GB2165545A - Pellicle structure for transmission of mid ultraviolet light - Google Patents

Pellicle structure for transmission of mid ultraviolet light Download PDF

Info

Publication number
GB2165545A
GB2165545A GB08523609A GB8523609A GB2165545A GB 2165545 A GB2165545 A GB 2165545A GB 08523609 A GB08523609 A GB 08523609A GB 8523609 A GB8523609 A GB 8523609A GB 2165545 A GB2165545 A GB 2165545A
Authority
GB
United Kingdom
Prior art keywords
pellicle
film
cellulose acetate
acetate butyrate
nanometers
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
Application number
GB08523609A
Other versions
GB2165545B (en
GB8523609D0 (en
Inventor
Joseph Gordon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toppan Photomasks Inc
Original Assignee
Du Pont Semiconductor Products Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Du Pont Semiconductor Products Inc filed Critical Du Pont Semiconductor Products Inc
Publication of GB8523609D0 publication Critical patent/GB8523609D0/en
Publication of GB2165545A publication Critical patent/GB2165545A/en
Application granted granted Critical
Publication of GB2165545B publication Critical patent/GB2165545B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/02Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
    • B29C41/12Spreading-out the material on a substrate, e.g. on the surface of a liquid
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F1/00Originals for photomechanical production of textured or patterned surfaces, e.g., masks, photo-masks, reticles; Mask blanks or pellicles therefor; Containers specially adapted therefor; Preparation thereof
    • G03F1/62Pellicles, e.g. pellicle assemblies, e.g. having membrane on support frame; Preparation thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2001/00Use of cellulose, modified cellulose or cellulose derivatives, e.g. viscose, as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2001/00Use of cellulose, modified cellulose or cellulose derivatives, e.g. viscose, as moulding material
    • B29K2001/08Cellulose derivatives
    • B29K2001/12Cellulose acetate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/0058Liquid or visquous
    • B29K2105/0073Solution
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2301/00Characterised by the use of cellulose, modified cellulose or cellulose derivatives
    • C08J2301/08Cellulose derivatives
    • C08J2301/14Mixed esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Preparing Plates And Mask In Photomechanical Process (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

A freely standing thin pellicle film of cellulose acetate butyrate is formed by spinning on a rotating substrate. After forming, the film is lifted off of the substrate and secured to a metallic frame. The pellicle is for use in the mid ultraviolet range of 280 to 360 nanometers, but can be used also in the deep ultraviolet range, e.g. wavelengths as low as about 240 nanometers. The pellicle prevents dust particles from being focused on a surface which is to be exposed by the ultraviolet radiation.

Description

SPECIFICATION Pellicle structure for transmission of mid ultraviolet light Background of the invention This invention relates to a pellicle structure used for the protection of photo masks and reticles in microlithography applications and, more specifically, relates to a novel pellicle structure which can transmit an average of about 90% or greater over a radiation band width beginning at about 240 nanometers.
Pellicles, which are free standing thin transparent organic films are commonly used to protect photo masks and reticles in order to increase die yield in microlithography during the manufacture of semiconductor devices. Such pellicles are normally attached to a mask used in the microlithography application and stand above the mask surface by a given distance. Thus, dust particles which may settle during the microlithography operation will settle on the pellicle and be defocused on the work surface.
Consequently, when used in a conventional photolithographic apparatus, one or more dust particles will not affect the yield of a given wafer. Die yield from such wafers is improved by up to and greater than 40% when the mask andlor reticle are pellicle protected.
Pellicles of this type are described in a publication by R. Hershel, Semiconductor International,8,97, (1981). Their use is also described in a publication by A. Rangappan, C. Kao, "SPIE Optical Microlithogra phy", Vol.334,52. (1982). Also see I. Ward, Dawn Duly, SPIE, Vol.470, Optical Microlithography Ill: Technology for the Next Decade (1984), pp. 147-156.
A standard pellicle being sold today, for example by the assignee of the present application, consists of a membrane which is commonly of nitrocellulose having a thickness of about 2.85 microns. Such nitrocellulose pellicles satisfy the light transmission requirements for most present microlithography applications. Films other than nitrocellulose are also known for use as pellicles. By way of example, films have been made of materials such as mylar, cellu lose acetate, parylene (poly(chloro-p-xycylene)) and cellulose acetate (without butyrate). Other materials are also known and the foregoing is not an exhaus tive list. Nitrocellular pellicles do not transmit suffi cient light at shorter wavelengths, for example below 360 nanometers.However, there is a growing need for pellicle materials which can transmit useful amounts of an input light in the mid range of ultraviolet wavelengths, particularly in the 280 to 360 nanometer range. Such materials must also permit relatively economical manufacture and have mecha nical durability which will enable them to exist as a free standing membranes which are not too rapidly degraded by ultraviolet radiation and can withstand at least minimal mechanical abuse during handling and cleaning. Moreover, the pellicle film must be capable of being made thin enough and of sufficient uniformity so as to not interfere with the optical properties of the microlithographic process.
Brief summary of the invention In accordance with the present invention, pellicle membranes of cellulose acetate butyrate in a range of formulations have been found to satisfy the ultraviolet transmissions and durability properties required of free standing membranes at ultraviolet frequencies in the deep and mid ultraviolet ranges of 240 to 290 nanometers and 290 to 360 nanometers, respectively. More particularly, the novel membrane of the invention is useful at frequencies beginning at about 240 nanometers, particularly when antireflection coatings are used. Indeed, the use of an antireflection coating on both surfaces of the cellulose acetate butyrate membrane of the invention permits transmission at frequencies as low as the cut-off transmission frequency of silica mask substrates which is approximately 190 nanometers.
A preferred cellulose acetate butyrate composition employs about 15% butyryl, and a 15 sec viscosity.
The butyryl content can vary from 5% to 40%. Its viscosity can vary from 5 sec to 20 sec. This material is available from Eastman Kodak under their catalog number 4623, CAS Registry No. 9004-36-8. This material is offered for sale by Eastman Kodak for use as a hot melt or as a strippable coating used for high-gloss coatings and protective coatings, respectively. Eastman Kodak cellulose acetal butyrate coatings are described in their bulletins No. 3.4A, E-101B, and E-184A, each of which is dated July, 1973.Note that these coatings are not suggested by Eastman Kodak to be capable of free standing use as a transparent film but are always intended to be fixed in surface to surface contact with a substrate such as a wooden surface which is to have a desired finish appearance or a metallic surface which is to be protected by the film which ordinarily adheres to its surface.
It was found that this material can be dissolved in a suitable solvent, preferably cyclohexanone, to a workable viscosity which enables the material to be filtered and then spin-coated on a glass substrate.
For example, from 3% to 10% of the cellulose acetate butyrate, by weight, solids content, can be dissolved in cyclohexanone. The substrate can be rotated at any appropriate speed selected from about 300 rpm to about 2,000 rpm and is spun for a time depending on the desired thickness to be obtained. This time will also depend upon atmospheric conditions and solvent concentration in the spinning appratus. It was found that the spin coating process inherently forms an acceptably thin coating and by suitable adjustment of speeds and other parameters a thick ness of 2.85 microns can be obtained in a repeatable manner within suitable tolerances by spinning at from 400 to 600 rpm, nominally, at 500 rpm. Film thicknesses from 1 micron to 5 microns can be made by appropriate adjustment of the process.
Thereafter, the substrate and film thereon is loaded into a water bath and the film is loosened from the glass substrate and secured to the end of a metal frame as by cementing with an epoxy type cement or the like.
The film may also be coated on one or both surfaces with an antireflection coating of known composition, for example calcium fluoride. The index of refraction of the cellulose acetate butyrate is approximately that of nitrocellulose so that the low reflectivity coating will be almost as effective on membranes of either material.
The novel pellicle film of the invention and having a thickness, for example of 2.85 microns has the novel characteristic in the mid ultraviolet range which extends between 280 nanometers and 360 nanometers that it transmits an average of about greater than 90% of incident light without the use of antireflection coatings. Moreover, there is substantial light transmission into the deep ultraviolet range which is less than about 280 nanometers. When the surfaces of the pellicle of the invention are provided with one or more antireflection coatings, transmission in the deep ultraviolet range is further improved such that an average greater than 90% transmission is obtained at frequencies above about 240 nanometers. When coated with one or more antireflection coatings, the film will transmit greater than about 90% of incident light and the band of 240 nanometers to 600 nanometers.
The pellicle was also found to have improved mechanical durability, better resistance to chemicals used to clean pellicles, and is not deteriorated adversely by mid ultraviolet radiation.
Brief description of the drawings Figure 1 is a top view of a portion of a silica mask which has a conductive coating thereon and a pellicle secured thereto.
Figure 2 is a cross-sectional view of Figure 1 taken across the section line 2-2 in Figure 1.
Figure 3 shows the spectral transmission for a prior art nitrocellulose pellicle having a thickness of 2.85 microns.
Figure 4 shows the spectral transmission charac teristicforthe nictocellulose pellicle of Figure 3 when it is coated with an antireflection coating on one side of the pellicle film.
Figure shows a prior art pellicle of the type shown in Figure 3 with antireflection coatings on both surfaces of the pellicle film.
Figure 6 shows the spectral transmission of a pellicle film of cellulose acetate butyrate made in accordance with the invention and demonstrates its improved transmission in the deeper ultraviolet regions.
Figure 7 illustrates the characteristics of the cellulose acetate butyrate pellicle film of Figure 6 when one side is covered with an antireflection coating.
Figure 8 shows the spectral transmission characteristic of the film of Figure 6 when both sides are coated with an antireflection coating.
Detailed description of the invention Figures 1 and 2 illustrate a conventional pellicleized mask wherein a silica mask 10 is a standard mask having a metallized pattern 11 on its upper surface (Figure 2). The pellicle shown in Figures 1 and 2 consists of a thin organic film 12 which is fastened to a rectangular metal frame 13 which will have a shape dependent upon the manner in which the mask is to be mounted in the projection aligner or step and repeat aligner used for the microlithography process. The film area can be any area desired or necessary in the microlithography application and will match the shape of the underlying mask.
Film 12 has been made of numerous materials in the past, notably nitrocellulose having a thickness of 2.85 microns. Other thicknesses have also been used, for example 0.865 microns. A commercially available pellicle manufactured by the assignee of the present application is a nitrocellulose film pellicle known as "Type 1" having a thickness of 2.85 microns and a spectral transmission characteristic which is shown in Figure 3.
In Figure 3, the horizontal axis of the graph is wavelength in nanometers of a standard high pressure mercury lamp while the vertical axis shows the percentage transmission of light through the pellicle.
Conventionally, the pellicle of Figure 3 is preferably operated at the i, hand g wavelengths which are shown in dotted lines in the band between 350 and 450 nanometers. Note particularly that the pellicle having the characteristic of Figure 3 cannot be used in relatively deep ultraviolet application since the transmission of light is sharply reduced below about 360 nanometers.
Nitrocellulose films having the characteristic of Figure 3 can be made by numerous processes, preferably a spinning process employing the weliknown technology used in spinning photoresists onto a substrate. The films are then conventionally lifted off in a water bath and cemented to frames such as the frame 13 of Figures 1 and 2 so that they are stretched tautly on the frame.
In order to improve its spectral transmission characteristics, it is known to apply an antireflection coating on one surface of the pellicle. This improves the characteristic to that shown in Figure 4 for the nitrocellulose film of 2.85 microns.
A still further improvement in the light transmission of the pellicle can be obtained by using an antireflective coating on both sides of the pellicle film as shown in Figure 5. These antireflection coatings can be any desired type, for example calcium fluoride coatings which are applied by conventional known processes.
In accordance with the present invention, the film 12 of Figures 1 and 2 is made of a cellulose acetate butyrate. In a preferred embodiment of the invention, the cellulose acetate butyrate contained about 15% butyryl and had a 15 sec viscosity. The material is commercially available from Eastman Kodak; catalog material No. 4623, CAS Registry No. 9004-36- 8. The viscosity can vary in the range of from 5 sec to 20 sec and the butyryl content can vary between 5% and 40%. Three percent to 10% solids by weight, preferably 6% of this material was dissolved in cyclohexanone to a workable viscosity and was then filtered and thereafter spin coated on a glass substrate. Other solvents can be used, for example, organic acetates, keytones, ethylene and propylene chlorides. These will produce good films, but cyclohexanone lent itself to good filtering.
The spinning process is essentially identical to conventional spin processes used for spinning photoresists onto a substrate. Thus, in solutions with 3% to 10% solids, spin rates of 300 to 2,000 rpm can be used to produce pellicles in a range of thicknesses from 1 micron to 5 microns. For a 2.85 micron thick pellicle, and using 6% solids by weight, the spin speed is from 400 to 600 rpm, nominally 500 rpm.
After forming the film, the substrate and film are placed in a water bath and the film is separated from the glass substrate. The film is then appropriately cemented to a support frame (support frame 13 of Figures 1 and 2) by a suitable epoxy cement and extends tautly across the frame.
When the pellicle film had a thickness of 2.85 microns, the spectral transmission characteristics shown in Figure 6 were obtained. When the film was coated on one surface or two surfaces respectively, the characteristics of Figures 7 and 8, respectively, were obtained.
In examining the spectral transmission characteristics of Figure 6, it will be observed that the spectral transmission of the 2.85 micron cellulose acetate butyrate film at 240 nanometers is greater than about .72% and, at 250 nanometers, peaks at about 90%. These transmission characteristics are adequate for application in the deep ultraviolet region in photomicrolithography applications. The transmission is substantially improved by use of antireflection coatings on one or both pellicle surfaces. Thus, in Figure 7, it will be seen that the transmission at 240 nanometers is substantially greater than 80%, and in Figure 8, approaches 90%.
Although the present invention has been described in connection with a preferred embodiment thereof, many variations and modifications will now become apparent to those skilled in the art. It is preferred, therefore, that the present invention be limited not by the specific disclosure herein, but only by the appended claims.

Claims (21)

1. A pellicle comprising a thin film of substantially uniform thickness which is tautly fixed to one edge of an enclosed frame; said thin film consisting of cellulose acetate butyrate.
2. The pellicle of claim 1, wherein said thin uniform film has a thickness of from about 1 micron to about 5 microns.
3. The pellicle of claim 1, wherein the opposite edge of said enclosed frame is adapted for mounting to a silica mask.
4. The pellicle of claim 1, wherein said thin film in the absence of antireflection coatings has a spectral transmission characteristic whereby an average greater than bout 90% of incident light in the band of frequencies from 280 nanometers to 360 nanometers is passed by said film.
5. The pellicle of claim 1, wherein said thin film has an antireflection coating on one of its surfaces.
6. The pellicle of claim 5, wherein said thin film transmits greater than about 90% of incident light in the band of 240 nanometers to 600 nanometers.
7. The pellicle of claim 3, wherein said thin uniform film has a thickness of about 2.85 microns.
8. The pellicle of claim 4, wherein said thin uniform film has a thickness of about 2.85 microns.
9. The pellicle of claim 5, wherein said thin uniform film has a thickness of about 2.85 microns.
10. The pellicle of claim 6, wherein said thin uniform film has a thickness of about 2.85 microns.
11. A process of making a pellicle comprising the steps of dissolving cellulose acetate butyrate in a solvent, filtering said dissolved cellulose acetate butyrate and solvent, spin coating said cellulose acetate butyrate and solvent on a spinning substrate and driving off said solvent to form a substantially uniformly thick film of cellulose acetate butyrate, lifting said film from said substrate and cementing said film to one end of a support frame with said film tautly stretched over said frame.
12. The process of claim 11, wherein said cellulose acetate butyrate contains from 5% to 40% butyryl, and has a viscosity of from 5 sec to 20 sec.
13. The process of claim 12, wherein said solvent is cyclohexanone.
14. The process of claim 11, wherein said cellulose acetate butyrate has about 15% butyryl and a viscosity of about 15 sec.
15. The process of claim 13, wherein said cellulose acetate butyrate has about 15% butyryl and a viscosity of about 15 sec.
16. The process of claim 11, wherein from 3% to 10% by weight of said cellulose acetate butyrate is dissolved in said solvent.
17. The process of claim 13, wherein from 3% to 10% by weight of said cellulose acetate butyrate is dissolved in said solvent.
18. The process of claim 16, wherein said spin rate is in the range of 300 to 2,000 rpm.
19. Pellicle film whenever made by the process claimed in any one of claims 11 to 18:
20. A pellicle film substantially as hereinbefore described with reference to and as shown in the accompanying drawings.
21. A process for making a pellicle substantially as hereinbefore described.
GB08523609A 1984-10-16 1985-09-25 Pellicle structure for transmission of mid ultraviolet light Expired GB2165545B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US66157784A 1984-10-16 1984-10-16

Publications (3)

Publication Number Publication Date
GB8523609D0 GB8523609D0 (en) 1985-10-30
GB2165545A true GB2165545A (en) 1986-04-16
GB2165545B GB2165545B (en) 1988-03-30

Family

ID=24654183

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08523609A Expired GB2165545B (en) 1984-10-16 1985-09-25 Pellicle structure for transmission of mid ultraviolet light

Country Status (5)

Country Link
JP (1) JPH065383B2 (en)
DE (1) DE3536708A1 (en)
FR (1) FR2573219B1 (en)
GB (1) GB2165545B (en)
IT (1) IT1187747B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0314418A2 (en) * 1987-10-26 1989-05-03 Mitsui Petrochemical Industries, Ltd. Dust-proof film

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5950467B2 (en) * 2013-09-24 2016-07-13 信越化学工業株式会社 Pellicle

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB716398A (en) * 1952-07-07 1954-10-06 Rose Rand Improvements in or relating to purses or handbags
GB1184008A (en) * 1967-12-15 1970-03-11 Polaroid Corp Optical Devices Comprising Cellulose Acetate and Cellulose Acetate Butyrate

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4453828A (en) * 1981-12-02 1984-06-12 Advanced Semiconductor Products, Inc. Apparatus and methods for measuring the optical thickness and index of refraction of thin, optical membranes
JPS58219023A (en) * 1982-06-15 1983-12-20 Daicel Chem Ind Ltd Manufacture of resin membrane
US4482591A (en) * 1983-03-08 1984-11-13 J. T. Baker Chemical Company Polyvinyl butyrate pellicle compositions and pellicles thereof for projection printing

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB716398A (en) * 1952-07-07 1954-10-06 Rose Rand Improvements in or relating to purses or handbags
GB1184008A (en) * 1967-12-15 1970-03-11 Polaroid Corp Optical Devices Comprising Cellulose Acetate and Cellulose Acetate Butyrate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0314418A2 (en) * 1987-10-26 1989-05-03 Mitsui Petrochemical Industries, Ltd. Dust-proof film
EP0314418A3 (en) * 1987-10-26 1991-01-30 Mitsui Petrochemical Industries, Ltd. Dust-proof film

Also Published As

Publication number Publication date
IT8522329A0 (en) 1985-10-02
GB2165545B (en) 1988-03-30
IT1187747B (en) 1987-12-23
JPS61106243A (en) 1986-05-24
FR2573219A1 (en) 1986-05-16
DE3536708A1 (en) 1986-04-17
GB8523609D0 (en) 1985-10-30
JPH065383B2 (en) 1994-01-19
FR2573219B1 (en) 1989-02-03

Similar Documents

Publication Publication Date Title
US4861402A (en) Method of making a cellulose acetate butyrate pellicle
US4657805A (en) Dust cover superior in transparency for photomask reticle use and process for producing the same
US4878973A (en) Process for producing a thin resin film
US5168001A (en) Perfluoropolymer coated pellicle
JP2758397B2 (en) Composite optical element having antireflection coating
US4996106A (en) Pellicle
CA1200947A (en) Pellicle compositions and pellicles thereof for projection printing
US5691088A (en) Pellicle for protection of photolithographic mask
US5008156A (en) Photochemically stable mid and deep ultraviolet pellicles
CA1265000A (en) Process for preparing thin film having high light transmittance
US4796973A (en) Pellicle structure for transmission of mid ultraviolet light
US6797207B2 (en) Process for producing organic thin film
GB2165545A (en) Pellicle structure for transmission of mid ultraviolet light
JPS6322576B2 (en)
JP2790946B2 (en) Method of manufacturing pellicle film
US5234742A (en) Pellicle for lithography
WO2012093834A2 (en) Pellicle membrane and method of manufacturing same
JPH06230560A (en) Pellicle
JP4371458B2 (en) Pellicle manufacturing method
JP3302268B2 (en) Pellicle manufacturing method
JPH04237055A (en) Pellicle structural body
CA1305627C (en) Pellicle
JP2790850B2 (en) Cellulose thin film for pellicle
JPH0262A (en) Photomask cover
JPH06100826B2 (en) Pellicle for lithograph

Legal Events

Date Code Title Description
732 Registration of transactions, instruments or events in the register (sect. 32/1977)
732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19980925