Simultaneous determination of dyes in wines by HPLC coupled to quadrupole orbitrap mass spectrometry.

A new method combining the QuEChERS (quick, easy, cheap, effective, rugged, and safe) method with ultra high performance liquid chromatography and ESI quadrupole Orbitrap high-resolution MS was developed for the highly accurate and sensitive screening of 69 dyes in wines. Response surface methodology was employed to optimize the QuEChERS sample preparation method for the determination of 69 different analytes in wines for the first time. After optimization, the maximum predicted recovery was 99.48% rate for canacert indigo carmine under the optimized conditions of 10 mL acetonitrile, 1.45 g sodium acetate, 107 mg primary secondary amine, and 96 mg C18 . For the matrices studied, the recovery rates of the other 68 compounds ranged from 87.2-107.4%, with coefficient of variation < 6.4%. The mass accuracy typically obtained is routinely better than 1.6 ppm and only needed to be calibrated once a week. The LODs for the analytes are in the range 1-1000 µg/kg. This method has been successfully applied on screening of dyes in commercial wines, and it is very useful for the fast screening of different food additives.

Influence of colloidal Fe(OH)3 on the adsorption characteristics of strontium in porous media from a candidate high-level radioactive waste geological disposal site.

Colloids in groundwater or geological barriers generally play a key role in the migration of special nuclides. Adsorption characteristics of strontium were investigated on porous media in the presence of colloidal Fe(OH)3 from the Beishan Site, the only high-level radioactive waste disposal site candidate in China. The effects of colloid amounts, solid contents, and pH were determined and studied by batch texts. The results revealed that the presence of colloidal Fe(OH)3 in porous media contributed to promotion of the sorption effect, and the influencing factors had a significant impact on the adsorption process. The sorption ability increased with increasing colloid amount when the equilibrium time was approximately 10 h under an optimal solid-liquid ratio of 20 g L-1. The sorption effect in alkaline conditions was better than that under acidic conditions. The sorption kinetics indicated that the strong chemical interaction and/or surface complexation contributed primarily to strontium sorption. The sorption isotherms and model fitting revealed that the sorption of strontium onto porous media in the presence of colloidal Fe(OH)3 was a monolayer adsorption, and the presence of colloidal Fe(OH)3 is an important factor that greatly influences the removal of strontium from aqueous solutions. These findings provide useful information for the treatment of strontium in radioactive waste disposal sites.

Effect of a humic acid colloid on the sorption behaviour of Sr onto soil in a candidate high-level radioactive waste geological disposal site.

We explored the effect of the presence or absence of humic acid (HA) on the sorption behaviour of Sr onto soil. We examined three different experimental cases for Sr sorption: (1) sorption in the presence of only colloidal HA, (2) sorption in the presence of only soil and (3) sorption in the presence of both colloidal HA and soil (HS). A batch technique was used to study the influencing factors, including the amount of colloidal HA, solid content, pH, initial concentration of Sr and contact time. The experiments showed that the influencing factors significantly affected the sorption process. For example, in the case of soil and HS, the sorption percentage increased rapidly with increasing solid content at m/V < 20 g/L, changing from 8.35% and 37.54% to 49.09% and 77.03%, respectively. Moreover, scanning electron microscopy and Fourier transform infrared spectroscopy were used to characterize samples. The kinetics and isotherms of Sr were best described by the pseudo-second-order and Langmuir models, which indicated that the process was controlled by chemisorption and uniform monolayer sorption with constant energy on the outer surface. These findings provide valuable information for predicting strontium migration in radioactive waste disposal sites.

Analysis of additives in dairy products by liquid chromatography coupled to quadrupole-orbitrap mass spectrometry.

A new method combining QuEChERS with ultrahigh-performance liquid chromatography and electrospray ionization quadrupole Orbitrap high-resolution mass spectrometry (UHPLC/ESI Q-Orbitrap) was developed for the highly accurate and sensitive screening of 43 antioxidants, preservatives and synthetic sweeteners in dairy products. Response surface methodology was employed to optimize a quick, easy, cheap, effective, rugged, and safe (QuEChERS) sample preparation method for the determination of 42 different analytes in dairy products for the first time. After optimization, the maximum predicted recovery was 99.33% rate for aspartame under the optimized conditions of 10 mL acetionitrile, 1.52 g sodium acetate, 410 mg PSA and 404 mgC18. For the matrices studied, the recovery rates of the other 42 compounds ranged from 89.4% to 108.2%, with coefficient of variation <6.4%. UHPLC/ESI Q-Orbitrap Mass full scan mode acquired full MS data was used to identify and quantify additives, and data-dependent scan mode obtained fragment ion spectra for confirmation. The mass accuracy typically obtained is routinely better than 1.5ppm, and only need to calibrate once a week. The 43 compounds behave dynamic in the range 0.001-1000 µg kg(-1) concentration, with correlation coefficient >0.999. The limits of detection for the analytes are in the range 0.0001-3.6 µg kg(-1). This method has been successfully applied on screening of antioxidants, preservatives and synthetic sweeteners in commercial dairy product samples, and it is very useful for fast screening of different food additives.