• Proceedings of the Korean Institute of Building Construction Conference
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• 2020.06a
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• pp.195-196
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• 2020

This study evaluated the mechanical properties and alkali silica reaction of mortar according to the mixing ratio of waste glass. As a result, as the mixing ratio of the waste glass increased, the compressive and flexible strength of the mortar decreased due to the slip of aggregate, and the alkali-silica reaction(ASR) increased. So, it is considered that research is needed to prevent slip and ASR of the waste glass aggregate in order to use the waste glass as a fine aggregate for concrete.

• Journal of the Korean Ceramic Society
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• v.39 no.5
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• pp.452-459
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• 2002

This paper addresses the hydrothermal reactivity of blast furnace slag and fly ash with lime, respectively. The test conditions were CaO-to-$SiO_2$ ratio (C/S), autoclaving temperature ($140{\circ}C$ and $180{\circ}C$) and time (20 to 60h). The study was carried out in terms of the hydrothermal reactivity between $SiO_2$ contained in each hydraulic material and (pure) lime and the compressive strength of autoclaved specimens. Porosity measurement and the XRD analysis were also made in order to ascertain the hydraulicity of the siliceous materials. Compressive strength of the specimens was interpreted in terms of porosity and the reactivity of CaO and $SiO_2$. And the XRD analysis showed the C/S change of the hydrates in the course of autoclaving process. $SiO_2$ in the blast furnace slag was more reactive with CaO than that in the fly ash and consequently the blast furnace slag specimens resulted in much higher compressive strength. A maximum compressive strength of $807kg/cm^2$ was obtained for the blast furnace slag at the autoclaving condition of $180{\circ}C$ and 40 h, while only $397kg/cm^2$ was maximally to achieve with fly ash.

• Journal of the Korean Society of Tobacco Science
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• v.3 no.2
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• pp.123-128
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• 1981

For evaluating the cigarette smoke quality of nonblended and commercial cigarettes, four modified smoke quality indexes were deduced from considering the reactivity of the thiol group in cystine (SH value) with the cigarette smoke constituents, and from the maximum limited contents of tar. nicotine, and carbon monoxide for the less harmful cigarettes. These results were discussed with respect to correlation coefficients between the indexes and tar/nicotine ratio which had been known reliable for smoke quality evaluation. Among the three indexes, the SH/[(N/O.6) +($\frac{C+T}{8}$)] index was found to be the most reliable and applicable.

• Bulletin of the Korean Chemical Society
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• v.20 no.1
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• pp.49-52
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• 1999

Various metal oxides such as Fe2O3, FeO, TiO2, MnO2, MoO3, WO3 and ZnO have been used as a catalyst for Gif-KRICT type cyclohexane oxidation. In this reaction, the conversion of cyclohexane to cyclohexanone and cyclohexanol and the selectivity ratio of cyclohexanone to cyclohexanol were greatly affected by the acidity of metal oxides. When metal oxide has more acidic property, the reactivity on oxidation is increased and the formation of cyclohexanone is more favored. From this result, we proposed a new mechanism for the biomimetic Gif-KRICT oxidation system.

• Bulletin of the Korean Chemical Society
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• v.15 no.6
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• pp.424-427
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• 1994

Effects of iron compounds in known biomimetic oxidation systems (Gif IV and GoAgg II) have been studied on activity and ketone/alcohol selectivity of cyclohexane oxidation. Both ketone/alcohol ratio and cyclohexane conversion were affected by counter-ion Z of iron compounds Z-Fe. When Z has a more electron withdrawing property, the reactivity is increased and the formation of ketone is favored. From these experimental results, a new mechanism is proposed for the biomimetic oxidation system.

• Journal of Korean Society for Atmospheric Environment
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• v.24 no.4
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• pp.393-403
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• 2008

In an effort to estimate secondary $PM_{10}$ concentrations and their diurnal variations at different photochemical activities, $PM_{10}$, CO, and $O_3$ concentrations obtained from the ambient air quality network located in Seoul are analyzed for the period from 2000 to 2005. In order to classify the photochemical activities on a daily basis, measured ${\Delta}O_{3,\;max-min}$ (maximum $O_3$-minimum $O_3$) and ${\int}(hv)dt$ which represents accumulated daily insolation, were used to classify each day into three regimes: 1) low photochemical reactivity; ${\Delta}O_{3,\;max-min}\;{\leq}\;40\;ppb$, and ${\int}(hv)dt\;{\leq}\;4000\;W/m^2$, 2) moderate photochemical reactivity; $40\;ppb\;<\;{\Delta}O_{3,\;max-min}\;{\leq}\;60\;ppb$, and $4000\;{\leq}\;{\int}(hv)de\;{\leq}\;6000\;W/m^2$, and 3) high photochemical reactivity; ${\Delta}O_{3,\;max-min}\;>\;60\;ppb$, and ${\int}(hv)dt\;{\geq}\;6000\;W/m^2$. The ratio of ($PM_{10}$/CO) obtained at low photochemical activity regime was used as an index of tracer for the estimation of secondary $PM_{10}$ at higher photochemical activity regimes. The results show that the estimated secondary $PM_{10}$ concentrations for moderate and high photochemical regimes are found to be 18.8% ($10.9\;{\mu}g/m^3$), and 35.0% ($26.2\;{\mu}g/m^3$), respectively. Diurnal variation of secondary $PM_{10}$ for the moderate photochemical regime shows weak but noticeable patterns. However, the highly activated photochemical regime shows strong diurnal variations of secondary $PM_{10}$ concentrations with the maximum value of $35.1\;{\mu}g/m^3$ at 1300LST.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2001.09a
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• pp.23-26
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• 2001

Batch test and column test were performed to develop the design factors for PRBs against the contaminated groundwater by ammonium and lead. Clinoptilolite, one of the natural zeolites having excellent cation exchange capacity(CEC), was chosen as the reactive material through the ion-exchange mechanism. In the batch test, the reactivity of Clinoptilolite to ammonium and lead was examined with varying the particle size of Clinoptilolite. The nit weight of Clinoptilolite showed removal efficiencies of 65 % against the ammonium and 98% against lead. The effect of particle size of Clinoptilolite was not noticeable. In the column test, the permeability was examined using flexible-wall permeameters with varying the particle size of Clinoptilolite. When the washed Clinoptilolite having the diameter of 0.42-0.85 nm was mixed with Jumunjin sands in 20:80 ratio (w/w), the highest permeability of 2$\times$10$^{-3}$ -7 x 10$^{-4}$ cm/s was achieved. The reactivity and the strength property of the mixed material were investigated using fixed wall column having 8 sampling ports on the wall and the direct shear test, respectively. Clinoptilolite was found to be a suitable material for PRBs against the contaminated groundwater with ammonium and/or heavy metals.

• International Journal of Concrete Structures and Materials
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• v.8 no.4
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• pp.315-326
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• 2014

This study evaluates the dosages of Class F fly ash, lithium nitrate and their combinations to suppress the excessive expansion caused by alkali-silica reactivity (ASR). In order to serve the proposed objective, the mortar bar specimens were prepared from (1) four dosages of Class F fly ash, such as 15, 20, 25 and 30 % as a partial replacement of Portland cement, (2) up to six dosages of lithium nitrate, such as lithium-to-alkali molar ratios of 0.59, 0.74, 0.89, 1.04, 1.19 and 1.33, and (3) the combination of lithium salt (lithium-to-alkali molar ratio of 0.74) and two dosages of Class F fly ash (15 and 20 % as a partial replacement of Portland cement). Percent contribution to ASR-induced expansion due to the fly ash or lithium content, test duration and their interaction was also evaluated. The results showed that the ASR-induced expansion decreased with an increase in the admixtures in the mortar bar. However, the specimens made with the both Class F fly ash and lithium salt produced more effective mitigation approach when compared to those prepared with fly ash or lithium salt alone. The ASR-induced expansions of fly ash or lithium bearing mortar bars by the proposed models generated a good correlation with those obtained by the experimental procedures.

• Bulletin of the Korean Chemical Society
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• v.29 no.4
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• pp.772-776
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• 2008

Second-order rate constants ($k_N$) have been measured spectrophotometrically for reactions of 3,4-dintrophenyl 2-furoate (2) with a series of secondary alicyclic amines in 80 mol % $H_2O$/20 mol % dimethyl sulfoxide (DMSO) at 25.0 ${^{\circ}C}$. The Bronsted-type plot exhibits a downward curvature for the aminolysis of 2, which is similar to that reported for the corresponding reactions of 2,4-dintrophenyl 2-furoate (1). Substrate 2 is less reactive than 1 toward all the amines studied but the reactivity difference becomes smaller as the amine basicity increases. Dissection of the second-order rate constants into the microscopic rate constants has revealed that the reaction of 2 results in a smaller $k_2/k_{-1}$ ratio but slightly larger $k_1$ value than that of 1. Steric hindrance has been suggested to be responsible for the smaller $k_1$ value found for the reactions of 1, since the ortho-substituent of 1 would inhibit the attack of amines (i.e., the $k_1$ process).

• Bulletin of the Korean Chemical Society
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• v.31 no.7
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• pp.1915-1919
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• 2010

Second-order rate constants $(k_N)$ have been measured for reactions of 2,4-dinitrophenyl phenyl carbonate (2) with a series of pyridines in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$ and compared with the $k_N$ values reported for the corresponding reactions of 2,4-dinitrophenyl benzoate (1) to investigate the effect of nonleaving group on reactivity and mechanism. The reactions of 2 result in larger $k_N$ values than those of 1. The Br${\o}$nsted-type plot for the reactions of 2 exhibits a downward curvature (i.e., ${\beta}2$ = 0.84 and ${\beta}1$ = 0.16), which is typical for reactions reported to proceed through a stepwise mechanism with a change in rate-determining step. The $pK_a$ at the center of the Br${\o}$nsted curvature, defined as $pK_a{^{\circ}}$, has been found to be 8.5 and 9.5 for the reactions of 2 and 1, respectively. Dissection of $k_N$ into the microscopic rate constants (e.g., $k_1$ and $k_2/k_{-1}$ ratio) has revealed that the reactions of 2 result in larger k1 values than those of 1, indicating that PhO behaves as a stronger electron-withdrawing group than Ph. However, the $k_2/k_{-1}$ ratio has been found to be independent of the electronic nature of Ph and PhO.