等离子喷涂 YSZ 涂层瞬态超高温冲蚀性能研究

目的研究等离子喷涂YSZ涂层的瞬态超高温烧蚀性能。方法借助超音速火焰喷涂设备实现超高温高速火焰,对等离子喷涂YSZ涂层进行瞬态冲蚀,通过火焰中加送氧化铝颗粒模拟对涂层的高温冲刷。采用常规手段评价涂层的抗瞬态超高温冲蚀性能,并对冲蚀部位进行微观观察,探讨涂层的失效机理。结果在3000 K、不添加砂粒的条件下,火焰冲击3 s后钢基体材料表面发生沸腾;喷涂0.6 mm YSZ的试样在火焰冲击60 s后涂层完好。在3000 K、添加砂粒的条件下,火焰冲击3 s后钢基体材料被冲刷出约1.0 mm深坑;喷涂0.6 mm YSZ试样的涂层被火焰冲刷剥落,但基体未受明显损伤;喷涂1 mm YSZ的试样,试验后仍保留部分涂层。结论在3000 K高温瞬态冲蚀条件下,热喷涂1 mm厚YSZ涂层可对材料表面形成有效防护。     

等离子喷涂耐高温抗氧化涂层的研究进展

利用等离子喷涂技术在工件表面制备抗高温氧化涂层,能显著提高工件的抗氧化性能。综述了目前国内外抗高温氧化涂层和热障涂层的研究现状。详细介绍了金属间化合物和MCrA lY两种耐高温抗氧化涂层的组织性能及其抗氧化原理。阐述了影响热障涂层性能的3种主要因素,分析了热障涂层由于热生长氧化层(TGO)的存在而引起的失效机制。指出了等离子喷涂制备耐高温抗氧化涂层存在的主要问题,并提出了几种解决思路,展望了等离子喷涂制备抗氧化涂层的应用前景。     

Cf/SiC 复合材料表面 HfO2涂层的制备及其抗热冲击性能研究

目的研究等离子喷涂条件下Cf/SiC复合材料表面HfO_2涂层的物相、显微组织及其抗热冲击性能。方法通过水热合成和喷雾造粒制备出HfO_2粉体,并利用等离子喷涂在Cf/SiC复合材料表面制备HfO_2涂层,研究涂层的物相、显微组织和抗热冲击性能。结果水热合成的纳米HfO_2为单斜相结构,颗粒的平均粒径为10~15nm;等离子喷涂制备的HfO_2涂层组织中存在微裂纹和孔隙,涂层为单斜相结构,且经1350℃热处理后涂层的相结构未发生改变。等离子喷涂的HfO_2涂层与Cf/SiC复合材料基体结合良好,未观察到涂层、基体间界面分离的现象。经1350℃、50周次的空冷热冲击试验后,涂层未发生破坏失效;在1350℃水冷热冲击条件下,热循环20次时涂层表面出现剥落,27次时脱落面积50%。结论通过等离子喷涂制备的HfO_2涂层与Cf/SiC复合材料基体结合良好,涂层能够抵御1350℃空冷、50周次热冲击,且未发生破坏失效,涂层的1350℃水冷热循环寿命达27次。     

低压等离子喷涂制备ZrB2-TiC复合涂层 及其烧蚀性能研究

目的探索低压等离子喷涂制备ZrB_2-TiC复合涂层工艺及其烧蚀性能。方法采用喷雾造粒技术制备适用于低压等离子喷涂的ZrB_2-TiC球形粉体,再采用低压等离子喷涂技术在高强石墨基体表面制备ZrB_2-TiC复合涂层。利用氧-乙炔火焰考核涂层的抗烧蚀性能,采用红外测温仪测试烧蚀过程中涂层的表面温度,分别采用扫描电镜、EDS及XRD分析涂层的表截面形貌、元素及物相。结果 ZrB_2-TiC复合涂层呈等离子喷涂层状结构特征,内部孔隙率达到10.8%,涂层与高强石墨之间的结合强度约5.4 MPa。喷涂后涂层产生了ZrTiB4、ZrTiC2新相。涂层经过2000℃氧乙炔烧蚀5min后,保持完整,未出现裂纹及剥落,烧蚀深度仅为2～5μm。结论采用低压等离子喷涂可在石墨表面制备性能优良的ZrB_2-TiC复合涂层,涂层可有效抵御氧乙炔火焰的烧蚀。     

ZrO2掺杂对La2Ce2O7力学和热物理性能 影响的研究

目的提高La_2Ce_2O_7(LC)陶瓷材料的断裂韧性。方法采用固相反应方法合成Y_2O_3稳定ZrO_2(YSZ)掺杂的La_2Ce_2O_7(LC)陶瓷材料(LCZ),研究LCZ块材的弹性模量、断裂韧性等力学性能,以及热膨胀系数、热传导率等热物理性能。结果 10%YSZ摩尔分数掺杂的LCZ块材的断裂韧性约为1.4 MPa·m1/2,比LC提高了近10%。YSZ掺杂有效地抑制了LC在200～400℃温度区间热膨胀系数下降的现象。在200～1200℃温度范围内,LCZ块材的热膨胀系数为10×10-6～12×10-6K-1,在1200℃的热导率约为0.75W/(m·K),比YSZ降低了50%以上,显示了优异的隔热性能。结论 YSZ的掺杂使LC中部分Zr4+取代了La3+,降低了晶格中的O空位浓度,原子的横向剪切运动被削弱,有效地抑制了LC在200～400℃温度区间热膨胀系数下降的现象。由于t-ZrO_2→m-ZrO_2的相变对微裂纹的愈合作用,10%YSZ掺杂使LC块材的断裂韧性得到有效提高。     

YSZ-W复合涂层的制备及抗烧蚀性能研究

目的在TC4表面制备均匀致密的YSZ-20%(体积分数)W(ZW2)复合涂层,以提高其抗烧蚀性能,并对其在超音速燃流中的烧蚀响应机制进行初步探究。方法以8YSZ和W粉为原料,采用喷雾干燥-真空烧结工艺制备喷涂用ZW2复合粉末,利用大气等离子喷涂技术(APS)制备ZW2复合涂层,采用超音速火焰冲刷法(SCF)测试涂层的抗烧蚀性能。结果在1500℃的真空环境下烧结2 h后,ZW2复合粉末原始颗粒之间的结合方式由PVA交联结合转变为冶金结合,烧结粉末的松装密度和流动性较造粒粉末分别提升632.3%和39.8%。APS制备的ZW2涂层的孔隙率为9.5%±0.8%,经SCF考核5 s后,500μm厚的ZW2涂层可以使TC4钛合金基体免于烧蚀,仅在ZW2涂层表面形成了厚度约为30μm的ZrO2-WO3疏松顶层。结论利用APS工艺可以制备均匀致密的ZW2复合涂层,真空烧结处理提高了ZW2复合粉末的APS工艺适应性。ZW2涂层有效地提高了TC4的抗烧蚀性能,烧蚀过程中低熔点WO3的形成缓解了烧蚀过程中涂层内部的热应力,从而避免了涂层提前剥落失效。     

超级爆炸喷涂镍基钴基涂层高温氧化及摩擦磨损性能

目的针对装备向高温高速发展的需求,开展NiCr-Cr_3C_2、CoMoCr及NiCr Al Y涂层的高温摩擦磨损性能对比研究。方法针对上述三种涂层,通过超级爆炸喷涂工艺进行涂层制备,并测试涂层孔隙率、显微硬度、结合强度等基本性能,开展650℃/260 h的抗氧化试验和400、650℃的销盘式摩擦磨损试验,对比涂层的各项性能和在高温条件下的氧化质量增量、摩擦系数、磨损质量损失。结果抗氧化试验后,NiCr-Cr_3C_2、CoMoCrSi及NiCrAlY涂层氧化增重0.18、0.1、0.005 mg/(cm~2·h)。650℃时,摩擦系数分别为0.5、1.0、0.6。结论超级爆炸喷涂工艺制备的涂层组织、结合强度均优于等离子喷涂等常规喷涂工艺。高温下的氧化产物Co_3O_4与Cr_2O_3对高温摩擦系数有不同的影响。NiCr-75Cr_3C_2和NiCrAlY涂层在400、650℃可作为与SG37A材料的对磨副材料。     

大气等离子和超音速火焰喷涂CoCrAlYSi-hBN涂层组织和性能对比

目的 针对航空发动机叶片榫头/榫槽摩擦副工作中的微动磨损问题,开展CoCrAlYSi-hBN抗微动磨损涂层研究.方法 通过大气等离子(APS)和超音速火焰(HVOF)喷涂工艺,制备CoCrAlYSi-hBN涂层,采用扫描电镜(SEM)研究涂层的形貌和微观组织,采用显微硬度计和拉伸试验机测试涂层的显微硬度和结合强度,采用SRV试验机探究涂层的摩擦磨损性能.结果 APS喷涂CoCrAlYSi-hBN涂层熔化更充分,显微组织均匀,具有更多高含量的hBN和孔隙;HVOF喷涂CoCrAlYSi-hBN涂层显微组织具有明显的层状结构,涂层致密,hBN和孔隙含量少;APS喷涂CoCrAlYSi-hBN涂层的硬度平均值为168.4HV0.3,结合强度平均值为44.6 MPa,远小于HVOF喷涂CoCrAlYSi-hBN涂层的硬度(327.1HV0.3)和结合强度平均值(59.5 MPa).相比HVOF喷涂CoCrAlYSi-hBN涂层,APS喷涂CoCrAlYSi-hBN涂层虽然有更低的摩擦系数(0.75),但涂层磨损更严重,涂层磨痕表面有明显的涂层剥落,HVOF喷涂CoCrAlYSi-hBN涂层磨痕则出现更多的犁沟.结论 HVOF喷涂工艺制备的CoCrAlYSi-hBN涂层的综合性能优于APS喷涂CoCrAlYSi-hBN涂层,在摩擦过程中,两种工艺制备的CoCrAlYSi-hBN涂层都会转移到对偶件上,从而减少对偶件的磨损,有作为叶片榫头抗微动磨损涂层的潜力.     

爆炸喷涂制备BaF2+CaF2+Cr3 C2/Ni-Cr涂层的组织及性能

采用爆炸喷涂工艺制备出BaF2＋CaF2＋Cr3C2／Ni—Cr涂层,为找到粉末性质对涂层性能的影响关系,利用XRD衍射分析、光学显微分析、扫描电镜分析、能谱分析及显微硬度分析等方法研究对比了不同种类粉末制备出的涂层的形貌、成分及显微硬度。研究结果表明,BaF2＋CaF2＋Cr3C2／Ni—Cr粉末在爆炸喷涂制备涂层的过程中氟化物会有损失,涂层中的Ca元素和Ba元素的质量分数低于其在粉末中的质量分数;包覆型粉的沉积效率高于机械混合型粉,前者制备的涂层中氟化物含量稍高于后者。     

Gd2O3-NiO 共掺对钇稳定氧化锆材料热物理性能的影响

目的研究Gd_2O_3-NiO共掺对钇稳定氧化锆材料热物理性能的影响。方法采用高温固相反应法制得Gd_2O_3-NiO共掺YSZ陶瓷材料。分别利用XRD、扫描电镜观察、激光导热仪、傅立叶红外光谱仪对陶瓷材料的晶体结构、微观结构、热扩散系数及红外透过率进行表征,并对其热导率进行分析。结果 Gd_2O_3-NiO共掺YSZ后,陶瓷材料单斜相含量减少,室温至1300℃的热导率相比YSZ降低,在2.5~5μm波长范围内红外透过率降低。结论 Gd_2O_3-NiO共掺对YSZ陶瓷材料热导率的影响机理为掺杂Gd_2O_3和NiO导致YSZ中单斜相(M)、四方相(T)和立方相(C)含量发生变化,同时YSZ晶格发生畸变。对YSZ辐射传热的影响机理为通过在YSZ中掺杂过渡金属元素Ni使陶瓷材料吸收特定波长的光,进而有效地降低在2.5~5μm短波长的红外透过率,降低其高温下的红外辐射传热。     

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.