基于重要抽样法的耐压球壳可靠性计算方法研究

目的 解决耐压球壳极小失效概率的可靠性计算问题。方法 在自适应Kriging的基础上,结合重要抽样法提出耐压球壳可靠性计算方法。该方法在较大失效概率下构建的Kriging模型基础上获得重要方向,在重要方向上计算得到较低失效概率下的设计点,以设计点为中心,构建小失效概率的Kriging模型,并通过此模型采用重要抽样法开展可靠性计算。结果 分别使用提出的重要抽样法和蒙特卡洛法计算了2个算例的失效概率,计算结果表明,该方法具有较高的精度和效率。使用该方法对某耐压球壳工作载荷下的失效概率进行了计算,计算得到该球壳失效概率为4.094×10^–96。结论 研究结果可为无失效方程下极低失效概率的可靠性计算问题提供参考。     

超高压深海环境下多结构并行疲劳试验技术研究

针对全海深载人潜水器2只载人舱缩比球壳模型的疲劳试验,通过理论方法对比分析了压差法与外压单独作用下球壳的应力状态,验证了超高压深海环境下内外压差法模拟球壳作业环境的可行性。同时,为降低球壳外部交变载荷对试验设备的损伤,并有效缩短试验时长,提出一种计及超高压深海环境下采用内外压差法开展的多结构并行疲劳试验技术。根据该试验技术进行了近7 000个循环周期的双球串联疲劳试验,有力地保证了全海深载人潜水器的研制周期。试验结果表明,该试验技术长期有效可靠,可为同类型试验提供技术依据和应用参考。     

Fluid30单元在同轴圆柱壳固有特性计算中的适用性分析

目的分析Fluid30单元用于内侧含环形间隙流体同轴圆柱壳固有特性计算的适用性。方法针对内侧含环形间隙流体的同轴圆柱壳模型,分别基于"Fluid30单元"和"理论流体附加质量"对壳体固有特性进行分析。通过变间隙宽度对比计算,探究壳体固有特性随无量纲半径比的变化规律,分析波动方程离散化对计算结果的影响,判定Fluid30单元的适用范围。结果半径比与固有频率之间呈非线性关系,半径比越小,壳体固有频率越低,固有频率随半径比变化率越大。波动方程离散化引起的误差随半径比减小而增大,以相对误差10%作为Fluid30单元适用性判别标准,(1,2)壳式频率对应的临界半径比为1.20,(1,3)壳式频率对应的临界半径比为1.03,其他壳式频率对应的临界半径比小于1.001。结论不同阶频率的Fluid30单元适用范围不同,当半径比小于临界值时,相关频率应基于理论流体附加质量迭代计算。     

提高深盲孔壳类零件温冲压模具寿命的措施

采用合理的模具结构、选择合适的模具材料、采用适宜的热处理工艺和表面强化工艺以及提高模具的加工质量等都可以显著提高温冲压模具的使用寿命。分析了超高强度钢制深盲孔壳体温冲压成形时,模具的工作条件及其失效形式,提出了能有效提高该壳体温冲压模具寿命的具体措施。     

毛细管气相色谱法测定椰子壳水解液中的糖

采用衍生化—萃取法处理含糖样品 ,毛细管气相色谱测定糖的方法 ,测定了椰子壳水解液中糖的含量。结果表明 ,该方法简便、可靠 ,方法的相对标准偏差小于 5 %     

柱壳液力成形弹性稳定性分析

利用非线性弹性稳定性理论 ,分析研究了壳体液力成形工艺中的开口圆柱壳弹性稳定性问题。计算结果表明不仅非线性弹性临界载荷远低于线性弹性临界载荷 ,而且更重要的是内压很大程度上有助于提高柱壳轴向弹性临界屈曲载荷 ,这样为内高压成形工艺提供了弹性失稳理论依据     

显像管玻壳铅尘在大气中的迁移扩散规律和污染特征

以石家庄市显像管玻壳厂排放的铅尘为研究对象，通过在该玻壳厂周围土壤表层布点采样，较系统地研究了铅尘在大气中的迁移转化规律及其污染特性。研究结果表明，用高斯模式能成功地预测铅尘在大气中的迁移扩散规律。     

Optimizing process parameters for the adsorption of phosphorus from synthetic wastewater on coconut shell based activated carbon

Activated carbon was prepared from coconut shell, an agricultural waste, for the removal of phosphorus from synthetic phosphorus‐containing wastewater. The activated carbon obtained from the coconut shell was characterized using Fourier‐transform infrared (FTIR) spectroscopy. Batch mode experiments were conducted to study the effects of pH, particle size, adsorbent dosage, and sorption time on the adsorptive potential of the prepared activated carbon. Response surface methodology was employed to study the interactions among the variables and to optimize the process conditions for the maximum removal of phosphorus using the coconut shell–based activated carbon (CNS). The characterization results from the FTIR showed the presence of variety of functional groups, such as ?OH, ?NH, C=O, C?H, C?N, CH₃, and CH₂, which explains the CNS's improved adsorption behavior on the colloidal particles. A maximum performance of 95.22% was obtained for CNS at the optimum conditions of adsorbent dosage = 1,000 milligrams (local variable), pH 2 (local variable), particle size = 0.2 millimeters (local variable), and sorption time = 4.2 hours (global variable).     

麻疯树籽壳生物质炭的制备及对六价铬离子的吸附研究

以麻疯树籽壳为原料经磷酸活化后炭化处理制备了生物质炭吸附剂。以六价铬离子为目标对象,考察了磷酸浓度、活化时间、炭化温度、炭化时间等制备条件对生物质炭吸附六价铬离子的能力,并探讨了生物质炭的投加量、溶液pH值等工艺条件对六价铬离子吸附能力的影响。结果表明:在磷酸浓度为2 mol/L,活化18 h,600℃下炭化1.5 h时所制得的生物质炭在投加量为5 g/L、溶液pH值为3时对铬离子的吸附效果最佳,铬离子去除率为74.5%。     

Synthesis of carbon-coated magnetic nanocomposite (Fe3O4@C) and its application for sulfonamide antibiotics removal from water

The occurrence of antibiotics in the environment has recently raised serious concerns regarding their potential threat to human health and aquatic ecosystem. A new magnetic nanocomposite, Fe304@C （Fe304 coated with carbon）, was synthesized, characterized, and then applied to remove five commonly-used sulfonamides （SAs） from water. Due to its combinational merits of the outer functionalized carbon shell and the inner magnetite core, Fe3O4@C exhibited a high adsorption affinity for selected SAs and a fast magnetic separability. The adsorption kinetics of SAs on Fe304 @ C could be expressed by the pseudo second-order model. The adsorption isotherms were fitted well with the Dual-mode model, revealing that the adsorption process consisted of an initial partitioning stage and a subsequent hole-filling stage. Solution pH exerted a strong impact on the adsorption process with the maximum removal efficiencies （74% to 96%） obtained at pH 4.8 for all selected SAs. Electrostatic force and hydrogen bonding were two major driving forces for adsorption, and electron-donor-acceptor interactions may also make a certain contribution. Because the synthesized Fe304@C showed comprehensive advantages of high adsorptivity, fast magnetic separability, and prominent reusability, it has potential applications in water treatment.