The largest database of trusted experimental protocols

Colorquest xe

Manufactured by HunterLab
Sourced in United States, China

The ColorQuest XE is a spectrophotometric instrument designed for color measurement and analysis. It utilizes state-of-the-art optics and a xenon flash lamp to provide accurate and reliable color data across a wide range of applications.

Automatically generated - may contain errors

60 protocols using colorquest xe

1

Color Difference Analysis of Blueberry Juice

Check if the same lab product or an alternative is used in the 5 most similar protocols
The color difference analyzer (Color Quest XE, Hunter Associates Laboratory, Inc., Fairfax, VA, USA) was used according to a reported method [29 (link)].
ΔE=(L*L0)2+(a*a0)2+(b*b0)2
where L* represents brightness; a* represents red intensity; b* represents yellow intensity; ΔE represents the total color change; and L0, a0, and b0 represent the color values of blueberry juice.
+ Open protocol
+ Expand
2

Colorimetric Analysis of Bromelain Hydrolysate

Check if the same lab product or an alternative is used in the 5 most similar protocols
The colour of the hydrolysate was measured using a colourimeter (ColorQuest XE; HunterLab, Reston, VA, USA), illuminant D65, 10° viewing angle in 20-mm glass transmission cell, and expressed as CIE L*, a* and b* (12 (link)). The pH of the hydrolysate at the end of bromelain hydrolysis was measured using a pH meter (PC700; Eutech Instruments) (7 (link)). The dry matter content of the hydrolysate was determined using the HR83 (Mettler Toledo) halogen moisture analyser (20 (link)). Its total nitrogen and crude protein content were examined using the Kjeldahl method (8 (link), 15 ).
+ Open protocol
+ Expand
3

Automated Mushroom Color Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The changes in color between raw and cooked samples were evaluated by an automatic colorimeter (ColorQuest XE, HunterLab, Shanghai, China) (24 (link)). Standard whiteboards and blackboards were used for calibration, and nine sites on the pileus surface were randomly selected to measure and record the values of L*, a*, and b*, representing lightness, greenness/redness, and blueness/yellowness, respectively. Then the hue angle (H), a/b values (h), chroma (C*), and total color difference (ΔE) were calculated according to the following formula:
+ Open protocol
+ Expand
4

Evaluation of UV-Induced Discoloration in Permutite

Check if the same lab product or an alternative is used in the 5 most similar protocols
The chroma values (L0*, a0*, b0*) of ion-exchanged permutite were measured by colorimeter (ColorQuest XE, Hunter Lab, Reston, VA, USA). The permutite samples were treated in a 254 nm UV irradiation box for of 5 cycles of 4 h, and measured again (L1*, a1*, b1*). In hunter whiteness formula, the whiteness of the fully reflected diffuser was defined as 100, and the whiteness of the sample was compared with the whiteness of the fully reflected diffuser. The whiteness of the sample was evaluated by calculating the color difference [18 (link)]. The hunter whiteness formula was calculated using Equation (1): W(L*,a*,b*)=(100L)2+(a*)2+(b*)2 
The discoloration properties of permutite samples were evaluated by the total color difference, as given by Equation (2) [19 (link)]: ΔE=(L0*L1*)2+(a0*a1*)2+(b0*b1*)2 
The nitrogen adsorption-desorption isotherms were measured by the volumetric method on an automatic adsorption instrument (ASAP 2010, Micromeritics, Norcross, GA, USA). The pore structure of permutite samples was analyzed by means of nitrogen sorption at 77.36 K. Specific surface area was calculated by the Brunauer-Emmett-Teller (BET) method based on the data in the p/p0 range between 0.05 and 0.25. A Barrett-Joyner-Halenda (BJH) analysis was carried out to calculate the mesopore volumes.
+ Open protocol
+ Expand
5

Colorimetric Analysis of Dried Gooseberries

Check if the same lab product or an alternative is used in the 5 most similar protocols
The colour of dried materials was determined using the CIELab system. The colour of the gooseberry fruits was measured with ColorQuest XE (Hunter Lab). Milled fruits were placed in a glass cuvette, and the colour was recorded using CIE L*a*b* 10°/D65 colour spaces, where L* indicates lightness, a* is the +a redness, and b* is the +b yellowness.
+ Open protocol
+ Expand
6

Colorimetric Analysis of Food Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Changes in color, sugar content, and pH were conducted by using a colorimeter (ColorQuest XE, Hunter-Lab, USA), refractometer (Brix/RI-Check, USA), and pH meter (FG-2, Mettler Toledo, USA), respectively.
+ Open protocol
+ Expand
7

Colorimetric Analysis of Coffee Bean Color

Check if the same lab product or an alternative is used in the 5 most similar protocols
The colorimeter (ColorQuest XE, HunterLab Inc.) was used to measure the color of the coffee bean (25 (link)). The colorimeter was calibrated using the white plate and packed coffee powder was added to a transparent preservative film and then placed on the detection port to obtain data. Results were calculated by the equipment using the Hunter Lab color scale. In this scale, L ranges from 0 (black) to 100 (white), a indicates degree of greenness (for negative a values) and degree of redness (for positive a results), b axis also ranges from negative to positive values indicating, respectively, degree of blueness to yellowness.
+ Open protocol
+ Expand
8

Film Color Characterization Method

Check if the same lab product or an alternative is used in the 5 most similar protocols
The Color Quest XE machine (Hunter Lab, Reston, VA, USA) was used to investigate the film’s color, according to the modified approach of Choi, et al. [29 (link)]. The L* (lightness), a* (red-green), and b* (yellow-blue) values of the film were recorded.
+ Open protocol
+ Expand
9

Color and Pigment Analysis of Fruit Peel

Check if the same lab product or an alternative is used in the 5 most similar protocols
The red saturation (a*) and yellow saturation (b*) of the peel were measured using a Color Quest XE color difference meter (Hunter Lab, Reston, VA, USA) on both sides of the abdomen of the fruit suture, and the ratio of red-green difference/yellow-blue difference was calculated (a*/b*). The average of two points was used as the corresponding index value of the fruit. The content of chlorophyll (Chl) in the pericarp was determined using the method of Lichtenthaler and Wellburn [15 (link)], followed by extraction with 95% ethanol and measuring the absorbance at 665 and 649 nm. The anthocyanin (Ant) content was determined in accordance with the method of Zapsalis and Francis [16 (link)], followed by extraction with 1% methanol solution of hydrochloric acid, and measuring the absorbance values at 650, 620 and 530 nm. Then, the content was calculated.
+ Open protocol
+ Expand
10

Colorimetric Analysis of Coffee Brews

Check if the same lab product or an alternative is used in the 5 most similar protocols
Colors of the hot and cold brew coffee were measured using a spectrophotometer (Hunterlab ColorQuest XE) at the transmission mode, D65 illuminant, 0.375 inch observation aperture, and 10° observation angle. A cuvette with a light path of 5 mm was applied in this study. The L*a*b* values of hot and cold brew coffee samples were determined after calibration. L* represents lightness, and a* and b* are chromaticity indexes. The total color difference (ΔE) of the two coffee was calculated via
ΔE=(L*cold L*hot)2+(a*colda*hot)2+(b*coldb*hot)2
+ 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!