• 유기물자원화
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• 제28권3호
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• pp.5-14
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• 2020

본 연구는 돈분과 사과착즙박 혼합 혐기소화액의 호기성 처리 과정에서 황산(H₂SO₄)을 이용한 혐기소화액의 pH를 7.0과 6.5 조절 처리가 암모니아 휘발과 화학적 특성 변화에 미치는 영향을 구명하기 위하여 수행하였다. 혐기소화액은 0.3 ㎥ air/㎥·min 조건에서 60일 동안 폭기처리를 실시하였다. 무처리구의 혐기소화액은 호기성 액비화 과정 중 pH가 상승하고, EC와 T-N 함량이 감소하는 경향을 나타내었다. 황산 무처리 혐기소화액은 pH가 높아 액비화 과정에 암모니아 농도가 172.6 mg/L로 높았으나 황산 처리 pH 조절 혐기소화액은 암모니아(NH₃) 발생이 유의적으로 감소되었다. 황산 무처리 혐기소화액은 액비화 과정 중 암모늄태 질소 함량이 47.2% 감소되었다. 혐기소화액의 pH 조절 처리구는 암모늄태 질소의 함량이 황산 처리 pH 조절 처리구에 비하여 높았다. 또한, 황산(H₂SO₄)처리는 혐기소화액에서 질소, 인산 함량의 증가에 영향을 주어 비료 성분이 높아지는 효과를 나타내었다. 따라서 혐기소화액의 황산 첨가에 의한 pH 조절은 호기성 액비화 공정에서 암모니아 휘산 저감과 질소 함량을 높이기 위한 유용한 방법으로 활용될 수 있을 것이다.

• 한국입자에어로졸학회지
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• 제17권4호
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• pp.91-106
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• 2021

Daily PM_2.5 was collected during summer period in 2020 in Gwangju to investigate its chemical and light absorption properties. In addition, real-time light absorption coefficients were observed using a dual-spot 7-wavelength aethalometer. During the study period, SO₄^2- was the most important contributor to PM_2.5, accounting for on average 33% (10-64%) of PM_2.5. The chemical form of SO₄^2- was appeared to be combination of 70% (NH₄)₂SO₄ and 30% NH₄HSO₄. Concentration-weighted trajectory (CWT) analysis indicated that SO₄^2- particles were dominated by local pollution, rather than regional transport from China. A combination of aethalometer-based and water-extracted brown carbon (BrC) absorption indicated that light absorption of BrC due to aerosol particles was 1.6 times higher than that due to water-soluble BrC, but the opposite result was found in absorption Ångström exponent (AAE) values. Lower AAE value by aerosol BrC particles was due to the light absorption of aerosol BrC by both water-soluble and insoluble organic aerosols. The BrC light absorption was also influenced by both primary sources (e.g., traffic and biomass burning emissions) and secondary organic aerosol formation. Finally the ATR-FTIR analysis confirmed the presence of NH₄⁺, C-H groups, SO₄^2-, and HSO₄^2-. The presence of HSO₄^2- supports the result of the estimated composition ratio of inorganic sulfate ((NH₄)₂SO₄) and bisulfate (NH₄HSO₄).

• 상하수도학회지
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• 제34권2호
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• pp.115-125
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• 2020

This study was aimed to examine inorganic fouling and fouling reduction method in direct contact membrane distillation(DCMD) process. Synthetic seawater of NaCl solution with CaCO₃ and CaSO₄ was used for this purpose. It was found in this study that both CaCO₃ and CaSO₄ precipitates formed at the membrane surface. More fouling was observed with CaSO₄(anhydrite) and CaSO₄·0.5H₂O(bassanite) than CaSO₄·2H₂O(gypsum). CaCO₃ and gypsum were detected at the membrane surface when concentrates of SWRO(seawater reverse osmosis) were treated by the DCMD process, while gypsum was found with MED(multi effect distillation) concentrates. Air backwash(inside to out) was found more effective in fouling reduction than air scouring.

• Kyungpook Mathematical Journal
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• 제60권3호
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• pp.551-570
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• 2020

We introduce the notion of Lie invariant normal Jacobi operators for real hypersurfaces in the complex hyperbolic quadric Q^m∗ = SO^o_m,2/SO_mSO₂. The invariant normal Jacobi operator implies that the unit normal vector field N becomes 𝕬-principal or 𝕬-isotropic. Then in each case, we give a complete classification of real hypersurfaces in Q^m∗ = SO^o_m,2/SO_mSO₂ with Lie invariant normal Jacobi operators.

• 대한수학회보
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• 제60권4호
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• pp.849-861
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• 2023

In this paper, we introduce the notion of semi-symmetric structure Jacobi operator for Hopf real hypersufaces in the complex quadric Q^m = SO_m+2/SO_mSO₂. Next we prove that there does not exist any Hopf real hypersurface in the complex quadric Q^m = SO_m+2/SO_mSO₂ with semi-symmetric structure Jacobi operator. As a corollary, we also get a non-existence property of Hopf real hypersurfaces in the complex quadric Q^m with either symmetric (parallel), or recurrent structure Jacobi operator.

• Nuclear Engineering and Technology
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• 제52권11호
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• pp.2543-2551
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• 2020

Calculations of chemical equilibrium for multicomponent aqueous systems of the HyBRID dissolution of magnetite were performed by using the HSC Chemistry. They were done by using a Pitzer-based aqueous solution model with the recipe of raw materials in experiments conducted at KAERI. The change in the amounts of species and ions and the pH values of the solution at equilibrium was observed as functions of temperature and raw amount of CuSO₄. Precipitation of Cu₂O occurred at a large amount of CuSO₄ added to the solution, while no precipitation of Cu(OH)₂ was found at any amounts of CuSO₄. The E-pH diagrams for Cu were constructed at various Cu concentrations to provide the effect of the Cu concentration on the pH values at boundaries where the coexistence of Cu⁺ ion and Cu₂O solid occurred. To prevent Cu⁺ ions from being precipitated to Cu₂O, the raw amount of CuSO₄ should be adjusted so that the pH value of the solution from the equilibrium calculation is less than that from the E-pH diagram. We provided guidelines for the raw amount of CuSO₄ and the pH value of the solution, which prevent the formation of Cu₂O precipitates in the HyBRID dissolution experiments for magnetite.

• 한국표면공학회지
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• 제53권3호
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• pp.87-94
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• 2020

Herein, sulfonated carbon nanotubes (CNT) have been prepared in dilute sulfuric acid (H₂SO₄) via a novel sulfonation approach based on gas-liquid interfacial plasma (GLIP) at room temperature. The sulfonic acid groups and total acid groups densities of CNT after GLIP treatment in 2 M H₂SO₄ for 45 min can reach to 0.53 mmol/g and 3.64 mmol/g, which is higher than that of sulfonated CNT prepared under 0.5 M / 1 M H₂SO₄. The plasma sulfonated CNT has been applied as catalysts for the conversion of microcrystalline cellulose to glucose. The effect of hydrolysis temperature and hydrolysis time on the conversion rate and product distribution have been discussed. It demonstrates that the total conversion rate of cellulose increasing with hydrolysis temperature and hydrolysis time. Furthermore, the GLIP sulfonated CNT prepared in 2 M H₂SO₄ for 45 min has shown high catalytic stability of 85.73 % after three cycle use.

• 한국자기공명학회논문지
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• 제21권2호
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• pp.67-71
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• 2017

At high temperature, the roles of $NH_4$ and $H_2O$ in $(NH_4)_2Fe(SO_4)_2{\cdot}6H_2O$ and $(NH_4)_2Zn(SO_4)_2{\cdot}6H_2O$ single crystals were investigated using a pulse NMR spectrometer. Temperature was shown to have a significant influence, causing changes in the deformation of $NH_4$ and $H_2O$. From the $^1H$ NMR and $^{14}N$ NMR spectrum, the forms of environment surrounding $^{14}N$ in $NH_4$ groups is more important than the loss of $H_2O$ groups. NMR studies indicate that $NH_4{^+}$ ions in Tutton salts play an important role in the changes of the crystal structure at high temperatures.

• 한국세라믹학회지
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• 제44권6호
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• pp.325-330
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• 2007

High porous AlO(OH) gel is used in precursor of ceramic material, coating material and porous catalyst. For use of these, not only physiochemical control for particle morphology, pore characteristic and peptization but also studies of synthetic method for preparation of high porous AlO(OH) gel were required. In this study, high porous AlO(OH) gel was prepared through the aging and filtration process of aluminum hydroxides gel precipitated by the hydrolysis reaction of $Na_2CO_3$ solution and $Al_2(SO_4)_3$ and $Na_2SO_4$ mixed solution. In this process, optimum synthetic condition of AlO(OH) gel having excellent pore volume as studying the effect of hydrolysis pH on gel precipitates has been studied. Hydrolysis pH brought about numerous changes on crystal morphology, surface area, pore volume and pore size. Physiochemical properties of gel were investigated as using XRD, TEM, TG/DTA, FT-IR and $N_2$ BET method.

• Nuclear Engineering and Technology
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• 제54권6호
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• pp.2329-2333
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• 2022

Base metal corrosion forms a significant issue during the chemical decontamination of the primary coolant loop in nuclear power plants as it is directly related to the economic and safety viability of decommissioning. In this technical note, potentiodynamic evaluations of several base metals (304 stainless steel, SA106 Grade B carbon steel, and alloy 600) were performed to determine their corrosion behavior during the hydrazine (N₂H₄)-based reductive ion decontamination (HyBRID) process. The results suggested that N₂H₄ protected the surface of the base metals in the HyBRID solution, which is primarily composed of H₂SO₄. The corrosion resistance of the carbon steel was further improved through the addition of CuSO₄ to the solution. The corrosion rate of carbon steel in the H₂SO₄-N₂H₄-CuSO₄ solution was lower than that exhibited in an oxalic acid solution, a commonly used reaction medium during commercial decontamination processes. These results indicate the superiority of the HyBRID process with respect to the base metal stability.