大规模风电接入电网的机组组合问题研究

伴随着风力发电规模的日益增加,风电并网需求量增大,大电网环境下与之相适应的火电机组的启停组合经济调度问题显得特别突出。针对此问题,通过对离散二进制粒子群算法进行优化改进,采用等耗量微增率迭代法整合优化方案,用于解决火电机组启停组合经济调度问题。仿真结果表明:该方案接近最优,在满足电力系统约束条件下得出的机组组合方式能够使得总运行费用最低,能够根据风电具体预测信息,为电网接入的火电机组经济调度提供可靠依据。     

Fe(Ⅱ)、Fe(Ⅲ)和Fe(Ⅵ)活化过硫酸盐氧化降解水中的菲

分别采用Fe(Ⅱ)、Fe(Ⅲ)和Fe(Ⅵ)活化过硫酸盐(PS)氧化降解水中的菲,考察了反应pH、药剂投加量及氧化时间等因素的影响,并对比了不同价态铁活化PS对菲的氧化降解效果.在反应pH为8、n(菲):n(Fe):n(PS)为1:2:2的优化条件下,反应60 min后Fe(Ⅱ)-PS和Fe(Ⅲ)-PS体系对菲的去除率分...     

白腐真菌发酵中胞外蛋白酶对MnP的产生及其稳定性的影响

在摇瓶试验中通过投加4种对应不同蛋白酶的抑制剂,研究了白腐真菌 Phanerochaete chrysosporium 固定化发酵过程中所产的胞外蛋白酶对其MnP的产生以及稳定性的影响.在培养1d后投加 Pepstatin A 可使MnP峰值提高且提前1d出现,而投加PMSF、EDTA后MnP峰值出现时间不变但峰值皆下降;培养4d后投加 PMSF 和Pepstatin A可使MnP酶活提高且稳定性增强;培养过程中投加 HgCl2 均会抑制菌体生长,使 MnP酶活水平较低.在培养1d后直接补人初级蛋白酶浓缩液.MnP 峰值酶活稍有提高.且第3d补入初级蛋白酶浓缩液会使MnP提前1d出现.在离体条件下,EDTA 和 HgCl2均可抑制MnP酶活;初级蛋白酶和次级蛋白酶均会导致MnP不稳定,但投加 PMSF 和 Pepstatin A 后,MnP稳定性增强.以上结果表明,在培养过程中初级蛋白酶部分组分对MnP的产生过程具有促进作用;初级蛋白酶和次级蛋白酶会导致离体MnP迅速失活,且证实其中2种组分--丝氨酸蛋白酶和天冬氨酸蛋白酶--可导致离体MnP不稳定.     

施用农药人员的安全与防护——ASTMF2669《旋用农药人员用防护服性能标准》介绍

本文主要介绍了ASTMF2669-2009《施用农药人员用防护服性能标准》的分级和检测要求、防护服材料性能要求、材料的抗渗透性指标等,并就施药人员的安全与防护以及完善防护服标准体系提出建议．以为我国广大相关领域人员了解标准和应用标准提供帮助．     

分子模拟方法在爆炸反应机理方面的应用进展

针对爆炸过程反应机理异常复杂,实验检测手段对其认识匮乏的现状,综述了量子化学、反应分子动力学等分子模拟方法的特点及研究进展,分析了分子模拟技术在燃爆机理研究中的应用进展,包括量子化学方法对于燃料热解/燃烧、瓦斯等可燃体系爆炸过程的微观基元反应步骤、反应能垒及热力学参数的计算,以及反应分子动力学(ReaxFF MD)在含能材料、可燃混合气等复杂爆炸体系获取可能的反应路径及中间自由基变化的应用。对分子模拟方法在爆炸领域研究的应用提出了建议及展望,指出ReaxFF MD和密度泛函理论(DFT)相结合是一种研究复杂爆炸体系微观反应机理极具潜力的方法,借助先进的分析检测手段对模拟方法的验证及修正,能获取更准确、全面的微观反应动力学模型。     

Acid Orange 7 degradation using methane as the sole carbon source and electron donor

• AO7 degradation was coupled with anaerobic methane oxidation. • Higher concentration of AO7 inhibited the degradation. • The maximum removal rate of AO7 reached 280 mg/(L·d) in HfMBR. • ANME-2d dominated the microbial community in both batch reactor and HfMBR. • ANME-2d alone or synergistic with the partner bacteria played a significant role. Azo dyes are widely applied in the textile industry but are not entirely consumed during the dyeing process and can thus be discharged to the environment in wastewater. However, azo dyes can be degraded using various electron donors, and in this paper, Acid Orange 7 (AO7) degradation performance is investigated using methane (CH₄) as the sole electron donor. Methane has multiple sources and is readily available and inexpensive. Experiments using ¹³C-labeled isotopes showed that AO7 degradation was coupled with anaerobic oxidation of methane (AOM) and, subsequently, affected by the initial concentrations of AO7. Higher concentrations of AO7 could inhibit the activity of microorganisms, which was confirmed by the long-term performance of AO7 degradation, with maximum removal rates of 8.94 mg/(L·d) in a batch reactor and 280 mg/(L·d) in a hollow fiber membrane bioreactor (HfMBR). High-throughput sequencing using 16S rRNA genes showed that Candidatus Methanoperedens, affiliated to ANME-2d, dominated the microbial community in the batch reactor and HfMBR. Additionally, the relative abundance of Proteobacteria bacteria (Phenylobacterium, Pseudomonas, and Geothermobacter) improved after AO7 degradation. This outcome suggested that ANME-2d alone, or acting synergistically with partner bacteria, played a key role in the process of AO7 degradation coupled with AOM.     

不同聚合度的聚磷酸铵灭火性能研究*

为考察聚磷酸铵（APP）干粉灭火剂的聚合度对其灭火性能的影响,选用3种不同聚合度的APP,结合其晶体结构、粒度分布及热性能测试,并通过粉体杯式燃烧器进行小尺寸灭火实验,对比3种样品的灭火性能及灭火机理,研究聚合度与其灭火性能的关系。热性能测试结果显示,聚合度的升高会导致APP的热稳定性下降,随着聚合度从80升至1 500,其初始分解温度从326.11 ℃降低至321.54 ℃,失重率从75.21%增加至79.66%。实验结果表明:随着APP聚合度的增加,火焰降温速率升高,最小灭火浓度（MEC）降低,灭火性能增强,当聚合度为1 500时,MEC为118.143 g/m3。聚合度的升高有助于APP在进入火场后更早、更充分地与火焰发生反应,从而使灭火性能得到提升。     

节能型焦化污水生物脱氮新工艺的生产性试验研究

采用节能型生物脱氮新工艺对黑龙江某焦化厂的污水处理站进行生产性试验研究,结果表明:处理后出水达到GB8978-1996《污水综合排放标准》一级,并可回用于熄焦。该工艺适合推广应用于焦化污水、垃圾渗滤液、养殖、化肥等高含氮有机污水的处理。     

Seasonal and spatial occurrence and distribution of atmospheric polycyclic aromatic hydrocarbons (PAHs) in rural and urban areas of the North Chinese Plain

Passive air sampling (PAS) was employed to study the occurrence of gaseous and particle-bound PAHs in the North Chinese Plain. The averaged concentrations of gaseous and particle-bound PAHs were 485 ± 209 ng/m³ and 267 ± 161 ng/m³, respectively. The PAHs concentrations at urban sites were generally higher than those at rural ones with ratios <1.5 in spring, summer and fall, but differences between them were not significant for the wintertime and annually averaged concentrations. This urban-rural distribution pattern was related to the PAHs emission sources. PAHs spatial variation can be partially (49%) explained by emission with a simple linear regression method. Both the gaseous and particle-bound PAHs were highest in winter and lowest in summer, with winter/summer ratios of 1.8 and 8, respectively. Emission strength was the most important factor for the seasonality.