Dalam kertas ini dibentangkan hasil kajian sifat fizikal dan terma komposit elektrolit berasaskan samarium terdop seria (Ce0.8Sm0.2O1.9, SDC) dan karbonat (67%mol Li2CO3/ 33%mol Na2CO3). Komposit SDC-(Li/Na)2CO3 adalah pengalir berion yang berpotensi digunakan sebagai bahan elektrolit sel fuel oksida pepejal bersuhu rendah (LT-SOFC). Pencirian komposit elektrolit ini meliputi morfologi, luas permukaan bahan, analisis terma dan keliangan pelet elektrolit. Komposit elektrolit SDC-(Li/Na)2CO3 disediakan dalam dua langkah: (1) penyediaan serbuk samarium terdop seria melalui kaedah sol-gel dan (2) pencampuran samarium terdop seria dan karbonat dalam pelbagai komposisi yang berbeza melalui kaedah tindak balas keadaan pepejal. Pelet elektrolit dihasilkan dengan tekanan mampatan 25, 50, 150 and 200 MPa pada suhu pensinteran 500, 600, 700 dan 800oC. Keputusan XRD menunjukkan bahawa penambahan karbonat tidak mengubah struktur fasa SDC. Keputusan FESEM menunjukkan bahawa sebatian karbonat adalah amorfus dan tersebar dengan baik dalam matriks SDC. Semakin tinggi kandungan karbonat dalam komposit, luas permukaan serbuk komposit didapati semakin kecil. Keputusan analisis terma menunjukkan bahawa takat lebur fasa karbonat berkurang dengan berkurangnya kandungan karbonat. Keliangan optimum yang sesuai bagi elektrolit LT-SOFC iaitu 3.38% dan 4.85% telah dicapai masing-masing untuk sampel dengan kandungan karbonat 20% (SDC8020) dan 30% (SDC7030) dengan suhu pensinteran 600oC dan tekanan mampatan 200 MPa.
The challenge in front of EDLC device is their low energy density compared to their battery counter parts. In the current study, a green plasticized nanocomposite sodium ion conducting polymer blend electrolytes (PNSPBE) was developed by incorporating plasticized Chitosan (CS) blended with polyvinyl alcohol (PVA), doped with NaBr salt with various concentration of CaTiO3 nanoparticles. The most optimized PNSPBE film was subsequently utilized in an EDLC device to evaluate its effectiveness both as an electrolyte and a separator. Structural and morphological changes were assessed using XRD and SEM techniques. The PNSPBE film demonstrated a peak ionic conductivity of 9.76×10-5 S/cm, as determined through EIS analysis. The dielectric and AC studies provided further confirmation of structural modifications within the sample. Both TNM and LSV analyses affirmed the suitability of the prepared electrolyte for energy device applications, evidenced by its adequate ion transference number and an electrochemical potential window of 2.86 V. Electrochemical properties were assessed via CV and GCD techniques, confirming non-Faradaic ion storage, indicated by the rectangular CV pattern at low scan rates. The parameters associated with the designed EDLC device including specific capacitance, ESR, power density (1950 W/kg) and energy density (12.3 Wh/kg) were determined over 1000 cycles.
Hydrogeochemical investigations had been carried out at the Amol-Babol Plain in the north of Iran. Geochemical processes and factors controlling the groundwater chemistry are identified based on the combination of classic geochemical methods with geographic information system (GIS) and geostatistical techniques. The results of the ionic ratios and Gibbs plots show that water rock interaction mechanisms, followed by cation exchange, and dissolution of carbonate and silicate minerals have influenced the groundwater chemistry in the study area. The hydrogeochemical characteristics of groundwater show a shift from low mineralized Ca-HCO3, Ca-Na-HCO3, and Ca-Cl water types to high mineralized Na-Cl water type. Three classes, namely, C1, C2, and C3, have been classified using cluster analysis. The spatial distribution maps of Na(+)/Cl(-), Mg(2+)/Ca(2+), and Cl(-)/HCO3 (-) ratios and electrical conductivity values indicate that the carbonate and weathering of silicate minerals played a significant role in the groundwater chemistry on the southern and western sides of the plain. However, salinization process had increased due to the influence of the evaporation-precipitation process towards the north-eastern side of the study area.
A series of batch laboratory studies were conducted to investigate the suitability of activated carbon SA2 for the removal of cadmium ions and zinc ions from their aqueous solutions. The single component equilibrium data were analyzed using the Langmuir and Freundlich isotherms. Overall, the Langmuir isotherm showed a better fitting for all adsorptions under investigation in terms of correlation coefficient and error analysis (SSE only 18.2 for Cd2+ and 47.95 for Zn2+). As the binary adsorption is competitive, extended Langmuir models could not predict the binary component isotherm well. The modified extended Langmuir models were used to fit the binary system equilibrium data. The binary isotherm data could be described reasonably well by the modified
extended Langmuir model, as indicated in the error analysis.
Phytoremediation is considered as a cost-effective and environmentally friendly
technique for decontaminating environments that have been contaminated with
heavy metal ions. The technique describes the use of plants and their concomitant
microbes to mitigate environmental contaminations. However, conventional
remediation techniques like chemical, thermal and physical treatment methods are
too costly, and may end of causing more contamination to the environment.
Phytoremediation practice provides a major information on the utilization of plants
and their materials in decontaminating polluted environments. Heavy metals and
other organic contaminants are among the most precarious substances released into
the environment which have an eminent level of toxicity and sturdiness of both
aquatic and terrestrial organisms. The review aimed at providing a broad
understanding of utilizing various plants and their materials in decontaminating
polluted environments with heavy metals and other organic contaminants. It also
provided the general methods used in treating the aforementioned contaminants in
an environment. The review further discussed the classes of phytoremediation like
phytoextraction, phytovolatilisation, phytostabilization, phytotransformation,
phytodegradation and phytofiltration. The generalized advantages and disadvantages
of phytoremediation were ultimately highlighted.
This review critically examines the effectiveness of ion-imprinted membranes (IIMs) in selectively recovering lithium (Li) from challenging sources such as seawater and brine. These membranes feature customized binding sites that specifically target Li ions, enabling selective separation from other ions, thanks to cavities shaped with crown ether or calixarene for improved selectivity. The review thoroughly investigates the application of IIMs in Li extraction, covering extensive sections on 12-crown-4 ether (a fundamental crown ether for Li), its modifications, calixarenes, and other materials for creating imprinting sites. It evaluates these systems against several criteria, including the source solution's complexity, Li+ concentration, operational pH, selectivity, and membrane's ability for regeneration and repeated use. This evaluation places IIMs as a leading-edge technology for Li extraction, surpassing traditional methods like ion-sieves, particularly in high Mg2+/Li+ ratio brines. It also highlights the developmental challenges of IIMs, focusing on optimizing adsorption, maintaining selectivity across varied ionic solutions, and enhancing permselectivity. The review reveals that while the bulk of research is still exploratory, only a limited portion has progressed to detailed lab verification, indicating that the application of IIMs in Li+ recovery is still at an embryonic stage, with no instances of pilot-scale trials reported. This thorough review elucidates the potential of IIMs in Li recovery, cataloging advancements, pinpointing challenges, and suggesting directions for forthcoming research endeavors. This informative synthesis serves as a valuable resource for both the scientific community and industry professionals navigating this evolving field.
The modification of jet shapes in Pb-Pb collisions, relative to those in pp collisions, is studied for jets associated with an isolated photon. The data were collected with the CMS detector at the LHC at a nucleon-nucleon center-of-mass energy of 5.02 TeV. Jet shapes are constructed from charged particles with track transverse momenta (p_{T}) above 1 GeV/c in annuli around the axes of jets with p_{T}^{jet}>30 GeV/c associated with an isolated photon with p_{T}^{γ}>60 GeV/c. The jet shape distributions are consistent between peripheral Pb-Pb and pp collisions, but are modified for more central Pb-Pb collisions. In these central Pb-Pb events, a larger fraction of the jet momentum is observed at larger distances from the jet axis compared to pp, reflecting the interaction between the partonic medium created in heavy ion collisions and the traversing partons.
Charge-dependent azimuthal particle correlations with respect to the second-order event plane in p-Pb and PbPb collisions at a nucleon-nucleon center-of-mass energy of 5.02 TeV have been studied with the CMS experiment at the LHC. The measurement is performed with a three-particle correlation technique, using two particles with the same or opposite charge within the pseudorapidity range |η|<2.4, and a third particle measured in the hadron forward calorimeters (4.4
The main objectives of this study are to synthesize a new solid-supported ionic liquid (SSIL) that has a covalent bond between the solid support, i.e., activated silica gel, with thiosalicylate-based ionic liquid and to evaluate the performance of this new SSIL as an extractant, labelled as Si-TS-SSIL, and to remove Pb(II) ions from an aqueous solution. In this study, 1-methyl-3-(3-trimethoxysilylpropyl) imidazolium thiosalicylate ([MTMSPI][TS]) ionic liquid was synthesized and the formation of [MTMSPI][TS] was confirmed through structural analysis using NMR, FTIR, IC, TGA, and Karl Fischer Titration. The [MTMSPI][TS] ionic liquid was then chemically immobilized on activated silica gel to produce a new thiosalicylate-based solid-supported ionic liquid (Si-TS-SSIL). The formation of these covalent bonds on Si-TS-SSIL was confirmed by solid-state NMR analysis. Meanwhile, BET analysis was performed to study the surface area of the activated silica gel and the prepared Si-TS-SSIL (before and after washing with solvent) with the purpose to show that all physically immobilized [MTMSPI][TS] has been washed off from Si-TS-SSIL, leaving only chemically immobilized [MTMSPI][TS] on Si-TS-SSIL before proceeding with removal study. The removal study of Pb(II) ions from an aqueous solution was carried out using Si-TS-SSIL as an extractant, whereby the amount of Pb(II) ions removed was determined by AAS. In this removal study, the experiments were carried out at a fixed agitation speed (400 rpm) and fixed amount of Si-TS-SSIL (0.25 g), with different contact times ranging from 2 to 250 min at room temperature. The maximum removal capacity was found to be 8.37 mg/g. The kinetics study was well fitted with the pseudo-second order model. Meanwhile, for the isotherm study, the removal process of Pb(II) ions was well described by the Freundlich isotherm model, as this model exhibited a higher correlation coefficient (R2), i.e., 0.99, as compared to the Langmuir isotherm model.
A detailed overview toward the advancement of amino acid-based electrochemical sensors on the detection of heavy metals is presented. Discussion is focused on the unique properties of various amino acids (AAs) and its composites which allow them being employed in a diverse range of sensing platforms. Formation of metal-ligand complexes in between metal ions and different AAs has been discussed. The essential insights on the interaction between amino acid-based sensors and target heavy metal ions (HMIs) are provided, along with the discussion on their pros and cons. Voltammetry analysis of metal ions based on various interfaces of electrochemical sensors has been highlighted, together with the incorporation of AAs with organic, inorganic and bio-materials. In all these cases, the amino acid modified electrodes have demonstrated large active surface area with abundant adsorption sites for HMIs. The developed sensors are promising for environmental applications, as evidenced by the high selectivity, high sensitivity, high catalytic activity, and low detection limits. The materials involved, fabrication techniques and its sensing mechanism were comprehensively discussed, and the future outlooks of electrochemical sensing platforms are emphasized in this review.
Charged particle therapy with carbon ions has advantages over conventional radiotherapy using x-ray beams. The application of charged particle therapy has rapidly increased over the last decades. This is due to its characteristic Bragg peak which has relatively low entrance doses and favourable doses distribution. In this research work, Geant4 based Monte Carlo simulation (MC) method has been used to calculate the radiation transportation and dose distributions in tissue-like media. The main objective of the work was to compare the Geant4 simulated depth dose distributions with experimental measurements and verify the capability of the geant4 simulation toolkit. The carbon ion beams for the therapeutic energy of 350 MeV/u and 400 MeV/u respectively were simulated, with the same settings as the experimental work carried out at the treatment room at Heavy Ion Medical Accelerator (HIMAC), National Institute of Radiological Sciences (NIRS), Chiba, Japan. The simulation results were verified with measurements data. The work was to measure the accuracy and quality of the dose distributions by Geant4 MC methods. The results show that the Bragg peak and spread out Bragg peak (SOBP) distributions in simulation has fairly good agreement with measurements.
Solid polymer blend electrolyte membranes (SPBEM) composed of chitosan and dextran with the incorporation of various amounts of lithium perchlorate (LiClO4) were synthesized. The complexation of the polymer blend electrolytes with the salt was examined using FTIR spectroscopy and X-ray diffraction (XRD). The morphology of the SPBEs was also investigated using field emission scanning electron microscopy (FESEM). The ion transport behavior of the membrane films was measured using impedance spectroscopy. The membrane with highest LiClO4 content was found to exhibit the highest conductivity of 5.16 × 10-3 S/cm. Ionic (ti) and electronic (te) transference numbers for the highest conducting electrolyte were found to be 0.98 and 0.02, respectively. Electrochemical stability was estimated from linear sweep voltammetry and found to be up to ~2.3V for the Li+ ion conducting electrolyte. The only existence of electrical double charging at the surface of electrodes was evidenced from the absence of peaks in cyclic voltammetry (CV) plot. The discharge slope was observed to be almost linear, confirming the capacitive behavior of the EDLC. The performance of synthesized EDLC was studied using CV and charge-discharge techniques. The highest specific capacitance was achieved to be 8.7 F·g-1 at 20th cycle. The efficiency (η) was observed to be at 92.8% and remained constant at 92.0% up to 100 cycles. The EDLC was considered to have a reasonable electrode-electrolyte contact, in which η exceeds 90.0%. It was determined that equivalent series resistance (Resr) is quite low and varies from 150 to 180 Ω over the 100 cycles. Energy density (Ed) was found to be 1.21 Wh·kg-1 at the 1st cycle and then remained stable at 0.86 Wh·kg-1 up to 100 cycles. The interesting observation is that the value of Pd increases back to 685 W·kg-1 up to 80 cycles.
This work presents some comments concerning the paper entitled 'Lattice Boltzmann simulation of alumina-water nanofluid in a square cavity' by Yurong He, Cong Qi, Yanwei Hu, Bin Qin, Fengchen Li and Yulong Ding which was published in Nanoscale Research Letters in 2011. The comments are related to the numerical parameters and the computed results of average Nusselt number.
In the title compound, [SbCl(2)(C(4)H(8)N(2)S)(2)]Cl, the coordination around the Sb atom can be described as distorted pseudo-octahedral. Both rings of the trimethylenethiourea ligands [alternatively 3,4,5,6-tetrahydropyrimidine-2(1H)-thione] adopt an envelope conformation. The molecules are connected into dimers in the ab plane by two intermolecular hydrogen bonds. The dimers are arranged into infinite one-dimensional chains along the a axis as a result of the Cl(-) ions forming intermolecular hydrogen bonds with three NH groups.
A study was carried out to determine the chemical composition of bulk precipitation, throughfall and stemflow in an urban forest in Kuala Lumpur, Malaysia. The mean weekly rainfall recorded during the period of study was 63.2 mm. Throughfall, stemflow and canopy interception of incident precipitation were 77.1%, 1.2% and 21.7% respectively. Bulk precipitation, througfall and stemflow were acidic, the pH recorded being 4.37, 4.71 and 4.15 respectively. In all cases the dominant ions were NO3, SO4, Cl, NH4, K, Ca and Na. Of the ions studied Ca, K, Cl, SO4, Mg and Mn showed net increases in passing through the forest canopy, while NH4, Na, NO3, Zn, H and Fe showed net retention. This study shows that the urban environment of Kuala Lumpur contributes considerable amounts of materials to the atmosphere, as reflected by the high ionic contents in bulk precipitation, throughfall and stemflow.
Analisis geokimia menggunakan kaedah ICP-MS menunjukkan taburan geokimia unsur di kawasan kajian dipengaruhi
oleh dua asalan sedimen berbeza iaitu daripada marin dan daratan. Unsur Ca dan Mg dikenal pasti sebagai unsur
marin, manakala unsur Al, Fe, Mn, Na, Cu, Cr, Zn dan Ni dikenal pasti sebagai unsur daratan. Unsur Ca dan Mg dikenal
pasti terhasil daripada proses penyahkapuran rangka dan hidupan marin seperti cengkerang moluska dan foraminifera.
Unsur benua berasal daripada granit dari Gunung Korbu dan Gunung Stong yang disaliri oleh Sungai Nenggiri dan
Sungai Galas, serta batuan argilit arenit yang berasal dari bahagian selatan dan tenggara Negeri Kelantan dari
Gunung Cintawangsa dan Gunung Stong dan disaliri oleh Sungai Lebir dan Sungai Galas. Unsur daripada batuan
induk membebaskan unsur kimia semasa luluhawa kimia dan telah dijerap oleh cas-cas negatif pada permukaan sedimen
halus seperti lempung dan lodak sebelum dimendapkan bersama di dalam kawasan kajian.
Type of bond is vital to understand the mechanism of interaction between corresponds atoms. We used three kinds of method
to determine the type of bond between diatomic cluster of platinum and hydrogen: types of element, electronegativity
and electron distribution. In this work, we found that the results from these three methods are not unanimously agreed
with each other for bond type forming in platinum-hydrogen diatomic cluster. Thus, we conclude that the type of bond
is hybrid of both: mainly covalent and slightly ionic.
Ionic polymer-metal composites (IPMC) are smart material transducers that bend in response to low-voltage stimuli and generate voltage in response to bending. IPMCs are mechanically compliant, simple in construction, and easy to cut into desired shape. This allows the designing of novel sensing and actuation systems, e.g., for soft and bio-inspired robotics. IPMC sensing can be implemented in multiple ways, resulting in significantly different sensing characteristics. This paper will review the methods and research efforts to use IPMCs as deformation sensors. We will address efforts to model the IPMC sensing phenomenon, and implementation and characteristics of different IPMC sensing methods. Proposed sensing methods are divided into active sensing, passive sensing, and self-sensing actuation (SSA), whereas the active sensing methods measure one of IPMC-generated voltage, charge, or current; passive methods measure variations in IPMC impedances, or use it in capacitive sensor element circuit, and SSA methods implement simultaneous sensing and actuation on the same IPMC sample. Frequency ranges for reliable sensing vary among the methods, and no single method has been demonstrated to be effective for sensing in the full spectrum of IPMC actuation capabilities, i.e., from DC to ∼100 Hz. However, this limitation can be overcome by combining several sensing methods.
There is limited information on the optimal processes to remove heavy metals in greywater. A Response Surface Methodology (RSM) via the Box-Behnken Design (BBD) approach was applied in this study to investigate and optimise the process variables of activation time (1.5-2.5 h), impregnation ratio (0.25-0.75) and zinc chloride (ZnCl2) percentage (20-60%) for the removal of heavy metal ions (Cd, Cu, Pb and Ni) associated with greywater treatment. The quadratic model was chosen to describe the effects of the process variables (activation time, impregnation ratio, ZnCl2 percentage) on predicting the responses (heavy metal ions removal) with low p-values (
Battery Monitoring System (BMoS) is an electronic system that monitors rechargeable battery cells or packs with various parameters, such as battery voltage, current and State-of-Charge (SoC). This system can be used to avoid overcharging or over-discharging of batteries to increase its shelf life. However, BMoS on the market is very expensive and not suitable for low cost embedded systems. As the Arduino Uno is widely used for low cost microcontroller boards, easy programming environment, and open-source platforms for building electronic projects, therefore, this study focuses on Arduino Uno BMoS based system. This system consists of current and voltage sensors, an Arduino Uno microcontroller and a liquid crystal display (LCD). In order to develop this system, there are three objectives to be achieved. First, the relationship between input and output of the sensors must be derived mathematically. The mathematical expression obtained can be verified by connecting and disconnecting the circuit with load and monitoring the value of output sensors. Then, a complete prototype of the BMoS was developed by connecting the LCD, current and voltage sensors to the Arduino Uno microcontroller. The complete prototype was tested using an 11.1 V of Lithium-ion battery and a DC motor as a load. From the results, the current sensor shows zero value when no load is connected as no current flow. The LCD also displays 11.1V of battery voltage when fully charged. Using the developed system, the user can monitor the current, the voltage and the SoC of the battery to ensure the battery is not overcharged and overused. The development of the BMoS can help to monitor the operation and performance of the batteries in any electronic systems. At the end of this study, the complete BMoS prototype gives benefits to the user and makes work easier.