• Journal of the Mineralogical Society of Korea
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• v.21 no.2
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• pp.117-127
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• 2008

The characteristics of phosphate adsorption-desorption on kaolinite was studied by batch adsorption experiments and detailed adsorbed state of phosphate on kaolinite surface was investigated using ATR-FTIR (Attenuated Total Reflectance-Fourier Transform Infrared) spectroscopy. The phosphorous contents were measured using UV-VIS-IR spectrophotometer with 820 nm wavelength. The adsorbed P was generally increased with increasing pH value in the range of pH 4 to pH 9, however it is not distinct. Moreover the adsorbed P was significantly changed with different initial phosphate concentration. The adsorption isotherms were well fitted with the Langmuir equation, Temkin equation, and Freundlich equation in descending order. The maximum Langmuir adsorption capacity of kaolinite KGa-2 is 232.5 ($204.1{\sim}256.5$) mg/kg and has very higher value than that of kaolinite KGa-1b. Most of adsorbed phosphate on kaolinite were not easily desorbed to aqueous solution, but might fixed on kaolinite surface. However it needs further research about the exact desorption experiment. It was impossible to recognize phosphorous adsorption bands on kaolinite in ATR-FTIR spectrum from kaolinite bands themselves, because the absorption peaks of phosphorous have very similar positions with those of kaolinite, and the intensities of the former were very weak in comparison with those of the latter.

• 한국생물공학회:학술대회논문집
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• 2001.11a
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• pp.586-589
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• 2001

In this study, phosphate was produced through the solublization of hydroxyapatite and rock phosphate by Pantoea agglomerans, and it was examined the possibility of solublizing insoluble phosphate salt by immobilized P. agglomerans on Ca-alginate bead as support. 520mg/L of phosphate was solublized when P. agglomerans was cultured in HY meclium at $30^{\circ}C$, pH7, 100rpm, during 48hours culture. And solublized phosphate amount was 86.09mg/L when hydroxyapatite in the HY medium was exchanged to rock phosphate. In case of being used immobilized P. agglomerans. 740mg/L of phosphate was solublized in the HY medium, during 120hrs in the same condition. And 182mg/L of phosphate was solublized when rock phosphate was added instead of hydroxyapatite.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2015.11a
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• pp.312-313
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• 2015

무전해 도금은 석출응력이 낮고 작업하기가 용이하기 때문에 산업분야에 있어서 중요한 역할을 한다. 무전해 도금 공정에 있어서, 니켈금속은 차아인산염, 아미노보레인 혹은 수소화붕소 화합물($HBF_4$)에 의한 니켈이온의 화학적 환원에 의해 도금된다. 환원반응이 진행함에 따라서 도금액 중에서 니켈과 차아인산염 이온은 감소한다. 이에 이러한 이온을 보충하기 위하여 도금액 중에 황산니켈과 차아인산나트륨이 일반적으로 첨가된다. 하지만 축적된 인산염, 황산염, 나트륨과 이외의 물질이 전착 박막의 품질을 떨어뜨리고 도금액은 폐기되기도 한다. 니켈회수 속도는 종래의 50% 이하였던 것이 90%이상으로 향상되었다. 이온교환법은 니켈도금 폐액으로부터 니켈회수에 필요한 친환경적이고 원가절감의 기술이라고 사료된다. 특히, 갈탄이 저렴하고 양이온 교환성능이 뛰어나다. 이유는 -COOH, -OH 등의 기능성 그룹을 갖기 때문이다. Fe-P 화합물은 식물에 유용하지 못하고 마그네슘과 칼슘 기반의 석출물은 저렴하고 취급이 용이하며 비료와 같이 재활용이 가능하기 때문에 일반적인 인의 제거 수단이 될 수 있다. 본고에서는 니켈도금 폐액으로부터 인을 제거하는 데 $Ca(OH)_2$, $CaCl_2$와 $CaCO_3$를 채택하여 인이 제거되는 정도를 비교하였고 니켈회수율을 높이기 위하여 갈탄을 사용하였다.

• Journal of the Korea Organic Resources Recycling Association
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• v.29 no.2
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• pp.25-30
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• 2021

This study investigated how the indicators of quality control are improved by proficiency in the measurement of phosphate concentration. In addition, analysis equipments were to be compared to see if there were any differences in measurements depending on the type of analysis device. In order to find out the effect of the proficiency of the analyst on the analysis results, three analysts measured phosphate concentration seven times in accordance with the Korean water pollution test standards, and met the quality control indices if repeated more than five times. The limit of quantification for phosphate was calculated at 0.02 mg/L. If the analysis devices are different, the absorbance and concentration of the samples near the limit of quantification are statistically significant difference.

• Proceedings of the KAIS Fall Conference
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• 2008.11a
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• pp.400-402
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• 2008

본 연구는 오염토양 내 구리를 효과적으로 고정화시키는 조건을 찾고자 고정화제의 주입농도를 변화시켜가며 실험을 진행하였으며, 실험결과 고정화제의 주입농도가 높을수록 구리제거효율도 높아지는 것으로 나타났으며 3mole의 인산염을 주입했을 때 98%이상의 높은 제거효율을 보였다. 또한 잔류인의 농도를 낮추고 고정화반응을 촉진시키기 위해 알칼리제를 투입하였을 때, 알칼리제의 농도가 높을수록 구리오염 농도와 잔류인의 농도가 더욱 낮아짐을 알 수 있었다.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.4
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• pp.241-248
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• 2009

A farming area located near an abandoned copper mine in GuPo-ri, Choongchung province is heavily contaminated with heavy metals such as As, Pb, Cd, Cu and Zn of which concentrations are higher than the values typically detected in Korean soil environment. In this work, laboratory and field studies were conducted to examine feasibility of using Ca-citrate-phosphate solution in stabilizing heavy metals in the polluted soils. In laboratory batch experiments with field soil, the addition of Ca-citrate-phosphate solution resulted in decrease of aqueous phase concentration of phosphate and improvement of heavy metal stabilization, compared to those for sterilized soil samples. This indicates that microbial uptake of phosphate may have provided positive effects on availability of phosphate toward heavy metal stabilization. According to microbial community analysis for the field experiment, the use of Ca-citrate-phosphate led to increased diversity of microbial populations, and strict anaerobic microorganisms such as Anaerofilum and Treponema became the most dominant populations in the solution-amended field experiments. These findings suggest that, when Ca-citrate-phosphate is used for heavy metal stabilization in soils, microbial processes may have important roles in improving the stabilization of heavy metals by providing reducing conditions to the treatment locations or/and by making phosphate available to heavy metal stabilization.

• Journal of the Mineralogical Society of Korea
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• v.22 no.4
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• pp.289-295
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• 2009

The characteristics of phosphate desorption on kaolinite was studied by batch adsorptiondesorption experiments. Desorption procedure was carried out through sequential extraction method at pH 4. The phosphorous contents were measured using UV-VIS-IR spectrophotometer with 820 nm wavelength. The adsorption-desorption reaction of P on kaolinite was irreversible, and most of adsorbed P on kaolinite were not easily dissolved to aqueous solution, but may might be fixed on kaolinite surface. The desorption isotherms were well fitted with the Freundlich and Temkin equations in the case of short reaction and long reaction time, respectively. The desorption reaction was divided into the early fast reaction and the later slow reaction. The percentage of desorption generally decreased with increasing adsorbed P concentration and increasing desorption reaction time.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.09a
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• pp.252-257
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• 2004

본 연구에서는 인산염을 이용여 납으로 오염된 Clay 사격장과 인위적으로 오염시킨 자연토양의 중금속의 고정화 실험을 수행하였다. 인산염 고정화제로는 DAP (diammonium phosphate)를 사용하였다. DAP를 투입한 중금속 오염토양을 고정화 실험과 TCLP로 용출 하였을 때, 99% 정도 고정화되었다. 인산염 투여양이 증가할수록 고정화 효율은 증가하는 것으로 나타났으며, 최적 인투입량은 128 mmol as P/kg인 것으로 나타났다. DAP 투입양이 증가할수록 토양의 pH는 증가하는 것으로 나타났으며, 토양의 초기 pH 변화에 따라 고정화 효율은 크게 변하지 않은 것으로 나타났으나, pH가 높을수록 고정화 효율은 작은폭으로 증가하는 것으로 나타났다.

• Journal of the Korea Institute of Building Construction
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• v.17 no.2
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• pp.135-140
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• 2017

As an elementary investigation to develop vegetation concrete with a relatively low pH value, magnesia-phosphate composites (MPC) were examined according to the phosphate types including Monoammonium, Monosodium, Monopotassium, Monocalcium, Diammonium, Disodium, Dipotassium, and Diacalcium phosphates. All of the MPC binders, the ratio of magnesia to phosphate was fixed to be 7:3. MPC mortars activated with Disodium, Dipotassium, and Diacalcium phosphates showed no compressive strength gain, even at age of 28 days. Meanwhile, MPC mortars with Monoammonium and Monosodium phosphates developed 28-day compressive strength of more than 34MPa, and showed a relatively low pH value below 9.8. Hence, Monoammonium and Monosodium phosphates have potentials as an activator for producing MPC-based vegetation concrete.

• The Science & Technology
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• s.529
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• pp.61-64
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• 2013