• Archives of Pharmacal Research
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• v.28 no.9
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• pp.1086-1091
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• 2005

An analytical method was developed for evaluating the cannabidiol (CBO), cannabinol (CBN), ${\Delta}^9-tetrahydrocannabinol$ $({\Delta}^9-THC)$ level in human hair using gas chromatography-mass spectrometry (GC-MS). Hair samples (50mg) were washed with isopropyl alcohol and cut into small fragments (< 1mm). After adding a deuterated internal standard, the hair samples were incubated in 1.0M NaOH for 10 min at $95^{\circ}C$. The analytes from the resulting hydrolyzed samples were extracted using a mixture of n-hexane-ethyl acetate (75:25, v/v). The extracts were then evaporated, derivatized, and injected into the GC-MS. The recovery ranges of CBD, CBN, and ${\Delta}^9-THC$ at three concentration levels were $37.9-94.5\%$ with good correlation coefficients $(r^2>0.9989)$. The intra-day precision and accuracy ranged from $-9.4\%\;to\;17.7\%$, and the inter-day precision and accuracy ranged from $-15.5\%\;to\;14.5\%$, respectively. The limits of detection (LOD) for CBD, CBN, and ${\Delta}^9-THC$ were 0.005, 0.002, and 0.006 ng/mg, respectively. The applicability of this method of analyzing the hair samples from cannabis abusers was demonstrated.

• Korean Chemical Engineering Research
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• v.50 no.1
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• pp.1-5
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• 2012

$Ba_{0.5}Sr_{0.5}Co_{0.8}Fe_{0.2}O_{3-{\delta}}$ hollow fiber with o.d. 1.02 mm and i.d. 0.437 mm were fabricated by a phase-inversion spinning technique.The starting $Ba_{0.5}Sr_{0.5}Co_{0.8}Fe_{0.2}O_{3-{\delta}}$ precursor was synthesized by the polymerized complex method and then calcined at $900^{\circ}C$. As-prepared powder was dispersed in a polymer solution, and extruded as form of hollow fiber through a spinneret. Finallydense $Ba_{0.5}Sr_{0.5}Co_{0.8}Fe_{0.2}O_{3-{\delta}}$ hollow fiber membrane was obtained by sintering for 2 h at $1,080^{\circ}C$ for the application of oxygen separation. In addition, despite a very thin membrane with 0.58 mm, the BSCF hollow fiber membrane possessed a proper mechanical strength of 602.5 MPa.

• Journal of Environmental Health Sciences
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• v.28 no.5
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• pp.4-12
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• 2002

It is well-known method to use Ethylene Oxide (ETO) as a fumigant to preserve cultural heritage from the attack of some bacteria and insects. In this article, we investigated co]or change of some cultural material upon treating ETO. The cultural material was selected from Korean paper (hanji), ancient books, blue prints, pigments (DA, DB, DC, DD, DE and DF). hemp cloths, and colored pictures (DG, DH, Dl, DJ, DK). The $\Delta$E value in chromaticity coordinates for each item was obtained upon treatment with ETO at concentration of 200, 250, 380, 500, 710 g/m$^3$ respectively. The $\Delta$E value was derived from the equation of L*at with the data checked 24 hr, 48 hr, and 72 hrs respectively. The Korean papers(hanji) showed slightly change in color by $\Delta$E 0.8. In the case of ancient books, it showed $\Delta$E 2.91 which was easily distinguishable with the naked eyes. For the almost 73％ of blue prints, the value of $\Delta$E was as much as more than 4.0 that it is recommended not to use. In the case of pigments, the value of $\Delta$E was ranged from 0.15 up to 4.0 so that it should be very careful before use. The hemp cloth dyed with natural indigo showed less than 1.00 in $\Delta$E, while various colored hemp cloth showed wide range of $\Delta$E from 1.00 to 4.00. Finally, from the fact that the color change was as small as less than 1.00 for the colored pictures, it is thought that treatment with ETO is one of method to be used to this purpose.

• Journal of Korea Water Resources Association
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• v.51 no.spc
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• pp.1079-1089
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• 2018

The majority of existing studies for quantifying uncertainties in climate change impact assessments suggest only the uncertainties of each stage, and not the total uncertainty and its propagation in the whole procedure. Therefore, this study has proposed a new method, the Uncertainty Delta Method (UDM), which can quantify uncertainties using the variances of projections (as the UDM is derived from the first-order Taylor series expansion), to allow for a comprehensive quantification of uncertainty at each stage and also to provide the levels of uncertainty propagation, as follows: total uncertainty, the level of uncertainty increase at each stage, and the percentage of uncertainty at each stage. For quantifying uncertainties at each stage as well as the total uncertainty, all the stages - two emission scenarios (ES), three Global Climate Models (GCMs), two downscaling techniques, and two hydrological models - of the climate change assessment for water resources are conducted. The total uncertainty took 5.45, and the ESs had the largest uncertainty (4.45). Additionally, uncertainties are propagated stage by stage because of their gradual increase: 5.45 in total uncertainty consisted of 4.45 in emission scenarios, 0.45 in climate models, 0.27 in downscaling techniques, and 0.28 in hydrological models. These results indicate the projection of future water resources can be very different depending on which emission scenarios are selected. Moreover, using Fractional Uncertainty Method (FUM) by Hawkins and Sutton (2009), the major uncertainty contributor (emission scenario: FUM uncertainty 0.52) matched with the results of UDM. Therefore, the UDM proposed by this study can support comprehension and appropriate analysis of the uncertainty surrounding the climate change impact assessment, and make possible a better understanding of the water resources projection for future climate change.

• Journal of Welding and Joining
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• v.5 no.2
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• pp.44-52
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• 1987

The fracture toughness, $J_{IC}$ of high frequency electric resistance welded steel pipe for smooth and side-grooved CT specimen was evaluated by unloading compliance method. The crack growth, .${\delta}a$ was obtained from the equation of Donald and Saxena & Hudak, and $J_{IC}$ was determined from the curve of J-${\delta}a$ relations. The crack growth on the experiment using unloading compliance method is underestimated as compared with ${\delta}a$ measured directly by the SEM, so the reliability of $J_{IC}$ from saxena & Hudak equation is large than that from Donald. The $J_{IC}$ value of side-grooved CT Specimen is estimated less than that of smooth, and this is the effect of the side-groove, the shear-lip of crack tip and the reduction of crack tunnelling phenomena.

• Journal of Technologic Dentistry
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• v.35 no.3
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• pp.185-192
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• 2013

Purpose: The aim of this study was to compare with color reproducibility of the coating method and dipping method using a colour liquid. Methods: Two groups of square-shaped specimens ($10mm{\times}10mm$ in diameter, 1.5mm thickness) were prepared for analysis(n=15/group). The CM(Coating Method) group was fabricated as full zirconia specimens with the coating coloring method and Group DM(Dipping Method) was prepared as specimens of 0.7 mm-thick zirconia plate using the dipping coloring method and veneered with 0.8mm-thick porcelain. Color parameters were measured with ShadeEye $NCC^{(R)}$ spectrophotometer and color differences were calculated using the equation ${\Delta}E^*= \{({\Delta}L^*)^2+({\Delta}a^*)^2+({\Delta}b^*)^2\}^{1/2}$. Non-parametric statistical methods, the Mann-Whitney test, and the Kruskal-Wallis test were used to analyze the data. Type one error rate was set at 0.05. Results: Color difference values larger than 7 were observed between specimens with the coating method and the dipping method, which were detectable difference in a clinical setting. Conclusion: Cautious application of the coating coloring method in a clinical setting and further researches to standardize the coating method are needed.

• Magazine of the Korean Society of Agricultural Engineers
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• v.16 no.3
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• pp.3539-3542
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• 1974

Maximum density and optimum moisture content of a soil may be one of the very important properties to be specified in the design of earth structures and their works. However, the determination of these soil properties may not be done without the necessary equipment and time-consuming field tests. This study was conducted to develop an easier method by determing the relations between the natural moisture content and optimum moisture content and between maximum density and optimum moisture content so determined. These velations are remarkably defferent according to the areas where the samples were taken, and thus analysis of the experimental results are shown by regions as follows: Eastern Districs:{{{{Tdmax= { 1} over {0.0090Wopt+0.417 } ( delta = +- 0.042, gamma =0.92) Wopt=0.251WN+8.5( delta = +- 2.41%, gamma =0.87) }}}} Southern Districts: {{{{Tdmax= { 1} over {0.0088Wopt+0.412 } (delta = +- 0.083, gamma =0.89) Wopt=0.332WN+8.42(delta = +- 3.41%, gamma =0.84)}}}}Central Districtsl1): {{{{Tdmax= { 1} over {0.0112Wopt+0.383} ( delta = +- 0.052, gamma =0.97) Wopt=0.758WN+2.606( delta = +- 4.72%, gamma =0.79)}}}}($\delta$:Standard Deviation, ${\gamma}$:Correlation Coefficient)

• Journal of the Korean Chemical Society
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• v.45 no.1
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• pp.7-13
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• 2001

The interaction of benzenesulfonate anion and its derivatives ($C_6H_5SO_3^-, p-$CH_3C_6H_4SO_3^-, and $p-C_2H_5C_6H_4SO_3^-$) with the micellar system of cationic surfactant TTAB(tetradecyltrimethylammonium bromide) was studied by UV/Vis spectrophotometric method. The solubilization constants($K_s$) of benzenesulfonate anions into the micellar phase of this surfactant have been measured with the change of temperature. The effects of additives(n-pentanol and NaBr) on the solubilization of benzenesulfonate anions by this surfactant system have been also measured. There was a great decrease on the values of $K_s$ and CMC simultaneously with these additives so that the measured values of ln$K_s$ were linear relationships with the values of lnCMC. For the thermodynamic study, various thermodynamic parameters(${\Delta}G^0_s$, ${\Delta}H^0_s$ and ${\Delta}S^0_s$) have been calculated and analyzed from the dependence of Ks values on temperature.

• Korean Chemical Engineering Research
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• v.50 no.2
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• pp.198-203
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• 2012

Salting-out technique was adopted to crystallize dye crystals from dye solution. In this research solubility of dye solution and crystallization kinetics of Reactive dye (RB-8, RB-49, RR-218) was investigated. The empirical expressions of salting-out crystallization kinetics for Reactive dye (RB-8, RB-49, RR-218) in continuous MSMPR crystallizer was RB-8 in crystal growth kinetics $G=7.1{\times}10^{-4}{\Delta}C^{0.67}$ and nucleation kinetics $B^0=3.1{\times}10^{15}{\Delta}C[1.2{\times}10^{-8}+{\Delta}C^{0.7}M_T{^2}]$, RB-49 in crystal growth kinetics $G=5.2{\times}10^{-4}{\Delta}C^{0.3441}$ and nucleation kinetics $B^0=7.2{\times}10^{15}{\Delta}C[3.3{\times}10^{-8}+({\Delta}C)^{0.7}M_T{^2}]$, RR-218 in crystal growth kinetics $G=4.4{\times}10^{-4}{\Delta}C^{0.2361}$ and nucleation kinetics $B^0=6.3{\times}10^{15}{\Delta}C[7.9{\times}10^{-8}+({\Delta}C)^{0.7}M_T{^2}]$. Also, comparison of calculated crystal size distribution applying to characteristic curve method with experimental crystal size showed good agreement.

• KOREAN JOURNAL OF CROP SCIENCE
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• v.42 no.1
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• pp.7-13
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• 1997

The composition and chemical structures of same individual components of essential oils from ginger flavor plants were estimated by gas chromatography and gas chromatography-mass spetrometric analysis with the aid of NBS and Wiley library and RI indice searches. Through gas chromatography and gas chromatography /mass spetrometry analysis of 43, 41, 32 essential oil components from flowers, leaves and stems from Lindera obstusiloba., respectively were identified, among which sabinene, $\beta$-myrcene, ι-limonene, phelandrene, ${\gamma}$-selinene, $\alpha$-terpinene, 2, 4a, 5, 6, 7, 8, 9, 9a -octahydro benzocycloheptane, $\delta$-cadinene, ${\gamma}$-terpinene, (Z) -3-hexen-1-ol acetate, ${\gamma}$-elemene, l-boreneol, $\delta$-guaiene, ledene, cis-3-hexanal, elemol, $\alpha$-chamigrene, $\beta$-endesmol: 9-octadecanal, 1-(1, 5-diMe-4-hexenyl)-4-Me. benzene were estimated to be major components.