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Ionpac as18 column

Manufactured by Thermo Fisher Scientific
Sourced in United States

The IonPac AS18 column is a high-performance ion chromatography column designed for the separation and detection of anions. It features a pellicular anion-exchange resin that provides efficient, reproducible separation of common inorganic and organic anions.

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3 protocols using ionpac as18 column

1

Measuring Flue Gas CO2 and Sulfate

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The concentration of CO2 sparged into the reactor was
confirmed using GasLab software and a cozIR wide-range 0–20%
CO2 sensor (CM-0123, Gas Sensing Solutions Ltd., Glasgow,
UK).
Sulfate concentrations accumulated, from the sparged simulated
flue gases, during the 50 h bioreactor experiment were quantified
using SulfaVer 4 Method 8051 (HACH, Loveland, CO, USA) with a HACH
DR6000 UV–Vis spectrophotometer (see Figures S3 & S4 in
the Supporting Information).
During
the cultured simulated flue gas trials, sulfate, phosphate,
and nitrate concentrations were measured in daily samples of the culture
medium (0.2 μm filtered) using an ion chromatograph (Thermo
Fisher ICS-2100) equipped with a Dionex IonPac AS18 column. Combined
Seven Anion Standard II (Dionex, Sunnyvale, CA) was used to calibrate
the instrument.
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2

Bench-scale Wastewater Analysis: Comprehensive Protocols

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Batch
experiment samples (solids and aqueous) were analyzed both on-site
and at the University of Illinois Urbana–Champaign (UIUC).
Hand-held probes were used to measure pH (Orion 3-Star portable pH
meter; Thermo Scientific), temperature, DO (Orion RDO dissolved oxygen
probe; Thermo Scientific), and ammonium concentrations (ProDSS multiparameter
digital water quality meter; YSI); each sensor was calibrated immediately
prior to use in the bench-scale experiments. Solids storage and analyses
for TSS and VSS were performed as in Bradley et al.21 (link),22 (link),31 (link)−33 Briefly, sample TSS
was determined by filtration through 0.7 μm glass fiber filters
(Whatman GF/F). After filtration, the filters were heated at 105 °C
for 1 h and desiccated for 30 min prior to weighing. VSS was determined
by combusting samples for 20 min at 550 °C.
Samples for
phosphate, nitrate, and nitrite were immediately filtered through
0.22 μm filters and frozen. After storage, aqueous samples were
thawed and refiltered prior to analysis via ion chromatography (Dionex
ICS-2100 ion chromatograph, Dionex IonPac AS18 column; Section S2 and Figures S3–S5 for calibration
curves). The MRL for phosphate was determined to be 0.027 mg-P·L–1 and the MRL range was 0.022 to 0.037 mg-P·L–1 (Section S2 and Table S3).
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3

Soil Nutrient and pH Analysis Protocol

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Mineral soil layers from each core were air-dried for determination of nutrient concentrations and pH. To measure pH, we placed 5 g of soil in a 50 ml centrifuge tube with 25 ml of 0.01 M CaCl2 and shook the mixture for 30 minutes. We let the mixture settle for two hours before using a Mettler Toledo Orion Dual Star to determine pH [20 (link)]. Soil cation and anions were determined by the method described by Quevauviller [21 ]. For this method, 2.5 g of soil into a centrifuge tube with 25 mL Milli-Q water and shaken for 3 hours at 15 rpm using a rotary shaker. Samples were then centrifuged at 5000 g for 10 minutes and subsequently filtered with a 0.45 μm filter. Afterwards, samples were analyzed for anions (Dionex IonPac AS18 column) and cations (Dionex IonPac CS12A column) with ion chromatography with a DionexICS-2000 using Chromeleon7 software in the Department of Soil Science of the University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
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