• 한국세라믹학회지
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• 제30권10호
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• pp.871-879
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• 1993

Effects of K2SO4 and Na2SO4 on C3S formation and its microstructure were investigated. C3S formation was not influenced by addition up to 6.0wt% of K2SO4 as SO3 base, however it was prevented by only 1.0wt% of Na2SO4 addition. C3S prevention by added Na2SO4 was the reason why C2S stabilized by Na+ and SO42- could not react to C3S. Added K2SO4 appeared as K2SO4, however added Na2SO4 appeared as the form of Na2xCa3-xAl2O6, (Na0.8Ca0.1)SO4 and Na2SO4 in interstitial phase.

• 한국세라믹학회지
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• 제30권12호
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• pp.1071-1079
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• 1993

Interaction of alkali oxides and SO3 and C3S formation and microstructure was studied using K2CO3 and Na2CO3 as alkali sources and (NH4)2SO4 for SO3. When SO3/K2O=1.43 as mole ratio, K2O and SO3 react to form K2SO4, this phase is immiscible with other oxide melt and thus could not affect C3S formation as well as its microstructure. In a condition of SO3/K2O 1, C3S crystals were round and grown in a much larger size. With addition of Na2O and SO3 by only 1wt% each, C3S formation was strongly hindered. Since C2S was stabilized by Na+ and SO4-2, it could not react to give C3S formation. However in the condition of SO3/Na2O=1.43, a little amount of C3S was formed. It is considered that small amount of Na2SO4 was formed, this phase was immiscible with clinker liquid, and the C3S crystals were formed locally in the liquid part of relatively low Na2O and SO3 compositions. These crystals had irregular and rough surfaces and contained more inclusions than those grown from K2O.SO3 system.

• 센서학회지
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• 제5권4호
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• pp.25-34
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• 1996

NASICON 전해질을 이용하여 대기환경 측정용의 SOx센서를 개발하였다. 다음 형태의 $Na_{2}SiO_{3}(Pt)$ 기준전극을 사용한 갈바니 셀을 조립하였다. Pt | $Na_{2}SiO_{3}$ | NASICON | $Na_{2}SO_{4}$ | Pt, $SO_{2}$, air $SO_{2}$ 와 NASICON의 반응을 피하기 위해 $Na_{2}SO_{4}(Pt)$를 지시전극으로 사용하였으며, $400{\sim}550^{\circ}C$ 범위에서 $5{\sim}95ppm$ 농도의 $SO_{2}$ 가스를 주입하고 나서 EMF를 측정하였다. $500^{\circ}C$ 이상의 온도에서 측정된 EMF는 계산치와 일치하였으나, $500^{\circ}C$ 이하에서는 불완전한 평형 때문에 센서의 거동이 불안정하였다. 감응시간은 약 10분 정도 이내였다. 이전지의 안정도와 응답시간으로 보건데, $Na_{2}SiO_{3}(Pt)$를 기준전극으로 하고 순수 $Na_{2}SO_{4}(Pt)$를 지시전극으로한 NASICON 고체전해질은 SOx 측정용의 상업적인 센서물질로써 가능성이 있다.

• Applied Biological Chemistry
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• 제36권6호
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• pp.434-439
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• 1993

중성염이 단백질의 거품성에 미치는 영향을 밝히기 위하여 NaF, $Na_2SO_4$, NaCl, $NaNO_3$ 및 NaSCN 등 5종 중성염을 가지고 0.1, 0.5, 1.0, 1.5 및 2.0 M 농도별로 sodium caseinate(5%, w/v)에 작용시켜 이들 염류가 거품성에 미치는 영향을 조사하였다. NaSCN을 제외한 모든 염류들은 거품형성능 증진효과가 있었고, 거품형성능을 위한 염류의 최적농도는 $Na_2SO_4$, NaCl 및 NaSCN에서 각각 0.5, 1.5 및 1.0 M이었으며, NaF 및 $NaNO_3$에서는 각각 0.5 및 2.0 M 농도에서 거품형성능이 양호하였다. 거품안정성은 0.5 M $Na_2SO_4$의 경우 37.0분(대조구 4.0) 으로서 가장 양호하였으며 0.5M NaF에서도 28.6분으로써 크게 증가하였으나, NaSCN의 경우는 역으로 모두 감소하였다. 거품안정성이 가장 양호한 것으로 나타난 0.5 M 농도의 경우, 거품안정성의 크기는 $Na_2SO_4$>NaF>$NaNO_3$>NaCl>NaSCN의 순으로 나타났으며 이는 음이온이 단백질의 염석효과를 나타내는 Hofmeister 계열순서와 거의 일치하였다. 본 실험의 중성염을 첨가하여 조제한 단백질 시료용액의 경우, 혼탁도, 표면장력 및 절대점도의 증감에 따른 거품성의 뚜렷한 변화는 나타나지 않았다.

• 한국표면공학회지
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• 제51권4호
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• pp.214-217
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• 2018

Stainless steel grade 430 with a composition of Fe-17%Cr was corroded in $Na_2SO_4$ and ($Na_2SO_4+NaCl$) salts at 800 and at $900^{\circ}C$ for up to 20 h. It corroded mainly to $Cr_2O_3$, along with a small amount of $Fe_2O_3$ and $Fe_3O_4$. The formed oxide scales were neither dense nor compact enough owing to their ensuing dissolution into the salt during corrosion, which facilitated internal corrosion. Corrosion occurred faster at $900^{\circ}C$ than $800^{\circ}C$. NaCl in $Na_2SO_4$ aggravated the scale adherence.

• 분석과학
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• 제16권2호
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• pp.159-165
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• 2003

아연산화광 황산침출액에 적용가능한 이온평형모델을 개발하기 위해 Vasil'ev식과 Pitzer식에 의한 해석방법을 비교하였다. 이온강도가 9 m정도로 증가할수록 Vasil'ev식보다는 Pitzer식에 의한 용액의 이온평형결과가 정확하였다. 아연산화광 황산침출액을 모사하기위해 $25^{\circ}C$에서 $ZnSO_4-Fe_2(SO_4)_3-Na_2SO_4-H_2SO_4-NaOH-H_2O$계에 대해 전해질의 농도를 변화시키며 혼합한 용액의 pH 측정값과 본 연구에서 계산한 pH값은 서로 잘 일치하였다.

• 한국세라믹학회지
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• 제30권7호
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• pp.543-548
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• 1993

Stability and formation of Pb(Mg1/3Nb2/3)O3 (PMN) phase synthesized in Li2SO4-Na2SO4 molten salts have been investigated. And powder characteristics of PMN have been studied with a variation of processing parameters such as temperature, time, amount of the salts, and excess PbO. More ratio of Li2SO4 to Na2SO4 influences the percentage of perovskite phase due to the difference of the eutectic point of the salts, but does not influence the powder characteristics. The shape of PMN particles shows faceted morphology with bimodal distribution consisting with large and submicron parts. Particle size of PMN increased greatly with increasing soaking time or amount of salts rather than temperature. The addition of excess PbO resulted in round PMN crystallites without submicron particles. These results are discussed by XRD, SEM and thermal analyses.

• 자원리싸이클링
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• 제11권1호
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• pp.19-25
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• 2002

$ZnSO_4$- $Na_2$$SO_4$-$H_2$$SO_4$-$NaOH-H_2$O계에 대해 전해질의 농도를 변화시키며 $25^{\circ}C$에서 용액의 pH를 측정하고, K-value방법을 이용하여 이온평형을 해석하였다. 물의 활동도와 용질의 활동도계수는 Pitzer식으로 계산하였다. 평형상태에서 존재하는 용질들의 농도와 활동도계를 전해질의 초기농도로부터 이온평형을 해석하여 구할 수 있었다 이온강도가 4 m정도로 진한 용액에서 pH측정값과 이온평형 해석으로 구한 pH 이론 값은 서로 잘 일치하였다. 액의 이온강도가 3.5에서 4.3사이의 실험조건에서 Pitzer식으로 구한 $ZnSO_4$의 평균이온 활동도계수는 문헌에 발표된 값과 잘 일치하였다.

• Journal of Plant Biology
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• 제34권3호
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• pp.185-190
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• 1991

Hypocotyl-derived callus cultures of Brassica pekinensis cv. Chungseng were grown on Murashige-Skoog medium containing NaCl, Na2SO4 and mannitol to clarify the effect of salts on callus growth, proline accumulation and water relations. Na2SO4 was more inhibitory than NaCl when survival rate, growth and fresh:dry weight ratios of established callus were measured. Fresh weight in 0.25% NaCl treatment was more than twice as increasable in comparison to the same concentration of Na2SO4 or control. Proline concentration was increased on either salt, attained at highest levels at the 5th subculture, and fluctuated as affected by both salts or mannitol. Concentrations of redeucing sugars were sharply increased after 2 or 3 times of subculture and decreased by increasing subculture. The water and osmotic potential in callus reached a maximum negative value after two weeks in culture, regardless of salt type and mannitol and tugor remained relatively constant on both salt and mannitol treatments.

• 한국전기전자재료학회논문지
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• 제13권5호
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• pp.451-457
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• 2000

Experimental investigations on the effect of two kinds of additives ; aqueous NaOH solution and ammonia(NH$_3$) for removal of NOx and SO$_2$ simultaneously by corona discharge were carried out. The simulated combustion flue gas was[NO(0.02[%])-SO$_2$(0.08[%])-$CO_2$-Air-$N_2$] Volume percentage of aqueous NaOH solution used was 20[%] and $N_2$flow rate was 2.5[$\ell$/min] for bubbling aqueous NaOH solution Ammonia gas(14.81[%]) balanced by argon was diluted by air. NH$_3$ molecular ratios(MR) based on [NH$_3$] and [NO+SO$_2$] were 1, 1.5 and 2.5 The vapour of aqueous NaOH solution and NH$_3$was introduced to the main simulated combustion flue gas duct through injection systems which were located at downstream of corona discharge reactor. NOx(NO+NO$_2$) removal rate by injecting the vapour of aqueous NaOH solution was much better than that by injecting NH$_3$however SO$_2$removal rate by injecting NH$_3$was much better than that by injecting the vapour of aqueous NaOH SO$_2$removal rate slightly increased with increasing applied voltage. When the vapour of aqueous NaOH solution and NH$_3$were simultaneously injection NOx and SO$_2$ removal rate were significantly increased.