EP2233548A1 - Method of producing ferro-coke - Google Patents
Method of producing ferro-coke Download PDFInfo
- Publication number
- EP2233548A1 EP2233548A1 EP07860587A EP07860587A EP2233548A1 EP 2233548 A1 EP2233548 A1 EP 2233548A1 EP 07860587 A EP07860587 A EP 07860587A EP 07860587 A EP07860587 A EP 07860587A EP 2233548 A1 EP2233548 A1 EP 2233548A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- molded product
- containing material
- coal
- ferrocoke
- carbon
- 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.)
- Granted
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B57/00—Other carbonising or coking processes; Features of destructive distillation processes in general
- C10B57/04—Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition
- C10B57/06—Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition containing additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
- C10B53/08—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form in the form of briquettes, lumps and the like
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/12—Making spongy iron or liquid steel, by direct processes in electric furnaces
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B5/00—Making pig-iron in the blast furnace
- C21B5/007—Conditions of the cokes or characterised by the cokes used
Definitions
- the present invention relates to a method of producing ferrocoke suitable for blast furnace feed by carbonization with use of raw materials of iron ore and coal.
- a continuous formed-coke producing method has been developed as a method of producing coke to be replaced with the coke producing method in chamber oven.
- a vertical shaft brick furnace build in chamotte brick not silica brick is used as carbonization oven. After coal is cold-molded into a predetermined size, it is charged into a shaft furnace and heated with use of circulating gas for heat carrier to carbonize a formed coal, and thereby a formed coke is produced.
- ferrocoke is a mixture of coal (hereinafter referred to as "carbon-containing material") and iron ore or iron material (hereinafter referred to as "iron oxide-containing material”)
- carbon-containing material a mixture of coal
- iron oxide-containing material iron ore or iron material
- the present invention was carried out in view of the above-mentioned problems and has an object to provide a method of producing ferrocoke by carbonization of a molded product composed of iron oxide-containing material and carbon-containing material, which method is capable of preventing thermal crack, crack that may occur in carbonization of the molded product, improving the original form ratio at the carbonization discharge side and preventing the ferrocoke from being cracked when being charged into the furnace thereby to prevent reduction of the yield.
- the present invention provides a method for producing ferrocoke by heating a molded product composed of a mixture of a carbon-containing material and an iron oxide-containing material to carbonize the molded product, wherein carbonization is performed at a heating rate of 20 °C/min or less in a temperature range where a temperature of a surface of the molded product ranges from 550 °C to 650 °C.
- the present invention in carbonizing of a molded product composed of a mixture of the iron oxide-containing material and carbon-containing material, it becomes possible to prevent occurrence of thermal stress inside the molded product, reduction of yield in producing of the ferrocoke and crack in the furnace or before being charged into the furnace.
- the heating rate referred to in the present invention is an instantaneous heating rate (temperature gradient (dT/dt) of the heating pattern), not an average heating temperature ( ⁇ T/t) obtained by dividing an increased temperature ⁇ T °C by a time t required for temperature rising.
- the inventors of the present invention have studied the method of producing ferrocoke, made measurement of the thermal and mechanical property of a molded product of mixed iron oxide-containing material and carbon-containing material as raw materials of ferrocoke, performed thermal stress analysis based on this property and found the heating method optimal for control cracking of the molded product of mixed iron oxide-containing material and carbon-containing material based on analysis results of deformation and cracking of the molded product in heat treatment under various conditions thereby completing the present invention.
- the iron oxide-containing material is a material such as iron ore containing as main component Fe 2 O 3 or Fe 3 O 4 , reduced iron containing iron oxide, and iron containing sludge.
- the carbon-containing material is a material such as coal, bituminous material and oil coke.
- the coal includes coal for coke making that shows caking property, coal for general use, such as semianthracite, anthracite and bituminous coal, that does not show caking property, and solvent refined coal such as swelling coal and SRC.
- the bituminous material includes coal such as pitch, soft pitch, middle softening point pitch, and hard pitch and petroleum bituminous material such as ASP (asphalt pitch) and PDA (propane deasphalting asphalt).
- the oil coke includes fluid coke and delayed coke.
- Figs. 1 and 2 the transition of maximum thermal stress occurring inside the molded product when the material is heated is illustrated in Figs. 1 and 2 .
- a raw material containing 100 mass% coal as carbon-containing material and a raw material containing 10 mass% iron ore as iron oxide-containing material and 90 mass% coal as carbon-containing material which are formed into molded products of volumes 18 cc, 50 cc and 92 cc.
- the molded products are heated at 5K (Kelvin)/min (5 °C/min) of constant temperature gradient.
- the transition of maximum thermal stress caused inside the molded product containing 100 mass% coal is illustrated in Fig.
- Fig. 2 the transition of maximum thermal stress caused inside the molded product containing mixture of 10 mass% iron ore and 90 mass% coal is illustrated in Fig. 2 .
- the thermal stress first, the density, thermal conductivity, specific heat, Young's modulus and temperature-dependent contraction coefficient of the coal and iron oxide-containing coal are measured and this measurement data is used as a basis to calculate the temperature dependency of the thermal stress by heat transfer and thermal stress calculation.
- the contraction coefficient is measured by a thermomechanical analyzer, using a test sample of a cylindrically molded product of diameter 5 mm and height 8 mm obtained by mixing predetermined amounts of coal and iron ore.
- the Young's modulus is measured by the resonance method, using a test sample obtained by mixing predetermined amounts of coal and iron oxide and cutting the mixture into a platy of width 15 mm, length 80 mm and thickness 10 mm.
- the Poisson's ratio is measured based on the method disclosed in the publication ( J.Fukai, T.Hashida, K.Suzuki, T.Miura and S.Ohtani: Tetsu-to-Hagané, vol.74 (1988), p.2209 ) and the specific heat, thermal conductivity and density are measured based on the methods disclosed in the publication ( K.Matsubara, O.Tajima, N.Suzuki, Y.Okada, Y.Nakayama and T.Kato: Tetsu-to-Hagané, vol.68 (1982), p.2148 ).
- Fig. 5 is a graph illustrating temperature dependency of contraction coefficient of a molded product composed of 100 mass% coal, a molded product composed of 90 mass% coal and 10 mass% iron ore and a molded product composed of 70 mass% coal and 30 mass% ore.
- the peak that is, secondary peak of the contraction coefficient
- the contractile rate of the surface becomes maximum when the surface temperature is around 750 °C, while as the temperature inside the material is lower than that of the surface, the contractile rate is relatively low as compared with that of the surface and there is higher possibility that cracking occurs due to contraction difference between the surface and inside of the molded product.
- the secondary peak is shown of the mixed molded product of coal and iron ore.
- the peak that is, primary peak of the contraction coefficient
- the Young's modulus of the coke as molded product composed of 100 mass% coal is small in this primary peak temperature range, as illustrated in Fig. 1 , the occurring thermal stress is relatively small and becomes insignificant.
- the contraction coefficient in Fig. 5 is shown.
- the thermal conductivity of the iron oxide-containing material is 100 times greater than that of the carbon-containing material, the temperature difference between the surface and inside of the molded product becomes smaller than that of the carbon-containing material only. The same tendency is shown even when the volume of the iron oxide-containing material is increased. Therefore, as illustrated in Fig. 2 , the peak of the thermal stress of the mixed molded product of the carbon-containing material and iron oxide-containing material becomes smaller to a degree that it can be ignored around the temperatures of 700 °C to 750 °C.
- the high peak of thermal stress is shown at the surface temperatures of the molded product ranging from 550 °C to 650 °C where the contraction coefficient ranges from its primary peak value to its minimum value.
- the Young's modulus is small in this temperature range and therefore, the thermal stress becomes insignificant.
- the molded product composed of a mixture of carbon-containing material and iron oxide-containing material, as the Young's modulus is larger due to influence of the iron oxide-containing material, larger thermal stress occurs even with slight change in strain in this temperature range.
- the mixture of the carbon-containing material and iron oxide-containing material shows the temperature of the thermal stress which is different from that of the only carbon-containing material. Therefore, as a new finding, in order to prevent occurrence of thermal stress and crack in carbonization, there is only need to control the heating method at the temperatures of 550 °C to 650 °C irrespective of the volume of the molded product, thereby completing the following invention.
- the following heating method at the temperatures of 550 °C to 650 °C used in the present invention is effective in carbonization of a molded product composed of a mixture of the carbon-containing material and iron oxide-containing material obtained by hot briquetting as well as by cold briquetting in which the content of the iron oxide-containing material is increased and a binder is used.
- the heating rate mentioned in the present invention is not a heating temperature ( ⁇ T/t) obtained by dividing an increased temperature ⁇ T °C by a time t required in temperature increase, but an instantaneous heating rate (temperature gradient of the heating pattern (dT/dt)).
- Fig. 3 the transition of the maximum thermal stress occurring inside the molded product composed of 100 mass% coal as carbon-containing material is illustrated in Fig. 3 and that of the molded product composed of 10 mass% iron ore as iron oxide-containing material and 90 mass% coal as carbon-containing material is illustrated in Fig. 4.
- Figs. 3 and 4 are graphs each illustrating the transition of the maximum thermal stress occurring inside the molded product when the 18 cc molded product is heated at the heating rates of 5, 10 and 20 K/min (°C/min) of constant temperature gradient. For each raw material, the smaller the heating rate, the smaller the maximum thermal stress.
- the upper limit of the heating rate at the temperatures of 550 °C to 650 °C in carbonization of the ferrocoke is 20 °C/min (K/min) and when it is heated at the heating rate of 20 °C/min or less that is instantaneous temperature gradient, there occurs almost no crack in the molded product.
- the mass% of the iron oxide-containing material as raw material of the preferable ferrocoke molded product of the present invention is 10 to 30 mass% and the rest is carbon-containing material.
- the volume of the preferable ferrocoke molded product of the present invention is 6 cc or more.
- the heating test of the ferrocoke molded product was performed using an electric furnace of which the heating rate is controllable and crack occurrence was investigated.
- ferrocoke raw materials were adjusted.
- the volatile portion, 35 mass% coal (coking coal) as carbon-containing material and iron ore containing 68 mass% Fe as iron oxide-containing material were selected and two raw materials of mixed coal and iron ore were prepared one having a mass ratio of 9:1 and the other having a mass ratio of 7:3.
- a double-roll type molding machine was used and three molded products were prepared with volumes of 6 cc, 18 cc and 50 cc. These molded products were heated in the electric furnace with various heating patterns.
- a few of molded products formed as mentioned above were arranged in the soaking area of the electric furnace, heated up to 900 °C with various heating patterns under the nitrogen atmosphere, cooled slowly under the nitrogen atmosphere to the ambient temperature and then, taken out of the electric furnace. Then, the appearance of molded products was checked and the ratio of ferrocoke still having its original form (original form ratio) was measured.
- the ferrocoke having its original form is ferrocoke obtained with no crack in the surface thereof.
- Table 1 shows results of original form ratio obtained when the molded products composed of coal and iron ore at a mass ratio of 7:3 are treated at the heating rate of constant temperature gradient in the temperature ranges of from 550 °C to 650 °C. The temperature rate outside the temperature range of 550 °C to 650 °C is changed appropriately and each temperature rate value is not constant.
- Table 1 shows results of original form ratio obtained when the molded products composed of coal and iron ore at a mass ratio of 7:3 are treated at the heating rate of constant temperature gradient in the temperature ranges of from 550 °C to 650 °C. The temperature rate outside the temperature range of 550 °C to 650 °C is changed appropriately and each temperature rate value is not constant.
- Table 1 shows results of original form ratio obtained when the molded products composed of coal and iron ore at a mass ratio of 7:3 are treated at the heating rate of constant temperature gradient in the temperature ranges of from 550 °C to 650 °C. The temperature rate outside the temperature range of 550
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Manufacturing & Machinery (AREA)
- Metallurgy (AREA)
- Coke Industry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
- The present invention relates to a method of producing ferrocoke suitable for blast furnace feed by carbonization with use of raw materials of iron ore and coal.
- As a method of producing ferrocoke by mixing fine iron ore into raw material coal and carbonizing the mixture in a conventional chamber oven, there have been considered 1) a method of charging fine mixture of coal and fine iron ore into a chamber oven and 2) a method of cold-molding coal and iron ore, that is, forming them at ambient temperatures and charging the molded product into a chamber oven (for example, see "COKE TECHNICAL REPORT", The Fuel Society of Japan, 1958, p.38). However, as the conventional chamber oven is built in silica brick, the iron ore charged therein reacts with silica which is a main ingredient of the silica brick to generate low-melting fayalite (2FeO SiO2), which gives damages to the silica brick. Hence, the method of producing ferrocoke in the chamber oven has not been performed industrially.
- Recently, a continuous formed-coke producing method has been developed as a method of producing coke to be replaced with the coke producing method in chamber oven. In the continuous formed-coke producing method, a vertical shaft brick furnace build in chamotte brick not silica brick is used as carbonization oven. After coal is cold-molded into a predetermined size, it is charged into a shaft furnace and heated with use of circulating gas for heat carrier to carbonize a formed coal, and thereby a formed coke is produced. Although it has been already confirmed that coke of strength equal to that produced in the conventional chamber oven can be produced by using a large amount of non-slightly caking coal that is inexpensive and rich in resource reserves, if the used coal is of high caking property, the formed coal is softened and fused in the shaft furnace, which makes the operation in the shaft furnace difficult and brings about degradation of coke such as deformation, crack and the like.
- In order to prevent fusion in the shaft furnace in the continuous coke producing method, there has been proposed a method of charging iron ore into coal so that the iron ore becomes 15 to 40 % of the total amount, cold-molding into a molded product and charging it into the shaft furnace (see Japanese Patent Application Laid-Open No.
6-55579 2004-217914 2005-53982 6-65579 2004-217914 2005-53982 - Meanwhile, as to production of the formed coke using only coal as main raw material, consideration has been given to a heating pattern in carbonization of the molded product, or formed coke, to prevent degradation of the coke such as deformation, crack and the like in carbonization and a method has been proposed of designing an optimal heating rate in accordance with the temperature of the molded product (see, for example, Japanese Patent Application Laid-Open Nos.
52-23103 7-102260 - As described above, in the method of producing ferrocoke using raw materials of coal and iron ore or iron material, the problems of deformation, crack and the like of the molded product in carbonization have not been solved. As the ferrocoke is a mixture of coal (hereinafter referred to as "carbon-containing material") and iron ore or iron material (hereinafter referred to as "iron oxide-containing material"), the thermal and mechanical property in heating is greatly different from that in producing of formed coke, and it is predicted deformation and crack behavior of the molded product in carbonization is different.
- The present invention was carried out in view of the above-mentioned problems and has an object to provide a method of producing ferrocoke by carbonization of a molded product composed of iron oxide-containing material and carbon-containing material, which method is capable of preventing thermal crack, crack that may occur in carbonization of the molded product, improving the original form ratio at the carbonization discharge side and preventing the ferrocoke from being cracked when being charged into the furnace thereby to prevent reduction of the yield.
- In order to solve these problems, the present invention provides a method for producing ferrocoke by heating a molded product composed of a mixture of a carbon-containing material and an iron oxide-containing material to carbonize the molded product, wherein carbonization is performed at a heating rate of 20 °C/min or less in a temperature range where a temperature of a surface of the molded product ranges from 550 °C to 650 °C.
- According to the present invention, in carbonizing of a molded product composed of a mixture of the iron oxide-containing material and carbon-containing material, it becomes possible to prevent occurrence of thermal stress inside the molded product, reduction of yield in producing of the ferrocoke and crack in the furnace or before being charged into the furnace.
- Here, the heating rate referred to in the present invention is an instantaneous heating rate (temperature gradient (dT/dt) of the heating pattern), not an average heating temperature (ΔT/t) obtained by dividing an increased temperature ΔT °C by a time t required for temperature rising.
-
-
Fig. 1 is a graph illustrating the relation between the maximum thermal stress and the surface temperatures of a coal molded product; -
Fig. 2 is a graph illustrating the relation between the maximum thermal stress and the surface temperatures of a molded product of 90% coal and 10% iron ore; -
Fig. 3 is a graph illustrating heating rate dependency of the maximum thermal stress and the surface temperatures of the coal molded product; -
Fig. 4 is a graph illustrating heating rate dependency of the maximum thermal stress and the surface temperatures of the molded product of 90% coal and 10% iron ore; and -
Fig. 5 is a graph illustrating the relation between the contraction coefficient and temperature of a mixture of coal and iron ore and of 100% coal. - The inventors of the present invention have studied the method of producing ferrocoke, made measurement of the thermal and mechanical property of a molded product of mixed iron oxide-containing material and carbon-containing material as raw materials of ferrocoke, performed thermal stress analysis based on this property and found the heating method optimal for control cracking of the molded product of mixed iron oxide-containing material and carbon-containing material based on analysis results of deformation and cracking of the molded product in heat treatment under various conditions thereby completing the present invention. Here, in the present invention, the iron oxide-containing material is a material such as iron ore containing as main component Fe2O3 or Fe3O4, reduced iron containing iron oxide, and iron containing sludge. Besides, the carbon-containing material is a material such as coal, bituminous material and oil coke. The coal includes coal for coke making that shows caking property, coal for general use, such as semianthracite, anthracite and bituminous coal, that does not show caking property, and solvent refined coal such as swelling coal and SRC. The bituminous material includes coal such as pitch, soft pitch, middle softening point pitch, and hard pitch and petroleum bituminous material such as ASP (asphalt pitch) and PDA (propane deasphalting asphalt). The oil coke includes fluid coke and delayed coke.
- As an example of various analysis results, the transition of maximum thermal stress occurring inside the molded product when the material is heated is illustrated in
Figs. 1 and 2 . There are prepared a raw material containing 100 mass% coal as carbon-containing material and a raw material containing 10 mass% iron ore as iron oxide-containing material and 90 mass% coal as carbon-containing material, which are formed into molded products of volumes 18 cc, 50 cc and 92 cc. Then, the molded products are heated at 5K (Kelvin)/min (5 °C/min) of constant temperature gradient. The transition of maximum thermal stress caused inside the molded product containing 100 mass% coal is illustrated inFig. 1 and the transition of maximum thermal stress caused inside the molded product containing mixture of 10 mass% iron ore and 90 mass% coal is illustrated inFig. 2 . Here, as to the thermal stress, first, the density, thermal conductivity, specific heat, Young's modulus and temperature-dependent contraction coefficient of the coal and iron oxide-containing coal are measured and this measurement data is used as a basis to calculate the temperature dependency of the thermal stress by heat transfer and thermal stress calculation. The contraction coefficient is measured by a thermomechanical analyzer, using a test sample of a cylindrically molded product of diameter 5 mm andheight 8 mm obtained by mixing predetermined amounts of coal and iron ore. The Young's modulus is measured by the resonance method, using a test sample obtained by mixing predetermined amounts of coal and iron oxide and cutting the mixture into a platy of width 15 mm, length 80 mm andthickness 10 mm. The Poisson's ratio is measured based on the method disclosed in the publication (J.Fukai, T.Hashida, K.Suzuki, T.Miura and S.Ohtani: Tetsu-to-Hagané, vol.74 (1988), p.2209) and the specific heat, thermal conductivity and density are measured based on the methods disclosed in the publication (K.Matsubara, O.Tajima, N.Suzuki, Y.Okada, Y.Nakayama and T.Kato: Tetsu-to-Hagané, vol.68 (1982), p.2148). Here, the above-mentioned heat transfer and thermal stress calculation uses the method based on the publication (T.Miura, H.Yoshino, S.Saito, S.Otani: Journal of the Fuel Society of Japan, vol.68 (1989), p.1045) - As illustrated in
Fig. 1 , when a molded product composed of only carbon-containing material is carbonized, a of maximum thermal stress is found around 700 °C to 750 °C of the surface temperature of the molded product. Reason for this result is explained with reference toFig. 5 . -
Fig. 5 is a graph illustrating temperature dependency of contraction coefficient of a molded product composed of 100 mass% coal, a molded product composed of 90 mass% coal and 10 mass% iron ore and a molded product composed of 70 mass% coal and 30 mass% ore. As illustrated inFig. 5 , in the heat treatment process of thecoal 100 mass% material, the peak (that is, secondary peak of the contraction coefficient) is observed around 750 °C. In this way, the contractile rate of the surface becomes maximum when the surface temperature is around 750 °C, while as the temperature inside the material is lower than that of the surface, the contractile rate is relatively low as compared with that of the surface and there is higher possibility that cracking occurs due to contraction difference between the surface and inside of the molded product. Likewise, the secondary peak is shown of the mixed molded product of coal and iron ore. Here, though the peak (that is, primary peak of the contraction coefficient) is also observed around 500 °C, as the Young's modulus of the coke as molded product composed of 100 mass% coal is small in this primary peak temperature range, as illustrated inFig. 1 , the occurring thermal stress is relatively small and becomes insignificant. - Besides, as illustrated in
Fig. 1 , as the molded product volume is larger, the temperature difference between the surface and the inside of the molded product is larger and therefore, the peak value of the maximum thermal stress becomes large. - Meanwhile, when the molded product composed of a mixture of the carbon-containing material and iron oxide-containing material is carbonized, the contraction coefficient in
Fig. 5 is shown. For example, as the thermal conductivity of the iron oxide-containing material is 100 times greater than that of the carbon-containing material, the temperature difference between the surface and inside of the molded product becomes smaller than that of the carbon-containing material only. The same tendency is shown even when the volume of the iron oxide-containing material is increased. Therefore, as illustrated inFig. 2 , the peak of the thermal stress of the mixed molded product of the carbon-containing material and iron oxide-containing material becomes smaller to a degree that it can be ignored around the temperatures of 700 °C to 750 °C. On the other hand, the high peak of thermal stress is shown at the surface temperatures of the molded product ranging from 550 °C to 650 °C where the contraction coefficient ranges from its primary peak value to its minimum value. In the case of the only carbon-containing material (coke of 100 mass% coal), the Young's modulus is small in this temperature range and therefore, the thermal stress becomes insignificant. In the case of the molded product (ferrocoke) composed of a mixture of carbon-containing material and iron oxide-containing material, as the Young's modulus is larger due to influence of the iron oxide-containing material, larger thermal stress occurs even with slight change in strain in this temperature range. If the size of the molded product is made smaller to reduce temperature distribution inside the material, Young's modulus dependency is much larger and therefore, the dependency on the molded product volume becomes smaller. In addition, as the bond strength between particles made of carbon-containing material is low in this temperature range, slight increase of occurring thermal stress has great influence on occurrence of crack. - Thus, the mixture of the carbon-containing material and iron oxide-containing material shows the temperature of the thermal stress which is different from that of the only carbon-containing material. Therefore, as a new finding, in order to prevent occurrence of thermal stress and crack in carbonization, there is only need to control the heating method at the temperatures of 550 °C to 650 °C irrespective of the volume of the molded product, thereby completing the following invention.
- Here, the following heating method at the temperatures of 550 °C to 650 °C used in the present invention is effective in carbonization of a molded product composed of a mixture of the carbon-containing material and iron oxide-containing material obtained by hot briquetting as well as by cold briquetting in which the content of the iron oxide-containing material is increased and a binder is used.
- As the method of controlling the heating at the temperatures of 500 °C to 650 °C, there is a method of controlling the heating rate. As the lower the heating rate, the smaller a temperature difference becomes between the surface and inside of the molded product, thereby to be able to prevent occurrence of the thermal stress. However, when the heating rate is decreased, carbonization time becomes longer, and unpreferably the product productivity is reduced. Then, it is necessary to set the upper limit of the heating rate. Here, the heating rate mentioned in the present invention is not a heating temperature (ΔT/t) obtained by dividing an increased temperature ΔT °C by a time t required in temperature increase, but an instantaneous heating rate (temperature gradient of the heating pattern (dT/dt)).
- For example, the transition of the maximum thermal stress occurring inside the molded product composed of 100 mass% coal as carbon-containing material is illustrated in
Fig. 3 and that of the molded product composed of 10 mass% iron ore as iron oxide-containing material and 90 mass% coal as carbon-containing material is illustrated inFig. 4. Figs. 3 and 4 are graphs each illustrating the transition of the maximum thermal stress occurring inside the molded product when the 18 cc molded product is heated at the heating rates of 5, 10 and 20 K/min (°C/min) of constant temperature gradient. For each raw material, the smaller the heating rate, the smaller the maximum thermal stress. - As a result of analysis of the cracking and deformation of the molded products that are subjected to heat treatment under various conditions, it is found that the upper limit of the heating rate at the temperatures of 550 °C to 650 °C in carbonization of the ferrocoke is 20 °C/min (K/min) and when it is heated at the heating rate of 20 °C/min or less that is instantaneous temperature gradient, there occurs almost no crack in the molded product.
- Here, the mass% of the iron oxide-containing material as raw material of the preferable ferrocoke molded product of the present invention is 10 to 30 mass% and the rest is carbon-containing material. The volume of the preferable ferrocoke molded product of the present invention is 6 cc or more.
- In order to clarify the relation between cracking of the ferrocoke and the ferrocoke thermal treatment conditions, the heating test of the ferrocoke molded product was performed using an electric furnace of which the heating rate is controllable and crack occurrence was investigated.
- First, ferrocoke raw materials were adjusted. The volatile portion, 35 mass% coal (coking coal) as carbon-containing material and iron ore containing 68 mass% Fe as iron oxide-containing material were selected and two raw materials of mixed coal and iron ore were prepared one having a mass ratio of 9:1 and the other having a mass ratio of 7:3. Next, a double-roll type molding machine was used and three molded products were prepared with volumes of 6 cc, 18 cc and 50 cc. These molded products were heated in the electric furnace with various heating patterns.
- A few of molded products formed as mentioned above were arranged in the soaking area of the electric furnace, heated up to 900 °C with various heating patterns under the nitrogen atmosphere, cooled slowly under the nitrogen atmosphere to the ambient temperature and then, taken out of the electric furnace. Then, the appearance of molded products was checked and the ratio of ferrocoke still having its original form (original form ratio) was measured. The ferrocoke having its original form is ferrocoke obtained with no crack in the surface thereof.
- Table 1 shows results of original form ratio obtained when the molded products composed of coal and iron ore at a mass ratio of 7:3 are treated at the heating rate of constant temperature gradient in the temperature ranges of from 550 °C to 650 °C. The temperature rate outside the temperature range of 550 °C to 650 °C is changed appropriately and each temperature rate value is not constant. Here, also for the molded products having raw materials of coal and iron ore at a mass ratio of 9:1, almost the same results were obtained as those of the molded product composed of, as raw material, coal and iron ore at a mass ratio of 7:3 and description of the results of the molded products composed of coal and iron ore at a mass ratio of 7:3 is omitted here.
- For molded products of all volumes and composed of coal and iron ore at both of mass ratios 9:1 and 7:3, no crack was observed at the
heating rate 10 °C/min or less at temperatures of 550 °C to 650 °C. In addition, cracked molded products at the heating rate 20 °C/min or less are less than 10% and so few that they do not have influence on the productivity. Meanwhile, when they were heated at the heating rate of 25 °C/min or more exceeding 20 °C/min, it was sure that many cracked ferrocokes were observed.TABLE 1 Heating rate in 550-650 °C original form ratio of 6cc molded product original form ratio of 18cc molded product original form ratio of 50cc molded product 5 °C/ min 0% 0% 0% 10 °C/ min 0% 0% 0% 15 °C/ min 1% 2% 3% 20 °C/min 3% 4% 7% 25 °C/min 18% 22% 25% 30 °C/min 36% 40% 46%
Claims (1)
- A method for producing ferrocoke by heating a molded product composed of a mixture of a carbon-containing material and an iron oxide-containing material to carbonize the molded product, wherein carbonization is performed at a heating rate of 20 °C/min or less in a temperature range where a temperature of a surface of the molded product ranges from 550 °C to 650 °C.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2007/075392 WO2009081506A1 (en) | 2007-12-26 | 2007-12-26 | Method of producing ferro-coke |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2233548A1 true EP2233548A1 (en) | 2010-09-29 |
EP2233548A4 EP2233548A4 (en) | 2014-04-09 |
EP2233548B1 EP2233548B1 (en) | 2016-09-07 |
Family
ID=40800825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07860587.0A Not-in-force EP2233548B1 (en) | 2007-12-26 | 2007-12-26 | Method of producing ferro-coke |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP2233548B1 (en) |
KR (1) | KR101246523B1 (en) |
CN (1) | CN101910364B (en) |
AU (1) | AU2007363032B2 (en) |
BR (1) | BRPI0722354A2 (en) |
WO (1) | WO2009081506A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10414986B2 (en) | 2014-05-19 | 2019-09-17 | Jfe Steel Corporation | Method for manufacturing coke, coke, and method for evaluating homogeneity of coal blend |
US11111441B2 (en) | 2015-06-24 | 2021-09-07 | Jfe Steel Corporation | Method for producing ferrocoke |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011108466A1 (en) * | 2010-03-03 | 2011-09-09 | Jfeスチール株式会社 | Process for producing ferro coke for metallurgy |
JP5763308B2 (en) * | 2010-07-28 | 2015-08-12 | Jfeスチール株式会社 | Ferro-coke manufacturing method |
CN102851049A (en) * | 2011-06-27 | 2013-01-02 | 宝山钢铁股份有限公司 | Coal blending method for high-reactivity coke for blast furnace |
EP2977429B1 (en) * | 2012-02-29 | 2018-06-06 | JFE Steel Corporation | Method for preparing coal for coke making |
CN108192679B (en) * | 2018-01-26 | 2020-12-22 | 上海泽玛克敏达机械设备有限公司 | Briquette and its preparation method and use |
CN113508169B (en) * | 2019-03-04 | 2024-09-13 | 杰富意钢铁株式会社 | Method for evaluating coal, method for producing mixed coal, and method for producing coke |
CN110093467B (en) * | 2019-06-05 | 2020-07-17 | 东北大学 | Preparation method of iron coke |
CN112980480A (en) * | 2021-02-25 | 2021-06-18 | 东北大学 | Method for preparing iron coke from steel slag and iron ore powder |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004217914A (en) * | 2002-12-25 | 2004-08-05 | Jfe Steel Kk | Method for producing and using ferrocoke and method for utilizing by-product gas in producing the ferrocoke |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5223102A (en) * | 1975-08-18 | 1977-02-21 | Nippon Steel Corp | Process for manufacturing formed coke |
JPS6012389B2 (en) | 1975-08-18 | 1985-04-01 | 新日本製鐵株式会社 | Manufacturing method of molded coke for metallurgy |
JPS603359B2 (en) * | 1978-05-11 | 1985-01-28 | 住金化工株式会社 | Method for manufacturing molded coke for metallurgy |
JPS5647234A (en) * | 1979-09-25 | 1981-04-28 | Aisin Warner Ltd | Manufacture of three-dimensional pin connector |
JPH0665579A (en) | 1992-08-19 | 1994-03-08 | Nippon Steel Corp | Method for compounding raw material of coal briquet for producing metallurgical formed coke |
JP3491092B2 (en) | 1993-10-05 | 2004-01-26 | Jfeスチール株式会社 | Manufacturing method of molded coke |
JP4267390B2 (en) | 2003-08-07 | 2009-05-27 | 新日本製鐵株式会社 | Method for producing ferro-coke for blast furnace |
JP5087868B2 (en) * | 2006-07-05 | 2012-12-05 | Jfeスチール株式会社 | Ferro-coke manufacturing method |
-
2007
- 2007-12-26 KR KR1020107013442A patent/KR101246523B1/en active IP Right Grant
- 2007-12-26 BR BRPI0722354-4A patent/BRPI0722354A2/en active Search and Examination
- 2007-12-26 WO PCT/JP2007/075392 patent/WO2009081506A1/en active Application Filing
- 2007-12-26 CN CN200780102093.7A patent/CN101910364B/en active Active
- 2007-12-26 AU AU2007363032A patent/AU2007363032B2/en not_active Ceased
- 2007-12-26 EP EP07860587.0A patent/EP2233548B1/en not_active Not-in-force
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004217914A (en) * | 2002-12-25 | 2004-08-05 | Jfe Steel Kk | Method for producing and using ferrocoke and method for utilizing by-product gas in producing the ferrocoke |
Non-Patent Citations (1)
Title |
---|
See also references of WO2009081506A1 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10414986B2 (en) | 2014-05-19 | 2019-09-17 | Jfe Steel Corporation | Method for manufacturing coke, coke, and method for evaluating homogeneity of coal blend |
US11111441B2 (en) | 2015-06-24 | 2021-09-07 | Jfe Steel Corporation | Method for producing ferrocoke |
Also Published As
Publication number | Publication date |
---|---|
AU2007363032A1 (en) | 2009-07-02 |
BRPI0722354A2 (en) | 2014-03-18 |
WO2009081506A1 (en) | 2009-07-02 |
EP2233548A4 (en) | 2014-04-09 |
EP2233548B1 (en) | 2016-09-07 |
CN101910364B (en) | 2014-05-14 |
KR20100077057A (en) | 2010-07-06 |
CN101910364A (en) | 2010-12-08 |
KR101246523B1 (en) | 2013-03-26 |
AU2007363032B2 (en) | 2012-01-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2233548B1 (en) | Method of producing ferro-coke | |
Hashemi et al. | Effects of resin and graphite content on density and oxidation behavior of MgO-C refractory bricks | |
CN102224120B (en) | Heat stable formed ceramic, apparatus and method of using the same | |
US20180194631A1 (en) | Method for producing graphite bodies | |
JP2008056777A (en) | Manufacturing method of molded product of raw material for ferrocoke and ferrocoke | |
JP4430448B2 (en) | Method for producing isotropic graphite material | |
JP2022158407A (en) | Method for predicting csr of blast furnace coke, method for predicting cri of blast furnace coke, and method for manufacturing blast furnace coke | |
JP5087868B2 (en) | Ferro-coke manufacturing method | |
JP4809675B2 (en) | Petroleum coke and method for producing the same | |
KR101433694B1 (en) | Process for producing needle coke for graphite electrode and stock oil composition for use in the process | |
Sharma et al. | Producing high coke strength after reactivity in stamp charged coke making | |
JP2007119602A (en) | Method for producing ferrocoke | |
JP5482837B2 (en) | Ferro-coke manufacturing method | |
JP6323394B2 (en) | Ferro-coke raw material molding method and ferro-coke manufacturing method | |
JP2007119601A (en) | Method for producing ferrocoke | |
JP7347462B2 (en) | Method for producing molded products and method for producing molded coke | |
JP5386835B2 (en) | Ferro-coke manufacturing method | |
JP5028946B2 (en) | Ferro-coke raw material molding and method for producing ferro-coke | |
KR102528277B1 (en) | Coke for melter-gasifier and method for manufacturing thereof | |
CN115466125A (en) | Preparation method of multifunctional C/SiC gradient furnace eye brick for ferrosilicon ore furnace | |
JP2021130580A (en) | Method for producing graphite material having high thermal expansion coefficient and the graphite material | |
JPH06322375A (en) | Production of formed coke | |
JPS5916588B2 (en) | Yakinyouseikeiko-kusunoseizouhou | |
JPH0797577A (en) | Method for production shaped coke | |
KR20120071081A (en) | Method for producing carbon composite metal oxide briquette |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20100622 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA HR MK RS |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20140312 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C10B 57/06 20060101AFI20140306BHEP Ipc: C10B 53/08 20060101ALI20140306BHEP |
|
17Q | First examination report despatched |
Effective date: 20150702 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
INTG | Intention to grant announced |
Effective date: 20160401 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAR | Information related to intention to grant a patent recorded |
Free format text: ORIGINAL CODE: EPIDOSNIGR71 |
|
INTG | Intention to grant announced |
Effective date: 20160630 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 826876 Country of ref document: AT Kind code of ref document: T Effective date: 20161015 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602007047868 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 10 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 826876 Country of ref document: AT Kind code of ref document: T Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20161208 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20161207 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20170107 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: BE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20170109 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602007047868 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
26N | No opposition filed |
Effective date: 20170608 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20161226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161231 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161231 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161226 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 11 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161226 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161226 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20171113 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20171220 Year of fee payment: 11 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20071226 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160907 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20161226 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602007047868 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20181231 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190702 |