同时测定人发中铜,铁,锌的分光光度法测定

本文提出了一种分光光度同时测定铜，铁，锌的新方法，在弱酸性介质及抗坏血酸和乳化剂ＯＰ存在下，以５－Ｂｒ－ＰＡＤＡＰ为显色剂，根据形成的配合光谱特征，选择５４５．５６６和７６０ｎｍ为测定波长，按系数倍率法和两波长标准加入法原理处理测量数据，直接测定了人发中铜，铁，锌的含量，结果满意。     

流动注射荧光分析法用于土壤及水系沉积物中铈（Ⅲ）含量的测定

研究表明Ｃｅ＾３＋在ｐＨ〈６．２ＫＣｌ介质中以２５４．０ｎｍ紫外光激发时，在３５２．０ｎｍ处发出具有恒定强度的荧光。因而可选择ｐＨ５－６作为测定酸度条件，利用Ａｌ２（ＳＯ４）３消除Ｆｅ＾３＋等离子的干扰，建立起Ｃｅ＾３＋的流动注射荧光分析法。方法的线性范围是２．０×１０＾－７—２．０×１０＾－６ｍｏｌ／ｌ，一元回归方程△Ｆ＝６６３６００Ｃ－０．０４１（ｎ＝１０，ｒ＝０．９９９７），检测限６．０×１     

电子受体及中间产物对厌氧氨氧化的影响

研究了厌氧氨氧化混合培养物对不同基质(硝酸盐、亚硝酸盐)的转化特性，确定了氨和硝酸盐、亚硝酸盐转化比例(物质的量)分别为1.085、0.897．亚硝酸盐转化成硝酸盐的比率为14.97％．在培养液中加入厌氧氨氧化的中间产物羟胺可以加速反应的进行．图3表2参9     

临沂地区蔬菜主要有害物质的调查

通过对全区蔬菜地布点取样调查，探明了蔬菜中有害物质（硝酸盐、亚硝酸盐、重金属、六六六、ＤＤＴ）以及６种重金属的残留量。结果，硝酸盐类是该区蔬菜中的主要有害物质，所检测的３种蔬菜中，硝酸盐和亚硝酸盐的超标率分别为７８．３％和３３．６％；重金属含量大多数未超标；ＤＤＴ全部未检出；六六六超标率平均为４．３％。     

临沂地区蔬菜主要有害物质的调查

通过对全区蔬菜地布点取样调查，探明了蔬菜中有害物质（硝酸盐、亚硝酸盐、重金属、六六六、ＤＤＴ）以及６种重金属的残留量。结果表明，硝酸盐类是该区蔬菜中的主要有害物质，所检测的３种蔬菜中，硝酸盐和亚硝酸盐的超标率分别为７８．３％和３３．６％；重金属含量大多数未超标；ＤＤＴ全部未检出；六六六超标率平均为４．３％。     

有机无机肥配合施用对菜园土壤及蔬菜硝酸盐类动态的影响

通过田间小区试验和室内测定，研究了有机肥与化肥以不同比例配合施用对小白菜硝酸盐和亚硝酸盐含量以及土壤硝酸盐含量的影响。结果表明：有机肥与化肥配合施用可以明显降低小白菜硝酸盐含量，减少硝酸盐在土壤剖面中向下淋溶，尤以有机肥与化肥施用比例为1：1(质量比)时小白菜产量较高，体内硝酸盐含量较低，土壤下层的硝酸盐含量也较低，达到蔬菜高产优质，生态环境清洁健康的目标。     

甲基纤维素在重量法测土壤硅中的应用研究

在重量法测定土壤全硅中，用甲基纤维素作凝聚剂，试验结果表明，用该凝聚剂与动物胶作凝聚剂测定土壤全硅的结果基本一致。甲基纤维素法的回收率为９３．８％—１０８．３％，标准差为０．３０％，变异系数最大为０．８８％；动物胶法的回收率为９２．３％—１０５．３％．用两种方法测定同一样品，两者间的绝对相差最大只有０．５％；ｔ检验表明，ｔ＝０．３６１＜ｔ（０．０５）＝２．２０，差异极不显著．因此，甲基纤维素可作为重量法测土壤硅的凝聚剂．     

栽培水分对采摘后油菜硝酸盐与亚硝酸盐含量的影响

采用盆栽方法栽培油菜(Brassicaca mpestrisL.),研究了灌水水平对采摘后油菜植株体硝酸盐与亚硝酸盐含量随时间变化的影响。共设高(灌水控制上限为田间持水量)、中(灌水控制上限为田间持水量的75%)和低(灌水控制上限为田间持水量的50%)3个灌水水平。油菜采摘后恒温贮存,定期测定油菜植株体内硝酸盐、亚硝酸盐含量。研究结果表明:不同灌水水平和贮存时间以及两者的交互作用都能显著地影响油菜植株体硝酸盐和亚硝酸盐含量;在采摘后的8d时间里,低灌水水平处理(0.50θf处理)的油菜植株体硝酸盐含量一直高于其它两处理;采摘后当天测定高灌水水平处理(1.00θf处理)的油菜植株体硝酸盐含量最低,以后则以中等灌水水平处理(0.75θf处理)的油菜植株体硝酸盐含量为最低。采摘后当天测定油菜植株体亚硝酸盐含量,亦以高灌水水平处理(1.00θf处理)为最低。采摘后油菜植株体硝酸盐和亚硝酸盐含量都经历一个先降低、后升高、再降低的变化过程。因此,从对人体健康及卫生的角度出发,以较高灌水水平栽培油菜,采摘后在一两天内食用,有利于将其硝酸盐和亚硝酸含量控制在较低水平。     

硝酸盐氮,亚硝酸盐氮总量紫外吸收快速测定

水体中尤其是海水中硝酸盐氮的测定较繁琐，干扰物质多，分析时间长，重现性差，准确性不高。文章通过实验介绍一种省时、省力、简便可行不消耗化学试剂且抗氯化物干扰、精度和准确度较高的硝酸盐氮、亚硝酸盐氮总量测定方法。     

低温反硝化过程中pH对亚硝酸盐积累的影响

以乙酸钠为单一碳源,在C/N比为3、温度为12—14℃的低C/N比、低温条件下通过间歇试验研究p H对反硝化亚硝酸盐积累规律影响.试验结果发现,在C/N为3时,p H值在7—9的范围内都能形成亚硝酸盐积累.反应时间为60 min时,亚硝酸盐积累率最大可达50%左右.低温SBR反应器连续试验研究表明,p H值为7.4±0.1和p H值为8.4±0.1时,序批式活性污泥法(SBR)出水亚硝酸盐积累率分别为51%和48%,取p H值为7.4±0.1条件下SBR反应器活性污泥进行酶活力测定发现,硝酸盐还原酶活力是亚硝酸盐还原酶活力的1.2倍,硝酸盐还原酶活力与亚硝酸盐还原酶活力对外界条件变化敏感程度不同,亚硝酸盐还原酶对外界条件变化更为敏感,其受到的抑制作用要大于硝酸盐还原酶,进而造成NO-2-N的积累.     

三氮的离子色谱法连续测定研究

本文首次提出用电导检测器和紫外检测器串联,对氮的三种形态(N-NO_2~-,N-NO_3~-,N-NH_4~+)进行连续测定;盐酸/甘氨酸作淋洗液,HPIC-CS_5作分离柱,建立了同时测定“三氮”灵敏的色谱方法,方法的线性相关系数大于0.999,各离子的相对标准偏差均小于0.5％,对样品的测定,回收率均在100％％+5％以内,与标准方法比较,结果颇为一致。     

Application of Synchronous Fluorescence Spectroscopy for Characterization of the Aromatic Hydrocarbons in Sediments of the Middle Adriatic

UV-fluorescence spectroscopy method with synchronous mode of scanning was used to characterize the types of aromatic hydrocarbons in surface sediments. the sampling stations were located on two transverses between Yugoslavian and the Italian coasts in the middle of the Adriatic Sea. the preparation of sediment samples was made according to IOC/UNESCO (1982). Synchronous excitation/emission scanning were done at wavelengths from 236/260 to 516/540 nm. Since the wavelength of maximum emission is a function of fused aromatic rings in a molecule, the fluorescence spectra of each sample were divided into three intervals: 300-340, 340-400, over 400 nm, corresponding to compounds with 2, 3 and 4,5 and more rings respectively.

Large qualitative differences were established between sediment samples. PAH with 5 and more rings are more prevalent near the Italian coast.     

Competition for electrons between reductive dechlorination and denitrification

It is common that 2,4,6-trichlorophenol (TCP) coexists with nitrate or nitrite in industrial wastewaters. In this work, simultaneous reductive dechlorination of TCP and denitrification of nitrate or nitrite competed for electron donor, which led to their mutual inhibition. All inhibitions could be relieved to a certain degree by augmenting an organic electron donor, but the impact of the added electron donor was strongest for TCP. For simultaneous reduction of TCP together with nitrate, TCP’s removal rate value increased 75% and 150%, respectively, when added glucose was increased from 0.4 mmol?L^–1 to 0.5 mmol?L^–1 and to 0.76 mmol?L^–1. For comparison, the removal rate for nitrate increased by only 25% and 114% for the same added glucose. The relationship between their initial biodegradation rates versus their initial concentrations could be represented well with the Monod model, which quantified their half-maximum-rate concentration (K _S value), and K _S values for TCP, nitrate, and nitrite were larger with simultaneous reduction than independent reduction. The increases in K _S are further evidence that competition for the electron donor led to mutual inhibition. For bioremediation of wastewater containing TCP and oxidized nitrogen, both reduction reactions should proceed more rapidly if the oxidized nitrogen is nitrite instead of nitrate and if readily biodegradable electron acceptor is augmented.

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珠江三角洲典型地区蔬菜硝酸盐与亚硝酸盐污染评价

研究了珠江三角洲典型地区中山市大型蔬菜生产基地中9种蔬菜30个样品中硝酸盐与亚硝酸盐的污染现状,初步摸清了蔬菜中硝酸盐及亚硝酸盐的污染状况。并以WHO/FAO规定的日允许摄入量换算得到的标准评价了其主要蔬菜品种的硝酸盐污染状况。结果表明:在被调查的蔬菜中,硝酸盐含量由高到低依次为菜心→白菜>芥菜→空心菜→生菜→瓜果类,菜心、芥菜和白菜为严重污染,生菜与空心菜为重污染,瓜果类蔬菜为轻污染;亚硝酸盐含量普遍较低,均未超标。因而有必要采取有效的污染防治措施控制该地区蔬菜中的硝酸盐污染状况。     

痕量亚硝酸根的极谱测定

在酸性介质中,次甲基蓝与亚硝酸根发生亚硝化反应,本文选用0.08mol/l的盐酸,其亚硝化产物在—0.65V(us.SCE)附近产生一灵敏的极谱波,亚硝酸根浓度在0.002—0.24ug/ml范围内与二次导数波高成直线关系,本法用于水样和蔬菜中亚硝酸根的测定,选择性好,灵敏度较     

Application of Synchronous Fluorescence Spectroscopy for Characterization of the Aromatic Hydrocarbons in Sediments of the Middle Adriatic

UV-fluorescence spectroscopy method with synchronous mode of scanning was used to characterize the types of aromatic hydrocarbons in surface sediments. the sampling stations were located on two transverses between Yugoslavian and the Italian coasts in the middle of the Adriatic Sea. the preparation of sediment samples was made according to IOC/UNESCO (1982). Synchronous excitation/emission scanning were done at wavelengths from 236/260 to 516/540 nm. Since the wavelength of maximum emission is a function of fused aromatic rings in a molecule, the fluorescence spectra of each sample were divided into three intervals: 300–340, 340–400, over 400 nm, corresponding to compounds with 2, 3 and 4,5 and more rings respectively.

Large qualitative differences were established between sediment samples. PAH with 5 and more rings are more prevalent near the Italian coast.     

FORMS OF NITROGEN (NO 3 - -N; NO 2 - -N AND NH 2 CONH 2 -N) AND THEIR RELATIONS TO A.O.U. IN THE INDIAN COASTAL WATERS OF ARABIAN SEA

The distribution of three important dissolved forms of nitrogen, viz. nitrate, nitrite and urea in the surface and bottom water samples collected from 27 selected hydrographic profiles, in the Arabian Sea, along the west coast of India is described. Of the three forms, nitrate concentrations were the highest and comparatively higher concentrations were observed in the bottom water. Decomposition of organic matter resulting in the release of the thermodynamically stable nitrogen species, i.e. nitrate, may be the major factor resulting in higher nitrate concentrations at these depths, where the water is also characterized by low values of dissolved oxygen and temperature. The significant positive correlation between A.O.U. and nitrate of the bottom water samples emphasizes the role of oxidative decomposition of organic matter which plays an active role in reducing the oxygen concentrations below the theoretical values since at this depth ( ≈200 m) the net production is taken to be zero. This is also evidenced by the negative correlation of nitrate with dissolved oxygen and temperature, for the bottom samples.     

Forms of Nitrogen (NO 3 - -N; NO 2 - -N and NH 2 CONH 2 -N) and their relations to A.O.U. in the Indian coastal waters of Arabian Sea

The distribution of three important dissolved forms of nitrogen, viz. nitrate, nitrite and urea in the surface and bottom water samples collected from 27 selected hydrographic profiles, in the Arabian Sea, along the west coast of India is described. Of the three forms, nitrate concentrations were the highest and comparatively higher concentrations were observed in the bottom water. Decomposition of organic matter resulting in the release of the thermodynamically stable nitrogen species, i.e. nitrate, may be the major factor resulting in higher nitrate concentrations at these depths, where the water is also characterized by low values of dissolved oxygen and temperature. The significant positive correlation between A.O.U. and nitrate of the bottom water samples emphasizes the role of oxidative decomposition of organic matter which plays an active role in reducing the oxygen concentrations below the theoretical values since at this depth ( , 200 m) the net production is taken to be zero. This is also evidenced by the negative correlation of nitrate with dissolved oxygen and temperature, for the bottom samples.     

Anaerobic degradation of 4‐chlorophenol under denitrifying conditions with nitrate as the only electron acceptor

A denitrifying bacterium was isolated from activated sludge after enrichment on 4‐chlorophenol under anoxic, denitrifying conditions, and the microbial degradation of 4‐chlorophenol by this bacterium, with nitrate as the only electron acceptor, was investigated. The bacterium was capable of degrading up to 5 mM 4‐chlorophenol with stoichiometric release of chloride under denitrifying conditions. Anaerobic degradation of 4‐chlorophenol was dependent on nitrate as an electron acceptor. Nitrate (10 mM) severely inhibited the growth by the toxic effect of the accumulated nitrite. The optimum nitrate concentration for cell growth and chlorophenol degradation was 6 mM.