WO1992004624A1 - Verfahren zur bestimmung der anzahl dissoziierfähiger teilchen in flüssigkeiten - Google Patents

Verfahren zur bestimmung der anzahl dissoziierfähiger teilchen in flüssigkeiten Download PDF

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Publication number
WO1992004624A1
WO1992004624A1 PCT/DE1991/000717 DE9100717W WO9204624A1 WO 1992004624 A1 WO1992004624 A1 WO 1992004624A1 DE 9100717 W DE9100717 W DE 9100717W WO 9204624 A1 WO9204624 A1 WO 9204624A1
Authority
WO
WIPO (PCT)
Prior art keywords
electrodes
liquid
particles
current
liquids
Prior art date
Application number
PCT/DE1991/000717
Other languages
German (de)
English (en)
French (fr)
Inventor
Wolfgang Dittrich
Original Assignee
HÜLS Aktiengesellschaft
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by HÜLS Aktiengesellschaft filed Critical HÜLS Aktiengesellschaft
Priority to KR1019930700731A priority Critical patent/KR930702671A/ko
Priority to FI931035A priority patent/FI931035L/fi
Publication of WO1992004624A1 publication Critical patent/WO1992004624A1/de
Priority to NO93930836A priority patent/NO930836L/no

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/06Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/42Measuring deposition or liberation of materials from an electrolyte; Coulometry, i.e. measuring coulomb-equivalent of material in an electrolyte
    • G01N27/423Coulometry

Definitions

  • the invention relates to a method for determining the number of dissociable particles (ion pairs) in liquids.
  • electrochemical methods for determining ions in liquids are known, which are all based on a conductivity measurement of the liquid.
  • an electrical voltage is applied to a pair of electrodes located in the liquid to be examined and the electrical current which then arises is measured by means of a measuring device.
  • Disassociable particles represent impurities in liquids and are generally in a dissociated and non-dissociated state.
  • the methods mentioned based on a conductivity measurement are therefore not able to exactly determine the number of dissociable particles in liquids, since during such a measurement some of the particles are always in undissociated form and therefore cannot contribute to the conductivity.
  • charge carriers are also continuously injected into the liquid, which also falsifies the result.
  • the invention is therefore based on the object of specifying a method which enables a simple but very precise determination of the number of dissociable particles in a liquid.
  • This object is achieved according to the invention by a method in which an electric field is applied to a pair of electrodes in the liquid which has a low injection capacity for charge carriers,
  • the particles already dissociated at the start of the method contribute to the measurement result, but also, since integration takes place over a certain period of time, the particles which are dissociated only later under the influence of the electric field.
  • the process is preferably carried out until the current flow practically no longer drops. Since generally certain residual flows always remain, it cannot be waited until the flow comes to a complete standstill. If such residual currents are present, their contribution to the current integral must of course be disregarded.
  • passivated electrodes can be used.
  • Electrodes are understood to be electrodes whose ability to inject electrodes has been greatly reduced by suitable pretreatment.
  • the passivation can be achieved with commercially available brass electrodes, for example, in a very simplified manner as follows.
  • the pair of electrodes to be passivated is placed in a cell with propylene carbonate (PC) and a field strength of, for example, 10 kV / c is applied to them. After a while, the electrodes are passivated. In the case of brass electrodes and PC, the passivation can be recognized by the brown discoloration of the electrode surfaces. The electrodes passivated in this way can then be used for the method according to the invention.
  • PC propylene carbonate
  • Another way of reducing the injectability of commercially available untreated (bare) electrodes is to cover them with ion-exchange membranes in the reverse direction.
  • the membrane prevents the ion from escaping into the liquid volume.
  • a disc is made up of ceramic, so that the fluid between the two plates is ⁇ and the electrodes of the plates can be fixed to the sides facing away from each of the liquid.
  • the present method is preferably carried out by applying a field of a few kV / cm. As a result, the method can be carried out in a sufficiently short time and it can be assumed that all particles capable of dissociation are dissociated.
  • the number of dissociable particles can be used to predict the cleaning time for the liquid.
  • PC propylene carbonate
  • Fig. 1 shows an apparatus for performing the method.
  • 2 shows a suitable measuring cell for the method.
  • 3 shows the course of the current which arises during the method.
  • the measuring cell 1 shown in FIG. 1 serves to hold the propylene carbonate 3 to be examined.
  • a pair of passivated electrodes 2 is connected to a voltage source 5.
  • a current recording device 4 is connected between one of the electrodes and the voltage source.
  • the recorder 6 of the current recording device prints out the temporal Stro veriauf. The start of the process is initiated by closing switch 7.
  • the electrodes are at a distance of 0.5 cm from one another, for example.
  • the applied voltage is between 100 and 1000 volts.
  • the resulting field has a strength of 200 to 2000 volts / cm.
  • Fig. 2 shows a specific embodiment for a measuring cell. It can be seen that it is a closed measuring cell 2.
  • the electrodes 1 contained therein are covered with ion exchange membranes 3. Alternatively, the passivated electrodes indicated in FIG. 1 could of course be used.
  • the current curve in FIG. 3 has a kink in the front area. This is a result of two overlapping processes. Initially, the particles that are already in dissociated form mainly contribute to the current flow. At the beginning, this leads to a high current flow I Q , which drops very quickly with a time constant T->. The current flow is thus brought about by the constantly newly disassociated particles. The decrease in this dominant stream proportion occurs
  • the course of the current can easily be determined by leveling out the area enclosed by it.
  • the present method has proven to be extremely advantageous when working in connection with the cleaning of propylene carbonate while simultaneously producing passivated electrodes.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Electrochemistry (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Molecular Biology (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Electrostatic Separation (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
PCT/DE1991/000717 1990-09-10 1991-09-05 Verfahren zur bestimmung der anzahl dissoziierfähiger teilchen in flüssigkeiten WO1992004624A1 (de)

Priority Applications (3)

Application Number Priority Date Filing Date Title
KR1019930700731A KR930702671A (ko) 1990-09-10 1991-09-05 용액중 해리성 입자수의 측정방법
FI931035A FI931035L (fi) 1990-09-10 1991-09-05 Foerfarande foer bestaemning av antalet dissocierbara partiklar vaetskor
NO93930836A NO930836L (no) 1990-09-10 1993-03-08 Fremgangsmaate til bestemmelse av antall dissosierbare partikler i vaesker

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4028716.5 1990-09-10
DE4028716A DE4028716A1 (de) 1990-09-10 1990-09-10 Verfahren zur bestimmung der anzahl dissoziierfaehiger teilchen in fluessigkeiten

Publications (1)

Publication Number Publication Date
WO1992004624A1 true WO1992004624A1 (de) 1992-03-19

Family

ID=6413977

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE1991/000717 WO1992004624A1 (de) 1990-09-10 1991-09-05 Verfahren zur bestimmung der anzahl dissoziierfähiger teilchen in flüssigkeiten

Country Status (9)

Country Link
EP (1) EP0548133A1 (enrdf_load_stackoverflow)
JP (1) JPH06501097A (enrdf_load_stackoverflow)
KR (1) KR930702671A (enrdf_load_stackoverflow)
CN (1) CN1059966A (enrdf_load_stackoverflow)
CA (1) CA2091347A1 (enrdf_load_stackoverflow)
DE (1) DE4028716A1 (enrdf_load_stackoverflow)
FI (1) FI931035L (enrdf_load_stackoverflow)
TW (1) TW240293B (enrdf_load_stackoverflow)
WO (1) WO1992004624A1 (enrdf_load_stackoverflow)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4425347B1 (ja) * 2008-10-21 2010-03-03 北斗電子工業株式会社 液体中の粒子のサイズの検出方法および装置

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2273590A1 (fr) * 1974-06-05 1976-01-02 Pechiney Aluminium Procede pour la determination en continu de la resistance interne d'une cuve d'electrolyse et appareillage pour la mise en oeuvre du procede
US4009998A (en) * 1975-09-05 1977-03-01 Phillips Petroleum Company Acid concentration measurement
EP0274396A2 (en) * 1987-01-09 1988-07-13 Hitachi, Ltd. Water quality control method, and method and apparatus for measuring electrical conductivity used in the water quality control

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2273590A1 (fr) * 1974-06-05 1976-01-02 Pechiney Aluminium Procede pour la determination en continu de la resistance interne d'une cuve d'electrolyse et appareillage pour la mise en oeuvre du procede
US4009998A (en) * 1975-09-05 1977-03-01 Phillips Petroleum Company Acid concentration measurement
EP0274396A2 (en) * 1987-01-09 1988-07-13 Hitachi, Ltd. Water quality control method, and method and apparatus for measuring electrical conductivity used in the water quality control

Also Published As

Publication number Publication date
EP0548133A1 (de) 1993-06-30
TW240293B (enrdf_load_stackoverflow) 1995-02-11
FI931035A7 (fi) 1993-04-06
CA2091347A1 (en) 1992-03-11
DE4028716A1 (de) 1992-03-12
KR930702671A (ko) 1993-09-09
CN1059966A (zh) 1992-04-01
FI931035L (fi) 1993-04-06
FI931035A0 (fi) 1993-03-09
JPH06501097A (ja) 1994-01-27

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