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| Polydimethylsiloxane | |
|---|---|
|
IUPAC name
poly(dimethylsiloxane) |
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Other names
PDMS |
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| Identifiers | |
| CAS number | 63148-62-9 Y |
| UNII | 92RU3N3Y1O Y |
| ATC code | P03AX05 |
| Properties | |
| Molecular formula | (C2H6OSi)n |
| Density | 965 kg m−3 |
| Melting point | N/A (vitrifies) |
| Boiling point | N/A (vitrifies) |
| Hazards | |
| NFPA 704 |
1
2
0
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| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Y (verify) (what is: Y/N?) | |
| Infobox references | |
Polydimethylsiloxane (PDMS) 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, and 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 also called dimethicone and 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 dimethicone makes hair shiny and slippery), food (antifoaming agent), caulking, lubricating oils, and heat-resistant tiles.
Contents
- 1 Structure
- 1.1 Branching and capping
- 2 Mechanical properties
- 3 Chemical compatibility
- 4 Applications
- 4.1 Surfactants and antifoaming agents
- 4.2 Hydraulic fluids and related applications
- 4.3 Soft lithography
- 4.4 Medicine and cosmetics
- 4.5 Foods
- 4.6 Domestic and niche uses
- 5 Safety and environmental considerations
- 6 See also
- 7 References
- 8 External links
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. Industrial synthesis can begin from dimethyldichlorosilane and water by the following net reaction:
- n Si(CH3)2Cl2 + n+1 H2O → HO[-Si(CH3)2O-]n H + 2n HCl
The polymerization reaction evolves hydrogen chloride. 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 two 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. http://pubs.acs.org/doi/abs/10.1021/ma000635i
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
Hardened PDMS cylinder on the glass of a stereomicroscope light.
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. In other words, 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 rolled into a sphere and thrown onto the same surface (short flow time), it will bounce like a rubber ball.
Although the viscoelastic properties of PDMS can be intuitively observed using the simple experiment described above, they can be more accurately measured using dynamic mechanical analysis. This involves using a specialized instrument to determine 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, but is typically in the range of 100 kPa to 3 MPa. The loss tangent is very low (tan δ ≪ 0.001).[2]
Chemical compatibility
After polymerization and cross-linking, solid PDMS samples will present an external hydrophobic surface.[3] This surface will appear metallic and shiny, although the substrate is clear. This surface chemistry makes it difficult for polar solvents (such as water) to wet the PDMS surface, and may lead to adsorption of hydrophobic contaminants. Plasma oxidation can be used to alter the surface chemistry, adding silanol (SiOH) groups to the surface. Atmospheric air plasma & argon plasma will work for this application. This treatment renders the PDMS surface hydrophilic, allowing water to wet (this is frequently required for water-based microfluidics). The oxidized surface resists adsorption of hydrophobic and negatively charged species. The oxidized surface can be further functionalized by reaction with trichlorosilanes. Oxidized surfaces are stable for ~30 minutes in air, after a certain time hydrophobic recovery of the surface is inevitable independently of the surrounding medium whether it is vacuum, air, or water.[4]
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,[3] making them incompatible with PDMS devices. 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.[5]
Applications
Surfactants and antifoaming agents
PDMS is a common surfactant and is a component of defoamers, which are used to suppress the formation of foams.[6] PDMS in a modified form is used as an herbicidal penetrant[7] and is a critical ingredient in water-repelling coatings, such as Rain-X.
Hydraulic fluids and related applications
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 pressurisations.[citation needed]
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.[8] 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.[9]
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. Once surface bonds are disrupted, usually a piece of glass slide is placed on the activated side of the PDMS (the side with imprints). Once the bonds relax to their normal state, the glass is 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.[10] PDMS can be cross-linked into networks and is a commonly used system for studying the elasticity of polymer networks.[citation needed] PDMS can be directly patterned by surface-charge lithography.[11]
PDMS is being used in the making of synthetic Gecko adhesion dry adhesive materials, to date only in laboratory test quantities.[12]
Some flexible electronics researchers use PDMS because of its low cost, easy fabrication, flexibility, and optical transparency.[13]
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.[14][15]
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[16] 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."[17]
Foods
PDMS can be found in many cooking oils and processed foods and fast food items such as McDonald's Chicken McNuggets, McDonald's French fries, and Wendy's French fries. {http://nutrition.mcdonalds.com/getnutrition/ingredientslist.pdf}
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.[18] 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, although this practice has decreased somewhat, due to safety concerns.
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.[19]
See also
- Silicone
- Siloxanes and other organosilicon compounds
- Polymethylhydrosiloxane (PMHS)
- Silicone rubber
References
- ^ "Linear Polydimethylsiloxanes" Joint Assessment of Commodity Chemicals, September 1994 (Report No. 26) ISSN 0773-6339-26.
- ^ 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. doi:10.1088/0960-1317/7/3/017.
- ^ a b McDonald, J. C.et al. (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.
- ^ H. Hillborg, J.F. Ankner, U.W. Gedde, G.D. Smith, H.K. Yasuda and 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.
- ^ 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.
- ^ Rainer Höfer, Franz Jost, Milan J. Schwuger, Rolf Scharf, Jürgen Geke, Josef Kresse, Herbert Lingmann, Rudolf Veitenhansl and Werner Erwied "Foams and Foam Control" Ullmann's Encyclopedia of Industrial Chemistry, 2000, Wiley-VCH, Weinheim. doi:10.1002/14356007.a11_465
- ^ "Pulse Penetrant". Retrieved 3 March 2009. [dead link]
- ^ PDMS in microfluidics : a review and tutorial
- ^ Waldner, Jean-Baptiste (2008). Nanocomputers and Swarm Intelligence. London: John Wiley & Sons. pp. 92–93. ISBN 1-84704-002-0.
- ^ Rogers, J. A.; Nuzzo, R. G. (2005). "February). Recent progress in soft lithography. In". Materials today 8 (2): 50–56. doi:10.1016/S1369-7021(05)00702-9.
- ^ 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.
- ^ Inspired by Gecko Feet, UMass Amherst Scientists Invent Super-Adhesive Material. 16 Feb 2012, UMass Press Release
- ^ Bowei Zhang, Quan Dong, Can E. Korman, Zhenyu Li, and Mona E. Zaghloul. "Flexible packaging of solid-state integrated circuit chips with elastomeric microfluidics".
- ^ William E. Prentice, Michael L. Voight (2001). Techniques in musculoskeletal rehabilitation. McGraw-Hill Professional. p. 369. ISBN 0-07-135498-0.
- ^ Richard H. Hunt, G. N. J. Tytgat, Axcan Pharma (1998). Helicobacter Pylori: Basic Mechanisms to Clinical Cure 1998. Springer. p. 447. ISBN 0-7923-8739-2.
- ^ 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.
- ^ 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.
- ^ Micro Total Analysis Systems, Silly Putty, and Fluorous Peptides
- ^ Hans-Heinrich Moretto, Manfred Schulze, Gebhard Wagner, "Silicones" Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a24_057
External links
- Amodimethicone Amodimethicone structure and properties
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UpToDate Contents
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- Safety Assessment of Dimethicone Crosspolymers as Used in Cosmetics.
- Becker LC1, Bergfeld WF2, Belsito DV2, Hill RA2, Klaassen CD2, Liebler DC2, Marks JG Jr2, Shank RC2, Slaga TJ2, Snyder PW2, Andersen FA3.
- International journal of toxicology.Int J Toxicol.2014 May 26;33(2 suppl):65S-115S. [Epub ahead of print]
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