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7500ce icp ms

Manufactured by Agilent Technologies
Sourced in United States

The 7500ce ICP-MS is an inductively coupled plasma mass spectrometer manufactured by Agilent Technologies. It is designed to perform high-sensitivity elemental analysis of a wide range of sample types. The 7500ce ICP-MS can detect and quantify trace elements at parts-per-trillion (ppt) levels with high accuracy and precision.

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30 protocols using 7500ce icp ms

1

Characterization of Copper Oxide Nanoparticles

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CuO NPs and bulk CuO were purchased from Shanghai Jingchun Reagent Limited Company, China. CuO NPs, with the purity is greater than 99.5 %, particle diameter is 40 nm and a surface area is 25–40 m2 g−1.The purity of bulk CuO is more than 99.9 %, particle diameter is 10 μm. The morphology of the CuO NPs was examined by transmission electron microscopy (TEM, JEOL 100CX, Japan). The particle diameter of CuO NPs in solution and the zeta potential of CuO NPs and bulk CuO in solution were measured using a 90 plus particle size analyzer (DR-525, Brookhave Instruments Corporation, USA) at 12 h after media preparation. The Cu2+ concentration that the nano-CuO released to the culture media was measured by ICP-MS 7500ce, Agilent, USA at 24 h after media preparation.
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2

Copper Removal from Aqueous Solutions

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300 mg of composite or ACFs was placed in a specially designed cartridge (details given in ESI), and cut glass fiber filters (0.4 μm, Macherey–Nagel) were placed in the inlet and outer caps of cartridge to avoid the release of fibers from the system. The prepared cartridge was rinsed with 0.01 M NaCl solution with the pH adjusted to 5.0 and 7.0 for 24 h at a flow rate of 150 mL h−1. Permeate samples were regularly collected and the concentration of copper in permeate was analyzed via ICP-MS (ICP-MS 7500 CE, Agilent). All tests were performed in duplicate.
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3

Quantifying Metal Ions in Bacterial Cells

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R1, Qpr6 KD, and Qpr6 Com strains were cultured to OD600 of 0.8 in 100 ml TGY media. The E. coli K-12 strain was cultured to OD600 of 0.4 in 50 ml LB media. The cells were then harvested by centrifugation at 10,000 g, 4°C for 10 min. The pellets were washed three times with 1 × PBS containing 1 mM EDTA and rinsed three times with 1 × PBS containing no EDTA. After centrifugation, the pellet was dried at 80°C for ~24 h, and the cell dry weight was measured. The cells were then resuspended in 2 ml of 30% nitric acid (GFS Chemicals) and incubated at 80°C for 4 h. After centrifugation at 12,000 g for 20 min, the supernatant was filtered against a 0.45 μM membrane (VWR) and serially diluted with ionized water to make the final concentration of nitric acid to 2%. The Mn2+ and Fe2+ concentrations were then measured using inductive coupled plasma mass spectrometry (ICP-MS 7500ce, Agilent). A blank control was prepared in the same manner but without cells. All data were replicated three times, and the means were used as representative values.
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4

ICP-MS Analysis of Iron Content

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Inductively coupled plasma mass spectrometer (ICP-MS) 7500CE (Agilent) was used for the determination of the iron content of different tissues. Before the measurement, samples were digested in order to destruct tissues and proteins, and obtain a limpid solution. Two milliliter aliquot of nitric acid (65%) and 1.5 ml of hydrogen peroxide (35%) were added. The mixture was placed in a Milestone MS-200 microwave oven and exposed at 250 W for 2 min, 0 W for 2 min, then 250 W for 6 min and 650 W for 5 min and 5 min of ventilation. After 20 min of cooling at room temperature, samples were ready for iron content determinations.
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5

Spectroscopic Characterization of Materials

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Ultraviolet photoemission spectroscopy was also carried out on an ESCALAB 250 Xi spectrometer using HeI resonance lines (21.2 eV). ICP-MS was performed on an Agilent ICPMS 7500CE. Powder XRD data were acquired on a Shimadzu X-ray diffractometer with Cu Kα radiation. TEM and EDX measurements were performed on a JEOL 2100 F TEM with an accelerating voltage of 200 kV. XPS measurements were carried out on a Thermo Electron Model with Al Kα as the excitation source.
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6

Copper Release in Membrane Filtration

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After day 1 of the MS2 removal test, the as-prepared filters were rinsed with 0.01 M NaCl solution prepared with water and adjusted to pH 5 or 7 (consistent with the experimental pH)
for 24 h at the same flux (160 L/m 2 •h). Permeate samples were regularly collected and the concentration of copper released during filtration was investigated via inductively coupled plasmamass spectrometry (ICP-MS 7500 CE, Agilent).
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7

Tissue Iron Content Analysis by ICP-MS

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Inductively coupled plasma mass spectrometer (ICP-MS) 7500CE (Agilent, Santa Clara, CA, USA) was used for the determination of the iron content of different tissues. Before the measurement, tissue samples were digested in order to destruct tissues and proteins and obtain a limpid solution. According to the sample, between 10 mg and 105 mg of tissue was available for digestion. Two milliliter aliquot of nitric acid (65%) and 1.5 ml of hydrogen peroxide (35%) were added. The mixture was placed in a Milestone MS-200 microwave oven and exposed, for brain samples, at 250 W for 2 min, 0 W for 2 min, then 250 W for 6 min and 650 W for 5 min and 5 min of ventilation. For liver and spleen samples, the digestion program was slightly different: 3 min at 250 W, 30 s at 0 W, then 5 min at 250 W, 30 s at 0 W, 5 min at 450 W, 30 s at 0 W, 5 min at 600 W and 25 min of ventilation. After 20 min of cooling at room temperature, samples were ready for iron content determinations.
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8

Elemental Analysis by ICP-MS

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Sixteen elements were determined in all samples with inductively coupled plasma mass spectrometry ICPMS (Agilent ICP-MS 7500ce, Waldbronn, Germany) at the following mass to charge ratios (m/z): As (m/z 75), Ca (m/z 43), Cr (m/z 52), Cu (m/z 65), Fe (m/z 56), K (m/z 39), Mg (m/z 24), Mn (m/z 55), P (m/z 31), V (m/z 51) and Zn (m/z 66). B (m/z 11), Mo (m/z 98), Pb (m/z 208) and U (m/z 238) were measured without collision or reaction gas, whereas all the other elements were measured in He mode.
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9

Elemental Analysis of Agricultural Samples

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Element concentrations in aqua regia digests (Ca, Cu, Fe, K, Mg, Mn, P, S and Zn), DTPA extracts (Cd, Cu, Fe, Mn and Zn), wheat shoot and grain digests (Ca, Cu, Fe, K, Mg, Mn, Na, P, S and Zn), mineral fertilizer digests (Ca, Cd, Cu, Fe, K, Mg, Mn, Na and Zn) and farmyard manure digests (Cd, Cu, Fe, K, Mn, P and Zn) were determined by inductively coupled plasma optical emission spectrometry (ICP-OES 5100, Agilent Technologies, Santa Clara, CA USA). Inductively coupled plasma mass spectrometry (ICP-MS 7500ce, Agilent Technologies, Santa Clara, CA USA) was used to measure Cd in aqua regia extracts, wheat shoot and grain digests and Cd, Cu, Mn and Zn in DGT extracts. Green manure digests were analysed by ICP-OES (Vista-MPX CCD Simultaneous, Varian Inc., Palo Alto, CA USA) for Ca, Fe, K, Mg, P and S and by ICP-MS (810, Varian Inc., Palo Alto, CA USA) for Cd, Cu, Mn and Zn.
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10

Comprehensive Material Characterization Protocols

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All chemical reagents and solvents were purchased from commercial sources and used as received without further purification. NMR spectra were recorded on a Bruker Avance DPX-250 spectrometer and Bruker AMX-400 Wide Bore for liquid and solid-state samples respectively. Mass spectra were acquired on a micrOTOF-QII ESI-MS instrument. Purity of all bulk material batches was confirmed by X-ray powder diffraction (XRPD) patterns collected on an X'Pert PRO MPD analytical diffractometer (Panalytical) at 45 kV, 40 mA using Cu Kα radiation (λ 1.5419 Å), and compared with single crystal simulated patterns. Thermogravimetric analyses were performed under nitrogen flow using a STA 449 F1 Jupiter-Simultaneous TGA-DSC from NETZSCH with a heat rate of 5°C/min. IR spectra were recorded in transmission mode on a Bruker Tensor 27FTIR equipped with a Golden Gate diamond ATR cell. Elemental Analysis measurements were performed on a Flash EA 2000 CHNS, Thermo Fisher Scientific analyser. Inorganic Elemental Analysis measurements were performed on an ICP-MS 7500ce, Agilent Technologies. Scanning electron microscope images were acquired on a FEI Quanta 650F working at an accelerating voltage of 2 kV and a beam current of 50 pA. Transmission electron microscope images were acquired on a JEOL JEM-1400 working at an accelerating voltage of 120 kV.
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