Ionic imbalance due to hydrogen carbonate from Asian dust

In an attempt to identify the ionic imbalance, hydrogen carbonate, HCO₃⁻ (bicarbonate), was determined together with the commonly determined nine major ions because the imbalance was frequently encountered in the chemical analysis of samples with high pHs. Titration method was applied for the determination of the samples with pH higher than 5.6. These samples amounted to 102 of the 1536 samples collected in Hokkaido, Northern Japan, from April 1998 to December 2002. Of the 102 samples, 74 (Group A) showed an acceptable ion balance without including HCO₃⁻. In the other 28 (Group B), however, inclusion of HCO₃⁻ successfully improved the ion balance. These results suggested that hydrogen carbonate was a potential candidate for explaining the imbalance. The hydrogen carbonate concentrations showed a strong correlation with the corresponding non-sea salt calcium (nss-Ca²⁺) concentrations, which implied that hydrogen carbonate was derived from calcium carbonate particles incorporated into falling raindrops or cloud droplets. For Group A, the relationship between hydrogen carbonate and the nss-calcium ion concentration was very similar to that for commonly suspended particles in Hokkaido. On the other hand, Group B exhibited a stronger but significantly different correlation. To the samples of Group B, a back-trajectory analysis was applied to demonstrate that the samples were associated with aerosol travelling from Northern China or Mongolia, which indicated that alkaline aerosol affected the chemistry. In consideration of these findings, the current standard of the ion balance should be critically reviewed for modification in regard to the contribution of hydrogen carbonate not only in source areas but also in receptor areas of alkaline aerosol.     

测定双酚A的流动注射化学发光法研究

在鲁米诺-高碘酸钾化学发光体系中加入双酚A,可以抑制该体系的化学发光,据此建立了双酚A的流动注射化学发光监测分析新方法。该法的线性范围为6 0×10-6～1 0×10-3g L,检测限为1 3×10-7g L。方法可用于水体中双酚A的测定。     

Activities of alkaline phosphatase in first trimester chorion biopsy tissue

We have determined the activity of alkaline phosphatase in chorionic villous tissue obtained in the first trimester of pregnancy, in order to obtain the normal range of values as a prerequisite for application to the prenatal diagnosis of the rare bone disease hypophosphatasia. The activities found were a combination of intestinal and liver/bone/kidney types; traces of placental type were present in only one sample.     

高锰酸钾与接触氧化协同除锰及硬度对除锰效果的影响

针对日益严重的地表水锰污染，本实验采用高锰酸钾与接触氧化的方法协同除锰；通过调配进水中Ca²⁺、Mg²⁺含量模拟我国不同地区硬度差异显著的地表水，探究水体硬度对锰的去除效果的影响.结果表明：Mn²⁺被高锰酸钾氧化并形成"锰质活性滤膜"，可在停药后实现稳定有效除锰.成熟滤池的除锰效果会显著受到硬度的影响，进水硬度在40、200、400 mg·L^-1及700 mg·L^-1（CaCO₃计）时，接触氧化滤池分别在48、56、64 d及72 d实现稳定除锰，而4根滤柱对Mn²⁺去除的极限浓度分别为1.8、1.7、1.2 mg·L^-1及0.7 mg·L^-1.     

重铬酸钾法测定化学需氧量的几点体会

重铬酸钾法是测定工业废水中化学需氧量的国家标准方法，通过大量的实验对CODCr的实验进行探索，提出几点体会，在CODCr的测定中有一定的实用性。     

切割钢渣活化过硫酸盐降解偶氮类染料酸性红73

切割钢渣是钢铁生产过程中的固体废弃物,如何有效处理和利用这些废渣具有减少环境污染、实现废物资源化的重要意义.本文选择河北邢台钢铁厂中切割钢渣为过硫酸盐(PS)活化剂,活化过硫酸盐(PS)去除水相中偶氮染料酸性红73(AR73),实验表明,25 mg·L~(-1) AR73在15 min内,其降解率为99.9%,TOC矿化率达58.6%.同时考察了钢渣投入量、PS浓度、初始pH值等影响因素对AR73降解效率的影响:随着PS浓度、钢渣投入量的增加,AR73的降解速率也逐渐增加;在pH为3～9时,AR73均可被有效去除,酸性条件更有利于AR73的去除.活性自由基猝灭实验表明,酸性红73的降解是通过自由基和非自由基两种机制实现的,且钢渣可多次回收重复利用.钢渣活化PS技术,还可有效去除蒽醌类染料(活性蓝19),其去除率为99.9%,矿化率可达92.0%;同时该技术对某印染废水(COD_(Cr)=5625 mg·L~(-1))的去除率达49.9%.本文所构建的切割钢渣活化过硫酸盐(PS)技术可应用于偶氮印染废水的处理,实现"以废治废"的目标.     

MERCK公司COD试剂的替代品开发

德国MERCK公司制造的COD测定仪器在我国环保行业、科研院所的水质监测工作中应用广泛,但配套试剂价格昂贵,限制了该仪器的使用。实验设计了高量程(100～1500mg/L)和低量程(25～100mg/L)COD替代试剂的开发方案。通过实验,确定了两个量程下COD替代试剂中K2Cr2O7、H2SO4-Ag2SO4、HgSO4的浓度和投加量以及测试方法。实验结果表明,在高量程和低量程范围内,使用COD替代试剂的测试结果与MERCK公司配套试剂的测试结果比较相符,反应时间也可缩短至30min。     

湖泊、水库水的强化混凝除藻的试验研究

就高锰酸钾复合药剂强化混凝对湖泊、水库水中藻类的去除进行了研究，试验表明：投加一定量的高锰酸钾复合药剂可显著提高水中藻类的去除率。将经与预氯化、预投加高锰酸钾除藻工艺进行比较，表明高锰 酸钾复合药剂强化混凝除藻效率明显优于传统预氯化、预投加高锰酸钾除藻工艺。     

溶济萃取法处理含硫酸及硫酸盐的废水

采用溶剂萃取法处理含硫酸及硫酸盐的工业废水，主产优质农用硫酸钾，副产氯化铵和氮钾复合肥，整个工艺过程基本无三废排放，实现了对该废水的综合有效治理。     

高铁酸钾对水中藻类及其次生嗅味污染物二甲基三硫醚同步去除研究

模拟高藻期碱性水源水,采用高铁酸钾对水中以颤藻和二甲基三硫醚为代表的藻类及微量嗅味污染物进行同步控制研究.在高铁酸钾与聚合氯化铁(PFC)单独混凝对藻类的控制效果对比的基础上,展开了高铁酸钾与高锰酸钾预氧化-PFC联用方法对藻类及嗅味污染物的控制效果对比,探讨了pH、预氧化时间和浊度等条件对控制效果的影响.结果表明,PFC单独混凝除藻率最高为90.6%,以Fe计的等量投加条件下,高铁酸钾控藻效果较PFC混凝好,除藻率可达92.4%.高锰酸钾对PFC具有强化混凝效果,可明显提高除藻率(94.5%).高铁酸钾较高锰酸钾预氧化对二甲基三硫醚的去除效果理想,且氧化时间大大缩短,高铁酸钾氧化时间1 min可去除92.5%二甲基三硫醚,高于高锰酸钾预氧化10 min后达到的去除率(74.6%).