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HPLC - UV/VIS Spectroscopy 
Fiber Optic and Diode Array Applications 
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> ION ANALYSIS
Overview Specifications Ordering Information Print Version Documentation
Overview
 
IsotachophoresisFor the separation of ionic components both chromatographic and electrophoretic techniques are used. Isotachophoresis (ITP) exploits differences in electrophoretic mobility in the presence of an electric field to effect the separation of ionic substances.
 
Non-continuous Electrolyte System
Characteristic for ITP is the use of a non-continuous system, which consists of two aqueous electrolytes, the so-called leading and trailing electrolytes. This system is usually realised within capillaries with internal diameters from 200 - 300 µm, in order to minimise heating due to the electric current and allow very high separation efficiencies to be achieved.
 
Minimum Sample Preparation
With chromatographic techniques the flow of the mobile phase usually causes the sample matrix to also be transported through the analytical column. This has the disadvantage, that often expensive and time-consuming sample preparation steps are required, before the analysis can be started.
 
In isotachophoresis it is generally possible to define conditions such that the sample matrix is not transported through the analytical separation path. The advantage of this is that practically all samples can be injected either directly or require only a simple dilution step before analysis can be started.
 
Application Possibilities
Isotachophoresis can in most cases be considered and used as a viable alternative to conventional ion chromatography. ITP brings maximum advantage when used for the analysis of complex matrixes. Typical examples in these areas are:

 
  • Organic acids in silage and fermentation
  • Trace impurities in H2O2, Glycerine, Inks
  • Anions in urine and serum
  • Taste enhancers, acidifiers, vitamins, food additives
  • Inorganic anions and cations in ground, surface or drinking water
  • Active agents and metabolites in creams and tablets
  • Proteins and amino acids
Additional information on Isotachophoresis is to be found under the Documentation link accessible from this page.
 
SpecificationsTop
Separation zoneTwo coupled capillaries
Pre-separation capillary800 µm I.D., FEP
Separating capillary300 µm I.D., fused silica
DetectionUp to three detectors possible depending on version supplied
Detection stage 1Contact-free conductivity detector integrated between the two capillaries
Detection stage 2Contact-free conductivity detector located after the second capillary
UV DetectorMeasuring cell integrated with the separating capillary
  • Deuterium lamp as light source
  • 4 wavelengths: 200, 220, 254, 280 nm
  • Fiber-optic coupling
DimensionsManual unit: 400 x 685 x 400 mm (W x H x D)
Automatic unit: 705 x 685 x 460 mm (W x H x D)
WeightManual unit: 20 kg
Automatic unit: 35 kg
Options
Diode array detectorAvailable as an option: Range 190 - 1100 nm, 1024 pixel, 0.8 nm/pixel, using fiber-optic coupling
AutosamplerThe Basic MARATHON and the TRIATHLON autosamplers are supported
All specifications may be subject to change for technical reasons.
Ordering InformationTop
81 657 02ItaChrom II – Manual Capillary Electrophoresis System
Separation unit: coupling of 2 capillaries
Detection: Two conductivity detectors and one UV detector with light guides
Control: PC controlled including software for Win95/98/NT
81 657 01ItaChrom II – Automated Capillary Electrophoresis System
Separation unit: coupling of 2 capillaries
Detection: Two conductivity detectors and one UV detector with light guides
Electrolyte unit: automated filling system for electrolyte
Autosampler: MARATHON (96 Vials)
Control: PC controlled including Software requires minimum WinNT4 SP5)
Spare Parts
51 595 43Pre-capillary, complete 90 mm/0,8
51 595 42Exchange detector, pre-column
51 595 45Separating capillary, complete 160 mm/0,3
52 001 00Exchange detector, separating column
51 595 57ITP Injection valve
52 001 01Exchange valve insert
51 595 53Bifurcation block
52 001 02Reservoir
52 001 03Filling tube with screw
51 553 72Cellophane membrane
52 001 04Fixing ring
52 001 05Screw
51 595 59O-Ring
52 001 06Needle valve
52 001 07Flange
52 001 08Washer
52 001 09Waste container
52 001 10Injection valve holder
52 001 11Valve body
52 001 12TE Reservoir
52 001 13High voltage unit
52 001 14HV Relay
52 001 15Cable set
52 001 16Oscillator card
51 595 51Controller
51 595 52Detector card
52 001 17LV Power supply
52 001 18Replacement lamp (254 nm)
51 595 40Replacement lamp (280 nm)
52 001 19UV Sensor
51 595 49UV Filter including holder and lense
51 595 50Lamp holder
52 001 20ITP Valve 300 µl
52 001 21CZE Valve
51 595 61Microprep. valve
ITP Electrolytes
51 595 01Leading electrolyte A1 pH = 6 / 250 ml
51 595 02Leading electrolyte A2 pH = 3.2 / 250 ml
51 595 03Leading electrolyte A3 pH = 3.5 / 250 ml
51 595 04Leading electrolyte A4 pH = 3.8 / 250 ml
51 595 05Leading electrolyte A5 pH = 4.5 / 250 ml
51 595 06Leading electrolyte A6 pH = 6 / 250 ml
51 595 07Leading electrolyte A7 pH = 9 / 250 ml
51 595 17Leading electrolyte A8 pH = 3.6 / 250 ml
51 595 10Trailing electrolyte A1 pH = 6 / 100 ml
51 595 25Trailing electrolyte A1 pH = 6 / 250 ml for automated ITP
51 595 11Trailing electrolyte A2 pH = 6 / 100 ml
51 595 26Trailing electrolyte A2 pH = 6 / 250 ml for automated ITP
51 595 12Trailing electrolyte A3 pH = 9 / 100 ml
51 595 19Trailing electrolyte A4 pH = 5 / 100 ml
51 595 27Trailing electrolyte A4 pH = 5 / 250 ml for automated ITP
51 595 20Trailing electrolyte A5 pH = 4 / 100 ml
51 595 08Leading electrolyte C1 pH = 5.2 / 250 ml
51 595 09Leading electrolyte C2 pH = 5.4 / 250 ml
51 595 18Leading electrolyte C3 pH = 5.2 / 250 ml
51 595 13Trailing electrolyte C1 pH = 3 / 100 ml
51 595 14Trailing electrolyte C2 pH = 5 / 100 ml
51 595 21Trailing electrolyte C3 pH = 5 / 100 ml
51 595 15Background electrolyte CZE pH = 5.2 / 250 ml
51 595 16Anti-convection reagent MHEC / 100 ml
51 595 22Leading electrolyte A9 pH = 3.5 / 250 ml
51 595 23Trailing electrolyte A10 pH = 6 / 250 ml
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