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Icpe 9000 spectrometer

Manufactured by Shimadzu
Sourced in Japan

The ICPE-9000 is a multi-element simultaneous inductively coupled plasma optical emission spectrometer (ICP-OES) capable of analyzing a wide range of elements. It utilizes high-frequency induction to generate a plasma that excites and ionizes the sample. The ICPE-9000 measures the intensity of the characteristic emission spectra produced by the excited elements to determine their concentrations in the sample.

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7 protocols using icpe 9000 spectrometer

1

Soil Chemical Analysis of Soybean Cultivation

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Soil samples were taken from each plot at a depth of approximately 0–30 cm using a polyvinyl chloride cylinder or soil sampler (DIK-1601; Daiki Rika Kogyo) on July 7 and November 17, 2016, which corresponded to the start and end of the soybean cultivation period, respectively. Samples were air-dried and passed through a 2-mm sieve, and the fine earth obtained was subjected to soil chemical analysis. The oven-dried weight of the fine earth was measured to obtain moisture correction factors that were used to convert nutrient contents of air-dried soil to a dry weight basis.
Total carbon and total nitrogen contents were determined using the dry combustion method with an elemental analyzer (Sumigraph NC-220F; Sumika Chemical Analysis Service, Osaka, Japan). Exchangeable bases (K+) extracted in 1 M ammonium acetate (pH 7) were measured with an inductively coupled plasma atomic emission spectroscopy (ICPE-9000 spectrometer, Shimadzu Corporation, Kyoto, Japan)62 . Available phosphorus was determined using the Bray-II method63 with a UV-1800 spectrophotometer (Shimadzu Corporation).
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2

Catalyst Characterization by XRD, TEM, and IR

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The crystalline structures of the catalysts were examined by powder XRD with a Rigaku RINT2400 diffractometer using a Cu-Kα X-ray source. TEM was conducted by a JEOL JEM-2010F microscope at an accelerating voltage of 200 kV. To prepare the TEM specimens, all samples were sonicated in carbon tetrachloride and dispersed on copper grids supported by an ultra-thin carbon film. CO pulse chemisorption was conducted at room temperature to estimate the Rh dispersion. The FT-IR spectra of adsorbed CO were measured with a JASCO FT/IR-430 spectrometer in transmission mode. A self-supporting wafer (20 mg cm–2) of the catalyst was placed in a quartz cell with CaF2 windows and attached to a glass circulation system. The catalyst was reduced at 450 °C for 30 min under H2 gas flow (60 mL min–1). Then, the catalyst was evacuated at the same temperature for 30 min, followed by cooling to room temperature. After the introduction of 5 Pa CO, spectra were repeatedly recorded at 1 cm–1 of resolution until the peak growth was saturated. ICP-AES analysis of the catalysts was performed using Shimadzu ICPE-9000 spectrometer. The catalysts were dissolved using aqua regia and a HF solution.
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3

Characterization of TS-1 Zeolites

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X-ray diffraction (XRD) measurements were performed on a Bruker Powder D8 Advance diffractometer (Billerica, MA, USA) at 40 kV and 40 mA using CuKa radiation (λ = 1.5418 Angstrom). DRUV/Vis spectra were recorded on a Shimadzu UV-2450 spectrophotometer (Kyoto, Japan) at 298 K using BaSO4 as a reference. FTIR spectra were recorded as KBr pellets on a Shimadzu IRPrestige-21 spectrometer (Kyoto, Japan). FTIR spectrum of pyridine adsorbed on TS-1 zeolites was tested at 298 K in a sealed reaction cell with KBr windows. A self-supporting disc (20 mg with 2.0 cm diameter) was prepared and evacuated at 723 K for 1 h. Subsequently, pyridine vapor was introduced and kept for 30 min. Excess pyridine was removed by vacuuming at 423 K for 30 min. The FTIR spectrum was collected in absorbance mode after the disc cooled to room temperature. Nitrogen adsorption–desorption isotherms were measured on a TriStar II 3020 sorption analyzer (Norcross, GA, USA) at 77 K. Elemental analyses (Si, Ti, and Na) were performed on an inductively coupled plasma optical emission spectrometer (Shimadzu ICPE-9000 spectrometer, Kyoto, Japan). Scanning electron microscopy (SEM) images were obtained on a JEOL JSM-7600F microscope (Tokyo, Japan) operated at 20 kV. Particle sizes were measured on a Malvern Zetasizer Nano ZS90 analyzer (Malvern, UK).
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4

Characterization of Sorbent Materials

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Elemental compositions of the sorbents obtained were determined using a Shimadzu ICPE-9000 spectrometer. The thermogravimetric (TG/DTG) and differential scanning calorimetric (DSC) data of samples were collected using a thermogravimetric analyzer (Netzsch STA 409 PC/PG) under an argon atmosphere. XRD data were obtained with a Shimadzu D6000 diffractometer with monochrome CuKα radiation (λ = 1.5418 Å). The BET surface properties of the samples were determined using a Tristar 320 surface area analyzer. The pore size distribution was calculated using the BJH method. The concentration of transition metals in the filtrates for every sorption experiment was determined using atomic adsorption with an AAS 300 Perkin-Elmer spectrometer. Sorbent particles of 0.1 mm were prepared for study by sieving.
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5

Trace Element Analysis by ICP-OES

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Inductively coupled plasma-optical
emission spectroscopy (ICP-OES) was carried out using an ICPE-9000
spectrometer (Shimadzu). Each sample was measured three times to ensure
the reproducibility of results.
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6

Cation Ratio Analysis by ICP-AES

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The cation ratio in the samples was additionally controlled by inductively coupled plasma atomic emission spectroscopy (ICP-AES) on a Shimadzu ICPE-9000 spectrometer (Kyoto, Japan). The samples were preliminarily dissolved in 12 M hydrochloric acid and the solutions obtained were diluted 100 times prior to their analysis.
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7

Quantitative Analysis via ICPE-9000

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Quantitative analysis was performed on a Shimadzu ICPE-9000 Spectrometer equipped with a highly efficient ionization and emission sources and CCD (charge-coupled device) detector. Its temperature was set at −14.89°C. Spectrum resolution, to avoid spectral interference was achieved automatically. A high-purity argon carrier gas was used. The flow rate of plasma gas (Ar) was maintained at 10 L/min, auxiliary gas (Ar) at 0.6 L/min, and carrier gas (Ar) at 0.7 L/min. The direction position AXIAL view, Rf power at 1.2 kW, pressure at 450 + 10 kPa. The rotation speed was adjusted to 20 rpm.
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