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词条 Capillary length
释义

  1. Origin

     Theoretical  Relationship with the Eötvös number  Experimental  Association with Jurin's Law  Association with a sessile droplet 

  2. History

  3. In nature

     Bubbles 

  4. See also

  5. References

The capillary length or capillary constant, is a length scaling factor that relates gravity and surface tension. It is a fundamental physical property that governs the behaviour of menisci, and is found when body forces (gravity) and surface forces (Laplace pressure) are in equilibrium.

The pressure of a static fluid does not depend on the shape, total mass or surface area of the fluid. It is directly proportional to the fluid's specific weight, - the force exerted by gravity over a specific volume, and it's vertical height. However, a fluid also experiences pressure that is induced by surface tension, commonly referred to as the Young-Laplace pressure.[1] Surface tension originates from cohesive forces between molecules, and in the bulk of the fluid, molecules experience attractive forces from all directions. The surface of a fluid is curved because exposed molecules on the surface have fewer neighbouring interactions, resulting in an net force that contracts the surface. There exists a pressure difference either side of this curvature, and when this balances out the pressure due to gravity, one can rearrange to find the capillary length.[2]

In the case of a fluid-fluid interface, for example a drop of water immersed in another liquid, the capillary length denoted or is most commonly given by the formula,

,

where is the surface tension of the fluid interface, is the gravitational acceleration and is the mass density difference of the fluids. The capillary length is sometimes denoted in relation to the mathetical notation for curvature. The term capillary constant is somewhat misleading, because it is important to recognise that is a composition of variable quantities, for example the value of surface tension will vary with temperature and the density difference will change depending on the fluids involved at an interface interaction. However if these conditions are known, the capillary length can be considered a constant for any given liquid, and be used in numerous fluid mechanical problems to scale the derived equations such that they are valid for any fluid.[3] For molecular fluids, the interfacial tensions and density differences are typically of the order of mN m-1 and g mL-1 respectively resulting in a capillary length of mm for water and air at room temperature on earth.[4] On the other hand, the capillary length would be mm for water-air on the moon. For a soap bubble, the surface tension must be divided by the mean thickness, resulting in a capillary length of about metres in air![5] The equation for can also be found with an extra term, most often used when normalising the capillary height.[6]

Origin

Theoretical

One way to theoretically derive the capillary length, is to imagine a liquid droplet at the point where surface tension balances gravity. If the droplet has an area of and a side length of ,

The characteristic Laplace pressure is:

,

where the capillary length is a magnitude of order estimate, and is surface tension. The pressure due to gravity is:

,

where is the force due gravity- (the fluids weight ), and is the area upon which the force is distributed.

With the mass and area:

and ,

.

At the point where the Laplace pressure balances out the pressure due to gravity, equivalent to

.

Relationship with the Eötvös number

We can use the above derivation when dealing with the Eötvös number, a dimensionless quantity that represents the ratio between the buoyancy forces and surface tension of the liquid. Despite being introduced by Loránd Eötvös in 1886, he has since become fairly dissociated with it, being replaced with Wilfrid Noel Bond such that it is now referred to as the Bond number in recent literature.

The Bond number can be written such that it includes a characteristic length- normally the radius of curvature of a liquid, and the capillary length[7]

,

with parameters defined above, and the radius of curvature.

Therefore we can write the bond number as

,

with the capillary length.

If the bond number is set to 1, then the characteristic length is the capillary length

Experimental

The capillary length can also be found through the manipulation of many different physical phenomenon. One method is to focus on capillary action, which is the attraction of a liquids surface to a surrounding solid.[8]

Association with Jurin's Law

Jurin's law is a quantitative law that shows that the maximum height that can be achieved by a liquid in a capillary tube is inversely proportional to the diameter of the tube. The law can be illustrated mathematically during capillary uplift, which is a traditional experiment measuring the height of a liquid in a capillary tube. When a capillary tube is inserted into a liquid, the liquid will rise or fall in the tube, due to an imbalance in pressure. The characteristic height is the distance from the bottom of the meniscus to the base, and exists when the Laplace pressure and the pressure due to gravity are balanced. One can reorganise to show the capillary length as a function of surface tension and gravity.

,

with the height of the liquid, the radius of the capillary tube, and the contact angle.

The contact angle is defined as the angle formed by the intersection of the liquid-solid interface and the liquid-vapour interface.[2] The size of the angle quantifies the wetability of liquid, i.e the interaction between the liquid and solid surface. Here we will consider a contact angle of , perfect wetting.

.

Thus the forms a cyclical 3 factor equation with .

This property is usually used by physicists to estimate the height a liquid will rise in a particular capillary tube, radius known, without the need for an experiment. When the characteristic height of the liquid is sufficiently less than the capillary length, then the effect of hydrostatic pressure due to gravity can be neglected.[9]

Using the same premises of capillary rise, one can find the capillary length as a function of the volume increase, and wetting perimeter of the capillary walls [11].

Association with a sessile droplet

{{See also|Sessile drop technique}}

Another way to find the capillary length is using different pressure points inside a sessile droplet, with each point having a radii of curvature, and equate them to the Laplace pressure equation. This time the equation is solved for the height of the meniscus level which again can be used to give the capillary length.

The shape of a sessile droplet is directly proportional to whether the radius is greater than or less than the capillary length. Microdrops are droplets with radius smaller than the capillary length, and their shape is governed solely by surface tension, forming a spherical cap shape. If a droplet has a radii larger than the capillary length, they are known as macrodrops and the gravitational forces will dominate. Macrodrops will be 'flattened' by gravity and the height of the droplet will be reduced.[10]

History

The investigations in capillarity stem back as far as Leonardo da Vinci, however the idea of capillary length wasn't developed until much later. Fundamentally the capillary length is a product of the work of Thomas Young and Pierre Laplace. They both appreciated that surface tension arose from cohesive forces between particles and that the shape of a liquid's surface reflected the short range of these forces. At the turn of the 19th century they independently derived pressure equations, but due to notation and presentation, Laplace often gets the credit. The equation showed that the pressure within a curved surface between two static fluids is always greater than that outside of a curved surface, but the pressure will decrease to zero as the radius approached infinity. Since the force is perpendicular to the surface and acts towards the centre of the curvature, a liquid will rise when the surface is concave and depress when convex.[11] This was a mathematical explanation of the work published by James Jurin in 1719[12], where he quantified a relationship between the maximum height taken by a liquid in a capillary tube and it's diameter- Jurin's Law.[13] The capillary length evolved from the use of the Laplace pressure equation at the point it balanced the pressure due to gravity, and is sometimes called the Laplace capillary constant, after being introduced by Laplace in 1806.[14]

In nature

Bubbles

Like a droplet, bubbles are round because cohesive forces pull it's molecules into the tightest possible grouping, a sphere. Due to the trapped air inside the bubble it's impossible for the surface area to shrink to zero, hence the pressure inside the bubble is greater than outside, because if the pressures were equal, then the bubble would simply collapse.[15] This pressure difference can be calculated from Laplace's pressure equation,

.

For a soap bubble, there exists two boundary surfaces, internal and external, and therefore two contributions to the excess pressure and Laplace's formula doubles to

.[16]

The capillary length can then be worked out the same way except the thickness of the film, must be taken into account as the bubble has a hollow centre unlike the droplet which is a solid. Instead of thinking of a droplet where each side is as in the above derivation, for a bubble is now

,

with and the radius and thickness of the bubble respectively.

As above, the Laplace and hydrostatic pressure are equated resulting in

.

Thus the capillary length contributes to a physio chemical limit that dictates the maximum size a soap bubble can take.[5]

See also

  • Capillarity
  • Surface tension
  • Pressure
  • Bond number
  • Jurin's law
  • Young-Laplace equation

References

1. ^{{Cite book|title=Colloidal science of flotation|last=V.|first=Nguyen, Anh|date=2004|publisher=Marcel Dekker|others=Schulze, Hans Joachim, 1938-|isbn=978-0824747824|location=New York|oclc=53390392}}
2. ^{{Citation|last=Yuan|first=Yuehua|title=Contact Angle and Wetting Properties|date=2013|work=Surface Science Techniques|volume=51|pages=3–34|editor-last=Bracco|editor-first=Gianangelo|publisher=Springer Berlin Heidelberg|doi=10.1007/978-3-642-34243-1_1|isbn=9783642342424|last2=Lee|first2=T. Randall|editor2-last=Holst|editor2-first=Bodil}}
3. ^{{Cite book|title=Microfluidics : modeling, mechanics and mathematics|last=E.|first=Rapp, Bastian|isbn=9781455731510|location=Kidlington, Oxford, United Kingdom|oclc=966685733|date = 2016-12-13}}
4. ^{{Cite journal|last=Aarts|first=D. G. A. L.|title=Capillary Length in a Fluid−Fluid Demixed Colloid−Polymer Mixture|journal=The Journal of Physical Chemistry B|language=en|volume=109|issue=15|pages=7407–7411|doi=10.1021/jp044312q|pmid=16851848|issn=1520-6106|year=2005}}
5. ^{{Cite journal|last=Clanet|first=Christophe|last2=Quéré|first2=David|last3=Snoeijer|first3=Jacco H.|last4=Reyssat|first4=Etienne|last5=Texier|first5=Baptiste Darbois|last6=Cohen|first6=Caroline|date=2017-03-07|title=On the shape of giant soap bubbles|journal=Proceedings of the National Academy of Sciences|language=en|volume=114|issue=10|pages=2515–2519|doi=10.1073/pnas.1616904114|issn=0027-8424|pmc=5347548|pmid=28223485}}
6. ^{{Cite journal|last=Boucher|first=E A|date=1980-04-01|title=Capillary phenomena: Properties of systems with fluid/fluid interfaces|journal=Reports on Progress in Physics|volume=43|issue=4|pages=497–546|doi=10.1088/0034-4885/43/4/003|issn=0034-4885}}
7. ^{{Cite journal|last=Liu|first=Tingyi “Leo”|last2=Kim|first2=Chang-Jin “CJ”|title=Contact Angle Measurement of Small Capillary Length Liquid in Super-repelled State|journal=Scientific Reports|language=en|volume=7|issue=1|pages=740|doi=10.1038/s41598-017-00607-9|issn=2045-2322|pmc=5428877|pmid=28389672|year=2017|bibcode=2017NatSR...7..740L}}
8. ^{{Cite book|title=Dictionary of energy|others=Cleveland, Cutler J.,, Morris, Christopher G.|isbn=9780080968124|edition=Second|location=Amsterdam, Netherlands|oclc=896841847|last1 = Cleveland|first1 = Cutler J.|last2=Morris|first2=Christopher G.|date=2014-10-20}}
9. ^{{Cite book|title=Physical electrochemistry : fundamentals, techniques and applications|last=Noam.|first=Eliaz|others=Gileadi, Eliʿezer 1932-|isbn=9783527341405|edition=Second|location=Weinheim|oclc=1080923071|date = 2018-09-13}}
10. ^{{Cite book|title=Microfluidics for biotechnology|last=1952-|first=Berthier, Jean|date=2010|publisher=Artech House|others=Silberzan, Pascal.|isbn=9781596934443|edition=2nd|location=Boston|oclc=642685865}}
11. ^{{Cite book|title=Respiratory Physiology : People and Ideas|last=B.|first=West, John|date=1996|publisher=Springer New York|isbn=9781461475200|location=New York, NY|oclc=852791684}}
12. ^{{Cite journal|title=Jurin|journal = Philosophical Transactions of the Royal Society of London|volume = 30|issue = 355|pages = 739–747|last=|first=|doi=10.1098/rstl.1717.0026|year = 1719}}
13. ^{{Cite journal|last=Kashin|first=V. V.|last2=Shakirov|first2=K. M.|last3=Poshevneva|first3=A. I.|title=The capillary constant in calculating the surface tension of liquids|journal=Steel in Translation|language=en|volume=41|issue=10|pages=795–798|doi=10.3103/S0967091211100093|issn=0967-0912|year=2011}}
14. ^L. Landau and B. Levich, “Dragging of a liquid by a moving plate,” Acta Physicochimica U.R.S.S., Vol. 17, No. 1-2, 1942, pp. 42-54
15. ^{{Cite book|url=https://books.google.co.uk/books?id=C-QhB0ObMT8C|title=IIT Physics-I|last=Agarwal|first=P.K|publisher=Krishna Prakashan Media|year=|isbn=|location=|pages=|language=en}}
16. ^{{Cite book|title=Materials science for dentistry|last=W.|first=Darvell, B.|isbn=9781845696672|edition=Ninth|location=Cambridge, England|oclc=874155175|date = 2009-04-29}}

1 : Fluid dynamics

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