• 한국세라믹학회지
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• 제29권5호
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• pp.396-402
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• 1992

Carbon solid was prepared from dormant mesophase pitch (DMPP) without using a binder and its properties were characterized. DMPP powder was stabilized with air or nitric acid in pretreatment stage so that it might not soften in later heat ttreatment stage. Optimum sintering properties were obtained from carbon powder with 2.36∼2.38 of C/H atomic ratio and 1.27∼1.40 of C/O atomic ration in air stabilization. In nitric acid stabilization, optimum sintering properties were obtained when 20∼40 vol.% of nitric acid solution was used. Compressive strength increased up to 1200$^{\circ}C$ of heat treatment temperature, and the highest compressive strength and bulk density of carbon solid from DMPP were 3000 kgf/㎤, respectively. The optical properties of carbon solid obtained was fine mosaic structure. Carbon solid after graphitization showed the properties of hard carbon due to stabilization and its shore hardness was 120.

• 한국분말재료학회지
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• 제3권2호
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• pp.112-119
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• 1996

Using rice husks pulverized by rotating knife cutter, the raw rice husk powder was solution treated by nitric and hydrochloric acids in order to separate phytolith from organic constituents. Because of the strong resistance of organic components of rice husk to acids, the raw powder had to be boiled in concentrated acids up to 300 min. By boiling in nitric acid for 60~120 min, all organic components were resolved while amorphous silica Powder of about 20 nm in size and of higher than 99.8% in purity was left behind. Inferior to the nitric acid, hydrochloric acid was not able to resolve organic component completely leaving unresolved matter of about 40% by weight even after 300 min of boiling. From the acid treatments and impurity analyses, it is considered that most of metallic elements in rice husks are combined to organic components that are easily soluble to acids.

• 한국표면공학회지
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• 제45권5호
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• pp.198-205
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• 2012

The corrosion properties of anodized films on aluminium 6070 alloy in a sulfuric acid have been studied. Comparison to evaluate the anodized A6070 and pure 6070 specimen, corrosion tests in $HNO_3$ vapor environment of the 20 wt.% were performed up to 72 hours. Characteristics of film formation and surface morphology were examined by optical microscopy, FE-SEM, and EDS. The oxide film anodized in the sulfuric acid solution contained 5 to 10 wt.% of sulfur. In the initial stages of corrosion, anodized specimens exhibited corrosion resistance than the pure specimen. However, the corrosion conditions in 24 hours, corrosion was far more anodized specimen than pure specimen. Therefore, anodized films contained sulfur, nitric acid vapor in the environment is thought to stimulate corrosion.

• 대한치과보철학회지
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• 제45권5호
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• pp.589-600
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• 2007

Statement of Problem: Titanium has many advantages of high biocompatibility, physical porperties, low-weight, low price and radiolucency, but it is incompatible with conventional dental porcelain due to titanium's oxidative nature. Many previous studies have shown that they used the method of sandblast surface treatment prior to porcelain application, the researchs are processing about the method of acid etching or surface coating. Purpose: The purpose of this research is to study the effect on bond strength between titanium and porcelain when using macro-surface treatment and micro-surface treatment and macro and micro surface treatment. Material and method: In this study, we evaluated the bond strength by using 3-point bending test based on ISO 9693 after classified 7 groups-group P : polished with #1200 grit SiC paper, group SS : sandblasted with $50{\mu}m$ aluminum oxides, group LS : sandblasted with $250{\mu}m$ alumium oxides, group HC : treated with 10% hydrochloric acid, group NF : treated with 17% solution of fluoric acid and nitric acid, group SHC : treated with 10% hydrochloric aicd after sandblsting with $50{\mu}m$ alumium oxides, group SNF treated with 17% solution of fluoric acid and nitric acid. Results : Within the confines of our research, the following results can be deduced. 1. Group SS which was sandblasted with $50{\mu}m$ aluminum oxides showed the highest bond strength of 61.74 MPa and significant differences(P<0.05). The bond strengths with porcelain in groups treated acid etching after sandblasting decreased more preferable than the group treated with sandblasting only. It gives significant differences(P<0.05). 2. After surface treatments, the group treated with sandblasting showed irregular aspect formed many undercuts, in the SEM photographs. The group treated with hydrochloric acid had the sharp serrated surfaces, the group treated with the solution of fluoric acid and nitric acid had the smooth surfaces, the group with sandblasting and hydrochloric acid had irrigular and porous structure, the group with sandblasting and the solution of fluoric acid and nitric acid had crater-like surfaces. But all of the groups treated with acid etching was not found and undercut. Conclusion: In above results, average surface roughness increase, bond strength also increase, but surface topographs influences more greatly on bond strengths.

• Journal of Acupuncture Research
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• 제23권4호
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• pp.115-121
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• 2006

Objectives : This study was designed to investigate the scavenging effect on Nitric Oxide of BUM. Methods : The scavenging effect on NO concentrations 2, 6, 12 and 24 hours after treatment with Vit C. and BUM at 1, 10, $100{\mu}g/ml$ were estimated. And those was compared with control group. Results : 1. The concentration of NO 2 hours after treatment with BUM at 1, 10, 1$100{\mu}g/ml$ were decreased compared with control group. 2. The conecntration of NO 6 hours after treatment with BUM at 1, 10, 1$100{\mu}g/ml$ were decreased compared with control group. 3. The concentration of NO 12 hours after treatment with BUM at 1, 10, $100{\mu}g/ml$ were decreased compared with control group. 4. The concentration of NO 24 hours after treatment with BUM at 1, $100{\mu}g/ml$ were decreased compared with control group. Conclusion : The scavenging effect of BUM on NO was dose-dependent.

• 한국환경과학회지
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• 제21권1호
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• pp.113-123
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• 2012

A unit emission reduction of nitrous oxide ($N_2O$) from anthropogenic sources is equivalent to a 310-unit $CO_2$ emission reduction because the $N_2O$ has the global warming potential (GWP) of 310. This greatly promoted very active development and commercialization of catalysts to control $N_2O$ emissions from large-scale stationary sources, representatively nitric acid production plants, and numerous catalytic systems have been proposed for the $N_2O$ reduction to date and here designated to Options A to C with respect to in-duct-application scenarios. Whether or not these Options are suitable for $N_2O$ emissions control in nitric acid industries is primarily determined by positions of them being operated in nitric acid plants, which is mainly due to the difference in gas temperatures, compositions and pressures. The Option A being installed in the $NH_3$ oxidation reactor requires catalysts that have very strong thermal stability and high selectivity, while the Option B technologies are operated between the $NO_2$ absorption column and the gas expander and catalysts with medium thermal stability, good water tolerance and strong hydrothermal stability are applicable for this option. Catalysts for the Option C, that is positioned after the gas expander thereby having the lowest gas temperatures and pressure, should possess high de$N_2O$ performance and excellent water tolerance under such conditions. Consequently, each de$N_2O$ technology has different opportunities in nitric acid production plants and the best solution needs to be chosen considering the process requirements.

• 공업화학
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• 제8권1호
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• pp.132-139
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• 1997

본 연구는 Nd, Pd, Ru, Zr, Mo 및 Fe 이 함유된 6성분계의 모의 방사성폐액을 대상으로 개미산 탈질에 의한 질산과 개미산의 분해속도 및 탈질 반응기구(mechanism)의 규명에 주안점을 두었다. 모든 실험은 반응온도 $90^{\circ}C$, 회분식계로 고정하여 수행하였으며, 초기 질산농도 1, 2, 3, 5M 및 $[HCOOH]/[HNO_3]$=1.25, 1,5. 1.75, 2.0에서 각각 탈질 시간을 330분까지 변화시켰다. 질산 및 개미산의 분해속도식은 각각 다음과 같으며, $\frac{d[HNO_3]}{dt}=-4.842{\times}10^{-2}[HNO_3][HCOOH],\;\frac{d[HCOOH]}{dt}=-8.911{\times}10^{-2}[HNO_3][HCOOH]$본 연구에서 제안한 반응기구는 초기 질산농도 2~5M 및 $[HCOOH]/[HNO_3]$=1.25~2.0의 범위에서 비교적 실험치와 이론치가 잘 일치하여, 이의 적용 타당성을 확인할 수 있었으나, 초기 질산농도 1M에서는 본 모델식에서 벗어나 다른 반응기구에 의해 분해됨을 추측할 수 있었다.

• 공업화학
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• 제27권3호
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• pp.319-324
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• 2016

본 연구에서는 피치계 탄소섬유의 표면처리를 위하여 탄소섬유를 산에 담지하여 전자선을 조사하고 각 처리 조건에 따른 탄소섬유의 표면 변화를 평가하였다. 산 담지용액은 질산과 과산화수소를 사용하였으며 전자선 조사량은 200, 400 kGy로 하였다. 과산화수소 담지보다 질산 담지가 탄소섬유 표면에 더 많은 산소관능기를 도입시켰으며, 질소관능기도 탄소섬유 표면에 도입되었다. 또한 전자선 조사량이 증가하면 탄소섬유에 도입되는 산소관능기가 증가하는 것을 알 수 있었다. 이는 과산화수소보다 질산이 전자선 조사에 의한 산화성 물질의 형성이 용이하고, 전자선 조사 에너지가 클수록 산화성 물질이 더 많이 형성되기 때문이다. 또한 질산 용액에서 전자선 조사에 의하여 생성되는 $NO_2$ 라디칼이 C-OH 관능기를 C=O 관능기로 산화시키는 반응이 주로 일어나므로 질산 담지 시 C=O 관능기의 생성이 유리한 것으로 나타났다.

• 자원리싸이클링
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• 제24권5호
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• pp.33-39
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• 2015

음이온 교환막을 이용한 확산투석에 의해 폐솔더 박리액으로부터 질산을 효율적으로 회수하기 위한 기초 연구를 실시하였다. 우선 모의용액 실험의 경우 유속, 유속비, 질산농도, 금속이온 종류 및 농도 등이 질산 회수율에 미치는 영향을 조사하였다. 유속이 증가함에 따라 질산 회수율은 감소하였고 급액에 대한 순수의 유속비(W/F)가 증가할수록 질산 회수율은 증가하여 유속비가 1.5이상에서 약 99%의 질산 회수율을 보였다. 급액중 질산용액의 농도가 증가함에 따라 3.0 M 까지는 산회수율이 증가 하였으나 3.0 M 이후로는 회수율은 점차 낮아 졌다. 확산투석막을 통과하는 금속이온의 투과율은 Pb, Na, Cu순 이었고, Fe과 Sn은 투과되지 않았다. 실제 폐솔더액을 사용하여 유속 $0.9L/hr-m^2$, W/F = 1.3 으로 확산 투석을 실시한 결과 약 94%의 질산 회수율을 얻을 수 있었다.

• Nuclear Engineering and Technology
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• 제53권10호
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• pp.3352-3358
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• 2021

Aiming at selective adsorption and separation of Y(III) from the Y(III)-Sr(II) group in acid solution, a silica-based TODGA impregnated adsorbent [(TODGA+1-dodecanol)/SiO₂-P-F600] has been prepared. Batch adsorption experiments were conducted under the effect of contact time, acid concentration, solution temperature, and adsorption capacity etc. Chromatography recovery of more than 90% Y(III) was successfully achieved under elution with 0.01 M DTPA solution in nitric acid adsorption system, and 0.1 M HCl solution in hydrochloride adsorption system, respectively.