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V 600

Manufactured by Jasco
Sourced in Japan

The V-600 is a versatile lab equipment designed for a range of applications. It features a compact and durable construction, and its core function is to provide precise measurements and analysis capabilities for various samples or materials.

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6 protocols using v 600

1

Sonocatalytic Degradation of Organic Pollutants

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The sonocatalytic activity of MXe/MIL-101(Cr) was assessed by measuring the decomposition of SD and AAP as pollutants in an aqueous solution at 25 °C. The entire sonocatalytic experiment was performed at 40 kHz in a MUJIGAE ultrasonic bath instrument (SD-D400H). Briefly, 25 mg of MXe/MIL-101(Cr) (1 g L-1) was added to 25 ml of a 10 mg L-1 solution of SD or AAP at pH 7.0. These mixtures were placed in the dark for 30 min to achieve adsorption–desorption equilibrium between the catalyst and the pollutant, and then H2O2 (2 ml, 2 mmol/L) was added. Following this, the sample was irradiated (180 W/L) using an ultrasonication bath at 303 K, and 1.5 ml volumes of the samples were collected and filtered at regular intervals through a 0.22 μm syringe filter. The filtrate adsorption intensities were then measured using a UV–Vis spectrophotometer (JASCO V-600) to determine pollutant concentrations. Experimental conditions such as pH (3–11), catalyst dosage (0.25–1.50 g/L), initial pollutant concentration (5–20 mg/L), H2O2 concentration (0.5–3 mM/L), radical scavenger species, ultrasonic irradiation power (90–225 W), and temperature (283–313 K) were varied to optimize the process. For recycling experiments, MXe/MIL-101(Cr) was washed thoroughly in DI water and dried at 60 °C in a vacuum for 6 h between cycles.
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2

Protein UV-Vis Absorbance Spectroscopy

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UV-visible absorption spectra of purified proteins were recorded using either a V-600 or a V-650 spectrophotometer (Jasco, Gross-Umstadt, Germany).
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3

Quantifying Hydrogen Peroxide in Sonocatalysis

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To quantify H2O2 evolution during sonocatalysis, a 2 ml sample of the reaction solution was filtered through a 0.22 μm syringe filter, and 1 ml of freshly prepared KI reagent (0.4 M KI, 0.05 M NaOH, and 1.6 × 10-4 M (NH4)6Mo7O24·4H2O) and 1 ml of 0.1 M KHC8H4O4 were mixed with 1 ml of filtrate and aged for 2 min. Absorption was then measured at 350 nm using a UV–vis spectrophotometer (JASCO V-600). A trapping experiment was conducted to investigate the contributions made by reactive oxygen species (ROS) to the decomposition of organic compounds. The following four scavengers were added to the sono-reactor containing AAP: 5 mM of AgNO3, an electron scavenger; EDTA, a hole scavenger; BQ, an O2•- scavenger; and t-BuOH, an •OH scavenger. In addition, different concentrations of humic acid (HA), t-BuOH (an •OH scavenger), and carbon tetrachloride (CCl4, an •OH promoter) were also added to investigate the reaction kinetics.
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4

Coordination of Titanium and Tannic Acid

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UV-vis spectroscopy was used to examine the coordination reaction of TA and TiIV in an aqueous solution. UV–vis spectra were obtained on a spectrophotometer (V-600, JASCO, MD) at room temperature. Three solutions were prepared prior to the measurements. Control samples of TA and TiIV solutions were prepared in oxygen-free deionized water at concentrations of 0.1 and 0.3455 wt%, respectively. The pH of the TA solution was controlled at 7. The TA-TiIV solution was prepared as above mentioned.
Fourier-transform infrared spectroscopy (FTIR, Jasco FT/IR-410) was employed to analyze chemical and coordination structures of metallogels. TA-TiIV metallogels were dried in liquid nitrogen under reduced pressure for 4 h. The dried TA-TiIV was grounded by a pestle and blended with KBr. The mixed powder was compressed into a pellet. FTIR was operated in a wavenumber range of 400 to 4000 cm−1.
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5

Inhibition Assay of Bisphenol Analogs

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The competent E. coli XL1-blue strain was purchased from Nippon Gene Co. Ltd. (Tokyo, Japan). Stock cultures were stored at −80 °C in a mixture containing LB media and 20% glycerol. Prior to each inhibition assay, the stock of E. coli strains (1 mL) was added in 100 mL of chemically defined mineral media reported by Cuellar et al. [35 ]. (see supporting information) and incubated aerobically overnight at 200 rpm and 37 °C. Then, 990 μL aliquots from the overnight grown cultures, which were diluted with test medium to an initial OD600 of approximately 0.15, were added to measuring cell for spectrophotometry. Then, the solution was mixed with 10 μL of the test solution of BPA, diBr-BPA, or diI-BPA (10 μM in DMSO) and incubated at 37 °C with shaking at 120 rpm. The growth curves were determined by measuring the OD600 of each cells every 2 h during 14 h on a spectral photometer JASCO V-600 (JASCO Co., Tokyo, Japan). Then, a final measurement was performed after 24 h. Two independent experiments were carried out. The statistical difference between the concentration of the means and standard errors of the OD600 measured at 24 h was determined by the Student's t-test.
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6

Photosynthetic Pigments and Hydrogen Peroxide Quantification

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Approximately 0.1 g of fresh leaf tissue was homogenized with sea sand, anhydrous magnesium carbonate and 80% acetone. The mixture was quantitatively transferred into test tubes and filtered using a vacuum pump. Filtrate absorbance was measured [Jasco-V600 (Jasco Inc., Japan)] at 647 nm (chlb) and 663 nm (chla) wavelengths. The concentration of photosynthetic pigments were calculated according to Lichtentahler (1987) .
Hydrogen peroxide Approximately 0.1 g of fresh leaf tissue was homogenized in 6 ml of cold acetone, quantitatively transferred into test tubes and centrifuged at 6,000 rpm for 5 minutes. Two ml of the supernatant was added to 0.8 ml of titanium reagent [0.04% (w/v) Ti 4+ in Ti(SO 4 ) form] and 1 ml of concentrated (30%) ammonia. The reaction mixture was mixed thoroughly and centrifuged at 6,000 rpm for 10 minutes. The upper layer of the mixture was discarded and the bottom layer (containing Ti-H 2 O 2 crystals) was supplemented with 2 ml of 2 M sulphuric acid. After syringe filtration (0.2 µm PTFE membrane), absorbance was measured at 415 nm (Mukherjee and Choudhuri, 1983) .
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