Leaching studies for tin recovery from waste e-scrap

Printed circuit boards (PCBs) are the most essential components of all electrical and electronic equipments, which contain noteworthy quantity of metals, some of which are toxic to life and all of which are valuable resources. Therefore, recycling of PCBs is necessary for the safe disposal/utilization of these metals. Present paper is a part of developing Indo-Korean recycling technique consists of organic swelling pre-treatment technique for the liberation of thin layer of metallic sheet and the treatment of epoxy resin to remove/recover toxic soldering material. To optimize the parameters required for recovery of tin from waste PCBs, initially the bench scale studies were carried out using fresh solder (containing 52.6% Sn and 47.3% Pb) varying the acid concentration, temperature, mixing time and pulp density. The experimental data indicate that 95.79% of tin was leached out from solder material using 5.5M HCl at fixed pulp density 50g/L and temperature 90°C in mixing time 165min. Kinetic studies followed the chemical reaction controlled dense constant size cylindrical particles with activation energy of 117.68kJ/mol. However, 97.79% of tin was found to be leached out from solder materials of liberated swelled epoxy resin using 4.5M HCl at 90°C, mixing time 60min and pulp density 50g/L. From the leach liquor of solder materials of epoxy resin, the precipitate of sodium stannate as value added product was obtained at pH 1.9. The Pb from the leach residue was removed by using 0.1M nitric acid at 90°C in mixing time 45min and pulp density 10g/L. The metal free epoxy resin could be disposed-of safely/used as filling material without affecting the environment.     

Study on integrated management of PCB containing waste and PCB contaminated waste: proposal of new congeners for quantification

In the present study, new congeners were selected for the efficient management of PCB containing waste and PCB contaminated waste, and the applicability of these new indicators was confirmed. As a result, 8 indicator congeners and 4 index peaks which were named “Proposed new method 1” and “Proposed new method 2” were selected. For the assessment of a novel quantitative method, comparative tests using conventional methods were conducted, and the factors for total PCB were calculated for each method. Results from these tests showed that the average values for the factors of CEN/TC19/WG22, DIN 51527, and the test method by the disposal regulation for ocean dumping in Korea were 1.86, 3.47, and 2.52, respectively, while those for the proposed new method 1 and proposed new method 2 were 2.98 and 5.56, respectively. For PCB contaminated waste, the factor was found to be 1.99, 3.42, and 3.02 using the conventional methods, 2.67 using the proposed new method 1, and 5.57 using the proposed new method 2. It is expected that, in accordance with the results of the present study, the management of PCB waste can be integrated, regardless of the type of waste involved.     

Catalytic wet oxidation of ammonia: why is N2 formed preferentially against NO3 -?

The role of catalyst and the reason for the preferential formation of N(2) in the catalytic oxidation reaction of ammonia in water over a Ru (3wt.%)/TiO(2) catalyst were elucidated. It was verified that the catalyst in the reaction had no direct relevance to the selective formation of N(2), but was responsible only for the oxidation of aqueous ammonia, NH(3)(aq), finally giving a molecule of nitrous acid. The preferential production of N(2) was experimentally demonstrated due to the homogeneous aqueous phase reaction of the nitrous acid-dissociated NO(2)(-) with NH(4)(+) ions. Even under the highly oxidizing condition, NO(2)(-) was much more likely to react with NH(4)(+) to form N(2) than being oxidized over the catalyst to NO(3)(-) as long as NH(4)(+) was available in solution.     

Utilization of coal fly ash as a slow-release granular medium for soil improvement

This work proposes a new potential application of waste coal fly ash as a K fertilizer support. Fly ash was reacted with KOH to facilitate the impregnation of K as well as to enhance the bonding force. In particular, the applied process resulted in a significant slow-releasing characteristic of fertilizer elements. To examine the effect of K impregnation, a few detailed leaching tests were carried out in terms of process variables such as reaction time and temperature, sintering time and temperature, and KOH concentration. The current experiment presented an optimum preparation condition that is competitive with conventional commercial fertilizers. The manufactured ash fertilizers inhibited release of the K elements. It was also found through the continuous leaching test with pure water that the ash fertilizer had excellent moisture absorbability. However, the effects of some trace elements in fly ash on soil health and crop productivity as well as environmental considerations need to be established with long-term studies.     

Influence of various reaction parameters on 2,4-D removal in photo/ferrioxalate/H(2)O(2) process

The influence of various reaction parameters on herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) removal were examined in the photo/ferrioxalate/H(2)O(2) system, with regard to: (1) sulfate, phosphate, and z.rad;OH scavenger, as solution constituent; and (2) light intensity, ferrioxalate, H(2)O(2), and oxalate concentration, as operating parameter. In terms of 2,4-D removal, the photo/ferrioxalate/H(2)O(2) system has always been superior to the photo/Ferric ion/H(2)O(2) system, despite the high presence of anions (sulfate 100 mM, phosphate 1 mM) or z.rad;OH scavenger. Not only the rate of 2,4-D removal, but also the decomposition rate of H(2)O(2) and oxalate proportionally increase with light intensity. The ferrioxalate concentration determines the light absorption fraction, and thus, controls the rates of 2,4-D removal, and the decomposition of H(2)O(2) and oxalate, are predicted from kinetic formulations. The optimal concentration of H(2)O(2) and oxalate, according to the extent of the z.rad;OH scavenging reaction with these reagents, has been demonstrated for 2,4-D removal. It was found that an increasing oxalate concentration, which bears the burden of increased dissolved organic carbon (DOC), does not occur. This is because its decomposition, as a result of the photochemical reduction of the ferric oxalate complex, results in a decrease of the equivalent DOC. The importance of the key reaction factors to be considered, when applying this system to real wastewater treatment, is also discussed.     

Factors influencing natural occurrence of fluoride-rich groundwaters: a case study in the southeastern part of the Korean Peninsula

Factors regulating the occurrence of fluoride in groundwater were investigated using natural isotope tracers and geochemical data in the southeastern part of Korea where about 10% of the total public water-supply wells (n=422) inspected in this study had fluoride levels exceeding the drinking water limit of Korea (1.5 mg/l). The F-rich public wells are mostly distributed along the major faults, especially in the terrain of the F-rich granitic rocks. The stable isotope analysis results provide substantial information for the relative ages of groundwaters. It is revealed that the F-rich groundwaters are deeply circulating paleogroundwaters and occur along the faults due to upward flow along the fault plane. While reacting with granitic rocks for a prolonged period, the F concentrations of groundwater are continuously enriched even after the groundwater reaches an equilibrium state with respect to fluorite (CaF2) due to removal of Ca by precipitation of calcite (CaCO3). These observations reflect that rock chemistry, groundwater age, well depth, and geologic structure are the important factors controlling the occurrence of high F groundwaters. However, high F groundwaters are rarely observed in the fault zones where the associated fractures are widely developed. Isotopic signature provides an evidence for deep penetration of recently recharged groundwater into the wide fault zone, indicating that the hydrologic condition of the fault is also an important factor controlling the occurrence of high F groundwaters.     

Simultaneous Measurements of Atmospheric Pollutants and Visibility with a Long-Path DOAS System in Urban Areas

In this paper, the applicability of a Long-Path Differential Optical Absorption Spectroscopy (LP-DOAS) system was checked for the feasibility of the simultaneous measurement of trace gases (such as O₃, NO₂, SO₂, and HCHO) and atmospheric visibility (light extinction by aerosols) in Asian urban areas. Field studies show that an LP-DOAS system can simultaneously measure the key pollutants (such as O₃, NO₂, SO₂, and HCHO) at detection limits in the ppb/sub-ppb range as well as the Mie extinction coefficient with an uncertainty of 0.1 km^–1 at time resolution of a few minutes. It is thus concluded that the use of LP-DOAS system is feasible for simultaneous measurement of gaseous pollutants as well as an atmospheric extinction coefficient which is tightly bound to fine particulate concentration.