• Environmental Engineering Research
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• v.23 no.2
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• pp.223-227
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• 2018

This study reports a cyanide resistant and/or tolerant fungus, isolated from the rhizosphere of Zea mays contaminated with cyanide-based pesticides. The isolate was characterised using molecular biology. The effect of free cyanide and heavy metals on the growth of isolate in a synthetic gold mine wastewater was examined. The molecular analyses identified the isolate as Fusarium oxysporum EKT01/02 (KU985430/KU985431). The isolate had a free cyanide degradation efficiency of 77.6%. The results indicated greater growth impairment in culture containing Arsenic (optical density 1.28 and 1.458) and cyanide (optical density 1.315 and 1.385). Higher growth was observed in all cultures supplemented with extracellular polymeric substance. This study showed that the isolate possesses wide substrate utilisation mechanism that could be deployed in environmental engineering applications.

• Journal of the Korean Professional Engineers Association
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• v.14 no.1
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• pp.22-29
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• 1981

This study concernes the decomposition of cyanide ion in electroplating plant wastewater and COD variation of photodeveloping wastewater under various conditions. Determinations of CN- concentration were carried out by AgNO$_3$ titration method. The sample solutions were pretreated by passing ozone and decompositions were checked as a function of time for ozone treatment. Analysis of film developing wastewater was carried out by KMnO$_4$ method. Electroplating plant wastewater was also examined at various pH; decomposition rate of cyanide ion was found to increase at higher pH. Time required for the decomposition could be shortened by removing the heavy metal ions under alkaline condition. The effect of temperature on decomposition was studied at 40$^{\circ}$ and 60$^{\circ}C$. The result was better at 40$^{\circ}C$ although time for decomposition was almost same at both temperatures. Analysis of film developing wastewater revealed that COD decrease was faster during the first 1 to 2 hours. However, further decrease could not be effected. The existence of unknown special organics resistant to the decomposition was believed to be the reason.

• 한국전기화학회:학술대회논문집
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• 1998.10a
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• pp.43-43
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• 1998

• Membrane Journal
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• v.4 no.2
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• pp.106-112
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• 1994

The ultrafiltration(UF) and reverse osmosis(RO) tests for a model metal plating wastewater prepared with zinc sulfate, showed the zinc ion rejection coefficient of over 99% and the permeate flux of $1.49 {\times} 10^{-3}cm/sec$ at pH = 8.3. The effect of cyanide on the zinc removal was investigated. When the amount of cyanide addition was same the zinc content, the zinc was removed over 99% and the cyanide was excluded about 93%. The addition of the surfactants such a LAS-Na and EDTA-Na was found to reduce the permeate flux down to $0.76 {\times} 10^{-3}cm/sec$ at the RO membrane.

• Korean Chemical Engineering Research
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• v.46 no.6
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• pp.1124-1129
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• 2008

Cokes wastewater is one of the most toxic industrial effluents since it contains high concentrations of pollutants, such as phenol, ammonia, thiocyanate and cyanides. Although biological pre-denitrification process has been used to treat this wastewater in Korea, unexpected failure in nitrogen removal occasionally occurs during summer season. In this study, therefore, we examined inhibitory effects of phenol, ammonia, thiocyanate, ferric cyanide and free cyanide on biological denitrification according to temperature variation ($20{\sim}38^{\circ}C$). Batch experiments showed that denitrification rate was faster in summer ($38^{\circ}C$) than other seasons, and removal rates of pollutants increased with increasing temperature. Phenol, ammonia, thiocyanate and ferric cyanide did not inhibit denitrification even at its high concentration (200 mg/L). However free cyanide above 0.5 mg/L seriously inhibited the bilolgical denitrification reaction. Inhibitory effect of these pollutants was reduced with increasing temperature.

• Resources Recycling
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• v.11 no.2
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• pp.3-13
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• 2002

The characteristics of cyanide decomposition in aqueous phase by hydrogen peroxide have been explored in an effort to develop a process to recycle waste water. The self-decomposition of $H_2O$$_2$at pH 10 or below was minimal even in 90 min., with keeping about 90% of $H_2O$$_2$undissociated. On the contrary, at pH 12 only 9% of it remained during the same time. In the presence of copper catalyst at 5 g Cu/L, complete decomposition of $H_2$O$_2$was accomplished at pH 12 even in a shorter time of 40 min. The volatility of free cyanide was decisively dependent on the solution pH: the majority of free cyanide was volatilized at pH 8 or below, however, only 10% of it was volatilized at pH 10 or above. In non-catalytic cyanide decomposition, the free cyanide removal was incomplete in 300 min. even in an excessive addition of $H_2$$O_2$at a $H_2$$O_2$/CN molar ratio of 4, with leaving behind about 8% of free cyanide. On the other hand, in the presence of copper catalyst at a Cu/CN molar ratio of 0.2, the free cyanide was mostly decomposed in only 16 min. at a reducedH202/CN molar ratio of 2. Ihe efnciency of HBO2 in cyanide decomposition decreased with increasing addition of H2O2 since the seu-decomposition rate of $H_2$$O_2$increased. At the optimum $H_2$$O_2$/mo1ar ratio 0.2 of and Cu/CN molar ratio of 0.05, the free cyanide could be completely decomposed in 70 min., having a self-decomposition rate of 22 mM/min and a H$_2$$O_2$ efficiency of 57%.

• Journal of environmental and Sanitary engineering
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• v.13 no.3
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• pp.85-92
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• 1998

In this study, the electrolytic treatment by one-stage electrolysis was investigated for electroplating wastewater containing $Cr^{6+}$ and $CN^{-}$. From the results, we concluded as follows : Optimum initial pH of wastewater was pH : 3. Amount of optimum addition of electroltyte(NaCl) was 0.1 wt%. Optimum potential for electrolysis was 5 volt. Concentration and removal efficiency for $Cr^{6+}$ and $CN^{-}$ were under 1 mg/L and above 99% at optimum conditions. And the feasibility of electrolytic treatment for electroplating wastewater containing $Cr^{6+}$ and $CN^{-}$ was certified.

• Resources Recycling
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• v.13 no.1
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• pp.28-38
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• 2004

The characteristics of cyanide decomposition in aqueous phase by electric oxidization have been explored in an effort to develop a process to recycle waste water. Considering current efficiency and voltage, the free cyanide decomposition experiment by electric oxidization indicated that 5 V of voltage and copper catalytic Cu/CN mole ratio 0.05 was the most appropriate condition, where current efficiency was 26%, and decomposition speed was 5.6 mM/min. High voltage and excess copper addition increased decomposition speed a little bit but not current efficiency. The experiment of free cyanide density change proves that high density cyanide is preferred because speed and current efficiency increase with density. Also, the overall decomposition reaction could be represented by the first order with respcect to cyanide with the rate constant of $1.6∼7.3${\times}$10^{-3}$ $min^{-1}$ The mass transfer coefficient of electric oxidization of cyanide came out as $2.42${\times}$10^{-5}$ $min^{-1}$ Furthermore, the Damkohler number was calculated as 5.7 in case of 7 V and it was found that the mass transfer stage was the rate determining step.

• Journal of Korean Society of Water and Wastewater
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• v.21 no.3
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• pp.279-285
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• 2007

Toxicity evaluations using oxygen uptake rate (OUR) on activated sludge process were investigated. On toxicity evaluations of heavy metals, all toxicants in experiments decreased OUR with respect to the concentrations of the toxicants, while high toxicities with cyanide and mercury were observed respectively. On toxicity evaluations of composite heavy metals, composite toxicities had similar results as to the total sum of each toxicants that presents accurate toxicity evaluation using OUR. From these results, it is concluded that activated sludge is effective indicator for toxicity evaluation on wastewater of biological treatment plants.

• Applied Chemistry for Engineering
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• v.8 no.3
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• pp.438-445
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• 1997

${\beta}-PbO_2$ electrode, which was electrodeposited on Ti madras, was prepared and for the decomposition of cyanide in electroplating wastewater. After the investigation of temperature and pH conditions for no hydrogen cyanide evolution during the decomposition of cyanide, the optimum current densities of ${\beta}-PbO_2$ electrodeposition and cyanide decomposition were determined in 500ppm NaCN solution, and durability of ${\beta}-PbO_2$ electrode was also investigated. Hydrogen cyanide was actively generated above $40^{\circ}C$ and was not evolved above pH 13. ${\beta}-PbO_2$ electrode electodeposited at $5A/dm^2$ showed the best cyanide decomposition efficiency The decompostion efficiency was about 70% at low decomposition current density ($0.08A/dm^2$), and it decreased gradually to about 10% as the decomposition current density increased up to $4A/dm^2$. The film of ${\beta}-PbO_2$ electrodeposited was corrosive at $20A/dm^2$ and was broken at $50A/dm^2$.