使用水溶液标准进行校准，不进行基体匹配。
Aqueous standards without matrix matching were used for calibration.
论述了研制镀铬溶液标准物质的必要性，介绍了镀铬溶液标准物质的研制过程。
The paper describes the necessity of developing the standard reference material chromeplating solution and introduces its developing process.
标准溶液的制备程序是怎样的？
用0.1M标准NaOH溶液滴定剂，滴定到溶液由红色变为橙色。
Use 0.1M standard NaOH solution titrant to titrate the solution from red colour to orange.
所以可采用使标准溶液和样品的性质更为相符的办法来解决这一问题。
This can be overcome by better matching of the properties of standards and sample.
记录并比较伴随地得到的供试溶液和标准溶液的光谱。
Record and compare the spectra concomitantly obtained for the test solution and the Standard solution.
这是通过度量标准溶液的吸收度来完成的。
This is accomplished by measuring the absorbance of standard solutions.
目的对按照2005年版《中国药典》方法配制和标定的盐酸标准溶液浓度进行不确定度评定。
Objective To evaluate uncertainty for concentration of hydrochloric acid standard solution prepared and standardized with the method in Chinese Pharmacopoeia (edition 2005).
介绍原子吸收光谱法检测过程中实验准备、标准溶液和样品制备方法、样品分析及数据处理等几个环节的质量控制措施。
The quality control of AAS measurement such as the test preparation, the standard solution and sample preparation method, the sample analysis and the data processing were introduced.
在不同的标准缓冲溶液中吡喃草酮光降解速度明显降低。
The tepraloxydim light degeneration speed reduces obviously in the different standard cushion solution.
结果表明，不同的氯标准溶液、显色剂与水样的加入顺序和显色时间对测定的结果均有干扰。
The results showed that the standard solution of chlorine, sequence of color-developing agent and water sample and coloration time had influences on the test results.
对测定过程中的标准溶液、准曲线、品称量以及使用仪器带来的不确定度进行了分析。
The uncertainties are evaluated under the individual analysis of standard solution, standard curve, weighing and the instrument and glassware used in the experiment.
根据其对系列标准溶液的实测结果，采用A类的评定方法，做出了该仪器测量不确定度评定。
Its uncertainty is obtained based on the measured results of series of standard solutions by Type a evaluation method.
在KCI的底液中，用KOH标准溶液进行直接滴定。
It is titrated with standard solution KOH in KCI supporting electrolyte.
用EDTA标准溶液滴定，可测得氧化钇的含量。
We can measure the contents of yttrium with EDTA standard solution titration.
方法分别选取猪源、牛源肝水解肽溶液，依据标准检测部分项目，并用分子排阻色谱法进行肽图分析。
Methods Several items of hepatolysate solution extracted from pig and cattle were tested based on standards, and using size-exclusion chromatography the peptide mappings were analyzed.
以PAN为指示剂用硫酸铜标准溶液滴定过量的EDTA标准溶液，从而求得镍的含量。
The excessive EDTA standard solution was titrated using copper sulfate with PAN as indicator so as to obtain nickel content.
用一定的标准溶液进行定量分析。
By the use of definite volumes of standard solutions or reagents.
负责对检验用设备、仪器、试剂、试液、标准品(或参考品)、标准溶液、培养基等化验检查用品制订管理制度，并监督实施。
Responsible for the management of analytical instrument, equipment, reagent, test solutions, standard substances, reference standards, standard solutions, culture and medium.
在标准分析方法中，采用原子荧光分光光度法测定水中砷、硒、汞所用的标准溶液系列必须每次配制，给工作带来很大的不方便。
For the standard analytical method, the series of standard solution for the determination of As, se and Hg in water by atomic fluorescence spectrophotometry must be prepared for every test.
自动进样器重复性的测试，一般取同一样品溶液至少重复进样10次，其相对标准偏差不应大于1%。
During automatic sampler repeatability test, a homogenous solution shall be at least sampled and injected for 10 times, and the RSD of results shall not be greater than 1%.
分析了以草酸钠为基准物标定高锰酸钾标准溶液浓度的反应原理，标定操作及温度、酸度、滴定速度等滴定条件对标定结果的影响。
This paper discusses the reaction principle and titrimetric operation in defining consistency of potassium permanganate titrant which sodium oxalate is regarded as the basis material.
加入标准溶液测定方法的回收率，消解条件对测定结果有影响。
Adding standard solution in the samples, the recovery ratio is determined.
每周测定标准水溶液中水的含量，按需要周期性的标定卡尔试剂。
Determine the water content of the water Solution weekly, and standardize the Reagent against it periodically as needed.
本文将给出水溶液中离子的绝对标准生成焓。
In this paper, the ionic absolute standard heat of formation is gotten.
应在线性浓度范围内制备标准溶液和样品溶液，并在同一波长处测定。
The standard and sample solutions should both be prepared in the linearconcentration range and measured at the same wavelength.
应在线性浓度范围内制备标准溶液和样品溶液，并在同一波长处测定。
The standard and sample solutions should both be prepared in the linearconcentration range and measured at the same wavelength.
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