WO2014023149A1 - 生物质燃料二氧化碳循环无氧气化方法及设备 - Google Patents
生物质燃料二氧化碳循环无氧气化方法及设备 Download PDFInfo
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- WO2014023149A1 WO2014023149A1 PCT/CN2013/079230 CN2013079230W WO2014023149A1 WO 2014023149 A1 WO2014023149 A1 WO 2014023149A1 CN 2013079230 W CN2013079230 W CN 2013079230W WO 2014023149 A1 WO2014023149 A1 WO 2014023149A1
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- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
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- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
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- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
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- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
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Definitions
- the invention relates to the field of gasification utilization of biomass as a raw material, and specifically relates to a biomass fuel carbon dioxide cycle non-oxygenation method and equipment. Background technique
- the main process for solving zero-emissions of greenhouse gases is to convert carbon dioxide as a reactant and convert it into a carbon-containing product through chemical reaction to achieve zero emissions.
- Invention patent authorization announcement number: CN102060662B a chemical power multi-generation energy system and method capable of recycling C0 2 , that is, by recovering C0 2 in chemical tail gas, a part of C0 2 is subjected to an oxygenation cycle to obtain syngas Another part of C0 2 is reformed by adding natural gas to finally obtain dimethyl ether or methanol.
- the invention patent can recycle C0 2 , but the process requires oxygen gasification, so the conversion of C0 2 in the gasification process is limited, and most of the co 2 needs to be converted by natural gas reforming reaction, thus having oxygen demand and demand.
- the object of the present invention is to provide a carbon dioxide cycle non-oxygenation method and apparatus for biomass fuel, which has the advantages of high fuel conversion rate, no oxygen consumption, simple process flow, and zero greenhouse gas carbon dioxide emissions of the entire system.
- the present invention provides a carbon dioxide cycle non-oxygenation method for biomass fuel, which uses only CO 2 as a gasification agent to vaporize biomass fuel into syngas, and syngas is used to produce chemical oil to realize
- the process of the overall oxygen-free cycle includes the following steps:
- a gasification unit to recover the synthesis gas and the synthesis gas itself C0 2 contained in the subsequent use of C0 2 generated as a gasifying agent, so that it violently reacts with the gasification of biomass fuel under the effect of external auxiliary energy source, Producing a high temperature synthesis gas whose main components are CO, C0 2 , CH 4 , H 2 , H 2 0, H 2 S, COS;
- Cooling unit The two-stage heat exchanger is cooled by the generated high-temperature syngas, wherein the first-stage heat exchanger uses the above-mentioned gasifying agent C0 2 as a cooling medium for preheating the gasifying agent C0 2 ;
- the secondary heat exchanger uses water as a cooling medium to obtain by-product water vapor;
- Washing unit performing cyclone dust removal and scrubbing tower washing treatment on the syngas cooled by two-stage heat exchange to obtain a clean synthesis gas which is further cooled;
- shifting reaction unit the obtained clean syngas is subjected to water gas reaction with the above-mentioned by-product water vapor, and a part of CO is converted into C0 2 to adjust the quality of the clean syngas to reach the H 2 /CO ratio range required for the catalytic synthesis reaction. ;
- Desulfurization unit Desulfurization of the cleaned syngas after quenching and tempering, and removing H 2 S and COS therein;
- Syngas decarbonization unit decarbonizes the clean synthesis gas after desulfurization, and separates C0 2 from it;
- catalytic synthesis unit synthesizing chemical oil by catalytic conversion reaction of clean synthesis gas after desulfurization and decarburization, and simultaneously generating C0 2 -rich tail gas;
- Exhaust gas decarburization unit Decarbonize the generated tail gas, separate the C0 2 from it, and discharge the remaining non-greenhouse gas directly or after treatment;
- Gasification agent circulation unit The C0 2 separated in step 6) and step 8) is reused as the cooling medium of the first stage heat exchanger in step 2), and the heat is cooled by the heat exchange of the high temperature synthesis gas to obtain preheating.
- the gasification agent C0 2 is used to carry out the gasification reaction in the step 1), and the cycle finally realizes zero greenhouse gas emission of the whole process.
- the temperature of the gasification reaction is 600 to 1300 ° C, and the temperature of the high temperature synthesis gas outlet is 700 to 1100 ° C; in the step 1), the temperature of the gasification reaction is 850 ° At 1250 ° C, the high temperature synthesis gas outlet temperature is 850 ⁇ 1100 °C.
- the external auxiliary energy source is a combination of one or more of plasma torch energy, microwave energy, solar energy, laser energy or electric induction energy, and the external auxiliary energy source accounts for unit time 10 to 30% of the total energy.
- the external auxiliary energy accounts for the total energy of the raw materials in the unit time. 15 ⁇ 20%.
- the ratio of the amount of the gasifying agent C0 2 to the gas yield per unit state is 0.36 to 0.51; in the step 1), the particle size of the biomass fuel is 50 mm or less, gasification
- the flow rate of the nozzle of the agent C0 2 is 30 ⁇ 60 m/s; in the step 2), the gasifying agent C0 2 is preheated to 350 ⁇ 600 °C by the first stage heat exchanger.
- the clean syngas component is adjusted to H 2 /CO of 2:1.
- Biomass fuel carbon dioxide cycle non-oxygenation equipment designed to achieve the above method, including gasifier, residual heat exchanger, waste heat boiler, cyclone, scrubber, shift reaction tower, desulfurization tower, syngas decarbonization tower , catalytic synthesis tower and tail gas decarbonization tower, the special features are:
- the synthesis gas outlet of the gasification furnace is connected to the heat medium input end of the waste heat heat exchanger, and the heat medium output end of the waste heat heat exchanger is connected to the heat source input end of the waste heat boiler, and the heat source output end of the waste heat boiler is
- the inlet end of the cyclone is connected, the outlet end of the cyclone is connected to the inlet of the scrubber, and the outlet of the scrubber is connected to the inlet of the shift reaction tower through a compressor, the waste heat boiler
- the steam output is connected to the steam inlet of the shift reaction column;
- the outlet of the shift reaction tower is connected to the input end of the desulfurization tower, the output end of the desulfurization tower is connected to the input port of the synthesis gas decarbonization tower, the output port of the synthesis gas decarbonization tower and the raw material of the catalytic synthesis tower
- the inlet of the catalytic synthesis tower is connected to the tail gas inlet of the tail gas decarbonization tower, and the C0 2 outlet of the tail gas decarbonization tower and the synthesis gas decarbonization tower is simultaneously connected with the cold medium input end of the waste heat heat exchanger.
- the cold medium output end of the waste heat exchanger is connected to the gasification agent inlet of the gasifier.
- the tail gas decarbonization tower and the C0 2 outlet of the syngas decarbonization tower are simultaneously connected to the inlet of the gas cabinet, and the outlet of the gas cabinet is connected to the cold medium input end of the waste heat heat exchanger through a blower.
- the inlet of the gas cabinet is also connected to the C0 2 output port of the starting calciner.
- a lower portion of the inner cavity of the gasification furnace is provided with an air distribution plate, and a main gasification agent inlet is disposed on the furnace wall below the air distribution plate, and a furnace wall above the air distribution plate is provided with auxiliary a gasification agent inlet, an external auxiliary energy inlet is disposed on the furnace wall above the auxiliary gasification agent inlet, and the cold medium output end of the waste heat exchanger is divided into two paths, one is connected to the main gasification agent inlet, and the other is connected All the way to the auxiliary gasification agent import.
- the gasification unit uses only carbon dioxide as a gasifying agent, and no oxygenation, which not only supplements the carbon source but also reduces the fuel combustion share, and has a high unit fuel conversion rate and a high effective gas content.
- FIG. 1 is a schematic view showing the connection structure of a biomass fuel carbon dioxide circulating oxygen-free apparatus according to the present invention.
- Figure 2 is a schematic view showing the structure of the gasification furnace of Figure 1.
- Figure 3 is a schematic cross-sectional view of the A_A of Figure 2;
- gasifier 1 residual heat exchanger 2, waste heat boiler 3, cyclone 4, scrubber 5, compressor 6, shift reaction tower 7, desulfurization tower 8, syngas decarbonization tower 9, catalysis Synthesis tower 10, exhaust decarbonization tower 11, gas cabinet 12, blower 13, fuel 14, external auxiliary energy inlet 15, auxiliary gasification agent inlet 16, feed inlet 17, syngas outlet 18, air distribution panel 19, main gas Chemical agent inlet 20, slag discharge port 21, feed device 22, slag cooler 23, steam 24, cold slag 25, fly ash 26, synthetic oil 27, synthetic tail gas 28, C0 2 gas 29, syngas 30, discharge Gas 31, starting calciner 32, limestone 33.
- the biomass fuel carbon dioxide cycle non-oxygenation equipment shown in the figure is mainly composed of gasifier 1, residual heat exchanger 2, waste heat boiler 3, cyclone 4, scrubber 5, shift reaction tower 7, desulfurization tower 8
- the synthesis gas decarbonization tower 9, the catalytic synthesis tower 10, and the tail gas decarbonization tower 11 are composed.
- the top of the gasification furnace 1 is provided with a synthesis gas outlet 18, and the bottom of the gasification furnace 1 is provided with a slag discharge port 21, and a central portion of the central portion of the gasification furnace is provided with a feed inlet 17 to which a feed inlet 17 is connected .
- An air distribution plate 19 is disposed at a lower portion of the inner cavity of the gasification furnace 1, and a main gasification agent inlet 20 is disposed on the furnace wall below the air distribution plate 19, and an auxiliary gasification agent inlet 16 is disposed on the furnace wall above the air distribution plate 19.
- An external auxiliary energy inlet 15 is disposed on the furnace wall above the auxiliary gasification agent inlet 16.
- the synthesis gas outlet 18 of the gasification furnace 1 is connected to the heat medium input end of the heat recovery heat exchanger 2, and the heat medium output end of the heat recovery heat exchanger 2 is connected to the heat source input end of the waste heat boiler 3, and the heat source output end of the waste heat boiler 3 is
- the inlet end of the cyclone 4 is connected, the outlet end of the cyclone 4 is connected to the inlet of the scrubber 5, and the outlet of the scrubber 5 is connected to the inlet of the shift reaction tower 7 via the compressor 6, the waste heat boiler
- the steam output of 3 is connected to the steam inlet of shift reaction column 7.
- the gas outlet of the shift reaction column 7 is connected to the input end of the desulfurization tower 8, and the output end of the desulfurization tower 8 is connected to the input port of the synthesis gas decarbonization column 9, the output port of the synthesis gas decarbonization column 9 and the raw material of the catalytic synthesis column 10.
- the inlet is connected, the by-product outlet of the catalytic synthesis column 10 is connected to the tail gas inlet of the tail gas decarbonization column 11, and the C0 2 outlet of the tail gas decarbonization column 11 and the synthesis gas decarbonization column 9 is simultaneously connected with the cold medium input end of the heat recovery heat exchanger 2.
- the cold medium output end of the heat recovery heat exchanger 2 is divided into two paths, one connected to the main gasifying agent inlet 20 and the other connected to the auxiliary gasifying agent inlet 16.
- the outlet of 0 2 is simultaneously connected to the inlet of the gas cabinet 12, and the outlet of the gas cabinet 12 is connected to the cold medium input end of the heat recovery heat exchanger 2 through the blower 13; the inlet of the gas cabinet 12 is also connected to the C0 2 output port of the start calciner 32. .
- the solid fuel 14 such as biomass is first fed into the gasification furnace 1 through the feeding device 22 through the feeding port 17, and the circulating gasifying agent C0 2 is blown in through the blower 13, and the gasifying agent C0 2 is divided into two.
- the road is introduced all the way through the main gasifying agent inlet 20, enters the gasification furnace 1 through the air distribution plate 19, and the other enters the gasification furnace 1 through the auxiliary gasification agent inlet 16 while introducing heat energy through the external auxiliary energy inlet 15.
- the high temperature reaction is carried out, and the pyrolysis gasification is initially carried out, and the main cracking generates CO, C0 2 , CH 4 , and semi-coke, because the reaction temperature in the furnace is controlled at 600 to 1600 ° C, and the semi-coke substance is mainly at a high temperature. versus.
- the amount of auxiliary energy of the fuel inlet can be 15-25% of the total, the reaction temperature of 800 ° C, for an amount of C0 2 circulation required biomass 0.48kg 0.51Nm 3,
- the volume composition of the outlet syngas is: CO: 50-55% C0 2 : 22-28% H 2 : 6 ⁇ 12%.
- the high-temperature synthesis gas 30 is taken out from the synthesis gas outlet 18 of the gasification furnace 1, and the fuel cold residue 25 is discharged from the slag discharge port 21, and discharged to the slag field through the slag cooler 23.
- the temperature of the reaction zone of the gasifier is controlled at 600 ⁇ 1300 °C, and 850 ⁇ 1250 °C is the optimum temperature.
- the syngas outlet temperature is controlled in the range of 800 ⁇ 1100 °C.
- Feeding carrier gas, process purge gas in gasification unit Both recycle C0 2 gas is utilized.
- the external input energy accounts for 15 ⁇ 30% of the energy of the processing raw materials.
- external energy types include microwave energy, solar energy, laser energy, electrical induction energy, and other energy types that can be converted into thermal energy.
- the circulation amount of the gasifying agent C0 2 can be appropriately adjusted according to the furnace temperature and the fuel condition.
- the flow rate of the gasification agent air distribution plate in the gasifier can be reasonably controlled according to the particle size of the fuel.
- a preferred example is a particle diameter of 50 mm or less, and a wind speed of 30 to 60 m/s.
- the start calciner 32 is used, and the limestone 33 is calcined by external heat to prepare high-purity C0 2 gas as the starting gas.
- the key to the design is to control the bed temperature and adjust the plasma power and carbon dioxide supply in real time. The control of the above-mentioned key factors can be achieved by the syngas outlet monitoring unit, and the interlock control can be realized, and the fully automated operation can be performed to improve the operational stability.
- the high temperature synthesis gas 30 then enters the heat recovery heat exchanger 2 and exchanges heat with the CO 2 gas 29 as a gasifying agent, thereby preheating the gasification agent and improving the gasification furnace conversion efficiency.
- the high-temperature syngas after the first-stage cooling then enters the waste heat boiler 3 to continue to cool down, and the by-product steam 24, after the two stages are cooled, the syngas is then passed through the cyclone 4 and the scrubber 5 to further cool and dedust the syngas, and separate it.
- the fly ash 26 is collected and discharged to the slag field, wherein the temperature of the preheated C0 2 is 350 to 600 °C.
- the cooled and purified syngas is then boosted by the compressor 6, pressurized, and then introduced into the shifting tower 7, and the syngas is subjected to quenching and tempering treatment in the shifting tower 7, and the main reaction is a water gas reaction, wherein the steam 24 is derived from the waste heat boiler. 3. This achieves the purpose of rational utilization of the overall process materials.
- the tempered syngas then enters the desulfurization tower 8 and the syngas decarbonization tower 9 for desulfurization and decarbonization purification treatment.
- the clean syngas from the synthesis gas decarbonization column 9 then enters the catalytic synthesis column 10, and the CO 2 gas 29 separated from the synthesis gas decarbonization column 9 is delivered to the gas cabinet 12 by the residual pressure.
- the syngas enters the catalytic synthesis column 10, and the synthesis gas is synthesized into a chemical oil 27 by a synthesis reaction, which is also accompanied by the formation of a synthetic tail gas.
- the synthetic tail gas 28 is then sent to the tail gas decarbonization tower 11, and the CO 2 gas 29 is separated in the tower, and the remaining greenhouse gas-free exhaust gas 31 is treated and discharged to the outside, thus achieving the overall process zero greenhouse gas emissions.
- the synthesis gas decarbonization column 9 and the CO 2 gas 29 separated from the exhaust gas decarbonization column 11 enter the gas cabinet 12, and are sent to the main gasification agent inlet 20 and the auxiliary gasification agent inlet 16 of the gasification furnace 1 through the blower 13 . At this point, the gasification cycle is carried out in this way.
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- Oil, Petroleum & Natural Gas (AREA)
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Description
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Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015525713A JP5965073B2 (ja) | 2012-08-09 | 2013-07-11 | バイオマス燃料の二酸化炭素の循環による無酸素ガス化方法および装置 |
| AU2013302099A AU2013302099B2 (en) | 2012-08-09 | 2013-07-11 | Method and device for biomass gasification by cycling of carbon dioxide without oxygen |
| KR1020157003071A KR101609809B1 (ko) | 2012-08-09 | 2013-07-11 | 산소없이 이산화탄소의 사이클링에 의한 바이오매스 가스화용 방법 및 장치 |
| DK13827090.5T DK2883940T3 (en) | 2012-08-09 | 2013-07-11 | Process and apparatus for biomass gasification by recirculation of the carbon dioxide without oxygen |
| RU2015108053/05A RU2604624C2 (ru) | 2012-08-09 | 2013-07-11 | Способ и устройство для газификации биомассы путем рециркуляции диоксида углерода без кислорода |
| EP13827090.5A EP2883940B1 (en) | 2012-08-09 | 2013-07-11 | Method and device for biomass gasification by cycling of carbon dioxide without oxygen |
| CA2881327A CA2881327A1 (en) | 2012-08-09 | 2013-07-11 | Method and device for biomass gasification by cycling of carbon dioxide without oxygen |
| US14/607,020 US9469820B2 (en) | 2012-08-09 | 2015-01-27 | Method and system for recycling carbon dioxide from biomass gasification |
| US15/261,988 US10077407B2 (en) | 2012-08-09 | 2016-09-11 | Method and system for recycling carbon dioxide from biomass gasification |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210282152.6 | 2012-08-09 | ||
| CN201210282152.6A CN102796561B (zh) | 2012-08-09 | 2012-08-09 | 生物质燃料二氧化碳循环无氧气化方法及设备 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US14/607,020 Continuation-In-Part US9469820B2 (en) | 2012-08-09 | 2015-01-27 | Method and system for recycling carbon dioxide from biomass gasification |
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| Publication Number | Publication Date |
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| WO2014023149A1 true WO2014023149A1 (zh) | 2014-02-13 |
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| Application Number | Title | Priority Date | Filing Date |
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| PCT/CN2013/079230 Ceased WO2014023149A1 (zh) | 2012-08-09 | 2013-07-11 | 生物质燃料二氧化碳循环无氧气化方法及设备 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US9469820B2 (zh) |
| EP (1) | EP2883940B1 (zh) |
| JP (1) | JP5965073B2 (zh) |
| KR (1) | KR101609809B1 (zh) |
| CN (1) | CN102796561B (zh) |
| AU (1) | AU2013302099B2 (zh) |
| CA (1) | CA2881327A1 (zh) |
| DK (1) | DK2883940T3 (zh) |
| RU (1) | RU2604624C2 (zh) |
| WO (1) | WO2014023149A1 (zh) |
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| CN102796561B (zh) * | 2012-08-09 | 2014-04-30 | 武汉凯迪工程技术研究总院有限公司 | 生物质燃料二氧化碳循环无氧气化方法及设备 |
| CN103045308B (zh) * | 2012-12-29 | 2014-12-03 | 中国科学院工程热物理研究所 | 一种基于煤炭的碳氢组分分级转化的发电方法及系统 |
| US9631553B2 (en) * | 2012-12-29 | 2017-04-25 | Institute Of Engineering Thermophysics, Chinese Academy Of Sciences | Process and equipment for coal gasification, and power generation system and power generation process thereof |
| CN103232857B (zh) * | 2013-04-24 | 2015-10-28 | 华东理工大学 | 一种co2零排放的煤基电力与化工品联产工艺 |
| CN103666580B (zh) * | 2013-11-29 | 2015-07-22 | 武汉凯迪工程技术研究总院有限公司 | 一种耦合式生物质加压热解工艺及系统 |
| CN105861057B (zh) * | 2016-04-22 | 2018-07-20 | 南京师范大学 | 一种二氧化碳近零排放的高经济性能源热转换系统及方法 |
| CN109780619A (zh) * | 2019-01-14 | 2019-05-21 | 江苏河海新能源股份有限公司 | 一种家用气化燃气一体化供热方法 |
| CN110387265A (zh) * | 2019-07-22 | 2019-10-29 | 苏钰山 | 一种生物质可燃气提取方法及提取设备 |
| CN110734788B (zh) * | 2019-10-21 | 2020-09-15 | 山东理工大学 | 一种高品质燃气制取系统 |
| EP3878807A1 (en) | 2020-03-13 | 2021-09-15 | Clariant International Ltd | Process for the production of synthesis gas via allothermic gasification with controlled carbon dioxide reduction |
| CN112646609B (zh) * | 2021-02-02 | 2025-03-18 | 上海浦合绿碳清洁能源科技有限公司 | 一种生物质气化制氢的装置及方法 |
| CN113717758B (zh) * | 2021-08-27 | 2024-02-09 | 山东津挚环保科技有限公司 | 合成气脱硫脱碳系统 |
| CN115011380A (zh) * | 2022-06-29 | 2022-09-06 | 西安交通大学 | 利用小型氟盐冷却高温堆余热热解垃圾制氢系统及方法 |
| CN115583630A (zh) * | 2022-09-20 | 2023-01-10 | 西南石油大学 | 一种光热催化分解硫化氢和二氧化碳制备合成气的方法 |
| CN117105175B (zh) * | 2023-08-26 | 2025-08-05 | 宁波四明化工有限公司 | 一种合成气脱碳液除杂工艺 |
| FI131724B1 (en) * | 2024-04-18 | 2025-10-20 | Teknologian Tutkimuskeskus Vtt Oy | Producing synthesis gas |
| FI20245495A1 (en) * | 2024-04-18 | 2025-10-19 | Teknologian Tutkimuskeskus Vtt Oy | Converting carbon dioxide formed during heat treatments into suitable components for use as fuel |
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Also Published As
| Publication number | Publication date |
|---|---|
| CN102796561A (zh) | 2012-11-28 |
| CN102796561B (zh) | 2014-04-30 |
| EP2883940A1 (en) | 2015-06-17 |
| CA2881327A1 (en) | 2014-02-13 |
| JP2015524504A (ja) | 2015-08-24 |
| RU2604624C2 (ru) | 2016-12-10 |
| KR20150027830A (ko) | 2015-03-12 |
| RU2015108053A (ru) | 2016-10-10 |
| EP2883940B1 (en) | 2018-09-26 |
| US10077407B2 (en) | 2018-09-18 |
| JP5965073B2 (ja) | 2016-08-03 |
| EP2883940A4 (en) | 2016-04-06 |
| KR101609809B1 (ko) | 2016-04-06 |
| AU2013302099A1 (en) | 2015-03-05 |
| AU2013302099B2 (en) | 2016-12-15 |
| DK2883940T3 (en) | 2019-01-21 |
| US20150141536A1 (en) | 2015-05-21 |
| US9469820B2 (en) | 2016-10-18 |
| US20160376513A1 (en) | 2016-12-29 |
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