• 제목/요약/키워드: SoP

검색결과 10,794건 처리시간 0.039초

UPnP 브리지를 위한 범용 MFD 구조 (General MFD Structure for UPnP Bridge)

  • 최용순;강정석;박홍성
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2007년도 심포지엄 논문집 정보 및 제어부문
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    • pp.289-290
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    • 2007
  • UPnP Bridge supporting diverse network interface has to meet standard requirements in order to be connected with legacy devices. It is able to provide or bridge a service description and device description according to a specification because IEEE1394 and USB have this standard requirements. But it is difficult to know whether it RS232C supports only serial communication and packet transfer. It need a document for the standard definition of communication protocol on UPnP device having such interface. By doing so, this document can understand device and packet type. This paper defines MFD(Message Field Description) and makes UPnP message converter. So it will be base to standardize supporting variable legacy device.

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p-Toluenesulfonate를 가진 새로운 코발트(II) 층상 화합물의 합성과 구조 분석 (Synthesis and Structural Analysis of a New Layered Cobalt(II) Compound with p-Toluenesulfonic Acid : $[Co(H_2O)_6](CH_3C_6H_4SO_3)_2$)

  • 김종혁;이석근
    • 분석과학
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    • 제13권4호
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    • pp.534-538
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    • 2000
  • The title compound, $[Co(H_2O)_6](CH_3C_6H_4SO_3)_2$, has been prepared and characterized by X-ray crystallography. The crystal structure of the compound demonstrates a layered material constituted by hexaaquacobalt (II) cations and p-toluenesulfonate anions. Geometrical environment of the cobalt atom is octahedrally coordinated by water molecules. The p-toluenesulfonate anions are arranged with the sulfonate groups turned toward opposite side of the layer, alternately. The layered structure is stabilized by the hydrogen bondings between the ligated water molecules and the anionic sulfonate oxygen atoms.

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(p, q)-LAPLACE TRANSFORM

  • KIM, YOUNG ROK;RYOO, CHEON SEOUNG
    • Journal of applied mathematics & informatics
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    • 제36권5_6호
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    • pp.505-519
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    • 2018
  • In this paper we define a (p, q)-Laplace transform. By using this definition, we obtain many properties including the linearity, scaling, translation, transform of derivatives, derivative of transforms, transform of integrals and so on. Finally, we solve the differential equation using the (p, q)-Laplace transform.

SO2 노출된 4개 수종의 엽내 광색소 함량 및 SOD 활성 변화 (Changes of Photosynthetic Pigment Contents and SOD Activity in the Leaves of Four Tree Species Exposed to SO2)

  • 이재천;한심희;권기원;우수영;최정호
    • 한국농림기상학회지
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    • 제5권1호
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    • pp.18-23
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    • 2003
  • 목본 식물을 대상으로 SO$_2$에 의해 나타나는 생리적인 반응을 구명하기 위하여 소나무, 오갈피나무, 현사시, 상수리나무를 대상으로 SO$_2$를 500 ppb, 800 ppb로 하루에 8시간씩 7일간 처리하여 잎의 광색소 함량과 SOD 활성을 비교 분석한 결과는 다음과 같았다. SO$_2$의 처리 농도가 증가할수록 4개 수목의 엽 내 엽록소 함량은 감소하였으며, 엽록소 a와 엽록소 b, 카로티노이드 함량의 변화는 수종별, 처리별로 다른 경향을 보였다. 오갈피나무와 상수리나무의 엽록소 b와 a의 비는 SO$_2$는 500 ppb 처리구에서는 증가하다가 800ppb 처리구에서는 감소하였다. 즉 500ppb에서는 엽록소 a가 파괴되며, 800ppb에서는 엽록소 b도 파괴될 수 있음을 보여 주었으며, SO$_2$에 대한 민감성은 엽록소 a가 엽록소 b보다 높은 것으로 나타났다. 4개 수종의 잎 SOD활성은 수종별, 처리별 큰 차이를 나타냈다. 오갈피나무와 상수리나무는 500 ppb 처리구에서는 SOD 활성이 증가하다가 더 높은 농도에서는 활성이 감소하였으며, 소나무와 현사시의 경우는 500ppb 처리와 800ppb 처리에서 높은 SOD활성을 유지하여 내성을 보인다. 그러나 광색소와 SOD 활성을 기준으로 판단해 볼 때, SO$_2$에 대한 저항성은 현사시가 가장 높은 것으로 판단된다.

In Vitro에서 $SO_2$ 수용액의 화학적 변화 (Chemical Changes of Dissolved Sulfur Dioxide In Vitro)

  • 이미순;이서래
    • Applied Biological Chemistry
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    • 제19권1호
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    • pp.51-56
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    • 1976
  • $SO_2$ 수용액의 화학적 변화를 in vitro system에서 조사하였다. 농도가 다른 수용액이 20시간 후에 비슷한 Eh값에 도달하였으며 산성용액에서는 Eh값이 그 이상 증가하지 않았다. Eh값은 알카리성용액에서 보다는 중성용액에서 크게 증가하였고 암흑에서 보다는 광조건하에서 다소 높은 경향을 나타냈다. 유리상태의 $SO_2$함량은 아황산염의 농도가 증가하거나, 광에 노출한 경우, 또는 pH가 높은 때에 크게 감소하였다. 발생기수소는 고농도의 $SO_2$나 산성용액에서 보다는 중성 혹은 알카리성 용액에서 더욱 많이 생성되었다.

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진주시 주변 산림에서 안개의 화학적 특성 (Chemical Characteristics of Fog at a Forested Area in Jinju)

  • 이총규
    • 농업생명과학연구
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    • 제46권6호
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    • pp.51-57
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    • 2012
  • 본 연구는 안개를 채취하여 화학적 조성을 분석하고 금후 산성안개의 대책에 필요한 기초자료로 활용하고자 수행하였다. 안개수의 pH는 2010년도가 4.3이었고, 2011년은 4.0으로서 강한 산성이었고, 전기전도도는 평균 477.2와 $562.7{\mu}s$이었다. 안개수의 음이온 중 봄철과 여름철 $NO_3{^-}$ 농도가 각각 267.1, 279.1 mg/L로서 가장 높았고, 다음으로 $SO{_4}^{2-}$ 농도가 각각 177.2, 198.6 mg/L이었다. 가을과 겨울철 $NO_3{^-}$ 농도가 각각 217.7, 237.9 mg/L로서 가장 높았고, 다음으로 $SO{_4}^{2-}$농도가 각각 164.2, 190.1 mg/L이었다(p<0.05). 양이온은 봄철과 여름철 $Ca^{2+}$농도가 각각 221.3, 233.7 mg/L로서 가장 높았고, $Na^+$ 농도가 각각 125.1, 131.7 mg/L이었다. 가을과 겨울철에 $Ca^{2+}$농도가 각각 196.8, 198.8 mg/L로서 가장 높았고, 다음으로 $Na^+$ 농도가 각각 97.1, 117.2 mg/L이었다(p<0.05). 산성안개를 일으키는 안개수의 pH와 $EC(r=-0.9861^{**})$, $NO_3{^-}(r=-0.9677^{**})$, $SO{_4}^{2-}$ ($r=-0.9510^{**}$), $Ca^{2+}$는 1% 수준에서 상관이 있었다. 산성안개수의 생성에 영향을 하는 인자의 회귀 방정식을 나타내면 $Y(pH)=6.4627+0.9723X_2(EC)+0.9364X_4(NO_3{^-})+0.9044X_5(SO{_4}^{2-})+0.8049X_{10}(Ca^{2+})+0.6709X_8(K^+)\;(r^2=0.8787)$로 추정되었다.

반건식 배연탈황법에 의한 연소 페가스 중 $SO_2$제거에 관한 연구 (A Study on $SO_2$Removal in Flue Gas by Semidry Flue Gas Desulfurization Method)

  • 송호철;이윤기;박진원
    • 한국대기환경학회지
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    • 제14권4호
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    • pp.273-280
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    • 1998
  • The investigation on the removal of 502 gas fro.In flue gas which causes serious air pollution was made by using a semi dry flue gas desulfurization method. Experiments were carried out as a function of process variables which would affect SO2 removal efficiency. Process variables inclilded SO2 inlet concentration, inlet temperature of simulated flue gas, sorbent weight fraction, and volume flow rate of sorbent slurry. In this study, used sorbent was Ca(OH), and simulated flue gas was prepared by mixing pure SO2 gas with air. Experimental conditions were varied at 140~18$0^{\circ}C$ of inlet temperature of the simulated flue gas, 500~2000ppm of inlet SO2 concentration, 0.4~1.0% of sorbent concentration, and 10~25 mL/min of flow rate of sorbent slurry. Among process variables, inlet concentration of SO2 was found to be the most significant factor to affect SO2 removal efficiency. The concentration of Ca(OH2) had a lower effect on SO2 removal than SO2 inlet concentration removal amount was 0.108, 0.141, 0.153 g SO2/g Ca(OH)2 respectively- As 200 mmol of HNO3 was added into slurry to improve removal efficiency, initial pH was maintained and solubility of slurry increased, so that removal efficiency elevated. Adding over 200 mmol of HNO3 into slurry caused removal efficiency lower. Therefore it could be concluded the optimum was 200 mmol of HNO3 input.

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Analysis of ceramide metabolites in differentiating epidermal keratinocytes treated with calcium or vitamin C

  • Kim, Ju-Young;Yun, Hye-Jeong;Cho, Yun-Hi
    • Nutrition Research and Practice
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    • 제5권5호
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    • pp.396-403
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    • 2011
  • Ceramides (Cer) comprise the major constituent of sphingolipids in the epidermis and are known to play diverse roles in the outermost layers of the skin including water retention and provision of a physical barrier. In addition, they can be hydrolyzed into free sphingoid bases such as $C_{18}$ sphingosine (SO) and $C_{18}$ sphinganine (SA) or can be further metabolized to $C_{18}$ So-1-phosphate (S1P) and $C_{18}$ Sa-1-phosphate (Sa1P) in keratinocytes. The significance of ceramide metabolites emerged from studies reporting altered levels of SO and SA in skin disorders and the role of S1P and Sa1P as signaling lipids. However, the overall metabolism of sphingoid bases and their phosphates during keratinocyte differentiation remains not fully understood. Therefore, in this study, we analyzed these Cer metabolites in the process of keratinocyte differentiation. Three distinct keratinocyte differentiation stages were prepared using 0.07 mM calcium (Ca$^{2+}$) (proliferation stage), 1.2 mM Ca$^{2+}$ (early differentiation stage) in serum-free medium, or serum-containing medium with vitamin C (50 ${\mu}L$/mL) (late differentiation stage). Serum-containing medium was also used to determine whether vitamin C increases the concentrations of sphingoid bases and their phosphates. The production of sphingoid bases and their phosphates after hydrolysis by alkaline phosphatase was determined using high-performance liquid chromatography. Compared to cells treated with 0.07 mM Ca$^{2+}$, levels of SO, SA, S1P, and SA1P were not altered after treatment with 1.2 mM Ca$^{2+}$. However, in keratinocytes cultured in serum-containing medium with vitamin C, levels of SO, SA, S1P, and SA1P were dramatically higher than those in 0.07- and l.2-mM Ca$^{2+}$-treated cells; however, compared to serum-containing medium alone, vitamin C did not significantly enhance their production. Taken together, we demonstrate that late differentiation induced by vitamin C and serum was accompanied by dramatic increases in the concentration of sphingoid bases and their phosphates, although vitamin C alone had no effect on their production.

황산고토와 수산화고토 비료가 토양 pH, EC 및 교환성 양이온 분포에 미치는 영향 비교 (Comparison of the Effects of Mg-Sulfate and Mg-Hydroxide on Soil pH, EC and Exchangeable Cation Distribution)

  • 이상조;이승호;신현진;조현종;김복진;정종배
    • 한국토양비료학회지
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    • 제36권3호
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    • pp.105-112
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    • 2003
  • 황산고토와 수산화고토는 용해도를 비롯한 화학적 특성이 크게 다르므로 이들을 비료로 토양에 시용하였을 때 토양의 화학성에 미치는 영향 또한 달리 나타날 것이다. 본 연구에서는 이들 고토 비료가 토양 pH, EC 및 교환성 양이온 분포에 미치는 영향을 조사하였다. 수산화고토는 토양 pH를 증가시켰으며, 이러한 현상은 수산화고토의 낮은 용해도 때문에 주로 표토에만 제한적으로 나타났다. 황산고토의 경우에는 토양 pH를 저하시켰으며, 이러한 영향은 조사된 20 cm 깊이까지 나타났다. 용해도가 높은 황산고토의 이러한 pH 저하 현상은 주로 토양용액의 이온 강도 증가에 기인한는 것으로 판단되었다. 토양 EC는 황산고토 처리에서 크게 증가하였으나 수신화고토 처리에서는 표토 일부에서 약간 증가하는 결과를 보였다. 교환성 $Mg^{2+}$ 함량 조사 결과를 보면 황산고토의 경우 용해도가 높으므로 일시에 다량의 마그네슘이 토양에 용출되며 관수에 따라서 쉽게 용탈될 수 있는 것으로 나티났으며, 반면 수산화고토의 경우에는 용해도가 낮으므로 표토에만 지속적으로 마그네슘을 공급할 수 있는 것으로 나타났다. 황산고토 처리의 경우 다량의 마그네슘을 용출되므로 수산화고토에 비하여 교환성 $Ca^{2+}$의 유실을 초래할 수 있는 것으로 나타났다. 이상의 결과를 고려할 때, 토양 환경 특성을 고려한 고토 비종의 선택이 필요할 것이며, 특히 산성토양 또는 염류집적 가능성이 높은 토양에서는 황산고토에 비해 수산화고토의 시용이 유리할 것으로 판단된다.

Effects of atmospheric environmental changes on annual ring growth of Cryptomeria japonica in Southern Korea

  • Luong, Thi-Hoan;Jang, Kyoung-Soo;Choi, Woo-Jung;Lee, Kye-Han
    • Journal of Ecology and Environment
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    • 제36권1호
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    • pp.31-38
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    • 2013
  • Annual ring formation is considered a source of information to investigate the effects of environmental changes caused by temperature, air pollution, and acid rain on tree growth. A comparative investigation of annual ring growth of Cryptomeria japonica in relation to environmental changes was conducted at two sites in southern Korea (Haenam and Jangseong). Three wood disks from each site were collected from stems at breast height and annual ring growth was analyzed. Annual ring area at two sites increased over time (p > 0.05). Tree ring growth rate in Jangseong was higher than that in Haenam. Annual ring area increment in Jangseong was more strongly correlated with environmental variables than that in Haenam; annual ring growth increased with increasing temperature (p < 0.01) and a positive effect of $NO_2$ concentration on annual ring area (p < 0.05) could be attributed to nitrogen deposition in Jangseong. The correlation of annual ring growth increased with decreasing $SO_2$ and $CO_2$ concentrations (p < 0.01) in Jangseong. Variation in annual growth rings in Jangseong could be associated with temperature changes and N deposition. In Haenam, annual ring growth was correlated with $SO_2$ concentration (p < 0.01), and there was a negative relationship between precipitation pH and annual ring area (p < 0.01) which may reflect changes in nutrient cycles due to the acid rain. Therefore, the combined effects of increased $CO_2$, N deposition, and temperature on tree ring growth in Jangseong may be linked to soil acidification in this forest ecosystem. The interactions between air pollution ($SO_2$) and precipitation pH in Haenam may affect tree growth and may change nutrient cycles in this site. These results suggested that annual tree ring growth in Jangseong was more correlated with environmental variables than that in Haenam. However, the further growth of C. japonica forest at two sites is at risk from the long-term effects of acid deposition from fossil fuel combustion.