Hysteresis system

There is appreciable contact angle hysteresis for many of the systems reported in Table X-2 the customary practice of reporting advancing angles has been followed. 

Cationic surfactants may be used [94] and the effect of salinity and valence of electrolyte on charged systems has been investigated [95-98]. The phospholipid lecithin can also produce microemulsions when combined with an alcohol cosolvent [99]. Microemulsions formed with a double-tailed surfactant such as Aerosol OT (AOT) do not require a cosurfactant for stability (see, for instance. Refs. 100, 101). Morphological hysteresis has been observed in the inversion process and the formation of stable mixtures of microemulsion indicated [102]. 

The question is not trivial such agreement is not assured in the case of systems showing hysteresis (see Section XVII-16), and it has been difficult to affirm it on rigorous thermodynamic grounds in the case of a heterogeneous surface. 

Below the critical temperature of the adsorbate, adsorption is generally multilayer in type, and the presence of pores may have the effect not only of limiting the possible number of layers of adsorbate (see Eq. XVII-65) but also of introducing capillary condensation phenomena. A wide range of porous adsorbents is now involved and usually having a broad distribution of pore sizes and shapes, unlike the zeolites. The most general characteristic of such adsorption systems is that of hysteresis as illustrated in Fig. XVII-27 and, more gener-... 

Abstract. A model of the conformational transitions of the nucleic acid molecule during the water adsorption-desorption cycle is proposed. The nucleic acid-water system is considered as an open system. The model describes the transitions between three main conformations of wet nucleic acid samples A-, B- and unordered forms. The analysis of kinetic equations shows the non-trivial bifurcation behaviour of the system which leads to the multistability. This fact allows one to explain the hysteresis phenomena observed experimentally in the nucleic acid-water system. The problem of self-organization in the nucleic acid-water system is of great importance for revealing physical mechanisms of the functioning of nucleic acids and for many specific practical fields. 

These results allows us to connect the observed hysteresis to the conformational changes in the NA molecule and consider it not as a macroscopic phenomenon like capillary hysteresis, but as natural property of the NA-water system. Our experimental and numerical results are in agreement with the data of other authors [13], [12], [14]. 

A characteristic feature of a Type IV isotherm is its hysteresis loop. The exact shape of the loop varies from one adsorption system to another, but, as indicated in Fig. 3.1, the amount adsorbed is always greater at any given relative pressure along the desorption branch FJD than along the adsorption branch DEF. The loop is reproducible provided that the desorption run is started from a point beyond F which marks the upper limit of the loop. 

The model proposed by Zsigmondy—which in broad terms is still accepted to-day—assumed that along the initial part of the isotherm (ABC of Fig. 3.1), adsorption is restricted to a thin layer on the walls, until at D (the inception of the hysteresis loop) capillary condensation commences in the finest pores. As the pressure is progressively increased, wider and wider pores are filled until at the saturation pressure the entire system is full of condensate. 

Both the cone-shaped and the wedge-like pore give rise to simple, hysteresis-free behaviour. The meniscus is nucleated at the apex of the cone (Fig. 3.14(a)) or at the intersection of the two planes of the wedge (Fig. 3.14(b)), giving a spherical meniscus in the first case and a cylindrical one in the second. In both systems the process of evaporation is the exact reverse of that of condensation, and hysteresis is therefore absent. 

The procedures are based on an imaginary emptying of the pores by the step-wise lowering of relative pressure, from the point already referred to where the mesopore system is taken as being full up a relative pressure of 0-95po is frequently adopted as starting point with isotherms having a hysteresis loop of Type A or Type E. (With Type B, as will appear later, the validity of pore size calculations is doubtful.)... 

Thus the hysteresis loop should close at a relative pressure determined by the tensile strength of the liquid adsorptive, no matter whether the pore system extends to finer pores than those characterized by or not. 

The limits of pore size corresponding to each process will, of course, depend both on the pore geometry and the size of the adsorbate molecule. For slit-shaped pores the primary process will be expected to be limited to widths below la, and the secondary to widths between 2a and 5ff. For more complicated shapes such as interstices between small spheres, the equivalent diameter will be somewhat higher, because of the more effective overlap of adsorption fields from neighbouring parts of the pore walls. The tertiary process—the reversible capillary condensation—will not be able to occur at all in slits if the walls are exactly parallel in other pores, this condensation will take place in the region between 5hysteresis loop and in a pore system containing a variety of pore shapes, reversible capillary condensation occurs in such pores as have a suitable shape alongside the irreversible condensation in the main body of pores. 

The computation of mesopore size distribution is valid only if the isotherm is of Type IV. In view of the uncertainties inherent in the application of the Kelvin equation and the complexity of most pore systems, little is to be gained by recourse to an elaborate method of computation, and for most practical purposes the Roberts method (or an analogous procedure) is adequate—particularly in comparative studies. The decision as to which branch of the hysteresis loop to use in the calculation remains largely arbitrary. If the desorption branch is adopted (as appears to be favoured by most workers), it needs to be recognized that neither a Type B nor a Type E hysteresis loop is likely to yield a reliable estimate of pore size distribution, even for comparative purposes. 

As pointed out earlier (Section 3.5), certain shapes of hysteresis loops are associated with specific pore structures. Thus, type HI loops are often obtained with agglomerates or compacts of spheroidal particles of fairly uniform size and array. Some corpuscular systems (e.g. certain silica gels) tend to give H2 loops, but in these cases the distribution of pore size and shape is not well defined. Types H3 and H4 have been obtained with adsorbents having slit-shaped pores or plate-like particles (in the case of H3). The Type I isotherm character associated with H4 is, of course, indicative of microporosity. 

It also is possible to develop square hysteresis loops via the sHp-iaduced anisotropy through plastic deformation. This technique had been employed ia the commercial processiag of Twistor memories (25) no longer used ia telephone electronic systems. 

Potassium Phosphates. The K2O—P20 —H2O system parallels the sodium system in many respects. In addition to the three simple phosphate salts obtained by successive replacement of the protons of phosphoric acid by potassium ions, the system contains a number of crystalline hydrates and double salts (Table 7). Monopotassium phosphate (MKP), known only as the anhydrous salt, is the least soluble of the potassium orthophosphates. Monopotassium phosphate has been studied extensively owing to its piezoelectric and ferroelectric properties (see Ferroelectrics). At ordinary temperatures, KH2PO4 is so far above its Curie point as to give piezoelectric effects in which the emf is proportional to the distorting force. There is virtually no hysteresis. 

AH three systems give similar tensile strength, elongation, and hardness properties. Hysteresis (heat buildup) measured by tan 5 shows an advantage for conventional and semi-EV systems and unaged fatigue follows the expected pattern. 

Trip Valves The trip valve is part of a system that is used where a specific valve action (i.e., fail up, Fail down, or lock in last position) is required when pneumatic supply pressure to the control valve falls befow a preset level. Trip systems are used primarily on springless piston ac tuators requiring fail-open or fail-closed acrion. An air storage or Volume tank and a check v ve are used with the trip valve to provide power to stroke the valve when supply pressure is lost. Trip valves are designed with hysteresis around the trip point to avoid instabihty when the trip pressure and the reset pressure settings are too close to the same value. 

The unbalanced voltage will produce an additional rotor current at nearly twice the supply frequency. For example, for a 2% slip, i.e. a slip of 1 Hz, the negative sequence stator current, due to an unbalanced supply voltage, will induce a rotor current at a frequency of (2/- 1) = 99 Hz for a 50 Hz system. These high-frequency currents will produce significant skin effects in the rotor bars and cause high eddy current and hysteresis losses (Section 1.6.2(A-iv)). Total rotor heat may be represented by... 

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