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Thermo tsq quantum access max

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Thermo TSQ Quantum Access MAX is a triple quadrupole mass spectrometer designed for high-performance liquid chromatography (HPLC) and ultra-high-performance liquid chromatography (UHPLC) applications. It features advanced ion optics and detection technologies to provide high sensitivity, selectivity, and quantitative accuracy for a wide range of analytes.

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2 protocols using thermo tsq quantum access max

1

Robenidine Hydrochloride Quantification Protocol

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Robenidine Hydrochloride (Purity ≥ 98%, Quality ratio, Dr. Ehrenstorfer GmbH, Augsburg, Germany), Robenidine-D8 Standard (Purity ≥ 98%, Quality ratio, Dr. Ehrenstorfer GmbH, Augsburg, Germany), and Robenidine Hydrochloride Raw Material (CAS 25875-50-7, Purity 98%, Shouguang Huachih Chemical Co., Shandong, China) were used. Ethyl acetate, hexane, and formic acid (chromatographic purity, J.T. Baker Co., NJ, USA). Anhydrous ethanol (analytically pure, Xilong Chemical Co., Ltd., Fujian, China), distilled water, soluble starch (analytically pure, Xiangzhong Chemical Reagent Supply Station, Shanghai, China), anhydrous magnesium sulfate (analytically pure, Sinopharm Chemical Reagent Co., Ltd., Shanghai, China), and heparin sodium (biological grade, Shanghai Biochemical Reagent Co., Ltd., Shanghai, China). Mettler-TOLE-DOAE-240 precision electronic balance (Mettler-Toledo, Zurich, Switzerland), 20PR-520 high-speed refrigerated centrifuge (Hitachi, Japan), speed mixer (Shanghai Kanghua, Shanghai, China), nitrogen blower (AOSHENG, Hangzhou Aosheng Instrument Co., Ltd., Zhejiang, China), rotary evaporator (Gongyi Yuhua, Henan, China), HPLC–Tandem Mass Spectrometer (Surveyor MS Pump Plus, Surveyor Autosampler Plus, Thermo TSQ Quantum Access MAX and Thermo LCquan 2.6 data acquisition system, Thermo Fisher Scientific, MA, USA).
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2

Extraction and Analysis of Organic Pollutants

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Sample extraction methodology was performed as described in Peterson et al. (2021) (link). Briefly, TSP filters were weighed individually, and two filters per sampled location were placed in a 50-mL centrifuge tube to ensure sufficient sample mass for analysis. Filters were spiked with internal standard (TCPP), and 45 mL methylene chloride:acetone (1:1) was added, followed by heated sonication (40 °C) for 1 hr. acetonitrile:water (1:1) was added to the centrifuge tube. Tubes were capped and placed on an orbital shaker platform (Model MaxQ 4000, Thermo Scientific, Waltham, MA) for 18 hrs at 350 rpm. Next, tubes were centrifuged (10 min; 3100 rpm) and supernatant was decanted into a second 50-mL centrifuge tube. Magnesium sulfate (4 g) and sodium chloride (1 g) salts were added, and tubes were vortexed for 1 min followed by centrifugation for 10 min at 3100 rpm. The final supernatant was then combined with the initial supernatant in the glass vial, evaporated under a stream of nitrogen at 35 °C, and reconstituted in 1 mL acetonitrile. Extract was vortexed for 10 s and syringe filtered (PTFE; 0.22 μm) into amber chromatography vials for subsequent analysis via triple quadrupole liquid chromatography tandem mass spectrometry with electrospray ionization (Thermo TSQ Quantum Access Max, Thermo Scientific, Waltham, MA), as described in Peterson et al. (2020) (link).
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