Sinking Concrete Repair Crystal Lake

Sinking Concrete Repair Crystal Lake

Concrete Repair Estimate Crystal Lake

Whether it's a residential driveway or a commercial sidewalk, the Smart Lift system is changing the game, one successful lift at a time. You've probably noticed the difference when you're out for a walk or driving through the neighborhood. It shows a commitment to maintenance and pride in ownership that resonates with current and prospective residents alike. Have you ever pondered the impact of sinking concrete on your property's value and safety? Learn more about Sinking Concrete Repair Crystal Lake here To combat the pervasive issue of sinking concrete, Acme Concrete has developed a cutting-edge solution that's both efficient and long-lasting.
You don't have to worry about lengthy construction times or being inconvenienced for days on end. The precision of the Smart Lift system means less mess and less time spent on repairs, letting you get back to your daily life faster. I'm thoroughly impressed.'Lisa G., another satisfied customer, says, 'I was skeptical about how much of a difference it would make, but the results speak for themselves. This Smart Lift system isn't just a repair method; it's a preventive measure against future settling.
As you dig deeper, you'll discover that the Smart Lift system represents just the beginning of a surge in high-tech solutions coming your way. They'll set a date to begin work, always aiming to minimize disruption to your daily routine. Imagine concrete raising methods that not only repair but also enhance the longevity and durability of your structures. You've probably noticed how sidewalks and driveways can quickly go from smooth surfaces to tripping hazards. Learn more about Acme Concrete Raising & Repair here.
Acme Concrete's pricing structure takes into account the severity of the concrete damage, the square footage of the area needing repair, and any special considerations unique to your project.

Concrete Raising Reviews

  1. Subgrade Stabilization
  2. Cracked Driveway Repair
  3. Concrete Crack Repair
  4. Slab Foundation Repair
  5. Affordable Slab Lifting Crystal Lake
  6. Concrete Raising Reviews
  7. Sidewalk Trip Hazard Fix
  8. Concrete Leveling
  9. Concrete Settling
  10. Subgrade Stabilization
  11. Cracked Driveway Repair
  12. Concrete Crack Repair
  13. Slab Foundation Repair
  14. Affordable Slab Lifting Crystal Lake
  15. Concrete Raising Reviews
  16. Sidewalk Trip Hazard Fix
  17. Concrete Leveling
  18. Concrete Settling
  19. Subgrade Stabilization
If you're a homeowner in Crystal Lake, there's a beacon of hope on the horizon. Furthermore, the durability of the repairs is outstanding. It's a question you're likely pondering as you consider the benefits of their innovative repair solutions.

The journey through these revelations will leave you questioning the status quo and curious about the innovative solutions that are setting new standards in concrete repair. You'll be amazed at how quickly the foam works - the lifting process often completes in minutes. This not only reduces the visual impact but also maintains the structural integrity of the slab far better than the heavier, more invasive mudjacking process. So, it's not just smart; it's a strategic move for any business looking to optimize their operations and presentation.

By sealing cracks and ensuring proper drainage, you're taking proactive steps to preserve your walkway's structure and aesthetic appeal. This minimizes disruption to your daily life and gets your property back to normal quickly. Elevating the charm of Crystal Lake, safer walkways contribute to the community's overall beauty and appeal.

Concrete Repair Estimate Crystal Lake

  • Concrete Settling
  • Affordable Slab Lifting Crystal Lake
  • Concrete Raising Reviews
  • Sidewalk Trip Hazard Fix
  • Concrete Leveling
  • Concrete Settling
  • Affordable Slab Lifting Crystal Lake
  • Concrete Raising Reviews
  • Sidewalk Trip Hazard Fix
  • Concrete Leveling
  • Concrete Settling
  • Affordable Slab Lifting Crystal Lake
  • Concrete Raising Reviews
  • Sidewalk Trip Hazard Fix
  • Concrete Leveling
  • Concrete Settling
  • Affordable Slab Lifting Crystal Lake
  • Concrete Raising Reviews
  • Sidewalk Trip Hazard Fix
  • Concrete Leveling


Acme's specialized techniques, including sealing and proper drainage implementation, ensure that water, ice, and chemicals don't penetrate and deteriorate the concrete. Navigating the rough waters of home maintenance, you've likely encountered the challenge of sinking concrete, a problem as pervasive as it is pesky.

Slab Leveling Solutions

  1. Concrete Leveling
  2. Concrete Settling
  3. Concrete Leveling
  4. Concrete Settling
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  20. Concrete Settling
Cracked Driveway Repair For Crystal Lake residents, this means you can maintain your property's safety and aesthetics without compromising on sustainability.

Early detection can mean simpler, more cost-effective repairs. They'll come to your location, inspect the condition of your concrete, and discuss what you're hoping to achieve. After our team worked their magic, he was amazed at the seamless finish. 'I wish I'd called Acme sooner.

Citations and other links

Porch Concrete Leveling Crystal Lake

Let's work together to make your home safer and more appealing. This can exacerbate the initial problem, leading to a vicious cycle of repairs. In most cases, the entire process is completed in just a few hours, minimizing disruption to your daily routine. Many homeowners face the challenge of aging concrete, which can significantly impact the safety and aesthetics of their property. Crystal Lake's landscape has been dramatically revitalized thanks to the innovative application of polyurethane concrete raising.

Cost-effectiveness is another key advantage. In most cases, the repair is completed within a few hours, and you can walk or drive on the surface almost immediately after. With Acme Concrete, you're investing in a safer tomorrow, today. It's designed to be long-lasting and doesn't degrade into pollutants over time.

By opting for concrete raising, you're preventing old concrete from ending up in landfills, which is a huge win for the environment. Slab Leveling Solutions This means you'll save money in the long run, avoiding the costs associated with repeated services. When you choose Acme Concrete's solution, you're not just fixing uneven slabs; you're also revitalizing the look of your sidewalks, driveways, and patios. For homeowners in Crystal Lake, opting for concrete raising can significantly enhance your property's appeal and safety.

The polyurethane foam used in this process is lighter on the environment, requiring less material and reducing the overall carbon footprint of your repair project. Moreover, the Smart Lift system enhances the safety and aesthetics of your property, potentially increasing its value. The system uses a specially formulated material that's both strong and eco-friendly, avoiding the need for chemical-laden solutions or the excessive waste often associated with older methods. Knowing Crystal Lake's climate and ground conditions allows them to tailor their services perfectly, ensuring the best possible outcome.

Porch Concrete Leveling Crystal Lake
Concrete Leveling and Lifting Crystal Lake

Concrete Leveling and Lifting Crystal Lake

From the environmental impact to the long-term costs and durability of the methods used, there's a significant shift happening in the industry. Marie from Oakwood Estates couldn't believe her eyes when she saw her driveway after Acme's team was done. 'It's like they waved a magic wand! Firstly, the weight of the slurry mixture used in mudjacking can lead to further settling over time. They're looking for cracks, sinking, and uneven surfaces that can pose safety risks or diminish the value of your home.

This traditional technique involves pumping a mixture of water, soil, and cement beneath settled concrete to raise it. It's a smart move, aligning with a more sustainable approach to home maintenance. The precision and control during this process mean there's less mess and disruption compared to traditional methods.

Our team brings years of expertise and a proven track record to the table, ensuring that your home stands on solid ground. First off, they use a unique polyurethane injection method that lifts and stabilizes sinking concrete slabs. Pool decks shouldn't be overlooked either.

At Acme Concrete, we've fine-tuned our repair process to ensure you get the most efficient and effective service possible. However, when you look at the long-term financial impact, the picture changes.

Concrete Settling

  1. Cracked Driveway Repair
  2. Concrete Crack Repair
  3. Slab Foundation Repair
  4. Affordable Slab Lifting Crystal Lake
  5. Concrete Raising Reviews
  6. Sidewalk Trip Hazard Fix
  7. Concrete Leveling
  8. Concrete Settling
  9. Cracked Driveway Repair
  10. Concrete Crack Repair
  11. Slab Foundation Repair
  12. Affordable Slab Lifting Crystal Lake
  13. Concrete Raising Reviews
  14. Sidewalk Trip Hazard Fix
  15. Concrete Leveling
  16. Concrete Settling
  17. Cracked Driveway Repair
  18. Concrete Crack Repair
  19. Slab Foundation Repair
  20. Affordable Slab Lifting Crystal Lake
But how exactly do they achieve these remarkable transformations, and what makes their method stand out from traditional repair techniques?

Concrete Raising Estimate Crystal Lake

It's also incredibly strong, able to support substantial weights shortly after application. Lastly, mudjacking doesn't address the underlying issue of soil erosion or compaction. Choosing Acme Concrete means you're opting for a durable, long-lasting solution to sunken concrete. Look for signs of uneven surfaces, cracks, or sinking areas that could benefit from Acme Concrete's innovative repair solutions. By addressing uneven surfaces, you're reducing the risk of trips and falls, making your property safer for everyone.

Here's how it works: First, small holes are drilled into the sunken concrete. Plus, it's less invasive and more cost-effective than traditional repair methods, like slab replacement. Enter Acme Concrete, a beacon in the murky waters of repair solutions, steering homeowners and business owners alike toward solid ground. Plus, it doesn't disturb the soil as much, preserving the existing ecological balance.

Choosing a method that aligns with sustainability not only benefits your property but also contributes to broader environmental well-being.

Slab Leveling Solutions

  1. Concrete Settling
  2. Concrete Raising Reviews
  3. Sidewalk Trip Hazard Fix
  4. Concrete Leveling
  5. Concrete Settling
  6. Concrete Raising Reviews
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  8. Concrete Leveling
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  10. Concrete Raising Reviews
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  14. Concrete Raising Reviews
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  16. Concrete Leveling
  17. Concrete Settling
  18. Concrete Raising Reviews
  19. Sidewalk Trip Hazard Fix
  20. Concrete Leveling
You won't have to worry about seasonal checks or frequent repairs. Having highlighted the benefits of Acme's Smart Lift System for businesses, it's crucial to examine how it stacks up against traditional concrete repair methods.

Cracked Driveway Repair

  • Void Filling
  • Concrete Raising Cost Estimate
  • Concrete Lifting
  • Foam Injection Contractors
  • Garage Apron Repair
  • Concrete Slab Stabilization
  • Sidewalk Trip Hazard Fix
  • Slabjacking
  • Illinois Concrete Repair
  • Soil Stabilization
  • Concrete Floor Repair
  • Concrete Raising Contractors
  • Pool Deck Repair
  • Concrete Support Injection
  • Affordable Slab Lifting Crystal Lake
  • Crystal Lake IL Contractors
Understanding the process of polyurethane raising begins with drilling small, strategically placed holes into the sunken concrete.

You've likely noticed how uneven sidewalks and driveways can pose serious tripping risks. The foam cures quickly, meaning the area can be used almost immediately after the procedure.

Subgrade Stabilization

  • Sunken Walkway Fix
  • Concrete Sinking
  • Soil Erosion Under Slab
  • Leveling Concrete Slabs
  • Concrete Leveling Companies
  • Sidewalk Leveling Experts
  • Concrete Void Filling
  • Sustainable Concrete Repair
  • Cracked Driveway Repair
  • Concrete Floor Leveling Contractors
  • Slab Foundation Repair
  • Water-Resistant Foam Injection
  • Sunken Step Repair
  • Concrete Joint Sealing
  • Curb Lifting
By fixing these issues, you're directly improving the safety of your community, making it a more welcoming place for walking, playing, and other outdoor activities.

Cracked Driveway Repair

  1. Concrete Repair Estimate Crystal Lake
  2. Slab Leveling Solutions
  3. Concrete Floor Repair
  4. Concrete Expansion Joint Repair
  5. Subgrade Stabilization
  6. Cracked Driveway Repair
  7. Concrete Crack Repair
  8. Slab Foundation Repair
  9. Affordable Slab Lifting Crystal Lake
  10. Concrete Raising Reviews
  11. Sidewalk Trip Hazard Fix
  12. Concrete Leveling
  13. Concrete Settling
  14. Slab Leveling Solutions
  15. Concrete Floor Repair
  16. Concrete Expansion Joint Repair
  17. Subgrade Stabilization
  18. Cracked Driveway Repair
You're likely aware that replacing concrete can be both expensive and disruptive.

Concrete Raising Estimate Crystal Lake
Concrete Leveling for Homes Crystal Lake
Concrete Leveling for Homes Crystal Lake

They're constantly exposed to water and chemicals, contributing to deterioration. Concrete Floor Repair You're not just saving money on the initial service; you're also minimizing disruption to your home or business. Typically, smaller repair jobs might cost less, while larger areas requiring extensive work will see a higher price tag. They've developed an innovative approach that not only saves you money but also extends the lifespan of your concrete, effectively turning a potentially costly endeavor into a savvy investment.
Initially, we'll conduct a thorough assessment of the affected area to identify the underlying issues causing the concrete to sink or settle. With Acme Concrete Raising & Repair, you're not just getting a service provider; you're gaining a partner who cares about the safety and aesthetics of your walkways. Plus, by maintaining the integrity of your concrete, you're ultimately preserving the value of your home.
Maintenance is virtually non-existent. The answer isn't as straightforward as you might hope, but it's certainly within reach. Read more about Sinking Concrete Repair Crystal Lake here Lastly, let's look at a commercial sidewalk outside a busy storefront.
Photos and a brief description of the problem areas will help them understand your needs better. This method conserves resources by utilizing the existing concrete, meaning there's no need for the production of new concrete, which in turn reduces carbon emissions associated with manufacturing and transporting new materials. Ignoring them can result in more extensive, and expensive, damage down the line.

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Choosing this smart solution not only addresses your immediate concrete issues but also invests in the longevity and aesthetics of your property. This means you're likely to need additional repairs sooner than you'd with more modern methods. Their team of skilled professionals takes pride in their work, paying close attention to detail to ensure every project meets their high standards. This allows them to assess the situation firsthand and propose the most effective solution. As you consider your own concrete issues, remember the success stories from your neighbors.
That's our proven process-designed to give you peace of mind and lasting results. What really sets them apart is their commitment to customer satisfaction. Another standout feature is its minimal environmental impact. This method lifts and levels your existing concrete, eliminating tripping hazards and improving drainage, which protects the walkway from future damage.
Understanding our concrete raising process from start to finish will give you peace of mind as we work on your property. You'll enhance the safety and appearance of your property while avoiding the higher costs associated with neglecting these issues. In recent years, Acme Concrete has integrated cutting-edge technological innovations to further enhance the effectiveness of its repair system.

Slab Foundation Repair

    Concrete Leveling This means you're looking at repairs that last longer and stand up to environmental challenges more effectively.
    You might wonder how it works. You'll be kept in the loop from start to finish, ensuring your needs are met and your questions are answered. The environmental footprint of concrete raising methods is a critical consideration for both consumers and professionals in the industry. Beyond enhancing safety, the advanced repair system dramatically improves the aesthetic appeal of your concrete surfaces.

    Explore Sinking Concrete Repair Crystal Lake here Concrete Crack Repair

    Void Filling

    1. Concrete Settling
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    3. Concrete Leveling
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    Basement Floor Leveling Crystal Lake
    Polyurethane synthesis: the urethane groups −NH−(C=O)−O− link the molecular units, resulting in a polymer consisting of an alternating chain of two monomers.
    A kitchen sponge made of polyurethane foam

    Polyurethane (/ËŒpÉ’liˈjÊŠÉ™rəˌθeɪn, -jʊəˈrÉ›θeɪn/;[1] often abbreviated PUR and PU) is a class of polymers composed of organic units joined by carbamate (urethane) links. In contrast to other common polymers such as polyethylene and polystyrene, polyurethane does not refer to a single type of polymer but a group of polymers. Unlike polyethylene and polystyrene, polyurethanes can be produced from a wide range of starting materials, resulting in various polymers within the same group. This chemical variety produces polyurethanes with different chemical structures leading to many different applications. These include rigid and flexible foams, and coatings, adhesives, electrical potting compounds, and fibers such as spandex and polyurethane laminate (PUL). Foams are the largest application accounting for 67% of all polyurethane produced in 2016.[2]

    A polyurethane is typically produced by reacting a polymeric isocyanate with a polyol.[3] Since a polyurethane contains two types of monomers, which polymerize one after the other, they are classed as alternating copolymers. Both the isocyanates and polyols used to make a polyurethane contain two or more functional groups per molecule.

    Global production in 2019 was 25 million metric tonnes,[4] accounting for about 6% of all polymers produced in that year.

    History

    [edit]
    Otto Bayer in 1952 demonstrating his creation

    Otto Bayer and his coworkers at IG Farben in Leverkusen, Germany, first made polyurethanes in 1937.[5][6] The new polymers had some advantages over existing plastics that were made by polymerizing olefins or by polycondensation, and were not covered by patents obtained by Wallace Carothers on polyesters.[7] Early work focused on the production of fibers and flexible foams and PUs were applied on a limited scale as aircraft coating during World War II.[7] Polyisocyanates became commercially available in 1952, and production of flexible polyurethane foam began in 1954 by combining toluene diisocyanate (TDI) and polyester polyols. These materials were also used to produce rigid foams, gum rubber, and elastomers. Linear fibers were produced from hexamethylene diisocyanate (HDI) and 1,4-Butanediol (BDO).

    DuPont introduced polyethers, specifically poly(tetramethylene ether) glycol, in 1956. BASF and Dow Chemical introduced polyalkylene glycols in 1957. Polyether polyols were cheaper, easier to handle and more water-resistant than polyester polyols. Union Carbide and Mobay, a U.S. Monsanto/Bayer joint venture, also began making polyurethane chemicals.[7] In 1960 more than 45,000 metric tons of flexible polyurethane foams were produced. The availability of chlorofluoroalkane blowing agents, inexpensive polyether polyols, and methylene diphenyl diisocyanate (MDI) allowed polyurethane rigid foams to be used as high-performance insulation materials. In 1967, urethane-modified polyisocyanurate rigid foams were introduced, offering even better thermal stability and flammability resistance. During the 1960s, automotive interior safety components, such as instrument and door panels, were produced by back-filling thermoplastic skins with semi-rigid foam.

    In 1969, Bayer exhibited an all-plastic car in Düsseldorf, Germany. Parts of this car, such as the fascia and body panels, were manufactured using a new process called reaction injection molding (RIM), in which the reactants were mixed and then injected into a mold. The addition of fillers, such as milled glass, mica, and processed mineral fibers, gave rise to reinforced RIM (RRIM), which provided improvements in flexural modulus (stiffness), reduction in coefficient of thermal expansion and better thermal stability. This technology was used to make the first plastic-body automobile in the United States, the Pontiac Fiero, in 1983. Further increases in stiffness were obtained by incorporating pre-placed glass mats into the RIM mold cavity, also known broadly as resin injection molding, or structural RIM.

    Starting in the early 1980s, water-blown microcellular flexible foams were used to mold gaskets for automotive panels and air-filter seals, replacing PVC polymers. Polyurethane foams are used in many automotive applications including seating, head and arm rests, and headliners.

    Polyurethane foam (including foam rubber) is sometimes made using small amounts of blowing agents to give less dense foam, better cushioning/energy absorption or thermal insulation. In the early 1990s, because of their impact on ozone depletion, the Montreal Protocol restricted the use of many chlorine-containing blowing agents, such as trichlorofluoromethane (CFC-11). By the late 1990s, blowing agents such as carbon dioxide, pentane, 1,1,1,2-tetrafluoroethane (HFC-134a) and 1,1,1,3,3-pentafluoropropane (HFC-245fa) were widely used in North America and the EU, although chlorinated blowing agents remained in use in many developing countries. Later, HFC-134a was also banned due to high ODP and GWP readings, and HFC-141B was introduced in early 2000s as an alternate blowing agent in developing nations.[8]

    Chemistry

    [edit]

    Polyurethanes are produced by reacting diisocyanates with polyols,[9][10][11][12][13][14] often in the presence of a catalyst, or upon exposure to ultraviolet radiation.[15] Common catalysts include tertiary amines, such as DABCO, DMDEE, or metallic soaps, such as dibutyltin dilaurate. The stoichiometry of the starting materials must be carefully controlled as excess isocyanate can trimerise, leading to the formation of rigid polyisocyanurates. The polymer usually has a highly crosslinked molecular structure, resulting in a thermosetting material which does not melt on heating; although some thermoplastic polyurethanes are also produced.

     
    Carbon dioxide gas and urea links formed by reacting water and isocyanate

    The most common application of polyurethane is as solid foams, which requires the presence of a gas, or blowing agent, during the polymerization step. This is commonly achieved by adding small amounts of water, which reacts with isocyanates to form CO2 gas and an amine, via an unstable carbamic acid group. The amine produced can also react with isocyanates to form urea groups, and as such the polymer will contain both these and urethane linkers. The urea is not very soluble in the reaction mixture and tends to form separate "hard segment" phases consisting mostly of polyurea. The concentration and organization of these polyurea phases can have a significant impact on the properties of the foam.[16]

    The type of foam produced can be controlled by regulating the amount of blowing agent and also by the addition of various surfactants which change the rheology of the polymerising mixture. Foams can be either "closed-cell", where most of the original bubbles or cells remain intact, or "open-cell", where the bubbles have broken but the edges of the bubbles are stiff enough to retain their shape, in extreme cases reticulated foams can be formed. Open-cell foams feel soft and allow air to flow through, so they are comfortable when used in seat cushions or mattresses. Closed-cell foams are used as rigid thermal insulation. High-density microcellular foams can be formed without the addition of blowing agents by mechanically frothing the polyol prior to use. These are tough elastomeric materials used in covering car steering wheels or shoe soles.

    The properties of a polyurethane are greatly influenced by the types of isocyanates and polyols used to make it. Long, flexible segments, contributed by the polyol, give soft, elastic polymer. High amounts of crosslinking give tough or rigid polymers. Long chains and low crosslinking give a polymer that is very stretchy, short chains with many crosslinks produce a hard polymer while long chains and intermediate crosslinking give a polymer useful for making foam. The choices available for the isocyanates and polyols, in addition to other additives and processing conditions allow polyurethanes to have the very wide range of properties that make them such widely used polymers.

    Raw materials

    [edit]

    The main ingredients to make a polyurethane are di- and tri-isocyanates and polyols. Other materials are added to aid processing the polymer or to modify the properties of the polymer. PU foam formulation sometimes have water added too.

    Isocyanates

    [edit]

    Isocyanates used to make polyurethane have two or more isocyanate groups on each molecule. The most commonly used isocyanates are the aromatic diisocyanates, toluene diisocyanate (TDI) and methylene diphenyl diisocyanate, (MDI). These aromatic isocyanates are more reactive than aliphatic isocyanates.

    TDI and MDI are generally less expensive and more reactive than other isocyanates. Industrial grade TDI and MDI are mixtures of isomers and MDI often contains polymeric materials. They are used to make flexible foam (for example slabstock foam for mattresses or molded foams for car seats),[17] rigid foam (for example insulating foam in refrigerators) elastomers (shoe soles, for example), and so on. The isocyanates may be modified by partially reacting them with polyols or introducing some other materials to reduce volatility (and hence toxicity) of the isocyanates, decrease their freezing points to make handling easier or to improve the properties of the final polymers.

    MDI isomers and polymer
    MDI isomers and polymer

    Aliphatic and cycloaliphatic isocyanates are used in smaller quantities, most often in coatings and other applications where color and transparency are important since polyurethanes made with aromatic isocyanates tend to darken on exposure to light.[page needed][18] The most important aliphatic and cycloaliphatic isocyanates are 1,6-hexamethylene diisocyanate (HDI), 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethyl-cyclohexane (isophorone diisocyanate, IPDI), and 4,4′-diisocyanato dicyclohexylmethane (H12MDI or hydrogenated MDI). Other more specialized isocyanates include Tetramethylxylylene diisocyanate (TMXDI).

    Polyols

    [edit]

    Polyols are polymers in their own right and have on average two or more hydroxyl groups per molecule. They can be converted to polyether polyols by co-polymerizing ethylene oxide and propylene oxide with a suitable polyol precursor.[19] Polyester polyols are made by the polycondensation of multifunctional carboxylic acids and polyhydroxyl compounds. They can be further classified according to their end use. Higher molecular weight polyols (molecular weights from 2,000 to 10,000) are used to make more flexible polyurethanes while lower molecular weight polyols make more rigid products.

    Polyols for flexible applications use low functionality initiators such as dipropylene glycol (f = 2), glycerine (f = 3), or a sorbitol/water solution (f = 2.75).[20] Polyols for rigid applications use higher functionality initiators such as sucrose (f = 8), sorbitol (f = 6), toluenediamine (f = 4), and Mannich bases (f = 4). Propylene oxide and/or ethylene oxide is added to the initiators until the desired molecular weight is achieved. The order of addition and the amounts of each oxide affect many polyol properties, such as compatibility, water-solubility, and reactivity. Polyols made with only propylene oxide are terminated with secondary hydroxyl groups and are less reactive than polyols capped with ethylene oxide, which contain primary hydroxyl groups. Incorporating carbon dioxide into the polyol structure is being researched by multiple companies.

    Graft polyols (also called filled polyols or polymer polyols) contain finely dispersed styrene–acrylonitrile, acrylonitrile, or polyurea (PHD) polymer solids chemically grafted to a high molecular weight polyether backbone. They are used to increase the load-bearing properties of low-density high-resiliency (HR) foam, as well as add toughness to microcellular foams and cast elastomers. Initiators such as ethylenediamine and triethanolamine are used to make low molecular weight rigid foam polyols that have built-in catalytic activity due to the presence of nitrogen atoms in the backbone. A special class of polyether polyols, poly(tetramethylene ether) glycols, which are made by polymerizing tetrahydrofuran, are used in high performance coating, wetting and elastomer applications.

    Conventional polyester polyols are based on virgin raw materials and are manufactured by the direct polyesterification of high-purity diacids and glycols, such as adipic acid and 1,4-butanediol. Polyester polyols are usually more expensive and more viscous than polyether polyols, but they make polyurethanes with better solvent, abrasion, and cut resistance. Other polyester polyols are based on reclaimed raw materials. They are manufactured by transesterification (glycolysis) of recycled poly(ethyleneterephthalate) (PET) or dimethylterephthalate (DMT) distillation bottoms with glycols such as diethylene glycol. These low molecular weight, aromatic polyester polyols are used in rigid foam, and bring low cost and excellent flammability characteristics to polyisocyanurate (PIR) boardstock and polyurethane spray foam insulation.

    Specialty polyols include polycarbonate polyols, polycaprolactone polyols, polybutadiene polyols, and polysulfide polyols. The materials are used in elastomer, sealant, and adhesive applications that require superior weatherability, and resistance to chemical and environmental attack. Natural oil polyols derived from castor oil and other vegetable oils are used to make elastomers, flexible bunstock, and flexible molded foam.

    Co-polymerizing chlorotrifluoroethylene or tetrafluoroethylene with vinyl ethers containing hydroxyalkyl vinyl ether produces fluorinated (FEVE) polyols. Two-component fluorinated polyurethanes prepared by reacting FEVE fluorinated polyols with polyisocyanate have been used to make ambient cure paints and coatings. Since fluorinated polyurethanes contain a high percentage of fluorine–carbon bonds, which are the strongest bonds among all chemical bonds, fluorinated polyurethanes exhibit resistance to UV, acids, alkali, salts, chemicals, solvents, weathering, corrosion, fungi and microbial attack. These have been used for high performance coatings and paints.[21]

    Phosphorus-containing polyols are available that become chemically bonded to the polyurethane matrix for the use as flame retardants. This covalent linkage prevents migration and leaching of the organophosphorus compound.

    Bio-derived materials

    [edit]

    Interest in sustainable "green" products raised interest in polyols derived from vegetable oils,[22][23][24] fatty acids,[25] lignin, sorbitol,[26] etc. These are mostly contributing to polyol part. There are attempts made to prepare isocyanate part using bio-derived material. However, as far as commercialization is concern, polyol part is more targeted being easy and required in more quantity than isocyanate part. Various oils used in the preparation polyols for polyurethanes include soybean oil, cottonseed oil, neem seed oil, algae oil,[27][28] and castor oil. Vegetable oils are functionalized in various ways and modified to polyetheramides, polyethers, alkyds, etc. Renewable sources used to prepare polyols may be fatty acids or dimer fatty acids.[29] Some biobased and isocyanate-free polyurethanes exploit the reaction between polyamines and cyclic carbonates to produce polyhydroxyurethanes.[30]

    Chain extenders and cross linkers

    [edit]

    Chain extenders (f = 2) and cross linkers (f ≥ 3) are low molecular weight hydroxyl and amine terminated compounds that play an important role in the polymer morphology of polyurethane fibers, elastomers, adhesives, and certain integral skin and microcellular foams.

    The elastomeric properties of these materials are derived from the phase separation of the hard and soft copolymer segments of the polymer, such that the urethane hard segment domains serve as cross-links between the amorphous polyether (or polyester) soft segment domains. This phase separation occurs because the mainly nonpolar, low melting soft segments are incompatible with the polar, high melting hard segments. The soft segments, which are formed from high molecular weight polyols, are mobile and are normally present in coiled formation, while the hard segments, which are formed from the isocyanate and chain extenders, are stiff and immobile. As the hard segments are covalently coupled to the soft segments, they inhibit plastic flow of the polymer chains, thus creating elastomeric resiliency. Upon mechanical deformation, a portion of the soft segments are stressed by uncoiling, and the hard segments become aligned in the stress direction. This reorientation of the hard segments and consequent powerful hydrogen bonding contributes to high tensile strength, elongation, and tear resistance values.[12][31][32][33][34] The choice of chain extender also determines flexural, heat, and chemical resistance properties.

    The most important chain extenders are ethylene glycol, 1,4-butanediol (1,4-BDO or BDO), 1,6-hexanediol, cyclohexane dimethanol and hydroquinone bis(2-hydroxyethyl) ether (HQEE). All of these glycols form polyurethanes that phase separate well and form well defined hard segment domains, and are melt processable. They are all suitable for thermoplastic polyurethanes with the exception of ethylene glycol, since its derived bis-phenyl urethane undergoes unfavorable degradation at high hard segment levels.[10] Diethanolamine and triethanolamine are used in flex molded foams to build firmness and add catalytic activity. Diethyltoluenediamine is used extensively in RIM, and in polyurethane and polyurea elastomer formulations.

    Table of chain extenders and cross linkers[35]
    Compound type Molecule Mol.
    mass
    Density
    (g/cm3)
    Melting
    pt (°C)
    Boiling
    pt (°C)
    Hydroxyl compounds – difunctional molecules Ethylene glycol 62.1 1.110 −13.4 197.4
    Diethylene glycol 106.1 1.111 −8.7 245.5
    Triethylene glycol 150.2 1.120 −7.2 287.8
    Tetraethylene glycol 194.2 1.123 −9.4 325.6
    Propylene glycol 76.1 1.032 Supercools 187.4
    Dipropylene glycol 134.2 1.022 Supercools 232.2
    Tripropylene glycol 192.3 1.110 Supercools 265.1
    1,3-Propanediol 76.1 1.060 −28 210
    1,3-Butanediol 92.1 1.005 207.5
    1,4-Butanediol 92.1 1.017 20.1 235
    Neopentyl glycol 104.2 130 206
    1,6-Hexanediol 118.2 1.017 43 250
    1,4-Cyclohexanedimethanol
    HQEE
    Ethanolamine 61.1 1.018 10.3 170
    Diethanolamine 105.1 1.097 28 271
    Methyldiethanolamine 119.1 1.043 −21 242
    Phenyldiethanolamine 181.2 58 228
    Hydroxyl compounds – trifunctional molecules Glycerol 92.1 1.261 18.0 290
    Trimethylolpropane
    1,2,6-Hexanetriol
    Triethanolamine 149.2 1.124 21
    Hydroxyl compounds – tetrafunctional molecules Pentaerythritol 136.2 260.5
    N,N,N′,N′-Tetrakis
    (2-hydroxypropyl)
    ethylenediamine
    Amine compounds – difunctional molecules Diethyltoluenediamine 178.3 1.022 308
    Dimethylthiotoluenediamine 214.0 1.208

    Catalysts

    [edit]

    Polyurethane catalysts can be classified into two broad categories, basic and acidic amine. Tertiary amine catalysts function by enhancing the nucleophilicity of the diol component. Alkyl tin carboxylates, oxides and mercaptides oxides function as mild Lewis acids in accelerating the formation of polyurethane. As bases, traditional amine catalysts include triethylenediamine (TEDA, also called DABCO, 1,4-diazabicyclo[2.2.2]octane), dimethylcyclohexylamine (DMCHA), dimethylethanolamine (DMEA), Dimethylaminoethoxyethanol and bis-(2-dimethylaminoethyl)ether, a blowing catalyst also called A-99. A typical Lewis acidic catalyst is dibutyltin dilaurate. The process is highly sensitive to the nature of the catalyst and is also known to be autocatalytic.[36]

    Another class of catalysts was published in a study in May 2024. In this study, polyurethane synthesis was investigated in the presence of acid catalysts, namely dimethylphosphite (DMHP), methanesulfonic acid (MSA), and trifluoromethanesulfonic acid (TFMSA). The thermodynamic profile was examined and described in detail through computational tools, showing that TFMSA had the best catalytic properties. The study aimed to open the door to a new class of catalysts.[37]

    Factors affecting catalyst selection include balancing three reactions: urethane (polyol+isocyanate, or gel) formation, the urea (water+isocyanate, or "blow") formation, or the isocyanate trimerization reaction (e.g., using potassium acetate, to form isocyanurate rings). A variety of specialized catalysts have been developed.[38][39][40]

    Surfactants

    [edit]

    Surfactants are used to modify the characteristics of both foam and non-foam polyurethane polymers. They take the form of polydimethylsiloxane-polyoxyalkylene block copolymers, silicone oils, nonylphenol ethoxylates, and other organic compounds. In foams, they are used to emulsify the liquid components, regulate cell size, and stabilize the cell structure to prevent collapse and sub-surface voids.[41] In non-foam applications they are used as air release and antifoaming agents, as wetting agents, and are used to eliminate surface defects such as pin holes, orange peel, and sink marks.

    Production

    [edit]

    Polyurethanes are produced by mixing two or more liquid streams. The polyol stream contains catalysts, surfactants, blowing agents (when making polyurethane foam insulation) and so on. The two components are referred to as a polyurethane system, or simply a system. The isocyanate is commonly referred to in North America as the 'A-side' or just the 'iso'. The blend of polyols and other additives is commonly referred to as the 'B-side' or as the 'poly'.[citation needed] This mixture might also be called a 'resin' or 'resin blend'. In Europe the meanings for 'A-side' and 'B-side' are reversed.[citation needed] Resin blend additives may include chain extenders, cross linkers, surfactants, flame retardants, blowing agents, pigments, and fillers. Polyurethane can be made in a variety of densities and hardnesses by varying the isocyanate, polyol or additives.

    Health and safety

    [edit]

    Fully reacted polyurethane polymer is chemically inert.[42] No exposure limits have been established in the U.S. by OSHA (Occupational Safety and Health Administration) or ACGIH (American Conference of Governmental Industrial Hygienists). It is not regulated by OSHA for carcinogenicity.

    Open-flame test. Top: untreated polyurethane foam burns vigorously. Bottom: with fire-retardant treatment.

    Polyurethanes are combustible.[43] Decomposition from fire can produce significant amounts of carbon monoxide and hydrogen cyanide, in addition to nitrogen oxides, isocyanates, and other toxic products.[44] Due to the flammability of the material, it has to be treated with flame retardants (at least in case of furniture), almost all of which are considered harmful.[45][46] California later issued Technical Bulletin 117 2013 which allowed most polyurethane foam to pass flammability tests without the use of flame retardants. Green Science Policy Institute states: "Although the new standard can be met without flame retardants, it does NOT ban their use. Consumers who wish to reduce household exposure to flame retardants can look for a TB117-2013 tag on furniture, and verify with retailers that products do not contain flame retardants."[47]

    Liquid resin blends and isocyanates may contain hazardous or regulated components. Isocyanates are known skin and respiratory sensitizers. Additionally, amines, glycols, and phosphate present in spray polyurethane foams present risks.[48]

    Exposure to chemicals that may be emitted during or after application of polyurethane spray foam (such as isocyanates) are harmful to human health and therefore special precautions are required during and after this process.[49]

    In the United States, additional health and safety information can be found through organizations such as the Polyurethane Manufacturers Association (PMA) and the Center for the Polyurethanes Industry (CPI), as well as from polyurethane system and raw material manufacturers. Regulatory information can be found in the Code of Federal Regulations Title 21 (Food and Drugs) and Title 40 (Protection of the Environment). In Europe, health and safety information is available from ISOPA,[50] the European Diisocyanate and Polyol Producers Association.

    Manufacturing

    [edit]

    The methods of manufacturing polyurethane finished goods range from small, hand pour piece-part operations to large, high-volume bunstock and boardstock production lines. Regardless of the end-product, the manufacturing principle is the same: to meter the liquid isocyanate and resin blend at a specified stoichiometric ratio, mix them together until a homogeneous blend is obtained, dispense the reacting liquid into a mold or on to a surface, wait until it cures, then demold the finished part.

    Dispensing equipment

    [edit]

    Although the capital outlay can be high, it is desirable to use a meter-mix or dispense unit for even low-volume production operations that require a steady output of finished parts. Dispense equipment consists of material holding (day) tanks, metering pumps, a mix head, and a control unit. Often, a conditioning or heater–chiller unit is added to control material temperature in order to improve mix efficiency, cure rate, and to reduce process variability. Choice of dispense equipment components depends on shot size, throughput, material characteristics such as viscosity and filler content, and process control. Material day tanks may be single to hundreds of gallons in size and may be supplied directly from drums, IBCs (intermediate bulk containers, such as caged IBC totes), or bulk storage tanks. They may incorporate level sensors, conditioning jackets, and mixers. Pumps can be sized to meter in single grams per second up to hundreds of pounds per minute. They can be rotary, gear, or piston pumps, or can be specially hardened lance pumps to meter liquids containing highly abrasive fillers such as chopped or hammer-milled glass fiber and wollastonite.[citation needed]

    The pumps can drive low-pressure (10 to 30 bar, 1 to 3 MPa) or high-pressure (125 to 250 bar, 12.5 to 25.0 MPa) dispense systems. Mix heads can be simple static mix tubes, rotary-element mixers, low-pressure dynamic mixers, or high-pressure hydraulically actuated direct impingement mixers. Control units may have basic on/off and dispense/stop switches, and analogue pressure and temperature gauges, or may be computer-controlled with flow meters to electronically calibrate mix ratio, digital temperature and level sensors, and a full suite of statistical process control software. Add-ons to dispense equipment include nucleation or gas injection units, and third or fourth stream capability for adding pigments or metering in supplemental additive packages.

    Tooling

    [edit]

    Distinct from pour-in-place, bun and boardstock, and coating applications, the production of piece parts requires tooling to contain and form the reacting liquid. The choice of mold-making material is dependent on the expected number of uses to end-of-life (EOL), molding pressure, flexibility, and heat transfer characteristics.

    RTV silicone is used for tooling that has an EOL in the thousands of parts. It is typically used for molding rigid foam parts, where the ability to stretch and peel the mold around undercuts is needed. The heat transfer characteristic of RTV silicone tooling is poor. High-performance, flexible polyurethane elastomers are also used in this way.

    Epoxy, metal-filled epoxy, and metal-coated epoxy is used for tooling that has an EOL in the tens of thousands of parts. It is typically used for molding flexible foam cushions and seating, integral skin and microcellular foam padding, and shallow-draft RIM bezels and fascia. The heat transfer characteristic of epoxy tooling is fair; the heat transfer characteristic of metal-filled and metal-coated epoxy is good. Copper tubing can be incorporated into the body of the tool, allowing hot water to circulate and heat the mold surface.

    Aluminum is used for tooling that has an EOL in the hundreds of thousands of parts. It is typically used for molding microcellular foam gasketing and cast elastomer parts, and is milled or extruded into shape.

    Mirror-finish stainless steel is used for tooling that imparts a glossy appearance to the finished part. The heat transfer characteristic of metal tooling is excellent.

    Finally, molded or milled polypropylene is used to create low-volume tooling for molded gasket applications. Instead of many expensive metal molds, low-cost plastic tooling can be formed from a single metal master, which also allows greater design flexibility. The heat transfer characteristic of polypropylene tooling is poor, which must be taken into consideration during the formulation process.

    Applications

    [edit]

    In 2007, the global consumption of polyurethane raw materials was above 12 million metric tons, and the average annual growth rate was about 5%.[51] Revenues generated with PUR on the global market are expected to rise to approximately US$75 billion by 2022.[52] As they are such an important class of materials, research is constantly taking place and papers published.[53]

    Degradation and environmental fate

    [edit]

    Effects of visible light

    [edit]
    Polyurethane foam made with an aromatic isocyanate, which has been exposed to UV light. Readily apparent is the discoloration that occurs over time.

    Polyurethanes, especially those made using aromatic isocyanates, contain chromophores that interact with light. This is of particular interest in the area of polyurethane coatings, where light stability is a critical factor and is the main reason that aliphatic isocyanates are used in making polyurethane coatings. When PU foam, which is made using aromatic isocyanates, is exposed to visible light, it discolors, turning from off-white to yellow to reddish brown. It has been generally accepted that apart from yellowing, visible light has little effect on foam properties.[54][55] This is especially the case if the yellowing happens on the outer portions of a large foam, as the deterioration of properties in the outer portion has little effect on the overall bulk properties of the foam itself.

    It has been reported that exposure to visible light can affect the variability of some physical property test results.[56]

    Higher-energy UV radiation promotes chemical reactions in foam, some of which are detrimental to the foam structure.[57]

    Hydrolysis and biodegradation

    [edit]

    Polyurethanes may degrade due to hydrolysis. This is a common problem with shoes left in a closet, and reacting with moisture in the air.[58]

    Microbial degradation of polyurethane is believed to be due to the action of esterase, urethanase, hydrolase and protease enzymes.[59] The process is slow as most microbes have difficulty moving beyond the surface of the polymer. Susceptibility to fungi is higher due to their release of extracellular enzymes, which are better able to permeate the polymer matrix. Two species of the Ecuadorian fungus Pestalotiopsis are capable of biodegrading polyurethane in aerobic and anaerobic conditions such as found at the bottom of landfills.[60][61] Degradation of polyurethane items at museums has been reported.[62] Polyester-type polyurethanes are more easily biodegraded by fungus than polyether-type.[63]

    See also

    [edit]
    • Botanol, a material with higher plant-based content
    • Passive fire protection
    • Penetrant (mechanical, electrical, or structural)
    • Polyaspartic
    • Polyurethane dispersion
    • Thermoplastic polyurethanes
    • Thermoset polymer matrix

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    [edit]
    • Center for the Polyurethanes Industry: information for EH&S issues related to polyurethanes developments
    • Polyurethane synthesis, Polymer Science Learning Center, University of Southern Mississippi
    • Polyurethane Foam Association: Industry information, educational materials and resources related to flexible polyurethane foam
    • PU Europe: European PU insulation industry association (formerly BING): European voice for the national trade associations representing the polyurethane insulation industry
    • ISOPA: European Diisocyanate & Polyol Producers Association: ISOPA represents the manufacturers in Europe of aromatic diisocyanates and polyols

     

    Polyurethane synthesis: the urethane groups −NH−(C=O)−O− link the molecular units, resulting in a polymer consisting of an alternating chain of two monomers.
    A kitchen sponge made of polyurethane foam

    Polyurethane (/ËŒpÉ’liˈjÊŠÉ™rəˌθeɪn, -jʊəˈrÉ›θeɪn/;[1] often abbreviated PUR and PU) is a class of polymers composed of organic units joined by carbamate (urethane) links. In contrast to other common polymers such as polyethylene and polystyrene, polyurethane does not refer to a single type of polymer but a group of polymers. Unlike polyethylene and polystyrene, polyurethanes can be produced from a wide range of starting materials, resulting in various polymers within the same group. This chemical variety produces polyurethanes with different chemical structures leading to many different applications. These include rigid and flexible foams, and coatings, adhesives, electrical potting compounds, and fibers such as spandex and polyurethane laminate (PUL). Foams are the largest application accounting for 67% of all polyurethane produced in 2016.[2]

    A polyurethane is typically produced by reacting a polymeric isocyanate with a polyol.[3] Since a polyurethane contains two types of monomers, which polymerize one after the other, they are classed as alternating copolymers. Both the isocyanates and polyols used to make a polyurethane contain two or more functional groups per molecule.

    Global production in 2019 was 25 million metric tonnes,[4] accounting for about 6% of all polymers produced in that year.

    History

    [edit]
    Otto Bayer in 1952 demonstrating his creation

    Otto Bayer and his coworkers at IG Farben in Leverkusen, Germany, first made polyurethanes in 1937.[5][6] The new polymers had some advantages over existing plastics that were made by polymerizing olefins or by polycondensation, and were not covered by patents obtained by Wallace Carothers on polyesters.[7] Early work focused on the production of fibers and flexible foams and PUs were applied on a limited scale as aircraft coating during World War II.[7] Polyisocyanates became commercially available in 1952, and production of flexible polyurethane foam began in 1954 by combining toluene diisocyanate (TDI) and polyester polyols. These materials were also used to produce rigid foams, gum rubber, and elastomers. Linear fibers were produced from hexamethylene diisocyanate (HDI) and 1,4-Butanediol (BDO).

    DuPont introduced polyethers, specifically poly(tetramethylene ether) glycol, in 1956. BASF and Dow Chemical introduced polyalkylene glycols in 1957. Polyether polyols were cheaper, easier to handle and more water-resistant than polyester polyols. Union Carbide and Mobay, a U.S. Monsanto/Bayer joint venture, also began making polyurethane chemicals.[7] In 1960 more than 45,000 metric tons of flexible polyurethane foams were produced. The availability of chlorofluoroalkane blowing agents, inexpensive polyether polyols, and methylene diphenyl diisocyanate (MDI) allowed polyurethane rigid foams to be used as high-performance insulation materials. In 1967, urethane-modified polyisocyanurate rigid foams were introduced, offering even better thermal stability and flammability resistance. During the 1960s, automotive interior safety components, such as instrument and door panels, were produced by back-filling thermoplastic skins with semi-rigid foam.

    In 1969, Bayer exhibited an all-plastic car in Düsseldorf, Germany. Parts of this car, such as the fascia and body panels, were manufactured using a new process called reaction injection molding (RIM), in which the reactants were mixed and then injected into a mold. The addition of fillers, such as milled glass, mica, and processed mineral fibers, gave rise to reinforced RIM (RRIM), which provided improvements in flexural modulus (stiffness), reduction in coefficient of thermal expansion and better thermal stability. This technology was used to make the first plastic-body automobile in the United States, the Pontiac Fiero, in 1983. Further increases in stiffness were obtained by incorporating pre-placed glass mats into the RIM mold cavity, also known broadly as resin injection molding, or structural RIM.

    Starting in the early 1980s, water-blown microcellular flexible foams were used to mold gaskets for automotive panels and air-filter seals, replacing PVC polymers. Polyurethane foams are used in many automotive applications including seating, head and arm rests, and headliners.

    Polyurethane foam (including foam rubber) is sometimes made using small amounts of blowing agents to give less dense foam, better cushioning/energy absorption or thermal insulation. In the early 1990s, because of their impact on ozone depletion, the Montreal Protocol restricted the use of many chlorine-containing blowing agents, such as trichlorofluoromethane (CFC-11). By the late 1990s, blowing agents such as carbon dioxide, pentane, 1,1,1,2-tetrafluoroethane (HFC-134a) and 1,1,1,3,3-pentafluoropropane (HFC-245fa) were widely used in North America and the EU, although chlorinated blowing agents remained in use in many developing countries. Later, HFC-134a was also banned due to high ODP and GWP readings, and HFC-141B was introduced in early 2000s as an alternate blowing agent in developing nations.[8]

    Chemistry

    [edit]

    Polyurethanes are produced by reacting diisocyanates with polyols,[9][10][11][12][13][14] often in the presence of a catalyst, or upon exposure to ultraviolet radiation.[15] Common catalysts include tertiary amines, such as DABCO, DMDEE, or metallic soaps, such as dibutyltin dilaurate. The stoichiometry of the starting materials must be carefully controlled as excess isocyanate can trimerise, leading to the formation of rigid polyisocyanurates. The polymer usually has a highly crosslinked molecular structure, resulting in a thermosetting material which does not melt on heating; although some thermoplastic polyurethanes are also produced.

     
    Carbon dioxide gas and urea links formed by reacting water and isocyanate

    The most common application of polyurethane is as solid foams, which requires the presence of a gas, or blowing agent, during the polymerization step. This is commonly achieved by adding small amounts of water, which reacts with isocyanates to form CO2 gas and an amine, via an unstable carbamic acid group. The amine produced can also react with isocyanates to form urea groups, and as such the polymer will contain both these and urethane linkers. The urea is not very soluble in the reaction mixture and tends to form separate "hard segment" phases consisting mostly of polyurea. The concentration and organization of these polyurea phases can have a significant impact on the properties of the foam.[16]

    The type of foam produced can be controlled by regulating the amount of blowing agent and also by the addition of various surfactants which change the rheology of the polymerising mixture. Foams can be either "closed-cell", where most of the original bubbles or cells remain intact, or "open-cell", where the bubbles have broken but the edges of the bubbles are stiff enough to retain their shape, in extreme cases reticulated foams can be formed. Open-cell foams feel soft and allow air to flow through, so they are comfortable when used in seat cushions or mattresses. Closed-cell foams are used as rigid thermal insulation. High-density microcellular foams can be formed without the addition of blowing agents by mechanically frothing the polyol prior to use. These are tough elastomeric materials used in covering car steering wheels or shoe soles.

    The properties of a polyurethane are greatly influenced by the types of isocyanates and polyols used to make it. Long, flexible segments, contributed by the polyol, give soft, elastic polymer. High amounts of crosslinking give tough or rigid polymers. Long chains and low crosslinking give a polymer that is very stretchy, short chains with many crosslinks produce a hard polymer while long chains and intermediate crosslinking give a polymer useful for making foam. The choices available for the isocyanates and polyols, in addition to other additives and processing conditions allow polyurethanes to have the very wide range of properties that make them such widely used polymers.

    Raw materials

    [edit]

    The main ingredients to make a polyurethane are di- and tri-isocyanates and polyols. Other materials are added to aid processing the polymer or to modify the properties of the polymer. PU foam formulation sometimes have water added too.

    Isocyanates

    [edit]

    Isocyanates used to make polyurethane have two or more isocyanate groups on each molecule. The most commonly used isocyanates are the aromatic diisocyanates, toluene diisocyanate (TDI) and methylene diphenyl diisocyanate, (MDI). These aromatic isocyanates are more reactive than aliphatic isocyanates.

    TDI and MDI are generally less expensive and more reactive than other isocyanates. Industrial grade TDI and MDI are mixtures of isomers and MDI often contains polymeric materials. They are used to make flexible foam (for example slabstock foam for mattresses or molded foams for car seats),[17] rigid foam (for example insulating foam in refrigerators) elastomers (shoe soles, for example), and so on. The isocyanates may be modified by partially reacting them with polyols or introducing some other materials to reduce volatility (and hence toxicity) of the isocyanates, decrease their freezing points to make handling easier or to improve the properties of the final polymers.

    MDI isomers and polymer
    MDI isomers and polymer

    Aliphatic and cycloaliphatic isocyanates are used in smaller quantities, most often in coatings and other applications where color and transparency are important since polyurethanes made with aromatic isocyanates tend to darken on exposure to light.[page needed][18] The most important aliphatic and cycloaliphatic isocyanates are 1,6-hexamethylene diisocyanate (HDI), 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethyl-cyclohexane (isophorone diisocyanate, IPDI), and 4,4′-diisocyanato dicyclohexylmethane (H12MDI or hydrogenated MDI). Other more specialized isocyanates include Tetramethylxylylene diisocyanate (TMXDI).

    Polyols

    [edit]

    Polyols are polymers in their own right and have on average two or more hydroxyl groups per molecule. They can be converted to polyether polyols by co-polymerizing ethylene oxide and propylene oxide with a suitable polyol precursor.[19] Polyester polyols are made by the polycondensation of multifunctional carboxylic acids and polyhydroxyl compounds. They can be further classified according to their end use. Higher molecular weight polyols (molecular weights from 2,000 to 10,000) are used to make more flexible polyurethanes while lower molecular weight polyols make more rigid products.

    Polyols for flexible applications use low functionality initiators such as dipropylene glycol (f = 2), glycerine (f = 3), or a sorbitol/water solution (f = 2.75).[20] Polyols for rigid applications use higher functionality initiators such as sucrose (f = 8), sorbitol (f = 6), toluenediamine (f = 4), and Mannich bases (f = 4). Propylene oxide and/or ethylene oxide is added to the initiators until the desired molecular weight is achieved. The order of addition and the amounts of each oxide affect many polyol properties, such as compatibility, water-solubility, and reactivity. Polyols made with only propylene oxide are terminated with secondary hydroxyl groups and are less reactive than polyols capped with ethylene oxide, which contain primary hydroxyl groups. Incorporating carbon dioxide into the polyol structure is being researched by multiple companies.

    Graft polyols (also called filled polyols or polymer polyols) contain finely dispersed styrene–acrylonitrile, acrylonitrile, or polyurea (PHD) polymer solids chemically grafted to a high molecular weight polyether backbone. They are used to increase the load-bearing properties of low-density high-resiliency (HR) foam, as well as add toughness to microcellular foams and cast elastomers. Initiators such as ethylenediamine and triethanolamine are used to make low molecular weight rigid foam polyols that have built-in catalytic activity due to the presence of nitrogen atoms in the backbone. A special class of polyether polyols, poly(tetramethylene ether) glycols, which are made by polymerizing tetrahydrofuran, are used in high performance coating, wetting and elastomer applications.

    Conventional polyester polyols are based on virgin raw materials and are manufactured by the direct polyesterification of high-purity diacids and glycols, such as adipic acid and 1,4-butanediol. Polyester polyols are usually more expensive and more viscous than polyether polyols, but they make polyurethanes with better solvent, abrasion, and cut resistance. Other polyester polyols are based on reclaimed raw materials. They are manufactured by transesterification (glycolysis) of recycled poly(ethyleneterephthalate) (PET) or dimethylterephthalate (DMT) distillation bottoms with glycols such as diethylene glycol. These low molecular weight, aromatic polyester polyols are used in rigid foam, and bring low cost and excellent flammability characteristics to polyisocyanurate (PIR) boardstock and polyurethane spray foam insulation.

    Specialty polyols include polycarbonate polyols, polycaprolactone polyols, polybutadiene polyols, and polysulfide polyols. The materials are used in elastomer, sealant, and adhesive applications that require superior weatherability, and resistance to chemical and environmental attack. Natural oil polyols derived from castor oil and other vegetable oils are used to make elastomers, flexible bunstock, and flexible molded foam.

    Co-polymerizing chlorotrifluoroethylene or tetrafluoroethylene with vinyl ethers containing hydroxyalkyl vinyl ether produces fluorinated (FEVE) polyols. Two-component fluorinated polyurethanes prepared by reacting FEVE fluorinated polyols with polyisocyanate have been used to make ambient cure paints and coatings. Since fluorinated polyurethanes contain a high percentage of fluorine–carbon bonds, which are the strongest bonds among all chemical bonds, fluorinated polyurethanes exhibit resistance to UV, acids, alkali, salts, chemicals, solvents, weathering, corrosion, fungi and microbial attack. These have been used for high performance coatings and paints.[21]

    Phosphorus-containing polyols are available that become chemically bonded to the polyurethane matrix for the use as flame retardants. This covalent linkage prevents migration and leaching of the organophosphorus compound.

    Bio-derived materials

    [edit]

    Interest in sustainable "green" products raised interest in polyols derived from vegetable oils,[22][23][24] fatty acids,[25] lignin, sorbitol,[26] etc. These are mostly contributing to polyol part. There are attempts made to prepare isocyanate part using bio-derived material. However, as far as commercialization is concern, polyol part is more targeted being easy and required in more quantity than isocyanate part. Various oils used in the preparation polyols for polyurethanes include soybean oil, cottonseed oil, neem seed oil, algae oil,[27][28] and castor oil. Vegetable oils are functionalized in various ways and modified to polyetheramides, polyethers, alkyds, etc. Renewable sources used to prepare polyols may be fatty acids or dimer fatty acids.[29] Some biobased and isocyanate-free polyurethanes exploit the reaction between polyamines and cyclic carbonates to produce polyhydroxyurethanes.[30]

    Chain extenders and cross linkers

    [edit]

    Chain extenders (f = 2) and cross linkers (f ≥ 3) are low molecular weight hydroxyl and amine terminated compounds that play an important role in the polymer morphology of polyurethane fibers, elastomers, adhesives, and certain integral skin and microcellular foams.

    The elastomeric properties of these materials are derived from the phase separation of the hard and soft copolymer segments of the polymer, such that the urethane hard segment domains serve as cross-links between the amorphous polyether (or polyester) soft segment domains. This phase separation occurs because the mainly nonpolar, low melting soft segments are incompatible with the polar, high melting hard segments. The soft segments, which are formed from high molecular weight polyols, are mobile and are normally present in coiled formation, while the hard segments, which are formed from the isocyanate and chain extenders, are stiff and immobile. As the hard segments are covalently coupled to the soft segments, they inhibit plastic flow of the polymer chains, thus creating elastomeric resiliency. Upon mechanical deformation, a portion of the soft segments are stressed by uncoiling, and the hard segments become aligned in the stress direction. This reorientation of the hard segments and consequent powerful hydrogen bonding contributes to high tensile strength, elongation, and tear resistance values.[12][31][32][33][34] The choice of chain extender also determines flexural, heat, and chemical resistance properties.

    The most important chain extenders are ethylene glycol, 1,4-butanediol (1,4-BDO or BDO), 1,6-hexanediol, cyclohexane dimethanol and hydroquinone bis(2-hydroxyethyl) ether (HQEE). All of these glycols form polyurethanes that phase separate well and form well defined hard segment domains, and are melt processable. They are all suitable for thermoplastic polyurethanes with the exception of ethylene glycol, since its derived bis-phenyl urethane undergoes unfavorable degradation at high hard segment levels.[10] Diethanolamine and triethanolamine are used in flex molded foams to build firmness and add catalytic activity. Diethyltoluenediamine is used extensively in RIM, and in polyurethane and polyurea elastomer formulations.

    Table of chain extenders and cross linkers[35]
    Compound type Molecule Mol.
    mass
    Density
    (g/cm3)
    Melting
    pt (°C)
    Boiling
    pt (°C)
    Hydroxyl compounds – difunctional molecules Ethylene glycol 62.1 1.110 −13.4 197.4
    Diethylene glycol 106.1 1.111 −8.7 245.5
    Triethylene glycol 150.2 1.120 −7.2 287.8
    Tetraethylene glycol 194.2 1.123 −9.4 325.6
    Propylene glycol 76.1 1.032 Supercools 187.4
    Dipropylene glycol 134.2 1.022 Supercools 232.2
    Tripropylene glycol 192.3 1.110 Supercools 265.1
    1,3-Propanediol 76.1 1.060 −28 210
    1,3-Butanediol 92.1 1.005 207.5
    1,4-Butanediol 92.1 1.017 20.1 235
    Neopentyl glycol 104.2 130 206
    1,6-Hexanediol 118.2 1.017 43 250
    1,4-Cyclohexanedimethanol
    HQEE
    Ethanolamine 61.1 1.018 10.3 170
    Diethanolamine 105.1 1.097 28 271
    Methyldiethanolamine 119.1 1.043 −21 242
    Phenyldiethanolamine 181.2 58 228
    Hydroxyl compounds – trifunctional molecules Glycerol 92.1 1.261 18.0 290
    Trimethylolpropane
    1,2,6-Hexanetriol
    Triethanolamine 149.2 1.124 21
    Hydroxyl compounds – tetrafunctional molecules Pentaerythritol 136.2 260.5
    N,N,N′,N′-Tetrakis
    (2-hydroxypropyl)
    ethylenediamine
    Amine compounds – difunctional molecules Diethyltoluenediamine 178.3 1.022 308
    Dimethylthiotoluenediamine 214.0 1.208

    Catalysts

    [edit]

    Polyurethane catalysts can be classified into two broad categories, basic and acidic amine. Tertiary amine catalysts function by enhancing the nucleophilicity of the diol component. Alkyl tin carboxylates, oxides and mercaptides oxides function as mild Lewis acids in accelerating the formation of polyurethane. As bases, traditional amine catalysts include triethylenediamine (TEDA, also called DABCO, 1,4-diazabicyclo[2.2.2]octane), dimethylcyclohexylamine (DMCHA), dimethylethanolamine (DMEA), Dimethylaminoethoxyethanol and bis-(2-dimethylaminoethyl)ether, a blowing catalyst also called A-99. A typical Lewis acidic catalyst is dibutyltin dilaurate. The process is highly sensitive to the nature of the catalyst and is also known to be autocatalytic.[36]

    Another class of catalysts was published in a study in May 2024. In this study, polyurethane synthesis was investigated in the presence of acid catalysts, namely dimethylphosphite (DMHP), methanesulfonic acid (MSA), and trifluoromethanesulfonic acid (TFMSA). The thermodynamic profile was examined and described in detail through computational tools, showing that TFMSA had the best catalytic properties. The study aimed to open the door to a new class of catalysts.[37]

    Factors affecting catalyst selection include balancing three reactions: urethane (polyol+isocyanate, or gel) formation, the urea (water+isocyanate, or "blow") formation, or the isocyanate trimerization reaction (e.g., using potassium acetate, to form isocyanurate rings). A variety of specialized catalysts have been developed.[38][39][40]

    Surfactants

    [edit]

    Surfactants are used to modify the characteristics of both foam and non-foam polyurethane polymers. They take the form of polydimethylsiloxane-polyoxyalkylene block copolymers, silicone oils, nonylphenol ethoxylates, and other organic compounds. In foams, they are used to emulsify the liquid components, regulate cell size, and stabilize the cell structure to prevent collapse and sub-surface voids.[41] In non-foam applications they are used as air release and antifoaming agents, as wetting agents, and are used to eliminate surface defects such as pin holes, orange peel, and sink marks.

    Production

    [edit]

    Polyurethanes are produced by mixing two or more liquid streams. The polyol stream contains catalysts, surfactants, blowing agents (when making polyurethane foam insulation) and so on. The two components are referred to as a polyurethane system, or simply a system. The isocyanate is commonly referred to in North America as the 'A-side' or just the 'iso'. The blend of polyols and other additives is commonly referred to as the 'B-side' or as the 'poly'.[citation needed] This mixture might also be called a 'resin' or 'resin blend'. In Europe the meanings for 'A-side' and 'B-side' are reversed.[citation needed] Resin blend additives may include chain extenders, cross linkers, surfactants, flame retardants, blowing agents, pigments, and fillers. Polyurethane can be made in a variety of densities and hardnesses by varying the isocyanate, polyol or additives.

    Health and safety

    [edit]

    Fully reacted polyurethane polymer is chemically inert.[42] No exposure limits have been established in the U.S. by OSHA (Occupational Safety and Health Administration) or ACGIH (American Conference of Governmental Industrial Hygienists). It is not regulated by OSHA for carcinogenicity.

    Open-flame test. Top: untreated polyurethane foam burns vigorously. Bottom: with fire-retardant treatment.

    Polyurethanes are combustible.[43] Decomposition from fire can produce significant amounts of carbon monoxide and hydrogen cyanide, in addition to nitrogen oxides, isocyanates, and other toxic products.[44] Due to the flammability of the material, it has to be treated with flame retardants (at least in case of furniture), almost all of which are considered harmful.[45][46] California later issued Technical Bulletin 117 2013 which allowed most polyurethane foam to pass flammability tests without the use of flame retardants. Green Science Policy Institute states: "Although the new standard can be met without flame retardants, it does NOT ban their use. Consumers who wish to reduce household exposure to flame retardants can look for a TB117-2013 tag on furniture, and verify with retailers that products do not contain flame retardants."[47]

    Liquid resin blends and isocyanates may contain hazardous or regulated components. Isocyanates are known skin and respiratory sensitizers. Additionally, amines, glycols, and phosphate present in spray polyurethane foams present risks.[48]

    Exposure to chemicals that may be emitted during or after application of polyurethane spray foam (such as isocyanates) are harmful to human health and therefore special precautions are required during and after this process.[49]

    In the United States, additional health and safety information can be found through organizations such as the Polyurethane Manufacturers Association (PMA) and the Center for the Polyurethanes Industry (CPI), as well as from polyurethane system and raw material manufacturers. Regulatory information can be found in the Code of Federal Regulations Title 21 (Food and Drugs) and Title 40 (Protection of the Environment). In Europe, health and safety information is available from ISOPA,[50] the European Diisocyanate and Polyol Producers Association.

    Manufacturing

    [edit]

    The methods of manufacturing polyurethane finished goods range from small, hand pour piece-part operations to large, high-volume bunstock and boardstock production lines. Regardless of the end-product, the manufacturing principle is the same: to meter the liquid isocyanate and resin blend at a specified stoichiometric ratio, mix them together until a homogeneous blend is obtained, dispense the reacting liquid into a mold or on to a surface, wait until it cures, then demold the finished part.

    Dispensing equipment

    [edit]

    Although the capital outlay can be high, it is desirable to use a meter-mix or dispense unit for even low-volume production operations that require a steady output of finished parts. Dispense equipment consists of material holding (day) tanks, metering pumps, a mix head, and a control unit. Often, a conditioning or heater–chiller unit is added to control material temperature in order to improve mix efficiency, cure rate, and to reduce process variability. Choice of dispense equipment components depends on shot size, throughput, material characteristics such as viscosity and filler content, and process control. Material day tanks may be single to hundreds of gallons in size and may be supplied directly from drums, IBCs (intermediate bulk containers, such as caged IBC totes), or bulk storage tanks. They may incorporate level sensors, conditioning jackets, and mixers. Pumps can be sized to meter in single grams per second up to hundreds of pounds per minute. They can be rotary, gear, or piston pumps, or can be specially hardened lance pumps to meter liquids containing highly abrasive fillers such as chopped or hammer-milled glass fiber and wollastonite.[citation needed]

    The pumps can drive low-pressure (10 to 30 bar, 1 to 3 MPa) or high-pressure (125 to 250 bar, 12.5 to 25.0 MPa) dispense systems. Mix heads can be simple static mix tubes, rotary-element mixers, low-pressure dynamic mixers, or high-pressure hydraulically actuated direct impingement mixers. Control units may have basic on/off and dispense/stop switches, and analogue pressure and temperature gauges, or may be computer-controlled with flow meters to electronically calibrate mix ratio, digital temperature and level sensors, and a full suite of statistical process control software. Add-ons to dispense equipment include nucleation or gas injection units, and third or fourth stream capability for adding pigments or metering in supplemental additive packages.

    Tooling

    [edit]

    Distinct from pour-in-place, bun and boardstock, and coating applications, the production of piece parts requires tooling to contain and form the reacting liquid. The choice of mold-making material is dependent on the expected number of uses to end-of-life (EOL), molding pressure, flexibility, and heat transfer characteristics.

    RTV silicone is used for tooling that has an EOL in the thousands of parts. It is typically used for molding rigid foam parts, where the ability to stretch and peel the mold around undercuts is needed. The heat transfer characteristic of RTV silicone tooling is poor. High-performance, flexible polyurethane elastomers are also used in this way.

    Epoxy, metal-filled epoxy, and metal-coated epoxy is used for tooling that has an EOL in the tens of thousands of parts. It is typically used for molding flexible foam cushions and seating, integral skin and microcellular foam padding, and shallow-draft RIM bezels and fascia. The heat transfer characteristic of epoxy tooling is fair; the heat transfer characteristic of metal-filled and metal-coated epoxy is good. Copper tubing can be incorporated into the body of the tool, allowing hot water to circulate and heat the mold surface.

    Aluminum is used for tooling that has an EOL in the hundreds of thousands of parts. It is typically used for molding microcellular foam gasketing and cast elastomer parts, and is milled or extruded into shape.

    Mirror-finish stainless steel is used for tooling that imparts a glossy appearance to the finished part. The heat transfer characteristic of metal tooling is excellent.

    Finally, molded or milled polypropylene is used to create low-volume tooling for molded gasket applications. Instead of many expensive metal molds, low-cost plastic tooling can be formed from a single metal master, which also allows greater design flexibility. The heat transfer characteristic of polypropylene tooling is poor, which must be taken into consideration during the formulation process.

    Applications

    [edit]

    In 2007, the global consumption of polyurethane raw materials was above 12 million metric tons, and the average annual growth rate was about 5%.[51] Revenues generated with PUR on the global market are expected to rise to approximately US$75 billion by 2022.[52] As they are such an important class of materials, research is constantly taking place and papers published.[53]

    Degradation and environmental fate

    [edit]

    Effects of visible light

    [edit]
    Polyurethane foam made with an aromatic isocyanate, which has been exposed to UV light. Readily apparent is the discoloration that occurs over time.

    Polyurethanes, especially those made using aromatic isocyanates, contain chromophores that interact with light. This is of particular interest in the area of polyurethane coatings, where light stability is a critical factor and is the main reason that aliphatic isocyanates are used in making polyurethane coatings. When PU foam, which is made using aromatic isocyanates, is exposed to visible light, it discolors, turning from off-white to yellow to reddish brown. It has been generally accepted that apart from yellowing, visible light has little effect on foam properties.[54][55] This is especially the case if the yellowing happens on the outer portions of a large foam, as the deterioration of properties in the outer portion has little effect on the overall bulk properties of the foam itself.

    It has been reported that exposure to visible light can affect the variability of some physical property test results.[56]

    Higher-energy UV radiation promotes chemical reactions in foam, some of which are detrimental to the foam structure.[57]

    Hydrolysis and biodegradation

    [edit]

    Polyurethanes may degrade due to hydrolysis. This is a common problem with shoes left in a closet, and reacting with moisture in the air.[58]

    Microbial degradation of polyurethane is believed to be due to the action of esterase, urethanase, hydrolase and protease enzymes.[59] The process is slow as most microbes have difficulty moving beyond the surface of the polymer. Susceptibility to fungi is higher due to their release of extracellular enzymes, which are better able to permeate the polymer matrix. Two species of the Ecuadorian fungus Pestalotiopsis are capable of biodegrading polyurethane in aerobic and anaerobic conditions such as found at the bottom of landfills.[60][61] Degradation of polyurethane items at museums has been reported.[62] Polyester-type polyurethanes are more easily biodegraded by fungus than polyether-type.[63]

    See also

    [edit]
    • Botanol, a material with higher plant-based content
    • Passive fire protection
    • Penetrant (mechanical, electrical, or structural)
    • Polyaspartic
    • Polyurethane dispersion
    • Thermoplastic polyurethanes
    • Thermoset polymer matrix

    References

    [edit]
    1. ^ "polyurethane". Dictionary.com Unabridged (Online). n.d.
    2. ^ Gama, Nuno; Ferreira, Artur; Barros-Timmons, Ana (27 September 2018). "Polyurethane Foams: Past, Present, and Future". Materials. 11 (10): 1841. Bibcode:2018Mate...11.1841G. doi:10.3390/ma11101841. PMC 6213201. PMID 30262722.
    3. ^ "Polyurethane". American Chemistry Council. Retrieved 2022-09-19.
    4. ^ "Polyurethane global market volume 2015-2026". Statista. Retrieved 23 July 2021.
    5. ^ Bayer, Otto (1947). "Das Di-Isocyanat-Polyadditionsverfahren (Polyurethane)". Angewandte Chemie. 59 (9): 257–72. Bibcode:1947AngCh..59..257B. doi:10.1002/ange.19470590901.
    6. ^ DE 728981, I.G. Farbenindustrie A.G., "Verfahren zur Herstellung von Polyurethanen bzw. Polyharnstoffen [Process for the production of polyurethanes or polyurea]", published 1942-12-07 
    7. ^ a b c Seymour, Raymond B.; Kauffman, George B. (1992). "Polyurethanes: A class of modern versatile materials". Journal of Chemical Education. 69 (11): 909. Bibcode:1992JChEd..69..909S. doi:10.1021/ed069p909.
    8. ^ Feske, Bert (October 2004). "The Use of Saytex RB-9130/9170 Low Viscosity Brominated Flame Retardant Polyols in HFC-245fa and High Water Formulations" (PDF). Polyurethanes Expo 2004. Las Vegas, NV: Alliance for the Polyurethane Industry Technical Conference. p. 309. Retrieved 2007-08-01.
    9. ^ n ≥ 2
    10. ^ a b Gum, Wilson; Riese, Wolfram; Ulrich, Henri (1992). Reaction Polymers. New York: Oxford University Press. ISBN 978-0-19-520933-4.
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    [edit]
    • Center for the Polyurethanes Industry: information for EH&S issues related to polyurethanes developments
    • Polyurethane synthesis, Polymer Science Learning Center, University of Southern Mississippi
    • Polyurethane Foam Association: Industry information, educational materials and resources related to flexible polyurethane foam
    • PU Europe: European PU insulation industry association (formerly BING): European voice for the national trade associations representing the polyurethane insulation industry
    • ISOPA: European Diisocyanate & Polyol Producers Association: ISOPA represents the manufacturers in Europe of aromatic diisocyanates and polyols