The aim of this work is to investigate the ability of a new functionalized graphene oxide 3-amino-5-phenylpyrazole (F-GO) in the adsorption and removal of Hg2+ from aqueous solution. Both untreated graphene oxide (GO) and F-GO were characterized using FT-IR, EDX, FE-SEM, XRD and TGA analysis. The effects of three operational variables (pH, adsorbent dose and initial metal ion concentrations) on Hg2+ adsorption capacity of F-GO were investigated by central composite design. This technique aims to find a simple way to optimize the adsorption process and to analyze the interaction between the significant parameters. A quadratic model suggested for the analysis of variance found that the adsorption of metal ions heavily depend upon pH of the solution. The adsorption mechanism has been determined by pseudo-first-order kinetic models and the adsorption behavior was modeled by Freundlich isotherm. Results demonstrated that the adsorption capacities of F-GO for removal of Hg2+ were generally higher than those of GO, which is attributed to a decrease in the agglomeration of graphene layers due to the presence of amino-functional moieties with their bulky phenyl groups. Thermodynamic data indicated that the functionalization significantly affects the thermostability of the GO precursor materials. The desorption study demonstrated favorable regenerability of the F-GO adsorbent, even after three adsorption–desorption cycles.

High performance polydimethylsiloxane (PDMS) membranes for n-butanol recovery were fabricated using a tri-functional crosslinker containing the phenyl group. In order to understand the role of the functional group structure and cross-linking density in pervaporation performance, PDMS membranes were prepared using tri-functional crosslinker containing other functional groups (hexyl and cyclohexyl) and conventional tetra-functional crosslinker. The relationship between the polymer structure-performance was discussed based on the sorption and diffusion properties of the membranes. As a result, the phenyl-based PDMS membrane exhibited the pervaporation performance owing to the strong hydrophobicity and chain rigidity of the phenyl group compared to other PDMS membranes even at high butanol concentration and high temperature conditions.

The organic light-emitting diodes are fabricated with six anthracene derivatives containing simple substituents such as phenyl or naphthyl group. The device structure is as in the following: Indium tin oxide (ITO) (180 nm)/4,4-4,4`,4``-tris[N-(1-naphthyl)-Nphenylamino] triphenylamine (2-TNATA) (30 nm)/4,4`-bis[N-(1-naphthyl)-N-phenyl-1-amino] biphenyl (NPB) (20 nm)/Emitting compound (30 nm)/2,2′,2"- (1,3,5-Benzinetriyl)-tris (1-phenyl-1-H–benz-imidazole) TPBi (40 nm)/lithium quinolate (Liq) (2 nm)/Al (100 nm). In the emitting layer the anthracene derivatives are used without any dopant. All the six devices show blue emissions. Among the tested diodes, the one with 9-(2-naphthyl)-10-(p-tolyl) anthracene (2-NTA) exhibited luminous efficiency, power and external quantum efficiencies of 3.26 cd/A, 0.98 lm/A, 2.8 % at 20 mA/cm .

This study was conducted to evaluate the health risk of workers exposed to phenyl glycidyl ether to prevent themfrom developing occupational diseases. The workplaces that coat floor with epoxy were selected and the sampleswere collected and analyzed with NIOSH 1619 Method. Unit risk was calculated according to the animalcarcinogenicity study. Excess cancer risk was also calculated by multiplying unit risk by exposure concentration.Monte Carlo simulation was performed to calculate the median, cumulative 90%, and cumulative 95% value.Phenyl glycidyl ether is a skin, eye irritator and can result in allergic reaction, nausea, intoxication. Unit risk wascalculated as 0.04 (mg/m³)-¹ based on the tumor incidence in rats. Geometric mean and geometric standarddeviation was also calculated as 0.112 ppm and 0.223, respectively by the workplace environment measurements.The median, cumulative 90%, and cumulative 95% value of excess cancer risk were calculated as 0.0244, 0.1328,0.1596, respectively. Not only cumulative 90% and cumulative 95% value but also the median of excess cancerrisk is much higher than 1×10-⁴ by the risk characterization, so there is a possibility of carcinogenesis to workers.Therefore, supervisors or managers of each workplace have to keep doing the risk management of their workplacesfor workers to reduce exposure to phenyl glycidyl ether.

낮은 농도와 높은 농도의 염 용액에서 Poly(styrene sulfonic acid)(PSSA) 겔의 팽윤도에 대한 이온 특성화 효과를 SO3-와 페닐 고리의 수소결합을 통하여 조사하였다. 낮은 농도에서 PSSA 수화 겔의 수축 정도는 SO3-와 물 사이의 수소 결합에 대한 음이온의 불안정화 영향 때문에 음이온에서는 SCN-〈Br-〈Cl-〈F-의 순서를 따랐다. 재 팽윤은 계에서 특별한 상호 작용이 있을 때 높은 농도에서 관찰되었다. 반면 양이온에서 PSSA 겔의 수축은 Li+〈Na+〈K+〈Ca+2 순서를 따랐다. Ca+2 이온에서의 큰 수축 효과는 이가 양이온(+2)에 의한 PSSA 겔의 물리적 가교 때문에 나타난 것으로 보인다. 양이온에서의 수축은 SO3-와 양이온 사이의 상호작용 정도에 비례하였다. PSSA의 팽윤에 대한 이온 특성화 효과는 SO3-와 페닐 고리의 수화 수소결합에 대한 이온의 영향 정도, 양이온과 π 전자의 상호작용, 소수성 상호작용, 그리고 분산력 등이 복합적으로 작용하여 나타난다고 볼 수 있다.

본 연구에서는 용매로 N-methyl-2-pyrrollidone을 사용하여, 상전환 방법으로 carboxylic acid를 함유한 음이온성 한외여과막을 제조하였다. 첨가제, 제막조건 및 운전조건에 따른 투과 특성을 알아보았다. Bovin serum albumin (BSA) 수용액의 pH에 따른 상대투과유속을 측정하여 fouling형성에 따른 투과 특성의 변화를 살펴보았다. 투과 특성은 막 제조환경과 투과 공정에 영향을 받았다. 이온교환용량과 측정 온도가 증가할수록, 그리고 BSA의 등전점으로부터 수용액의 pH값이 멀어질수록 상대투과유속이 증가하였다.

Among the efforts to increase the efficiency of organic light-emitting device (OLED), there is a way: doping phosphorescent materials. As a phosphorescent material, complexes of heavy transition metal, platinum, were synthesized. Cl- ion and phenyl group were used as ancillary ligands with 2-(2-pyridyl)benzimidazole (pbi) as a chromophore. The complexes were analysed by FAB-mass spectrometer and absorption and emission spectra were obtained. A phenyl group was able to shift the emission band of the complex even if it's not a chromorphore.

In this study, benzoxazolo carbocyanine is of industrial importance as green-sensitizing dye in the spectral sensitization. Sensitizing dye was prepared by the reaction of 2-methyl-3-sulfopropyl-4,5-benzoxazolium (inner salt) with triethyl orthobenzoate in the presence of triethylamine. The product was identified by using various analytical tools such as elemental analyzer, IR spectrophotometer, UV-Vis spectrophotometer, 1H-NMR spectrometer, TGA and DSC. The maximum absorption peak in methanol solvent was 507 nm. Therefore, it was concluded that benzoxazolo carbocyanine dye can be used as sensitizing dye for the spectral sensitization of photographic emulsion and color cosmetics.

상전환 방법으로 제조된 음이온 성 Poly(his[4-(3-aminophenoxy)phenyl]sulfone pyromellite)imide(ACPI) 한외여과막의 순수 투과유속과 용질 배재도 측정치로 투과성능을 연구하였다. ACPI 한외여과막의 투과성능은 캐스팅 용액의 조성과 막 제조 및 측정조건에 영향을 받았다. Bovine serum albumin (BSA) 용액을 pH 2.5-9.0 상태에서 ACPI 한외여과 막의 상대투과유속과 membrane filtration index (MFI) 측정한 결과 BSA의 등전점에서 멀어 질수록 상대투과유속은 증가하고 막 오염정도를 나타내는 MFI는 감소하였다. 또한, 친수성인 ACPI 한외여과막의 이온교환용량(IEC)이 증가할수록 상대투과유속은 증가하고, MFI는 감소하였다.

In this paper, it was studied about the red-sensitive layer. UV-Vis data of the dye at monomeric and J-state were considered with respect to their performance(contrast, speed, density and fog) in photographic emulsion. The sensitizing effect of the dye is found to be strongly structure-dependent. Naphthctbiazolo carbocyanine dye can be used as red sensitizing dye for the spectral sensitization of photographic emulsion.

2-phenyl-N-methyl-1,3-thiazolium perchlorate(PTP)derivatives were synthesized via addition and substitution reactions. PTP was hydrolyzed under aqueous hydrochloride. The structures of the compounds were conformed by N.M.R.,I.R., and elemental analysis.

In this study, sensitizing dye was prepared by the reaction of 2-methyl-3-sulfopropyl-4,5-naphthothiazolium(inner salt) with triethyl orthobenzoate in the presence of triethylamine. The product was identified by using various analytical tools such as elemental analyzer, IR spectrophotometer, UV-Vis spectrophotometer, 1H-NMR spectrometer, TGA and DSC. Therefore, it was concluded that 9-phenyl-3,3'-bis(3-sulfopropyl)-4,5,4',5'-naphthothiazolo carbocyanine triethyl ammonium salt can be used as red-sensitizing dye for the spectral sensitization of photographic emulsion.

The rate constant of Nucleophilic addition of sodium thiophenoxide to nitrone were determined by UV Spectrophotometry and a rate equation which can be applied over wide pH range was obtained. Base on the rate equation, general base effect, substituent effect and final product, plausible mechanism of addition reaction have been proposed. Blow pH 3.0, the reaction was initiated of thiophenol, and in the range of pH 3.0~10.0, proceeded by the competitive addition of thiophenol and thiophenoxide anion. Above the pH 10.0, the reaction proceeded through the addition of a thiophenoxide anion.

The rate constant of the nucleophilic addition of 1-propanethiol to α-phenyl-N-iso-propylnitrone derivatives were determined at various pH and a rate equation which can be applied over wide pH range is obtained. Final product of the addition reaction was α-thiopropyl-p-phenylbenzylideneamine. Base on the rate equation, general base effect, substituent effect and final product, plausible mechanism of addition reaction have been proposed. Below pH 3.0, the reaction was initiated by the addition of 1-propanthiol, and in the range of pH 3.0-10.0, proceeded by the competitive addition of 1-propanethiol and propanethiolate. Above the pH 10.0, the reaction proceeded through the addition of propanethiolate.

The rate constants of hydrolysis of α-phenly-N-iso-propylnitrone and its derivatives have been determined by UV spectrophotometry at 25℃ and a rate equation which can be applied over a wide pH range was obtained. On the basis of rate equations derived and judging from the hydrolysis products obtained and general base and substituent effects, plausible mechanism of hydrolysis in various pH range have been proposed. Below pH 4.5, the hydrolysis was initiated by the protonation and followed by the addition of water to α-carbon. Above pH 10.0, the hydrolysis was proceeded by the addition of hydroxide ion to α-carbon. In the range of 4.5~10.0, the addition of water to nitrone was rate controlling step.

(2,3-Dibromopropyl) phenyl lauroyl phosphate[DPPL] was synthesized by adding lauric acid to (2,3-dibromopropyl)chloro phenyl phosphate [DPP]. which prepared from phenyl phosphoric acid dichloride with 2,3-dibromo propyl alcohol. Flame retardants of DPPF and DPPLF were prepared respectively. DPPF was a water soluble flame retardant, and DPPLF was o/w type emulsion flame retardant. After flame retardant treating two kinds of flame retardants to the various synthetic fabrics respectively. the flame retardancy and tear strength were measured. As the results of the measurement. DPPF had only name retardancy, but DPPLF had both of flame retardancy and softness.

2,4,6-Triamino-5-nitrosopyrimidine was prepared using malononitrile and guanidine carbonate, and acetylated refluxing in acetic acid with acetic anhydride in order to activate the nitroso group for nucleophilic attack. Nucleophilic attack of phenylpyrimidium bromide on the nitroso group of 2,4,6-triacetamido-5-nitrosopyrimidine gave the intermediate, which lost pyrdidine to give the nitrone derivative. Addition of the methanethiol anion to nitrone gave 2,4-diacetamido-7-phenyl-6-methylthiopteridine which was hydrolyzed to give 2,4-diamino-7-phenyl-6-methylthiopteridine. Spectral data (IR, M.S, NMR) were provided to identify the reaction products during synthesis.