U.S. patent application number 17/279321 was filed with the patent office on 2021-12-23 for polyolefin resin foam sheet.
This patent application is currently assigned to SEKISUI CHEMICAL CO., LTD.. The applicant listed for this patent is SEKISUI CHEMICAL CO., LTD.. Invention is credited to Yoshito ARAI, Yasunari KUSAKA, Daisuke MUKOHATA, Asami NAGAI.
Application Number | 20210395476 17/279321 |
Document ID | / |
Family ID | 1000005870532 |
Filed Date | 2021-12-23 |
United States Patent
Application |
20210395476 |
Kind Code |
A1 |
NAGAI; Asami ; et
al. |
December 23, 2021 |
POLYOLEFIN RESIN FOAM SHEET
Abstract
The present invention provides a polyolefin resin foam sheet
having an area density of 5 g/m.sup.2 or more and 400 g/m.sup.2 or
less, and satisfying at least one of the following conditions (1)
and (2) in thermogravimetric-mass spectrometry carried out at a
heating rate of 10.degree. C.min over an entire measurement
temperature range of a 200 to 550.degree. C. measurement
temperature, condition (1): a combustion gas generation ratio X
defined as a ratio of a peak area value of an amount of a
combustion gas P having a mass-to-charge ratio m/z of 55 generated
at a measurement temperature of 200 to 364.degree. C. with respect
to the peak area value of an amount of the combustion gas P
generated over the entire measurement temperature range is 25% or
less; and condition (2): a combustion gas generation ratio Y
defined as a ratio of a peak area value of an amount of a
combustion gas Q having a mass-to-charge ratio m/z of 69 generated
at a measurement temperature of 200 to 364.degree. C. with respect
to the peak area value of an amount of the combustion gas Q
generated over the entire measurement temperature range is 25% or
less. According to the present invention, a polyolefin resin foam
sheet can be provided that has a high fire retardancy while
maintaining a lightweight property.
Inventors: |
NAGAI; Asami; (Saitama-shi,
Saitama, JP) ; MUKOHATA; Daisuke; (Saitama-shi,
Saitama, JP) ; KUSAKA; Yasunari; (Mishima-gun, Osaka,
JP) ; ARAI; Yoshito; (Suita-shi, Osaka, JP) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
SEKISUI CHEMICAL CO., LTD. |
Osaka-shi, Osaka |
|
JP |
|
|
Assignee: |
SEKISUI CHEMICAL CO., LTD.
Osaka-shi, Osaka
JP
|
Family ID: |
1000005870532 |
Appl. No.: |
17/279321 |
Filed: |
September 27, 2019 |
PCT Filed: |
September 27, 2019 |
PCT NO: |
PCT/JP2019/038393 |
371 Date: |
March 24, 2021 |
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C08J 2323/16 20130101;
C08K 5/0066 20130101; C08J 2323/12 20130101; C08K 5/521 20130101;
C08J 5/18 20130101; C08J 2323/06 20130101; C08K 5/136 20130101;
C08J 9/0061 20130101; C08J 2203/04 20130101; C08J 9/103 20130101;
C08J 2201/03 20130101 |
International
Class: |
C08J 9/00 20060101
C08J009/00; C08J 9/10 20060101 C08J009/10; C08K 5/00 20060101
C08K005/00; C08K 5/136 20060101 C08K005/136; C08K 5/521 20060101
C08K005/521; C08J 5/18 20060101 C08J005/18 |
Foreign Application Data
Date |
Code |
Application Number |
Sep 28, 2018 |
JP |
2018-185670 |
Claims
1. A polyolefin resin foam sheet having an area density of 5
g/m.sup.2 or more and 400 g/m.sup.2 or less, and satisfying at
least one of the following conditions (1) and (2) in
thermogravimetric-mass spectrometry carried out at a heating rate
of 10.degree. C.min over an entire measurement temperature range of
a 200 to 550.degree. C. measurement temperature, condition (1): a
combustion gas generation ratio X defined as a ratio of a peak area
value of an amount of a combustion gas P having a mass-to-charge
ratio m/z of 55 generated at a measurement temperature of 200 to
364.degree. C. with respect to the peak area value of an amount of
the combustion gas P generated over the entire measurement
temperature range is 25% or less; and condition (2): a combustion
gas generation ratio Y defined as a ratio of a peak area value of
an amount of a combustion gas Q having a mass-to-charge ratio m/z
of 69 generated at a measurement temperature of 200 to 364.degree.
C. with respect to the peak area value of an amount of the
combustion gas Q generated over the entire measurement temperature
range is 25% or less.
2. The polyolefin resin foam sheet according to claim 1, wherein
the polyolefin resin foam sheet has a thickness of 15 mm or
less.
3. The polyolefin resin foam sheet according to claim 1, wherein a
polyolefin resin constituting the polyolefin resin foam sheet is
one or more selected from the group consisting of a polyethylene
resin and a polypropylene resin.
4. The polyolefin resin foam sheet according to claim 3, wherein
the polyolefin resin is a combination of a polyethylene resin and a
polypropylene resin.
5. The polyolefin resin foam sheet according claim 1, wherein the
polyolefin resin foam sheet comprises a fire retardant.
6. The polyolefin resin foam sheet according to claim 5, wherein
the fire retardant is at least one of a phosphorus fire retardant
and a halogen fire retardant.
7. The polyolefin resin foam sheet according to claim 6, wherein
the phosphorus fire retardant is one or more selected from the
group consisting of a phosphate, a polyphosphate, and a phosphorus
spiro compound.
8. The polyolefin resin foam sheet according to claim 6, wherein
the halogen fire retardant is a bromine fire retardant.
Description
TECHNICAL FIELD
[0001] The present invention relates to a polyolefin resin foam
sheet obtained by foaming a polyolefin resin, and in particular to
a polyolefin resin foam sheet used for an impact absorbing material
installed in an aircraft.
BACKGROUND ART
[0002] Conventionally, polyolefin resin foams have excellent
properties, such as a lightweight property, thermal insulation
property, impact absorption, water resistance, chemical resistance,
and mechanical strength, and therefore have been used in a wide
range of fields such as building materials, electrical appliances,
automobiles, and aircraft. Since polyolefin resin foams are
flammable, various kinds of fire retardants are blended in a
relatively large amount when used in applications that require fire
retardancy. For example, Patent Literature 1 discloses a
non-halogen fire retardant resin foam obtained by cross-linking and
foaming a resin composition containing 100 parts by weight of a
resin component composed of 90 to 30% by weight of a specific
ethylene copolymer, 50 to 150 parts by weight of a predetermined
metal hydroxide, 2 to 25 parts by weight of red phosphorus, 2 to 25
parts by weight of titanium oxide, and 0.1 to 5 parts by weight of
a heat stabilizer.
CITATION LIST
Patent Literature
[0003] PTL1: JP 3580556 B
SUMMARY OF INVENTION
Technical Problem
[0004] When a large amount of fire retardant is blended in a resin
composition as in the resin foam described in Patent Literature 1,
the viscosity is outside of a proper range, so that a foaming
property deteriorates and a foam density increases. As a result,
the weight of the foam sheet increases, which makes it difficult to
use for applications requiring a lightweight property, such as in
aircraft, for example.
[0005] The present invention has been made in view of the
conventional circumstances described above, and an object of the
present invention is to provide a polyolefin resin foam sheet
having a high fire retardancy while maintaining a lightweight
property.
Solution to Problem
[0006] The present inventors have diligently performed
investigations to solve the above-described problem. As a result,
the present inventors discovered that a polyolefin resin foam sheet
having both a lightweight property and fire retardancy can be
obtained by setting an area density to a predetermined range, and
setting in thermogravimetric-mass spectrometry, a peak area value
of the amount of a combustion gas having a specific mass-to-charge
ratio m/Z generated in a specific measurement range, relative to
the peak area value of the amount generated over the entire
measurement range, to a certain value or less, thereby completing
the present invention.
[0007] That is, the gist of the present invention is described in
the following [1] to [8].
[0008] [1] A polyolefin resin foam sheet having an area density of
5 g/m.sup.2 or more and 400 g/m.sup.2 or less, and satisfying at
least one of the following conditions (1) and (2) in
thermogravimetric-mass spectrometry carried out at a heating rate
of 10.degree. C.min over an entire measurement temperature range of
a 200 to 550.degree. C. measurement temperature, condition (1); a
combustion gas generation ratio X defined as a ratio of a peak area
value of an amount of a combustion gas P having a mass-to-charge
ratio m/z of 55 generated at a measurement temperature of 200 to
364.degree. C. with respect to the peak area value of an amount of
the combustion gas P generated over the entire measurement
temperature range is 25% or less; and condition (2): a combustion
gas generation ratio Y defined as a ratio of a peak area value of
an amount of a combustion gas Q having a mass-to-charge ratio m/z
of 69 generated at a measurement temperature of 200 to 364.degree.
C. with respect to the peak area value of an amount of the
combustion gas Q generated over the entire measurement temperature
range is 25% or less.
[0009] [2] The polyolefin resin foam sheet according to [1],wherein
the polyolefin resin foam sheet has a thickness of 15 mm or
less.
[0010] [3] The polyolefin resin foam sheet according to [1] or
[2],wherein a polyolefin resin constituting the polyolefin resin
foam sheet is one or more selected from the group consisting of a
polyethylene resin and a polypropylene resin.
[0011] [4] The polyolefin resin foam sheet according to [3],
wherein the polyolefin resin is a combination of a polyethylene
resin and a polypropylene resin.
[0012] [5] The polyolefin resin foam sheet according to any of [1]
to [4],wherein the polyolefin resin foam sheet comprises a fire
retardant.
[0013] [6] The polyolefin resin foam sheet according to [5],wherein
the fire retardant is at least one of a phosphorus fire retardant
and a halogen fire retardant.
[0014] [7] The polyolefin resin foam sheet according to [6],wherein
the phosphorus fire retardant is one or more selected from the
group consisting of a phosphate, a polyphosphate, and a phosphorus
spiro compound.
[0015] [8] The polyolefin resin foam sheet according to [6] or
[7],wherein the halogen fire retardant is a bromine fire
retardant.
Advantageous Effects of Invention
[0016] According to the present invention, a polyolefin resin foam
sheet can be provided that has a high fire retardancy while
maintaining a lightweight property.
DESCRIPTION OF EMBODIMENTS
[Polyolefin Resin Foam Sheet]
[0017] The polyolefin resin foam sheet of the present invention
(hereinafter, also referred to as "foam sheet") has an area density
of 5 g/m.sup.2 or more and 400 g/m.sup.2 or less, and satisfies at
least one of the following conditions (1) and (2) in
thermogravimetric-mass spectrometry carried out at a heating rate
of 10.degree. C.min over an entire measurement temperature range of
a 200 to 550.degree. C. measurement temperature,
[0018] condition (1): a combustion gas generation ratio X defined
as a ratio of a peak area value of an amount of a combustion gas P
having a mass-to-charge ratio m/z of 55 generated at a measurement
temperature of 200 to 364.degree. C. with respect to the peak area
value of an amount of the combustion gas P generated over the
entire measurement temperature range is 25% or less; and
[0019] condition (2): a combustion gas generation ratio Y defined
as a ratio of a peak area value of an amount of a combustion gas Q
having a mass-to-charge ratio m/z of 69 generated at a measurement
temperature of 200 to 364.degree. C. with respect to the peak area
value of an amount of the combustion gas Q generated over the
entire measurement temperature range is 25% or less.
[0020] In the present invention, the foam sheet has an area density
of 5 g/m.sup.2 or more and 400 g/m.sup.2 or less, and therefore has
a light weight and can be used for applications requiring reduced
weight, such as aircraft. Further, in thermogravimetric-mass
spectrometry, the foam sheet of the present invention satisfies at
least one of the above-described conditions (1) and (2), and
therefore has excellent fire retardancy.
[0021] A polyolefin resin foam sheet of the present invention will
now be described in more detail.
<Area Density>
[0022] The foam sheet of the present invention has an area density
of 5 g/m.sup.2 or more and 400 g/m.sup.2 or less. If the area
density is less than 5 g/m.sup.2, the density of the foam sheet
becomes too small, so that the mechanical strength is reduced and
the impact absorption is also reduced. On the other hand, if the
area density exceeds 400 g/m.sup.2, the weight of the foam sheet
increases, which means that the foam sheet can no longer be used
for applications requiring a lightweight property, such as in
aircraft, and the fire retardancy also deteriorates. From these
viewpoints, the area density of the foam sheet is preferably 10
g/m.sup.2 or more, more preferably 20 g/m.sup.2 or more, and
further preferably 30 g/m.sup.2 or more, and is preferably 350
g/m.sup.2 or less, more preferably 300 g/m.sup.2 or less, and
further preferably 250 g/m.sup.2 or less. Generally, a foam sheet
containing a fire retardant tends to have a high area density, but
in the present invention, the above-described range can be achieved
and a light-weight foam sheet can be obtained by adjusting the
crosslinking degree, the foaming ratio, and the amount of the fire
retardant.
[0023] In the present invention, the area density can be measured
by the method described in the Examples.
[Conditions (1) and (2) in Thermogravimetric-Mass Spectrometry]
[0024] The foam sheet of the present invention satisfies at least
one of the following conditions (1) and (2) in
thermogravimetric-mass spectrometry carried out at a heating rate
of 10.degree. C.min over an entire measurement temperature range at
a 200 to 550.degree. C. measurement temperature,
[0025] condition (1): a combustion gas generation ratio X defined
as a peak area value of an amount of a combustion gas P having a
mass-to-charge ratio m/z of 55 generated at a measurement
temperature of 200 to 364.degree. C. with respect to the peak area
value of an amount of the combustion gas P generated over the
entire measurement temperature range is 25% or less; and
[0026] condition (2): a combustion gas generation ratio Y defined
as a peak area value of an amount of a combustion gas Q having a
mass-to-charge ratio m/z of 69 generated at a measurement
temperature of 200 to 364.degree. C. with respect to the peak area
value of an amount of the combustion gas Q generated over the
entire measurement temperature range is 25% or less.
[0027] Thermogravimetric-mass spectrometry (TG-MS analysis) is a
method in which a gas generated by heating a sample in
thermogravimetric (TG) measurement is introduced into a mass
spectrometer (MS) online to obtain a mass spectrum. In
thermogravimetric-mass spectrometry, it is possible to measure the
weight change of the sample due to heating, and the kind
(mass-to-charge ratio) and amount of the combustion gas generated
by the decomposition of the measurement sample due to heating.
Generally, when a polyolefin resin such as polyethylene resin or
polypropylene resin is heated, at least one of a combustion gas P
having a mass-to-charge ratio m/z of 55 and a combustion gas Q
having a mass-to-charge ratio m/z of 69 is generated.
[0028] The condition (1) specifies that a combustion gas generation
ratio X defined as a ratio of a peak area value of an amount of a
combustion gas P having a mass-to-charge ratio m/z of 55 generated
at a measurement temperature of 200 to 364.degree. C. with respect
to the peak area value of an amount of the combustion gas P
generated over the entire measurement temperature range is 25% or
less. The combustion gas generation ratio X can be determined based
on the following formula.
[0029] Combustion gas generation ratio X=100.times.Peak area value
of an amount of combustion gas P generated at measurement
temperature of 200 to 364.degree. C./peak area value of an amount
of combustion gas P generated over an entire measurement
temperature range (200 to 550.degree. C.)
[0030] By satisfying the condition (1), the foam sheet of the
present invention can have a reduced heating value and excellent
fire retardancy. From the viewpoint of further improving fire
retardancy, the combustion gas generation ratio X in the
above-described condition (1) is preferably 23% or less, more
preferably 20% or less, and further preferably 16% or less. The
heating value is the heating value measured by the method described
in the Examples.
[0031] The condition (2) specifies that a combustion gas generation
ratio Y defined as a ratio of a peak area value of an amount of a
combustion gas Q having a mass-to-charge ratio m/z of 69 generated
at a measurement temperature of 200 to 364.degree. C. with respect
to the peak area value of an amount of the combustion gas Q
generated over the entire measurement temperature range is 25% or
less. The combustion gas generation ratio Y can be determined based
on the following formula.
[0032] Combustion gas generation ratio Y=100.times.Peak area value
of amount of combustion gas Q generated at measurement temperature
of 200 to 364.degree. C./peak area value of amount of combustion
gas Q generated over an entire measurement temperature range (200
to 550.degree. C.)
[0033] By satisfying the condition (2), the foam sheet of the
present invention can have a reduced heating value and excellent
fire retardancy. From the viewpoint of further improving fire
retardancy, the combustion gas generation ratio Y in the
above-described condition (2) is preferably 23% or less, more
preferably 20% or less, and further preferably 16% or less.
[0034] The foam sheet of the present invention may satisfy at least
one of the above conditions (1) and (2), but from the viewpoint of
further reducing the heating value and improving the fire
retardancy, it is preferable to satisfy both the conditions (1) and
(2). The value of the each of the combustion gas generation ratios
X and Y in the conditions (1) and (2) can be set to a value of a
certain value or less by adjusting the kind and content of the fire
retardant.
<Apparent Density>
[0035] In the present invention, the foam sheet has an apparent
density of preferably 45 kg/m.sup.3 or less. When the apparent
density of the foam sheet is 45 kg/m.sup.3 or less, the foam sheet
can have a sufficiently reduced weight. From the viewpoint of
reducing the weight of the foam sheet, the foam sheet has an
apparent density of more preferably 40 kg/m.sup.3 or less, and
further preferably 35 kg/m.sup.3 or less. On the other hand, the
foam sheet has an apparent density of preferably 10 kg/m.sup.3 or
more, and more preferably 20 kg/m.sup.3 or more. When the apparent
density of the foam sheet is 10 kg/m.sup.3 or more, it is possible
to secure the mechanical strength while maintaining a lightweight
property.
[0036] When the foam sheet contains a fire retardant as in the
present invention, the viscosity of the expandable composition
increases, which means that it is difficult to increase the
expansion ratio and reduce the density. However, in the present
invention, by using a fire retardant like that used in Examples
described later, because expansion is made to occur while adjusting
the crosslinking degree and the like, it is possible to adjust the
apparent density to be within the above-described range.
<Crosslinking Degree (Gel fraction)>
[0037] From the viewpoint of improving mechanical strength even
when lightweight, the foam sheet of the present invention is
preferably crosslinked. In that case, the crosslinking degree (gel
fraction) is preferably 20 to 60% by mass. When the gel fraction is
equal to or more than this lower limit value, sufficient crosslinks
are formed in the foam sheet, and therefore the mechanical strength
tends to increase. Further, when the crosslinking degree is equal
to or less than the upper limit value, it is easier to secure the
flexibility of the foam sheet. Further, by setting the crosslinking
degree to be within the above-described range, it is easier to
adjust the area density to be within the above-described range.
From such a viewpoint, the crosslinking degree is more preferably
25 to 55% by mass, further preferably 30 to 55% by mass, and even
further preferably 32 to 45% by mass.
[0038] The crosslinking degree can be measured by the measurement
method described later.
<Thickness>
[0039] From the viewpoint of improving mechanical strength and
impact absorption, the foam sheet of the present invention has a
thickness of preferably 15 mm or less, more preferably 2 to 15 mm,
and further preferably 3 to 14 mm.
<25% Compressive Strength>
[0040] The foam sheet has a 25% compressive strength of preferably
10 to 100 kPa. When the 25% compressive strength is equal to or
less than the upper limit value, the flexibility of the foam sheet
is improved, and conformability to the adherend is improved when
used as a pressure-sensitive adhesive tape, for example. On the
other hand, when the 25% compressive strength is equal to or more
than the lower limit value, impact absorption and impact resistance
are both improved. From these viewpoints, the foam sheet has a 25%
compressive strength of more preferably 15 to 80 kPa, and further
preferably 20 to 75 kPa.
[0041] The 25% compressive strength can be measured according to
the method described in the Examples described later.
<Polyolefin Resin>
[0042] The polyolefin resin foam sheet of the present invention
contains a polyolefin resin. Examples of the polyolefin resin
include a polyethylene resin, a polypropylene resin, an
ethylene-vinyl acetate copolymer, and the like. Among these, it is
preferable to use one or more selected from the group consisting of
a polyethylene resin and a polypropylene resin, and it is more
preferable to use a polyethylene resin and a polypropylene resin in
combination. By using a polyethylene resin and a polypropylene
resin in combination, it is easier to adjust the crosslinking
degree and expansion ratio, and therefore it is easier to obtain a
foam sheet having an excellent lightweight property.
<<Polyethylene Resin>>
[0043] Examples of the polyethylene resin include a low density
polyethylene resin (0.93 g/cm.sup.3 or less, LDPE), a medium
density polyethylene resin (more than 0.930 g/cm.sup.3 and less
than 0.942 g/cm.sup.3, MDPE), and a high density polyethylene resin
(0.942 g/cm.sup.3 or more, HDPE). Further, a suitable specific
example of the low density polyethylene resin is a linear low
density polyethylene resin (LLDPE).
[0044] Among these, a linear low density polyethylene resin and a
high density polyethylene resin are preferable, and a linear low
density polyethylene resin is more preferable. By using these
resins, it is easier to obtain a foam sheet having an excellent
lightweight property.
[0045] The linear low density polyethylene resin has a density of
preferably 0.90 g/cm.sup.3 or more, and more preferably 0.91
g/cm.sup.3 or more and 0.93 g/cm.sup.3 or less. The high density
polyethylene resin has a density of preferably 0.98 g/cm.sup.3 or
less, and more preferably 0.95 g/cm.sup.3 or more and 0.97
g/cm.sup.3 or less. By setting the density of the high density
polyethylene resin or linear low density polyethylene resin to be
within these ranges, it is easier to obtain a foam sheet having an
excellent lightweight property.
[0046] The polyethylene resin may be a homopolymer of ethylene, but
may also be a copolymer or the like of ethylene and a small amount
of an .alpha.-olefin, in which ethylene is the main component
(preferably 75% by mass or more, and more preferably 90% by mass or
more, of all the monomers). Examples of the .alpha.-olefin include
an .alpha.-olefin having 3 to 12 carbon atoms, and more preferably
4 to 10 carbon atoms. Specifically, examples include 1-butene,
1-pentene, 1-hexene, 4-methyl-1-pentene, 1-heptene, 1-octene, and
the like. In the copolymer, these .alpha.-olefins can be used alone
or in combination of two or more.
[0047] Further, the polyethylene resin may be used alone or in
combination of two or more.
<<Polypropylene Resin>>
[0048] The polypropylene resin may be homopolypropylene, which is a
homopolymer of propylene, or may be a copolymer of propylene with a
small amount of ethylene and a small amount of .alpha.-olefin other
than propylene, in which propylene is the main component
(preferably 75% by mass or more, and more preferably 90% by mass or
more, of all the monomers).
[0049] Examples of the copolymer include a block copolymer, a
random copolymer, a random block copolymer, and the like. Among
these, a random copolymer (that is, a random polypropylene) is
preferable.
[0050] Examples of the .alpha.-olefin other than propylene include
an .alpha.-olefin having about 4 to 10 carbon atoms, such as
1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-heptene, and
1-octene. Among these, ethylene is preferable from the viewpoint of
a formability and heat resistance. In the copolymer, these
.alpha.-olefins can be used alone or in combination of two or
more.
[0051] Further, the polypropylene resin may be used alone or in
combination of two or more.
[0052] Examples of the ethylene-vinyl acetate copolymer used as the
polyolefin resin include an ethylene-vinyl acetate copolymer
containing 50% by mass or more of an ethylene-derived structural
unit.
[0053] In the present invention, any of a polyethylene resin, a
polypropylene resin, or a mixture thereof, which have been
polymerized with a polymerization catalyst such as a Ziegler-Natta
compound, a metallocene compound, or a chromium oxide compound may
be used. By using a polyethylene resin obtained using a metallocene
compound polymerization catalyst, particularly a linear low density
polyethylene, it is easier to obtain a foam sheet having high
flexibility and high impact absorption.
<Fire Retardant>
[0054] The foam sheet of the present invention preferably includes
a fire retardant. The fire retardant is preferably at least one of
a phosphorus fire retardant and a halogen fire retardant. By using
such a fire retardant, the above-described combustion gas
generation ratio can be effectively reduced. It is presumed that
this is because an inert gas generated from the fire retardant
reduces the amount of combustion gas generated from the resin and
the like of the foam sheet. Further, since such a fire retardant
prevents the viscosity of the expandable composition from being
excessively high in relation to the foaming agent described later,
it is easier to adjust the apparent density of the foam sheet to be
within the above-described range. Therefore, by using the fire
retardant, it is easier to obtain a foam sheet having both fire
retardancy and a lightweight property. From this viewpoint, the
phosphorus fire retardant is preferably one or more selected from
the group consisting of a phosphate, a polyphosphate, and a
phosphorus spiro compound, which are described later. In addition,
as the halogen fire retardant, a bromine fire retardant described
later is preferable.
<<Phosphorus Fire Retardant>>
[0055] Examples of the phosphorus fire retardant include a
phosphate such as melamine orthophosphate and piperazine
orthophosphate, a polyphosphate such as ammonium polyphosphate,
melamine polyphosphate, and melamine polyphosphate-melam-melem, a
phosphazene compound, a phosphorus spiro compound, and the like.
Among these, a phosphate, a polyphosphate, and a phosphorus spiro
compound are more preferable from the viewpoint that their
influence on the viscosity of the expandable composition is small
and the expansion ratio can be easily adjusted.
[Phosphate and Polyphosphate]
[0056] Examples of the phosphate include melamine orthophosphate,
piperazine orthophosphate, melamine pyrophosphate, piperazine
pyrophosphate, calcium phosphate, magnesium phosphate, and the
like.
[0057] Examples of the polyphosphate include ammonium
polyphosphate, melamine polyphosphate, melamine
polyphosphate-melam-melem, piperazine polyphosphate, and the
like.
[0058] Among these, one or more selected from the group consisting
of melamine pyrophosphate, piperazine pyrophosphate, and ammonium
polyphosphate is preferable, and it is more preferable to use
piperazine pyrophosphate and melamine pyrophosphate in combination.
When piperazine pyrophosphate and melamine pyrophosphate are used
in combination, a mass ratio of the melamine pyrophosphate to the
piperazine pyrophosphate (melamine pyrophosphate/piperazine
pyrophosphate) is preferably 0.25 or more and 1.0 or less.
[0059] The "melamine" or "piperazine" in the above-described
examples of the phosphate and the polyphosphate may be substituted
for compounds having the name N,N,N',N'-tetramethyldiaminomethane,
ethylenediamine, N,N'-dimethylethylenediamine,
N,N'-diethylethylenediamine, N,N-dimethylethylenediamine,
N,N-diethylethylenediamine, N,N,N',N'-tetramethylethylenediamine,
N,N,N',N'-diethylethylenediamine, 1,2-propanediamine,
1,3-propanediamine, tetramethylenediamine, pentamethylenediamine,
hexamethylenediamine, 1, 7-diaminoheptane, 1,8-diaminooctane,
1,9-diaminononane, 1,10-diaminodecane,
trans-2,5-dimethylpiperazine, 1,4-bis(2-aminoethyOpiperazine,
1,4-bis(3-aminopropy0piperazine, acetoguanamine, benzoguanamine,
acrylic guanamine, 2,4-diamino-6-nonyl-1,3,5-triazine,
2,4-diamino-6-hydroxy-1,3,5-triazine,
2-amino-4,6-dihydroxy-1,3,5-triazine,
2,4-diamino-6-methoxy-1,3,5-triazine,
2,4-diamino-6-ethoxy-1,3,5-triazine,
2,4-diamino-6-propoxy-1,3,5-triazine,
2,4-diamino-6-isopropoxy-1,3,5-triazine,
2,4-diamino-6-mercapto-1,3,5-triazine,
2-amino-4,6-dimercapto-1,3,5-triazine, ammeline,
phthalodiguanamine, melamine cyanurate, melamine pyrophosphate,
butylene diguanamine, norbornene diguanamine, methylene
diguanamine, ethylene dimelamine, trimethylene dimelamine,
tetramethylene dimeramine, hexamethylene dimelamine, or
1,3-hexylene melamine.
[0060] In the present invention, when the above-described phosphate
and polyphosphate are used, they may be used alone, or two or more
selected from the group consisting of the phosphate and the
polyphosphate may be mixed and used as an intumescent fire
retardant. Further, as an intumescent fire retardant, one or more
selected from the group consisting of the above-described phosphate
and polyphosphate and a metal oxide may be mixed and used.
[0061] Examples of the metal oxide used in combination with one or
more selected from the group consisting of the phosphate and the
polyphosphate include zinc oxide, magnesium oxide, calcium oxide,
silicon dioxide, titanium oxide, manganese oxide (MnO, MnO.sub.2),
iron oxide (FeO, Fe.sub.2O.sub.3, Fe.sub.3O.sub.4), copper oxide,
nickel oxide, tin oxide, aluminum oxide, calcium aluminate, and the
like. Among these, zinc oxide, magnesium oxide, and calcium oxide
are preferable.
[0062] In the case of using one or more selected from the group
consisting of the phosphate and the polyphosphate mixed with the
metal oxide, it is preferable to adjust the mass ratio thereof as
follows. From the viewpoint of improving fire retardancy, the mass
ratio of the one or more selected from the group consisting of the
phosphate and the polyphosphate to the metal oxide [total mass of
phosphate and polyphosphate/mass of metal oxide] is preferably 4 or
more and 100 or less, more preferably 6 or more and 50 or less, and
further preferably 10 or more and 35 or less.
[0063] Examples of commercially available products of the fire
retardant including one or more selected from the group consisting
of the phosphate and the polyphosphate include "ADK STAB FP-2100J",
"ADK STAB FP-2200S", and "ADK STAB FP-2500S" manufactured by ADEKA
Corporation, "EXOLIT AP422" and "EXOLIT AP462" manufactured by
Clariant Japan K.K., and the like.
[Phosphazene Compound]
[0064] The phosphazene compound is an organic compound having a
-P.dbd.N-bond in the molecule. The phosphazene compound is
preferably a compound represented by the following formula (1)
because such a compound has a relatively high decomposition
temperature.
##STR00001##
[0065] In the above formula (1), R.sub.1 to R.sub.6 each
independently represent any of an alkyl group having 1 to 12 carbon
atoms, an alkoxy group having 1 to 12 carbon atoms, an aryloxy
group having 6 to 12 carbon atoms, an amino group, or a halogen
atom.
[0066] Examples of such a phosphazene compound include "SPB-100"
and the like, which is commercially available from Otsuka Chemical
Co., Ltd.
[Phosphorus Spiro Compound]
[0067] The phosphorus spiro compound is not particularly limited as
long as it is a spiro compound having a phosphorus atom. A spiro
compound is a compound having a structure in which two cyclic
compounds share one carbon, and a spiro compound having a
phosphorus atom is a compound in which at least one of the elements
constituting the two cyclic compounds is a phosphorus atom.
[0068] As the phosphorus spiro compound, for example, it is
preferable to use a compound having a structure represented by the
following formula (2) in the molecule. In formula (2),* indicates a
linking portion with another substituent.
##STR00002##
<<Halogen Fire Retardant>>
[0069] In the present invention, a halogen fire retardant may be
used. The halogen fire retardant stabilizes active OH radicals by a
radical trapping effect in the gas phase. Further, during
combustion, active OH radicals and H radicals that act as
combustion promoters are trapped and stabilized by hydrogen halides
generated from the halogen fire retardant. In addition, the
hydrogen halides generated from the halogen fire retardant during
combustion are nonflammable, and therefore they bring about a
dilution effect and also an oxygen blocking effect.
[0070] The halogen fire retardant is not particularly limited as
long as it is a fire retardant containing halogen in its molecular
structure. Examples of the halogen fire retardant include a bromine
fire retardant and a chlorine fire retardant, and among them, a
bromine fire retardant is preferable.
[0071] The bromine fire retardant is not particularly limited as
long as it is a fire retardant containing bromine in its molecular
structure. Examples of the bromine fire retardants include
decabromodiphenyl ether, octabromodiphenyl ether,
tetrabromobisphenol A (TBBA), TBBA epoxy oligomer, TBBA carbonate
oligomer, TBBA bis(dibromopropyl ether), TBBA bis(aryl ether),
bis(pentabromophenyl)ethane, 1,2-bis(2,4,6-tribromophenoxy)ethane,
2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine, 2,6- or
(2,4-)dibromophenol homopolymer, brominated polystyrene,
polybrominated styrene, ethylenebistetrabromophthalimide,
hexabromocyclododecane, hexabromobenzene, pentabromobenzyl acrylate
monomer, pentabromobenzyl acrylate polymer, and the like. Among
these, bis(pentabromophenyl)ethane is preferable from the viewpoint
of fire retardancy and foaming property. One of these bromine fire
retardants may be used alone, or two or more may be mixed and
used.
[0072] In the case of using the halogen fire retardant, an antimony
fire retardant aid may be used in combination therewith. Based on a
synergistic effect with the halogen fire retardant, the antimony
fire retardant aid can reduce the above-described combustion gas
generation ratios X and Y, can improve the fire retardancy of the
foam sheet, and contain lower the content of the halogen fire
retardant. When an antimony fire retardant aid is used, the
antimony fire retardant aid reacts with the halogen fire retardant
during combustion and turns into a nonflammable halogenated
antimony. As a result, an oxygen blocking effect is produced.
[0073] Examples of the antimony fire retardant aid include antimony
trioxide and antimony pentoxide, and commercially available
products include, for example, "PATOX-M", "PATOX-MK", "PATOX-K",
and the like, manufactured by Nihon Seiko Co., Ltd.
[0074] From the viewpoint of a synergistic effect with the halogen
fire retardant, the blended amount of the antimony fire retardant
aid is preferably 20 to 80 parts by mass, more preferably 30 to 70
parts by mass, and further preferably 40 to 60 parts by mass, with
respect to 100 parts by mass of the halogen fire retardant.
<<Melting Point of Fire Retardant>>
[0075] The melting point of the fire retardant used in the present
invention is preferably about the same as or higher than the
foaming temperature of the foam sheet. When the melting point of
the fire retardant is about the same as or higher than the foaming
temperature, the fire retardant tends to melt due to the heat
during combustion, and combustion of the foam sheet can be
suppressed. From this viewpoint, the melting point of the fire
retardant is preferably 240 to 600.degree. C., more preferably 250
to 550.degree. C., and further preferably 255 to 500.degree. C.
[0076] The content of the fire retardant in the foam sheet is
preferably 1 to 100 parts by mass, more preferably 3 to 80 parts by
mass, and further preferably 5 to 50 parts by mass, with respect to
100 parts by mass of the polyolefin resin. By setting the content
of the fire retardant to be 1 part by mass or more, the fire
retardancy of the foam sheet is improved, and by setting the
content to be 100 parts by mass or less, the weight of the foam
sheet is maintained and processability and the like is
improved.
<Foaming Agent>
[0077] The foam sheet of the present invention can be obtained by
foaming an expandable composition including a polyolefin resin and
a foaming agent. As the foaming agent, a thermally decomposable
foaming agent is preferable.
[0078] An organic foaming agent and an inorganic foaming agent can
be used as the thermally decomposable foaming agent. Examples of
the organic foaming agent include an azo compound such as
azodicarbonamide, an azodicarboxylic acid metal salt (such as
barium azodicarboxylate), and azobisisobutyronitrile, a nitroso
compound such as N,N'-dinitrosopentamethylenetetramine, a hydrazine
derivative such as a hydrazodicarbonamide,
4,4'-oxybis(benzenesulfonyl hydrazide), and toluenesulfonyl
hydrazide, a semicarbazide compound such as toluenesulfonyl
semicarbazide, and the like.
[0079] Examples of the inorganic foaming agent include ammonium
carbonate, sodium carbonate, ammonium hydrogencarbonate, sodium
hydrogencarbonate, ammonium nitrite, sodium borohydride, monosoda
anhydrous citrate, and the like.
[0080] Among these, from the viewpoint of obtaining fine cells, and
from the viewpoint of economy and safety, an azo compound is
preferable, and azodicarbonamide is more preferable.
[0081] The thermally decomposable foaming agent may be used alone
or in combination of two or more.
[0082] The content of the foaming agent in the expandable
composition is preferably 1 part by mass or more and 40 parts by
mass or less, more preferably 5 parts by mass or more and 35 parts
by mass or less, and further preferably 10 parts by mass or more
and 30 parts by mass or less, with respect to 100 parts by mass of
the polyolefin resin. By setting the blended amount of the foaming
agent to be 1 part by mass or more, the expandable sheet can be
appropriately foamed, and it is possible to impart appropriate
flexibility and impact absorption to the foam sheet. Further, by
setting the blended amount of the foaming agent to be 30 parts by
mass or less, it is possible to prevent the foam sheet from foaming
more than necessary and the mechanical strength of the foam sheet
can be improved.
<Additives>
[0083] A crosslinking aid may be blended in the expandable
composition. As the crosslinking aid, a polyfunctional monomer can
be used. By adding a crosslinking aid to the polyolefin resin, the
amount of ionizing radiation irradiated in step (2) described later
is reduced, and cleaving and degradation of the resin molecules
from the irradiation of the ionizing radiation is prevented.
[0084] Specifically, examples of the crosslinking aid include a
compound having three functional groups in one molecule such as
trimethylolpropane trimethacrylate, trimethylolpropane triacrylate,
trimellitic acid triallyl ester, 1,2,4-benzenetricarboxylic acid
triallyl ester, and triallyl isocyanurate, a compound having two
functional groups in one molecule such as 1,6-hexanediol
dimethacrylate, 1,9-nonanediol dimethacrylate, 1,10-decanedliol
dimethacrylate, and divinylbenzene, diallyl phthalate, diallyl
terephthalate, diallyl isophthalate, ethyl vinylbenzene, neopentyl
glycol dimethacrylate, lauryl methacrylate, stearyl methacrylate,
and the like.
[0085] These crosslinking aids are used alone or in combination of
two or more.
[0086] The amount of the crosslinking aid added is preferably 0.5
to 10 parts by mass, more preferably 1.0 to 8 parts by mass, and
further preferably 1.5 to 5 parts by mass, with respect to 100
parts by mass of the polyolefin resin. By setting the addition
amount to be 0.5 parts by mass or more, the crosslinking degree
desired for the foam sheet can be stably obtained, and by setting
the addition amount to be 10 parts by mass or less, the
crosslinking degree of the foam sheet can be easily controlled.
[0087] A decomposition temperature adjusting agent may be blended
in the expandable composition. The decomposition temperature
adjusting agent is blended to reduce the decomposition temperature
of the thermally decomposable foaming agent and to increase or
adjust the decomposition rate. Specific examples of such a compound
include zinc oxide, zinc stearate, urea, and the like.
[0088] The decomposition temperature adjusting agent is blended in
an amount of, for example, 0.01 to 5 parts by mass with respect to
100 parts by mass of the polyolefin resin in order to adjust the
surface condition of the foam sheet.
[0089] An antioxidant may be blended in the expandable composition.
Examples of the antioxidant include a phenolic antioxidant such as
2,6-di-t-butyl-p-cresol, a sulfur antioxidant such as
dilaurylthiodipropionate, a phosphorus antioxidant, an amine
antioxidant, and the like. The antioxidant is blended in an amount
of, for example, 0.01 to 5 parts by mass with respect to 100 parts
by mass of the polyolefin resin.
[0090] In addition to these, additives generally used in a foam,
such as a heat stabilizer, a colorant, an antistatic agent, and a
filler, may also be blended in the expandable composition.
[0091] In the foam sheet, the polyolefin resin is the main
component, and the content of the polyolefin resin is, for example,
45% by mass or more, preferably 50% by mass or more, and more
preferably 55% by mass or more, based on the total amount of the
foam sheet.
<Method for Producing Foam Sheet>
[0092] The foam sheet of the present invention can be produced by
foaming the polyolefin resin by a general method. The production
method is not limited, and the foam sheet can be produced by
crosslinking the expandable composition including at least the
polyolefin resin and the foaming agent as necessary, and then
foaming.
[0093] Specifically, the foam sheet of the present invention can be
produced by a method having the following steps (1) to (3), for
example.
[0094] Step (1): A step of obtaining an expandable composition in
the form of a sheet by feeding the polyolefin resin, the thermally
decomposable foaming agent, and other additives to an extruder,
melt-kneading, and extruding into a sheet from the extruder.
[0095] Step (2): A step of cross-linking the expandable composition
in the form of a sheet.
[0096] Step (3): A step of heating the crosslinked sheet-like
expandable composition, foaming the thermally decomposable foaming
agent, and preferably stretching in one or both of the MD direction
and the TD direction.
[0097] In addition to this method, the cross-linked polyolefin
resin foam sheet can also be produced by the method described in WO
2005/007731 (A).
[0098] The method for foaming the expandable composition is not
particularly limited, and examples thereof include a method of
heating the expandable composition with hot air, a method of
heating the expandable composition with infrared rays, a method of
heating the expandable composition in a salt bath, a method of
heating the expandable composition in an oil bath, and the like.
These methods may be used in combination.
[0099] The foaming of the expandable composition is not limited to
examples in which a thermally decomposable foaming agent is used,
and physical foaming with butane gas or the like may be used.
[0100] Examples of the method of cross-linking the expandable
composition include a method in which the expandable composition is
irradiated with ionizing radiation such as an electron beam,
.alpha.-rays, .beta.-rays, and .gamma.-rays, a method in which an
organic peroxide is blended in the expandable composition in
advance and the expandable composition is heated to decompose the
organic peroxide, and the like. These methods may be used in
combination. Among these, a method of irradiating ionizing
radiation is preferable.
[0101] The irradiation amount of the ionizing radiation is
preferably 0.5 to 20 Mrad, and more preferably 1.0 to 12 Mrad, so
that the gel fraction is within the above-described range.
[0102] Examples of the organic peroxide used for crosslinking
include 1,1-bis(t-butylperoxy)3,3,5-trimethylcyclohexane,
1,1-bis(t-butylperoxy)cyclohexane, and the like. These may be used
alone or in combination of two or more. The added amount of the
organic peroxide is preferably 0.01 to 5 parts by mass, and more
preferably 0.1 to 3 parts by mass, with respect to 100 parts by
mass of the polyolefin resin. When the added amount of the organic
peroxide is within the above-described range, crosslinking of the
expandable composition proceeds more easily, and the amount of
decomposed residue of the organic peroxide in the obtained
cross-linked polyolefin resin foam sheet is suppressed.
[0103] The polyolefin resin foam sheet of the present invention is
preferably stretched as described above. The stretching may be
performed after foaming the expandable composition to obtain the
foam sheet, or may be performed while foaming the expandable
composition. When the foam sheet is stretched after foaming the
expandable composition to obtain the foam sheet, it is better to
immediately stretch the foam sheet while maintaining a molten state
at the time of foaming without cooling the foam sheet. However, the
foam sheet may also be stretched after cooling the foam sheet and
then again heating the foam sheet to be in a molten or softened
state.
[0104] Further, the stretching ratio of the polyolefin resin foam
sheet in the MD direction is preferably 1.1 to 3.0 times, and more
preferably 1.3 to 2.8 times. By setting the stretching ratio of the
polyolefin resin foam sheet in the MD direction to be equal to or
more than the lower limit value, the flexibility and tensile
strength of the polyolefin resin foam sheet tend to be better. On
the other hand, by setting the stretching ratio to be equal to or
less than the upper limit value, the foam sheet can be prevented
from breaking during the stretching, and it is possible to prevent
a reduction in the expansion ratio due to the foaming gas escaping
from the foam sheet during foaming, and as a result the flexibility
and tensile strength of the polyolefin resin foam sheet are better
and the quality tends to be more uniform. Further, the polyolefin
resin foam sheet may be stretched in the TD direction in a
stretching ratio in the above-described range.
[Pressure-Sensitive Adhesive Tape]
[0105] In the present invention, the foam sheet according to the
present invention may be used as a base material, and a
pressure-sensitive adhesive layer may be provided on one or both
sides of the foam sheet to form a pressure-sensitive adhesive tape.
The thickness of the pressure-sensitive adhesive tape is usually
about 2 to 16 mm.
[0106] The thickness of the pressure-sensitive adhesive layer
constituting the pressure-sensitive adhesive tape is preferably 5
to 200 .mu.m, more preferably 7 to 150 .mu.m, and further
preferably 10 to 100 .mu.m. When the thickness of the
pressure-sensitive adhesive layer constituting the
pressure-sensitive adhesive tape is 5 to 200 .mu.m, the thickness
of the pressure-sensitive adhesive tape can be thinner.
[0107] The pressure-sensitive adhesive constituting the
pressure-sensitive adhesive layer provided on one or both sides of
the foam sheet is not particularly limited, and for example, an
acrylic pressure-sensitive adhesive, a urethane pressure-sensitive
adhesive, a rubber pressure-sensitive adhesive, and the like is
used.
[0108] Examples of the method of applying the pressure-sensitive
adhesive to the foam sheet and laminating the pressure-sensitive
layer on the foam sheet include a method in which the
pressure-sensitive adhesive is applied to at least one side of the
foam sheet using an application machine such as a coater, a method
in which the pressure-sensitive adhesive is sprayed and applied on
at least one side of the foam sheet using a spray, a method in
which the pressure-sensitive adhesive is applied on one side of the
foam sheet using a brush, and the like.
[0109] The pressure-sensitive adhesive tape using the foam sheet of
the present invention can be suitably used as an impact absorbing
material in an aircraft. Further, the pressure-sensitive adhesive
tape can also be used as an impact absorbing material or the like
installed in the main body of an electronic device.
EXAMPLE
[0110] The present invention will be now described in more detail
by way of examples, but the present invention is not limited to
these examples.
[Measurement Methods]
[0111] The methods for measuring each physical property in this
specification are as follows.
<Apparent Density and Area Density>
[0112] The apparent density of the foam sheet was measured in
accordance with JIS K7222: 2005.
[0113] The area density of the foam sheet was calculated based on
the apparent density and thickness.
<25% Compressive Strength>
[0114] The 25% compressive strength of the foam sheet was measured
at 23.degree. C. in accordance with JIS K6767.
<Thermogravimetric-Mass Spectrometry>
[0115] Using the foam sheet of each example and comparative example
as a sample, thermogravimetric-mass spectrometry (TG-MS analysis)
was performed as follows to determine the combustion gas generation
ratio X and the combustion gas generation ratio Y. The measurement
conditions other than those described above were as follows.
(Conditions)
[0116] Apparatus: STA449F1 and QMS403 manufactured by NETZSCH
Sample: 25 mg
[0117] TG measurement conditions: After vacuum degassing the sample
chamber at 40.degree. C., the sample chamber was returned to normal
pressure with air (He/0.sub.2 =4/1 volume ratio), the temperature
was increased to 550.degree. C. at a heating rate of 10.degree.
C.min while introducing the sample into the sample chamber at 50
ml/min, and the sample was then held for 10 minutes at 550.degree.
C.
[0118] MS measurement: SCAN mode
[0119] Transfer line temperature: 280.degree. C.
[0120] Inlet system temperature: 250.degree. C.
[0121] The data obtained by measuring under the conditions
described above was analyzed using "Proteus Thermal Analysis" from
NETZSCH. In order to determine the combustion gas generation
ratios, a graph was plotted with temperature on the horizontal
axis, TG/% on a first vertical axis (or right vertical axis), and
ionic strength on a second vertical axis (or left vertical axis).
The combustion gas generation ratios were calculated from the ratio
of the peak area at a measurement temperature of 200.degree. C. to
364.degree. C. with respect to the total peak area of 200.degree.
C. to 550.degree. C. when the mass-to-charge ratio m/z of 55 or 69
was plotted on the graph. For the baseline type, a left tangent was
used when determining the peak area from 200.degree. C. to
364.degree. C., and a straight line was used when determining the
total peak area value from 200.degree. C. to 550.degree. C.
(Combustion Gas Generation Ratio X)
[0122] Combustion gas generation ratio X (%)=100.times.Peak area
value of amount of combustion gas P generated at measurement
temperature of 200 to 364.degree. C./peak area value of amount of
combustion gas P generated over an entire measurement temperature
range (200 to 550.degree. C.)
(Combustion Gas Generation Ratio Y)
[0123] Combustion gas generation ratio Y (%)=100.times.Peak area
value of amount of combustion gas Q generated at measurement
temperature of 200 to 364.degree. C./peak area value of amount of
combustion gas Q generated over an entire measurement temperature
range (200 to 550.degree. C.)
<Maximum Heating Value and Total Heating Value>
[0124] The maximum heating value and the total heating value of the
foam sheet were measured in accordance with FAR PART 25 Appendix F
Part IV.
<Crosslinking Degree (Gel Fraction)>
[0125] Approximately 100 mg of a sample piece was collected from
the foam sheet, and a weight A (mg) of the sample piece was
precisely weighed. Next, the sample piece was dipped in 30 cm.sup.3
of xylene at 120.degree. C., left for 24 hours, then filtered
through a 200 mesh wire mesh to collect the insoluble matter on the
wire mesh. The insoluble matter was vacuum dried, and a weight B
(mg) of the insoluble matter was precisely weighed. From the
obtained values, the crosslinking degree (% by mass) was calculated
based on the following formula.
Crosslinking degree (% by mass)=(B/A).times.100
<Evaluation of Fire Retardancy>
[0126] The fire retardancy of the foam sheet was evaluated based on
the above-described maximum heating value and total heating
value.
[0127] Specifically, cases in which the maximum heating value
during a 5-minute test was 65 kW/m.sup.2 or less and the total
heating value for 2 minutes after the start of the test was 65
kWmin/m.sup.2 or less were evaluated as a pass, and other cases
were evaluated as a fail.
<Starting Materials Used>
[0128] The materials used in the examples and comparative examples
are as follows.
[Polyolefin Resin]
[0129] Polypropylene: Ethylene-propylene random copolymer, "EG7F"
manufactured by Japan Polypropylene Corporation [0130]
Polyethylene: Linear low density polyethylene, "5220G" manufactured
by Dow Chemical Co., Ltd.
[Crosslinking Aid]
[0130] [0131] Crosslinking aid: Trimethylolpropane
trimethacrylate
[Foaming Agent]
[0131] [0132] Thermally decomposable foaming agent:
Azodicarbonamide
[Antioxidant]
[0132] [0133] Antioxidant A: 2,6-di-t-butyl-p-cresol [0134]
Antioxidant B: Dilaurylthiodipropionate
[Fire Retardant]
[0134] [0135] Fire retardant A: Phosphorus fire retardant, Teijin
Limited "Fireguard FCX-210", melting point 257.degree. C. [0136]
Fire retardant B: Bis(pentabromophenyl)ethane, Albemarle Japan Co.,
Ltd. "SAYTEX8010", melting point 350.degree. C. [0137] Fire
retardant C: Phosphoric acid ester, Daihachi Chemical Industry Co.,
Ltd., "TMCPP"
[Fire Retardant Aid]
[0137] [0138] Fire retardant aid: Antimony trioxide, Nihon Seiko
Co., Ltd. "PATOX-M", melting point 656.degree. C.
Example 1
[0139] An expandable composition was prepared by mixing and
kneading 80 parts by mass of polypropylene, 20 parts by mass of
polyethylene, 3.2 parts by mass of crosslinking aid, 20 parts by
mass of thermally decomposable foaming agent, 15 parts by mass of
fire retardant A, 0.5 parts by mass of antioxidant A, and 0.3 parts
by mass of antioxidant B with a laboplast mill. Then, a 2 mm
sheet-like expandable composition (hereinafter referred to as
"expandable sheet") was prepared by heat-pressing the expandable
composition at 180.degree. C. and 15 MPa.
[0140] Next, an electron beam with an acceleration voltage of 1000
kV and 1.4 Mrad was irradiated from both sides of the prepared
expandable sheet. Then, the expandable sheet was placed in a hot
air oven set to 250.degree. C. for 4 minutes, and then promptly
taken out to obtain a polyolefin resin foam sheet.
[0141] Table 1 shows the evaluation results of the obtained foam
sheet.
Examples 2 to 4 and Comparative Examples 1 to 2
[0142] The same procedures as in Example 1 were carried out, except
that the blend of the expandable composition was changed as shown
in Table 1 and the dosage at the time of cross-linking was adjusted
so as to achieve the crosslinking degree (gel fraction) shown in
Table 1.
[0143] Table 1 shows the evaluation results of the obtained foam
sheets.
TABLE-US-00001 TABLE 1 Comparative Example Example 1 2 3 4 1 2
Blend (phr) Polyolefin Polypropylene 80 80 80 80 80 80 resin
Polyethylene 20 20 20 20 20 20 Antioxidant 2,6-di-t-butyl-p-cresol
0.5 0.5 0.5 0.5 0.5 0.5 dilaurylthiodipropionate 0.3 0.3 0.3 0.3
0.3 0.3 Crosslinking trimethylolpropane 3.2 3.2 3.2 3.2 3.2 3.2 aid
trimethacrylate Thermally azodicarbonamide 20 20 20 20 20 20
decomposable foaming agent Fire retardant Fire retardant A 15 15 0
0 0 0 Fire retardant B 0 30 15 15 0 0 Fire retardant C 0 0 0 0 0 12
fire retardant aid 0 0 0 8 0 0 Specification Sheet thickness (mm) 5
9 6 6 3 5 Density (kg/m.sup.3) 28 23 28 42 40 24 Area density
(g/m.sup.2) 140 207 168 252 120 120 25% Compressive strength (kPa)
58 52 73 71 77 42 Gel fraction 43 34 36 43 45 36 Thermogravimetric-
Combustion gas generation ratio X 10 19 20 14 29 26 mass
spectrometry (mass-to-charge ratio m/z: 55) Combustion gas
generation ratio Y 12 21 21 13 29 29 (mass-to-charge ratio m/z: 69)
Fire retardancy Evaluation pass pass pass pass fail fail Maximum
heating value (kw/m.sup.2) 63 42 43 59 70 80 Total heating value
(kW min/m.sup.2) 36 33 29 50 35 35
[0144] As is clear from the above results, the polyolefin resin
foam sheet of the present invention has a high fire retardancy
while maintaining a lightweight property, and therefore can be
suitably used for applications requiring reduced weight, such as
aircraft.
* * * * *