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Ea3000 elemental analyzer

Manufactured by Eurovector
Sourced in Italy

The EA3000 elemental analyzer is a versatile and reliable instrument designed for the determination of carbon, hydrogen, nitrogen, and sulfur in a wide range of organic and inorganic samples. It features a compact and user-friendly design, making it a suitable choice for laboratories that require precise and efficient elemental analysis.

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8 protocols using ea3000 elemental analyzer

1

Characterization of Mg-CNT Composites

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Scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) analyses were performed using a Hitachi SU8010 SEM (Japan). Transmission electron microscopy (TEM) was performed using a JEM-2100F (JEOL, Japan). X-ray diffraction (XRD) analyses were performed on Bruker D8 Adv. (Germany) using Cu Kα radiation and operating conditions of 40 kV and 30 mA to identify the crystal phases of the as-prepared composites. The crystal groups of Mg–CNTs before and after the reaction were investigated by attenuated total reflectance Fourier transform infrared spectroscopy (FT-IR, PE1700 PerkinElmer, US). The elemental composition was analyzed by an Elemental Analyzer (EA3000, Euro Vector, Italy) and inductively coupled plasma atomic emission spectrometry (ICP-AES, Perkin Elmer Optima 8000, US.). Raman spectra were recorded on a LabRam HR800 (Horiba Jobin-Yvon, France). The Brunauer–Emmett–Teller (BET) surface area and pore distribution of the composites were calculated from N2 adsorption–desorption isotherms obtained on an Autosorb-iQ (Quantachrome, US).
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2

Comprehensive Materials Characterization

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A SEM image of the freeze-dried
sample was taken on a Hitachi S-4800 microscope, as described previously.53 (link) XRD sample characterizations were performed
on a Bruker D8 ADVANCE diffractometer. Diffraction patterns were obtained
at diffraction angles between 10 and 60° at room temperature.
EA for silicium in each sample was tested with Agilent 7700×
inductively coupled plasma–mass spectrometry (Agilent Technologies,
USA) after dissolving with HF. EA for carbon (C), hydrogen (H), nitrogen
(N), and oxygen (O) was implemented using the Elemental Analyzer EA3000
(Euro Vector, Italy). The hydrophilicity or hydrophobicity of each
sample was evaluated by surface-contact-angle measurement between
thesessile water drop and sample surface. WCA measurement was performed
using Attension Theta Lite (Biolin Scientific, Finland). A drop of
water (20 μL) was dropped over the sample using an automatic
microsyringe, and then, static images for each surface were taken.
Mercury intrusion porosimetry was performed with PoreMaster 60GT (Quantachrome
Instruments, USA), following an earlier report.54 (link)
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3

Foliar Nutrient Use Efficiency Analysis

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Oven‐dried foliage was ground into a fine powder with a JXMF‐03 grinding mill (Shanghai Jingxin Industrial Development Co., Ltd.). The leaf nitrogen concentration (LNC) was determined by an EA3000 elemental analyzer (EuroVector). The leaf phosphorus concentration (LPC) was determined by a Prodigy inductively coupled plasma atomic emission spectrometer (ICP‐AES) (Teledyne Leeman Labs.). The foliar photosynthetic N‐use efficiency (PNUE) and photosynthetic P‐use efficiency (PPUE) were calculated as follows: PNUE=AaLNC/SLA;
PPUE=AaLPC/SLA
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4

Soil Characterization of Remediated Sites

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The physicochemical characteristics of soils subjected to the different remediation strategies were determined at the beginning (day 0) and the end (day 126) of the experiment. The moisture content and electrical conductivity (EC) were measured, using a TPY-7PC soil analyzer (Zhejiang Top Technology Co.; Ltd., Zhejiang, China). Total carbon (TC), total organic carbon (TOC), and total nitrogen (TN) were determined, using an EA3000 Elemental Analyzer (Euro Vector S.P.A.; Italy). Total phosphorus (TP) was measured, using the molybdenum–antimony anti-spectrophotometric method [30 ].
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5

Cryoconite Nutrient Composition Analysis

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Three cryoconite samples from each time point were analyzed for TOC, IC, and TN. All eight cryoconite samples from each time point were analyzed for solid phase nitrogen and phosphorus speciation. Dried cryoconite samples (105°C, overnight) were analyzed for total organic carbon (TOC) and total nitrogen (TN) on a Eurovector EA3000 Elemental Analyzer. Detection limits for TOC and TN were 100 μg C g−1 and 100 μg N g−1 respectively, with coefficients of variation for duplicate analyses of 9.5 and 5.3%. Exchangeable NH+4, NO3, and NO2 in wet cryoconite were extracted using a 2M KCl method (Telling et al., 2011 (link)). Extracts were analyzed on a Bran and Luebbe Autoanalyzer 3. Results were converted to dry weights after weighing cryoconite before and after oven drying. The average coefficients of variation for duplicate NH+4 and NO3 analyses were 35.7 and 37.8%, respectively. Potentially bioavailable and residual phosphorus (Presidual) in dried cryoconite were analyzed using a three stage sequential digestion method using (1) 1 M MgCl2, (2) 0.1 M NaOH and (3) acid persulfate. Extracts were analyzed on a Shimadzu mini UV-vis spectrophotometer. The average coefficients of variation for duplicate cryoconite samples for the MgCl2, NaOH, and persulfate digestion steps were 10.1, 6.2, and 10.3%, respectively.
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6

Nanometal Fluids: Interfacial Tension and Thermal Cracking

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Nanometal fluids of different mass fractions were prepared, and the surface tension and oil–water interfacial tension of different concentrations of fluids were tested by a spinning drop interfacial tensiometer TX-500C (Shanghai Geology Instrument Institute, Shanghai, China). All of the interfacial tension measurements were conducted at 25 °C under atmospheric pressure. The thermal catalytic cracking effect of nanometal fluids on Bohai heavy oil at different heating rates was carried out using the Q50 thermogravimetric analyzer (TGA, TA Instruments, New Castle, DE, USA), under a nitrogen atmosphere. A Q2000 differential scanning calorimeter (DSC, TA Instruments, New Castle, DE, USA) was applied to investigate the thermal behavior of the heavy oil. A EA3000 elemental analyzer (EuroVector, Pavia, Italy) was used to determine the content of carbon and hydrogen in the heavy oil.
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7

Biomass Properties: Sawdust, Corncob, Rice Husk

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Three types of
biomass samples were investigated in this study: sawdust (SD), corncob
(CC), and rice husk (RH). The samples were collected from Hubei province,
China. The samples were first dried and pulverized, sieved to 180–250
μm and dried at 105 °C for 12 h before each experiment.
The properties of biomass samples are listed in Table 1, proximate and ultimate analyses were performed
using a YSRZY-8 industrial analyzer (Yongxin, China) and an EA3000
elemental analyzer (Euro Vector, Italy), respectively. The fixed carbon
and volatile matter mass fractions of SD, CC, and RH were 19.67, 14.82,
9.32%, and 69.38, 74.15, 64.56%, respectively. SD has the highest
fixed carbon content, and CC has the highest volatile matter content.
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8

GC-MS and Elemental Analysis of Bio-crudes

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The chemical composition of bio-crudes was analyzed by GC-MS. GC analysis was performed using a 6890 Model Gas Chromatograph with helium as the carrier gas and a mass spectroscopy detector (Agilent) using a thin film (30 m × 0.32 mm, 0.5 μm film thickness) HP-MS5 capillary column supplied from HP. Bio-crudes were diluted in acetone with dilution ratio 1:10 and subjected to a fixed temperature Journal Pre-proof ramping profile: 40 °C (held 4 min) to 280 °C at a rate of 10 °C/ min (held 20 min). The injector temperature was 250 °C and the injector split ratio was set to 30:1. Compounds were identified using the NIST spectrum library.
The elemental composition of bio-crudes and bio-chars was measured using a Eurovector EA3000 elemental analyzer. The total organic carbon (TOC) of the aqueous phases was determined using a Shimadzu TOC-L series analyzer.
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