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    <title>DSpace Collection: Institutt for prosess-, energi- og miljøteknologi</title>
    <link>http://hdl.handle.net/2282/256</link>
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  <item rdf:about="http://hdl.handle.net/2282/440">
    <title>Carbon dioxide emission reduction by increased utilization of waste-derived fuels in the cement industry</title>
    <link>http://hdl.handle.net/2282/440</link>
    <description>Title: Carbon dioxide emission reduction by increased utilization of waste-derived fuels in the cement industry
&lt;br/&gt;
&lt;br/&gt;Authors: Tokheim, Lars-André; Brevik, Per
&lt;br/&gt;
&lt;br/&gt;Abstract: Considerable reductions in Norway's emissions of greenhouse gases like CO2 are required to&#xD;
meet the commitments of the Kyoto Protocol. CO2 emissions from cement clinker production&#xD;
originate from decarbonation of limestone as well as fuel combustion, and the cement plants&#xD;
in Norway have to comply with requirements given by the pollution control authorities via the&#xD;
national emissions trading system.&#xD;
There are several ways of reducing CO2 emissions from the cement industry. Utilizing CO2-&#xD;
neutral waste fuels as a replacement for fossil fuels is an attractive means of reducing the net&#xD;
CO2 emissions. Using modern kiln technology is another important measure facilitating lower&#xD;
emissions.&#xD;
The Norcem plant in Brevik carried out an extensive modernization project in 2004-5, and as&#xD;
a result of this the plant in Brevik currently uses close to 100,000 tons of CO2-neutral wastefuels&#xD;
every year. The outcome of this is a reduction in fuel-generated CO2 emissions of about&#xD;
25 % from 1995 to 2005.&#xD;
Reduction of CO2 emissions by secondary methods such as post-combustion measures using&#xD;
amine absorption for the capture of CO2 in the exhaust gas from the cement plant is&#xD;
technically feasible, but expensive and risky.</description>
  </item>
  <item rdf:about="http://hdl.handle.net/2282/436">
    <title>Assessment of mercury emission at Norcem's cement kiln by use of 203 Hg tracer</title>
    <link>http://hdl.handle.net/2282/436</link>
    <description>Title: Assessment of mercury emission at Norcem's cement kiln by use of 203 Hg tracer
&lt;br/&gt;
&lt;br/&gt;Authors: Eriksen, Dag Øistein; Tokheim, Lars-André; Eriksen, T.A.; Meyer, Julien; Qvenild, Carsten
&lt;br/&gt;
&lt;br/&gt;Abstract: In manufacture of cement clinker, mercury is introduced in the cement kiln system via the fuels and as constituents in the raw materials, i.e.,&#xD;
limestone, iron ore, etc. The permissible emission of Hg to air is very low (0.05 mg/Nm3) due to its toxicity. Thus, it is important to know how&#xD;
mercury distributes and behaves in the kiln system. The objective of the study was to measure the distribution of mercury in the kiln system, to&#xD;
measure the hold up time of Hg, to measure the portion of emission through the chimneys, and to see the dependence of the injection sites on these&#xD;
parameters. The results showed that the amounts of mercury being emitted through the exhaust gases were largely dependent on where it was&#xD;
injected. The residence time of mercury in the system was nevertheless long, after 10 hours it was still increase in the count rate of the mercury&#xD;
absorbed. There was also an immediate increase in the filter dust, but nothing could be measured in the clinker. This knowledge is needed for the&#xD;
reduction of mercury emissions.
&lt;br/&gt;
&lt;br/&gt;Description: The original&#xD;
publication is available at www.springerlink.com</description>
  </item>
  <item rdf:about="http://hdl.handle.net/2282/369">
    <title>Nosé-Hoover simulations of aqueous mixtures of small alcohols</title>
    <link>http://hdl.handle.net/2282/369</link>
    <description>Title: Nosé-Hoover simulations of aqueous mixtures of small alcohols
&lt;br/&gt;
&lt;br/&gt;Authors: Holta, Randi Toreskås
&lt;br/&gt;
&lt;br/&gt;Abstract: We have performed constant energy and constant temperature equilibrium molecular&#xD;
dynamics simulations of model liquids of water, methanol, and ethanol, and of the binary aqueous mixtures of the alcohols at mole fractions alcohol of 0.25, 0.50, and&#xD;
0.75 at room temperature. The total number of molecules is 256 and the integration&#xD;
timestep is 0.5fs.&#xD;
The molecules are modelled with rigid, nonpolarizable effective site potentials. The&#xD;
TIP4P model is applied for water, and the OPLS models for methanol and ethanol&#xD;
(trans).&#xD;
The thermostatically controlled simulations are performed within the Nose-Hoover&#xD;
formalism, with separate temperature control of the translational and rotational degrees&#xD;
of freedom. Reservoir coupling in the mixtures is determined as a weighted average&#xD;
of the liquid values.&#xD;
We present enthalpies of vaporization and excess configurational energies for the&#xD;
mixtures. Further, we show all radial site-site correlation functions for the self- and&#xD;
cross-interactions. We also present results for self-diffusion coefficients for the components,&#xD;
and the velocity auto correlations functions.&#xD;
The NVT simulations are investigated with respect to the possibility of reproducing&#xD;
the canonical ensemble. We find that the simulations are not entirely within the premises&#xD;
of the canonical ensemble. We suggest that this is due to a too weak coupling&#xD;
(too large heat bath mass). The results are nevertheless found to be in good agreement&#xD;
with experiments and published simulational studies.&#xD;
The NVE simulations for the mixtures reproduce the desired temperature well.&#xD;
The energy conservation is good and improves with decreasing water content.&#xD;
Effects of using only trans-ethanol might be seen for the self-diffusion coefficients.&#xD;
Structural results for both the model alcohols are found to be consistent with V-chains.&#xD;
Upon addition of water, methyl-methyl coordination numbers for both alcohols&#xD;
decrease less than the hydroxyl coordination numbers.
&lt;br/&gt;
&lt;br/&gt;Description: Avhandling (dr.ing.) - Høgskolen i Telemark / Norges teknisk-naturvitenskapelige universitet</description>
  </item>
  <item rdf:about="http://hdl.handle.net/2282/362">
    <title>Investment cost estimates and investment decisions</title>
    <link>http://hdl.handle.net/2282/362</link>
    <description>Title: Investment cost estimates and investment decisions
&lt;br/&gt;
&lt;br/&gt;Authors: Emhjellen, Kjetil; Emhjellen, Magne; Osmundsen, Petter
&lt;br/&gt;
&lt;br/&gt;Abstract: When evaluating new investment projects, oil companies traditionally use the discounted cashflow method. This method requires&#xD;
expected cashflows in the numerator and a risk-adjusted required rate of return in the denominator in order to calculate net present&#xD;
value. The capital expenditure (CAPEX) of a project is one of the major cashflows used to calculate net present value. Usually the&#xD;
CAPEX is given by a single cost figure, with some indication of its probability distribution. In the oil industry and many other&#xD;
industries, it is a common practice to report a CAPEX that is the estimated 50/50 (median) CAPEX instead of the estimated&#xD;
expected (expected value) CAPEX. In this article, we demonstrate how the practice of using a 50/50 (median) CAPEX, when the cost&#xD;
distributions are asymmetric, causes project valuation errors and therefore may lead to wrong investment decisions with acceptance&#xD;
of projects that have negative net present values.</description>
  </item>
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