HNS多点阵列装药慢速烤燃试验研究

研究多点阵列冲击片雷管装药的热安全性。方法针对φ3 mm×3 mm、φ4 mm×4 mm、φ5 mm×5 mm、φ4mm×8mm共四种不同尺寸的HNS多点阵列装药开展慢速烤燃试验研究,得到HNS多点阵列装药在3.3℃/h、5、10℃/min三种不同升温速率下的响应特性。结果同规格装药情况下,随着升温速率的提高,其热烤响应剧烈程度有加剧趋势;同升温速率条件下,试样药量越大,反应剧烈程度有加剧趋势。结论阵列装药有利于分散HNS装药在热烤条件下的热积累,降低热烤试验的响应强度,提升装药的热安全性。     

装药结构热安全性试验方法及其特点分析

目的 在装药结构的热安全性试验时选择合理的加热方法.方法 从燃料、加热速率、温度范围、温度可控性、温区可控性、对试件影响等方面对开放油池火烧、可控喷射火烧、红外辐射灯阵、电加热带、电加热箱等常用的加热方式进行对比分析.结果 对于快烤加载,红外辐射灯阵兼具开放油池火烧和可控喷射火烧的优势,能够实现温度为800～1200℃、升温速率不低于200℃/s、温度控制偏差不大于5％的模拟火烧温度稳定控制,且具备清洁环保的优势;对于慢烤加载,红外辐射灯阵兼具电加热带和电加热炉加载的优势,能够实现温升速率3.3℃/h～1.0℃/min可调节,加热温度不低于400℃,温度分区不低于4个的分区慢速烤燃温度控制,且不会给试样反应等级带来额外影响.结论 合理选择慢烤、快烤加热方式,避免对装药结构的反应等级产生影响,是装药结构的热安全性试验时需重视的一个问题.     

圆孔装药固体火箭发动机的慢速烤燃特性研究

目的 研究圆孔装药固体火箭发动机的慢速烤燃特性.方法 针对装填高能推进剂的固体火箭发动机,建立了二维瞬态慢速烤燃模型.其中AP/HTPB推进剂的化学动力学模型为两步总包反应模型.在升温速率分别为3.6、7.2、10.8 K/h的工况下,进行固体火箭发动机的烤燃数值模拟,并具体分析慢速烤燃工况下固体火箭发动机的传热特性和...     

固体发动机装药热安全性数值分析

目的研究固体火箭发动机遭受火烤时的安全性。方法建立发动机有限元模型,计算推进剂在慢速烤燃和快速烤燃工况下的温度分布和爆炸延迟时间。结果推进剂慢烤47 h后达到临界温度,其值为352℃;快烤推进剂加热697 s后达到临界温度,临界温度为355℃。结论推进剂在快速烤燃模式下的热扩散速率大于慢速烤燃工况下,但是温度梯度则相反。两种工况下推进剂达到临界温度后开始反应的位置不同,推进剂厚度决定了其储热能力。     

PBT基推进剂热分解特性与慢烤行为关系研究

目的 研究PBT(3,3–二叠氮甲基氧丁环–四氢呋喃共聚醚)基推进剂慢速烤燃响应情况与热分解特性之间的关系。方法 采用差示量热扫描仪和慢速烤燃试验,研究推进剂在不同固含量(通过改变高氯酸铵含量来调整)和不同铝粉含量下的热分解温度变化情况,计算不同组分含量下推进剂的热分解动力学参数,对比分析PBT基推进剂固、铝粉含量变化对热分解特性及慢速烤燃行为影响。结果 固含量从78%下降至75%时,配方中AP(高氯酸铵)的高、低温热分解温度和热分解活化能均会下降。铝粉质量分数从18%下降至5%时,配方中AP的高、低温热分解温度和热分解活化能均会下降。当采用78%的固含量时,配方无法通过慢烤试验,而采用75%的固含量,铝粉质量分数为18%、5%时,均能通过慢烤试验。结论 根据热分析及慢烤试验结果可认为,固含量变化对慢烤响应程度变化有较大影响,Al粉含量变化对配方慢烤响应程度的影响较小。影响配方慢烤响应程度主要由AP高温分解控制,AP高温分解活化能越低,越有利于推进剂通过慢速烤燃测试。     

炸药缓慢加热条件实验技术进展

为降低炸药装药意外热刺激起爆后对武器平台、后勤系统和人员损伤的严重程度及概率,适应不敏感弹药发展过程中对炸药热危险性综合评定的需要,有针对性地分析了以美国为主的炸药和弹药装药慢烤燃实验相关文献、STANAG 4382《北约弹药缓慢加热测试标准》调查报告以及西安近代化学研究所开展的密闭系统的模拟弹慢速烤燃实验研究成果。分析结果发现,尚需解决的问题为3.3℃/h温升速率条件起源未知,小型模型实验技术是目前开展的重点,可视化/量化反应状态的实验技术及仿真预测试验反应剧烈程度的模型研究是发展重点,试验反应剧烈性抑制技术研究是未来的发展趋势。     

不同升温速率下模块装药的烤燃特性分析

目的 研究不同升温速率下模块装药烤燃特性的变化.方法 基于模块装药结构及其烤燃化学反应机理,提出基本假设,建立二维非稳态烤燃计算模型,通过数值模拟计算分析研究模块装药在不同工况下的烤燃特性.结果 在3.30、5.25、7.20 K/h的加热条件下,模块装药发生烤燃响应的着火温度分别为476.6、473.1、477.1 ...     

不敏感发射药检测与评估技术研究综述

为了深入研究不敏感发射药,从全尺寸发射药不敏感性能试验、实验室感度试验及小型模拟试验三个方面,综述了发射药在各类刺激源下响应特性检测评估技术的研究进展,重点阐述了具有发射药特点的小型模拟检测手段和方法。如热碎片传导点火试验、小规模慢速烤燃装置试验及发射药床临界直径试验方法等,提出了不敏感发射药检测与评估迫切需要发展的方向。研究发射药小型模拟试验及评估技术,该类方法可研究发射药配方组分、药型等对其敏感性响应规律及机理,有望减少或替代全尺寸发射药装药的外场响应试验;发展适用于发射药多孔离散状结构的试验方法、反应判据及评估标准,促进高能不敏感发射药的研究和应用;开展发射装药对弹药生存能力影响评估技术,结合典型弹药研究装药结构等对其反应等级的影响规律。     

微波辐照程序升温与恒温解吸载甲苯活性炭

利用微波作为加热手段,采用恒温解吸和程序升温解吸两种方法对吸附了甲苯的活性炭进行了解吸研究。两种方法的操作条件分别为:1.恒温400℃;2.程序升温,初始温度及升温幅度均为100℃,每个温度点保持时间10min,终温500℃保持5min。结果表明,微波恒温解吸和程序升温解吸产生的甲苯气体浓度最高可达到56.7g/m3、28.7g/m3;两种解吸方法都可以在45min左右使活性炭达到90%以上的解吸效率。对两种方法的能量消耗进行分析后发现,相比400℃恒温解吸,程序升温解吸的能量消耗可以降低23.7%。     

含能材料热安全性研究进展

分析了国内外关于含能材料烤燃试验和烤燃数值模拟的研究进展,主要是炸药和推进剂等烤燃试验研究成果,以及装填含能材料的弹药系统的烤燃数值模拟研究成果。结果发现,小型含能材料烤燃试验技术是目前烤燃试验开展的重点,其中烤燃过程可视化、烤燃响应程度的量化是烤燃试验的关键技术。小型烤燃试验研究结合烤燃数值模拟是评估弹药系统热安全性的重要方法。针对烤燃数值模型的完善(热-机械-化学耦合烤燃模型)是未来的发展趋势。     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.