Bioleaching of molybdenum from coal liquefaction catalyst residues

It has been shown that the bacterium Thiobacillus ferrooxidans can solubilize MoS 2 from coal liquefaction catalyst residues. The MoS 2 is formed during the liquefaction process from a molybdenum catalyst precursor. MoS 2 is insoluble; in order to be recovered and reused, it must be converted to a s...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Fuel (Guildford) 1993, Vol.72 (12), p.1613-1618
Hauptverfasser: Blaustein, Bernard D., Hauck, John T., Olson, Gregory J., Baltrus, John P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1618
container_issue 12
container_start_page 1613
container_title Fuel (Guildford)
container_volume 72
creator Blaustein, Bernard D.
Hauck, John T.
Olson, Gregory J.
Baltrus, John P.
description It has been shown that the bacterium Thiobacillus ferrooxidans can solubilize MoS 2 from coal liquefaction catalyst residues. The MoS 2 is formed during the liquefaction process from a molybdenum catalyst precursor. MoS 2 is insoluble; in order to be recovered and reused, it must be converted to a soluble form. T. ferrooxidans can oxidatively solubilize the molybdenum in MoS 2 to molybdate, in which form it can be recovered as a soluble or HCl extractable material. Bioleaching experiments show that with a starting cell concentration of 1.0 × 10 7 cells ml −1, or greater, a significant amount of the molybdenum in the residue was solubilized. These experiments indicate that the amount of molybdenum biologically solubilized from the liquefaction residues is dependent on inoculum size, with all strains of T. ferrooxidans tested having equal ability, and on the particle size of the residue. An important factor in the solubilization of MoS 2 by T. ferrooxidans is the inhibitory effect of molybdate. Literature reports that as little as 10 ppm molybdate is inhibitory to growth or ferrous iron oxidation. However, leachates containing in excess of 70 ppm molybdenum (equivalent to 116 ppm molybdate) were generated as a result of bioleaching of the liquefaction residue. When cells from previous leaching experiments were used to inoculate flasks containing fresh media and additional liquefaction residue, the bacteria were able to bioleach the fresh residue. Recent experiments have focused on the ability of T. ferrooxidans to produce protective agents in the leachate that minimize the inhibitory effects of molybdate. We found that production of the protective factor(s) did not depend on previous exposure of the cells to molybdenum or liquefaction residue.
doi_str_mv 10.1016/0016-2361(93)90344-2
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16974942</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0016236193903442</els_id><sourcerecordid>16974942</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-8c55db8f2ea71262b80ec94357f91b4d2cd23245df49d7b3ef1c0a0385f71bb43</originalsourceid><addsrcrecordid>eNqFkD1PwzAQhi0EEqXwDxgyIARDwF-J4wWJVnxJlVhgthz7DEZOXOwUqf-elFaMsNwtz_ve6UHolOArgkl9jcdRUlaTC8kuJWacl3QPTUgjWClIxfbR5Bc5REc5f2CMRVPxCZrNfAygzbvv34roii6GdWuhX3WFS7ErTNShCP5zBU6bwce-MHrQYZ2HIkH2dgX5GB04HTKc7PYUvd7fvcwfy8Xzw9P8dlEazshQNqaqbNs4CloQWtO2wWAkZ5VwkrTcUmMpo7yyjksrWgaOGKwxayonSNtyNkXn295liuM_eVCdzwZC0D3EVVakloJLTv8HOeOU03oE-RY0KeacwKll8p1Oa0Ww2phVG21qo01Jpn7Mqk3_2a5fZ6ODS7o3Pv9mmZBEsGrEbrYYjFK-PCSVjYfegPUJzKBs9H_f-Qaa64ws</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>14342426</pqid></control><display><type>article</type><title>Bioleaching of molybdenum from coal liquefaction catalyst residues</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Blaustein, Bernard D. ; Hauck, John T. ; Olson, Gregory J. ; Baltrus, John P.</creator><creatorcontrib>Blaustein, Bernard D. ; Hauck, John T. ; Olson, Gregory J. ; Baltrus, John P.</creatorcontrib><description>It has been shown that the bacterium Thiobacillus ferrooxidans can solubilize MoS 2 from coal liquefaction catalyst residues. The MoS 2 is formed during the liquefaction process from a molybdenum catalyst precursor. MoS 2 is insoluble; in order to be recovered and reused, it must be converted to a soluble form. T. ferrooxidans can oxidatively solubilize the molybdenum in MoS 2 to molybdate, in which form it can be recovered as a soluble or HCl extractable material. Bioleaching experiments show that with a starting cell concentration of 1.0 × 10 7 cells ml −1, or greater, a significant amount of the molybdenum in the residue was solubilized. These experiments indicate that the amount of molybdenum biologically solubilized from the liquefaction residues is dependent on inoculum size, with all strains of T. ferrooxidans tested having equal ability, and on the particle size of the residue. An important factor in the solubilization of MoS 2 by T. ferrooxidans is the inhibitory effect of molybdate. Literature reports that as little as 10 ppm molybdate is inhibitory to growth or ferrous iron oxidation. However, leachates containing in excess of 70 ppm molybdenum (equivalent to 116 ppm molybdate) were generated as a result of bioleaching of the liquefaction residue. When cells from previous leaching experiments were used to inoculate flasks containing fresh media and additional liquefaction residue, the bacteria were able to bioleach the fresh residue. Recent experiments have focused on the ability of T. ferrooxidans to produce protective agents in the leachate that minimize the inhibitory effects of molybdate. We found that production of the protective factor(s) did not depend on previous exposure of the cells to molybdenum or liquefaction residue.</description><identifier>ISSN: 0016-2361</identifier><identifier>EISSN: 1873-7153</identifier><identifier>DOI: 10.1016/0016-2361(93)90344-2</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; bioleaching ; Energy ; Exact sciences and technology ; Fuel processing. Carbochemistry and petrochemistry ; Fuels ; molybdenum ; Solid fuel processing (coal, coke, brown coal, peat, wood, etc.) ; Thiobacillus ferrooxidans</subject><ispartof>Fuel (Guildford), 1993, Vol.72 (12), p.1613-1618</ispartof><rights>1993</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-8c55db8f2ea71262b80ec94357f91b4d2cd23245df49d7b3ef1c0a0385f71bb43</citedby><cites>FETCH-LOGICAL-c431t-8c55db8f2ea71262b80ec94357f91b4d2cd23245df49d7b3ef1c0a0385f71bb43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0016236193903442$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,4010,4036,4037,23909,23910,25118,27900,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3791735$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Blaustein, Bernard D.</creatorcontrib><creatorcontrib>Hauck, John T.</creatorcontrib><creatorcontrib>Olson, Gregory J.</creatorcontrib><creatorcontrib>Baltrus, John P.</creatorcontrib><title>Bioleaching of molybdenum from coal liquefaction catalyst residues</title><title>Fuel (Guildford)</title><description>It has been shown that the bacterium Thiobacillus ferrooxidans can solubilize MoS 2 from coal liquefaction catalyst residues. The MoS 2 is formed during the liquefaction process from a molybdenum catalyst precursor. MoS 2 is insoluble; in order to be recovered and reused, it must be converted to a soluble form. T. ferrooxidans can oxidatively solubilize the molybdenum in MoS 2 to molybdate, in which form it can be recovered as a soluble or HCl extractable material. Bioleaching experiments show that with a starting cell concentration of 1.0 × 10 7 cells ml −1, or greater, a significant amount of the molybdenum in the residue was solubilized. These experiments indicate that the amount of molybdenum biologically solubilized from the liquefaction residues is dependent on inoculum size, with all strains of T. ferrooxidans tested having equal ability, and on the particle size of the residue. An important factor in the solubilization of MoS 2 by T. ferrooxidans is the inhibitory effect of molybdate. Literature reports that as little as 10 ppm molybdate is inhibitory to growth or ferrous iron oxidation. However, leachates containing in excess of 70 ppm molybdenum (equivalent to 116 ppm molybdate) were generated as a result of bioleaching of the liquefaction residue. When cells from previous leaching experiments were used to inoculate flasks containing fresh media and additional liquefaction residue, the bacteria were able to bioleach the fresh residue. Recent experiments have focused on the ability of T. ferrooxidans to produce protective agents in the leachate that minimize the inhibitory effects of molybdate. We found that production of the protective factor(s) did not depend on previous exposure of the cells to molybdenum or liquefaction residue.</description><subject>Applied sciences</subject><subject>bioleaching</subject><subject>Energy</subject><subject>Exact sciences and technology</subject><subject>Fuel processing. Carbochemistry and petrochemistry</subject><subject>Fuels</subject><subject>molybdenum</subject><subject>Solid fuel processing (coal, coke, brown coal, peat, wood, etc.)</subject><subject>Thiobacillus ferrooxidans</subject><issn>0016-2361</issn><issn>1873-7153</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0EEqXwDxgyIARDwF-J4wWJVnxJlVhgthz7DEZOXOwUqf-elFaMsNwtz_ve6UHolOArgkl9jcdRUlaTC8kuJWacl3QPTUgjWClIxfbR5Bc5REc5f2CMRVPxCZrNfAygzbvv34roii6GdWuhX3WFS7ErTNShCP5zBU6bwce-MHrQYZ2HIkH2dgX5GB04HTKc7PYUvd7fvcwfy8Xzw9P8dlEazshQNqaqbNs4CloQWtO2wWAkZ5VwkrTcUmMpo7yyjksrWgaOGKwxayonSNtyNkXn295liuM_eVCdzwZC0D3EVVakloJLTv8HOeOU03oE-RY0KeacwKll8p1Oa0Ww2phVG21qo01Jpn7Mqk3_2a5fZ6ODS7o3Pv9mmZBEsGrEbrYYjFK-PCSVjYfegPUJzKBs9H_f-Qaa64ws</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>Blaustein, Bernard D.</creator><creator>Hauck, John T.</creator><creator>Olson, Gregory J.</creator><creator>Baltrus, John P.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>1993</creationdate><title>Bioleaching of molybdenum from coal liquefaction catalyst residues</title><author>Blaustein, Bernard D. ; Hauck, John T. ; Olson, Gregory J. ; Baltrus, John P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-8c55db8f2ea71262b80ec94357f91b4d2cd23245df49d7b3ef1c0a0385f71bb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Applied sciences</topic><topic>bioleaching</topic><topic>Energy</topic><topic>Exact sciences and technology</topic><topic>Fuel processing. Carbochemistry and petrochemistry</topic><topic>Fuels</topic><topic>molybdenum</topic><topic>Solid fuel processing (coal, coke, brown coal, peat, wood, etc.)</topic><topic>Thiobacillus ferrooxidans</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blaustein, Bernard D.</creatorcontrib><creatorcontrib>Hauck, John T.</creatorcontrib><creatorcontrib>Olson, Gregory J.</creatorcontrib><creatorcontrib>Baltrus, John P.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Fuel (Guildford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blaustein, Bernard D.</au><au>Hauck, John T.</au><au>Olson, Gregory J.</au><au>Baltrus, John P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioleaching of molybdenum from coal liquefaction catalyst residues</atitle><jtitle>Fuel (Guildford)</jtitle><date>1993</date><risdate>1993</risdate><volume>72</volume><issue>12</issue><spage>1613</spage><epage>1618</epage><pages>1613-1618</pages><issn>0016-2361</issn><eissn>1873-7153</eissn><abstract>It has been shown that the bacterium Thiobacillus ferrooxidans can solubilize MoS 2 from coal liquefaction catalyst residues. The MoS 2 is formed during the liquefaction process from a molybdenum catalyst precursor. MoS 2 is insoluble; in order to be recovered and reused, it must be converted to a soluble form. T. ferrooxidans can oxidatively solubilize the molybdenum in MoS 2 to molybdate, in which form it can be recovered as a soluble or HCl extractable material. Bioleaching experiments show that with a starting cell concentration of 1.0 × 10 7 cells ml −1, or greater, a significant amount of the molybdenum in the residue was solubilized. These experiments indicate that the amount of molybdenum biologically solubilized from the liquefaction residues is dependent on inoculum size, with all strains of T. ferrooxidans tested having equal ability, and on the particle size of the residue. An important factor in the solubilization of MoS 2 by T. ferrooxidans is the inhibitory effect of molybdate. Literature reports that as little as 10 ppm molybdate is inhibitory to growth or ferrous iron oxidation. However, leachates containing in excess of 70 ppm molybdenum (equivalent to 116 ppm molybdate) were generated as a result of bioleaching of the liquefaction residue. When cells from previous leaching experiments were used to inoculate flasks containing fresh media and additional liquefaction residue, the bacteria were able to bioleach the fresh residue. Recent experiments have focused on the ability of T. ferrooxidans to produce protective agents in the leachate that minimize the inhibitory effects of molybdate. We found that production of the protective factor(s) did not depend on previous exposure of the cells to molybdenum or liquefaction residue.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/0016-2361(93)90344-2</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0016-2361
ispartof Fuel (Guildford), 1993, Vol.72 (12), p.1613-1618
issn 0016-2361
1873-7153
language eng
recordid cdi_proquest_miscellaneous_16974942
source Elsevier ScienceDirect Journals Complete
subjects Applied sciences
bioleaching
Energy
Exact sciences and technology
Fuel processing. Carbochemistry and petrochemistry
Fuels
molybdenum
Solid fuel processing (coal, coke, brown coal, peat, wood, etc.)
Thiobacillus ferrooxidans
title Bioleaching of molybdenum from coal liquefaction catalyst residues
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T06%3A45%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bioleaching%20of%20molybdenum%20from%20coal%20liquefaction%20catalyst%20residues&rft.jtitle=Fuel%20(Guildford)&rft.au=Blaustein,%20Bernard%20D.&rft.date=1993&rft.volume=72&rft.issue=12&rft.spage=1613&rft.epage=1618&rft.pages=1613-1618&rft.issn=0016-2361&rft.eissn=1873-7153&rft_id=info:doi/10.1016/0016-2361(93)90344-2&rft_dat=%3Cproquest_cross%3E16974942%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=14342426&rft_id=info:pmid/&rft_els_id=0016236193903442&rfr_iscdi=true