• 제목/요약/키워드: H&N Ca.

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Effects of Long-Term Fertilization for Cassava Production on Soil Nutrient Availability as Measured by Ion Exchange Membrane Probe and by Corn and Canola Nutrient Uptake

  • Hung T. Nguyen;Anh T. Nguyen;Lee, B.W.;J. Schoenau
    • 한국작물학회지
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    • 제47권2호
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    • pp.108-115
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    • 2002
  • The effects of long-term fertilization on soil properties and nutrient availability are not well documented for cassava cultivation in Vietnam. In 1990, a field research plots were established with 12 treatments to test the effect of different rates of nitrogen (N), phosphorus (P) and potassium (K) on soil properties in Acrisols at Thai Nguyen University in Northern Vietnam. In 1999, composite soil samples (0 to 20cm depth) were collected from eight selected plots for measurements of nutrient supply rates by ion exchange membrane probes and for growing corn and canola in a growth chamber with and without added lime. Generally, long-term nitrogen (N) fertilization increased available N supply rates but decreased available potassium (K) and magnesium (Mg). Long-term phosphorus(P) applications increased canola N, calcium (Ca) and Mg uptake. Canola P uptake increased with increased P rates only when lime was added. Long-term K applications increased canola N, K, Ca, Mg uptake but only significantly increased corn N uptake. Liming significantly increased uptake of N, P, K, Ca, Mg and S for both corn and canola. However, N $H_{4-}$N, K and Mg soil supply rates were reduced when lime was added, due to competition between Ca from the added lime and other nutrients.

수산화 인산칼슘의 합성 (Synthesis of Hydroxycalciumphosphate)

  • Hwang, Young-Gil;Kim, Youn-Soo;Kim, Jae-Il
    • 자원리싸이클링
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    • 제5권3호
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    • pp.50-55
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    • 1996
  • CaO를 $HNO_3$로 용해하여 제조한 (NO$Ca_3$)$_2$용액을 $NH_4$OH로 pH를 조절하고, 상압하의 온도에서 (NH$_4$)$_2$HPO$_4$를 주입시켜서 소정의 시간동안 Ca,,(PO$_4$),(OH)$_2$합성실험을 하였다. Ca,,(PO$_4$),(OH)$_2$는 pH 10~13 범위에서 생성되었고 이 HAP의 입경을 전자현미경으로 조사한 결과 0.1~0.5$mu extrm{m}$이었다. 반응온도는 $40~70^{\circ}C$, 결정화온도 $90^{\circ}C$이며 반응시간은 30분이 적당하였다. 생성된 Ca\ulcorner(PO$_4$)\ulcorner(OH)$_2$$500^{\circ}C$, 1시간동안 하소하여도 변화하지 않으나 80$0^{\circ}C$에서 1시간동안 하소한 시료는 $Ca_3$($PO_4$)$_2$와 HAP, CaO로 변화되었고, 구형의 미립자로 되어 있었다.

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Tsukamurella sp. 26A에 의한 생물계면활성제의 생산 (Production of Biosurfactant by Tsukamurella sp. 26A)

  • 최경숙;김순한;정영기;장경립;이태호
    • 미생물학회지
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    • 제33권3호
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    • pp.187-192
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    • 1997
  • 토양으로부터 biosurfactant를 생산하는 미생물을 분리하여 Tsukamurella sp. 26A로 동정하였다. Biosurfactant 생산을 위한 최적 배지 조성은 n-hexadecane 7%, $NaNO_{3}$ 0.2%, $K_2HPO_4$ 0.001%, $MgSO_{4}$ center dot $7H_{2}O$ 0.02%, $CaCl_2$ center dot $2H_{2}O$ 0.02%, yeast extract 0.02%(pH 6.8-7.0, 30^{\circ}C.$ )이었으며 배양액의 최저 표면장력과 계면장력은 각각 30mN/m, 1.5mN/m였다. 유화기질로서 hydrocarbon류, edible oil류, 그리고 petroleum oil등에 작용시켰을 경우 비교적 높은 유화활성과 유화 안정도를 나타내었다.

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Salen-Aluminum Complexes as Host Materials for Red Phosphorescent Organic Light-Emitting Diodes

  • Bae, Hye-Jin;Hwang, Kyu-Young;Lee, Min-Hyung;Do, Young-Kyu
    • Bulletin of the Korean Chemical Society
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    • 제32권9호
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    • pp.3290-3294
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    • 2011
  • The properties of monomeric and dimeric salen-aluminum complexes, [salen(3,5-$^tBu)_2$Al(OR)], R = $OC_6H_4-p-C_6H_6$ (H1) and R = [salen(3,5-$^tBu$)AlOPh]C$(CH_3)_2$ (H2) (salen = N,N'-bis-(salicylidene)-ethylenediamine) as host layer materials in red phosphorescent organic light-emitting diodes (PhOLEDs) were investigated. H1 and H2 exhibit high thermal stability with decomposition temperature of 330 and $370^{\circ}C$. DSC analyses showed that the complexes form amorphous glasses upon cooling of melt samples with glass transition temperatures of 112 and $172^{\circ}C$. The HOMO (ca. -5.2~-5.3 eV) and LUMO (ca. -2.3~-2.4 eV) levels with a triplet energy of ca. 1.92 eV suggest that H1 and H2 are suitable for a host material for red emitters. The PhOLED devices based on H1 and H2 doped with a red emitter, $Ir(btp)_2$(acac) (btp = bis(2-(2'-benzothienyl)-pyridinato-N,$C^3$; acac = acetylacetonate) were fabricated by vacuum-deposition and solution process, respectively. The device based on vacuum-deposited H1 host displays high device performances in terms of brightness, luminous and quantum efficiencies comparable to those of the device based on a CBP (4,4'-bis(Ncarbazolyl) biphenyl) host while the solution-processed device with H2 host shows poor performance.

Green Light-Emitting Phosphor, Ba2xCaMgSi2O8:Eux

  • Kim, Jeong-Seog;Piao, Ji-Zhe;Choi, Jin-Ho;Cheon, Chae-Il;Park, Joo-Suk
    • 한국세라믹학회지
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    • 제42권3호
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    • pp.145-149
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    • 2005
  • [ $Eu^{2+}$ ]-activated barium magnesium silicate phosphor, $(Ba,Ca)_{3}MgSi_{2}O_{8}:Eu_{x}$, has been known to emit blue-green light. In this study we report the manufacturing processes for producing either pure green or pure blue light-emitting phosphor from the same composition of $Ba_{2-x}Ca_{2}CaMgSi_{2}O_{8}:Eu_{x}$ (0 < x < 1) by controlling heat treatment conditions. Green light emitting phosphor of $Ba_{1.9}CaMgSi_{2}O_{8}:Eu_{0.1}$ can be produced under the sample preparation condition of highly reducing atmosphere of $23\%\;H_2/77\%\;N_2$, while blue or blue-green light emitting phosphor under reducing atmosphere of $5\~20\%\;H_2\;/\;95\~80\%$ N_2. The green light-emitting phosphors are prepared in two steps: firing at $800\~1000^{\circ}C$ for $2\~5$ h in air then at $1100\~1350^{\circ}C$ for 2-5 h under reducing atmo­sphere $23\%$ $H_2/77\%\;N_2$. The excitation spectrum of the green light-emitting phosphor shows a broadband of $300\~410$ nm. The emission spectrum has a maximum intensity at the wavelength of about 501 nm. The CIE value of green light emission is (0.162, 0.528). The pure blue light-emitting phosphors can be produced using the $Ba{2_x}CaMgSi_{2}O_{8}:Eu_{x}$ by introducing additional firing step at $1150\~1300^{\circ}C$ in air before the final reducing treatment. The XRD analysis shows that the green light-emitting phosphor mainly consisted of $Ba_{1.31}Ca_{0.69}SiO_{4}$ (JCPDS $\#$ 36-1449) and other minor phases i.e., $MgSiO_3$ (JCPDS $\#$ 22-0714) and $Ca_{2}BaMgSi_{2}O_{8}$ (JCPDS $\#$ 31-0128). The blue light-emitting phosphor mainly consisted of $Ca_{2}BaMgSi_{2}O_{8}$ phase.

Activation of acetylcholine receptor elicits intracellular Ca2+ mobilization, transient cytotoxicity, and induction of RANKL expression

  • Heo, Seong-Jong;Kim, Min Seuk
    • International Journal of Oral Biology
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    • 제41권3호
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    • pp.119-123
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    • 2016
  • Acetylcholine receptors (AChR) including muscarinic and nicotinic AChR are widely expressed and mediate a variety of physiological cellular responses in neuronal and non-neuronal cells. Notably, a functional cholinergic system exists in oral epithelial cells, and nicotinic AChR (nAChR) mediates cholinergic anti-inflammatory responses. However, the pathophysiological roles of AChR in periodontitis are unclear. Here, we show that activation of AChR elicits increased cytosolic $Ca^{2+}([Ca^{2+}]_i)$, transient cytotoxicity, and induction of receptor activator of nuclear factor kappa-B ligand (RANKL) expression. Intracellular $Ca^{2+}$ mobilization in human gingival fibroblast-1 (hGF-1) cells was measured using the fluorescent $Ca^{2+}$ indicator, fura-2/AM. Cytotoxicity and induction of gene expression were evaluated by measuring the release of glucose-6-phosphate dehydrogenase and RT-PCR. Activation of AChR in hGF-1 cells by carbachol (Cch) induced $[Ca^{2+}]_i$ increase in a dose-dependent manner. Treatment with a high concentration of Cch on hGF-1 cells caused transient cytotoxicity. Notably, treatment of hGF-1 cells with Cch resulted in upregulated RANKL expression. The findings may indicate potential roles of AChR in gingival fibroblast cells in bone remodeling.

Diazidophenylmethane 유도체들의 가수분해반응 메카니즘에 대한 반응속도론적 연구 (Kinetics and Mechanism of the Hydrolysis of Diazidophenylmethane Derivatives)

  • 권기성;서지형;이용구
    • 대한화학회지
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    • 제41권6호
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    • pp.313-319
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    • 1997
  • Diazidophenylmethane 유도체들(X: p-H, $p-OCH_3,\;p-F,\;p-CH_3$)을 합성하여 25$^{\circ}C$의 50:50(v/v) MeOH/$H_2O$ 혼합용매(${\mu}=0.1$ : KCl)에서의 pH 변화에 따른 가수분해 반응 속도상수를 측정하여 유도된 반응속도식과 치환기효과, 용매효과, 염효과, 열역학적 활성화 파라미터, 그리고 생성물분석의 결과로부터 낮은 $pH(0{\leq}pH<2)$에서는 $S_N2_CA$, 중간 pH(2$S_N1$, 그리고 높은 $pH(12에서는 $S_N2$ 반응메카니즘을 각각 제안하였다.

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New Oxide Crystals as Substrates for GaN-based Blue Light Emitting Devices

  • Fukuda, T.;Shimamura, K.;Tabata, H.;Takeda, H.;Futagawa, N.;Yoshikawa, A.;Kochurikhin, Vladimir-V.
    • 한국결정성장학회:학술대회논문집
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    • 한국결정성장학회 1999년도 PROCEEDINGS OF 99 INTERNATIONAL CONFERENCE OF THE KACG AND 6TH KOREA·JAPAN EMG SYMPOSIUM (ELECTRONIC MATERIALS GROWTH SYMPOSIUM), HANYANG UNIVERSITY, SEOUL, 06월 09일 JUNE 1999
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    • pp.3-26
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    • 1999
  • We have successfully grown <111>-oriented (La,Sr)(Al,Ta)$O_3$(LSAT) mixed-perovskite single crystals and <0001>-oriented $Ca_8La_2(PO_4)_6O_2$(CLPA) single crystals with the apatite structure by the Czochralski method. The compositional and lattice parameter uniformity of the crystals are discussed in relation to the growth conditions. Since LSAT and CLPA single crystals have excellent lattice matching with GaN, they ar promising as new substrates for the growth of high quality GaN epitaxial layers.

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플라즈마 처리에 의한 양액 성분 변화 (Change of Hydroponic Components by Plasma Treatment)

  • 김동석;박영식
    • 한국환경과학회지
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    • 제21권3호
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    • pp.363-368
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    • 2012
  • The influence of plasma discharge on the nutrient components ($NO_3$-N, $NH_4$-N, $PO_4$-P, K, Ca, and Mg) and water quality [pH, ORP (oxidation-reduction potential) and electric conductivity] of hydroponic water were investigated. It was observed that the $NH_4$-N, $PO_4$-P, K, Ca, and Mg were kept at the constant concentrations for plasma discharging of 90 min. On the other hand, $NO_3$-N concentration was increased with proceeding of the plasma discharge. The increase of $NO_3$-N concentration was considered with the fact that nitric acid was created from nitrogen among supplying air for the insulation of inside of dielectric barrier. ORP and electric conductivity was increased with plasma discharging time. However, pH was decrease with what because of the generation of the nitric acid. When adjusting the hydroponic ingredients, pH and conductivity must to be considered because of the change of pH and conductivitiy with the discharging.

대두재배 농가포장 토양의 화학적 특성 (Chemical properties of soybean-cultivated field soils)

  • 유순호;노희명;이상호;김찬섭
    • 한국토양비료학회지
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    • 제23권4호
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    • pp.275-280
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    • 1990
  • 대두의 안전증수를 위하여 합리적인 비배관리 및 토양관리에 필요한 기초 자료를 얻고자 일반 농가의 대두재배 포장을 대상으로 대두엽과 토양을 채취 분석하였다. 본조사에서는 경기도 13개, 충청남도 5개 및 충청북도 6개 포장 등 24개 대두재배 포장에서 대두 생육기(파종 50~60일 후, 1988년 7월)에 토양과 대두엽을, 수확 직후 (1988년 10월)와 이듬해 파종 전(1989년 4월)에 토양을 채취하였다. 이들을 분석한 결과는 다음과 같다. 1. 토양의 pH는 4.8~6.8범위였으며, 수확기의 pH는 평균 5.4로서 생육기의 5.7에 비하여 낮았다. 2. 토양중 교환성과 활성 Al함량은 토양의 pH와 밀접한 관련이 있었다. 토양의 pH가 낮을수록 교환성과 활성 Al함량은 높았으며, pH 5.8이상에서 교환성 Al은 거의 검출되지 않았다. 3. 수확기의 토양의 전질소와 유효인산 함량은 생육기에 비하여 낮았다. 특히, 유효인산은 생육기와 수확기는 물론 파종기에 채취한 토양에서도 상당히 높았다. 4. 토양중 교환성 Ca과 Mg함량은 수확기와 생육기간에 별 차가 없었으나, 교환성 K함량은 수확기의 경우 생육기에 비하여 감소하였다. 5. 대두엽중 질소함량은 토양중 전질소함량과는 상관이 없었으나 대두엽중 K함량과는 상관이 높았다. 대두엽중 Mg함량 역시 대두엽중 Ca함량과 상관이 높았으며, 다른 성분과는 달리 토양중 Mg함량과도 상관이 높았다.

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