scholarly journals Magnetite-Functionalized Horse Dung Humic Acid (HDHA) for the Uptake of Toxic Lead(II) from Artificial Wastewater

2021 ◽  
Vol 2021 ◽  
pp. 1-15
Author(s):  
Rahmat Basuki ◽  
Bambang Rusdiarso ◽  
Sri Juari Santosa ◽  
Dwi Siswanta
Keyword(s):  
Humic Acid ◽  
Xrd Analysis ◽  
Desorption Process ◽  
X Ray ◽  
Ft Ir ◽  
Magnetic Strength ◽  
The Stability ◽  
Ir Study ◽  
Average Size ◽  
Adsorption Rates

Magnetite-functionalized horse dung humic acid (HDHA) has been successfully prepared by the coprecipitation method, and the as-prepared adsorbent (MHDHA) has been applied as an easy-handling adsorbent for toxic Pb(II) in artificial wastewater. The MHDHA was characterized by Fourier transform-infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray (EDX), and vibrating sample magnetometer (VSM). The FT-IR study showed that the MHDHA had the characteristics peaks of HA and Fe-O stretching. The XRD analysis revealed that the MHDHA had the 2 θ characteristic for magnetite. The TEM image and EDX analysis exhibited that the MHDHA with an average size of ∼14 nm was partially aggregated and contained ( w / w ) 9.89% carbon, 2.89% nitrogen, and 32.74% oxygen based on functional groups of HDHA. The stability improvement of MHDHA was showed by decreasing HDHA dissolved from 95% to less than 30% at pH 12 after magnetite functionalization. The post-adsorption handling improvement was evidenced by easy and quick retraction by an external magnet with a 62.95 emu/g magnetic strength value. The adsorption capacities were influenced by the pH and ionic strength, whilst the adsorption rates were well simulated by the Ho pseudo-second-order model. The removal uptake of Pb(II) ions increased when the initial concentration was increased and fitted well with the Langmuir isotherm model when the monolayer adsorption capacity was 2.78 × 10 − 4   mol / g (equal to 57.64 mg/g). The value of Dubinin-Radushkevich adsorption energy ( E D − R ) found in this study was 14.78 kJ/mol, which implied that ion exchange is the main mechanism involved in the adsorption process. The regeneration studies of MHDHA show that there was no significant change in composition, morphology, crystallinity, and functional group after five consecutive cycles of the adsorption-desorption process.

scholarly journals Functional Attributes of Myco-Synthesized Silver Nanoparticles from Endophytic Fungi: A New Implication in Biomedical Applications

Biology ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 473
Author(s):  
Prabu Kumar Seetharaman ◽  
Rajkuberan Chandrasekaran ◽  
Rajiv Periakaruppan ◽  
Sathishkumar Gnanasekar ◽  
Sivaramakrishnan Sivaperumal ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Culture Filtrate ◽  
Morphological Changes ◽  
Xrd Analysis ◽  
Penicillium Oxalicum ◽  
Breast Cancer Cell Lines ◽  
Face Centered Cubic ◽  
Tem Analysis ◽  
X Ray ◽  
Average Size

To develop a benign nanomaterial from biogenic sources, we have attempted to formulate and fabricate silver nanoparticles synthesized from the culture filtrate of an endophytic fungus Penicillium oxalicum strain LA-1 (PoAgNPs). The synthesized PoAgNPs were exclusively characterized through UV–vis absorption spectroscopy, Fourier Transform Infra-Red spectroscopy (FT-IR), X-ray powder diffraction (XRD), and Transmission Electron Microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX). The synthesized nanoparticles showed strong absorbance around 430 nm with surface plasmon resonance (SPR) and exhibited a face-centered cubic crystalline nature in XRD analysis. Proteins presented in the culture filtrate acted as reducing, capping, and stabilization agents to form PoAgNPs. TEM analysis revealed the generation of polydispersed spherical PoAgNPs with an average size of 52.26 nm. The PoAgNPs showed excellent antibacterial activity against bacterial pathogens. The PoAgNPs induced a dose-dependent cytotoxic activity against human adenocarcinoma breast cancer cell lines (MDA-MB-231), and apoptotic morphological changes were observed by dual staining. Additionally, PoAgNPs demonstrated better larvicidal activity against the larvae of Culex quinquefasciatus. Moreover, the hemolytic test indicated that the as-synthesized PoAgNPs are a safe and biocompatible nanomaterial with versatile bio-applications.

A study on using expanded perlite with hydroxyapatite: Reinforced bio-composites

2021 ◽  
pp. 095441192199656
Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu
Keyword(s):  
Body Fluid ◽  
Xrd Analysis ◽  
Cold Isostatic Pressing ◽  
Expanded Perlite ◽  
X Ray Diffraction ◽  
Pressing Method ◽  
X Ray ◽  
Infra Red ◽  
Ft Ir

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.

scholarly journals Effects of Gum Arabic-Coated Magnetite Nanoparticles on the Removal of Pb Ions from Aqueous Solutions

2021 ◽  
pp. 889-896
Author(s):  
Hanan J. Mustafa ◽  
Tagreed M. Al-Saadi
Keyword(s):  
Aqueous Solutions ◽  
Crystallite Size ◽  
Magnetite Nanoparticles ◽  
Gum Arabic ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Absorption Bands ◽  
X Ray ◽  
Ft Ir ◽  
Pb Ions

To study the removal of lead (Pb) ions from aqueous solutions, novel magnetite nanoparticles (NPs) of Ni0.31Mg0.15Ag0.04Fe2.5O4 were synthesized by coprecipitation synthesis using metal sulfates, and then coated with Gum Arabic (GA). The prepared NPs were analyzed using various spectroscopic and analytical methods, such as X-Ray diffraction analysis (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray spectroscopy (EDX), Fourier Transform Infra-Red spectroscopy (FT-IR), and Atomic Absorption Spectrophotometer (AAS). By using XRD analysis, the cubic inverse spinel structure of the prepared NPs was proven, showing average values of crystallite size, lattice constant, and density of 28.57nm, 8.32582Å, and 5.2890 g/cm3, respectively. FE-SEM analysis revealed the sphere-like shape of the nanoparticles with a measured crystallite size of 25.93nm. The existence of constituent elements was evidenced by EDX. FT-IR test proved the success of the coating process of magnetite NPs by the presence of the main characteristic absorption bands of GA in the FT-IR spectrum of GA-magnetite NPs. The adsorption of Pb ions by GA- magnetite NPs was shown by AAS analysis, where the concentration of Pb ions decreased from 25ppm to 6.6ppm, reaching 1.1ppm at the time of 25min. The porosity of the NPs and the carboxyl groups in GA played an important role in the process.

scholarly journals STARCH MEDIATED SYNTHESIS OF HYDROXYAPATITE NANOPARTICLE FOR BIOMEDICAL APPLICATIONS

2015 ◽  
Vol 2 (1) ◽  
pp. 15-17
Author(s):  
Indira J
Keyword(s):  
Biomedical Applications ◽  
Soluble Starch ◽  
Morphological Properties ◽  
Spherical Nanoparticles ◽  
Hydroxyapatite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Average Size ◽  
Controllable Size

Hydroxyapatite (HAP) nanoparticles with uniform morphologies and controllable size have been synthesized by template directed method. The environment and eco-friendly polysaccharide soluble starch is used as a template to regulate size and shape of the nanoparticles synthesized. Structural and morphological properties of as-synthesized hydroxyapatite nanoparticles have been examined through the techniques like Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Diffraction (XRD) and Scanning Electron Microscopy(SEM), respectively. The results indicate that the obtained particles are uniform discrete spherical nanoparticles. The average size of the hydroxyapatite nanoparticles were ranged from 45 to 60 nm.

Preparation and Characterization of CdSe Nanoparticles Synthesized Using the Ultrasonic Irradiation

2007 ◽  
Vol 124-126 ◽  
pp. 1229-1232 ◽  
Author(s):  
Myoung Seok Sung ◽  
Yoon Bok Lee ◽  
Yong Jin Kim ◽  
Yang Do Kim
Keyword(s):  
Ultrasonic Irradiation ◽  
Photoelectron Spectroscopy ◽  
Irradiation Time ◽  
Xrd Analysis ◽  
Cdse Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Emission ◽  
Transmission Electron ◽  
Average Size

Cadmium selenide(CdSe) nanoparticles were prepared in the aqueous solution containing isopropyl alcohol by the ultrasonic irradiation at room temperature. The cadmium chloride (CdCl2) and sodium selenosulfate (Na2SeSO3) were used as the cadmium and selenium source, respectively. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-Vis absorption spectra and PL spectra were used to characterize the CdSe nanoparticles. XRD analysis revealed the formation of cubic structure CdSe. TEM images showed aggregated CdSe nanoparticles with the size of nanometer scale. Average size of CdSe nanoparticles were about 3.9, 5.0 and 5.1nm with sonication time of 6, 30 and 40 minutes, respectively. The surface emission became less intensive and shifted to red with increasing irradiation time. This paper presents the effects of ultrasonic on the formation of CdSe nanoparticles and its characteristics.

Preparation and Characterization the Cheap Mineral (Calcium Compound): The Preliminary Survey in the Natural Material

2013 ◽  
Vol 770 ◽  
pp. 303-306
Author(s):  
A. Montree ◽  
K. Teanchai ◽  
Wichian Siriprom
Keyword(s):  
Molecular Composition ◽  
Natural Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Conventional Analysis ◽  
Calcium Compound ◽  
Egg Shells ◽  
Ft Ir ◽  
Ir Study ◽  
Ir Spectroscopic

The present work reports the production of biomaterial, while the potential in bio mineralization were studied with three conventional analysis techniques, X-Ray Diffraction (XRD) were confirm the crystal structure, Energy Dispersive X-Ray Fluorescence (EDXRF) and Fourier Transform Infrared Spectroscopy (FT-IR) study trace element and molecular composition, respectively. The results of XRD reveal that, the egg shells have a crystalline of calcium carbonate in phase calcite and fishbone have a crystalline of calcium phosphate in phase hydroxyapatite, respectively. The composition of both mineral and the level of metals element were investigated by EDXRF. The major composition was identified as Calcium (Ca) and other element are Potassium (K), Phosphorus (P) Sulfur (Al), Zinc (Zn), Ferrum (Fe), Copper (Cu) and Strontium (Sr). In addition, the deeply investigate molecular composition both mineral used using FT-IR spectroscopic analysis.

X-ray diffraction and FT-IR study of caprine and ovine hide

2005 ◽  
Vol 29 (1) ◽  
pp. 55-62 ◽  
Author(s):  
Clark A. Maxwell ◽  
Nancy Bell ◽  
Craig J. Kennedy ◽  
Tim J. Wess
Keyword(s):  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Ir Study

The Study and Characterization of a Novel Structure of 1,3,5-Benzenetricarboxylic Acid

2013 ◽  
Vol 830 ◽  
pp. 202-206
Author(s):  
Hai Yan Tan ◽  
Cheng Liu ◽  
Jin Ping Wu
Keyword(s):  
Relevant Information ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
X Ray ◽  
Novel Structure ◽  
Ft Ir ◽  
Benzenetricarboxylic Acid ◽  
The Stability ◽  
Lamella Structure

A novel ten-interpenetrating structure of 1,3,5-benzenetricarboxylic acid was grown under solvothemal condition after heated it 16 hours. It was characterized by FT-IR, HNMR, X-ray diffraction, HRTEM. HRTEM obtain the relevant information of structural morphologies. The result of HRTEM showsed this material owned special lamella structure. X-ray diffraction showed the crystal of the new structure is of monoclinic system, space groupP1 with a=26.5039(17), b=16.4121(17),c=26.550(2)Å,α=90.00, β=91.533(2), γ=90.00, V=11544.4(17)Å3, Z=8, Dc=1.451g/cm3,μ=0.126mm-1,F(000)=5184, R=0.0891 and w (R)=0.1819 for 11318 observed reflection with I>2(I),hydrogen bond contributed to the stability of the structure. The fluorescence spectra indicated that the title compound had two stronger emission peak at 346nm and 400nm. Keywords:1, 3, 5-benzenetricarboxylic acid; novel structure; ten-interpenetrating

scholarly journals Synthesis of SiO2-TiO2:Yb3+ glass-ceramics and characterization of structure and optical properties

2017 ◽  
Vol 1 (T1) ◽  
pp. 114-121
Author(s):  
Thanh Tat Huynh ◽  
Van Thi Thanh Tran
Keyword(s):  
Sol Gel ◽  
Glass Ceramics ◽  
Xrd Analysis ◽  
Silica Matrix ◽  
Photoluminescence Intensity ◽  
Raman Spectroscopic ◽  
Characteristic Emission ◽  
Ft Ir ◽  
Average Size ◽  
20 Nm

In this work, the monoliths of 85 % SiO2-15 % TiO2 doped Yb3+ ions at different contents have been prepared by sol-gel method. The measurement of FT-IR, Raman spectroscopic and XRD analysis show the formation of anatase TiO2 nanocrystals with average size about 15–20 nm in silica matrix. Moreover, the pyrochlore crystals of Yb2Ti2O7 begin to form in the samples when content of Yb3+ reaches to 1 mol %. TiO2 Yb3+ 2F7/2 2F5/2 truyền năng lƣợng kích thích UV EV EC mức khuyết tật 974 nm The energy transferred from TiO2 crystals to Yb3+ ions is proven by the characteristic emission spectrum of Yb3+ at the wavelength of 980 nm when the samples are excited by the wavelength of 300 nm. The photoluminescence intensity is highest at 0.1% mol of Yb3+ and gradually decreases with doping content

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