The chemistry and technology of furfural and its many by-products:
Gespeichert in:
| Format: | Elektronisch E-Book |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
Amsterdam
Elsevier
2000
|
| Schriftenreihe: | Sugar series
13 |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Beschreibung: | 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 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 Includes bibliographical references and index |
| Beschreibung: | 1 Online-Ressource (1 online resource (xv, 358 p.)) |
| ISBN: | 9780444503510 044450351X |
Internformat
MARC
| LEADER | 00000nmm a2200000zcb4500 | ||
|---|---|---|---|
| 001 | BV039827912 | ||
| 003 | DE-604 | ||
| 005 | 20130315 | ||
| 007 | cr|uuu---uuuuu | ||
| 008 | 120124s2000 sz |||| o||u| ||||||eng d | ||
| 020 | |a 9780444503510 |9 978-0-444-50351-0 | ||
| 020 | |a 044450351X |9 0-444-50351-X | ||
| 035 | |a (OCoLC)162130560 | ||
| 035 | |a (DE-599)BVBBV039827912 | ||
| 040 | |a DE-604 |b ger |e aacr | ||
| 041 | 0 | |a eng | |
| 044 | |a sz |c XA-CH | ||
| 049 | |a DE-91 |a DE-1046 | ||
| 082 | 0 | |a 547/.592 |2 22 | |
| 084 | |a CHE 647f |2 stub | ||
| 084 | |a CHE 672f |2 stub | ||
| 245 | 1 | 0 | |a The chemistry and technology of furfural and its many by-products |c Karl J. Zeitsch |
| 264 | 1 | |a Amsterdam |b Elsevier |c 2000 | |
| 300 | |a 1 Online-Ressource (1 online resource (xv, 358 p.)) | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 490 | 0 | |a Sugar series |v 13 | |
| 500 | |a 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. | ||
| 500 | |a 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. | ||
| 500 | |a A comprehensive list of physical properties, some never published before, make the book an indispensable companion for producers, users and researchers alike | ||
| 500 | |a 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 | ||
| 500 | |a Includes bibliographical references and index | ||
| 650 | 4 | |a Furfural | |
| 650 | 4 | |a Furfural / Derivatives | |
| 650 | 4 | |a Furfural / Derives | |
| 650 | 0 | 7 | |a Furfural |0 (DE-588)4272610-4 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Furfuralderivate |0 (DE-588)4319833-8 |2 gnd |9 rswk-swf |
| 689 | 0 | 0 | |a Furfural |0 (DE-588)4272610-4 |D s |
| 689 | 0 | 1 | |a Furfuralderivate |0 (DE-588)4319833-8 |D s |
| 689 | 0 | |5 DE-604 | |
| 700 | 1 | |a Zeitsch, Karl J. |e Sonstige |4 oth | |
| 856 | 4 | 0 | |u http://www.sciencedirect.com/science/book/9780444503510 |x Verlag |3 Volltext |
| 912 | |a ZDB-33-ESD |a ZDB-33-EBS | ||
| 940 | 1 | |q FAW_PDA_ESD | |
| 940 | 1 | |q TUM_PDA_ELSEVIER_erworben | |
| 940 | 1 | |q FLA_PDA_ESD | |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-024687916 | ||
Datensatz im Suchindex
| _version_ | 1804148764154265600 |
|---|---|
| any_adam_object | |
| building | Verbundindex |
| bvnumber | BV039827912 |
| classification_tum | CHE 647f CHE 672f |
| collection | ZDB-33-ESD ZDB-33-EBS |
| ctrlnum | (OCoLC)162130560 (DE-599)BVBBV039827912 |
| dewey-full | 547/.592 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547/.592 |
| dewey-search | 547/.592 |
| dewey-sort | 3547 3592 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Chemie |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>04553nmm a2200541zcb4500</leader><controlfield tag="001">BV039827912</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20130315 </controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">120124s2000 sz |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780444503510</subfield><subfield code="9">978-0-444-50351-0</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">044450351X</subfield><subfield code="9">0-444-50351-X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)162130560</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV039827912</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">aacr</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">sz</subfield><subfield code="c">XA-CH</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-91</subfield><subfield code="a">DE-1046</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547/.592</subfield><subfield code="2">22</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">CHE 647f</subfield><subfield code="2">stub</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">CHE 672f</subfield><subfield code="2">stub</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">The chemistry and technology of furfural and its many by-products</subfield><subfield code="c">Karl J. Zeitsch</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Amsterdam</subfield><subfield code="b">Elsevier</subfield><subfield code="c">2000</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (1 online resource (xv, 358 p.))</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="490" ind1="0" ind2=" "><subfield code="a">Sugar series</subfield><subfield code="v">13</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">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. </subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">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. </subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">A comprehensive list of physical properties, some never published before, make the book an indispensable companion for producers, users and researchers alike</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">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</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Furfural</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Furfural / Derivatives</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Furfural / Derives</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Furfural</subfield><subfield code="0">(DE-588)4272610-4</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Furfuralderivate</subfield><subfield code="0">(DE-588)4319833-8</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Furfural</subfield><subfield code="0">(DE-588)4272610-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Furfuralderivate</subfield><subfield code="0">(DE-588)4319833-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zeitsch, Karl J.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.sciencedirect.com/science/book/9780444503510</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-33-ESD</subfield><subfield code="a">ZDB-33-EBS</subfield></datafield><datafield tag="940" ind1="1" ind2=" "><subfield code="q">FAW_PDA_ESD</subfield></datafield><datafield tag="940" ind1="1" ind2=" "><subfield code="q">TUM_PDA_ELSEVIER_erworben</subfield></datafield><datafield tag="940" ind1="1" ind2=" "><subfield code="q">FLA_PDA_ESD</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-024687916</subfield></datafield></record></collection> |
| id | DE-604.BV039827912 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-10T00:12:19Z |
| institution | BVB |
| isbn | 9780444503510 044450351X |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-024687916 |
| oclc_num | 162130560 |
| open_access_boolean | |
| owner | DE-91 DE-BY-TUM DE-1046 |
| owner_facet | DE-91 DE-BY-TUM DE-1046 |
| physical | 1 Online-Ressource (1 online resource (xv, 358 p.)) |
| psigel | ZDB-33-ESD ZDB-33-EBS FAW_PDA_ESD TUM_PDA_ELSEVIER_erworben FLA_PDA_ESD |
| publishDate | 2000 |
| publishDateSearch | 2000 |
| publishDateSort | 2000 |
| publisher | Elsevier |
| record_format | marc |
| series2 | Sugar series |
| spelling | The chemistry and technology of furfural and its many by-products Karl J. Zeitsch Amsterdam Elsevier 2000 1 Online-Ressource (1 online resource (xv, 358 p.)) txt rdacontent c rdamedia cr rdacarrier Sugar series 13 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 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 Includes bibliographical references and index Furfural Furfural / Derivatives Furfural / Derives Furfural (DE-588)4272610-4 gnd rswk-swf Furfuralderivate (DE-588)4319833-8 gnd rswk-swf Furfural (DE-588)4272610-4 s Furfuralderivate (DE-588)4319833-8 s DE-604 Zeitsch, Karl J. Sonstige oth http://www.sciencedirect.com/science/book/9780444503510 Verlag Volltext |
| spellingShingle | The chemistry and technology of furfural and its many by-products Furfural Furfural / Derivatives Furfural / Derives Furfural (DE-588)4272610-4 gnd Furfuralderivate (DE-588)4319833-8 gnd |
| subject_GND | (DE-588)4272610-4 (DE-588)4319833-8 |
| title | The chemistry and technology of furfural and its many by-products |
| title_auth | The chemistry and technology of furfural and its many by-products |
| title_exact_search | The chemistry and technology of furfural and its many by-products |
| title_full | The chemistry and technology of furfural and its many by-products Karl J. Zeitsch |
| title_fullStr | The chemistry and technology of furfural and its many by-products Karl J. Zeitsch |
| title_full_unstemmed | The chemistry and technology of furfural and its many by-products Karl J. Zeitsch |
| title_short | The chemistry and technology of furfural and its many by-products |
| title_sort | the chemistry and technology of furfural and its many by products |
| topic | Furfural Furfural / Derivatives Furfural / Derives Furfural (DE-588)4272610-4 gnd Furfuralderivate (DE-588)4319833-8 gnd |
| topic_facet | Furfural Furfural / Derivatives Furfural / Derives Furfuralderivate |
| url | http://www.sciencedirect.com/science/book/9780444503510 |
| work_keys_str_mv | AT zeitschkarlj thechemistryandtechnologyoffurfuralanditsmanybyproducts |