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Dionex ics

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Dionex ICS is an ion chromatography system designed for the analysis of ionic compounds. It is used for the separation, identification, and quantification of anions, cations, and other ionic species in a wide range of sample types.

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Lab products found in correlation

3 protocols using dionex ics

1

Anammox-CdS Biohybrid System for Nitrogen Removal

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After constructing the anammox-CdS biohybrid system, the supernatant of the vial was poured out and then the vial was added 100 mL the medium containing 25 mg-N/L NH4+-N, and 0.1 g cystine. Helium gas was sparged to remove the possible remained oxygen before refilling the medium, and the experimental vial was irradiated with a LED lamp (490 nm) at a constant temperature of 35°C. The control group without anammox biomass was the non-biological control group, the one without CdS nanoparticles was the positive control group, and the one without LED light was the negative control group. The other conditions of the control groups were kept as the same with experimental groups. The qualities of NH4+-N, NO2-N and NO3-N were determined by an ion chromatograph (DIONEX ICS, Thermo Fisher, USA); the quality of cysteine was detected by high performance liquid chromatography (HPLC, LC-20A, SHIMADZU, Japan); the qualities of N2 and N2O were detected by gas chromatograph (GC7900, Tianmei, China).
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2

Formation Water Geochemical Analyses

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Formation water samples for geochemical analyses were taken during field collection and upon arrival at the Texas laboratory. Analyses were performed by Intertek (Houston, TX, USA; Supplementary Material File S1). Concentrations of anions and organic acids were measured by ion chromatography using a Dionex ICS (Thermo Scientific, Waltham, MA, USA). Concentrations of Al, Ba, B, Cd, Ca, Cr, Cu, Fe, Pb, Li, Mg, Mn, Ni, P, K, Si, Na, Sr and Zn were determined using inductively coupled plasma spectroscopy.
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3

Quantifying Glycogen-Derived Glucose via HPAE-PAD

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A Dionex ICS (Thermo Scientific) was used to measure glucose released from glycogen. After glycogen hydrolysis, 10 μl samples were injected for analysis. Each sample was injected twice. An isocratic 10-min method with the high-pH mobile phase consisting of 98% buffer B (100 mM NaOH, pH 13.0) and 2% buffer D (1 M sodium acetate, 100 mM NaOH) was used along with a Dionex CarboPac PA10 (2 × 250 mm) anion-exchange column. A fresh glucose standard curve was prepared by serially diluting glucose (Sigma # G6918; 100 ml) to obtain concentrations between 4000 μM and 0 μM in 0.1 M sodium acetate (pH 4.8) supplemented with 0.5 mg/ml BSA. Glucose peak areas were manually integrated, and glucose concentrations were interpolated from the standard curve. Nonlinear regression analysis using the Michaelis–Menten equation were performed on Prism (GraphPad). One-way ANOVA with Fisher’s LSD as the post hoc test was performed using Prism (GraphPad) with an n = 7 (14 total measurements on the Dionex ICS) for precursor rhGAA, an n = 5 (10 total measurements) for processed rhGAA, an n = 3 (6 total measurements) for rhGAA–kif, and an n = 2 (4 total measurements) for all other samples.
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