Solid polymer electrolyte based on methyl cellulose (MC)-lithium triflate (LiCF3SO3) plasticised with ethylene carbonate (EC) was prepared using solution cast technique. The X-ray diffraction (XRD) studies proved that the amorphous nature of the electrolyte systems was increases due to the addition of salt and plasticiser. The improved surface morphology of plasticised polymer system ensures it has good electrode-electrolyte contact during performance testing. The polymer electrolyte was found to have high thermal stability indicating that the electrolyte can be used at higher temperature. The ionic conductivity increased up to 1.24 x 10-4 S cm-1 at optimum amount of EC plasticiser associated to the effect of plasticiser that initially leads to the formation of Li+-EC complex. Consequently, it reduces the fraction of polymer-Li+ complex which contributes to the increase of the segmental chain flexibility in the plasticized system. Temperature dependent studies indicate ionic conductivity increase due to the temperature increase and is in line with Arrhenius behaviour pattern. An activation energy of 0.26 eV at highest conductivity sample was obtained. The addition of plasticiser lowers the activation energy thus increasing the ion mobility of the system and contributing to ionic conductivity increment. The plasticization method is a promising means to dealing with the solid polymer electrolyte problem and producing electrolytes that meet the needs of electrochemical devices.
The discharge of electroplating waste containing nickel ions has led to environmental issues owing to the toxicity problem mainly to the aquatic organisms and humans. Liquid-liquid extraction offers a great potential treatment for nickel removal with several advantages of simple, high efficiency and high separation factor. In this study, a green synergistic liquid-liquid extraction of nickel ions from electroplating waste solution using chelating oxime (LIX63) and organophosphorus (D2EHPA) carriers individually as well as their synergistic mixture has been studied. The result demonstrated that about 83% of nickel ions have been successfully extracted via the mixture system of 0.08M LIX63 +0.02M D2EHPA with the maximum synergistic enhancement factor, Rmax of 29.56. Meanwhile, the back extraction study also revealed that HNO3 was the most suitable stripping agent while the diluent screening also showed that palm oil has high potential to be incorporated as a diluent in the green synergistic liquid-liquid extraction of nickel.
This paper contains data from the elemental and phytochemical profiling of black pepper oleoresin extracts using the LC-MS QToF and ICP-MS analysis. In recent years studies have shown the medicinal properties of extracts from these two cultivars of Piper nigrum. The medicinal properties are attributed to the presence of many secondary metabolites and mineral element in them. The phytochemical profiling was conducted using a Liquid Chromatography equipped with an electrospray time-of-flight mass spectrometer detectors. The mass spectrometer was equipped with an electrospray ionization sources operated in positive ion mode. The alkaloid compounds in the optimized black pepper extract were tentatively characterized in accordance with their ions׳ mass fragmentation.
The paper presents the results of ample investigations performed on industrial and traditional ceramics of fired clay used in processes of water potabilization in the last stage of filtration, after that of active charcoal. Using the data obtained through the scanning electron microscope coupled with energy dispersive X-ray analysis (SEM-EDX) and pH analyses, on the basis of the atomic composition and free concentration of hydronium ions, the normal caustic (Si/Al) and summative [(Si+Ti+FeIII+Cl)/(Al+Ca+Mg+Na+K)] modules were assessed, which were correlated with the free acidity and, respectively, the capacity of absorption and ionic exchange of the Fe3+ and Al3+ ions. The study allowed the selection, on the basis of the caustic module, of the ceramics with high capacity for ionic exchange.
In this work, epoxidized natural rubber 50 (ENR-50) has been used as a host polymer for the preparation of electrolyte system. Attenuated total reflection-fourier transform infrared spectroscopic analyses showed the presence of lithium saltENR interactions. The glass transition temperature displayed an increasing trend with the increase in salt concentration indicating that the ionic conductivity was not influenced by segmental motion of the ENR-50 chains. The increase in
glass transition temperature with the addition of salt was due to the formation of transient cross-linking between ENR-50 chains via the coordinated interaction between ENR-50 chains and salt. The highest room temperature ionic conductivity obtained was in the order of 10-5 S cm-1 for the film containing 50 wt% of lithium salt. The ionic conductivity of this electrolyte system increased with increasing temperature and obeyed the Vogel-Tamman-Fulcher behavior. The increase in ionic conductivity of the electrolyte system with salt concentration could also be correlated to the charge carriers concentration and/or migration rate of charge carriers.
This paper is focussed on conductivity and dielectric properties of Poly (vinyl) chloride (Pvc)- ammonium triflate (NH4CF3SO3) - butyltrimethyl ammonium bis (trifluoromethyl sulfonyl) imide (Bu3MeNTf2N) ionic liquid, electrolyte system. The electrolyte is prepared by solution cast technique. In this work, the sample containing 30 wt. % NH4CF3SO3 exhibits the highest room temperature conductivity of 2.50 x 10-7 S cm' . Ionic liquid is added in various quantities to the 70 wt. % Pvc-30 wt. % NH4CF3SO3 composition in order to enhance the conductivity of the sample. The highest conductivity at room temperature is obtained for the sample containing 15 wt. % Bu3MeNTf2N with a value of 1.56 x 10 -4 S cm' . The effects of ionic liquid addition on the frequency dependent dielectric properties of PVC based electrolytes is investigated by electrochemical impedance spectroscopy (Eis) at room temperature. The values of dielectric constant were found to increase with increasing conductivity of the samples. Analysis of the ac conductivity data showed the electrolytes to be of the non-Debye type.
Bacillus pumilis was isolated and identified from limestone and the ability towards carbon dioxide (CO) sequestration was demonstrated. B . pumilus (S3 SC_1), isolated from Gua Tempurung, Gopeng, Perak was able to form calcite in the presence of calcium ions. B. pumilus was successfully characterized by using conventional biochemical characterization and 16s rDNA sequencing. Three types of experimental systems with B. pumilus, without B. pumilus and without continuous supply of CO2 with the presence of B. pumilus which could produce extracellular carbonic were studied to determine the effects of bacterially produced carbonic anhydrase (CA) by B. pumilus in removing CO2 as calcite. Through our current study, CO2 sequestration ability of B . pumilus was proven.
Structural and luminescence properties of borophosphate glasses with different modifier doped with transition metal ions have been investigated in this study. The glass sample from the series of xPb 30 4:0 .2Sb20 3:0.3B 20 3:(0 .5-x)P 20 5 and ySb 20 3:0 .2Pb 30 4:(0 .5-y)B 20 3:0 .3P 20 5where x 20 mol% and 0 y 0 .1 5mol% , respectively, were doped with 0.01 mol% of Fe 20 3 system have been prepared using the melt-quenching technique. The structural properties of samples had been studied using fourier transform infrared (FT-m) spectroscopy. The FT-IR study showed the network structure of the studied glasses based on the B 20 3-P 20 5host with the 5b203 and Pb203 modifiers. The results of FT-IR showed traces of B03 and B04 with the introduction of 5b203 and Pb203 modifiers. With the increasing content of B203 which replacing content of P205 in the glass network, the intensity of the borate band decreases and shifted to lower frequency. uv-Vis spectroscopy analysed the transition of Fe3+ from ground state to excited state in the ultraviolet spectral region. The photoluminescence of samples were studied using photoluminescence spectroscopy. The result of photoluminescence spectroscopy showed the effect of photoluminescence enhancement by doping Fe3+ as activator.
PM2.5 mass concentration and associated water-soluble ionic species in a sub-urban coastal area of Kuala Terengganu, Malaysia were investigated intermittently from year 2006 to 2009. A total of 78 weekly PM2.5 samples were analyzed. The mass concentration of PM2.5 exhibited annual, seasonal and diurnal variations. Temporal distributions of rainfall, sporadic haze episodes and local air flow (sea breeze circulation) were factors controlling PM2.5 mass variations in the study area. Although the PM2.5 concentrations were increased during haze episodes in 2006 (August and October) and2007 (October), their concentrations however, were still within the international guidelines. The average concentration of individual ions was in decreasing trend; SO42-> NH4+> K+> Na+> NO3-> Cl-> Ca2+. The concentrations of SO42- and NH4+ accounted for > 70% of the water-soluble aerosol mass. More than 80% of ionic species associated with PM2.5 are from non-marine sources. Major processes affecting the ionic composition of PM2.5 are biomass burning, crustal loading and sea spray. Air quality mitigation strategies should focus on anthropogenic activities emitting SO2, which promotes aerosol SO42- formation.
Epoxy shape memory foam (ESM) was produced by an advanced aqueous method. Mixture of epoxy, sodium bicarbonate,
hardener and ammonium chloride was premixed and emulsified in distilled water by using high speed stirring (at 1200
rpm). The content of sodium bicarbonate used was 5, 10, 15 and 20 phr. Besides that, ammonium chloride was used
(based on stoichiometrical content) to also function as acidifying agent in initiating the decomposition process of sodium
bicarbonate at lower foaming temperature. The foam morphology was observed using SEM. It was found that higher
sodium bicarbonate produced more porosity, more cell size, thinner cell wall and more cell interconnection. Epoxy shape
memory foam with 10 phr of sodium bicarbonate exhibited good shape memory property and better compression set.
Shape memory behaviour was measured by the recovered time of the transformed sample to its original shape.
A new crosslinked chitosan grafted with methyl methacrylate (M-CTS) adsorbent was synthesized via free radical polymerization for effective removal of Cu(II) ions from aqueous solution. Crosslinked chitosan (1 g) was grafted with 29.96 × 10-1 M methyl methacrylate in the presence of 2.63 × 10-1 M ammonium persulfate as initiator at 60 °C for 2 h to give grafting and yield percentages of 201% and 67%, respectively. Batch adsorption experiment was performed as a function of solution pH, initial metal ion concentration and contact time. The isotherm data were adequately described by Langmuir model, while kinetic study revealed that the pseudo-second order rate model best fitted for the experimental data. The maximum adsorption capacity for M-CTS at pH 4 was 192.31 mg g-1. Furthermore, the reusability of over six adsorption-desorption cycles suggested that M-CTS is a durable adsorbent and good candidate for metal ions treatment.
This study aimed to investigate the transport mechanisms of ions during forward-osmosis-driven (FO-driven) dewatering of microalgae using molecular dynamics (MD) simulations. The dynamical and structural properties of ions in FO systems of varying NaCl or MgCl2 draw solution (DS) concentrations were calculated and correlated. Results indicate that FO systems with higher DS concentration caused ions to have lower hydration numbers and higher coordination numbers leading to lower diffusion coefficients. The higher hydration number of Mg2+ ions resulted in significantly lower ionic permeability as compared to Na+ ions at all concentrations (p = 0.002). The simulations also revealed that higher DS concentrations led to higher accumulation of ions in the membrane. This study provides insights on the proper selection of DS for FO systems.
Preparation of selective magnetic adsorbents for dispersive micro-solid phase extraction often involves multi-step reactions which are time consuming. This study demonstrates a simplified method for the synthesis of a magnetic adsorbent, which is selective towards the adsorption of mercury(ii) ions (Hg2+). In this method, the incorporation of a metal capturing ligand (3-oxo-1,3-diphenylpropyl-2-(naphthalen-2-ylamino) ethylcarbamodithioate) and the coating of magnetic particles with silica gel was performed in a single step. This adsorbent was then used in solid-phase microextraction for the preconcentration of Hg2+ in water. In this study, a mercury analyzer was used to quantify the Hg2+. Under optimized conditions, the developed analytical method achieved a low detection limit (4.0 ng L-1), satisfactory enrichment factor (96.4) and wide linearity range (50.0-5000 ng L-1) with a good coefficient of determination (0.9985) and good repeatability (<7%). The preconcentration factor of this method was 100. This proposed method was also successfully utilized for the determination of Hg2+ in drinking water, tap water and surface water with good recovery (>91%) and high intra-day and inter-day precision.
Environmental monitoring is important to determine the extent of eco-system pollution and degradation so that effective remedial strategies can be formulated. In this study, an environmentally friendly and cost-effective sensor made up of novel carbon electrode modified with cellulose and hydroxyapatite was developed for the detection of trace lead ions in aqueous system and palm oil mill effluent. Zinc, cadmium, and copper with lead were simultaneously detected using this method. The electrode exhibited high tolerance towards twelve common metal ions and three model surface active substances - sodium dodecyl sulfate, Triton X-100, and cetyltrimethylammonium bromide. Under optimum conditions, the sensor detected lead ions in palm oil mill effluent in the concentration range of 10-50 μg/L with 0.11 ± 0.37 μg/L limit of detection and 0.37 ± 0.37 μg/L limit of quantification. The validation using tap water, blood serum and palm oil mill effluent samples and compared with Atomic Absorption Spectroscopy, suggested excellent sensitivity of the sensor to detect lead ions in simple and complex matrices. The cellulose produced based on "green" techniques from agro-lignocellulosic wastes, in combination with hydroxyapatite, were proven effective as components in the carbon electrode composite. It has great potential in both clinical and environmental use.
The functionalization of surface charges on oil palm empty fruit bunch (EFB) fibers was modified by grafted carboxylic
acid and polymer amine groups. Single and binary adsorption of Cu(II), Ni(II), Mo(VI) and As(V) were investigated
by competitiveness in the adsorbents. The mechanism of each metal ion was deliberately studied on kinetics-diffusion
(intraparticle diffusion) and isotherm adsorption models (Langmuir and Freundlich). Competitiveness of metal ions was
found in the selectivity of Cu(II) > Ni(II) and Mo(VI) > As(V) in the binary solution. The regeneration of adsorbents
was performed up to five cycles of an adsorption/desorption process and the reduction of adsorption performance was
less than 14.5%. Therefore, this promises low-cost adsorbents for metal ion uptake, showing potential for removal and
recovery in industrial wastewater treatment.
Currently, heavy metals and dyes are some of the most critical pollutants in the aquatic environment. So, in this paper "waste-to-resource conversion", as a new application of modified mine silicate waste to remove Pb2+ ion and methylene blue (MB) dye, adsorption properties, mechanism of action and recycling were studied. Silicate wastes are located in the alteration zone and the margin of molybdenum ore, these wastes are under the influence of hydrothermal solutions which are impregnated with iron and manganese ions. Hence, acid and base modifications have been commonly used. So, in this study, a highly porous nanostructure of modified silicate waste was used to remove MB and Pb2+ ion, in subsequent to our previous study on the application of the raw material of the same in the removal of malachite green. Acid, base, and acid/base treatments were used to activate and modify the adsorbent. Results show a significantly higher potential of modified adsorbent in the removal of MB and Pb2+ compared to the raw material. According to the isotherm and kinetic studies for MB and Pb2+ the Langmuir and Temkin and pseudo-second-order models were investigated with experimental data. Modified nanomaterial was used for several adsorption and desorption processes, without a significant decrease in the capability of the adsorbent in the removal of MB and Pb2+ pollutants. Leached iron and manganese ions (as production of modification) are deposited in the form of sludge using a simple pH adjustment and precipitation process and can be used to recover iron and manganese metals in the long run. The comparison of monolayer adsorption capacity using for Pb2+ ion and MB dye are as ((untreated SW: 29.41, 1.05); (NaOH treated: 21.74, 100); (Nitric Acid treated: 16.67, 142.86); (Citric Acid treated: 40, 125); (Nitric/Citric Acids treated: 15.63, 111.11) and (Nitric/Citric Acids/NaOH treated: 15.15, 83.33)), respectively. Higher adsorption capacity and re-generable properties of this adsorbent suggest the usage of this natural and abundant mine waste to treat wastewater containing toxic elements and dyes.
Water pollution is one of the most concerning global environmental problems in this century with the severity and complexity of the issue increases every day. One of the major contributors to water pollution is the discharge of harmful heavy metal wastes into the rivers and water bodies. Without proper treatment, the release of these harmful inorganic waste would endanger the environment by contaminating the food chains of living organisms, hence, leading to potential health risks to humans. The adsorption method has become one of the cost-effective alternative treatments to eliminate heavy metal ions. Since the type of adsorbent material is the most vital factor that determines the effectiveness of the adsorption, continuous efforts have been made in search of cheap adsorbents derived from a variety of waste materials. Fruit waste can be transformed into valuable products, such as biochar, as they are composed of many functional groups, including carboxylic groups and lignin, which is effective in metal binding. The main objective of this study was to review the potential of various types of fruit wastes as an alternative adsorbent for Pb(II) removal. Following a brief overview of the properties and effects of Pb(II), this study discussed the equilibrium isotherms and adsorption kinetic by various adsorption models. The possible adsorption mechanisms and regeneration study for Pb(II) removal were also elaborated in detail to provide a clear understanding of biochar produced using the pyrolysis technique. The future prospects of fruit waste as an adsorbent for the removal of Pb(II) was also highlighted.
In this study, the combination of novel valinomycin doped chitosan-graphene oxide (C-GO-V) thin film and surface plasmon resonance (SPR) system for potassium ion (K+) detection has been developed. The novel C-GO-V thin film was deposited on the gold surface using spin coating technique. The system was used to monitor SPR signal for K+ in solution with and without C-GO-V thin film. The K+ can be detected by measuring the SPR signal when C-GO-V thin film is exposed to K+ in solution. The sensor produces a linear response for K+ ion up to 100ppm with sensitivity and detection limit of 0.00948°ppm-1 and 0.001ppm, respectively. These results indicate that the C-GO-V film is high potential as a sensor element for K+ that has been proved by the SPR measurement.
In this work, batch adsorption experiments were carried out to investigate the suitability of prepared acid activated carbons in removing heavy metal ions such as nickel(II), lead(II) and chromium(VI). Acid activated carbons were obtained from oil palm and coconut shells using phosphoric acid under similar activation process while the differences lie either in impregnation condition or in both pretreatment and impregnation conditions. Prepared activated carbons were modified by dispersing hydrated iron oxide. The adsorption equilibrium data for nickel(II) and lead(II) were obtained from adsorption by the prepared and commercial activated carbons. Langmuir and Freundlich models fit the data well. Prepared activated carbons showed higher adsorption capacity for nickel(II) and lead(II). The removal of chromium(VI) was studied by the prepared acid activated, modified and commercial activated carbons at different pH. The isotherms studies reveal that the prepared activated carbon performs better in low concentration region while the commercial ones in the high concentration region. Thus, a complete adsorption is expected in low concentration by the prepared activated carbon. The kinetics data for Ni(II), Pb(II) and Cr(VI) by the best selected activated carbon fitted very well to the pseudo-second-order kinetic model.
Plant litter decomposition is not only the major source of soil carbon and macronutrients, but also an important process for the biogeochemical cycling of trace elements such as iron (Fe), manganese (Mn), zinc (Zn), and copper (Cu). The concentrations of plant litter trace elements can influence litter decomposition and element cycling across the plant and soil systems. Yet, a global perspective of the patterns and driving factors of trace elements in plant litter is missing. To bridge this knowledge gap, we quantitatively assessed the concentrations of four common trace elements, namely Fe, Mn, Zn, and Cu, of freshly fallen plant litter with 1411 observations extracted from 175 publications across the globe. Results showed that (1) the median of the average concentrations of litter Fe, Mn, Zn, and Cu were 0.200, 0.555, 0.032, and 0.006 g/kg, respectively, across litter types; (2) litter concentrations of Fe, Zn, and Cu were generally stable regardless of variations in multiple biotic and abiotic factors (e.g., plant taxonomy, climate, and soil properties); and (3) litter Mn concentration was more sensitive to environmental conditions and influenced by multiple factors, but mycorrhizal association and soil pH and nitrogen concentration were the most important ones. Overall, our study provides a clear global picture of plant litter Fe, Mn, Zn, and Cu concentrations and their driving factors, which is important for improving our understanding on their biogeochemical cycling along with litter decomposition processes.