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Thermocline software

Manufactured by Newport Scientific
Sourced in Australia

Thermocline software is a data analysis tool developed by Newport Scientific. It is designed to process and visualize temperature profile data collected from various aquatic environments. The software provides users with the ability to view, analyze, and interpret temperature variations within water bodies.

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5 protocols using thermocline software

1

Rheological Analysis of Flour-Water Systems

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Pasting properties of flour-water systems were analysed using a rapid visco analyser (RVA) (RVA super 4, Newport Scientific, Warriewood, Australia), following a method adjusted from Do et al. (2019) (link). To examine hot swelling properties, chickpea flours were dispersed in demineralised water to obtain suspensions at desired concentrations (6-24% (w/w)). Additionally, a sample with potato starch (PS) (1-3.5% (w/w)) was used, as this is a frequently used thickening agent in the food industry. Samples were stirred overnight at 4 °C to achieve maximal hydration and afterwards homogenised for 15 s at 8000 rpm using an Ultra-Turrax.
Of these samples, 25 g was added to an aluminium canister and a plastic rotation paddle was inserted for stirring. Samples were equilibrated at 25 °C for 2 min, heated to 95 °C at 6 °C/min, held at 95 °C for 10 min, cooled down to 25 °C at 6 °C/min and held at 25 °C for 10 min. The first 10 s the paddle speed was 900 rpm to homogenise the sample, afterwards paddle speed was kept constant at 80 rpm. Thermocline Software (Newport Scientific) was used to analyse the data. All samples were measured in duplicate and at least two flour batches were measured per flour.
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2

Starch Pasting Behavior Analysis

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Pasting behavior of samples was measured with a Rapid Visco Analyser (Model RVA-Super 3, Newport Scientific, Warrie-wood, NSW, Australia), which was controlled by the Thermocline software (version 2.3, Newport Scientific Pty Ltd.). A starch suspension sample prepared by mixing starch in deionized water at a ratio of 7:100 (w/w) was gradually heated (while being stirred at 160 rpm) from 50°C to 95°C at a rate of 7.5°C/min, and held at 95°C for 5 minutes. After that, the mixture was cooled from 95°C to 50°C at the same rate and then held at 50°C for 20 minutes. The viscosity of starch suspension samples was expressed by the rapid viscosity unit (RVU). The peak viscosity (maximum viscosity during pasting), breakdown viscosity (difference between the peak viscosity and minimum paste viscosity), setback viscosity (difference between the final viscosity and minimum viscosity during pasting), final viscosity, and pasting temperature were also determined.
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3

Rapid Visco Analysis of Starch Slurry

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It was determined by using Rapid Visco Analyzer (Newport Scientific, Sydney, Australia) according to the method of Alamri, Mohamed and Hussain [20 (link)]. Sample (3 g) at 14% moisture basis was weighed in RVA aluminum canister and distill water was added to make slurry of total weight of 28 g. Paddle speed was kept at 960 rpm for initial 10 s and then decreased to 160 rpm throughout the experiment. A programmed heating and cooling cycle was designed. Resultant slurry was kept at 50 °C for 30 s, heated from 50 °C to 95 °C in 4.40 min at rate of 10.23 °C/min, kept at 95 °C for 4 min. Afterwards, it was cooled from 95 °C to 50 °C in 4.40 min at rate of 10.23 °C/min, and finally maintained at 50 °C for 2 min. All measurements were done in triplicate and data was processed by Thermocline software (Newport Scientific, Sydney, Australia).
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4

Pasting Properties of Dry Bean Powders

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The pasting properties of fine and coarse edible dry bean powders blended with corn starch were investigated using a Rapid Visco Analyzer (RVA, Model 4, Newport Scientific Pty. Ltd., Warriewood, NSW, Australia). Reference samples and reference blends were evaluated for comparison. The sample (3.5 g) was dispersed in distilled water (25 g), scaling both the sample and water weight on a 14 g/100 g sample moisture basis. The suspensions were subjected to Standard Method 2 (Thermocline Software, Newport Scientific Pty. Ltd., Warriewood, NSW, Australia), thus suspensions were kept at 50 °C for 1.5 min, heated at 6 °C/ min up to 95 °C, kept at 95 °C for 5 min, cooled at 3.5 °C/min down to 50 °C and kept at 50 °C for 1.8 min. From the resulting RVA pattern, the following indices were extrapolated: peak viscosity (PV, cP; maximum paste viscosity achieved during the heating phase); breakdown (BD, cP; index of viscosity decrease during the holding period, corresponding to the PV minus the viscosity after the holding period at 95 °C); final viscosity (FV, cP; paste viscosity reached at the end of the cooling cycle), and setback (SB, cP; index of the paste viscosity increase during cooling, corresponding to the difference between FV and the viscosity reached after the holding period at 95 °C). For each sample, results are the average of three measurements.
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5

Starch Pasting Properties Analysis

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Pasting properties of the starch were analyzed using a Rapid Visco-Analyzer (Newport Scientific, Sydney, Australia) following the methods of Ao and Jane (2007) , with minor modifications. A starch suspension (6%, dsb, w/w) was used for the RVA analysis. The pasting temperature, and the peak, breakdown, and final viscosities were determined using the Thermocline software (Newport Scientific).
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