To use effectively the solar energy in greenhouse heating, a high performance solar collector should be developed. And then the size of the solar collector and thermal storage tank should be determined through the calculation of heating load. The solar collector must be set in the optimum tilt angle and direction to take daily solar radiation maximally, and the flow rate of heat transfer fluid through the solar collector should be kept in the optimum range. In this research, the performance tests of a capillary tube solar collector were performed to determine the optimum water flow rate and the results summarized as follows. 1. The regressive equations for efficiency estimations of the capillary tube solar collector in the open loop were modeled in the water flow rate of 700-l,000 l/hr. 2. The optimum water flow rate of the solar collector was estimated by the second order polynomial regression and the maximum efficiency was 80% at the water flow rate of 850 l/hr. 3. The solar thermal storage system consisted of a capillary tube solar collector and a water storage tank was tested at the water flow rate of 850 l/hr in the closed loop, and obtained the solar thermal storage efficiency of 55.2%. 4. As the capillary tube solar collector engaged in this experiment was made of non-corrosive polyolefin tubes, its weight was as light as 1/30 of the flat plate solar collector made of copper tubes. Therefore it was considered to be suitable for the greenhouse heating system.

This study demonstrated a rapid and simple method for the determination of seven anions including halides and oxyhalides from the KURT underground water sample by capillary electrophoresis with UV detection. In nuclear waste disposal, some anions such as iodine, selenium, and technetium have been of great concern due to its high mobility and toxicity with a long half-life. It has been needed for a reliable analysis of anionic speciation because the high mobility of anions is easily affected by environmental conditions especially pH and salinity of underground water. Here this project is to develop a fast separation of seven anions including iodide, iodate, and selenite using capillary electrophoresis. The electroosmotic flow (EOF) was suppressed using a poly (ethyleneglycol) -coated capillary (DB-WAX capillary). As a result, anions migrated depending on their mobility under a reverse polarity condition (-15 kV) and the analysis time was within 15 min. UV detection was used at 200 nm. The RSDs for migration time were between 0.7% and 1.3% except for selenite of 5.1%. The RSDs for peak area were obtained between 2.9% and 7.4%. The calibration curves were linear from 10 to 200 mg/L with correlation coefficients greater than 0.9952. The LODs were 7.3, 10.9, 11.3, 12.9, 13.0, 13.9, and 17.4 mg/L for iodide, nitrate, bromide, selenite, bromate, tungstate and iodate. The KURT underground water sample spiked with seven anions at 50 mg/L were analyzed. The recoveries of spiked KURT sample ranged from 93.4% to 99.3%. The proposed method was successfully applied to determine seven anions in underground water sample.

Higenamine [1-(4-hydroxy-6, 7-dihydroxy-l, 2, 3, 4-tetrahydroisoquinoline) is a cardiotonic constituent of Aconiti tuber, one of the most widely prescribed oriental medicines. S-(-)higenamine was reported to have a stronger cardiotonic activity than R-(+)-higenamine and known as a central intermediate in the biosynthesis of various benzyl isoquionoline alkaloids in plants. The separation of higenamine enantiomers has been accomplished with capillary electrophoresis using cyclodextrins (CDs) as chiral selectors. Good resolution of this enantiomers was obtained using a 50 mM sodium phosphate buffer containing hydroxypropyl β-CDs using 27 cm fused silica capillary (50μm i.d., 20 cm to detector) at 25 ℃. With the electric field of 340 V/cm, the separation time of higenamine enantiomers was less than 6 min. Under this optimum conditions, the relative standard deviations of migration time and peak area were less than 1.6% and 3.2%. A 512-channel diode array detector was confirmed for the higenamine. The detection limits (S/N = 3) of these enantiomers are 1.5mutextrmm/mL. We confirmed the chiral form of higenamine in medicinal plants.