GB2097324A - Shrink films of ethylene/ alpha - olefin copolymers - Google Patents
Shrink films of ethylene/ alpha - olefin copolymers Download PDFInfo
- Publication number
- GB2097324A GB2097324A GB8211739A GB8211739A GB2097324A GB 2097324 A GB2097324 A GB 2097324A GB 8211739 A GB8211739 A GB 8211739A GB 8211739 A GB8211739 A GB 8211739A GB 2097324 A GB2097324 A GB 2097324A
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- GB
- United Kingdom
- Prior art keywords
- film
- ethylene
- copolymer
- octene
- shrink
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 239000005977 Ethylene Substances 0.000 title claims abstract description 28
- 229920006300 shrink film Polymers 0.000 title claims abstract description 20
- 239000004711 α-olefin Substances 0.000 title abstract 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 title description 4
- 229920001577 copolymer Polymers 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 22
- 238000002844 melting Methods 0.000 claims abstract description 18
- 230000008018 melting Effects 0.000 claims abstract description 18
- 229920001519 homopolymer Polymers 0.000 claims abstract description 6
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 22
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 8
- 238000000113 differential scanning calorimetry Methods 0.000 claims description 6
- 229920005684 linear copolymer Polymers 0.000 claims description 5
- 229920001038 ethylene copolymer Polymers 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 230000005855 radiation Effects 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 abstract description 13
- 230000003287 optical effect Effects 0.000 abstract description 6
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 239000004698 Polyethylene Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 4
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000002952 polymeric resin Substances 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012967 coordination catalyst Substances 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
- B29C61/003—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor characterised by the choice of 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0049—Heat shrinkable
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2007/00—Flat articles, e.g. films or sheets
- B29L2007/008—Wide strips, e.g. films, webs
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
Abstract
A shrink film having high optical clarity, good shrink properties, and good mechanical properties is obtained by stretching biaxially a film made of a copolymer of ethylene with at least one C8-C18 alpha -olefin, which copolymer has two distinct crystallite melting points below 128 DEG C, the difference between these melting points being at least 15 DEG C, and stretching being carried within the temperature range defined by these melting points. The above copolymer may be blended with a homopolymer of ethylene or copolymer of ethylene with an ethylenically unsaturated comonomer, which may constitute up to about 95 weight % of the blend.
Description
SPECIFICATION
Shrink films of ethylenela-olefin copolymers BACKGROUND OF THE INVENTION
This invention relates to shrink films based on selected linear, low density copolymers of ethylene with certain a-olefins, which films have outstanding optical properties and a good balance of other physical properties and shrink properties.
Shrink films of oriented polyethylene and various copoI,'mers of ethylene are well known; see, for example, U.S. Patents 3,299,194 to Golike and 3,663,662 to Golike et al.
A polyolefin shrink film, used mainly for wrapping food products and a variety of consumer goods, should have good optical clarity; otherwise, the consumer appeal of the packaged article within the wrapping-would be diminished or lost. For practical applications, the film should shrink within a temperature range of approximately 100 to 1 200C to a degree of at least 15% in the direction of orientation and with sufficient force to provide a tight-fitting skin around the article enclosed within the wrapping. The film also should have good mechanical properties, such as tensile strength and modulus, so that it will stretch and then shrink without tearing, will maintain good physical contact with the packaged article at all times, and will not get easily damaged in handling.
One prior art technique for making ethylene polymer shrink films required polymer crosslinking prior to stretching in order to impart to the film greater mechanical strength. This crosslinking usually was accomplished by irradiation with high energy particles or with gamma rays.
In order to obtain a resin composition yielding films with satisfactory properties for shrink film applications without crosslinking prior to stretching, it has been generally necessary in the past to blend low density and high density ethylene polymers. Naturally, it would be desirable to be able to make shrink films from a single low density ethylene polymer resin. In this context, the term "low density" means 0.940 g/cm3 or less, and "high density" means more than 0.940 g/cm3.
A recent commercial offering of the Dow Chemical Company, DOWLEX~ low density "polyethylene" resins, are described in a Dow bulletin as giving blown film having excellent optics and superior strength properties. Yet, the same bulletin indicates that these resins are not suitable for making shrink films because they will shrink less than conventional low density polyethylene film and will shrink within a narrower temperature range. DOWLEX~ resins are in fact copolymers of ethylene with 1 -octene.
SUMMARY OF THE INVENTION
According to this invention; there is now provided a shrink film having high optical clarity, good shrink properties, and good mechanical properties, said film being obtained by stretching at least three times its original linear dimension in at least one direction a film made of the following homogeneous polymeric composition:
(1) 5-100 weight % of afleast one linear copolymer of ethylene with at least one C8~C18 a-olefin, said copolymer having the following characteristics:
(a) melt index of 0.1-4.0 g/1 0 min;
(b) density of 0.900 to 0.940 g/cm3;
(c) stress exponent above 1.3; and
(d) two distinct crystallite melting regions below 1 280C as determined by differential scanning calorimetry (DSC), the temperature difference between those regions being at least 1 5 C; and
(2) 0~95 weight % of at least one polymer selected from the group consisting of ethylene homopolymers and copolymers of ethylene with an ethylenically unsaturated comonomer, said polymer having only one crystallite melting point below 1 28 C; with the proviso that stretching is done within the temperature range defined by the two crystallite melting points of the linear copolymers of ethylene with C8-C18 a-olefin of the above paragraph (1).
BRIEF DESCRIPTION OF THE DRAWINGS
The drawings represent DSC plots for three different resins. FIG. 1 is the plot for polyethylene,
FIG: 2 for a commercial linear ethylene/i -octene copolymer, and FIG. 3 for a blend of high and low density ethylene polymers.
DETAILED DESCRIPTION OF THE INVENTION
The principal resin used in the compositions of the present invention is a linear copolymer of ethylene with an a-olefin. Typical #-olefins which can be copolymerized with ethylene are 1 -octene, 1 -decene, 1 -undecene, 1 -dodecene, and 1 -hexadecene. The copolymers are prepared at a low to moderate pressure (about 29.4 MPa) in the presence of a coordination catalyst according to the generally known technique of the so-called Ziegler and Natta processes. Typical catalysts are various organoaluminum, organotitanium, and organovanadium compounds, and especially titanium-modified organoaluminum compounds. The preparation of ethylene copolymers with a-olefins is taught, for example, in U.S.Patents 4,076,698 to Anderson et al. and"4,205,021 to Morita et al.
Suitable commercially available copolymers of ethylene with higher a-olefins include the above mentioned DOWLEX~ resins, and the preferred copolymer is that with 1 -octene. As the proportion of a-olefin in the copolymer or the molecular weight of a-olefin increases the density of the copolymer decreases. For 1 -octene, the amount of this a-olefin in the copolymer normally will be between about 3 and 16 weight percent. However, the amount of each such comonomer will be so chosen that proper values of melt index, density, and stress exponent of the copolymer are obtained. These proportions are easily established from known relationships and can be verified experimentally by means of standard techniques.Thus, the melt index is determined according to ASTM method D1238 (condition E) and the density according to ASTM D 505. The stress exponent is the slope of the plot of log flow rate versus log extrusion force. Since the plot is not linear, the slope is determined according to ASTM D1238 using 2160 g and 640 g weights, both at 1900C.
The copolymers should give two distinct crystallite melting peaks, which means that they have two different groups of crystallites, each having its own distinct melting region. For ethylene/i -octene copolymers, such regions will be at about 1 070C and 1250 C. FIG. 1 is a typical DSC plot of AH in milliwatts vs. temperature in C for conventional polyethylene having a density of 0.91 7. This polymer has only one peak, which lies at about 1 070C. A DSC plot for DOWLEX 2045 ethylene/1 -octene copolymer (d = 0.920) is presented in FIG. 2. The higher temperature peak is in reality a doublet, and the high melting temperature of the doublet is taken as characteristic of this peak.FIG. 3 is a DSC plot for a blend of linear high density ethylene/1 -octene copolymer with the conventional polyethylene. The blend density is 0.926. It can be seen that the peaks of the blend correspond to those of the DOWLEX~ resins shown in FIG. 2. DSC is a well-known technique for measuring polymer crystallite melting temperatures. Linear copolymers of ethylene with 1 -octene or another a-olefin, wherein the a-olefin comonomer is present is such small amounts that a second DSC peak is not observed are not suitable in the present invention. The existence of two crystallite melting regions in the ethylene ~-olefin copolymers is their most outstanding characteristic because films made from these copolymers can be oriented between those two temperatures.Shrink films made from these copolymers have excellent properties, quite comparable with those of shrink films made from blends of low density and high density ethylene polymers, for example, those described in U.S. Patent 3,299,194.
However, it has been found that the presence of as little as 5 weight percent of an ethylene/cr- olefin copolymer of this class in a blend with a conventional ethylene homopolymer or copolymer having only one crystallite melting region below 1 280C can sometimes improve the properties of the latter copolymer so significantly that excellent shrink films having desirable physical properties, including high optical clarity, can be made therefrom. Such conventional homopolymers or copolymers can be both high density and low density, linear and branched, made at high pressure or at low pressure. The copolymers may be those with any comonomer, including for example, a!-olefins. vinyl esters, alkyl acrylates and methacrylates, and acrylonitrile. Many such polymers are commercially available from several sources.The blends can be prepared by any conventional technique capable of producing a uniform, homogeneous material.
Film is made from the above copolymers or blends by a suitable melt extrusion process. The film is either tubular or flat. It is stretched, preferably biaxially, in the plane of the film to the extent of at least 3 times in each direction, preferably at least 5 times. A convenient process, which combines extrusion and orientation of polymeric films is described in U.S. Patent 3,141,912 to Goldman et al.
When subjected to a temperature of about 100 to 1200 C, an oriented, unconstrained film will shrink at least about 15%, and this shrinking will be accompanied by a considerable force, usually at least 1400 KPa. The preferred shrink films will shrink at least 30% at a temperature just below the higher crystallite melting peak, at least 15% at 1 OOOC. The shrink force at 1 000C should be greater than about 350 kPa. Haze should be less than 4%, especially less than 2%. Gloss should be greater than 90, preferably greater than 110.
A limited amount of crosslinking can be introduced after stretching but prior to shrinking, if desired. This can be accomplished with a minimum amount of high energy radiation, normally less than 8 Mrad, as described, for example, in U.S. Patent 3,663,662 to Golike et al. Irradiated oriented films have improved melt strength and are less sensitive to temperature differences in the shrink tunnel.
This invention is now illustrated by the following representative examples, where all parts and proportions are by weight. In all cases the thickness of shrink film was about 0.025 mm.
All data obtained in units other than SI have been converted to SI units.
The shrinkage of oriented films was determined by scribing a fixed length, usually 100 mm, on a strip of unconstrained film in a 1 000C temperature bath for 10 seconds and calculating shrinkage as the percent change of length.
The shrink force was determined according to ASTM 2838. Modulus, tensile strength, and elongation at break were determined according to ASTM D412.
The ethylene resins used in the examples are listed in Table I, below:
TABLE I
Melt
Temp., C Density Stress Melt 1-Octene
Resin (by DSC) g/cm3 Exponent Index % Description
A 124; 107 0.920 1.4 1.0 14 Linear, low density
copolymer
B 126 0.950 1.8 0.45 1.7 Linear, high density
copolymer
C 103 0.917 - 4.0 - Branched, low density
homopolymer
D 126 0.940 1.9 0.45 3.6 Linear, low density
copolymer
EXAMPLE 1
Oriented tubular film was prepared by the process of U.S. 3,141,912 to Goldman. A 5 cm extruder
operated at 2300C and at a feed rate of 0.9 kg of ethylene polymer resin per hour produced film at the rate of 2.7 m/min. The hot tubular film was quenched, reheated to 1 5-1 200C, and blown at an internal pressure of 2 kPa.The blowing was controlled with a quench ring to give a fivefold stretch in the transverse direction. The take-up rolls were operated to give a fivefold stretch in the longitudinal direction.
Shrink film made from resin A according to the present invention was compared with a prior art shrink film made from a blend of resins B and C (in a respective ratio of 26 :74) according to the teachings of U.S. 3,299,194 to Golike. The films were placed about objects, hot wire sealed, and shrunk in a tunnel maintained at 1 67 C. The appearance of packages in both cases was identical. The properties of both shrink films are compared in Table II, below. All properties other than haze and gloss are given as a ratio: machine direction/transverse direction.
TABLE II B+C
Resin Type* A (26:74)
Modulus, MPa i; 295/260 360/330
Tensile, MPa 115/108 69/56
Elongation, % 240/195 152/128 Tear, g/mm 1480/1280 267/462 Shrinkage(1000C)% 19/25 27/30 Shrink Force (1000C) kPa 1810/3590 2960/3450 Haze, % 3.5 3.6
Gloss 85 93
* See Table I for resin description.
EXAMPLE 2
Resin blends were prepared as shown in Table III, below, melt blended in a standard single-screw mixing extruder, and melt pressed into 5 x 5-cm films. These were stretched fivefold at 1 200C in each direction in a laboratory stretcher (T. M. Long Co., Inc., Somerville, N.J.).
The physical properties of the films of this invention (A/B and A/D blends) are compared in Table Ill with those of prior art films made of ethylene polymer blends (B/C and C/D blends). The improvement of the physical properties, especially of optical properties, in the films of the present invention is apparent.
TABLE III
Resin Blend*
Higher Density Component
Type** B D 8 D 26 26 37 20 30
Lower Density Component
Type** C C A A
% 74 63 80 70
Film Properties
Modulus, MPa 367 458 583 508
Tensile, MPa 82 64 106 119 Elongation, % 80 106 131 114
Tear, g/mm 295 336 380 380 Shrinkage(1000C)% 8 8 6 10 Shrink Force (1000C) kPa 1170 965 1420 1240
Haze, /O 6.5 4.3 3.8 2.4
Gloss. 65 66 73 121
* Proportions were chosen to give blend density of 0.926 g/cm3.
** See Table I for resin description.
EXAMPLE 3
Oriented films were prepared from blends of resins A and C (see Table I). Stretching was carried out at 110-11 20C using the same technique and equipment as in Example 2. The physical properties of the stretched films are shown in Table IV, below. It can be seen that all the properties change as the proportion of the conventional low density polyethylene (Resin C) increases. The most striking change is the large decrease of the shrink force with retention of the high level of shrinkage.
TABLEV Proportion of Resin C
in A/C Resin Blend, % 0 25 50 75
Film Properties
Modulus, MPa 364 273 240 240 Tensile,MPa 144 69 42 30 Elongation, % 129 162 144 131
Tear, g/mm 104 510 580 260
Shrinkage(100 C) % 16 20 16 18 ShrinkForce(1000C)kPa 2250 2100 1670 . 1210 Haze, % 1.0 1.7 2.4 1.6
Gloss 140 139 119 100
Claims (9)
1. A shrink film made by stretching at least three times its original linear dimension in at least one direction a film made of the following homogeneous polymeric composition:
(1) 5-100 weight % of at least one linear copolymer of ethylene with at least one C8-C18 a-olefin, said copolymer having the following characteristics:
(a) melt index of 0.1-4.0 g/1 0 min;
(b) density of 0.900 to 0.940 g/cm3;
(c) stress exponent above 1.3; and
(d) two distinct crystallite melting regions below 1 280C as determined by differential scanning calorimetry (DSC), the temperature difference between those regions being at least 1 50C; and
(2) 0-95 weight % of at least one polymer selected from the group consisting of ethylene
homopolymers and copolymers of ethylene with an ethylenically unsaturated comonomer, said polymer
having only one crystallite melting point below 1 280C; with the proviso that stretching is carried out within the temperature range defined by the two crystallite melting points of the ethylene copolymer with C8-C18 a-olefin of the above paragraph (1).
2. A film of Claim 1, which is made of a copolymer of ethylene with 1 -octene.
3. A film of Claim 2 wherein the proportion of 1 -octene is about 3-1 6 weight percent.
4. A film of Claim 1, which is made of a blend of a copolymer of ethylene with 1 -octene having
two crystallite melting points with a copolymer of ethylene with 1 octene having only one crystallite
melting point by differential scanning calorimetry.
5. A film of Claim 1 which is stretched biaxially to the extent of at least five times in each direction
6. A film of Claim 5 which is subjected after stretching but prior to shrinking to high energy
radiation in an amount of less than about 8 Mrad.
7. In a process for wrapping an article in an oriented polyolefin film and heat-shrinking the film to
provide a tightly fitting overwrap about the article, the improvement of using a film of Claim 1.
8. The improvement of Claim 7 wherein the film is a copolymer of ethylene with 1 -octene.
9. A film as claimed in Claim 1, prepared by a procedure substantially as described in the
foregoing Examples section.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25681281A | 1981-04-23 | 1981-04-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2097324A true GB2097324A (en) | 1982-11-03 |
| GB2097324B GB2097324B (en) | 1984-06-06 |
Family
ID=22973685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8211739A Expired GB2097324B (en) | 1981-04-23 | 1982-04-22 | Shrink films of ethylene/ -olefin copolymers |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS57181828A (en) |
| BE (1) | BE892927A (en) |
| CA (1) | CA1174423A (en) |
| DE (1) | DE3215120A1 (en) |
| FR (1) | FR2504537B1 (en) |
| GB (1) | GB2097324B (en) |
| IT (1) | IT1151736B (en) |
| NL (1) | NL189515C (en) |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0092897A2 (en) * | 1982-04-26 | 1983-11-02 | American National Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| FR2561246A1 (en) * | 1983-11-10 | 1985-09-20 | Charbonnages Ste Chimique | POLYMER COMPOSITIONS BASED ON COPOLYMERS AND ETHYLENE HOMOPOLYMERS AND THEIR APPLICATION TO THE INSULATION OF METAL CONDUCTORS, ESPECIALLY TELEPHONE WIRES |
| EP0240705A2 (en) * | 1986-03-03 | 1987-10-14 | Kohjin Co., Ltd. | Heat shrinkable film |
| EP0299750A2 (en) * | 1987-07-13 | 1989-01-18 | Mitsubishi Kasei Corporation | Linear polyethylene film and process for producing the same |
| EP0346944A2 (en) * | 1982-04-26 | 1989-12-20 | American National Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| EP0359440A2 (en) * | 1988-09-01 | 1990-03-21 | Mitsui Petrochemical Industries, Ltd. | Polyethylene resin composition and film thereof |
| EP0374783A2 (en) * | 1988-12-19 | 1990-06-27 | Viskase Corporation | Heat shrinkable very low density polyethylene terpolymer film |
| US4976898A (en) * | 1985-06-17 | 1990-12-11 | Viskase Corporation | Process for making puncture resistant, heat-shrinkable films containing very low density polyethylene |
| US5032463A (en) * | 1988-07-18 | 1991-07-16 | Viskase Corporation | Very low density polyethylene film from blends |
| US5059481A (en) * | 1985-06-17 | 1991-10-22 | Viskase Corporation | Biaxially stretched, heat shrinkable VLDPE film |
| EP0461848A2 (en) * | 1990-06-12 | 1991-12-18 | Mitsui Petrochemical Industries, Ltd. | Ethylene-pentene-1 copolymer compositions and their use |
| US5256351A (en) * | 1985-06-17 | 1993-10-26 | Viskase Corporation | Process for making biaxially stretched, heat shrinkable VLDPE films |
| US5256428A (en) * | 1985-06-17 | 1993-10-26 | Viskase Corporation | Puncture resistant, heat-shrinkable films containing very low density polyethylene |
| WO1994007954A1 (en) * | 1992-10-02 | 1994-04-14 | E.I. Du Pont De Nemours And Company | Improved shrink film and methods relating thereto |
| WO1995013187A1 (en) * | 1993-11-08 | 1995-05-18 | W.R. Grace & Co. - Conn. | Multilayered, bioriented, heat shrinkable film |
| USRE35285E (en) * | 1985-09-30 | 1996-06-25 | W. R. Grace & Co.-Conn. | Thermoplastic multi-layer packaging film and bags made therefrom |
| US6514583B1 (en) | 1992-11-13 | 2003-02-04 | Cryovac, Inc. | High impact strength film containing single site catalyzed copolymer |
| WO2004011546A1 (en) * | 2002-07-29 | 2004-02-05 | Borealis Technology Oy | Schrink film |
| EP3453532B1 (en) | 2014-04-09 | 2021-03-31 | Dow Global Technologies LLC | Oriented polyethylene films and a method for making the same |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57188323A (en) * | 1981-05-16 | 1982-11-19 | Nippon Telegr & Teleph Corp <Ntt> | Manufacture of heat shrinkable tape |
| JPS59229317A (en) * | 1983-06-13 | 1984-12-22 | Showa Denko Kk | Preparation of low temperature heat-shrinkable film |
| JPS61112627A (en) * | 1984-11-08 | 1986-05-30 | Showa Denko Kk | Low-temperature heat-shrink film |
| JPS61123516A (en) * | 1984-11-21 | 1986-06-11 | Showa Denko Kk | Film heat-shrinkable at low temperature |
| JPH0720664B2 (en) * | 1985-05-29 | 1995-03-08 | 三菱化学株式会社 | Method for producing low density polyethylene biaxially stretched film |
| JPH0613192B2 (en) * | 1986-03-03 | 1994-02-23 | 株式会社興人 | Heat shrinkable film |
| JPH085172B2 (en) * | 1987-01-13 | 1996-01-24 | 株式会社興人 | Polyolefin-based heat-shrinkable laminated film |
| JPH0729378B2 (en) * | 1987-08-14 | 1995-04-05 | 株式会社興人 | Method for producing polyethylene heat-shrinkable film |
| WO1990001409A1 (en) * | 1988-08-15 | 1990-02-22 | Kohjin Co., Ltd. | Process for producing heat-shrinkable polyethylene film |
| JPH0664039A (en) * | 1992-08-20 | 1994-03-08 | Mitsui Petrochem Ind Ltd | Method and apparatus for production of biaxially oriented film and shrink film |
| US6287613B1 (en) | 1994-12-12 | 2001-09-11 | Cryovac Inc | Patch bag comprising homogeneous ethylene/alpha-olefin copolymer |
| US20080118692A1 (en) * | 2006-11-21 | 2008-05-22 | Fina Technology, Inc. | Polyethylene useful for producing film and molded articles in a process which uses solid state stretching |
| JP2010270227A (en) * | 2009-05-21 | 2010-12-02 | Tohcello Co Ltd | Biaxially oriented ethylene-based copolymer film |
| ES2659232T3 (en) | 2013-02-20 | 2018-03-14 | Prime Polymer Co., Ltd. | Biaxially stretched film, and ethylene type polymer composition |
| WO2016039275A1 (en) | 2014-09-10 | 2016-03-17 | 三井化学東セロ株式会社 | Biaxially oriented ethylene polymer film and packaging |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU41935A1 (en) * | 1961-06-26 | 1962-12-22 | ||
| GB1035887A (en) * | 1964-04-15 | 1966-07-13 | Du Pont | Improvements relating to films |
| JPS5952643B2 (en) * | 1977-01-27 | 1984-12-20 | 三井化学株式会社 | ethylene copolymer |
| JPS56144926A (en) * | 1980-04-15 | 1981-11-11 | Mitsubishi Petrochem Co Ltd | Monoaxially stretched product of ethylenic resin |
-
1982
- 1982-03-30 CA CA000399852A patent/CA1174423A/en not_active Expired
- 1982-04-20 JP JP57064859A patent/JPS57181828A/en active Granted
- 1982-04-20 FR FR8206750A patent/FR2504537B1/en not_active Expired
- 1982-04-22 NL NLAANVRAGE8201675,A patent/NL189515C/en active Search and Examination
- 1982-04-22 GB GB8211739A patent/GB2097324B/en not_active Expired
- 1982-04-22 BE BE0/207891A patent/BE892927A/en not_active IP Right Cessation
- 1982-04-22 IT IT20883/82A patent/IT1151736B/en active
- 1982-04-23 DE DE19823215120 patent/DE3215120A1/en active Granted
Cited By (39)
| Publication number | Priority date | Publication date | Assignee | Title |
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| EP0346944A2 (en) * | 1982-04-26 | 1989-12-20 | American National Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| US4457960A (en) * | 1982-04-26 | 1984-07-03 | American Can Company | Polymeric and film structure for use in shrink bags |
| EP0092897A3 (en) * | 1982-04-26 | 1985-01-23 | American Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| EP0092897A2 (en) * | 1982-04-26 | 1983-11-02 | American National Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| EP0346944A3 (en) * | 1982-04-26 | 1990-07-25 | American National Can Company | Polymeric composition of matter, oriented polymeric films and shrink bags made therefrom |
| USRE35567E (en) * | 1982-04-26 | 1997-07-22 | American National Can Company | Polymeric and film structure for use in shrink bags |
| FR2561246A1 (en) * | 1983-11-10 | 1985-09-20 | Charbonnages Ste Chimique | POLYMER COMPOSITIONS BASED ON COPOLYMERS AND ETHYLENE HOMOPOLYMERS AND THEIR APPLICATION TO THE INSULATION OF METAL CONDUCTORS, ESPECIALLY TELEPHONE WIRES |
| US4976898A (en) * | 1985-06-17 | 1990-12-11 | Viskase Corporation | Process for making puncture resistant, heat-shrinkable films containing very low density polyethylene |
| US5439717A (en) * | 1985-06-17 | 1995-08-08 | Viskase Corporation | Shrunken bag made from biaxially stretched, VLDPE film |
| US5256428A (en) * | 1985-06-17 | 1993-10-26 | Viskase Corporation | Puncture resistant, heat-shrinkable films containing very low density polyethylene |
| US5059481A (en) * | 1985-06-17 | 1991-10-22 | Viskase Corporation | Biaxially stretched, heat shrinkable VLDPE film |
| US5256351A (en) * | 1985-06-17 | 1993-10-26 | Viskase Corporation | Process for making biaxially stretched, heat shrinkable VLDPE films |
| USRE35285E (en) * | 1985-09-30 | 1996-06-25 | W. R. Grace & Co.-Conn. | Thermoplastic multi-layer packaging film and bags made therefrom |
| EP0240705A3 (en) * | 1986-03-03 | 1989-12-06 | Kohjin Co., Ltd. | Heat shrinkable film |
| EP0240705A2 (en) * | 1986-03-03 | 1987-10-14 | Kohjin Co., Ltd. | Heat shrinkable film |
| EP0299750A2 (en) * | 1987-07-13 | 1989-01-18 | Mitsubishi Kasei Corporation | Linear polyethylene film and process for producing the same |
| EP0299750A3 (en) * | 1987-07-13 | 1990-12-12 | Mitsubishi Kasei Corporation | Linear polyethylene film and process for producing the same |
| US5032463A (en) * | 1988-07-18 | 1991-07-16 | Viskase Corporation | Very low density polyethylene film from blends |
| US5089322A (en) * | 1988-09-01 | 1992-02-18 | Mitsui Petrochemical Industries, Ltd. | Polyethylene resin composition and film thereof |
| EP0359440A3 (en) * | 1988-09-01 | 1991-01-30 | Mitsui Petrochemical Industries, Ltd. | Polyethylene resin composition and film thereof |
| EP0359440A2 (en) * | 1988-09-01 | 1990-03-21 | Mitsui Petrochemical Industries, Ltd. | Polyethylene resin composition and film thereof |
| US6197909B1 (en) | 1988-12-19 | 2001-03-06 | Curwood, Inc. | Heat shrinkable C2C4C6 terpolymer film |
| US5434010A (en) * | 1988-12-19 | 1995-07-18 | Viskase Corporation | Heat shrinkable very low density polyethylene terpolymer film |
| EP0374783A3 (en) * | 1988-12-19 | 1990-09-19 | Viskase Corporation | Heat shrinkable very low density polyethylene terpolymer film |
| EP0374783A2 (en) * | 1988-12-19 | 1990-06-27 | Viskase Corporation | Heat shrinkable very low density polyethylene terpolymer film |
| US6100357A (en) * | 1988-12-19 | 2000-08-08 | Viskase Corporation | Heat shrinkable very low density polyethylene terpolymer film |
| EP0461848A2 (en) * | 1990-06-12 | 1991-12-18 | Mitsui Petrochemical Industries, Ltd. | Ethylene-pentene-1 copolymer compositions and their use |
| US5262228A (en) * | 1990-06-12 | 1993-11-16 | Mitsui Petrochemical Industries, Ltd. | Ethylene/pentene-1 copolymer compositions and their use |
| EP0461848A3 (en) * | 1990-06-12 | 1993-03-17 | Mitsui Petrochemical Industries, Ltd. | Ethylene-pentene-1 copolymer compositions and their use |
| WO1994007954A1 (en) * | 1992-10-02 | 1994-04-14 | E.I. Du Pont De Nemours And Company | Improved shrink film and methods relating thereto |
| US6514583B1 (en) | 1992-11-13 | 2003-02-04 | Cryovac, Inc. | High impact strength film containing single site catalyzed copolymer |
| WO1995013187A1 (en) * | 1993-11-08 | 1995-05-18 | W.R. Grace & Co. - Conn. | Multilayered, bioriented, heat shrinkable film |
| US6106934A (en) * | 1993-11-08 | 2000-08-22 | Cryovac, Inc. | Multilayered, bioriented, heat shrinkable film, method for the manufacture thereof and use thereof for packaging food products and consumer goods |
| US6197244B1 (en) | 1993-11-08 | 2001-03-06 | Cryovac, Inc. | Method for the manufacture of multilayer film |
| AU686271B2 (en) * | 1993-11-08 | 1998-02-05 | Cryovac, Inc. | Multilayered, bioriented, heat shrinkable film |
| WO2004011546A1 (en) * | 2002-07-29 | 2004-02-05 | Borealis Technology Oy | Schrink film |
| US7517941B2 (en) | 2002-07-29 | 2009-04-14 | Borealis Technology Oy | Shrink film |
| EP3453532B1 (en) | 2014-04-09 | 2021-03-31 | Dow Global Technologies LLC | Oriented polyethylene films and a method for making the same |
| EP3129225B1 (en) | 2014-04-09 | 2021-07-21 | Dow Global Technologies LLC | Oriented polyethylene films and a method for making the same |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2504537A1 (en) | 1982-10-29 |
| DE3215120C2 (en) | 1991-07-25 |
| CA1174423A (en) | 1984-09-18 |
| JPH0354048B2 (en) | 1991-08-19 |
| FR2504537B1 (en) | 1986-10-03 |
| NL8201675A (en) | 1982-11-16 |
| DE3215120A1 (en) | 1982-12-09 |
| IT8220883A0 (en) | 1982-04-22 |
| JPS57181828A (en) | 1982-11-09 |
| NL189515C (en) | 1993-05-03 |
| BE892927A (en) | 1982-10-22 |
| GB2097324B (en) | 1984-06-06 |
| IT1151736B (en) | 1986-12-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PE20 | Patent expired after termination of 20 years |
Effective date: 20020421 |