离子色谱法测定工业废水中丙酸

建立了用离子色谱法测定工业废水中丙酸的方法,结果表明,常规阴离子对本方法的测定没有干扰,校准曲线线性相关系数高,并且能在很大范围内呈现线性。运用该方法实测标样和水样,精密度和准确度都能满足需求,表明该方法测定结果可靠,具有一定的应用价值。对实际废水样品进行分析,丙酸的回收率分别为95．0％～103．8％。本方法分析速度快,所需样品量少,且无需要复杂的前处理,简便、灵敏、可靠。     

离子色谱法同时测定工业废气中丁酸和异丁酸

建立了用离子色谱法测定有组疲废气和无组织废气中丁酸和异丁酸的新方法。对实际废气样品进行分析,丁酸和异丁酸的回收率分别为93．0％～103．3％和94．0％～104％。本方法分析速度快,所需样品量少,且无需要复杂的前处理,简便、灵敏、可靠。     

乌鲁木齐近十二年(1997~2009)降水中化学组分变化趋势分析

通过对乌鲁木齐市近12年(1997~2009)降水的化学组分分析,表明大气环境中的年际pH值在6.04~7.42间波动。∑阴离子所占百分比约为∑阳离子2倍。SO^2-₄和Ca²⁺分别是阴离子和阳离子中占比重最大的离子,直接影响降水的化学性质。近年来,SO^2-₄在阴离子中所占比重呈下降趋势,而NO^-₃则逐年增加,说明乌鲁木齐市在控制燃煤型污染方面采取的措施取得了一定效果,而机动车尾气污染日益加重,大气环境中各阴离子的组分比例在不断变化。     

甲胺、二甲胺及三甲胺的气相色谱测定

采用气相色谱法、大口径毛细管柱分离了甲胺、二甲胺、三甲胺.用氮磷检测器(NPD)检测,得到了良好的分离效果和很高的灵敏度,检测限可达0.025mg/L.同时,对甲胺类在NPD和氢火焰离子化检测器(FID)上的灵敏度作了比较,发现甲胺类物质在NPD上的灵敏度大大高于FID,因此,前者特别适用于检测环境试样中低含量甲胺类有机物的监测.     

Use of polymeric sub-micron ion-exchange resins for removal of lead, copper, zinc, and nickel from natural waters

This research investigated the removal capacity of polymeric sub-micron ion-exchange resins(SMR) for removal of lead, copper, zinc, and nickel from natural waters in competition with natural organic matter(NOM). Polymeric SMR particles were created and tested to ensure that they were adequately dispersed in the solution. They removed little NOM(10%or less) from river water and wastewater, indicating that competition from NOM was not a major concern. SMR were able to remove 82% ± 0.2% of lead, 46% ± 0.6% of copper, 55% ±20% of zinc, and 17% ± 2% of nickel from river water spiked with 500 μg/L of each. Similarly,in wastewater, they were able to remove 86% ± 0.1% of lead, 38% ± 0.8% of copper, 28% ± 1%of zinc, and 11% ± 1% of nickel.     

Determination of carazolol in pharmaceutical formulations by gas‐liquid‐chromatography (GLC)

A gas‐liquid‐chromatographic procedure for the quantitative determination of authentic carazolol and carazolol in tablets (Conducton^(R)?) has been described. Carazolol in tablets was extracted with absolute alcohol before injecting onto the gas Chromatograph. The concentration range adopted varied between 0.2 mg to 1.0 mg/ml of carazolol in alcohol solution. The results obtained were 97.6%±3.2 and 98.4%±2.6 for the stated and added amounts respectively.     

Organochlorine insecticide residues in Egyptian mothers’ milk

Two hundred ninety‐two mother's milk samples were collected during 1994 from ten Egyptian governorates representing rural, metropolitan, and newly reclaimed desert areas. The samples were analyzed for 14 organochlorine insecticides and metabolites using electron capture gas chromatography and confirmed by gas chromatography/mass spectrometry (GC/MS). The overall samples average showed that the most abundant organochlorine insecticide residues were p,p'‐DDE, α‐endosulfan, β‐HCH and, p,p’‐DDT. Residues in the range of not detectable to less than 14μg/l whole milk were recorded for α‐HCH, heptachlor, heptachlor epoxide, aldrin, dieldrin, endrin endrin aldehyde and p,p'‐DDD. The percentage of samples exceeding the acceptable daily intake for children (ADIs) set by the FAO/WHO ranged from 19% to 44% in all governorates included in the study except the governorate of Minia in which only 2.6% of the samples exceeded the ADI values. The insecticides exceeding ADI values are mostly heptachlor and heptaclor epoxide (ADI = 3.12 μg/1 whole milk).     

The effect of Oja-titun market effluent on the chemical quality of receiving OPA reservoir in Ile-Ife, Nigeria

The effect of market effluent from the Oja-titun market in Ile-Ife, Nigeria on the chemical quality of the Opa Reservoir located 3.5 km downstream was investigated between February and November 2000. Water samples were collected in February, May, August and November from 16 sites, four along each of the market drainage channels (MDC), market stream, tributary stream and the Opa River and Reservoir. The peak level of each variable-biochemical oxygen demand, temperature, total alkalinity, Na(+), K(+), Ca(2+), Mg(2+), PO(4)(3+), SO(4)(2+), Cl(-), NO(3)(-), Pb and Zn-occurred at the MDC, and decreased significantly downstream, except pH, conductivity and dissolved oxygen, which increased. Seasonal fluctuation in most variables was pronounced. Generally, there were high values in the early dry and dry seasons and low values in the rainy and early rainy seasons. Comparison of the reservoir water with international limitation standards for drinking water supply showed that the quality of the reservoir water was very low and that treatment required to achieve minimum limitation standards for drinking water would be both intensive and expensive. The study concluded that the stream borne effluent from the market impacts significantly on the chemical quality of the reservoir water although other tributaries within the Reservoir's catchment are other possible sources of pollutants in the reservoir.     

Alkaline Degradation of Cellulose: Mechanisms and Kinetics

Cellulose powder and softwood sawdust were subjected to alkaline degradation under conditions representative of a cementitious environment for periods of 7 and 3 years, respectively. During the first 3 years, sampling was frequent, and data on the degradation of cellulose and production of isosaccharinic acid was used for establishing long-term prediction models. Samples after an additional period of 4 years were compared to the predicted values. The total rate of degradation was measured as the increase in total organic carbon (TOC) in corresponding solutions. A previously published theoretical model of degradation kinetics gave a good approximation of the present experimental data. Peeling-off, stopping, and alkaline hydrolysis reaction rate constants were obtained as model parameters, and the results suggested that the transformation of the glucose end group is the rate-limiting step in the cellulose peeling-off reaction and also determines the pH dependence of that reaction. After 3 years, isosaccharinic (ISA) acid represented 70–85% of all degradation products as quantified by capillary zone electrophoresis. The long-term prediction model indicated that all of the cellulose would be degraded after only 150–550 years. The control sampling after 7 years points toward a lower degradation of cellulose and production of ISA than predicted by the model, reflecting either a degradation of ISA that was faster than the production or a termination of the ISA production.     

离子色谱法测定植物叶片中氟的探讨

植物叶片中氟的测定一般采用离子选择电极法,离子色谱法对其测定还鲜见报道,本文对用离子色谱方法测定植物叶片中的氟进行了探讨。