Investigation of low-molecular weight organic acids and their spatiotemporal variation characteristics in Hongfeng Lake, China

The identities and concentrations of low-molecular-weight organic acids (LMWOAs) were determined by ion chromatography throughout a 20-m water column in Hongfeng Lake, China. The spatiotemporal variations of LMWOAs and their contributions to dissolved organic matter (DOM) in a research period of 24 hr were also investigated. The results demonstrated that five LMWOAs (lactic, acetic, pyruvic, sorbic, oxalic acid) were detected, and their total concentration and proportion in DOC were 6.55 μmol/L and 7.47%. Their average levels were 2.50, 0.65, 2.35, 0.96 and 0.09 μmol/L, respectively. LMWOAs were higher during daytime (10:00-18:00 on Jun 13, 2008) than nighttime (21:00-6:00 the next morning), in particular 4.99 μmol/L high in the epilimnion ( 1 m water depth), reflecting the fact that direct import from terrigenous sources and photochemical production from humic materials were dominant during LMWOAs’ origin and accumulation. The same factors caused LMWOAs to be 0.63 μmol/L in the epilimnion higher than in the hypolimnion. The rapid decrease of total organic acid (TOA) up until 18:00 mainly resulted from bio-uptake and mineralization in the hypolimnion (>1 m water depth). Pyruvic acid increased with time in the epilimnion and decreased in the hypolimnion, largely related to the two contrary processes of continuous degradation and synthesis of macromolecular organic matter during life materials’ cycle mediated by organisms. Simultaneously, plankton behavior and thermal stratification played a pivotal role in LMWOAs’ behavior in the water column, causing decreasing and increasing profiles. The distribution of LMWOAs represents an interesting resource for biogeochemical research of DOM in aquatic ecosystems.     

Preparation of MgO/B2O3 coatings by plasma spraying on SUS304 surface and effects of heat-resistant

This study mainly deals with the preparation of MgO/B₂O₃ coatings by plasma spraying on the SUS304 surface and the effects of heatresistant. The power materials of low thermal conductivity were selected to control the heat divergent performance of high temperature parts. The reticular micro-structure between the cover thermal layer and the substrate was prepared by using the plasma spraying method. The powder mixture of MgO and B₂O₃ were selected as spraying materials and the SUS304 was used as the substrate material. The MgO/B₂O₃ coating was prepared on the surface of the SUS304 to provide better cover thermal performance. The properties of the microstructures and the morphologies were studied by Optical Microscope, Scanning Electron Microscope, Electron Probe Microanalyzer, and X-ray Diffraction. The results showed that the cover thermal performance has been improved.     

航空发动机叶片高应力振动疲劳试验技术研究

在电动振动台上对航空发动机叶片进行了高应力振动疲劳试验,详细研究了试验机理,提出了辅助点监测叶片最大振动应力、共振峰后定频率激励等试验方法,并成功利用振动台开环控制技术有效稳定了叶片的振动应力水平,从而获得可靠的疲劳数据。另外,从试验角度出发,对振动台激励与叶片振动应力响应之间的关系进行了研究。     

热脱附-气相色谱-质谱法测定环境空气中5种挥发性卤代烃

建立热脱附-气相色谱-质谱联用测定环境空气中三氯甲烷、四氯化碳、三氯乙烯、四氯乙烯、溴仿等5种挥发性卤代烃的分析方法。该方法在一定浓度范围内工作曲线线性良好,相关系数均在0．9990～0．9998之间,加标回收率在94．0％～106．6％之间,RSD为2．18％-7．62％,检出限为0．22μg／m3～0．30μg／m3。该方法具有操作简单、分析快速、准确度高、灵敏高的特点,用热脱附-气相色谱-质谱联用测定环境空气中5种挥发性卤代烃,结果令人满意。     

硫酸羟胺的自加速分解温度和稳定性研究

通过快速筛选热分析试验对硫酸羟胺热危险性进行定性分析,对其热分解过程进行初步研究,获得温度、压力变化规律;再运用C80微量热仪对硫酸羟胺进行深入分析,得到硫酸羟胺的化学反应动力学参数,根据Semenov模型计算其自加速分解温度（SADT）。试验结果表明：由RSD初步筛选试验得到硫酸羟胺在164．2℃时即发生分解放热;用C80法得到硫酸羟胺的起始热分解温度为137．1℃,并计算了该物质在3种典型包装下的自加速分解温度。由SADT得到储存、运输过程中硫酸羟胺的控制温度,从而为减少硫酸羟胺事故的发生提供必要的参考数据。     

搭接结构件腐蚀疲劳试验技术

腐蚀疲劳试验是评估腐蚀环境对结构件疲劳寿命影响的有效方法。从试验件设计、疲劳载荷谱加载方式、典型腐蚀环境的施加、试验数据的处理原则等方面对搭接结构件腐蚀疲劳试验技术进行了较全面的介绍。     

预腐蚀铝合金材料裂纹萌生寿命评估

铝合金在航空工业中广泛应用,因此对于铝合金构件的寿命评估很重要。利用扫描电子显微镜(SEM)原位观测技术,研究了预腐蚀铝合金试件在循环应力作用下的疲劳裂纹萌生和扩展行为。结果表明腐蚀坑对于裂纹萌生扩展行为具有强烈的影响。基于局部应变法,提出了一种预测带有腐蚀损伤的铝合金疲劳裂纹萌生寿命的评估公式。     

基于人体皮肤热模型的热防护服评价方法研究

在热防护服热防护性能测试装置基础上,用自行研制的新型耐高温模拟皮肤传感器代替铜片热流计测量通过应急热防护服装面料的热流量,将热流量作为热波皮肤模型边界条件,得到人体皮肤表层下80μm处的温度值,从而得到一定条件下人体真实皮肤达到二级烧伤所需时间,用其评价热防护服用织物的热防护性能,并将热波皮肤模型(TWMBT)的测试值与Pennes模型以及铜片热流计的测试结果进行分析比较。采用热波皮肤模型分析织物层下的"皮肤"防热时间更接近实际皮肤达到二级烧伤时间值,可较为精确的量化织物热防护性能,为应急救援热防护服装的热设计提供理论依据。     

污水污泥间壁热干燥实验研究

研究了污泥间壁热干燥的工艺过程,分析了其工艺参数、冷凝水水质和产生的污染气体,探讨了有机物水解机理.结果表明,污泥含水率与停留时间呈负指数函数相关.收集到的干燥冷凝水属高浓度有机废水,其总有机碳（TOC）、挥发性有机酸（VFA）和氨氮（NH₃-N）浓度均很高,pH值保持在9～9.5.干燥冷凝水中挥发性有机酸和氨氮来源于2部分：低温110 ～130℃时,主要发生蛋白质的水解,生成有机酸和氨氮;高温140～150℃时,主要发生脂肪类的水解,生成有机酸.干燥温度低于150 ℃时,污泥间壁热干燥过程无污染气体产生.     

酸和热处理对海泡石结构及吸附Pb2+、 Cd2+性能的影响

通过X射线衍射、傅里叶变换红外光谱及比表面积分析等研究了酸和热处理对天然海泡石结构的影响,并考察不同处理后的海泡石样品吸附重金属Pb2+、Cd2+性能.结果表明,海泡石比表面积均随盐酸浓度、处理时间的增加而略有增大,而结构无明显变化,0.5 mol·L-1 HCl处理时,天然海泡石中的CaCO3未能被完全去除,6.0 mol·L-1 HCl处理72 h时,海泡石比表面积达到最大301.47 m2·g-1.盐酸热处理并不能提高海泡石的比表面积,也不会使海泡石结构产生明显变化.不同类型酸处理对海泡石比表面积提高顺序依次为:HCl>HNO3>H2SO4;海泡石经焙烧后比表面积迅速下降,由100℃的21.44 m2·g-1下降到900℃的0.17 m2·g-1.重金属吸附实验表明,盐酸处理浓度和时间对海泡石吸附Pb2+、Cd2+离子性能无明显影响;不同酸处理对海泡石吸附Pb2+、Cd2+离子性能存在一定影响,H2SO4处理后海泡石对Pb2+、Cd2+离子吸附量明显高于HCl和HNO3处理.海泡石焙烧处理后对Pb2+离子吸附量无明显影响,但对Cd2+离子吸附量在焙烧700℃以上时增加明显.