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Lovis 2000 m me rolling ball viscometer

Manufactured by Anton Paar
Sourced in Austria

The Lovis 2000 M/ME is a rolling ball viscometer designed for determining the dynamic viscosity of Newtonian and non-Newtonian fluids. It measures the rolling time of a steel ball through a sample-filled measuring cell, which is used to calculate the dynamic viscosity of the fluid.

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3 protocols using lovis 2000 m me rolling ball viscometer

1

Viscosity Measurement of Particle Suspension

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The viscosity of the 0.1 wt% model particle suspension in water was measured using the Lovis 2000 M/ME rolling ball viscometer (Anton Paar, Graz, Austria) at 20 °C.
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2

Viscosity Analysis of DNA-Ligand Complexes

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The viscosities of the DNA-ligand complexes were determined by the Lovis 2000 M/ME Rolling-ball viscometer (Anton Paar GmbH, Graz, Austria), based on the falling ball principle. The temperature was controlled at ±0.005 K through an internal Peltier thermostat. A calibrated 1.59 mm glass capillary containing a steel ball was filled with the sample for measuring the ball falling time at angles in the range from 20° to 70°. The kinematic, as well as dynamic viscosities at 25 °C, were estimated based on the ball falling time and densities DNA solution was prepared in 100 mM Tris-HCl (pH 7.4) and viscosity was measured while each derivative 12c and 12a (5 µM) was added to CT-DNA solution (50 µM). Ethidium bromide, Harmine and Hoechst 33258 at different concentrations were used as controls. Data was represented graphically as (ŋ/ŋ0)1/3 vs. the ratio of the concentration of the hybrid to CT-DNA, where ŋ is the viscosity of CT-DNA in the presence of the various concentrations of derivatives and ŋ0 is the viscosity of CT-DNA solution.
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3

Density and Viscosity of Deep Eutectic Solvents

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A total of five different natural deep eutectic solvents (NADES; Table 1) were prepared using the standard heating and stirring method [23 (link)]. For this purpose, the components of the desired NADES were weighed into a round bottomed flask at the selected molar ratio (Table 1), and stirred over a water bath for at least 30 min. To reduce viscosity and facilitate handling, the prepared solvents were diluted further with 25% ultrapure water before use (NADES/water, 75%:25% w:w).
The densities (ρ, kg m−3) of these mixtures (NADES/water, 75%:25% w:w) were determined in the temperature range between 5 °C and 60 °C (278.15–333.15 K), in increments of 5 °C at an ambient pressure of 0.1 MPa using a DMA 5000 M vibrating tube densimeter (Anton Paar, Graz, Austria). The set temperatures were stable within the interval ± 0.005 °C, while the repeatability of the measurements was within ±5 × 10−3 kg m−3.
In addition, the dynamic viscosities (η, mPa·s) were measured in the same temperature range (from 5 °C to 60 °C) using a Lovis 2000 M/ME rolling-ball viscometer (Anton Paar, Austria). The diameter of the capillary used was 1.8 mm and was chosen according to the optimal run time of the measurements. Gilded rolling-balls were used to avoid corrosion of the rolling balls. The capillary was calibrated with the viscosity standard before use.
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