Determining gaseous composition of fluid inclusions with quadrupole mass spectrometer

Quadrupole mass spectrometer (QMS) is an instrument for effectively determining gaseous composition of fluid inclusion. The gaseous component is extracted from inclusions with thermal decrepitation method and then determined with the sensitive QMS instrument. The method is characterized by high sensitivity and high accuracy with the relative standard deviation (RSD,n=6) of less than 3%. It has been successfully used for analyzing fluid inclusions. The analytical results meet the requirement of geological study.

四极杆质谱仪中扫描速率对PFTBA信号强度和噪声的影响研究

Using quadrupole mass spectrometer,calibration gas PFTBA was turned on in constant flow to get the signal intensity,and off to get the noise value.Different scan time and dwell time was used separately for full scan mode and SIM to find out the effect of scan rate on signal intensity and noise.

毒物分析中四极杆质谱仪扫描速率对灵敏度影响研究

To find out the effect of scan rate on sensitivity in quadrupole mass spectrometer,DDV and 11 common hypnotic drugs were chosen for GC-MS analysis.Different scan time and dwell time was used separately for full scan mode and SIM.Then charasteristic ions were extracted to calculate signal to noise values.

A Predictive Instrument for Sensitive and Expedited Measurement of Ultra-Barrier Permeation

The reliable operation of flexible display devices poses a significant engineering challenge regarding the metrology of high barriers against water vapor.No reliable results have been reported in the range of 10–6 g∙(m^(2)∙d)1,and there is no standard ultra-barrier for calibration.To detect trace amount of water vapor permeation through an ultra-barrier with extremely high sensitivity and a greatly reduced test period,a predictive instrument was developed by integrating permeation models into high-sensitivity mass spectrometry measurement based on dynamic accumulation,detection,and evacuation of the permeant.Detection reliability was ensured by means of calibration using a standard polymer sample.After calibration,the lower detection limit for water vapor permeation is in the range of 10–7 g∙(m^(2)∙d)1,which satisfies the ultra-barrier requirement.Predictive permeation models were developed and evaluated using experimental data so that the steady-state permeation rate can be forecasted from non-steady-state results,thus enabling effective measurement of ultra-barrier permeation within a significantly shorter test period.

Simultaneous quantification of eighteen constituents in traditional Chinese medicine XiaoShuanTongLuo by UPLCMS/ MS

XiaoShuanTongLuo （XSTL） is an important multi-herbal formula widely used as a traditional Chinese medicine （TCM）. In this paper, an ultra-performance liquid chromatography-electrospray ionization tandem mass spectrometric method （UPLC-ESI-MS/MS） was developed for the simultaneous identification and quantification of 18 chemical constituents in the extract of XSTL. The analysis was performed in multiple-reaction monitoring （MRM） mode using positive and negative electrospray ionization （ESI）. A BEH C18 （2.1 mm× 100 mm, 1.7 μm） column with a gradient mobile phase of methanol-0.1% aqueous formic acid solution at a flow rate of 0.2 mL/min was used for separation. The standard curves of most components showed good linearity over the concentration range of 0.001-0.5 μg/mL with r = 0.9896-0.9996. The relative standard deviations （RSD） of intra-day and inter-day precision were all lower than 15% at low, middle, and high concentration levels. The RSD of stability analysis in 24 h were also lower than 15%. The validated method was employed to quantify 18 active components simultaneously in four different commercial brands of XSTL products in various dosage forms. The developed method was rapid, accurate, sensitive, and reproducible for the quality control of XSTL.

In situ Rb-Sr dating of mica by LA-ICP-MS/MS

Mica exhibits a relatively high Rb/Sr ratio and possesses a closure temperature for the Rb-Sr isotope system that is higher than the ore-forming temperature range of low-to medium-temperature deposits.Consequently,utilizing the laser ablation(LA)technique for in situ Rb-Sr dating in mica constitutes a significant methodology for resolving the mineralization chronology of low-to medium-temperature hydrothermal ore deposits.In this study,we employed a combination of a triple quadrupole inductively coupled plasma mass spectrometer(ICP-MS/MS)and 193 nm LA system with SF_6as the reaction gas to achieve interference removal of~(87)Rb~+on~(87)Sr~+.We then developed an in situ Rb-Sr dating method for mica.In addition,an investigation was conducted to identify the factors that could influence the analytical accuracy of the method.Subsequently,we applied the developed method to carry out in situ Rb-Sr dating for the ZBH-25 biotite,a national primary reference material(GBW04439)for K-Ar dating,and yielded a younger age(ca.12%,relative standard deviation,RSD)than the reference K-Ar age when using NIST SRM 610 as the reference material for external calibration.This finding indicated that in the process of determining Rb-Sr ages for mica by LA-ICP-MS/MS,there are significant matrix effects between the NIST SRM 610 and the mica samples,resulting in inaccurate Rb-Sr ages.In response to this issue,a two-step calibration method is proposed here.Based on external calibration using NIST SRM 610,ZBH-25 biotite is employed as a second external reference material to perform a second calibration of the sample data to correct the matrix effect between the glass standards and the natural mica samples,thereby improving the accuracy of Rb-Sr dating by LA-ICP-MS/MS.Using the proposed method,in situ Rb-Sr dating by LA-ICP-MS/MS was performed on mica samples from monzonite exposed in Mt.Dromedary,New South Wales,Australia,porphyritic granodiorite in Fangshan pluton and albionite granite in the Gyirong area of Tibet.The obtained Rb-Sr age results show agreement with the recommended values within the analytical uncertainty,which serves to validate the accuracy and effectiveness of the proposed method.