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Publication Date
Wed Jul 16 2014
Journal Name
Transactions Of The Asabe
Volume
57
Issue Number
3
DOI
10.13031/trans.57.10512
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Scopus (5)
Articles
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Sorption Isotherms for Triticale Seed
EMC curve
Equilibrium moisture content
Moisture content
Static method (desiccation jars)
Water activity
Mahmoud K. A. Khedher Agha
W. S. Lee
Ray A Bucklin
Arthur A Teixeira
Ann Blount
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Triticale is being evaluated as a substitute for corn in animal feed and as a forage crop for Florida. Storage of triticale seed is difficult in Florida's hot and humid climate, and more information about the relationships between equilibrium moisture content (EMC) and equilibrium relative humidity (ERH) at constant temperature (sorption isotherms) of triticale is needed to develop improved storage methods. Therefore, the primary research objective was to measure the EMC for triticale seed at different ERH values at three different constant temperatures (5°C, 23°C, and 35°C) using six desiccation jars containing different saturated salt concentrations. The secondary objective was to determine the best fit equation describing these relationships. The six saturated salt solutions provided relative humidity (RH) values of 11%, 23%, 33%, 58%, 75%, and 84% at 25°C. An average of ten weeks was required to reach equilibrium when the initial moisture content (MC) of the seed was 13.35% (wet basis). The results of this experiment were used to develop three prediction equations, (modified Henderson, modified Chung-Pfost, and modified Oswin equations) representing the relationship between ERH and EMC. The results show that the modified Chung-Pfost equation represented this relationship most accurately, with a standard error of 2.4% and a coefficient of determination obtained from the scatter plot for the predicted vs. measured RH (R2) equal to 0.99. Overall, this result will aid the development and improvement of drying and storage methods for triticale seed.

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D. Fatima Abdel-Maliki
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2
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2
3-triazole was reported [2]
[3]. The existence of relatively basic nitrogen atoms in the 1
2
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and the possibility of introducing additional donor groups in the substituents (Fig. 1)
made the CuAAC “click” reaction an attractive method to prepare differently substituted 1
2
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and can be carried out with a variety of Cu(I) catalysts and solvents
including aqueous conditions. The Cu(I) catalysts overcome the high activation energy barrier of the non-catalyzed Huisgen reaction by changing the mechanism of the reaction. A large variety of copper catalysts can be used for the CuAAC reaction
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as well as for organic syntheses. We recently reported on the synthesis of a series of differently substituted 1
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see Fig. 2 middle
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CH3 (L2)
OCH3 (L3)
COOH
F
Cl
CN
CF3
O(CH2)3CH3 and N(CH3)2. These versatile ligands were found to coordinate to various first row transition metals
such as manganese
cobalt and nickel [6]. Here we extend the series to include more first row transition metal(II) coordination compounds
iron
copper and zinc
as well as a second row transition metal(II) coordination compound
cadmium
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2
3-triazol-1-yl)pyridine chromophore (Fig. 2 right with R = CH3). This series of seven novel coordination compounds is the first series of pyridyl-triazole based transition metal coordination compounds where seven different transition metals are coordinated to the same 1
2
3-triazole chromophore
namely 2-(1-(4-methyl-phenyl)-1H-1
2
3-triazol-1-yl)pyridine.
Kinaan M
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