Meniscus Forces and Profiles: Theory and Its Applications to Liquid-Mediated Interfaces

1998 ◽  
Vol 120 (2) ◽  
pp. 358-368 ◽  
Author(s):  
Chao Gao ◽  
Peihua Dai ◽  
Andy Homola ◽  
Joel Weiss

A theory for obtaining meniscus forces and profiles for any given liquid-mediated interface is presented that includes the effects of surface interactions, adsorption and evaporation of liquid films. The meniscus force is obtained from the derivative of the total free energy of liquid-mediated interface, which requires the meniscus profile to be known. The meniscus profile is the solution of a second-order differential equation, as derived from Pascal’s law for static incompressible liquids with inclusion of surface interactions. For nonvolatile liquid films, the total liquid amount at the interface is a conserved quantity, whereas for volatile liquids, the liquid films are in thermodynamic equilibrium with their respective vapor phase. Two typical types of initial liquid conditions are considered. Type I represents the case in which one surface is wet and the other is initially dry, having a finite contact angle with the liquid. Type II represents the situation in which both surfaces are wet by either a liquid or by two different liquids before making contact. If two or more types of liquids are involved at the interface, miscibility of the liquids and interactions due to other liquid(s) have to be also considered. For contacts with azimuthal geometry, which is merely a mathematical convenience, such as ellipsoidal/spherical, conical or crater, the theory generates several analytical formulae for calculating meniscus forces without involving meniscus profiles. These formulae can be handily applied to various surface probes techniques such as Scanning Probe Microscopy or Surface Force Apparatus. The proposed theory is also applicable to “meniscus rings” formed around crater geometry, such as encountered in laser-textured magnetic disks. In this case, the outer meniscus ring can be asymmetric to the inner meniscus ring if no liquid passage exists between the inner and outer meniscus ring. Even for the case of spherical contact geometry, the calculated meniscus profile is very nonspherical with a much larger volume than that of the widely assumed spherical meniscus profile for Type I conditions, leading to an under-estimation of the meniscus force in the previous models. It is found that for a spherical or a crater contact geometry, the surface interactions have little effect on the meniscus force provided the lateral meniscus dimension is much smaller than the radius of the sphere or of the crater. However the surface interactions have a large effect on the meniscus force for other contact geometries, such as conical contact geometry. The calculated meniscus forces are compared with the normal component of the stiction force measured at the laser textured surfaces and good agreement is found. The calculated meniscus profiles are also found in good agreement with that measured using light interferometer technique between two cross cylinders. One very interesting finding of our theory is that the meniscus volume grows first and may then shrink, as observed experimentally by others, because the initially dry surface become wetted and the boundary conditions change over from Type I to Type II.

1981 ◽  
Author(s):  
V Sachs ◽  
R Dörner ◽  
E Szirmai

Anti human plasminogen sera of the rabbit precipitate human plasma in the agar gel diffusion test by means of intra-basin absorption with plasminogenfree human plasma with three different types: type I is represented by one strong precipitation line, type II by two lines, a big one and a small one, and type III by three slight but distinct lines. The following frequencies of the different types have been observed in a sample of 516 human plasmas: type I 65%, type II 33% and type III 2%. Suppose the types are phenotypical groups of a diallelic system where the types I and III represent the homozygous genotypes and the type II the heterozygous the estimated gene frequencies are in good agreement with the expected values. There is also a good agreement of the distribution of plasminogen groups determined by electrofocussing from RAUM et al. and HOBART. The plasminogen groups possibly may have also a biological meaning because the plasmas of type III always have a lesser fibrinolytic activity than the plasmas of the other types.


2006 ◽  
Vol 2 (S238) ◽  
pp. 117-122
Author(s):  
Andrew Lawrence

AbstractThe standard torus picture for explaining the difference between Type I and Type II AGN is physically unlikely and provides no natural explanation for a number of simple facts - the average covering factor, the broad range of covering factors, and the characteristic reprocessing distance. Parsec scale warped discs are a strong alternative. A very simple “misaligned disc” model produces good agreement with covering factor statistics, but predicts too many off-axis emission line cones. I discuss possible ways to improve such a model.


Author(s):  
Marion C. Schäfer ◽  
Svilen Bobev

Studies of the K–Ba–Ga–Sn system produced the clathrate compounds K0.8(2)Ba15.2(2)Ga31.0(5)Sn105.0(5)[a= 17.0178 (4) Å], K4.3(3)Ba11.7(3)Ga27.4(4)Sn108.6(4)[a= 17.0709 (6) Å] and K12.9(2)Ba3.1(2)Ga19.5(4)Sn116.5(4)[a= 17.1946 (8) Å], with the type-II structure (cubic, space groupFd\overline{3}m), and K7.7(1)Ba0.3(1)Ga8.3(4)Sn37.7(4)[a= 11.9447 (4) Å], with the type-I structure (cubic, space groupPm\overline{3}n). For the type-II structures, only the smaller (Ga,Sn)24pentagonal dodecahedral cages are filled, while the (Ga,Sn)28hexakaidecahedral cages remain empty. The unit-cell volume is directly correlated with the K:Ba ratio, since an increasing amount of monovalent K occupying the cages causes a decreasing substitution of the smaller Ga in the framework. All three formulae have an electron count that is in good agreement with the Zintl–Klemm rules. For the type-I compound, all framework sites are occupied by a mixture of Ga and Sn atoms, with Ga showing a preference for Wyckoff site 6c. The (Ga,Sn)20pentagonal dodecahedral cages are occupied by statistically disordered K and Ba atoms, while the (Ga,Sn)24tetrakaidecahedral cages encapsulate only K atoms. Large anisotropic displacement parameters for K in the latter cages suggest an off-centering of the guest atoms.


1987 ◽  
Vol 57 (03) ◽  
pp. 332-336 ◽  
Author(s):  
Jeffrey D Hall ◽  
Dean W Willis ◽  
Bruce L Evatt ◽  
Debra W Jackson

SummaryThree monoclonal antibodies produced against vWF:Ag by conventional hybridoma technique did not inhibit factor VIII coagulant activity (F.VIII:C) but did inhibit VIII ristocetin cofactor activity. The antibodies were used in an indirect competitive ELISA for quantifying von Willebrand’s antigen (vWF: Ag) and compared with values obtained by the Laurell technique using commercial antibody by means of a ratio: ELISA/Laurell. For one monoclonal BD2-CC9, vWF:Ag values obtained in the two assays were in good agreement for normal and hemophilia A plasmas (normal, n = 19, ratio = 1.13 ± .17, hemophilia A, n = 10, ratio = 0.91 ± .15). However, type II vWD patients had a disproportionately low value of vWF: Ag with the ELISA. Use of the ratio normalized the difference among individual plasma values and allowed a significant separation of type II vWD plasma (n = 9, ratio = 0.46 ± .19) from normal plasma (p = .0001) and type I vWD plasma (n = 8, ratio = 1.52 ± .34) from type II vWD plasma (p = .0003) using BD2-CC9. Although the sample size was small, the greater degree of discrimination among the vWD plasmas tested with BD2-CC9 (compared with the other two antibodies [CA3-AE4, CC6-BG10]) suggests that this antibody may recognize conformational epitopes that reflect the degree of multimeric polymerization of the vWF molecule rather than simply recognize a decreased number of antigenic sites in a basic subunit. BD2-CC9 may be valuable in investigating the various types of vWD and/or the process of polymerization of this complex protein.


Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.


Author(s):  
G. D. Gagne ◽  
M. F. Miller ◽  
D. A. Peterson

Experimental infection of chimpanzees with non-A, non-B hepatitis (NANB) or with delta agent hepatitis results in the appearance of characteristic cytoplasmic alterations in the hepatocytes. These alterations include spongelike inclusions (Type I), attached convoluted membranes (Type II), tubular structures (Type III), and microtubular aggregates (Type IV) (Fig. 1). Type I, II and III structures are, by association, believed to be derived from endoplasmic reticulum and may be morphogenetically related. Type IV structures are generally observed free in the cytoplasm but sometimes in the vicinity of type III structures. It is not known whether these structures are somehow involved in the replication and/or assembly of the putative NANB virus or whether they are simply nonspecific responses to cellular injury. When treated with uranyl acetate, type I, II and III structures stain intensely as if they might contain nucleic acids. If these structures do correspond to intermediates in the replication of a virus, one might expect them to contain DNA or RNA and the present study was undertaken to explore this possibility.


Author(s):  
T.A. Fassel ◽  
M.J. Schaller ◽  
M.E. Lidstrom ◽  
C.C. Remsen

Methylotrophic bacteria play an Important role in the environment in the oxidation of methane and methanol. Extensive intracytoplasmic membranes (ICM) have been associated with the oxidation processes in methylotrophs and chemolithotrophic bacteria. Classification on the basis of ICM arrangement distinguishes 2 types of methylotrophs. Bundles or vesicular stacks of ICM located away from the cytoplasmic membrane and extending into the cytoplasm are present in Type I methylotrophs. In Type II methylotrophs, the ICM form pairs of peripheral membranes located parallel to the cytoplasmic membrane. Complex cell wall structures of tightly packed cup-shaped subunits have been described in strains of marine and freshwater phototrophic sulfur bacteria and several strains of methane oxidizing bacteria. We examined the ultrastructure of the methylotrophs with particular view of the ICM and surface structural features, between representatives of the Type I Methylomonas albus (BG8), and Type II Methylosinus trichosporium (OB-36).


1987 ◽  
Vol 48 (C5) ◽  
pp. C5-525-C5-528 ◽  
Author(s):  
K. J. MOORE ◽  
P. DAWSON ◽  
C. T. FOXON
Keyword(s):  
Type I ◽  
Type Ii ◽  

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