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188 protocols using cary 630

1

Membrane Characterization via Hydrophobicity, Microscopy, and Spectroscopy

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Membrane hydrophobicity was evaluated via water contact angle measurements with a calibrated tensiometer (Biolin Scientific, AZ, USA) using the sessile drop method with one water droplet of 20 μl. The top surface and cross section of the membranes were imaged by field-emission SEM (FESEM) using secondary and backscattered electron detectors (JEOL, Tokyo, Japan). Membrane samples were coated with 5 nm of carbon thread before taking images. The average pore size, porosity, and thickness of the membranes were extracted from FESEM images at various locations using ImageJ software (National Institute of Health, MD, USA). Five SEM images from similarly fabricated alumina membranes were used for ImageJ analysis and the surface pore size was considered to be the longest distance between two points on the pore boundaries (or the Feret’s diameter). Elemental compositions of the membranes were quantified using an energy-dispersive x-ray spectroscopy detector (Oxford Instruments, Oxfordshire, UK) coupled with the FESEM system operating at an accelerating voltage of 15 kV. FTIR was conducted using a spectrometer with a diamond attenuated total reflection module (Cary 630, CO, USA).
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2

Characterization of Precipitated CaCO3 Crystals

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For characterization of the precipitated CaCO3, a X-ray diffraction (XRD, DX-2700BH), a Fourier-transform infrared (FTIR, Cary 630) spectrometer and a scanning electron microscopy (SEM, phenom pro) was used. The resulting powders crystalline phases of was carried out using a Cu Kα source was used over a 2θ range of 20° to 60° and a step size of 0.02° with dwell time of 0.05 s was applied during the analyses. From intensity peaks of XRD patterns, the compositions of vaterite were estimated by eqn (4) as follows:32 (link) where IC and IV are the intensity of calcite and vaterite respectively, three suffixes are Miller indexes of each phase, and fV is the content of vaterite in precipitates.
Fourier transmission infrared spectroscopy was performed on uniaxially pressed powder pellets mixed with KBr. The FTIR analyses were carried out in the 4000–400 cm−1 range with a resolution of 4 cm−1 and with 32 spectral scan repeats for each sample. The size and morphological structures of the precipitated CaCO3 were examined by scanning electron microscopy. Powder samples for SEM were uncoated and observed at a working distance of 3.5 mm and an accelerating voltage of 0.7 kV.
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3

Spectroscopic Characterization of Compounds

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FT-IR analyses were performed on Cary 630 FT-IR with ATR. NMR analyses were recorded on a Bruker Fourier 300. 1H NMR spectra of samples were recorded in CDCl3 at 300 MHz, chemicals shifts were reported in parts per million (CDCl3 residual signal at δ = 7.26 ppm). 13C NMR spectra of samples were recorded at 75 MHz (CDCl3 signal at δ = 77.16 ppm). HRMS were recorded by the PLANET platform at URCA on a Micromass GC-TOF.
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4

Comprehensive Characterization of As-Prepared Materials

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The crystalline phase of the as-prepared materials was confirmed by X-ray diffractometer (XRD, XD-2) from 10–80° with a scan rate of 4° min−1. The apparent morphology and distribution of elements were obtained by transmission electron microscope (TEM, FEI Tecnai G2 F20 X-Twin) with an energy dispersive X-ray spectrometer (EDS). The specific surface area was collected by surface area analyzer (BET, Gemini VII 2390). Functional groups and molecular structure were analyzed by the Fourier transform infrared spectrometer (FTIR, Cary 630) from 4000–400 cm−1. The element kinds, contents, and valence states were determined by X photoelectron spectroscopy (XPS, ThermoFisher ESCALAB Xi+, Waltham, MA, USA) from 0–1350 eV.
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5

Characterization of Cyanopropyl T8 Particles

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The microstructure and morphology of the synthesized cyanopropylT8 particles were observed by SEM.
SEM images in Figure 10 show that particles
are micrometer-sized. They are well dispersed in size and ranges from
1 to 200 μm.
The attenuated total reflectance FTIR method via
a Cary 630 instrument
was used to identify the absorption bands and assign them to the bonds
within the compound. In accordance with the literature,6 (link),11 (link) the typical FTIR characteristic data obtained include stretching
vibrations at 2245.8 cm–1 for the −CN group,
stretching vibration at 2939.8 cm–1 (C–H),
and bending vibration at 1406.0 cm–1 (C–H).
Also, vibration at 747.4 cm–1 corresponds to Si–C,
while that at 1096 cm–1 corresponds to Si–O
stretch.
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6

FTIR and LPG Spectroscopy Analysis

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Fourier transform infrared spectrometry (FTIR) was performed using a Cary 630 spectrometer with wavenumber accuracy of 0.05 cm -1 . Measurements were performed at 25°C, with 64 scans per sample, after subtracting a background spectrum measured over an average of 16 scans between 4000 -650 cm -1 . The spectra from the LPG were measured using a CCD spectrometer (Ocean Optics, HR4000, UK) with 0.11 nm wavelength accuracy and a tungsten-halogen light source (Ocean Optics, HL-2000, UK).
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7

FTIR Analysis of Synthetic Smectite Clays

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All synthetic smectite clay mineral samples were dried at 110 °C for 18 h before FTIR spectra were collected to limit the contribution of vH-O–H stretching bands from water around 3400 cm−1 and 1630 cm−1. Samples were measured using an Agilent Cary 630 FTIR equipped with a 1 bounce diamond attenuated total reflectance (ATR) cell with a spectral resolution of 2 cm−1 from 4000 to 400 cm−1. Before each sample was analyzed the ATR cell was cleaned with ethanol, allowed to dry, and 256 background scans were run. The samples were immediately transferred onto the ATR cell and 128 scans were collected.
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8

Comprehensive Characterization of Nanomaterials

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The TEM measurements were conducted using an FEI Tecnai G2 F30 transmission electron microscope (FEI, USA). Fourier transform infrared spectrophotometric (FTIR) spectra were recorded on a Cary 630 (Agilent, USA) spectrometer using the KBr pellet technique. Small-angle X-ray diffraction (SXRD) was performed on a SmartLab (RIGAKU, Japan). Thermogravimetric analysis (TGA) was performed on a TGA/DSC3+ instrument (METTLER TOLEDO, Switzerland) with a heating rate of 10 °C min−1 under a nitrogen flow. Zeta potentials were determined on a Nano-ZS90 laser particle size and zeta potential analyzer (Malvern, UK). The fluorescence spectra were examined with an F-7100 fluorescence spectrophotometer (Hitachi, Japan).
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9

Compatibility of Nanoemulsion Components

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The compatibility between CO and other components of the nanoemulsion was studied viaFT-IR spectroscopy (Agilent Technologies Cary 630). The spectrum of CO and CON was recorded as being inthe region of 4000 to 400 cm−1 [24 (link)].
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10

FTIR Analysis of Biomaterials

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FTIR analysis of BTs has been performed with the scan range 400–4000 cm−1 at the resolution of 8 cm−1 using ATR accessory on Agilent Cary 630 FTIR spectrometer.
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