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Hunter lab colorimeter

Manufactured by HunterLab
Sourced in United States

The Hunter Lab colorimeter is a device used to measure and quantify the color of materials. It provides an objective and standardized way to assess color properties such as lightness, hue, and chroma. The colorimeter employs specialized sensors and algorithms to analyze the reflected light from a sample, producing numerical color data that can be used for quality control, product development, and other applications.

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26 protocols using hunter lab colorimeter

1

Colorimetric Analysis of Film Samples

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A Hunter Lab colorimeter (Color Flex, Hunter Lab Inc., Reston, VA, USA) was used to determine the color values of the film. L (lightness/brightness), a (+a: redness/−a: greenness) and b (+b: yellowness/–b: blueness) values expressed the film color. Five measurements (one at the centre and four around the perimeter) were taken on each film and the mean values recorded. The whiteness index (WI) and total difference in color (ΔE*) were calculated according to eqn (2) and (3), respectively, as suggested by ref. 26 (link). where subscripts R and S represent the Hunter color values for the reference and sample, respectively.
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2

Characterization of Date Fruit Melanin

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The method of Hou et al.38 (link) was followed for preliminary identification of extracted melanin. Solubility of date fruit melanin (10 mg) was tested in acetic acid, acetone, chloroform, distilled water, Dimethyl sulfoxide (DMSO), ethanol, ethyl acetate, methanol, 1 M hydrochloric acid, 1 M sodium hydroxide/sodium carbonate (20 mL each) after shaking and letting stand for 3 h. The pigment was also precipitated with 1% FeCl322 (link). The color of the melanin samples was measured as l*, a*, and b* color values using Hunter Lab colorimeter (Hunter Lab Inc., Reston, VA, USA). Melanin samples (0.5 g) were dissolved in NaOH (0.01 M 100 mL) to get 0.5% melanin solution, and after 5 min of sonication, its UV–visible spectra were scanned from the range of 200–700 nm using a BioTek EPOCH 2 Microplate spectrophotometer (Agilent, Santa Clara, USA)39 (link). Attenuated total reflectance spectroscopy (ATR-FTIR) was performed using Spectrum Two IR coupled with Universal ATR (Perkin-Elmer inc., Norwalk, CT, USA). Date fruit melanin was placed on the ATR diamond crystal plate and scanned in the spectral range from 4000 cm−1 to 400 cm−1 at room temperature.
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3

Strawberry Preservation Protocol: Chroma and Browning

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Strawberries with uniform size and commercial maturity were selected for the preservation study. They were purchased at a local market and used without any additional treatment. The sample luminosity was measured with a Hunter lab colorimeter every 24 h for eight days. With this parameter, the chroma (Cab*) for strawberries was obtained using Equation (1).
the Cab*=(a*2+b*2
where a* represents the red and green colors; b* the yellow and blue colors. The browning index (IP) was calculated with Equation (2) [23 (link)].
IP=100×X0.310.172
where
X=a*+1.75L5.645L+a*3.012b*
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4

Meat Color, Lipid Oxidation, and Composition

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The color parameters [L* (lightness), a* (redness), and b* (yellowness)] of raw and cooked meat samples (cubes, 2 cm) were measured by Hunter Lab colorimeter (Color Flex EZ, USA) following the procedure described in (Wattanachant et al., 2005 (link)). The Lipid peroxidation was measured by a 2-thiobarbituric acid test (TBA) (Fernández-López et al., 2005 (link)). Total volatile bases nitrogen (TVBN) was estimated according to Botta et al. (1984) . The pH value of minced meat samples was assessed using a pH meter (pH 211 HANNA instruments Inc. Woonsocket, USA). The chemical composition of meat was also estimated by Wattanachant et al., 2005 (link). Moisture content was determined by oven method (AOAC, 2005 ); protein was determined by Kjeldahl method (AOAC, 2005 ); fat was estimated by the Soxhlet apparatus method (AOAC, 2005 ); and a muffin assessed ash at 600 °C (AOAC, 2005 ).
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5

Characterizing Cookie Physical Properties

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Diameter and thickness of some selected cookies, as well as the optimized cookie, were determined with a Vanier calliper at three different points. The colour of the cookie sample was determined by a method described by Olawoye and Gbadamosi (2020b) . The colour which include L∗, lightness (0 = black, 100 = white), a∗ (-a = greenness, +a = redness) and b∗ (-b = blueness, +b = yellowness) of the cookies were obtained using HunterLab colorimeter coupled with an optical sensor (HunterLab, U.S.A.). Hardness analysis was performed with a TA-XT2i Texture Analyser (Stable Micro Systems, UK) fitted with a shape blade-cutting probe as described by (Sharma et al., 2016 ).
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6

Evaluating Color and Rancidity of Iron-Fortified Flours

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The color of all samples (control and Fe-fortified) from split desi seeds (dal), desi flour and kabuli flour was evaluated using a HunterLab Colorimeter (Hunter Associates Laboratory Inc., Reston, VA, USA). Iron-fortified samples were compared to unfortified controls. The color values (L*, a* and b*) for each sample were recorded at three-month intervals over a one-year period [32 ].
The fortified desi and kabuli flours along with controls were assessed for rancidity. The samples were stored individually for 6 and 12 months in plastic bags at room temperature (19–22 °C) and a relative humidity of 45%–55%. The moisture contents ranged from 8.3%–9.3%. Five-gram samples were weighed and transferred into test tubes, followed by the addition of 50 mL of methylene chloride to each tube. The flour and methylene chloride mixture was pressed in a syringe and enough oil–solvent mixture collected to recover approximately 1g of oil. The solvent was removed using a rotary evaporator (BUCHI Rotavapoor R-200, Brinkmann Instruments, Inc., Westbury, NY, USA) and the oil was transferred to a 5 mm diameter NMR tube [33 (link)]. The samples were analyzed in an NMR spectrometer (Ultrashield 500 MHz/54 mm, Bruker AG, Fallanden, Switzerland) for 1 h to obtain a signal for hydroperoxide, the primary product of lipid oxidation [34 (link)].
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7

Automated Chicken Meat Color Analysis

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The 210 chicken breast meats were obtained from a processing line and separated using the L* value, which was determined using a HunterLab colorimeter, into three color characteristics; these included dark-colored samples (L*<50), normal-colored samples (50≤L*≤56), and light-colored samples (L*>56). The RGB color values of the samples were determined using imaging analysis. The R, G, and B values of the samples were then converted to L*, a*, and b* values using the EasyRGB color calculator. Thereafter, the accuracy of determining the characteristics of each sample, using imaging analysis, was evaluated by comparing the L* value obtained by the imaging analysis with that obtained using the HunterLab colorimeter; then, the percentages of correct and incorrect data were calculated.
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8

Color Analysis of SDEW Instant Noodles

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Color characteristics, including lightness (L*), redness (a*), and yellowness (b*), were recorded at random points on the fried SDEW instant noodle with the aid of the Hunter LAB colorimeter (Hunter Associates Laboratory, Inc., Reston, VA, USA). The total color characteristics of the noodles were calculated using the L*, a*, and b* values by following the equation proposed by Tiga et al. [56 (link)].
ΔE*=ΔL*2+Δa*2+Δb*2
where Δ L*, Δ a*, and Δ b* represents the lightness, redness, and yellowness of the color characteristics of the SDEW instant noodles, respectively. Δ E* is the total color value.
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9

Measuring Color Difference in ECC Samples

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The color analysis of the EC was performed using a HunterLab colorimeter (HunterLab, Reston, VA, USA), which employs a D65 illuminant to simulate daylight. The color was expressed in terms of the L*, a*, and b* parameters according to the CIELab scale. The color difference (∆E*) between the ECC and the control FS was calculated using Equation (6).
E*=(L*)2+(a*)2+(b*)2
where:

E*: Total color difference between the ECC Sample and the base color standard FS.

(L*): Difference in luminosity between the ECC sample and the base color standard FS.

(a*): Shift in the green-red color between the ECC sample and the base color standard FS.

(b*): Shift in the blue-yellow color between the ECC sample and the base color standard FS.

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10

Colorimetric Analysis of Freeze-Dried Noodle Powder

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The cooked noodles were freeze-dried and milled through 60 mesh (HY-04A, Beijing Huanyatianyuan Instrument Co., Ltd., Beijing, China). The color of the cooked noodle powder was measured by a HunterLab colorimeter (DP-9000 D25A, Hunter Associates Laboratory, Reston, VA, USA) with a 40 mm aperture and a halogen tungsten lighting source lamp equipped with a C illuminant and 2° standard observer. The results were expressed as L* (lightness/darkness), a* (greenness/redness) and b* (blueness/yellowness) values. The instrument was calibrated with standard whiteboards and blackboards. Color value averages were calculated from triplicate measurements. The ΔE value representing the comprehensive value of the noodle was calculated as follows:
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