WO2000039035A1 - Process for the treatment of waste water containing heavy metals - Google Patents
Process for the treatment of waste water containing heavy metals Download PDFInfo
- Publication number
- WO2000039035A1 WO2000039035A1 PCT/NL1999/000815 NL9900815W WO0039035A1 WO 2000039035 A1 WO2000039035 A1 WO 2000039035A1 NL 9900815 W NL9900815 W NL 9900815W WO 0039035 A1 WO0039035 A1 WO 0039035A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- metals
- waste water
- process according
- precipitated
- separated
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/34—Biological treatment of water, waste water, or sewage characterised by the microorganisms used
- C02F3/345—Biological treatment of water, waste water, or sewage characterised by the microorganisms used for biological oxidation or reduction of sulfur compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/02—Aerobic processes
- C02F3/10—Packings; Fillings; Grids
- C02F3/105—Characterized by the chemical composition
- C02F3/107—Inorganic materials, e.g. sand, silicates
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/28—Anaerobic digestion processes
- C02F3/2806—Anaerobic processes using solid supports for microorganisms
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/006—Radioactive compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/101—Sulfur compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/20—Heavy metals or heavy metal compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S210/00—Liquid purification or separation
- Y10S210/902—Materials removed
- Y10S210/911—Cumulative poison
- Y10S210/912—Heavy metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S210/00—Liquid purification or separation
- Y10S210/902—Materials removed
- Y10S210/911—Cumulative poison
- Y10S210/912—Heavy metal
- Y10S210/913—Chromium
Definitions
- the present invention relates to the treatment of waste water containing sulphate and heavy metals involving biological reduction and precipitation of water-insoluble metal species.
- the biological reduction can be a reduction of a metal to a lower valence in which form the metal precipitates as a metal sulphide, metal carbonate, metal oxide or hydroxide, metal phosphate or as the elemental metal, or it can be a reduction of a sulphur components such as sulphate to produce hydrogen sulphide which chemically precipitates the metal as a metal sulphide, or it can be both reduction of the metal and of the sulphur components with precipitation of metal sulphide.
- the metal precipitates are separated from the waste water.
- a process in which sulphates are biologically reduced to sulphide which precipitate metals as metal sulphides is known from WO 80/02281, WO 91/16269 and WO 97/29055.
- the metal sulphides are formed in conventional bioreactors and separated off in settling tanks. These processes are not very suitable for dilute waste water streams, i.e. containing heavy metal ions in the ppm range, since the hydraulic limitations would necessitate the use of relatively large bioreactor volumes and would make the process too expensive.
- a continuous process has now been found, which solves the problem of treating dilute waste waters containing heavy metals, whilst producing a non-diluted residue.
- the process is characterised in that the biological reduction of metals and/or sulphur components present in the waste water or added to the waste water, and the precipitation of metals or metal compounds are performed in a sand bed.
- Sand particles in the sand bed at least partly immobilise the bacteria and retain the precipitated metal species.
- Treated waste water is separated from the sand particles and from the metal precipitates, preferably by gravitation.
- the sand particles are washed, separating the precipitated metals and part of the biomass from the sand. Any small amounts of residual sulphide in the effluent can be biologically or chemically removed downstream from the sand bed.
- the sand bed is a so-called moving sand bed, i.e. a sand bed which is in continuous movement so as to allow simultaneous filtration of the metal precipitates from the waste water and separation of the metal precipitates from the sand particles.
- a suitable moving sand bed is a so-called dynamic sand filter as described in EP-A- 590705, and schematically depicted in figure 1.
- a dynamic sand bed to be used according to the invention is different from a fluidised bed, which is essentially a static bed. In such a dynamic sand filter, a reducing biomass is immobilised on the sand particles as a result of biofilm formation. The sand at the bottom is continuously removed upward e.g.
- a gas flow nitrogen or air
- the rate at which the sand is removed and subsequently cleaned can be controlled according to the method of WO 98/39255, which ensures that the metals will end up in a concentrated stream.
- the gas supply can be controlled as a function of the sand bed resistance for a clean sand bed.
- the process of the invention can be used for removing metals which can be precipitated, after biological reduction to a suitable valence state, as such or as a salt with anions that are normally present in waste water (hydroxide, carbonate, oxide, sometimes phosphate or sulphate) or can be added (pH increase).
- the reduced metals form insoluble precipitates, which are separated from the sand particles and from the waste water.
- selenium and tellurium can be precipitated in the elemental form (e.g. Se + — > Se - Se°i)
- chromium can be precipitated as hydroxide (e.g.
- uranium (IV) and vanadium (IN) can be precipitated as hydroxide, oxide or carbonate (e.g. ⁇ f + — » LT + — > UO 2 >t), and manganese can be precipitated as carbonate (e.g. M " — > Mn — >• Mn — > MnCO ).
- the process can also be used for removing metals which require additional reagents to be precipitated, in particular sulphide ions; the metals are then, if necessary after reduction, contacted with sulphide to form insoluble metal sulphides which are separated off.
- the sulphide is produced in situ by biological reduction of sulphur components having a higher oxidation state, such as sulphate, sulphite, thiosulphate, elemental sulphur. These sulphur components may already be present in the waste water containing the heavy metals, as in the case of e.g. sulphate in mine effluents, or be added, e.g. in the form of elemental sulphur.
- Metals that can be precipitated as sulphide include (monovalent:) Ag, Tl, In, (divalent:) Cu, Zn, Cd, Ni, Fe, Pb, Sn, Hg, Co, Mn, (trivalent:) As, Sb, Bi, Cr, (tetravalent:) Mo, Ti. Some of these may be biologically reduced from higher valence states such Fe + , As + , Sb + , Bi + , Tl + , In 3+ , Mn + etc, prior to the precipitation step.
- Suitable bacteria for reducing sulphur components to sulphide in the anaerobic sand bed reactor include sulphur and sulphate reducing bacteria, such as species from the genera: Desulforomonas sp. (mesophilic), Desulfotomaculum KT7 (thermophilic), the species Desulforolobus ambivalens, Acidianus infernus, Acidianus brierley, Stygiolobus azoricus (mesophilic), Thermoproteus neutrophilus, Thermoproteus tenax, Thermodiscus maritimus (thermophilic), Pyrobaculum is/andicum, Pyrodictium occultum, Pyrodictium brockii (hyperthermophilic), and other species of the genera Desulfov ⁇ brio, Desulfotomaculum, Desulfomonas, Thermodesulfobacterium, Desulfobulbus, Desulfobacter, Des ⁇ dfoc
- Suitable bacteria for biological reduction of metals include metal reducing bacteria such as species of the genera Geobacter, Pseudomonas, Shewanella, Desidfovibrio, Desulfobacterium, Desulfomicrobium, Desulforomonas, Alteromonas. In general, these bacteria are available as mixed populations from various anaerobic cultures and/or grow spontaneously in the anaerobic reactor.
- the process can be operated at mesophilic conditions (15-40°C) or at thermophilic conditions (40-90°C), depending on the temperature of the waste water. Normally mesophilic conditions are expected.
- the pH can range from 5 to 9, most preferably between 6 and 8. It will usually be necessary to add an electron donor in order to reduce the sulphur compounds to sulphide, especially in the case of treating water which does not contain organic waste.
- the following nutrients can be added: hydrogen, carbon monoxide, methanol, ethanol or other alcohols, short-chain fatty acids and other organic compounds such as sugars, starch and organic waste.
- nutrient elements in the form of nitrogen and phosphate are added as well. The addition of trace elements will only exceptionally be necessary, when they are not sufficiently available in the metal-containing water.
- waste water containing heavy metals that can be treated using the process of the invention are ground water, mine effluents, effluents from metallurgical plants and sites, industrial waste water, cooling water or run-off water streams, containing relatively low levels of heavy metals, in particular lower than 100 ppm.
- effluents of existing water treatment systems can be treated to lower the metal concentrations even further.
- water streams containing metals in such an oxidation state that they cannot be removed by only raising the pH such as in conventional lime treatment systems.
- dissolved oxidised selenium components can be removed biologically according to the invention by reducing the metal to the elemental selenium form which precipitates out.
- uranium can be removed biologically by reducing the valence from 6+ to 4+ and subsequent precipitation as an oxide, carbonate, hydroxide or the like.
- the metal-containing waste water (1) is led into a mixing tank (M) in which the temperature and pH are adjusted if necessary and electron donor can be added (15). Due to the wash water recycle stream recycle (13) the redox potential of the water (2) entering the moving bed sand filter (B) is lowered which enhances the biological activity in the filter. Water flows from the bottom to the top (3) through the sand particles moving slowly from the top to the bottom (11). The recirculation of sand particles is created by means of inserting gas (5) in a small inner tube (t). Due to the gas a mammoth pump is created and water, sand and metal precipitates captured in the sand are transported upwards (9) to the sand metal separation system (SI).
- SI sand metal separation system
- the metal precipitates are loosened from the sand particles due to the turbulence in the tube (t) and based on difference in settling velocity the large sand particles are returned to the sand bed using gravity (10) and metal precipitates and part of the loosened biomass are removed by means of the wash water stream (12).
- This stream is led to liquid solid separator (S2) in which the metal precipitates and biomass is separated from the water and removed from the system through (14).
- the cleared water is returned to the mixing tank (M).
- the gas (5) inserted in the inner tube (t) is either removed through 7 or preferably recycled through 8. If no gas recycle is used or hydrogen gas is used as electron donor fresh gas is added through 6.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Hydrology & Water Resources (AREA)
- Biodiversity & Conservation Biology (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Removal Of Specific Substances (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Biological Treatment Of Waste Water (AREA)
- Separation Of Solids By Using Liquids Or Pneumatic Power (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19990964779 EP1147063B1 (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
CA 2354388 CA2354388C (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
US09/869,346 US6630071B1 (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
MXPA01006638A MXPA01006638A (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals. |
BR9916629A BR9916629A (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
JP2000590954A JP2002533218A (en) | 1998-12-29 | 1999-12-29 | Method of treating wastewater containing heavy metals |
AU30818/00A AU3081800A (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
DE69906148T DE69906148T2 (en) | 1998-12-29 | 1999-12-29 | METHOD FOR TREATING HEAVY METAL CONTAINERS |
AT99964779T ATE234793T1 (en) | 1998-12-29 | 1999-12-29 | METHOD FOR TREATING WASTEWATER CONTAINING HEAVY METALS |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98204463.8 | 1998-12-29 | ||
EP19980204463 EP1016633A1 (en) | 1998-12-29 | 1998-12-29 | Process for the treatment of waste water containing heavy metals |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000039035A1 true WO2000039035A1 (en) | 2000-07-06 |
Family
ID=8234567
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1999/000815 WO2000039035A1 (en) | 1998-12-29 | 1999-12-29 | Process for the treatment of waste water containing heavy metals |
Country Status (13)
Country | Link |
---|---|
US (1) | US6630071B1 (en) |
EP (2) | EP1016633A1 (en) |
JP (1) | JP2002533218A (en) |
CN (1) | CN1281524C (en) |
AT (1) | ATE234793T1 (en) |
AU (1) | AU3081800A (en) |
BR (1) | BR9916629A (en) |
CA (1) | CA2354388C (en) |
DE (1) | DE69906148T2 (en) |
ES (1) | ES2192099T3 (en) |
MX (1) | MXPA01006638A (en) |
WO (1) | WO2000039035A1 (en) |
ZA (1) | ZA200104623B (en) |
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SE396552B (en) * | 1976-03-03 | 1977-09-26 | Nordstjernan Rederi Ab | PROCEDURE FOR FILTERING A SUSPENSION OR EMULSION AND FILTERING APPARATUS FOR PERFORMING THE PROCEDURE |
JPS6034796A (en) * | 1983-08-05 | 1985-02-22 | Kurita Water Ind Ltd | Treating apparatus of waste water containing heavy metal utilizing activated sludge |
JPS6377508A (en) * | 1986-09-20 | 1988-04-07 | Akashi Jiyouka:Kk | Moving bed type water treating apparatus |
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-
1998
- 1998-12-29 EP EP19980204463 patent/EP1016633A1/en not_active Withdrawn
-
1999
- 1999-12-29 JP JP2000590954A patent/JP2002533218A/en active Pending
- 1999-12-29 ES ES99964779T patent/ES2192099T3/en not_active Expired - Lifetime
- 1999-12-29 AT AT99964779T patent/ATE234793T1/en not_active IP Right Cessation
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- 1999-12-29 WO PCT/NL1999/000815 patent/WO2000039035A1/en active IP Right Grant
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- 1999-12-29 US US09/869,346 patent/US6630071B1/en not_active Expired - Lifetime
- 1999-12-29 AU AU30818/00A patent/AU3081800A/en not_active Abandoned
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2001
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JP2004526561A (en) * | 2001-03-09 | 2004-09-02 | カウンシル・オブ・サイエンティフィック・アンド・インダストリアル・リサーチ | Process and backflow loop reactor for sewage purification |
DE10238957B4 (en) * | 2002-08-24 | 2005-12-01 | Forschungszentrum Rossendorf Ev | Method for reducing uranium (VI) concentration in flowing waters |
CN103253753A (en) * | 2013-06-04 | 2013-08-21 | 江苏省环境科学研究院 | Recycling method of iron-containing resin desorption waste liquid |
WO2018007297A1 (en) | 2016-07-04 | 2018-01-11 | Paques I.P. B.V. | Recovery of heavy metals by selective precipitation |
WO2019218412A1 (en) * | 2018-05-15 | 2019-11-21 | 中国环境科学研究院 | Immobilized microbial agent for in situ remediation of contaminated sediments, preparation method and use |
US11993527B2 (en) | 2018-05-15 | 2024-05-28 | Chinese Research Academy Of Environmental Sciences | Immobilized microbial agent for in situ restoration of contaminated sediments, preparation method and application thereof |
CN108977395A (en) * | 2018-07-31 | 2018-12-11 | 李昕 | Passivation solidifies the preparation method of the hexavalent chromium polluted Bio-Nano-Materials of rehabilitating soil |
CN108977395B (en) * | 2018-07-31 | 2022-03-22 | 李昕 | Preparation method of biological nano material for repairing hexavalent chromium pollution in soil through passivation and solidification |
WO2023175163A1 (en) | 2022-03-18 | 2023-09-21 | Wageningen Universiteit | Process for the generation of hydrogen sulfide in the presence of pyrite as catalyst |
NL2031328B1 (en) | 2022-03-18 | 2023-09-29 | Univ Wageningen | Process for the generation of hydrogen sulfide in the presence of pyrite as catalyst |
Also Published As
Publication number | Publication date |
---|---|
DE69906148T2 (en) | 2003-09-25 |
AU3081800A (en) | 2000-07-31 |
CN1281524C (en) | 2006-10-25 |
ES2192099T3 (en) | 2003-09-16 |
CN1332701A (en) | 2002-01-23 |
MXPA01006638A (en) | 2002-07-02 |
EP1147063B1 (en) | 2003-03-19 |
CA2354388C (en) | 2011-11-22 |
DE69906148D1 (en) | 2003-04-24 |
ATE234793T1 (en) | 2003-04-15 |
BR9916629A (en) | 2001-10-16 |
EP1016633A1 (en) | 2000-07-05 |
JP2002533218A (en) | 2002-10-08 |
US6630071B1 (en) | 2003-10-07 |
EP1147063A1 (en) | 2001-10-24 |
ZA200104623B (en) | 2003-02-06 |
CA2354388A1 (en) | 2000-07-06 |
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