The esterification of the reactants of Jatropha oil and methanol added by propyleneglycol was done using p-TSA catalyst. And then the emulsification of triglyceride and methanol was conduced by 1.0vol% GMS. The emulsified reactants were transesterified at 65℃ using TMAH and mixed catalyst (50wt%-TMAH+50wt%-NaOH) respectively. The esterification conversion at the 1:8 molar ratio of free fatty acid to methanol using 8.0wt% p-TSA was 94.7% within 80min. The overall conversion at the 1:8 molar ratio of mixed fat(50wt% Beef Tallow) to methanol and 65℃ using mixed catalyst was 95.4% The cloud point of Biodiesel decreased with the addition of petroleum diesel.

To improve the filtration efficiency of porous materials used in filters, an extensive specific surface area is required to serve as a site for adsorption of impurities. In this paper, a method for creating a hybridized porous alloy using a powder metallurgical technique to build macropores in an Al-4 wt.% Cu alloy and subsequent surface modification for a microporous surface with a considerably increased specific surface area is suggested. The macropore structure was controlled by granulation, compacting pressure, and sintering; the micropore structure was obtained by a surface modification using a dilute NaOH solution. The specific surface area of surface-modified specimen increased about 10 times compare to as-sintered specimen that comprised of the macropore structure. Also, the surface-modified specimens showed a remarkable increase in micropores larger than 10 nm. Such a hybridized porous structure has potential for application in water and air purification filters, as well as membrane pre-treatment and catalysis.

Based on the importance of coastal saline-alkali soil remediation in Yellow River Delta, China, the Cl-、Na+ transferring tendency in soil and the saline-alkali soil eco-remediation effects were researched by measuring soil Cl-、Na+ 、soluble salt、soil respire rate and dry biomass weight of reed, etc. periodically. The results shows: the concentration of irrigated soil Cl-、Na+ and soluble salt were decreased 57.7-70%、45.7-47.1% and 53.2-59.7%, respectively, and soil salt decreasing level were little influenced by the hydraulic load, inundation depth varies in some degree, but it was influenced by dry-wet alternative irrigating mode The concentration of soil total nitrogen、organic mass、microbial respire rate, and the reed biomass above ground were increased averagely to 2.17、1.20、1.46 and 1.34 multiple respectively afterirrigation with wastewater, which have complex remediation effects on the coastal saline-alkali wetland, but there are some differences among the different irrigating crafts.

Non-sintering cement was manufactured with briquette ash. Alkali activator for compression bodies used a NaOH solution. In order to apply alkali-activated briquette ash and the non-sintering cement to concrete, several experimental studies were performed. It was necessary to study the binder obtained by means of a substitute for the cement. This study concentrated on strength development according to the concentration of NaOH solution, the curing temperature, and the curing time. The highest compressive strength of compression bodies appeared as 353kgf/cm2 cured at 80˚C for 28 days. This result indicates that a higher curing temperature is needed to get a higher strength body. Also, geopolymerization was examined by SEM and XRD analysis after the curing of compression bodies. According to SEM and XRD, the main reaction product in the alkali activated briquette ash is aluminosilicate crystal.

The esterification of free fatty acid in Jatropha oil added by propylene glycol using p-TSA catalyst was done, and then the transesterification of Jatropha oil added by 1.0vol% GMS as an emulsifier using TMAH, and mixed catalyst(60wt%-TMAH+ 40wt%-KOH) respectively was followed at 60℃. The esterification conversion at the 1:8 molar ratio of free fatty acid to methanol using 8.0wt% p-TSA was 94.7% within 60min. The overall conversion at the 1:8 molar ratio of Jatropha oil to methanol and 60℃ using mixed catalyst was 95.4%. The kinematic viscosity of Biodiesel using TMAH and mixed catalyst in 24h met the ASTM D-6751 above 30℃, and showed a little more than its criterion.

As the durability, reparability and maintainability of reinforced concrete structures are emphasized, the early perfomance degradation of concrete structures becomes a serious problem. Moreover, defects in construction materials and constructions inconsistent with the design promote the degradation of perfomance. Some worst buildings have fallen into an irreparable state within a few years. In particular, carbonation in concrete structures has been handled as the most fundamental and critical factor related to the durability of reinforced concrete. As a result, there have been efforts to develop repair materials to control carbonation. As one of these efforts, alkali recovery agents have been presented as materials for increasing the re-alkalization and durability of carbonated concrete structures. However, in applying them in the field, the performance and quality of concrete recovered after an alkali recovery agent is applied has not been fully assessed. Therefore, to examine the recovered perfomance of concrete structures resulting from the application of an alkali recovery agent, the present study assessed the depth of carbonation and the degree of deterioration of 20 years or older reinforced concrete structures, and analyzed the quality of concrete after applying an alkali recovery agent to the structures. This study aimed at providing basic infomation for the application of alkali recovery agents in the fleld. In this experiment, alkali recovery agents of the lithium silicate line, which are most common in Korea, were applied and cured using concrete of the same size. The degree of recovery was investigated according to the length of time in the initial curing stage, and based on the investigation, the maintenance perfomance of the alkali recovery agent was assessed according to the age of exposure to the open air. For these tasks, this experiment sampled concrete of different degrees of deterioration, applied alkali recovery agents to them, and observed re-alkalization and changes in the internal texture of the concrete.

Concrete Carbonation is usually measured as discoloration, as it has one of strengths to be economical, and simple and immediately confirm the given results in the spot. And, when Carbonation is measured as Phenolphthalein Solution, it is possible to confirm the scope of alkali through acid and basic reaction. Then, Concrete Basic Reaction is decided according to alkali concentration depending on Potassium Hydroxide Now that Carbonation is gradually produced toward inner side from outer side, with time going by, it doesn’t work, to some adequate depth, in as fast time as compulsory facilitating test. Thus, this research thesis made a comparative analysis on concrete phenomenal discoloration borderline following Phenolphthalein Solution, as part of a bid to measure Carbonation. Also, the thesis measured 'Concrete Alkali Concentration. The result showed that concrete coloring is classified into red and scarlet according to alkali concentration, and into borderline breakpoint of the speckle of scarlet and carbonation reaction. The higher chroma becomes with concrete decolorizing, the higher alkali concentration becomes. Also, it was demonstrated that for long-term concrete discoloration borderline, discoloration degree can be determined by amounts of Potassium Hydroxide. Such result proved that limiting the extent of only red color as alkali, in the process of deciding on the scope of concrete alkali, can be served as an error in measuring service life of Concrete Carbonation.

This paper presents results and observations obtained from a study of the optical and thermal properties of alkali tellurite depending on the composition. Fourier transform infrared (FT-IR) spectra showed evidence of chemical modification from TeO4 trigonal bipyramids (tbp) to TeO3 trigonal pyramids (tp) in tellurite glasses. The optical band gaps of the different glass samples calculated using Tauc's method were found to range from 3.5-3.8 eV. The glass transition temperature (Tg) and glass stability (δT) of alkali tellurite glasses were investigated, as M2O [M: Li, Na, K] amounted to 25 mol%, through the use of differential thermal analysis (DTA). The coefficient of thermal expansion (CTE) was measured in a thermo mechanical analysis (TMA) with a slow heating rate after the glass samples were annealed. The results confirm that the optical band gap of alkali tellurite glasses depends on the Te-O-Te structural relaxation related to the ratio of bridging/non bridging oxygen (BO/NBO). In contrast, the thermal properties are related to the ionic field strength of the Te-O-M and M-O-M bonds, and the Te-O-Te breakage depends on the ratio of BO/NBO.

Carbonized concrete structure becomes superannuated gradually and its accelerated subsequent deterioration process leads to corrosion of steel while it ages. Recently economical and environmental concern about remodeling such superannuated concrete, including the basic structure of concrete, has been rapidly growing. Alkali restorative, which restores alkalinity in carbonized concrete structure, is used in the field of remodeling in order to improve the property of concrete structure. There have been many different kinds of materials which restore alkalinity in carbonized concrete. They can be classified according to their structural elements. This study focuses on the alkali restorative which mainly consists of silicic lithium metallic salt while examining the durable effectiveness of the factors (such as water permeation, surface erosion, elution of alkali, etc.), which will continuously affect concrete as deteriorating factors even after the restoration of alkali. The result shows that the alkali restorative consisting mainly of silicic lithium contributes to water-resistance, surface strength, and long term durability of alkali due to water permeation in carbonized concrete.

질산, 불산 및 과염소산을 사용하여 플루토늄 옥사이드 을 녹여 Pu 기준용액을 제조한후 UV-Visible-Near IR 분광기를 이용하여 Pu 흡수 스펙트럼 특성을 관찰하였다. 산성, 중성 및 알칼리 매질에서 Pu(III), Pu(IV) 및 Pu(VI)에 대한 분광학적 특성을 조사하였다. 또한 알칼리 및 산 농도 증가에 따른 Pu(VI) 흡수 스펙트럼에 대한 특성 피크 세기 및 위치를 관찰하였다. 염산 및 수산화나트륨 매질에서 환원제 첨가에 따른 Pu(VI) 산화수 변화를 측정하였다.

The transesterifications of beef tallow and the mixture of beef tallow and rapeseed oil were conducted at 65℃ respectively using TMAH, NaOH and their mixed catalysts. The reactants were emulsified with 1vol% emulsifier and propylene glycol. The overall conversion of beef tallow was 95% at such optimum conditions as the 1:8 of molar ratio and 0.8 wt% TMAH. The overall conversion of mixed fat at the 1:8 of molar ratio and mixed catalyst of 70 wt% TMAH 30 wt% NaOH was close to 97% which appeared at 0.8 wt% TMAH in 80min. And the kinematic viscosity of biodiesel mixture using the mixed catalyst was 6.5mm2/s at 40℃.

The esterification of palmitic acid in rapeseed oil and methanol emulsified by propylene glycol with PTSA(p-toluene sulfonic acid) was followed by the transesterification of rapeseed oil into biodiesel with 1(w/v)% GMS(glycerol monostearate) as an emulsifier using TMAH(tetramethyl ammonium hydroxide) catalysts at 60℃. The former reaction was optimized at the 1:20 of molar ratio of oil to methanol and 5wt% PTSA, and the latter was optimized at the 1:8 of molar ratio of oil to methanol and 0.8wt% TMAH. The overall conversion into biodiesel was 98% after 60min of reaction time at the 1:8 of molar ratio, 0.8wt% TMAH and 60℃. TMAH was a good catalyst to control the viscosity of biodiesel mixture.

Competitive solvent extraction of the mixure of alkali metal and alkaline earth cation from water into organic solvent containing the crown ether carboxylic acid and anlogous crown ether phosphonic acid was investigated as follows. The lipophilic group is found to strongly influence to the selective extraction in the mixed systems from only alkali metal cation for sym-(n-decyldibenzo)-16-crown-5-oxyacetic acid _1 to mostly alkaline earth metal cation for sym-bis[4(5)-tert-butylbenzo]-16-crown-5-oxyacetic acid _3. Monoethyl sym-(n-decyldibenzo)-16-crown-5-oxymethylphosphonic acid _2. and monoethyl-sym- bis]4(5)-tert-butylbenzo]-16-crown-5-oxymethylphosphonic acid _4 showed good selectivity for Na+ over Mg2+, the second extracted ion. Structural variation in the crown ether phosphonic acid somewhat was influenced to the extraction selectivity in the mixed systems. when variation of the ionized group is influenced in the mixed systems, the selectivity of Na+ as the second extracted ion was much better crown ether carboxylic acid _1 than crown ether phosphonic acid _2, while the efficiency of Na+ extraction was better _2 (83% total loading) than _1 (32%).

A comparison of alkali metal cation and alkaline earth cation solvent extraction was made for three additional monoionizable crown ethers and one diionizable crown ether. sym-(n-Octyldibenzo)-16-crown-5-oxyacetic acid _1 exhibited high efficiency and selecvity in solvent extraction of alkali metal cations with respect to that observed with alkaline earth cations. Sizes of Na+ and Ca2+ appropriately match with the cavity size of monoethyl sym-bis[4(5)-tert-butylbenzo]-16-crown-5-oxymethylphosphonic acid _3. As the result, Na+ and Ca2+ are the best extracted. sym-(n-Octyldibenzo)-16-crown-5-oxymethyldiphosphonic acid _4was found to be somewhat selective for Na+ over Li+ and other alkaline earth metal cations. In the complexation of alklaine earth cations by crown ether diphosphonic acid _4, Ca2+ and Sr2+ are the appropriate sizes, but lager Ba2+ may be due to favorable formation of a sandwich type complex between the crown ether cavity and the dianion of the deprotonated crown ether phoaphonic acid moiety.