The largest database of trusted experimental protocols

Agilent 8900 icp ms

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 8900 ICP-MS is an inductively coupled plasma mass spectrometer designed for elemental analysis. It provides sensitive and accurate detection of trace elements in various sample types.

Automatically generated - may contain errors

5 protocols using agilent 8900 icp ms

1

Analyzing Urinary Arsenic Speciation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Urine specific gravity was analyzed using a handheld refractometer with automatic temperature compensation (PAL-10S; ATAGO Co Ltd). An Agilent LC 1260 equipped with a Hamilton PRP-100X column interfaced with an Agilent 8900 ICP-MS in collision cell mode was used to measure concentrations of urinary arsenic species, i.e., iAs (arsenite and arsenate), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), and arsenobetaine (AsB), at the Trace Element Analysis Core at Dartmouth College. The arsenic species limit of detection (LOD) ranged from 0.06 to 0.10 μg/L across batches (Table S1). Total arsenic in tap water samples was measured with the Agilent 8900 ICP-MS in direct solution acquisition mode with a LOD of 0.04 μg/L.
+ Open protocol
+ Expand
2

Characterizing Luminescent Solid Solutions

Check if the same lab product or an alternative is used in the 5 most similar protocols
The crystal structures of the as-synthesized products were characterized with an Xray powder diffractometer (Cu Kα radiation, λ = 1.5406 Å). The structure was optimized by the GSAS program. The morphologies and the actual doping concentration of Mn4+ in a solid solution crystal were obtained with a scanning electron microscope (SEM, Quanta 250, FEI, St. Leonards, NSW, Australia) and Agilent 8900 ICP-MS (Santa Clara, CA, USA), respectively. Photoluminescence spectra (PL), photoluminescence excitation spectra (PLE), and temperature-dependent luminescence properties were tested employing a Hitachi F-4600 Fluorescence analyzer (Tokyo, Japan) equipped with a 150 W Xe lamp as an excitation light source. The diffuse reflection spectra of the samples were tested with a spectrophotometer (UV-3600, Shimadzu, Tokyo, Japan) and BaSO4 was used as the reflective material. The quantum efficiency (QE) of the samples was measured by a fluorescence spectrometer with an integrating sphere (Horiba FluoroMax-4, Tokyo, Japan). The WLEDs were tested by a high-precision array spectrometer (HSP 6000) under a steady current of 700 mA.
+ Open protocol
+ Expand
3

Quantifying Ag-NP Bioaccumulation in Zebrafish

Check if the same lab product or an alternative is used in the 5 most similar protocols
Zebrafish samples from vehicle, 0.03, 0.3, and 3 ppm Ag-NP exposure groups were analyzed at 3 and 5 dpf to quantify tissue concentrations of Ag. Samples were analyzed in triplicate with 22 to 26 larval zebrafish/sample obtained from 3 separate spawnings. Zebrafish samples, triplicate method blanks (200 µL 18.2 MΩ/cm water), and triplicate NIST1640a digestion quality control standards (200 µL NIST1640a Trace Elements in Natural Water - National Institute of Standards and Technology) were digested by adding 30 µL concentrated TraceMetal Grade HNO3 (Fisher Scientific) and 100 µL concentrated TraceMetal Grade HCl (Fisher Scientific) then heating in a hot block that was ramped up to 95 ºC over 30 min, followed by digestion at 95 ºC for 1 h. 550 µL 30% ULTREX II H2O2 (J.T. Baker) was added incrementally to room temperature samples with heating between additions. The following increments were used: 50 µL at 4 ºC for 15 min, 100 µL at 67 ºC for 10 min, 100 µL at 85 ºC for 45 min, 150 µL at 95 ºC for 25 min, and 150 µL at 95 ºC for 1 h. The samples were allowed to cool, then brought to a final volume of 1 mL with 18.2 MΩ-cm water prior to analysis by the Interdisciplinary Center for Plasma Mass Spectrometry at the University of California at Davis (ICPMS.UCDavis.edu) using an Agilent 8900 ICP-MS (Agilent Technologies).
+ Open protocol
+ Expand
4

Arsenic Species Analysis in Food Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Arsenic species were analyzed at the Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition in College Park, MD, USA, using a single laboratory validated method described previously.61 (link),62 (link) Briefly, ~ 0.25 g portions of each sample were extracted with 15 mL of DI water by heating at 90 °C for 30 min with a 45 min ramp (DigiPREP MS, SCP Science, Quebec, CA). Cooled extracts were centrifuged and syringe filtered (0.45 μm pore size). Following a further 1:3 dilution with DI water, anionic arsenic species were determined using an Agilent 1260 HPLC (Santa Clara, CA, USA) equipped with a PRP-X100 anion exchange guard column (Hamilton Company, Reno, NV) in line with an Agilent 8900 ICP-MS operated in He collision mode to reduce ArCl isobaric interference.
+ Open protocol
+ Expand
5

Arsenic Species Analysis in Food Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Arsenic species were analyzed at the Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition in College Park, MD, USA, using a single laboratory validated method described previously.61 (link),62 (link) Briefly, ~ 0.25 g portions of each sample were extracted with 15 mL of DI water by heating at 90 °C for 30 min with a 45 min ramp (DigiPREP MS, SCP Science, Quebec, CA). Cooled extracts were centrifuged and syringe filtered (0.45 μm pore size). Following a further 1:3 dilution with DI water, anionic arsenic species were determined using an Agilent 1260 HPLC (Santa Clara, CA, USA) equipped with a PRP-X100 anion exchange guard column (Hamilton Company, Reno, NV) in line with an Agilent 8900 ICP-MS operated in He collision mode to reduce ArCl isobaric interference.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!