U.S. patent application number 12/517103 was filed with the patent office on 2010-03-25 for multimodal polyethylene resin for pipe made by a single-site catalyst.
This patent application is currently assigned to BOREALIS TECHNOLOGY OY. Invention is credited to Per-ola Hagstrand, Solveig Johansson, Sune Olsson, Magnus Palmlof.
Application Number | 20100075087 12/517103 |
Document ID | / |
Family ID | 38016706 |
Filed Date | 2010-03-25 |
United States Patent
Application |
20100075087 |
Kind Code |
A1 |
Palmlof; Magnus ; et
al. |
March 25, 2010 |
Multimodal Polyethylene Resin for Pipe Made by a Single-site
Catalyst
Abstract
The present invention relates to a polyethylene composition
comprising a polyethylene base resin, which comprises a. an
ethylene copolymer as fraction (A), and b. an ethylene homo- or
copolymer as fraction (B), with fraction (A) having a lower
molecular weight than fraction (B), wherein the polyethylene base
resin is obtainable in a polymerisation process in which a
single-site catalyst. (SSC) is used in the polymerisation of at
least one of fractions (A) and (B), and the base resin has (i) a
density of below 940 kg/m.sup.3, and (ii) a MFR.sub.2 at 190
.degree. C./2.16 kg of 0.001 to 10 g/10 min, and the composition
has (iii) a flexural modulus of from 300 to 820 MPa, and to a
process for the production of such a composition, and to a pipe
produced from such a composition.
Inventors: |
Palmlof; Magnus; (Vastra
Frolunda, SE) ; Johansson; Solveig; (Stenungsund,
SE) ; Hagstrand; Per-ola; (Stenungsund, SE) ;
Olsson; Sune; (Odsmal, SE) |
Correspondence
Address: |
MILBANK, TWEED, HADLEY & MCCLOY LLP
INTERNATIONAL SQUARE BUILDING, 1850 K STRET, N.W., SUITE 1100
WASHINGTON
DC
20006
US
|
Assignee: |
BOREALIS TECHNOLOGY OY
Porvoo
FI
|
Family ID: |
38016706 |
Appl. No.: |
12/517103 |
Filed: |
November 21, 2007 |
PCT Filed: |
November 21, 2007 |
PCT NO: |
PCT/EP2007/010092 |
371 Date: |
June 30, 2009 |
Current U.S.
Class: |
428/36.9 ;
525/240 |
Current CPC
Class: |
C08F 210/16 20130101;
Y10T 428/139 20150115; C08L 2314/06 20130101; C08F 4/65925
20130101; C08F 4/65916 20130101; C08L 23/02 20130101; C08L 23/02
20130101; C08L 23/0815 20130101; C08L 23/06 20130101; C08L 2666/06
20130101; C08F 4/65912 20130101; C08L 23/0815 20130101; C08F 2/001
20130101; C08L 2205/02 20130101; C08L 2666/06 20130101 |
Class at
Publication: |
428/36.9 ;
525/240 |
International
Class: |
C08L 23/04 20060101
C08L023/04; B32B 1/08 20060101 B32B001/08 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 1, 2006 |
EP |
06024952.1 |
Claims
1. A polyethylene composition comprising a polyethylene base resin,
which comprises a. an ethylene copolymer as fraction (A), and b. an
ethylene homo- or copolymer as fraction (B), with fraction (A)
having a lower molecular weight than fraction (B), wherein the
polyethylene base resin is obtainable in a polymerisation process
in which a single-site catalyst (SSC) is used in the polymerisation
of at least one of fractions (A) and (B), and the base resin has
(i) a density of below 940 kg/m.sup.3, (ii) a MFR.sub.2 at
190.degree. C./2.16 kg of 0.01 to 10 g/10 min and the composition
has (iii) a flexural modulus of from 400 to 820 MPa.
2. The polyethylene composition according to claim 1, wherein the
polyethylene composition has a Charpy impact strength at 0.degree.
C. of at least 10 kJ/m.sup.2, measured according to ISO 179.
3. The polyethylene composition according to claim 1, wherein the
polyethylene composition has a critical temperature in the RCP-S4
test of +2.degree. C. or lower, measured according to ISO
13477.
4. The polyethylene composition according to claim 1, wherein the
polyethylene composition has a slow crack growth value in a pipe
notch test
5. The polyethylene composition according to claim 1, wherein the
polyethylene composition has an MRS rating of at least 6.3,
measured according to ISO/TR 9080.
6. The polyethylene composition according to claim 1, wherein the
molecular weight distribution of the polyethylene base resin is
from 5 to 25.
7. The polyethylene composition according to claim 1, wherein
fraction (A) is a copolymer of ethylene and C.sub.4 to C.sub.20
alpha-olefin comonomers.
8. The polyethylene composition according to claim 1, wherein
fraction (A) has a density from 920 to 962 kg/m3.
9. The polyethylene composition according to claim 1, wherein
fraction (A) has a melt flow rate (190.degree. C./2.16 kg)
MFR.sub.2 of 10 to 300 g/10 min.
10. The polyethylene composition according to claim 1, wherein in
the poly-ethylene resin the weight ratio between fraction (A) and
fraction (B) is between 60:40 to 40:60.
11. A process for the production of a polyethylene composition
comprising a polyethylene base resin, which comprises a. an
ethylene copolymer as fraction (A), and b. an ethylene homo- or
copolymer as fraction (B), with fraction (A) having a lower
molecular weight than fraction (B), wherein in the polymerisation
of at least one of fractions (A) and (B) a single-site catalyst
(SSC) is used, wherein the base resin produced (i) has a density of
below 940 kg/m.sup.3, and (ii) a MFR, at 190.degree. C./2.16 kg of
0.001 to 10 g/10 min, and the composition has (iii) a flexural
modulus from 400 to 820 MPa.
12. A pipe made of a polyethylene composition according to claim
1.
13. (canceled)
Description
[0001] The present invention relates to a polyethylene composition
comprising a polyethylene resin produced by a polymerisation
process in the presence of a single-site catalyst (SSC).
Furthermore, the present invention relates to the use of such a
polyethylene composition for the production of pipes, and to pipes,
in particular to pressure pipes, made of such a polyethylene
composition.
[0002] Pipes, in particular pressure pipes, are used in various
applications like the transport of drinking water, sewage,
different industrial applications, gas and more.
[0003] Based on the polymer strength, polyethylene pipes for
pressurised systems can be classified in different categories, such
as PE63, PE80 or PE100. The higher the number, the longer the
service life under high pressure.
[0004] Presently, the best polyethylene resins for pressure pipes
are prepared in a multistage process with Ziegler-Natta catalysts.
The densities of such polyethylene resins are high in order to
reach a high pressure resistance of the pipes produced. However,
high density gives a high stiffness, which is a drawback e.g. when
installing the pipes.
[0005] In the end of the 80ies Kaminsky et al. presented a
metallocene catalyst type of single-site catalysts. Intensive
research on metallocene catalysts has been done but still the
introduction of polyolefin resins prepared by metallocene catalysts
into the market is low. The main areas where single-site resins
have been introduced are film or extrusion coating as disclosed in
e.g. WO 03/066699. The films disclosed in this document have
excellent mechanical properties and outstanding sealability.
[0006] However, it is known that the catalytic activity of
single-site catalysts is moderate and the highest activity is
reached in the medium to low density regions.
[0007] To meet the PE80 requirements with multimodal polyolefin
resins manufactured by conventional Ziegler-Natta catalyst, the
density must be at least 940 kg/m.sup.3, and to meet PE100
requirements the density must even be above 945 kg/m.sup.3.
Pressure pipe resins prepared by single-site catalysts of the state
of the art, as it is described e.g. in WO 02/34829, also have a
density higher than 940 kg/m.sup.3. The consequence of the use of
such high density resins is that the flexibility of the pipes
produced therefrom is rather low.
[0008] Furthermore, for the production of pressure pipes it is
necessary that the polyethylene compositions used have a suitable
melt flow rate and molecular weight distribution, in order to
ensure a good processability of the composition during the
extrusion process.
[0009] Hence, the object of the present invention is to provide a
polyethylene composition for the manufacturing of pipes, especially
pressure pipes, which simultaneously has a good processability, is
flexible enough for easy handling and fulfils the requirements of
pressure class PE63 or higher.
[0010] It has now surprisingly been found that such a polyethylene
composition can be provided if a single-site catalyst is used in
its production, and the base resin of the composition has a density
of below 940 kg/m.sup.3.
[0011] Therefore, the present invention provides a polyethylene
composition comprising a polyethylene base resin, which comprises
[0012] a. an ethylene copolymer as fraction (A), and [0013] b. an
ethylene homo- or copolymer as fraction (B), with fraction (A)
having a lower molecular weight than fraction (B), wherein the
polyethylene base resin is obtainable in a polymerisation process
in which a single-site catalyst (SSC) is used in the polymerisation
of at least one of fractions (A) and (B), and the base resin has
[0014] (i) a density of below 940 kg/m.sup.3, and [0015] (ii) a
MFR.sub.2 at 190.degree. C./2.16 kg of 0.01 to 10 g/10 min, and the
composition has [0016] (iii) a flexural modulus from 300 to 820
MPa.
[0017] As demonstrated below, the invention enables preparation of
more flexible pipes still meeting the requirements for high
pressure resistance.
[0018] Hence, for example, the compositions of the invention allow
for the production of more flexible pipes which can be bended more
easily and thus more easily be coiled into a roll. This offers the
advantage that installing the pipes is much simplified.
[0019] At the same time, a much improved pressure resistance is
obtained so that the pipes can be used for applications for which
conventionally only pipes made of a polyolefin composition with
higher density could be used.
[0020] The term "base resin" denotes the entirety of polymeric
components in the polyethylene composition according to the
invention, usually making up at least 90 wt % of the total
composition. Preferably, the base resin is consisting of fractions
(A) and (B), optionally further comprising a prepolymer fraction in
an amount of up to 20 wt %, preferably up to 10 wt %, more
preferably up to 5 wt % of the total base resin.
[0021] The density of the base resin contained in the polyethylene
composition of the present invention lies in the medium range, i.e.
below 940 kg/m.sup.3, more preferably in the range of 910 to below
940 kg/m.sup.3, even more preferably in the range of 915 to below
940 kg/m.sup.3, and most preferably in the range of 920 to below
939 kg/m.sup.3, measured according to ISO 1183.
[0022] Despite a 5 to 10 kg/m.sup.3 units lower density of the base
resin compared to conventional resins, the pipes made of the
composition of the invention fulfill high pressure
classifications.
[0023] The melt flow rate (MFR) and the flow rate ratio (FRR) are
important properties of the polyethylene base resin, because MFR
and FRR are indications of the flowability and thus processability
of the polymer. The higher the melt flow rate, the lower the
viscosity of the polymer. The MFR is measured according to ISO
1133, indicated in g/10 min and determined at a temperature of
190.degree. C. and different loadings such as 2.16 kg (MFR.sub.2;
ISO 1133), 5.0 kg (MFR.sub.5; ISO 1133) or 21.6 kg (MFR.sub.21; ISO
1133). The flow rate ratio, FRR is the ratio between
MFR.sub.weight1 and MFR.sub.weight2, i.e. FRR.sub.21/5 means the
ratio between MFR.sub.21 and MFR.sub.5.
[0024] In the present invention, the polyethylene base resin
preferably has an MFR.sub.2 of 0.01 to 5.0 g/10 min, more
preferably of 0.02 to 1.0 g/10 min, and most preferably of 0.10 to
0.50 g/10 min.
[0025] The modulus of elasticity (E-modulus) is determined
according to ISO 527. The polyethylene composition according to the
present invention preferably has a modulus of elasticity from 400
to 900 MPa, more preferable from 425 to 850 MPa, and most
preferably from 450 to 800 MPa.
[0026] It is furthermore preferred that the flexural modulus of the
polyethylene composition is from 400 to below 800 MPa, more
preferably from 450 to 700 MPa, and most preferably from 450 to 650
MPa.
[0027] Charpy impact test at low temperature assesses impact
toughness and therefore provides a way to evaluate resistance to
rapid crack propagation (RCP).
[0028] In a preferred embodiment of the present invention, the
polyethylene composition has a Charpy impact strength at 0.degree.
C. of at least 8 kJ/m.sup.2, and more preferably of at least 10
kJ/m.sup.2, measured according to ISO 179.
[0029] The rapid crack propagation resistance of polyethylene
compositions may also be determined by a method called S4 (Small
Scale Steady State), which has been developed at Imperial College,
London, and is described in ISO 13477:1977 (E). The pipes of the
present invention preferably reach a critical temperature, i.e.
RCP-S4 value, of +2.degree. C. or lower, more preferably of
+1.degree. C. or lower.
[0030] The slow crack propagation resistance may be determined
according to ISO 13479:1997 in terms of the number of hours a
notched pipe withstands a certain pressure at a certain temperature
before failure.
[0031] The polyethylene composition of the pipe according to the
present invention preferably has slow crack propagation resistance
of at least 165 hours, more preferably of at least 500 hours, still
more preferably of at least 1000 hours, and most preferably of at
least 4000 hours, at 5.4 MPa hoop stress and 80.degree. C.
according to ISO 1167.
[0032] A further important pipe property is the design stress
rating, which is the circumferential stress a pipe is designed to
withstand for 50 years without failure and is determined at
different temperatures in terms of the Minimum Required Strength
(MRS) according to ISO/TR 9080. Thus, MRS 8.0 means that the pipe
is a pipe withstanding a hoop stress of 8.0 MPa gauge for 50 years
at 20.degree. C., and similarly MRS 10.0 means that the pipe
with-stands a hoop stress of 10 MPa gauge for 50 years at
20.degree. C.
[0033] The polyethylene composition of the pipe according to the
invention preferably has a MRS rating of at least 6.3, more
preferably of at least 8.0, and most preferably of 10.0.
[0034] The shear thinning index (SHI) is the ratio of the
viscosities of the polyethylene base resin at different shear
stresses and may serve as a measure of the broadness of the
molecular weight distribution. In the present invention, the shear
stresses at 2.7 kPa and 210 kPa as well as at 5 kPa and 300 kPa are
used for the determination of SHI of the polyethylene base resin.
The definition and measurement conditions are described in detail
on page 8, line 29 to page 11, line 25 of WO 00/22040.
[0035] The polyethylene base resin has preferably an
SHI.sub.(2.7/210) of below 20, more preferably of below 15, and
most preferably of below 10. It is preferred the range of
SHI.sub.(2.7/210) is from 1 to below 20.
[0036] It is also preferred that the SHI.sub.(5/300) is below 35,
more preferred below 30 and most preferred below 25. The preferred
range of the SHI.sub.(5/300) is between 5 to below 35.
[0037] It should be noted that the polyethylene composition of the
present invention, and therefore also the pipes produced therefrom,
is characterized not by a single one of the above defined features,
but by the combination of all features as defined in claim 1. By
the unique combination of the features it is possible to obtain a
polymer composition for pipes of superior performance, in
particular with regard to flexibility, processability, pressure
performance, impact strength, slow crack and rapid crack
propagation resistance.
[0038] Moreover, it is significant to point out the importance of a
good processability of the polyethylene composition intended for
pipe applications. High molecular weight is needed for meeting good
pressure resistance and low creep. Improved processability is
reached by the multimodal design. This means at least one low
molecular weight fraction giving easier processability and one
fraction with a high molecular weight contributing to mechanical
strength, are present in the composition used for pipes of the
invention.
[0039] Usually, a polyethylene composition comprising at least two
polyethylene fractions which have been produced under different
polymerisation conditions resulting in different (weight average)
molecular weights for the fractions, is referred to as
"multimodal". The prefix "multi" relates to the number of different
polymer fractions the composition is consisting of. Thus, for
example, a composition consisting of two fractions only is called
"bimodal".
[0040] The form of the molecular weight distribution curve, i.e.
the appearance of the graph of the polymer weight fraction as
function of its molecular weight, of such multimodal polyethylene
will show two or more maxima or at least be distinctly broadened in
comparison with the curves for individual fractions.
[0041] For example, if a polymer is produced in a sequential
multistage process, utilising reactors coupled in series and using
different conditions each reactor, the polymer fractions produced
in different reactors will each have their own molecular weight
distribution and weight average molecular weight. When the
molecular weight distribution curve of such a polymer is recorded,
the individual curves from these fractions are superimposed into
the molecular weight distribution curve for total resulting polymer
product, usually yielding a curve with two or more distinct
maxima.
[0042] The polyethylene base resin of the composition of the
invention is a multimodal-, or preferably a bimodal, polyethylene
resin, which comprises at least two polyethylene fractions (A) and
(B), wherein fraction (A) has a lower molecular weight than
fraction (B). The term molecular weight where used herein denotes
the weight average molecular weight M.
[0043] The polyethylene base resin of the present invention
preferably has a molecular weight distribution (MWD) defined as the
ratio of the weight average molecular weight M.sub.w and the number
average molecular weight M.sub.n of 5 to 25, more preferably of 5
to 20, and most preferably of 5 to 15.
[0044] It is previously known that in order to produce multimodal,
in particular bimodal, olefin polymers, such as the polyethylene
base resin of the present invention, two or more reactors or zones
connected in series as described in EP 517 868, which is hereby
incorporated by way of reference in its entirety, can be used.
[0045] The main polymerisation stages are preferably carried out as
a combination of slurry polymerisation/gas-phase polymerisation.
The slurry polymerisation is preferably performed in a so-called
loop reactor. Optionally and advantageously, the main
polymerisation stages may be preceded by a prepolymerisation, in
which case most preferably 1 to 5% by weight of the total amount of
polymers is produced. The pre-polymer may be an ethylene homo- or
copolymer.
[0046] If a pre-polymerisation takes place, in this case all of the
catalyst is preferably charged into the first pre-polymerisation
reactor and the pre-polymerisation is performed as slurry
polymerisation. Such a polymerisation leads to less fine particles
being produced in the following reactors and to a more homogeneous
product being obtained in the end. Generally, this technique
results in a multimodal polymer mixture through polymerisation with
the aid of a catalyst, in the present invention with the aid of a
single-site catalyst.
[0047] The single-site catalyst used in the examples of the present
invention has been disclosed in EP 1 462 464, example 5, catalyst
3.
[0048] In the process of the invention for producing the base resin
of the polymer composition of the invention, at least fraction (A)
or fraction (B) are produced in a polymerisation reaction in the
presence of a single-site catalyst. For example, fraction (A), or
alternatively (B), may be produced in the presence of a single-site
catalyst and fraction (B), or alternatively (A), may be produced in
the presence of a Ziegler-Natta catalyst.
[0049] It is, however, preferred that both fractions (A) and (B)
are prepared in the presence of a single-site catalyst.
[0050] Furthermore, it is preferred that fraction (A) and fraction
(B) are polymerised in the presence of the same single-site
catalyst.
[0051] In the production of a polyethylene base resin of the
present invention it is preferred that fraction (A) is produced in
a loop reactor under certain conditions with respect to hydrogen,
monomer and comonomer concentration, temperature, pressure, and so
forth.
[0052] Furthermore, it is preferred that fraction (B) is produced
in a gas-phase reactor.
[0053] Still further, preferably, after the polymerisation fraction
(A) including the catalyst is transferred to the reactor,
preferably a gas-phase reactor, where fraction (B) is produced
under different conditions.
[0054] The resulting end product consists of an intimate mixture of
the polymers from the two main reactors and optionally the
prepolymer fraction, the different molecular-weight-distribution
curves of these polymers together forming a
molecular-weight-distribution curve having a broad maximum or two
maxima, i.e. the end product is a bimodal polymer mixture.
[0055] Owing to the flexibility with respect to reaction conditions
thus obtained, it is most preferred that the polymerization is
carried out in a pre-polymerization reactor/a loop reactor/a
gas-phase reactor. Preferably, the polymerization conditions in the
preferred three-step method are chosen so that fraction (A) is
produced in one step, preferably the second reactor, whereas
fraction (B) is produced in another step, preferably the third
reactor. The order of these steps may, however, be reversed.
[0056] In the present invention it is preferred that the
pre-polymerisation operates at a temperature between 40 to
70.degree. C., more preferred between 50 to 65.degree. C. and
preferably at a pressure of 50 to 70 bar, more preferably of 55 to
65 bar.
[0057] In the second reactor the polymerisation temperature is
preferably between 60 to 100.degree. C., more preferably between 70
to 90.degree. C., and preferably at a pressure of 40 to 70 bar,
more preferably of 50 to 60 bar.
[0058] In the third reactor the temperature is preferably between
60 to 105.degree. C., more preferably between 70 and 90.degree. C.
and preferably at a pressure of 10 to 40 bar, more preferably of 15
to 20 bar.
[0059] The weight ratio of fractions (A) and (B) is preferably from
60:40 to 40:60, more preferably 55:45 to 45:55.
[0060] In the present invention fraction (A) is an ethylene
copolymer and fraction (B) can be an ethylene homo- or copolymer.
It is preferred that also fraction (B) is an ethylene
copolymer.
[0061] The used comonomers of both fractions may be equal or
different.
[0062] As comonomers various alpha-olefins with 4 to 20 carbon
atoms may be used, but the comonomers are preferably selected from
the group of 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene,
1-heptene, 1-octene, 1-decene and 1-eicosene. In particularly
preferred embodiment, the comonomer is 1-butene and/or
1-hexene.
[0063] Preferably, fraction (B) is an ethylene copolymer, and the
comonomer used is an alpha-olefin with 4, more preferably 6, or
more carbon atoms, more preferably is 1-hexene or 1-octene.
[0064] At least on of the fractions (A) and (B) may also consist of
ethylene and two or more different comonomer units, e.g. may
consist of a terpolymer.
[0065] If the composition of the invention comprises a terpolymer,
preferably this is a terpolymer of ethylene and C.sub.4 to C.sub.12
alpha-olefin-comonomers, and preferably the terpolymer is fraction
(B).
[0066] The amount of the comonomer used in fraction (A) preferably
is between 0.1 to 3.0 mole-%, more preferably 0.2 to 2.0 mole-%,
even more preferably 0.5 to 1.5 mole-%.
[0067] The amount of the comonomer used in fraction (B) preferably
is between 0.1 to 2.0 mole-%, more preferably 0.1 to 1.5 mole-%,
even more preferably 0.2 to 1.0 mole-%.
[0068] Furthermore, it is preferred that fraction (A) has a density
from 920 to 962 kg/m.sup.3, more preferred from 925 to 945
kg/m.sup.3, most preferred from 925 to 940 kg/m.sup.3.
[0069] Moreover, the melt flow rate MFR.sub.2 (190.degree. C./2.16
kg) of fraction (A) preferably is between 10 to 300 g/10 `min, more
preferably between 50 to 140 g/10 min.
[0070] The polyethylene composition of the invention may also
comprise additives like process aids, antioxidants, pigments,
UV-stabilizers and the like. Usually, the amount of those additives
is 10 wt % or lower, based on the total composition.
[0071] The present invention also relates to a pipe, in particular
a pressure pipe, comprising the polyethylene composition as
described hereinbefore, as well as to the use of such a composition
for the production of a pipe, in particular a pressure pipe.
[0072] The pipe of the present invention may be prepared in any
conventional manner, preferably by extrusion of the polyolefin
composition in an extruder. This is a technique well known to the
person skilled in the art.
[0073] The pipe of the present invention shows good stress
resistance as well as a high flexibility.
METHODS AND EXAMPLES
[0074] Melt Flow Rate (MFR)
[0075] The MFR is determined according to ISO 1133 and is indicated
in g/10 min. For polyethylene resins a temperature of 190.degree.
C. is applied. The MFR is determined at different loadings such as
2.16 kg (MFR.sub.2), 5 kg (MFR.sub.5) or 21.6 kg (MFR.sub.21).
[0076] Molecular Weight
[0077] The weight average molecular weight M.sub.w and the
molecular weight distribution (MWD=M.sub.w/M.sub.n, wherein M.sub.n
is the number average molecular weight and M.sub.w is the weight
average molecular weight) is measured by based on ISO 1014-4:2003.
A Waters 150CV plus instrument was used with column
3.times.HT&E styragel from Waters (divinylbenzene) and
trichlorobenzene (TCB) as solvent at 140.degree. C. The column set
was calibrated using universal calibration with narrow MWD PS
standards (the Mark Houwings constant K: 9.54*10.sup.-5 and a:
0.725 for PS, and K: 3.92* 10.sup.-4 and a: 0.725 for PE). The
ratio of M.sub.w and M.sub.n is a measure of the broadness of the
distribution, since each is influenced by opposite end of the
"population".
[0078] Rapid Crack Propagation (S4)
[0079] The rapid crack propagation (RCP) resistance of a pipe is
determined according to ISO 13477 (E). According to the RCP-S4
method a pipe is tested which has an axial length not below 7 pipe
diameters. The outer diameter of the pipe is about 110 mm or
greater and its wall thickness about 10 mm or greater. When
determining the RCP properties of a pipe in connection with the
present invention the outer diameter and the wall thickness have
been selected to be 110 mm and 10 mm respectively. While the
exterior of the pipe is at ambient pressure (atmospheric pressure),
the pipe is pressurized internally and the internal pressure in the
pipe is kept constant at a pressure of 0.5 MPa positive pressure.
The pipe and the equipment surrounding it are thermostated to a
predetermined temperature. A number of discs have been mounted on a
shaft inside the pipe to prevent decompression during the test. A
knife projectile is shot, with well-defined forms, towards the pipe
close to its end in the so-called initiating zone in order to start
a rapidly running axial crack. The initiating zone is provided with
an abutment for avoiding unnecessary deformation to the pipe. The
test equipment is adjusted in such a manner that crack initiation
takes place in the material involved and a number of tests are
effected at varying temperatures. The axial crack length in the
measuring zone, having a total length of 4.5 diameters, is measured
for each test and is plotted against the set test temperature. If
the crack length exceeds 4 diameters the crack is assessed to
propagate. If the pipe passes the test at a given temperature, the
temperature is lowered successively until a temperature
(T.sub.critical) is reached, at which the pipe no longer passes the
test.
[0080] Pressure Test on Un-Notched Pipes
[0081] The pressure test on un-notched 32 mm pipes is carried out
according to ISO 1167. The time to failure is determined in
hours.
[0082] Pressure Test on Notched Pipes
[0083] The pressure test on notched 110 mm pipes is carried out
according to ISO 13479.
[0084] Charpy Notch Impact Test
[0085] The impact strength is determined as Charpy Impact Strength
according to ISO 179-1 non-instrumented or ISO 179-2
instrumented.
[0086] Flexural Modulus
[0087] The flexural modulus is determined according to ISO 178 at a
constant speed of 2 mm/min.
[0088] E-modulus
[0089] The modulus of elasticity is determined according to ISO
527-2 (test specimen 1B), at a constant speed of 1 mm/min.
[0090] Rheological Parameters
[0091] Rheological parameters such as Shear Thinning Index SHI and
viscosity are determined by using a rheometer, preferably a Physica
MCR 300 Rheometer from Anton Paar. The definition and measurement
conditions are described in detail on page 8, line 29 to page 11,
line 25 of WO 00/22040.
Examples
Example 1
[0092] Into a 50 dm.sup.3 loop reactor 32 kg/h propane and 8.3 g/h
hydrogen and ethylene were added. The operating temperature was
60.degree. C. and the operating pressure was 61 bar.
[0093] The slurry was taken out of the reactor and transferred into
a 500 dm.sup.3 loop reactor. The reactor was operated at 85.degree.
C. and 58 bar pressure. The single site catalyst prepared as
disclosed in EP 1 462 464 was continuously fed at a rate of 29
g/min into the loop reactor. Additional ethylene, 1-butene, propane
diluent and hydrogen were continuously introduced into the reactor
so that the rate of polymer production was 35 kg/h and the
MFR.sub.2 of the polymer was 110 g/10 min and the density of
polymer was 939 kg/m.sup.3.
[0094] The slurry was continuously withdrawn from the reactor to a
flash stage where hydrocarbons were removed from the polymer. The
polymer was then transferred into a gas phase reactor, where the
polymerisation was continued. The reactor was operated at
80.degree. C. temperature and 20 bar pressure. Ethylene, hydrogen
and 1-hexene were fed into the reactor to obtain such conditions
that the rate of polymer production was 34 kg/h. The productivity
of the catalyst was 2.4 kg/g catalyst.
[0095] The ratio between polymer amounts produced in the slurry
(reactor 2) and gas phase (reactor 3) reactors was 51:49.
[0096] The polymer was then compounded in with 1500 ppm Calcium
stearate and 3000 ppm Irganox B225. The final compound had a
density of 937 kg/m.sup.3 and MWD of 9.1.
[0097] The compounded material was then extruded into pipes having
an external diameter of about 110 mm and thickness of about 10 mm
and 32 mm and a thickness of 3 mm respectively.
[0098] Data of the polymerisation conditions, the resin/composition
and the pipe produced therefrom are given in Table 1.
Comparative Example 1
[0099] A pipe resin was produced by means of a three-step process
in a pre-polymerisation loop-reactor followed by first a
loop-reactor and then a gas phase-reactor, as described in Example
1. The split was 2:42:56. No comonomer was used in the two
consecutive loop-reactors, while 1-butene was used as comonomer in
the high molecular weight fraction produced in the gas-phase
reactor in an amount such that the 1-butene comonomer content of
the total resulting polymer was 2.9% by weight. A Ziegler-Natta
type catalyst as disclosed in EP 688 794 was used. The M.sub.n of
the final polymer was found to be 8600 g/mol and the M.sub.w was
240000 g/mol. M.sub.w/M.sub.n thus was 28. Further data are given
in Table 1 below.
[0100] The material was then compounded with stabilisers and carbon
black and extruded into pipes having an external diameter of about
110 mm and thickness of about 10 mm and a diameter of 32 mm and a
thickness of 3 mm respectively.
TABLE-US-00001 TABLE 1 Comparative units Example 1 Example 1
PREPOLYMERISATION REACTOR Temperature .degree. C. 60 50 Pressure
bar 61 64.2 Split wt-% 0 2 LOOP REACTOR Temperature .degree. C. 85
95 Pressure bar 58 64 C.sub.2 concentration mol % 5.7 3.5
H.sub.2/C.sub.2 ratio mol/kmol 0.46 950 C.sub.4/C.sub.2 ratio
mol/kmol 92 0 Split wt-% 51 44 MFR.sub.2 g/(10 min) 110 325 Density
kg/m.sup.3 939 972 Comonomer butene-1 GAS PHASE REACTOR Temperature
.degree. C. 80 85 Pressure bar 20 19.5 H2/C2 ratio mol/kmol 0 50
C4/C2 ratio mol/kmol -- 200 C6/C2 ratio mol/kmol 4 -- Split wt-% 49
54 Comonomer Hexene-1 Butene-1 Density-base resin kg/m.sup.3 936
940 COMPOUNDING EXTRUDER JSW CIM90P JSWCIM460P Feed kg/hr 217 SEI
kWh/t 277 235 Melt temperature .degree. C. 222 285 PROPERTIES OF
COMPOUNDED RESIN/PRODUCED PIPE Hexene-1 content wt-% 1.3 0 Butene-1
content wt-% 1.6 2.9 MFR2 g/(10 min) 0.45 MFR5 g/(10 min) 1.4 0.85
MFR21 g/(10 min) 19 M.sub.w g/mol 157,000 240,000 M.sub.n g/mol
17,200 8,600 MWD 9.1 28 Density-compound kg/m.sup.3 937.2 951
SHI.sub.(2.7/210) 8.6 29.4 SHI.sub.(5/300) 15.2 52.5 Eta.sub.0.05
Pa s 23450 52400 E-modulus MPa 640 Flexural Modulus MPa 596 845
Impact strength at 0.degree. C. kJ/m.sup.2 10 16 Impact strength at
kJ/m.sup.2 5.9 -20.degree. C. Pressure test on un-notched 32 mm
pipes 10.0 MPa at 20.degree. C. h >4719 12.0 MPa at 20.degree.
C. h 4144 4.6 MPa at 80.degree. C. h 6321 5.1 MPa at 80.degree. C.
h 2 5.4 MPa at 80.degree. C. h 6259 Pressure test on notched 110 mm
pipes 4.0 MPa at 80.degree. C. h >5000 4.45 MPa at 80.degree. C.
h 2731 RCP-resistance, T.sub.critical .degree. C. +1 -4
* * * * *