Q235钢在海洋铁细菌作用下的腐蚀行为研究

采用开路电位、电化学极化曲线、电化学阻抗谱(EIS)等方法研究了海洋铁细菌作用下Q235钢的腐蚀行为与腐蚀机理。扫描电子显微镜(SEM)形貌分析结果表明有大量的杆状铁细菌附在Q235钢铁表面。在海洋微生物的影响下,Q235钢的开路电位变小,腐蚀倾向与腐蚀率变大。EIS结果表明在海洋铁细菌作用下Q235钢的交流阻抗模值减少,而且大大降低了Q235钢的极化电阻和表面膜的电阻。微生物的附着促进了钢材表面的溶解,使其表面氧化膜层消失,进而形成了疏松不致密的生物膜层,从而加速了其腐蚀进程。     

有机/无机缓蚀剂在模拟混凝土孔隙液中对钢筋缓蚀作用对比研究

目的检测和评价五种有机/无机缓蚀剂在含3.5%NaCl的模拟混凝土孔隙液(SCP)中对Q235碳钢的缓蚀效果。方法采用动电位极化曲线和电化学交流阻抗谱(EIS)测试方法。结果综合评价后可知,0.0015 mol/L的D-葡萄糖酸钠具有最好的缓蚀效果,浸泡30 d后的Rct可达到282.7^4×104Ω·cm^2,此时的IE为99.99%,对Q235碳钢在模拟海水混凝土孔隙液中的腐蚀具有最佳应用价值。结论各缓蚀剂均存在最优浓度/配比,可使钢筋在含Cl-的SCP溶液中的点蚀电位(Eb)和电荷转移电阻(Rct)显著提高,且缓蚀效率(IE)随浸泡时间的延长而增大。     

黑色金属材料在长江淡水中的腐蚀行为

通过现场暴露试验,获得了2种碳钢、3种不锈钢及1种不锈钢与碳钢复合板材料在武汉长江淡水中的4年腐蚀试验结果,总结了它们的腐蚀行为。结果表明,Q235和16Mn碳钢在武汉长江中有较高的腐蚀率和明显的点蚀,稳定腐蚀率为0.055 mm/a;暴露4 a,奥氏体不锈钢304和316L没有明显腐蚀,而马氏体不锈钢430有较明显的点蚀和缝隙腐蚀;马氏体不锈钢0Cr13Ni5Mo与Q345C复合钢板在长江淡水中使用4 a后,0Cr13Ni5Mo发生严重的点蚀,说明马氏体不锈钢在淡水中的应用应慎重。     

黑色金属材料在长江淡水中的腐蚀行为

通过现场暴露试验,获得了2种碳钢、3种不锈钢及1种不锈钢与碳钢复合板材料在武汉长江淡水中的4年腐蚀试验结果,总结了它们的腐蚀行为。结果表明,Q235和16Mn碳钢在武汉长江中有较高的腐蚀率和明显的点蚀,稳定腐蚀率为0．055mm／a;暴露4a,奥氏体不锈钢304和316L没有明显腐蚀,而马氏体不锈钢430有较明显的点蚀和缝隙腐蚀;马氏体不锈钢0Crl3Ni5Mo与Q345c复合钢板在长江淡水中使用4a后,OCrl3Ni5Mo发生严重的点蚀,说明马氏体不锈钢在淡水中的应用应慎重。     

两种不锈钢在冷却塔冷凝酸液中的耐蚀性能

目的分析304不锈钢和316L不锈钢在电厂冷却塔内海水及烟气形成的模拟冷凝酸液环境中的耐蚀性能。方法利用浸泡试验和电化学试验方法测试两种不锈钢在模拟冷凝酸液中的腐蚀形貌、腐蚀率和极化曲线。结果 304不锈钢在模拟冷凝酸液中的耐蚀性能较差,其腐蚀率及钝态稳定性受冷凝酸液pH值的影响较大;316L不锈钢在模拟冷凝酸液中的耐蚀性能较好,其腐蚀率及钝态稳定性受冷凝酸液pH值的影响较小。结论 316L不锈钢在冷却塔冷凝酸液中的耐蚀性能明显优于304不锈钢。     

海水中阴极极化对X80钢应力腐蚀及氢脆敏感性的影响

目的研究不同p H值海水中阴极极化对X80管线钢应力腐蚀及氢脆的抑制作用。方法采用慢应变速率拉伸试验、电化学测试、微观组织观察等分析方法。结果 X80钢在天然海水中的析氢电位约为-940m V(vs.SCE,下同),海水p H为3.5时析氢电位发生正移。其应力腐蚀敏感性与极化电位有很大关系,随着极化电位负移,X80钢的氢脆敏感性增加。天然海水中当极化电位负于-950 m V时,断口出现准解理断裂特征形貌。在-1050 m V极化电位下,钢材进入氢脆断裂区发生脆性断裂。海水p H为3.5时,-900 m V钢材有发生氢脆的危险。结论与天然海水相比,X80钢在p H为3.5的酸性海水中具有较高的应力腐蚀敏感性,两种海水介质中X80钢的应力腐蚀敏感性均随极化电位负移而增加。     

钢铁材料在黄河三门峡水库中的腐蚀行为

目的获取典型钢铁材料在黄河三门峡水库中长期暴露的腐蚀结果和腐蚀行为。方法采用暴露腐蚀试验,将1种碳钢、3种低合金钢和3种不锈钢材料在三门峡水库中暴露1,2,5,8 a,用金相显微镜测量各材料的点蚀深度,观察腐蚀形貌,并计算其腐蚀速率。结果在三门峡水库中暴露8 a,碳钢和低合金钢的腐蚀行为基本相同,4种钢暴露1 a的平均腐蚀速度接近,为0.047~0.050 mm/a,暴露1~8 a,Q235B的平均腐蚀速度为0.040 mm/a,X70,X80和D36钢的平均腐蚀速度与Q235B相差不大,分别为0.039,0.034,0.037 mm/a。暴露1 a后,0Cr13表面有蚀点,最大点蚀深度为0.010 mm,暴露8 a后,0Cr13试样的边角、钻孔处出现溃烂、穿孔。暴露8 a后,304和316L的最大点蚀深度均小于0.1 mm。结论 Q235B,X70,X80,D36在黄河三门峡水库中的腐蚀行为基本相同,它们在第1年的腐蚀速度较大,暴露1 a后腐蚀速度略有降低。0Cr13腐蚀严重,暴露8 a,发生腐蚀溃烂、穿孔现象。304和316L在三门峡水库中有很好的耐蚀性。     

45#钢和Q235在不同水环境中的腐蚀行为研究

目的研究碳钢在不同水环境条件下的腐蚀行为。方法通过开展45#钢及Q235两种典型的碳钢材料在淡海水交替、海水及淡水自然环境下2年的暴露试验,将三种环境下材料的腐蚀形貌、腐蚀速率进行对比,总结3种材料在不同水环境下的腐蚀规律,对其腐蚀机理进行了简要的探讨,并对其长周期的腐蚀行为进行预测。结果对45#钢来说,淡海水环境对其的影响是海水环境下的92%,淡水环境的影响是海水环境下的46%;对Q235来说,淡海水环境对其的影响是海水环境下的88%,淡水环境的影响是海水环境的53%。结论碳钢在海水环境下耐蚀性最差,在淡海水交替自然环境下次之,在淡水环境下的耐蚀性能最好。     

几种合金涂层在变电站土壤中的腐蚀行为研究

目的研究Al,Al Si,Ni Al,316L不锈钢四种合金涂层在变电站土壤及其溶液中的腐蚀行为。方法采用高速电弧喷涂方法在Q235钢表面上分别制备纯Al,Al Si,Ni Al,316L不锈钢合金涂层,通过对四种涂层钢在湖南220 k V毛家塘变电站中进行埋样和土壤溶液里的电化学实验,研究四种涂层在变电站土壤及其溶液中的耐蚀性能,并利用扫描电子显微镜(SEM)和X射线电子能谱(EDS)对埋样的腐蚀产物进行观察和分析。结果 Al Si涂层具有最好的耐土壤腐蚀性,其次是Ni Al涂层和316L不锈钢涂层,而纯铝涂层长时间埋地容易鼓泡,耐土壤腐蚀性不佳。结论四种合金涂层显著提高了Q235钢的耐蚀性,可用于接地网材料防腐。     

两种不锈钢在港口海水环境中的腐蚀行为和规律研究

目的研究304和316L不锈钢在我国不同港口海水全浸区浸泡不同周期后的腐蚀规律。方法进行港口海域实海全浸试验,利用三维视频拍摄、质量损失分析及图像处理等手段,对比分析不锈钢在青岛、舟山、三亚港口海水全浸区的腐蚀形貌、腐蚀速率、腐蚀深度和海生物附着面积。结果两种不锈钢表面以点蚀和缝隙腐蚀为主,304不锈钢表面还产生严重的隧道腐蚀。不同港口海水中,304和316L不锈钢的腐蚀速率均较低,316L不锈钢的耐蚀性优于304不锈钢。三港口海域不锈钢表面形貌的差异明显,三亚试样表面海生物附着最多,舟山试样表面附着大量泥沙,三亚港口海域不锈钢的腐蚀速率小于舟山港口海域。结论不同港口海水环境对不锈钢表面海生物种类及附着面积的影响显著,而不锈钢表面状态直接影响其腐蚀形貌。     

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.