• Proceedings of the Membrane Society of Korea Conference
• /
• 2004.05a
• /
• pp.207-210
• /
• 2004

The pore-filled anion-exchange membranes were prepared in this study with an asymmetric poly(vinylidene fluoride)(PVDF) membrane as a nascent membrane and poly(vinylbenzyl chloride)(PVBCl) as a polyelectrolyte. The solution of PVBCI having the chloromethylate aryl ring of 80 percents and 1,4-diaminobicyclo [2,2,2]octane(DABCO) was made with the solvent of tetrahydrofuran(THF) and N,N-Dimethylformamide(DMF), which is in the rotio of 8:2. A new preparation method in this study, i.e. in-situ crosslinking, enabled us to produce the pore-filled membranes without change of size, and to control the properties of final membrane with various degree of cross-linking. From the result of surface morphologies of SEM and AFM the polyelectrolyte exists in the pores of nascent membrane as a certain configuration. From the investigation of the solvent affecting much to the permeability and rejection, it was found. that the membranes using DMF and THF showed better performances than the membranes produced by THF only. The water permeability of the final membrane at low pressure(100㎪) showed a typical ultrafiltation membrane's permeability (8-10kg/㎡hr) and good values of rejection(55∼60 percent).

• Journal of the Korea Academia-Industrial cooperation Society
• /
• v.7 no.1
• /
• pp.27-32
• /
• 2006

We separated semiconducting single-walled carbon nanotubes(sem-SWCNT) from the HiPco-SWCNTS by dispersion with octadecylamine(ODA). The mixture of acid-treated SWCWTS and ODA was heated at $120^{\circ}C$ for 120hours. ODA physisorbs selectively on the side-wall of sem-SWCNTS. The ODA-treated CNTs were dispersed in tetrahydrofuran(THF) via sonication. The ODA-physisorbed sem-SWCNT can be retained in the supernatant of THF, but met-SWCNT and unabsorbed sem-SWCNT were precipitated in THF. Raman spectra with 514 nm and 1074 nm were investigated. The amount of sem-SWCNT in the supernatant and precipitant was about 94 % and 50 %, respectively.

• Bulletin of the Korean Chemical Society
• /
• v.22 no.8
• /
• pp.837-841
• /
• 2001

The electronic absorption and Raman spectra of $\alpha\omega-diphenylpolyenyl$, anions Ph(CH)nPh- (DPn- , n = 3, 5, 7, 9, and 13), with odd number of carbons at the polyene part, have been studied in the tetrahydrofuran (THF) solutions and in their solid film states, respectively. In the case of Raman spectra for DPn- , the frequencies and relative intensities of some Raman peaks regularly change with the increase of polyene chain length. The spectral patterns of anions (DPn- ) are very similar with those of radical anion (DPn${\cdot}$- ). However, the C=C stretching peaks of DPn- anions are observed in the 25-35 cm-1 higher frequency region than those of DPn${\cdot}$- radical anions. In the case of long chain models such as DP9- and DP13- , the C=C stretching peaks are observed in even higher frequency region than those of the corresponding neutral polyenes such as DP8, DP10, and DP12. The Raman patterns of DPn- anions in the THF solutions are similar with those in their solid film states. On the other hand, their electronic absorption spectra show a considerable difference each other. The n- ${\pi}*$ electronic absorption bands of DPn- anions in the THF solutions have been observed in the 0.27-0.39 eV lower energy region than those in their solid film states due to the solvent effects on polyene anions.

• Journal of Adhesion and Interface
• /
• v.18 no.3
• /
• pp.109-117
• /
• 2017

Poly(N-vinyl carbazole) (PVK) homopolymer, poly(4-vinylpyridine) (PVP) homopolymer, and PVK-b-PVP block copolymer were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization and the polymers were used to prepare non-aqueous graphene dispersions with four different solvents, ethanol, N-methyl-2-pyrrolidone (NMP), dichloromethane (DCM), and tetrahydrofuran (THF). $^1H-$ and $^{13}C-NMR$ spectroscopy, size exclusion chromatography (SEC), and differential scanning calorimetry (DSC) were carried out to confirm the chemical structure of the polymers. Stability of graphene dispersions was measured by on-line turbidity measurement. Time-dependent Turbiscan Stability Index (TSI) values were interpreted in terms of surface tension (${\sigma}$) and solubility parameter (${\delta}$) among solvents, polymers, and graphene. It was confirmed that the solubilities of polymer and surface tension between solvent and graphene affected the dispersion stability of graphene. PVK-b-PVP block copolymer could effectively maintain the low TSI values of graphene dispersions in ethanol and THF, which have been known as poor solvents for graphene dispersions. It can also be noted that DCM shows good dispersion stability comparable to NMP, which has been known as the best solvent for graphene dispersion.

• Journal of the Korean Chemical Society
• /
• v.52 no.2
• /
• pp.140-147
• /
• 2008

.A new approach for a cloud point extraction-electrothermal atomic absorption spectrometric method was used for determining bismuth. The aqueous analyte was acidified with sulfuric acid (pH 3.0-3.5). Triton X-114 was added as a surfactant and natriumdiethyldithiocarbaminat (Na-DDTC) was used as a complexing agent. After phase separation at 50oC based on the cloud point separation of the mixture, the surfactant-rich phasen was diluted using tetrahydrofuran (THF). Twenty microliters (20 L) of the enriched solution and 10 l of 0.1% (w/v) Pd(NO3)2 as chemical modifier were dispersed into the graphite tube and the analyte determined by electrothermal atomic absorption spectrometry. After optimizing extraction conditions and instrumental parameters, a preconcentration factor of 195 was obtained for a sample of only 10 mL. The detection limit was 0.04 ng ml-1 and the analytical curve was linear for the concentration range of 0.04-0.70 ng mL-1. Relative standard deviations were <5%. The method was successfully applied for the extraction and determination of bismuth in water samples.

• Applied Chemistry for Engineering
• /
• v.2 no.4
• /
• pp.340-347
• /
• 1991

Siloxane containing copolyimide (SPI) was synthesized from 3, 3', 4, 4'-benzophenonetetracarboxylic dianhydride(BTDA), 4, 4'-methylene dianiline(MDA), 4, 4'-oxydianiline(ODA) and amine-terminated polydimethyl-siloxane(PDMS). Homopolyamic acid(HPAA) in tetrahydrofuran(THF) was reacted with PDMS to obtain siloxane containing polyamic acid(SPAA) followed by the thermal curing to manufacture SPI. SPAA and HPAA exhibited inherent viscosity value of 0.35~0.48dl/g. Glass transition temperature of SPI ranged in $258^{\circ}C{\sim}264^{\circ}C$. SPI had a lower $T_g$ than that of HPI. ODA based HPI and SPI showed slightly higher $T_g$ values, thermal stability, and water content.

• Journal of the Microelectronics and Packaging Society
• /
• v.8 no.2
• /
• pp.25-29
• /
• 2001

This study examined the effects of carbon surface modification by the epoxy resin coating on the electrochemical performance. The mesocarbon microbeads(MCMB) carbon was surface-modified by coating the epoxy resin and its electrochemical properties as an anode was examined. The surface coating of MCMB was carried out by refluxing the MCMB powders in a dilute H2SO4 solution, and mixing them with the epoxy resin-dissolved tetrahydrofuran(THF) solution. Under heat-treatment of the coated MCMB at the temperature over $1000^{\circ}C$, the epoxy-resin coating layer was converted into amorphous phase which was identified by a high resolution transmission electron microscope (HRTEM). The epoxy resin coated MCMB has higher Brunauer-Emmett-Teller (BET) surface area, higher charge/ discharge capacity and better cycleability than a raw MCMB without coating. The reason for the enhancement of cell performance by the epoxy resin coating were considered as the epoxy resin coating layer plays an important role to be a barrier for carbon reacting with electrolyte and to retard the formation of passivation layer.

• Korean Chemical Engineering Research
• /
• v.53 no.1
• /
• pp.103-110
• /
• 2015

In this work, the performance of various promoters was investigated used in $CO_2$ separation from the gases emitted from steel-making process using gas hydrate technology. The studied promoters are tetrahydrofuran (THF), propylene oxide and 1,4-dioxane, which are all expected to form a structure II hydrate, and the target gases include $CO_2/N_2$ mixed gases ($CO_2/N_2$ = 20/80 and 40/60) and Blast Furnace Gas (BFG). The phase equilibrium points were measured when each promoter was added with various concentrations. For fast acquisition of abundant data, the "continuous" Quartz crystal microbalance (QCM) method was employed. In addition, the crystal structure of each gas hydrate was analyzed by Powder X-ray diffraction (PXRD).

• Journal of the Korean Chemical Society
• /
• v.50 no.4
• /
• pp.307-314
• /
• 2006

The redox characteristics of 2-ketohydrazono-3-phenyl-5-substituted-2,3-dihydro-1,3,4-thiadiazoles and its derivatives (1a-h) has been investigated in nonaqueous solvents such as 1,2-dichloroethane (DCE), dichloromethane (DCM), acetonitrile (AN), tetrahydrofuran (THF), and dimethylsulfoxide (DMSO) containing 0.1 mol.dm-3 tetra n-butylammonium perchlorate (TBAP) as supporting electrolyte at platinum ectrode. Through controlled potential electrolysis, the oxidation and reduction products of the investigated compounds can be separated and indentified. The redox mechanism is suggested and proved. It was found that all the investigated compounds are oxidized in two irreversible one-electron processes following the well known pattern of EC-mechanism. On the other hand, these compounds are reduced in a single two electron or in a successive two one electron processes following the well known pattern of EEC-mechanism according to the nature of the substituent

• Clean Technology
• /
• v.14 no.1
• /
• pp.35-39
• /
• 2008

In this study, we successfully fabricated a super-hydrophobic polymer layer on the surface of slide glass using the solubility difference of a polymer at two different solvents. After dissolving polystyrene (PS) resins in tetrahydrofuran (THF) as a good solvent and then adding ethanol(EtOH) as a poor solvent, we were able to fabricate super-hydrophobic surface. We also investigated the effect of EtOH addition, coating methods, solution mixing time and speed, and other alcohols on the surface hydrophobicity. The water contact angle (WCA) of the fabricated surface revealed $WCA>150^{\circ}$ and the microporous surface structure composed of microparticles with the size less than $5\;{\mu}m$.