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3364 PDF UVNN GENESYS BEER CRAFT UG

BeerCraft User Guide
Introduction
Getting
Started
The Thermo Scientific™ BeerCraft™ software is a valuable addition to any brewery for the testing of wort, yeast,
malt, hops and finished beer samples to ensure the perfect batch every time. It features 20 of the most important
ASBC methods which are programed into the software enabling simple sample analysis and results calculation. The
selection of methods is easy with the GENESYS™ UV-Vis spectrophotometer’s large high-resolution touch screen
and convenient method descriptions. Results can be saved using custom batch names to associate each experiment
with a particular brew and printed or saved locally, to a USB stick, or to a network with a Wi-Fi adapter.
If not done so already, refer to the GENESYS Family Spectrophotometers User Guide for information on how to
update your GENESYS software and activate methods packages using the following sections:
• Updating Software
• Activating Methods Packages
Once this has been completed and the BeerCraft software has been activated, select the BeerCraft icon on the
GENESYS Home Screen to access the available beer methods.
Revision A 269-336400
© 2019 Thermo Fisher Scientific Inc.
All rights reserved.
BeerCraft
Methods
Beer
Bitterness
Units
ASBC. Beer 23. Beer Bitterness, A. Bitterness Units. This method serves as a measurement of the overall bitterness of
beer by measuring the absorbance of an acidified and extracted beer solution at 275 nm.
Iso-α-Acids
ASBC. Beer 23. Beer Bitterness, F. Iso-α-Acids by Solvent Extraction. This method determines the concentration of
iso-α-acids in beer by measuring the absorbance of the sample at 255 nm.
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Wort
Bitterness
Units
ASBC. Wort 23. Wort Bitterness, A. Bitterness Units by Spectrophotometry. The international bitterness units in
wort are determined by measuring the absorbance of an acidified and extracted wort solution at 275 nm.
Alcohol Low
Concentrations
ASBC. Beer 4. Alcohol, F. Enzymatic Method for Low Alcohol Concentrations. The ethanol content in low or no
alcohol samples is determined using an assay kit by measuring the absorbance of NADH at 340 nm.
Adjust the parameters to
correspond to your assay kit.
Measure the absorbance of the pre-reagent blank,
standard, and samples before adding alcohol
dehydrogenase reagent. Then take the
post-reagent measurements.
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Free Amino
Nitrogen
ASBC. Beer 31. Free Amino Nitrogen. The free amino nitrogen in wort or beer is determined by measuring the
absorbance at 570 nm after reacting with ninhydrin color reagent.
Enter the sample dilution
Measure the Blank, Standard, and Samples
in triplicate
Flocculation
ASBC. Yeast 11. Flocculation, B. Absorbance Method. The flocculation of a yeast sample is determined by reacting
with a buffered calcium sulfate solution and measuring the absorbance at 600 nm.
Measure the absorbance of Tube A and
Tube B. The degree of flocculence will be
reported as nonflocculent, moderately
flocculent, or very flocculent.
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Thiobarbituric
Acid Index
ASBC. Wort 21. Thiobarbituric Acid Index 2009. The thiobarbituric acid index of beer and wort is determined by
measuring the absorbance at 448 nm following a colorimetric reaction.
Enter the sample dilution
Measure the Blank, Standard, and Samples
in triplicate
Total
Polyphenols
ASBC. Beer 35. Total Polyphenols. The concentration of polyphenols in beer is determined by measuring the
absorbance of a solution at 600 nm following a colorimetric reaction.
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Total
Carbohydrate
ASBC. Beer 41. Total Carbohydrate, A. By spectrophotometry. Dextrin, the primary carbohydrate present in beer
reacts to produce a colored complex that is measured spectrophotometrically at 490 nm to determine the total
carbohydrate in beer.
Enter the sample dilution
Measure the Blank, Standard, and Samples
in triplicate
Beer Color
ASBC. Beer 10. Color, A. Spectrophotometric Color Method. The color of beer is determined by measuring the
absorbance at 430 nm of a sample free of turbidity.
Enter the sample dilution
Enter a Pathlength Conversion Factor of
1.27 if using a 1-cm cell or 1 if using a ½-in
cell.
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Beer Protein
ASBC. Beer 11. Protein, C. By spectrophotometer. The protein content of beer stabilized with polyvinyl
polypyrrolidone (PVPP), beer not treated with PVPP, or dark beer is determined using absorbance measurements at
215 nm and 225 nm.
Select Unstabilized, Stabilized, or
Dark
Enter the sample weights
Enter the Total Polyphenol
concentration
Enter a value for density of sample to
calculate the protein concentration in
mg/mL.
Otherwise leave blank to obtain the
concentration in %wt/wt.
Tristimulus
Color
ASBC. Beer 10. Color, C. Tristimulus Analysis. This method provides a representation of beer color in
three-dimensional color space by mathematically transforming %T values measured between 380 nm and 780 nm
into L*, a*, b* values.
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α-and ß-Acids
ASBC. Hops 6. α-and ß-Acids in Hops and Hop Pellets, A. α-and ß-Acids by Spectrophotometry. The percentage of
α- and ß- acids in hops is determined by measuring the absorbance of an extracted hops solution at 275 nm,
325 nm, and 355 nm. The hop storage index (HSI) is also calculated.
Enter the sample dilution
Diacetyl
ASBC. Beer 25. Diacetyl. The diacetyl content in beer is determined my measuring the absorbance of a sample
solution at 530 nm. The workflow is similar to the Quant application described in the GENESYS Family
Spectrophotometers User Guide.
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Alpha-Amylase
Beer Total
Sulfur Dioxide
ASBC. Malt 7. Alpha-Amylase, B. Fixed Time and Variable Color Method. This method evaluates the activity of
α-amylase in malt using a fixed time and variable color procedure where the %T at 650 nm is measured. The
workflow is similar to the Quant application described in the GENESYS Family Spectrophotometers User Guide.
ASBC. Beer 21. Total Sulfur Dioxide, A. p-Rosaniline Method. The total sulfur dioxide content of beer is measured
using the p-rosaniline method by measuring the color development at 550 nm. The workflow is similar to the Quant
application described in the GENESYS Family Spectrophotometers User Guide.
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Iron
ASBC. Beer 18. Iron, A. Analysis by Colorimetry. The iron content in beer is determined spectrophotometrically by
measuring the absorbance at 520 nm when using 2,2-bipyridine as a color reagent or at 505 nm when using
orthophenanthroline as a color reagent. The workflow is similar to the Quant application described in the
GENESYS Family Spectrophotometers User Guide.
Select 2,2-bipyridine or
orthophenanthroline
Malt Sulfur
Dioxide
ASBC. Malt 11. Sulfur Dioxide. The sulfur dioxide content of malt is measured using the p-rosaniline method by
measuring the color development at 560 nm. The workflow is similar to the Quant application described in the
GENESYS Family Spectrophotometers User Guide.
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Reducing
Sugar
ASBC. Malt 6. Diastatic Power, B. Diastatic Power (Rapid Method). The production of reducing sugars in malt is
determined by measuring the absorbance at 415 nm of a digested starch solution. The workflow is similar to the
Quant application described in the GENESYS Family Spectrophotometers User Guide.
Dissolved
Oxygen
ASBC. Beer 34. Dissolved Oxygen. This method determines the amount of dissolved oxygen in beer by the reaction
of oxygen with reduced indigo carmine by measuring the absorbance of the solution at 615 nm. The workflow is
similar to the Quant application described in the GENESYS Family Spectrophotometers User Guide.
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Cell Changer
Operation
with Beer
Methods
The following beer methods can utilize a cell changer for more efficient measurement:
• Beer Bitterness Units
• Iso-α-Acids
• Wort Bitterness Units
• Total Polyphenols
• Beer Color
• Tristimulus Color
• α-and ß-Acids
• Diacetyl
• Alpha-Amylase
• Beer Total Sulfur Dioxide
• Iron
• Malt Sulfur Dioxide
• Reducing Sugar
• Dissolved Oxygen
For general operation of GENESYS cell changers, refer to the GENESYS Family Spectrophotometers User Guide.
Select SETUP
Select the currently
installed cell changer
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Saving with a
Batch Name
When ending an experiment, the option is available to save the results using a batch name in addition to the
individual name of the saved experiment. If multiple beer methods are being utilized on the same batch of beer, the
batch name will enable these experiments to be associated together as a specific batch. This will enable the results of
multiple tests on the same batch to be easily compiled together in the Data Viewer.
Enter batch name
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Filter results in Data Viewer for a
specific batch
Using
SmartStart
with Beer
Methods
SmartStart™ can be used to create shortcuts to favorite beer methods on the Home screen using the same procedure
highlighted in the GENESYS Family Spectrophotometers User Guide under the SmartStart section.
Selected Smart Methods will be
highlighted
Mark method as Smart Method
Toggle to unselect
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Navigate to Settings and then to SmartStart and select Switch to SmartStart Mode.
Only Smart Methods are displayed
Reset to
Factory
Default
Reset to Factory Default can be accessed from the beer methods home page. It removes all user settings for every beer
method and resets the software back to the default settings. This can be utilized if a user changes the settings in
multiple beer methods and would like to revert them all back to the original settings at once.
Select to gain access to
factory settings reset
Select to reset settings
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