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The promise of fine new music is as real as the instruments you ve already made Let me introduce one last term: theatric listening If you close your eyes when you listen to sound, any sound, and let your mind s eye illustrate the sound, this visualization may help you compose with the sound This is theatric listening It may take a little practice But if you lose yourself within a sound or a music, your closed-eye field of vision will not remain blank Something will appear For me, this something is instructive and, if you ll bear with me here, it tells me what it needs I imagine the accompanying sounds just as I might imagine the harmony to a singer s lyrics in a more traditional song But that s just me one of the ways I compose with experimental, unusual sound forms.

Nx N0 1 p 2 px 1 2-88

(continued)

Neglecting the weights of the end groups, the weight fraction wx of x-mers (i.e., the weight fraction of the molecules that contains x structural units) is given by wx xNx =N0 and Eq. 2-88 becomes

wx x 1 p 2 px 1 2-89

Equations 2-86 and 2-89 give the number- and weight-distribution functions, respectively, for step polymerizations at the extent of polymerization p. These distributions are usually referred to as the most probable or Flory or Flory Schulz distributions. Plots of the two distribution functions for several values of p are shown in Figs. 2-9 and 2-10. It is seen that on a

THE UNITED STATES IN THE TWENTIETH CENTURY: 1946 1990

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You ll soon develop your own personal style of playing and composing with the bent instruments you ve designed Wanting to learn more about electronics is a natural outgrowth of circuit-bending I highly encourage further research and study Bending and true-theory electronics are actually good friends No matter how bent your circuits are, when you use the generic line-output scheme, you re already incorporating true-theory technique The two approaches to design, although outrageously dissimilar, are yet complementary And as a bender, you have a unique advantage to entering real electronics: not only experience, but also honest inspiration..

the hydroxyl and nitrogen functions. The metal is separated by ltration of the polymer and can be recovered from the polymer by changing the pH. Other chelating polymers have been studied for removal of pertechnetate ion, TcO , from contaminated groundwater at nuclear 4 reactor facilities [Alexandratos and Natesan, 1999; Bonnesen et al., 2000]. Polymers containing crown ether or cryptand macrocyclic ligands bind and separate various cations [Jaycox and Smid, 1981; Mathias and Al-Jumah, 1980]. Polymers containing chiral groups are useful for resolving racemic mixtures into the individual enantiomers [Kiniwa et al., 1987; Mathur et al., 1980; Wulff et al., 1980]. For example, the copper(II) complex of XXXXIII (either the R- or S-enantiomer) resolves racemates of amino acids [Sugden et al., 1980]. The separation is based on the formation of a pair of diastereomeric complexes from the reaction of the polymer reagent with the two enantiomers. One of the enantiomers is complexed more strongly than the other and this achieves separation of the enantiomers. A polymer drug can be synthesized by the covalent bonding of a drug to a polymer or the synthesis and (co)polymerization of a monomer containing the drug moiety [Callant and Schacht, 1990; Donaruma and Vogl, 1978; Hsieh, 1988; Levenfeld et al., 1990; Ottenbrite

and Sunamoto, 1986] (Ionic bonding or complexing of a drug to the polymer are other approaches) Polymer drugs are of interest since they offer a number of potential advantages relative to the corresponding low-molecular-weight drugs The action of a polymer drug usually depends on in vivo hydrolytic or enzymatic cleavage of the drug moiety from the polymer This gives the advantage of a delayed and sustained release of the drug over a longer time period with a corresponding decrease in side effects such as irritation, intolerance, and toxicity There is the potential to tailor-make a polymer drug with a speci c required solubility, rate of diffusion, and increased or decreased activity by appropriate choice of the polymer and drug Other possibilities include the synthesis of polymer drugs with negligible absorptivity for situations where localized drug action is desired (eg.

Table 51 Prices and Yields of Long-Term U.S. Government Securities: 1946 1989

, skin treatment), the ability to design drugs capable of getting to a speci c organ (via appropriate af nity groups) in the desired amounts at the required time, and the coupling of two or more drugs onto the same polymer to achieve enhanced or synergistic activity The term polymer drug also includes the physical encapsulation of a low-molecular-weight drug by a polymer Drug action requires the hydrolytic or enzymatic degradation of the polymer Such materials can show many of the advantages of polymer drugs in which the drug is chemically bound to a polymer Also of interest are polymer drugs that do not depend on release of a lowmolecular-weight drug moiety for activity but possess activity as polymers Polymeric agricultural chemicals such as polymer herbicides, fertilizers, and insecticides have also been studied [Lohmann and d Hondt, 1987; Scher, 1977; Shambhu et al, 1976].

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