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The importance of the health monitoring system has already been brie y mentioned in the section on the engine and transmission system The importance of Health and Usage Monitoring Systems, or HUMS as they are also known (in abbreviated parlance) are now considered to be so important that the UK Civil Aviation Authority (CAA) now speci es the equipment as mandatory for all helicopters certi ed in the UK There are two notable aspects to the use of HUMS The rst relates to criticality and ight safety, the second to cost savings If the correct critical parameters in an engine and transmission system are monitored then it is possible to identify deterioration of components before a critical failure occurs This is done by establishing a time-history of the parameter during normal operation of the aircraft, and carrying out trend analysis using computers and data reduction techniques.



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Figure 64-1 RTP can be viewed as a sublayer of the transport layer From the application developer's perspective, however, RTP is not part of the transport layer but instead part of the application layer This is because the developer must integrate RTP into the application Specifically, for the sender side of the application, the developer must write code into the application which creates the RTP encapsulating packets; the application then sends the RTP packets into a UDP socket interface Similarly, at the receiver side of the application, the RTP packets enter the application through a UDP socket interface; the developer therefore must write code into the application that extracts the media chunks from the RTP packets This is illustrated in Figure 64-2





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Despite the variety of polymer/poor solvent pairs that could in principle achieve light-responsive phase separation, the systems investigated to date are not numerous. Polymers in organic solvents were considered as early as in the 1980s by Irie and colleagues, with azobenzene-modi ed polystyrene in carbon disul de (Irie and Iga, 1986). Recent reconsideration of polystyrene-based systems have pointed that the desolvatation and precipitation may considerably slow down the chain dynamics (T{Tg), which in turn traps the photoproduced aggregates in a frozen (insoluble) state (Shulkin and Stover, 2003). Thus the aggregates may not redissolve, but the photocontrol of precipitation kinetics could nevertheless nd

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promising developments for the synthesis of nanoparticles with complex shapes or porosity Similarly, solvent effects switch azo-containing polypeptide chains between their coil conformation in good solvent and a phototriggered folded structure (helix formation; Fig 72a), although no precipitation occurs In this case, the desolvatation is usually achieved by mixing water with alcohol or other additives (Pieroni et al, 2001; Willner and Rubin, 1996) But the vast majority of systems developed to date correspond to phase separation in aqueous solutions, using the low critical solubility temperature (LCST) displayed by most water-soluble chains In short, macromolecules with known LCST behavior can be modi ed by inclusions of azobenzene groups to obtain a water-soluble chain containing a few mol% of azo monomers The hydrophobicity of photochromes causes the LCST to shift toward signi cantly lower temperature (Fig 7.

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2b), but does not change the qualitative properties of high solubility (respectively swelling of a gel or of isolated chains) at low temperature and low solubility (respectively gel shrinkage or collapse of the chain) at temperature beyond the modi ed LCST The generality of this effect is re ected by the diverse chemical structures of macromolecules found in literature, including derivatives of poly(N-isopropylacrylamide) (Liu et al, 2001; Irie, 1993; Mamada et al, 1990), copolymers of isopropylacrylamide and hydroxyalkylacrylamide (Menzel et al, 1995), methyl and hydroxypropyl cellulose derivatives (Zheng et al, 2004), elastinlike polypeptides (Alonso et al, 2001), collagenlike systems (Kusebauch et al, 2006; Strzegowski et al, 1994) The LCST of a modi ed chain decreases typically in proportion to the fraction of azobenzene hydrophobes (Alonso et al, 2001; Menzel et al, 1995) (Eq 71) Fig 7.

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