• Macromolecular Research
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• 제11권1호
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• pp.53-61
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• 2003

A molecular-thermodynamic model is developed for the salt-induced protein precipitation. The protein molecules interact through four intermolecular potentials. An equation of state is derived based on the statistical mechanical perturbation theory with the modified Chiew's equation for the fluid phase, Young's equation for the solid phase as the reference system and a perturbation based on the protein-protein effective two body potential. The equation of state provides an expression for the chemical potential of the protein. In a single protein system, the phase separation is represented by fluid-fluid equilibria. The precipitation behaviors are simulated with the partition coefficient at various salt concentrations and degree of pre-aggregation effect for the protein particles. In a binary protein system, we regard the system as a fluid-solid phase equilibrium. At equilibrium, we compute the reduced osmotic pressure-composition diagram in the diverse protein size difference and salt concentrations.

• 자원리싸이클링
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• 제26권5호
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• pp.39-47
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• 2017

본 연구에서는 희토류 황산수용액으로부터 희토류 원소를 철로부터 분리/회수하고자, 황산나트륨을 이용한 희토류 황산복염 침전반응에 관하여 고찰하였다. 네오디뮴(Nd)은 황산나트륨과 결합하여 복염으로 침전이 용이하게 일어나는 반면에 디스프로슘(Dy)은 황산복염으로 침전되기 위해서 과량의 황산나트륨이 필요하였다. 또한 황산수용액에서 네오디뮴의 존재는 디스프로슘 황산복염 침전을 촉진시켜서 디스프로슘 황산복염 침전률을 증가시켰다. 본 연구에서 사용된 네오디뮴 함량 23.39 mg/ml, 디스프로슘 함량 8.67 mg/ml인 황산수용액으로부터 반응온도 $60^{\circ}C$, 반응 3시간에서 황산나트륨을 7 당량 첨가하였을 때, 네오디뮴 복염 침전률은 99.7%, 디스프로슘 복염 침전률은 94.3%이었다. 또한 네오디뮴과 디스프로슘의 황산복염 침전특성을 이용한 두 원소의 분리 가능성을 고찰한 결과, 염화나트륨 첨가에 의한 염석효과가 디스프로슘 품위 증가에 중요한 역할을 하며 본 연구조건에서 최대 98.7% 품위의 디스프로슘을 얻을 수 있었다.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제50권3호
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• pp.130-135
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• 2001

In this paper, the distribution characteristics of salt contaminants with the distance from sea in East coast, from Sokcho to Pusan of Korea peninsula were investigated to evaluate the design standard of KEPCO. To get the equivalent salt deposit density(ESDD), conventional brush wiping method was used. As the measuring period is comparatively short, and the measuring interval is long to check the maximum value, acquired ESDD data is very lower than the recommended value in the standard. The measured data didn't follow normal distribution, so it should take the statistical treatment. Through normalizing method, we could get a reliable probability data. In the past investigation, the accumulation characteristics of Japan is consulted to set the criterion, but the climatic condition of Korea is different to Japan. With the comparison of precipitation data and some measured data for long tern accumulation, we could set appropriate accumulation factor.

• 한국세라믹학회지
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• 제33권9호
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• pp.1031-1037
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• 1996

• 대한화학회지
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• 제46권1호
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• pp.7-13
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• 2002

자화수가 특이한 물리화학적 성질을 갖고 있음은 여러 학자들에 의하여 꾸준히 연구되어 왔는데, 아직도 자화수의 특성이 명확하게 설명되지 못하고 있는 실정이다. 본 연구에서는 자화수가 염류들의 침전반응 및 석고의 가수 경화반응에 미치는 영향을 다음과 같이 관찰하였다. $25^{\circ}C$ 항온조 내부에서 실시한 salt filter assay 방법으로 침전반응을 조사하였으며, $20^{\circ}C$ 실온에서 석고의 가수 경화반응 시간을 Gillmore needle의 방법으로 측정함으로써 석고의 가수 경화 속도를 조사하였다. 0.1M 염 이온들을 반응시킨 염류의 침전 반응 결과, $BaSO_4,\;BaCO_3,\;CaCO_3$의 침전 생성물의 양은 대조군의 증류수에 비하여 자화수에서 각각 약 3.6%, 3.8%, 4.4% 씩 증가되었으며, 석고의 최종 경화시간은 대조군의 증류수에 비하여 자화수에서 현저하게 감소되었으므로 자화수가 석고의 가수 경화속도를 촉진시키는 것으로 나타났다. 이는 대조군의 증류수에 비하여 자화수는 물분자가 치밀하게 구조화되어서 수많은 cluster들을 형성함으로서 물분자 사이의 결합 및 반응력이 증가되며, $Ba^{2+}$ 또는 $Ca^{2+}$ 같은 염류들에 대하여 특징적으로 반응해 침전반응 속도와 가수 경화 반응 속도가 증가된 것으로 추측된다.

• The Korean Journal of Ecology
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• 제20권2호
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• pp.133-143
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• 1997

From 1984 to 1989 reclaimed coastal lands in Choongnam Province of the western coast of Korea were studied for soil texture at three sites(Daeho, Hyundai A and Hyundai B) and for desalination one site(Hyundai B). The soil textures of varied sites in Hyundai A were horizontally similar and composed of 39-40% clay, 40-49% silt and 8-14% sand. But those in Da돼 and Hyundai B differed horizontally in the same area and vertically at the same site. Soil texures of Da돼 were composed of 15-17% clay, 30-45% silt and 40-55% sand and those of Hyundai B were composed of 22-45% clay, 26-49% silt and 17-31% sand. The measured electrical conductivity(EC), which represents whole salt content of the reclaimed soil, decreased year by year. The vertical distribution of the EC changed temporally and spatially in the upper zone above a 50 cm depth but not in The lower zone below a 50 cm depth. The EC valus of the soil were inversely proportional to the magnitued of annual precipitation, evaporation and the numbers of rainy days with r equalling -0.97. But the annual decrease of the EC was directly proportional to climatic factors with r=0.7. Salt in the reclaimed land was leached out by the percolative action of surplus rain water, or moved up by evaporation and carried away by running rain water. The running out of the salt on the soil surface was most efficiently carried out over 10 mm precipitation per day.

• 한국결정성장학회지
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• 제22권2호
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• pp.99-104
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• 2012

BCP(biphasic calcium phosphate) 분말을 제조하기 위하여 $Ca(NO_3)_2{\cdot}4H_2O$, $(NH_4)_2HPO_4$를 출발 물질로 공침법(co-precipitation process)을 이용하여 합성하였다. 합성된 분말의 열처리 전 후의 HAp(Hydroxyapatite)/${\beta}$-TCP(${\beta}$-Tricalcium phosphate) 결정상 비율 및 분광학적 특성을 XRD 및 FT-IR를 이용하여 분석하였다. BCP 분말의 생체활성 거동을 평가하기 위하여 Hanks' Balanced Salt Solution(HBSS)에 침적시켜 시간에 따라 형상, 이온농도의 변화 및 결정상을 분석한 결과 낮은 결정화도의 HAp가 생성됨을 확인하였다. BCP분말의 세포독성 평가에서도 대조군에 비하여 세포성장률이 우수함을 관찰하였다.

• Membrane and Water Treatment
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• 제3권4호
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• pp.253-266
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• 2012

In this work, the effect of hybrid salts precipitation-nanofiltration (SP-NF) process on the scale deposits in thermal and membrane desalination processes has been studied. The analysis was carried out to study the scale formation from the Arabian Gulf seawater in MSF and RO reference processes by changing the percentage of pretreatment from 0 to 100%. Four different SP-NF configurations were suggested. A targeted Top Brine Temperature (TBT) of $130^{\circ}C$ may be achieved if 30% portion is pretreated by SP and/or NF processes. As a rule of thumb, each 1% pretreatment portion increases the reference TBT of $115^{\circ}C$ by $0.6^{\circ}C$. For both MSF and RO, parallel pretreatment of certain percentage of the feed by SP and the rest by NF, showed the lowest scale values. The case showed the best values for sulfate scale prevention and the highest values of increasing the monovalent ions relative to the divalent scale forming ions. Sulfate scale is significant in MSF process while carbonate scale is significant in RO. Salt precipitation was suggested because it is less costly than nanofiltration, but nanofiltration was used here because it is efficient in sulfate ions removal.

• 한국세라믹학회지
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• 제27권7호
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• pp.851-860
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• 1990

The hydrolysis-precipitation reaction of mixed aluminum salt solutions of aluminum sulfate, aluminum nitrate, and urea has been investigated to obtain narrow-sized and unagglomerated fine spherical precipitates of aluminum hydroxide required for coating core particles. The hydrolysis-precipitatin reaction could be controlled to be appropriate to coating processes by usign urea as a pH control-agent. As the concetration of total Al3+ ion and the molar ratio of SO42-/Al3+ in starting solutions became smaller and also as the vol. ratio of water/solution for hydrolyzing mixed aluminum salt solution became larger, the morphology of precipitates tended to be more unagglomerated and spherical, while their size(0.5longrightarrow0.05${\mu}{\textrm}{m}$) to be smaller. The optimum hydrolysis condition for coating processes was to hydrolyze the mixed aluminum salt solution, in which the molar ratio of SO42-/Al3+ was 0.75, while the amount of water corresponding to the vol. ratio of water/solution of 15. The precipitate was the aluminum hydroxide which sulfate ions were strongly adsorbed on and the maximum yield in the hydrolysis-precipitation reaction was about 20%.

• 한국세라믹학회지
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• 제31권10호
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• pp.1181-1187
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• 1994

Sr-ferrite powders were synthesized by molten salt method. The process of powder formation was investigated by controlling the size and shape (sphere and acicular) of starting materials. The morphology of resulting ferrite was plate-like regardless of the shape of starting materials, Fe2O3 powders. As a result, the formation of Sr-ferrite in the molten salt was proceeded by solution-precipitation.