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The Deformation and Breaking Load of the Fishing Hook by the Tensile Test (인장시험에 의한 낚시의 변형과 파단하중)

  • KO Kwan-Soh;KIM Yong-Hae
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.14 no.4
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    • pp.269-275
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    • 1981
  • The fishing hooks were tested for breaking and unbending due to plastic deformation of the material. Study of tensile test is not complicated, but has not even worked out fully enough, especially when the test specimen is subjected to plastic deformation. The fishing hook is subjected to unbending stress and the critical section is a Point which is furthest from the line of action of the forces. The dynamic force of fish during jerks depends on their speed of movement and body weight, the kinetic energy corresponding to it and also on the rlastic displacement of the rigging which absorb the energy. Six kinds of hook were tested by the dynamometer under tensile speed 290mm/min (subscript s) and 780mm/min (subscript f). According to their results, the breaking load(B: kg) can be induced with the formula $B={\alpha}wd^2+\beta$ where w(mm) is the distance between the barb base and the lower shank and d(mm) is diameter. The coefficients of the formula for the round hooks(R) and the angular hooks(A) are approximately as follows: $$R:\;\alpha_{s}=0.5,\;\beta_{s}=1.6,\;\alpha_{f}=0.4,\;\beta_{f}=1.4$$ $$A:\;\alpha_{s}=1.1,\;\beta_{s}=2.0,\;\alpha_{f}=1.0,\;\beta_{f}=0.9$$ The ratio of $B_{f}\;to\;B_{s}$ is corresponding to 0.8. The ratio of deformation(X) that is moved distance of barb base at break to the distance(H) between head base and barb base is about $50\%$. Further study should be carried out on the subject of impact and fatigue test under the same condition which is exerted force by the hooked fish.

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Holding Strength of Screw in Domestic Particleboard and Medium Density Fiberboard(II) -Predicting Formula of Withdrawal Strength of Screw- (국산(國産) 파티클보드와 중밀도섬유판의 나사못유지력(維持力)(II) -나사못 유지력(維持力) 예측식(預測式)-)

  • Lee, Phil-Woo;Park, Hee-Jun;Han, Yu-Soo
    • Journal of the Korean Wood Science and Technology
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    • v.19 no.4
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    • pp.43-51
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    • 1991
  • This study was carried out to determine the withdrawal strength of various screws according to root diameter of screw and embeded length on the face and edge of domestic particleboard and medium density fiberboard. The obtained results were as follows: 1. The withdrawal strength of screw in domestic particleboard and medium density fiberboard was closely related to embeded length of the screw but less dependent on root diameter of the screw. 2. The withdrawal strength on the face and edge of domestic particleboard could be predicted by means of the following expression: $F_{Pf}=4.60{\times}D^{0.24}{\times}L^{1.14}(R^2=0.87)$ $F_{Pe}=0.54{\times}D^{0.43}{\times}L^{1.73}(R^2=0.84)$ Where: $F_{Pf}$ : withdrawal strength on the face of particleboard(kgf) $F_{Pe}$=withdrawal strength on the edge of particleboard(kgf) D=diameter of the screw(mm) L=embeded length(mm) 3. The withdrawal strength on the face and edge of domestic medium density fiberboard could he predicted by means of the following expression: $FM_f=1.53{\times}D^{0.53}{\times}L^{1.39}(R^2=0.93)$ $F_{Me}=1.14{\times}D^{0.66}{\times}L^{1.36}(R^2=0.87)$ where: $F_{Mf}$ = withdrawal strength on the face of medium density fiberboard(kgf) $F_{Mf}$=withdrawal strength on the edge of medium density fiberboard(kgf).

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Mating Behavior, Mycotoxin Production, and Vegetative Compatibility of Gibberella fujikuroi Species Complex from Sorghum in Korea

  • Lim, Sun-Hee;Yun, Sung-Hwan;Lee, Yin-Won
    • The Plant Pathology Journal
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    • v.17 no.5
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    • pp.276-280
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    • 2001
  • Fusarium isolates of Gibberella fujikuroi species complex were obtained from sorghum grown in five provinces of Korea in 1996 and 1997. These isolates were characterized based on their mating behavior, mycotoxin production, and vegetative compatibility. Only three mating populations (A, D, and F) were recovered from a total of 155 isolates examined. The relative frequency of the mating populations was significantly different: F was predominant (80%), while D and A were observed at low frequencies of 9% and 3%, respectively. Female fertile isolates were more common within F (44 our of 124) than D (2 out of 14), while none of the five A isolates were female fertile. The inbreeding effective population sizes ($\textrm{N}_e$)for mating type and male/hermaphrodite ratios in mating populations A and D produced significant amounts of fumonisins, while F isolates produced none or only traces of fumonisin B$_1$. In contrast. F isolates produced higher amounts of moniliformin (average of 3,820 ppm) than A and D isolates (averages of 77 and 1,819 ppm, respectively). Fifty-one isolates were tested for vegetative compatibility using nitrogen non-utilization mutants of each isolate, and 44 vegetative compatibility groups (VCGs) were identified. A single VC type (VC1) was found in all of the five A isolates examined. Six of the D isolates examined consisted of three VC types: two for VC2, two for VC3, and the rest for VC4. All of the F isolates tested were incompatible in every combination and , thus, each constituted a unique VCG.

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The Crystal Structure of $C_{13}H_{15}N_3O_3$ ($C_{13}H_{15}N_3O_3$의 결정 구조)

  • Park, Hai-Yoon;Kim, Moon-Jib;Park, Ho-Jong
    • Korean Journal of Crystallography
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    • v.15 no.1
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    • pp.24-28
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    • 2004
  • The structure of $C_{12}H_{15}N_3O_3$ has been determined by X-ray diffraction methods. The crystal system is monoclinic, space group $P2_1/c$, unit cell constants, a = 12.9955(9) ${\AA}$, b = 7.7137(5) ${\AA}$, c = 13.4699(11) ${\AA}$, ${\beta}$ = 107.86(1)$^{\circ}$, V = 1285.2(1) ${\AA}^3$, T = 296 K, Z = 4, $D_c$ = 1.350 $Mgm^{-3}$. The intensity data were collected on an Enraf-Nonius CAD-4 Diffractometer with graphite monochromated Mo $K{\alpha}$ radiation (${\lambda}$ = 1.71073 ${\AA}$). The molecular structure was solved by direct methods and refined by full-matrix least squares to a final R = 4.19% for 1644 unique observed $F_0\;>\;4{\sigma}(F_0)$ reflections 193 parameters.

Genetic analysis of protoplast fusants of candida pseudotropicalis (Candida pseudotropicalis 융합세포의 유전적 분석)

  • Chun, Soon-Bai;Bai, Suk
    • Korean Journal of Microbiology
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    • v.26 no.2
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    • pp.82-87
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    • 1988
  • The genetic analysis and characterization of protoplast fusion hybrids between complementary auxotrophic mutants of Candida pseudotropicalis were carried out. Nuclear fusion appeared to occur in fusion hybrids (e.g., F15 and F33), as strongly suggested by isolation of recombinants after mitotic segregation of parental genetic markers. This was confirmed by KNA content, nuclear staining and comparison of survival rate to UV light. After keeping fusion hybrids for approximately one year, the frequency of spontaneous mitotic segregation was $3.0\times 10^{-4}$ - $8.1\times 10^{-4}$ while that of induced mitotic segregation was $1.4\times 10^{-3}$- $1.7\times 10^{-3}$. These results suggested that they maintained stable karyogamy state. It was also found that the production of $\beta$-D-galactosidase from F15, F33 and F158 was somewhat increased when compared with that from either auxotrophic parents or wild type.

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Two New Steroidal Saponins from the Tuberss of Liriope spicata

  • Lee, Do-Yong;Son, Son-Ho;Do, Jae-Chul;Kang, Sam-Sik
    • Archives of Pharmacal Research
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    • v.12 no.4
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    • pp.295-299
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    • 1989
  • Two novel steroidal saponins designated as spicatosides A(1) and B(2) were isolated from the tubers of Liriope spicata and their structures were elucidated as 25(S)-rus-cogenin -1-0- fJ - D-glucopyranosyl (1$\rightarrow$2)- [$\beta$ - D-xylopyranosyl (1$\rightarrow$3)] -$\beta$- D- fucopyranoside (1) and 26-0-$\beta$-D-glucopyranosyI25(S)-22-0-methyl-furost-5-en-l$\beta$, 3$\beta$, 26-trioll-0-fJ -D¬glucopyranosyl (1$\rightarrow$2)- [$\beta$- D-xylopyranosyl (1$\rightarrow$3)] - $\beta$- D- fucopyranoside (2), respectively.

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Design and analysis of highly selective ultrawide stopband lowpass filter using lumped and distributed equivalent circuit models

  • Pankaj Singh Tomar;Manoj Singh Parihar
    • ETRI Journal
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    • v.46 no.4
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    • pp.716-726
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    • 2024
  • An ultrawide stopband lowpass filter is reported using three stepped impedance resonators with high selectivity. The filter extends the stopband frequency range and attenuation, and two quarter-wave open stubs and three circular ground slots are introduced. The lumped and distributed equivalent models are derived and analyzed. The corresponding results are validated experimentally in a fabricated prototype. The prototype lowpass filter has a 3 dB cutoff frequency (fc) of 2.9 GHz, and the stopband is extended up to 35 GHz (12.07fc), with an attenuation level better than 20 dB throughout. The passband-to-stopband transition (3 dB-20 dB) bandwidth is 0.18 GHz, and the roll-off factor is 135 dB/GHz at 30 dB. The insertion loss is 0.3 dB at 1.6 GHz. The normalized circuit size of the proposed filter with respect to the guided wavelength is 0.04.

Synthesis of wagnerite and its analogues for ceramic pigments (ll) (도자기 유약용 Wagnerite의 합성(II))

  • Yong- Sun Chung;Keun Ho Auh
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.7 no.4
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    • pp.648-657
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    • 1997
  • In order to investigate the polymorphism of wagnerite, the single phase of$Mg_3(PO_4)_2$ was synthesized by heating the stoichiometric mixture of $Mg_3(PO_4)_2$ and $MgF_2$ in a sealed platinum tube at $1040^{\circ}C$ (or 3 hours, One reversible inversion was detected at $1255^{\circ}C$ and the thermal decomposition was not observed until it reached the melting point. As a result, wagnerite is thermally stable enough to be used as pigments for glazes and plastics if substituted with divalent metal ions. The contractions of d-values in $Zn_4P_2O_8F_2$ and $Zn_3MgP_2O_8F_2$ phases were observed by the substitution with metal ions which resulted in intense purple, gold and green colors. Among the several attempts of charge - coupled sub-stitution, only $A^{1+}A_3^{2+}X^{5+}X^{6+}O_8_F2$ compositions were successful to synthesize the wagnerite phase.

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The Crystal Structure of Cantharidin $(C_{10}H_{12}O_{4})$ (Cantharidin$(C_{10}H_{12}O_{4})$의 결정 구조)

  • 김문집;박호종;김대영;이종수
    • Korean Journal of Crystallography
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    • v.13 no.2
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    • pp.91-95
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    • 2002
  • The structure of Cantharidin (Hexahydro-3a,7a-dimethy1-4,7-epoxyisobenzofuran-1,3-dione, C/sub 10/H/sub 12/O/sub 4/)has been determined by X-ray diffraction methods. The crystal system is orthorhombic, space group Pna2/sub 1/, unit cell constants, a=11.0731(9) (equation omitted), b=6.7344(4) (equation omitted), c=12.5000(9) (equation omitted), α=β=γ=90°, V=932.13(12) (equation omitted), T=296K, Z=4, D/sub c/=1.398Mgm/sup -3/. The intensity data were collected on an Enraf-Nonius CAD-4 Diffractometer with graphite monochromated MoKα radiation(λ=0.71073(equation omitted)). The molecular structure was solved by direct methods and refined by full-matrix least squares to a final R=4.42% for 759 unique observed F/sub o/>4σ(F/sub o/) reflections and 140 parameters.

Automated Synthesis of [$^{18}F$]Fallypride for Routine Clinical Use (자동합성장치를 이용한 [$^{18}F$]Fallypride의 합성)

  • Park, Jun-Hyung;Moon, Byung-Seok;Lee, Hong-Jin;Lee, Hyo-Jun;Lee, In-Won;Lee, Byung-Chul;Kim, Sang-Eun
    • The Korean Journal of Nuclear Medicine Technology
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    • v.14 no.2
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    • pp.104-109
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    • 2010
  • Purpose: $[^{18}F]$Fallypride plays an effective radiotracer for the study of dopamine $D_2/D_3$ receptor occupancy, neuropsychiatric disorders and aging in humans. This tracer has the potential for clinical use, but automated labeling efficiency showed low radiochemical yields about 5~20% with relatively long labelling time of fluorine-18. In present study, we describe an improved automatic synthesis of [$^{18}F$]Fallypride using different base concentration for routine clinical use. Materials and Methods: Fully automated synthetic process of [$^{18}F$]Fallypride was perform using the TracerLab $FX_{FN}$ synthesizer under various labeling conditions and tosyl-fallypride was used as a precursor. [$^{18}F$]Fluoride was extracted with various concentration of $K_{2.2.2.}/K_2CO_3$ from $^{18}O$-enriched water trapped on the ion exchange cartridge. After azeotropic drying, the labeling reaction proceeded in $CH_3CN$ at $100^{\circ}C$ for 10 or 30 min. The reaction mixture was purified by reverse phase HPLC and collected organic solution was exchanged by tc-18 Sep-Pak for the clinically available solution. Results: The optimal labeling condition of [$^{18}F$]Fallypride in the automatic production was that 2 mg of tosyl-fallypride in acetonitrile (1 mL) was incubated at $100^{\circ}C$ for 10 min with $K_{2.2.2.}/K_2CO_3$ (11/0.8 mg). [$^{18}F$]Fallypride was obtained with high radiochemical yield about $66{\pm}1.4%$ (decay-corrected, n=28) within $51{\pm}1.2$ min including HPLC purification and solid-phase purification for the final formulation. Conclusion: [$^{18}F$]Fallypride was prepared with a significantly improved radiochemical yield with high specific activity and shorten synthetic time. In addition, this automated procedure provides the high reproducibility with no synthesis failures (n=28).

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