Search by property

From Battery Knowledge Base

This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

Search by property

A list of all pages that have property "Text"Text" is a predefined property that represents text of arbitrary length and is provided by <a rel="nofollow" class="external text" href="https://www.semantic-mediawiki.org/wiki/Help:Special_properties">Semantic MediaWiki</a>." with value "Type of usage of a certain budget". Since there have been only a few results, also nearby values are displayed.

Showing below up to 26 results starting with #1.

View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)


    

List of results

  • TrimethoxyMethylSilane  + (TrimethoxyMethylSilane)
  • Tris222TrifluoroethylBorate  + (Tris222TrifluoroethylBorate)
  • TrisPentafluorophenylBorane  + (TrisPentafluorophenylBorane)
  • Trondheim  + (Trondheim)
  • TubularPlate  + (TubularPlate)
  • Tufts University  + (Tufts University)
  • Tulsa  + (Tulsa)
  • Tungsten  + (Tungsten)
  • TungstenAtom  + (TungstenAtom)
  • TungstenBasedElectrode  + (TungstenBasedElectrode)
  • TungstenOxideElectrode  + (TungstenOxideElectrode)
  • TungstenSymbol  + (TungstenSymbol)
  • Turbidity Measurement  + (Turbidity Measurement)
  • Tutorial  + (Tutorial)
  • Tutorial  + (Tutorium)
  • TwinVECTOR  + (TwinVECTOR)
  • Power Shift Summit  + (Two full days of interactive discussions cross-energy sector and cross-economic sector, national workshops, expo and networking opportunities.)
  • StrippingVoltammetry  + (Two-step electrochemical measurement in whTwo-step electrochemical measurement in which 1) material is accumulated at an electrode and 2) the amount of an accumulated species is measured by voltammetry. The measured electric current in step 2 is related to the concentration of analyte in the solution by calibration. Anodic stripping voltammetry (ASV) was historically used to measure concentrations of metal ions in solution using cathodic accumulation with mercury to form an amalgam. Due to the toxicity of mercury and its compounds, inductively coupled plasma optical emission spectrometry and inductively coupled plasma mass spectrometry have frequently replaced ASV at mercury electrodes in the laboratory, often sacrificing the probing of speciation and lability in complex matrices. Mercury has now been replaced by non-toxic bismuth or anti- mony as films on a solid electrode support (such as glassy carbon) with equally good sensi- tivity and detection limits. Because the accumulation (pre-concentration) step can be prolonged, increasing the amount of material at the electrode, stripping voltammetry is able to measure very small concentrations of analyte. Often the product of the electrochemical stripping is identical to the analyte before the accumulation. Stripping voltammetry is a calibrated method to establish the relation between amount accumulated in a given time and the concentration of the analyte in solution. Types of stripping voltammetry refer to the kind of accumulation (e.g. adsorptive stripping voltammetry) or the polarity of the stripping electrochemistry (anodic, cathodic stripping voltammetry). (anodic, cathodic stripping voltammetry).)
  • PotentiometricStrippingAnalysis  + (Two-step electrochemical measurement in whTwo-step electrochemical measurement in which 1) material is accumulated at an electrode and 2) the material is removed by chemical reaction or electrochemically at constant current with measurement of electrode potential. Historically for the analysis of metal ions, mercury ions were added to the test solution to form a mercury amalgam when reduced. Alternatively, an HMDE or MFE was used and the oxidizing agent added after amalgam formation. However, the toxicity of mercury and its compounds have all but precluded the present-day use of mercury. The accumulation is similar to that used in stripping voltammetry. The stripping potentiogram shows staircase curves of potential as a function of time. Frequently, the first derivative is displayed (dE/dt=f(t)), as this produces peak-shaped signals. The time between transitions (peaks) is proportional to the concentration of analyte in the test solution. The time between changes in potential in step 2 is related to the concentration of analyte in the solution. concentration of analyte in the solution.)
  • TwoFluoropyridine  + (TwoFluoropyridine)
  • TwoManifold  + (TwoManifold)
  • TwoMeTHF  + (TwoMeTHF)
  • TwoSidedHeating  + (TwoSidedHeating)
  • TwoStepCharging  + (TwoStepCharging)
  • GibbsEnergy  + (Type of thermodynamic potential; useful for calculating reversible work in certain systems.)