Site coefficients suitable to China site category

The basis for the NEHRP site coefficients is summarized in the paper. The comparison of site classification between China and US code provisions has been carried out. The relationship between two site classifications has been found by the analysis of wave velocity of site soil. Thus amplitude-dependent site amplification factors for China site classification has been gained by transformation from US amplification factors. Two amplification factors are specified： Fa for short periods and Fv for longer periods. On the contrast, there is only one long period factor and not a short period factor in the current China code provision.

Newmark design spectra considering earthquake magnitudes and site categories

Newmark design spectra have been implemented in many building codes, especially in building codes for critical structures. Previous studies show that Newmark design spectra exhibit lower amplitudes at high frequencies and larger amplitudes at low frequencies in comparison with spectra developed by statistical methods. To resolve this problem, this study considers three suites of ground motions recorded at three types of sites. Using these ground motions, influences of the shear-wave velocity, earthquake magnitudes, source-to-site distances on the ratios of ground motion parameters are studied, and spectrum amplification factors are statistically calculated. Spectral bounds for combinations of three site categories and two cases of earthquake magnitudes are estimated. Site design spectrum coefficients for the three site categories considering earthquake magnitudes are established. The problems of Newmark design spectra could be resolved by using the site design spectrum coefficients to modify the spectral values of Newmark design spectra in the acceleration sensitive, velocity sensitive, and displacement sensitive regions.

Method study and uncertainty analysis of calibration coefficients validation based on the Inner Mongolia test site

Calibration coefficients validation is the foundation for ascertaining the sensor performance and carrying out the quantitative application.Based on the analysis of the differences between the calibration and validation,two calibration coefficients validation methods were introduced in this paper.Taking the HJ-1A satellite CCD1 camera as an example,the uncertainties of calibration coefficients validation were analyzed.The calibration coefficients validation errors were simulated based on the measured data at an Inner Mongolia test site.The result showed that in the large view angle,the ground directional reflectance variation and the atmospheric path variation were the main error sources in calibration coefficients validation.The ground directional reflectance correction and atmospheric observation angle normalization should be carried out to improve the validation accuracy of calibration coefficients.

Sorbent Concentration Effect on Adsorption of Methyl Orange on Chitosan Beads in Aqueous Solutions

The adsorption of methyl orange（MO） on chitosan（CS） beads in aqueous solutions was investigated by a batch equilibration technique. Special emphasis was focused on the effect of sorbent concentration（cs） on the adsorp- tion equilibration of MO on CS beads. An obvious Cs-effect was observed in the adsorption equilibration, i.e., the ad- sorption amount（F） was declined with Cs increase. The classical Langmuir model adequately described the adsorption isotherm for each given cs. However, it could not be used to predict the cs-effect observed. The applicability of the Langmuir-SCA isotherm, a surface component activity（SCA） model equation, to fit the cs-effect data was examined. In the SCA model, the activity coefficient of sorbent surface sites, fsH2O, was assumed to be a function of cs due to the deviation of a real adsorption system from an ideal one, arisen from sorbent particle-particle interactions in real systems. The results show that the Langmuir-SCA isotherm could accurately describe the c：effect observed under the studied conditions. Furthermore, the effects of temperature（t）, pH, and electrolyte（NaNO3） concentration（ CNaNO3 ） on fsH2O were examined. The results show that fsH2O clearly decreased with increasing t（20-35℃） and pH（5-8）, but no obvious change in fsH2O was observed as CNaNO3 varied in a range 0.001-0.010 mol/L. These results give a better understanding of the cs-effect.