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My below code is working fine for convert excel document to PDF but its not Convert ... public short excel2Pdf(string originalXlsPath, string pdfPath) ... /how-to​-convert-excel-workbook-to-pdf-without-using-excel-interop-library.

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7-123

+ dt) -

d M1 Ka Kt M1 d M2 M2 7-124

X(t).



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where Ka and Kt have been independently determined as 0.4 and 0.3, respectively. The greater reactivity of a-pyrrolidone in the copolymerization with E-caprolactam can then be attributed to the greater acidity of a-pyrrolidone (by a factor of $2.5) and the greater nucleophilicity of the a-pyrrolidone anion in the transacylation equilibrium (by a factor of $3.3). 7-12b Monomers with Different Functional Groups

(8.44)





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Copolymerization between monomers containing different functional groups is selective. One of the cross-propagation steps in a contemplated copolymerization may be highly unfavorable because of the wide variations in the types of propagating centers involved and, often, in the energies of the bonds being broken during propagation. Copolymerization between certain types of monomers does not occur and that between others is dif cult to achieve, while some copolymerizations occur with relative ease. Thus, the combination of a lactam with any other type of monomer, such as a lactone, epoxide, or alkene, is incompatible because of differences in their propagation mechanisms. For example, anionic copolymerization of a lactam with an epoxide does not occur since the anion derived from the epoxide terminates by proton abstraction from lactam monomer. Epoxides readily undergo anionic copolymerization with lactones and cyclic anhydrides because the propagating centers are similar alkoxide and carboxylate [Aida et al., 1985; Cherdron and Ohse, 1966; Inoue and Aida, 1989; Luston and Vass, 1984]. Most of the polymerizations show alternating behavior, with the formation of polyester, but the mechanism for alternation is unclear. There are few reports of cationic copolymerizations of lactones and cyclic ethers other than the copolymerizations of b-propiolactone with tetrahydrofuran and 3,3-bis(chloromethyl)oxetane, probably indicative of the difference in propagating centers (dioxocarbocation and oxonium ion, respectively) [Yamashita et al., 1966]. The copolymerizations tend toward ideal behavior with the product containing large amounts of the cyclic ether. Anionic copolymerization of an episul de and epoxide shows extreme ideal behavior with only small amounts of epoxide incorporated into the copolymer, since episul des are much more reactive than epoxides. Cationic copolymerization does not occur to any extent because sulfonium ion centers do not add epoxide, although oxonium ion centers do add episul de.

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Moreover, as X (t) is a continuous process, its increment will also be continuous [i.e., Y(dt, x, t) - t 0 as dt - t 0], and it will be a smooth (differentiable) function of X(t) and t. Now let us divide the interval of time from t to t + dt into s subintervals of equal length dt j s delimited by the times tk = t + (dt j s) k, where k = 0, ... , s. Then we see that Y must satisfy the following self-consistency condition:

There are very few reported copolymerizations between cyclic monomers and carbon carbon double-bond monomers. Such copolymerizations would require a careful selection of the monomers and reaction conditions to closely match the reactivities of the different monomers and propagating centers. The almost complete absence of successes indicates that the required balancing of reactivities is nearly impossible to achieve. There are a few reports of copolymerizations between carbon carbon double-bond monomers and cyclic ethers or acetals [Higashimura et al., 1967; Inoue and Aida, 1984; Yamashita et al., 1966]. Some copolymerizations have been studied where one of the reactants is a compound not usually considered as a monomer. These include copolymerizations of epoxides and higher cyclic ethers with carbon dioxide, episul des with carbon dioxide and carbon disul de, and epoxides with sulfur dioxide [Aida et al., 1986; Baran et al., 1984; Chisholm et al., 2002; Inoue and Aida, 1989; Soga et al., 1977]. The copolymers are reported to be either 1 : 1 alternating copolymers or contain 1 : 1 alternating sequences together with blocks of the cyclic monomer. 7-12c Block Copolymers

{X(tk) - X(tk_l)} = LY(dtjs, X(tk_l), tk-l). (8.45)

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save Excel file in format of pdf in c# C# .NET - NullSkull.com
Aug 2, 2011 · I had created an excel file in C# and want to change it's format in pdf and save my file in a path in my computer ;I used the suggested Code,but I ...












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