The largest database of trusted experimental protocols

27 protocols using haake mars

1

Rheological Characterization of Protein Solutions

Check if the same lab product or an alternative is used in the 5 most similar protocols
Shear stress and apparent viscosity of the protein solution were measured with a dynamic rheometer (HAAKE MARS, Thermo Fisher Scientific, Pittsburgh, PA, USA) equipped with the P60 probe with a gap of 1 mm, and the protein solution was evenly applied to the plate and preserved for 5 min before assays. The parameters were set as follows: the shear rate, temperature, and time were 10 s−1~400 s−1, 25 °C, and 330 s, respectively.
The dynamic rheological properties of proteins solution were measured using a dynamic rheometer (HAAKE MARS, Thermo Fisher Scientific, Pittsburgh, USA) according to the method of Kang et al. [22 (link)]. A 50 mm parallel steel plate geometry with a 0.5 mm gap was used. The raw protein solution was placed between the flat parallel plates with its perimeter coated with a thin layer of silicone oil to prevent dehydration. The sample was heated at a rate of 2 °C/min and continuously sheared in an oscillatory mode at a fixed frequency of 0.1 Hz. The storage modulus (G′) and loss modulus(G″) were recorded continuously from 20 °C to 80 °C.
+ Open protocol
+ Expand
2

Rheological Characterization of Hydrolysates

Check if the same lab product or an alternative is used in the 5 most similar protocols
The hydrolysate viscosities were determined using a modular advanced rheometer system (Haake Mars, Thermo Electron Corp., Germany). The system is equipped with a stainless steel measuring plate (MP 660, 60 mm) and a rotor (PP60H, 60 mm). The temperature was set to 30°C, the frequency was maintained at 1.5 Hz, and the gap between the parallel plates was kept at 1 mm. The hydrolysed samples were measured for 5 min at different shear rates ranging from 50 to 500 s−1.
+ Open protocol
+ Expand
3

Rheological Characterization of CHT-mPEG Blends

Check if the same lab product or an alternative is used in the 5 most similar protocols
Rheometric analysis was conducted for CHT-alone (yield value ≈ 0.1670 Pa) and CHT/mPEG blend mixtures (yield value ≈ 0.2406 Pa) to assess the mechanical transitions inherent within the polymeric solution phase. A cone-and-plate Haake MARS (Modular Advanced Rheometer System) rheometer (Thermo Electron Corporation, Karlsruhe, Germany) with cone diameter of 35 mm, cone angle = 1° (sensor C35/1°) Ti, A-factor = 8.905e+04 Pa/Nm, M-factor = 57.01 (1/s)/(rad/s), inertia = 1.721e−06 kg m2, damping = 30.00, thermal expansion coefficient: 1.100 µm/°C, compliance = 0.003157 rad/Nm, and a cone/plate gap of 0.51 mm. The temperature was maintained at 20 °C using a MARS II Universal Temperature Controller and a solvent trap was employed to prevent evaporation of the sample. Oscillation frequency sweeps were conducted over a frequency range of 10–0.01 Hz at a constant stress value of 2.0 Pa which was within the linear viscoelastic region of 0.1–7.0 Pa (stress sweep analysis conducted at 0.01 Hz). The variation and behaviour of elastic and loss moduli with reference to increasing frequency (angular frequency—ω) was studied and reported as mechanical characteristics. Further details of the method and equipment settings can be found in author’s previous report published elsewhere73 (link).
+ Open protocol
+ Expand
4

Rheological Characterization of Polymer Solutions

Check if the same lab product or an alternative is used in the 5 most similar protocols
The rheological properties of polymer solutions were investigated with a rheometer (Haake Mars, Thermo Fisher Scientific, America).The shear rate (γ) varied from 1 to 100 s−1 for each sample and test temperature was 150 °C.
+ Open protocol
+ Expand
5

Rheological Characterization of Corn Starch

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pasting properties were evaluated using the rheometer HAAKE MARS, Thermo Scientific, Darmstadt, Germany. Pasting profiles of samples were recorded using 15% corn suspensions (calculated on a dry matter basis) with the addition of 60 mL distilled water. Each sample was held at 25 °C for 3 min, followed by heating to 95 °C, after which the temperature was held constant at 95 °C for 15 min before cooling to 25 °C. The heating and cooling rates were set at 1.5 °C/min, while a shear rate of 10 s−1 was applied. The recorded parameters were initial viscosity (IV) (at the beginning of the heating phase), peak viscosity (PV) (timepoint at which most of the granules reached maximum swelling), final viscosity (FV), and gelatinization temperature (Tg) (temperature when the viscosity starts to rise due to the beginning of starch granule swelling). The measurements were repeated in triplicate.
+ Open protocol
+ Expand
6

Emulsion Preparation and Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following apparatus were used in the extraction and preparation of the emulsions: Hei-Standard MR 3001 magnetic stirrer (Heidolph Instruments, Schwabach, Germany), centrifuge (Centrifuge 2-5, Sigma, Osterode am Harz, Germany), InoLab pH meter (WTW, Weilheim, Germany), T25 digital Ultra-Turrax homogenizer, equipped with an S 25 N-18 G dispersive element (IKA, Staufen, Germany) and LHDM502 Universal Ultrasonic Generator Homogenizer (Colo, Novo Mesto, Slovenia). Measurements of the emulsion droplet size were conducted using a Mastersizer 2000 (Malvern Panalytical Ltd., Malvern, UK). The microphotographs were taken using an optical stereo microscope ZEISS STEMI 508 with a AXIOCM ERc 5s camera (Carl Zeiss Microscopy GmbH, Jena, Germany), while the obtained images were processed using ZenBlue Software 3.4 (White Plains, NY, USA) The determination of the rheological properties was performed using HAAKE MARS (Thermo Scientific, Karlsruhe, Germany).
+ Open protocol
+ Expand
7

Characterization and Release Kinetics of Iron Oxide Nanoparticle-Loaded Composite Matrices

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphologies of the as-prepared IONP-CM were observed under an AFM (Signal Hill, CA, United States of America) and a field-emission SEM (Zeiss Supra 40 Gemini, Germany). The mechanical characteristics of the prepared IONP-CM were assessed using a universal material testing machine (Shimadzu Co., Japan). The rheological features of the IONP-CM were determined using a modular advanced rheometer system (HAAKE MARS, Thermo Fisher Scientific, United States of America). This involved conducting strain–sweep measurements over a range of 0.01%–10% strain amplitude at a frequency of 6.28 rad/s, as well as frequency–sweep measurements at frequencies ranging from 1 to 30 rad/s with a fixed 1% strain amplitude. For the IONP release test, the IONP-loaded CM scaffolds were precisely shaped into uniform squares (10 mm × 10 mm). After that, they were co-incubated with 1.5 mL of PBS at 37°C. The concentration of Fe ions released from the scaffolds was determined at predetermined time intervals spanning a 7-day period using inductively coupled plasma atomic emission spectrometry (ICP-OES, Agilent 5800, United States).
+ Open protocol
+ Expand
8

Rheological Characterization of Swollen Cryogels

Check if the same lab product or an alternative is used in the 5 most similar protocols
The rheological
properties of swollen cryogels were evaluated by a rheometer (Haake
Mars, ThermoFisher Scientific, Germany) with a rotating-plate (diameter
35 mm) measuring setup. Measurements were carried out in oscillatory
amplitude sweep mode at a temperature T of 25 °C,
frequency f of 1 Hz, and shear stress τ in
the range 0.1–1000 Pa. Storage modulus G
(Pa) and loss modulus G” (Pa) representing
the solid-state behavior and liquid-state behavior of the sample,
respectively, were recorded. In the logarithmic-scale diagram of G’ and G” plotted against
τ, the linear viscoelastic (LVE) region is the region where
the gel returns to its original form when stress is withdrawn, and
declining point is the point where elastic deformation is limited
and plastic deformation begins (Figure S.6). Declining point is determined as the point where the G’ value declines more than 10% from its average value in the
LVE region. Beyond this point, the gel network structure begins to
break, collapse, or fracture.
+ Open protocol
+ Expand
9

Characterization of TBR PU/GE Nanofiber Membrane

Check if the same lab product or an alternative is used in the 5 most similar protocols
The rheological behavior of the doping solutions was investigated with a rheometer (HAAKE MARS, Thermo Fisher Scientific). The morphology of the TBR PU/GE nanofiber membrane was observed using field emission scanning electron microscopy (FESEM, Nova Nano 230, Netherlands FEI), confocal scanning microscopy (CSM, Zeiss CSM 700, Germany) and transmission electron microscopy (TEM, H7650, Hitachi, Japan). The pore size and the distribution of the as-prepared membrane was determined using capillary flow porometry (POROLUX1000, Belgium). The membrane porosity was determined using the gravimetric method.27,28 (link) The static contact angle was measured using a contact angle goniometer (DSA 100, KRÜSS, Germany). The mechanical properties of the TBR PU/GE nanofiber membrane were tested using an electronic stretching machine (M350-5Kn, SDLATLAS, British) at room temperature.
+ Open protocol
+ Expand
10

Rheological Characterization of Viscoelastic Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Viscosity and viscoelasticity were measured with a rheometer (Haake Mars, Thermo Scientific) with a 1°×R35 cone rotor. The viscosity (Epa (Pa s)), stress (Tau (Pa)), and loss tangent (tan δ) were measured each second. The conditions for measurement of viscosity were a sample amount of 0.2 mL and a gap of 0.051 mm. Recovery of viscosity was measured with a shear rate of 0–500 s−1(90 min) → 500–0 s−1(90 min). The conditions for measurement of viscoelasticity were a sample amount of 2 mL, a gap of 1 mm, and stress of 1 Pa → 10 Pa.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!