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Cary 100 scan uv vis spectrophotometer

Manufactured by Agilent Technologies
Sourced in United States

The Cary 100 Scan UV–vis spectrophotometer is a laboratory instrument designed to measure the absorption of ultraviolet and visible light by samples. It is capable of scanning across a wide range of wavelengths to analyze the spectral properties of various materials.

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7 protocols using cary 100 scan uv vis spectrophotometer

1

UV/Vis Spectroscopy of Dye-Surfactant Interactions

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Ultraviolet/visible (UV/vis) absorption
spectra were recorded for wavelengths of 200 to 800 nm using a Cary
100 Scan UV/vis spectrophotometer (Agilent, US). One ml of sample
solution was filled into a semimicro UV cuvette and spectra were taken
directly after sample preparation as well as after 1, 2, and 7 days
of aging. The latter helped to access the colloidal stability of the
samples. More information is given in the Supporting Information. The method of continuous variations, also known
as Job’s plot (details in the Supporting Information), was applied in order to resolve the stoichiometry
of ion pair formation between SSY and C16TAB. Job’s
plots have been used in previous work for the investigation of dye-surfactant
binding interactions.6 (link),38 (link)−41 (link) For a description of the working
principle and experimental results from the application of the Jobs
method the reader is referred to the Supporting Information.
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2

Elemental Composition Analysis

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The elemental composition was determined with an Elementar Vario MICRO cube C,H,N-analyzer (Langenselbold, Germany) equipped with a thermal desorption column and spectrophotometrically using a Cary 100 Scan UV-Vis spectrophotometer (Agilent Technologies, Santa Clara, CA, USA) after Schoniger method combustion (for F) and after decomposition by concentrated sulfuric acid as heteropoly acid according to Kjeldahl method (for P).
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3

Equilibrium Adsorption of Methylene Blue

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The equilibrium MB uptake capacity
of GO and GO-LCTS composites was
evaluated by batch mode using fixed amounts of adsorbent in sealed
glass vials. The adsorption isotherms obtained by such batch mode
conditions used a dosage of 5 mg adsorbent with 7 mL MB solution (pH
= 7) at variable initial MB (100–1000 μM). Samples were
mixed on a horizontal shaker (SCILOGEX SK-O330-Pro) for 24 h to ensure
equilibrium. A 1 mM stock solution of MB in water was prepared, and
other solutions were obtained by appropriate dilution. Absorption
measurements were carried out at λ = 664 nm, and a linear calibration
curve for MB absorbance at variable concentration was obtained with
a slope of 0.0615 = Abs664nm/[MB]. After 24 h shaking to
achieve equilibrium, the sample powders were separated from the solution
by centrifugation and the residual (MB) was measured using UV–vis
spectroscopy (Varian Cary 100 Scan UV–vis spectrophotometer).
The equilibrium uptake of MB was calculated using eq 2. where Qe (mg g–1) is the MB adsorbed per unit mass of adsorbent, C0 (mM) is the initial dye concentration, Ce (mM) is the residual amount of MB, V (L) is the volume of the MB solution, and m (g) is the weight of the adsorbent.
The GO composite was tested
for its regeneration properties over several adsorption–desorption
cycles with MB, as described in further detail in the Supporting Information.
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4

Characterization of Colloidal AuNPs

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The spectra of a colloidal solution of AuNPs were obtained by using quartz cells with a Varian Cary 100 Scan UV/Vis spectrophotometer. The initial parameters were: absorbance scan range: λ=300–700 nm, number of reads=5. Photometric accuracy for standard solution methods: ±0.01 Abs, wavelength accuracy at λ=656.1 nm: λ±0.02 nm, wavelength accuracy at λ=486.0 nm: λ±0.04 nm.
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5

Synthesis and Characterization of Dimers

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Reactions for the synthesis of dimers were monitored by thin layer chromatography (TLC) on precoated silica gel plates F254 (Merck, Darmstadt, Germany) and column chromatography was performed on Merck Kieselgel 60 (70–230 mesh). For the ESI MS analyses, a Micromass ZQ Instrument (Waters, Milan, Italy) equipped with an electrospray source was used. MALDI TOF mass spectrometric analyses were performed on a Voyager-De Pro MALDI mass spectrometer (PerSeptive Biosystems, Framingham, MA, USA). Absorption spectra were measured with a Cary 100 Scan UV-Vis spectrophotometer (Varian, Santa Clara, CA, USA) using a 1-cm path length quartz cell.
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6

Characterization of DOM UV-Vis Spectra

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The 5 mgC L−1 of each DOM and its constituent was prepared by dilution of the corresponding stock solution for characterization of UV–Vis spectra. The process was carried out with 1 cm quartz cuvette in Varian Cary 100 scan UV–Vis spectrophotometer, and the absorbance of each DOM at 254 nm and 365 nm was acquired, respectively.
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7

Characterization of AuNC Nanoparticles

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High-resolution transmission electron microscopy (HRTEM) measurements were recorded on a JEOL 2010 transmission electron microscope (Tokyo, Japan) operating at an accelerating voltage of 200 kV. Proton nuclear magnetic resonance (1H NMR) spectra were performed on a Bruker AC 400 NMR spectrometer (Rheinstetten, Karlsruhe, Germany) in concentrated D2O solutions. At the same time, the fractions were investigated by a matrix-assisted laser desorption ionization time-of-flight mass spectrometer (MALDI-TOF MS) (Autoflex, Bruker, Germany). X-ray photoelectron spectroscopy (XPS) measurements were conducted with a Leybold Heraeus SKL-12 X-ray photoelectron spectrometer (Shenyang, China) modified with a VG CLAM 4 multichannel hemispherical analyzer using a Mg Kα excitation source at 1253.6 eV (10 kV, 20 mA). Thermogravimetric analysis (TGA) measurements were conducted with a Perkin-Elmer TGA 6 thermogravimetric analyzer (Waltham, MA, USA). In addition, the UV–vis absorption spectra of the crude AuNC product and the AuNC fractions were recorded on a Cary 100 Scan UV–vis spectrophotometer (Varian, Palo Alto, CA, USA). The PL properties of the samples were acquired on a QM4 spectrofluorometer (Photon Technology International, Lawrenceville, NJ, USA).
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