Difference between revisions of "What is soft matter"

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====Aggregates====
 
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Aggregation occurs between colloidal particles in a fluid when the particles have a strong enough attraction to permanently attach to one another. Aggregated colloids are known to increase the viscosity of the fluid through the same methods as dispersed colloids and through a different mechanism called screening. When a fluid with aggregates is subjected to shear flow the aggregates screens the fluid or forces the fluid to go around the aggregate therefore increasing the viscosity of the fluid.
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Aggregation occurs between colloidal particles in a fluid when the particles have a strong enough attraction to permanently attach to one another. Aggregated colloids are known to increase the viscosity of the fluid through the same methods as dispersed colloids and through a different mechanism called screening. When a fluid with aggregates is subjected to shear flow the aggregates screens the fluid or forces the fluid to go around the aggregate therefore increasing the viscosity of the fluid. This is due to their fractal structure.
  
 
====Polymers====
 
====Polymers====

Revision as of 16:08, 22 September 2008

Back to Topics.

Structured and fluid

In a few words, soft matter is:

  • Things that don’t hurt your hand when you hit them.
  • Synonymous with “complex fluids”
  • Examples: hair gel, mayonnaise, shaving cream, colloidal crystals, polymer solutions and blends

The amazing properties of soft materials come from their a 'subtle balance' between energy and entropy which leads to rich phase behavior and spontaneous (and often surprising) complexity (Jones 2002). They are considered 'structured fluids' because they have the local mobility of liquids, but their constituents are polyatomic structures.

Macosko Fig 5-3-3.gif Homberg Fig 2-1.gif Weitz 339-60-1989.png
Macosko Fig. 5-3-3 Homberg Fig. 2.1 Weitz Nature 339,60,1989.

Comments on Figures: Elaborate HERE!

The image on the left demonstrates the "Weissenberg effect". A rod is ratated at a speed of 20<math>pi</math>/s in Oil(a) and Polyisobutylene(PIB)(b). Picture(a) shows what is observed for a simple Newtonian fluid where centrifugal forces created by rotating the rod deplete fluid from the region immediately adjacent to it and create a vortex in the liquid near the rod. Picture (b), on the other hand, the polymer solution is drawn towards the rod and climbs up. This is a typical elastic fluid response which rises from the existence of normal stress differences in shear, in other words, entanglements of long-chained polymers. (Rodriguez, Cohen, Ober, Archer, Principles of Polymer Systems 5ed,Taylor&Francis)

The image on the right shows transmission electron micrographs of clusters of gold, silica and polystyrene. The left column is showing structures in DLCA regime (diffusion-limited colloid aggregation), whereas the right one shows structures in RLCA regime (reaction-limited colloid aggregation). “Diffusion-limited colloid aggregation occurs when there is negligible repulsive force between the colloidal particles, so that the aggregation rate is limited solely by the time taken for clusters to encounter each other by diffusion. Reaction-limited colloid aggregation occurs when there is still a substantial, but not insurmountable repulsive force between the particles, so that the aggregation rate is limited by the time taken for two clusters to overcome this repulsive barrier by thermal activation” (Weitz, Nature 1989). The structures are fractal in both DLCA and RLCA, which means that mass scales proportional to (r/a)^4, where r is radius of gyration and a is radius of particles in the structure. DCLA clusters tend to be more open and thin, understandable considering their fractal dimension is below 2. On the other hand RLCA clusters appear to be more compact with fractal dimension above 2. Still, resemblance between different structures in the same regime is remarkable.


Classes of Structured Fluids

Colloids

Witten states:

The interaction energy of two colloidal particles in a given solvent is also magnified because of their bulk. Consequently, small changes in the solvent can have a large effect on the interaction energy. This makes it possible to change the interaction between two colloidal particles abruptly from an effective hard-core repulsion to an attraction whose strength is many times the thermal energy kbT. With such an attraction the particles must stick together when they encounter each other. The particles flocculate or precipitate

Does anyone know if this process is reversible? or will the particles typically remained clumped despite reversing the changes in the solvent.

The reason that the colloids flocculate is due to the Van der Waals forces that now allow them to stick together (http://en.wikipedia.org/wiki/Colloid). I would imagine that simply changing the solvent will not weaken these forces (once the colloids were allowed to interact). The only way to deflocculate the suspension would be to mechanically agitate it.

Aggregates

Aggregation occurs between colloidal particles in a fluid when the particles have a strong enough attraction to permanently attach to one another. Aggregated colloids are known to increase the viscosity of the fluid through the same methods as dispersed colloids and through a different mechanism called screening. When a fluid with aggregates is subjected to shear flow the aggregates screens the fluid or forces the fluid to go around the aggregate therefore increasing the viscosity of the fluid. This is due to their fractal structure.

Polymers

The word "Polymer" is originally Greek. Poly means 'many' and mer comes from merous which roughly means 'parts'.

Polymers are large molecules with Molecular Weights that are high enough to allow for chain entanglements. Typically, Molecular Weight of polymer is greater than 5000 g/mole. These materials may be organic, inorganic, or organometallic, and synthetic or natural in origin. Polymers are essential materials for almost every industry as adhesives, building materials, paper, cloths, fibers, coatings, plastics, ceramics, concretes, liquid crystals, photoresists, and coatings. Natural inorganic polymers include diamonds, graphite, sand, asbestos, agates, chert, feldspars, mica, quartz, and talc.

Natural organic polymers include polysaccharides (or polycarbohydrates) such as starch and cellulose, nucleic acids, and proteins. Synthetic inorganic polymers include boron nitride, concrete, many high-temperature superconductors, and a number of glasses. Siloxanes or polysiloxanes represent synthetic organometallic polymers. See also Silicone resins.

Synthetic polymers used for structural components weigh considerably less than metals, helping to reduce the consumption of fuel in vehicles and aircraft. They even outperform most metals when measured on a strength-per-weight basis. Polymers have been developed which can also be used for engineering purposes such as gears, bearings, and structural members.


Single Polymer Chains AFM.jpg

This is how real linear polymer chains "look" like as recorded using an atomic force microscope under liquid medium. Chain thickness is 0.4 nm. (Attribution should be given to the work: Y. Roiter and S. Minko)


Thermal Transition

Thermal trans.gif (http://www.uwsp.edu/chemistry/polyed/images/thermal_trans.gif)

In the solid state many polymers are amorphous rather than crystalline. However, many polymers, especially those high ordered structures do crystallize. These polymers are known as semi-crystalline materials, because typically only part of the macromolecular chain is involved in crystallization. The glass transition temperature (Tg) is the temperature at which an amorphous polymer undergoes a change from a rigid solid to a more flexible rubbery material. This temperature marks the onset of segmental motion in amorphous polymer samples. In semi-crystalline polymers, both the glass and malt transition temperature (Tm) may be observed since both amorphous and crystalline domain exist in the polymer structure. In this material, the glass transition temperature lies below the melt transition temperature. Another important thermal transition in semi-crystalline polymers is the crystalline transition temperature (Tc). This is the temperature at which the polymer sample undergoes crystallization. This crystallization happens between the glass and the melt transition temperature.

Surfactant assemblies

Associated structures

Witten: Association is a temporary joining together of the structures. The structure thus joined can transmit forces and thus alter mechanical properties strongly, but at the same time they are weak enough to break and reform over the time of an experiment. Thus the associations alter themselves in response to the local stress or flow in the liquid. Typical examples are micelles. Gk2x20.gif



Properties of soft matter

  • Viscoelasticity

Some materials exhibit properties of both elastic and viscous materials. When strain is applied to viscoelastic material, its viscosity results in a strain rate that depends on time. However, one the strain is removed, the material will slowly return to its original configuration. Examples of such materials include amorphous polymers, semicrystalline polymers, and biopolymers.

  • Turbidity/opacity

Turbidity is the cloudiness or haziness of a liquid due to particles suspended in the liquid. Turbidity is one of the many standards placed upon drinking water in the USA. The upper limit on turbidity for drinking water is 0.3 NTU or Nephelometric Turbidity Units measured by a nephlometer. Fun names!

  • Irreversible fragility

When you say irreversible fragility, do you mean a form of hysteresis? If so, there is some interesting mention of some of the thermodynamically irreversible propoerties found in surface interactions in Israelachvili's book (like with adhesion on p 323). --BPappas 05:12, 22 September 2008 (UTC)

  • Temperature sensitivity


Indian boot - de Gennes 1996.gif 2500 years ago, South American Indians take sap from a hevea tree, cover their feet, wait about 20 minutes, and a pair of boots is created. The latex is crosslinked by oxidation only, so is weak. In 1830 Charles Goodyear decides to boil the hevea latex with sulfur (heaven only knows why), the crosslinking is much, much better, and eventually the radial tire is created. (de Gennes, 1996, p.4)
Video: Cholesteric Liquid Crystals Changing Color responding to changes in temperature. [1]

Length scales and order

When studying soft matter, it is important to be aware of the length scales which control the macroscopic behavior. Jones (Soft Condensed Matter, 2002) points out that the length scales of soft condensed matter fall in between atomic and macroscopic scales. This makes course-grained models appropriate for studying these materials. Such models focus on the topological features of the system, rather than specific details of the chemistry. Despite the mesoscopic length scales, fluctuations from Brownian motion are still important; typical bond energies are on the order of thermal energies (kT).

Polymers in solution.png Surfactants in solution.png Particles in dispersion.png
Polymers in solution Surfactant solutions Particle dispersions

Comments:




De Gennes 1997 p 29.gif De Gennes 1997 Fig 1-1.gif De Gennes 1997 Fig III-3.gif
Structure and size, de Gennes, 1997, p.29 Motion and size, de Gennes,1997, Fig I-1 Structure and concentration, de Gennes, 1993, Fig. III-1
Fractals Random walk eqn.png Polymer cStar eqn.png

Comments:






Ink making for soft matter physicists

Soot - de Gennes 1996.gif Poor dispersion - de Gennes 1996.gif Good dispersion - de Gennes 1996.gif
de Gennes, 1996, p.29

If you think this is primitive, check out how newpaper ink is make.

Most newspapers in the United States now use soy based inks rather than petroleum based inks. Since these inks take a longer time to dry than other types of ink, typically they are used on papers that absorb most of the ink. When a person reads a newspaper, the ink has often not yet dried and will still rub off on their hands. Until recently, all soy-based inks still contained some petroleum resin. One recently patented ink does not contain any soy. I cannot find any information on what the challenges were production and chemical-wise for switching entirely from petroleum. Does anyone know why petroleum products (especially resins) were still needed in the soy-based inks?

Comment: Apparently the main problem with soy-only inks is that they do not dry and harden properly, and that the only way to produce a soy-only ink would be to use oxidative polymerization of the unsaturated fatty acids contained in the soy oil. This does not produce as absorbent or as spreadable an ink as is needed for paper production today, but according to this piece (I just put the HTML version here, not the pdf), almost all inks were vegetable-only before the 1950s. In order for the ink to harden using today's printing techniques like heatset, there needs to be a resin present. Also, some papers won't absorb the soy oil if they are not porous enough, and thus need lower viscosity petroleum additives to draw the ink into the printing material [2] --BPappas 04:58, 22 September 2008 (UTC)


This is a quote from a US department of agriculture document on the relative benefits of soy verses petroleum inks: "The newspaper industry is a large user of soy inks. Soy inks account for more than 90 percent of all colored inks and about one-third of black inks used by U.S. newspapers. Soy inks produce better colors and provide greater clarity with reduced rub-off on readers' hands. The lighter color of soybean oil makes it ideal for color inks because the true color of the pigments can show through. Newspaper pictures are composed ofa pattern of dots, which with petroleum-based inks increase in size during the press run, reducing the clarity of the picture. With soy inks, the dots remain relatively the same size, keeping picture clarity constant throughout the press run. Moreover,soy inks can be used for printing newspapers without a change in equipment or printing methods. Soy ink has been found to be a better carrier of pigments, driers, and other agents than other ink vehicles, which can result in less press time, lower cost, and higher quality results." (http://www.bioplastic.org/industrial-use-1997.html)

(http://en.wikipedia.org/wiki/Soy_ink, http://pubs.acs.org/cen/whatstuff/stuff/7646scit2.html)





Soft matter - Ice cream!

Plain frozen cream is as hard as rock, but the micro-scale structure of ice cream turns it into a wonderful dessert. Ice cream is a three phase mixture of pure water crystals, concentrated cream and sugar, and air pockets. The cream solution can remain liquid, since the sugar lowers the freezing point below 0 C. It coats each of the millions of ice crystals and lightly binds them together. The texture of ice cream is further improved by air pockets introduced during mixing. These air pockets are stabilized by fat molecules from the cream. The air weakens the network of crystals and cream, making the ice cream easier to serve and to eat. Several variations of ice cream have evolved over the centuries. American ice cream traditionally uses a combination of milk and cream, whereas French ice cream uses lower-fat milk, with egg yolks as a stabilizer. Italian gelato also uses egg yolks, but contains less air, resulting in a denser product. Low-fat ice cream utilizes additives such as corn syrup, powdered milk, and vegetable gums. Indian kulfi is based on a recipe from the 16th century, in which milk is boiled down to concentrate the proteins and sugar, then frozen without stirring.
Ice cream - Hamley.gif TEM of a typial ice-cream. (a) Ice crystals, average size 50 nm, (b) air cells, average size 100-200 mm, (c) unfrozen material. (W.S. Arbuckle, Ice Cream, 2nd ed., Avi Publishing, 1972. also, Hamley, Fig. 3.20)
For more information about ice cream, see On Food and Cooking, 2nd ed., Scribner, 2004. by Harold McGee (pp. 39-45), from which this section is based.




From great biology to great physics

Connect these scientists:

  • Thomas Graham (1805-1869)
  • Robert Brown (1773-1858)
  • Michael Faraday (1791-1867)
  • Ludwig Boltzmann (1844-1906)
  • Albert Einstein (1897-1955)
  • Jean Perrin (1870-1942)

Hint: Size dependence of diffusion




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