• Korean Chemical Engineering Research
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• 제43권5호
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• pp.637-640
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• 2005

극성과 비극성의 물질인 methyl tert-butyl ether(MTBE)와 2,2,4-trimethylpentane 혼합물과 methyl ethyl ketone(MEK)와 2,2,4-trimethylpentane 2성분의 액체혼합물 그리고 극성의 물질인 MTBE과 MEK 2성분 액체혼합물의 밀도를 densitometer를 사용하여 278.15 K, 288.15 K, 298.15 K에서 각각 측정하였다. 측정한 밀도로부터 얻은 2성분계 과잉몰부피의 측정값과 Huron-Vidal의 혼합법칙을 사용한 Peng-Robinson-Stryjek-Vera(PRSV)의 3차 상태방정식으로부터 계산한 계산값이 잘 일치하였으며 극성물질을 포함한 혼합물의 몰부피 계산에 3차의 PRSV 상태방정식이 이용될 수 있음을 확인하였다.

• 한국토양비료학회지
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• 제21권1호
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• pp.49-54
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• 1988

고추의 연작장해(連作障害) 요인(要因)을 분석(分析)하여 연작지토양개량(連作地土壤改良)을 위(爲)한 기초자료(基礎資料)를 얻고자 1985~1986년(年) 2개년(個年) 동안 전북(全北) 임실군(任實郡) 관촌(館村)의 고추 주산단지(主産團地)에서 시험(試驗)을 수행(遂行)하였던바 그 결과(結果)를 요약(要約)하면 다음과 같다. 1. 조사지역(調査地域)의 연작면적비율(連作面積比率)은 2년연작(年連作)이 12.7%였으며 3년연작(年連作)이 6.8%, 4년이상연작(年以上連作)은 48.9% 였다. 2. 연작지(連作地)의 토양이화학성(土壤理化學性) 특성(特性)은 토양경도(土壤硬度)가 높고 토양삼상중(土壤三相中) 기상(氣相)의 비(比)가 낮았으며 유효인산(有效燐酸)은 508 ppm, 치환성가리(置換性加里) 0.86me/100g로 적정치(適正値)보다 월등(越等)히 높았다. 3. 토양미생물(土壤微生物)의 균류(菌類)에 대(對)한 세균수(細菌數)(B/F비(比))와 방선균수(放線菌數)(A/F비(比))는 연작연한(連作年限)이 많을 수록 낮아지는 경향(傾向)이었다. 4. 토양선충밀도(土壤線蟲密度)는 1년재배지(年栽培地) 359, 2년연작지(年連作地) 391, 3년연작지(年連作地) 495, 4년이상연작지(年以上連作地)가 524마리/100g이였으며 경사(傾斜)가 심(甚)하고 배수(排水)가 양호(良好)할수록 낮았다. 5. 역병발생(疫病發生)은 4년이상연작지(年以上連作地)의 이병주율(罹病株率)이 14.3%로 1년재배지(年栽培地)의 0.7%에 비(比)해 월등(越等)히 높았으며 경사(傾斜)가 완만할수록 탄저병(炭疽病)은 감소(減少)되고 역병(疫病)은 증가(增加)되는 경향(傾向)이였다.

• 한국농공학회지
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• 제25권4호
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• pp.50-60
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• 1983

305 samples of alluvial deposit in inland and harbour districts were selected and consolidation charateristics of the alluvium were put in order statiscally. The correlations between them were as follows. 1. The relationships between LL(liguid limit) and Cc (compression index) were explained as Cc=0. 03(LL-21. 7) in case of inland district soil and as Cc=0. 019(LL-19) in case of harbour district soil. As compared with formular proposed by Skernpton, the gradient of this linear line was slight steep. 2. The relationships between PI(plastic index) and Cc were explained as Cc=0. 063 PI-0. 52 in case of inland district soil and Cc=0. 043 PI-0. 31 in case of harbour district soil. 3. As void ratio and natural moisture content were increased, Cc was increased, and as wet density was increased, Cc was decreased with a gentle curve. 4. As LL and P1 increased, mv(coefficient of volume compressibility) was increased but if LL and P1 was increased beyond a certain extend, mv has a tendency of constant value, that is, mv show a tendency to take constant value in the very soft clay. and mv in P=2. 5kg/cm$^2$ was about l${\times}$ l0-$^1$cm$^2$/kg in case of land district soil and 6x 10-$^1$crn$^2$/kg in case of harbour district soil lower than that in P=0. 25kg/crn2. 5. Cv(coefficient of consolidation) was a tendency to decrease with a gentle curve as LL was increased, and Cv in P=0. 25kg/crn2 was about 3x l0-$^1$crn$^2$/min larger than that in P=2. 5kg/crn$^2$. 6. Relationships between Py(pre-consolidation pressure) which is included over consolidation soil and ∑r1h(effective over-burden pressure) were explained as Py=l. 12 ∑r'h in case of land district soil and as Py=l. l5∑r'h in case of harbour district soil. 7. Some of the properties show good correlations between them, practical and effective applications of these correlations are expected in the planning and excution of soil investigation and also in the evaluation of the results.

• Journal of Periodontal and Implant Science
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• 제26권2호
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• pp.469-490
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• 1996

The initial events required for periodontal regeneration is the attachment, spreading, and proliferation of appropriated cells at the healing sites. These have been reported that minocycline stimulates the attachment of periodontal ligament cells, and also $TGF-{\beta}1$ enhances the proliferation of periodontal ligament cells. The purpose of the present study was to evaluate the effects of $TGF-{\beta}1$ on the cellular activity of minocycline treated human periodontal ligament cells. Periodontal ligament cells were obtained from the explants of healthy periodontal ligaments of extracted 3rd molars or premolar teeth extracted from the patients for orthodontic treatment. The cells were cultured in minimal essential medium(${\alpha}-MEM$) supplemented with 10.000units/ml penicillin, $10,000{\mu}g/ml$ streptomycin and 10% FBS(fetal bovine serum) at $37^{\circ}C$ in a humidified atmosphere of 5% carbon dioxide and the 5th to the 8th passages of the cells were used. To evaluate the effect of minocycline on cell attachment, the cells were seeded at a cell density of $1.5{\times}10^4$ cells/well in 24-well culture plates and treated with $20{\mu}g/ml$ and $100{\mu}g/ml$ of minocycline for 1.5 h. After trypsinization, the cells were counted with hemocytometer and were taken photographs for observation of cellular morphology. To evaluate the effect of $TGF-{\beta}1$ on minocycline-pretreated periodontal ligament cells, the cells were seeded at a cell density of $1{\times}10^4$ cells/ well in 24-well culture plates and treated with $20{\mu}g/ml$ and $100{\mu}g/ml$ of minocycline for 1.5 h. After incubation, 1 and 10ng/ml of $rh-TGF-{\beta}1$ were also added to the each well and incubated for 1 and 2 days, respectively. Then, MTT assay, DNA synthesis($^3H-thymidine\;assay$), and protein and collagen assay(3H-proline assay) were carried out. In the MIT assay, after 200ul MTT solutionlconeentration of 5mg/ml) were added to the each well of the 24-well plates and incubated for 3 hours, and 200 ul DMSO were added so as to dissolve insoluble blue formazan crystals which was formed in incubated period. Then it read plates on a ELISA reader. For mitogenic assay, 1 uCi/ml $^3H-thymidine$ was added to each well for the final 2 hours of the incubation periods. After labeling, the wells were washed 3 times with ice cold PBS and 4 times with 5% TCA to remove unincorporated label and precipitate the cellular DNA. DNA, with the incorporated $^3H-thymidine$, was solubilized with 500 ul of 0.1% NaOH/0.1% SDS. A 250 ul aliquot was removed from each well and placed in a scintillation vial with 4ml of scintillation cocktail. Using an liguid scintillation counter, counts per minute(CPM) were determined for each samples. 3 uCi/ml $^3H-proline$ was added to each well for the final 4 hours of the incubation periods and total protein and percent collagen synthesis were carried out. The results indicate that minocycline treated group with $100{\mu}g/ml$ concentration for 1.5 hours significantly increased than that of control in cell attachment, and cell process is also evident compared with that of control in cell morphology, and the cellular activity and DNA synthesis rate of cells treated minocycline and $TGF-{\beta}1$ significantly increased than that of control values, but were below to values of the $TGF-{\beta}1$ only treated group in MIT assay and $^3H-thymidine\;assay$, and the total protein synthesis of minocycline and $TGF-{\beta}1$ treated group also significantly increased than that of control values, but the percent collagen synthesis of tested group significantly decreased to compared with control. On the above the findings, the tested group of minocycline and $TGF-{\beta}1$ did not increase the effect on the cell activity than $TGF-{\beta}1$ only tested group and the tested group of minocycline inhibited cell activity. This results indicate that minocycline was effective on cell attachment in early stage, but it is harmful to cell activity, that inhibitory effect of minocycline was compensated with stimulatory effect of $TGF-{\beta}1$.