EP1044289A2 - Plasmaborierung - Google Patents
PlasmaborierungInfo
- Publication number
- EP1044289A2 EP1044289A2 EP98965249A EP98965249A EP1044289A2 EP 1044289 A2 EP1044289 A2 EP 1044289A2 EP 98965249 A EP98965249 A EP 98965249A EP 98965249 A EP98965249 A EP 98965249A EP 1044289 A2 EP1044289 A2 EP 1044289A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- boron
- gas
- medium
- reactor
- plasma
- 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
- 238000005271 boronizing Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 claims abstract description 67
- 229910052796 boron Inorganic materials 0.000 claims abstract description 64
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 63
- 238000011282 treatment Methods 0.000 claims abstract description 49
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- 239000007789 gas Substances 0.000 claims description 62
- 230000008569 process Effects 0.000 claims description 21
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000011261 inert gas Substances 0.000 claims description 6
- 229910052786 argon Inorganic materials 0.000 claims description 5
- 238000004140 cleaning Methods 0.000 claims description 5
- 229910052756 noble gas Inorganic materials 0.000 claims description 5
- 238000009826 distribution Methods 0.000 claims description 2
- 238000005259 measurement Methods 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 11
- 239000002245 particle Substances 0.000 abstract description 11
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 21
- 238000005755 formation reaction Methods 0.000 description 11
- 239000011148 porous material Substances 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 3
- 229910015900 BF3 Inorganic materials 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 238000001994 activation Methods 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000001636 atomic emission spectroscopy Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002912 waste gas Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000010849 ion bombardment Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- CMIAIUZBKPLIOP-YZLZLFLDSA-N methyl (1r,4ar,4br,10ar)-7-(2-hydroperoxypropan-2-yl)-4a-methyl-2,3,4,4b,5,6,10,10a-octahydro-1h-phenanthrene-1-carboxylate Chemical compound C1=C(C(C)(C)OO)CC[C@@H]2[C@]3(C)CCC[C@@H](C(=O)OC)[C@H]3CC=C21 CMIAIUZBKPLIOP-YZLZLFLDSA-N 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000007725 thermal activation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/36—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases using ionised gases, e.g. ionitriding
- C23C8/38—Treatment of ferrous surfaces
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/36—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases using ionised gases, e.g. ionitriding
Definitions
- the present invention relates to a method for producing a boride layer on a surface by plasma working, a gas medium containing a boron donor medium being fed to a reactor and a glow discharge being generated in the reactor, and a corresponding device for using such a method.
- Boroning which is part of the thermochemical treatment process, preferably enables the creation of wear-resistant surface layers on metallic components, which provide excellent protection against high abrasive and adhesive wear.
- Industrial boriding processes have so far frequently worked with solid boron dispensing media in the form of e.g. B. powders or pastes.
- these methods have a number of disadvantages that limit the generation of bonds to specific applications for which there are no alternative treatments with a comparable protection against wear and tear. These disadvantages include e.g. B. the high manual effort due to handling. The component has to be packed in powder or the borating paste has to be spread and then the remaining borating agent has to be removed. The residues of borating agent should be disposed of in suitable landfills for ecological reasons.
- the known methods are often not or not sufficiently controllable. Automation of the processes is not possible.
- the invention further relates to a device for producing a boride layer on a surface by plasma working, comprising a reactor with a treatment space, to which a gas medium containing a boron donor medium is fed and in which a glow discharge is produced with the features of claim 20.
- This device is for carrying out the The method according to the invention is suitable according to one of the aforementioned variants and is described in more detail below.
- the method according to the invention is described in more detail in its various alternatives. Extensive tests have shown that when it comes to plasma processing, it is essential to choose the parameters for the generation of the plasma generated in the treatment room of the reactor. It was surprisingly found that these parameters should advantageously be selected so that an increased proportion of excited boron particles in the plasma is obtained. If the plasma contains large amounts of excited boron, this leads to low-pore layers. This could be demonstrated in the course of development work on the method according to the invention, for example by optical emission spectroscopy or plasma analysis. If, on the other hand, BCI particles with a high content are contained in the plasma, this leads to layers with a large number of pores, which should be avoided for the reasons already mentioned above.
- the glow discharge is preferably generated with a pulsed DC voltage.
- the pulse duty factor defined as the ratio between the time length of the voltage pulse to the subsequent pulse pause enables the desired generation of an increased content of excited boron particles and thus control of the process for plasma generation in the desired sense.
- this duty cycle should be greater than 1.1, preferably it is in the range between approximately 1.25: 1 to 5: 1, more preferably in the range between 1.5: 1 and 3.5: 1.
- the period duration, ie the sum of the duration of the voltage pulse and the pulse pause is preferably less than about 230 ⁇ s and in particular> 50 ⁇ s.
- the period duration in the process according to the invention in one variant is below approximately 230 ⁇ s and above 50 ⁇ s, eg. B. at about 210 ⁇ s.
- the voltage applied for the pulsed direct current for generating the glow discharge is preferably in the range between approximately 500 volts and approximately 1000 volts, preferably in the range between approximately 600 volts and approximately 900 volts, further preferably in the range between approximately 650 volts and about 800 volts. It has also been found that the use of a longer pulse pause is advantageous when working with a higher voltage. However, a good result can also be achieved when a lower voltage is applied, preferably within the voltage ranges specified above, the composition of the individual components of the gas medium fed to the reactor also being able to exert an influence here.
- a boron donor medium in the form of a boron trihalide eg., As the first component of the gas medium fed to the reactor.
- Gaseous hydrogen is preferably used as the second component of the gas medium and, if appropriate, an inert gas, e.g. B. Argon. It has been found that when argon is used as the third component, good boride layers can be produced even when using lower voltages in the process according to the invention.
- the content of boron trihalide as boron donor medium in the gas medium supplied generally influences the results of the process according to the invention.
- the boron trihalide content must not be too low and should generally not be less than 1% by volume, since then usually no suitable boride layer is obtained.
- the boron trihalide content is preferably in the range from about 2% by volume to 50% by volume, but if the contents are too high it should be noted that a relatively high boron trihalide loss is obtained. This loss of boron trihalide can be found in the waste gas from the reactor and thus also leads to increased expenditure in the disposal or cleaning of the waste gas.
- the boron trihalide content is preferably in the range between about 2% by volume and 10% by volume, for example about 7.5% by volume of boron trihalide.
- an inert gas is used as the third component of the gas medium in the process according to the invention, then the content of the inert gas, eg. B. argon, preferably in the range between about 0 vol .-% and about 20 vol .-%.
- Gaseous hydrogen is preferably used as the second component in an amount which corresponds to the residual content of the gas medium which results from the preferred ranges given above for the two other components, boron trihalide and noble gas.
- the process according to the invention is preferably carried out in the low pressure range, for example in a range between approximately 0.5 and approximately 15 hPa, preferably in a range between approximately 1 to 10 hPa.
- the setting of the desired parameters to achieve the desired effect can be done e.g. B. make so that the proportion of excited boron particles in the plasma is determined analytically and then one or more of the process parameters for generating the glow discharge such as voltage, duty cycle, frequency, temperature, pressure etc. are changed accordingly.
- the boride layer can also be produced in several stages, z. B. works in a first stage at a lower treatment temperature, thereby avoiding the halide formation in the plasma, which is also responsible for the formation of pores.
- a thinner but closed boride layer is first produced which is more resistant to a corrosive attack.
- the treatment temperature can then be raised in a second treatment stage in order to promote the diffusion of the boron particles and thus the formation of a layer with increasing layer thickness.
- the other process parameters must also be selected in such a way that an increased content of excited boron particles in the plasma is obtained as possible in order to favor the boride formation reaction and to avoid a corrosive attack.
- the current which can be set via the plasma generally has a significant influence in the context of the method according to the invention.
- the influencing of the layer characteristics or the suppression of pore formation, caused by the chlorine species present in the treatment atmosphere, and the favoring of the boride formation, as two competing reactions, are determined via this and the other plasma parameters.
- a plasma state can be achieved via a defined voltage, which is characterized by a high particle density of boron-releasing species, so that the boride formation takes place preferentially.
- the analysis of the plasma states can be carried out, for example, using optical emission spectroscopy.
- the signals for the excited boron, the excited BCI and the Cl + signal can be used to optimize the layer characteristics.
- Procedures in which the analysis methods show high B signals have proven to be favorable. This is possible, for example, with voltages in a middle range of preferably about 650 volts to 800 volts, the content of boron trihalide in the gas medium and the pulse duty factor of the pulsed direct current also playing a role.
- the method according to the invention is suitable for industrial applications and could be developed for series production. Compared to other known boriding processes of the type mentioned at the outset, which work with solid boron dispensing media, plasma working with a gaseous boron dispensing medium shows enormous potential for improvement.
- the handling of the components to be treated could be reduced to a minimum.
- the method according to the invention is suitable for automation. By changing the treatment time, a change in the gas composition is possible within the scope of the method according to the invention, so that the layer formation can be influenced thereby, special attention being paid to avoiding the formation of FeB. Furthermore, the method according to the invention takes account of the environmental concept, since the boroning agent residues to be disposed of can be minimized.
- Industrial areas of application for the method according to the invention are e.g. B. the boronization of metal parts to increase the wear resistance of the surfaces of components that are subject to particularly high abrasive or adhesive loads.
- the procedure according to the invention is suitable for. B. for application to components in the automotive industry, for example for gears, hydraulic tappets, camshafts, oil pump drives z. B. with crossed axes, helical gears, continue for extruder screws and other components that are exposed to increased stress.
- the present invention further relates to a device for producing a boride layer on a surface by plasma working, comprising a reactor to which a gas medium containing a boron donor medium can be fed and in which a glow discharge is generated.
- the device according to the invention is characterized in that it has a plasma generator which supplies a pulsed DC voltage with a variable pulse width and / or pulse pause.
- the device according to the invention preferably has at least one mass flow meter for measuring and / or adjusting the composition and / or the flow of one or more of the gases in the gas medium. It can be measured at any time which instantaneous gas composition the gas medium supplied to the reactor has and can then change the composition of the gas medium and / or change the respective flow rate of one or more of the gases contained in the gas medium. This makes it possible to influence the process. You can, for example, influence the layer formation by changing the gas composition during the process, this in turn depending on the results of the analysis of the determined particle composition in the plasma.
- a gas medium which contains two or three components, for example a boron trihalide, hydrogen and an inert gas, is preferably used. There are therefore preferably three mass flow meters, each for measuring and / or adjusting the flow of each of these three components.
- a gas meter-independent pressure meter is preferably used for the device according to the invention in order to measure the treatment pressure.
- This gas meter-independent pressure meter is preferably controlled by a computer.
- the distribution of the gas in the treatment room of the reactor can e.g. B. make a gas shower.
- a thermally decomposable boron dispenser it has proven to be advantageous to use a cooled gas inlet, since in this way a better utilization of the boron medium introduced can be achieved.
- a gas cleaning device for the exhaust gas treatment in order to minimize the boron content in the exhaust gas and thus the environmental impact of the method.
- an arrangement of this type can be used in which the gas cleaning device is connected downstream of a vacuum pump connected to the treatment room.
- the reactor can have an additional heater.
- the present invention also relates to a method of the type mentioned at the outset, which is carried out by means of a device having the features of one of the device claims 16 to 25.
- Fig. 1 is a schematic simplified representation of a plant according to the invention for producing a boride layer on a surface by plasma working
- Fig. 2 is a diagram relating to the temporal change in the voltage in the pulsed direct current which is used for a method according to the invention.
- FIG. 1 shows a diagram of the plant structure of a plant as can be used in the method according to the invention for producing a boride layer on a surface by plasma working.
- the system comprises a reactor 10 with a treatment room 11, in which the plasma is generated.
- the treatment room 11 of the reactor 10 is charged with a boron dispensing medium which enters the treatment room 11 via a gas inlet 12 and the feed line 13.
- a total of three feed lines are connected to the feed line 13, via which the individual components of the treatment gas are fed.
- these components are Boron trihalide, e.g. B. boron trichloride or boron trifluoride, which is supplied via the branch line 14, which opens into the supply line 13.
- the second component is hydrogen gas, which is supplied via the branch line 15, which likewise opens into the supply line 13.
- the third component is an inert gas, e.g. B. argon which is supplied via the branch line 16, which also opens into the supply line 13.
- Mass flow meters 17, 18 and 19 are provided for all three components, by means of which the flow of the respective component of the treatment gas can be set and measured.
- the reactor 10 further comprises a charging plate 20, which is located in the reactor space 11 and rests on two support insulators and the current-carrying support (not shown).
- the supply of voltage for generating the glow discharge takes place via the schematically illustrated voltage supply line 21.
- the plasma generator supplies a pulsed DC voltage with a variable pulse width or pulse pause, as will be explained further below.
- the composition and the flow of the treatment gas are adjusted with the aid of the mass flow meters 17, 18, 19.
- the treatment pressure is measured using a pressure meter that is independent of the gas type and is also controlled by a computer.
- the pressure measurement and pressure control is carried out by means of the device designated 22 in the diagram, which is connected to the treatment room 11 via the line 23.
- a vacuum pump 24 is connected to this line 23 downstream of the pressure control 22. Downstream of this vacuum pump 24 is a device 25 for exhaust gas purification in this exhaust gas line, which ensures adequate exhaust gas treatment.
- the temperature of the plasma generator is controlled via the temperature control device 26 and the line 27.
- the system according to the invention also has an additional heater 28, which is accommodated in the reactor 10 in order to achieve the desired treatment temperature in the treatment room 11.
- the inventive method for producing a boride layer preferably works in the low pressure range, for. B. in the range of 1 to 10 hPa, and is supported by an electrical activation of the gas atmosphere.
- the components to be treated (borating) are cathodically against the container wall of the Treatment room switched.
- the preferably made of boron trihalide, e.g. B. boron trichloride or boron trifloride, hydrogen and noble gas existing gas medium is placed in the treatment room 11 and undergoes thermal activation as well as electrical activation by glow discharge.
- the treatment temperature is dependent on the material of the respective components to be borated and is, for example, above 700 ° C., preferably at 800 ° C. or above.
- a pulsed DC voltage is preferably applied in order to enable the surface to be activated by the noble gas ion bombardment before the treatment phase.
- active excited boron particles are generated during the treatment, which reach the surface of the component and form borides there primarily by diffusion.
- the reduction of the halogen present in the atmosphere, which is generated from the boron trihalide, is favored by the atomic hydrogen generated in the plasma, which is produced from the H 2 gas supplied.
- the diagram according to FIG. 2 shows an example of a possible voltage curve as a function of the time for a pulsed direct current, as is particularly advantageous for a method according to the invention.
- the voltage is z. B. in a medium range at 650 volts, the voltage pulse is maintained, for example, 160 ⁇ s and the pulse pause is, for example, 50 ⁇ s.
- the pulse pause is therefore about a factor of 3 shorter than the duration of the DC voltage pulse.
- the period in the exemplary embodiment is 210 ⁇ s and thus the frequency is 4.762 kHz.
- the pulse duty factor defined as the ratio of the length of the pulse duration to the pulse pause within a pulse is 3.2 in the exemplary embodiment. It has been found that a longer pulse pause is required when using a relatively high voltage.
- argon in the treatment gas can also be used at relatively low voltages, e.g. B. achieve good results in the range above 500 volts.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Chemical Vapour Deposition (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Electron Sources, Ion Sources (AREA)
- Primary Cells (AREA)
- Apparatus For Radiation Diagnosis (AREA)
- Plasma Technology (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01110904A EP1143031A3 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19755595 | 1997-12-15 | ||
DE19755595 | 1997-12-15 | ||
PCT/EP1998/008079 WO1999031291A2 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01110904A Division EP1143031A3 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
EP01110904.8 Division-Into | 2001-05-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1044289A2 true EP1044289A2 (de) | 2000-10-18 |
EP1044289B1 EP1044289B1 (de) | 2002-03-27 |
Family
ID=7851902
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01110904A Ceased EP1143031A3 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
EP98965249A Expired - Lifetime EP1044289B1 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01110904A Ceased EP1143031A3 (de) | 1997-12-15 | 1998-12-11 | Plasmaborierung |
Country Status (8)
Country | Link |
---|---|
US (1) | US6783794B1 (de) |
EP (2) | EP1143031A3 (de) |
JP (1) | JP4588213B2 (de) |
KR (1) | KR100583262B1 (de) |
CN (1) | CN1198953C (de) |
AT (1) | ATE215132T1 (de) |
DE (1) | DE59803574D1 (de) |
WO (1) | WO1999031291A2 (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE524493C2 (sv) * | 2002-02-25 | 2004-08-17 | Telia Ab | Uppskattningsenhet och metod för att bestämma positionen för en mobil station i ett mobilt kommunikationssystem |
US7767274B2 (en) * | 2005-09-22 | 2010-08-03 | Skaff Corporation of America | Plasma boriding method |
CA2649525A1 (en) * | 2006-04-20 | 2007-11-01 | Habib Skaff | Mechanical parts having increased wear resistance |
CA2680858A1 (en) * | 2007-03-22 | 2008-09-25 | Skaff Corporation Of America, Inc. | Mechanical parts having increased wear-resistance |
US8338317B2 (en) * | 2011-04-06 | 2012-12-25 | Infineon Technologies Ag | Method for processing a semiconductor wafer or die, and particle deposition device |
CN104233425B (zh) * | 2014-09-29 | 2017-01-25 | 河海大学常州校区 | 微弧渗硼催化溶液和微弧渗硼溶液以及微弧渗硼方法 |
KR102084296B1 (ko) * | 2016-12-15 | 2020-03-03 | 도쿄엘렉트론가부시키가이샤 | 성막 방법, 붕소 막 및 성막 장치 |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3677799A (en) * | 1970-11-10 | 1972-07-18 | Celanese Corp | Vapor phase boron deposition by pulse discharge |
JPS5118944A (ja) * | 1974-08-07 | 1976-02-14 | Suwa Seikosha Kk | Kisohokaho |
JPS56105627A (en) * | 1980-01-28 | 1981-08-22 | Fuji Photo Film Co Ltd | Manufacture of amorphous semiconductor |
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- 1998-12-11 JP JP2000539186A patent/JP4588213B2/ja not_active Expired - Fee Related
- 1998-12-11 EP EP01110904A patent/EP1143031A3/de not_active Ceased
- 1998-12-11 DE DE59803574T patent/DE59803574D1/de not_active Expired - Lifetime
- 1998-12-11 CN CNB988121832A patent/CN1198953C/zh not_active Expired - Fee Related
- 1998-12-11 KR KR1020007006436A patent/KR100583262B1/ko not_active IP Right Cessation
- 1998-12-11 EP EP98965249A patent/EP1044289B1/de not_active Expired - Lifetime
- 1998-12-11 WO PCT/EP1998/008079 patent/WO1999031291A2/de active IP Right Grant
- 1998-12-11 AT AT98965249T patent/ATE215132T1/de not_active IP Right Cessation
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2000
- 2000-06-15 US US09/594,905 patent/US6783794B1/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
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See references of WO9931291A2 * |
Also Published As
Publication number | Publication date |
---|---|
ATE215132T1 (de) | 2002-04-15 |
EP1143031A2 (de) | 2001-10-10 |
EP1143031A3 (de) | 2004-04-28 |
JP4588213B2 (ja) | 2010-11-24 |
JP2002508448A (ja) | 2002-03-19 |
CN1198953C (zh) | 2005-04-27 |
KR20010033075A (ko) | 2001-04-25 |
US6783794B1 (en) | 2004-08-31 |
KR100583262B1 (ko) | 2006-05-25 |
CN1282383A (zh) | 2001-01-31 |
WO1999031291A3 (de) | 1999-09-10 |
DE59803574D1 (de) | 2002-05-02 |
EP1044289B1 (de) | 2002-03-27 |
WO1999031291A2 (de) | 1999-06-24 |
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