• 한국세라믹학회지
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• 제27권6호
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• pp.747-754
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• 1990

Aluminum hydrate gels were prepared from the mixtures of bauxite and ammonium sulfate by wet acid process. Optimum conditions for obtaining the maximum yield( 99%) of aluminum hydrates from the same amount of bauxite were confirmed as follows ; 1. Mixing ratio ; addition of 25mole% of ammonium sulfate to 1mole of bauxite. 2. Calcination ; heated at 350℃ for 1hr. 3. Extraction ; leached at 95℃ in 1% H2SO4 for 90min. 4. pH of precipitating solution; slight below 7.0. Amorphous aluminum hydrates were precipitated at the pH lower than 8.5, but the precipitates crystallized to bayerite at the pH was 10. Mean diameter of α-Al2O3 powders which were obtained by calcining the aluminum hydrates was below 0.2㎛, and EDS analysis revealed than SiO2 was it's primary impurity.

• 한국환경보건학회지
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• 제35권1호
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• pp.53-57
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• 2009

In order to treat the complex wastewater containing organic compound and solids, pre-treatment system associated with molecular separation process were investigated. The reductions of COD and turbidity were obtained after coagulation processes using Alum (Aluminium sulfate, $Al_2(SO_4)_2{\cdot}18H_{2}O$) and PACl (poly aluminium chloride as 17% $Al_{2}O_{3}$). The results of study were as follows: using variable dosage of Alum, COD removal was highest at 4,000 mg/l, and the reduction of COD and turbidity was 42% and 92%, respectively. The optimum coagulation would be effective at pH 7.3 than pH 9.0 by the addition of alum at a concentration of 6,000 mg/l and PACl was add at 4.25% in raw complex wastewater with 2,000 mg/l alum at pH 7.3, the reduction of COD was reduced by 32%. But coagulation aid experiments indicated that PACl would be more effective in sludge separation ability than COD removal efficiency.

• Journal of the Korean Wood Science and Technology
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• 제38권3호
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• pp.230-241
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• 2010

본 연구는 산염이 첨가된 아세톤 용액으로 목질바이오매스를 가수분해하여 효과적으로 화학적 조성분을 분리할 수 있는 최적조건을 확립하는데 있다. 아세톤에 의한 목질바이오매스의 가수분해에서 $Al_2(SO_4)_3$은 우수한 촉매로 작용하였으며, 최적 농도는 0.01 M (6.3 wt%)였다. 본 실험에서는 아세톤과 물의 비율을 9 : 1로 맞추고 $Al_2(SO_4)_3$의 최적 농도조건에서 신갈나무재와 소나무재를 $200^{\circ}C$에서 45분 동안 가수분해하여 각각 92.7%와 92.4% 분해율을 나타냈다. 아세톤과 물의 비율이 8 : 2에서는 반응시간을 60분으로 연장하였을 경우 신갈나무재의 가수분해율은 92.7%였으나, 소나무재는 반응온도를 $210^{\circ}C$로 상승시켜야 신갈나무재에 버금가는 가수분해율을 얻을 수 있었다. 가수분해 온도와 시간을 증가시키면 가수분해산물로부터 분리, 회수되는 리그닌은 증가하였으나, 탄수화물 함량은 급격히 감소하는 경향을 보였다. 리그닌과 당의 회수량을 고려해 보면, 목질바이오매스의 최적 가수분해 조건은 아세톤과 물의 비율 8 : 2, 아세톤 용액에 대한 $Al_2(SO_4)_3$ 농도는 6.3 wt%, 가수분해 온도와 시간은 각각 $190^{\circ}C$와 60분으로 나타났고, 이 조건에서 당의 회수율은 목질바이오매스 전건중량 기준으로 신갈 나무재와 소나무재에서 각각 47.6%와 51.4%로 나타났고, 리그닌 회수율은 각각 18.2%와 13.7%로 측정되었다.

• 한국세라믹학회지
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• 제25권5호
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• pp.449-454
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• 1988

The effects of salts which was used as a catalysis in formation of $\alpha$-calciumusulfate hemihydrate from dicalcium sulfate hydrate were investigated on the hydration of $\alpha$-calciumsulfate hemihydrate. The hydration of $\alpha$-calciumsulfate hemihydrate was studied by the measurements of crystalline water, heat evolution. Also the hydrates were analyzed by XRD, DSC and SEM. The promotive effect each salts on the hydration was as follows: NaCl>NH4Cl>NaNO3>NH4NO3, and the hydration rate was accelerated with concentration of salts. The effect of Al2(SO4)3 and potassium sodium tartrate on the hydration was slmilar to water, whereas sodium succinate and gelatin retarded the hydration in comparision with water. These salts affected the hydration time but total heat evoution was similar.

• 상하수도학회지
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• 제24권5호
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• pp.537-548
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• 2010

Recently the Government has announced updated water quality standards for wastewater treatment effluent (become effective in 2012). That includes highly enforced regulations for T-P, BOD and COD, and a large budget, in particular for phosphorus removal, was set by the Ministry of environment. Chemical coagulation destabilizes colloidal particles so that particles grow to larger flocs, and solid particles are removed by solid-liquid separation. The efficiency of chemical coagulation depends on a various factors, including coagulant types and costs, construction and operation costs for the treatment facilities and so on. The proper selection should be based on the treatment efficiency of coagulants and underlying costs. The current research was to evaluate the treatment efficiencies of coagulants on a variety of wastewater influents and to develop saturation curves for several water quality parameters. Typical $Al_2(SO_4)_3$ and $FeCl_3$ were tested under a range of coagulant concentrations. The pollutant removal efficiencies of chemical treatment both for the $Al_2(SO_4)_3$ and $FeCl_3$ were especially high for T-P, followed by SS, BOD and COD. Correlation test also proved the highest relationship between SS and T-P.

• Geomechanics and Engineering
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• 제33권2호
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• pp.121-131
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• 2023

Clay sedimentation has been widely analyzed for its application in a variety of geotechnical constructions such as mine tailing, artificial islands, dredging, and reclamation. Chemical flocculants such as aluminum sulfate (Al₂(SO₄)₃), ferric chloride (FeCl₃), and ferric sulfate (Fe(SO₄)₃), have been adopted to accelerate the settling behaviors of clays. As an alternative clay flocculant with natural origin, this study investigated the settling of xanthan gum-treated kaolinite suspension in deionized water. The sedimentation of kaolinite in solutions of xanthan gum biopolymer (0%, 0.1%, 0.5%, 1.0%, and 2.0% in a clay mass) was measured until the sediment height was stabilized. Kaolinite was aggregated by xanthan gum via a direct electrical interaction between the negatively charged xanthan gum molecules and positively charged edge surface and via hydrogen bonding with kaolinite particles. The results revealed that the xanthan gum initially bound kaolinite aggregates, thereby forming larger floc sizes. Owing to their greater floc size, the aggregated kaolinite flocs induced by xanthan gum settled faster than the untreated kaolinite. Additionally, X-ray computed tomography images collected at various depths from the bottom demonstrated that the xanthan gum-induced aggregation resulted in denser sediment deposition. The findings of this study could inspire further efforts to accelerate the settling of kaolinite clays by adding xanthan gum.

• 대한치과교정학회지
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• 제27권5호
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• pp.839-852
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• 1997

Crystal growth 용액인 황화이온을 함유한 폴리아크릴산 용액에 의한 법랑질 표면처리는 법랑질 표면에 crystal growth를 유도함으로써 통상적인 산부식법을 대체하여 교정용 브라켓을 접착하기 위한 법랑질 전처치의 방법으로 사용될 수 있음이 제안된 바 있다. 이 연구는 crystal growth후 교정용 브라켓 접착제로 브라켓을 접착하는 방법의 임상적용 가능성을 구명하기 위하여 시행되었다. 발거된 사람소구치의 법랑질 표면을 $25\%$ 폴리아크릴산과 0.3M 황산을 함유한 기본 crystal growth 용액, 각각 0.3M lithium sulfate, 0.3M magnesium sulfate, 0.3M potassium sulfate를 첨가한 crystal growth 용액, $37\%$ 인산용액, 퍼미스로 각각 처리한 후, 교정용 광중합형 글래스아이오노머 시멘트와 교정용 레진접착제로 금속브라켓을 접착하였다. $37^{\circ}C$의 증류수에 24시간 침지시킨 후, 브라켓 전단결합강도를 측정하고 접착 파절양태를 관찰하였으며 표면처리된 법랑질 표면과 브라켓 제거후의 법랑질 표면을 주사전자현미경으로 관찰하여 다음과 같은 결과를 얻었다. Crystal growth후 광중합형 글래스아이오노머 시멘트로 브라켓 접착시 0.3M magnesium sulfate를 함유한 군의 브라켓 전단결합강도가 가장 높았다(p<0.01). Crystal growth후 광중합형 글래스아이오노머 시멘트로 접착한 군의 브라켓 전단결합강도는 crystal growth 후 레진접착제로 접착한 군보다 높았다(p<0.001). Magnesium sulfate, 또는 potassium sulfate를 함유한 crystal growth 용액으로 법랑질 표면을 처리한 후 글래스아이오노머시멘트로 접착한 군의 브라켓 전단결합강도는 산부식 후 레진 접착제로 접착한 군과 유의한 차이를 보이지 않았다. 브라켓 제거시 잔류접착제의 양은 글래스아이오노머 시멘트로 접착한 것이 가장 적었다. 이상의 결과는 magnesium sulfate나 potassium sulfate를 함유한 crystal growth 용액으로 법랑질 표면처리 후 교정용 광중합형 글래스 아이오노머 시멘트로 브라켓을 접착하는 방법이 통상적으로 사용되는 산부식 후 교정용 레진접착제에 의한 브라켓 접착법을 대체할 수 있음을 시사한다.

• 한국가금학회지
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• 제31권4호
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• pp.213-219
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• 2004

본 시험은 깔짚에 3가지 화학제재($FeSO_4,\;AlCl_3\;+\;CaCO_3$ 및 $KMnO_4$)를 처리하였을 때 육계 생산성에 대한 영향과 계사내 암모니아, 이산화탄소 발생량에 대한 6주 동안의 변화와 저감 효과를 규명하기 위해서 수행하였다. 사양시험은 육계 초생추 총 96수(6처리$\times$4반복$\times$4수)를 공시하여 42일 동안 실시하였다. 화학제재는 깔짚 kg당 $FeSO_4$ $\cdot$ $7H_2O$ 200 g, $AlCl_3$ $\cdot$ $6H_2O$ 200 g + $CaCO_3$ 50 g 및 $KMnO_4$ 비율로 top dressing하였으며 대조구는 화학제재를 첨가하지 않았다. 육계 생산성은 화학제재 처리구와 대조구 간에 유의차가 없었다. 그러나 대조구와 비교한 $FeSO_4$와 $AlCl_3$+$CaCO_3$ 처리구의 암모니아 발생량은 6주째에서 각각 $91\%$와 $53\%$가 감소되었고(P<0.05), $KMnO_4$ 처리구의 암모니아 발생량은 대조구보다 6주째에서 $69\%$ 감소되어 통계적 유의차를 보였다(P<0.05). 깔짚에서 생성된 이산화탄소 발생량은 $AlCl_3+CaCO_3$와 $KMnO_4$ 처리구가 대조구와 비교할 때 6주째에서 각각 $59\%$와 $65\%$ 감소되었다(P<0.01). 결론적으로 깔짚에 화학제재를 처리했을 경우 암모니아와 이산화탄소 가스 발생량은 현저하게 감소되며, 육계생산성에는 영향을 주지 않는 것으로 나타났다.

• 한국균학회지
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• 제32권2호
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• pp.125-129
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• 2004

섬유소분해효소(CMCase)를 산업적으로 이용하기 위한 기초자료를 제공하고자 섬유소분해능이 우수한 L. japonicus로부터 CMCase를 분리 정제하였다. L. japonicus의 배양액으로부터 4단계를 거쳐 분자량이 42 kDa인 CMCase를 분리 정제하였다. 이 효소는 pH 6.0에서 최적의 활성을 보여주는 acidic CMCase로서 $30^{\circ}C$에서 최대 활성을 나타냈다. EDTA에 의해 활성이 저해되는 것으로 보아 metalloenzyme으로 추정되며, SDS에 의해 저해되는 것으로 보아 S-S기를 갖고 있는 효소로 판단된다. $Al_{2}(SO_{4})_{3}$와 $BaCl_{2}$에서는 효소 활성이 높았으나 그 이외의 금속염에서는 효소 활성이 낮았다.

• Asian Journal of Atmospheric Environment
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• 제8권3호
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• pp.126-139
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• 2014

In order to estimate the influence of sources on $PM_{2.5}$ in the industrial area of Japan, we carried out a source analysis using chemical component data of $PM_{2.5}$. $PM_{2.5}$ samples were collected intermittently at an industrial area in Japan from July 2010 to November 2012. Water soluble ions ($Cl^-$, $NO_3{^-}$, $SO{_4}^{2-}$, $Na^+$,$NH_4{^+}$, $K^+$, $Mg^{2+}$, $Ca^{2+}$), elements (Al, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Cd, Sb, Pb), and carbonaceous species (OC, EC) of the $PM_{2.5}$ (a total of 198 samples) were analyzed. Positive Matrix Factorization (PMF) model was applied to the data of those chemical components to identify the source of $PM_{2.5}$. At this observation site, nine factors were extracted. The major contributors of $PM_{2.5}$ were secondary sulfate 1, in which loading factors of $SO{_4}^{2-}$ and $NH_4{^+}$ were large (percentage source contribution: 20.9%), traffic, in which loading factors of OC (organic carbon) and EC (elemental carbon) were large (20.8%), secondary sulfate 2, in which loading factors of K and $SO{_4}^{2-}$ were large (8.0%), steel mills (7.8%), secondary chloride and nitrate (7.0%), soil (5.0%), heavy oil combustion (3.8%), sea salt (3.8%), and coal combustion (2.3%). The conditional probability function (CPF) and the potential source contribution function (PSCF) were carried out to examine the influence of a regional source and a broad-based source, respectively. CPF results supported local source influences such as steel mills, sea salt, traffic, coal combustion, and heavy oil combustion. PSCF results suggested that ships in the East China Sea, an industrial area of the east coastal region of China, and an active volcano in the Kyushu region of Japan were potential regional sources of secondary sulfate 1. Secondary sulfate 2 was affected by the burning of biomass fields and by coal combustion in Chinese urban areas such as Beijing, Hebei, and western Inner Mongolia. Source characterization using continuous data from one site showed a potential source representing fossil fuel combustion is affected both by regional and broad-based sources.