首页> 外文期刊>Journal of liquid chromatography and related technologies >Development and Validation of a Gradient-HPLC-PDAD Method for the Identification of Ballpoint Pen Ink Components: Study of Their Decomposition on Aging for Forensic Science Appplications
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Development and Validation of a Gradient-HPLC-PDAD Method for the Identification of Ballpoint Pen Ink Components: Study of Their Decomposition on Aging for Forensic Science Appplications

机译:鉴定圆珠笔墨水成分的梯度HPLC-PDAD方法的开发和验证:法医学应用的老化分解研究

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A reverscd-phase high performance liquid chromatographic (RP-HPLC) method, using nuilti step gradient elution, is described for the simultaneous determination of ball point pen inks: blue violet, fuchsin, pararosaniline, crystal violet, and victoria blue. The analytical column, an [nertsii ODS-3 5 m, 250 x 4 mm, was operated at ambient temperature. The elution solvents were classified as A: CH_3COONH_4 0.05 M, B: CH.iCN and C: CH3OH. The samples were eluted according to the following ternary gradient: 50% in A, 30% in B and 20% in C as initial conditions, changing to 20% in A, 30% in B and 50% in C in 10 min, and ending to 50% in B and 50% in C after 10 min. A final isocratic step at the composition of 50% in B and 50% in C was incorporated for 5 min. Elution was performed at a flow rate of 0.8 mL/min and observed inlet pressure ranged from 105 to 270 kg/cm~2. A diode-array detector performed monitoring of ink components at 594 nm for the blue inks and 540 nm for red inks. Identification of examined compounds was made by comparing their retention time values and UV spectra in the range 390-596 nm with commercial standards stored in a data library. Detection limits of 0.1-2 ng were obtained per 20 L injection volume, while linearity held up to 50 ng L. The statistical evaluation of the method was examined performing intra-day (n = 6) and inter-day calibration (n = 6) and was found to be satisfactory, with high accuracy and precision results. Six commercial ballpoint pens were examined, among them 3 blue and 3 black pens. These samples were analyzed over a period of 20 weeks in order to establish a useful tool for dating entries on documents.
机译:描述了使用nuilti阶梯梯度洗脱的反相高效液相色谱(RP-HPLC)方法,用于同时测定圆珠笔墨水:蓝紫色,品红,品红苯胺,结晶紫和维多利亚蓝。分析柱[nertsii ODS-3 5 m,250 x 4 mm]在环境温度下运行。洗脱溶剂分类为A:CH_3COONH_4 0.05 M,B:CH 3 CN和C:CH 3 OH。根据以下三元梯度洗脱样品:A的50%,B的30%和C的20%作为初始条件,在10分钟内更改为A的20%,B的30%和C的50%,以及10分钟后在B中达到50%,在C中达到50%。在B中50%和C中50%组成的最终等度步骤中加入5分钟。洗脱以0.8 mL / min的流速进行,观察到的入口压力范围为105至270 kg / cm〜2。二极管阵列检测器对蓝色墨水在594 nm处以及红色墨水在540 nm处进行墨水成分监视。通过将化合物的保留时间值和390-596 nm范围内的UV光谱与数据库中存储的商业标准品进行比较,可以鉴定受检化合物。每20 L进样量可获得0.1-2 ng的检出限,而线性最高可达50 ngL。在日内(n = 6)和日间校准(n = 6)下对该方法的统计评估进行了检查),并被认为是令人满意的,具有高精度和高精度的结果。检查了六支商业圆珠笔,其中3支蓝色和3支黑色笔。在20周的时间内对这些样品进行了分析,以建立一个用于对文档上的条目进行约会的有用工具。

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