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Figure 5.9 Dissociation equilibrium shift (negative logarithm of the ion product Kw [mol kg 1]2) in pure water under different p-T conditions up to 1000 MPa and 1000 C (a) and with adiabatic lines (--) up to 140 C extrapolated up to 1400 MPa (b) (60, 65).

Description Sample precision in bits (can be 8 or 12) Image height in pixels Image width in pixels Number of components in the image

in binding length and angle Vintrinsic as well as solvational properties Vsolvational (Eq. 5.21): V = Vintrinsic + Vsolvational (5.21)

2 59

For industrial applications, such property changes of food matrices are important. Figure 5.10 shows in situ pH shifts in food systems (milk, pea soup, baby mashed carrots with maize, herring with tomato sauce; for the detailed ingredients, see Annex) and N-(2-Acetamido)-2-aminoethanesulfonic acid ACES buffer in dependence of temperature. To remove all external effects, all data were divided by the pH-values of the temperature stable phosphate buffer. Hence, in Fig. 5.10, pH differences between food and phosphate buffer are shown. ACES buffer had the highest pH shift and all other food systems had lower temperature dependencies. To investigate the temperature and pressure dependence of the dissociation equilibrium shift, different buffer systems were modeled. The created p-T diagrams of the calculated pKa value have shown different changes (Fig. 5.11). Different initial temperatures and the adiabatic heating (dashed line) due to the pressure buildup process required the implementation of the speci c temperature dependences, respectively. These temperature dependences can be very high and could compensate the advantages of the low isothermal pressure dependence. The diversity of iso-pKa lines in buffer solutions resulted mainly from the different dissociation reactions and consequently different standard molar enthalpies ( rH0) or reaction volumes ( V).

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1.10 1.05

6 3 1 1 1 1 1

Description Component identifier JPEG allows this to be 0 to 255 JFIF restricts it to 1 (Y), 2 (Cb), or 3 (Cr) The 4 high-order bits specify the horizontal sampling for the component The 4 low-order bits specify the vertical sampling Either value can be 1, 2, 3, or 4 according to the standard We do not support values of 3 in our code The quantization table identifier for the component Corresponds to the identifier in a DQT marker Can be 0, 1, 2, or 3

1.10 1.05 1.00 0.95 0.90 0.85 0.80 0.75 0.70 0 10 20 30 40 50 60 70 80 90

pHX /pHPBS [-]

Cache Distributed Transaction Coordinator ICMP IP LogicalDisk Memory Network Interface Objects Paging File PhysicalDisk Process Processor Redirector Server Server Work Queues System TCP Terminal Services Terminal Services Session UDP 9 1 1 1 42

1.00 0.95 0.90 0.85 0.80 0.75 0.70

Temperature [ C]

The SOS (Start of Scan) marker marks the beginning of compressed data for a scan in a JPEG stream Its structure is illustrated in Table 57 After the component count comes a component descriptor for each component (shown in Table 58) This is followed by 3 bytes of data used only in progressive mode The compressed scan data immediately follows the marker

attack are also counted as two opposite attack characteristics between the Rootkit and Security Audit attacks in Table 86 Most of the attacks have unique mean decrease characteristics in multiple objects

Figure 5.10 Real pH shift in food systems (milk, pea soup, baby mashed carrots with maize, herring with tomato sauce) and 0.01 M ACES buffer in dependence of temperature (65).

PBS (2nd)

5. 0

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