关于高层建筑的地震动输入

简单地叙述了目前高层建筑地震反应分析中常用的地震动输入方法,用相同的高层建筑和四种不同的场地组建成四个结构－场地一体化模型,通过对四种模型计算得到了场地地表反应、结构顶点水平运动、结构要部的等效输入相对射波的传递函数的幅值谱和结构单元内力的比较,论证了影响高层建筑等效输入地震动的主要因素,并说明了在结构地震反应分析中考虑结构－土相互作用的影响的必要性。     

时间积分声光相关器相关峰提取技术的实验研究

本文根据声光相关原理,针对时间积分声光相关器的相关峰提取问题,提出了系统实施方案,建立了实验系统的数学模型,设计和制作了系统的光路和电路,最终成功地提取出了相关峰,得到了与理论分析一致的实验结果,使系统增益达到５１．９ｄＢ。     

Dipole moments of copolymers in relation to the distribution of polar monomer unit sequences

A method for evaluating the dipole moments of copolymers in relation to the distribution of polar unit sequences is proposed. Experimental data on the synthesis and dipole moments of styrene-p-chlorostyrene and styrene-p-methoxystyrene copolymers were used to calculate the effective dipole moment of a polar unit in a copolymer. For this purpose, we assumed the following effective moment values for the corresponding polar unit sequences along the copolymer chains: when both of the nearest neighbours are polar, μ_PP, when one of the nearest neighbours is polar and the other is non-polar, μ_PS, and when both of the nearest neighbours are non-polar, μ_SS. The relative magnitudes of μ_SS, μ_PS and μ_PP calculated for both copolymers reflect the influence of dipole-dipole interactions on the effective dipole moment of a polar unit in a copolymer molecule.     

Quasielastic scattering from dilute polymer solutions

The initial slope $\text{Ω(q)}$ of the time-dependent scattering function and the static structure factor S(q) of macromolecules in good solvents are calculated without using the Gaussian assumption. For S(q), the scaling relation S(q)～q^?1.7 is confirmed in the intermediate q range, whereas no q dependent cross-over behaviour can be observed. The calculation of $\text{Ω(q)}$ reveals a q³ dependence in this range and no evidence is seen for an exponent apart from 3. The time-dependent scattering function S(q,t) is treated within the framework of the Gaussian assumption. Hydrodynamic as well as excluded volume interactions are incorporated. It has been found that excluded volume effects decrease the decay of the scattering function in comparison with the Gaussian chain.     

Selective solvation of polystyrene in tetralin/cyclohexane mixtures

Refractive index increments and density increments have been measured at 307.6K for polystyrene in binary solvents of 1,2,3,4-tetrahydronaphthalene (tetralin, TET) and cyclohexane over the whole range of solvent composition. Comparison of these increments with the corresponding values obtained at dialysis equilibrium (i.e. at constant chemical potential of low molecular weight species) yielded the coefficients of selective adsorption (γ₁) of TET by the polymer. Positive values of γ₁ were exhibited at solvent compositions up to 78% (v/v) of the thermodynamically better solvent, TET. Theoretical curves of γ₁ vs. composition were calculated on the basis of, firstly, relevant interaction parameters and, secondly, interaction parameters in conjunction with solubility parameters. Both procedures afforded self-consistent results, which were, however, uniformly lower than the experimental values of γ₁.     

Ion-dipole interactions between adsorbed CO and support cations in Pt/K-LTL

The adsorption of carbon monoxide on a non-acidic Pt/K-LTL catalyst has been studied by diffuse reflectance and transmission IR spectroscopy. The CO spectrum is strongly dependent on the experimental conditions. Adsorption on the small Pt clusters in the presence of water gives linear-CO bands between 2060 and 1990 cm^–1 and a bridging-CO band around 1800 cm^–1. In the absence of water, the linear bands are red shifted to about 1940 and 1720 cm^–1, respectively. The frequency shift is attributed to an ion-dipole interaction between adsorbed CO and support cations. The ion-dipole interaction is screened by the adsorbed water leading to a smaller red shift in the CO stretching frequency.     

Chemical interactions between soil N and alkaline-hydrolysing N fertilizers

Chemical interactions between soil N and alkaline-hydrolysing N fertilizers labelled with¹⁵N were studied in the laboratory using twelve-irradiated soils. Fertilizer was recovered in the soil organic N fraction via the process of NH₃ fixation. NH₃ fixation at day 7 varied from 1.8 to 4.6% of the N added as aqua ammonia at 1000 mg kg^–1 soil. The amount of NH₃ fixed increased with increasing rates of application of NH_3(aq) and urea. The rate of NH₃ fixation decreased with time, with more than 55% of the total NH₃ fixation in 28 days occurring in the first week following application of 2000 mg urea-N kg^–1 soil. Soil pH and NH₃ fixation varied in response to N source, and increased in the order of di-ammonium phosphate 3 fixation, resulting in the release of unlabelled ammonium (deamination) and a real added nitrogen interaction in all but two of the soils studied. The release of NH ₄ ⁺ initially increased up to a pH of 7.5, was inhibited between pH 8.5 and 9.0, but increased thereafter. The balance (N_bal) between NH₃ fixation and deamination was either positive or negative, depending on the pH of the fertilized soil, which was directly related to N source and concentration for a given soil.     

Clustering of platinum atoms into nanoscale particle and network on NaY zeolite

Platinum has been supported on NaY zeolite by ion exchange of Pt(NH₃)₄ ²⁺. Clustering of Pt atoms into a 1 nm cluster, and three-dimensional quantum-size wire (3 nm thick) network (greater than 100 nm) from reduction of the Pt species has been investigated by extended X-ray absorption fine structure transmission electron microscopy and xenon adsorption measurements.     

Enantiomers of methyl substituted analogs of (Z)-5-decenyl acetate as probes for the chirality and complementarity of its receptor inAgrotis segetum 1: Synthesis and structure-activity relationships

The enantiomers of analogs of (Z)-5-decenyl acetate, a pheromone component ofAgrotis segetum, substituted by a methyl group in the 2, 3, 4, 7, and 8 positions and dimethyl substituted in the 4,7 positions, have been synthesized and studied by an electrophysiological single-cell technique and by molecular mechanics calculations. The results demonstrate that the electrophysiological activity as well as the ability of the (Z)-5-decenyl acetate receptor to differentiate between enantiomers depends on the position of the methyl substituent. For analogs methyl substituted in the 2, 4, or 8 position, no differences in the activities of the enantiomers could be observed. In contrast, the enantiomers of the 3- and 7-methyl analogs display a significant difference in the activities, theR-enantiomers being more active than theS-enantiomers. From an analysis of the structure-activity results of the enantiomers of the 4,7-dimethyl-substituted analogs, the chiral sense of the alkylchain of the natural pheromone component on binding to its receptor could be deduced.Schiff., Lepidoptera: Noctuidae.     

Systemic Induction of Allelochemicals in Glanded and Glandless Isogenic Cotton by Spodoptera exigua Feeding

Induction of systemic resistance to feeding of beet armyworm, Spodoptera exigua, was investigated in two isogenic lines of Stoneville 213 cotton, Gossypium hirsutum, that differed in the presence of pigment glands. In laboratory bioassays, larvae strongly preferred to feed on glandless cotton plants when presented a choice between undamaged terminal leaves of undamaged glanded and glandless plants. Feeding damage inflicted by S. exigua larvae on the two oldest leaves of glanded plants seven days prior to feeding bioassays caused larvae to prefer by 33-fold the undamaged terminal foliage from undamaged plants compared to that from damaged plants. Feeding damage on glandless plants caused only a 2.6-fold greater preference for terminal foliage from undamaged plants over foliage from previously damaged plants. Extracts of terminal foliage from glanded cotton damaged seven days earlier had significantly greater quantities of terpenoid aldehydes (hemigossypolone, gossypol, and heliocides) than did foliage from undamaged glanded plants. Terpenoid aldehydes were undetectable in extracts of both undamaged and previously damaged glandless plants. The profile of volatile compounds collected from the headspace of mechanically damaged terminal leaves of undamaged glanded and glandless plants differed. Both cotton isolines released large quantities of lipoxygenase products (hexenyl alcohols, acetates, and butyrates), but glandless plants released only small amounts of mono- and sesquiterpenes compared to glanded plants. Glandless plants damaged seven days prior to volatile collection released significantly greater quantities of lipoxygenase products, -ocimene, and - and -farnesene than did undamaged glandless plants. Previously damaged glanded plants released significantly greater quantities of all mono- and sesquiterpenes and hexenyl acetates and butyrates, but not alcohols. The relative importance of volatile compounds versus terpenoid aldehydes in induced feeding deterrence in cotton to S. exigua larvae is still unclear.