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Author Zeitsch, Karl J.

Title The chemistry and technology of furfural and its many by-products / Karl J. Zeitsch.

Imprint Amsterdam ; New York : Elsevier, 2000.

Copies

Location Call No. OPAC Message Status
 Axe Elsevier ScienceDirect Ebook  Electronic Book    ---  Available
Description 1 online resource (xv, 358 pages) : illustrations
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
Series Sugar series ; vol. 13
Sugar series ; 13.
Summary This book is a "world first", since the furfural industry has been traditionally secretive to the point of appearing shrouded in clouds of mystery. Even renowned encyclopedic works have published but scant and often erroneous information on the subject. Striking a healthy balance between theory and practice, the book leads the reader from reaction mechanisms and kinetics to the technology of making furfural by various old and new processes, using conventional raw materials or sulfite waste liquor. Detailed discussions of means of increasing the yield are of great chemical and technological interest as well as of immense economic importance. From furfural proper, the treatise shifts to the fascinating field of wanted and unwanted by-products ranging from largely unutilized carboxylic acids to troublesome impurities such as 5-methyl furfural and 2-furyl methyl ketone, and then to extremely valuable serendipitous flavor compounds such as diacetyl and 2,3-pentanedione. A wide variety of derivatives are discussed; considerable space is devoted to polytetrahydrofuran, an important building block of stretchable synthetic fibers, while furan resins from both furfural and furfuryl alcohol are given the attention commensurate with their industrial importance. Notable supplementary chapters cover the in-line measurement of furfural, the treatment of furfural waste water, and various aspects of corrosion. A chapter on the applications of furfural elaborates not only traditional uses in extracting petroleum and vegetable oils but also the sensational discovery that furfural is a highly effective "indirect nematocide". Without becoming toxic, it changes the microflora of the soil by stimulating bacteria antagonistic to nematodes, thereby reducing the nematode population to zero, at an unprecedented low price. It is believed that this application will be the principal outlet for furfural in the future. A comprehensive list of physical properties, some never published before, make the book an indispensable companion for producers, users and researchers alike
Contents Selected chapter headings: Introduction. The Reactions Leading to Furfural. Acid Catalysis. The Kinetics of Pentose Formation from Pentosan. The Kinetics of Xylose Disappearance. Furfural Loss Reactions. The "Paradox" of Furfural Yields. The Discoloration of Furfural. Raw Materials. Furfural Processes. Distillation of Furfural. In-line Measurement of Furfural. Treatment of Furfural Waste Water. Applications of Furfural. Carboxylic Acids. Diacetyl and 2,3-Pentanedione. Furfuryl Alcohol. Furan. Furoic Acid. Difurfural (5,5'-Diformyl-2,2'-Difuran). 2-Hydroxyfuranone-5. Acetoin. Pyrazines. Tetrahydrofuran. Polytetrahydrofuran. Xylose. Furan Dialdehyde. Furan Resins. Tetrahydrofurfuryl Alcohol. Dihydropyran. Maleic Acid. Methylfuran. Pyrolysis of Furfural. Appendices. Subject index.
Bibliography Includes bibliographical references and index.
Note Print version record.
Subject Furfural.
Furfural -- Derivatives.
Furaldehyde
Furfural.
Furfural -- Dérivés.
SCIENCE -- Chemistry -- Organic.
Furfural
Other Form: Print version: Zeitsch, Karl J. Chemistry and technology of furfural and its many by-products. Amsterdam ; New York : Elsevier, 2000 044450351X 9780444503510 (DLC) 99058936 (OCoLC)42921345
ISBN 9780444503510
044450351X
9780080528991 (electronic bk.)
0080528996 (electronic bk.)
Standard No. AU@ 000051860382
CHNEW 001005702
DEBBG BV039827912
DEBSZ 367751992
DEBSZ 482351977
NZ1 12434577

 
    
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