• 한국산학기술학회논문지
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• 제18권6호
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• pp.1-7
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• 2017

분무식 노즐(spray nozzle)은 액체의 표면을 증가시키기 위해 에너지를 공급하여 액체를 다수의 액적으로 미립화시키는 장치로 연소과정에서의 연료의 미립화 또는 표면이나 입자의 코팅 등 여러 산업분야에 다양한 목적으로 응용된다. 초음파 미립화 노즐은 진동 발생장치로부터 고진동수의 전기에너지를 받아 같은 진동수의 기계적 에너지로 변환시키는 변환기를 갖고 있다. 변환된 에너지를 액체에 부가하여 고주파 진동에 의해 미세한 액적을 생성하여 분사한다. 코팅작업에서 가압되지 않은 저속의 분무는 액적이 튕겨나가지 않고 표면에 달라붙어 과도하게 분사되는 양을 줄일 수 있다. 초음파 미립화 노즐은 초음파 진동부 외벽에 공기를 공급해 줄 수 있는 공간을 통해 생성된 보조 공기흐름을 이용하여 저속의 액적을 운반하여 분무특성이나 분무형상을 조절할 수 있다. 따라서 주위 공기의 흐름을 이용하여 원하는 분무특성을 얻을 수 있다. 본 연구에서는 액적의 분사 운동을 모사하기 위해 라그랑지안 분산상 모델(DPM)을 적용한 상용코드 FLUENT를 사용하여 액적 주위의 공기흐름을 동반하는 초음파 미립화 노즐을 해석하였다. 노즐 수축부 형상, 액적의 크기 그리고 공기 측 압력차의 크기를 변화시키며 수치해석을 수행하여 코팅용 분무를 위한 최적 조건을 연구하였다.

• Journal of Periodontal and Implant Science
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• 제26권2호
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• pp.429-447
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• 1996

Transforming growth factor $-{\beta}$ is one of the polypeptide growth factors that mediate the activity of mesenchymal cells and regulate wound healing process via cell proliferation, migration and extracellular matrix formation. The purposes of this study is to evaluate the effects of transforming growth factor $-{\beta}$ on the protein synthetic activity of human periodontal ligament cells and human gingival fibroblasts. The cells which were prepared were primary cultured gingival fibroblasts and periodontal ligament cells from humans, and the fourth or sixth subpassage were used in the experiments. Cells were seeded and at a confluent state, 0, 0.5, I, 2.5, 5, 10 ng/ml $TGF-{\beta}$ and $2{\mu]Ci/ml\;[^3H]$ proline were added to the cells and cultured for 24 hours. Then, 1 and 5 ng/ml concentrations were selected and added to confluent cells and cultured for 24 and 48 hours. They were labeled with $2{\mu}Ci/ml\;[^3H]$ proline for 24 hours and a collagen assay was done by the Peterkofsky and Diegelman method. The results were presented as the mean disintegration per minute (dpm) per well and S.D. of four determinations, The results were as follows. : The total protein, collagen and noncollagenous protein synthesis in periodontal ligament cells and gingival fibroblasts were increased dose- dependently by transforming growth factor-p to 2.5-5 ng/ml concentration and decreased at 10 ng/ml concentration. The percent of collagen was slightly changed according to the concentration of transforming growth factor-po The effect of transforming growth $factor-{\beta}$ was not specific for collagen synthesis since it increased the total, noncollagenous and collagenous protein, simultaneously. In the comparison of protein synthetic activity between the human periodontal ligament cells and human gingival fibroblasts, the human gingival fibroblasts had higher activities than the human periodontal ligament cells at all times and concentrations of $TGF-{\beta}$. In the comparison of protein synthetic activity between the 24 hour effect and the 48 hour effect of $TGF-{\beta}$, the 48 hour cultured cells' synthetic activity decreased more than the 24 hour cultured cells at human periodontal ligament cells and human gingival fibroblasts. In conclusion, $TGF-{\beta}$ has important roles in the stimulation of protein synthesis in human periodontal ligament cells and human gingival fibroblasts. Thus, it may be useful for clinical application in periodontal regenerative procedures.