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Sample Javascript code to use PDFTron SDK's built-in rasterizer to render PDF images on the fly and save the resulting images in various raster image formats ...

Byzantine and Arab gold coins began to circulate in Europe, and the mobility of money increased Currencies continued in frightful confusion and were progressively debased and called down, but silver mining in Hungary and Saxony was rapidly developing This was the period when the towns of northern Europe obtained power and autonomy (202) They built walls Municipalities were organized, financed, and dominated by the new merchant class, the burghers Many Italian cities achieved their freedom Rising population led to land reclamation along the estuaries of the North Sea and the founding of new towns which were often populated by escaped serfs Urban artisans began forming craft fraternities to control the quality and price of their wares (203) Education spread, partly because the new merchant class, although.

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For 2,4-tolylene diisocyanate analysis of the experimental data at low conversion shows the para isocyanate group at be 27 times as reactive as the ortho groups However, the effective difference in reactivity of the two functional groups is much greater k1 =k2 11:9 , since the reactivity of the ortho group drops an additional factor of approximately 4 after reaction of the para isocyanate group The reactivity differences of the two functional groups in 2,4-tolylene diisocyanate result from its unsymmetric and aromatic structure The environments (steric and electrostatic) of the two isocyanate groups are different to begin with, and the effect of reaction of one group is ef ciently transmitted through the conjugated p-electron system of the aromatic ring.

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These differences disappear for a reactant such as 1,4-cyclohexylene diisocyanate, which is symmetric to begin with and possesses no aromatic system to transmit the effect of the reacted isocyanate group to the unreacted group The change in reactivity of one functional group upon reaction of the other has been noted in several systems as a diference in the reactivity of monomer compared to the other-sized species, although all other species from dimer on up had the same reactivity [Hodkin, 1976; Yu et al, 1986] This behavior usually occurs with monomers having two functional groups in close proximity and where polymerization involves a signi cant change in the electrondonating or electron-withdrawing ability of the functional group Thus the reactivity of the hydroxyl group in ethylene glycol (V) toward esteri cation is considerably higher than the hydroxyl of a half-esteri ed glycol (VI) [Yamanis and Adelman, 1976] The nucleophilicity.

javascript convert pdf to tiff

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often ex-pirates and adventurers, found education advantageous in their business. Venice now had many wealthy merchants with extensive shipping interests. She dominated the Adriatic and had developed a monopoly of transport to all the dependencies of Constantinople. (204) Commenda contracts, which involved sleeping partnerships and insurance, became widespread. Genoa, however, was just beginning its recovery. In spite of this evidence of progress, the new economic activity was still small scale. Detailed records of credit and credit forms are lacking for another century or so. The Church had been the indispensable moneylender for centuries. (205) It had liquid capital which it advanced to nobles, usually secured by a form of census called a land gage, a live gage when the revenue contributed to repayment of principal, or a dead gage (mortgage) when the debt was not reduced by the payments. (206) In this century commercial credit developed in forms more fully reported at later dates.

of a hydroxyl group is enhanced more by an adjacent hydroxyl relative to an adjacent ester group. Similarly, in the polymerization of sodium p- uorothiophenoxide (an A B reactant), nucleophilic substitution at the aromatic C F bond occurs faster at uorophenyl end groups of a growing polymer compared to monomer [Lenz et al., 1962]. The electron-donating effect of the para S group in the monomer decreases the electron de ciency of the para carbon more than does a fS group in species larger than monomer. Polymerization of terephthalic acid with 4,6-diamino-1,3-benzenediol via oxazole formation (Eq. 2-219) proceeds with a sharp and continuous decrease in reaction rate with increasing polymer molecular weight [Cotts and Berry, 1981]. Reaction becomes progressively more diffusion-controlled with increasing molecular size due to the increasing rigid-rod structure of the growing polymer. Trifunctional monomers constitute an important class of monomers. One often encounters such reactants in which the various functional groups have different reactivities. Thus, the polyesteri cation of glycerol (VII) with phthalic anhydride proceeds with incomplete

acrylonitrile, acrylamide), and 3-14e ( uoropolymers). Other copolymers include uorocarbon elastomers such as vinylidene uoride with hexa uoropropene or 1-hydropenta uoropropene (with and without tetra uoroethylene as a third monomer) and per uoro(methyl vinyl ether) with vinylidene uoride or tetra uoroethylene (trade names: Fluorel, Tecno on, Viton) [Lynn and Worm, 1987]. The uorocarbon elastomers show superior performance in hostile environments (high and low temperature, chemicals, oils, fuels). Applications include engine oil and drivetrain seals, fuel system hoses and O-rings, and a variety of similar parts in the petroleum and chemical industry as well as in other high-performance machinery. Copolymerization of tetra uoroethylene with X yields per uorosulfonate ionomers (trade

javascript convert pdf to tiff

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javascript convert pdf to tiff

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javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff

javascript convert pdf to tiff