• Journal of the Korean Society of Clothing and Textiles
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• v.27 no.7
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• pp.862-871
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• 2003

Kenaf has been estimated as an economic and environmentally compatible crop. This study purposed to enlarge the use of kenaf as textile materials and to develope high value-added textile fibers. Kenaf has been cultivated successfully and grown fast in Jeju. The height of kenaf stalks was about 220cm at 105 DAP and 400cm at 150 DAP, After harvesting at 105 DAP and seperating the basts from harvested kenaf stalks, decorticated kenaf basts were rotted in water at 15~$25^{\circ}C$ for biological rotting and were treated with 1%, 4% and 7% NaOH at 9$0^{\circ}C$ for chemical retting. The properties of extracted fibers were compared: such as fiber diameter. Transversal and longitudinal views, colors, crystallinities, strengths and elongations etc. The diameter of kenaf bast fibers was 15~25 ${\mu}{\textrm}{m}$. Biologically rotted kenaf bast fibers had well developed lumens which were diminished after chemical retting. The degree of crystallinities of biologically rotted kenaf bast fiber was about 92~96% showed higher than those of chemically rotting. The biologically rotted fibers were bright and had creamy color. Yelloweness increased at chemically rotted fibers. Fiber bundle strengths were from maximum 98076.9 (gf/g) to minimum 63749.5 (gf/g). Fiber bundle strengths of biologically rotted kenaf fibers appeared greater than those of chemically rotted fibers. Alkali treatments of chemical rotting could make strength lower and elongation higher. Rotting method might be one of the most importance factors affecting to final fiber properties.

• Journal of Life Science
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• v.16 no.3 s.76
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• pp.534-539
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• 2006

In the ozone disinfection unit process of a piston type batch reactor with continuous ozone analysis using a flow injection analysis (FIA) system, the CT values for 1 log inactivation of Cryptosporidium parvum by viability assays of DAPI/PI and excystation were $1.8{\sim}2.2\;mg/L{\cdot}min$ at $25^{\circ}C$ and $9.1mg/L{\cdot}min$ at $5^{\circ}C$, respectively. At the low temperature, ozone requirement rises $4{\sim}5$ times higher in order to achieve the same level of disinfection at room temperature. In a 40 L scale pilot plant with continuous flow and constant 5 minutes retention time, disinfection effects were evaluated using excystation, DAPI/PI, and cell infection method at the same time. About 0.2 log inactivation of Cryptosporidium by DAPI/PI and excystation assay, and 1.2 log inactivation by cell infectivity assay were estimated, respectively, at the CT value of about $8mg/L{\cdot}min$. The difference between DAPI/PI and excystation assay was not significant in evaluating CT values of Cryptosporidium by ozone in both experiment of the piston and the pilot reactors. However, there was significant difference between viability assay based on the intact cell wall structure and function and infectivity assay based on the developing oocysts to sporozoites and merozoites in the pilot study. The stage of development should be more sensitive to ozone oxidation than cell wall intactness of oocysts. The difference of CT values estimated by viability assay between two studies may partly come from underestimation of the residual ozone concentration due to the manual monitoring in the pilot study, or the difference of the reactor scale (50 mL vs 40 L) and types (batch vs continuous). Adequate If value to disinfect 1 and 2 log scale of Cryptosporidium in UV irradiation process was 25 $mWs/cm^2$ and 50 $mWs/cm^2$, respectively, at $25^{\circ}C$ by DAPI/PI. At $5^{\circ}C$, 40 $mWs/cm^2$ was required for disinfecting 1 log Cryptosporidium, and 80 $mWs/cm^2$ for disinfecting 2 log Cryptosporidium. It was thought that about 60% increase of If value requirement to compensate for the $20^{\circ}C$ decrease in temperature was due to the low voltage low output lamp letting weaker UV rays occur at lower temperatures.