Plasticizer

It was commonly thought that plasticizers work by embedding themselves between the chains of polymers, spacing them apart (increasing the "free volume"),[3][4] or swelling them and thus significantly lowering the glass transition temperature for the plastic and making it softer; however it was later shown that the free volume explanation could not account for all of the effects of plasticization.[5] The classical picture on the mobility of polymer chain is more complex in the presence of plasticizer than that drawn by Fox&Flory for simple polymer chain. The molecules of plasticizer take control over mobility of the chain, and polymer chain does not show an increase of the free volume around polymer ends; in the case that the plasticizer/ water creates hydrogen bonds with hydrophilic parts of polymer, the associated free volume can be decreased. [6] For plastics such as PVC, the more plasticizer added, the lower their cold flex temperature will be. Plastic items containing plasticizers can exhibit improved flexibility and durability. Plasticizers can become available for exposure due to migration and abrasion of the plastic since they are not bound to the polymer matrix. The "new car smell" is often attributed to plasticizers or their degradation products.[7] However, multiple studies on the makeup of the smell do not find phthalates in appreciable amounts, likely due to their extremely low volatility and vapor pressure.[8]

The effect of plasticizers on elastic modulus is dependent on both temperature and plasticizer concentration. Below a certain concentration, referred to as the crossover concentration, a plasticizer can increase the modulus of a material. The material's glass transition temperature will decrease however, at all concentrations. In addition to a crossover concentration a crossover temperature exists. Below the crossover temperature the plasticizer will also increase the modulus.

Migration of plasticizers out of their host plastics leads to loss of flexibility, embrittlement, and cracking. This decades-old plastic lamp cord crumbles when flexed, due to loss of the plasticizers.

Over the last 60 years more than 30,000 different substances have been evaluated for their suitability as polymer plasticizers. Of these, only a small number – approximately 50 – are today in commercial use.[9]

Ester plasticizers are selected based upon cost-performance evaluation. The rubber compounder must evaluate ester plasticizers for compatibility, processibility, permanence and other performance properties. The wide variety of ester chemistries that are in production include sebacates, adipates, terephthalates, dibenzoates, gluterates, phthalates, azelates, and other specialty blends. This broad product line provides an array of performance benefits required for the many elastomer applications such as tubing and hose products, flooring, wall-coverings, seals and gaskets, belts, wire and cable, and print rolls. Low to high polarity esters provide utility in a wide range of elastomers including nitrile, polychloroprene, EPDM, chlorinated polyethylene, and epichlorohydrin. Plasticizer-elastomer interaction is governed by many factors such as solubility parameter, molecular weight, and chemical structure. Compatibility and performance attributes are key factors in developing a rubber formulation for a particular application.[10]

Plasticizers used in PVC and other plastics are often based on esters of polycarboxylic acids with linear or branched aliphatic alcohols of moderate chain length. These compounds are selected on the basis of many critieria including low toxicity, compatibility with the host material, nonvolatility, and expense. Phthalate esters of straight-chain and branched-chain alkyl alcohols meet these specifications and are common plasticizers. Ortho-phthalate esters have traditionally been the most dominant plasticizers, but regulatory concerns have led to the move away from classified substances to non-classified which includes high molecular weight ortho-phthalates and other plasticisers, especially in Europe.

Antiplasticizers are polymer additives that have effect opposite to those of plasticizers. They increase the modulus while decreasing the glass transition temperature.

Bis(2-ethylhexyl) phthalate is a common plasticizer.

Substantial concerns have been expressed over the safety of some polymer plasticizers, especially because some low molecular weight ortho-phthalates have been classified as potential endocrine disruptors with some developmental toxicity reported.[11]

• Phthalate-based plasticizers are used in situations where good resistance to water and oils is required. Some common phthalate plasticizers are:

• Low Molecular Weight Ortho Phthalates
  • Diisobutyl phthalate (DIBP)
  • Di-n-butyl phthalate (DBP), used for cellulose plastics, food wraps, adhesives, perfumes, and cosmetics - about a third of nail polishes, glosses, enamels, and hardeners contain it, together with some shampoos, sunscreens, skin emollients, and insect repellents
  • Butyl benzyl phthalate (BBzP) is found in vinyl tiles, traffic cones, food conveyor belts, artificial leather, and plastic foams
  • Bis(2-ethylhexyl) phthalate (DEHP), used in construction materials and medical devices
  • Dioctyl phthalate (DOP), historically used in flooring materials, carpets, notebook covers, and high explosives, such as Semtex. Together with DEHP it was the most common plasticizers but both have largely been replaced now with higher molecular weight versions

• High Molecular Weight Ortho Phthalates
  • Diisononyl phthalate (DINP), used in flooring materials, found in garden hoses, shoes, toys, and building materials
  • Bis(2-propylheptyl) phthalate (DPHP), used in cables, wires and roofing materials
  • Diisodecyl phthalate (DIDP), used for insulation of wires and cables, car undercoating, shoes, carpets, pool liners
  • Diisoundecyl phthalate (DIUP), used for insulation of wires and cables, car undercoating, shoes, carpets, pool liners. Good high temperature and outdoor weathering performance
  • Ditridecyl phthalate (DTDP) is the highest molecular weight phthalate plasticizer, providing greater performance at high temperature. It is the preferred plasticizer for automotive cable and wire application.

• Trimellitates are used in automobile interiors and other applications where resistance to high temperature is required. They have extremely low volatility.
  • Tri-(2-ethylhexyl)trimellitate (TEHTM)(TOTM)
  • Tri-(isononyl)trimellitate (TINTM)
  • Tri-(isodecyl)trimellitate (TIDTM)
  • Tri-(isotridecyl)trimellitate (TITDTM)

• Adipate-based plasticizers are used for low-temperature or resistance to ultraviolet light. An example is:
  • Bis(2-ethylhexyl)adipate (DEHA)
• Sebacate- based plasticizers are provides excellent compatibility with a range of plastic materials and synthetic rubbers (specially nitrile rubber and neoprene), superior properties at low temperatures, and good oil resistivity. Some examples are:
  • Dibutyl sebacate (DBS)
  • Di-(2ethylhexyl)sebacate, Di-octyl Sebacate (DOS)

Plasticizers with better biodegradability and presumably lower environmental toxicity are being developed. Some such plasticizers are:

• Glycerol Triacetate (Triacetin) can be used as food additives
• Alkyl citrates, used in food packagings, medical products, cosmetics, and children's toys
  • Triethyl citrate (TEC)
  • Acetyl triethyl citrate (ATEC), higher boiling point and lower volatility than TEC
  • Tributyl citrate (TBC) compatible with PVC and vinyl acetate homopolymers and copolymers
  • Acetyl tributyl citrate (ATBC), compatible with PVC and vinyl chloride copolymers
  • Tri-(2ethylhexyl)citrate (TOC), also used for gums and controlled release medicines
  • Acetyl trioctyl citrate (ATOC), also used for printing ink
  • Trihexyl citrate (THC), compatible with PVC, also used for controlled release medicines
  • Acetyl trihexyl citrate (ATHC), compatible with PVC
  • Butyryl trihexyl citrate (BTHC, trihexyl o-butyryl citrate), compatible with PVC
• Vegetable Oil based plasticizers
  • Epoxidized soybean oil (ESBO or ESO) is used as secondary plasticizer and heat stabilizer in PVC.
  • Epoxidized Linoleic Oil (ELO) similar use as ESO

• Azelates
• Dibenzoates used in vinyl flooring, adhesives and sealants
• Terephthalates such as Bis(2 ethyl hexyl terephthalate (DEHT) (Eastman Chemical Company Trademark: Eastman 168). Dibutyl terephthalate (DBT)(Eastman Chemical Trademark: Eastman Effusion)
• 1,2-Cyclohexane dicarboxylic acid diisononyl ester (BASF trademark: Hexamoll DINCH)
• Alkyl sulphonic acid phenyl ester (ASE). Lanxess Chemical Trademark: Mesamoll)
• Organophosphates impart an inherent fire retarding property
  • [[Tricresyl (methyl phenyl) phosphate (TCP)
  • [[2-ethylhexyldiphenyl phosphate
• Glycols and polyethers
  • Triethylene glycol di-2hexanoate (Eastman Chemical Trademark: Eastman TEG-EH)
• Polymeric plasticizers

• Note: Bisphenol A, or BPA, is not a plasticizer, despite what the popular media says. BPA is a monomer and sometimes other additive for plastics, but it is not a plasticizer according to any scientific definition.

In the concrete technology, plasticizers and superplasticizers are also called high range water reducers. When added to concrete mixtures, they confer a number of properties including improve workability and strength. The strength of concrete is inversely proportional to the amount of water added, i.e., the water-cement (w/c) ratio. In order to produce stronger concrete, less water is added (without "starving" the mix), which makes the concrete mixture less workable and difficult to mix, necessitating the use of plasticizers, water reducers, superplasticizers, fluidizer or dispersants.[12]

Plasticizers are also often used when pozzolanic ash is added to concrete to improve strength. This method of mix proportioning is especially popular when producing high-strength concrete and fiber-reinforced concrete.

Adding 1-2% plasticizer per unit weight of cement is usually sufficient. Adding an excessive amount of plasticizer will result in excessive segregation of concrete and is not advisable. Depending on the particular chemical used, use of too much plasticizer may result in a retarding effect.

Plasticizers are commonly manufactured from lignosulfonates, a by-product from the paper industry. Superplasticizers have generally been manufactured from sulfonated naphthalene condensate or sulfonated melamine formaldehyde, although newer products based on polycarboxylic ethers are now available. Traditional lignosulfonate-based plasticisers, naphthalene and melamine sulfonate-based superplasticisers disperse the flocculated cement particles through a mechanism of electrostatic repulsion (see colloid). In normal plasticisers, the active substances are adsorbed on to the cement particles, giving them a negative charge, which leads to repulsion between particles. Lignin, naphthalene, and melamine sulfonate superplasticisers are organic polymers. The long molecules wrap themselves around the cement particles, giving them a highly negative charge so that they repel each other.

Polycarboxylate ether superplasticizer (PCE) or just polycarboxylate (PC), work differently from sulfonate-based superplasticizers, giving cement dispersion by steric stabilisation. This form of dispersion is more powerful in its effect and gives improved workability retention to the cementitious mix.[13]

Plasticizers can be added to wallboard stucco mixtures to improve workability. In order to reduce the energy consumed drying wallboard, less water is added, which makes the gypsum mixture very unworkable and difficult to mix, necessitating the use of plasticizers, water reducers, or dispersants. Some studies also show that too much lignosulfonate dispersant could result in a set-retarding effect. Data showed that amorphous crystal formations occurred that detracted from the mechanical needle-like crystal interaction in the core, preventing a stronger core. The sugars, chelating agents in lignosulfonates such as aldonic acids and extractive compounds are mainly responsible for set retardation. These low range water reducing dispersants are commonly manufactured from lignosulfonates, a by-product from the paper industry.

High range superplasticizers (dispersants) have generally been manufactured from sulfonated naphthalene condensate, although polycarboxylic ethers represent more modern alternatives. Both of these high range water reducers are used at 1/2 to 1/3 of the lignosulfonate types.[14]

Traditional lignosulfonate and naphthalene sulfonate-based plasticisers disperse the flocculated gypsum particles through a mechanism of electrostatic repulsion (see Colloid). In normal plasticisers, the active substances are adsorbed on to the gypsum particles, giving them a negative charge, which leads to repulsion between particles. Lignin and naphthalene sulfonate plasticizers are organic polymers. The long molecules wrap themselves around the gypsum particles, giving them a highly negative charge so that they repel each other.[15]

Energetic material pyrotechnic compositions, especially solid rocket propellants and smokeless powders for guns, often employ plasticizers to improve physical properties of the propellant binder or of the overall propellant, to provide a secondary fuel, and ideally, to improve specific energy yield (e.g. specific impulse, energy yield per gram of propellant, or similar indices) of the propellant. An energetic plasticizer improves the physical properties of an energetic material while also increasing its specific energy yield. Energetic plasticizers are usually preferred to non-energetic plasticizers, especially for solid rocket propellants. Energetic plasticizers reduce the required mass of propellant, enabling a rocket vehicle to carry more payload or reach higher velocities than would otherwise be the case. However, safety or cost considerations may demand that non-energetic plasticizers be used, even in rocket propellants. The solid rocket propellant used to fuel the Space Shuttle solid rocket booster employs HTPB, a synthetic rubber, as a non-energetic secondary fuel.

Here are some energetic plasticizers used in rocket propellants and smokeless powders:

• Nitroglycerine (NG, aka "nitro", glyceryl trinitrate)
• Butanetriol trinitrate (BTTN)
• Dinitrotoluene (DNT)
• Trimethylolethane trinitrate (TMETN, aka Metriol trinitrate, METN)
• Diethylene glycol dinitrate (DEGDN, less commonly DEGN)
• Triethylene glycol dinitrate (TEGDN, less commonly TEGN)
• Bis(2,2-dinitropropyl)formal (BDNPF)
• Bis(2,2-dinitropropyl)acetal (BDNPA)
• 2,2,2-Trinitroethyl 2-nitroxyethyl ether (TNEN)

Due to the secondary alcohol groups, NG and BTTN have relatively low thermal stability. TMETN, DEGDN, BDNPF, and BDNPA have relatively low energies. NG and DEGN have relatively high vapor pressure.[16]