EP3485189A1 - Method for determining time to brittle failure of a pipe made of polypropylene - Google Patents

Method for determining time to brittle failure of a pipe made of polypropylene

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Publication number
EP3485189A1
EP3485189A1 EP17735595.5A EP17735595A EP3485189A1 EP 3485189 A1 EP3485189 A1 EP 3485189A1 EP 17735595 A EP17735595 A EP 17735595A EP 3485189 A1 EP3485189 A1 EP 3485189A1
Authority
EP
European Patent Office
Prior art keywords
stress
time
polypropylene composition
brittle failure
specimen
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.)
Withdrawn
Application number
EP17735595.5A
Other languages
German (de)
French (fr)
Inventor
Dimphna Johanna Maria Van Beek
Patrick Elisabeth Luc Voets
Henrica Norberta Alberta M. STEENBAKKERS-MENTING
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SABIC Global Technologies BV
Original Assignee
SABIC Global Technologies BV
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by SABIC Global Technologies BV filed Critical SABIC Global Technologies BV
Publication of EP3485189A1 publication Critical patent/EP3485189A1/en
Withdrawn legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N3/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N3/08Investigating strength properties of solid materials by application of mechanical stress by applying steady tensile or compressive forces
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N3/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N3/08Investigating strength properties of solid materials by application of mechanical stress by applying steady tensile or compressive forces
    • G01N3/10Investigating strength properties of solid materials by application of mechanical stress by applying steady tensile or compressive forces generated by pneumatic or hydraulic pressure
    • G01N3/12Pressure testing
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N3/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N3/08Investigating strength properties of solid materials by application of mechanical stress by applying steady tensile or compressive forces
    • G01N3/18Performing tests at high or low temperatures
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16LPIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
    • F16L9/00Rigid pipes
    • F16L9/12Rigid pipes of plastics with or without reinforcement
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/0001Type of application of the stress
    • G01N2203/0012Constant speed test
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/0014Type of force applied
    • G01N2203/0016Tensile or compressive
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/0058Kind of property studied
    • G01N2203/006Crack, flaws, fracture or rupture
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/0058Kind of property studied
    • G01N2203/0069Fatigue, creep, strain-stress relations or elastic constants
    • G01N2203/0071Creep
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/0058Kind of property studied
    • G01N2203/0069Fatigue, creep, strain-stress relations or elastic constants
    • G01N2203/0075Strain-stress relations or elastic constants
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/02Details not specific for a particular testing method
    • G01N2203/0202Control of the test
    • G01N2203/0212Theories, calculations
    • G01N2203/0218Calculations based on experimental data
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2203/00Investigating strength properties of solid materials by application of mechanical stress
    • G01N2203/02Details not specific for a particular testing method
    • G01N2203/022Environment of the test
    • G01N2203/0222Temperature

Definitions

  • the present invention relates to a method for determining the time to brittle failure of a pipe made of a polypropylene composition.
  • ISO 1 167 specifies the method of preparation of test pieces, the equipment used to pressurize test pieces, the testing procedure to be applied and the test report. The time to failure and the type of failure (brittle, ductile or mixed) at predetermined hoop stresses are determined by this test. Such methods require large volumes of material and long testing times of more than one year. These extremely long testing times are a serious concern in using these methods for determination of time to failure behavior of resins and manufactured pipes as well as in the development of new grades, in batch release testing and quality control.
  • Resistance to slow crack growth of a pipe made of a high density polyethylene can be determined by the measurement of the strain hardening modulus according to IS018488.
  • the slow crack growth behavior of HDPE can be regarded as a
  • the disentanglement capability of HDPE will determine its resistance against slow crack growth.
  • the strain hardening modulus of HDPE is a measure of the disentanglement capability of the tie molecules of this polymer and is an intrinsic property. Thus, the measurement of the strain hardening modulus of HDPE will give an insight on the slow crack growth behavior or HDPE.
  • the present invention provides a method for determining the time to brittle failure of a pipe made of a polypropylene composition, comprising:
  • step d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus G p from the true stress- strain curve, according to the method as described in ISO/DIS 18488,
  • the inventors have found that the quotient G p Y and the time to brittle failure show a correlation.
  • the determination of G p Y can be performed much easier than the measurement of the time to brittle failure.
  • the time to brittle failure of a given pipe made of a polypropylene composition can be estimated by determining G p Y of the same material.
  • the correlation can be obtained by measuring the time to brittle failure and G p Y for a sufficient number of pipes of different polypropylene composition. Once the correlation is obtained, it is no longer necessary to actually measure the time to brittle failure for new pipes.
  • the measurement of G p Y can be used to estimate the time to brittle failure with a relatively high accuracy.
  • time to brittle failure of a pipe made of polypropylene cannot be determined only by the tensile strain hardening modulus like with the Full Notched Creep Test (FNCT) of a pipe made of HDPE.
  • FNCT Full Notched Creep Test
  • the inventors have found that the determination of the time to brittle failure of a pipe made of polypropylene composition requires the measurement of the yield stress Y in addition to the tensile strain hardening modulus. step a)
  • the method according to the invention comprises a) providing a specimen of the polypropylene composition having a predetermined shape.
  • step a) involves compression molding a sheet from a polypropylene composition according to ISO 1873-2 and punching a specimen having a geometry of the test specimen described in ISO/DIS 18488 from the sheet.
  • the geometry of the test specimen is described in section 6.1 of ISO/DIS 18488.
  • the sheets After compression molding of the sheets, the sheets are stored for minimal 7 days at room temperature. After 7 days the sheets are annealed to remove any orientation or thermal history and maintain isotropic sheets. Annealing of the sheets are performed by conditioning the sheet for 1 h in an oven at a temperature of 95 to 120 °C, preferably 96 to 1 10 °C, more preferably 97 to 105 °C, more preferably 98 to 102 °C, most preferably around 100 °C and slowly cooling down to room temperature by switching off the closed temperature chamber. The period of conditioning is preferably 1 h, but may also be shorter or longer, e.g. 0.5 to 2 h. During this operation free movement of the sheets is allowed. After cooling down, specimens having the predetermined shape as described in ISO/DIS 18488 are punched from the sheet. step b)
  • the method according to the invention comprises b) elongating the specimen at a constant traverse speed at a predetermined temperature.
  • the constant traverse speed is 5-40 mm/min, more preferably 10-30 mm/min, more preferably 15-25 mm/min, more preferably about 20 mm/min.
  • the predetermined temperature is 95-105 °C, preferably 100 °C. step c)
  • the method according to the invention comprises c) measuring the load sustained by the specimen during the elongation of step b). A stress-strain curve is obtained. In step c), the yield stress Y is also measured. The Yield stress is the tensile stress at the first point on the stress- strain curve where some further increase in strain occurs without any increase in stress.
  • steps b) and c) are performed as follows:
  • the sample shall remain between the clamps for a certain period, e.g. at least 1 minute, before the load is applied and measurement starts.
  • test specimen A sufficient number (e.g. 5) of test specimen is subjected to the measurement and averages are measured to obtain the final results. Preferably, if straining of the test specimen takes place in the clamps, the test results are discarded. step d)
  • the method according to the invention comprises d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus G p from the true stress-strain curve, according to the method as described in ISO/DIS 18488.
  • the method of the calculations are described in ISO/DIS 18488, section 8 "Data treatment".
  • the draw ratio, ⁇ is calculated from the length, /, and the gauge length, / 0 , as shown by formula 1 .
  • ⁇ / is the increase in the specimen length between the gauge marks.
  • the true stress, o irue is calculated according to formula 2, which is derived on the assumption of conservation of volume between the gauge marks:
  • Neo-Hookean constitutive model (formula 3, see Annex A of ISO/DIN 18488) is used to fit and extrapolate the data from which ⁇ Gp> (MPa) for 8 ⁇ ⁇ ⁇ 12 is calculated.
  • the method according to the invention comprises e) calculating a quotient of the tensile strain hardening modulus G p divided by the yield stress Y. step f)
  • the method according to the invention comprises f) determining the time to brittle failure of the pipe based on the quotient G p Y. Preferably, the time to brittle failure of the pipe at 4.2 MPa and 95 °C is determined.
  • step f) involves comparing the quotient G p /Y determined for the pipe to a reference formula which shows the relationship between the brittle time to failure and the quotient Gp Y for pipes made of polypropylene composition.
  • the reference formula which shows the relationship between the brittle time to failure and the quotient Gp/Y for pipes made of polypropylene composition may be a calibration curve which is a best fit of plots taking time to brittle measurements performed on pipes on one axis and Gp/Y measurements performed on test specimens on another axis.
  • the axis for the time to brittle may be on a logarithmic scale.
  • each of the pipes was prepared according to ISO 1 167-2.
  • the measurement of time to brittle failure was performed at 95 °C and at a hoop stress of 4.2 MPa measured according to IS03213.
  • G p Y The measurement of G p Y was performed on test specimens made according to IS01873-2 and ISO/DIS18488 at a constant traverse speed of 20 mm/min and a temperature of 100 °C.
  • the polypropylene composition of the pipe for which the time to brittle failure is determined may contain additives, in particular additives suitable for use in pipes.
  • additives suitable for use in pipes include but are not limited to nucleating agents, stabilizers, anti-oxidants pigments and/or colorants, impact modifiers, flame retardants, acid scavengers, anti-microbials and the like.
  • Such additives are well known in the art. The skilled person will choose the type and amount of additives such that they do not detrimentally influence the aimed properties of the composition.
  • the polypropylene composition may consist of a propylene polymer or may consist of a propylene polymer and additives.
  • the amount of the additive in the polypropylene composition is chosen from 0 to 5 wt% based on the total weight of the polypropylene composition (the polypropylene composition comprises 95 to 100 wt% of the propylene polymer), preferably the amount of additive is from 0.01 to 3 wt%, for example from 0.1 to 2 wt%, based on the total weight of the polypropylene composition.
  • propylene polymer as used herein is meant propylene homopolymer, a random or a block copolymer of at least 70 wt% of propylene with up to 30 wt% of an a-olefin having 2 or 4 to 10 C-atoms.
  • the examples of ⁇ -olefin in the random or block propylene copolymer include ethylene, 1 -butene, 1 -pentene, 4-methyl-1 -pentene, 1 -hexene, 1 -heptene or 1 -octene, preferably ethylene.
  • the propylene copolymer may consist of at least 70 wt% of propylene and up to 30 wt% of a-olefin, preferably 1 -10 wt% of a-olefin, based on the total weight of the propylene copolymer.
  • Polypropylene homopolymer and the copolymer of propylene with an ⁇ -olefin can be made by any known polymerization technique as well as with any known
  • polymerization catalyst system Regarding the techniques, reference can be given to slurry, solution or gas phase polymerizations; regarding the catalyst system reference can be given to Ziegler-Natta, metallocene or single-site catalyst systems. All are, in themselves, known in the art.
  • the propylene-based polymer used in the invention is a propylene homopolymer or a copolymer of propylene with ethylene, wherein the amount of ethylene is 1 -10 wt% based on the copolymer.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
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  • General Health & Medical Sciences (AREA)
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Abstract

The invention relates to a method for determining the time to brittle failure of a pipe made of a polypropylene composition, comprising: a) providing a specimen of the polypropylene composition having a predetermined shape, b) elongating the specimen at a constant traverse speed at a predetermined temperature, c) measuring the load sustained by the specimen during the elongation to obtain a stress-strain curve and measuring the yield stress Y, d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus Gp from the true stress- strain curve, according to the method as described in ISO/DIS 18488, e) calculating a quotient of the tensile strain hardening modulus Gp divided by the yield stress Y and f) determining the time to brittle failure of the pipe based on the quotient Gp/Y.

Description

METHOD FOR DETERMINING TIME TO BRITTLE FAILURE OF A PIPE MADE OF
POLYPROPYLENE
The present invention relates to a method for determining the time to brittle failure of a pipe made of a polypropylene composition.
One of the most important properties of a polymer material used for hot and cold water pressure pipes is its resistance to internal pressure at different temperatures. A standardized method to measure the internal pressure at different temperatures of pipes is described in ISO 1 167. ISO 1 167 specifies the method of preparation of test pieces, the equipment used to pressurize test pieces, the testing procedure to be applied and the test report. The time to failure and the type of failure (brittle, ductile or mixed) at predetermined hoop stresses are determined by this test. Such methods require large volumes of material and long testing times of more than one year. These extremely long testing times are a serious concern in using these methods for determination of time to failure behavior of resins and manufactured pipes as well as in the development of new grades, in batch release testing and quality control.
Additionally, material wastage, energy costs and water use in traditional methods are undesirable from a sustainability point of view.
Resistance to slow crack growth of a pipe made of a high density polyethylene (HDPE) can be determined by the measurement of the strain hardening modulus according to IS018488. The slow crack growth behavior of HDPE can be regarded as a
combination of yield stress and the capability of disentanglement of tie molecules. The disentanglement capability of HDPE will determine its resistance against slow crack growth. The strain hardening modulus of HDPE is a measure of the disentanglement capability of the tie molecules of this polymer and is an intrinsic property. Thus, the measurement of the strain hardening modulus of HDPE will give an insight on the slow crack growth behavior or HDPE.
It is desirable if the time to brittle failure of a pipe made of a polypropylene composition can be estimated by a method which requires less amount of pipe and less time.
Accordingly, the present invention provides a method for determining the time to brittle failure of a pipe made of a polypropylene composition, comprising:
a) providing a specimen of the polypropylene composition having a predetermined shape, b) elongating the specimen at a constant traverse speed at a predetermined temperature,
c) measuring the load sustained by the specimen during the elongation to obtain a stress-strain curve and measuring the yield stress Y,
d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus Gp from the true stress- strain curve, according to the method as described in ISO/DIS 18488,
e) calculating a quotient of the tensile strain hardening modulus Gp divided by the yield stress Y and
f) determining the time to brittle failure of the pipe based on the quotient Gp Y.
The inventors have found that the quotient Gp Y and the time to brittle failure show a correlation. The determination of Gp Y can be performed much easier than the measurement of the time to brittle failure. Hence, the time to brittle failure of a given pipe made of a polypropylene composition can be estimated by determining Gp Y of the same material. The correlation can be obtained by measuring the time to brittle failure and Gp Y for a sufficient number of pipes of different polypropylene composition. Once the correlation is obtained, it is no longer necessary to actually measure the time to brittle failure for new pipes. The measurement of Gp Y can be used to estimate the time to brittle failure with a relatively high accuracy.
It is particularly noted that the time to brittle failure of a pipe made of polypropylene cannot be determined only by the tensile strain hardening modulus like with the Full Notched Creep Test (FNCT) of a pipe made of HDPE. The inventors have found that the determination of the time to brittle failure of a pipe made of polypropylene composition requires the measurement of the yield stress Y in addition to the tensile strain hardening modulus. step a)
The method according to the invention comprises a) providing a specimen of the polypropylene composition having a predetermined shape.
Preferably, step a) involves compression molding a sheet from a polypropylene composition according to ISO 1873-2 and punching a specimen having a geometry of the test specimen described in ISO/DIS 18488 from the sheet. In particular, the geometry of the test specimen is described in section 6.1 of ISO/DIS 18488.
Preferably, the following steps are followed after the compression molding:
After compression molding of the sheets, the sheets are stored for minimal 7 days at room temperature. After 7 days the sheets are annealed to remove any orientation or thermal history and maintain isotropic sheets. Annealing of the sheets are performed by conditioning the sheet for 1 h in an oven at a temperature of 95 to 120 °C, preferably 96 to 1 10 °C, more preferably 97 to 105 °C, more preferably 98 to 102 °C, most preferably around 100 °C and slowly cooling down to room temperature by switching off the closed temperature chamber. The period of conditioning is preferably 1 h, but may also be shorter or longer, e.g. 0.5 to 2 h. During this operation free movement of the sheets is allowed. After cooling down, specimens having the predetermined shape as described in ISO/DIS 18488 are punched from the sheet. step b)
The method according to the invention comprises b) elongating the specimen at a constant traverse speed at a predetermined temperature. Preferably, the constant traverse speed is 5-40 mm/min, more preferably 10-30 mm/min, more preferably 15-25 mm/min, more preferably about 20 mm/min.
Preferably, the predetermined temperature is 95-105 °C, preferably 100 °C. step c)
The method according to the invention comprises c) measuring the load sustained by the specimen during the elongation of step b). A stress-strain curve is obtained. In step c), the yield stress Y is also measured. The Yield stress is the tensile stress at the first point on the stress- strain curve where some further increase in strain occurs without any increase in stress.
Preferably, steps b) and c) are performed as follows:
Measurement of the exact dimensions (with accuracy of 0.01 mm) of width (b) and (with an accuracy of 0.005 mm) of thickness (h) of each individual test specimen. Conditioning of the test specimens for a period of time, e.g. at least 30 minutes, in the temperature chamber set at said predetermined temperature prior to starting the test.
Clamping of the test piece in the upper grip of the elongation device. The clamps are chosen to avoid damage and slippage of the test piece.
Closure of the temperature chamber.
After reaching said predetermined temperature, clamp the test piece with the lower grip.
The sample shall remain between the clamps for a certain period, e.g. at least 1 minute, before the load is applied and measurement starts.
Add a pre-stress e.g. of 0.4 MPa reached with a speed of e.g. 5 mm/min.
During the test, the load sustained by the specimen and the elongation are measured.
Extend the test specimen at said constant traverse speed until the test specimen breaks.
A sufficient number (e.g. 5) of test specimen is subjected to the measurement and averages are measured to obtain the final results. Preferably, if straining of the test specimen takes place in the clamps, the test results are discarded. step d)
The method according to the invention comprises d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus Gp from the true stress-strain curve, according to the method as described in ISO/DIS 18488.
The method of the calculations are described in ISO/DIS 18488, section 8 "Data treatment". The draw ratio, λ, is calculated from the length, /, and the gauge length, /0, as shown by formula 1 .
k k
(1 )
where
Δ/ is the increase in the specimen length between the gauge marks. The true stress, oirue, is calculated according to formula 2, which is derived on the assumption of conservation of volume between the gauge marks:
(2)
where
F is the measured force (N).
It is important that the initial cross section A shall be determined for each individual test bar.
The Neo-Hookean constitutive model (formula 3, see Annex A of ISO/DIN 18488) is used to fit and extrapolate the data from which <Gp> (MPa) for 8 < λ < 12 is calculated.
J t + C
20 λ I
(3)
where
C is a mathematical parameter of the constitutive model describing the yield stress extrapolated to λ = 0.
Accuracy of fit of data (R2) greater than 0.9 shall be achieved. step e)
The method according to the invention comprises e) calculating a quotient of the tensile strain hardening modulus Gp divided by the yield stress Y. step f)
The method according to the invention comprises f) determining the time to brittle failure of the pipe based on the quotient Gp Y. Preferably, the time to brittle failure of the pipe at 4.2 MPa and 95 °C is determined.
Preferably, step f) involves comparing the quotient Gp/Y determined for the pipe to a reference formula which shows the relationship between the brittle time to failure and the quotient Gp Y for pipes made of polypropylene composition.
The reference formula which shows the relationship between the brittle time to failure and the quotient Gp/Y for pipes made of polypropylene composition may be a calibration curve which is a best fit of plots taking time to brittle measurements performed on pipes on one axis and Gp/Y measurements performed on test specimens on another axis. The axis for the time to brittle may be on a logarithmic scale.
An example of a graph made from (1 ) time to brittle measurements performed on pipes and (2) Gp/Y measurements performed on test specimens is shown in Figure 1 . 12 different types of propylene compositions were used with varying molecular weight, co- monomer content and/or nucleating agent.
For the measurement on pipes, each of the pipes was prepared according to ISO 1 167-2. The measurement of time to brittle failure was performed at 95 °C and at a hoop stress of 4.2 MPa measured according to IS03213.
The measurement of Gp Y was performed on test specimens made according to IS01873-2 and ISO/DIS18488 at a constant traverse speed of 20 mm/min and a temperature of 100 °C.
From figure 1 , the relationship between Gp Y and the time to brittle failure at a hoop stress of 4.2 MPa and 95 °C can be determined. polypropylene composition
The polypropylene composition of the pipe for which the time to brittle failure is determined may contain additives, in particular additives suitable for use in pipes. Additives suitable for use in pipes include but are not limited to nucleating agents, stabilizers, anti-oxidants pigments and/or colorants, impact modifiers, flame retardants, acid scavengers, anti-microbials and the like. Such additives are well known in the art. The skilled person will choose the type and amount of additives such that they do not detrimentally influence the aimed properties of the composition.
The polypropylene composition may consist of a propylene polymer or may consist of a propylene polymer and additives. The amount of the additive in the polypropylene composition is chosen from 0 to 5 wt% based on the total weight of the polypropylene composition (the polypropylene composition comprises 95 to 100 wt% of the propylene polymer), preferably the amount of additive is from 0.01 to 3 wt%, for example from 0.1 to 2 wt%, based on the total weight of the polypropylene composition. With propylene polymer as used herein is meant propylene homopolymer, a random or a block copolymer of at least 70 wt% of propylene with up to 30 wt% of an a-olefin having 2 or 4 to 10 C-atoms. The examples of α-olefin in the random or block propylene copolymer include ethylene, 1 -butene, 1 -pentene, 4-methyl-1 -pentene, 1 -hexene, 1 -heptene or 1 -octene, preferably ethylene. In case of a block copolymer, the propylene copolymer may consist of at least 70 wt% of propylene and up to 30 wt% of a-olefin, preferably 1 -10 wt% of a-olefin, based on the total weight of the propylene copolymer.
Polypropylene homopolymer and the copolymer of propylene with an α-olefin can be made by any known polymerization technique as well as with any known
polymerization catalyst system. Regarding the techniques, reference can be given to slurry, solution or gas phase polymerizations; regarding the catalyst system reference can be given to Ziegler-Natta, metallocene or single-site catalyst systems. All are, in themselves, known in the art.
Preferably, the propylene-based polymer used in the invention is a propylene homopolymer or a copolymer of propylene with ethylene, wherein the amount of ethylene is 1 -10 wt% based on the copolymer.

Claims

A method for determining the time to brittle failure of a pipe made of a
polypropylene composition, comprising:
a) providing a specimen of the polypropylene composition having a predetermined shape,
b) elongating the specimen at a constant traverse speed at a predetermined
temperature,
c) measuring the load sustained by the specimen during the elongation to obtain a stress-strain curve and measuring the yield stress Y,
d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus Gp from the true stress-strain curve, according to the method as described in ISO/DIS 18488, e) calculating a quotient of the tensile strain hardening modulus Gp divided by the yield stress Y and
f) determining the time to brittle failure of the pipe based on the quotient Gp Y.
The method according to claim 1 , wherein step f) involves comparing the quotient Gp Y determined for the pipe to a reference formula which shows the relationship between the time to brittle failure and the quotient Gp/Y for pipes made of polypropylene composition.
The method according to claim 2, wherein the reference formula is obtained by measurements of the time to brittle failure and the quotient Gp/Y of at least 10 types of pipes made of polypropylene composition.
The method according to any one of the preceding claims, wherein step a) involves compression molding a sheet from a polypropylene composition according to ISO 1873-2 and punching a specimen having a geometry of the test specimen described in ISO/DIS18488 from the sheet.
The method according to claim 4, wherein the sheet is annealed after the compression molding and before the punching at a temperature of 95 to 120 °C, preferably 96 to 1 10 °C, more preferably 97 to 105 °C, more preferably 98 to 102 °C, most preferably 100 °C, wherein the annealing is performed for 0.5 to 2 h. The method according to any one of the preceding claims, wherein the constant traverse speed is 5-40 mm/min, preferably 20 mm/min.
The method according to any one of the preceding claims, wherein the predetermined temperature is 95-105 °C, preferably 100 °C.
The method according to any one of the preceding claims, wherein the polypropylene composition of the pipe for which the time to brittle failure is determined comprises 95 to 100 wt% of a propylene polymer and 0 to 5 wt% of additives.
EP17735595.5A 2016-07-14 2017-07-11 Method for determining time to brittle failure of a pipe made of polypropylene Withdrawn EP3485189A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP16179399 2016-07-14
PCT/EP2017/067342 WO2018011177A1 (en) 2016-07-14 2017-07-11 Method for determining time to brittle failure of a pipe made of polypropylene

Publications (1)

Publication Number Publication Date
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