Displaying publications 21 - 40 of 92 in total

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  1. Ahmed, Al-Halemi, Jaafar, M.S.
    MyJurnal
    Radon-222 emanation from selected locally produced samples of building materials, used in Malaysia were measured using the Professional Continuous Radon Monitor Model 1027, which is a patented electronic detecting-junction photodiode sensor to measure the concentration of radon gas. Each sample was placed for 72 hours inside a 3.11 x 10 -2 m 3 sealed container. It was found that the average radon concentration Bqm -3 of air for concrete bricks, concrete brick with cemented coatings, concrete brick with cemented coatings and paint samples were, 303.7 Bq/m 3, 436.6 Bqm -3, and 410.7 Bqm -3, respectively. (Bqm -3 ) for brown clay brick, brown clay brick with cemented coatings, brown clay brick with cemented coatings and paint were 166.5 Bqm -3, 166.5 Bqm -3, and 148 Bqm -3, respectively. (Bqm -3 ) for sample of compact ceramic tile was 0 Bqm -3. The findings show that concrete brick samples are important source of radon emanation, while brown clay brick have been accepted as the recommendation of the U.S. Environmental Protection Agency (EPA), and ceramic tiles had no emanation of radon gas due to their compact surface, or the glazed layer created on the tile surface during the manufacturing process, which blocks radon emanation. A positive correlation between radon emanation and radium content has been observed for both brown clay brick and concrete brick samples whereas a negative correlation for ceramic tile has been observed. Consequently from the findings, in order to reduce radon emanation and radon exposure in house dwellings and in addition to EPA recommendation of sealed cracks and established good ventilation, we recommend concrete walls to be painted and concrete floors to be paved with ceramic tiles.
    Matched MeSH terms: Aluminum Silicates
  2. Halimah Muhamad, Nashriyah Mat, Tan, Yew Ai, Ismail, B.S.
    MyJurnal
    The adsorption equilibrium time and effects of pH and concentration of ¹⁴C-labeled chlorpyrifos
    O,O-diethyl O-(3, 5, 6 trichloro-2-pyridyl)-phosphorothiote in soil were investigated. Two types of Malaysian soil under oil palm were used in this study; namely clay loam and clay soil obtained from the Sungai Sedu and Kuala Lumpur International Airport (KLIA) Estates, respectively. Equilibrium studies of chlorpyrifos between the agricultural soil and the pesticide solution were conducted. Adsorption equilibrium time was achieved within 6 and 24 hours for clay loam and clay soil, respectively. It was found that chlorpyrifos adsorbed by the soil samples was characterized by an initial rapid adsorption after which adsorption remained approximately constant. The percentage of ¹⁴C-labeled chlorpyrifos adsorption on soil was found to be higher in clay loam than in clay soils. Results of the study demonstrated that pH affected the adsorption of chlorpyrifos on both clay loam and clay soils. The adsorption of chlorpyrifos on both types of soil was higher at low pH with the adsorption reduced as the pH increased. Results also suggest that chlorpyrifos sorption by soil is concentration dependent.
    Matched MeSH terms: Aluminum Silicates
  3. Nashriyah Mat, Mazleha Maskin, Kubiak, Roland
    MyJurnal
    The soil plant transfer coefficient or f factor of 14 C-carbofuran pesticide was studied in outdoor lysimeter experiment consisting of Brassica sp. vegetable crop, riverine alluvial clayey soil and Bungor series sandy loam soil. Soil transfer coefficients at 0-10 cm soil depth were 4.38 + 0.30, 5.76 + 1.04, 0.99 + 0.25 and 2.66 + 0.71; from 1X recommended application rate in alluvial soil, 2X recommended application rate in alluvial soil, 1X recommended application rate in Bungor soil and 2X recommended application rate in Bungor soil, respectively. At 0-25 cm soil depth, soil plant transfer coefficients were 8.96 + 0.91, 10.40 + 2.63, 2.34 + 0.68 and 6.19 + 1.40; from 1X recommended application rate in alluvial soil, 2X recommended application rate in alluvial soil, 1X recommended application rate in Bungor soil and 2X recommended application rate in Bungor soil, respectively. At 77 days after treatment (DAT), the soil plant transfer coefficient was significantly higher in riverine alluvial soil than Bungor soil whereas shoot and root growth was significantly higher in Bungor soil than in riverine alluvial soil. At both 0-10 cm Brassica sp. rooting depth and 0-25 cm soil depth, the soil plant transfer coefficient was significantly higher in 2X recommended application rate of 14 C-carbofuran as compared to 1X recommended application rate, in both Bungor and riverine alluvial soils.
    Matched MeSH terms: Aluminum Silicates
  4. Meor Yusoff, M.S., Latifah Amin
    MyJurnal
    XRF analysis was done on a local zircon samples and the result shows it has a high Fe, Th and U content. The high Fe content in Malaysian zircon had made the mineral to be classified as of a low-grade zircon. Presence of Fe in this mineral may be resulted from clay mineral coating found on the zircon surface. Chemical leaching technique was used for the removal of this Fe and the study also shows that a 600 o C heat pretreatment stage is important for the effectiveness of this process. Other parameters studied are the HCl concentration, leaching temperature and time. By using the optimum leaching parameters, the Fe content had been reduced to 0.049% and thus qualified it to be categorised as a premium grade zircon.
    Matched MeSH terms: Aluminum Silicates
  5. Mohd Basyaruddin Abdul Rahman, Uswatun Hasanah Zaidan, Mahiran Basri, Siti Salhah Othman, Raja Noor Zaliha Raja Abdul Rahman, Abu Bakar Salleh
    MyJurnal
    The land area of Tanah Putih, Gua Musang, Kelantan (Malaysia) is well-known for its wealth in industrial mineral resources, especially aluminosilicate of feldspar and mica. Natural feldspar and mica were physicochemically characterized with regard to X-ray diffraction (XRD), nitrogen sorption analysis and transmission electron microscopy (TEM) techniques for qualitative and quantitative identification of feldspar and mica. They show a good crystallinity, high surface area and uniformity of mesoporous structures. For the purpose of this experiment, the aluminosilicate of feldspar was modified either by acid treatment, or grafting the silanol groups present with various functional groups including aminopropyl-, octyl-, vinyl-, mercapto- and glycidoxy-triethoxysilanes, or activation of pre-treated support with glutaraldehyde. These support derivatives were used for further utilization in the immobilization of lipase from Candida rugosa and resulted in various interaction mechanisms between enzyme and introduced supports. It seemed that the features of the functionalized feldspar surfaces provide a preferable environmental host to enable the adsorption of lipase via interfacial adsorption method. Lipase immobilization onto feldspar support were further confirmed by scanning electron microscopy (SEM) coupled with energy dispersive X-ray microanalysis (EDX), transmission electron microscopy (TEM) and infra-red spectroscopy (FTIR) techniques. Enhancement of protein loading (up to 8.22 mg protein/g support) and immobilization yield (up to 78%) were shown by modified feldspar-lipase derivatives compared to unmodified feldspar support.
    Matched MeSH terms: Aluminum Silicates
  6. Jamaliah Sharif, Khairul Zaman Mohd Dahlan, Wan Md Zin Wan Yunus
    MyJurnal
    Effects of organoclay concentration on the properties of radiation crosslinked natural rubber (NR)/ ethylene vinyl acetate (EVA)/clay nanocomposites were investigated. The NR/EVA blend with a ratio of 40/60 was melt blended with different concentration of either dodecyl ammonium montmorillonite (DDA-MMT) or dimethyl dihydrogenated tallow quarternary ammonium montmorillonite (C20A). Composite of NR/EVA blend with unmodified clay (Na-MMT) was also prepared for comparison purposes. The composites were irradiated with electron beam (EB) at an optimum irradiation dose. The formation of radiation-induced crosslinking depends on the type and concentration of the organoclay used in the preparation of nanocomposites as measured by gel content. Changes in the interlayer distance of the silicate layers with the increase of organoclay concentration were shown by the XRD results. Variation in the tensile properties of the nanocomposites with the increase of organoclay concentration depends on the formation of crosslinking as well as reinforcement effect of the organoclay. Improvement in thermal stability of the NR/EVA blend was also observed with the presence of organoclay.
    Matched MeSH terms: Aluminum Silicates
  7. Ahmad Saat, Zaini Hamzah
    MyJurnal
    Clay has been regarded as very important natural industrial materials. All these industries exploit the properties that clay can be molded into any shape and fired to dry without losing its form. A study was carried out on clay samples from eight sites in the north-eastern part of Peninsular Malaysia. The study was accomplished by using X-ray diffraction (XRD) technique. The x-ray diffraction spectra obtained enable the determination of the lattice spacing associated with the types of clay and nonclay minerals present in the samples. Results of the study shows that the major components of clay minerals present in all samples studied are kaolinite and illite. The presence of kaolinite is confirmed by firing test in which the kaolinite diffraction peaks disappeared upon heating the samples at 600 o C. The presence of non-clay minerals such as quartz, mica, feldspar and chlorite are also observed.
    Matched MeSH terms: Aluminum Silicates
  8. Halimah Muhamad, Tan, Yew Ai, Nashriyah Mat, Ismail Sahid
    MyJurnal
    The purpose of this study was to determine the adsorption coefficient (Koc) of chlorpyrifos in clay soil by measuring the Freundlich adsorption coefficient (Kads(f)) and desorption coefficient (1/n value) of chlorpyrifos. It was found that the Freundlich adsorption coefficient (Kads(f)) and the linear regression (r 2 ) of the Freundlich adsorption isotherm for chlorpyrifos in the clay soil were 52.6 L/kg and 0.5344, respectively. Adsoprtion equilibrium time was achieved within 24 hours for clay soil. This adsoprtion equilibrium time was used to determine the effect of concentration on adsorption. The adsorption coefficient (Koc) of clay soil was found to be 2783 L/kg with an initial concentration solution of 1 µg/g, soil-solution ratio (1:5) at 30 o C when the equilibrium between the soil matrix and solution was 24 hours. The Kdes decreased over four repetitions of the desorption process. The chlorpyrifos residues may be strongly adsorbed onto the surface of clay.
    Matched MeSH terms: Aluminum Silicates
  9. Mohamed Haneef INH, Mohd Shaffiar N, Buys YF, Syed Shaharuddin SI, Abdul Hamid AM, Widiyati K
    J Biomed Mater Res B Appl Biomater, 2022 11;110(11):2574-2588.
    PMID: 35661579 DOI: 10.1002/jbm.b.35105
    Halloysite nanotubes (HNTs) have recently been the subject of extensive research as a reinforcing filler. HNT is a natural nanoclay, non-toxic and biocompatible, hence, applicable in biomedical fields. This review focuses on the mechanical, thermal, and functional properties of polymer nanocomposites with HNT as a reinforcing agent from an experimental and theoretical perspective. In addition, this review also highlights the recent applications of polymer/HNT nanocomposites in the biomedical fields.
    Matched MeSH terms: Aluminum Silicates
  10. Lisuzzo L, Cavallaro G, Pasbakhsh P, Milioto S, Lazzara G
    J Colloid Interface Sci, 2019 Jul 01;547:361-369.
    PMID: 30974251 DOI: 10.1016/j.jcis.2019.04.012
    The filling of halloysite nanotubes with active compounds solubilized in aqueous solvent was investigated theoretically and experimentally. Based on Knudsen thermogravimetric data, we demonstrated the water confinement within the cavity of halloysite. This process is crucial to properly describe the driving mechanism of halloysite loading. In addition, Knudsen thermogravimetric experiments were conducted on kaolinite nanoplates as well as on halloysite nanotubes modified with an anionic surfactant (sodium dodecanoate) in order to explore the influence of both the nanoparticle morphology and the hydrophobic/hydrophilic character of the lumen on the confinement phenomenon. The analysis of the desorption isotherms allowed us to determine the water adsorption properties of the investigated nanoclays. The pore sizes of the nanotubes' lumen was determined by combining the vapor pressure of the confined water with the nanoparticles wettability, which was studied through contact angle measurements. The thermodynamic description of the water confinement inside the lumen was correlated to the influence of the vacuum pumping in the experimental loading of halloysite. Metoprolol tartrate, salicylic acid and malonic acid were selected as anionic guest molecules for the experimental filling of the positively charged halloysite lumen. According to the filling mechanism induced by the water confinement, the vacuum operation and the reduced pressure enhanced the loading of halloysite nanotubes for all the investigated bioactive compounds. This work represents a further and crucial step for the development of halloysite based nanocarriers being that the filling mechanism of the nanotube's cavity from aqueous dispersions was described according to the water confinement process.
    Matched MeSH terms: Aluminum Silicates
  11. Ali M, Yekeen N, Pal N, Keshavarz A, Iglauer S, Hoteit H
    J Colloid Interface Sci, 2022 Feb 15;608(Pt 2):1739-1749.
    PMID: 34742087 DOI: 10.1016/j.jcis.2021.10.080
    HYPOTHESIS: Actualization of the hydrogen (H2) economy and decarbonization goals can be achieved with feasible large-scale H2 geo-storage. Geological formations are heterogeneous, and their wetting characteristics play a crucial role in the presence of H2, which controls the pore-scale distribution of the fluids and sealing capacities of caprocks. Organic acids are readily available in geo-storage formations in minute quantities, but they highly tend to increase the hydrophobicity of storage formations. However, there is a paucity of data on the effects of organic acid concentrations and types on the H2-wettability of caprock-representative minerals and their attendant structural trapping capacities.

    EXPERIMENT: Geological formations contain organic acids in minute concentrations, with the alkyl chain length ranging from C4 to C26. To fully understand the wetting characteristics of H2 in a natural geological picture, we aged mica mineral surfaces as a representative of the caprock in varying concentrations of organic molecules (with varying numbers of carbon atoms, lignoceric acid C24, lauric acid C12, and hexanoic acid C6) for 7 days. To comprehend the wettability of the mica/H2/brine system, we employed a contact-angle procedure similar to that in natural geo-storage environments (25, 15, and 0.1 MPa and 323 K).

    FINDINGS: At the highest investigated pressure (25 MPa) and the highest concentration of lignoceric acid (10-2 mol/L), the mica surface became completely H2 wet with advancing (θa= 106.2°) and receding (θr=97.3°) contact angles. The order of increasing θa and θr with increasing organic acid contaminations is as follows: lignoceric acid > lauric acid > hexanoic acid. The results suggest that H2 gas leakage through the caprock is possible in the presence of organic acids at higher physio-thermal conditions. The influence of organic contamination inherent at realistic geo-storage conditions should be considered to avoid the overprediction of structural trapping capacities and H2 containment security.

    Matched MeSH terms: Aluminum Silicates
  12. Yusof AM, Keat LK, Ibrahim Z, Majid ZA, Nizam NA
    J Hazard Mater, 2010 Feb 15;174(1-3):380-5.
    PMID: 19879040 DOI: 10.1016/j.jhazmat.2009.09.063
    The removal of ammonium from aqueous solutions using zeolite NaY prepared from a local agricultural waste, rice husk ash waste was investigated and a naturally occurring zeolite mordenite in powdered and granulated forms was used as comparison. Zeolite NaY and mordenite were well characterized by powder X-ray diffraction (XRD), energy dispersive X-ray (EDX) analysis and the total cation exchange capacity (CEC). CEC of the zeolites were measured as 3.15, 1.46 and 1.34 meq g(-1) for zeolite Y, powdered mordenite and granular mordenite, respectively. Adsorption kinetics and equilibrium data for the removal of NH(4)(+) ions were examined by fitting the experimental data to various models. Kinetic studies showed that the adsorption followed a pseudo-second-order reaction. The equilibrium pattern fits well with the Langmuir isotherm compared to the other isotherms. The monolayer adsorption capacity for zeolite Y (42.37 mg/g) was found to be higher than that powdered mordenite (15.13 mg/g) and granular mordenite (14.56 mg/g). Thus, it can be concluded that the low cost and economical rice husk ash-synthesized zeolite NaY could be a better sorbent for ammonium removal due to its rapid adsorption rate and higher adsorption capacity compared to natural mordenite.
    Matched MeSH terms: Aluminum Silicates/chemistry*
  13. Mishra RK, Ramasamy K, Lim SM, Ismail MF, Majeed AB
    J Mater Sci Mater Med, 2014 Aug;25(8):1925-39.
    PMID: 24831081 DOI: 10.1007/s10856-014-5228-y
    The present study investigates the development of methyl cellulose (MC)-sodium alginate (SA)-montmorillonite (MMT) clay based bionanocomposite films with interesting wound healing properties. The differential scanning calorimetry analysis of the composite films revealed presence of single glass transition temperature (Tg) confirming the miscible nature of the ternary blended films. The increase in MMT ratio in the composite films reduced the mobility of biopolymer chains (MC/SA) which increased the Tg of the film. Thermogravimetric analysis showed that dispersion of clay (MMT) at nano level significantly delayed the weight loss that correlated with higher thermal stability of the composite films. It was observed that the developed films were able to exhibit antimicrobial activity against four typical pathogenic bacteria found in the presence of wound. The developed films were able to significantly inhibit (10 mg/ml) the growth of Enterococcus faecium and Pseudomonas aeruginosa. In vitro scratch assay indicated potential wound closure activities of MC-2-4 bionanocomposite films at their respective highest subtoxic doses. In conclusion, these ternary bionanocomposite films were found to be promising systems for wound healing applications.
    Matched MeSH terms: Aluminum Silicates*
  14. Adzmi F, Meon S, Musa MH, Yusuf NA
    J Microencapsul, 2012;29(3):205-10.
    PMID: 22309479 DOI: 10.3109/02652048.2012.659286
    Microencapsulation is a process by which tiny parcels of an active ingredient are packaged within a second material for the purpose of shielding the active ingredient from the surrounding environment. This study aims to determine the ability of the microencapsulation technique to improve the viability of Trichoderma harzianum UPM40 originally isolated from healthy groundnut roots as effective biological control agents (BCAs). Alginate was used as the carrier for controlled release, and montmorillonite clay (MMT) served as the filler. The encapsulated Ca-alginate-MMT beads were characterised using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). The FTIR results showed the interaction between the functional groups of alginate and MMT in the Ca-alginate-MMT beads. Peaks at 1595, 1420 and 1020 cm(-1) characterised alginate, and peaks at 1028 and 453 cm(-1) characterised MMT; both sets of peaks appeared in the Ca-alginate-MMT FTIR spectrum. The TGA analysis showed an improvement in the thermal stability of the Ca-alginate-MMT beads compared with the alginate beads alone. SEM analysis revealed a homogeneous distribution of the MMT particles throughout the alginate matrix. T. harzianum UPM40 was successfully encapsulated in the Ca-alginate-MMT beads. Storage analysis of the encapsulated T. harzianum UPM40 showed that the low storage temperature of 5°C resulted in significantly (p 
    Matched MeSH terms: Aluminum Silicates
  15. Al-Maqtari AA, Lui JL
    J Prosthodont, 2010 Jul;19(5):347-56.
    PMID: 20456026 DOI: 10.1111/j.1532-849X.2010.00593.x
    The purpose of this in vitro study was to determine if packable resin composite with/without flowable resin composite has the ability to prevent coronal leakage in restored endodontic access openings following aging.
    Matched MeSH terms: Aluminum Silicates/chemistry
  16. Zal U’yun Wan Mahmood, Zaharudin Ahmad, Che Abd Rahim Mohamed, Abdul Kadir Ishak, Norfaizal Mohammed
    MyJurnal
    The distribution, enrichment and pollution status of metals in sediment cores from the Sabah-Sarawak coastal waters were studied. Seven sediment cores were taken in July 2004 using a gravity box corer. The metals of Cu, Zn and Pb were analyzed by ICP-MS to assess the pollution status of the sediments. The sediment fine fraction and organic carbon content was also analyzed. Enrichment Factor (EF), Geoaccumulation Index (Igeo) and Pollution Load Index (PLI) was calculated as criteria of possible contamination. The results showed that collected sediments were composed with clay, silt and sand as 12 – 74%, 27 – 72% and 0 – 20%, respectively. Meanwhile, organic carbon contents were relatively low and constant over time, based on sediment depth profiles, and it did not exceed 5% at any sampling station. The average metal concentrations in sediment cores at all sampling station were distributed in the ranges of 1.66 ± 1.36 – 6.61 ± 0.12 μgg-1 for Cu, 26.55 ± 1.04 – 57.94 ± 1.58 μgg-1 for Zn and 3.99 ± 0.10 – 14.48 ± 0.32μgg-1 for Pb. According to calculations of EF, Igeo and PLI, it can be concluded that concentrations of Cu, Zn and Pb were not significantly affected by pollution from anthropogenic sources at the seven sampling locations. Thus, the metal content of Cu, Zn and Pb in sediment should not cause pollution problem to the marine environment of Sabah-Sarawak coastal waters and further response measures are not needed.
    Matched MeSH terms: Aluminum Silicates
  17. Mohajerani A, Burnett L, Smith JV, Kurmus H, Milas J, Arulrajah A, et al.
    Materials (Basel), 2019 Sep 20;12(19).
    PMID: 31547011 DOI: 10.3390/ma12193052
    Nanoparticles are defined as ultrafine particles sized between 1 and 100 nanometres in diameter. In recent decades, there has been wide scientific research on the various uses of nanoparticles in construction, electronics, manufacturing, cosmetics, and medicine. The advantages of using nanoparticles in construction are immense, promising extraordinary physical and chemical properties for modified construction materials. Among the many different types of nanoparticles, titanium dioxide, carbon nanotubes, silica, copper, clay, and aluminium oxide are the most widely used nanoparticles in the construction sector. The promise of nanoparticles as observed in construction is reflected in other adoptive industries, driving the growth in demand and production quantity at an exorbitant rate. The objective of this study was to analyse the use of nanoparticles within the construction industry to exemplify the benefits of nanoparticle applications and to address the short-term and long-term effects of nanoparticles on the environment and human health within the microcosm of industry so that the findings may be generalised. The benefits of nanoparticle utilisation are demonstrated through specific applications in common materials, particularly in normal concrete, asphalt concrete, bricks, timber, and steel. In addition, the paper addresses the potential benefits and safety barriers for using nanomaterials, with consideration given to key areas of knowledge associated with exposure to nanoparticles that may have implications for health and environmental safety. The field of nanotechnology is considered rather young compared to established industries, thus limiting the time for research and risk analysis. Nevertheless, it is pertinent that research and regulation precede the widespread adoption of potentially harmful particles to mitigate undue risk.
    Matched MeSH terms: Aluminum Silicates
  18. Jamil NH, Abdullah MMAB, Pa FC, Mohamad H, Ibrahim WMAW, Amonpattaratkit P, et al.
    Materials (Basel), 2021 Mar 10;14(6).
    PMID: 33801862 DOI: 10.3390/ma14061325
    Kaolin, theoretically known as having low reactivity during geopolymerization, was used as a source of aluminosilicate materials in this study. Due to this concern, it is challenging to directly produce kaolin geopolymers without pre-treatment. The addition of ground granulated blast furnace slag (GGBS) accelerated the geopolymerization process. Kaolin-GGBS geopolymer ceramic was prepared at a low sintering temperature due to the reaction of the chemical composition during the initial stage of geopolymerization. The objective of this work was to study the influence of the chemical composition towards sintering temperature of sintered kaolin-GGBS geopolymer. Kaolin-GGBS geopolymer was prepared with a ratio of solid to liquid 2:1 and cured at 60 °C for 14 days. The cured geopolymer was sintered at different temperatures: 800, 900, 1000, and 1100 °C. Sintering at 900 °C resulted in the highest compressive strength due to the formation of densified microstructure, while higher sintering temperature led to the formation of interconnected pores. The difference in the X-ray absorption near edge structure (XANES) spectra was related to the phases obtained from the X-ray diffraction analysis, such as akermanite and anothite. Thermal analysis indicated the stability of sintered kaolin-GGBS geopolymer when exposed to 1100 °C, proving that kaolin can be directly used without heat treatment in geopolymers. The geopolymerization process facilitates the stability of cured samples when directly sintered, as well as plays a significant role as a self-fluxing agent to reduce the sintering temperature when producing sintered kaolin-GGBS geopolymers.
    Matched MeSH terms: Aluminum Silicates
  19. Faris MA, Abdullah MMAB, Muniandy R, Abu Hashim MF, Błoch K, Jeż B, et al.
    Materials (Basel), 2021 Mar 09;14(5).
    PMID: 33803313 DOI: 10.3390/ma14051310
    Geopolymer concrete has the potential to replace ordinary Portland cement which can reduce carbon dioxide emission to the environment. The addition of different amounts of steel fibers, as well as different types of end-shape fibers, could alter the performance of geopolymer concrete. The source of aluminosilicate (fly ash) used in the production of geopolymer concrete may lead to a different result. This study focuses on the comparison between Malaysian fly ash geopolymer concrete with the addition of hooked steel fibers and geopolymer concrete with the addition of straight-end steel fibers to the physical and mechanical properties. Malaysian fly ash was first characterized by X-ray fluorescence (XRF) to identify the chemical composition. The sample of steel fiber reinforced geopolymer concrete was produced by mixing fly ash, alkali activators, aggregates, and specific amounts of hook or straight steel fibers. The steel fibers addition for both types of fibers are 0%, 0.5%, 1.0%, 1.5%, and 2.0% by volume percentage. The samples were cured at room temperature. The physical properties (slump, density, and water absorption) of reinforced geopolymer concrete were studied. Meanwhile, a mechanical performance which is compressive, as well as the flexural strength was studied. The results show that the pattern in physical properties of geopolymer concrete for both types of fibers addition is almost similar where the slump is decreased with density and water absorption is increased with the increasing amount of fibers addition. However, the addition of hook steel fiber to the geopolymer concrete produced a lower slump than the addition of straight steel fibers. Meanwhile, the addition of hook steel fiber to the geopolymer concrete shows a higher density and water absorption compared to the sample with the addition of straight steel fibers. However, the difference is not significant. Besides, samples with the addition of hook steel fibers give better performance for compressive and flexural strength compared to the samples with the addition of straight steel fibers where the highest is at 1.0% of fibers addition.
    Matched MeSH terms: Aluminum Silicates
  20. Channa IA, Chandio AD, Rizwan M, Shah AA, Bhatti J, Shah AK, et al.
    Materials (Basel), 2021 May 12;14(10).
    PMID: 34065936 DOI: 10.3390/ma14102496
    Organic photovoltaics (OPVs) die due to their interactions with environmental gases, i.e., moisture and oxygen, the latter being the most dangerous, especially under illumination, due to the fact that most of the active layers used in OPVs are extremely sensitive to oxygen. In this work we demonstrate solution-based effective barrier coatings based on composite of poly(vinyl butyral) (PVB) and mica flakes for the protection of poly (3-hexylthiophene) (P3HT)-based organic solar cells (OSCs) against photobleaching under illumination conditions. In the first step we developed a protective layer with cost effective and environmentally friendly methods and optimized its properties in terms of transparency, barrier improvement factor, and bendability. The developed protective layer maintained a high transparency in the visible region and improved oxygen and moisture barrier quality by the factor of ~7. The resultant protective layers showed ultra-flexibility, as no significant degradation in protective characteristics were observed after 10 K bending cycles. In the second step, a PVB/mica composite layer was applied on top of the P3HT film and subjected to photo-degradation. The P3HT films coated with PVB/mica composite showed improved stability under constant light irradiation and exhibited a loss of <20% of the initial optical density over the period of 150 h. Finally, optimized barrier layers were used as encapsulation for organic solar cell (OSC) devices. The lifetime results confirmed that the stability of the OSCs was extended from few hours to over 240 h in a sun test (65 °C, ambient RH%) which corresponds to an enhanced lifetime by a factor of 9 compared to devices encapsulated with pristine PVB.
    Matched MeSH terms: Aluminum Silicates
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