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Icap 7400 radial

Manufactured by Thermo Fisher Scientific
Sourced in United States

The ICAP-7400 Radial is an inductively coupled plasma optical emission spectrometer (ICP-OES) designed for elemental analysis. It is capable of detecting and quantifying a wide range of elements in various sample types. The ICAP-7400 Radial provides high-performance analysis with a robust and reliable plasma source.

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3 protocols using icap 7400 radial

1

Comprehensive Analytical Techniques for (Bio)dissolution

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The analytic process for the liquid sample during the (bio)dissolution process is shown in Fig. 1a. The dissolved Fe2+ and Fe3+ were quantified through the o-phenanthroline spectrophotometry method40 (link) with a microplate reader (BOX 998, Biotek Instruments, HIGHLAND PARK, USA). Iron, Cu2+, and Zn2+ concentrations were analyzed by inductively coupled plasma-atomic emission spectrometry (ICP-AES) (ICAP-7400 Radial, Thermo Fisher Scientific, MA, USA); meanwhile, the pH and oxidation–reduction potential (ORP) values were monitored with a pH meter (PHSJ-4A, Shanghai LEICI Co., Shanghai, China) and ORP meter (BPH-221, Dalian BELL Co., Dalian, China), respectively. The bacterial density was detected using a hemocytometer in a bright field microscope (CX31RTSF, Tokyo OLYMPUS Co., Tokyo, Japan). The mineralogical contents of bornite and marmatite were detected by XRF (Axios MAX, PANalytical B.V., Almelo, Holland). All electrochemical experiments were performed by electrochemical TAB (CHI700E, Shanghai CH Instruments, Shanghai, China). The mineralogical phases of bornite, marmatite and the residues were analyzed by SR-XRD at beam line of 4B9A of the Beijing Synchrotron Radiation Facility (BSRF). The mineralogical changes were detected by a confocal micro-Raman spectrometer (inVia Qontor, Renishaw, United Kingdom).
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2

Comprehensive Analytical Characterization of Raw Materials

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The elemental analysis of raw material was carried out by X-ray fluorescence (XRF, XRF-1800, Shimadzu, Kyoto, Japan, instrument working voltage 40 kV, working current 95 mA, prt 8 mL min−1). The crystalline phases and surface morphology of raw material and important solid roasted material were examined and scanned by X-ray diffraction (XRD, TTRAX III, Japan, Cu-Kα radiation, tube current 700 mA, tube voltage 40 kV, step sizes 0.2°, scanning range 2θ = 5°–90°, scanning rate 10° min−1), scanning electron microscopy (SEM, Nova NanoSEM 450, FEI, USA, acceleration voltage: 50 V to 30 kV, magnification 20–1000k). The aluminum content in aluminum liquid was determined by an inductively coupled plasma-optical emission spectrometer (ICP-OES, ICAP7400 Radial, Thermo Scientific, USA). The carbon contents analysis was performed via an infrared carbon and sulfur analyzer (CS 2000, ELTRA, Germany). The particle size distribution was measured using Rise-2002 laser particle size analyzer (Jinan Runzhi Technology Co., Ltd.).
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3

Quantifying Iron Concentrations by ICP-OES

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Total iron concentrations were analyzed in the supernatant solutions after separation of the solid phases after immediately diluting and acidifying with 1% HNO3. Iron measurements were carried out by ICP-OES (Thermo Fisher iCAP 7400 Radial) with a calibration between 1 and 100 ppm. The quality of the measurements was controlled through duplicate analyses of the samples and analysis of QC check-standards before and after the analysis.
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