This study investigates the paste mixing of positive active materials which, affect the life cycle of batteries in Pb-Ca-Sn grids, and generation of 4BS in a curing process and considers the effects of these things on the initial charge characteristics and life cycle. In the results of the experiments applied in this study, it was possible to reduce the curing time in which the fine 4BS was formed by the mixing of the positive active materials of lead acid battery applied at high temperature compared to that of the existing coarse 4BS and that represented some improvements in the life cycle performance.

A stability to the spreading solvent, which is acetonitrile, benzene, chloroform and acetonitrile-benzene(1:1, v/v) of (3-Alkyl benzimidazdium)-TCNQ(1:2) complex was investigated by UV-visible spectrometer and was confirmed stabilized on acetonitrile, acetonitrile-benzene (1:1, v/v) for five hours. Using Ultra pure water as subphase for Langmuir-Blodgett(LB) films, it was achived successively to fabricate the Y-type LB films of (3-Alkyl benzimidazolium)-TCNQ(1:2) complex. For the identification of (3-Alkyl benzimidazolium)-TCNQ(1:2) complex, UV-visible spectra was recorded on HP 8452A spectrometer.

A Stability to spreading solvent, which is acetonitrile, dichloromethane, benzene, chloroform, and acetonitrile-benzene (1:1, v/v) of (N-docosyl quinolinium)-TCNQ(1:2) complex was investigated by UV-visible spectrometer and was confirmed stabilized on acetonitrile, dichloromethane, and acetonitrile-benzene(1:1, v/v) for 7 hours. Using buffer solution(ph≑6.0) as subphase for Langmuir-Blodgett(LB) film, it was achieved successively to fabricate the Y type LB films of (N-docosyl quinolinium)-TCNQ(1:2) complex. For the identification of deposition of (N-docosyl quinolinium)-TCNQ(1:2) complex, UV-visible spectra was recorded on HP 8452A spectrometer.

Ultra thin organic films, (3-docosyl benzimidazolium)-TCNQ(1:1)complex, were deposited onto ordinary microscope slide glass substrates with a Langmuir-Blodgett technique. II-A isotherms were studied to find optimum conditions of deposition by varying temperature. Anisotropic de electrical conductivities were measured at room temperature. They are about 5.21×10-12S/cm along the direction of film surface, and (2.73~4.40)×10-16S/cm in the vertical direction.

In relation to the preparation of Langmuir-Blodgett thin film, four kinds of N-alkylpyridiniurn bromide were synthesized. The values of surface tensions of these materials, measured with a Traube stalagmometer, gave the relationship between the critical micells hydrophobic radical and between CMC and temperature. Values of thermodynamic properties(δH0m, δS0m, δG0m,) for the formatoin of micelle were also obtained. Experiments gave the following results; at the temperature range between 40 and 60℃, CMC of Hexadecyl-, Octadecyl-, Eicosyl-, and Docosyl-Pyridinium Bromide were 7.64×10-4~9.13×10-4, 3.85×10-4~4.60×10-4, 2.00×10-4~2.39×10-4, and 1.07×10-4~1.28×10-4 mol/l, respectively. Surface tension, γCMC, of those were 33.49~36.00, 34.78~37.61, 35.49~37.61 and 38.76~55.80 dyne/cm, respectively, The relationship between CMC and the mumber of carbon atoms in the hydrophobic radical, N was expressed as follows : Log(CMC)=A-BN where A and B are constants. At the temperature range between 40 and 60℃, the change of Gibbs evergy (δGm) for one methylene group (-CH2-) were -0.65RT, respectively, The minus values of enthalpy change (δHm) suggest that the formation of micelle is exothermic. Additionally, the overall increase in the entropy change (δSm) with respect to the temperature increase suggests that the formation of micelle is attained by a exothermic enthalpy directed process.