民航维修系统建立风险管理的探索

中国民航维修系统正在建立安全管理体系,本文介绍了风险管理目的、构建原则并举例说明风险管理的实施步骤。为中国民航维修系统建立风险管理进行了有益的探索。     

浅议AP1000核电建造过程本质安全化

为推进我国核电产业技术水平的整体跨越,实现我国第三代核电AP1000的自主化过程中的安全,国家核电技术公司（以下简称“国家核电”）在建造过程中通过加强从业人员安全培训、企业安全文化建设和依托项目的安全管理,大力提升人的本质安全化水平;广泛采用新技术、改进施工工艺,实行模块化、专业化施工,加大安全基础设施投入力度,强化建造过程中的安全控制,努力打造核电建造过程中物的本质安全;完善安全管理制度,建设安全责任体系和监督体系,持续提高管理上的本质安全。     

阻挡放电光催化净化低浓度含H2S废气试验研究

采用介质阻挡放电光催化方法对低浓度含H2S废气进行试验研究.正交试验结果表明,外加电压对H2S去除率的影响最为显著,其次为初始浓度以及模拟废气停留时间.H2S去除率随外加电压的上升而升高,随初始浓度的增大而降低,随模拟废气停留时间的增长而升高.填料表面负载纳米TiO2光催剂化可有效提高H2S去除率,在外加电压达到22 kV时,有光催化剂比无光催化剂时去除率提高11.9%.研究表明:介质阻挡放电协同光催化净化低浓度含H2S废气能达到85%以上的去除率,且不易产生二次污染.     

单兵用主动式听力保护技术研究现状分析

战场噪声是造成单兵听力损伤的重要原因,通常要求单兵处于大于85dBA的噪声环境中需佩戴听力保护装置。听力保护装置通常包括耳罩式和耳塞式。新型单兵用耳塞式听力保护装置具有听力保护、环境声音的监听、持续及脉冲噪声抑制、通信接入等多种功能。     

1780-1819年华北平原水旱灾害社会响应方式的转变

历史时期水旱灾害的社会响应典型案例重建是气候变化影响与适应研究的重要方向。选取1780-1819年间华北平原发生的4次典型水旱灾害(1785、1792、1813年旱灾及1801年水灾),基于清代档案资料和历史气候重建结果提取代用指标,对其灾情严重程度、政府救灾力度和灾民行为进行了量化描述和对比分析,发现:①4次灾害中赈济密度(赈灾物资数/成灾州县数)逐次下降,1813年旱灾中降至不足1785年旱灾的1/6,政府救灾力度遭到严重削弱;②灾民行为日益失控,从1792年旱灾和1801年水灾中的大规模跨区域迁徙,发展到1813年旱灾中大量加入盗匪和起义军,走向暴力。这一转变的发生,是在自然(气候突变、灾害增多)、社会(政府财政危机、人地矛盾激化)不利背景之下,政府与灾民的互动关系日趋消极的结果。     

我国中东部不同地区冬季颗粒物垂直分布的车载移动观测

利用中山大学环境气象综合观测车（载有3D可视型激光雷达、多普勒风廓线激光雷达、转动拉曼温廓线激光雷达）于2018年冬季在全国范围内（厦门-北京）的走航观测资料,对我国中东部不同地区和城市的边界层结构以及颗粒物分布特征进行了研究.结果表明：(1)在从南向北走航的过程中,边界层内各个高度的温度以及边界层高度呈下降趋势.(2)不同高度发生颗粒物污染的气象成因有所差别,其中1000 m高度左右发生颗粒物污染的主要成因是较高的水平风速将周围地区的颗粒物输送过来而导致;500 m及近地面附近发生颗粒物污染主要是由水平风速较小导致局地来源的颗粒物堆积以及上游地区颗粒物的输送两者共同作用.(3)逆温结构和上升气流会导致颗粒物在边界层顶堆积,而下沉气流使得颗粒物由在某一高度堆积扩散至整层均匀分布.     

新烟碱类农药呋虫胺对映体选择性研究进展

农业生产中,呋虫胺以外消旋体的形式销售和使用,在进入生态环境后出现对映体选择性降解、吸收、代谢、排泄等.不区分对映体间差异的传统风险评估给呋虫胺的合理使用与生态安全带来了诸多隐患.研究指出S-呋虫胺既是高毒体也是高活体,其生态毒性为R-呋虫胺的13.9~145.9倍,但R-呋虫胺也表现出较高的杀虫活性,且作物中优先降解,开发高比例的R体农药有利于维持杀虫活性的同时降低对非靶生物和生态环境的负效应.本文旨在综述呋虫胺对映体选择性生物活性、生态毒性及环境行为研究进展,为其科学难题的解决提供新思路,也为其科学有效管理提供理论依据.     

城市空气质量达标规划的逻辑框架

针对环境空气质量达标规划目前没有明确规划编制的基本要求和主要内容之间的关联原则、未将长期规划方案落实到日常管理方案、过于重视长期空气质量目标与减排情景方案而对污染物减排方案重视不足、未将规划的成本效益分析作为主要方案设计依据等逻辑不清的问题,从人群健康的角度出发,构建达标规划的逻辑框架：提出空气质量目标和人群健康目标相一致的目标体系;设计与空气质量目标一致的污染物减排方案,通过成本效益或成本有效性分析明确优先序,按照重污染日（周）、重污染月、采暖期等优先序实施区域内污染物排放量的绝对减排,并落实到排污许可证中;实施空气质量“日”管理,根据预测模型对未来重污染天气进行污染源排放管理,并对污染源减排方案实施持续动态评估和调整.     

Efficient degradation of Rhodamine B by magnetically recoverable Fe3O4-modified ternary CoFeCu-layered double hydroxides via activating peroxymonosulfate

Environment-friendly nano-catalysts capable of activating peroxymonosulfate (PMS) have received increasing attention recently. Nevertheless, traditional nano-catalysts are generally well dispersed and difficult to be separated from reaction system, so it is particularly important to develop nano-catalysts with both good catalytic activity and excellent recycling efficiency. In this work, magnetically recoverable Fe₃O₄-modified ternary CoFeCu-layered double hydroxides (Fe₃O₄/CoFeCu-LDHs) was prepared by a simple co-precipitation method and initially applied to activate PMS for the degradation of Rhodamine B (RhB). X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller method (BET), and vibrating sample magnetometer (VSM) were applied to characterize morphology, structure, specific surface area and magnetism. In addition, the effects of several key parameters were evaluated. The Fe₃O₄/CoFeCu-LDHs exhibited high catalytic activity, and RhB degradation efficiency could reach 100% within 20 min by adding 0.2 g/L of catalyst and 1 mmol/L of PMS into 50 mg/L of RhB solution under a wide pH condition (3.0-7.0). Notably, the Fe₃O₄/CoFeCu-LDHs showed good super-paramagnetism and excellent stability, which could be effectively and quickly recovered under magnetic condition, and the degradation efficiency after ten cycles could still maintain 98.95%. Both radicals quenching tests and electron spin resonance (ESR) identified both HO? and SO₄^?? were involved and SO₄^?? played a dominant role on the RhB degradation. Finally, the chemical states of the sample's surface elements were measured by X-ray photoelectron spectroscopy (XPS), and the possible activation mechanism in Fe₃O₄/CoFeCu-LDHs/PMS system was proposed according to comprehensive analysis.     

Identification of close relationship between atmospheric oxidation and ozone formation regimes in a photochemically active region

Understanding ozone (O₃) formation regime is a prerequisite in formulating an effective O₃ pollution control strategy. Photochemical indicator is a simple and direct method in identifying O₃ formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O₃ formation. Thus, it may impact accuracy in signaling O₃ formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O₃ formation regimes during a long-lasting O₃ exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O₃ formation regime. Over eastern PRD, O₃ formation was mainly in a NO_x-limited regime when HO₂/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO₂/OH ratio higher than 5 and lower than 2 was indicative of NO_x-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O₃ formation regime by HO₂/OH ratio. In comparison with other commonly used photochemical indicators, HO₂/OH ratio had the best performance in differentiating O₃ formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O₃ formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O₃ pollution over a photochemically active region.