• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2015년도 추계학술논문요약집
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• pp.465-466
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• 2015

In this study, different amount of (fe(0)) were dissolve into different strength of phosphoric ($H_3PO_4$) acid and the optimum solubility was observed at 0.89M Fe(0) into 4M of $H_3PO_4$ acid. Different concentration of oxalic acid was added to determine the optimum precipitated condition. The dissolution kinetics of Fe(0) into $H_3PO_4$ acid was investigated at $40-50^{\circ}C$. The optimum Fe-oxalate precipitate was dried and thermal decomposition using DSC-TG was conducted. Approximately 52 wt(%) of oxalic acid was removed at $300^{\circ}C$. Iron oxides such as magnetite and hematite that may be formed on the surface of nuclear waste were also dissolved into the $H_3PO_4$ acid and the optimum solubility for magnetite is 0.005M while that for hematite is 0.02M in 8M $H_3PO_4$ acid, respectively.

• Membrane and Water Treatment
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• 제2권3호
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• pp.187-205
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• 2011

The electric transport of the mixture of hydrochloric and phosphoric acids through strong base (Neosepta ACM) and weak base (Selemion AAV) anion-exchange membranes was investigated. The instantaneous efficiency of HCl removal from the cathode solution, $CE_{Cl}$, with and without $H_3PO_4$ was determined. It was found that $CE_{Cl}$ was 0.8-0.9 if the number of moles of elementary charge passed through the system, $n_F$, did not exceed ca. 80% of the initial number of HCl moles in the cathode solution, $n_{Cl,ca,0}$. The retention efficiency of $H_3PO_4$ in that range was close to one. The transport of acid mixtures was satisfactorily described by a model based on the extended Nernst-Planck and Donnan equations for $n_F$ not exceeding $n_{Cl,ca,0}$. Among the tested model parameters, most important were: concentration of fixed charges, the porosity-tortuosity coefficient, and the partition coefficient of an undissociated form of $H_3PO_4$. For the both membranes, the obtained optimal values of fixed charge concentration, $\bar{c}_m$, were up to 40% lower than the literature values of $\bar{c}_m$ obtained from the equilibrium measurements. Regarding the $H_3PO_4$ equilibria, it was sufficient to consider $H_3PO_4$ as a monoprotic acid.

• 한국표면공학회지
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• 제50권4호
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• pp.231-236
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• 2017

The present work addresses how to measure the amount of dissolved aluminum in phosphoric acid, based on volumetric and gravimetric measurements of the precipitates formed by reaction between the $H_3PO_4$ solution containing dissolved aluminum ions and 10 % KF solution. The volume of the precipitates increased with dilution of the dissolved aluminum-containing $H_3PO_4$ solution up to 1/4 dilution above which it decreased with further dilution. The lowered amounts of the precipitates at low dilution less than 1/4 and high dilution more than 1/4 are attributed to high acidity of the solution and decreased amount of dissolved aluminum in the solution, respectively. Volumetric measurement of the amount of precipitates was found not to be very reliable with the experiments, while weight measurement of the precipitates after drying for 80 min at $60^{\circ}C$ appeared to be very reproducible. In the present work, it is suggested that the amount of Al dissolved in 85 % $H_3PO_4$ solution can be calculated by multiplying 50 to the weight of precipitate obtained by reacting 8 ml of 1/4 diluted $H_3PO_4$ solution containing dissolved aluminum ions with 6 ml of 10 % KF solution.

• Journal of Electrochemical Science and Technology
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• 제2권2호
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• pp.76-84
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• 2011

Potentiostatic oxidation of Pb-1.7%Sb alloy used in the manufacture of grids of lead-acid batteries over the potential range from -1.0V to 2.3V in 5M $H_2SO_4$ in the absence and the presence of 0.4M $H_3PO_4$ and the self-discharge characteristics of the oxide layer formed is studied by electrochemical impedance spectroscopy (EIS). Depending on the potential value, sharp variations in resistance and capacitance of the alloy are recorded during the oxidation and they can be used for identification of the various substances involved in passive layer. Addition of $H_3PO_4$ is found to deteriorate the insulating properties of the passive layer by the retardation of the formation of $PbSO_4$. $H_3PO_4$ completely inhibits the current and impedance fluctuations recorded in $H_3PO_4$-free solutions in the potential range 0.5 V-1.7 V. These fluctuations are attributed to the occurrence of competitive redox processes that involve the formation of $PbSO_4$, $PbOSO_4$, PbO and $PbO_2$ and the repeated formation and breakdown of the passive layer. Self-discharge experiments indicate that the amount of $PbO_2$ formed in the presence of $H_3PO_4$ is lesser than in the $H_3PO_4$-free solutions. The start of transformation of $PbSO_4$ into $PbO_2$ is greatly shortened. $H_3PO_4$ facilitates the diffusion process of soluble species through the passive layer ($PbSO_4$ and basic $PbSO_4$) but impedes the diffusion process through $PbO_2$.

• Korean Chemical Engineering Research
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• 제57권6호
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• pp.891-897
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• 2019

본 연구에서는 Phosphoric acid ($H_3PO_4$)와 Vanadium (V) pentoxide ($V_2O_5$), Molybdenum (VI) trioxide ($MoO_3$)으로 부터 조성을 달리하여, heteropoly acid의 PVMo 촉매를 활성탄 지지체에 담지하였다. 촉매의 반응성 조사를 위해, 기상의 포름알데히드를 $140^{\circ}C$의 온도에서 1시간 동안 반응시켰다. 반응전후의 촉매는 XRD와 BET 분석을 수행하였으며, 촉매의 산도 측정을 위해 $NH_3-TPD$을 수행하였다. 포름알데히드의 전환율은 $MoO_3$와 $H_3PO_4$ 성분이 감소하고 $V_2O_5$ 성분이 증가함에 따라 증가하였다. 대부분의 촉매에서 비교적 낮은 촉매 결정성이 관찰되었으며, 비표면적은 반응후 다소 감소하는 것으로 나타났다. $NH_3-TPD$ 분석 결과, $400^{\circ}C{\sim}500^{\circ}C$에 해당하는 강한 산점의 비율이 $MoO_3$와 $H_3PO_4$ 성분의 함량이 감소하고 $V_2O_5$ 성분의 함량이 증가함에 따라 증가하였다. 이러한 강한 산점의 비율이 포름알데히드의 전환율에 영향을 미치는 것으로 나타났다.

• 대한소아치과학회지
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• 제45권3호
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• pp.290-298
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• 2018

이 연구는 유전치 비와동성 우식 병소에 레진침투법을 시행할 때 sodium hypochlorite(NaOCl) 제단백 후 phosphoric acid($H_3PO_4$) 산부식 처리에 따른 법랑질 표면구조 및 레진 침투깊이 변화를 알아보았다. 90개의 발치된 비와동성 병소의 유전치를 전처리에 따라 5개 군으로 나누었다 : I군 hydrochloric acid(HCl) 2분; II군 NaOCl 1분, $H_3PO_4$ 1분; III군 NaOCl 2분, $H_3PO_4$ 1분; IV군 NaOCl 1분, $H_3PO_4$ 2분; V군 NaOCl 2분, $H_3PO_4$ 2분. 그 중 15개는 전계방사주사전자현미경을 통해 표면을 관찰하였고, 75개는 레진침투 후 공초점레이저주사현미경을 통해 병소 깊이와 레진 침투깊이를 측정하여 레진 침투도를 도출했다. NaOCl 적용 시간이 길어질수록 법랑질 산부식 I, II형 비율이 증가하였다. 레진 침투도는 V군이 II, III군에 비해 통계학적으로 유의하게 높았고(p < 0.05), IV, V군은 유의할 만한 차이가 없었다. 레진침투법은 유전치 초기 우식 병소의 치료로 사용될 수 있으며, 전처리 제로 15% HCl 산부식 대신 5.25% NaOCl 제단백 후 35% $H_3PO_4$ 산부식이 대안으로 고려될 수 있다.

• 대한화학회지
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• 제19권5호
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• pp.325-330
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• 1975

철(III) 이온과 인산간의 착물형성에 관하여 넓은 인산산성범위(0${\sim}40{\%}$)에서 가시부스펙트럼과 용액으로 부터 분리해낸 화합물을 검토함으로써 연구하였다. 철(III)함유 인산용액의 전자흡수 스펙트럼은 19.2kK 및 24.1kK에서 철(III)-인산 착물형성을 나타내는 두개의 가시부 흡수를 나타내었다. 24.1kK 밴드의 인산농도에 따른 흡광도 변화의 측정으로부터 아마도 $[Fe(H_xPO_4)]^{x+}\;및\;[Fe_2 (H_xPO_4)]^{(3+x)+}$등 두개의 형태가 틀린 철(III)-인산착물이 존재함을 알 수 있었다. 이들 두화합물중 몰비가 1:1인 착물은 고체상태로 분리하는데 성공하였으며 인산이온은 염기도 1인 상태로 금속에 배위되어 있음을 알 수 있으나, 이합체로 생각되는 화합물은 분리해낼 수 없었다.

• 한국토양비료학회지
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• 제19권3호
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• pp.217-221
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• 1986

토양중(土壤中)에서 납(Pb)의 용출경감효과(溶出輕減效果)를 구명(究明)하기 위(爲)하여 토양(土壤)에 납을 $PbCl_2$로 310.8ppm 처리(處理)하고 경감제(輕減劑)로서 소석회(消石灰), 석고(石膏), 과석(過石), 인산(燐酸)을 처리(處理)하여 담수후(湛水後) 실온(室溫)에 보관(保管)하면서 납 용출량(溶出量) 및 Ca, $PO_4$, $SO_4$와 pH, Eh를 측정(測定)한 결과(結果)는 다음과 같다. 1. 납 용출량(溶出量)은 경감제시용량(輕減劑施用量)이 증가(增加)할수록 감소(減少)되었으며 $H_3PO_4$ 및 과석(過石)이 용출억제효과(溶出抑制效果)가 좋았다. 2. 토양(土壤)의 pH는 소석회(消石灰)가 높고 인산구(燐酸區)가 낮으며 토양(土壤)의 Eh는 반대(反對)의 경향(傾向)이었다. 3. 토양중(土壤中)의 수용성(水溶性) Ca, $PO_4$ 및 $SO_4$ 함량(含量)은 경감제(輕減劑) 시용량(施用量)이 증가(增加)할수록 증가(增加)되었다. 4. 시험후(試驗後) 토양(土壤)의 가용성(可溶性) 납함량(含量)은 과석(過石), 인산(燐酸), 소석회(消石灰), 석고(石膏), 대조(對照)의 순(順)으로 낮은 경향(傾向)이었다.

• Transactions on Electrical and Electronic Materials
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• 제4권2호
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• pp.1-4
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• 2003

The purpose of this study was to investigate the characteristics of slurry including phosphoric acid for chemical-mechanical planarization of copper and tantalum nitride. In general, the slurry for copper CMP consists of alumina or colloidal silica as an abrasive, organic acid as a complexing agent, an oxidizing agent, a film forming agent, a pH control agent and additives. Hydrogen peroxide (H$_2$O$_2$) is the material that is used as an oxidizing agent in copper CMP. But, the hydrogen peroxide needs some stabilizers to prevent decomposition. We evaluated phosphoric acid (H$_3$PO$_4$) as a stabilizer of the hydrogen peroxide as well as an accelerator of the tantalum nitride CMP process. We also estimated dispersion stability and zeta potential of the abrasive with the contents of phosphoric acid. An acceleration of the tantalum nitride CMP was verified through the electrochemical test. This approach may be useful for the development of the 2$\^$nd/ step copper CMP slurry and hydrogen peroxide stability.

• 한국세라믹학회지
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• 제55권5호
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• pp.480-491
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• 2018

Calcium phosphates (CaP) were prepared by a wet chemical method. Micro-crystalline dicalcium phosphate (DCPD) was precipitated at $37^{\circ}C$ and pH 5.0 using $Ca(OH)_2$ and $H_3PO_4$. The precipitated DCPD solution was kept at $37^{\circ}C$ for 96 h. Artificial bone cement was composed of DCPD, $Ca(H_2PO_4)_2{\cdot}H_2O$ (MCPM), and $CaSO_4{\cdot}1/2H_2O$, $H_2O$ and aqueous poly-phosphoric acid solution. The wet prepared CaP powder was used as a matrix for the bone cement recipe. With the addition of aqueous poly-phosphoric acid, the cement hardening reaction was started and the CaP bone cement blocks were fabricated for the mechanical strength measurement. For the tested blocks, the mechanical strength was measured using a universal testing machine, and the microstructure phase analysis was done by field emission scanning electron microscopy and X-ray diffraction. The cement hardening reaction occurred through the decomposition and recrystallization of MCPM and $CaSO_4{\cdot}1/2H_2O$ added on the surface of the wet prepared CaP, and this resulted in grain growth in the bone cement block.