• 한국환경농학회지
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• 제24권3호
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• pp.253-260
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• 2005

국내 시설하우스의 경우 화학비료를 비롯한 각종 농자재의 투입으로 인하여 비료 성분이 집적되었고 이는 작물의 수분흡수 장해를 유발하여 영양장해와 품질저하를 초래하고 있다. 또한 일부 지역에서는 농작물 가식 부위로의 ${NO_3}^-$ 축적과 질소 및 인의 용탈로 인한 수질 오염이 우려 된다. 본 연구에서는 연작장해가 발생한 시설채소재배지 토양의 물리화학적 특성을 평가하고 염류성분을 흡착 고정화할 수 있는 흡착제를 처리하여 토양용액에 존재하는 염류성분을 경감시킬수 있는 최적의 흡착제를 선별하고자 하였다. 실험에 사용된 토양은 유효인산$(1431{\sim}6516mg\;kg^{-1})$, 질산성 질소$(117.60{\sim}395.73mg\;kg^{-1})$, 치환성 칼슘$(4.06{\sim}11.07\;cmol_c\;kg^{-1})$ 및 마그네슘$(2.59{\sim}18.76\;cmol_c\;kg^{-1})$ 성분이 기준치를 과도하게 초과하여 염류장해를 유발하는 요인으로 작용하였다. 염류집적 토양에 대한 미강처리는 토양용액 내의 인산과 질산이온을 $93{\sim}100%$ 감소시켰으며 처리효율은 미강 > 혼합이온교환수지 > 분말형 제올라이트 순으로 나타났다. 미강을 제외한 모든 처리구는 pH $7.98{\sim}8.11$의 범위를 나타내었으며 미강 처리구에서는 토양의 pH가 6.61로 감소되었다. 미강 처리구의 경우 토양의 종류에 따른 차이는 있었으나 음이온에 대한 흡착능력이 매우 뛰어남을 알 수 있었다. 토양용액 중의 칼슘 이온에 대한 제거효율은 제올라이트 $1{\sim}65%$, 혼합이온교환수지 $7{\sim}61%$의 범위를 나타냈으며 미강의 경우 일부 토양에서는 토양용액 중의 칼슘 농도를 증가시키는 것으로 나타났으며 양이온교환수지의 경우 암모니움 이온과 칼륨 및 나트륨 이온에 대해서도 가장 뛰어난 흡착특성을 나타내었다. 이상의 결과를 통하여 양이온의 경우에는 혼합이온 교환수지 처리가 그리고 음이온의 경우 미강 처리가 토양용액 중의 염류성분의 흡착 제거에 뛰어난 효과가 있는 것으로 평가되었으며 경제적인 측면에서도 적용 가능할 것으로 판단되었다.

• 해양환경안전학회지
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• 제25권7호
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• pp.914-919
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• 2019

알칼리성 산업부산물의 혼합에 따른 연안 오염퇴적물의 성상 변화를 평가하기 위해 해수 교환을 고려한 mesocosm 실험을 수행하였다. 실험시작 1개월 후 실험구의 인산인 농도는 대조구 대비 간극수와 직상수에서 각각 19.0, 0.4 mg/L 낮게 검출되었다. 이는 GCA에서 용출된 칼슘이온과 인산인의 흡착반응을 통한 간극수 내의 인 고정 및 직상수로의 용출 억제에 따른 결과로 판단된다. 실험구의 간극수 내 황화수소 농도는 5.0 mg/L로 112.5 mg/L인 대조구에 비해 매우 낮게 나타났으며, 실험구 직상수의 DO 농도는 대조구에 비해 3.47 mg/L 높게 나타났다. 이상의 결과로부터 알칼리성 산업부산물인 GCA는 연안 오염퇴적물의 개선에 효과적인 재료임을 확인하였다.

• 상하수도학회지
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• 제32권3호
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• pp.253-259
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• 2018

Cu(II) can cause health problem for human being and phosphate is a key pollutant induces eutrophication in rivers and ponds. To remove of Cu(II) and phosphate from solution, chitosan as adsorbent was chosen and used as a form of hydrogel bead. Due to the chemical instability of hydrogel chitosan bead (HCB), the crosslinked HCB by glutaraldehyde (GA) was prepared (HCB-G). HCB-G maintained the spherical bead type at 1% HCl without a loss of chitosan. A variety of batch experiment tests were carried out to determine the removal efficiency (%), maximum uptake (Q, mg/g), and reaction rate. In the single presence of Cu(II) or phosphate, the removal efficiency was obtained to 17 and 16%, respectively. However, the removal efficiency of Cu(II) and phosphate was increased to 50~55% at a mixed solution. The maximum uptake (Q) for Cu(II) and phosphate was enhanced from 11.3 to74.4 mg/g and from 3.34 to 36.6 mg/g, respectively. While the reaction rate of Cu(II) and phosphate was almost finished within 24 and 6 h at single solution, it was not changed for Cu(II) but was retarded for phosphate at mixed solution.

• 한국농공학회논문집
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• 제55권1호
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• pp.49-57
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• 2013

The present study was conducted to investigate phosphate removal from aqueous solution using industrial wastes, red mud (RM), acid treated red mud (ATRM) and converter furnace steel slag (CFSS). The chemical composition of adsorbents was analyzed using X-ray fluorescence (XRF). Batch experiments and elution experiments using water tank were performed to examine environmental factors that influences on phosphate removal. Kinetic sorption data of RM, ATRM, and CFSS were described well by the pseudo second-order kinetic sorption model, and equilibrium sorption data of all adsorbents obeyed Freundlich isotherm model. The adsorption capacities of adsorbents followed order: ATRM (7.06 mg/g)>RM (4.34 mg/g)>CFSS (1.88 mg/g). Increasing pH from 3 to 11, the amount of adsorbed phosphate on all RM, ATRM, and CFSS were decreased. The presence of sulfate and carbonate decreased the phosphate removal of RM and ATRM but did not influence on the performance of CFSS. The phosphate removal of RM, ATRM, and CFSS was greater in seawater than deionized water, resulting from the presence of cations in seawater. The water tank elution experiments showed that RM capping blocked the elution of phosphate effectively. It was concluded that the adsorbents can be successfully used for the removal of the phosphate from the aqueous solutions.

• 상하수도학회지
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• 제31권6호
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• pp.521-527
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• 2017

Phosphorus is one of the limiting nutrients for the growth of phytoplankton and algae and is therefore one of leading causes of eutrophication. Most phosphorous in water is present in the form of phosphates. Different technologies have been applied for phosphate removal from wastewater, such as physical, chemical precipitation by using ferric, calcium or aluminum salts, biological, and adsorption. Adsorption is one of efficient method to remove phosphates in wastewater. To find the optimal media for phosphate removal, physical characteristics of media was analysed, and the phosphate removal efficiency of media (silica sand, slag, zeolite, activated carbon) was also investigated in this study. Silica sand showed highest relative density and wear rate, and phosphate removal efficiency. Silica sand removed about 36% of phosphate. To improve the phosphate removal efficiency of silica sand, Fe coating was conducted. Fe coated silica sand showed 3 times higher removal efficiency than non-coated one.

• Ocean and Polar Research
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• 제31권3호
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• pp.247-255
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• 2009

We measured phosphate benthic fluxes and conducted phosphate adsorption experiments in order to find out the effects of adsorption on phosphate benthic fluxes in the intertidal sediments of Keunso Bay during summer and winter. Organic carbon contents showed little variation with season at St. S1, but noticeable changes were observed at St. S2, which were three times higher in winter than in summer. The higher organic carbon contents in winter resulted from the bloom of benthic algae in surface sediments. Pore water phosphate concentrations were much higher in summer than in winter. The higher phosphate concentration in summer was probably due to the faster remineralization rate of organic matter in summer. At St. S1, benthic fluxes of phosphate showed a negative value in summer and a positive value in winter. However, St. S2 had a negative benthic flux both in summer and winter. The negative benthic flux was ascribed to the phosphate adsorption on iron oxides in surface sediments. The equilibrium concentrations of phosphate obtained from the adsorption experiment were three times higher at St. S1 than at St. S2. The relatively high adsorption coefficient and low equilibrium concentration indicated that phosphate was strongly adsorbed on the surface sediments of Keunso Bay. The strong adsorption affinity significantly reduced benthic fluxes of phosphate in the intertidal sediments.

• 분석과학
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• 제6권1호
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• pp.47-55
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• 1993

구리 착물을 수은 방울 전극에 흡착시키는 방법을 이용하여 음극 벗김 전압전류법으로 황화이온 존재하에서 미량의 시안화물을 효과적으로 정량할 수 있는 방법을 연구하였다. 염화칼륨과 인산염의 완충 용액(pH=7.0) 중에서 구리 이온 농도를 $1.0*10^{-3}M$로 유지하고서 석출 전위 -0.30V, 석출 시간 3.0분에서 약 500배의 황화이온이 있을 때 시안화이온의 검출 한계는 $2.0*10^{-7}M$이었다.

• 상하수도학회지
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• 제31권4호
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• pp.281-287
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• 2017

Mill scale, an iron waste, was used to separate magnetite particles for the adsorption of phosphate from aqueous solution. Mill scale has a layered structure composed of wustite (FeO), magnetite ($Fe_3O_4$), and hematite ($Fe_2O_3$). Because magnetite shows the highest magnetic property among these iron oxides, it can be easily separated from the crushed mill scale particles. Several techniques were employed to characterize the separated particles. Mill scale-derived magnetite particles exhibited a strong uptake affinity to phosphate in a wide pH range of 3-7, with the maximum adsorptive removal of 100%, at the dosage of 1 g/L, pH 3-5. Langmuir isotherm model well described the equilibrium data, exhibiting maximum adsorption capacities for phosphate up to 4.95 and 8.79 mg/g at 298 and 308 K, respectively. From continuous operation of the packed-bed column reactor operated with different EBCT (empty bed contact time) and adsorbent particle size, the breakthrough of phosphate started after 8-22 days of operation. After regeneration of the column reactor with 0.1N NaOH solution, 95-98% of adsorbed phosphate could be detached from the column reactor.

• 한국환경과학회지
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• 제12권10호
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• pp.1055-1060
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• 2003

Adsorption on goethite of individual component from a solution containing phosphate, sulfate, or copper ion was investigated. Competitive adsorption in the binary and ternary solution systems composed of phosphate, sulfate, and copper ions was also investigated. In competitive adsorption systems with phosphate and sulfate ions, the presence of phosphate ion reduced the adsorption of sulfate ion largely. On the other hand, the presence of sulfate ion caused only a small decrease in phosphate adsorption. This result suggests that phosphate ion is a stronger competitor for adsorption on goethite than sulfate ion, which is consistent with the higher affinity of phosphate for the surface compared to sulfate ion. Compared to the results from single-sorbate systems, adsorption of copper ion in the binary system of sulfate ion and copper ion was found to be enhanced in the presence of sulfate ion. Addition of sulfate ion to the binary system of copper ion and phosphate ion resulted in a small enhancement in copper sorption. This result implies that the presence of sulfate ion promotes adsorption of the ternary complex FeOHCuSO$_4$. The adsorption isotherms could be well described by the Langmuir adsorption equation.

• 한국토양비료학회지
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• 제21권3호
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• pp.241-245
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• 1988

야산지(野山地)를 경작지(耕作地)로 전환(轉換)하기 위한 기초자료(基礎資料)를 얻고자 영남지역(嶺南地域)을 중심(中心)으로 야산지(野山地) 토양(土壤)의 특성(特性)을 조사(調査)하였다. 일반적(一般的) 이화학성(理化學性)은 기경지(旣耕地) 토양(土壤)에 비해 불량(不良)하였다. 경사지(傾斜地)에서는 침식성인자(浸蝕性因子) K치(値)가 높고 입단안전성(粒團安定性)이 낮아 침식(浸蝕)에 의(依)한 표토(表土)의 유실(流失)이 있을 것으로 추정(推定)되었다. 주구성점토광물(主構成粘土鑛物)은 Kaoline계(系)이고 영일(迎日)II는 Bentonite로 판단(判斷)되었다. 이들지역(地域)의 토양(土壤)은 치환성(置換性) Al 및 Fe함량(含量)이 높고 인산흡착계수(燐酸吸着係數)가 246~551(Pmg/100g)으로 높았다. 따라서 야산지(野山地)를 경작지(耕作地)로 전환(轉換)하기 위해서는 물리(物理) 및 화학적(化學的) 성질(性質)의 개량(改良)이 선결(先決)되어야 하겠다.