Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K7/00—Use of ingredients characterised by shape
  • C08K7/02—Fibres or whiskers
  • C08K7/04—Fibres or whiskers inorganic
  • C08K7/14—Glass
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
  • C08G75/02—Polythioethers
  • C08G75/0204—Polyarylenethioethers
  • C08G75/0209—Polyarylenethioethers derived from monomers containing one aromatic ring
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
  • C08J5/0405—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres
  • C08J5/043—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres with glass fibres
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
  • C08L81/02—Polythioethers; Polythioether-ethers
• • 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

Definitions

• the invention relates to polyphenylene sulfide polymer compositions having significantly improved water aging properties.
• the invention further relates to articles incorporating the polyphenylene sulfide polymer compositions.
• Reinforced polyphenylene sulfide (“PPS”) polymer compositions are advantageously used in applications setting in which the PPS polymer is in contact with water.
• the PPS polymer compositions are reinforced with E-glass fiber, to provide for a PPS polymer composition having high strength (e.g. tensile strength), in addition to the inherently desirable chemical resistance of the composition. Due to the high strength and desirable chemical resistance, such compositions are especially desirable in drinking water applications.
• the strength of the PPS polymer composition degrades significantly, requiring replacement of the corresponding part including the PPS polymer composition. Accordingly, there is an ever present desire to increase the retention of mechanical properties of reinforced PPS polymer compositions during prolonged contact with water.
• PPS polyphenylene sulfide
• MFR low melt flow rate
• PPS polymer compositions including E-CR glass fibers in conjunction with a low MFR PPS polymer and a high MFR PPS polymer had unexpected synergies with respect to water aging performance, relative to corresponding polymer compositions including E-CR glass fibers and either a low MFR PPS polymer or a high MFR PPS polymer. Due at least in part to the improved water aging performance, the PPS polymer compositions can be advantageously incorporated into application settings where the polymer composition is in contact with water. Examples include, but are not limited to, drinking water applications.
• the PPS polymer composition has improved retention of tensile strength and improved retention of tensile elongation at break after water aging.
• tensile elongation at break is sometimes referred to as "tensile elongation.”
• an ISO 527-2 tensile bar molded from the PPS polymer composition in submersed in deionized water and maintained at a temperature of 135°C for a selected period of time. Water aging is described in more detail in the Examples. Retention of tensile strength refers to 100 times the difference in (1) the tensile strength of an as molded (e.g.
• ISO 527-2 tensile bar molded from the PPS polymer composition and (2) the tensile strength of an ISO 527-2 tensile bar molded from the PPS polymer composition after water aging for a selected amount of time, relative to the tensile strength of the as molded ISO 527-2 tensile bar molded from the PPS polymer composition.
• a lower value of the retention of tensile strength indicates a lesser change to the tensile strength during water aging.
• the PPS polymer has retention of tensile strength after 250 hours of water aging of no more than 30 %, preferably no more than 28 %, more preferably no more than 26 %, even more preferably no more than 24 %, still more preferably no more than 22 %, most preferably no more than 20 %. In some embodiments, the PPS polymer has a retention of tensile strength after 500 hours of water aging of no more than 30 %, preferably no more than 25 %, most preferably no more than 23 %.
• the PPS polymer has a retention of tensile strength after 1000 hours of water aging of no more than 34 %, preferably no more than 30 %, even more preferably no more than 28 %, still more preferably no more than 27 %.
• retention of tensile elongation refers to 100 times the difference in (1) the tensile elongation of an as molded ISO 527-2 tensile bar molded from the PPS polymer composition and (2) the tensile elongation of an ISO 527-2 tensile bar molded from the PPS polymer composition after water aging for a selected amount of hours at 135°C, relative to the tensile elongation of the as molded ISO 527-2 tensile bar molded from the PPS polymer composition.
• a lower value of the retention of tensile elongation indicates a lesser change to the tensile elongation during water aging.
• the PPS polymer composition has a retention of tensile elongation after 250 hours of water aging of no more than 35 %, preferable no more than 30 %, most preferably no more than 25 %. In some embodiments, the PPS polymer composition has a retention of tensile elongation after 500 hours of water aging of no more than 35 %, preferably no more than 30 %, more preferably no more than 25 %, most preferably no more than 20 %. In some embodiments, the PPS polymer composition has a retention of tensile elongation after 1000 hours of water aging, of no more than 30 %, preferably no more than 25 %.
• the PPS polymer compositions described herein have, in addition to improved retention of tensile strength and retention of tensile elongation, desirable tensile strength and tensile resistance.
• the PPS polymer composition can have a tensile strength of at least 120 mega Pascals ("MPa"), preferably at least 140 MPa, more preferably at least 160 MPa, still more preferably at least 170 MPa, even more preferably at least 175 MPa, still more preferably at least 180 MPa, even more preferably at least 185 MPa, most preferably at least 190 MPa.
• MPa mega Pascals
• Tensile strength can be measured as described in the Examples below.
• the PPS polymer composition has a tensile elongation at break of at least 1 %, preferably at least 1.5 %, most preferably at least 1.6 %. Tensile elongation at break can be measured as described in the Examples.
• the PPS polymer composition includes a low MFR PPS polymer and, optionally, a high MFR PPS polymer.
• a PPS polymer refers to any polymer having at least 50 mol % of a recurring unit (Rpps), relative to the total number of recurring units in the PPS polymer.
• the PPS polymer has at least 60 mol %, at least 70 mol %, at least 80 mol %, at least 90 mol %, at least 95 mol % or at least 99 mol % recurring unit (Rpps), relative to the total number of recurring units in the PPS polymer.
• Recurring unit (RPPS) is represented by the following formula :
• a dashed bond indicates a bond to an atom outside the recurring unit.
• the dashed bond can be a bond to an identical recurring unit, a different recurring unit, or an atom of a non-recurring unit (e.g. an end-capper).
• the PPS polymer can include one or more additional recurring units (R*pps) according to Formula (1). In such cases, each additional recurring unit (R*pps) is distinct from each other and from recurring unit (Rpps).
• the total concentration of recurring unit (Rpps) and one or more additional recurring units (R*pps), is at least 50 mol % and, in some embodiments, at least 60 mol %, at least 70 mol %, at least 80 mol %, at least 90 mol %, at least 95 mol % or at least 99 mol %, relative to the total number of recurring units in the PPS polymer.
• the low MFR PPS polymer contains at least 50 mol % of a recurring unit (Rpps) according to Formula (1) and the high MFR PPS polymer contains at least 50 mol % of a recurring unit according to Formula (1), which can be the same or different that recurring unit (Rpps) of the low MFR PPS polymer.
• Rpps recurring unit
• a low MFR PPS polymer has a melt flow rate of no more than 170 grams/10 minutes ("g/10 min.”), preferably no more than 150 g/10 min., more preferably no more than 140 g/10 min., most preferably no more than 130 g/10 min.
• the low MFR PPS polymer has a melt flow rate of at least 50 g/10 min., preferably at least 60 g/10 min., more preferably at least 65 g/10 min., most preferably at least 70 g/10 min.
• the PPS polymer composition includes a high MFR PPS polymer in addition to the low MFR PPS polymer.
• a high MFR PPS polymer has a melt flow rate of at least 700 g/10 min., preferably at least 900 g/10 min., most preferably at least 1000 g/10 min. In some embodiments, additionally or alternatively, the high MFR PPS polymer has a melt flow rate of no more than 2500 g/10 min., preferably no more than 2200 g/10 min., most preferably no more than 2000 g/10 min.
• melt flow rate refers to the melt flow rate at 316°C, measured using a 5 kilogram ("kg”) weight according to ASTM D1238B.
• the total concentration of the low MFR PPS polymer and the high MFR is the total concentration of the low MFR PPS polymer and the high MFR
• PPS polymer can be at least 30 wt. %, preferably at least 35 wt. %, most preferably at least 40 wt. %. Additionally or alternatively, the total concentration of the low MFR PPS polymer and high MFR PPS can be no more than 65 wt. %, preferably no more than 60 wt. %, most preferably no more than 55 wt. %. For clarity, in embodiments in which the high MFR PPS polymer is not present, the aforementioned concentration ranges refer the concentration of the low MFR PPS polymer. As used herein, wt. % is relative to the total weight of the PPS polymer composition, unless explicitly noted otherwise.
• the relative concentration of the low MFR PPS polymer to the high MFR PPS polymer is from 1 : 1 to 3: 1, preferably 1 : 1 to 2.5:1, more preferably 1 :1 to 2: 1, most preferably 1 : 1 to 1 : 1.5.
• the polymer composition includes an E-CR glass fiber.
• E-CR glass fiber is a boron-free modified E-Glass fiber, used for improved resistance to corrosion by most acids and as defined according to ASTM D578/D578M - 05 (2011).
• the concentration of the E-CR glass fiber is from 30 wt. % to 60 wt. %, preferably from 35 wt. % to 55 wt. %.
• E glass fiber includes boron (generally as boric oxide).
• boric oxide is included to help reduce the melt viscosity of the glass, thereby allowing the glass fiber to be fabricated at lower processing temperatures.
• concentration of boric oxide in the glass fiber is at least 2 wt. %, and can be as high as 8 wt. % or even higher, relative to the total weight of the glass fiber.
• E glass fibers further include fluoride as a fluxing agent to aid in the fiber forming process.
• E-CR glass fibers are free of boron and, optionally fluoride free.
• a glass fiber free of boron has a boron concentration of less than 1 wt. %, preferably less than 0.5 wt. %, more preferably less than 0.1 wt. %, even more preferably less than 0.05 wt. %, still more preferably less than 0.03 wt. %, most preferably less than 0.02 wt. %, relative to the total weight of the glass fiber.
• a glass fiber free of fluoride has a fluoride concentrate of less than 0.04 wt. %, preferably less than 0.01 wt. %, relative to the total weight of the glass fiber. Boron concentration and fluoride concentration can be measured by inductively coupled plasma-atomic emission spectrometry ("ICP-AES”), as described in the Examples.
• ICP-AES inductively coupled plasma-atomic emission spectrometry
• E-CR glass fibers further include titanium dioxide to reduce the melt viscosity of the glass fiber.
• the concentration of titanium in the glass fiber is at least 0.1 wt. %, preferably at least 0.15 wt. %, most preferably at least 0.17 wt. %, relative to the total weight of the E-CR glass fiber.
• the E-CR glass fiber additionally or alternatively, has a titanium concentration of no more than 0.25 wt. %, preferably no more than 0.20 wt. %, most preferably 0.19 wt. %, relative to the total weight of the glass fiber. Titanium concentration can be measured by ICP-AES.
• the E-CR glass fibers can further include potassium oxide as a fluxing agent.
• the E-CR glass fiber has a potassium concentration of at least 0.2 wt. %, preferably at least 0.25 wt. %, more preferably at least 0.3 wt. %, most preferably at least 0.35 wt. %, relative to the total weight of the E-CR glass fiber.
• the E-CR glass fiber additionally or alternatively, has a potassium concentration of no more than 0.5 wt. %, preferably no more than 0.45 wt. %, relative to the total weight of the E-CR glass fiber. Potassium concentration can be measured by ICP-AES.
• the E-CR glass fibers have a reduced sodium oxide concentration, relative to E-glass fibers.
• the E-CR glass fiber has a sodium concentration of less than 0.5 wt. %, preferably less than 0.3 wt. %, more preferably less than 0.1 wt. %, most preferably less than 0.05 wt. %, relative to the total weight of the E-CR glass fiber.
• the E-CR glass fiber has a sodium concentration of at least 0.01 wt.%, preferably at least 0.02 wt.%.
• the E-CR glass fiber has a strontium concentration of less 0.1 wt.
• the E-CR glass fiber has a strontium concentration of at least 0.01 wt.%. Sodium and strontium concentration can be measured by ICP-AES.
• the PPS polymer composition can optionally include reinforcing fillers; lubricants; processing aids; plasticizers; flow modifiers; flame retardants; anti-static agents; extenders; pigments, dyes or colorants; and metal deactivators.
• additives When present to total concentration of additives can be from 0.1 wt. % to
• the PPS polymer compositions can be desirably incorporated into drinking water applications settings as well as automotive application settings.
• a plumbing fixtures include the PPS polymer composition.
• the plumbing fixture can be selected from the group consisting of a water pump, a water meter, a faucet, a valve, a manifold, a spout and a pipe.
• an automotive fluid reservoir includes the PPS polymer composition.
• an automotive fluid reservoir is a container for holding automotive fluid that is delivered to (and optionally returned from) an automobile component.
• the automotive fluid reservoir is selected from the group consisting of an engine coolant reservoir and a windshield wiper fluid reservoir.
• the PPS polymer composition When incorporated into a drinking water or automotive application settings, the PPS polymer composition is intended to be in contact with water or automotive fluid during expected use of the of the plumbing fixture and automotive fluid reservoir, respectively. Put another way, when used as intended, the PPS polymer composition is in contact with water or automotive fluid when the PPS polymer composition is incorporated into a plumbing fixture and automotive fluid reservoir, respectively.
• Each composition contained a PPS polymer having a melt flow rate of 70 g/10 min. ("low MFR PPS”) or 1500 g/10 min. (“high MFR PPS”).
• Some compositions incorporated glass fiber ("GF"), either E-glass fiber obtained as ThermoFlow ® 770 from Johns Manville (“E-GF 1"); E-glass fiber obtained as ECS 03 T779DE from Nippon Electric Glass America (“E-GF 2”) or E-CR glass fiber (3B DS 8800-1 IP from 3B-The Fibreglass Company).
• the boron concentration in the glass fibers were measured using ICP-AES.
• ICP-AES ICP-AES analysis
• a clean dry plastic container was placed onto an analytical balance, and the balance was zeroed.
• One half to three gram of sample was weighed and the weight was recorded to 0.0001 g.
• the sample was then dissolved in hydrofluoric acid.
• the solution was neutralized with boric hydroxide before testing commenced in the ICP-AES.
• ICP-AES analysis was performed using inductively-coupled plasma emission spectrometer Perkin-Elmer Optima 8300 dual view.
• the spectrometer was calibrated using a set of NIST traceable multi-element mixed standards with analyte concentration between 0.0 and 10.0 mg/L.
• a linear calibration curve was obtained in a whole range of concentrations with a correlation coefficient better than 0.9999 for each of 48 analytes.
• the standards were run before and after every ten samples to ensure instrument stability. The results were reported as an average of three replicates.
• the concentration of elemental impurities in the sample was calculated with the following equation:
• A concentration of element in the sample in mg/kg
• E-GF1, E-GF2 and E-CR glass fiber had boron concentrations of 1.31 wt.%, 1.53 wt.% and less than 0.019 wt.% boron, respectively.
• compositions included a high density polyethylene lubricant or a color package containing a blend of dyes.
• the parameters for each sample composition are listed in Table 1. TABLE 1
• samples having E-CR glass fiber had surprisingly improved water aging performance relative to samples having E glass fiber.
• sample CE2 E glass fiber
• sample E2 E-CR glass
• sample E2 E-CR glass
• sample E2 had a relative change in tensile strength of 18.8 %, 22.0 % and 26.3 % after 250 hours, 500 hours and 1000 hours, respectively, of water aging.
• sample with E-CR glass showed a 19.5 %, 18.6 % and 15.9 % difference (improvement) in retention of tensile strength after 250 hours, 500 hours and 1000 hours, respectively, relative to sample CE2. Additionally, sample E2 also had increased tensile strength relative to sample CE2 initially and, therefore, also after water aging. Similar results were seen for sample El by comparison with sample CE1.
• sample E2 E- CR glass fiber
• CE2 E glass fiber
• sample El E-CR glass fiber
• sample El had a 12.5 %, 19.1 % and 21.1 % improvement in the retention of tensile elongation after, respectively, 250 hours, 500 hours and 1000 hours of water aging, relative to sample CE1 (E glass fiber).
• sample El had a greater initial tensile elongation relative to sample CE1.
• samples El to E3 all showed improved (lower) or the same retention of tensile elongation relative to the corresponding values after 250 hours of water aging.
• samples CEl to CE3 all showed the same or reduced retention of tensile elongation relative to the corresponding values after 250 hours of water aging.
• sample E2 low MFR PPS
• sample E3 high MFR PPS
• initial tensile strength of sample El low MFR PPS and high MFR PPS
• sample El also had significantly decreased relative change in tensile strength after water aging for 250 hours (17.9 %), relative to samples E2 (18.8 %) and E3 (22.4 %). With respect to tensile elongation, similar results were obtained. For example, sample El had a significantly decreased relative change in tensile elongation after water aging for 250 hours (23.5 %), relative to samples E2 (33.3 %) and E3 (28.3 %). After 500 hours of water aging, sample El had a reduced relative change in tensile elongation (17.6 %), relative to samples E2 (33.3 %) and E3 (25 %). Similar results were obtained after 1000 hours of water aging.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Inorganic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Manufacturing & Machinery (AREA)
• Materials Engineering (AREA)
• Compositions Of Macromolecular Compounds (AREA)

Priority Applications (5)

Applications Claiming Priority (4)

Publications (1)

Family

ID=62235973

Family Applications (1)

Country Status (6)

Cited By (2)

Citations (3)

Family Cites Families (20)

• 2018
  • 2018-05-24 JP JP2019568082A patent/JP7317720B2/ja active Active
  • 2018-05-24 EP EP18726807.3A patent/EP3635031B1/en active Active
  • 2018-05-24 CN CN201880037814.9A patent/CN110719938B/zh active Active
  • 2018-05-24 WO PCT/EP2018/063586 patent/WO2018224314A1/en not_active Ceased
  • 2018-05-24 KR KR1020197036440A patent/KR102563177B1/ko active Active
  • 2018-05-24 US US16/619,295 patent/US11180637B2/en active Active

Patent Citations (3)

Also Published As

Similar Documents

Legal Events