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I tend to build Web pages in two phases: Generally, I first lay out my text and images to create the overall design, and then I add details and make alterations to get the page just right. The second phase of Web page design often requires that I make a small adjustment to the HTML code, typically through the Property inspector, but occasionally I need to go right to the source the code. Dreamweaver offers a feature for making minor, but essential alterations to the code: the Quick Tag Editor. The Quick Tag Editor is a small pop-up window that appears in the Document window and enables you to edit an existing tag, add a new tag, or wrap the current selection in a tag. One other feature makes the Quick Tag Editor even quicker to use: A handy list of tags or attributes cuts down on typing. To call up the Quick Tag Editor, use any of the following methods: n Choose Modify Quick Tag Editor. n Press the keyboard shortcut Ctrl+T (Command+T). n Click the Quick Tag Editor icon on the Property inspector. The Quick Tag Editor has three modes: Insert HTML, Wrap Tag, and Edit HTML. Although you can get to all three modes from any situation, which mode appears initially depends on the current selection. The Quick Tag Editor s window (see Figure 6-23) appears above the current selection when you use either the menu or keyboard method of opening it or next to the Property inspector when you click the icon. In either case, you can move the Quick Tag Editor window to a new location onscreen by dragging its title bar. FIGURE 6-23

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The USB library enables you to work with the USB 2.0 port on your PSP, which is also backwards-compatible with USB 1.1.

<photo id= 24910877 owner= 54256647@N00 secret= 8c15a21389 title= STA_0724 ispublic= 1 isfriend= 0 isfamily= 0 /> ... <photo id= 24865509 owner= 54256647@N00 secret= 53e7584368 title= IMG_0713 ispublic= 1 isfriend= 0 isfamily= 0 /> <photo id= 24865497 owner= 54256647@N00 secret= 4c6f065c3d title= IMG_0729 ispublic= 1 isfriend= 0 isfamily= 0 /> <photo id= 24865488 owner= 54256647@N00 secret= 155fc590f0 title= IMG_0709 ispublic= 1 isfriend= 0 isfamily= 0 /> </photos> </rsp> server= 23 ;

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In contrast, methylnaphthalene is the main product in the dehydrocyclization of n-pentylbenzene 18 Formation of aromatics also takes place over molecular-sieve catalysts. This is an essential reaction over the newer-generation zeolite-cracking catalysts. They differ from earlier catalysts (amorphous silica-alumina) in that the product gasoline they produce contains less olefins and more aromatics. This is the result of more dominant hydrogen-transfer reactions between cyclic hydrocarbons and alkenes producing aromatics and paraffins. The recent high demand for aromatic compounds, however, has resulted in the development of additional new processes based on zeolites. In contrast with conventional reforming catalysts, zeolites are capable of transforming light hydrocarbons (CrC s alkanes and alkenes) to aromatics. H-ZSM-5 was found to be an excellent catalyst with prolonged catalytic activity 19,220 The first reaction in the multistep process leading ultimately to aromatics is the formation of small alkenes by cracking and dehydrogenation of small alkanes. Alkenes then undergo oligomerization and disproportionation to form a near-equilibrium mixture of higher olefins. Finally, these higher alkenes cyclize to cycloalkenes, which, in turn, participate in dehydrogenation and hydrogen transfer with olefins to give aromatics. The rapid olefin equilibration compared to further processes accounts for the observation that H-ZSM-5 transforms varied feeds (smaller and higher hydrocarbons, methanol, Fischer-Tropsch products, triglycerides) to products of very similar product distribution consisting mainly of C r C4 aliphatics and C6-C lO aromatics 20,221 As a result of shape selectivity, ZSM-5 does not generate appreciable amounts of aromatics higher than C lO Since they are considered to be coke precursors, the lack of higher aromatic compounds ensures sustained catalytic activity. Aromatization over H-ZSM-5, however, has the stoichiometric restriction to produce 3 mol of alkanes per one mole of aromatic compound. It was later observed

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How to add a PDF417 Barcode ActiveX to a MS Excel sheet. Start the Excel and create a new sheet or open an already existing sheet. Now go to the menu ...

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Select a file from the batch list and click the Remove button to remove it from the batch list. The file itself is unaffected.

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blur() (Windows only) focus() (Windows only)

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