无线家庭网络印制倒F型天线的分析与设计

从电波传播机理出发,分析室内电波的退极化现象,研究WHAN对天线的极化、辐射及阻抗匹配特性的特殊要求.从传输线理论入手,推导出印制IFA输入阻抗的解析式,并据此分析其输入阻抗随其水平分枝长度变化的规律.根据印制IFA各分枝的电流分布特性,得出其空间辐射电场的解析式,从而证明其辐射既具有等向特性又具有交叉极化特性.仿真印制IFA各尺寸参数变化对其输入阻抗和谐振频率的影响效果,给出其规律及设计方法,并设计出一例适用于蓝牙WHAN的小尺寸印制IFA.测试结果表明,在2.4GHz频率附近,电压驻波比为2.0时的带宽约为490MHz,可完全覆盖蓝牙的工作频段2.400~2.484GHz,而且所测方向图也进一步印证该天线确实具有等向辐射特性和交叉极化特性.此外,该天线可与蓝牙模块合为一体,其各种蓝牙产品均已商用,并获江苏省科技进步一等奖.     

燃烧源PM2.5微粒润湿性能

利用W ashburn动态渗透压力法研究了燃煤电厂与垃圾焚烧发电厂PM2.5微粒的润湿性能及其与微粒形态和组分的关系,并考察了添加润湿剂(十二烷基苯磺酸钠(SDBS)、十二烷基硫酸钠(SDS)、JFC、FS-310、Silanol w22)对水润湿燃烧源PM2.5的改善作用.利用扫描电镜和X-射线能谱分析了微粒的形态和化学组分.结果表明:微粒的形态和组分对润湿性能有较大影响,垃圾焚烧发电厂PM2.5微粒的水润湿性能优于燃煤电厂PM2.5;不同润湿剂改善燃烧源PM2.5微粒润湿性的效果与微粒特性密切相关,SDS,Silanol w22可明显改善燃煤电厂PM2.5微粒的润湿性能,而FS-310,JFC则对垃圾焚烧电厂PM2.5微粒有显著改善作用;研究结果可为利用蒸汽相变提高燃烧源PM2.5脱除效果及湿法除尘提供重要基础.     

膜生物反应器净化污水的硝化反硝化性能

比较了膜生物反应器(MBR)和传统活性污泥工艺(CAS)在相同运行条件下处理生活污水的硝化和反硝化性能.结果表明,MBR对NH4 -N和TN的去除率分别比CAS高54.8%和37.3%.2种工艺的亚硝化、反硝化作用均呈零级反应,对应降解速率常数MBR分别约为CAS的2.2倍和2.5倍;CAS中硝化作用为零级反应,而MBR中硝化作用随时间推移趋于平缓.MBR中的细菌总数、硝酸菌、亚硝酸菌和反硝化菌数量分别比CAS工艺中相应菌种高1~2个数量级.通过控制曝气强度或减小回流通道断面限制缺氧区溶解氧质量浓度,可提高MBR中的反硝化效果.     

超启发式DE算法求解零等待发酵工艺调度

为解决具备间歇过程特点的零等待发酵工艺调度过程中易变质的难点,提出了一种超启发式差分算法,并将最小化最大完工时间设置为优化目标。此算法分为2层,高层为改进的自适应差分进化算法,来对低层的启发式操作进行选择排序。而低层组合排序成了新的算法对问题域进行操作,加入模拟退火算法避免陷入局部最优。所提出的方法具有学习的机制,对不同问题具有较强的泛化能力。通过测试算例和实际生产进行算法的比较和求解验证了此算法的有效性,结果表明所提出的算法比传统的启发式算法性能更优。     

Study on the application of active balancing device to solve the vibration problem for the rotor with bending fault

The rotor with bending faults that occurrs on the rotating machinery usually vibrates seriously. This paper investigates to apply the active balancing device on a flexible rotor with bending faults to solve the vibration problem. Two problems are studied by finite element method firstly： Where the balance actuator is fixed on the shaft and how much the balancing capacity of the active balancing device is needed. The experiment is then carried out on the test rig, which consists of a flexible rotor with bending faults. The test results indicate that the bending rotor peak vibration response can be decreased from 550~m to 40~tm below by using the active balancing device. The peak vibration response decreases approximately by 93 %. The synchronous vibration due to the rotor bending faults can be controlled effectively by using ac- tive balancing device. The active balancing device is especially adapted to solve the problem caused by thermal distortion with time-variation and randomness, which is varied with working conditions, thus it has good practical value in practice.     

基于GIS、GPS、GSM的救护车智能管理系统研究

文章提出了一种救护车智能管理系统。该系统基于GIS、GPS、GSM技术,它能在发生紧急事故时,提供救护车到达出事地点,再从出事地点到达最近医院的最佳路径,该系统能够使救护车始终处于监控之下。我们通过设计有效的数据结构和算法来实现系统的上述功能。     

德士古渣油气化系统数学模拟

对德士古渣油气化系统进行了过程分析,建立了单元设备物料和热量衡算的数学模型,提出了计算气化炉微量组分的方法。运用序贯模块法对该系统进行了稳态模拟计算,结果同设计值和工厂值吻合较好。     

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

We defined the genetic landscape of balanced chromosomal rearrangements at nucleotide resolution by sequencing 141 breakpoints from cytogenetically interpreted translocations and inversions. We confirm that the recently described phenomenon of 'chromothripsis' (massive chromosomal shattering and reorganization) is not unique to cancer cells but also occurs in the germline, where it can resolve to a relatively balanced state with frequent inversions. We detected a high incidence of complex rearrangements (19.2%) and substantially less reliance on microhomology (31%) than previously observed in benign copy-number variants (CNVs). We compared these results to experimentally generated DNA breakage-repair by sequencing seven transgenic animals, revealing extensive rearrangement of the transgene and host genome with similar complexity to human germline alterations. Inversion was the most common rearrangement, suggesting that a combined mechanism involving template switching and non-homologous repair mediates the formation of balanced complex rearrangements that are viable, stably replicated and transmitted unaltered to subsequent generations.     

A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis

To identify susceptibility loci for ankylosing spondylitis, we performed a two-stage genome-wide association study in Han Chinese. In the discovery stage, we analyzed 1,356,350 autosomal SNPs in 1,837 individuals with ankylosing spondylitis and 4,231 controls; in the validation stage, we analyzed 30 suggestive SNPs in an additional 2,100 affected individuals and 3,496 controls. We identified two new susceptibility loci between EDIL3 and HAPLN1 at 5q14.3 (rs4552569; P = 8.77 × 10(-10)) and within ANO6 at 12q12 (rs17095830; P = 1.63 × 10(-8)). We also confirmed previously reported associations in Europeans within the major histocompatibility complex (MHC) region (top SNP, rs13202464; P < 5 × 10(-324)) and at 2p15 (rs10865331; P = 1.98 × 10(-8)). We show that rs13202464 within the MHC region mainly represents the risk effect of HLA-B*27 variants (including HLA-B*2704, HLA-B*2705 and HLA-B*2715) in Chinese. The two newly discovered loci implicate genes related to bone formation and cartilage development, suggesting their potential involvement in the etiology of ankylosing spondylitis.     

A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia

Non-obstructive azoospermia (NOA) is one of the most severe forms of male infertility. Its pathophysiology is largely unknown, and few genetic influences have been defined. To identify common variants contributing to NOA in Han Chinese men, we performed a three-stage genome-wide association study of 2,927 individuals with NOA and 5,734 controls. The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)). These findings implicate genetic variants at 1p13.3, 1p36.32 and 12p12.1 in the etiology of NOA in Han Chinese men.