Formation and dissolution kinetics of Al(OH) sub 3 (s) in synthetic freshwater solutions
The precipitation of Al in aqueous solutions can be described as a two-step process. When acidic inorganic Al solutions (pH 4.5) were titrated with NaOH to pH levels between 5.5 and 6.0, an amorphous Al (OH){sub 3} (s) phase was formed instantaneously. During the first 5 min, the apparent half time...
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Veröffentlicht in: | Water resources research 1991-03, Vol.27:3 |
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description | The precipitation of Al in aqueous solutions can be described as a two-step process. When acidic inorganic Al solutions (pH 4.5) were titrated with NaOH to pH levels between 5.5 and 6.0, an amorphous Al (OH){sub 3} (s) phase was formed instantaneously. During the first 5 min, the apparent half time for the reduction in dissolved Al species (t {1/2}) was 0.162 {plus minus} 0.07 hours (n = 4). The decrease of dissolved Al species continued during the following 24 hours, but at a far slower rate. The highest precipitation rates were found in the solution of highest pH, and at approximately identical pH, the highest rate was found in the solution of highest temperature. The dissolution of amorphous Al(OH){sub 3} (s) can also be described as a two-step process. When the amorphous Al solutions (pH between 5.5 and 6.0) were acidified to pH about 4.5 (HCl), the initial dissolution was relatively fast, but not as instantaneous as in the first step of precipitation. After 24 hours of storage 40 to 50% of the original Al(OH){sub 3} (s) remained in the solid phase. This is explained by the presence of a far lower dissolution rate in a second step, i.e., the remaining Al(OH){sub 3} (s) was less soluble. Results suggest that a total dissolution of Al (97%) will occur after 15.3 {plus minus} 4.9 days. The implication of these findings are discussed with reference to the current geochemical models pretending to simulate and predict aluminum chemistry in soils and surface runoff. |
doi_str_mv | 10.1029/90WR02409 |
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When acidic inorganic Al solutions (pH 4.5) were titrated with NaOH to pH levels between 5.5 and 6.0, an amorphous Al (OH){sub 3} (s) phase was formed instantaneously. During the first 5 min, the apparent half time for the reduction in dissolved Al species (t {1/2}) was 0.162 {plus minus} 0.07 hours (n = 4). The decrease of dissolved Al species continued during the following 24 hours, but at a far slower rate. The highest precipitation rates were found in the solution of highest pH, and at approximately identical pH, the highest rate was found in the solution of highest temperature. The dissolution of amorphous Al(OH){sub 3} (s) can also be described as a two-step process. When the amorphous Al solutions (pH between 5.5 and 6.0) were acidified to pH about 4.5 (HCl), the initial dissolution was relatively fast, but not as instantaneous as in the first step of precipitation. After 24 hours of storage 40 to 50% of the original Al(OH){sub 3} (s) remained in the solid phase. This is explained by the presence of a far lower dissolution rate in a second step, i.e., the remaining Al(OH){sub 3} (s) was less soluble. Results suggest that a total dissolution of Al (97%) will occur after 15.3 {plus minus} 4.9 days. The implication of these findings are discussed with reference to the current geochemical models pretending to simulate and predict aluminum chemistry in soils and surface runoff.</description><identifier>ISSN: 0043-1397</identifier><identifier>EISSN: 1944-7973</identifier><identifier>DOI: 10.1029/90WR02409</identifier><language>eng</language><publisher>United States</publisher><subject>540320 - Environment, Aquatic- Chemicals Monitoring & Transport- (1990-) ; ACID RAIN ; ALUMINIUM COMPOUNDS ; ALUMINIUM OXIDES ; AQUEOUS SOLUTIONS ; ATMOSPHERIC PRECIPITATIONS ; CHALCOGENIDES ; CHEMICAL REACTION KINETICS ; CHEMISTRY ; DISPERSIONS ; DISSOLUTION ; ENVIRONMENTAL SCIENCES ; FRESH WATER ; GEOCHEMISTRY ; HYDROGEN COMPOUNDS ; KINETICS ; MIXTURES ; OXIDES ; OXYGEN COMPOUNDS ; PH VALUE ; RAIN ; REACTION KINETICS ; SIMULATION ; SOLUTIONS ; WATER</subject><ispartof>Water resources research, 1991-03, Vol.27:3</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/5716240$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Lydersen, E.</creatorcontrib><creatorcontrib>Salbu, B.</creatorcontrib><creatorcontrib>Poleo, A.B.S.</creatorcontrib><creatorcontrib>Muniz, I.P.</creatorcontrib><title>Formation and dissolution kinetics of Al(OH) sub 3 (s) in synthetic freshwater solutions</title><title>Water resources research</title><description>The precipitation of Al in aqueous solutions can be described as a two-step process. When acidic inorganic Al solutions (pH 4.5) were titrated with NaOH to pH levels between 5.5 and 6.0, an amorphous Al (OH){sub 3} (s) phase was formed instantaneously. During the first 5 min, the apparent half time for the reduction in dissolved Al species (t {1/2}) was 0.162 {plus minus} 0.07 hours (n = 4). The decrease of dissolved Al species continued during the following 24 hours, but at a far slower rate. The highest precipitation rates were found in the solution of highest pH, and at approximately identical pH, the highest rate was found in the solution of highest temperature. The dissolution of amorphous Al(OH){sub 3} (s) can also be described as a two-step process. When the amorphous Al solutions (pH between 5.5 and 6.0) were acidified to pH about 4.5 (HCl), the initial dissolution was relatively fast, but not as instantaneous as in the first step of precipitation. After 24 hours of storage 40 to 50% of the original Al(OH){sub 3} (s) remained in the solid phase. This is explained by the presence of a far lower dissolution rate in a second step, i.e., the remaining Al(OH){sub 3} (s) was less soluble. Results suggest that a total dissolution of Al (97%) will occur after 15.3 {plus minus} 4.9 days. The implication of these findings are discussed with reference to the current geochemical models pretending to simulate and predict aluminum chemistry in soils and surface runoff.</description><subject>540320 - Environment, Aquatic- Chemicals Monitoring & Transport- (1990-)</subject><subject>ACID RAIN</subject><subject>ALUMINIUM COMPOUNDS</subject><subject>ALUMINIUM OXIDES</subject><subject>AQUEOUS SOLUTIONS</subject><subject>ATMOSPHERIC PRECIPITATIONS</subject><subject>CHALCOGENIDES</subject><subject>CHEMICAL REACTION KINETICS</subject><subject>CHEMISTRY</subject><subject>DISPERSIONS</subject><subject>DISSOLUTION</subject><subject>ENVIRONMENTAL SCIENCES</subject><subject>FRESH WATER</subject><subject>GEOCHEMISTRY</subject><subject>HYDROGEN COMPOUNDS</subject><subject>KINETICS</subject><subject>MIXTURES</subject><subject>OXIDES</subject><subject>OXYGEN COMPOUNDS</subject><subject>PH VALUE</subject><subject>RAIN</subject><subject>REACTION KINETICS</subject><subject>SIMULATION</subject><subject>SOLUTIONS</subject><subject>WATER</subject><issn>0043-1397</issn><issn>1944-7973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqNjr2KAjEURoMoOP4UvsHFSovRGxMNKWVR7AQRtBvGmGGiYwJzI-Lbr8pub3X44HxwGBtwnHCc6anGww5nEnWDJVxLmSqtRJMliFKkXGjVZh2iCyKX84VK2HEd6lseXfCQ-zOcHVGo7p99dd5GZwhCActqtN2Mge4nEDCiMTgP9PSxfBtQ1JbKRx5tDf9v6rFWkVdk-3_ssuF6tf_ZpIGiy8i4aE1pgvfWxGyu-OIVLb6SfgENv0Ye</recordid><startdate>19910301</startdate><enddate>19910301</enddate><creator>Lydersen, E.</creator><creator>Salbu, B.</creator><creator>Poleo, A.B.S.</creator><creator>Muniz, I.P.</creator><scope>OTOTI</scope></search><sort><creationdate>19910301</creationdate><title>Formation and dissolution kinetics of Al(OH) sub 3 (s) in synthetic freshwater solutions</title><author>Lydersen, E. ; Salbu, B. ; Poleo, A.B.S. ; Muniz, I.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_57162403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>540320 - Environment, Aquatic- Chemicals Monitoring & Transport- (1990-)</topic><topic>ACID RAIN</topic><topic>ALUMINIUM COMPOUNDS</topic><topic>ALUMINIUM OXIDES</topic><topic>AQUEOUS SOLUTIONS</topic><topic>ATMOSPHERIC PRECIPITATIONS</topic><topic>CHALCOGENIDES</topic><topic>CHEMICAL REACTION KINETICS</topic><topic>CHEMISTRY</topic><topic>DISPERSIONS</topic><topic>DISSOLUTION</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>FRESH WATER</topic><topic>GEOCHEMISTRY</topic><topic>HYDROGEN COMPOUNDS</topic><topic>KINETICS</topic><topic>MIXTURES</topic><topic>OXIDES</topic><topic>OXYGEN COMPOUNDS</topic><topic>PH VALUE</topic><topic>RAIN</topic><topic>REACTION KINETICS</topic><topic>SIMULATION</topic><topic>SOLUTIONS</topic><topic>WATER</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lydersen, E.</creatorcontrib><creatorcontrib>Salbu, B.</creatorcontrib><creatorcontrib>Poleo, A.B.S.</creatorcontrib><creatorcontrib>Muniz, I.P.</creatorcontrib><collection>OSTI.GOV</collection><jtitle>Water resources research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lydersen, E.</au><au>Salbu, B.</au><au>Poleo, A.B.S.</au><au>Muniz, I.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation and dissolution kinetics of Al(OH) sub 3 (s) in synthetic freshwater solutions</atitle><jtitle>Water resources research</jtitle><date>1991-03-01</date><risdate>1991</risdate><volume>27:3</volume><issn>0043-1397</issn><eissn>1944-7973</eissn><abstract>The precipitation of Al in aqueous solutions can be described as a two-step process. When acidic inorganic Al solutions (pH 4.5) were titrated with NaOH to pH levels between 5.5 and 6.0, an amorphous Al (OH){sub 3} (s) phase was formed instantaneously. During the first 5 min, the apparent half time for the reduction in dissolved Al species (t {1/2}) was 0.162 {plus minus} 0.07 hours (n = 4). The decrease of dissolved Al species continued during the following 24 hours, but at a far slower rate. The highest precipitation rates were found in the solution of highest pH, and at approximately identical pH, the highest rate was found in the solution of highest temperature. The dissolution of amorphous Al(OH){sub 3} (s) can also be described as a two-step process. When the amorphous Al solutions (pH between 5.5 and 6.0) were acidified to pH about 4.5 (HCl), the initial dissolution was relatively fast, but not as instantaneous as in the first step of precipitation. After 24 hours of storage 40 to 50% of the original Al(OH){sub 3} (s) remained in the solid phase. This is explained by the presence of a far lower dissolution rate in a second step, i.e., the remaining Al(OH){sub 3} (s) was less soluble. Results suggest that a total dissolution of Al (97%) will occur after 15.3 {plus minus} 4.9 days. The implication of these findings are discussed with reference to the current geochemical models pretending to simulate and predict aluminum chemistry in soils and surface runoff.</abstract><cop>United States</cop><doi>10.1029/90WR02409</doi></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | 540320 - Environment, Aquatic- Chemicals Monitoring & Transport- (1990-) ACID RAIN ALUMINIUM COMPOUNDS ALUMINIUM OXIDES AQUEOUS SOLUTIONS ATMOSPHERIC PRECIPITATIONS CHALCOGENIDES CHEMICAL REACTION KINETICS CHEMISTRY DISPERSIONS DISSOLUTION ENVIRONMENTAL SCIENCES FRESH WATER GEOCHEMISTRY HYDROGEN COMPOUNDS KINETICS MIXTURES OXIDES OXYGEN COMPOUNDS PH VALUE RAIN REACTION KINETICS SIMULATION SOLUTIONS WATER |
title | Formation and dissolution kinetics of Al(OH) sub 3 (s) in synthetic freshwater solutions |
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