高超声速飞行器主动式气膜冷却防热技术研究

目的针对未来高超声速飞行器(飞行速度20 Ma),提出一种主动式气膜冷却防热技术,并计算验证其有效性。方法通过求解三维N-S方程组,采用PARK-1的5组分(N2,O2,N,O,NO)17方程有限速率化学反应模型,考虑了真实气体效应;针对典型的钝头体外形,在头部驻点处构造单个气膜冷却微孔,向外喷射冷却气体,计算了飞行马赫数为20、高度在30 km以下的气膜冷却效率。结果与无气膜冷却相比,有气膜冷却时,气膜孔附近等温壁面(300 K)热流密度的最高降幅约90%,冷却气体有效覆盖面积可达到约孔出口面积的10倍。结论气膜冷却在未来高超声速飞行器防热中具有广阔的应用前景。     

高超声速飞行器翼前缘射流降热研究

目的获得高超声速飞行器翼前缘射流降热机理。方法通过计算流体力学(CFD)方法,针对典型高超声速带翼飞行器开展飞行马赫数为15条件下的射流干扰热环境规律研究,分析无射流翼前缘气动加热特性,确定热流严酷射流开孔区域,分别在翼前缘激波干扰及翼后段布置射流孔,并设计射流流动参数,开展射流总压与来流总压比率在0.002～0.02范围内的流场仿真计算,获得局部流动及表面热流分布特性,针对计算结果进行对比分析。结果随着总压比率逐渐增大,激波干扰以及机翼后段射流孔区域热流均显著降低,降幅达76%～99%。翼中段无射流典型位置总压比率为0.002时热流增高,增幅为11%～24%,随着射流总压增大热流降低,降幅达68%～86%。高射流总压比率局部射流孔前热流增大2倍以上。结论射流影响下降热机理是射流将高温气体推离壁面,局部表面热流显著降低。低射流总压比率亚音速射流作用区域向下游延伸距离短,不会引起局部再附热流增大。高射流总压比率音速射流降热影响向下游明显延伸,增强射流强度可以增加延伸区长度,同时会诱导局部射流孔前再附热流显著增大。     

高超声速飞行器异型气膜孔无喷流热增量研究

目的获取高超声速飞行器气膜孔不喷流时的热负荷增量。方法通过计算流体力学(CFD)方法针对典型高超声速飞行器50km、飞行马赫数为15条件下的无开孔、有开孔气膜冷、有开孔无喷流3种工况开展壁面热流分布研究。结果无开孔的最大热流分布在头部滞止点附近,约为2.2 MW/m~2,有气膜冷却的工况热流最高值在侧面气膜孔没有覆盖到的部位,约为1.4 MW/m~2,有异型孔但是不喷流的工况,热流密度最大值主要分布在开孔附近,最大值大于3.3 MW/m~2。结论对于在高超声速飞行器表面开孔采用气膜冷却方式冷却时,如果由于某种原因气膜孔不喷流,那么在孔的附近乃至整个滞止区域附近的热流负荷将会大幅度升高。     

再入攻角对弹头锥身气动热环境及结构热响应影响研究

目的分析再入弹头锥身气动热环境及结构热响应,研究再入攻角振荡对其影响规律。方法建立基于工程法的气动热/结构热响应耦合计算方法,并采用该方法开展锥身典型位置气动热环境及结构热性计算分析。结果随着再入攻角的振荡衰减,各典型子午面冷壁热流密度曲线围绕90°子午面热流密度曲线振荡,其振幅呈现先振荡增大、后振荡衰减的变化规律。与90°子午面相比,各子午面总加热量均有所增大。再入攻角振荡引起的金属层外壁面温度最大振荡幅值为3K,但对最终时刻结构温度影响较小。结论计算弹道条件下,再入飞行攻角振荡对气动热环境及结构热响应影响较小,可通过增加余量的方式给予考虑。     

高超声速飞行器综合热管理及关键技术研究进展

从高超声速飞行器面临的内外热环境特点、热防护与舱内热管理的需求入手,面对热源增大、热沉受限的现状,提出需对高超声速飞行器舱外热防护与舱内热管理开展综合热管理与一体化设计,并分别针对热防护、舱内热管理以及综合热管理现有技术手段、应用特点以及发展趋势等方面开展综合论述与分析。在此基础上,对美国已经提出的一系列综合热管理计划的发展状况与关键技术点进行了综合论述。最后,从先进热管理单点技术、高超声速飞行器内外一体化耦合设计以及综合热管理系统快速建模与分析3方面分析了高超声速飞行器综合热管理关键技术。     

陶瓷基复合材料连接结构失效分析方法

目的分析陶瓷基复合材料的结构强度。方法围绕C/SiC陶瓷基复合材料连接结构失效分析问题,提出模量突降和渐进损伤两种分析方法,基于Abaqus软件平台编写UMAT有限元分析子程序,结合试验数据分析多种不同失效准则在陶瓷基复合材料结构强度分析中的适用性。结果基于改进三维Hashin失效准则,针对典型C/SiC复合材料连接结构进行了失效行为计算,获得结构的失效模式与试验结果规律一致,破坏载荷的预测误差在10%以内。结论通过与试验结果的对比分析,验证了两种方法的有效性,研究方法能够为高超声速飞行器、天地往返飞行器复合材料热结构的强度分析提供技术支撑。     

SiO2气凝胶隔热性能的影响因素研究

目的 在不同热流条件下,通过调整SiO2气凝胶的孔隙率、涂层厚度等,以满足合适的隔热要求。方法 针对中短程飞行器飞行时外壁面承受短时高热流的特点,在分析孔隙率对SiO2气凝胶热导率影响规律的基础上,通过数值仿真研究不同气凝胶孔隙率、气凝胶厚度及热流作用下的温度响应。结果 得到了不同条件下满足隔热要求的气凝胶最小厚度,以及气凝胶表面的最高温度。高温情况下,气凝胶孔隙率为96%时,有效热导率最低,孔隙率超过96%时,隔热性能变差。结论 当飞行器内壁面温度满足要求时,增大气凝胶的孔隙率,则需要减小气凝胶的厚度,相应的气凝胶表面温度会升高,但升幅很小。当飞行器外壁面承受长时间大热流时,仅调整气凝胶的厚度和孔隙率不能达到结构的隔热要求。     

再入飞行器振动环境工程预示方法

目的为再入飞行器振动环境设计提供方法支撑,并为结构设计和地面环境试验条件制定提供载荷输入。方法分析再入飞行器振动环境主要特征及其诱导因素,结合飞行试验实测振动数据研究小攻角对飞行振动环境的影响规律,辨识出脉动压力与动压、马赫数以及攻角的关系式。在传统脉动压力预测方法基础上,建立涉及攻角影响的再入飞行均方根脉动压力预测模型,并给出再入振动环境工程预示方法。结果构建模型计算的脉动压力变化趋势与实测振动量值变化趋势基本一致,辨识出来的脉动压力与攻角、动压以及马赫数之间的关系式是基本合理的。结论基于实测数据及脉动压力特性建立了再入飞行器振动环境工程预示模型,结合实测振动数据和气动载荷数据可预测出再入飞行器振动环境,能够实现再入飞行器振动环境载荷的精细化设计,并为结构设计提供载荷输入。     

发动机燃烧室内壁材料热环境的气动热试验模拟技术研究

利用超声速矩形湍流导管和等离子电弧加热器模拟了发动机燃烧室内流和高超声速飞行器外壁面外流热环境,进行了平板表面冷壁热流测量和燃烧室内壁材料考核试验。结果表明:由于辐射换热的影响,在选取的两个典型来流条件下,发动机燃烧室内流热环境下的冷壁热流比外流热环境下的高出21%和40%,但是冷壁热流的增量基本相当,约为0.70~0.80MW/m²。随着冷壁热流的增加,辐射换热产生的热流增量的影响力会逐渐减小。材料考核时,相同配方的C/SiC复合材料在内流热环境下的表面温度高出约400℃,背面温度高出约90℃,这种差异对于发动机燃烧室内壁面材料考核至关重要,必须在材料考核试验中加以考虑。      

C/SiC复合材料波纹点阵结构进气道前缘设计与制备

目的 C/SiC复合材料进气道前缘轻量化设计与制备。方法基于进气道气动外形和结构要求,建立波纹点阵夹芯结构的进气道前缘有限元模型,然后按照德国航空中心H2K超声速风洞试验室试验的数据进行反演,得到进气道前缘的热流密度分布,据此进行边界条件加载,在模型中考虑固体导热、表面辐射以及空腔辐射三种传热方式。采用瞬态传热算法,求解100 s下进气道前缘的温度场,为了进一步降低C/SiC复合材料波纹点阵结构进气道前缘的最高温度,设计不同的进气道前缘尖端半径,并进行优化。最后根据优化得到的波纹点阵进气道几何参数,采用PIP法制备出C/SiC复合材料点阵结构进气道前缘。结果进气道尖端半径小于0.5mm时,最高温度高于1800℃,超过C/SiC复合材料极限温度;进气道尖端半径大于1.0 mm时,最高温度为1520℃,低于C/SiC复合材料极限温度;进气道尖端半径大于2.0 mm时,增大半径对降低进气道前缘最高温度没有明显的作用。不同进气道前缘尖端半径下,最高温度达到稳态的时间不一样,半径等于0.5 mm时,进气道前缘达到稳态的时间约为30 s左右。随着前缘尖端半径增大,最高温度达到稳态的时间增加,半径为1.0 mm时,达到稳态时间约为60 s。结论进气道前缘最高温度随着尖端半径增大明显降低,当半径大于2.0 mm时,增大半径对降低进气道前缘最高温度没有明显的作用。     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

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Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.