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94 protocols using v 750

1

Leaf Optical Properties and Chlorophyll Analysis

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The reflection and transmission spectra of the third leaf (fully expanded and unshaded leaf) from the top of the plant were measured using a spectrophotometer (V-750, JASCO Corporation, Tokyo, Japan) with an integrating sphere unit (ISV-922, JASCO Corporation, Tokyo, Japan) at 10 DAT. The range of the measured light spectrum was 400–700 nm. Eight and four plants in each treatment in Experiments 1 and 2 were sampled, respectively. Absorptance was calculated for each wavelength as follows:
Chlorophyll pigment was extracted from the third leaf from the top of the plant with N,N-dimethylformamide at 10 DAT, according to the protocol described by Porra et al. [81 (link)]. For chlorophyll concentration analysis, four leaves from four plants in each treatment were sampled. The chlorophyll concentration was determined on a dry weight basis by measuring the absorbance of the leaf extracts at 663.8, 646.8, and 750.0 nm using an ultraviolet-visible spectrophotometer (V-750, JASCO Corporation, Tokyo, Japan).
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2

Photocatalytic Degradation of Organic Dyes

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Example 3

Photocatalytic Activity

The photocatalytic activity of Bi2S3—CdS was evaluated through photocatalytic degradation of methyl orange and methyl green under UV light irradiation for 120 min using Xenon lamp (300 W) as light source. In each experiment (carried out separately for each dye) 50 mg of Bi2S3—CdS was dispersed in 50 mL of aqueous dye solution of methyl orange (10 mg/L) or methyl green (14 mg/L). In order to ensure the adsorption-desorption equilibrium between the photocatalyst and dye, solution was stirred in dark for 1 hour and then illuminated under Xenon lamp (300 W). After 15 min time interval, 4 mL of the suspension was collected and centrifuged to remove Bi2S3—CdS catalyst. The concentration of dye was assessed using a UV-Visible spectrophotometer (JASCO V-750) by measuring the absorbance of dyes at their respective wavelength. The degradation efficiency was calculated as:
Degradation rate (%)=(C0−C)/C0×100  (equation 1)where C0 is the initial concentration of the methyl orange or methyl green and C is the time-dependent concentration of methyl orange or methyl green after each irradiation (see FIG. 6).

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3

UV-Vis Absorption Spectra of r-BS Powders

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The UV-Vis absorption spectra of the r-BS powders were measured using spectrophotometer (V-750, Jasco, Tokyo, Japan) with an integration sphere unit at room temperature.
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4

Storage Stability and Kinetics of Laccase

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The storage stability of free and immobilized enzyme stored at 4 °C was examined over 30 days. Briefly, ABTS was used as a substrate, to which 10 mg of free or immobilized laccase was added. Changes in the concentration of the substrate were measured spectrophotometrically (λ=420 nm), using a Jasco V-750 (Japan) spectrophotometer. For the storage stability study, the initial value of the activity of the free or immobilized enzyme was defined as 100%. The inactivation constant (kD), and half-life (t1/2) were evaluated based on the linear regression slope.
The same reaction was used to evaluate the kinetic parameters: the Michaelis-Menten constant (Km) and the maximum rate of reaction (Vmax). For this purpose solutions of the substrate at concentrations ranging from 1 to 100 mM were used, and the experiments were carried out under optimum assay reaction conditions. The Hanes-Woolf plot was used to calculate the apparent kinetic parameters of the free and immobilized enzyme. All measurements were made in triplicate, and the results are presented as average ± standard deviation.
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5

Multianalytical Characterization of MnFe2O4 Composites

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The MnFe2O4 phase on silica and GO was analyzed using high-angle XRD instrument (Miniflex 600, Rigaku, Tokyo, Japan). The textural features of two supports were measured using the N2 adsorption technique (ASAP-2020 plus, Micromeritics, Norcross, GA, USA). The morphological variations of manganese ferrite nanoparticles over the silica and GO support was investigated using transmission electron microscopy (TEM, JEM2100F, JEOL, Tokyo, Japan). The sample preparation procedure was described in our previous publication [14 (link)]. The superparamagnetic properties of the two composites were analyzed using vibrating sample magnetometer (VSM), LDJ electronics, 9600, Troy MI, USA. The ferrite nanoparticle chemical coordination was analyzed using DRS-UV-visible spectroscopy analysis (JASCO V-750, Tokyo, Japan).
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6

Catechin Degradation in Tea Analysis

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The degradation of catechins in tea was studied in details with assistance of high-performance liquid chromatography (HPLC: pump-PU-4180/detector-UV-4075, JASCO Corp.) by applying reverse phase chromatography with an ODS column was utilized. Standard catechins of EGC, EGCg, EC, ECg, GC and GCg, (Funakoshi Co., Ltd) were used to confirm the catechins type appear in HPLC spectra. The color changing in different degraded solution was confirmed by transmittance measurement on an UV–visible spectroscopy (UV–vis: V-750, JASCO Corp.). The chemical component besides the standard catechins was identified by a LC mass spectroscopy with time-of-flight detector (LC-TOF–MS, Waters Corp.). In addition, the metal ions diluted from glaze through degradation were confirmed by inductivity coupled plasma optical emission spectrometer (ICP-OES: ICPE-9820, Shimadzu Corp.)
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7

Synthesis and Characterization of β-Nb2ZnO6 Nanoparticles

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Niobium chloride (0.270 g) and zinc nitrate (0.2974 g) were weighed and shifted to a Teflon-lined autoclave with 20 mL of distilled water. After stirring, urea (0.2402 g) and ammonium fluoride (0.148 g) were added to the mixture. After stirring, the autoclave was heated at 200 °C for 12 h. The obtained precipitation was centrifuged and washed repeatedly using deionized water, followed by washing with ethanol, and dried overnight (60 °C). The samples were calcined at 500 °C and 700 °C in the furnace and assigned as (A) and (B), respectively.
The morphology and size of β-Nb2ZnO6 nanoparticles (A) and (B) were determined by a transmission electron microscope (TEM) (FEI, Morgagni 268, Brno, Czech Republic) and X-ray diffraction (Rigaku, Japan) quantified with Cu-Kα radiation (λ = 1.5418 Ǻ) with a 1° per minute speed of scanning (range 10–80°). Surface area (BET) was determined by Micromeritics ASAP 2020 PLUS (Norcross, GA, USA) by degassing the samples (180 °C) and by employing N2 adsorption data with a range of relative pressure (P/P0) from 0.0 to 1.0. A diffuse reflectance UV-visible spectrophotometer was used for recording the UV-Visible spectra (UV-Vis, JASCO V-750, Great Dunmow, Essex, UK).
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8

Dye-coupled Film Absorbance Spectra

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Absorbance spectra of dye-coupled films were measured by an ultraviolet and visible light
spectrophotometer with an integrating sphere unit (V-750 and PIV-756, JASCO Corp., Tokyo,
Japan). Plain polyethylene films were used to obtain baseline absorbance. Absorbance was
measured in the wavelength ranging from 300 to 800 nm at 1 nm spectral bandwidth. Maximum
absorbance values around 500 nm were used for comparison between the implanted film and
the non-implanted same lot.
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9

Photocatalytic Degradation of Methyl Orange

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Example 4

Photocatalytic Activity

The photocatalytic activity of zinc oxide nanoflowers and nanospheres was evaluated through the photocatalytic degradation of methyl orange under UV light irradiation for 120 min using a xenon lamp (300 W) as the light source. In each experiment, 10 mg, 30 mg, and 50 mg of catalyst (zinc oxide nanoflowers or nanospheres) was dispersed in 100 mL of an aqueous solution of methyl orange dye, the dye having a concentration of 10 mg/L. In order to ensure the adsorption-desorption equilibrium between catalyst and dye, the solution was stirred in the dark for 1 h before irradiating with the xenon lamp. At 15 min time intervals, 4 mL samples of the suspension were collected and centrifuged to remove the zinc oxide nanoflowers or nanospheres, and the concentration of dye in the supernatant was assessed with a UV-Visible spectrophotometer (JASCO V-750) by measuring the absorbance at 465 nm. The change in 200-800 nm absorbance over time is shown in FIGS. 10 and 11. The degradation efficiency was calculated as:
Degradation efficiency (%)=(C0−C)/C0×100%,where C0 is the initial concentration of the methyl orange dye, and C is the time-dependent concentration of methyl orange upon irradiation. The change in degradation efficiency over time is shown in FIGS. 6-9.

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10

Characterization of Zinc Oxide Nanostructures

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Example 3

Physical Characterization

The morphologies of the zinc oxide nanoflowers and nanospheres were examined by scanning electron microscopy (SEM, FEI INSPECT S50), as shown in FIGS. 2A-2B and FIGS. 3A-3B, respectively. The crystallinity and crystal phases of the zinc oxide nanoflowers or nanospheres were studied by an X-ray diffractometer (XRD Rigaku, Japan) using Cu-Kα radiation (λ=1.5418 {acute over (Å)}) in the range of 10°-80° with 1°/min scanning speed. The XRD patterns for both nanoflowers and nanospheres arc shown in FIG. 1. UV-Vis diffuse reflectance spectra of zinc oxide nanoflowers and nanospheres, as shown in FIG. 4, were recorded on a diffuse reflectance UV-Vis spectrophotometer (JASCO V-750). Micromeritics ASAP 2020 PLUS nitrogen adsorption apparatus (USA) was employed for BET surface area determination. Before surface area analysis, samples were degassed at 180° C., and the surface area was then determined using N2 adsorption data in the relative pressure (P/P0) range of 0.05-0.3, as shown in FIG. 5. The BET surface area of zinc oxide nanoflowers was observed as 22.54 m2/g (pore size: 22.92 nm; pore volume 0.1291 cm3/g) while for nanospheres, the surface area was 9.51 m2/g (pore size: 30.74 nm; pore volume 0.0780 cm3/g).

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