• Journal of the Korean Chemical Society
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• v.37 no.9
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• pp.787-792
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• 1993

Semiempirical MNDO calculations are employed to study relation properties on bridging OH group with Al-O(P-O) bond length and Al-O-P bond angle of structural characteristics using birdging $(OH)_3AlOP(OH)_3$ and $(OH)_3AlOHP(OH)_3^+$ model culster. We know that the O-H bond dissociation energy of bridging OH group is increased with increasing Al-O(P-O) bond length and decreasing Al-O-P bond angle. The bridging OH group is formed into enlarged Al-O(P-O) bond length and shortened Al-O-P bond angle in bridging oxygen atom by a hydrogen migration. The negative net charge of bridging oxygen atom is increased with longer Al-O-P bond angle, while the positive net charge is decreased with longer Al-O-P bond angle.

• Journal of the Korean Society of Marine Environment & Safety
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• v.22 no.2
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• pp.187-194
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• 2016

In this paper, as a basic research for the restoration and construction of easuary saltmarsh, To observe the habitat environment for reed, we observed sediment environment (Particle size, water content, pH, nutrient analysis ($NH_4-N$, $PO_4-P$)), ground water level, ground level, individual numbers of reed, maximum reed height. As a result of this study, sediment particle size and moisture content of soil on the study area not effected reed habitat, pH showed no difference in each site. $NH_4-N$ and $PO_4-P$ concentration also no difference in each site. Ground level of reed habitat area is more higher than none reed habitat. However Ground water level of reed habitat area is more lower than none reed habitat. As a results of analyzing the influence factors for reed habitat in Nakdong estuary saltmarsh, ground water level and ground level is most influenced factor for reed habitat.

• Journal of the Korean Electrochemical Society
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• v.11 no.4
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• pp.268-272
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• 2008

$LiFePO_4$ material was synthesized by electrospinning method to obtain optimal particle size($50{\sim}100\;nm$) without carbon coating or ball milling. This material showed an orthorthombic structure with Pnma space group without any impurities, such as FeP or $Fe_2P$, in the XRD pattern. The particle morphology and particle shape were observed by SEM analysis. Li/$LiFePO_4$ cell showed a high initial discharge capacity of 135 mAh/g, at current density of $0.1\;mA/cm^2$ with a cut-off voltage of 2.8 to 4.0V. This cell exhibited a perfect cycle performance over 99.9% cycle retention rate up to 50 cycles.

• Bulletin of the Korean Chemical Society
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• v.28 no.6
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• pp.921-928
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• 2007

Three different phosphonated trisbipyridine ruthenium complexes, [(4-CH3-4'-CH2PO(OH)2-2,2'-bipyridine)- (bpy)2Ru]·(PF6)2 (Ru-P1), [(4-CH3-4'-CH2PO(OH)2-2,2'-bipyridine)3Ru]·(PF6)2 (Ru-P2), and [(4,4'-CH2PO- (OH)2-2,2'-bipyridine)3Ru]·(PF6)2 (Ru-P3) were synthesized and their photochemical and electrochemical properties were studied. These ruthenium complexes were strongly adsorbed on the surface of the layered metal oxide semiconductor K4Nb6O17 that was partially acid-exchanged and sensitized up to pH 10, while the carboxylated ruthenium complex, (4,4'-COOH-2,2'-bipyridine)3Ru·Cl2 (Ru-C) that was previously studied was sensitized only below pH 4. The visible light water reduction at K4Nb6O17 that was internally platinized and sensitized by these phosphonated Ru-complexes was comparatively studied using a reversible electron donor iodide.

• Korean Journal of Crystallography
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• v.12 no.3
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• pp.145-149
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• 2001

The hydrothermal reaction between zinc(II) nitrate Zn₃(PO₄)₂(H₂O) and potassium phosphate dibasic (K₂HPO₄) in the presence of pyrazine gave a three-dimensional zinc-phosphate coordination polymer with an empirical formula of Zn₃(PO₄)₂(H₂O) (1). Compound 1 was characterized by IR spectroscopy, and X-ray diffraction. Crystallographic data for 1: monoclinic space group. P2₁/c, a=8.970(1)Å, b=4.901(1)Å, c=16.759(3)Å, β=94.98(2)°, Z=4, R(wR₂)=0.0332(0.0927).

• Korean Journal of Environmental Agriculture
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• v.42 no.2
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• pp.83-92
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• 2023

Excess N and P from the livestock manure applied to farmlands, have entered the water systems and poses a serious threat to the natural environment. Consequently, there has been recent awareness towards the management of livestock manure and its related fields. In this study, piggery wastewater was collected from a piggery in Pohang city, Korea. At 800℃, thermal decomposition of a natural stone, magnesite (MgCO₃), yielded powered MgO with particle sizes ranging between 10 to 100 ㎛. Furthermore, NH₄⁺-N and PO₄^3--P were recovered as struvite precipitates from the piggery wastewater, by adjusting the pH with MgO and H₃PO₄. At pH 10, the recovery efficiencies of NH₄⁺-N and PO₄^3--P were found to be 86.1% and 94.1%, respectively. Using an X-ray Diffractometer (XRD), the struvite in the precipitate was confirmed to be consistent with standard pure struvite. Further, the purity of the struvite precipitate was analyzed using an energy dispersive X-ray (EDX) and thermal gravimetry-differential thermal analysis (TG-DTA), and found to be between 79.2% and 93.0%. Additionally, struvite-containing piggery wastewater and sawdust were mixed in a weight ratio of 2.5:1 and processed into a mature compost. The newly manufactured compost passed all quality standards required for first-class graded livestock composts. Moreover, this compost was sprayed directly onto the soil at the test site, and various parameters of the soil's effluent, such as total organic carbon (TOC), total nitrogen (T-N), total phosphorus (T-P), and dissolved oxygen (DO), were analyzed and measured. Based on these results, it is determined that the newly manufactured compost can more significantly reduce water pollution than commercial compost.

• Proceedings of the Korea Water Resources Association Conference
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• 2009.05a
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• pp.602-607
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• 2009

논에서 수질변화특성에 관한 메카니즘은 매우 복잡하다. 영양물질의 농도특성을 정확히 파악하기 위해서는 영농활동에 따른 체계적인 모니터링을 통한 다양한 측정 자료가 필요하다. 그러나 현재 논에서 토양의 산화환원에 관한 연구 자료는 많지 않기 때문에 그의 특성을 파악하기에는 어려운 실정에 있다. 본 연구의 목적은 충북대학교 부속농장 필지논에서 2008년 영농기간을 중심으로 논에서의 영양물질인 총인(TP), 인산성 인($PO_4-P$) 및 산화환원전위(Eh)의 변화특성을 파악함으로써, 논으로부터의 영양물질 유출제어에 관한 기초 자료를 제공하는데 있다. 이 연구는 2008년 6월부터 10월까지 필지논에서 논 표면수의 TP 와 $PO_4-P$의 농도변화와 토양의 산화환원전위(Eh)와의 관계 특성을 파악하였다. 관개기의 논에서 인은 분얼비 시기에 인성분이 시비되지 않았는데도 불구하고 분얼비 직후와 분얼비 1주일 후에 TP농도가 높게 나타났는데 이는 담수의 영향으로 논이 환원상태로 되어, 논바닥에 침전된 철이온에 흡착되어 있던 인이 철이온의 환원으로 함께 용출하기 때문이라고 생각된다. 산화환원전위(Eh)는 높아지면 산화경향을, 낮아지면 환원경향을 나타낸다. 본 연구기간 동안의 산화환원전위(Eh) 값은 비 관개기에 $201^{\sim}405$ mV로 높게 나타났고, 관개기에는 $93^{\sim}195$ mV로 낮게 나타났다. 필지논 표면수의 인농도는 분얼비 직후 1주일후까지 TP 와 $PO_4-P$ 농도는 같이 상승하다가 TP농도는 약 2주일까지 더 상승하여 2008년 최대값을 나타냈고 $PO_4-P$농도는 하강하였는데 이는 논 토양이 환원상태로 되면서 바닥에 있던 입자성 인이 논 표면으로 떠올랐기 때문으로 사료된다. 그 후에 담수가 끝나는 시점까지 농도는 낮아졌다. 강우량이 적은 관개초기에 인의 농도는 비교적 높게 나타났지만 강우량이 많은 여름에는 작물의 생장에 필요한 영양물질 섭취 등으로 인농도가 낮게 나타나 논은 인의 유출을 억제하고 있는 것으로 나타났다. 이와 같이 인의 유출특성 및 산화환원전위(Eh)의 변화에 따른 논에서의 유출부하 특성이 규명된다면, 환경부하가 적은 효과적인 물관리가 가능해 질 것으로 판단된다.

• Journal of the Korean Ceramic Society
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• v.31 no.11
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• pp.1337-1345
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• 1994

Glasses in the system of 45CaO-25TiO2-30P2O5 containing 1 mole% of M2O(M=Li, Na, K) were melted and crystallized. And their crystal phases were Ca3(PO4)2, CaTi4(PO4)6, and TiO2. Porous glass-ceramics with skeleton of two crystal phase CaTi4(PO4)6 and TiO2 were prepared by selective leaching of Ca3(PO4)2 with 0.1 N-HCl. Glass transition temperature(Tg) and crystallization temperature(Tc) were decreased by addition of 1 mole% alkali metal oxide. Pore size of porous glass-ceramics was increased with increasing heat treatment temperature and its dependence on heat treatment temperature was decreased with addition of Na2O and K2O. It was found that porous glass-ceramics of parent glass and containing 1mole% M2O(M=Li, Na, K) composition had maximum specific surface area, porosity and maximum of crystallzed phase by heat treatment at 80$0^{\circ}C$, 76$0^{\circ}C$, 78$0^{\circ}C$, 80$0^{\circ}C$ respectively.

• Journal of the korean academy of Pediatric Dentistry
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• v.45 no.3
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• pp.290-298
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• 2018

This study aimed to evaluate surface morphology and resin tag penetration of resin infiltration into primary anterior teeth after enamel deproteinization with sodium hypochlorite (NaOCl) prior to phosphoric acid ($H_3PO_4$) etching. Ninety primary anterior teeth with non-cavitated caries lesion were devided five groups according to enamel pretreatment as follows, group I-15% hydrochloric acid (HCl) 2min. ; group II-5.25% NaOCl 1min., 35% $H_3PO_4$ 1min. ; group III-5.25% NaOCl 2min., 35% $H_3PO_4$ 1min. ; group IV-5.25% NaOCl 1min., 35% $H_3PO_4$ 2min. ; group V-5.25% NaOCl 2min., 35% $H_3PO_4$ 2min. Fifteen teeth were examined etched surface structure using field emission-scanning electron microscope. Seventy five teeth were infiltrated with resin, maximum penetration depth and percentage penetration were analysed using dual fluorescence confocal microscopy. As the application time of NaOCl increased, ratio of enamel type I, II were increased. Percentage penetration (PP) was higher in group V than group II, III (p < 0.05). PP of group IV, V did not show any differences. Non-cavitated caries of primary anterior teeth can be treated with resin infiltration. Enamel deproteinization with NaOCl prior to 35% $H_3PO_4$ etching could be an alternative of 15% HCl etching in resin infiltration.

• Applied Biological Chemistry
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• v.7
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• pp.45-52
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• 1966

This study was carried out to determine how the water soluble, the available $P_2O_5$ and urea-N would change in the course of time, when the mixtures of calcium superphosphate and urea with lime for fertilizer which occurred in Korea and largely contained calcium carbonate were made. Three kinds of materials, i. e., calcium superphosphate, urea and lime for fertilizer were used in this study. Three kinds of mixed fertilizer, i. e., A, B and C were made up by mixing these materials to satisfy the following formula. $$1)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_2H_2(PO_4)+H_2CO_3+NH_3$$ $$2)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_3(PO_4)_2+H_2CO_3+NH_3$$ $$3)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_3(PO_4)_2+H_2CO_3+CaCO_3+NH_3$$ A,B and C were placed in desiccators respectively a six month period. During the time of storage, the water soluble, the available phosphoric acid and urea-N were measured once a month, seven times with the control measurement. The results may be summarized as follows. 1. None of A, B and C showed any change in the urea-N with the lapse of time. This fact indicated that the combination of calcium superphosphate and urea with lime for fertilizer was not unfavourable. 2. A, B and C decreased in the amount of water soluble $P_2O_5$ with the passage of time. This fact indicated that the mixing of calcium superphosphate and urea with lime for fertilizer was unfeasible. 3. The available $P_2O_5$ in any of A,B and C did not undergo a change as time went by. This fact suggested that the combination of calcium superphate and urea with lime for fertilizer was favourable.