Showing posts with label High heat plastics. Show all posts
Showing posts with label High heat plastics. Show all posts

Tuesday, 19 November 2024

High Performance Thermoplastic Selection - Imide-Based Polymers (PEI, PAI, PESI, TPI, PI) and Polybenzimidazoles (PBI, PBI+PEEK, PBI+PEKK) [Part 2B]

Hello and welcome to the Part 2B of our High Performance Thermoplastics selection blog series. Today we discuss imide-based polymers and Polybenzimidazoles, their chemistry and production processes, their main properties, processing methods, and applications.

We will discuss six major high performance thermoplastics families (“the magnificent six”) which are outlined in the following enumeration

1. Introduction to High Performance Polymers

2. Short profile of the "magnificent six" families:

-Part 2A: Polysulfides (Polyphenylene sulfide - PPS), Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR)

-Part 2B: Imide-Based Polymers (PEI, PAI, PESI, TPI, PI) and Polybenzimidazoles (PBI, PBI+PEEK, PBI+PEKK)

-Part 2C: Polyether (PPE, PAEK, PEEK, PEKK)

-Part 2D: Liquid Crystal Polymers (LCP) and High-performance Polyesters (Polycyclohexylene terephthalate - PCT)

-Part 2E: Semi- and Fully Aromatic Polyamides (PARA, PPA, Aramid)

-Part 2F: Polyhalogenolefins (PTFE, PCTFE, FEP, PVDF, ECTFE)

Imide-Based Polymers (PEI, PAI, PESI, TPI, PI) 

Polyetherimide (PEI)

In the 1980s, Joseph G. Wirth developed PEI at General Electric’s Plastics Division and it found its way into the market as Ultem. When Saudi Basic Industries Corporation (SABIC) bought the GE Plastics business in 2007, it took over the PEI patents and continued its marketing and development. 

Chemistry and Production Process

Polyetherimide (PEI) is an amorphous high-performance polymer known for its excellent thermal stability, mechanical strength, and electrical properties. Its chemical structure consists of aromatic rings linked by ether and imide groups. This unique structure contributes to its exceptional properties.
The production of PEI typically involves a multi-step process. One common method is the reaction between bisphenol A and trimellitic anhydride. This reaction forms a precursor, which is then subjected to thermal imidization to yield the final PEI polymer.

Main Properties
  • Excellent Thermal Stability: PEI exhibits outstanding resistance to high temperatures, making it suitable for applications in harsh environments. The glass transition temperature (Tg) is at 217°C and the Relative Thermal Index (RTI) of PEI is 180°C.
  • High Mechanical Strength: It possesses excellent tensile strength, flexural strength, and impact resistance.
  • Good Electrical Properties: PEI offers good dielectric strength, arc resistance, and low moisture absorption, making it ideal for electrical and electronic applications.
  • Chemical Resistance: It is resistant to a wide range of chemicals, including acids, bases, and solvents. PEI is able to retain its strength and resist stress corrosion cracking when exposed to aliphatic hydrocarbons, alcohols, automotive and aircraft fluids, acids, weak aqueous solutions , and acids.
  • Flame Retardancy: PEI is inherently flame-retardant, reducing the risk of fire hazards.
  • Transparent: PEI can be colored, both transparent and opaque. 
  • Biocompatibility: For example Ultem 1010 is biocompatible and it holds NSF 51 certification for food contact. Additionally, it is capable of withstanding steam sterilization.
  • Alternative to Sulfones: PEI is an alternative to replace Polysulfones in certain applications. PEI has a higher UV resistance compared to PSU, PESU, and PPSU. Also, PEI has good mechanical properties, together with low moisture uptake and higher dimensional stability. Figure 1 compares the properties of PEI and Polysulfones (PSU, PESU, and PPSU).
Figure 1: Property comparison of PEI vs Polysulfones (PSU, PESU, PPSU).
  • Low smoke generation: in case of burning, PEI generates low amounts of smoke, making it an ideal interior material for railway, aeroplanes, and aerospace applications. Additionally, it shows low toxicity making it a material which performs excellent in Flame, Smoke, Toxicity (FST) tests.
  • Flexible: PEI is flexible and can be used in simple spring applications as well as for frame in eyewear.
Processing Methods

PEI can be processed using various methods, including:
  • Injection Moulding: This method is commonly used to produce complex parts with high precision.
  • Extrusion: PEI can be extruded into films, sheets, and profiles.
  • Thermoforming: This process allows for the shaping of PEI sheets into various forms.
  • Additive manufacturing: apart from the costly materials such as PEEK and PEKK for 3D printing, the amorphous PEI is a more economic alternative. It is used as a filament for FDM 3D printers, and it is compatible with high-performance FDM/FFF printers (incl. Stratasys printers).
Applications

PEI's exceptional properties make it suitable for a wide range of applications:
  • Electronics: It is used in printed circuit boards, connectors, and other electronic components due to its excellent electrical properties and thermal stability.
  • Aerospace: PEI is employed in aircraft components, such as engine parts and structural elements, owing to its high temperature resistance and mechanical strength.
  • Automotive: It is used in automotive components, including under-the-hood parts, due to its resistance to heat, chemicals, and mechanical stress.
  • Medical Devices: PEI's biocompatibility and sterilisation resistance make it suitable for medical devices like surgical instruments and medical device housings.
  • Food Processing Equipment: Its chemical resistance and high temperature tolerance make it ideal for food processing equipment.
Main manufacturer and trade names

SABIC: Ultem™ PEI, Siltem™ polyetherimide(PEI)-siloxane copolymer, Extem™ amorphous PI

Economic Aspects

PEI is a high-performance polymer, and its cost is generally higher than that of more common plastics. However, its exceptional properties often justify the higher cost, especially in demanding applications where performance is critical.
In conclusion, Polyetherimide (PEI) is a versatile high-performance polymer with excellent thermal, mechanical, and electrical properties. Its wide range of applications, coupled with its superior performance, makes it a valuable material in various industries.

Polyamide-Imide (PAI): An amorphous high-performance polymer which can be still melt processed

Polyamide-Imide (PAI) is an extremely strong, rigid and wear-resistant high performance polymer with use temperature form -200°C till up to 260°C.  Additionally, PAI can keep its mechanical properties over the whole use temperature range and is not melting when reaching the glass transition temperatures. Reason is a post curing process after processing turning the material into a thermoset-like structure. Polyamide-imide was developed by DuPont in the mid-1950s and in 1973, chemical company Amoco commercialized PAI as Torlon® to the market. Nowadays, the newly formed chemical company Syensqo, which routes back to Ernest Solvay and the Solvay company, produces and market this high performance polymer. 

Chemistry and Production Process

Polyamide-imide (PAI) is a high-performance polymer that combines the properties of polyamides (nylons) and polyimides. It is synthesized through a multi-step process involving the reaction of diamines with dianhydrides. The resulting polymer chains have alternating amide and imide groups, providing a unique combination of properties.

Main Properties

PAI exhibits a remarkable set of properties:
  • High Temperature Resistance: With a glass-transition temperature (Tg) of 275°C, PAI can withstand continuous use at temperatures up to 260°C and short-term exposure to even higher temperatures.
  • Excellent Mechanical Properties: It offers high tensile strength, flexural modulus, and impact resistance.
  • Chemical Resistance: PAI is resistant to a wide range of chemicals, including acids, bases, and solvents.
  • Good Electrical Properties: It has low dielectric constant and dissipation factor, making it suitable for electronic applications.
  • High compressive strength: PAI has a compressive strength which is double that of PEEK when unfiled. Compared to PEI it is about 40% higher.  
  • Extreme low wear and friction: PAI has a dynamic friction coefficient around 0.4; by adding additives such as graphite, it can be lowered to 0.3.
Figure 2: Wear during dry running of PAI vs PI and PTFE.

  • Flame Retardancy: PAI is inherently flame-retardant, reducing the risk of fire.
  • Dimensional Stability: It exhibits excellent dimensional stability, maintaining its shape even at high temperatures. It has a low thermal expansion, even with reinforcements (low CLTE values). 
  • Moisture uptake: PAI absorbs water up to 3.5%, however with a controlled curing process, water can be removed and extreme dimension stable parts in injection moulding with only 1% shrinkage.
Processing Methods

Due to its high melting temperature, PAI is typically processed using specialized techniques:
  • Injection Moulding: High-temperature injection moulding machines are required to process PAI.
  • Extrusion: PAI can be extruded into films, sheets, and profiles.
  • Compression Moulding: This technique is suitable for complex shapes and parts with a diameter larger than 25 mm. 
  • Machining: PAI can be machined for creating prototype parts or precision finished parts.
Applications

PAI's exceptional properties make it suitable for a wide range of applications:
  • Aerospace: Components like engine parts, hydraulic systems, and structural elements.
  • Automotive: High-temperature components such as engine covers, turbocharger housings, and under-hood components.
  • Electronics: Printed circuit boards, connectors, and electronic packaging.
  • Industrial Machinery: Bearings, gears, and other high-performance components.
  • Medical Devices: Sterilizable components and peristaltic pump rollers and bushings for prosthetics (long life due to low wear).
Trade Names and Economic Aspects
  • Syensqo (former Solvay): Torlon PAI
The cost of PAI is higher than that of many other engineering plastics due to its complex manufacturing process and high-performance properties. However, its long-term durability and reliability often offset the initial cost.

Polyamide-imide (PAI) is a versatile high-performance polymer that offers a unique combination of properties. Its excellent thermal, mechanical, and chemical resistance make it a valuable material for demanding applications across various industries.

Polyimides (PI): A Versatile Polymer

Introduction

Polyimides (PIs) are a class of high-performance polymers renowned for their exceptional thermal and chemical resistance, mechanical strength, and electrical insulation properties. PIs show a wide range of use temperatures, from cryogenic up to 400°C and the mechanical properties remain the same in this range. PIs combine low thermal expansion, high wear resistance, and low creeping with high purity and low off-gassing. Their unique combination of properties makes them indispensable in a wide range of applications, from aerospace and electronics to automotive and medical industries.

Chemistry and Production Process
  • Chemistry: PIs are synthesized through a two-step process involving the reaction of a dianhydride with a diamine. This reaction, known as polycondensation, results in the formation of a polyamic acid, an intermediate product. The polyamic acid is then subjected to thermal or chemical imidization to form the final polyimide.
  • Production Process:
1. Monomer Synthesis: High-purity dianhydrides and diamines are synthesized through various chemical processes.
2. Polymerization: The monomers are reacted in a suitable solvent to form a polyamic acid solution.
3. Imidization: The polyamic acid solution is converted into polyimide through thermal curing or chemical imidization. Thermal curing involves heating the solution to drive off water and form the imide rings. Chemical imidization uses a dehydrating agent to accelerate the process.
4. Processing: The polyimide can be processed into various forms, such as films, fibers, coatings, and composites, depending on the desired application.

Main Properties
  • Excellent Thermal Stability: PIs exhibit outstanding thermal stability, with heat deflection temperatures above 300°C and decomposition temperatures above 400°C. No softening and glass transition temperature can be noticed. SHort term use temperatures are up to 500°C. PI behaves like a thermoset with a linear property profile over the whole temperature range. 
  • Chemical Resistance: They are resistant to a wide range of chemicals, however they can be attacked by strong acids, and bases. PIs are hygroscopic and are not resistant towards hydrolysis. 
  • Mechanical Strength: PIs possess high tensile strength, flexural strength, and impact resistance.
  • Electrical Insulation: They are excellent electrical insulators with low dielectric constants and high dielectric strength.
  • Flame Retardancy: Many PIs are inherently flame-retardant.
Processing Methods
  • Solution Processing: Polyimide solutions can be cast into films, coated onto substrates, or spun into fibers.
  • Press-sintering: is used for making higher amounts of parts; otherwise cutting the part out of semi-finished shapes is done. 
  • Melt processing: thermoplastic Polyimides (TPIs) are injection moldable and extrusion prossable PIs. The major two commercially available are Ultem PEI (PI based on bisphenol A bisether-4-diphthalic anhy-dride [BEPA]) and Aurum TPI (PI based on Pyromellitic dianhydride [PMDA]). Aurum TPI has a Tg of 245°C. 
  • Copper enamel coating: Polyesterimides (PEsI) are used for wire enamel with excellent thermal properties. These kinds of  wires are widely used for compressors, washing machine motors, explosion-proof motors, dry transformers, and electric tools.
  • Additive Manufacturing: PIs are being explored for 3D printing applications, enabling the fabrication of intricate components.
Applications
  • Electronics: PIs are used in flexible printed circuit boards, high-temperature wire insulation, and semiconductor packaging (combination of high dielectric strength with low dissipation factors at various frequencies makes it a excellent insulation material)
  • Aerospace: They are employed in aircraft components, such as engine seals, heat shields, and structural reinforcements.
  • Automotive: PIs are used in engine components, electrical connectors, and thermal insulation.
  • Medical Devices: They are used in medical devices, catheters, and drug delivery systems.
  • Other Applications: PIs find applications in various industries, including energy storage, filtration, and protective coatings.

Trade Names and Economic Aspects
  • DuPont: Vespel® S, SP, SCP, and Kapton®
  • Mitsui: Aurum® TPI
The global polyimide market is growing steadily, driven by increasing demand from electronics, aerospace, and automotive industries. However, the high cost of raw materials and complex manufacturing processes can limit the widespread adoption of PIs.
In conclusion, polyimides are a versatile class of high-performance polymers with a wide range of applications. Their unique combination of properties, including exceptional thermal and chemical resistance, mechanical strength, and electrical insulation, makes them indispensable in many industries.

Polybenzimidazole (PBI) - the ultra high performance plastic which was developed in cooperation with NASA

Polybenzimidazole (PBI) is a high-performance polymer known for its exceptional thermal stability, chemical resistance, and mechanical properties. Its unique structure, consisting of a repeating benzimidazole unit, imparts these remarkable characteristics. In the 1950s Dr. Carl Shipp Marvel, often referred to by the nickname "Speed", developed PBI and in cooperation with NASA created a lightweight, high heat, low friction, high chemical and radiation resistant polymer which can be used in space and aircraft applications. Nowadays the application field of  PBI is much broader and it is used in electric & electronic appliances too. Its unique structure, consisting of a repeating benzimidazole unit, imparts these remarkable characteristics. PBI has a glass transition point of 427°C and its high purity makes it ideal for cable insulation powder coatings, friction parts and housings.

Chemistry and Production

PBI is synthesized through a condensation polymerization reaction between a diamine, typically 3,3′-diaminobenzidine, and a dicarboxylic acid, such as terephthalic acid or isophthalic acid. The reaction involves the formation of amide bonds between the amine and carboxylic acid groups, leading to the formation of the PBI polymer chain.

The production process of PBI typically involves the following steps:
1. Monomer Preparation: The diamine and dicarboxylic acid monomers are purified to remove impurities that could affect the polymerization reaction.
2. Polymerization: The purified monomers are combined under controlled conditions, such as temperature, pressure, and solvent, to initiate the polymerization reaction.
3. Polymer Isolation: The resulting PBI polymer is isolated from the reaction mixture through techniques like filtration or precipitation.
4. Purification: The polymer is further purified to remove any residual monomers or byproducts.
5. Processing: The PBI polymer is processed into various forms, such as fibers, films, or composites, depending on the desired application.

Properties of PBI

PBI exhibits a range of properties that make it suitable for demanding applications:
  • Thermal Stability: PBI possesses excellent thermal stability with a glass transition temperature of 427°C, capable of withstanding temperatures up to 500°C without significant degradation. This property is attributed to the aromatic nature of the benzimidazole unit and the strong intermolecular forces between polymer chains. Figure 3 shows an overview of the PBI and PBI blends as well as PBI compounds with their glass transition temperature.  
Figure 3: Overview Tg of PBI, PBI blends, and PBI compounds [2].

  • Chemical Resistance: PBI is highly resistant to a variety of chemicals, including acids, bases, and solvents. This makes it ideal for applications in corrosive environments and applications where high temperatures and aggressive chemicals are combined present.
  • Mechanical Properties: PBI offers good mechanical properties, such as tensile strength, modulus, and toughness. Its mechanical performance can be further enhanced through reinforcement with fibers or other materials.
  • Wear resistance: PBI has low friction properties with a coefficient of friction of 0.4. The wear of PBI is low too.  The PBI grade Celazole TL-60 is a very good wear grade material, reaching a PV of 225,000 psi-ft/min at 200 fpm. 
  • Flame Resistance: PBI is inherently flame-resistant and can be used in applications where fire safety is a critical concern.
  • Barrier Properties: PBI can serve as an effective barrier to gases and vapors, making it useful in applications such as filtration and gas separation.
Processing Methods

PBI can be processed using various methods, depending on the desired form and properties:
  • Solution Processing: PBI can be dissolved in suitable solvents and processed into films, coatings, or fibers through techniques like casting, spinning, or printing.
  • Melt Processing: Although PBI has a high melting point, it can be processed using melt-spinning or melt-extrusion techniques under specific conditions. Also blending PBI with PEEK and PEKK enables processing in injection moulding and extrusion. 
  • Composite Processing: PBI can be combined with other materials to form composites, such as carbon fiber-reinforced PBI, which offer enhanced mechanical properties and thermal stability.
  • Compression moulding: can be used to make semi-finished shapes such as rods, films, sheets, and tubes. 
Applications of PBI
PBI's unique combination of properties makes it suitable for a wide range of applications, including:
  • High-Temperature Applications: PBI is used in components for aerospace isolations, aircraft engines, industrial furnaces, and heat exchangers due to its exceptional thermal stability.
  • Chemical Processing:  PBI is used in chemical processing equipment, such as filters, gaskets, and valves, due to its chemical resistance.
  • Protective Clothing: PBI is used in protective clothing for firefighters, industrial workers, and military personnel due to its flame resistance and thermal protection.
  • Gas Separation: PBI membranes are used in gas separation processes to selectively separate different gases.
  • Fuel Cells: PBI is used as a polymer electrolyte membrane in fuel cells, enabling efficient energy conversion.
Trade Names and Economic Aspects
There is only one major company producing the polymer PBI and offering it under various trade names, including:
  • PBI Polymer: Celazole(R)
  • PBI Advanced Materials (PBi-am; SATO Group): 7000 series
The market for PBI is relatively small compared to other polymers, but it is expected to grow due to increasing demand in niche applications. The economic aspects of PBI production and processing are influenced by factors such as the cost of raw materials, energy consumption, and market demand.

Conclusion
PBI is a high-performance polymer with exceptional properties that make it suitable for demanding applications. Its thermal stability, chemical resistance, and mechanical properties have led to its use in various industries, including aerospace, chemical processing, and protective equipment. As the demand for high-performance materials continues to grow, PBI is expected to play an increasingly important role in various technological advancements.

In the upcoming Part 2C we will discuss the Polyether high performance polymers such as PPE, PAEK, PEEK, and PEKK.

Thanks for reading & #findoutaboutplastics

Greetings, 
Literature: 
[1] https://pbipolymer.com/wp-content/uploads/2016/05/Polymer-Protects-Firefighters-Military-Civilians.pdf
[2] https://www.pbi-am.com/en/base-polymers/pbi
[3] Dynamic Mechanical Analysis of High Temperature Polymers, Ning Tian, Aixi Zhou, The University of North Carolina
[4] https://pbipolymer.com/wp-content/uploads/2021/07/Dynamic-Mechanical-Analysis-High-Temperature-Polymers.pdf
[5] https://pbipolymer.com/wp-content/uploads/2016/05/High_PV_Wear_Study_of_Six_High_Performance_Polymers.pdf
[6] https://www.pbi-am.com/en/base-polymers/pbi
[7] https://www.sabic.com/en/products/specialties/ultem-resin-family-of-high-heat-solutions/ultem-resin
[8] https://www.3dnatives.com/en/ultem-030820204/#!
[9] https://www.ensingerplastics.com/en/thermoplastic-materials/torlon-pai-polyamid-imide
[10] https://www.researchgate.net/publication/329955339_Thermoplastic_Polyimide_TPI
[11] https://pmc.ncbi.nlm.nih.gov/articles/PMC7240679/
[12] https://www.sciencedirect.com/science/article/abs/pii/S001191642400211X#:~:text=Nanofiltration%20(OSN).-,Abstract,temperatures%2C%20and%20low%20fuel%20crossover.

Wednesday, 6 November 2024

Design Properties for Engineers: Dynamic Mechanical Analysis (DMA) of Ultra Performance Polymers (PBI and PBI blends)

Hello and welcome to a new post on design properties for engineers. In today’s post we discuss the storage modulus E’ measured by DMA of the ultra performance polymer Polybenzimidazole (PBI). Check out my other post on DMA of high performance polymers here. DMA is an essential tool for polymer material selection, allowing you to immediately capture the mechanical behaviour over a wide temperature range. 

What is Polybenzimidazole (PBI)?

PBI is the ultra high performance plastic which was developed in cooperation with NASA to have a lightweight, high heat, low friction, high chemical and radiation resistant polymer which can be used in space and aircraft applications. Nowadays the application field of  PBI is much broader and it is used in electric & electronic appliances too. Its unique structure, consisting of a repeating benzimidazole unit, imparts these remarkable characteristics. PBI has a glass transition point of 427°C and its high purity makes it ideal for cable insulation powder coatings, friction parts and housings. 

Storage Modulus E’ of PBI and PBI-blends

Figure 1 shows the storage modulus vs. temperature behaviour of PBI, PBI-PEEK blend, PAI, and PEI. They all show a significant drop in modulus in the glass transition region, expect of PBI. Before reaching the Tg, the neat PBI polymer still has a storage modulus of 3 GPa, where else the other presented polymers have already reached the zero level at this temperature. Blending PBI with PEEK makes it easier for melt processing and still up to 200°C a high level of modulus can be achieved. Among the amorphous high performance polymers, PAI has with 275 °C the highest glass transition temperature. A continuous use temperature of 260°C is feasible. PAI is melt processable in an injection moulding machine and needs an annealing step after moulding. 

Figure 1: Storage modulus E' of PBI and PBI blends [1]

Literature:

Sunday, 8 September 2024

High Performance Thermoplastic Selection - Polysulfides (Polyphenylene sulfide - PPS), Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR) [Part 2A]

Hello and welcome to the second part of our High Performance Thermoplastics selection blog series. The second part will focus on the introduction of high performance polymers, their chemistry and production processes, their main properties, their processing methods, and last but not least, applications.

Here you can jump to Part 1.

There are six major high performance thermoplastics families (“the magnificent six”) which we will discuss: 

-Part 2A: Polysulfides (Polyphenylene sulfide - PPS), Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR)

-Part 2B: Imide-Based Polymers (PEI, PAI, PESI, TPI, PI) and Polybenzimidazoles (PBI, PBI+PEEK, PBI+PEKK)

-Part 2C: Polyether (PPE, PAEK, PEEK, PEKK)

-Part 2D: Liquid Crystal Polymers (LCP)

-Part 2E: Semi- and Fully Aromatic Polyamides (PARA, PPA, Aramid)

-Part 2F: Polyhalogenolefins (PTFE, PCTFE, FEP, PVDF, ECTFE)

All thermoplastics can be visualized by using the performance pyramid, as shown in Figure 1. Based on production volumes, performance, and price, thermoplastics can be categorized as commodity plastics such as Polyolefins, engineering plastics such as Polyamide, and high performance polymers. Polysulfides (PPS), Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR) are highlighted since they will be discussed in this post.

Figure 1: Plastics Performance Pyramid highlighting PPS, Polysulfones, and PAR. 

Polysulfides (Polyphenylene sulfide - PPS), Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR)

The first major family we discuss is the Polysulfide family which contains Polyphenylene sulfide (PPS), followed by Polysulfones (PSU, PESU, PPSU), and Polyarylates (PAR). Polyphenylene ether (PPE) can be added to this family too, however I placed it in the family of Polyethers together with Polyetheretherketone (PEEK). 

Polyphenylene sulfide (PPS) - The polymer that thinks it’s metal…

Everyone who had already a part made out of PPS in his hand and let it drop will immediately recognize its metal-like sound. Thus, sometimes PPS is referred to as the “polymer that thinks it’s metal”. 

Chemistry and Production

PPS is a semi-crystalline polymer and its backbone consists of aromatic rings (phenylene groups) linked by sulfide bridges. This unique structure grants PPS its remarkable properties. The production process typically involves step-growth polymerization, where para-dichlorobenzene reacts with sodium sulfide under specific conditions in a solvent like N-methylpyrrolidone (NMP). However, numerous modifications and post-treatments can be employed to create specific PPS grades with tailored properties. There are two main routes making PPS and depending which route was taken, a so-called cured PPS (“flash PPS”, referring to the flash evaporation of water and solvent at the end of the two-step process; first step: sodium hydroxide reacts with solvent N-Methyl-2-pyrrolidone (NMP); step two: hydrogen sulfide gas introduced and a suspension is the result; curing by air is needed to increase the molecular weight; it leads to chain elongation and branching; typical MW before curing: 18,000 – 22,000 and after: 45,000) or linear PPS (“quench PPS”, where the reaction takes place in a solvent and it is continuous without having to remove water; "quench" or "quenching" = process of rapidly heating and mixing the slurry from the reactor with a quench medium, usually water and/or steam, leading to polymerization determination). The flash process has a higher yield efficiency (>92 %), good operational stability with better quality control. The quench process results in higher MW directly ( MW ~50,000) and lower yield efficiency (~88%).

Cured (“branched”) PPS has a dark brown color and in the beginning, linear PPS grades showed superior toughness, less off-gasing, lower flash appearance, and improved weldline strength. Parts ade out of cured PPS show an improved dimensional stability and creep performance. However, over time and with production improvements, differences were minimized.  

Well-known trade names for PPS include Ryton® (Syensqo), Torelina® (Toray), Fortron® (Celanese), Durafide® (Polyplastics), Xytron® (Envalior) and DIC PPS (DIC).

Properties of PPS

  • High-temperature performance: PPS boasts a melting point around 280°C (536°F) and can withstand continuous use (UL 746B) at temperatures exceeding 200°C (424°F). This makes it ideal for applications that encounter extreme heat.
  • Chemical resistance: PPS exhibits exceptional resistance to a wide range of chemicals, including strong acids, bases, and solvents. This allows it to function in harsh chemical environments. Concentrated nitric acid is one of the few chemicals which can dissolve PPS, apart from that there are no other chemicals which can dissolve PPS at a temperature below 200°C. 
  • Dimensional stability: PPS maintains its shape remarkably well at elevated temperatures, minimizing warping or shrinkage. For medium sized parts, 0.1% of its given dimension can be held and for large parts, 0.2% of the set dimension can be held.
  • Flame retardant: PPS is inherently flame retardant and self-extinguishing, making it a safe choice for applications requiring fire resistance. It can achieve the UL94 V0 at 0.75 mm and has a limiting oxygen index (LOI) which is estimated according to ISO 4589, of 45%.
  • Creep performance (long-term properties): PPS exhibits minimal changes in strain (creep) and stress relaxation under constant force or strain, respectively. It could be demonstrated that branched PPS compounds offer superior creep and stress relaxation resistance compared to super tough and linear PPS, highlighting differences in visco-flexural characteristics.
  • Electrical insulator: The non-polar structure of PPS makes it a good electrical insulator. 
  • Excellent flow properties: allowing to fill thin wall thicknesses. Amount of crystallization is around 50%. 

Table 1 summarizes selected mechanical properties of non reinforced PPS, cured PPS, and linear PPS moulding compounds. Often questions around the part marking code for highly filled PPS compounds arise. According to ISO 11469, the 65 wt% PPS compound R-7-120NA has following part marking code, which is in line with the VDA 260 too: >PPS-(GF+MD)65<.

Table 1: Selected mechanical properties of non reinforced PPS, cured PPS, and linear PPS moulding compounds [1].

Processing Methods

PPS can be processed using various techniques:

  • Injection Moulding: This is the most common method for shaping PPS into complex parts. Mould temperatures of minimum 135°C are needed to have a proper crystallization of the polymer. 
  • Extrusion: PPS can be extruded into sheets, rods, tubes, and pipes for diverse applications.
  • Machining:  PPS exhibits good machinability, allowing for the creation of precise components.
  • Coating: PPS powders can be used to coat metal sureafce such as kitchen pans. 

Applications of PPS

Due to its exceptional properties, PPS finds applications in a variety of industries:

  • Automotive:  PPS is used for pump components, engine parts close to the combustion engine, and electrical connectors due to its heat and chemical resistance. Also for e-mobility, PPS plays a key role, especially for high temperature electronics. Currently, a typical internal combustion engine (ICE) has around 700 grams of PPS polymer on board. New numbers form Asia reveal that there will be 3 to 4 kg of PPS in electric vehicles (EVs) and hybrid electric vehicles (HEVs).
  • Chemical Processing: PPS is ideal for pipes, valves, and pump housings due to its excellent chemical resistance.
  • Electrical & Electronics: PPS is a valuable material for connectors, circuit boards, and other electrical components because of its electrical insulating properties.
  • Aerospace: PPS finds use in aircraft components due to its lightweight nature and high-temperature performance.

Economic Aspects

PPS is a high-performance polymer, and its production costs are typically higher than those of some commodity plastics. However, PPS prices are still much lower compared to other high performance polymers such as PEEK. PPS and its exceptional properties often translate into longer lifespans, reduced maintenance needs, and improved performance, justifying the initial investment.

PPS stands out as a versatile and high-performance thermoplastic. Its unique combination of properties makes it a valuable material for demanding applications across various industries. As polymer engineering continues to evolve, PPS is certain to remain a key player for years to come.


Polysulfones (PSU, PESU, PPSU) - Take me to the moon

Polysulfones (PSFs) are an amorphous class of high-performance thermoplastics renowned for their exceptional properties, including heat resistance, chemical resistance, and dimensional stability. These attributes make them ideal for applications requiring materials that can withstand harsh conditions and maintain their integrity over time. Polysulfone was used as an external sun protection helmet visor for the Apollo 11 crew which landed on the moon on  July 20th 1969. 

Chemistry and Production

The chemical structure of polysulfones is characterized by a repeating ether sulfone unit (-O-SO2-). This unique structure contributes to the material's excellent properties.

Polysulfones are typically produced through a nucleophilic aromatic substitution reaction between bisphenol A and a dichlorosulfone. The reaction is carried out in a polar aprotic solvent, such as dimethyl sulfoxide (DMSO), in the presence of a base.

Main Properties

  • Heat resistance: Polysulfones have a glass transition between 190°C (374 °F) for PSU and 220°C (428 °F) for PESU and PPSU, leading to a  high heat deflection temperature, making them suitable for applications in hot environments.
  • Chemical resistance: They are resistant to a wide range of chemicals, including acids, bases, and solvents.
  • Dimensional stability: Polysulfones exhibit excellent dimensional stability, maintaining their shape and size even under varying conditions.
  • Flame retardancy: Many polysulfone grades are inherently flame-retardant and fulfil the UL94 V0.
  • Hydrolytic stability: They are resistant to hydrolysis, making them suitable for applications in contact with water. PSU and PPSU polymers exhibit excellent resistance to hydrolysis, remaining stable under high-temperature steam and water exposure. This characteristic makes them suitable for medical instruments requiring repeated autoclaving. For example, PSU performs well even after 100 autoclave cycles at 134°C. PPSU on the other hand, maintains its original physical properties like rigidity and ductility up to 1000 cycles at the same temperature.
  • Biocompatibility: There are polysulfone (PSU) and polyphenylene sulfone (PPSU) grades which have been developed for usage in medical devices that require long-term biocompatibility. For example, there are PSU and PPSU grades such as Syensqo's Eviva PSU and Veriva PPSU grades which are biocompatible polymers developed for long-term medical implants. They meet regulatory standards for devices in contact with bodily tissue/fluids for 30+ days and are manufactured following ISO 13485 and cGMP guidelines. In addition, standard grades of polysulfone and PPSU are used in medical devices that are in contact with bodily fluids and tissue short-term, or less than 24 hours.

Differences between polysulfone (PSU), polyethersulfone (PESU) and polyphenylene sulfone (PPSU)

While all three materials - polysulfone (PSU), polyethersulfone (PESU), and polyphenylene sulfone (PPSU) - are high-performance thermoplastics with similar properties, there are some key differences between them.

  • Polysulfone (PSU): The repeating unit in PSU is a bisphenol A sulfone. PSU offers good heat resistance, chemical resistance, and dimensional stability.
  • Polyethersulfone (PESU): PESU has a repeating unit of bisphenol S ether sulfone. It exhibits excellent heat resistance, hydrolytic stability, and chemical resistance, making it suitable for applications in harsh environments.
  • Polyphenylene Sulfone (PPSU): PPSU has a repeating unit of biphenyl sulfone. It offers exceptional heat resistance, mechanical strength, and flame retardancy. It has the highest stress crack resistance and notched impact strength of all three types of Polysulfones. 

Table 2 compares the different properties of PSU, PESU, and PPSU to each other. 

Table 2: Comparison of the the different properties of PSU, PESU, and PPSU.

Processing Methods
Polysulfones can be processed using various methods, including:
  • Injection molding: This is the most common method for producing polysulfone parts.
  • Extrusion: Polysulfones can be extruded into sheets, films, and profiles.
  • Blow molding: This process is used to produce hollow objects from polysulfone.
  • Thermoforming: Polysulfones can be thermoformed into complex shapes.

Applications
  • PSU: Automotive components, electronics, medical devices, and food processing equipment.
  • PESU: Medical devices, electronics, water filtration, and chemical processing.
  • PPSU: Aerospace components, electronics, medical devices, and high-temperature applications.
Trade Names and Economic Aspects
There are a hand full of  major chemical companies which produce polysulfones, including:
  • BASF: Ultrason® E PESU; Ultrason® P PSU; Ultrason® S PPSU;
  • Syensqo: Udel® (PSU), Veradel® (PESU), Radel® (PPSU)
  • Sumitomo Chemical: Sumikaexcel® PESU
The market for polysulfones is expected to continue to grow due to their versatility and performance advantages. However, the high cost of polysulfones compared to other engineering thermoplastics can limit their use in some applications. For lower end applications it is competing against Polycarbonate (PC) and in the high-performance segment with Polyetherimide (PEI). 

Polysulfones are a valuable class of high performance thermoplastics with a wide range of applications. Their exceptional properties, including heat resistance, chemical resistance, and dimensional stability, make them ideal for demanding environments. As the demand for high-performance materials continues to grow, the use of polysulfones is expected to increase in the coming years.


Polyarylates (PARs) - UV protection with excellent retention of optical properties, combined with high temperature resistance

Polyarylates (PARs) is an aromatic polyester derived from aromatic dicarboxylic acids and bisphenols. They possess a combination of excellent properties, including high heat resistance, chemical resistance, and mechanical strength, making them suitable for a wide range of applications.

Chemistry and Production
The synthesis of polyarylates typically involves a condensation polymerization reaction between aromatic dicarboxylic acids and bisphenols. The most common monomers used are terephthalic acid (TPA) and bisphenol A (BPA) or bisphenol S (BPS). However, other monomers can be used to tailor the properties of the resulting polymer.

The reaction is typically carried out in a melt polymerization process, where the monomers are heated in the presence of a catalyst. The reaction proceeds by forming ester linkages between the carboxylic acid and phenolic groups. Based on the used monomers we can distingish between Type 1 and Type 2 PAR. 

Type 1 vs. Type 2 Polyarylates: A Key Distinction
Polyarylates can be broadly categorized into two types based on their chemical structure and properties: Type 1 and Type 2 (Table 3).

Type 1 Polyarylates
  • Structure: Typically composed of only aromatic hydroxycarboxylic acid. Most common Type 1 PAR is the Poly-4-hydroxybenzoate (PHB) which consists of aromatic rings linked by ester groups.
  • Properties: Known for their excellent heat resistance, dimensional stability, and chemical resistance. They often exhibit a balance of properties, making them suitable for a wide range of applications.

Type 2 Polyarylates
  • Structure: Typically composed of terephthalic acid (TPA) and bisphenol A (BPA) or other aromatic dicarboxylic acids or bisphenols, such as isophthalic acid or bisphenol S. Most common Type 2 is the Polybisphenol-A terephthalate (PBAT).
  • Properties: May exhibit enhanced properties in specific areas, such as higher toughness, lower water absorption, or improved flame retardancy. The choice of monomers can be tailored to meet specific application requirements.
Table 3: Structure and property comparison of Type 1 and Type 2 PAR. 


Main Properties
Polyarylates exhibit a number of desirable properties, including:
  • High heat resistance: They have excellent thermal stability, allowing them to be used in high-temperature applications. BPAT has a Tg of 196°C (384.8 F), allowing for a short term usage up to 170°C. The heat deflection temperature (1.8 MPa) of BPAT is 174°C (345.2 F) and 40°C higher compared to PC (Tg=148°C; HDT = 135°C). 
  • Chemical resistance: They are resistant to a wide range of chemicals, including acids, bases, and solvents. They are especially resistant towards oils and alcohols when blended with PET, still keeping their transparency. Resistance towards alkali, ketones, and aromatic hydrocarbons is slow.   Also, neat PAR resins are more sensitive to stress cracking. 
  • UV stability: The UV-stability of PARs is high, since UV radiation causes the formation of a protective layer which in turn serves as UV protection. PARs are able to prevent the passage of ultraviolet light at and below 350 nm and transmit almost 90% light at a wavelength of 400 nm or more. It could be shown in various 8,000-hour long-term tests that PAR, in contrast to PS and PC, retains its almost untarnished shine even under the influence of UV. 
    • Why is there such a high ultraviolet absorption capacity and high weathering durability? PAR absorbs UV energy and causes a so-called Fries rearrangement reaction. This reaction produces a benzophenone structure on the resin surface. As a consequence, PAR is able to block light of 400 nm or less. The tone of color (yellowing) changes of PAR too due to the Fries rearrangement.
  • Mechanical strength: They have good mechanical properties, including high tensile strength, flexural strength, and impact resistance. In general, they can be placed between Polycarbonate and Polysulfones. Strength and stiffness are better compared to PC. Impact strength is high at lower temperatures (-40°C), however not as high as with PC. Additionally, the elongation at break is not as good as that of PC.
  • Dimensional stability: They exhibit low shrinkage and excellent dimensional stability. PARs have excellent elastic recovery which makes them a suitable material for spring applications. 
  • Electrical properties: They have good electrical properties, such as high dielectric strength and low water absorption.
  • Optical properties: almost as transparent as Polycarbonate and PMMA. PARs have a slight yellow color and transmit almost 90% light.
  • Good for blending with other polymers: 
    • with PET and PETG, to decrease shrinkage and warpage of PET; 
    • with PC and PBT, in order to increase the thermal heat resistance.
    • with PC, PET and PETG, to integrate a permanent UV protection. 

Processing Methods
Polyarylates can be processed using various methods, including:
  • Injection moulding: This is the most common method for processing polyarylates, allowing for the production of complex parts. PARs have a high melt viscosity and processing is harder. As a result, flow enabler such as adding special groups or atoms, mineral filler/glass fiber reinforcement, and alloying with other polymers, resulting PAR/PET, PAR/PA, PAR/ PC is done. Since the structure of PAR is similar to PC, it can be processed by the same injection moulds. 
  • Extrusion: Polyarylates can be extruded into sheets, films, and profiles.
  • Thermoforming: This process involves heating a sheet of polyarylate and forming it into a desired shape.
  • Compression moulding: This method is suitable for producing large, thick-walled parts.

Applications
Polyarylates are used in a wide range of applications, including:
  • Automotive industry: Components such as engine covers, under-hood parts, and interior trim.
  • Electrical and electronics: Connectors, circuit boards, and housings.
  • Medical devices: Surgical instruments, implants, and diagnostic equipment.
  • Aerospace: Structural components and protective coatings.
  • Industrial equipment: Pump housings, valves, and pipes.
Trade Names and Economic Aspects
Following major chemical companies produce polyarylates under various trade names, including:
  • Unitika: U-Polymer®
  • Westlake Plastics: Ardel® (only semi-finished products)
The market for polyarylates is growing at an average of 3% p.a., driven by increasing demand in various industries. The high performance and versatility of polyarylates make them attractive to manufacturers seeking materials with superior properties.

Outlook to Part 2B
In Part 2B we continue with the detailed discussion of Imide-based polymers (PEI, PAI, PESI, TPI, PI) and Polybenzimidazoles (PBI, PBI+PEEK, PBI+PEKK).


Thank you for reading!
Greetings and #findoutaboutplastics
Herwig Juster
[3] https://www.celanese.com/products/fortron-polyphenylene-sulfide

[4] https://plastics-rubber.basf.com/global/de/performance_polymers/products/ultrason

[5] https://www.syensqo.com/en/brands/radel-ppsu

[6] https://www.unitika.co.jp/plastics/e/products/par/upolymer/

[7] Kaiser - Kunststoffchemie für Ingenieure

[8] https://www.mueller-ahlhorn.com/par-polyarylat-ein-polymer-mit-vielseitigen-eigenschaften/

[9] https://www.genesismedicalplastics.com/what-is-polysulfone/?no_cache=1725462936

[10] https://www.syensqo.com/en/chemical-categories/specialty-polymers/healthcare/implantable-devices

[11] https://m.ky-plastics.com/news/similar-to-pc-but-more-advanced-polymer-poly-49365791.html

[12] https://www.unitika.co.jp/plastics/e/products/par/unifiner/

[13] https://www.unitika.co.jp/plastics/e/products/par/upolymer/p-series/ps-01.html

[14] http://www.enexinternational.com/PPS_Presentation_for_Web.pdf

[15] https://patents.google.com/patent/WO2016099694A1/en

Monday, 4 March 2024

High Heat Plastics Selection: Liquid Crystal Polymers (LCP) - Decreasing Wall Thickness, Increasing Tensile Strength?

Hello and welcome to this blog post in which we discuss the high heat polymer Liquid Crystal Polymer (LCP) and its specific properties. In general, defining the part requirements can be seen as a common starting point in polymer material selection. However when selecting high heat plastics, short and long time temperature performance plays a key role too. Also, implementing design features such as thin wall part design is another drive of the usage of high performance polymers. However, what happens if the wall thickness of LCP parts is decreased. Will the tensile strength keeps constant or is there a different behaviour to be observed?

Introduction to Liquid Crystal Polymers

Based on their superiority in high heat solder resistance, high-temperature strength, dimensional stability, overall good chemical resistance, low flammability, and low water absorption, liquid crystalline polymers (LCPs) are widely employed in many types of electric and electronic parts (connectors). Since LCPs have an exceptionally low melt viscosity, they have better thin-wall fluidity and mouldability compared to any other engineering plastics. LCPs are currently utilized for the most highly precise applications, also where Surface Mounting Technology (SMT) is needed. Electric and electronic devices moulded using LCPs have grown in significance in recent years for the IT-related industries as well as many consumer markets. Recent developments of high heat LCPs include the usage as high-heat EV battery module insulation [2].

Not to be overlooked is the fact that every LCP has a unique chemical structure. This implies that although the term "liquid crystalline polymer" refers to the overall set of features, each manufacturer of LCP may have unique chemical structures and this is similar to polyamides. For example, PA6 and PA 4.6 show significantly differing thermal resistance, yet they both absorb more water than polyesters and have poorer dimension stability. While each polyamide has a unique chemical structure that determines its different thermal resistance, the amide-bonding group determines the increased water absorption property.

Looking into the literature [1] of polymer chemistry, we can distinguish between

-Type I LCP (HDT a 1.82 MPa > 260°C), 

-Type II LCP (HDT = 210-260°C), and

-Type III (HDT < 210°C). 

All three types contain a p-hydroxybenzoic group and are called  “thermotropic” LCP ( in contract to “lyotropic” LCP = liquid crystals can be seen in solvent as a solution). The crystals stay solid in the melt phase and can be modelled as matchsticks during the injection moulding filling process. Applying shear to the polymer will result in a very good alignment of the matchsticks.

Discovery of LCP - Friedrich Reinitzer and Otto Lehmann

In 1888, Friedrich Reinitzer, an Austrian chemist and botanist, observed unusual temperature-dependent behavior in cholesteryl benzoate. He noticed it melted into a hazy liquid at one temperature and then became clear at a higher temperature, exhibiting color changes upon cooling before solidifying. Puzzled by these two melting points, Reinitzer sent his findings and the material to German physicist Otto Lehmann. Lehmann used a heated microscope to further investigate and identified the hazy liquid as a new state of matter with crystalline properties, which he named a "liquid crystal." While this discovery by Reinitzer and Lehmann around the turn of the 20th century generated initial scientific interest and the identification of nearly 200 similar compounds, practical applications were not immediately apparent, leading to a decline in research focus.

Summarizing the key pros and cons of LCP:

Pros:

-High thermal resistance (up to 260 °C)

-Barrier properties (due to dense skin layer)

-Excellent soldering resistance for lead-free reflow soldering processes

-Solvent stability (except alkali & steam)

-Superior high flowability

-High flame retardancy (UL 94 V-0 @0.3 mm)

Cons:

-Strong anisotropy in moulded parts

-Lower weld line strength

Thermal properties: CUT vs. HDT of LCP 

The short term temperature resistance of engineering polymers can be improved by adding glass-fiber reinforcement, however the long term temperature resistance stays on a similar level. This is different with high heat plastics such as PEEK, PPS, LCP, Polyarylates (PAR), Polysulfones (PSU, PESU, PPSU), and Polyimides (PEI, PAI, PI). They combine a high short- and long term thermal resistance. Figure 1 compares the Continuous Use temperature (CUT) to the Heat Deflection Temperature (HDT; short term temperature resistance) of high performance and engineering polymers.  LCP has an excellent short- and long-term temperature stability.

Figure 1: Short-term (HDT 1.8 MPa) vs. long-term temperature resistance (CUT) of engineering and high performance polymers such as LCP, PEEK, and PPS.

What is the glass transition and melt temperature of LCP?

LCPs do not have a “glass transition” temperature in the classical way of definition (Alpha temperature transition enabling the movement of more than 40 C-atoms in backbone [3]). They have a liquid crystal temperature. Figure 2 shows the DMA curves of PESU (amorphous; Tg = 220°C), PEEK (semi-crystalline; Tg=143°C; Tm =334°C), and LCP (Tlc = 300-380°C). LCP does not have a glass transition temperature, nor a melting temperature. It has a liquid crystalline temperature where the crystals  remain solid, however the linkages between the solid crystals can move [1]. If you examine in detail the literature, a small transition temperature of LCP was found at 120°C. LCP can keep a high mechanical strength level up to 300 °C, outperforming PEEK and PESU. 

Figure 2: DMA of high performance polymers (PEEK, PESU, LCP) - LCP has a liquid crystalline transition area (300°C-380°C).

Wall thickness and tensile strength

Moving back to the question from the beginning of this post: what is the relationship between wall thickness and tensile strength of LCP? 

The skin layer's thickness of LCP is almost 200 μm and is a result of the strong orientation of the solid crystal elements (“matchsticks”). The ratio of the skin layer to the total thickness increases proportionately as the thickness decreases. The skin layer has strong mechanical properties since it is made up of highly aligned fibrous semi-crystals of stiff rod molecules. Because of this, LCP's strength will progressively rise as its thickness decreases. Figure 3 shows this relationship of a LCP, and comparing it to a PBT and PESU. This is a common and unique feature of LCP that isn't seen in traditional polymers. 

Figure 3: Tensile strength as a function of wall thickness of LCP, PESU, and PBT. 

Conclusions

Designing parts with high performance polymers such as LCP is not more difficult compared to engineering or commodity polymers. It is different and the dependency of mechanical properties as a function of wall thickness allows applications made out of LCP to be really thin and still fulfill stringent requirements such as temperature, flame retardancy, and strength.

More on high performance polymers can be found here and here.

Thanks for reading and #findoutaboutplastics

Greetings,

Herwig Juster 

Literature: 

[1] https://www.sumitomo-chem.co.jp/sep/english/products/pdf/lcp_users_manual_v31_e.pdf

[2] https://www.solvay.com/en/press-release/solvay-introduces-new-polymer-high-heat-ev-battery-module-insulation

[3] https://www.findoutaboutplastics.com/2018/12/dynamic-mechanical-analysis-dma-as.html

[4] https://www.azom.com/article.aspx?ArticleID=13872

[5] https://www.ptonline.com/articles/tracing-the-history-of-polymeric-materials-part-27-lcp

[6] Zeus- Introduction to LCP