SANS 11885-1996
水质.电感耦合等离子体原子发射光谱法测定33种元素

Water quality - Determination of 33 elements by inductively coupled plasma atomic emission spectroscopy


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标准号
SANS 11885-1996
发布日期
1996年
实施日期
废止日期
2008-03-28
发布单位
ZA-SANS
代替标准
SANS 11885-2008
适用范围
Field of application This International Standard specifies a method for the determination of dissolved, particulate or total elements in raw, potable and waste water for the following elements: aluminium, antimony, arsenic, barium, beryllium, bismuth, boron, cadmium, calcium, chromium, cobalt, copper, iron, lead, lithium, magnesium, manganese, molybdenum, nickel, phosphorus, potassium, selenium, silicon, silver, sodium, strontium, sulfur, tin, titanium, tungsten, vanadium, zinc, zirconium. Table 1 lists these elements along with the recommended wavelengths and typical estimated instrumental detection limits using conventional pneumatic nebulization. Actual working detection limits are sample-dependent and as the sample matrix varies, these concentrations can also vary. Because of the differences between various makes and models of satisfactory instruments, no detailed instrumental operating instructions can be provided. Instead, the analyst will need to refer to the instructions provided by the manufacturer of the particular instrument. 2 Interferences Table 2 lists elements and the most important spectral interferences at the wavelengths recommended for analysis. Several types of interference effects can contribute to inaccuracies in the determination of trace elements. They can be summarized as follows. a) Spectral interferences, categorized as: 1) overlap of a spectral line from another element; these effects can be compensated by utilizing computer correction of the raw data; 2) unresolved overlap of molecular band spectra; these effects can possibly be overcome by selection of an alternative wavelength. If the appropriate equipment is available, wavelength scanning can be performed to detect potential spectral interferences. b) Background influences, categorized as: 2) background contribution from continuous or recombination phenomena; 3) background contribution from stray light from the line emission of elements in high concentration. The effect of background interferences can usually be compensated by background correction adjacent to the analyte line.




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