyword(s):  
Thermal Cycle ◽  
Visual Inspection ◽  
Acoustic Microscopy ◽  
Scanning Acoustic Microscopy ◽  
3D Measurement ◽  
X Ray ◽  
Wide Range ◽  
Electronic Parts ◽  
Testing Awareness

Abstract The electronics supply chain is being increasingly infiltrated by non-authentic, counterfeit electronic parts, whose use poses a great risk to the integrity and quality of critical hardware. There is a wide range of counterfeit parts such as leads and body molds. The failure analyst has many tools that can be used to investigate counterfeit parts. The key is to follow an investigative path that makes sense for each scenario. External visual inspection is called for whenever the source of supply is questionable. Other methods include use of solvents, 3D measurement, X-ray fluorescence, C-mode scanning acoustic microscopy, thermal cycle testing, burn-in technique, and electrical testing. Awareness, vigilance, and effective investigations are the best defense against the threat of counterfeit parts.

Human Dentine Remineralization Under Non-colagen Materials Action

2017 ◽  
Vol 68 (5) ◽  
pp. 928-932
Author(s):  
Agripina Zaharia ◽  
Viorica Ghisman Plescan ◽  
Elena Maria Anghel ◽  
Viorica Musat
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Artificial Saliva ◽  
Composite Layer ◽  
X Ray ◽  
Micro Raman Spectroscopy ◽  
Agarose Hydrogel ◽  
Human Dentine ◽  
Dentine Surface ◽  
Scanning Electron

The purpose of this work is to induce biomimetic remineralization of acid etched coronal human dentine in artificial saliva (AS) under agarose (A) hydrogel or chitosan (CS)-A hydrogel action. The investigations focused on the morphology, chemical composition and crystalline structure of the new remineralized layers grown onto the etched dentinal surface (R) using scanning electron microscopy coupled with energy dispersive X-ray spectrometry and micro-Raman spectroscopy. Experimental results showed that remineralized layers grown in the presence of A or CS-A hydrogels consist in B-type Ca-deficient hydroxyapatite (HAP). After 7 days treatment into artificial saliva under agarose hydrogel, nanorod-like extrafibrilar HAP crystals randomly self-assembled in a discontinuous layer were formed, while in presence of chitosan-agarose hydrogel a continuous compact CS-HAP composite layer was obtained. The new biomimetic layer (A-CS4) formed after 4 days on dentine surface under A-CS hydrogel has higher crystallinity. Longer exposed (7 days) dentine in the presence of agarose hydrogel shows a higher mineral-to-collagen ratio (A7). Since dentine mineralization increases, the collagen quality factor decreases in succession A-CS4]R]A7. Results show a benefic effect of chitosan on remineralization of etched dentine.

Pharmaceutical Co-Crystals - Design, Development and Applications

2020 ◽  
Vol 10 (3) ◽  
pp. 169-184
Author(s):  
Rachna Anand ◽  
Arun Kumar ◽  
Arun Nanda
Keyword(s):  
Physicochemical Properties ◽  
Crystal Engineering ◽  
Pharmacological Action ◽  
Physicochemical Characteristics ◽  
Research Area ◽  
Dissolution Profile ◽  
Design Development ◽  
Drug Molecule ◽  
Wide Range ◽  
Major Factors

Background: Solubility and dissolution profile are the major factors which directly affect the biological activity of a drug and these factors are governed by the physicochemical properties of the drug. Crystal engineering is a newer and promising approach to improve physicochemical characteristics of a drug without any change in its pharmacological action through a selection of a wide range of easily available crystal formers. Objective: The goal of this review is to summarize the importance of crystal engineering in improving the physicochemical properties of a drug, methods of design, development, and applications of cocrystals along with future trends in research of pharmaceutical co-crystals. Co-crystallization can also be carried out for the molecules which lack ionizable functional groups, unlike salts which require ionizable groups. Conclusion: Co-crystals is an interesting and promising research area amongst pharmaceutical scientists to fine-tune the physicochemical properties of drug materials. Co-crystallization can be a tool to increase the lifecycle of an older drug molecule. Crystal engineering carries the potential of being an advantageous technique than any other approach used in the pharmaceutical industry. Crystal engineering offers a plethora of biopharmaceutical and physicochemical enhancements to a drug molecule without the need of any pharmacological change in the drug.

scholarly journals Biodiesel Production on Monometallic Pt, Pd, Ru, and Ag Catalysts Supported on Natural Zeolite

Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 48
Author(s):  
Pawel Mierczynski ◽  
Magdalena Mosińska ◽  
Lukasz Szkudlarek ◽  
Karolina Chalupka ◽  
Misa Tatsuzawa ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Natural Zeolite ◽  
Noble Metals ◽  
Methyl Esters ◽  
Physicochemical Characteristics ◽  
Biodiesel Production ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yield Values ◽  
Temperature Programmed

Biodiesel production from rapeseed oil and methanol via transesterification reaction facilitated by various monometallic catalyst supported on natural zeolite (NZ) was investigated. The physicochemical characteristics of the synthesized catalysts were studied by X-ray diffraction (XRD), Brunauer–Emmett–Teller method (BET), temperature-programmed-reduction in hydrogen (H2-TPR), temperature-programmed-desorption of ammonia (NH3-TPD), Scanning Electron Microscope equipped with EDX detector (SEM-EDS), and X-ray photoelectron spectroscopy (XPS) methods. The highest activity and methyl ester yields were obtained for the Pt/NZ catalyst. This catalyst showed the highest triglycerides conversion of 98.9% and fatty acids methyl esters yields of 94.6%. The activity results also confirmed the high activity of the carrier material (NZ) itself in the investigated reaction. Support material exhibited 90.5% of TG conversion and the Fatty Acid Methyl Esters yield (FAME) of 67.2%. Introduction of noble metals improves the TG conversion and FAME yield values. Increasing of the metal loading from 0.5 to 2 wt.% improves the reactivity properties of the investigated catalysts.

scholarly journals Use of WetSEM® capsules for convenient multimodal scanning electron microscopy, energy dispersive X-ray analysis, and micro Raman spectroscopy characterisation of technetium oxides

2021 ◽  
Author(s):  
D. J. Bailey ◽  
M. C. Stennett ◽  
J. Heo ◽  
N. C. Hyatt
Keyword(s):  
Raman Spectroscopy ◽  
Low Cost ◽  
Powder Materials ◽  
Spectroscopy Analysis ◽  
X Ray ◽  
Micro Raman Spectroscopy ◽  
Hazard And Risk ◽  
Sem Imaging ◽  
General User ◽  
532 Nm

AbstractSEM–EDX and Raman spectroscopy analysis of radioactive compounds is often restricted to dedicated instrumentation, within radiological working areas, to manage the hazard and risk of contamination. Here, we demonstrate application of WetSEM® capsules for containment of technetium powder materials, enabling routine multimodal characterisation with general user instrumentation, outside of a controlled radiological working area. The electron transparent membrane of WetSEM® capsules enables SEM imaging of submicron non-conducting technetium powders and acquisition of Tc Lα X-ray emission, using a low cost desktop SEM–EDX system, as well as acquisition of good quality μ-Raman spectra using a 532 nm laser.

scholarly journals Preparation of Synthetic Zeolites from Coal Fly Ash by Hydrothermal Synthesis

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1267
Author(s):  
David Längauer ◽  
Vladimír Čablík ◽  
Slavomír Hredzák ◽  
Anton Zubrik ◽  
Marek Matik ◽  
...  
Keyword(s):  
Fly Ash ◽  
Coal Combustion ◽  
Power Plants ◽  
Coal Fly Ash ◽  
Thermal Power ◽  
Product Analysis ◽  
Coal Combustion Products ◽  
X Ray ◽  
Wide Range ◽  
Silica Alumina

Large amounts of coal combustion products (as solid products of thermal power plants) with different chemical and physical properties cause serious environmental problems. Even though coal fly ash is a coal combustion product, it has a wide range of applications (e.g., in construction, metallurgy, chemical production, reclamation etc.). One of its potential uses is in zeolitization to obtain a higher added value of the product. The aim of this paper is to produce a material with sufficient textural properties used, for example, for environmental purposes (an adsorbent) and/or storage material. In practice, the coal fly ash (No. 1 and No. 2) from Czech power plants was firstly characterized in detail (X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX), particle size measurement, and textural analysis), and then it was hydrothermally treated to synthetize zeolites. Different concentrations of NaOH, LiCl, Al2O3, and aqueous glass; different temperature effects (90–120 °C); and different process lengths (6–48 h) were studied. Furthermore, most of the experiments were supplemented with a crystallization phase that was run for 16 h at 50 °C. After qualitative product analysis (SEM-EDX, XRD, and textural analytics), quantitative XRD evaluation with an internal standard was used for zeolitization process evaluation. Sodalite (SOD), phillipsite (PHI), chabazite (CHA), faujasite-Na (FAU-Na), and faujasite-Ca (FAU-Ca) were obtained as the zeolite phases. The content of these zeolite phases ranged from 2.09 to 43.79%. The best conditions for the zeolite phase formation were as follows: 4 M NaOH, 4 mL 10% LiCl, liquid/solid ratio of 30:1, silica/alumina ratio change from 2:1 to 1:1, temperature of 120 °C, process time of 24 h, and a crystallization phase for 16 h at 50 °C.

scholarly journals Adsorption Studies of Arsenic(V) by CuO Nanoparticles Synthesized by Phyllanthus emblica Leaf-Extract-Fueled Solution Combustion Synthesis

2021 ◽  
Vol 13 (4) ◽  
pp. 2017
Author(s):  
Sadia Saif ◽  
Syed F. Adil ◽  
Mujeeb Khan ◽  
Mohammad Rafe Hatshan ◽  
Merajuddin Khan ◽  
...  
Keyword(s):  
Leaf Extract ◽  
Solution Combustion Synthesis ◽  
Copper Oxide Nanoparticles ◽  
Maximum Adsorption Capacity ◽  
Phyllanthus Emblica ◽  
Adsorption Efficiency ◽  
Solution Combustion ◽  
X Ray ◽  
Cuo Nps ◽  
Crystalline Nature

In the present study, a simple and eco-friendly route for the synthesis of copper oxide nanoparticles (CuO NPs) using leaf extract of Phyllanthus emblica as fuel has been demonstrated, as P. emblica is a locally available abundant plant. The formation of the as-prepared CuO NPs was confirmed by using various techniques, such as UV–Vis absorption spectroscopy, cold field scanning electron microscopy (CF–SEM), energy dispersive X-ray analysis (EDX), dynamic light scattering (DLS), and X-ray photoelectron (XPS). The hydrodynamic size of the CuO NPs was found to be 80 nm, while the zeta potential of −28.6 mV was obtained. The elemental composition was confirmed by EDX analysis accompanied with elemental mapping, while the crystalline nature was substantiated by the XRD diffractogram. The as-synthesized CuO NPs were studied for their use as an adsorbent material for the removal of As(V) from water. It was confirmed that the CuO NPs effectively removed As(V) via adsorption, and the adsorption efficiency was found to be best at a higher pH. The maximum adsorption capacity of CuO for As(V) was found to be 1.17 mg/g calculated using the Langmuir equation.

scholarly journals Multidimensional Ln-Aminophthalate Photoluminescent Coordination Polymers

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  
Keyword(s):  
Water Content ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Low Cost ◽  
Microwave Assisted Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The development of straightforward reproducible methods for the preparation of new photoluminescent coordination polymers (CPs) is an important goal in luminescence and chemical sensing fields. Isophthalic acid derivatives have been reported for a wide range of applications, and in addition to their relatively low cost, have encouraged its use in the preparation of novel lanthanide-based coordination polymers (LnCPs). Considering that the photoluminescent properties of these CPs are highly dependent on the existence of water molecules in the crystal structure, our research efforts are now focused on the preparation of CP with the lowest water content possible, while considering a green chemistry approach. One- and two-dimensional (1D and 2D) LnCPs were prepared from 5-aminoisophthalic acid and Sm3+/Tb3+ using hydrothermal and/or microwave-assisted synthesis. The unprecedented LnCPs were characterized by single-crystal X-ray diffraction (SCRXD), powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM), and their photoluminescence (PL) properties were studied in the solid state, at room temperature, using the CPs as powders and encapsulated in poly(methyl methacrylate (PMMA) films, envisaging the potential preparation of devices for sensing. The materials revealed interesting PL properties that depend on the dimensionality, metal ion, co-ligand used and water content.

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