CN100541179C - A kind of plasmatron spectrographic analysis hybrid ionic standard substance - Google Patents
A kind of plasmatron spectrographic analysis hybrid ionic standard substance Download PDFInfo
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- CN100541179C CN100541179C CNB2004100252691A CN200410025269A CN100541179C CN 100541179 C CN100541179 C CN 100541179C CN B2004100252691 A CNB2004100252691 A CN B2004100252691A CN 200410025269 A CN200410025269 A CN 200410025269A CN 100541179 C CN100541179 C CN 100541179C
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Abstract
The present invention relates to metrology and measurement standard transmission of quantity value technical field, especially relate to a kind of research of departments such as metallurgy, geology, environmental protection, medical and health, agricultural, chemical industry, food and plasmatron spectrographic analysis hybrid ionic standard substance (standard model) of monitoring of being widely used in.Contain gold (Au) 1.00~10.00mg, iridium (Ir) 1.00~10.00mg, palladium (Pd) 1.00~10.00mg, platinum (Pt) 1.00~10.00mg, rhodium (Rh) 1.00~10.00mg, antimony (Sb) 1.00~10.00mg, tin (Sn) 1.00~10.00mg, tellurium (Te) 1.00~10.00mg, lytic agent 100mL in its 1L capacity, all the other are element body (mL).The present invention not only can provide the material of tracing to the source for daily emission spectrographic analysis test, and has widened technical foundation for the measurement verification work of country, has also remedied the blank spot of national standard substance in hybrid metal ion standard substance field simultaneously.
Description
Technical field
The present invention relates to metrology and measurement standard transmission of quantity value technical field, especially relate to a kind of research of departments such as metallurgy, geology, environmental protection, medical and health, agricultural, chemical industry, food and plasmatron spectrographic analysis hybrid ionic standard substance (standard model) of monitoring of being widely used in.
Background technology
In industries such as metallurgy, geology, environmental protection, medical and health, with emission spectrographic analysis as conventional method of analysis.Emission spectrographic analysis is a kind of relative measurement method, must trace to the source by the standard substance of respective element in the middle of The whole analytical process.At present, China is used for national calibration hybrid metal ion standard substance and quite lacks, and this is embodied in two aspects: (1) hybrid metal element kind is few; (2) concentration series is incomplete, so that many laboratories can only be uneven according to the interim preparation of standard substance and the kind of analyzed object purchase one matter.For example, environmental monitoring department will carry out water analysis, and adopting plasma emission spectrometer is a kind of desirable method.Yet, in order to finish this analysis must move liquid, dilution, constant volume preparation hybrid ionic respectively from the standard substance of a plurality of one matters standard substance.This be one not only loaded down with trivial details but also bring the course of work of hidden danger can for the inaccuracy of data.Careless slightly, just can not make science, comprehensive, the accurate analysis to the analysis transmission of standard value.Above-mentioned state can't adapt to the needs of the numerous technical field analytical tests of China.Present domestic such standard substance that still do not have, the external report that such standard substance is not arranged yet.So the national standard substance of development hybrid metal ion is that various circles of society are engaged in the needs of carrying out the work in the laboratory of emission spectrographic analysis, plasma emission spectrometer metering needs of tracing to the source especially.
Summary of the invention
Technical matters to be solved by this invention provides a kind of highly sensitive, accuracy good, analysis speed is fast plasmatron spectrographic analysis hybrid ionic standard substance.The technical scheme that the present invention solves its technical matters employing is: a kind of plasmatron spectrographic analysis hybrid ionic standard substance, contain gold (Au) 1.00~10.00mg in its 1L capacity, iridium (Ir) 1.00~10.00mg, palladium (Pd) 1.00~10.00mg, platinum (Pt) 1.00~10.00mg, rhodium (Rh) 1.00~10.00mg, antimony (Sb) 1.00~10.00mg, tin (Sn) 1.00~10.00mg and tellurium (Te) 1.00~10.00mg and lytic agent 100mL, all the other are element body, the unit of element body is mL, lytic agent is technology ultrapure rank nitric acid 50mL and the ultrapure rank hydrochloric acid of technology 50mL, and element body is that titanium steams water.The present invention is owing to adopt technique scheme, not only can provide the material of tracing to the source for daily emission spectrographic analysis test, and be that technical foundation has been widened in national measurement verification work, also remedied the blank spot of national standard substance simultaneously in hybrid metal ion standard substance field.
Gold among the present invention (Au), iridium (Ir), palladium (Pd), platinum (Pt), rhodium (Rh), antimony (Sb), tin (Sn), tellurium (Te) are for providing the material of tracing to the source of emission spectrographic analysis test, and it is that ultrapure rank nitric acid of element body, technology and the ultrapure rank hydrochloric acid of technology can dissolve above-mentioned metal one matter as lytic agent that titanium steams water.Above-mentioned metal one matter (standard substance) should meet the regulation of " country of JJG1006-94 People's Republic of China (PRC) metering technology normalized ".All components among the present invention all at home market buy.
Compound method of the present invention is as follows: adopt the electronic balance of 100,000/precision to take by weighing a certain amount of metal one matter and place beaker, with the ultrapure rank nitric acid of technology and the ultrapure rank hydrochloric acid of technology ratio dissolution of metals one matter in 1: 1, after dissolving finishes, be transferred in the recorder jar of 1L capacity, blend titanium steaming water and evenly allocate and be diluted to 1L.Ultrapure rank nitric acid of technology among the present invention and the ultrapure rank hydrochloric acid of technology are respectively 50mL (account for 5% of 1L respectively, promptly concentration is 5%).
Embodiment
Embodiment 1: adopt the electronic balance of 100,000/precision to take by weighing respectively that gold (Au), iridium (Ir), palladium (Pd), platinum (Pt), rhodium (Rh), antimony (Sb), tin (Sn), tellurium (Te) 1.00mg place beaker and with other nitric acid 50mL of technology extra-pure grade and the ultrapure rank hydrochloric acid of technology 50mL dissolving, after dissolving finishes, be transferred in the recorder jar of 1L volume, blend titanium steaming water and evenly allocate and be diluted to 1L.
Embodiment 2: adopt the electronic balance of 100,000/precision to take by weighing respectively that gold (Au), iridium (Ir), palladium (Pd), platinum (Pt), rhodium (Rh), antimony (Sb), tin (Sn), tellurium (Te) 5.00mg place beaker and with other nitric acid 50mL of technology extra-pure grade and the ultrapure rank hydrochloric acid of technology 50mL dissolving, after dissolving finishes, be transferred in the recorder jar of 1L volume, blend titanium steaming water and evenly allocate and be diluted to 1L.
Embodiment 3: adopt the electronic balance of 100,000/precision to take by weighing respectively that gold (Au), iridium (Ir), palladium (Pd), platinum (Pt), rhodium (Rh), antimony (Sb), tin (Sn), tellurium (Te) 10.00mg place beaker and with other nitric acid 50mL of technology extra-pure grade and the ultrapure rank hydrochloric acid of technology 50mL dissolving, after dissolving finishes, be transferred in the recorder jar of 1L volume, blend titanium steaming water and evenly allocate and be diluted to 1L.
Using method of the present invention is with reference to prior art.
Claims (1)
1. plasmatron spectrographic analysis hybrid ionic standard substance, it is characterized in that: contain gold (Au) 1.00~10.00mg in its 1L capacity, iridium (Ir) 1.00~10.00mg, palladium (Pd) 1.00~10.00mg, platinum (Pt) 1.00~10.00mg, rhodium (Rh) 1.00~10.00mg, antimony (Sb) 1.00~10.00mg, tin (Sn) 1.00~10.00mg and tellurium (Te) 1.00~10.00mg and lytic agent 100mL, all the other are element body, the unit of element body is mL, lytic agent is technology ultrapure rank nitric acid 50mL and the ultrapure rank hydrochloric acid of technology 50mL, and element body is that titanium steams water.
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CNB2004100252691A CN100541179C (en) | 2004-06-18 | 2004-06-18 | A kind of plasmatron spectrographic analysis hybrid ionic standard substance |
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CNB2004100252691A CN100541179C (en) | 2004-06-18 | 2004-06-18 | A kind of plasmatron spectrographic analysis hybrid ionic standard substance |
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CN1710409A CN1710409A (en) | 2005-12-21 |
CN100541179C true CN100541179C (en) | 2009-09-16 |
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Families Citing this family (2)
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CN101398419B (en) * | 2008-11-04 | 2011-11-30 | 钢铁研究总院 | Concourse type metallurgy standard sample for minimal invasion analysis, preparation method and application thereof |
CN101576497B (en) * | 2009-03-06 | 2011-09-21 | 刘征涛 | Plasma emission spectrum detection method of content of platinum, palladium and rhodium in ceramic materials |
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2004
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Non-Patent Citations (6)
Title |
---|
原油金属元素标准物质的研制. 于燕,韩琴.油气田地面工程,第20卷第4期. 2001 |
原油金属元素标准物质的研制. 于燕,韩琴.油气田地面工程,第20卷第4期. 2001 * |
多金属矿石与精矿、金和银矿石国家标准物质. 有色金属,第1期. 2005 |
多金属矿石与精矿、金和银矿石国家标准物质. 有色金属,第1期. 2005 * |
混合金属离子标准物质的研制,GBW(E) 080674. 应劼,王虎,崔启明.化学分析计量,第17卷第5期. 2008 |
混合金属离子标准物质的研制,GBW(E) 080674. 应劼,王虎,崔启明.化学分析计量,第17卷第5期. 2008 * |
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