Displaying publications 561 - 580 of 1298 in total

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  1. Dasan YK, Guan BH, Zahari MH, Chuan LK
    PLoS One, 2017;12(1):e0170075.
    PMID: 28081257 DOI: 10.1371/journal.pone.0170075
    Lanthanum substituted Ni-Zn ferrite nanoparticles (Ni0.5Zn0.5LaxFe1-xO4; 0.00 ≤x≤ 1.00) synthesized by sol-gel method were presented. X-ray diffraction patterns reveal the typical single phase spinel cubic ferrite structure, with the traces of secondary phase for lanthanum substituted nanocrystals. In addition, the structural analysis also demonstrates that the average crystallite size varied in the range of 21-25 nm. FTIR spectra present the two prominent absorption bands in the range of 400 to 600 cm-1 which are the fingerprint region of all ferrites. Surface morphology of both substituted and unsubstituted Ni-Zn ferrite nanoparticle samples was studied using FESEM technique and it indicates a significant increase in the size of spherical shaped particles with La3+ substitution. Magnetic properties of all samples were analyzed using vibrating sample magnetometer (VSM). The results revealed that saturation magnetization (Ms) and coercivity (Hc) of La3+ substituted samples has decreased as compared to the Ni-Zn ferrite samples. Hence, the observed results affirm that the lanthanum ion substitution has greatly influenced the structural, morphology and magnetic properties of Ni-Zn ferrite nanoparticles.
    Matched MeSH terms: Microscopy, Electron, Scanning
  2. Loh KS, Lee YH, Musa A, Salmah AA, Zamri I
    Sensors (Basel), 2008 Sep 18;8(9):5775-5791.
    PMID: 27873839
    Magnetic nanoparticles of Fe₃O₄ were synthesized and characterized using transmission electron microscopy and X-ray diffraction. The Fe₃O₄ nanoparticles were found to have an average diameter of 5.48 ±1.37 nm. An electrochemical biosensor based on immobilized alkaline phosphatase (ALP) and Fe₃O₄ nanoparticles was studied. The amperometric biosensor was based on the reaction of ALP with the substrate ascorbic acid 2-phosphate (AA2P). The incorporation of the Fe₃O₄ nanoparticles together with ALP into a sol gel/chitosan biosensor membrane has led to the enhancement of the biosensor response, with an improved linear response range to the substrate AA2P (5-120 μM) and increased sensitivity. Using the inhibition property of the ALP, the biosensor was applied to the determination of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). The use of Fe₃O₄ nanoparticles gives a two-fold improvement in the sensitivity towards 2,4-D, with a linear response range of 0.5-30 μgL-1. Exposure of the biosensor to other toxicants such as heavy metals demonstrated only slight interference from metals such as Hg2+, Cu2+, Ag2+ and Pb2+. The biosensor was shown to be useful for the determination of the herbicide 2, 4-D because good recovery of 95-100 percent was obtained, even though the analysis was performed in water samples with a complex matrix. Furthermore, the results from the analysis of 2,4-D in water samples using the biosensor correlated well with a HPLC method.
    Matched MeSH terms: Microscopy, Electron, Transmission
  3. Mawlud SQ
    PMID: 30359852 DOI: 10.1016/j.saa.2018.10.032
    Enhanced red and orange fluorescence emissions of Sm3+ Rare earth (RE) ions were observed in sodium‑zinc tellurite glasses embedded with silver and gold nanoparticles (NPs). The fine distribution of NPs in the glass matrix with an average diameter ~ 11.09 nm and ~3.86 nm for Ag and Au NPs respectively were confirmed by using transmission electron microscope (TEM). The embedding of Ag and Au NPs into the glass structure caused an increasing in the transition emission intensity of Sm3+ ions, which is ascribed to the progress of the presence of the localized surface Plasmon resonance (LSPR) indicating from the characteristic absorption peaks. The luminescence and absorption spectra have been discussed using a standard hypothesis Judd-Ofelt theory for a certain absorption transitions 6P3/2, 4I11/2, 6F11/2, 6F9/2, 6F7/2, 6F5/2, 6F3/2, 6H15/2, 6F1/2 and emission transitions 6H5/2, H7/2, 6H9/2 and H11/2 under 409 nm excitation of the Sm3+ ions. The decay life time curve exhibited a non-exponential behavior of the studied glass samples and the results were compared with the similar reported glasses. An efficient red and orange fluorescence emission illustrate that the Sm3+-doped sodium‑zinc tellurite embedded with Ag and Au NPs are potential materials for the laser illumination.
    Matched MeSH terms: Microscopy, Electron, Transmission
  4. Prathumratana L, Kim R, Kim KW
    Environ Geochem Health, 2020 Mar;42(3):1033-1044.
    PMID: 30206754 DOI: 10.1007/s10653-018-0186-9
    Lead contamination in topsoil of the mining and smelting area of Mitrovica, Kosovo, was investigated for total concentrations and chemical fractions by sequential extraction analysis, mineralogical fractions by X-ray diffraction (XRD) and scanning electron microscopy with energy-dispersive X-ray spectrometer (SEM-EDX). The study revealed that all samples contained Pb exceeding USEPA standard of 400 mg kg-1. The highest total concentration of Pb (125,000 mg kg-1) was the soil from the former smelter. Sequential extraction results showed that the predominant form of Pb was associated with Fe-Mn oxide-bound fraction which ranged from 45.37 to 71.61% of total concentrations, while carbonate and silicate Pb-binding fractions were dominant when physical measurements (XRD and SEM-EDX) were applied. Application of Pb isotope ratios (206Pb/207Pb and 208Pb/206Pb), measured by inductively coupled plasma mass spectrometry, identified that Pb contamination is originated from similar anthropogenic source. The results reflected that the Pb contamination in the soil of this area is serious. In order to provide proper approaches on remediation and prevention of health impacts to the people in this area, a continuous monitoring and health risk assessment are recommended.
    Matched MeSH terms: Microscopy, Electron, Scanning
  5. Che Engku Noramalina Che-Engku-Chik, Nor Azah Yusof, Jaafar Abdullah, Siti Sarah Othman, Helmi Wasoh
    MyJurnal
    A novel DNA biosensing platform was designed by the functionalization of iron oxide (Fe3O4)
    with the carboxylic group via capping agent, mercaptopropionic acid (MPA) and conjugated
    with nanocellulose crystalline (NCC) surface modified with surfactant cetyltrimethylammonium
    bromide (CTAB) to assist in the DNA sensing capability. The product of nanocomposites
    compound was drop-casted on screen printed carbon electrode (SPCE). Characterization by field
    emission scanning electron microscope (FESEM) and energy dispersive X-Ray (EDX)
    spectroscopy showing that carboxyl functionalized iron oxide (COOH-Fe3O4) can be hybridized
    with NCC-CTA+ via electrostatic interaction.
    Matched MeSH terms: Microscopy, Electron, Scanning
  6. Mohd Chachuli SA, Hamidon MN, Mamat MS, Ertugrul M, Abdullah NH
    Sensors (Basel), 2018 Aug 01;18(8).
    PMID: 30071579 DOI: 10.3390/s18082483
    High demand of semiconductor gas sensor works at low operating temperature to as low as 100 °C has led to the fabrication of gas sensor based on TiO₂ nanoparticles. A sensing film of gas sensor was prepared by mixing the sensing material, TiO₂ (P25) and glass powder, and B₂O₃ with organic binder. The sensing film was annealed at temperature of 500 °C in 30 min. The morphological and structural properties of the sensing film were characterized by field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD). The gas sensor was exposed to hydrogen with concentration of 100⁻1000 ppm and was tested at different operating temperatures which are 100 °C, 200 °C, and 300 °C to find the optimum operating temperature for producing the highest sensitivity. The gas sensor exhibited p-type conductivity based on decreased current when exposed to hydrogen. The gas sensor showed capability in sensing low concentration of hydrogen to as low as 100 ppm at 100 °C.
    Matched MeSH terms: Microscopy, Electron, Scanning
  7. Zin, M.H., Abdan, K., Norizan, M.N., Mazlan, N.
    MyJurnal
    The main focus of this study was to obtain the optimum alkaline treatment for banana fibre and the its effect on the mechanical and chemical properties of banana fibre, its surface topography, its heat resistivity, as well as its interfacial bonding with epoxy matrix. Banana fibre was treated with sodium hydroxide (NaOH) under various treatment conditions. The treated fibres were characterised using FTIR spectroscopy. The morphology of a single fibre observed under a Digital Image Analyser indicated slight reduction in fibre diameter with increasing NaOH concentration. The Scanning Electron Microscope (SEM) results showed the deteriorating effect of alkali, which can be seen from the removal of impurities and increment in surface roughness. The mechanical analysis indicates that 6% NaOH treatment with a two-hour immersion time gave the highest tensile strength. The adhesion between single fibre and epoxy resin was analysed through the micro-droplet test. It was found that 6% NaOH treatment with a two-hour immersion yielded the highest interfacial shear stress of 3.96 MPa. The TGA analysis implies that alkaline treatment improved the thermal and heat resistivity of the fibre.
    Matched MeSH terms: Microscopy, Electron, Scanning
  8. Anne JM, Boon YH, Saad B, Miskam M, Yusoff MM, Shahriman MS, et al.
    R Soc Open Sci, 2018 Aug;5(8):180942.
    PMID: 30225083 DOI: 10.1098/rsos.180942
    In this work, we reported the synthesis, characterization and adsorption study of two β-cyclodextrin (βCD) cross-linked polymers using aromatic linker 2,4-toluene diisocyanate (2,4-TDI) and aliphatic linker 1,6-hexamethylene diisocyanate (1,6-HDI) to form insoluble βCD-TDI and βCD-HDI. The adsorption of 2,4-dinitrophenol (DNP) on both polymers as an adsorbent was studied in batch adsorption experiments. Both polymers were well characterized using various tools that include Fourier transform infrared spectroscopy, thermogravimetric analysis, Brunauer-Emmett-Teller analysis and scanning electron microscopy, and the results obtained were compared with the native βCD. The adsorption isotherm of 2,4-DNP onto polymers was studied. It showed that the Freundlich isotherm is a better fit for βCD-TDI, while the Langmuir isotherm is a better fit for βCD-HMDI. The pseudo-second-order kinetic model represented the adsorption process for both of the polymers. The thermodynamic study showed that βCD-TDI polymer was more favourable towards 2,4-DNP when compared with βCD-HDI polymer. Under optimized conditions, both βCD polymers were successfully applied on various environmental water samples for the removal of 2,4-DNP. βCD-TDI polymer showed enhanced sorption capacity and higher removal efficiency (greater than 80%) than βCD-HDI (greater than 70%) towards 2,4-DNP. The mechanism involved was discussed, and the effects of cross-linkers on βCD open up new perspectives for the removal of toxic contaminants from a body of water.
    Matched MeSH terms: Microscopy, Electron, Scanning
  9. Othman N, Masarudin MJ, Kuen CY, Dasuan NA, Abdullah LC, Md Jamil SNA
    Nanomaterials (Basel), 2018 Nov 07;8(11).
    PMID: 30405074 DOI: 10.3390/nano8110920
    The combination of compounds with different classes (hydrophobic and hydrophilic characters) in single chitosan carrier is a challenge due to the hydrophilicity of chitosan. Utilization of l-ascorbic acid (LAA) and thymoquinone (TQ) compounds as effective antioxidants is marred by poor bioavailability and uptake. Nanoparticles (NPs) solved the problem by functioning as a carrier for them because they have high surface areas for more efficient delivery and uptake by cells. This research, therefore, synthesized chitosan NPs (CNPs) containing LAA and TQ, CNP-LAA-TQ via ionic gelation routes as the preparation is non-toxic. They were characterized using electron microscopy, zetasizer, UV⁻VIS spectrophotometry, and infrared spectroscopy. The optimum CNP-LAA-TQ size produced was 141.5 ± 7.8 nm, with a polydispersity index (PDI) of 0.207 ± 0.013. The encapsulation efficiency of CNP-LAA-TQ was 22.8 ± 3.2% for LAA and 35.6 ± 3.6% for TQ. Combined hydrophilic LAA and hydrophobic TQ proved that a myriad of highly efficacious compounds with poor systemic uptake could be encapsulated together in NP systems to increase their pharmaceutical efficiency, indirectly contributing to the advancement of medical and pharmaceutical sectors.
    Matched MeSH terms: Microscopy, Electron
  10. Azis RS, Che Muda NN, Hassan J, Shaari AH, Ibrahim IR, Mustaffa MS, et al.
    Materials (Basel), 2018 Nov 06;11(11).
    PMID: 30404131 DOI: 10.3390/ma11112190
    This paper investigates the effect of the ratio of ammonium nitrate (AN) on the structural, microstructural, magnetic, and alternating current (AC) conductivity properties of barium hexaferrite (BaFe12O19). The BaFe12O19 were prepared by using the salt melt method. The samples were synthesized using different powder-to-salt weight ratio variations (1:3, 1:4, 1:5, 1:6 and 1:7) of BaCO₃ + Fe₂O₃ and ammonium nitrate salt. The NH₄NO₃ was melted on a hot plate at 170 °C. A mixture of BaCO₃ and Fe₂O₃ were added into the NH₄NO₃ melt solution and stirred for several hours using a magnetic stirrer under a controlled temperature of 170 °C. The heating temperature was then increased up to 260 °C for 24 hr to produce an ash powder. The x-ray diffraction (XRD) results show the intense peak of BaFe12O19 for all the samples and the presence of a small amount of the impurity Fe₂O₃ in the samples, at a ratio of 1:5 and 1:6. From the Fourier transform infra-red (FTIR) spectra, the band appears at 542.71 cm - 1 and 432.48 cm - 1 , which corresponding to metal⁻oxygen bending and the vibration of the octahedral sites of BaFe12O19. The field emission scanning electron microscope (FESEM) images show that the grains of the samples appear to stick each other and agglomerate at different masses throughout the image with the grain size 5.26, 5.88, 6.14, 6.22, and 6.18 µm for the ratios 1:3, 1:4, 1:5, 1:6, and 1:7 respectively. From the vibrating sample magnetometer (VSM) analysis, the magnetic properties of the sample ratio at 1:3 show the highest value of coercivity Hc of 1317 Oe, a saturation magnetization Ms of 91 emu/g, and a remnant Mr of 44 emu/g, respectively. As the temperature rises, the AC conductivity is increases with an increase in frequency.
    Matched MeSH terms: Microscopy, Electron, Scanning
  11. Alim S, Kafi AKM, Rajan J, Yusoff MM
    Int J Biol Macromol, 2019 Feb 15;123:1028-1034.
    PMID: 30465828 DOI: 10.1016/j.ijbiomac.2018.11.171
    This work reports on a novel glucose biosensor based on co-immobilization of glucose oxidase (GOx) and horseradish peroxidase with polymerized multiporous nanofiber (MPNFs) of SnO2 onto glassy carbon electrode with chitosan. Multiporous nanofibers of SnO2 were synthesized by electrospinning method from the tin precursor which possesses high surface area good electrical conductivity, and the nanofibers were polymerized with polyaniline (PANI). GOx and HRP were then co-immobilized with the nanofibers on the surface of the glassy carbon electrode by using chitosan. The polymerized nanofibers play a significant role in facilitating the direct electron transfer between the electroactive center of the immobilized enzyme and the electrode surface. The morphology of the nanofiber and polymerized nanofiber has been evaluated by field emission scanning electron microscopy (FESEM). Cyclic Voltammetry and amperometry were employed to study and optimize the performance of the fabricated biosensor. The PANI/SnO2-NF/GOx-HRP/Ch/GC biosensor displayed a linear amperometric response towards the glucose concentration range from 5 to 100 μM with a detection limit of 1.8 μM (S/N = 3). Also, the anti-interference study and real sample analysis was investigated. Furthermore, the biosensor reported in this work exhibited excellent stability, reproducibility, and repeatability.
    Matched MeSH terms: Microscopy, Electron, Scanning
  12. Arshad S, Ahmad M, Saboor A, Ibrahim FH, Mustafa MRU, Zafar M, et al.
    Microsc Res Tech, 2019 Feb;82(2):92-100.
    PMID: 30511479 DOI: 10.1002/jemt.23106
    Climate change is the most realistic theory of this era. Sudden and drastic changes are happening on the earth and the survival of mankind is becoming questionable in the future. The plants play the key role in controlling the climate change. The study emphasizes on role of trees in the cop up or damaging the climate of this earth, whether they are medicinal trees or economically important trees. Due to the overgrazing and intense deforestation the climate is being affected hazardously. The global warming phenomenon is occurring due to the less availability of trees and more carbon dioxide in the atmosphere. In total 20 plants were collected from across the Pakistan on the basis of their abundance and their key roles. Out of which seeds of eight plants were scanned through scanning electron microscope for correct authentication and importance of these medicinally important trees in mitigating the climate change. RESEARCH HIGHLIGHTS: The role of forest sector in the climate's change mitigation. Medicinally and economically important tree species across Pakistan. By using SEM, Ultra seed sculpturing features as an authentication tool. To formulate some policies to stop or control deforestation.
    Matched MeSH terms: Microscopy, Electron, Scanning
  13. Meriam Suhaimy SH, Lai CW, Tajuddin HA, Samsudin EM, Johan MR
    Materials (Basel), 2018 Oct 23;11(11).
    PMID: 30360462 DOI: 10.3390/ma11112066
    There are various approaches to enhancing the catalytic properties of TiO₂, including modifying its morphology by altering the surface reactivity and surface area of the catalyst. In this study, the primary aim is to enhance the photocatalytic activity by changing the TiO₂ nanotubes' architecture. The highly ordered infrastructure is favorable for a better charge carrier transfer. It is well known that anodization affects TiO₂ nanotubes' structure by increasing the anodization duration which in turn influence the photocatalytic activity. The characterizations were conducted by FE-SEM (fiend emission scanning electron microscopy), XRD (X-ray diffraction), RAMAN (Raman spectroscopy), EDX (Energy dispersive X-ray spectroscopy), UV-Vis (Ultraviolet visible spectroscopy) and LCMS/MS/MS (liquid chromatography mass spectroscopy). We found that the morphological structure is affected by the anodization duration according to FE-SEM. The photocatalytic degradation shows a photodegradation rate of k = 0.0104 min-1. It is also found that a mineralization of Simazine by our prepared TiO₂ nanotubes leads to the formation of cyanuric acid. We propose three Simazine photodegradation pathways with several intermediates identified.
    Matched MeSH terms: Microscopy, Electron, Scanning
  14. Kassim, S., Tahrin, R.A.A., Rusdi, N.F., Harun, N.A.
    ASM Science Journal, 2018;11(101):86-95.
    MyJurnal
    A feasible production of poly (methyl methacrylate)@alloy (gold-silver) core shell has
    been presented as candidate in enhanced detection of surface enhanced Raman scattering
    (SERS). Free emulsifier- emulsion synthesised PMMA sphere with average size of 419 nm in
    diameter were used as core material for incorporation of alloy nanoparticles (6 nm) resulting
    a core-shell structure. The fabrication of PMMA@alloy SERS substrate was successfully
    done via self-assembly thus the produced SERS substrate that comprise of unique optical
    properties combination arising from periodic core arrangement and plasmonic activity of
    alloy nanoparticles. Alloy is bimetallic nanoparticles in which the combination of silver
    (Ag) and gold (Au) present an absolutely improved light resistance as compared to single
    metal alone with great surface plasmon resonance. Morphology and elemental analysis was
    performed through scanning electron microscope (SEM) and the analysis showing species of
    both Au and Ag in single alloy nanoparticles. The alloy nanoparticles were also observed to
    homogenously coating the PMMA sphere. Surface plasmon resonance activity was maximum
    at 476 nm obtained from UV-Visible spectroscopy. High surface production was observed
    to have periodically arranged PMMA@alloy core -shell and potentially to be used as SERS
    substrate.
    Matched MeSH terms: Microscopy, Electron, Scanning
  15. Mehamod, F.S., Kadir, M.A., Jusoh, N., Yusof, N.F., Suah, F.B.
    ASM Science Journal, 2018;11(101):114-123.
    MyJurnal
    The development of new adsorbent has rapidly increased in order to overcome the problem
    of waste water treatment from heavy metal pollution. The ability of nickel (II)-ion imprinted
    polymer (Ni-IIP) as an alternative adsorbent for the removal of nickel ion from aqueous has
    been investigated. The Ni-IIP was prepared via bulk polymerization by using functional
    monomers; methylacrylic acid (MAA) with picolinic acid as a co-monomer. Nickel ion was
    used as template, AIBN as initiator and EGDMA as cross-linking agent. Non-imprinted control
    polymer (NIP) was prepared in the same manner as Ni-IIP but in the absence of nickel
    ion. The resultant of Ni-IIP and NIP were characterized by using Fourier Transform Infrared
    (FTIR) spectroscopy and Scanning Electron Microscope (SEM). Result showed that, the adsorption
    of nickel ion onto Ni-IIP increased as the adsorbent dosage increased and contact
    time is prolonged. The adsorption isotherm model for Ni-IIP and NIP were fitted well with
    Freundlich and Langmuir, respectively. Kinetic study for both Ni-IIP and NIP were followed
    the pseudo-second order, indicates that the rate-limiting step is the surface adsorption that
    involves chemisorption. Selectivity studies showed that the distribution coefficient of Ni2+
    was higher compared to Zn2+, Mg2+ and Pb2+. The present work has successfully synthesized
    Ni-IIP particles with good potential in recognition of Ni2+ ions in an aqueous medium.
    Matched MeSH terms: Microscopy, Electron, Scanning
  16. Jannah, A.N., Erwana, N.Y., Jamion, N.A.
    MyJurnal
    This study was carried out to investigate the electrical properties of YBCO sample as superconductor
    and the effect of addition of Co3O4 on the superconducting properties of YBCO superconductor. The
    YBCO sample was prepared by solid state reaction route. The samples were prepared by each with
    weight percentage of cobalt oxide of x= 0.00, x= 0.01, x= 0.02 and x= 0.03. Electrical Conduction by
    Multimeter, Fourier Transform Infrared (FTIR), Critical temperature (Tc) measurement, X-ray
    Diffraction (XRD), and Scanning Electron Microscopy (SEM) were conducted for analysis.
    Multimeter showed all samples were in electric conduction, FTIR showed that carbonyl compound in
    the sample was removed after calcinations. Tc measurement showed that the critical temperature of
    sample of x= 0.02 was increased compared to sample of x= 0.00. XRD showed all samples have
    orthorhombic structure and SEM showed that the grain size was increased as increased the cobalt
    addition in YBCO superconductor. Besides, the EDX also showed the composition of elements
    YBCO were tally with chemicals used for pure YBCO and addition cobalt oxide into YBCO
    superconductor.
    Matched MeSH terms: Microscopy, Electron, Scanning
  17. Ramakrishnan R, Gimbun J, Ramakrishnan P, Ranganathan B, Reddy SMM, Shanmugam G
    Curr Drug Deliv, 2019;16(10):913-922.
    PMID: 31663478 DOI: 10.2174/1567201816666191029122445
    BACKGROUND: This paper presents the effect of solution properties and operating parameters of polyethylene oxide (PEO) based nanofiber using a wire electrode-based needleless electrospinning.

    METHODS: The feed solution was prepared using a PEO dissolved in water or a water-ethanol mixture. The PEO solution is blended with Bovine Serum Albumin protein (BSA) as a model drug to study the effect of the electrospinning process on the stability of the loaded protein. The polymer solution properties such as viscosity, surface tension, and conductivity were controlled by adjusting the solvent and salt content. The morphology and fiber size distribution of the nanofiber was analyzed using scanning electron microscopy.

    RESULTS: The results show that the issue of a beaded nanofiber can be eliminated either by increasing the solution viscosity or by the addition of salt and ethanol to the PEO-water system. The addition of salt and solvent produced a high frequency of smaller fiber diameter ranging from 100 to 150 nm. The encapsulation of BSA in PEO nanofiber was characterized by three different spectroscopy techniques (i.e. circular dichroism, Fourier transform infrared, and fluorescence) and the results showed the BSA is well encapsulated in the PEO matrix with no changes in the protein structure.

    CONCLUSION: This work may serve as a useful guide for a drug delivery industry to process a nanofiber at a large and continuous scale with a blend of drugs in nanofiber using a wire electrode electrospinning.

    Matched MeSH terms: Microscopy, Electron, Scanning
  18. Rohaizar MH, Sepeai S, Surhada N, Ludin NA, Ibrahim MA, Sopian K, et al.
    Heliyon, 2019 Nov;5(11):e02790.
    PMID: 31768436 DOI: 10.1016/j.heliyon.2019.e02790
    Continuing trend in silicon wafer thickness directed at cost reduction approaches basic boundaries created by: (a) mismatch between Al paste and Si wafer thermal expansion and (b) incomplete optical absorption. With its symmetrical front and back electrical contacts, the bifacial solar cell setup reduces stress due to mismatch thermal expansion, decreases metal use and increases high temperature efficiency. Efficiency improvement is accomplished in bifacial solar cells by capturing light from the back surface. Partially transparent wafers provide an option to improve near-infrared radiation absorption within Si wafer. To fully absorb optical radiation, three-dimensional texture of these kinds of wafers is essential. Pulsed laser interactions, thermal oxidation, and wet chemical etching are included in this research. A feature of its energy and pattern setup is the interaction of pulsed laser with Si, running at 1.064 μm wavelength and micro-second length. Two experimental settings were explored: (a) post-laser chemical etching with potassium hydro-oxide etching with thermal oxide as etching mask and (b) post-laser heat Si surface oxidation. Due to fast melting and recrystallization, laser pulsed processing inherently produces its own texture. Some of these spherically-shaped, randomly focused characteristics improve inner scattering and boost near-infrared absorption within the wafer. These characteristics are separated during chemical etching with the thermally-grown oxide layer as an etch mask. Comparison of optical absorption in both surfaces shows almost a rise in the magnitude of absorption in non-etched surfaces. Detailed optical (optical microscope and IR absorption), morphological (field emission scanning electron microscope) and heat imaging (far IR camera) analyses were performed to comprehend physical processes that contribute to near-IR absorption improvement. Such kinds of partially-transparent, three-dimensional textured Si wafers are anticipated to discover applications for bifacial solar cells as substrates.
    Matched MeSH terms: Microscopy, Electron, Scanning
  19. Fatimah I, Prakoso NI, Sahroni I, Musawwa MM, Sim YL, Kooli F, et al.
    Heliyon, 2019 Nov;5(11):e02766.
    PMID: 31844705 DOI: 10.1016/j.heliyon.2019.e02766
    In this work, TiO2/SiO2 composite photocatalysts were prepared using biogenic silica extracted from bamboo leaves and titanium tetraisopropoxide as a titania precursor via a sol-gel mechanism. A study of the physicochemical properties of materials as a function of their titanium dioxide content was conducted using Fourier transform infrared spectroscopy, a scanning electron microscope, a diffuse reflectance ultraviolet-visible (UV-vis) spectrophotometer, and a gas sorption analyzer. The relationship between physicochemical parameters and photocatalytic performance was evaluated using the methylene blue (MB) photocatalytic degradation process under UV irradiation with and without the addition of H2O2 as an oxidant. The results demonstrated that increasing the TiO2 helps enhance the parameters of specific surface area, the pore volume, and the particle size of titanium dioxide, while the band gap energy reaches a maximum of 3.21 eV for 40% and 60% Ti content. The composites exhibit photocatalytic activity with the MB degradation with increasing photocatalytic efficiency since the composites with 40 and 60% wt. of TiO2 demonstrated the higher degradation rate compared with TiO2 in the presence and absence of H2O2. This higher rate is correlated with the higher specific surface area and band gap energy compared with those of TiO2.
    Matched MeSH terms: Microscopy, Electron, Scanning
  20. Sukor NF, Jusoh R, Kamarudin NS, Abdul Halim NA, Sulaiman AZ, Abdullah SB
    Ultrason Sonochem, 2020 Apr;62:104876.
    PMID: 31796331 DOI: 10.1016/j.ultsonch.2019.104876
    Phenolic acids of oak gall were extracted using ultrasonic-probe assisted extraction (UPAE) method in the presence of ionic liquid. It was compared with classical ultrasonic-bath assisted extraction (CUBAE) and conventional aqueous extraction (CAE) method, with and without the presence of ionic liquid. Remarkably, the UPAE method yielded two-fold higher extraction yield with the presence of ionic liquid, resulting 481.04 mg/g for gallic acids (GA) and 2287.90 mg/g for tannic acids (TA), while a decreased value of 130.36 mg/g for GA and 1556.26 mg/g for TA were resulted with the absence of ionic liquid. Intensification process resulted the highest yield of 497.34 mg/g and 2430.48 mg/g for GA and TA, respectively, extracted at temperature 50 °C with sonication intensity of 8.66 W/cm2 and 10% duty cycle, diluted in ionic liquid, 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, [Bmim][Tf2N] at concentration of 0.10 M with sample-to-solvent ratio 1:10 for 8 h. Peleg's model successfully predicted the UPAE process confirming that extraction capacity is the controlling factor in extracting phenolic acids. Hence, it can be concluded that UPAE method and ionic liquid have synergistic effect as it effectively enhanced the extraction efficiency to increase the bioactive constituents yield.
    Matched MeSH terms: Microscopy, Electron, Scanning
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