The largest database of trusted experimental protocols

Minolta colorimeter

Manufactured by Konica Minolta
Sourced in Japan, United States, Germany

The Minolta colorimeter is a device designed to measure and quantify color. It captures and analyzes the spectral characteristics of light, providing precise color data.

Automatically generated - may contain errors

38 protocols using minolta colorimeter

1

Biocomposite Surface Color Evaluation

Check if the same lab product or an alternative is used in the 5 most similar protocols
The surface colour of the biocomposites were measured using chroma-meter (Konica Minolta Colorimeter, Bangi, Malaysia) according to the CIE L*a*b* colour system by Lab Colour Space. The lightness (L*) and two chromaticity coordinates (a* and b*) were measured for independent specimens at four different positions on each.
+ Open protocol
+ Expand
2

Colorimeter-based Fish Fillet Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The color analysis was done using a Minolta colorimeter (Minolta Co. Ltd., Japan) under the hunter lab system. The color measurements of L * (lightness), a * (redness), and b * (yellowness) were recorded at three different locations on the fish fillets surface and determined the mean value. (10)
+ Open protocol
+ Expand
3

Quantitative Color Analysis of Fish Fillets

Check if the same lab product or an alternative is used in the 5 most similar protocols
Color readings were taken in the L*, a* and b* color space (CIELAB color space, D65 standard illumination and a 2° observer) and repeated 3 times using a Konica Minolta colorimeter (Osaka, Japan). The evaluated color parameters were lightness (L*), red–green chromaticity (a*), yellow–blue chromaticity (b*), the saturation or intensity of the color chroma (C*) and the hue angle (h), as recommended by the International Commission on Illumination [30 ,31 (link),32 (link)]. The analyses were performed in triplicate for each sample. The color evaluation was carried out in two dorsal regions of the fillets along the cephalocaudal direction.
+ Open protocol
+ Expand
4

Color Analysis of Painted Glass Slides

Check if the same lab product or an alternative is used in the 5 most similar protocols
On the same samples, color measurements were made according to Giacomucci et al. (2012) (link) by taking five measurements at random positions on the painted glass slides. A Konica Minolta colorimeter with a CR-300 measuring head (8 mm diameter viewing area) was used under the following conditions: illuminant D65 and observer 2º. Color measurements were analyzed by considering the CIELAB color system (CIE 1986) , which represents each color by means of three coordinates: L*, lightness of color, which varies from 0 (absolute black) to 100 (absolute white); a*, associated with changes in rednessgreenness (positive a* is red and negative a* is green); and b*, associated with changes in yellowness-blueness (positive b* is yellow and negative b* is blue). The total color difference (ΔE*ab) after immersion assays was calculated as follows:
+ Open protocol
+ Expand
5

Physicochemical Analysis of Beef Patties

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pH values of raw and cooked patties were measured with a digital pH meter (Mettler Toledo, MP230, Schwerzenbach, Switzerland) using 3 g of sample homogenized with 20 mL of distilled water.
The color of raw and cooked patties was measured using a Konica Minolta Colorimeter (Chroma meter, CR-300, Japan). The apparatus was standardized through a white ceramic plate (Y = 93.5, X = 0.3132, y = 0.3198), and lightness (L*), redness (a*), and yellowness (b*) values were recorded.
Release water percentage (RW%) was measured based on a method described by Joo [16 ]. The cooking loss (CL%) was determined as a percentage method adopted by Biswas et al. [17 (link)] using the following formula: Cooking loss (%) = (Weight of the patties after cooking/Weight of the patties before cooking) × 100.
Warner-Bratzler shear force (WBSF) was determined on the cooked sample using the established AMSA procedure [18 ]. The shrinkage percentage of the patties’ diameter was measured at four different locations both before and after cooking. A total of 18 (nine raw and nine cooked) patties were allocated for physiochemical analysis.
+ Open protocol
+ Expand
6

Assessing Broiler Meat Quality Attributes

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pH of breast meat was detected using a pH device (Mettler-Toledo, Greisensee, Switzerland) 45 min after slaughter, as described by Hu et al. [25 (link)]. The meat color of the breast was detected using a Minolta colorimeter (Konica-Minolta, Tokyo, Japan) according to lightness (L*), redness (a*), and yellowness (b*). The cooking loss (CL), drip loss (DL) and water loss rate (WLR) were measured as described by Hu et al. [25 (link)]. The breast meat was weighed (WInitial), steamed in a pot for 30 min, and then reweighted (WFinal). The equation of CL is: CL (%) = (WInitial − WFinal)/WInitial × 100. To measure DL, the breast meat was weighed (WInitial) and placed in a plastic bag at 4 °C. After 24 h, the meat sample was reweighted (WFinal). The equation of DL is: DL (%) = (WInitial − WFinal)/WInitial × 100. To measure WLR, the breast was weighed (WInitial) and placed in 18 layers of filter paper. Then, the sample was pressed at 2000 psi for 60 s. The meat sample was reweighed immediately (WFinal). The equation of WLR is: WLR (%) = (WInitial − WFinal)/WInitial × 100.
+ Open protocol
+ Expand
7

Color Analysis of Raw and Cooked Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Color determination of raw and cooked samples was carried out using a Minolta Colorimeter (model CR-310, Konica Minolta Co. Ltd, Osaka, Japan) equipped with a standard illuminant D65 and 8 mm viewing port. The measurements are presented in the CIE L*, a*, b* color scale (CIE, 1986 ). The assessments were carried out on 3 preselected locations at the surface of each sample. Before measurement, the apparatus was calibrated according to the white reference standard Y = 94.2; x = 0.313; y = 0.324. L* (lightness, black = 0, white = 100), a* (redness >0, greenness <0), b* (yellowness, b*>, blue <0), C (Chroma, 0 at the center of the color sphere), and hue° (hue angle, red = 0°, yellow = 90°, green = 180°, blue = 270°) were quantified on each samples using a 10° position of the standard observer. Chroma (C), hue angle (h°), and the individual differences (ΔE) in L*, a* and b* values were calculated using the following equations (CIE, 1986 ): C=(a*2+b*2)1/2 h° = tg−1 (b*/a*), were h° = 0° for reddish hue and h° = 90° for yellowish hue. ΔE=[(ΔL*)2+(Δa*)2+(Δb*)2]1/2
+ Open protocol
+ Expand
8

Microcapsule Powder Color Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Digital images of microcapsule powder were taken using a computer vision system with a digital camera (Canon Inc., Model EOS1000D, Taiwan). Parameters of the camera were calibrated using 30 color charts with a Minolta colorimeter, and the red, green, and blue color values (RGB) were obtained using the Adobe Photoshop CS3 software v10.0.1 (Adobe Systems Incorporated, 2007). The RGB values were converted to CIEL*a*b* space using the colorimetric converter of the colorizer website (https://colorizer.org/ accessed on 7 October 2023).
+ Open protocol
+ Expand
9

Colorimetric Analysis of Fish Fillets

Check if the same lab product or an alternative is used in the 5 most similar protocols
The analysis on the fillets was carried out using a Konica Minolta colorimeter (Osaka, Japan), and the results were reported according to the CIE system (CIE 1976). L*, a*, b*, and ΔE* representing lightness, redness/greenness, yellowness/blueness, and the total difference in color were reported.
ΔE* (CIE 1986) was calculated as: ΔE=(ΔL)2+(Δa)2+(Δb)2
where ΔL*, Δa*, and Δb*are the differentials among the color parameters of the samples over the shelf life and the color parameters of the samples at T0.
+ Open protocol
+ Expand
10

Colorimetric Analysis of Exocarp

Check if the same lab product or an alternative is used in the 5 most similar protocols
The color of the exocarp was calculated using a Minolta colorimeter (Minolta Co. Ltd., Osaka, Japan), as defined by (Mc Gire, 1992) . After one day from all storage periods, the L*, a*, and b* parameters were registered, and three replicates in three trays were evaluated per treatment, and the hue angle (HUE) was recorded as H0= tan-1(b*/a*).
+ 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!