Polydimethylsiloxane

Polydimethylsiloxane (PDMS), also known as dimethylpolysiloxane or dimethicone, belongs to a group of polymeric organosilicon compounds that are commonly referred to as silicones.[1] PDMS is the most widely used silicon-based organic polymer due to its versatility and properties leading to many applications.[2]

Polydimethylsiloxane
Names
IUPAC name
poly(dimethylsiloxane)
Other names
PDMS
dimethicone
dimethylpolysiloxane
E900
Identifiers
3D model (JSmol)
ChemSpider
  • none
ECHA InfoCard 100.126.442
E number E900 (glazing agents, ...)
UNII
Properties
(C2H6OSi)n
Density 965 kg/m3
Melting point N/A (vitrifies)
Boiling point N/A (vitrifies)
Pharmacology
P03AX05 (WHO)
Hazards
NFPA 704 (fire diamond)
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

It is particularly known for its unusual rheological (or flow) properties. PDMS is optically clear and, in general, inert, non-toxic, and non-flammable. It is one of several types of silicone oil (polymerized siloxane). Its applications range from contact lenses and medical devices to elastomers; it is also present in shampoos (as it makes hair shiny and slippery), food (antifoaming agent), caulking, lubricants and heat-resistant tiles.

Structure

The chemical formula for PDMS is CH3[Si(CH3)2O]nSi(CH3)3, where n is the number of repeating monomer [SiO(CH3)2] units.[3] Industrial synthesis can begin from dimethyldichlorosilane and water by the following net reaction:

The polymerization reaction evolves hydrochloric acid. For medical and domestic applications, a process was developed in which the chlorine atoms in the silane precursor were replaced with acetate groups. In this case, the polymerization produces acetic acid, which is less chemically aggressive than HCl. As a side-effect, the curing process is also much slower in this case. The acetate is used in consumer applications, such as silicone caulk and adhesives.

Branching and capping

Hydrolysis of Si(CH3)2Cl2 generates a polymer that is terminated with silanol groups (−Si(CH3)2OH]). These reactive centers are typically "capped" by reaction with trimethylsilyl chloride:

2 Si(CH3)3Cl + [Si(CH3)2O]n−2[Si(CH3)2OH]2 → [Si(CH3)2O]n−2[Si(CH3)2O Si(CH3)3]2 + 2 HCl

Silane precursors with more acid-forming groups and fewer methyl groups, such as methyltrichlorosilane, can be used to introduce branches or cross-links in the polymer chain. Under ideal conditions, each molecule of such a compound becomes a branch point. This can be used to produce hard silicone resins. In a similar manner, precursors with three methyl groups can be used to limit molecular weight, since each such molecule has only one reactive site and so forms the end of a siloxane chain.

Well-defined PDMS with a low polydispersity index and high homogeneity is produced by controlled anionic ring-opening polymerization of hexamethylcyclotrisiloxane. Using this methodology it is possible to synthesize linear block copolymers, heteroarm star-shaped block copolymers and many other macromolecular architectures.

The polymer is manufactured in multiple viscosities, ranging from a thin pourable liquid (when n is very low), to a thick rubbery semi-solid (when n is very high). PDMS molecules have quite flexible polymer backbones (or chains) due to their siloxane linkages, which are analogous to the ether linkages used to impart rubberiness to polyurethanes. Such flexible chains become loosely entangled when molecular weight is high, which results in PDMS' unusually high level of viscoelasticity.

Mechanical properties

PDMS is viscoelastic, meaning that at long flow times (or high temperatures), it acts like a viscous liquid, similar to honey. However, at short flow times (or low temperatures), it acts like an elastic solid, similar to rubber. Viscoelasticity is a form of nonlinear elasticity that is common amongst noncrystalline polymers.[4] The loading and unloading of a stress-strain curve for PDMS do not coincide; rather, the amount of stress will vary based on the degree of strain, and the general rule is that increasing strain will result in greater stiffness. When the load itself is removed, the strain is slowly recovered (rather than instantaneously). This time-dependent elastic deformation results from the long-chains of the polymer. But the process that is described above is only relevant when cross-linking is present; when it is not, the polymer PDMS cannot shift back to the original state even when the load is removed, resulting in a permanent deformation. However, permanent deformation is rarely seen in PDMS, since it is almost always cured with a cross-linking agent.  

If some PDMS is left on a surface overnight (long flow time), it will flow to cover the surface and mold to any surface imperfections. However, if the same PDMS is poured into a spherical mold and allowed to cure (short flow time), it will bounce like a rubber ball.[3] The mechanical properties of PDMS enable this polymer to conform to a diverse variety of surfaces. Since these properties are affected by a variety of factors, this unique polymer is relatively easy to tune. This enables PDMS to become a good substrate that can easily be integrated into a variety of microfluidic and microelectromechanical systems.[5][6] Specifically, the determination of mechanical properties can be decided before PDMS is cured; the uncured version allows the user to capitalize on myriad opportunities for achieving a desirable elastomer. Generally, the cross-linked cured version of PDMS resembles rubber in a solidified form. It is widely known to be easily stretched, bent, compressed in all directions.[7] Depending on the application and field, the user is able to tune the properties based on what is demanded.

Fabric embedded within PDMS. This technique enables a user to retain a thin layer of PDMS as a substrate while achieving a higher stiffness through the insertion of reinforcement.
Linear relationship in Sylgard 184 PDMS between curing temperature and Young's modulus

Overall PDMS has a low elastic modulus which enables it to be easily deformed and results in the behavior of a rubber.[8][9][10] Viscoelastic properties of PDMS can be more precisely measured using dynamic mechanical analysis. This method requires determination of the material's flow characteristics over a wide range of temperatures, flow rates, and deformations. Because of PDMS's chemical stability, it is often used as a calibration fluid for this type of experiment.

The shear modulus of PDMS varies with preparation conditions, and consequently dramatically varies in the range of 100 kPa to 3 MPa. The loss tangent is very low (tan δ ≪ 0.001).[10]

Chemical compatibility

PDMS is hydrophobic.[6] Plasma oxidation can be used to alter the surface chemistry, adding silanol (SiOH) groups to the surface. Atmospheric air plasma and argon plasma will work for this application. This treatment renders the PDMS surface hydrophilic, allowing water to wet it. The oxidized surface can be further functionalized by reaction with trichlorosilanes. After a certain amount of time, recovery of the surface's hydrophobicity is inevitable, regardless of whether the surrounding medium is vacuum, air, or water; the oxidized surface is stable in air for about 30 minutes.[11] Alternatively, for applications where long-term hydrophilicity is a requirement, techniques such as hydrophilic polymer grafting, surface nanostructuring, and dynamic surface modification with embedded surfactants can be of use. [12]

Solid PDMS samples (whether surface-oxidized or not) will not allow aqueous solvents to infiltrate and swell the material. Thus PDMS structures can be used in combination with water and alcohol solvents without material deformation. However most organic solvents will diffuse into the material and cause it to swell.[6] Despite this, some organic solvents lead to sufficiently small swelling that they can be used with PDMS, for instance within the channels of PDMS microfluidic devices. The swelling ratio is roughly inversely related to the solubility parameter of the solvent. Diisopropylamine swells PDMS to the greatest extent; solvents such as chloroform, ether, and THF swell the material to a large extent. Solvents such as acetone, 1-propanol, and pyridine swell the material to a small extent. Alcohols and polar solvents such as methanol, glycerol and water do not swell the material appreciably.[13]

Applications

Surfactants and antifoaming agents

PDMS is a common surfactant and is a component of defoamers.[14] PDMS, in a modified form, is used as an herbicide penetrant[15] and is a critical ingredient in water-repelling coatings, such as Rain-X.[16]

Dimethicone is also the active silicone fluid in automotive viscous limited slip differentials and couplings. This is usually a non-serviceable OEM component but can be replaced with mixed performance results due to variances in effectiveness caused by refill weights or non-standard pressurizations.

Soft lithography

PDMS is commonly used as a stamp resin in the procedure of soft lithography, making it one of the most common materials used for flow delivery in microfluidics chips.[17] The process of soft lithography consists of creating an elastic stamp, which enables the transfer of patterns of only a few nanometers in size onto glass, silicon or polymer surfaces. With this type of technique, it is possible to produce devices that can be used in the areas of optic telecommunications or biomedical research. The stamp is produced from the normal techniques of photolithography or electron-beam lithography. The resolution depends on the mask used and can reach 6 nm.[18]

In biomedical (or biological) microelectromechanical systems (bio-MEMS), soft lithography is used extensively for microfluidics in both organic and inorganic contexts. Silicon wafers are used to design channels, and PDMS is then poured over these wafers and left to harden. When removed, even the smallest of details is left imprinted in the PDMS. With this particular PDMS block, hydrophilic surface modification is conducted using plasma etching techniques. Plasma treatment disrupts surface silicon-oxygen bonds, and a plasma-treated glass slide is usually placed on the activated side of the PDMS (the plasma-treated, now hydrophilic side with imprints). Once activation wears off and bonds begin to reform, silicon-oxygen bonds are formed between the surface atoms of the glass and the surface atoms of the PDMS, and the slide becomes permanently sealed to the PDMS, thus creating a waterproof channel. With these devices, researchers can utilize various surface chemistry techniques for different functions creating unique lab-on-a-chip devices for rapid parallel testing.[5] PDMS can be cross-linked into networks and is a commonly used system for studying the elasticity of polymer networks. PDMS can be directly patterned by surface-charge lithography.[19]

PDMS is being used in the making of synthetic gecko adhesion dry adhesive materials, to date only in laboratory test quantities.[20]

Some flexible electronics researchers use PDMS because of its low cost, easy fabrication, flexibility, and optical transparency.[21]

Stereo lithography

In stereo lithography (SLA) 3D printing, light is projected onto photocuring resin to selectively cure it. Some types of SLA printer are cured from the bottom of the tank of resin and therefore require the growing model to be peeled away from the base in order for each printed layer to be supplied with a fresh film of uncured resin. A PDMS layer at the bottom of the tank assists this process by absorbing oxygen : the presence of oxygen adjacent to the resin prevents it adhering to the PDMS, and the optically clear PDMS permits the projected image to pass through to the resin undistorted.

Medicine and cosmetics

Activated dimethicone, a mixture of polydimethylsiloxanes and silicon dioxide (sometimes called simethicone), is often used in over-the-counter drugs as an antifoaming agent and carminative.[22][23] It has also been at least proposed for use in contact lenses.[24]

Silicone breast implants are made out of a PDMS elastomer shell, to which fumed amorphous silica is added, encasing PDMS gel or saline solution. [25]

In addition, PDMS is useful as a lice or flea treatment because of its ability to trap insects.[26] It also works as a moisturizer that is lighter and more breathable than typical oils.

Skin

PDMS is used variously in the cosmetic and consumer product industry as well. For example, PDMS can be used in the treatment of head lice on the scalp[26] and dimethicone is used widely in skin-moisturizing lotions where it is listed as an active ingredient whose purpose is "skin protection." Some cosmetic formulations use dimethicone and related siloxane polymers in concentrations of use up to 15%. The Cosmetic Ingredient Review's (CIR) Expert Panel, has concluded that dimethicone and related polymers are "safe as used in cosmetic formulations."[27]

Hair

PDMS compounds such as amodimethicone, are effective conditioners when formulated to consist of small particles and be soluble in water or alcohol/act as surfactants[28][29] (especially for damaged hair[30]), and are even more conditioning to the hair than common dimethicone and/or dimethicone copolyols.[31]

Contact Lenses

A proposed use of PDMS is contact lens cleaning. Its physical properties of low elastic modulus and hydrophobicity have been used to clean micro and nano pollutants from contact lens surfaces more effectively than multipurpose solution and finger rubbing; the researchers involved call the technique PoPPR (polymer on polymer pollution removal) and note that it is highly effective at removing nanoplastic that has adhered to lenses.[32]

Flea treatment for pets

Dimethicone is the active ingredient in a liquid applied to the back of the neck of a cat or dog from a small one time use dose disposable pipette. The parasite becomes trapped and immoblised in the substance and thus breaks the life cycle of the insect.

Foods

PDMS is added to many cooking oils (as an antifoaming agent) to prevent oil splatter during the cooking process. As a result of this, PDMS can be found in trace quantities in many fast food items such as McDonald's Chicken McNuggets, french fries, hash browns, milkshakes and smoothies[33] and Wendy's french fries.[34]

Under European food additive regulations, it is listed as E900.

Condom lubricant

PDMS is widely used as a condom lubricant.[35][36]

Domestic and niche uses

Many people are indirectly familiar with PDMS because it is an important component in Silly Putty, to which PDMS imparts its characteristic viscoelastic properties.[37] Another toy PDMS is used in is Kinetic Sand. The rubbery, vinegary-smelling silicone caulks, adhesives, and aquarium sealants are also well-known. PDMS is also used as a component in silicone grease and other silicone based lubricants, as well as in defoaming agents, mold release agents, damping fluids, heat transfer fluids, polishes, cosmetics, hair conditioners and other applications. PDMS has also been used as a filler fluid in breast implants.

It can be used as a sorbent for the analysis of headspace (dissolved gas analysis) of food.[38]

Safety and environmental considerations

According to Ullmann's Encyclopedia, no "marked harmful effects on organisms in the environment" have been noted for siloxanes. PDMS is nonbiodegradable, but is absorbed in waste water treatment facilities. Its degradation is catalyzed by various clays.[39]

See also

References
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  2. Wolf, M.P., G.B. Salieb-Beugelaar, and P. Hunziker, PDMS with designer functionalities-Properties, modifications strategies, and applications. Progress in Polymer Science, 2018. 83: p. 97-134 https://doi.org/10.1016/j.progpolymsci.2018.06.001
  3. Mark, J. E.; Allcock, H. R.; West, R. “Inorganic Polymers” Prentice Hall, Englewood, NJ: 1992. ISBN 0-13-465881-7.
  4. Courtney, Thomas H. (2013). Mechanical Behavior of Materials. McGraw Hill Education (India). ISBN 978-1259027512. OCLC 929663641.
  5. Rogers, J. A.; Nuzzo, R. G. (2005). "Recent progress in Soft Lithography. In". Materials Today. 8 (2): 50–56. doi:10.1016/S1369-7021(05)00702-9.
  6. McDonald, J. C.; Duffy, D. C.; Anderson, J. R.; Chiu, D. T.; Wu, H.; Schueller, O. J. A.; Whitesides, G. M. (2000). "Fabrication of microfluidic systems in poly(dimethylsiloxane)". Electrophoresis. 21 (1): 27–40. doi:10.1002/(SICI)1522-2683(20000101)21:1<27::AID-ELPS27>3.0.CO;2-C. PMID 10634468.
  7. Wang, Zhixin (2011). Polydimethylsiloxane Mechanical Properties Measured by Macroscopic Compression and Nanoindentation Techniques. OCLC 778367553.
  8. Johnston, I. D.; McCluskey, D. K.; Tan, C. K. L.; Tracey, M. C. (2014-02-28). "Mechanical characterization of bulk Sylgard 184 for microfluidics and microengineering". Journal of Micromechanics and Microengineering. 24 (3): 035017. Bibcode:2014JMiMi..24c5017J. doi:10.1088/0960-1317/24/3/035017. ISSN 0960-1317.
  9. Liu, Miao; Sun, Jianren; Sun, Ying; Bock, Christopher; Chen, Quanfang (2009-02-23). "Thickness-dependent mechanical properties of polydimethylsiloxane membranes". Journal of Micromechanics and Microengineering. 19 (3): 035028. Bibcode:2009JMiMi..19c5028L. doi:10.1088/0960-1317/19/3/035028. ISSN 0960-1317.
  10. Lotters, J. C.; Olthuis, W.; Veltink, P. H.; Bergveld, P. (1997). "The mechanical properties of the rubber elastic polymer polydimethylsiloxane for sensor applications". J. Micromech. Microeng. 7 (3): 145–147. Bibcode:1997JMiMi...7..145L. doi:10.1088/0960-1317/7/3/017.
  11. H. Hillborg; J. F. Ankner; U. W. Gedde; G. D. Smith; H. K. Yasuda; K. Wikstrom (2000). "Crosslinked polydimethylsiloxane exposed to oxygen plasma studied by neutron reflectometry and other surface specific techniques". Polymer. 41 (18): 6851–6863. doi:10.1016/S0032-3861(00)00039-2.
  12. O'Brien, Daniel Joseph; Sedlack, Andrew J. H.; Bhatia, Pia; Jensen, Christopher J.; Quintana-Puebla, Alberto; Paranjape, Makarand (2020). "Systematic Characterization of Hydrophilized Polydimethylsiloxane". Journal of Microelectromechanical Systems: 1–9. arXiv:2007.09138. doi:10.1109/JMEMS.2020.3010087. ISSN 1057-7157. S2CID 220633559.
  13. Lee, J. N.; Park, C.; Whitesides, G. M. (2003). "Solvent Compatibility of Poly(dimethylsiloxane)-Based Microfluidic Devices". Anal. Chem. 75 (23): 6544–6554. doi:10.1021/ac0346712. PMID 14640726.
  14. Rainer Höfer, Franz Jost, Milan J. Schwuger, Rolf Scharf, Jürgen Geke, Josef Kresse, Herbert Lingmann, Rudolf Veitenhansl, Werner Erwied (2000). "Foams and Foam Control". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_465.CS1 maint: multiple names: authors list (link)
  15. "Pulse Penetrant". Archived from the original on February 20, 2012. Retrieved 3 March 2009.
  16. Rain X The Invisible Windshield Wiper. householdproducts.nlm.nih.gov
  17. PDMS in microfluidics : a review and tutorial. elveflow.com
  18. Waldner, Jean-Baptiste (2008). Nanocomputers and Swarm Intelligence. London: John Wiley & Sons. pp. 92–93. ISBN 978-1-84704-002-2.
  19. S. Grilli; V. Vespini; P. Ferraro (2008). "Surface-charge lithography for direct pdms micro-patterning". Langmuir. 24 (23): 13262–13265. doi:10.1021/la803046j. PMID 18986187.
  20. Inspired by Gecko Feet, UMass Amherst Scientists Invent Super-Adhesive Material Archived 2012-02-23 at the Wayback Machine. 16 Feb 2012, UMass Press Release
  21. Zhang, B.; Dong, Q.; Korman, C. E.; Li, Z.; Zaghloul, M. E. (2013). "Flexible packaging of solid-state integrated circuit chips with elastomeric microfluidics". Scientific Reports. 3: 1098. Bibcode:2013NatSR...3E1098Z. doi:10.1038/srep01098. PMC 3551231.
  22. Prentice, William E. & Voight, Michael L. (2001). Techniques in musculoskeletal rehabilitation. McGraw-Hill Professional. p. 369. ISBN 978-0-07-135498-1.
  23. Hunt, Richard H.; Tytgat, G. N. J. & Pharma, Axcan (1998). Helicobacter Pylori: Basic Mechanisms to Clinical Cure 1998. Springer. p. 447. ISBN 978-0-7923-8739-8.
  24. Horn, Gerald. "Silicone polymer contact lens compositions and methods of use Patent US 20050288196". Retrieved 17 July 2015.
  25. Evaluation of sustained release of antisense oligonucleotide from poly DL (lactide-co-glycolide) microspheres targeting fibrotic growth factors CTGF and TGF-β1 (PDF).
  26. Burgess, Ian F. (2009). "The mode of action of dimeticone 4% lotion against head lice, Pediculus capitis". BMC Pharmacology. 9: 3. doi:10.1186/1471-2210-9-3. PMC 2652450. PMID 19232080.
  27. Nair, B; Cosmetic Ingredients Review Expert Panel (2003). "Final Report on the Safety Assessment of Stearoxy Dimethicone, Dimethicone, Methicone, Amino Bispropyl Dimethicone, Aminopropyl Dimethicone, Amodimethicone, Amodimethicone Hydroxystearate, Behenoxy Dimethicone, C24-28 Alkyl Methicone, C30-45 Alkyl Methicone, C30-45 Alkyl Dimethicone, Cetearyl Methicone, Cetyl Dimethicone, Dimethoxysilyl Ethylenediaminopropyl Dimethicone, Hexyl Methicone, Hydroxypropyldimethicone, Stearamidopropyl Dimethicone, Stearyl Dimethicone, Stearyl Methicone, and Vinyldimethicone". International Journal of Toxicology. 22 (2 Suppl): 11–35. doi:10.1177/1091581803022S204. PMID 14555417.
  28. Schueller, Randy; Romanowski, Perry (1999). Conditioning Agents for Hair and Skin. CRC Press. p. 273. ISBN 978-0-8247-1921-0. Amodimethicone is recognized for its extremely robust conditioning and for its ability to form clear products when used in high-surfactant shampoos. Amodimethicone is a useful ingredient in conditioners, gels, mousses, and permanents, but its use in shampoos has proved troublesome due to interactions between the cationic and the anionic surfactants, which can result in compatibility problems. However, the amodimethicone emulsion can be made compatible in high-surfactant-level shampoos
  29. Goddard, E. Desmond; Gruber, James V. (1999). Principles of Polymer Science and Technology in Cosmetics and Personal Care. CRC Press. p. 299. ISBN 978-0-8247-1923-4. Amodimethicone is typically an emulsion-polymerized polymer; however, utilizing linear processing technology amodimethicone fluids may be prepared as neat fluids, and then emulsified by a mechanical process as desired. The most widely utilized amodimethicone emulsions contain as the surfactant pair either (1) tallowtrimonium chloride (and) nonoxy- nol-10, or (2) cetrimonium chloride (and) trideceth-10 or -12. These "uncapped" amino- functional silicone compounds may be characterized by a linear or branched structure. In either case, amodimethicone polymers will undergo a condensation cure reaction during drying to form a somewhat durable elastomeric film on the hair, providing wet- and dry- combing benefits, lowering triboelectric charging effects, and increasing softness of the dry hair. They are excellent conditioning agents, often found in conditioners, mousses, setting lotions, and less frequently in 2-in-1 shampoos
  30. Iwata, Hiroshi (2012). Formulas, Ingredients and Production of Cosmetics: Technology of Skin- and Hair-Care Products in Japan. Springer Science & Business Media. p. 144. ISBN 978-4-431-54060-1. Amodimethicone is the most widely used amino-modified silicone. It has an aminopropyl group attached to the methyl group of Dimethicone. Amodimethicone of various degrees of amino modification are available as well as those that have POP, POE, or an alkyl group attached. Amino-modified silicones are cationic and affinitive to hair keratin. They are particularly highly affinitive to damaged hair, which is anionic due to the presence of cysteic acid
  31. Barel, André O.; Paye, Marc; Maibach, Howard I. (2014). Handbook of Cosmetic Science and Technology, Fourth Edition. CRC Press. p. 567. ISBN 978-1-84214-564-7. ...and amodimethicone, which is an amino-substituted silicone and silicone quats, which contain permanently quaternized ammonium groups. In general, amodimethicones and silicone quats condition better than dimethicones, which condition better than dimethicone copolyols
  32. Burgener, Katherine; Bhamla, M. Saad (2020-05-19). "A polymer-based technique to remove pollutants from soft contact lenses". Contact Lens and Anterior Eye. arXiv:2005.08732. doi:10.1016/j.clae.2020.05.004. ISSN 1367-0484.
  33. "McDonald's Food Facts: Ingredients" (PDF). McDonald's Restaurants of Canada Limited. 2013-09-08. p. 13.
  34. "Wendy's: Menu: French Fries". Wendy's International, Inc.
  35. Coyle, Tiernan; Anwar, Naveed (2009). "A novel approach to condom lubricant analysis: In-situ analysis of swabs by FT-Raman Spectroscopy and its effects on DNA analysis". Science & Justice. 49 (1): 32–40. doi:10.1016/j.scijus.2008.04.003. PMID 19418926.
  36. Blackledge, R. D.; Vincenti, M. (1994). "Identification of polydimethylsiloxane lubricant traces from latex condoms in cases of sexual assault". Journal of the Forensic Science Society. 34 (4): 245–256. doi:10.1016/s0015-7368(94)72928-5. PMID 7844517.
  37. Micro Total Analysis Systems, Silly Putty, and Fluorous Peptides. fluorous.com. January 18, 2008
  38. Bicchi, C.; Iori, C.; Rubiolo, P.; Sandra, P. (2002). "Headspace Sorptive Extraction (HSSE), Stir Bar Sorptive Extraction (SBSE), and Solid Phase Microextraction (SPME) Applied to the Analysis of Roasted Arabica Coffee and Coffee Brew". Journal of Agricultural and Food Chemistry. 50 (3): 449–59. doi:10.1021/jf010877x. PMID 11804511.
  39. Moretto, Hans-Heinrich; Schulze, Manfred and Wagner, Gebhard (2005) "Silicones" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. doi:10.1002/14356007.a24_057
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