• 한국대기환경학회지
• /
• 제21권3호
• /
• pp.343-355
• /
• 2005

Cloud/fog water was collected at Daegwallyeong, a typical clean environmental area, by using an active fog sampler during the foggy period in 2002, The pH ranged from 3,7 to 6,5 with a mean of 5,0, but the pH calculated from average concentrations of $H^+$ was 4.4. $SO_4^{2-},\;NO_3^-\;and\;NH_4^+$ were predominant ions with average concentrations of 473,3, 463,3 and $576,0\;{\mu}eq/L$, respectively, This showed that cloud/fog water was slightly acidified, but the concentrations of major pollutants were as high as those for polluted area, suggesting effect from long range transported pollutants, Samples were categorized into four groups (E, W, S, N) by applying 48-h back trajectory analysis using the Hybrid Single-Particle Largrangian Integrated Trajectory (HYSPLIT) model. Concentrations of seasalt $(Na^+\;and\;Cl^-)$ were the highest for group E, indicating large input of seasalts by air masses transported from the East Sea. The concentrations of $SO_4^{2-}$ were slightly higher in group W but the difference was not significant. However, the concentrations of $NO_3^-$ were significantly higher in group W than those in other three groups, The median values of cloud/fog water pH for group N and W were below 4,5, which is significantly lower than median values in group E and group S, This suggests that the acidifying pollutants were transported from the Asia continents and Seoul metropolitan area cause acidification of the cloud/fog water in Daegwallyeong.

• 한국생물공학회:학술대회논문집
• /
• 한국생물공학회 2003년도 생물공학의 동향(XIII)
• /
• pp.159-159
• /
• 2003

• 한국응용곤충학회지
• /
• 제14권1호
• /
• pp.7-12
• /
• 1975

벼 흰빛잎마름병의 병원균(Xanthomonas oryzae)을 이용하여 항생제의 일종인 Agrepto에 대한 약제저항성형성을 조사하기 위하여 세대 경과에 따른 약제처리효과를 Optical Density로 간접 측정하여 다음과 같은 결과를 얻었다. 1. Agrepto는 액체배양기에 첨가되었을 때 처리 제1세대 30ppm까지의 낮은 농도 처리에서도 세균증식에 현저한 저지 효과를 나타내었다. 2. 동일농도의 4세대간 처리에서 세대의 경과에 따라 세균 증식량이 현저히 증가하였고 증식율은 10ppm 처리구에서 보다 30ppm 처리구에서 더욱 뚜렷하였다. 3. 전세대 20ppm 처리구의 선발집단의 경우 세대가 경과할수록 더욱 내성의 증가 현상을 나타내었다. 4. 고농도 처리구에서 선발된 세균이 저농도처리구에서 선발된 세균의 경우보다 저항성 형성이 현저히 증가되는 경향을 보였다.

• Korea-Australia Rheology Journal
• /
• 제14권4호
• /
• pp.189-201
• /
• 2002

The interaction between hydrophobically modified hydroxyethyl cellulose (hmHEC), containing approximately 1 wt% side-alkyl chains of $C_{16}$, and an anionic sodium dodecyl sulphate (SDS) surfactant was investigated. For a semi-dilute solution of 0.5 wt% hmHEC, the previously observed behaviour of a maximum in solution viscosity at intermediate SDS concentrations, followed by a drop at higher SDS concentrations, until above the cmc of surfactant when the solution resembles that of the unsubstituted polymer, was confirmed. Additionally, a two-phase region containing a hydrogel phase and a water-like supernatant was found at low SDS concentrations up to 0.2 wt%, a concentration which is akin to the critical association concentration, cac, of SDS in the presence of hmHEC. Above this concentration, SDS molecules bind strongly to form mixed micellar aggregates with the polymer alkyl side-chains, thus strengthening the network junctions, resulting in the observed increase in viscosity and elastic modulus of the solution. The shear behaviour of this polymer-surfactant complex during steady and step stress experiments was examined In great detail. Between SDS concentrations of 0.2 and 0.25 wt%, the shear viscosity of the hmHEC-polymer complex network undergoes shear-induced thickening, followed by a two-stage shear-induced fracture or break-up of the network. The thickening is thought to be due to structural rearrangement, causing the network of flexible polymers to expand, enabling some polymer hydrophobic groups to be converted from intra- to inter-chain associations. At higher applied stress, a partial local break-up of the network occurs, while at even higher stress, above the critical or network yield stress, a complete fracture of the network into small microgel-like units, Is believed to occur. This second network rupture is progressive with time of shear and no steady state in viscosity was observed even after 300 s. The structure which was reformed after the cessation of shear is found to be significantly different from the original state.

• 한국대기환경학회지
• /
• 제11권1호
• /
• pp.57-68
• /
• 1995

Precipitation samples were collected by a wet-only automatic acid precipitation sampler at Kangwha island on the western coast in Korea, through January until December 1992. pH, electric conductivity and the concentrations of major water-soluble ion components such as N $H_{4}$$^{+}$, $Ca^{2+}$, $K^{+}$, $Mg^{2+}$, N $a^{+}$, N $O_{3}$$^{[-10]}$ , S $O_{4}$$^{2-}$ and C $l^{[-10]}$ were measured. From the result of checking the validity for assesment of pollution level of precipitation samples by pH using correlation analysis between pH and major components, and t-test of chemical composition between acid rain and non-acid rain, pH proved to be not satisfactory for its pillution level. A more comprehensive method is therefore required. In order to estimate the monthly analytical result of chemical composition of precipitation samples comprehensively, a cluster analysis was used among the various multivariate statistical analysis. As a result of making a cluster analysis for separating the monthly precipitation samples into homogeneous patterns by setting the concentrations of nine major water-soluble ion components as a variable, three homogeneous patterns were obtained. The first pattern was a group of months having average ion concentrations, the second a guoup of months having low ion concentration, and the third a group of months having high ion concentrations. Thus, it was indicated that the pollution level of precipitation was higher on February and lower on May, June, August and September than the other months. As a result, this analysis method could be estimated the chemical coposition of precipitation regionally as well as monthly.monthly.

• 한국산업보건학회지
• /
• 제26권2호
• /
• pp.170-177
• /
• 2016

Objectives: This study was conducted to evaluate the total heavy metals contents and chemical forms in the animal manure compost. Materials and methods: A total of 109 compost samples were collected throughout the country and classified into three groups in accordance with the raw materials; pig manure, poultry manure and mixed(pig+poultry+cattle) manure. The compost samples were analyzed for total metal content and sequential chemical extraction to estimate the quantities of metals. Results: Concentrations of Zn and Cu in several compost samples were higher than the maximum acceptable limits by the Korea Compost Quality Standards. Concentrations of Zn, Cu, and Cd in compost samples were 257~5,102, 68~1,243, and 0.02~2.54 mg/kg respectively, while Cr, Ni, As, and Pb were < 20 mg/kg. The concentrations of heavy metals in pig manure compost were higher than those of both the poultry and the mixed manure compost. The predominant forms for extracted metals were Cr, Ni, Zn, As, and Pb, residual; Cu, organic; and Cd, carbonate. Conclusions: Results indicate that the Zn and Cu contents in compost were higher than other heavy metals and the heavy metal contents were greater in pig manure compost followed by mixed and poultry manure compost. To prevent the accumulation of heavy metals in soil where animal manure compost is applied, strategy for reducing heavy metal concentrations in animal manure and compost must be considered.

• 한국입자에어로졸학회지
• /
• 제4권1호
• /
• pp.1-7
• /
• 2008

Temporal trends of the PM10 and PM2.5 mass concentrations, and the concentrations of chemical species (sulfate, nitrate, ammonium, OC, and EC) in PM2.5 at Seoul are compared with the reported results from other mega cities in the world. The mass concentrations of PM10 and PM2.5 at Seoul show decreasing trend. However, the concentration levels are still higher than other cities except Beijing. The sulfate concentration at Seoul has decreased while those of nitrate and ammonium have increased. The concentrations of OC and EC show no apparent trend.

• 한국응용과학기술학회지
• /
• 제18권2호
• /
• pp.79-94
• /
• 2001

• Korean Chemical Engineering Research
• /
• 제48권5호
• /
• pp.609-614
• /
• 2010

본 연구는 주단량체로 2-에틸헥실아크릴레이트(2-EHA), n-부틸아크릴레이트(n-BA), 메틸메타크릴레이트(MMA) 그리고 기능성 단량체로 아크릴산(AAc)을 사용한 유화중합에서 아크릴계 점착제를 합성하기 위한 최적의 합성 조건을 구하고자 한다. 이를 위하여 계면활성제 농도의 영향, 계면활성제 Hydrophilic lipophilic Balance(HLB) 값, 중합개시제의 농도와 완충제가 아크릴계 점착제의 물성에 미치는 영향을 연구하였다. 그 결과 계면활성제는 단량체 사용량에 대하여 3~5 wt%를 사용하였을 때, HLB 값이 12.3일 때 가장 안정한 점착체를 얻을 수 있었으며, 중합 개시제의 농도가 1 wt% 이상 사용하였을 때는 중합 속도는 증가하였으나 안정성이 저하되었다. 완충제로 sodium bicarbonate를 사용할 경우 0.4 wt% 이상 사용하여야 충분한 완충 효과가 있었으며, 단량체의 종류에 따라 약간의 차이는 있으나 완충제의 농도가 0.6~0.8 wt%가 적당하여 4성분계 유화중합에서 최적의 중합 조건을 제시할 수 있었다.

• 한국대기환경학회지
• /
• 제34권1호
• /
• pp.16-37
• /
• 2018

In this study, difference in chemical composition of $PM_{2.5}$ observed between the year 2013 and 2015 at six air quality intensive monitoring stations (Bangryenogdo (BR), Seoul (SL), Daejeon (DJ), Gwangju (GJ), Ulsan (US), and Jeju (JJ)) was investigated and the possible factors causing their difference were also discussed. $PM_{2.5}$, organic and elemental carbon (OC and EC), and water-soluble ionic species concentrations were observed on a hourly basis in the six stations. The difference in chemical composition by regions was examined based on emissions of gaseous criteria pollutants (CO, $SO_2$, and $NO_2$), meteorological parameters (wind speed, temperature, and relative humidity), and origins and transport pathways of air masses. For the years 2013 and 2014, annual average $PM_{2.5}$ was in the order of SL ($${\sim_=}DJ$$)>GJ>BR>US>JJ, but the highest concentration in 2015 was found at DJ, following by GJ ($${\sim_=}SJ$$)>BR>US>JJ. Similar patterns were found in $SO{_4}^{2-}$, $NO_3{^-}$, and $NH_4{^+}$. Lower $PM_{2.5}$ at SL than at DJ and GJ was resulted from low concentrations of secondary ionic species. Annual average concentrations of OC and EC by regions had no big difference among the years, but their patterns were distinct from the $PM_{2.5}$, $SO{_4}^{2-}$, $NO_3{^-}$, and $NH_4{^+}$ concentrations by regions. 4-day air mass backward trajectory calculations indicated that in the event of daily average $PM_{2.5}$ exceeding the monthly average values, >70% of the air masses reaching the all stations were coming from northeastern Chinese polluted regions, indicating the long-range transportation (LTP) was an important contributor to $PM_{2.5}$ and its chemical composition at the stations. Lower concentrations of secondary ionic species and $PM_{2.5}$ at SL in 2015 than those at DJ and GJ sites were due to the decrease in impact by LTP from polluted Chinese regions, rather than the difference in local emissions of criteria gas pollutants ($SO_2$, $NO_2$, and $NH_3$) among the SL, DJ, and GJ sites. The difference in annual average $SO{_4}^{2-}$ by regions was resulted from combination of the difference in local $SO_2$ emissions and chemical conversion of $SO_2$ to $SO{_4}^{2-}$, and LTP from China. However, the $SO{_4}^{2-}$ at the sites were more influenced by LTP than the formation by chemical transformation of locally emitted $SO_2$. The $NO_3{^-}$ increase was closely associated with the increase in local emissions of nitrogen oxides at four urban sites except for the BR and JJ, as well as the LTP with a small contribution. Among the meterological parameters (wind speed, temperature, and relative humidity), the ambient temperature was most important factor to control the variation of $PM_{2.5}$ and its major chemical components concentrations. In other words, as the average temperature increases, the $PM_{2.5}$, OC, EC, and $NO_3{^-}$ concentrations showed a decreasing tendency, especially with a prominent feature in $NO_3{^-}$. Results from a case study that examined the $PM_{2.5}$ and its major chemical data observed between February 19 and March 2, 2014 at the all stations suggest that ambient $SO{_4}^{2-}$ and $NO_3{^-}$ concentrations are not necessarily proportional to the concentrations of their precursor emissions because the rates at which they form and their gas/particle partitioning may be controlled by factors (e.g., long range transportation) other than the concentration of the precursor gases.