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Semi micro ph electrode

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Semi Micro pH electrode is a laboratory instrument used for measuring the pH of small sample volumes. It is designed to provide accurate pH measurements in applications where sample size is limited.

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2 protocols using semi micro ph electrode

1

Ferrihydrite Reduction Monitoring Protocol

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Ferrihydrite reduction was monitored by measuring the concentration of aqueous Fe(II) and total Fe(II) (total Fe(II) is comprised of aqueous Fe(II) and Fe(II) extracted from the solids by 0.75 M HCl) with the ferrozine assay [24 ]. Briefly, 1 mL of HEPES (50 mM)-buffered ferrozine reagent [25 (link)] was added to 0.05 mL of sample, and the Fe(II) concentration was measured at 562 nm with a spectrophotometer. The concentrations of sulfate and phosphate in samples were determined by using an ion chromatograph (Dionex 3000) with an IonPac AS11 analytical column (250 x 2 mm, Dionex) and 1–20 mM KOH at a flow rate of 0.5 mL min-1 (Dionex Corporation, Sunnyvale, CA, USA). The concentrations of glucose and acetate, lactate, and other organic acids were measured by high-performance liquid chromatography (HPLC) with an Agilent 1100 series HPLC equipped with refractive index and ultraviolet absorbance detectors (Aglient Technologies, Santa Clara, CA, USA). The samples were diluted with an equal volume of 10 mM H2SO4, and 50 μL of the diluted sample was injected on a Bio-Rad Aminex HPX-87H ion-exchange column (7.8 × 300 mm; Bio-Rad Laboratories, Hercules, CA, USA). The column was eluted isocratically with 5 mM H2SO4 at a flow rate of 0.6 mL min-1 at 50°C, with analyte detection at 210 nm. The aqueous-phase pH was measured by Semi Micro pH electrode (Thermo Scientific, Waltham, MA, USA).
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2

Quantifying Ferrihydrite Reduction and Sulfate Dynamics

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The reduction of ferrihydrite was assessed by measuring the Fe(II) in the suspensions by acid extraction and analysis by the ferrozine method (Stookey 1970 ) using HEPES-buffered ferrozine reagent (Sørensen 1982 (link)) as described by O'Loughlin et al. (2019) . Sulfate reduction was monitored by measuring sulfate concentration using the method of Kolmert et al. (2000) (link), scaled for 0.5 mL of sample. Briefly, 0.5 mL of sample was combined with 0.5 mL of conditioning reagent and 30 mg of BaCl2 powder was added and the mixture was immediately mixed (vortexed) for 30 s. Immediately after mixing, the mixture was poured into a microcuvette and the absorbance at 430 nm was measured; the detection limit was 0.2 mM SO42-. Aqueous phase Sb concentrations were determined by inductively coupled plasma-optical emission spectroscopy (ICP-OES) using a PerkinElmer 4300DV instrument. Measurement of the Sb emission line at 217.582 nm in radial view mode provided a detection limit of 5 μM. An Agilent 1100 series high performance liquid chromatograph (HPLC) was used to determine the concentrations of acetate, lactate, and propionate as described by Kwon et al., 2014 , Kwon et al., 2014 . The pH of aqueous solutions was measured using a Semi Micro pH electrode (Thermo Scientific Inc.) calibrated with NIST-traceable pH standards to a precision of 0.01 pH units.
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