EP3208015B1 - Method of sintering electrically conducting powders - Google Patents
Method of sintering electrically conducting powders Download PDFInfo
- Publication number
- EP3208015B1 EP3208015B1 EP16382069.9A EP16382069A EP3208015B1 EP 3208015 B1 EP3208015 B1 EP 3208015B1 EP 16382069 A EP16382069 A EP 16382069A EP 3208015 B1 EP3208015 B1 EP 3208015B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- sintering
- activation
- comprised
- current density
- voltage
- 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.)
- Active
Links
- 238000005245 sintering Methods 0.000 title claims description 82
- 239000000843 powder Substances 0.000 title claims description 59
- 238000000034 method Methods 0.000 title claims description 36
- 230000004913 activation Effects 0.000 claims description 75
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims 1
- 238000009706 electric current assisted sintering Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 238000007088 Archimedes method Methods 0.000 description 4
- 238000000280 densification Methods 0.000 description 4
- 238000002490 spark plasma sintering Methods 0.000 description 4
- 238000007596 consolidation process Methods 0.000 description 3
- 230000001788 irregular Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910009043 WC-Co Inorganic materials 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009707 resistance sintering Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/105—Sintering only by using electric current other than for infrared radiant energy, laser radiation or plasma ; by ultrasonic bonding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/003—Apparatus, e.g. furnaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
- B22F3/087—Compacting only using high energy impulses, e.g. magnetic field impulses
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/14—Both compacting and sintering simultaneously
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/105—Sintering only by using electric current other than for infrared radiant energy, laser radiation or plasma ; by ultrasonic bonding
- B22F2003/1051—Sintering only by using electric current other than for infrared radiant energy, laser radiation or plasma ; by ultrasonic bonding by electric discharge
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2201/00—Treatment under specific atmosphere
- B22F2201/50—Treatment under specific atmosphere air
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2202/00—Treatment under specific physical conditions
- B22F2202/06—Use of electric fields
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2301/00—Metallic composition of the powder or its coating
- B22F2301/15—Nickel or cobalt
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2301/00—Metallic composition of the powder or its coating
- B22F2301/20—Refractory metals
- B22F2301/205—Titanium, zirconium or hafnium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2301/00—Metallic composition of the powder or its coating
- B22F2301/40—Intermetallics other than rare earth-Co or -Ni or -Fe intermetallic alloys
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/16—Both compacting and sintering in successive or repeated steps
- B22F3/164—Partial deformation or calibration
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C14/00—Alloys based on titanium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/08—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/10—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on titanium carbide
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/0047—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
- C22C32/0052—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides
Definitions
- the present invention belongs to the field of methods for obtaining sintered parts, which consists in the application of heat and pressure to powders for finally obtaining dense parts, in particular wherein the heat is obtained via electrical currents that are forced to pass through conductive powders.
- ECAS electric current assisted sintering
- ECAS techniques can be classified with respect to the discharge time. Conventionally, 0.1 s discharge time can be assumed as the threshold between fast and ultrafast ECAS. However, confusion should be avoided between fast termed herein and the FAST acronym (field activated/assisted sintering technique) frequently encountered in the scientific literature. Here, fast simply refers to either a high processing rate or a low processing time.
- ultrafast ECAS techniques typically employ either one or up to three repeated (capacitor) discharges. Each discharge lasts less than 0.1 s.
- the current pulse density can be on the order of 10 kA/cm 2 .
- Ultrafast ECAS is generally referred to as electric discharge compaction (EDC) or EFS (Electro Forging Sintering). Representative examples of these methods were explained in the following patents: EP 2198993 A1 from Fais, US4929415 and US4975412 from Okazaki. Main problem of these methods is that the capacitors discharge the stored energy in a sudden an uncontrolled way and thus they did not permit tailoring of the power input to the powder mass.
- JP H03 236402 discloses an apparatus for carrying out the sintering of electrically conducting powders.
- the present invention proposes a method of sintering electrically conducting powders in an air atmosphere for obtaining a sintered product, comprising the following sequence of steps:
- the method of the present invention comprises, between step b) and step c), applying to the powders an activation current density lower than the sintering current density at an activation voltage greater than the sintering voltage during an activation time lower than the sintering time, to reduce the electrical resistance of the powders, the activation current density and the sintering current density being constant.
- the application of the activation current density and sintering current density is carried out while the pressure is being applied to the powders.
- the activation current density applied to the powders at a voltage greater than the voltage used for sintering in step c) during a lower time than step c) produces a current discharge that breaks the oxide layer in the surface of the powders and creates bridges between the particles of powders, obtaining a more uniform and cleaner particle surface which reduces the electrical resistance to the flow of the current through the powders such that the sintering current density applied in step c) is distributed more homogeneously through the powders in the mold.
- the activation current density is greater than 0,5 kA/cm 2
- the activation voltage is greater than 10V
- the activation time is lower than 300ms, for generating a current discharge of low intensity at a high voltage in a very reduced time, to assure an homogeneous superficial de-oxidation of the powders and formation of bridges among particles.
- the time between the removal of the activation current density and the application of the sintering current density is lower than 20 ms to assure an optimal distribution of the sintering current density.
- the sintering current density is applied immediately after the application of the activation current density, i.e just after the activation time is run out.
- the method of the invention comprises the control of the two electrical power units which enables to optimize the processing time and the energy consumption, altogether with the installation costs.
- FIG. 2 the time pressure/ current/voltage diagram corresponding to the implementation of the method according to the invention for obtaining a sintered WC-Co is shown.
- the process starts with the step consisting in placing an electrically conducting powder in an electrically insulating mold.
- a pressure between 100 and 500 MPa is applied inside the mold, preferably with two pistons, in this case around 300 MPa.
- an activation step is carried out, consisting in applying an activation current density at an activation voltage for an activation time and carried out by employing a first electrical power unit (2).
- a low current density around 2 kA/cm 2
- a high voltage around 30V
- the pulse is about two tenths of a second.
- a waiting step is carried out wherein no current and/or voltage are applied.
- This step consists in the switching of the power units, that is, to switch from a power unit (2) to another power unit (3).
- the waiting time is that needed for carrying out said switching by the control unit (4), in the present case a PLC.
- the switching time is about 2 tenth of a second.
- the proper sintering step is performed, which consists in applying a sintering current density at a sintering voltage during a sintering time carried out by employing the second electrical power unit (3).
- the intensity is higher (around 10 kA), but the voltage is reduced to 5 V.
- the current density is applied using two opposite electrodes.
- the pistons can be used as opposite electrodes.
- the invention also relates to an apparatus (1) for carrying out the inventive method.
- the apparatus comprises:
- the means for providing current and voltage for an activation step is a first electrical power unit (2) and the means for providing current and voltage for a sintering step is a second electrical power unit (3).
- the first power unit (2) is arranged to provide through the electrodes (7) an activation current density comprised between 0.5 and 5 KA/cm 2 and an activation voltage comprised between 10 and 100 V whereas the second power unit (3) is arranged to provide through electrodes (7) a sintering current density comprised between 3 and 15 kA/cm 2 and a sintering voltage lower than 15 V.
- the apparatus further comprises:
- the means for controlling the duration of the current density and voltage provided by the first power unit (2) are able to control a predetermined discharge time (activation time) comprised in the range going from 50 to 300 ms and the means for controlling the duration of the current and voltage provided by the second power unit (3) are able to control a predetermined discharge time (sintering time) comprised in the range going from 500 to 1500 ms.
- Each power unit (2, 3) comprise a transformer (21, 31) and an inverter (22, 32), and the two power units (2, 3) are controlled by a single control unit (4), which is preferably a programmable logic controller.
- This PLC includes:
- a WC-6Co or WC-10Co disk is produced with the disclosed apparatus with a thickness of 16 mm and a diameter of 22 mm.
- the agglomerated powder was spherical with an agglomerate size of less than 100 microns.
- a current density between 2 and 4 kA/cm 2 during 100-200 ms was applied in order to activate the powder.
- a voltage between 15-50 V is needed for this activation step.
- the density of the final disk measured by the Archimedes method, is around 13-14.8 g/cm 3 . It is possible to obtain fully dense samples with hardness around 1800-2100 HV30.
- a titanium disk is produced with the disclosed apparatus with a thickness of 10 mm and a diameter of 22 mm.
- the shape of the particles of the powder was irregular with a maximum particle size around 75 microns.
- a current density between 1-3 kA/cm 2 was applied during 90-100 ms in order to activate the powder.
- a voltage between 10-50 V is needed for the activation stage.
- sintering stage a current density between 4-7 kA/cm 2 was applied during 500-1000 ms to obtain a densified sample with a voltage lower than 10 V. Between stages, activation and sintering, a minimum time of 10 ms was established. Pressure, from 100-500 MPa, was applied from the beginning of the process.
- the density of the final disk measured by the Archimedes method, is around 3.5-4.4 g/cm 3 . It is possible to obtain fully dense samples.
- a TiC-25Ni and TiC-25Fe disks are produced with the disclosed apparatus with a thickness of 16 mm and a diameter of 22 mm.
- the agglomerated powder was irregular with a particle size of less than 30 microns.
- a current density between 1-3 kA/cm 2 was applied during 100-200 ms in order to activate the powder.
- a voltage between 15-50 V is needed for this activation stage.
- a current density between 6-9 kA/cm 2 was applied during 500-1000 ms to obtain a densified sample with a voltage lower than 10 V.
- a minimum time of 10 ms was stablished.
- the density of the final disk was around 5.1-5.5 g/cm 3 for TiC-25Ni and 5.1-5.4 g/cm 3 for TiC-25Fe. It is possible to obtain fully dense samples with hardness around 1600-2000 HV30.
- An aluminium disk was produced with the disclosed apparatus with a thickness of 12 mm and a diameter of 12 mm.
- the powder was irregular with a particle size of less than 150 microns.
- a current density between 0.5-2 kA/cm 2 was applied during 100-200 ms in order to activate the powder.
- a voltage between 30-80 V is needed for this activation stage.
- the density of the final disk was around 2.5-2.7 g/cm 3 .
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Powder Metallurgy (AREA)
Description
- The present invention belongs to the field of methods for obtaining sintered parts, which consists in the application of heat and pressure to powders for finally obtaining dense parts, in particular wherein the heat is obtained via electrical currents that are forced to pass through conductive powders.
- ECAS (electric current assisted sintering) gathers a family of consolidation methods in which mechanical pressure is combined with electric and thermal fields to enhance interparticle bonding and densification. The starting materials can be in the form of either powders or green compacts. The primary purpose of imposed electric currents is to provide the required amount of resistive heat.
- ECAS techniques can be classified with respect to the discharge time. Conventionally, 0.1 s discharge time can be assumed as the threshold between fast and ultrafast ECAS. However, confusion should be avoided between fast termed herein and the FAST acronym (field activated/assisted sintering technique) frequently encountered in the scientific literature. Here, fast simply refers to either a high processing rate or a low processing time.
- On one hand, fast ECAS techniques are known with different acronyms mainly depending on the electric current waveform: SPS (Spark Plasma Sintering), PECS (Pulsed Electric Current Sintering), RS (Resistance Sintering), etc. The bases of the process were developed by INOUE (
US3241956 A ). The electric current is normally applied as pulses and also was reported the possibility of the application of various superimposed currents with different frequencies and two stages of pressure to increase densification. The application of the load was also described inUS3508029 A . These two processes are characterized by the low intensity of the electric pulses (< 1 kA/cm2) and high duration of the cycles (from seconds to minutes). In addition, the manufacturing of fast ECAS equipment is complex with the need of protective atmosphere (or vacuum). - On the other hand, ultrafast ECAS techniques typically employ either one or up to three repeated (capacitor) discharges. Each discharge lasts less than 0.1 s. The current pulse density can be on the order of 10 kA/cm2. Ultrafast ECAS is generally referred to as electric discharge compaction (EDC) or EFS (Electro Forging Sintering). Representative examples of these methods were explained in the following patents:
EP 2198993 A1 from Fais,US4929415 andUS4975412 from Okazaki. Main problem of these methods is that the capacitors discharge the stored energy in a sudden an uncontrolled way and thus they did not permit tailoring of the power input to the powder mass. The use of high current and high voltage resulted in inconsistent densification and inhomogeneity of parts manufactured using these consolidation processes, because the resistance of the powders is not homogeneous due to porosity, surface oxidation, compaction or bonding between the particles, and it is well known that the current always follows the lowest resistive path. Other problems are the low size of the samples that can be produced and the sparks in the electrodes produced by the high current and high voltage. - Other ultrafast processes used low voltage equipment like the patents developed by Cremer (
US2355954 ), Knoess (US5529746 ) and Bauer (US7361301 ). Knoess and Bauer obtained good densification with high conductive powders like iron and copper. Knoess used various pulses of very high current (>100 kA/cm2) and Bauer an intensity lower that 10 kA/cm2, voltage lower than 10V using a sintering time around 1 s. The problem may occur when high electrical resistance samples are manufactured (due to the high resistivity of the powder or because of the large size of the parts), it will not be possible to close the electric circuit so the current can pass the whole material of the parts. For that reason, with these techniques it will not be possible to obtain larger samples or the consolidation of powders with higher resistivity due to the low voltage used. -
JP H03 236402 - To overcome the drawbacks of the prior art, the present invention proposes a method of sintering electrically conducting powders in an air atmosphere for obtaining a sintered product, comprising the following sequence of steps:
- a) placing the powders in an electrically isolating mold,
- b) applying a pressure to the powders between 100 and 500MPa,
- c) applying to the powders a sintering current density at a sintering voltage during a sintering time, for sintering the powders.
- The method of the present invention comprises, between step b) and step c), applying to the powders an activation current density lower than the sintering current density at an activation voltage greater than the sintering voltage during an activation time lower than the sintering time, to reduce the electrical resistance of the powders, the activation current density and the sintering current density being constant.
- The application of the activation current density and sintering current density is carried out while the pressure is being applied to the powders.
- The activation current density applied to the powders at a voltage greater than the voltage used for sintering in step c) during a lower time than step c) produces a current discharge that breaks the oxide layer in the surface of the powders and creates bridges between the particles of powders, obtaining a more uniform and cleaner particle surface which reduces the electrical resistance to the flow of the current through the powders such that the sintering current density applied in step c) is distributed more homogeneously through the powders in the mold. Thus is possible to sinter large size parts and parts made of material with a high electrical resistivity.
- Preferably the activation current density is greater than 0,5 kA/cm2, the activation voltage is greater than 10V and the activation time is lower than 300ms, for generating a current discharge of low intensity at a high voltage in a very reduced time, to assure an homogeneous superficial de-oxidation of the powders and formation of bridges among particles.
- According to the invention, the time between the removal of the activation current density and the application of the sintering current density is lower than 20 ms to assure an optimal distribution of the sintering current density. Most preferably the sintering current density is applied immediately after the application of the activation current density, i.e just after the activation time is run out.
- According to a preferred aspect of the invention:
- The activation current density is applied by employing a first electrical power unit.
- The sintering current density is applied by employing a second electrical power unit.
- The first and second electrical power units are operated independently.
- The method of the invention comprises the control of the two electrical power units which enables to optimize the processing time and the energy consumption, altogether with the installation costs.
- Further it allows to program and monitor at all times the power that is being introduced in the powder, thus allowing the process to be controlled very accurately and repetitively, both in the application of the activation current density and in the application of the sintering current density.
- Furthermore, it has been found that the precise control enabled by this method, allows a considerable increase in the parts size, their geometry, and the types of materials that can be sintered.
- According to a preferred embodiment of the invention:
- The activation current density is comprised in the range going from 0.5 to 5 kA/cm2;
- The activation voltage is comprised in the range going from 10 to 100 V;
- The activation time is comprised in the range going from 50 to 300 ms;
- The sintering current density is comprised in the range going from 3 to 15 kA/cm2;
- The sintering voltage is lower than 15 V;
- The sintering time is comprised in the range going from 500 to 1500 ms,
- According to a most preferred embodiment of the invention:
- The activation current density is comprised in the range going from 0.5 to 4 kA/cm2;
- The activation voltage is comprised in the range going from 10 to 100 V;
- The activation time is comprised in the range going from 90 to 200 ms;
- The sintering current density is comprised in the range going from 3 to 10 kA/cm2;
- The sintering voltage is lower than 10 V;
- The sintering time is comprised in the range going from 500 to 1500 ms,
- The skilled person will select the precise values of these parameters for each conductive powder, but always bearing in mind that the activation current density applied to one conductive powder must be lower than the sintering current density applied and the activation voltage greater than the sintering voltage. Thus it is not possible to choose a value of 4 kA/cm2 for the activation current density and a value of 3 kA/cm2 for the sintering current density. Same applies to the activation and sintering voltages where is not possible to apply a activation voltage of 10 V and a sintering voltage of 15 V. Some examples of parameters selections are disclosed in the description of preferred embodiments.
- To complete the description and in order to provide for a better understanding of the invention, a set of drawings is provided. Said drawings form an integral part of the description and illustrate an embodiment of the invention, which should not be interpreted as restricting the scope of the invention, but just as an example of how the invention can be carried out. The drawings comprise the following figures:
-
FIG. 1 is a block diagram of an apparatus according to a preferred embodiment. -
FIG. 2 is a time plot of the pressure and the voltage/current when the inventive method is applied to a WC-Co powder. - In
FIG. 2 the time pressure/ current/voltage diagram corresponding to the implementation of the method according to the invention for obtaining a sintered WC-Co is shown. - The process starts with the step consisting in placing an electrically conducting powder in an electrically insulating mold.
- Then a pressure between 100 and 500 MPa is applied inside the mold, preferably with two pistons, in this case around 300 MPa.
- Then an activation step is carried out, consisting in applying an activation current density at an activation voltage for an activation time and carried out by employing a first electrical power unit (2). As shown, in this step a low current density (around 2 kA/cm2) and a high voltage (around 30V) are applied. The pulse is about two tenths of a second.
- Then a waiting step is carried out wherein no current and/or voltage are applied. This step consists in the switching of the power units, that is, to switch from a power unit (2) to another power unit (3). The waiting time is that needed for carrying out said switching by the control unit (4), in the present case a PLC. In
FIG. 2 the switching time is about 2 tenth of a second. A technical possibility would be to use a single power unit but with instantaneously variable current and voltage. However, the control requirements for the current and voltage levels and the discharge times would imply very sophisticated equipment that would make the method uneconomic at industrial level. - Then, the proper sintering step is performed, which consists in applying a sintering current density at a sintering voltage during a sintering time carried out by employing the second electrical power unit (3). In this case the intensity is higher (around 10 kA), but the voltage is reduced to 5 V.
- The current density is applied using two opposite electrodes. In an embodiment the pistons can be used as opposite electrodes.
- As shown in
FIG 1 , and according to a preferred embodiment, the invention also relates to an apparatus (1) for carrying out the inventive method. - The apparatus comprises:
- means for applying current and voltage to the powders, represented by the power units (2, 3);
- an electrically insulating mold (5) containing the conductive powders (6), which is closed in its ends by two pistons for applying mechanical pressure and which form the electrodes (7) as well.
- As shown in
FIG. 1 , the means for providing current and voltage for an activation step is a first electrical power unit (2) and the means for providing current and voltage for a sintering step is a second electrical power unit (3). - The first power unit (2) is arranged to provide through the electrodes (7) an activation current density comprised between 0.5 and 5 KA/cm2 and an activation voltage comprised between 10 and 100 V whereas the second power unit (3) is arranged to provide through electrodes (7) a sintering current density comprised between 3 and 15 kA/cm2 and a sintering voltage lower than 15 V. These ranges allow to sinter most of the commercially interesting conductive powders for typical applications, with a single machine, which parameters have to be set prior to the sintering.
- The apparatus further comprises:
- Means for switching between the first 2 and the second 3 electrical power unit;
- Means for controlling the duration of the current density and voltage provided by the first power unit (2);
- means for controlling the duration of the current density and voltage provided by the second power unit (3);
- connections (23, 33) between each of the power units (2, 3) and the electrodes (7) of the mold (5).
- means for controlling the pistons that apply pressure in the mold.
- The means for controlling the duration of the current density and voltage provided by the first power unit (2) are able to control a predetermined discharge time (activation time) comprised in the range going from 50 to 300 ms and the means for controlling the duration of the current and voltage provided by the second power unit (3) are able to control a predetermined discharge time (sintering time) comprised in the range going from 500 to 1500 ms.
- Each power unit (2, 3) comprise a transformer (21, 31) and an inverter (22, 32), and the two power units (2, 3) are controlled by a single control unit (4), which is preferably a programmable logic controller.
- This PLC includes:
- means for switching between the first (2) and the second (3) electrical power unit,
- means for controlling the duration of the current and voltage provided by the first power unit (2),
- means for controlling the duration of the current and voltage provided by the second power unit (3); and
- means for controlling the pistons that apply pressure in the mold.
- Now, specific examples of application of the method of the invention to different metal powders are described.
- A WC-6Co or WC-10Co disk is produced with the disclosed apparatus with a thickness of 16 mm and a diameter of 22 mm. The agglomerated powder was spherical with an agglomerate size of less than 100 microns.
In the activation step a current density between 2 and 4 kA/cm2 during 100-200 ms was applied in order to activate the powder. A voltage between 15-50 V is needed for this activation step. - In the subsequent sintering stage a current density between 6-10 kA/cm2 was applied to obtain a densified sample with a voltage lower than 10 V during 500-1000 ms. Between stages, activation and sintering, a minimum time of 10 ms was established. Pressure, from 100-500 MPa, was applied from the beginning of the process.
- The density of the final disk, measured by the Archimedes method, is around 13-14.8 g/cm3. It is possible to obtain fully dense samples with hardness around 1800-2100 HV30.
- A titanium disk is produced with the disclosed apparatus with a thickness of 10 mm and a diameter of 22 mm. The shape of the particles of the powder was irregular with a maximum particle size around 75 microns.
- In the activation step a current density between 1-3 kA/cm2 was applied during 90-100 ms in order to activate the powder. A voltage between 10-50 V is needed for the activation stage.
- In the sintering stage a current density between 4-7 kA/cm2 was applied during 500-1000 ms to obtain a densified sample with a voltage lower than 10 V. Between stages, activation and sintering, a minimum time of 10 ms was established. Pressure, from 100-500 MPa, was applied from the beginning of the process.
- The density of the final disk, measured by the Archimedes method, is around 3.5-4.4 g/cm3. It is possible to obtain fully dense samples.
- A TiC-25Ni and TiC-25Fe disks are produced with the disclosed apparatus with a thickness of 16 mm and a diameter of 22 mm. The agglomerated powder was irregular with a particle size of less than 30 microns.
- In the activation step a current density between 1-3 kA/cm2 was applied during 100-200 ms in order to activate the powder. A voltage between 15-50 V is needed for this activation stage.
- In the subsequent sintering step a current density between 6-9 kA/cm2 was applied during 500-1000 ms to obtain a densified sample with a voltage lower than 10 V. Between stages, activation and sintering, a minimum time of 10 ms was stablished. Pressure, from 100-500 MPa, was applied from the beginning of the process.
- The density of the final disk, measured by the Archimedes method, was around 5.1-5.5 g/cm3 for TiC-25Ni and 5.1-5.4 g/cm3 for TiC-25Fe. It is possible to obtain fully dense samples with hardness around 1600-2000 HV30.
- An aluminium disk was produced with the disclosed apparatus with a thickness of 12 mm and a diameter of 12 mm. The powder was irregular with a particle size of less than 150 microns.
- In the activation step a current density between 0.5-2 kA/cm2 was applied during 100-200 ms in order to activate the powder. A voltage between 30-80 V is needed for this activation stage.
- In the subsequent sintering stage a current density between 3-4 kA/cm2 was applied during 500-1000 ms to obtain a densified sample with a voltage lower than 10 V. Between stages, activation and sintering, a minimum time of 10 ms was established. Pressure, from 100-300 MPa, was applied from the beginning of the process.
- The density of the final disk, measured by the Archimedes method, was around 2.5-2.7 g/cm3.
- In this text, the term "comprises" and its derivations should not be understood in an excluding sense, that is, these terms should not be interpreted as excluding the possibility that what is described and defined may include further elements, steps, etc.
- The invention is obviously not limited to the specific embodiments described herein, but also encompasses any variations that may be considered by any person skilled in the art, within the general scope of the invention as defined in the claims.
Claims (8)
- Method of sintering electrically conducting powders in an air atmosphere for obtaining a sintered product, comprising the following sequence of steps:a) placing the powders in an electrically isolating mold,b) applying a pressure to the powders between 100 and 500MPa,c) applying to the powders a sintering current at a sintering voltage during a sintering time, for sintering the powders,characterized by applying to the powders, between step b) and step c), an activation current density lower than the sintering current density at an activation voltage greater than the sintering voltage during an activation time lower than the sintering time, to reduce the electrical resistance of the powders, the activation current density and the sintering current density being constant
- Method according to claim 1, wherein the activation current density is greater than 0.5 kA/cm2, the activation voltage is greater than 10V and the activation time is lower than 300ms,
- Method according to any of the previous claims, wherein:- The application of the sintering current density and sintering voltage are carried out by employing a first electrical power unit (2);- The application of the activation current density and activation voltage are carried out by employing a second electrical power unit (3);- The first and second electrical power units (2, 3) operate independently.
- Method according to any of the previous claims, wherein:- The activation current density is comprised in the range going from 0.5 to 5 kA/cm2;- The activation voltage is comprised in the range going from 10 to 100 V;- The activation time is comprised in the range going from 50 to 300 ms;- The sintering current density is comprised in the range going from 3 to 15 kA/cm2;- The sintering voltage is lower than 15 V;- The sintering time is comprised in the range going from 500 to 1500 ms,and wherein the activation current density is lower than the sintering current density and the activation voltage is greater than the sintering voltage.
- Method according to claims 1 to 4, wherein:- The powders are WC-6Co powders or WC-10Co;- The activation current density is comprised in the range going from 2 to 4 kA/cm2;- The activation voltage is comprised in the range going from 15 to 50 V;- The activation time is comprised in the range going from 100 to 200 ms;- The sintering current density is comprised in the range going from 6 to 10 kA/cm2;- The sintering voltage is lower than 10 V;- The sintering time is comprised in the range going from 500 to 1000 ms.
- Method according to claims 1 to 4, wherein:- The powders are titanium powders;- The activation current density is comprised in the range going from 1 to 3- KA/cm2;- The activation voltage is comprised in the range going from 10 to 50 V;- The activation time is comprised in the range going from 90 to 110 ms;- The sintering current density is comprised in the range going from 4 to 7 kA/cm2;- The sintering voltage is lower than 10 V;- The sintering time is comprised in the range going from 500 to 1000 ms.
- Method according to claims 1 to 4, wherein:- The powders are a mixture of TiC-25Ni powders and TiC-25Fe powders;- The activation current density is comprised in the range going from 1 to 3 kA/cm2;- The activation voltage is comprised in the range going from 15 to 50 V;- The activation time is comprised in the range going from 100 to 200 ms;- The sintering current density is comprised in the range going from 6 to 9 kA/cm2;- The sintering voltage is lower than 10 V;- The sintering time is comprised in the range going from 500 to 1000 ms.
- Method according to claims 1 to 4, wherein:- The powders are an aluminium powders;- The activation current density is comprised in the range going from 0.5 to 2 kA/cm2;- The activation voltage is comprised in the range going from 30 to 80 V;- The activation time is comprised in the range going from 100 to 200 ms;- The sintering current density is comprised in the range going from 3 to 4 kA/cm2;- The sintering voltage is lower than 10 V;- The sintering time is comprised in the range going from 500 to 1000 ms.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP16382069.9A EP3208015B1 (en) | 2016-02-19 | 2016-02-19 | Method of sintering electrically conducting powders |
ES16382069T ES2738627T3 (en) | 2016-02-19 | 2016-02-19 | Method for sintering electrically conductive powders |
DK16382069.9T DK3208015T3 (en) | 2016-02-19 | 2016-02-19 | Method for sintering electrically conductive powders |
US15/436,844 US20170259336A1 (en) | 2016-02-19 | 2017-02-19 | Method of sintering electrically conducting powders and an apparatus for carrying out said method |
CN201710089756.1A CN107096919B (en) | 2016-02-19 | 2017-02-20 | Method for sintering conductive powder and apparatus for carrying out said method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP16382069.9A EP3208015B1 (en) | 2016-02-19 | 2016-02-19 | Method of sintering electrically conducting powders |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3208015A1 EP3208015A1 (en) | 2017-08-23 |
EP3208015B1 true EP3208015B1 (en) | 2019-05-01 |
Family
ID=55446727
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP16382069.9A Active EP3208015B1 (en) | 2016-02-19 | 2016-02-19 | Method of sintering electrically conducting powders |
Country Status (5)
Country | Link |
---|---|
US (1) | US20170259336A1 (en) |
EP (1) | EP3208015B1 (en) |
CN (1) | CN107096919B (en) |
DK (1) | DK3208015T3 (en) |
ES (1) | ES2738627T3 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3702065A1 (en) * | 2019-02-28 | 2020-09-02 | Siemens Aktiengesellschaft | Sintering device with decoupled sinter pressure and sinter flow, method for producing an electric contact material using the sintering device, electric contact material and use of the electric contact material |
CN111375758A (en) * | 2020-04-23 | 2020-07-07 | 王伟东 | Sintering method of titanium or titanium alloy powder |
CN111748717B (en) * | 2020-06-30 | 2021-06-08 | 马鞍山海华耐磨材料科技有限公司 | Wear-resistant casting made of metal-based ceramic composite material and machining process of wear-resistant casting |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2355954A (en) | 1942-03-04 | 1944-08-15 | Hardy Metallurg Company | Powder metallurgy |
US3241956A (en) | 1963-05-30 | 1966-03-22 | Inoue Kiyoshi | Electric-discharge sintering |
US3508029A (en) | 1967-02-22 | 1970-04-21 | Lockheed Aircraft Corp | Servocontrol system for discharge sintering |
US3656946A (en) * | 1967-03-03 | 1972-04-18 | Lockheed Aircraft Corp | Electrical sintering under liquid pressure |
US4975412A (en) | 1988-02-22 | 1990-12-04 | University Of Kentucky Research Foundation | Method of processing superconducting materials and its products |
US4929415A (en) | 1988-03-01 | 1990-05-29 | Kenji Okazaki | Method of sintering powder |
JP2796156B2 (en) * | 1990-02-13 | 1998-09-10 | 住友石炭鉱業株式会社 | Spark sintering equipment |
DE4407593C1 (en) | 1994-03-08 | 1995-10-26 | Plansee Metallwerk | Process for the production of high density powder compacts |
CN1203946C (en) * | 1996-07-12 | 2005-06-01 | Fmc生物聚合物有限公司 | Plasma technology for activating sintered material |
US6612826B1 (en) | 1997-10-15 | 2003-09-02 | Iap Research, Inc. | System for consolidating powders |
CN2471452Y (en) * | 2001-01-13 | 2002-01-16 | 昆明理工大学 | Plasma activating material sintering apparatus |
CN1292863C (en) * | 2001-01-20 | 2007-01-03 | 昆明理工大学 | Nano zirconium oxide plasma activation sintering method |
US20050237698A1 (en) * | 2004-04-23 | 2005-10-27 | Postage Bradley R | Reduced ESR through use of multiple wire anode |
CN1959878B (en) * | 2005-11-02 | 2010-09-15 | 四川大学 | Method for preparing permanent magnetism block body of nano crystal neodymium, boron |
EP2198993B1 (en) | 2008-12-19 | 2012-09-26 | EPoS S.r.L. | Sintering process and corresponding sintering system |
-
2016
- 2016-02-19 EP EP16382069.9A patent/EP3208015B1/en active Active
- 2016-02-19 DK DK16382069.9T patent/DK3208015T3/en active
- 2016-02-19 ES ES16382069T patent/ES2738627T3/en active Active
-
2017
- 2017-02-19 US US15/436,844 patent/US20170259336A1/en not_active Abandoned
- 2017-02-20 CN CN201710089756.1A patent/CN107096919B/en active Active
Non-Patent Citations (1)
Title |
---|
None * |
Also Published As
Publication number | Publication date |
---|---|
US20170259336A1 (en) | 2017-09-14 |
CN107096919B (en) | 2021-04-06 |
DK3208015T3 (en) | 2019-07-29 |
CN107096919A (en) | 2017-08-29 |
EP3208015A1 (en) | 2017-08-23 |
ES2738627T3 (en) | 2020-01-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Samuel et al. | Power metallurgy tool electrodes for electrical discharge machining | |
Orrù et al. | Consolidation/synthesis of materials by electric current activated/assisted sintering | |
EP3208015B1 (en) | Method of sintering electrically conducting powders | |
EP3389862B1 (en) | Method of producing spheroidal dehydrogenated titanium alloy particles | |
Grasso et al. | Electric current activated/assisted sintering (ECAS): a review of patents 1906–2008 | |
Groza | Field-activated sintering | |
JP2016522313A (en) | Powder material solidification apparatus and method | |
US20130266473A1 (en) | Method of Producing Sintered Magnets with Controlled Structures and Composition Distribution | |
EP3218325B1 (en) | Method for consolidation of powder materials | |
US5196264A (en) | Porous sintered body and method of manufacturing same | |
EP3184205A1 (en) | Composite tantalum powder, preparation method therefor, and capacitor positive electrode prepared by using tantalum powder | |
WO2018132854A1 (en) | Method for additive manufacturing | |
US2175899A (en) | Process for making metal articles | |
RU2495732C1 (en) | Method of compacted powder production | |
Alferov et al. | Characteristics of DC vacuum arc in the transverse axially symmetric magnetic field | |
EP3093857A1 (en) | Method for producing magnets using powder metallurgy | |
CN109609792A (en) | A method of preparing tungsten-copper alloy | |
Xianhui et al. | Effect of TiB2 particle size on erosion behavior of Ag-4wt% TiB2 composite | |
Shvetsov et al. | Erosion of explosively compacted Mo/Cu electrodes in high-current arc discharges | |
CN103878364B (en) | A kind of preparation method of the middle pressure tantalum powder for improving proof voltage energy | |
Olevsky et al. | Resistance Sintering | |
EP2191921B1 (en) | Process for producing a copper-chromium contact element for medium-voltage switchgear assemblies | |
US3445625A (en) | Method for making porous low density metal member from powdered metal | |
KR101459196B1 (en) | Manufacturing Methods of MAX Phases TiAlN Bulk Materials and Micro Electrical Discharge Drilling Method threeof | |
RU2802693C1 (en) | Method for producing tungsten-titanium-cobalt hard alloy from powders obtained by electroerosive dispersion of t5k10 alloy waste in kerosene |
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 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20180220 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20180413 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: B22F 3/16 20060101ALN20181102BHEP Ipc: B22F 3/105 20060101ALI20181102BHEP Ipc: B22F 3/087 20060101AFI20181102BHEP Ipc: C22C 21/00 20060101ALN20181102BHEP Ipc: C22C 29/08 20060101ALN20181102BHEP Ipc: C22C 14/00 20060101ALN20181102BHEP Ipc: C22C 32/00 20060101ALN20181102BHEP Ipc: B30B 11/00 20060101ALI20181102BHEP Ipc: B01J 19/08 20060101ALI20181102BHEP Ipc: C22C 29/10 20060101ALN20181102BHEP |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C22C 14/00 20060101ALN20181113BHEP Ipc: C22C 21/00 20060101ALN20181113BHEP Ipc: C22C 29/10 20060101ALN20181113BHEP Ipc: C22C 29/08 20060101ALN20181113BHEP Ipc: B22F 3/087 20060101AFI20181113BHEP Ipc: C22C 32/00 20060101ALN20181113BHEP Ipc: B01J 19/08 20060101ALI20181113BHEP Ipc: B30B 11/00 20060101ALI20181113BHEP Ipc: B22F 3/16 20060101ALN20181113BHEP Ipc: B22F 3/105 20060101ALI20181113BHEP |
|
INTG | Intention to grant announced |
Effective date: 20181214 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM 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 Ref country code: AT Ref legal event code: REF Ref document number: 1126251 Country of ref document: AT Kind code of ref document: T Effective date: 20190515 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602016013155 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 Effective date: 20190724 |
|
REG | Reference to a national code |
Ref country code: SE Ref legal event code: TRGR |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20190501 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NO 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: 20190801 Ref country code: AL 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: 20190501 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: 20190901 Ref country code: HR 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: 20190501 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: 20190501 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: 20190501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: RS 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: 20190501 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: 20190801 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: 20190501 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1126251 Country of ref document: AT Kind code of ref document: T Effective date: 20190501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20190901 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2738627 Country of ref document: ES Kind code of ref document: T3 Effective date: 20200124 |
|
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: 20190501 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: 20190501 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: 20190501 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: 20190501 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: 20190501 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602016013155 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM 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: 20190501 |
|
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: 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: 20190501 |
|
26N | No opposition filed |
Effective date: 20200204 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20190501 |
|
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: 20190501 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20200229 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200219 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: 20190501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 |
|
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: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200229 |
|
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 FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190501 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: 20190501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK 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: 20190501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20190501 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230525 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20231218 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20231218 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20240301 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FI Payment date: 20240226 Year of fee payment: 9 Ref country code: DE Payment date: 20240228 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20240307 Year of fee payment: 9 Ref country code: IT Payment date: 20240222 Year of fee payment: 9 Ref country code: DK Payment date: 20240226 Year of fee payment: 9 |