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C18 guard column

Manufactured by Merck Group
Sourced in Germany

The C18 guard column is a component of high-performance liquid chromatography (HPLC) systems. Its primary function is to protect the analytical column from contaminants and particulates that could otherwise compromise the performance and lifespan of the analytical column. The C18 guard column contains a stationary phase material similar to that of the analytical column, allowing it to effectively retain and filter out unwanted compounds before they reach the analytical column.

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2 protocols using c18 guard column

1

Wastewater Characterization and Analysis

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The feed wastewater characterization and reactor performance were monitored by wet analyses. For the suspended solid (TSS) parameter, standard methods (APHA, 1998) were applied. COD is one of the most important parameters in determining the degree of organic pollution in wastewaters. COD analyses were carried out using the microdigestion and titration method specified in the standard methods (SM 5220B) [20 ].
An HPLC (Shimadzu) equipped with a Diode-Array Detection (DAD) detector and LC-QTOF-MS/MS (Agilent 6530 Accurate Mass–ESI Interface, Santa Clara, CA, USA) was used for liquid chromatography analysis. To achieve the chromatographic separation, the Purospher Star RP-18 column (125 mm × 2.0 mm, particle size 5 µm) was supplied with a C18 guard column by Merck (Darmstadt, Germany). The analyses were performed in Positive Ionization mode with eluent A (acetonitrile-methanol (2:1)) and eluent B (ammonium acetate 5 mM at pH 4.7 (acetic acid)). The flow rate was selected as 0.3 mL/min, and the injection volume was determined as 10 µL. According to the selected method, the eluent gradient started from 5% and rose to 95% of eluent A in 5 min (was held for 4 min) and turned to the initial condition in 5 min.
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2

Liquid Chromatography-Mass Spectrometry Quantification

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Instrumental analysis was performed by LC, using a Symbiosis™ Pico (SP104.002, Spark, Holland), connected in series with a 4000 QTRAP Hybrid Triple Quadrupole -Linear Ion Trap-MS equipped with a Turbo Ion Spray source (Applied Biosystems-Sciex, Foster City, CA, USA). Target compounds were separated on a Purospher Star RP-18 end-capped column (125 mm×2.0 mm, particle size 5 μm) with a C18 guard column (4×2.0 mm), both supplied by Merck (Darmstadt, Germany). The optimized separation conditions were as follows: solvent (A) water (0,1 % formic acid) and (B) methanol (10 mM ammonium acetate) at a flow rate of 0.25 mL/min. The gradient elution was: 50% (B) for initial and hold for 1 min; 80% (B) at 3 min and hold for 1 min; 90% (B) at 9 min and hold for 8 min; 100% (B) at 22 min and hold for 9 min. 50% (B) at 32 min and hold for 5 min to return to initial mode. The total chromatographic time was 37 min. The sample injection was 10 µL (Santín et al., 2016) .
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