光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2010年
4期
1126-1129
,共4页
紫外分光光度法%火焰原子吸收光谱法%青稞%矿质元素%含量
紫外分光光度法%火燄原子吸收光譜法%青稞%礦質元素%含量
자외분광광도법%화염원자흡수광보법%청과%광질원소%함량
Ultraviolet spectrophotometry%Flames atomic absorption spectrometry (FAAS)%Hullessbarley%Mineral elements%Content
采用紫外分光光度-硫酸钡比浊法和干灰化-火焰原子吸收分光光度法对5个品系青稞中的S,Zn,Ca,Mg,K,Na,Fe,Cu,Mn 9种矿质元素含量进行了测定,并对方法的精密度、准确度、稳定性和重复性进行了分析.结果显示各元素检测方法的精密度在1.2%~3.7%之间,加标回收率在97.44%~101.52%之间,准确度在1.3%~3.8%之间,说明该方法具有较高的精密度和准确度;各元素检测方法的重复性在2.6%~6.1%之间,且样品溶液在室温下放置24 h后各元素含量基本不变,说明该方法具有较好的重复性和稳定性.在所有青稞样品中,各元素平均含量依次为K>s>Mg>Ca>Fe>Na>Zn>Mn>Cu,且与人体健康密切相关的Zn,Fe,Mn元素的含量均相对较高.其测定结果可为青稞的进一步开发利用提供科学依据.
採用紫外分光光度-硫痠鋇比濁法和榦灰化-火燄原子吸收分光光度法對5箇品繫青稞中的S,Zn,Ca,Mg,K,Na,Fe,Cu,Mn 9種礦質元素含量進行瞭測定,併對方法的精密度、準確度、穩定性和重複性進行瞭分析.結果顯示各元素檢測方法的精密度在1.2%~3.7%之間,加標迴收率在97.44%~101.52%之間,準確度在1.3%~3.8%之間,說明該方法具有較高的精密度和準確度;各元素檢測方法的重複性在2.6%~6.1%之間,且樣品溶液在室溫下放置24 h後各元素含量基本不變,說明該方法具有較好的重複性和穩定性.在所有青稞樣品中,各元素平均含量依次為K>s>Mg>Ca>Fe>Na>Zn>Mn>Cu,且與人體健康密切相關的Zn,Fe,Mn元素的含量均相對較高.其測定結果可為青稞的進一步開髮利用提供科學依據.
채용자외분광광도-류산패비탁법화간회화-화염원자흡수분광광도법대5개품계청과중적S,Zn,Ca,Mg,K,Na,Fe,Cu,Mn 9충광질원소함량진행료측정,병대방법적정밀도、준학도、은정성화중복성진행료분석.결과현시각원소검측방법적정밀도재1.2%~3.7%지간,가표회수솔재97.44%~101.52%지간,준학도재1.3%~3.8%지간,설명해방법구유교고적정밀도화준학도;각원소검측방법적중복성재2.6%~6.1%지간,차양품용액재실온하방치24 h후각원소함량기본불변,설명해방법구유교호적중복성화은정성.재소유청과양품중,각원소평균함량의차위K>s>Mg>Ca>Fe>Na>Zn>Mn>Cu,차여인체건강밀절상관적Zn,Fe,Mn원소적함량균상대교고.기측정결과가위청과적진일보개발이용제공과학의거.
The contents of nine mineral elements, including sulphur, zinc, calcium, magnesium, potassium, sodium, iron, cop-per and manganese in five hulless barley (Hordeum vulgate L. var. nudum Hook. f.) lines were determined by ultraviolet spectrophotometry and flames atomic absorption spectrometry (FAAS). For the determination of sulphur, the samples were dis-solved by magnesia and anhydrous sodium carbonate at 250 ℃ for 0. 5 h and at 550 "C for 3 h in the muffle furnace, and then a certain amount of barium chloride was put into the sample solution for colorimetry of the UV-Vs spectrophotometer. For the de-termination of other eight mineral elements, all of the samples were dissolved by a kind of incinerating method, first, the sample was put into the muffle furnace at 250 ℃ for 0. 5 h and at 550 ℃ for 2. 5 h, then two droplets of 50%HNO_3 were distributed in-to each sample, and the last step was putting the sample into the muffle furnace at 550 ℃ for 0. 5 h. And then all of the ash was dissolved by 50%HNO_3to 50 milliliter and determined by flames atomic absorption spectrometry. The precision, accuracy, re-peatability and stability of the method were discussed too. The results showed that the relative standard deviations (RSD) were between 1.2% and 3.7%; The average recoveries were 97. 44%-101. 52% and the relative standard deviations (RSD) of sample determination were 1.3%-3.8%. The repeatability experiment showed that the relative standard deviations (RSD) were 2.6%-6.1%. And the content of each mineral element was the same after 24 hours; All these showed that the method has a good preci-sion, accuracy, repeatability and stability. In all the hulless barley samples, the average contents were in the order of K>S>Mg >Ca>Fe>Na>Zn>Mn>Cu, and the contents of zinc, iron and manganese closely related to people's health were relatively higher than other crops. The data of the experiment could provide an accurate and credible evidence for the deeper exploitation of the hulless barley.