CA1279440C - Non-crosslinked foam - Google Patents
Non-crosslinked foamInfo
- Publication number
- CA1279440C CA1279440C CA000546873A CA546873A CA1279440C CA 1279440 C CA1279440 C CA 1279440C CA 000546873 A CA000546873 A CA 000546873A CA 546873 A CA546873 A CA 546873A CA 1279440 C CA1279440 C CA 1279440C
- Authority
- CA
- Canada
- Prior art keywords
- foam
- butene
- polymer
- propylene
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D53/00—Sealing or packing elements; Sealings formed by liquid or plastics material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08J2323/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S264/00—Plastic and nonmetallic article shaping or treating: processes
- Y10S264/05—Use of one or more blowing agents together
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S264/00—Plastic and nonmetallic article shaping or treating: processes
- Y10S264/18—Cross-linking a thermoplastic linear foam during molding
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49789—Obtaining plural product pieces from unitary workpiece
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49826—Assembling or joining
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49826—Assembling or joining
- Y10T29/49863—Assembling or joining with prestressing of part
- Y10T29/4987—Elastic joining of parts
- Y10T29/49872—Confining elastic part in socket
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49826—Assembling or joining
- Y10T29/49908—Joining by deforming
- Y10T29/49915—Overedge assembling of seated part
- Y10T29/49917—Overedge assembling of seated part by necking in cup or tube wall
Abstract
1-3904 (US) WkBB:sl NON-CROSSLINKED FOAM
Abstract of the Disclosure A non-crosslinked foam of a composition comprising:
(A) 72 to 98% by weight of a 1-butene polymer; and (B) 28 to 2% by weight of a propylene polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer.
Abstract of the Disclosure A non-crosslinked foam of a composition comprising:
(A) 72 to 98% by weight of a 1-butene polymer; and (B) 28 to 2% by weight of a propylene polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer.
Description
T-3904 (US) '~KBB:sl ~X~7~4~3 ,............... .
NON-CROSS~INKED FOAM
Back~round of the Invention This invention relates to a non-crosslinked foam of a composition comprising a major proportion of a l-butene polymer and a minor proportion of a propylene polymer. More specifically7 it relates to a non-crosslinked foam of a composition comprising a l-butene polymer and a propylene polymer having excellent heat resistance, sealability and heat creep resistance. It i9 contemplated that this foam could be used 8S a cap liner or for other applications, such as foam cushion packaging, other flexible packaging end uses, backing for - wear surfaces, and other typical foam applications.
In recent years, cans for holding beverages have been superseded by bottles. Ampoules for holding pharmaceuticals are also desired to be replaced by bottles with screw caps because glass fragments are likely to get into the contents upon opening. The most important property required of caps used in such bottles is sealability7 and to secure this property, foams of high-pressure low-deusity polyethylene have gained widespread use as cap liners of thermoplastic resins.
Containers holding pharmaceuticals and drinks are usually ~ubjected to sterilization treatment at high temperatures7 or retorting7 after filling. The sterilizing temperature has recently tended to become higher for shortening the sterilizing time and increasing productivity7 and nowadays, the sterilization treatment is carried out ~ainly at temperatures as high as at least 100C.
High-pressure low-density polyethylene foams have low heat-; resistant temperatures and cannot be sterilized at high temperatures of at least 100C and therefore cannot be used for such an application.
On the other hand7 polypropy]ene has excellent heat resistance but a uniform foam of polyp~lopylene alone is very difficult to obtain.
9~
Japanese Patent Publication No. 40,167/1981 discloses a foamprepared from a mixture of 90 to 30% by weight of polypropylene and 10 to 70% by weight of polybutene-l. The patent publication states that this foam has excellent heat resistance, high-temperature creep characteristics, mechanical strength and thermal insulating property and - is suitable for use as a thermally insulating material for high-temperature structures. It also states that when the mixing proportions of polyproyplene and polybutene-l fall outside the above-specified ranges, a good foam cannot be obtained.
1~Japanese Laid-Open Patent Publication No. 129,025/1983 discloses a polyolefin ~oam prepared from a mixture of (a) 60 to 98% by weight of a propylene/ethylene block copolymer having a melt index of 0.5 to 2.0 and an ethylene content of 5 to 15%, (b) 1 to 20% by weight of polybutene or a butene copolymer having a melt index of 2 to 10, and 15(c) 1 to 2070 by weight of low-density polyethylene having a melt index of 2 to 10.
It is an object of this invention to provide a novel non-crosslinked foam of a composition comprising a 1-butene polymer and a propylene polymer. The term "non-crosslinked" has the same meaning ~as "nou-vulcanized" which, is the foam is produced without vulcanizing crosslinking) agents or irradiations for vulcanizing (crosslinking).
The term "foam" means foamed and expanded materials or sponge-like materials which have many small cells.
Another object of this invention is to provide a non-crosslinked foam suitable for use as a cap liner, such as a bottle closure, having excellent flexibility, sealability, heat resistance, heat creep resistance and hygienic property.
Further objects of this invention along with its advantages will become apparent from ~he following description.
~ ~7g4~(3 Summary of the Invention The objects and advantages of this invention are achieved by a non-crosslinked foam of a composition comprising:
(A) 72 to 98% by weight of a 1-butene polymer, and (B) 2~ to 2% by weight of a propylenP polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer~
The 1-butene polymer (A) used in this invention includes, for example, a homopolymer of 1-butene and copolymers of at least 80 moleh, preferably at least 90 mole%, of polymerized units of 1-butene and not more than 20 mole%, preferably not more than 10 mole%, of polymerized units of an alpha-olefin having 2 to 20 carbon atoms other than l-butene. The preferred olefins usable with the 1-butene are ethylene and propylene.
Examples o the other alpha-olefin having 2 to 20 carbon atoms include ethylene, p~opylene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-tetradecene, and 1-octadecene.
For easy production of a foam, the 1-butene polymer tA) (A) is preferably a crystalline polymer having a melt flow rate tMFR: ASTM
20 D1238, E) of 0.05 to 50 g/10 min., preferably 0.1 to 20 g/10 min.
The melting point of the 1-butene polymer (A) is preferably at least 100C, more preferably at least 120C, in order to give a foam having good heat resistance.
The propylene polymer (B) used in this invention includes, for exampIe, a homopolymer of propylene and copolymers composed of at least mole /O~ preferably at least 90 mole%, of polymerized units of propylene and not more than 30 mole%, preferably not more than 10 mole/0, of polymerized units of an alpha-olefin having 2 to 10 carbon atoms other than propylene. The preferred olefins usable with the present invention are butene and ethylene.
~L~7944~) Examples of the other alpha olefin having 2 to 10 carbon atoms other than propylene include ethylene, l-butene, 4-methyl-1-pentene, l-hex~ne, 1-octene, and 1-decene.
For easy praduction of a foam, the proylene polymer (B~ is S preferably a crystalline poiymer having a melt flow rate (MER: ASTM
D1238, L) of 0.1 to 50 g/10 min., more preferably 0.5 to 20 g/10 min.
The non-crosslinked foam of this Invention is composed of 72 to 98% by weight, preferably 75 to 95% by weight of the l-butene polymer (A) and 28 to 2% by weight, preferably 25 to 5% by weight, of the propylene polymer (B) because with such a composition, the foam can be easily produced and has flexibility.
The non-crosslinked foam of this invention preferably has an expansion ratio of Y.5 to 8, especially 1.7 to 4. It has good flexibility and contains a small proportion of open cells. When it is applied as a cap liner, it has excellent sealability. Sealability, as used herein is regarded as the ability of the material to form a liquid-tight seal. Continued pressure reduction resistance value (airtightness value) is an Index of Sealability. If the value is higher (maxiwn value is 334 mmHg), sealability is better.
The expansion ratio denotes the ratio of the true density (do) of the unfoamed composition from which the foam is prepared to the : apparent density (d) of the resulting foam, (do/d).
One preferred method of producing the non-crosslinked foam of this invention is a so-called extrusion foaming method which comprises extruding a composition comprising the l-butene polymer (A), the propylene polymer (B), and a blowing agent in the molten or softened state from a die to release the extrudate into an atmosphere under normal atmospheric pressure from a high pressure state, thereby expanding the gas generated from the blowing agent in the composition.
The blowing agent in such an extrusion foaming method is used generally in an amount of 0.2 to 5 parts by weight, preferably 0.4 to 2 parts by ~ ~ 8723601 ~ ;~794~
weight, per 100 parts by weight of the l-butene polymer (A) and the propylene polymer (B) co~bined. If the amount of the blowing agent is less than 0.2 part by weight, the expansion ratio is low and a good foam ".
~ ay not be obtained. If it exceeds 5 parts by weight, the expansion ratio becomes too high, and the proportion of open cells tends to become larger. Hence, the sealability of the resulting form as a cap liner is reduced.
Specific examples of the blowing agent are evaporable blowing agents, for example fluorinated aliphatic hydrocarbons such as trichloromonofluoromethane and dicholorotetrafluoroethane, and aliphatic hydrocarbons such as propane, methyl chloride, isobutane, pentane and hexane; and decomposable blowing agents such as sodium bicarbonate, ammonium car~onate, azodicarbonamide, barium azodicarboxylate, N,N'-dinitrosopentamethylenetetramine, 4,4-hydroxybis(benzenesulfonyl ` 15 hydrazide), diphenylsulfone-3,3-disulfonyl hydrazide, p-toluenesulfonyl ..
semicarbazide, trihydrazinotriazine and biurea. The evaporable blowing agents which completely volatilize leaving no residue and therefore are free from a hygenic problem, and azodicarbonamide and sodium bicarbonate as the decomposable blowing agent are preferred among them.
The composition used in this invention may contain additives normally used in polyolefins, sllch as heat stabilizers, slip agents and antistatic agents, in ~addition to the blowing agent. The amounts of these additives are such as not to impair the objects of the present i~vention. I
Amount of additives to be blended within the scope of the present invention is recommended as follows:
- heat stabilizers ; 0.1 0.5 wt%
slip agents ; 0.1 ~ 1 wt%
antistatic agents; 0.1 ~ 1 wt%
".
~.~
~79~
The ~on-crosslinked foam of this invention rnay be in various forms such as sheets, pipes, rods and tubes by properly changing the die of the extruder. A packing material such as a bot~le closure may be produced using the non-crosslinked foam of this invention by, for example, punching out (cutting out) a cap liner of a predetermined shape from the foam in a sheet or rod shape, and as required, fitting it into a metallic outer shell of a crown cap, for example, or bonding it to the shell by an adhesive or otherwise.
Since th~e no~-crosslinked foam of this invention has excellent flexibility, sealability, heat resistance, heat creep resistance and hy~ienic property, they can be used as a lining material for example of bottle closures such as various types of crown caps, pilfer-proof caps, and side seal caps. Such caps can be used for holing pharmaceuticals and beverages and can be subjected to sterilizirlg treatment at high temperatures. This foam can be mo~ified to include other additives such as flame retardants.
The following Examples illustrate the present invention in greater detail. It ,should be understood, however that the present invention is not limited in any way to these examples unless it departs from its spirit and scope.
Production of a non-crosslinked foamed sheet:
One hundred parts by weight of a resin mixture (PB-I + PP-I) composed of 95% by weight of a l-butene homopolymer (PB-I; MFR=0.4 gtlO
min.; [~]: 2.6 dl/g; melting point: 125C) and 5% by weight of a propylene ho~opolymer (PP-I; MFR=0.5 g/10 min.) were mixed by a tumbler with 0.2 trqde ~rj~
part by weight of azo'dicarbonamide (ADCA:Vinfor AC#3, a tradcna~. for a *., product of Eiwa Chemical Industry Co., Ltd.) and 0.3 part by weight of . sodium bicarbonate. The mixture was melt-kneaded in a single-screw extruder (screw diameter 40 mm; set temperature 120C) and extruded from a pipe forming die (set temperature 120C) to give a pipe-~AX8723601 1~944~3 like foam. The pipe-like foam was cut open to give a sheet-like foam having a thickness of 2 mm. The resulting foam was closed-cellular and showed a good foamed condition. The term "closed cells" used herein-means cells in which bubbles are surrounded by resin membranes in the foam and are not interconnected to one another within the foam. The term "open cells" means cells interconnected to one another within the foam. The respective percentages of these two types of cells are determined by the following equations after measuring the real volume (~V) of a test specimen of a foam by an air substitution method.
- 10 Closed cell percentage ~V - WS/dp ---- x 100 (Vol. ~) Vs " ~
Open cell percentage Vs - ~
-~ x 100 (Vol. %) Vs Vs: The apparent.volume of the test specimen.
WS: The weight of the test specimen.
QV: The real volume of the test specimen.
dp: The density of the plastic material constituting specimen.
It had an apparent density of 0.53 g/cm3 and a surface harness, deter-mined in accordance with JIS K-6301, of 82.
- Evaluation of the properties of the foam as a cap liner:
A packing material, 27.5 mm in diameter, punched out from the resulting sheet-like foam was pushed and fitted into the inner surface of an aluminum cap having a diameter of 28 mm. Hot water at 80C was poured in an amount of 110 ml into glass bottle having a capacity of 120 ml and a mouth diameter of 25 mm, and immediately then, the glass bottle was sealed up with the resulting cap by using a capping machine (made by Shibasaki Seisakusho). The glass bottle was then left to stand in a 30 retorting kettle at 121C for 30 minutes and taken out. It was laid . ~. . down and allowed to cool at room temperature for 24 hours. Then, the HA~8723601 34~
, - 8 -bottle was checked for leakage of the water it held. Thereafter, the airtightness value and the opening torque value of the glass bottle were measured by the following methods.
Continued pressure reduction resistance value (airtightness value) (mmHg):
A pressure gauge was thrusted into the cap of the glass bottle, and the pressure of the inside of the bo-ttle was measured.
If the bottle is completely sealed up, the pressure of the inside of the bottle ought to be 334 mmHg as a difference between the 10vapor pressure (355 mmHg) at 80C of water and the vapor pressure (21 mmHg) of water at room temperature (23C). The sealability of the glass bottle is better as the airtightness value is nearer to 334 mmHg. When there is leakage, the pressure is O mmHg.
Opening torque value (kg-cm):
15The torque of the cap at the time of opening the bottle was measured by using a torque meter and used as a measure of the ease of bottle opening. To secure good sealability with a screw cap, it is generally sufficient to close it tightly. If, however, it is closed too tightly, it cannot be easily opened by a humau power. The torque value which permits easy opening by aged people, women and children is ", considered to be not more than 10 kg-cm.
The results are shown in Table 1.
Example 1 was repeated except that a propylene/ethylene random 25copolymer (PEC~ PR: 0.5 g/10 min.; ethylene content: 3 mole%) in the amounts indicated in Table 1 was used instead of PP-I used in Example 1. The results were good as shown in Table 1.
Example 1 was repeated except that PEC-I used in Example 2 was used in the amount indicated in Table 1 instead of PP-I used in Example HA~8723601 1~'34~() 1. Probably because the cap liner composed of the resulting foam had too high a hardness, its adhesion to the bottle mouth was poor, and as shown in Table 1 leakage occurred. The airtightness value was as low as 20 mmHg. The opening torque value was also low.
Example 1 was repeated except that PEC-I used in Example 1 was used in the amount indicated in Table 1 instead of PP-I used in Example 1. ThP foamed state of the resulting foam was bad, and the expansion ratio was not so high. The foam was not closed-cellular, but open-cellular. The properties of the foam as a cap liner were also poor.
The results are shown in Table 1.
1~AX8723601 - ~794~3 --1 o. --._ .
~ ~ o o o ~ ~
E !a Z Z Z ::~
U~ ~ ~ 1~
t~l G . .___ .
H ~ I 00 ~_ 1~ l a ~ E
P~ ~ Q) ~ 00 ~ .q ~ o~
j ~ .....
~ ~ ~ 04 ~: ,~ o o o c~J o r~ ~ C~J
1~ ~ ~
_ . ~ .
_~
o u~ ~ ~ O In o u, ~ ~ . 00 o~
h p~ 4 .
~ _ , _ .~ ~ ~
.- O rl ~ ~ ~ ~ ~0 H 00 O O O, O O
~3 ~ ~q ..... _.__ O ~
~ ~ ~ ~ ~C ~ ~ , E ~ C 4-1 0 O O O O O
~ C O ~ O O O O O O
O O rl I E C~
~ u J~
.: _ _ . _ ~1~
~.: .,1 ~ p~
~ ~ C ~ ~
O ~ ~0 . . . , .
~ . ,~ . o o o o o :~ . ~: ~ æ
3 _ ~' O ~ ~-.: p:~ ~ ~.1 ~ C~ ~1 C'~ C`l ~ C~ O O O O
_ , . ._ _ _ ~ 37 I ~ O
.' . . _ _ ~ ~ I
;~ P-~ 3 IJ~
~:4 _ _ :~ ~
~ 3 ~7 L~ O
~ ., C
: ~ ~
~- ~ r ~o ~1 _ _ .~
..
NON-CROSS~INKED FOAM
Back~round of the Invention This invention relates to a non-crosslinked foam of a composition comprising a major proportion of a l-butene polymer and a minor proportion of a propylene polymer. More specifically7 it relates to a non-crosslinked foam of a composition comprising a l-butene polymer and a propylene polymer having excellent heat resistance, sealability and heat creep resistance. It i9 contemplated that this foam could be used 8S a cap liner or for other applications, such as foam cushion packaging, other flexible packaging end uses, backing for - wear surfaces, and other typical foam applications.
In recent years, cans for holding beverages have been superseded by bottles. Ampoules for holding pharmaceuticals are also desired to be replaced by bottles with screw caps because glass fragments are likely to get into the contents upon opening. The most important property required of caps used in such bottles is sealability7 and to secure this property, foams of high-pressure low-deusity polyethylene have gained widespread use as cap liners of thermoplastic resins.
Containers holding pharmaceuticals and drinks are usually ~ubjected to sterilization treatment at high temperatures7 or retorting7 after filling. The sterilizing temperature has recently tended to become higher for shortening the sterilizing time and increasing productivity7 and nowadays, the sterilization treatment is carried out ~ainly at temperatures as high as at least 100C.
High-pressure low-density polyethylene foams have low heat-; resistant temperatures and cannot be sterilized at high temperatures of at least 100C and therefore cannot be used for such an application.
On the other hand7 polypropy]ene has excellent heat resistance but a uniform foam of polyp~lopylene alone is very difficult to obtain.
9~
Japanese Patent Publication No. 40,167/1981 discloses a foamprepared from a mixture of 90 to 30% by weight of polypropylene and 10 to 70% by weight of polybutene-l. The patent publication states that this foam has excellent heat resistance, high-temperature creep characteristics, mechanical strength and thermal insulating property and - is suitable for use as a thermally insulating material for high-temperature structures. It also states that when the mixing proportions of polyproyplene and polybutene-l fall outside the above-specified ranges, a good foam cannot be obtained.
1~Japanese Laid-Open Patent Publication No. 129,025/1983 discloses a polyolefin ~oam prepared from a mixture of (a) 60 to 98% by weight of a propylene/ethylene block copolymer having a melt index of 0.5 to 2.0 and an ethylene content of 5 to 15%, (b) 1 to 20% by weight of polybutene or a butene copolymer having a melt index of 2 to 10, and 15(c) 1 to 2070 by weight of low-density polyethylene having a melt index of 2 to 10.
It is an object of this invention to provide a novel non-crosslinked foam of a composition comprising a 1-butene polymer and a propylene polymer. The term "non-crosslinked" has the same meaning ~as "nou-vulcanized" which, is the foam is produced without vulcanizing crosslinking) agents or irradiations for vulcanizing (crosslinking).
The term "foam" means foamed and expanded materials or sponge-like materials which have many small cells.
Another object of this invention is to provide a non-crosslinked foam suitable for use as a cap liner, such as a bottle closure, having excellent flexibility, sealability, heat resistance, heat creep resistance and hygienic property.
Further objects of this invention along with its advantages will become apparent from ~he following description.
~ ~7g4~(3 Summary of the Invention The objects and advantages of this invention are achieved by a non-crosslinked foam of a composition comprising:
(A) 72 to 98% by weight of a 1-butene polymer, and (B) 2~ to 2% by weight of a propylenP polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer~
The 1-butene polymer (A) used in this invention includes, for example, a homopolymer of 1-butene and copolymers of at least 80 moleh, preferably at least 90 mole%, of polymerized units of 1-butene and not more than 20 mole%, preferably not more than 10 mole%, of polymerized units of an alpha-olefin having 2 to 20 carbon atoms other than l-butene. The preferred olefins usable with the 1-butene are ethylene and propylene.
Examples o the other alpha-olefin having 2 to 20 carbon atoms include ethylene, p~opylene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-tetradecene, and 1-octadecene.
For easy production of a foam, the 1-butene polymer tA) (A) is preferably a crystalline polymer having a melt flow rate tMFR: ASTM
20 D1238, E) of 0.05 to 50 g/10 min., preferably 0.1 to 20 g/10 min.
The melting point of the 1-butene polymer (A) is preferably at least 100C, more preferably at least 120C, in order to give a foam having good heat resistance.
The propylene polymer (B) used in this invention includes, for exampIe, a homopolymer of propylene and copolymers composed of at least mole /O~ preferably at least 90 mole%, of polymerized units of propylene and not more than 30 mole%, preferably not more than 10 mole/0, of polymerized units of an alpha-olefin having 2 to 10 carbon atoms other than propylene. The preferred olefins usable with the present invention are butene and ethylene.
~L~7944~) Examples of the other alpha olefin having 2 to 10 carbon atoms other than propylene include ethylene, l-butene, 4-methyl-1-pentene, l-hex~ne, 1-octene, and 1-decene.
For easy praduction of a foam, the proylene polymer (B~ is S preferably a crystalline poiymer having a melt flow rate (MER: ASTM
D1238, L) of 0.1 to 50 g/10 min., more preferably 0.5 to 20 g/10 min.
The non-crosslinked foam of this Invention is composed of 72 to 98% by weight, preferably 75 to 95% by weight of the l-butene polymer (A) and 28 to 2% by weight, preferably 25 to 5% by weight, of the propylene polymer (B) because with such a composition, the foam can be easily produced and has flexibility.
The non-crosslinked foam of this invention preferably has an expansion ratio of Y.5 to 8, especially 1.7 to 4. It has good flexibility and contains a small proportion of open cells. When it is applied as a cap liner, it has excellent sealability. Sealability, as used herein is regarded as the ability of the material to form a liquid-tight seal. Continued pressure reduction resistance value (airtightness value) is an Index of Sealability. If the value is higher (maxiwn value is 334 mmHg), sealability is better.
The expansion ratio denotes the ratio of the true density (do) of the unfoamed composition from which the foam is prepared to the : apparent density (d) of the resulting foam, (do/d).
One preferred method of producing the non-crosslinked foam of this invention is a so-called extrusion foaming method which comprises extruding a composition comprising the l-butene polymer (A), the propylene polymer (B), and a blowing agent in the molten or softened state from a die to release the extrudate into an atmosphere under normal atmospheric pressure from a high pressure state, thereby expanding the gas generated from the blowing agent in the composition.
The blowing agent in such an extrusion foaming method is used generally in an amount of 0.2 to 5 parts by weight, preferably 0.4 to 2 parts by ~ ~ 8723601 ~ ;~794~
weight, per 100 parts by weight of the l-butene polymer (A) and the propylene polymer (B) co~bined. If the amount of the blowing agent is less than 0.2 part by weight, the expansion ratio is low and a good foam ".
~ ay not be obtained. If it exceeds 5 parts by weight, the expansion ratio becomes too high, and the proportion of open cells tends to become larger. Hence, the sealability of the resulting form as a cap liner is reduced.
Specific examples of the blowing agent are evaporable blowing agents, for example fluorinated aliphatic hydrocarbons such as trichloromonofluoromethane and dicholorotetrafluoroethane, and aliphatic hydrocarbons such as propane, methyl chloride, isobutane, pentane and hexane; and decomposable blowing agents such as sodium bicarbonate, ammonium car~onate, azodicarbonamide, barium azodicarboxylate, N,N'-dinitrosopentamethylenetetramine, 4,4-hydroxybis(benzenesulfonyl ` 15 hydrazide), diphenylsulfone-3,3-disulfonyl hydrazide, p-toluenesulfonyl ..
semicarbazide, trihydrazinotriazine and biurea. The evaporable blowing agents which completely volatilize leaving no residue and therefore are free from a hygenic problem, and azodicarbonamide and sodium bicarbonate as the decomposable blowing agent are preferred among them.
The composition used in this invention may contain additives normally used in polyolefins, sllch as heat stabilizers, slip agents and antistatic agents, in ~addition to the blowing agent. The amounts of these additives are such as not to impair the objects of the present i~vention. I
Amount of additives to be blended within the scope of the present invention is recommended as follows:
- heat stabilizers ; 0.1 0.5 wt%
slip agents ; 0.1 ~ 1 wt%
antistatic agents; 0.1 ~ 1 wt%
".
~.~
~79~
The ~on-crosslinked foam of this invention rnay be in various forms such as sheets, pipes, rods and tubes by properly changing the die of the extruder. A packing material such as a bot~le closure may be produced using the non-crosslinked foam of this invention by, for example, punching out (cutting out) a cap liner of a predetermined shape from the foam in a sheet or rod shape, and as required, fitting it into a metallic outer shell of a crown cap, for example, or bonding it to the shell by an adhesive or otherwise.
Since th~e no~-crosslinked foam of this invention has excellent flexibility, sealability, heat resistance, heat creep resistance and hy~ienic property, they can be used as a lining material for example of bottle closures such as various types of crown caps, pilfer-proof caps, and side seal caps. Such caps can be used for holing pharmaceuticals and beverages and can be subjected to sterilizirlg treatment at high temperatures. This foam can be mo~ified to include other additives such as flame retardants.
The following Examples illustrate the present invention in greater detail. It ,should be understood, however that the present invention is not limited in any way to these examples unless it departs from its spirit and scope.
Production of a non-crosslinked foamed sheet:
One hundred parts by weight of a resin mixture (PB-I + PP-I) composed of 95% by weight of a l-butene homopolymer (PB-I; MFR=0.4 gtlO
min.; [~]: 2.6 dl/g; melting point: 125C) and 5% by weight of a propylene ho~opolymer (PP-I; MFR=0.5 g/10 min.) were mixed by a tumbler with 0.2 trqde ~rj~
part by weight of azo'dicarbonamide (ADCA:Vinfor AC#3, a tradcna~. for a *., product of Eiwa Chemical Industry Co., Ltd.) and 0.3 part by weight of . sodium bicarbonate. The mixture was melt-kneaded in a single-screw extruder (screw diameter 40 mm; set temperature 120C) and extruded from a pipe forming die (set temperature 120C) to give a pipe-~AX8723601 1~944~3 like foam. The pipe-like foam was cut open to give a sheet-like foam having a thickness of 2 mm. The resulting foam was closed-cellular and showed a good foamed condition. The term "closed cells" used herein-means cells in which bubbles are surrounded by resin membranes in the foam and are not interconnected to one another within the foam. The term "open cells" means cells interconnected to one another within the foam. The respective percentages of these two types of cells are determined by the following equations after measuring the real volume (~V) of a test specimen of a foam by an air substitution method.
- 10 Closed cell percentage ~V - WS/dp ---- x 100 (Vol. ~) Vs " ~
Open cell percentage Vs - ~
-~ x 100 (Vol. %) Vs Vs: The apparent.volume of the test specimen.
WS: The weight of the test specimen.
QV: The real volume of the test specimen.
dp: The density of the plastic material constituting specimen.
It had an apparent density of 0.53 g/cm3 and a surface harness, deter-mined in accordance with JIS K-6301, of 82.
- Evaluation of the properties of the foam as a cap liner:
A packing material, 27.5 mm in diameter, punched out from the resulting sheet-like foam was pushed and fitted into the inner surface of an aluminum cap having a diameter of 28 mm. Hot water at 80C was poured in an amount of 110 ml into glass bottle having a capacity of 120 ml and a mouth diameter of 25 mm, and immediately then, the glass bottle was sealed up with the resulting cap by using a capping machine (made by Shibasaki Seisakusho). The glass bottle was then left to stand in a 30 retorting kettle at 121C for 30 minutes and taken out. It was laid . ~. . down and allowed to cool at room temperature for 24 hours. Then, the HA~8723601 34~
, - 8 -bottle was checked for leakage of the water it held. Thereafter, the airtightness value and the opening torque value of the glass bottle were measured by the following methods.
Continued pressure reduction resistance value (airtightness value) (mmHg):
A pressure gauge was thrusted into the cap of the glass bottle, and the pressure of the inside of the bo-ttle was measured.
If the bottle is completely sealed up, the pressure of the inside of the bottle ought to be 334 mmHg as a difference between the 10vapor pressure (355 mmHg) at 80C of water and the vapor pressure (21 mmHg) of water at room temperature (23C). The sealability of the glass bottle is better as the airtightness value is nearer to 334 mmHg. When there is leakage, the pressure is O mmHg.
Opening torque value (kg-cm):
15The torque of the cap at the time of opening the bottle was measured by using a torque meter and used as a measure of the ease of bottle opening. To secure good sealability with a screw cap, it is generally sufficient to close it tightly. If, however, it is closed too tightly, it cannot be easily opened by a humau power. The torque value which permits easy opening by aged people, women and children is ", considered to be not more than 10 kg-cm.
The results are shown in Table 1.
Example 1 was repeated except that a propylene/ethylene random 25copolymer (PEC~ PR: 0.5 g/10 min.; ethylene content: 3 mole%) in the amounts indicated in Table 1 was used instead of PP-I used in Example 1. The results were good as shown in Table 1.
Example 1 was repeated except that PEC-I used in Example 2 was used in the amount indicated in Table 1 instead of PP-I used in Example HA~8723601 1~'34~() 1. Probably because the cap liner composed of the resulting foam had too high a hardness, its adhesion to the bottle mouth was poor, and as shown in Table 1 leakage occurred. The airtightness value was as low as 20 mmHg. The opening torque value was also low.
Example 1 was repeated except that PEC-I used in Example 1 was used in the amount indicated in Table 1 instead of PP-I used in Example 1. ThP foamed state of the resulting foam was bad, and the expansion ratio was not so high. The foam was not closed-cellular, but open-cellular. The properties of the foam as a cap liner were also poor.
The results are shown in Table 1.
1~AX8723601 - ~794~3 --1 o. --._ .
~ ~ o o o ~ ~
E !a Z Z Z ::~
U~ ~ ~ 1~
t~l G . .___ .
H ~ I 00 ~_ 1~ l a ~ E
P~ ~ Q) ~ 00 ~ .q ~ o~
j ~ .....
~ ~ ~ 04 ~: ,~ o o o c~J o r~ ~ C~J
1~ ~ ~
_ . ~ .
_~
o u~ ~ ~ O In o u, ~ ~ . 00 o~
h p~ 4 .
~ _ , _ .~ ~ ~
.- O rl ~ ~ ~ ~ ~0 H 00 O O O, O O
~3 ~ ~q ..... _.__ O ~
~ ~ ~ ~ ~C ~ ~ , E ~ C 4-1 0 O O O O O
~ C O ~ O O O O O O
O O rl I E C~
~ u J~
.: _ _ . _ ~1~
~.: .,1 ~ p~
~ ~ C ~ ~
O ~ ~0 . . . , .
~ . ,~ . o o o o o :~ . ~: ~ æ
3 _ ~' O ~ ~-.: p:~ ~ ~.1 ~ C~ ~1 C'~ C`l ~ C~ O O O O
_ , . ._ _ _ ~ 37 I ~ O
.' . . _ _ ~ ~ I
;~ P-~ 3 IJ~
~:4 _ _ :~ ~
~ 3 ~7 L~ O
~ ., C
: ~ ~
~- ~ r ~o ~1 _ _ .~
..
Claims (15)
1. A non-crosslinked foam of a composition comprising:
(A) 72 to 98% by weight of a 1-butene polymer, and (B) 28 to 2% by weight of a propylene polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer.
(A) 72 to 98% by weight of a 1-butene polymer, and (B) 28 to 2% by weight of a propylene polymer, the percentages being based on the total weight of the 1-butene polymer and the propylene polymer.
2. The foam of claim 1 wherein the 1-butene polymer is a 1-butene homopolymer.
3. The foam of claim 1 wherein the 1-butene polymer is a copolymer composed of at least 80 mole% of polymerized units of 1-butene and not more than 20 mole% of an alpha-olefin having 2 to 20 carbon atoms other than 1-butene.
4. The foam of claim 1 wherein the 1-butene polymer has a melt flow rate of 0.05 to 50 g/10 min.
5. The foam of claim 1 wherein the propylene polymer is a propylene homopolymer.
6. The foam of claim 1 wherein the propylene polymer is a copolymer composed of at least 70 mole% of polymerized units of propylene and not more than 30 mole% of polymerized units of an alpha-olefin having 2 to 10 carbon atoms other than propylene.
7. The foam of claim 1 wherein the propylene polymer has a melt flow rate of 0.1 to 50 g/10 min.
8. The foam of claim 1 which comprises 75 to 95% by weight of the 1-butene polymer and 25 to 5% by weight of the propylene polymer.
9. The foam of claim 1 which has an expansion ratio of from 1.5 to 8.
10. The foam of claim 1 which has an expansion ratio of from 1.7 to 4.
11. A cap liner comprising a non-crosslinked foam of a composition comprising:
72 to 98% by weight of a 1-butene polymer, and
72 to 98% by weight of a 1-butene polymer, and
12 61815-3234 28 to 2% by weight of a propylene polymer, the percentages being based on the total weight of the 1-butene polymer and the pxopylene polymer.
12. A process for makiny a non-crosslinked foam comprising the steps of:
blending 72 to 98% by weiyht of a 1-butene polymer with 28 to 2% by weight of a propylene polymer in a mixer;
melt-kneading the mixture in an extruder;
extruding the melt-kneaded mixture from a die therein forming a foam sheet;
punching out cap inserts from the foam sheet;
disposing the punched out inserts on the inner surface of a bottle cap forming a lined cap; and sealing a bottle with the lined cap.
12. A process for makiny a non-crosslinked foam comprising the steps of:
blending 72 to 98% by weiyht of a 1-butene polymer with 28 to 2% by weight of a propylene polymer in a mixer;
melt-kneading the mixture in an extruder;
extruding the melt-kneaded mixture from a die therein forming a foam sheet;
punching out cap inserts from the foam sheet;
disposing the punched out inserts on the inner surface of a bottle cap forming a lined cap; and sealing a bottle with the lined cap.
13. The foam of claim 3 wherein the other alpha-olefin is a member of the group consisting of ethylene and propylene.
14. The foam of claim 6 wherein the other alpha-olefin is a member of the group consisting of butene and ethylene.
15. A process for making a non-crosslinked form comprising the steps of:
blending 72 to 98% by weight of a 1-butene polymer selected from the group consisting of a homopolyer, and copolymer composed of at least 80 mole % of polymerized units of 1-butene and not more than 20 mole % of an alpha-olefin having 2 to 20 carbon atoms other than 1-butene and mixtures thereof with 28 to 2% by weight of a propylene polymer selected from the group consisting of a homopolymer, and a copolymer composed of at least 70 mole % of polymerized units of propylene and not more than 30 mole % of polymerized units of an alpha-olefin having 2 to 10 carbon atoms other than propylene and mixtures thereof, and a blowing agent in a mixer;
melt-kneading the mixture in an extruder;
extruding the melt-kneading mixture from a die therein forming a foam sheet;
punching out cap inserts from the foam sheet;
disposing the punched out inserts on the inner surface of a bottle cap forming a lined cap; and sealing a bottle with the lined cap.
blending 72 to 98% by weight of a 1-butene polymer selected from the group consisting of a homopolyer, and copolymer composed of at least 80 mole % of polymerized units of 1-butene and not more than 20 mole % of an alpha-olefin having 2 to 20 carbon atoms other than 1-butene and mixtures thereof with 28 to 2% by weight of a propylene polymer selected from the group consisting of a homopolymer, and a copolymer composed of at least 70 mole % of polymerized units of propylene and not more than 30 mole % of polymerized units of an alpha-olefin having 2 to 10 carbon atoms other than propylene and mixtures thereof, and a blowing agent in a mixer;
melt-kneading the mixture in an extruder;
extruding the melt-kneading mixture from a die therein forming a foam sheet;
punching out cap inserts from the foam sheet;
disposing the punched out inserts on the inner surface of a bottle cap forming a lined cap; and sealing a bottle with the lined cap.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61215844A JPH0660255B2 (en) | 1986-09-16 | 1986-09-16 | Non-crosslinked foam |
JP215844/86 | 1986-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1279440C true CA1279440C (en) | 1991-01-22 |
Family
ID=16679205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000546873A Expired - Lifetime CA1279440C (en) | 1986-09-16 | 1987-09-15 | Non-crosslinked foam |
Country Status (6)
Country | Link |
---|---|
US (2) | US4739547A (en) |
EP (1) | EP0264193B1 (en) |
JP (1) | JPH0660255B2 (en) |
AT (1) | ATE77399T1 (en) |
CA (1) | CA1279440C (en) |
DE (1) | DE3779854T2 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07116309B2 (en) * | 1987-02-28 | 1995-12-13 | 三井石油化学工業株式会社 | Composition for non-crosslinked foam |
JPH0712648B2 (en) * | 1987-09-11 | 1995-02-15 | 三井石油化学工業株式会社 | Laminate based on non-crosslinked foam |
US5208266A (en) * | 1992-04-28 | 1993-05-04 | Toshimichi Yamazaki | Lightly crosslinked polymeric foams and process for making same |
US5585411A (en) * | 1993-08-11 | 1996-12-17 | Shell Oil Company | Plastic foams made from polybutylene blends |
FR2710089B1 (en) * | 1993-09-17 | 1995-12-01 | Hopenko Marie Francoise | Isophonic anti-lifting wedge. |
US5542892A (en) * | 1994-08-15 | 1996-08-06 | Unisen, Inc. | Supporting chassis for a treadmill |
US5929129A (en) | 1994-09-19 | 1999-07-27 | Sentinel Products Corp. | Crosslinked foamable compositions of silane-grafted, essentially linear polyolefins blended with polypropylene |
US5883144A (en) | 1994-09-19 | 1999-03-16 | Sentinel Products Corp. | Silane-grafted materials for solid and foam applications |
DE69528941T2 (en) | 1994-09-19 | 2003-09-18 | Sentinel Products Corp | Cross-linked foam structures of mainly linear polyolefins and manufacturing processes |
US5932659A (en) | 1994-09-19 | 1999-08-03 | Sentinel Products Corp. | Polymer blend |
US5844009A (en) | 1996-04-26 | 1998-12-01 | Sentinel Products Corp. | Cross-linked low-density polymer foam |
CA2203595A1 (en) | 1996-04-26 | 1997-10-26 | Robert F. Hurley | Cross-linked polyolefin tape |
US5876813A (en) | 1996-07-09 | 1999-03-02 | Senitnel Products Corp | Laminated foam structures with enhanced properties |
US5882776A (en) | 1996-07-09 | 1999-03-16 | Sentinel Products Corp. | Laminated foam structures with enhanced properties |
US5938878A (en) | 1996-08-16 | 1999-08-17 | Sentinel Products Corp. | Polymer structures with enhanced properties |
US5962543A (en) * | 1996-11-15 | 1999-10-05 | Mitsui Chemicals, Inc. | Foam processable rubber compositions and vulcanized rubber foam molded products of the same |
JP4126491B2 (en) * | 2003-03-06 | 2008-07-30 | 住友化学株式会社 | Foamable resin composition and propylene-based resin foam |
JP6720172B2 (en) * | 2014-12-19 | 2020-07-08 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | Soft and flexible polyolefin composition |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE570550A (en) * | 1957-12-09 | |||
US3062758A (en) * | 1959-06-10 | 1962-11-06 | Chemical Products Corp | Plastisol compositions and method of making them |
DE2613939C3 (en) * | 1976-04-01 | 1978-10-05 | Chemische Werke Huels Ag, 4370 Marl | Process for the production of foamed plastic and plastic-elastic polyolefin compositions |
JPS5311965A (en) * | 1976-07-20 | 1978-02-02 | Sumitomo Chemical Co | Process for manufacture of polyolefin foam |
JPS57197132A (en) * | 1981-05-29 | 1982-12-03 | Sumitomo Chem Co Ltd | Manufacture of polypropylene foam |
DE3471671D1 (en) * | 1983-04-05 | 1988-07-07 | Kanegafuchi Chemical Ind | Pre-expanded particle of polyolefin and process for preparing the same |
JPS60110734A (en) * | 1983-11-21 | 1985-06-17 | Japan Styrene Paper Co Ltd | Pre-expanded particle of uncrosslinked polypropylene resin |
JPS60123540A (en) * | 1983-12-07 | 1985-07-02 | Japan Styrene Paper Co Ltd | Noncrosslinked polypropylene resin prefoamed particle |
JPS60168632A (en) * | 1984-02-13 | 1985-09-02 | Japan Styrene Paper Co Ltd | Expanded molding of bridged polypropylene resin |
JPS61103944A (en) * | 1984-10-29 | 1986-05-22 | Mitsubishi Yuka Badische Kk | Foamable polypropylene particle |
JPS61115940A (en) * | 1984-11-09 | 1986-06-03 | Mitsubishi Yuka Badische Kk | Polypropylene foam particle |
-
1986
- 1986-09-16 JP JP61215844A patent/JPH0660255B2/en not_active Expired - Fee Related
-
1987
- 1987-09-11 US US07/096,100 patent/US4739547A/en not_active Expired - Lifetime
- 1987-09-15 CA CA000546873A patent/CA1279440C/en not_active Expired - Lifetime
- 1987-09-16 AT AT87308191T patent/ATE77399T1/en active
- 1987-09-16 DE DE8787308191T patent/DE3779854T2/en not_active Expired - Fee Related
- 1987-09-16 EP EP87308191A patent/EP0264193B1/en not_active Expired - Lifetime
- 1987-11-16 US US07/121,497 patent/US4791147A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0264193A3 (en) | 1988-11-23 |
US4739547A (en) | 1988-04-26 |
ATE77399T1 (en) | 1992-07-15 |
JPH0660255B2 (en) | 1994-08-10 |
US4791147A (en) | 1988-12-13 |
EP0264193B1 (en) | 1992-06-17 |
JPS6372733A (en) | 1988-04-02 |
DE3779854D1 (en) | 1992-07-23 |
DE3779854T2 (en) | 1993-02-04 |
EP0264193A2 (en) | 1988-04-20 |
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