Transparent conductive oxide (TCO) glass is one of most important components in dyesensitized solar cell (DSSC) device. In addition to its high electrical conductivity, transparency is another important requirement that must be achieved in fabricating TCO. One TCO film is fluorine-doped tin oxide (FTO), which can be considered as the most promising substitution for indium-doped tin oxide (ITO), since the latter is very expensive. However, the fabrication techniques for TCO film need to be carefully selected; the synthesis parameters must be properly optimized to provide the desired properties. In this work, FTO glass has been fabricated by the ultrasonic spray pyrolisis technique with different precursors, i.e. tin (II) chloride dihydrate (SnCl 2 .2H 2 O) and anhydrous tin (IV) chloride (SnCl 4 ), as well as different solvents, i.e. ethanol and methanol. For both conditions, ammonium fluoride (NH 4 F) was used as the doping compound. The resulting thin films were characterized by use of a scanning electron microscope (SEM), x-ray diffraction (XRD), ultraviolet-visible (UV-Vis) spectroscopy and a four-point probe test. The results of the investigation show that the highest transmittance of 88.3% and the lowest electrical resistivity of 8.44×10 -5 Ω.cm were obtained with the FTO glass processed with 20 minutes of spray pyrolysis deposition and 300 o C substrate heating, using SnCl 4 as the precursor and methanol as the solvent. It can be concluded that TCO fabrication with tin chloride precursors and ammonium fluoride doping using ultrasonic spray pyrolisis can be considered as a simple and low cost method, as well as a breakthrough in manufacturing conductive and transparent glass.
Lithium minerals become a sub-economic raw material for lithium production to fulfill the lithium demand. This study is about lithium extraction from mica schist using the roasting and leaching processes. The mica schist located in Kebumen, Indonesia was used to study the phenomena during the lithium extraction process. Sodium sulfate was used as a roasting agent while 0.36 M sulfuric acid was used as a leaching agent. Solid/liquid ratio (1:5, 1:10, 1:15 and 1:20 (g/mL)) and leaching time (30, 60, 90 and 120 minutes) were used as variables in this study. The roasting process was done at 700 °С for 40 minutes while the leaching process was done at 70 °С and 350 rpm. The ratio of additive and mica schist was 1.5:1 (g/g). XRD, ICP-OES, and SEM were used to observe the formed compounds, chemical composition and morphology of the materials. HighScore Plus (HSP) was used to interpret the content of each compound in mica schist, roasted mica schist, and residue. ICP analysis confirmed that the mica schist contains 45.28 ppm of lithium. It is supported by XRD that lithium exists in mica schist as lepidolite (KLi2AlSi4O10(F,OH)2). Sulfate roasting did not affect the type of lepidolite but the lepidolite reactivity against the chemical agent. SEM analysis shows that the roasting process reduced the average particle size from 32.17 to 27.16 µm. ICP analysis of roasted mica schist shows that lithium concentration was reduced from 45.28 to 1.27 ppm. The optimum result from this study was 97.66 % extraction of lithium while solid/liquid ratio was 1:5 (g/ml) and leaching time was 30 minutes. HSP shows that lepidolite contents in initial mica schist, roasted mica schist and residue were 60.6; 24.3 and 18.7 %, respectively. Lithium concentration in the residue according to ICP analysis is 1.06 ppm.
Experiments have been carried out to remove magnesium ions from brine water using limestone, Rembang, Indonesia. The aim of the study was to produce brine water concentrates that were rich in lithium and did not contain magnesium elements. Brine water used has the following chemical composition: 74.67 ppm Li; 877.891 ppm Na; 1549.81 ppm K; 147.23 ppm Mg; 38.49 ppm Ca and others. The initial stages were 200 g of natural lime calcined at 900 °C for 3 hours using a furnace as a precipitation agent. It is then added to 1000 ml of brine water with a variation of 0.336 g, 1 g, 10 g, 20 g, 30 g, 40 g, 50 g by stirring for 3 hours at atmospheric pressure. The results showed that the magnesium removal from brine water began to be seen in the addition of roasted limestone of 1 g with the dominant phase as Mg0.03Ca0.97CO3 in the precipitated residue. On the addition of 10 g and 20 g of roasted limestone into brine water, the percentage of magnesium removal was almost maximum of 98.8% and 99.8% with the precipitated residues as Mg(OH)2 phases. This experiment was successful to remove magnesium from brine water so that the lithium concentration of brine water increased to 104.32 ppm Li and 105.86 ppm Li with the addition of roasted limestone of 10 g and 20 g, respectively. These results indicate that the use of roasted limestone to eliminate magnesium from brine water with low lithium grade is recommended.
The purpose of this study was to investigate whether lithium was precipitated along with the removal of Ca and Mg elements from brine water using limestone and oxalic acid. The first stage was Mg removal by adding CaO at room temperature for 3 hours. The second stage was the Ca removal by adding oxalic acid at a ratio of 2; 3; 4; 5; 10; 15; 20; 30; and 40 ml / 100 ml brine water and pH : 0, 1, and 4 at room temperature for 3 hours. The results showed the most optimal addition of CaO was 20 gr/1 l of brine water with the Mg element can be removed above 99 %, while Li was only reduced by about 1 ppm, and the Ca content only increased by around 28 ppm. The use of oxalic acid will also reduce the amount of lithium besides the Ca removal in the form a precipitate of calcium oxalate. The use of oxalic acid at pH 0 and 4 would reduce the Li content more than at pH 1. At the use of oxalic acid up to 40 ml at pH 1, brine water still contained about 78% Li element.
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