U.S. patent application number 10/653099 was filed with the patent office on 2004-03-11 for pellicle.
This patent application is currently assigned to ASAHI GLASS COMPANY LIMITED. Invention is credited to Irisawa, Jun, Matsukura, Ikuo, Shirota, Naoko.
Application Number | 20040048005 10/653099 |
Document ID | / |
Family ID | 18591080 |
Filed Date | 2004-03-11 |
United States Patent
Application |
20040048005 |
Kind Code |
A1 |
Matsukura, Ikuo ; et
al. |
March 11, 2004 |
Pellicle
Abstract
A pellicle for a photolithographic patterning process by means
of a light having a wavelength of at most 200 nm, comprising a
frame and a pellicle membrane bonded to the frame by means of an
adhesive, wherein the pellicle membrane or the adhesive comprises
the following fluorine-containing polymer (A): fluorine-containing
polymer (A): a substantially linear fluorine-containing polymer
having a chain of carbon atoms as the main chain, and containing as
carbon atoms in its main chain, a carbon atom having one or two
hydrogen atoms bonded thereto and a carbon atom having no hydrogen
atom bonded thereto and having a fluorine atom or a
fluorine-containing organic group bonded thereto.
Inventors: |
Matsukura, Ikuo; (Kanagawa,
JP) ; Shirota, Naoko; (Kanagawa, JP) ;
Irisawa, Jun; (Kanagawa, JP) |
Correspondence
Address: |
OBLON, SPIVAK, MCCLELLAND, MAIER & NEUSTADT, P.C.
1940 DUKE STREET
ALEXANDRIA
VA
22314
US
|
Assignee: |
ASAHI GLASS COMPANY LIMITED
TOKYO
JP
|
Family ID: |
18591080 |
Appl. No.: |
10/653099 |
Filed: |
September 3, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10653099 |
Sep 3, 2003 |
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10351354 |
Jan 27, 2003 |
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6660346 |
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10351354 |
Jan 27, 2003 |
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09803965 |
Mar 13, 2001 |
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6548129 |
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Current U.S.
Class: |
428/14 ; 428/421;
428/422; 430/5 |
Current CPC
Class: |
Y10T 428/31544 20150401;
G03F 1/64 20130101; G03F 1/62 20130101; Y10T 428/3154 20150401 |
Class at
Publication: |
428/014 ;
428/422; 428/421; 430/005 |
International
Class: |
B32B 027/00 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 15, 2000 |
JP |
2000-072718 |
Claims
What is claimed is:
1. A pellicle for a photolithographic patterning process by means
of a light having a wavelength of at most 200 nm, comprising a
frame and a pellicle membrane bonded to the frame by means of an
adhesive, wherein the pellicle membrane or the adhesive comprises
the following fluorine-containing polymer (A): fluorine-containing
polymer (A): a substantially linear fluorine-containing polymer
having a chain of carbon atoms as the main chain, and containing as
carbon atoms in its main chain, a carbon atom having one or two
hydrogen atoms bonded thereto and a carbon atom having no hydrogen
atom bonded thereto and having a fluorine atom or a
fluorine-containing organic group bonded thereto.
2. The pellicle according to claim 1, wherein the
fluorine-containing polymer (A) is a polymer having monomer units
formed by polymerization of a monomer (b) represented by
CHR.sup.1.dbd.CR.sup.2R.sup.3, wherein each of R.sup.1, R.sup.2 and
R.sup.3 which are independent of one another, is a hydrogen atom, a
fluorine atom or a monovalent organic group, and monomer units
formed by polymerization of a monomer (c) represented by
CFR.sup.4.dbd.CR.sup.5R.sup.6, wherein each of R.sup.4, R.sup.5 and
R.sup.6 which are independent of one another, is a fluorine atom or
a monovalent fluorine-containing organic group, or R.sup.4 and
R.sup.5 together form a bivalent fluorine-containing organic group
and R.sup.6 is a fluorine atom or a monovalent fluorine-containing
organic group, or R.sup.5 and R.sup.6 together form a bivalent
fluorine-containing organic group and R.sup.4 is a fluorine atom or
a monovalent fluorine-containing organic group.
3. The pellicle according to claim 2, wherein the monomer (b) is at
least one monomer selected from olefins and fluoroolefins having a
hydrogen atom bonded to a carbon atom in an unsaturated group, and
the monomer (c) is a fluorine-containing unsaturated alicyclic
monomer which may have an oxygen atom as an atom constituting the
ring.
4. The pellicle according to claim 1, wherein the
fluorine-containing polymer (A) is a polymer having monomer units
formed by cyclic polymerization of a monomer (d) represented by
CH.sub.2.dbd.CR.sup.7-Q-CR- .sup.8.dbd.CF.sub.2, wherein each of
R.sup.7 and R.sup.8 which are independent of each other, is a
hydrogen atom, a fluorine atom or a monovalent fluorine-containing
organic group, and Q is a bivalent fluorine-containing organic
group.
5. The pellicle according to claim 1, wherein the
fluorine-containing polymer (A) is a polymer having monomer units
formed by polymerization of a fluorine-containing unsaturated
alicyclic monomer which may have an oxygen atom as an atom
constituting the ring, represented by
CFR.sup.4.dbd.CR.sup.5R.sup.6, wherein R.sup.4 and R.sup.5 together
form a bivalent fluorine-containing organic group and R.sup.6 is a
fluorine atom or a monovalent fluorine-containing organic group, or
R.sup.5 and R.sup.6 together form a bivalent fluorine-containing
organic group and R.sup.4 is a fluorine atom or a monovalent
fluorine-containing organic group, and monomer units formed by
cyclic polymerization of a monomer (d) represented by
CH.sub.2.dbd.CR.sup.7-Q-CR.sup.8.dbd.CF.sub.2, wherein each of
R.sup.7 and R.sup.8 which are independent of each other, is a
hydrogen atom, a fluorine atom or a monovalent fluorine-containing
organic group, and Q is a bivalent fluorine-containing organic
group.
6. The pellicle according to claim 4 or 5, wherein the monomer (d)
is a monomer represented by
CH.sub.2.dbd.CH--R.sup.f--O--CF.dbd.CF.sub.2, wherein R.sup.f is a
C.sub.1-4 perfluoroalkylene group.
7. A pellicle for a photolithographic patterning process by means
of a light having a wavelength of at most 200 nm, comprising a
frame and a pellicle membrane bonded to the frame by means of an
adhesive, wherein the pellicle membrane comprises a
fluorine-containing polymer which is the following
fluorine-containing polymer (A) and which has an alicyclic
structure in its main chain, provided that a part of atoms
constituting the alicyclic structure may be oxygen atoms:
fluorine-containing polymer (A): a substantially linear
fluorine-containing polymer having a chain of carbon atoms as the
main chain, and containing as carbon atoms in its main chain, a
carbon atom having one or two hydrogen atoms bonded thereto and a
carbon atom having no hydrogen atom bonded thereto and having a
fluorine atom or a fluorine-containing organic group bonded
thereto.
8. The pellicle according to claim 7, wherein the
fluorine-containing polymer (A) is a copolymer of at least one
monomer selected from olefins and fluoroolefins having a hydrogen
atom bonded to a carbon atom in an unsaturated group, and a
fluorine-containing unsaturated alicyclic monomer which may have an
oxygen atom as an atom constituting the ring, represented by
CFR.sup.4.dbd.CR.sup.5R.sup.6, wherein R.sup.4 and R.sup.5 together
form a bivalent fluorine-containing organic group and R.sup.6 is a
fluorine atom or a monovalent fluorine-containing organic group, or
R.sup.5 and R.sup.6 together form a bivalent fluorine-containing
organic group and R.sup.4 is a fluorine atom or a monovalent
fluorine-containing organic group.
9. The pellicle according to claim 7, wherein the
fluorine-containing polymer (A) is a polymer having monomer units
formed by cyclic polymerization of a monomer (d) represented by
CH.sub.2.dbd.CR.sup.7-Q-CR- .sup.8.dbd.CF.sub.2, wherein each of
R.sup.7 and R.sup.8 which are independent of each other, is a
hydrogen atom, a fluorine atom or a monovalent fluorine-containing
organic group, and Q is a bivalent fluorine-containing organic
group.
10. The pellicle according to claim 7, wherein the
fluorine-containing polymer (A) is a polymer having monomer units
formed by polymerization of a fluorine-containing unsaturated
alicyclic monomer which may have an oxygen atom as an atom
constituting the ring, represented by
CFR.sup.4.dbd.CR.sup.5R.sup.6, wherein R.sup.4 and R.sup.5 together
form a bivalent fluorine-containing organic group and R.sup.6 is a
fluorine atom or a monovalent fluorine-containing organic group, or
R.sup.5 and R.sup.6 together form a bivalent fluorine-containing
organic group and R.sup.4 is a fluorine atom or a monovalent
fluorine-containing organic group, and monomer units formed by
cyclic polymerization of a monomer (d) represented by
CH.sub.2.dbd.CR.sup.7-Q-CR.sup.8.dbd.CF.sub.2, wherein each of
R.sup.7 and R.sup.8 which are independent of each other, is a
hydrogen atom, a fluorine atom or a monovalent fluorine-containing
organic group, and Q is a bivalent fluorine-containing organic
group.
11. The pellicle according to claim 9 or 10, wherein the monomer
(d) is a monomer represented by
CH.sub.2.dbd.CH--R.sup.f--O--CF.dbd.CF.sub.2, wherein R.sup.f is a
C.sub.1-4 perfluoroalkylene group.
12. A pellicle for a photolithographic patterning process by means
of a light having a wavelength of at most 200 nm, comprising a
frame and a pellicle membrane bonded to the frame by means of an
adhesive, wherein the adhesive comprises the following
fluorine-containing polymer (A): fluorine-containing polymer (A): a
substantially linear fluorine-containing polymer having a chain of
carbon atoms as the main chain, and containing as carbon atoms in
its main chain, a carbon atom having one or two hydrogen atoms
bonded thereto and a carbon atom having no hydrogen atom bonded
thereto and having a fluorine atom or a fluorine-containing organic
group bonded thereto.
13. The pellicle according to claim 12, wherein the
fluorine-containing polymer (A) is a fluorine-containing polymer
having an alicyclic structure in its main chain, provided that a
part of atoms constituting the alicyclic structure may be oxygen
atoms.
14. The pellicle according to claim 12 or 13, wherein the
fluorine-containing polymer (A) is a fluorine-containing polymer
having functional groups.
15. The pellicle according to claim 12, wherein the
fluorine-containing polymer (A) is a fluorine-containing polymer
having no alicyclic structure in its main chain.
16. A photolithographic patterning process by means of a light
having a wavelength of at most 200 nm in photolithography, which
comprises using the pellicle as defined in claim 1, 7 or 12.
17. The photolithographic patterning process according to claim 16,
wherein the light having a wavelength of at most 200 nm is a
fluorine gas excimer laser light.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a pellicle for
photolithography using a light having a wavelength of at most 200
nm.
[0003] 2. Discussion of Background
[0004] A pellicle is a dustproof integral device to be mounted on a
photomask or a reticle (hereinafter they will be referred to as a
mask) so as to prevent dust particles from depositing on the mask
and to prevent pattern failure during exposure, used in
photolithography as one step in production of semiconductor devices
or liquid crystal display boards. As its structure, usually a
transparent thin membrane bonded to a frame by using adhesives is
mounted on the mask at some distance from the mask surface.
[0005] In fields of production of semiconductor devices and liquid
crystal display panels in which such a pellicle is used, the
wavelength of light sources to be used has been shortened rapidly
also in photolithography, along with minimization of wiring and
wiring interval. In a conventional exposure technique with a
minimum pattern dimension of at least 0.3 .mu.m, a process
employing an i-beam light source (365 nm) has been mainly used, and
as a material of a transparent thin membrane of a pellicle
(hereinafter referred to as a pellicle membrane), a cellulose
nitrate type material has been used.
[0006] In recent years, for a photolithographic patterning process
with a minimum pattern dimension of at most 0.3 .mu.m, a KrF
excimer laser is being introduced, but its irradiation wavelength
is 248 nm, and the cellulose nitrate type membrane material is
inadequate in view of durability. Further, it has been found that
an amorphous perfluoropolymer is effective as a membrane material
in the case where a light having a short wavelength such as an
excimer laser is employed (Japanese Patent No. 2951337 or Japanese
patent No. 2952962).
[0007] On the other hand, for a photolithographic patterning
process with a minimum pattern dimension of at most 0.2 .mu.m under
development in recent years, as a laser emitting a light having a
wavelength of at most 200 nm, use of e.g. an argon fluoride excimer
laser emitting a light having a wavelength of 193 nm (hereinafter
referred to as an ArF excimer laser) or a fluorine gas excimer
laser emitting a light having a wavelength of 157 nm (hereinafter
referred to as a F.sub.2 excimer laser) has been proposed.
[0008] However, since these laser lights have an extremely high
energy, even the above amorphous perfluoropolymer as disclosed in
Japanese Patent No. 2951337 is inadequate in view of durability.
For example, of "CYTOP" (Japanese tradename) which is a
perfluoropolymer used in the above patent, transmission of light
and durability suddenly decrease at a wavelength shorter than 170
nm. This perfluoropolymer has a significantly low transmission of
the F.sub.2 excimer laser light having a wavelength of 157 nm.
Therefore, development of a pellicle membrane which can be used for
F.sub.2 excimer laser light has been desired.
[0009] Moreover, with respect to adhesives for bonding the pellicle
membrane to a frame, there are similar problems of degradation due
to reflected light or scattering light of the laser. Thus the
adhesive having a high durability has also been desired.
SUMMARY OF THE INVENTION
[0010] The present inventors have found a fluorine-containing
polymer having a high durability and a high transmission of a laser
light for irradiation which has a wavelength of at most 200 nm
(particularly at most 180 nm) (hereinafter referred to as a
short-wavelength laser light). The present invention relates to a
pellicle employing this fluorine-containing polymer as a pellicle
membrane or as an adhesive.
[0011] Namely, the present invention provides a pellicle for an
exposure treatment by means of a light having a wavelength of at
most 200 nm, comprising a frame and a pellicle membrane bonded to
the frame by means of an adhesive, wherein the pellicle membrane or
the adhesive comprises the following fluorine-containing polymer
(A):
[0012] fluorine-containing polymer (A): a substantially linear
fluorine-containing polymer having a chain of carbon atoms as the
main chain, and containing as carbon atoms in its main chain, a
carbon atom having one or two hydrogen atoms bonded thereto and a
carbon atom having no hydrogen atom bonded thereto and having a
fluorine atom or a fluorine-containing organic group bonded
thereto.
BRIEF DESCRIPTION OF THE DRAWING
[0013] FIG. 1 is a diagram illustrating transmissions of light
through membranes comprising a polymer A, a polymer B, a polymer C,
a polymer D and a polymer E, respectively, as against a
wavelength.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0014] The pellicle of the present invention is particularly
suitable as a pellicle for a photolithographic patterning process
by means of a light having a wavelength of at most 180 nm, which is
a light having a wavelength shorter than that of an ArF excimer
laser light. Specifically, it is suitable as a pellicle for a
photolithographic patterning process by means of a F.sub.2 excimer
laser light having a wavelength of 157 nm.
[0015] The fluorine-containing polymer (A) of the present invention
is a substantially linear fluorine-containing polymer having a
chain of carbon atoms as the main chain. The chain of carbon atoms
as the main chain of the polymer comprises chains of two carbon
atoms constituting a polymerizable unsaturated bond of a monomer
connected in principle. Therefore, with respect to the
fluorine-containing polymer (A), "containing as carbon atoms in its
main chain, a carbon atom having one or two hydrogen atoms bonded
thereto and a carbon atom having no hydrogen atom bonded thereto
and having a fluorine atom or a fluorine-containing organic group
bonded thereto" means that in a case of a homopolymer obtained by
polymerization of a monomer having one polymerizable unsaturated
group, it is a polymer of a monomer having two carbon atoms
constituting a polymerizable unsaturated bond of the monomer, one
carbon atom having a hydrogen atom bonded thereto and the other
carbon atom having no hydrogen atom bonded thereto (hereinafter
referred to as a monomer (a)).
[0016] In a case of a copolymer, it may be a copolymer of a monomer
having two carbon atoms constituting a polymerizable unsaturated
bond, at least one of the two carbon atoms having a hydrogen atom
bonded thereto (hereinafter referred to as a monomer (b)) and a
monomer having two carbon atoms constituting a polymerizable
unsaturated bond, both of the two carbon atoms having no hydrogen
atom bonded thereto (hereinafter referred to as a monomer (c)).
[0017] Further, the fluorine-containing polymer (A) may be a
copolymer of at least two types of the monomer (a), or it may be a
copolymer of the monomer (a) and another monomer. Further, it may
be a copolymer of the monomer (b), the monomer (c) and another
monomer.
[0018] The fluorine-containing polymer (A) may be a polymer
obtained by cyclic polymerization of a monomer having two
polymerizable unsaturated bonds. In the case of this polymer,
usually four carbon atoms constituting the two polymerizable
unsaturated bonds form the main chain of the polymer. Therefore,
said fluorine-containing polymer (A) is a polymer obtained by
cyclic polymerization of a monomer having four carbon atoms
constituting two polymerizable unsaturated bonds, at least one of
the carbon atoms having a hydrogen atom bonded thereto, and at
least one of the carbon atoms having no hydrogen atom bonded
thereto (hereinafter referred to as monomer (d)).
[0019] In a case of a copolymer, it may be a copolymer of a monomer
having four carbon atoms, each having no hydrogen atom bonded
thereto (hereinafter referred to as monomer (e)) and a monomer
which has a carbon atom having a hydrogen atom bonded thereto in a
polymerizable unsaturated bond (said monomer may be a monomer
having two polymerizable unsaturated bonds, which may undergo
cyclic polymerization, or may be a monomer having one polymerizable
unsaturated bond) (hereinafter referred to as monomer (f)).
Further, the fluorine-containing polymer (A) may be a copolymer of
the monomer (d) and another monomer, or it may be a copolymer of
the monomer (e), the monomer (f) and another monomer.
[0020] Since the fluorine-containing polymer (A) is a polymer
having fluorine, the above monomers (a), (c), (d) and (e) have to
have a fluorine atom or a fluorine-containing organic group bonded
to a carbon atom in the polymerizable unsaturated bond. It is not
essential for the monomers (b) and (f) to have a fluorine atom or a
fluorine-containing organic group is bonded to a carbon atom in the
polymerizable unsaturated bond. However, they may have such an atom
or a group bonded to a carbon atom.
[0021] As the fluorine-containing organic group, preferred are a
monovalent group and a bivalent group. In the case of a bivalent
fluorine-containing organic group, it may be bonded to each of two
carbon atoms in the polymerizable unsaturated bond (whereby a ring
containing the two carbon atoms is formed), or it may be bonded to
one of the two carbon atoms (whereby a ring containing said one
carbon atom is formed, and the other carbon atom is a carbon atom
outside the ring).
[0022] The monomers (a) to (f) may have an atom, an organic group
or another substituent other than a hydrogen atom, a fluorine atom
and a fluorine-containing organic group, on the carbon atom in the
polymerizable unsaturated bond. For example, they may have a
halogen atom other than a fluorine atom, such as a chlorine atom,
or an organic group such as an alkyl group. However, with respect
to a polymer having a large number of organic groups such as alkyl
groups in its side chains, hydrogen atoms bonded to the carbon
atoms tend to decrease the durability, thus the number of such
substituents is preferably small.
[0023] As the monovalent fluorine-containing organic group, the
preferred one is a fluorine-containing alkyl group or a
fluorine-containing alkoxy group. The carbon number of such a group
is preferably at most 10, particularly preferably at most 4. Such a
group preferably contains no hydrogen, and preferred is a group
containing fluorine atoms alone (i.e. a perfluoroalkyl group or a
perfluoroalkoxy group), or a perhalo-polyfluoroalkyl group or a
perhalo-polyfluoroalkoxy group containing fluorine atoms and a
small number of chlorine atoms as compared with the number of
fluorine atoms. Further, in a case of the fluorine-containing
polymer (A) to be used as an adhesive, a fluorine-containing
organic group having a functional group effective for improvement
in adhesion may be contained. The monovalent fluorine-containing
organic group is not limited to a linear one, and may be
branched.
[0024] As the bivalent fluorine-containing organic group, preferred
is a polyfluoroalkylene group having a carbon number of at most 10
(particularly preferably at most 6) which may contain an etherial
oxygen atom. As the polyfluoroalkylene group, preferred is a
perfluoroalkylene group or a perhalo-polyfluoroalkylene group
containing a small number of chlorine atoms. The etherial oxygen
atom may be present on one terminal of the polyfluoroalkylene
group, may be present on each terminal, or may be present between
carbon atoms. The bivalent fluorine-containing organic group is not
limited to a linear one, and may be branched.
[0025] As a monovalent organic group other than the monovalent
fluorine-containing organic group, preferred is an alkyl group or
an alkoxy group containing no fluorine atom or monovalent
fluorine-containing organic group as mentioned above. The carbon
number of the alkyl group or alkoxy group is preferably at most 10,
particularly preferably at most 4. As said monovalent organic group
other than the monovalent fluorine-containing organic group,
particularly preferred is a methyl group.
[0026] A polymer having crystalline property tends to decrease
transmission due to light scattering and to cause distortion of a
reticle image. Therefore, the fluorine-containing polymer (A) is
preferably amorphous with a crystalline property of at most 30%,
particularly preferably at most 20%. The crystalline property of
the polymer can be lowered by introducing a bulky structure into a
polymer chain. Therefore, it is preferred to make an alicyclic
structure having a bulky structure be present in the main chain of
the polymer to reduce crystallization of the polymer and to obtain
an amorphous polymer having a high transparency. Therefore, as the
fluorine-containing polymer (A), particularly preferred is a
fluorine-containing polymer having an alicyclic structure in its
main chain.
[0027] "Having an alicyclic structure in its main chain" means that
at least one carbon atom in the main chain is a carbon atom
constituting the alicyclic structure. This alicyclic structure is
preferably a fluorine-containing alicyclic structure having a
fluorine atom or a fluorine-containing organic group bonded to at
least one carbon atom constituting the alicyclic structure.
Further, a part of atoms constituting the alicyclic structure may
be an atom other than a carbon atom, such as an oxygen atom or a
nitrogen atom. Preferred as the alicyclic structure is a 4- to
8-membered fluorine-containing alicyclic structure having one or
two oxygen atoms.
[0028] By using a monomer having a polymerizable unsaturated group
in an alicyclic structure, a polymer having an alicyclic structure
in its main chain can be obtained. The monomer (d) or (e) forms a
polymer having an alicyclic structure in its main chain by cyclic
polymerization. "Having a polymerizable unsaturated group in an
alicyclic structure" means that a polymerizable unsaturated group
is present between carbon atoms constituting the alicyclic
structure, or a polymerizable unsaturated group is present between
a carbon atom constituting the ring and a carbon atom outside the
ring. As the alicyclic structure, preferred is a
fluorine-containing alicyclic structure, and it may have an oxygen
atom as an atom constituting the ring, as mentioned above.
[0029] Hereinafter the monomer having a polymerizable unsaturated
group in a fluorine-containing alicyclic structure will be referred
to as a fluorine-containing unsaturated alicyclic monomer. As atoms
constituting the ring in the fluorine-containing unsaturated
alicyclic monomer, one or two oxygen atoms may be contained in
addition to carbon atoms. The monomer (c) is preferably a
fluorine-containing unsaturated alicyclic monomer. The monomer (a),
(b) or (f) may be a fluorine-containing unsaturated alicyclic
monomer.
[0030] As the monomer (a), preferred is vinylidene fluoride or
trifluoroethylene. However, a homopolymer of such a monomer tends
to be crystalline, and tends to have a low transparency.
[0031] As the monomer (b), preferred is a monomer represented by
CHR.sup.1.dbd.CR.sup.2R.sup.3, wherein each of R.sup.1, R.sup.2 and
R.sup.3 which are independent of one another, is a hydrogen atom, a
fluorine atom or a monovalent organic group. Each of R.sup.1 and
R.sup.2 is preferably a hydrogen atom or a fluorine atom, and
R.sup.3 is preferably a hydrogen atom, a fluorine atom or a
monovalent organic group having a carbon number of at most 4.
Specifically, an olefin such as ethylene or propylene, or a
fluoroolefin having a hydrogen atom bonded to a carbon atom in a
polymerizable unsaturated group, such as vinyl fluoride,
1,2-difluoroethylene, vinylidene fluoride or trifluoroethylene, may
be mentioned. As the monomer (b), preferred are a C.sub.2-3 olefin
and a C.sub.2-3 fluoroolefin. Particularly preferred as the monomer
(b) are an olefin selected from ethylene and propylene and a
fluoroolefin selected from vinyl fluoride, 1,2-difluoroethylene and
vinylidene fluoride.
[0032] As the monomer (c), preferred is a monomer represented by
CFR.sup.4.dbd.CR.sup.5R.sup.6, wherein each of R.sup.4, R.sup.5 and
R.sup.6 which are independent of one another, is a fluorine atom or
a monovalent fluorine-containing organic group, or R.sup.4 and
R.sup.5 together form a bivalent fluorine-containing organic group
and R.sup.6 is a fluorine atom or a monovalent fluorine-containing
organic group, or R.sup.5 and R.sup.6 together form a bivalent
fluorine-containing organic group and R.sup.4 is a fluorine atom or
a monovalent fluorine-containing organic group. The monomer (c)
wherein R.sup.4 and Rs together form a bivalent fluorine-containing
organic group and R.sup.6 is a fluorine atom or a monovalent
fluorine-containing organic group, or R.sup.5 and R.sup.6 together
form a bivalent fluorine-containing organic group and R.sup.4 is a
fluorine atom or a monovalent fluorine-containing organic group, is
one type of a fluorine-containing unsaturated alicyclic monomer,
and hereinafter such a monomer will be referred to as a
fluorine-containing unsaturated alicyclic monomer (c).
[0033] As the monomer (c), specifically, a polyfluoroolefin having
no hydrogen atom, such as tetrafluoroethylene,
chlorotrifluoroethylene or hexafluoropropylene, perfluoro(alkyl
vinyl ether) or a fluorine-containing unsaturated alicyclic monomer
(c) represented by the following formula 1, 2 or 3, may, for
example, be mentioned. Particularly preferred as the monomer (c) is
perfluoro(2,2-dimethyl-1,3-dioxole) i.e. a compound represented by
the formula 1 wherein both R.sup.11 and R.sup.12 are
trifluoromethyl groups. 1
[0034] In the above formulae 1 to 3, each of R.sup.11 to R.sup.16
which are independent of one another, is a fluorine atom or a
fluorine-containing organic group, and as the fluorine-containing
organic group, preferred is a perfluoroalkyl group, and
particularly preferred is a perfluoroalkyl group having a carbon
number of 1 or 2.
[0035] The fluorine-containing polymer (A) comprising a copolymer
of the monomers (b) and (c) may be a polymer having no
fluorine-containing alicyclic structure in its main chain, such as
an ethylene/tetrafluoroeth- ylene copolymer, a
propylene/tetrafluoroethylene copolymer, a propylene/vinylidene
fluoride/tetrafluoroethylene copolymer or a vinylidene
fluoride/hexafluoropropylene copolymer, but their transparency is
not adequate. However, they are useful as an adhesive for bonding a
membrane to a frame. Preferred as the fluorine-containing polymer
(A) is a copolymer of the monomer (b) with the fluorine-containing
unsaturated alicyclic monomer (c) represented by the above formula
1, 2 or 3. In such a case, as the monomer (b), preferred is at
least one monomer selected from olefins such as ethylene and
fluoroolefins having a hydrogen atom bonded to a carbon atom in the
unsaturated group.
[0036] The proportion of monomer units formed by polymerization of
the monomer (b) (hereinafter referred to as monomer units (b), and
the same applies to the other monomer units) in the copolymer of
the monomer (b) and the monomer (c) to the total of the monomer
units (b) and the monomer units (c) is preferably from 10 to 70 mol
%. In a case where the monomer (b) is a monomer having at least two
hydrogen atoms (hydrogen atoms bonded to a carbon atom in a
polymerizable unsaturated bond) such as ethylene, it is preferably
from 10 to 50 mol %. The proportion of the monomer units (b) is
particularly preferably from 20 to 40 mol %. In the case of the
fluorine-containing polymer (A) for an adhesive, a polymer having a
proportion of the monomer units (b) to the total of the monomer
units (b) and the monomer units (c) of from 40 to 85 mol % is also
preferred.
[0037] Here, the proportion of the total of the monomer units (b)
and the monomer units (c) to the total monomer units in the polymer
is preferably from 50 to 100 mol %, particularly preferably from 80
to 100 mol %. The most preferred polymer is a copolymer of the
monomer (b) and the monomer (c) alone, provided that each monomer
may consist of at least two types.
[0038] As the monomer (d), preferred is a monomer represented by
CH.sub.2.dbd.CR.sup.7-Q-CR.sup.8.dbd.CF.sub.2, wherein each of
R.sup.7 and R.sup.8 which are independent of each other, is a
hydrogen atom, a fluorine atom or a monovalent fluorine-containing
organic group, and Q is a bivalent fluorine-containing organic
group. As R.sup.7, preferred is a hydrogen atom or a fluorine atom,
and particularly preferred is a hydrogen atom. As R.sup.8,
preferred is a fluorine atom or a perfluoroalkyl group having a
carbon number of at most 2, and particularly preferred is a
fluorine atom.
[0039] As Q, preferred is a perfluoroalkylene group having a carbon
number of at most 10, which may have an etherial oxygen atom. The
etherial oxygen atom may be present at one terminal of the
perfluoroalkylene group, may be present on each terminal, or may be
present between carbon atoms. In a case of a perfluoroalkylene
group having no etherial oxygen atom, the carbon number is more
preferably from 2 to 6, in the case of a perfluoroalkylene group
having an etherial oxygen atom on one terminal or between carbon
atoms, the carbon number is more preferably from 1 to 4, and in the
case of a perfluoroalkylene group having an etherial oxygen atom on
each terminal, the carbon number is more preferably from 1 to 3.
The total number of oxygen atoms and carbon atoms excluding carbon
atoms at a branched moiety, is most preferably from 2 to 4.
[0040] As Q, preferred is a perfluoroalkylene group having a carbon
number of at most 4 and having an etherial oxygen atom at a
2,2-difluorovinyl group side, a perfluoroalkylene group having a
carbon number of at most 4 and having an etherial oxygen atom
between carbon atoms, or a perfluoroalkylene group having a carbon
number of at most 4 and having no etherial oxygen atom. More
preferred as Q is a perfluoroalkylene group having a carbon number
of at most 4 and having an etherial oxygen atom at a
2,2-difluorovinyl group side.
[0041] That is to say, the most preferred monomer (d) is a monomer
represented by CH.sub.2.dbd.CH--R.sup.f--O--CF.dbd.CF.sub.2,
wherein R.sup.f is a C.sub.1-4 perfluoroalkylene group. This
monomer is polymerized easily by cyclopolymerization, and, a
polymer having a high transmission to a short-wavelength light and
having a high mechanical strength can be obtained (JP-A-63-238111,
JP-A-63-238113). As R.sup.f, preferred is a perfluoroalkylene group
having a carbon number of from 1 to 3 excluding a branch. In a case
where R.sup.f is branched, the branch is preferably a
trifluoromethyl group, and the number of the branch is preferably
from 1 to 2.
[0042] Here, by cyclic polymerization of
CH.sub.2.dbd.CR.sup.7-Q-CR.sup.7.- dbd.CF.sub.2, monomer units
represented by e.g. the following formula 4, 5 or 6 are usually
formed. As the monomer (d) represented by
CH.sub.2.dbd.CR.sup.7-Q-CR.sup.8.dbd.CF.sub.2, the following
compounds may, for example, be mentioned. 2
CH.sub.2.dbd.CHCF.sub.2CF.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CHCF.sub.2CF.sub.2CF.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CHCF.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CHCF(CF.sub.3)CF.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CHCF.sub.2OCF.sub.2CF.dbd.CF.sub.2,
CH.sub.2.dbd.CHCF.sub.2CCl.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CFCF.sub.2CF.sub.2OCF.dbd.CF.sub.2,
CH.sub.2.dbd.CFCF(CF.sub.3)CF.sub.2OCF.dbd.CF.sub.2.
[0043] The fluorine-containing polymer (A) may be a homopolymer of
the monomer (d), provided that it may be a copolymer of at least
two types of the monomer (d), or may be a copolymer of the monomer
(d) with another monomer. As said another monomer, the monomer (a),
(b), (c) or (e) may, for example, be mentioned. As the copolymer,
preferred is a copolymer of the monomer (d) and the monomer (c) or
a copolymer of the monomer (d) and the monomer (e), and more
preferred is a copolymer of the monomer (d) and the monomer (c). In
such a case, as the monomer (c), preferred is the above
fluorine-containing unsaturated alicyclic monomer (c).
[0044] The proportion of the monomer units (d) to the total monomer
units in the fluorine-containing polymer (A) is suitably from 30 to
100%, preferably from 50 to 100%, and most preferably 100%.
[0045] As the monomer (e), preferred is a monomer having all
hydrogen atoms bonded to carbon atoms in the polymerizable
unsaturated group in the monomer (d) replaced by fluorine atoms or
perfluoroalkyl groups. More preferred is a monomer represented by
CF.sub.2.dbd.CR.sup.9-Q-CR.sup.10.d- bd.CF.sub.2, wherein each of
R.sup.9 and R.sup.10 which are independent of each other, is a
fluorine atom or a monovalent fluorine-containing organic group,
and Q is as defined above. However, the position or the number of
the etherial oxygen atom in Q is not restricted. Specifically, the
following monomers may be mentioned.
CF.sub.2.dbd.CFCF.sub.2CF.sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFCF.sub.2CF.sub.2CF.sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFCF.sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFCF(CF.sub.3)CF.sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFOCF.sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFOC(CF.sub.3).sub.2OCF.dbd.CF.sub.2,
CF.sub.2.dbd.CFCF.sub.2CCl.sub.2OCF.dbd.CF.sub.2.
[0046] As the monomer (f), the above monomer (a) or (b) may be
used. The monomer (b) is particularly preferred. In
copolymerization of the monomer (e) and the monomer (f), the
monomer (e) forms monomer units having a fluorine-containing
alicyclic structure by cyclic polymerization, and a copolymer
having the monomer units (e) and the monomer units (f) will be
formed. The copolymer having the monomer units (e) and the monomer
units (f) may further have another monomer units such as the above
monomer units (c).
[0047] In the copolymer of the monomer (e) and the monomer (f), the
proportion of the monomer units (f) to the total of the monomer
units (e) and the monomer units (f) is preferably from 10 to 70 mol
%. In the case of the monomer (f) having at least two hydrogen
atoms (hydrogen atoms bonded to carbon atoms in the polymerizable
unsaturated bond) such as ethylene, it is preferably from 10 to 60
mol %. The proportion of the monomer units (f) is particularly
preferably from 20 to 50 mol %. Here, the proportion of the total
of the monomer units (e) and the monomer units (f) to the total
monomer units in the polymer is preferably from 50 to 100 mol %,
particularly preferably from 70 to 100 mol %.
[0048] The fluorine-containing polymer (A) is preferably a polymer
containing monomer units having a fluorine-containing alicyclic
structure, as mentioned above. The proportion of the monomer units
having a fluorine-containing alicyclic structure to the total
monomer units in the fluorine-containing polymer (A) is preferably
at least 20 mol %, particularly preferably at least 40 mol %.
[0049] Particularly preferred as the fluorine-containing polymer
(A) are a copolymer of ethylene and
perfluoro(2,2-dimethyl-1,3-dioxole), a homopolymer of the monomer
(d) and the copolymer of the fluorine-containing unsaturated
alicyclic monomer (c) and the monomer (d).
[0050] According to studies by the present inventors, it is
considered that if carbon atoms having a fluorine atom bonded
thereto (particularly CF.sub.2 groups) alone are continuously
present in a large amount in the chain of carbon atoms in the main
chain of the fluorine-containing polymer (A), the electron
transition energy of said part will decrease, whereby a light
having a wavelength of at most 170 nm tends to be absorbed, and a
transmission will be lowered. It is considered that the same
applies to a case where carbon atoms having hydrogen atoms bonded
thereto (particularly CH.sub.2 groups) alone are continuously
present in a large amount. Therefore, it is unfavorable that a
block of continuous monomer units such as the monomer units (c) or
(e) alone in a large amount is present in the polymer (the same
applies to the other monomer units such as the monomer units (b) or
(f)).
[0051] With respect to the above chain of the monomer units alone,
the number of the monomer units is preferably at most 10,
particularly preferably at most 8, on the average in the entire
polymer. Therefore, the fluorine-containing polymer (A) as a
copolymer is preferably a random copolymer, as well as having the
above proportion of the monomer units.
[0052] A pellicle membrane is usually produced by using a solution
of the fluorine-containing polymer (A). The solvent is not
particularly limited so long as it dissolves the polymer, and
preferred is a fluorine-containing solvent in which the polymer is
highly soluble. For example, the following fluorine-containing
solvents may be used.
[0053] Polyfluoroaromatic compounds such as perfluorobenzene,
pentafluorobenzene and 1,3-bis(trifluoromethyl)benzene.
Polyfluorotrialkylamine compounds such as perfluorotributylamine
and perfluorotripropylamine. Polyfluorocycloalkane compounds such
as perfluorodecalin and perfluorocyclohexane. Polyfluorocyclic
ether compound such as perfluoro(2-butyltetrahydrofuran).
[0054] Polyfluoroalkanes such as perfluorooctane, perfluorodecane,
1,3-dichloro-1,1,2,2,3-pentafluoropropane, 2H,3H-perfluoropentane
and 1H-perfluorohexane. Polyfluoroethers such as methyl
perfluoroisopropyl ether, methyl perfluorobutyl ether, methyl
(perfluorohexylmethyl) ether, methyl perfluorooctyl ether and ethyl
perfluorobutyl ether.
[0055] As a method of producing a pellicle membrane from the
polymer solution, a method of forming a thin membrane of the
polymer on a substrate by means of several coating methods from the
solution, such as roll coating, casting, dip coating, spin coating,
water casting, die coating or Langmuir Blodgett, may be employed.
The thickness of the membrane is usually selected within a range of
from 0.01 to 50 .mu.m. In the case of a pellicle membrane,
extremely strict membrane thickness control is required, and
therefore it is more preferred to employ spin coating. As the
substrate, preferred is a silicon wafer, quartz glass or the like
having a smooth surface.
[0056] As the fluorine-containing polymer (A) for an adhesive,
preferred is a polymer similar to the fluorine-containing polymer
(A) preferred as a pellicle membrane. For example, a copolymer of
the fluorine-containing unsaturated alicyclic monomer (c) and the
monomer (b), a polymer of the monomer (d) or a copolymer of the
monomer (e) and the monomer (f) is preferred. Further, for the
fluorine-containing polymer (A) for an adhesive, a high
transparency is not necessarily required, and therefore it may be
the polymer having no fluorine-containing alicyclic structure in
its main chain. Therefore, a copolymer of the monomer (b) and the
monomer (c) other than the fluorine-containing unsaturated
alicyclic monomer (c) (i.e. the fluorine-containing polymer (A)
having no alicyclic structure in its main chain) may also be used
as a preferred adhesive.
[0057] The fluorine-containing polymer (A) having no alicyclic
structure in its main chain may, for example, be a
propylene/vinylidene fluoride/tetrafluoroethylene copolymer or a
vinylidene fluoride/hexafluoropropylene copolymer. In such a
polymer, the proportion of the monomer units (b) to the total of
the monomer units (c) and the monomer units (b) is preferably from
40 to 85 mol %, particularly preferably from 50 to 80 mol %.
[0058] Further, in a case where the fluorine-containing polymer (A)
is used as an adhesive for bonding a pellicle membrane to a frame
for a pellicle, it is preferred to use the fluorine-containing
polymer (A) having functional groups effective for improvement in
adhesion introduced thereinto. Here, the fluorine-containing
polymer (A) for a pellicle membrane preferably contains no
functional group from the viewpoint of transmission of light.
[0059] The functional group in the fluorine-containing polymer (A)
containing functional groups, is not particularly limited so long
as it can present adhesion to a frame or a pellicle membrane, and a
carboxylic acid group, a sulfonic acid group, a group having an
ester linkage, an alkenyl group, a hydrolyzablel silyl group, a
hydroxyl group, a maleimide group, an amino group, a cyano group or
an isocyanate group may, for example, be mentioned. As the
functional group, particularly suitable is a carboxylic acid group
from the viewpoint of excellent adhesion to a metal such as
aluminum as a frame material, excellent storage stability and
effective adhesion obtainable at a relatively low temperature.
[0060] The number of the functional groups in the
fluorine-containing polymer (A) is preferably from 0.001 to 1 mmol
per g of the polymer. In a case where the number of the functional
groups exceeds 1 mmol, there is a possibility that absorption by
the functional groups may impair durability of the adhesive.
[0061] A polymer having a fluorine-containing alicyclic structure
in its main chain and having adhesive functional groups introduced
thereinto and a production method thereof are known (JP-A-4-189880,
JP-A-4-226177, JP-A-6-220232). The known polymer having a
fluorine-containing alicyclic structure in its main chain is a
copolymer of the above monomer (c) or a polymer of the monomer
(e).
[0062] Also with respect to the fluorine-containing polymer (A)
having functional groups, functional groups can be introduced in
the same manner as the above known polymer. For example, a method
of utilizing terminal groups of the polymer obtained by
polymerization, a method of copolymerizing a monomer having an
alkoxycarbonyl group and subjecting the resulting polymer to
hydrolysis, or a method of subjecting a polymer to a
high-temperature treatment so that side chains or terminals of the
polymer undergo oxidative destruction to form functional groups,
may, for example, be mentioned.
[0063] Further, with the fluorine-containing polymer (A) or the
fluorine-containing polymer (A) containing functional groups to be
used as an adhesive, an adhesion promotor such as a silane type,
epoxy type, titanium type or aluminum type coupling agent, may be
mixed so as to improve adhesion. Further, it is also possible to
thinly coat the fluorine-containing polymer (A) containing
functional groups on a frame, and to apply the fluorine-containing
polymer (A) having no functional group thereto, so as to obtain
strong adhesion.
[0064] Now, the present invention will be explained in further
detail with reference to Examples. However, it should be understood
that the present invention is by no means restricted to such
specific Examples.
EXAMPLE 1
[0065] Synthesis Example of Fluorine-Containing Polymer (A)
[0066] 20 g of 1,1,2,4,4,5,5-heptafluoro-3-oxa-1,6-heptadiene
(CH.sub.2.dbd.CHCF.sub.2CF.sub.2OCF.dbd.CF.sub.2) and 40 g of
trichlorotrifluoroethane were put in an autoclave made of
pressure-resistant glass having an internal volume of 200 ml, the
atmosphere in which was replaced by nitrogen. As a polymerization
initiator, 20 mg of bis(heptafluorobutyryl)peroxide was added, the
atmosphere in the autoclave was replaced by nitrogen again, and
polymerization was carried out at 18.degree. C. for 10 hours. As a
result, 10 g of an amorphous polymer having a fluorine-containing
alicyclic structure in its main chain (hereinafter referred to as
polymer A) was obtained.
[0067] The intrinsic viscosity [.eta.] of the polymer A was 0.96 in
1,3-bis(trifluoromethyl)benzene at 30.degree. C. The polymer A had
a glass transition temperature of 90.degree. C., was a tough
transparent vitreous polymer, and had a refractive index of
1.36.
[0068] On the other hand, the polymer A obtained by the same method
as mentioned above, was subjected to a heat treatment in air at
320.degree. C. for 3 hours and soaked in water for modification.
From IR spectrum measurement of the modified polymer A, a peak
assigned to carboxyl groups was confirmed, with an amount of 0.005
mmol/g. Hereinafter this modified polymer A will be referred to as
adhesive A.
EXAMPLE 2
[0069] Synthesis Example of Fluorine-Containing Polymer (B)
[0070] Perfluoro(2,2-dimethyl-1,3-dioxole) (hereinafter referred to
as PDD) and ethylene with a molar ratio of 70:30 were subjected to
radical polymerization using diisopropyl peroxydicarbonate as an
initiator to obtain an amorphous polymer having a
fluorine-containing alicyclic structure in its main chain
(hereinafter referred to as polymer B) having a glass transition
temperature of 80.degree. C. and a 10% heat decomposition
temperature of 330.degree. C. The polymer B was a tough transparent
polymer having an elastic modulus of 1.6 GPa at room temperature,
and had a refractive index of 1.35.
EXAMPLE 3
[0071] Synthesis Example of Fluorine-Containing Polymer (C)
[0072] 30 g of
1,1,2,4,5,5-hexafluoro-3-oxa-4-trifluoromethyl-1,6-heptadie- ne
(CH.sub.2.dbd.CHCF(CF.sub.3)CF.sub.2OCF.dbd.CF.sub.2) and 70 g of
1H-perfluorohexane(CF.sub.3CF.sub.2CF.sub.2CF.sub.2CF.sub.2CF.sub.2H)
were put in an autoclave made of pressure-resistant glass having an
internal volume of 100 ml, the atmosphere in which was replaced by
nitrogen.
[0073] 17 mg of bis(heptafluorobutyryl)peroxide as a polymerization
initiator was added, and the atmosphere in the autoclave was
replaced by nitrogen again, and polymerization was carried out at
25.degree. C. for 20 hours. As a result, 24 g of an amorphous
polymer having a fluorine-containing alicyclic structure in its
main chain (hereinafter referred to as polymer C) was obtained.
[0074] The intrinsic viscosity [.eta.] of the polymer C was 0.60 in
perfluoro(2-butyltetrahydrofuran) at 30.degree. C. The polymer C
had a glass transition temperature of 108.degree. C., was a tough
transparent vitreous polymer at room temperature, and had a
refractive index of 1.34.
EXAMPLE 4
[0075] Synthesis Example of Fluorine-Containing Polymer (D)
[0076] 20 g of
1,1,2,4,5,5-hexafluoro-3-oxa-4-trifluoromethyl-1,6-heptadie- ne,
7.5 g of PDD and 70 g of 1H-perfluorohexane were put in an
autoclave made of pressure-resistant glass having an internal
volume of 100 ml, the atmosphere in which was replaced by
nitrogen.
[0077] 23 mg of bis(heptafluorobutyryl)peroxide as a polymerization
initiator was added, the atmosphere in the autoclave was replaced
by nitrogen again, and polymerization was conducted at 25.degree.
C. for 30 hours. As a result, 15 g of an amorphous polymer having a
fluorine-containing alicyclic structure in its main chain
(hereinafter referred to as polymer D) was obtained.
[0078] The intrinsic viscosity [.eta.] of the polymer D was 0.45 in
perfluoro(2-butyltetrahydrofuran) at 30.degree. C. The polymer D
was a tough transparent vitreous polymer at room temperature.
EXAMPLE 5
[0079] Synthesis Example of Perfluoropolymer
[0080] 35 g of perfluoro(butenyl vinyl ether), 150 g of deionized
water, 6 g of methanol as a chain transfer agent and 90 mg of
diisopropyl peroxydicarbonate as a polymerization initiator were
put in an autoclave made of pressure-resistant glass having an
internal volume of 200 ml. The atmosphere in the autoclave was
replaced by nitrogen, and suspension polymerization was carried out
at 40.degree. C. for 22 hours to obtain 33 g of an amorphous
perfluoropolymer having a fluorine-containing alicyclic structure
in its main chain and having terminal groups (--COF groups) derived
from the initiator.
[0081] The intrinsic viscosity [.eta.] of the polymer was 0.35 in
perfluoro(2-butyltetrahydrofuran) at 30.degree. C., and the glass
transition temperature was 108.degree. C. The polymer was a tough
transparent vitreous polymer at room temperature, and had a 10%
thermal decomposition temperature of 465.degree. C.
[0082] This polymer was dissolved in perfluorotributylamine so that
the concentration became 6%, the solution was put in an autoclave
made of nickel having an internal volume of 1 Q, and a 20% fluorine
gas was introduced until the pressure became 0.7 MPa.G, followed by
fluorination with stirring at 195.degree. C. for 10 hours, to
obtain a polymer having no terminal group derived from the
initiator (hereinafter referred to as polymer E). The infrared
absorption spectrum of the compression molded film of the obtained
polymer was measured, whereupon no characteristic absorption at
1,883 cm.sup.-1 derived from --COF groups was confirmed.
[0083] On the other hand, the amorphous perfluoropolymer having
terminal groups (--COF groups) derived from the initiator, obtained
by the same method as mentioned above, was subjected to heat
treatment in air at 320.degree. C. for 3 hours and then soaked in
water for modification. By measuring IR spectrum of the modified
polymer, a peak assigned to carboxyl groups was confirmed with an
amount of 0.02 mmol/g. Hereinafter the modified polymer will be
referred to as an adhesive E.
EXAMPLE 6
[0084] 7 g of the polymer A and 93 g of
1,3-bis(trifluoromethyl)benzene were put in a flask made of glass,
followed by heating at 40.degree. C. for 24 hours with stirring. As
a result, a uniform colorless and transparent solution without
turbidity was obtained. This solution was coated on a polished
glass plate by spin coating for 10 seconds at 500 rpm and for 20
seconds at 2,000 rpm, followed by heat treatment for 1 hour at
80.degree. C. and further for 1 hour at 180.degree. C. to obtain a
uniform transparent membrane on the glass plate.
[0085] On the other hand, a solution obtained by treating 7 g of
the adhesive A and 93 g of 1,3-bis(trifluoromethyl)benzene in the
same manner as mentioned above, was coated on an aluminum frame,
followed by drying at room temperature for 2 hours. Then, the
aluminum frame was put on a hot plate at 120.degree. C. so that the
adhesive surface turned up, followed by heating for 10 minutes, and
the above glass plate having the membrane of the polymer A formed
thereon was press-bonded on the frame so that the membrane face the
frame, and the assembly was held at 120.degree. C. for 10 minutes
to complete bonding. Then, the membrane was separated from the
glass plate to obtain a pellicle comprising the aluminum frame and
a uniform self-supporting membrane of about 1 .mu.m thickness
comprising the polymer A bonded to the frame.
[0086] Using 7 g of the polymer B and 93 g of
1,3-bis(trifluoromethyl)benz- ene, using 7 g of the polymer C and
93 g of perfluorotributylamine, and using 7 g of the polymer D and
93 g of perfluorotributylamine, pellicles comprising an aluminum
frame and a uniform self-supporting membrane of about 1 .mu.m
thickness comprising each polymer bonded to the frame, were
obtained. Each of these membranes had a transmission of light
having a wavelength of 157 nm of at least 95%.
[0087] The pellicles having a membrane comprising each of the
polymers A to D were subjected to an irradiation test by means of a
F.sub.2 excimer laser light having a wavelength of 157 nm, to be
used for photolithography, whereupon the membranes comprising each
of the polymers A to D showed excellent durability. Further, no
separation of the membrane was observed, and the adhesive A also
showed a good durability.
EXAMPLE 7
[0088] Using as an adhesive a propylene/vinylidene
fluoride/tetrafluoroeth- ylene copolymer (copolymer having a
content (mol %) of propylene units: vinylidene fluoride units:
tetrafluoroethylene units of 25:35:40, and having an intrinsic
viscosity [.eta.] of 0.58 in tetrahydrofuran at 30.degree. C.), and
using a butyl acetate solution of this adhesive and the polymer C
as a membrane material, a pellicle comprising a frame and a uniform
membrane of about 1 .mu.m thickness comprising the polymer C bonded
to the frame was obtained in the same manner as in Example 6.
[0089] The obtained pellicle had adequate adhesion to air blow
without elongation or sag of the membrane. This pellicle was
evaluated by an irradiation test by means of a F.sub.2 excimer
laser light having a wavelength of 157 nm, to be used for
photolithography, whereupon no separation of the membrane was
confirmed even after irradiation of 10,000 pulse, and the adhesive
also showed a good durability.
EXAMPLE 8
[0090] Using as an adhesive a vinylidene
fluoride/hexafluoropropylene copolymer (copolymer having a content
(mol %) of vinylidene fluoride units: hexafluoropropylene units of
78:22, and having an intrinsic viscosity [.eta.] of 0.60 in
tetrahydrofuran at 30.degree. C.), and using an ethyl acetate
solution of this adhesive and the polymer C as a membrane material,
a pellicle comprising a frame and a uniform membrane of about 1
.mu.m thickness comprising the polymer C bonded to the frame was
obtained in the same manner as in Example 6.
[0091] The obtained pellicle had adequate adhesion to air blow
without elongation or sag of the membrane. The pellicle was
evaluated by an irradiation test by means of an F.sub.2 excimer
laser light having a wavelength of 157 nm, to be used for
photolithography, whereupon no separation of the membrane was
confirmed even after irradiation of 10,000 pulse, and the adhesive
also showed a good durability.
EXAMPLE 9
[0092] 9 g of the polymer E obtained in Example 5 and 91 g of
perfluorotributylamine were put in a flask made of glass, followed
by heating at 50.degree. C. for 24 hours with stirring. As a
result, a uniform colorless and transparent solution without
turbidity was obtained. The solution was coated on a polished glass
plate by spin coating at a spin rate of 500 rpm for 10 seconds and
at 4,000 rpm for 20 seconds, followed by heat treatment for 1 hour
at 80.degree. C. and further for 1 hour at 180.degree. C. to obtain
a uniform transparent membrane on the glass plate.
[0093] Then, using a perfluorotributylamine solution of the
adhesive E, the above glass plate having the membrane of the
polymer E formed thereon was press-bonded on an aluminum frame
having the adhesive E coated thereon in the same manner as in
Example 6, to obtain a pellicle comprising an aluminum frame and a
uniform self-supporting membrane of about 1 .mu.m thickness
comprising the polymer E bonded to the frame. This pellicle was
evaluated by an irradiation test by means of a F.sub.2 excimer
laser, whereupon significant loss or breakage of the membrane
comprising the polymer E occurred, and it could not be used.
Further, separation of the membrane was observed, and durability of
the adhesive E was also inadequate.
EXAMPLE 10
[0094] Each of the solutions of the polymers A to D and the polymer
E used in Examples 6 and 9 was coated on a polished glass plate by
spin coating in the same manner as mentioned above, followed by
drying to obtain a uniform transparent membrane of about 10 .mu.m
thickness. With respect to each of the obtained membranes,
transmission of light was measured, and the results are shown in
FIG. 1. It was found that a light having a wavelength of 157 nm was
transmitted through each of the membranes comprising the polymers A
to D with a high transmission, but substantially no light having a
wavelength of 157 nm was transmitted through the membrane
comprising the polymer E.
[0095] The pellicle using the fluorine-containing polymer (A) of
the present invention has a high transmission at the
short-wavelength region at a wavelength of at most 200 nm
(particularly at most 180 nm), and has a high durability against a
short-wavelength laser light to be used for finer processing in the
future. Accordingly, it has excellent effects as a dust-proof
membrane for a mask to be used for next-generation
photolithography, and is effective to improve the yield of
products.
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