GB2109012A - Novel and improved diamond like film and process for producing same - Google Patents
Novel and improved diamond like film and process for producing same Download PDFInfo
- Publication number
- GB2109012A GB2109012A GB08229792A GB8229792A GB2109012A GB 2109012 A GB2109012 A GB 2109012A GB 08229792 A GB08229792 A GB 08229792A GB 8229792 A GB8229792 A GB 8229792A GB 2109012 A GB2109012 A GB 2109012A
- Authority
- GB
- United Kingdom
- Prior art keywords
- film
- pair
- amorphous
- electrodes
- substrate
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/22—Surface treatment of glass, not in the form of fibres or filaments, by coating with other inorganic material
-
- 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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/26—Deposition of carbon only
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/28—Other inorganic materials
- C03C2217/282—Carbides, silicides
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2218/00—Methods for coating glass
- C03C2218/10—Deposition methods
- C03C2218/15—Deposition methods from the vapour phase
- C03C2218/152—Deposition methods from the vapour phase by cvd
- C03C2218/153—Deposition methods from the vapour phase by cvd by plasma-enhanced cvd
Landscapes
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Vapour Deposition (AREA)
- Carbon And Carbon Compounds (AREA)
- Surface Treatment Of Glass (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
An amorphous, carbonaceous, diamond-like film has an extremely low hydrogen content and stress, below 10<10> dynes/cm<2> is resistant to both acids and alkalis, and adheres tenaciously to many types of substrates including glasses, plastics, metals, and semiconductors. The film is produced by radio frequency plasma decomposition of an alkane and a pair of spaced carbon electrodes.
Description
SPECIFICATION
Novel and improved diamond-like film and process for producing same
This invention relates to an improved amorphous, carbonaceous, diamond-like film. Additionally, the invention pertains to an improved process for producing such an amorphous, carbonaceous film having diamond-like properties.
Carbonaceous diamond-like film orfilms having diamond-like properties, of the kind to which this invention relates, are well-known in the prior art. These films are particularly useful in applications such as the coating of optical lenses to increase the optical transmission through the lens and the coating of mirrors to improve the light reflectivity from the mirror. Such films also find useful applications as protective films in abrasive applications, such as the coating of writing instruments, as a general antireflective coating, and as a dielectric or protective coating for silicon and silicon-containing devices.In fact, the diamond-like films disclosed in this invention find many other useful applications in commerce and industry where films which are clear, extremely hard, extremely adherent, abrasion-resistant, corrosion-resistant, and which possess good optical properties, are needed.
While the amorphous, carbonaceous, diamond-like films of the prior art have much to commend them, the search has continued for improved amorphous, carbonaceous films having diamond-like properties. Particularly such a film having increased hardness and increased adherence to various substrates has continued to be sought, as well as a process for producing such a film.
The novel and improved carbonaceous diamond-like film of this invention is an improvement over presently-known films in that it has an extremely low stress, has the ability to tenaciously adhere to many, varied substrates, has a low hydrogen content, and is extremely hard.
With this invention, there is produced a novel and improved, amorphous, carbonaceous, diamond-like film which has an extremely low hydrogen content and an extremely low stress. This film is resistant to both acids and alkalis and has a hardness similar to that of diamond. The film has a refractive index, a dielectric constant, and a thermal coefficient of expansion similar to that of diamond.
In addition, the film adheres well to many types of substrates, such as glasses, plastics, metals, semiconductors and the like.
The improved amorphous, carbonaceous, diamond-like film of this invention, in addition to possessing the above-enumerated properties and qualities, differs from other presently-known carbonaceous films in that it possesses an extremely low hydrogen content; on the order of about one atomic percent or less of hydrogen. The prior art carbonaceous films contain hydrogen in an amount of up to about 25 atomic percent or more.
The diamond-like film of this invention additionally differs from prior art carbonaceous films in that it has an extremely low stress; the stress may be either a compressive or a tensile stress. The film of this invention exhibits a stress on the order of 107 to 1 Os dynes/cm2, while the films of the prior art exhibit a stress on the order of 10" dynes/cm2. It is believed that the stress of these carbonaceous films is related to their hydrogen content, and that the lower the hydrogen content of the film, the lower the stress in the film. Due to the extremely low stress, the film of this invention is extremely adherent and adheres tenaciously to a great number and variety of substrates on which it is deposited.
The carbonaceous, diamond-like films of this invention are extremely resistant to acids, such as H2S04, HF, HCi, and HCI:HNO3, and alkalis such as NaQH, KOH, RbOH, and CsOH.
The amorphous, carbonaceous, diamond-like film of this invention is produced by a hybrid process in a deposition chamber using a radio frequency plasma decomposition from an alkane, such as n-butane, using a pair of spaced, generally parallel, carbon electrodes, preferably ultra pure carbon electrodes. While most films in the following examples were deposited using normal butane, other alkanes, such as methane, ethane, propane, pentane, and hexane can be substituted in the process of this invention to produce the improved carbonaceous, diamond-like film thereof.
The deposition chamber, such as a stainless steel chamber, includes a pair of generally parallel and horizontai, vertically spaced, pure carbon electrodes with the substrate to be coated positioned on the lower carbon electrode. The electrodes are typically positioned about 2 up to about 8 centimeters apart from each other, with the preferred electrode spacing being approximately 2.5 centimeters. The chamber is evacuated to its ultimate pressure, generally in the region of about 10-7 torr, and then backfilled with an alkane, such as n-butane, to a pressure of approximately 8x 10-4 torr. Thereafter, the vacuum system is throttled to a pressure in the range of approximately 25 to 100 millitorr.After stabilization of the pressure, the radio frequency power is applied to the pair of pure carbon electrodes with the lower electrode (substrate target) being biased in the range of about O to about -100 volts, and the upper electrode being biased in the range of about -200 to about -3500 volts. Radio frequency plasma decomposition is begun, and an amorphous, carbonaceous, diamond-like film is deposited onto the substrate at rates varying between about 8 up to about 35 angstroms per minute, to produce a film of up to about 5 micrometers in thickness.
The films produced by the above process have an extremely low stress. The stress for the films produced by the process has been measured and determined to be in the range of about 107 to 1 os dynes/cm2. As has been previously stated, the stress may be either a compressive or tensile stress. It has been determined that the resultant stress of the film produced by this process, be it either a compressive or tensile stress, is dependent on the potential applied to the upper carbon electrode.
The following specific examples are included in order to illustrate the invention and the improvements thereof with greater particularity. However, it is to be understood that these examples are not intended to limit the invention in any way.
Example I
In this example, a stainless steel deposition chamber, as described above, was prepared for deposition of the improved carbonaceous diamond-like film of this invention. The deposition chamber was stabilized with n-butane at a deposition pressure of approximately 50 millitorr with the pair of ultra pure carbon electrodes being horizontally positioned and at a vertical spacing of approximately 6 centimeters from each other. A glass substrate for deposition of the film was positioned on the lower carbon electrode. The lower electrode (substrate target) was maintained at a potential of -50 volts and the upper electrode was maintained at a potential of -500 volts.
A film was then deposited by radio frequency plasma decomposition from n-butane onto the glass substrate under the above conditions at a rate of about 10 angstroms per minute to a thickness of approximately 1.45 micrometers. The stress of the resultant film was measured and determined to be a stress of about 7 x 108 dynes/cm2, tensile stress. The resultant film had a hydrogen content of less than 1.0 atomic percent.
In a similar experiment, it was determined that when the potential of the upper electrode was decreased and maintained at a -300 volts, while maintaining the potential of the lower electrode (substrate target) at -50 volts, the film deposited under such conditions at a rate of approximately 10 angstroms per minute to a thickness of 1.5 micrometers had a compressive stress.
The stress of the film in this experiment was measured and determined to be about 8x 108 dynes/cm2, compressive stress. The hydrogen content of the film obtained in this experiment was measured and determined to be less than 1.0 atomic percent hydrogen.
In a series of additional experiments, similar to the above, improved carbonaceous diamond-like films, like the above, were deposited on other substrates. These substrates included metals, such as stainless steel, molybdenum, tungsten, and tantalum; various glasses, silicon, silicon dioxide, and aluminum oxide, as well as plastics, such as polycarbonate, styrene, acrylic, styrene/acrylic copolymer, and other resins.
Example II
In this example, a series of experiments were performed as in Example I to deposit the improved carbonaceous, diamond-like film of this invention under a variety of potentials applied to the upper electrode and lower electrode or substrate target. The voltages employed and the results obtained in each of these experiments are set forth hereinbelow::
Lower electrode
Upper electrode (substrate target) Film thickness Film stress (T-Tensile,
No. potential-volts potential-volts (micrometers) C-Compressive) dyne/cm2
1 -450 -50 1.44 7.01x107(T) 2 -450 -50 0.72 2.80x 107 (T) 3 -450 -50 1.50 1.97x107(T) 4 -400 -50 0.42 3.22x108 (T)
5 -400 -50 2.75 9.02x108(T) 6 -400 -50 0.82 9.61x106(T) 7 -350 -50 0.25 5.95x108(T) 8 -350 -50 1.00 1.15x108(T)
9 -300 -50 0.22 1.52x108(C) 10 -250 -50 0.18 3.91x108(C) 11 -250 -50 0.0 & 0.08 7.45x 108 (C) The hydrogen content of the above films was measured and determined to be less than 1.0 atomic percent hydrogen.
Example Ill
In this example, a number of high quality plastic lenses were coated with the improved carbonaceous, diamond-like film of this invention using the stainless steel deposition chamber and process of this invention as described in Example I. After evacuation, the chamber was backfilled with normal butane and stabilized at a deposition pressure of approximately 80 millitorr. The pair of ultra pure carbon electrodes were positioned at a spacing of about 2.5 centimeter with the plastic lens to be coated positioned on the lower electrode. This lower electrode (substrate target) was maintained at a potential of --50 volts while the upper electrode was maintained at a potential of -2500 volts. A film was then r.f. plasma deposited onto the plastic lens under these conditions at a rate of approximately 25 angstroms per minute to a thickness of 1100 angstroms. Another lens was coated on both of its sides with the film of this invention, with the film on each side having a thickness of 1100 angstroms.
A third plastic lens was coated on one side with the film of this invention to a thickness of 11,000 angstroms. In all cases, the films of this example exhibited the same low stress and low hydrogen content as the films produced in the previous examples set forth above. Additionally, the optical properties (absorption, transmission, and reflection) of the coated plastic lenses were maintained at approximately the same level, and in many cases these optical properties were improved by the film of this invention having been coated on their surface.
Claims (21)
1. An amorphous, carbonaceous film having diamond-like properties and having a stress below 1 o10 dynes/cm2.
2. An amorphous, carbonaceous film as defined in claim 1 wherein said film has a stress in the order of 107 or 108 dynes/cm2.
3. An amorphous, carbonaceous film as defined in claim 1 or 2 wherein said film has a hydrogen content of one or less atomic percent.
4. An amorphous, carbonaceous film as defined in claim 1,2 or 3 wherein said stress of said film is a tensile stress.
5. An amorphous, carbonaceous film as defined in claim 1,2 or 3 wherein said stress of said film is a compressive stress.
6. An article of manufacture comprising an amorphous, carbonaceous film as defined in any preceding claim deposited on a substrate.
7. An article of manufacture as defined in claim 6 wherein said substrate is selected from the group consisting of glasses, plastics, metals, and semiconductor materials.
8. A process for forming an amorphous, carbonaceous film on a substrate comprising the steps of:
(a) providing a pair of spaced, generally parallel carbon electrodes,
(b) positioning said substrate closely adjacent one of said pair of electrodes, and
(c) depositing said film on said substrate by a radio frequency plasma decomposition of a lower alkane.
9. A process as defined in claim 8 wherein said lower alkane is an alkane containing from 1 up to about 6 carbon atoms.
10. A process as defined in claim 8 wherein said alkane is n-butane.
11. A process as defined in claim 8, 9 or 10 wherein said spacing of said parallel electrodes is from about 2 up to about 8 centimeters.
12. A process as defined in any of claims 8-11 1 wherein said one electrode of said pair of electrodes most closely adjacent said substrate is biased in the range of from about 0 to about -100 volts and the other of said pair of electrodes is biased in the range of from about -200 to about -3500 volts.
13. A process for depositing an amorphous, carbonaceous film on a substrate comprising the steps of:
(a) providing an evacuated deposition chamber haying an internal pair of generally horizontal and parallel carbon electrodes, said pair of electrodes being vertically spaced a distance of from about 2 up to about 8 centimeters, and means for applying radio frequency power to said pair of electrodes;
(b) positioning said substrate on the lower electrode of said pair of electrodes;
(c) stabilizing said deposition chamber with a lower alkane at a pressure of from about 25 up to about 100 millitorr;
(d) applying radio frequency power to said pair of electrodes; and
(e) biasing the upper electrode of said pair in the range of from about200 to about3500 volts and said lower electrode in the range of from about 0 to about -100 volts, whereby said film deposits on said substrate by radio frequency plasma decomposition of said lower alkane.
14. A process as defined in claim 13 wherein said vertical spacing of said pair of electrodes is from about 2.5 to about 6.0 centimeters.
1 5. A process as defined in claim 13 wherein said deposition chamber is stabilized at a pressure of from about 35 up to about 85 millitorr.
1 6. A process as defined in claim 1 3 wherein said upper electrode is biased in the range of from about -250 to about -2500 volts.
1 7. A process as defined in claim 1 3 wherein said lower electrode is biased in the range of from about -25 to about -75 volts.
1 8. A process as defined in claim 1 3 wherein said lower alkane is n-butane.
1 9. A novel amorphous, carbonaceous film substantially as hereinbefore described.
20. A novel filmed article of manufacture substantially as hereinbefore described.
21. A process for forming an amorphous, carbonaceous film on a substrate substantially as hereinbefore described according to any of the examples or experiments set forth.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8131794 | 1981-10-21 | ||
US34802182A | 1982-02-11 | 1982-02-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2109012A true GB2109012A (en) | 1983-05-25 |
GB2109012B GB2109012B (en) | 1986-09-03 |
Family
ID=26281036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08229792A Expired GB2109012B (en) | 1981-10-21 | 1982-10-19 | Novel and improved diamond-like film and process for producing same |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPH0699807B2 (en) |
CA (1) | CA1202598A (en) |
DE (1) | DE3237851A1 (en) |
FR (1) | FR2514743B1 (en) |
GB (1) | GB2109012B (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3442208A1 (en) * | 1984-11-19 | 1986-05-28 | Leybold-Heraeus GmbH, 5000 Köln | Process and apparatus for producing hard carbon layers |
GB2174038A (en) * | 1985-03-23 | 1986-10-29 | Canon Kk | Thermal recording head |
GB2174580A (en) * | 1985-03-22 | 1986-11-05 | Canon Kk | Heat generating resistor |
DE3706340A1 (en) * | 1987-02-27 | 1988-09-08 | Winter & Sohn Ernst | METHOD FOR APPLYING A WEAR PROTECTIVE LAYER AND PRODUCT PRODUCED THEREOF |
US4783369A (en) * | 1985-03-23 | 1988-11-08 | Canon Kabushiki Kaisha | Heat-generating resistor and heat-generating resistance element using same |
US4804974A (en) * | 1985-03-23 | 1989-02-14 | Canon Kabushiki Kaisha | Thermal recording head |
US4847639A (en) * | 1985-06-10 | 1989-07-11 | Canon Kabushiki Kaisha | Liquid jet recording head and recording system incorporating the same |
US4870388A (en) * | 1985-03-22 | 1989-09-26 | Canon Kabushiki Kaisha | Heat-generating resistor and heat-generating resistance element using same |
US4983993A (en) * | 1985-03-25 | 1991-01-08 | Canon Kabushiki Kaisha | Thermal recording head |
GB2240114A (en) * | 1990-01-18 | 1991-07-24 | Stc Plc | Film nucleation process for growing diamond film |
GB2257986A (en) * | 1991-07-23 | 1993-01-27 | Flouroware Inc | Diamond coated carrier for carrying wafers requiring chemical processing |
GB2286347A (en) * | 1994-02-10 | 1995-08-16 | Atomic Energy Authority Uk | Improved load-bearing polymeric materials |
WO2007057478A1 (en) * | 2005-11-15 | 2007-05-24 | Fundacion Tekniker | Part having an outer polymer surface with a metallic finish, production method thereof and use of same |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4640744A (en) * | 1984-01-23 | 1987-02-03 | Standard Oil Company (Indiana) | Amorphous carbon electrodes and their use in electrochemical cells |
JPS62202899A (en) * | 1986-03-03 | 1987-09-07 | Nippon Gakki Seizo Kk | Production of decorative article |
JPH0676666B2 (en) * | 1987-02-10 | 1994-09-28 | 株式会社半導体エネルギ−研究所 | Carbon film production method |
JPH01103310A (en) * | 1987-10-16 | 1989-04-20 | Sumitomo Electric Ind Ltd | Surface acoustic wave element |
DE3815457A1 (en) * | 1988-05-06 | 1989-11-16 | Sipra Patent Beteiligung | KNITTING MACHINE |
JP2574934Y2 (en) * | 1993-03-02 | 1998-06-18 | シチズン時計株式会社 | Parts for knitting machines |
JPH0676383U (en) * | 1993-04-06 | 1994-10-28 | シチズン時計株式会社 | Textile related machine parts |
JP2003035707A (en) * | 2001-06-18 | 2003-02-07 | Doko Cho | Substrate for bio chip with implanted gene or protein and method of manufacturing the same |
US10249495B2 (en) * | 2016-06-28 | 2019-04-02 | Applied Materials, Inc. | Diamond like carbon layer formed by an electron beam plasma process |
JP7122316B2 (en) * | 2017-09-25 | 2022-08-19 | 住友電気工業株式会社 | Method for producing hard carbon-based coating, and member with coating |
JP2021006649A (en) * | 2017-09-26 | 2021-01-21 | 住友電気工業株式会社 | Production method of hard carbon film |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3961103A (en) * | 1972-07-12 | 1976-06-01 | Space Sciences, Inc. | Film deposition |
US4060660A (en) * | 1976-01-15 | 1977-11-29 | Rca Corporation | Deposition of transparent amorphous carbon films |
JPS5838952B2 (en) * | 1976-01-22 | 1983-08-26 | 日本電気株式会社 | semiconductor laser equipment |
GB1582231A (en) * | 1976-08-13 | 1981-01-07 | Nat Res Dev | Application of a layer of carbonaceous material to a surface |
JPS6023406B2 (en) * | 1977-05-18 | 1985-06-07 | 日本電気株式会社 | magnetic disk |
JPS5825041B2 (en) * | 1979-08-03 | 1983-05-25 | 日本電信電話株式会社 | Method for manufacturing diamond-like carbon film |
DE3064976D1 (en) * | 1979-11-20 | 1983-10-27 | Nat Res Dev | Infra red reflectors |
EP0032788B2 (en) * | 1980-01-16 | 1989-12-06 | National Research Development Corporation | Method for depositing coatings in a glow discharge |
JPS56108876A (en) * | 1980-02-04 | 1981-08-28 | Citizen Watch Co Ltd | Silver plated exterior decorative parts for watch and their manufacture |
DE3172609D1 (en) * | 1980-08-21 | 1985-11-14 | Nat Res Dev | Coating infra red transparent semiconductor material |
EP0049032B1 (en) * | 1980-08-21 | 1986-09-17 | National Research Development Corporation | Coating insulating materials by glow discharge |
GB2083841B (en) * | 1980-08-21 | 1985-03-13 | Secr Defence | Glow discharge coating |
GB2082562B (en) * | 1980-08-21 | 1983-12-14 | Secr Defence | Coating germanium of silicon with carbon |
JPS57106513A (en) * | 1980-12-22 | 1982-07-02 | Nippon Telegr & Teleph Corp <Ntt> | Formation of carbon film |
-
1982
- 1982-10-04 FR FR8216600A patent/FR2514743B1/en not_active Expired
- 1982-10-12 CA CA000413200A patent/CA1202598A/en not_active Expired
- 1982-10-13 DE DE19823237851 patent/DE3237851A1/en active Granted
- 1982-10-19 GB GB08229792A patent/GB2109012B/en not_active Expired
- 1982-10-20 JP JP18534882A patent/JPH0699807B2/en not_active Expired - Lifetime
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3442208C3 (en) * | 1984-11-19 | 1998-06-10 | Leybold Ag | Method and device for producing hard carbon layers |
DE3442208A1 (en) * | 1984-11-19 | 1986-05-28 | Leybold-Heraeus GmbH, 5000 Köln | Process and apparatus for producing hard carbon layers |
GB2174580A (en) * | 1985-03-22 | 1986-11-05 | Canon Kk | Heat generating resistor |
US4851808A (en) * | 1985-03-22 | 1989-07-25 | Canon Kabushiki Kaisha | Heat-generating resistor and heat-generating resistance device by use of said heat-generating resistor |
US4870388A (en) * | 1985-03-22 | 1989-09-26 | Canon Kabushiki Kaisha | Heat-generating resistor and heat-generating resistance element using same |
GB2174038A (en) * | 1985-03-23 | 1986-10-29 | Canon Kk | Thermal recording head |
US4783369A (en) * | 1985-03-23 | 1988-11-08 | Canon Kabushiki Kaisha | Heat-generating resistor and heat-generating resistance element using same |
US4804974A (en) * | 1985-03-23 | 1989-02-14 | Canon Kabushiki Kaisha | Thermal recording head |
GB2174038B (en) * | 1985-03-23 | 1989-03-22 | Canon Kk | Thermal recording head |
US4845513A (en) * | 1985-03-23 | 1989-07-04 | Canon Kabushiki Kaisha | Thermal recording head |
US4983993A (en) * | 1985-03-25 | 1991-01-08 | Canon Kabushiki Kaisha | Thermal recording head |
US4847639A (en) * | 1985-06-10 | 1989-07-11 | Canon Kabushiki Kaisha | Liquid jet recording head and recording system incorporating the same |
DE3706340A1 (en) * | 1987-02-27 | 1988-09-08 | Winter & Sohn Ernst | METHOD FOR APPLYING A WEAR PROTECTIVE LAYER AND PRODUCT PRODUCED THEREOF |
GB2240114A (en) * | 1990-01-18 | 1991-07-24 | Stc Plc | Film nucleation process for growing diamond film |
GB2240114B (en) * | 1990-01-18 | 1993-03-24 | Stc Plc | Film nucleation process |
GB2257986A (en) * | 1991-07-23 | 1993-01-27 | Flouroware Inc | Diamond coated carrier for carrying wafers requiring chemical processing |
GB2286347A (en) * | 1994-02-10 | 1995-08-16 | Atomic Energy Authority Uk | Improved load-bearing polymeric materials |
GB2286347B (en) * | 1994-02-10 | 1998-04-29 | Atomic Energy Authority Uk | Improved load-bearing polymeric materials |
WO2007057478A1 (en) * | 2005-11-15 | 2007-05-24 | Fundacion Tekniker | Part having an outer polymer surface with a metallic finish, production method thereof and use of same |
Also Published As
Publication number | Publication date |
---|---|
FR2514743B1 (en) | 1986-05-09 |
GB2109012B (en) | 1986-09-03 |
JPH0699807B2 (en) | 1994-12-07 |
DE3237851A1 (en) | 1983-04-28 |
JPS5879807A (en) | 1983-05-13 |
CA1202598A (en) | 1986-04-01 |
FR2514743A1 (en) | 1983-04-22 |
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