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Vibra s60

Manufactured by Harvard Bioscience
Sourced in United Kingdom

The Vibra S60 is a laboratory shaker designed for mixing and agitating samples. It features a compact and robust construction, providing a consistent and reliable shaking motion. The Vibra S60 is suitable for a variety of applications that require gentle to moderate mixing of liquids, suspensions, or solids in various laboratory settings.

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Lab products found in correlation

6 protocols using vibra s60

1

Sonochemical Oxidation of Rhodamine B

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To quantitatively analyze the sonochemical oxidation process, the degradation of rhodamine B was evaluated using a spectrophotometric method measured at 554 nm (Vibra S60, Biochrom Ltd., UK). The initial concentration of the rhodamine B solution was 5 mg L–1, where the solution was prepared with tap water. No significant difference in water quality was observed during the experiments. The ultrasound irradiation time was 180 min and the concentration of rhodamine B was monitored at 20 min intervals. All measurements were repeated three times; the average values are reported herein.
The sonochemically active zone was visualized using luminol solution (0.1 g L–1 luminol and 1 g L–1 NaOH) in a completely dark room [14] , [26] (link). SCL images were acquired using an exposure-controlled digital camera (α58; Sony Corp., JPN).
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2

Ultrasound-Assisted Bead Desorption and Aluminum Foil Erosion

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Three types of beads with mean diameters of 0.2, 1.0, and 4.0 mm were used in this process. For the desorption tests, the beads were coated with red paint using oil-based spray paint and exposed to ultrasound irradiation in water, with a bead ratio of 5:1 [11] (link). The turbidity induced by the paint desorption was measured using a UV–vis spectrophotometer (Vibra S60, Biochrom Ltd., UK). The irradiation time was kept at 3 min.
Aluminum foil erosion tests were conducted using aluminum foil and a cylindrical frame with three diameters of 45, 62, and 80 mm. The frame was used to avoid moving the foil using ultrasound and ultrasound-induced liquid flow. The aluminum foil with a thickness of 16 μm was wrapped around the frame. The irradiation time was 30 s. Afterward, the damaged foil was dried, scanned, and analyzed visually.
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3

Sonochemical Oxidation Kinetics Quantification

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The sonochemical oxidation activity was quantified using KI dosimetry [11] . A high concentration of 10 g/L KI was applied to maximize the reaction of oxidizing radicals generated by cavitation, and the I3 ions generated by the sonochemical oxidation reactions were quantified with an ultraviolet–visible spectrophotometer (Vibra S60, Biochrom Ltd., UK). The concentration of I3 ion was measured every 2 min, and the measured data were interpreted assuming a zero-order reaction to calculate the kinetic constants.
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4

Ultrasonic Desorption and Visualization of Coated Beads

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Three kinds of beads with mean diameters of 1.0, 2.0, and 4.0 mm were tested to investigate the mechanism of ultrasonic washing processes. For desorption tests, the beads were coated with a red paint using an oil-based spray paint and exposed to ultrasound irradiation under the water : beads ratios of 3:1, 5:1, and 10:1. The turbidity induced by the detachment of the paint was measured using a UV–vis spectrophotometer (Vibra S60, Biochrom Ltd., UK). For the visualization of cavitational active zone, uncoated/transparent beads were used in the luminol solution (0.1 g/L luminol and 1 g/L NaOH). SCL (Sonochemiluminescence) images were obtained using an exposure-controlled digital camera (α58, Sony Corp., JPN) in a completely dark room [29] , [30] . The aluminum foil tests were conducted to visualize the sonophysical effects. The thickness of aluminum foil was 15 μm [25] .
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5

Quantifying Sonochemical Oxidation via UV-Vis and SCL

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The sonochemical oxidation was quantified using a KI solution (10 g/L KI) and visualized using a luminol solution (0.1 g/L luminol and 1 g/L NaOH) [26] (link), [31] (link), [32] (link). The concentration of I3 ions was measured using a UV–vis spectrophotometer (Vibra S60, Biochrom Ltd., UK). The ultrasound irradiation time was maintained at 3 min. All tests and measurements were repeated three to five times, and the average values are reported in this study. Sonochemiluminescence (SCL) images were obtained using a luminol solution and an exposure-controlled digital camera (DSC-RX100M7; Sony Corp., Japan) in a completely dark room. The exposure time was 20 s.
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6

Analysis of Nitrite, Nitrate, and Hydrogen Peroxide

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The concentrations of nitrite (NO2) and nitrate (NO3) ions were measured using an ion chromatography (IC) system (ICS-2100; Dionex, USA) equipped with an autosampler (AS-DV; Dionex, USA) [2] (link). The concentration of sonochemically generated H2O2 was spectrophotometrically analyzed using solution A (0.10 M potassium biphthalate), solution B (0.4 M KI, 0.06 M sodium hydroxide, and 10-4 M ammonium molybdate), and a UV–vis spectrophotometer (Vibra S60, Biochrom ltd., UK) [22] , [23] (link).
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