The largest database of trusted experimental protocols

Agilent 5110

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 5110 is an inductively coupled plasma optical emission spectrometer (ICP-OES) designed for elemental analysis. It provides quantitative determination of trace elements in a wide range of sample types, including environmental, food, and geological samples. The 5110 employs a vertical plasma configuration and an echelle optics system to deliver high-performance multi-element analysis.

Automatically generated - may contain errors

28 protocols using agilent 5110

1

Degradation Kinetics of Chitosan Scaffolds

Check if the same lab product or an alternative is used in the 5 most similar protocols
The scaffolds (diameter = 6 mm, height = 2 mm) and CS coating (5 × 5 cm, 200 mg) were subjected to vacuum drying, and the initial mass was recorded as M0. Subsequently, the scaffolds were immersed in 0.05 M Tris-HCL buffer (pH = 7.4), and the CS coatings were, respectively, immersed in a 0.1 M NH4HCO3 buffer (pH = 7.4) with or without lipase (1.25 mg/mL). The proportions used in the above experiments was 200 mg/mL. The solution was refreshed every 2 days, and the scaffolds and CS coating were weighed and recorded as Mt after washing with PBS and vacuum-drying at the designated time point (3rd, 7th, 14th, and 21st days). The weight loss ratio is calculated as follows: Weight Loss%=(M0Mt)M0×100
The ion concentrations of Mg2+ and PO43− were measured simultaneously at the specified time points (3rd, 7th, 14th, and 21st days) using an inductively coupled plasma optical emission spectrometer (ICP-OES, Agilent 5110, Santa Clara, CA, USA).
+ Open protocol
+ Expand
2

Quantifying Matrix-Associated Iron in Biofilm

Check if the same lab product or an alternative is used in the 5 most similar protocols
For estimating the matrix associated iron [26 (link)] 3-day old colony biofilm was dispersed in 15 mL PBS, sonicated, and centrifuged at 14,000 rpm for 1 min, the supernatant was collected and filtered using 0.22 µ filter. Fe content in the samples was estimated at 238 nm using ICP-OES Agilent 5110. The statistical test used for analysis is unpaired t-test using GraphPad Prism5.
+ Open protocol
+ Expand
3

Microwave-Assisted Elemental Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Similarly as described before,65 the as-prepared nanoparticles were weighted into PTFE tubes and mixed with 6 mL 65% HNO3 p.a. (Merck) and 1 mL 30% H2O2 p.a. (Merck). The samples were then digested in a microwave and elements were quantified with an ICP-OES (Agilent 5110, Santa Clara, CA, USA). Due to the high silicate content and thus incomplete Si dissolution, the Si percentage was underestimated in some samples. For these samples, the residual mass was assumed to be Si as well.
+ Open protocol
+ Expand
4

Elemental Analysis of Plant Roots

Check if the same lab product or an alternative is used in the 5 most similar protocols
Approximately 0.15 g of dried root tissue powder was transferred into a beaker containing 4 mL of nitric acid overnight. The mixture was heated on a stirring hotplate at 200 °C for 3 h, and 2 mL of H2O2 was gradually added during the digestion process, with the solution evaporating to 1 mL using residual heat. The solution was deliquated to 10 mL with Milli Q water and then filtered through 0.22 μm filters to quantify the element content of Magnesium (Mg), Iron (Fe), Copper (Cu), and Zinc (Zn) via inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-OES) (Agilent 5110, Agilent, Santa Clara, CA, USA).
+ Open protocol
+ Expand
5

Comprehensive Characterization of Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphology and structure of the as-prepared nanoparticles were examined by transmission electron microscopy (TEM; JEM-2100; JEOL, Tokyo, Japan). Nitrogen adsorption/desorption isotherms and pore size distributions were obtained with an adsorption analyzer (Micromeritics, Norcross, GA, USA). Fourier-transform infrared spectra were measured on a Nexus 670 spectrometer (Thermo Fisher Scientific). The wide-angle X-ray diffraction (XRD) patterns were obtained on a D8 ADVANCE powder diffractometer using Cu Kα1 radiation (1.5405 Å). Dynamic light scattering was conducted by using a BI-200SM multiangle dynamic/static laser scattering instrument (Brookhaven Instruments Corporation, Holtsville, NY, USA). Zeta potential was detected by a Zetasizer Nano ZS Nanosizer (Malvern Instruments, Malvern, UK). UV-Vis spectra were recorded on a UV-3101PC Shi-madzu spectroscope (Shimadzu, Kyoto, Japan). The content of Si was determined by Agilent 5110 inductively coupled plasma-optical emission spectroscopy (Agilent Technologies, Santa Clara, CA, USA).
+ Open protocol
+ Expand
6

Sulfur Content Analysis in Plant Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
Sulfur was measured for 21-d-old shoot and root dry samples by digestion method, using 2 mL freshly prepared 1% HNO3 (trace metal grade, Fisher Scientific) that was added to the preweighed shoot and root samples. After digestion, 1 mL of samples were transferred to volumetric test tubes and diluted to a final volume of 50 mL with 1% HNO3. The concentration of sulfur was determined using ICP-OES (Agilent 5110, Agilent Technologies) with the following conditions: 1.2 KW RF power, 0.7 L/min nebulizer flow, 12.0 L/min plasma flow, 1.0 L/min auxiliary flow, argon gas, 8-mm viewing height, and axial viewing mode.
+ Open protocol
+ Expand
7

Comprehensive Characterization of Catalysts

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphologies of samples were characterized via TEM (Technai G20 S-TWIN, FEI, Hillsboro, OR, USA) with a 200 kV acceleration voltage. The element distribution was studied using HAADF-STEM-EDX mapping. The phase of catalysts was analyzed using XRD (D8, Brook, Nordrhein-Westfalen, Germany) with Cu Kα radiation (λ = 0.15418 nm). The chemical states of surface elements were characterized via X-ray photoelectron spectroscopy (Thermo Fisher Scientific K-Alpha, ESCALAB 250XI, Waltham, MA, USA). Thermogravimetric analysis (STA, 2500) for the carbon content was conducted from 30 °C to 800 °C under an O2 atmosphere. The content of each element in the sample was analyzed by inductively coupled plasma atomic emission spectrometry (ICP-AES, Agilent 5110, Santa Clara, CA, USA).
+ Open protocol
+ Expand
8

Cultivation and Zinc Treatment of P. aeruginosa

Check if the same lab product or an alternative is used in the 5 most similar protocols
PAO1 was purchased from American Type Culture Collection (#15692, ATCC; Manassas, VA, USA). P. aeruginosa containing a triple hemagglutinin tag on its czcR N-terminus (CzcR-HA PAO1) was kindly provided by Dr. Karl Perron (University of Geneva; Geneva, Switzerland) [41 (link)]. P. aeruginosa was cultured in LB (Alfa Aesar, #3339936; Haverhill, MA, USA) overnight at 200 rpm and 37 °C, then diluted to 5 × 107 CFU/mL in LB (as a control) or LB containing zinc (800 µM, as ZnSO4, except for growth curve as indicated), and incubated for 16 h at 37 °C (shaking at 200 rpm). Zinc concentration was confirmed using Inductively Coupled Plasma-Optical Emission Spectrometer (ICP-OES; Agilent 5110; Agilent Technologies, Santa Clara, CA, USA) [66 (link)].
+ Open protocol
+ Expand
9

Quantifying Microbial Impact on Fluid Chemistry

Check if the same lab product or an alternative is used in the 5 most similar protocols
To assess the impact of microbes on the fluid chemistry, inductively coupled plasma-optical emission spectroscopy (ICP–OES) was employed using an Agilent 5110 (Agilent, Milton Keynes, UK) at the Open University, as previously described [47 (link)]. Fluid samples were taken at the end of the growth experiments from both the biotic and abiotic test groups and filtered using 0.22 μm filters (Starlab, Milton Keynes, UK) and acidified through the addition of 1% nitric acid (Sigma-Aldrich, Gillingham, UK) prior to analysis.
+ Open protocol
+ Expand
10

Degradation Analysis of Mg-Zn-Y-Nd Alloy

Check if the same lab product or an alternative is used in the 5 most similar protocols
The surface morphology of the leached samples before and after removal of the degradation products was observed by scanning electron microscopy (FEI Quanta 200, Eindhoven, Holland), and the elemental composition of each surface was also detected using the scanning electron microscopy matching energy dispersion spectrometer.26 (link) To investigate the mechanical property of the degraded Mg-Zn-Y-Nd alloy, surface hardness was detected as reported.27 According to American Society for Testing Materials G1-03, the degradation products of surface deposition were removed by chromic acid solution for Mg alloy samples. The inductively coupled plasma optical emission spectrometry (ICP-OES, Agilent 5110, Palo Alto, CA, USA) was used to measure the concentration of Mg2+, Zn2+, Y3+, Nd3+ in the extract and culture medium.
+ 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!