EP1567682A1 - Method and system for extracting metal from glass waste - Google Patents

Method and system for extracting metal from glass waste

Info

Publication number
EP1567682A1
EP1567682A1 EP20030769011 EP03769011A EP1567682A1 EP 1567682 A1 EP1567682 A1 EP 1567682A1 EP 20030769011 EP20030769011 EP 20030769011 EP 03769011 A EP03769011 A EP 03769011A EP 1567682 A1 EP1567682 A1 EP 1567682A1
Authority
EP
European Patent Office
Prior art keywords
glass particles
solution
glass
tank
period
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP20030769011
Other languages
German (de)
English (en)
French (fr)
Inventor
Larry Lee Lough
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tri E Holding
Original Assignee
Tri E Holding
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US10/310,411 external-priority patent/US6666904B1/en
Priority claimed from US10/376,206 external-priority patent/US6669757B1/en
Application filed by Tri E Holding filed Critical Tri E Holding
Publication of EP1567682A1 publication Critical patent/EP1567682A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B43/00Obtaining mercury
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B13/00Obtaining lead
    • C22B13/04Obtaining lead by wet processes
    • C22B13/045Recovery from waste materials
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B7/00Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
    • C22B7/006Wet processes
    • C22B7/007Wet processes by acid leaching
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Definitions

  • the present invention is related to treatment of glass waste products, and more specifically to a method and systems for extracting heavy metals from glass waste.
  • recycling glass is manually intensive and expensive. This is so because one vendor of glass may use different concentrations of lead in their glass products than another glass vendor. As a result, in order to recycle the glass waste, the waste must be separated into vendor specific categories so that each vendor receives glass waste that can be reused by them. Glass waste with different concentrations of lead will melt, spread, and solidify at different temperatures, and therefore glass vendors can only reuse glass waste that has the proper amount of lead concentrations that is used in their glass manufacturing process. Waste disposal facilities receive glass waste that is not separated by vendor, and the waste disposal facilities have no effective techniques for automatically separating different glass vending wastes from one another. Because of the expense and time consuming nature associated with recycling glass waste, many waste disposal facilities have resorted to illegal disposal of glass waste. This is where the glass waste is not properly treated according to state and federal Environmental Protection Agencies (EPAs). This is extremely dangerous to the people that live near any such facility.
  • EPAs Environmental Protection Agencies
  • smelting melts the glass of the monitor at an extremely high temperature and then extracts the lead off the top of the liquid produced.
  • the EPA has authorized this process only as a stop gap measure since no other viable technique presently exist to safely dispose of monitor glass.
  • the reason why the EPA has only temporarily authorized this processes is because the process produces toxic gas as a byproduct and cross contaminates the glass with other toxins.
  • Some toxins and other heavy metals produced by the smelting process include Selenium arsenic. Therefore, the EPA realizes that it cannot continue to permit the smelting process to continue indefinitely and is actively pursuing and promoting research to replace the process.
  • CRT disposal or television disposal is a major environmental challenge for the United States, this challenge continues to escalate as more and more organizations and people continue to buy and dispose of CRT monitors and televisions at alarming rates.
  • the EPA has only authorized two methods of disposal for these monitors; the first is to recycle the monitors by separating glass waste into the appropriate manufacturers associated with the waste (glass- to-glass recycling).
  • the second technique is the smelting process, which the EPA has only approved as a stopgap or emergency measure.
  • CRT waste is the number two contributor to hazardous lead waste in the United States. This problem will only continue to grow over the next several years as liquid crystal and/or plasma screen technology is integrated into the industry and individuals/organizations accelerate their disposal rates of the CRT monitors. Accordingly, there is a need for improved techniques to extract heavy metals from glass waste products.
  • the techniques should be environmentally safe, efficient, and practical so that the techniques are readily embraced and adopted by waste disposal facilities.
  • a method and systems are provided for extracting heavy metals from glass waste products.
  • the glass waste is crushed to a small size and treated with a solution of water and acid.
  • the acid extracts the heavy metals from the surface of the glass waste.
  • the glass particles and solution are then separated.
  • a method to extract metal from glass is presented.
  • Glass is crushed into glass particles.
  • the glass particles having sizes that are greater than or equal to 10 nanometers and less than 2 millimeters in diameter size are filtered out from the glass particles of larger diameter sizes.
  • the tank is filled with the filtered glass particles and a solution of water (H 2 0) and Nitric acid (HN0 3 ). Furthermore, the solution and glass particles are circulated within the tank. Next, the solution is removed from the tank.
  • a system for extracting metal from glass includes a grinding device, a screen, a conveyor, a circulating pump, and a solution pumping device.
  • the grinding device crushes glass into glass particles.
  • the screen filters glass particles having a size having a diameter size of greater than about 10 nanometers and less than about 2 millimeters.
  • the conveyor transports the filtered glass to a tank having a solution of water (H 2 0) and acid.
  • the circulating pump device circulates the filtered glass particles and the solution for a period of time.
  • the solution-pumping device pumps the solution out of the tank.
  • a system for extracting metal from glass is provided.
  • the system includes a conveyor device, a solution pump, and a separating device.
  • the conveyor device transports glass particles having a diameter size between about 10 nanometers and about 2 millimeters to a processing tank.
  • the solution pump fills the processing tank with a solution of water and acid, where the acid removes lead from the surface of the glass particles.
  • the separating device removes the glass particles from the tank and the solution.
  • FIG. 1 is a flowchart of a method for extracting metal from glass.
  • FIG. 2 is a diagram of a system for extracting metal from glass.
  • FIG. 3 is a diagram of another system for extracting metal from glass.
  • FIG. 1 illustrates a flowchart of one method 100 for extracting metal from glass, according to one embodiment of the present invention.
  • the method 100 is achieved through the use of standard waste disposal equipment or devices.
  • the method 100 can also be processed in any custom made equipment designed to process method 100.
  • glass waste particularly glass waste associated with CRT monitors or televisions, includes unacceptable levels of lead, or other heavy metals (e.g., cadmium, mercury, selenium, arsenic, and the like), that needs to be removed or decreased to acceptable levels before the glass waste can be disposed of in a landfill.
  • lead, or other heavy metals e.g., cadmium, mercury, selenium, arsenic, and the like
  • glass waste includes varying levels of lead or other heavy metals recycling is not a practical solution because the glass waste must be separated by glass manufacture to be of any recycling use.
  • glass waste can economically and safely be disposed of well within the current EPA standards by safely and efficiently removing lead and other heavy metals from the glass waste.
  • the glass waste is provided to a grinding device.
  • the glass waste is fed to the grinding device by a variable speed screw conveyor made of stainless steel material.
  • the grinding device is a high-speed hammer mill, such as the high-speed hammer mill manufactured by Andela Tool of Richfield Springs, New York. The grinding device reduces the size of the glass waste by approximately 55% per pass through the grinding device.
  • the grinding device reduces is capable of reducing a diameter size of the glass waste to a submicron layer or approximately 10 nanometers.
  • a grinding device is Cyclo Mill produced by Dayton Color, of Ohio.
  • the grinding device uses Tungsten Carbide media that is cobalt enriched. It is capable of producing a force that approaches approximately three times the force of standard gravity.
  • the diameter size of the glass waste reaches approximately 10 nanometers.
  • a trommel separation device classifies the glass particles into particles of glass that are between about 10 nanometers and less than about 2 millimeters (mm) in diameter from those that are larger than 10 nanometers or 2 mm in diameter.
  • the trammel separation device can be configured to classify the particles into sizes between less than 2 mm and sizes greater than approximately 10 nanometers. Particles with diameters of a configurable size between approximately 10 nanometers or approximately less than 2 mm are allowed to pass through a screen onto a conveyor device, such as a screw conveyor of stainless steel construction. Thus, at 110, glass particles between about 10 nanometers and 2mm in diameter or less are filtered out of the supply of glass waste. Particles that are larger are reintroduced to the grinding device through a feedstock for continued grinding until all glass particles have achieved a desired diameter size between about 10 nanometers and about 2 mm or less and are filtered onto the conveyor device. The filtered glass particles are transported on the conveyor device to a chemical processing tank.
  • the chemical processing tank is filled with the filtered glass particles until approximately 75% of the tank is filled with the filtered glass particles.
  • a solution of acid and water is added to the tank to completely fill the tank at 115.
  • the acid solution is approximately 14% Nitric acid (HNO ) and 86% tap water (H 2 0). Due to the small size of the filtered glass particles and the acid solution, the mixture in the tank makes a slurry mixture.
  • a different acid other than Nitric Acid (HN0 3 ) can be used, such as Hydrochloric acid (HCL), Phosphoric acid (H P0 ), or the like.
  • HCL Hydrochloric acid
  • H P0 Phosphoric acid
  • different concentrations of acid to water can be used without departing from the present disclosure.
  • the slurry mixture is then circulated for a period of time within the tank by use of a tank pump.
  • the tank pump is a laminar flow pump that circulates the slurry at a rate of approximately 100 gallons per minute (gpm). The period is configurable between about 1 minute and 6 hours in duration.
  • a 1 minute period can be achieved when the diameter of the filtered glass particles are approximate 10 nanometers in size, and when the solution is heated to a temperature of approximately 155 degrees Fahrenheit.
  • a period between 2 to 6 hours in duration can be achieved when the diameter of the glass particles are approximate 2 mm in size and the solution is at ambient temperature.
  • a period of approximately 40 minutes in duration can be achieved when the glass particles are approximately 2 mm in size and the solution is raised to a temperature between approximately 155 to 160 degrees Fahrenheit.
  • a 5 minute period can be achieved when the diameter size of the filtered glass particles are at a submicron size and the temperature of the solution is elevated to approximately 120 degrees Fahrenheit.
  • the period of circulating can be configurable based on the diameter size of the glass particles and/or the temperature of the solution, which is used during the circulating cycle.
  • the period of circulation decreases.
  • the diameter size of the filtered glass particles decrease the period of circulation decreases. So, by reducing the diameter size of the filtered glass particles to approximately 10 nanometers and elevating the temperature to approximately 155 degrees Fahrenheit a period of 1 minute can be achieved.
  • the acid solution is removed from the tank at 125, or the treated and filtered glass particles are filtered from the solution and the tank. Moreover, by elevating the temperature of the solution the solubility of the solution increases.
  • the filtered glass particles are then subjected to a wash cycle starting at 130, where regular tap water is pumped into the tank.
  • the tap water and filtered glass particle mixture is the circulated within the tank for a second period of time at 135.
  • the second period of time is about 1 hour in duration.
  • Lime is then injected into the mixture to neutralize its acidity at 140. In one embodiment, about 10% lime is injected for 90% water.
  • the filtered glass particles are subjected to a wash cycle or rinsing with tap water as the filtered and treated glass particles are transported to a final destination.
  • the treated glass particles are fully treated and safe for disposal once transported from a conveying device to their final destination. Thus, no second period is required at all in these embodiments.
  • transportation and rinsing techniques can be used once the treated glass particles exit the circulating or mixing cycle. All such techniques are intended to fall within the broad scope of the present disclosure.
  • the mixture is then separated such that the neutralized tap water is separated from the filtered glass particles.
  • this separation occurs by diverting the filtered glass particles to a vorta sieve via a screw conveyor for final storage.
  • the remaining water effluent is diverted to a bag filter to remove any suspended solids and than through a combination charcoal filter and reverse osmosis filter in order to remove any residual soluble lead or other heavy metals.
  • the tap water and the filtered glass particles can be safely disposed of in an environmentally safe manner.
  • the acid solution can be reused with another cycle of glass treatment.
  • the acid solution can be reused with more than 50 cycles, depending upon the heavy metal content of the acid solution.
  • the tap water used for rinsing or washing the filtered glass particles is safe to dispose of in any municipality's water supply and conforms to all EPA regulations. When the acid solution has reached its useful life it can be treated as an ordinary hazardous waste stream and disposed of according to EPA regulations.
  • the filtered and treated glass particles have heavy metals removed from their surface and any lead (or other heavy metals) remaining in the particles cannot be released because the force required to further break the glass particles of between about 10 nanometers or about less than 2mm far exceeds any force that may be applied in a landfill or if the glass particles are used as a sand mixture for blacktop or concrete. In fact, any force will be dispersed throughout the particles and will not be concentrated in any specific single glass particle. As a result, the filtered and treated glass particles far exceed existing EPA regulations and can be disposed of or used in other products without environmental concern that the particles will rupture or expose the environment to lead or other heavy metals.
  • the glass particles when the glass particles are circulated with the acid solution and then again, in some embodiments, with the tap water the glass particles become smooth removing any jagged edges. In fact the glass particles form the texture and appearance of typical sand.
  • the acid solution can remain in the tank with the glass particles filtered and transported to another tank for rinsing, or the glass particles can be rinsed as they are transported to a final destination. All such variations on the steps of method 100 are intended to fall within the broad scope of the present invention.
  • FIG. 2 illustrates a diagram of one system 200 for extracting heavy metals from glass, according to one embodiment of the present invention.
  • the metal extraction system 200 includes a grinding device 210, a screen filter 220, a conveyor 230, a circulating pump device 240, and a solution-pumping device 250.
  • the configuration of the various components of the metal extraction system 200 are presented for purposes of illustration only and are not intended to limit the present invention, since a variety of additional components and configurations can be used to achieve the teachings of the present invention. Thus, all such additional components and configurations fall within the scope of the present invention.
  • the components are well known and readily available to those of ordinary skill in the art.
  • the grinding or crushing device 210 grinds glass waste into small particles.
  • One such grinding device 210 that can be used is a high-speed hammer mill, such as one manufactured by Andela Tool Inc., of Richfield, New York.
  • Other grinders such as the Cyclo Mill from Dayton Color of Dayton,
  • the glass waste can be a CRT monitor and a magnetic device can be applied to the feeding end of the grinding device 210 to extract metal waste material from the glass waste.
  • a screen filter 220 onto a conveyor device.
  • the glass particles having a diameter of greater than configured diameter size are resent to the grinding device 210 until all the glass waste has been crushed to a diameter size desired (e.g., between about 10 nanometers and less than about 2 mm).
  • the screen filter 220 can be associated with a trommel separation device an exit end of the grinding device 210.
  • the conveyor device 230 transports the filtered glass particles to a chemical treatment tank 235.
  • the conveyor device 230 is a screw conveyor of stainless steel construction.
  • the conveyor device 230 continues to deposit the filtered glass particles into the tank 235 until a desired level or weight is achieved within the tank 235.
  • the conveyor device 230 continues to deposit the filtered glass particles into the tank 235 until the tank is approximately 75% full of filtered glass particles.
  • an acid water solution 255 is pumped into the tank 235 to fill the tank 235 to capacity with the filtered glass particles and the added acid solution 255.
  • the solution 255 is approximately 86% water (H 2 0) and 14% Nitric acid (HN0 3 ).
  • the acid used can be Hydrochloric acid (HCL), Phosphoric acid (H 3 P0 ), or other acids.
  • the concentrations of acid to water can be altered without departing from the present disclosure.
  • a solution-pumping device 250 is used to supply and remove the solution 255.
  • the slurry mixture is mixed within the tank 235 for a configurable period of time by using a circulating pump device 240, such as a laminar flow pump adapted to the bottom of the tank 235.
  • the circulating pump device 240 circulates the slurry mixture at a rate of approximately 100 gpm.
  • the period of time during which the slurry mixture is mixed or circulated within the tank 235 is a duration having a range of approximately 1 minute to approximately 6 hours. The period is determined based on the size of the diameter of the filtered glass particles and any elevated temperature of the solution 255 used during the mixing or circulation. Thus, the duration of the period is decreased as the filtered glass particles' diameter size decreases and/or as a solution's temperature is elevated above ambient temperature.
  • the circulating pump device 240 is shut down and the solution 255 is removed from the tank 235 using the solution- pumping device 250, or any other device designed to remove the solution 255.
  • the solution 255 is then stored in its original holding tank (not depicted in FIG. 2) and be reused for a plurality of additional treatment cycles on additional glass waste.
  • the solution 255 can be reused for approximately 50 iterations (depending upon the concentration levels of the heavy metal in the solution 255) of treatment cycles.
  • the tank 235 is filled with regular tap water to wash or rinse the filtered glass particles of any acidic residue left by the solution 255.
  • the tap water is supplied to the tank 235 through a water supply device 260. Moreover, the tap water is supplied until the tank 235 is completely full.
  • the water and filtered glass particles are then circulated within the tank 235 for a second period of time. In one embodiment, the second period of time is about 1 hour.
  • the treated or filtered glass particles are strained or filtered from the solution 255 and rinsed as the filtered glass particles are transported to their final destination.
  • no second period of time is needed at all before the filtered glass particles are ready for environmentally safe disposal.
  • the circulating pump device 240 is shut down.
  • lime is supplied to the water and filtered glass particle mixture to neutralize the acidity. In one embodiment, this is achieved by adding 10% lime for 90% tap water.
  • the neutralized water and lime mixture is then pumped to a filter separator with the filtered glass particles diverted (e.g., via a vorta sieve, and the like) onto a screw conveyor for final storage.
  • a filter separator with the filtered glass particles diverted (e.g., via a vorta sieve, and the like) onto a screw conveyor for final storage.
  • other neutralizing or precipitation agents can be used other than lime. All such agents are intended to fall within the broad scope of the present invention.
  • the glass particles do not have heavy metals on their surface due to the mixing cycles with the solution 255 and the tap water. Moreover, any heavy metal remaining within the filtered glass particles cannot be extracted from the filtered glass particles without a substantial and focused force directed on a single glass particle. As a practical matter conventional landfill processes will not achieve this force. Moreover, other products, such as road materials and others, can use the filtered glass particles with assurance that no exerted force that the products are subjected to will be enough to crack the filtered glass particles and release enough lead or other heavy metal (e.g., cadmium, mercury, arsenic, selenium, and others) to be considered hazardous by the EPA.
  • heavy metal e.g., cadmium, mercury, arsenic, selenium, and others
  • the neutralized water can then be supplied to a water treatment device 270 to make the water safe for disposal in a municipality's water supply.
  • the water treatment device 270 is a carbon filtering system combined with a reverse osmosis filtering system. After treatment, the water can be safely discharged to a sewage system of a municipality.
  • glass waste particularly waste associated with CRT monitor disposal
  • these techniques adhere to and exceed current EPA regulations and provide a mechanism for waste disposal facilities to economically dispose of glass waste.
  • the treated glass particles have the consistency of sand, since the circulating cycles have smoothed the edges of the very small glass particles.
  • further processing can produce spherical particles.
  • the glass particles are no more harmful than sand would be if ingested or if they were to enter an open wound. Therefore, the glass particles can be used in a plurality of other products such as foundations for roads, mixtures for concrete, and others.
  • FIG. 3 illustrates a diagram of another system 300 for extracting heavy metals from glass, according to one embodiment of the present invention.
  • the metal extraction system 300 includes a conveyor device 310, a solution-pumping device 320, and a separating device 330. Untreated glass particles having a diameter of less than about 2mm are deposited onto the conveyor device 310. Any technique of grinding/crushing device can be used to originally deposit the glass particles onto the conveyor device 310.
  • the conveyor device 310 in one embodiment, is a screw conveyor of stainless steel construction.
  • the conveyor device 310 deposits the glass particles into a processing tank 330 until a desired level or weight is reached within the tank 330.
  • the conveyor device 310 is configured to halt depositing glass particles into the tank 330 when the tank 330 is about 75% filled with the glass particles.
  • the solution pumping device 320 pumps an acidic solution of acid and water mixture 322 into the tank 330 to bring the tank 330 to a full capacity level.
  • the acid solution 322 is a mixture of water (H 2 0) and Nitric acid (HN0 3 ).
  • the acid can be Hydrochloric acid (HCL), Phosphoric acid (H 3 P0 ), or other acids.
  • the concentration of HNO 3 to water within the acidic solution is approximately 14%.
  • concentrations of HNO 3 can be used and different acids can be used without departing from the present invention.
  • the acidic solution 322 and the glass particles are mixed or circulated within the tank 330 for a period of time.
  • Mixing can occur with a solution-circulating device, such as a laminar flow pump where the mixture is circulated at a rate of approximately 100 gpm.
  • the circulation rate and the period of time are configurable settings that can be adjusted without departing from the present invention.
  • the period of time can range between as little as 1 minute in duration and as much as 6 hours in duration. The period is determined based on the diameter size of the glass particles and any elevated temperature above ambient temperature that is used to heat the solution 322.
  • a heating device 323, can be applied directly to the solution 322 or to the tank 330 to elevate the temperature of the solution 322 that is mixed in the tank 330 with the glass particles.
  • the solution 322 is removed from the tank 330 via a separation device 340, such as a screen filter and the like.
  • the solution 322 can then be returned to its original holding tank and reused for a number of different treatment cycles. In one embodiment, the solution 322 is reused for approximately 53 treatment cycles on new untreated glass particles.
  • a rinsing device 350 supplies ordinary tap water to the tank 330.
  • the tank 330 has the glass particles, and the glass particles and tap water are circulated within the tank for a second period of time that is also configurable. In one embodiment, the second period of time is about 1 hour in duration.
  • the water can be brought to the appropriate pH level by injecting lime (or other neutralizing or precipitation agents) into the water.
  • the separating device 340 separates the glass particles and water, and the glass is now safe to use with other products or to be disposed of in an environmentally safe and approved manner.
  • the second period is negligible or non existent because the glass particles are rinsed using the rinsing device 350 as the treated glass particles are transported to their final destination.
  • the tap water used for rinsing is subjected to a water treatment device 360, such as a carbon filtering process and or a reverse osmosis process. Upon the conclusion of this treatment, the water is safe to dispose of in the sewage of a municipality's water supply.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Manufacturing & Machinery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Processing Of Solid Wastes (AREA)
  • Extraction Or Liquid Replacement (AREA)
  • Manufacture And Refinement Of Metals (AREA)
EP20030769011 2002-12-05 2003-11-25 Method and system for extracting metal from glass waste Withdrawn EP1567682A1 (en)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US10/310,411 US6666904B1 (en) 2002-12-05 2002-12-05 Method and system for extracting metal from glass waste
US310411 2002-12-05
US10/376,206 US6669757B1 (en) 2002-12-05 2003-02-26 Method for extracting metal from glass waste
US376206 2003-02-26
US10/691,282 US6893606B2 (en) 2002-12-05 2003-10-22 Method and system for extracting metal from glass waste
US691158 2003-10-22
US10/691,158 US6893605B2 (en) 2002-12-05 2003-10-22 Method and system for extracting metal from glass waste
US691282 2003-10-22
PCT/US2003/037456 WO2004053174A1 (en) 2002-12-05 2003-11-25 Method and system for extracting metal from glass waste

Publications (1)

Publication Number Publication Date
EP1567682A1 true EP1567682A1 (en) 2005-08-31

Family

ID=32512534

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20030769011 Withdrawn EP1567682A1 (en) 2002-12-05 2003-11-25 Method and system for extracting metal from glass waste

Country Status (4)

Country Link
EP (1) EP1567682A1 (enExample)
JP (1) JP2006511718A (enExample)
AU (1) AU2003291826A1 (enExample)
WO (1) WO2004053174A1 (enExample)

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Publication number Priority date Publication date Assignee Title
JP4918839B2 (ja) * 2006-10-06 2012-04-18 三菱マテリアル株式会社 表示パネル廃棄物の処理方法
CN102372431B (zh) * 2010-08-09 2013-06-26 深圳市格林美高新技术股份有限公司 一种处理废旧含铅玻璃的方法
EP2455500A1 (en) * 2010-11-22 2012-05-23 Costech International S.p.A. Process of treating end-of-life cathode ray tubes for lead and soluble silicates recovery
US20140345326A9 (en) * 2011-03-29 2014-11-27 Greene Lyon Group, Inc. Systems and methods for processing lead-containing glass
KR101659748B1 (ko) * 2012-02-06 2016-09-26 톳토리 프리펙쳐 유리로부터의 중금속류의 분리 방법
CN104162536A (zh) * 2014-08-01 2014-11-26 西安建筑科技大学 一种废旧阴极无害化处理与资源利用方法
ITUA20161987A1 (it) * 2016-03-24 2017-09-24 E V H S R L Processo per il trattamento dei tubi catodici a fine vita

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US5350121A (en) * 1991-12-09 1994-09-27 Falcon United Ltd. Method for recycling glass
US6129779A (en) * 1997-05-13 2000-10-10 First Solar, Llc Reclaiming metallic material from an article comprising a non-metallic friable substrate
JP2002302720A (ja) * 2001-04-04 2002-10-18 Nisso Kinzoku Kagaku Kk タリウムを含むガラス屑からタリウムを回収する方法

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AU2003291826A1 (en) 2004-06-30
JP2006511718A (ja) 2006-04-06
WO2004053174A1 (en) 2004-06-24

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