Plasticizers for polymers are either solids or low-volatility liquids. According to 2017 data, the total global market for plasticizers was 7.5 million metric tonnes. In North America the 2017 volume was ~1.01 million metric tonnes and in Europe the figure was 1.35 million metric tonnes, split between various end-use applications with a chemical type trend moving to higher molecular weight (HMW) orthophthalates and alternative types following regulatory issues concerning lower molecular weight (LMW) orthophthalates. Almost 90% of polymer plasticizers, most commonly
phthalate esters, are used in
PVC, giving this material improved flexibility and durability. Other polymers which can contain high loadings of plasticizers include
acrylates and
cellulose-type plastics, such as
cellulose acetate,
nitrocellulose and
cellulose acetate butyrate.
Mechanism of action The molecules of the plasticizer are immobilized within the matrix formed by the polymer, rather than being part of the polymer. It was commonly thought that plasticizers work by embedding themselves between the chains of
polymers, spacing them apart (increasing the "free volume"), or swelling them and thus significantly lowering the
glass transition temperature for the plastic and making it softer. It was later shown that the free volume explanation could not account for all of the effects of plasticization. The mobility of a polymer chain is more complex in the presence of plasticizer than what the
Flory–Fox equation predicts for a simple polymer chain. The molecules of plasticizer take control over mobility of the chain; a polymer chain does not show an increase of the free volume around polymer ends. If plasticizer/water creates hydrogen bonds with hydrophilic parts of the polymer, the associated free volume can be decreased. 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 decrease 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.
Selection 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.
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,
glutarates,
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. 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 Antiplasticizers are
polymer additives that have effect opposite to those of plasticizers. They increase the modulus while decreasing the glass transition temperature. is a common plasticizer.
Safety and toxicity 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. Plasticizers can escape plastics 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, 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.
Common polymer plasticizers Ortho phthalates •
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 •
Dimethyl phthalate (DMP), used in fragrances, as an insect repellent, and in several industrial processes as a solvent/carrier •
Diethyl phthalate (DEP), used in fragrances as a carrier and extender/fixative •
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 (benzyl butyl phthalate, BBzP) is found in vinyl tiles, traffic cones, food
conveyor belts,
artificial leather, and plastic foams •
Bis(2-ethylhexyl) phthalate (DEHP) also commonly known as (dioctyl phthalate, DOP or diethylhexyl phthalate), historically used in flooring materials, medical devices, myriad consumer
products, and high
explosives, such as
Semtex. DEHP was the most common plasticizer for decades and still holds that title globally even as it has largely been replaced now with higher molecular weight phthalates and alternatives in the US and Europe •
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.
Terephthalates •
Terephthalates are isomeric with ortho phthalates but have proven to have cleaner toxicological results due to their inability to form stable monoesters during hydrolysis and metabolic breakdown. •
Bis(2-ethylhexyl) terephthalate (DEHT; Dioctyl terephthalate, DOTP) (Eastman Chemical Company Trademark: Eastman 168™), used as a replacement for DEHP and DINP • Diisopentyl terephthalate (DiPT)(Evonik Industries Trademark: ELATUR® DPT), used as a replacement for DBP and DiBP • Dibutyl terephthalate (DBT)(Eastman Chemical Trademark: Eastman Effusion™), used as a replacement for DBP and DiBP
Trimellitates •
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, Trioctyl Trimellitate plasticizer) •
Tri(isononyl)trimellitate (TINTM) •
Tri(isodecyl)trimellitate (TIDTM) •
Tri(isotridecyl)trimellitate (TITDTM)
Adipates & Sebacates •
Adipate-based plasticizers are used for low-temperature or resistance to
ultraviolet light. An example is: •
Bis(2-ethylhexyl)adipate (DEHA, dioctyl adipate plasticizer) •
Sebacate- based plasticizers provide excellent compatibility with a range of plastic materials and synthetic rubbers (specifically nitrile rubber and neoprene), superior properties at low temperatures, and good oil resistivity. Some examples are: •
Dibutyl sebacate (DBS) •
Di(2-ethylhexyl)sebacate, Di-octyl Sebacate (or DOS plasticizer)
Organophosphates •
Organophosphates include the following: •
Tricresyl phosphate (TCP) •
2-Ethylhexyl diphenyl phosphate Other •
1,2-Cyclohexane dicarboxylic acid diisononyl ester (BASF Trademark: Hexamoll DINCH) • Bis(2-ethylhexyl) cyclohexane-1,4-dicarboxylate (Hanwha Trademark: Eco-DEHCH) • Alkyl sulphonic acid phenyl ester (ASE). (Lanxess Chemical Trademark: Mesamoll) • Triethylene glycol di-2ethylhexanoate (Eastman Chemical Trademark: Eastman TEG-EH) Bio-based plasticizers have been investigated, such as
glycerol triacetate (Triacetin) and
acetyltributylcitrate. They are used in niche applications.
Epoxidized soybean oil is used broadly as a secondary plasticizer in many vinyl applications. • Note:
Bisphenol A, or BPA, is not a plasticizer, although it is often wrongly described as one. ==For inorganic materials==