WO2007036334A2 - Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien - Google Patents
Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien Download PDFInfo
- Publication number
- WO2007036334A2 WO2007036334A2 PCT/EP2006/009267 EP2006009267W WO2007036334A2 WO 2007036334 A2 WO2007036334 A2 WO 2007036334A2 EP 2006009267 W EP2006009267 W EP 2006009267W WO 2007036334 A2 WO2007036334 A2 WO 2007036334A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pyrolysis
- chamber
- combustion
- furnace
- oxygen
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B7/00—Working 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
- C22B7/001—Dry processes
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/02—Obtaining noble metals by dry processes
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/02—Obtaining noble metals by dry processes
- C22B11/021—Recovery of noble metals from waste materials
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/02—Incineration of waste; Incinerator constructions; Details, accessories or control therefor with pretreatment
- F23G5/027—Incineration of waste; Incinerator constructions; Details, accessories or control therefor with pretreatment pyrolising or gasifying stage
- F23G5/0273—Incineration of waste; Incinerator constructions; Details, accessories or control therefor with pretreatment pyrolising or gasifying stage using indirect heating
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/08—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating
- F23G5/14—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating including secondary combustion
- F23G5/16—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating including secondary combustion in a separate combustion chamber
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/50—Control or safety arrangements
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/003—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals for used articles
- F23G7/006—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals for used articles wires, cables
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27B—FURNACES, KILNS, OVENS, OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
- F27B5/00—Muffle furnaces; Retort furnaces; Other furnaces in which the charge is held completely isolated
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2207/00—Control
- F23G2207/10—Arrangement of sensing devices
- F23G2207/102—Arrangement of sensing devices for pressure
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2207/00—Control
- F23G2207/30—Oxidant supply
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2208/00—Safety aspects
- F23G2208/10—Preventing or abating fire or explosion, e.g. by purging
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2209/00—Specific waste
- F23G2209/14—Gaseous waste or fumes
- F23G2209/141—Explosive gases
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the invention relates to methods for and corresponding devices for the burning of precious metal-containing materials.
- AquaCat® ® process Johnson Matthey. It can be used to recycle precious metal waste containing carbon and organic compounds, especially gold, silver, platinum and palladium waste from industry, the watch and jewelery sector.
- the organic components are oxidized in supercritical water under pressure with oxygen, leaving behind the precious metal as an oxidic residue. Again, the material must be continuously transportable. The method further requires a pressure reactor.
- Siemens KWU has developed a process that combines pyrolysis and high-temperature combustion using pyrolysis gases (Ullmann's 6th ed., 2003 CD-ROM release, "Waste" Ref. 320: KJ Thome-Kozmiensky: Thermal Waste Treatment EF-Verlag for energy and environmental technology, Berlin 1994), where it depends crucially on the generation of energy during incineration (waste-to-energy plant)
- Another possible method is the gasification of the organic components of metal-containing waste 2 , which in turn with high Apparative effort is required and always presupposes appreciable gasifiable shares, because the gas is ultimately used to generate energy.
- DE 94 20 410 U1 relates to a plant for a thermal recycling process for metallic objects which are mixed or contaminated with organic substances, such as e.g. Oil drums, but also on a smaller scale waste containing precious metals from jewelery workshops or small businesses in the jewelery industry.
- organic substances such as e.g. Oil drums
- a pollination with pyrolysis phase and an oxidation phase in a smoldering chamber is recommended, wherein the oxidation takes place with the introduction of an exhaust gas with combustible oxygen content.
- a similar system is used according to DE 35 18 725 A1 of the thermal stripping - there with combustion of the carbonization.
- the two methods are not suitable for liquids with organic components that burn with great energy.
- the invention relates to the burnup of noble metal-containing materials with organic fractions which burn with great energy, in at least two steps, of which the first (A) involves pyrolysis or carbonization with reduced oxygen supply and at least one further step (B) comprises an oxidative combustion , During the first process step, there is no hot flame. In the subsequent oxidative combustion of the pyrolysis residue flame and Rußaustrag are limited. Preferably, a Rußaustrag is excluded.
- the noble metal-containing materials with organic components are in particular carbon, solvents or plastics. Such materials generally have a calorific value of 20 to 50 KJ / g, in particular 40 KJ / g and are potentially explosive.
- the steps A and B are carried out in an indirectly heated oven directly successively in a furnace chamber.
- the pyrolysis which is also referred to as smoldering in Germany, takes place in an atmosphere with reduced oxygen content.
- the chamber is purged with inert gas, in particular nitrogen or argon.
- the oxygen content is at most 6% by weight, in particular at most 4% by weight.
- the end of the pyrolysis is detected by a sensor, in particular a pressure sensor.
- the pyrolytically treated material has at the end of process step A low volatility substances with high carbon content.
- the atmosphere is changed by air or oxygen supply and thus initiated directly step B.
- oxygen into the furnace which has already been heated to 400 to 900 ° C., in particular 500 to 800 ° C., without causing an explosion.
- This process step saves considerable logistical effort, considerable energy input and shortens the time required.
- the energy consumption can be further reduced, in which two furnaces alternately perform steps A and B side by side and are equipped with a single exhaust gas treatment.
- two furnaces alternately perform steps A and B side by side and are equipped with a single exhaust gas treatment.
- pyrolysis and combustion exhaust gases in the exhaust gas treatment plant This reduces the volume flow and thus the energy requirement.
- the combustion chamber of the furnace is equipped with a sensor in order to be able to determine the pyrolysis end. Furthermore, it is significant that the pyrolysis furnace under inert gas as well as under air or oxygen atmosphere can be operated and a switching device is provided by the Protective gas filling the furnace chamber to an air flow or oxygen flow can change. The changeover must be controlled by the result of the sensor.
- steps A and B are carried out successively in a chamber, the end of the pyrolysis is determined, and after the end of the pyrolysis an atmosphere change takes place from a protective gas-containing atmosphere to air or oxygen atmosphere. This saves batch change and the associated expenditure of time and energy.
- the oven has a continuous conveyor for liquids or pastes.
- liquids or pastes are the 300 0 C to 700 0 C, especially 350 0 C to 600 0 C hot furnace continuously promoted during pyrolysis in the pyrolysis chamber. The risk of explosion is thereby avoided, in which the furnace is operated under slight overpressure.
- Pastes are heated to the point that they behave like liquids. By conveying liquid substances or liquefied pastes through a pipeline, the oxygen input is kept so low that explosion limits can not be achieved.
- the precious metal content of the waste can vary widely depending on the origin, e.g. from 0.01 to 60%. In addition to the precious metals, other metals may be included.
- a precious metal content of between 10 and 1000 ppm (0.001 and 0.1% by weight), in particular between 10 and 100 ppm (0.001 and 0.01% by weight) enrichment with the continuous conveyor into the pyrolysis is particularly suitable. Since continuous enrichment already during pyrolysis, a considerable enrichment can be achieved within a tub. Due to the continuous delivery, it is possible to pyrolyze a multiple of liquid volume within a tub, based on the tub volume.
- the furnace of the invention is particularly important to recycle rhodium, platinum, palladium, gold and iridium.
- the promotion of the liquids during the pyrolysis distributes the carbonization evenly over the pyrolysis process duration.
- the carbonization gas produced during pyrolysis reduces the natural gas consumption of thermal afterburning.
- the thermal afterburning is therefore on the one hand to lower volumetric flows interpretable and on the other hand requires due to the continuous carbonization gas supply lower energy consumption.
- the following measures are preferably taken, which can be used individually or in combination with each other.
- a The process is advantageously carried out in a chamber furnace.
- the pyrolysis can be carried out and then the combustion, while in the second already the next pyrolysis takes place. While then switching to combustion in the second chamber, the first can already be re-charged with material for pyrolysis.
- the pyrolysis step naturally takes place under extensive exclusion of oxygen.
- the relevant chamber is purged prior to pyrolysis with inert gas, preferably nitrogen.
- the temperature control is usually within the range of 100 to 1200, in particular 200 to 800 0 C, at step A 100 to 1200, preferably from 200 to 800 0 C, at step B from 500 to 1200, preferably 600 to 800 ° C.
- the material supply of liquids for the pyrolysis step A is preferably not in portions, but slowly and continuously.
- step B precious metal components and ash are expediently taken up in drip pans, which are arranged below the combustion material supply or pyrolysis material supply.
- Figure 1 is a schematic drawing of the two chambers.
- FIG. 1 An expedient embodiment can be taken from the diagram of FIG. 1, in which 1. The two combustion chambers with heating.
- drip pans which are arranged under the fuel supply or Pyrolysegutzu operation for receiving precious metal shares and ashes.
- the invention thus also relates to a device for carrying out the method according to the invention comprising two heatable combustion chambers 1, depending on at least one Brenngutzu entry 3 and at least one collecting trough 2, disposed below the Brenngutzu entry.
- the residue is burned off under air supply at an oxygen content of 14 to 16% and at a temperature of 600 to 800 °.
- a chamber furnace is equipped with approximately 1,100 kg of different precious metal-containing waste.
- 32 trays with a filling volume of 60 l each are introduced into the kiln.
- 14 of the tubs are each filled with 30 kg of a 0.1 wt.% Palladium-containing coal.
- 5 wells are filled with 20 kg of platinum oxide, wherein the platinum oxide is present at 80 wt.% And is contaminated with 20 wt.% Of a solvent based on xylene.
- 5 wells are filled with 20 kg each of a paste from the production of ceramic colors, the paste has about 10 wt.% Gold. 8 empty tubs are set in the topmost position of the oven. The tubs are kept in a batch rack.
- the oven is then switched to pyrolysis mode. For this purpose, inert gas is introduced into the furnace until the oxygen content has fallen below 4%. Then the loaded at 200 0 C furnace is heated within 4 hours at 600 0 C. The oven is then held at 600 C for two hours.
- the pyrolysis in the loaded tubs is largely completed.
- This is followed by a metered addition of 500 l of organic liquid of a homogeneous catalyst based on rhodium in triphenylphosphine with additions of methyl isobutyl ketone.
- the content of rhodium is 10 ppm (0.001 wt.%).
- the solution is continuously added to the 8 walls. pumped and largely evenly distributed.
- the pumping capacity is a maximum of 200 l / h and is regulated by the utilization rate of the thermal afterburning.
- the thermal afterburning is equipped with a temperature sensor, which reduces the pump power when the temperature rises above 1,100 ° C.
- the end of pyrolysis is reached after 2 1/2 hours at the earliest, at higher calorific values according to the regulation by the thermal afterburning later.
- the temperature of the furnace is increased within about 30 minutes at 800 0 C.
- the overpressure of 5 mbar set by the protective gas increases for a short time due to progressive pyrolysis. After the determined with a pressure sensor overpressure has fallen back to the pressure of the nitrogen purge, this state is maintained at 800 0 C for 20 minutes. If no further increase in pressure takes place during this test period, atmospheric air is supplied to the furnace chamber and the oxidation phase is thus started without cooling the chamber. A second furnace, which is connected to the same thermal afterburning as the furnace which has meanwhile been transferred to the combustion phase, is released for the start of pyrolysis. The thermal afterburning is set to 1,100 0 C and is used more efficiently by the interlocking. The interlocking causes a smoothing of the liberated Schwelgasmengen over the processes A and B.
- the thermal afterburning is designed in essence for an oven and is actually operated with two ovens. This saves on an effort in terms of sizing and in particular the energy costs to keep the temperature at 1100 0 C. Furthermore, the natural gas consumption of the thermal afterburning is reduced by the introduction of the carbonization gases. This happens all the more efficiently, the more homogeneously the carbonization gas is introduced, which according to the invention is achieved by coupling the afterburning of a furnace which is in process B with an oven which is driven in process A.
- the oxidation is completed in a known manner, whereupon the furnace is cooled to 200 0 C and charge is removed.
- the inventive method can prepare different batches without mixing with each other. For example, batches of different customers can be processed in parallel, whereby the batches can be of different nature.
- the supply of liquids also has the advantage that the Schwelgasmenge is made uniform in order to save costs in the thermal afterburning costs.
- the liquids supplied at 600 ° C may also be liquefied pastes or suspensions. These liquids are particularly explosive at high temperatures in the presence of oxygen. The risk of explosion is excluded according to the invention, in which the oxygen content is kept below 6%. This surprisingly explosive materials are supplied to a furnace at high temperatures.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Organic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Processing Of Solid Wastes (AREA)
- Incineration Of Waste (AREA)
- Gasification And Melting Of Waste (AREA)
- Catalysts (AREA)
Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2006296760A AU2006296760B2 (en) | 2005-09-27 | 2006-09-25 | Method and device for treating materials containing precious metals |
CN2006800354851A CN101273147B (zh) | 2005-09-27 | 2006-09-25 | 用于后处理含贵金属材料的方法和设备 |
AT06805827T ATE471995T1 (de) | 2005-09-27 | 2006-09-25 | Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien |
PL06805827T PL1951919T3 (pl) | 2005-09-27 | 2006-09-25 | Sposób i urządzenie do przeróbki materiałów zawierających metale szlachetne |
DE200650007286 DE502006007286D1 (de) | 2005-09-27 | 2006-09-25 | Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien |
CA 2623699 CA2623699C (en) | 2005-09-27 | 2006-09-25 | Method and device for burning-off precious metal-containing materials |
JP2008532642A JP4950997B2 (ja) | 2005-09-27 | 2006-09-25 | 貴金属含有材料を焼却するための方法および装置 |
ES06805827T ES2347910T3 (es) | 2005-09-27 | 2006-09-25 | Procedimiento y dispositivo para el tratamiento de materiales que contienen metales nobles. |
BRPI0616432-3B1A BRPI0616432B1 (pt) | 2005-09-27 | 2006-09-25 | Forno de reciclagem, método para o processamento de materiais com partes orgânicas contendo metais nobres e dispositivo para realização do método. |
EP20060805827 EP1951919B1 (de) | 2005-09-27 | 2006-09-25 | Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien |
US12/056,524 US8188329B2 (en) | 2005-09-27 | 2008-03-27 | Method and device for burning-off precious metal-containing materials |
US13/461,114 US8377382B2 (en) | 2005-09-27 | 2012-05-01 | Recycling furnace for burning off precious metal-containing materials |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005046275 | 2005-09-27 | ||
DE102005046275.8 | 2005-09-27 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/056,524 Continuation US8188329B2 (en) | 2005-09-27 | 2008-03-27 | Method and device for burning-off precious metal-containing materials |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007036334A2 true WO2007036334A2 (de) | 2007-04-05 |
WO2007036334A3 WO2007036334A3 (de) | 2007-11-29 |
Family
ID=37441803
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/009267 WO2007036334A2 (de) | 2005-09-27 | 2006-09-25 | Verfahren und vorrichtung zur aufbereitung edelmetallhaltiger materialien |
Country Status (19)
Country | Link |
---|---|
US (2) | US8188329B2 (de) |
EP (1) | EP1951919B1 (de) |
JP (1) | JP4950997B2 (de) |
KR (1) | KR101018927B1 (de) |
CN (1) | CN101273147B (de) |
AR (1) | AR058674A1 (de) |
AT (1) | ATE471995T1 (de) |
AU (1) | AU2006296760B2 (de) |
BR (1) | BRPI0616432B1 (de) |
CA (1) | CA2623699C (de) |
DE (1) | DE502006007286D1 (de) |
ES (1) | ES2347910T3 (de) |
MY (1) | MY145641A (de) |
PL (1) | PL1951919T3 (de) |
PT (1) | PT1951919E (de) |
RU (1) | RU2380436C1 (de) |
TW (1) | TWI393781B (de) |
WO (1) | WO2007036334A2 (de) |
ZA (1) | ZA200802623B (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2500442A1 (de) | 2011-03-18 | 2012-09-19 | Heraeus Precious Metals GmbH & Co. KG | Prozess zur Rückgewinnung von Edelmetall aus funktionalisierten edelmetallhaltigen Adsorptionsmaterialien |
EP3118337A1 (de) * | 2015-07-15 | 2017-01-18 | Heraeus Deutschland GmbH & Co. KG | Verfahren und vorrichtung zum abbrand von edelmetallhaltigen materialien |
WO2018152484A1 (en) | 2017-02-17 | 2018-08-23 | Heraeus Deutschland GmbH & Co. KG | Process for the incineration of activated coal-supported pgm catalysts |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4950997B2 (ja) | 2005-09-27 | 2012-06-13 | ヘレーウス マテリアルズ テクノロジー ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディートゲゼルシャフト | 貴金属含有材料を焼却するための方法および装置 |
RU2010114611A (ru) | 2007-09-14 | 2011-10-20 | Баррик Гольд Корпорейшн (CA) | Способ восстановления металлов платиновой группы с использованием восстановителей |
JP5268398B2 (ja) * | 2008-03-14 | 2013-08-21 | Jx日鉱日石金属株式会社 | 貴金属スクラップの処理方法 |
DE102011016860A1 (de) * | 2011-04-13 | 2012-10-18 | Umicore Ag & Co. Kg | Verfahren zur Bereitstellung edelmetallhaltiger Stoffgemische für die Rückgewinnung von Edelmetallen |
CN103924086B (zh) * | 2014-04-02 | 2016-05-18 | 上海交通大学 | 电子废弃物破碎分选后的混合金属富集体的分离回收方法 |
US9850433B2 (en) | 2015-12-31 | 2017-12-26 | Chz Technologies, Llc | Multistage thermolysis method for safe and efficient conversion of E-waste materials |
KR102658327B1 (ko) * | 2016-02-08 | 2024-04-18 | 뉴사우스 이노베이션즈 피티와이 리미티드 | 복합 폐기물 소스를 처리하기 위한 방법, 장치 및 시스템 |
CN107166403B (zh) * | 2017-07-04 | 2019-03-05 | 于向真 | 一种贵金属碳催化剂焚烧炉及焚烧工艺 |
US10640711B2 (en) | 2018-06-05 | 2020-05-05 | Chz Technologies, Llc | Multistage thermolysis method for safe and efficient conversion of treated wood waste sources |
EP3810325A4 (de) * | 2018-06-21 | 2022-02-09 | Heraeus Deutschland GmbH & Co. KG | Edelmetallkatalysatorbriketts, verfahren zu deren herstellung und deren verbrennung |
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EP2500442A1 (de) | 2011-03-18 | 2012-09-19 | Heraeus Precious Metals GmbH & Co. KG | Prozess zur Rückgewinnung von Edelmetall aus funktionalisierten edelmetallhaltigen Adsorptionsmaterialien |
US8475749B2 (en) | 2011-03-18 | 2013-07-02 | Heraeus Precious Metals Gmbh & Co. Kg | Process for recovery of noble metals from functionalised, noble metal-containing adsorption materials |
EP3118337A1 (de) * | 2015-07-15 | 2017-01-18 | Heraeus Deutschland GmbH & Co. KG | Verfahren und vorrichtung zum abbrand von edelmetallhaltigen materialien |
WO2017008955A3 (de) * | 2015-07-15 | 2017-08-24 | Heraeus Deutschland GmbH & Co. KG | Verfahren und vorrichtung zum abbrand von edelmetallhaltigen materialien |
US10724116B2 (en) | 2015-07-15 | 2020-07-28 | Heraeus Deutschland GmbH & Co. KG | Process and device for burn-off of precious metal-containing materials |
WO2018152484A1 (en) | 2017-02-17 | 2018-08-23 | Heraeus Deutschland GmbH & Co. KG | Process for the incineration of activated coal-supported pgm catalysts |
US10393374B2 (en) | 2017-02-17 | 2019-08-27 | Heraeus Deutschland & Gmbh & Co. Kg | Process for the incineration of activated coal-supported PGM catalysts |
Also Published As
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US20080295749A1 (en) | 2008-12-04 |
WO2007036334A3 (de) | 2007-11-29 |
EP1951919B1 (de) | 2010-06-23 |
AU2006296760A1 (en) | 2007-04-05 |
DE502006007286D1 (de) | 2010-08-05 |
ES2347910T3 (es) | 2010-11-25 |
AU2006296760B2 (en) | 2009-12-10 |
JP4950997B2 (ja) | 2012-06-13 |
BRPI0616432A2 (pt) | 2011-06-21 |
CN101273147B (zh) | 2011-05-18 |
MY145641A (en) | 2012-03-15 |
RU2380436C1 (ru) | 2010-01-27 |
PT1951919E (pt) | 2010-09-28 |
ATE471995T1 (de) | 2010-07-15 |
EP1951919A2 (de) | 2008-08-06 |
US8377382B2 (en) | 2013-02-19 |
US8188329B2 (en) | 2012-05-29 |
JP2009510381A (ja) | 2009-03-12 |
TWI393781B (zh) | 2013-04-21 |
BRPI0616432B1 (pt) | 2014-04-15 |
RU2008116593A (ru) | 2009-11-10 |
ZA200802623B (en) | 2009-04-29 |
US20120227643A1 (en) | 2012-09-13 |
CN101273147A (zh) | 2008-09-24 |
AR058674A1 (es) | 2008-02-20 |
PL1951919T3 (pl) | 2010-11-30 |
TW200716766A (en) | 2007-05-01 |
KR20080050439A (ko) | 2008-06-05 |
CA2623699C (en) | 2012-04-24 |
KR101018927B1 (ko) | 2011-03-02 |
CA2623699A1 (en) | 2007-04-05 |
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