试论攀钢基地的矿产资源体系

攀钢基地位于康淇地轴中段两侧边缘一个古裂谷带中。裂谷带地质构造复杂,成矿条件优越,形成储量丰富、种类齐全的矿产资源,其中钒、铁地质储量名列全国第一,钛矿资源居世界之首,钒矿占世界第三位,铁矿仅次于鞍本地区,名列全国第二位。 攀钢基地矿产资源体系由核心资源(铁矿和炼焦煤)和辅助原料资源(动力煤、熔剂石灰岩、白云岩、耐火粘土、菱镁矿等)构成。在核心资源中,以攀西铁矿运在六盘水和以六盘水的炼焦煤运在攀钢,构成钟摆式运输系统。基地矿产资源体系和钟摆式运输,基本上能满足攀钢基地对矿产资源的要求。 攀钢基地矿产资源体系和攀西—六盘水之间钟摆式运输系统的形成,决定了攀钢二基地必须建在攀西(渡口至西昌)地区。否则,将造成不良后果。     

贵金属氧化物阳极电解处理乙醇模拟废水的研究

采用热分解法在钛基体上制备了5种电极，并分别对乙醇模拟废水进行电解以降低COD值，研究了电极中SnO2含量对降低乙醇模拟有机废水COD的影响，并探讨了其机理。     

Emissions of intermediate volatility organic compound from waste cooking oil biodiesel and marine gas oil on a ship auxiliary engine

Ship auxiliary engines contribute large amounts of air pollutants when at berth.Biodiesel,including that from waste cooking oil(WCO),can favor a reduction in the emission of primary pollutant when used with internal combustion engines.This study investigated the emissions of gaseous intermediate-volatile organic compounds(IVOCs) between WCO biodiesel and marine gas oil(MGO) to further understand the differences in secondary organic aerosol(SOA) production of exhausts.Results revealed that WCO exhaust exhibited similar IVOC composition and volatility distribution to MGO exhaust,despite the differences between fuel contents.While WCO biodiesel could reduce IVOC emissions by 50% as compared to MGO,and thus reduced the SOA production from IVOCs.The compositions and volatility distributions of exhaust IVOCs varied to those of their fuels,implying that fuel-component-based SOA predicting model should be used with more cautions when assessing SOA production of WCO and MGO exhausts.WCO biodiesel is a cleaner fuel comparing to conventional MGO on ship auxiliary engines with regard to the reductions in gaseous IVOC emissions and corresponding SOA productions.Although the tests were conducted on test bench,the results could be considered as representative due to the widely applications of the test engine and MGO fuel on real-world ships.     

压载舱锌阳极失效原因分析及实验室研究

目的 找到压载舱锌阳极失效原因,并提出整改方案。方法 对服役环境进行调研、阳极化学成分检测、电化学性能检测以及阳极表面形貌检测。结果 干湿交替以及高温的环境是造成锌阳极发生钝化的主要原因。在干湿交替环境下,阳极腐蚀表面晶粒松散,晶界宽度大,发生晶间腐蚀和晶粒脱落,造成了阳极失效。结论 通过该项目的实验研究,得出了锌阳极的适用条件,在干湿交替的环境以及高温环境(50 ℃)下,不推荐使用锌阳极,建议使用铝阳极。     

投加FeSO4对序批式生物膜反应器中DHA、EPS和处理效果的影响

针对化学协同生物除磷过程,研究了序批式生物膜反应器(SBBR)中FeSO_4对悬浮相活性污泥脱氢酶活性(DHA)、胞外聚合物(EPS)及系统处理效果的影响.结果表明,少量FeSO_4对DHA和EPS的分泌具有促进作用,但最佳投加量不一致,分别为0.10 mmol·L-1和0.20 mmol·L-1;大量的FeSO_4则会引发抑制.FeSO_4投加量少于0.30 mmol·L-1时会使污泥MLVSS、MLVSS/MLSS增加,超过0.30 mmol·L-1时则使MLVSS、MLVSS/MLSS下降,但MLSS和SVI随着FeSO_4投加量的增加分别持续增加和下降.FeSO_4对COD和TN的去除具有抑制作用,但并不显著,去除率分别在77%和72%左右;TP的去除效果明显改善,在投加量为0.30 mmol·L-1时效果最好.投加FeSO_4协同生物除磷时建议最佳投加量为0.30 mmol·L-1,此时污泥DHA被轻微抑制,但污泥浓度、EPS、TP去除率均已达到最大,出水水质满足一级A排放标准.     

电容器阳极铝箔工艺研究现状与发展

论述了影响中高压铝电解电容器用高纯铝阳极箔立方织构比例及力学性能的各种因素,分析了阳极箔生产过程中均匀化退火、热轧、预备退火、成品退火等工艺过程对立方织构及综合性能的影响,提出了提高阳极箔性能的工艺发展方向。     

洗涤剂富磷污染及其对策

介绍了国内湖海水域富磷污染的现状,指出含磷洗涤剂的使用是造成富磷污染的主要原因,提出了解决富磷污染的对策及适合中国国情的洗涤剂发展方向。     

抛石环境中铝合金阳极性能评价及其对海底隧道钢壳保护效果评估

目的 解决埋覆介质中牺牲阳极电化学性能评价的不确定性,实现非匀质介质中牺牲阳极电容量测试结果的评价和对比.方法 模拟沉管隧道埋覆的环境介质,对铝合金牺牲阳极的电容量和溶解形貌进行评测.为区别于现有的海水等匀质介质中阳极的检测方法,建立非匀质介质中铝阳极电化学性能评价方法.另外,在上述埋覆介质中,测定阳极和阴极的极化曲线,修正仿真计算的边界条件,有利于模拟这种高电阻率介质环境下阴极保护电位分布.结果 测试箱所测电阻率与商用便携式电导率仪测定精度相当.A1阳极在低电阻率的海水中(25～40?·cm)性能稳定,电容量稳定在2500 A·h/kg,溶解性能良好;在40?·cm海淡水+回填石的混合介质中,电容量测试值数据波动大,重现性差.B1阳极在海水(25～40?·cm)中的电容量和A1阳极相当,未见到差异,在40?·cm海淡水+回填石混合介质中,电容量数值分散性小,电化学活性高.结论 混合介质中的评价试验体现了海淡水、混合介质电阻率和回填石对阳极溶解产物阻滞的综合效应,提高了抛石环境中铝阳极寿命评估的准确性,尤其适用于沉管隧道钢壳用铝合金阳极电化学性能评价和牺牲阳极保护效果评估.     

阳极材料对苯酚废水处理效果的影响研究

应用自制电化学反应器研究了不同阳极材料对苯酚废水的电催化氧化处理效果的影响.实验结果表明,在相同的实验条件下,钛基RuO2和钛基SnO2种新型阳极处理苯酚废水的电催化氧化效果要远好过传统的阳极材料石墨.     

Dechlorination of carbon tetrachloride by the catalyzed Fe-Cu process

The electrochemical reduction characteristics of carbon tetrachloride (CT) were investigated using cyclic voltammetry in this study. In addition, the difference in reduction mechanisms of CT between Master Builders' iron and the catalyzed Fe-Cu process was discussed. The results showed that CT was reduced directly on the surface of copper rather than by atomic hydrogen produced at the cathode in the catalyzed Fe-Cu process. The reduction was realized largely by atomic hydrogen in Master Builders' iron. The entire CT in 350 ml aqueous solution with 320 mgL was reduced to trichloromethane and dichloromethane in 2.25 h when 100 g of scrap iron with FeCu ratio of 10:1 (ww) were used. Moreover, the reduction rate slowed with time. CT could be reduced at acidic, neutral and alkaline pH from solution by Fe-Cu bimetallic media, but the mechanisms were di?erent. The degradation rate was not significantly in?uenced by pH in the catalyzed Fe-Cu process; in Master Builders' iron it clearly increased with decreasing pH. The kinetics of the reductions followed pseudo-first order in both cases. Furthermore, the reductions under acidic conditions proceeded faster than that under the neutral and alkaline conditions. The catalyzed Fe-Cu process was superior to Master Builders' iron in treating CT-containing water and this advantage was particularly noticeable under alkaline conditions. The reduction was investigated in the cathode (Cu) and anode (Fe) compartments respectively, the results showed that the direct reduction pathway played an important role in the reduction by the catalyzed Fe-Cu process. The catalyzed Fe-Cu process is of practical value.