US20020166772A1 - Maintenance of an electrolyte - Google Patents

Maintenance of an electrolyte Download PDF

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Publication number
US20020166772A1
US20020166772A1 US10/104,127 US10412702A US2002166772A1 US 20020166772 A1 US20020166772 A1 US 20020166772A1 US 10412702 A US10412702 A US 10412702A US 2002166772 A1 US2002166772 A1 US 2002166772A1
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US
United States
Prior art keywords
electrolyte
ion
ion exchanger
exchanger
further characterized
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
US10/104,127
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English (en)
Inventor
Jan Hendriks
Josephus Weel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MacDermid Enthone Inc
Original Assignee
Enthone Inc
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 Enthone Inc filed Critical Enthone Inc
Assigned to ENTHONE INC. reassignment ENTHONE INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WEEL, JOSEPHUS H.M., HENDRIKS, JAN J.M.
Publication of US20020166772A1 publication Critical patent/US20020166772A1/en
Abandoned legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D21/00Processes for servicing or operating cells for electrolytic coating
    • C25D21/16Regeneration of process solutions
    • C25D21/22Regeneration of process solutions by ion-exchange
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D21/00Processes for servicing or operating cells for electrolytic coating
    • C25D21/12Process control or regulation

Definitions

  • the invention pertains to a method for the care and maintenance of an electrolyte.
  • Insoluble anodes are predominantly used in acidic gold electrolytes. Therefore, supplementation of the electrolyte with a gold salt is necessary. Such gold salts predominantly contain potassium as cations. In addition, it is typical for the flushing water to be fed back into the plating bath for the purpose of cost reduction. Thus, in the course of the bath operation, the concentration of potassium ions increases and leads to a large increase in the density of the bath, which results in a reduction of the bath operating time.
  • insoluble anodes results in problematic shifts in pH during operation. This also depresses cathode efficiency below 100%, so that hydrogen ions are reduced in addition to gold ions, thereby raising the pH.
  • acid is typically added to the electrolyte to control the pH to within certain limits. This can be, e.g., sulfuric acid or also an organic acid.
  • one object of the invention is based the provision of a simple method for maintaining an electrolyte, which is capable of lengthening the lifetime of the electrolyte in an electrolytic process by maintaining a substantially constant ion concentration and ion composition in the electrolyte.
  • Another object of the invention is the provision of a method to maintain the pH of an electrolyte in an electrolytic process without the formation of precipitates.
  • a related object of the invention is the provision of a method to maintain the pH of an electrolyte in an electrolytic process without wasteful addition of costly chemicals to the electrolyte.
  • the invention is directed to a method for maintenance of an electrolyte.
  • the method is characterized in that at least one ion exchanger controls ion concentration and ion composition of the electrolyte.
  • the invention is also directed to a method for the control of the composition of an electrolyte comprising alkali metal ions during a gold plating operation.
  • the electrolyte is circulated through an acidic cation exchanger to exchange the alkali metal cations of the electrolyte with acidic counterions from the exchanger, and the electrolyte is returned to the gold plating operation.
  • the invention is further directed to a device for care and maintenance of an electrolyte.
  • the device comprises an ion exchanger for exchanging an ion of the electrolyte with a cation from the ion exchanger.
  • the present invention proposes to adjust the ion composition and the ion concentration in the electrolyte by means of an ion exchanger.
  • the electrolyte is guided through the ion exchanger and, during the exchange process, the counterions in the matrix of the ion exchanger are exchanged with ions from the electrolyte.
  • the method according to the invention allows the ion composition of the electrolyte and the corresponding ion concentration to be controlled in an advantageous way.
  • the method according to the invention is particularly advantageous in that, through the use of the ion exchanger, ions that negatively affect the bath quality can be exchanged with ions that are necessary to maintain a substantially constant bath quality.
  • the composition of the electrolyte and the corresponding ion concentration can be adjusted in an advantageous way.
  • the method according to the invention provides an unexpected solution to the problem in the state of the art that the bath composition must be adjusted with an expensive process using additives, which, e.g., for gold baths, increases the risk of forming deposits as described above.
  • the present invention discloses a method for the care and maintenance of electrolytes that is extremely advantageous because conventional means that negatively influence the lifetime of an electrolyte bath are avoided and, further, because environmental benefits are gained through reduced chemical usage.
  • the method according to the invention is less expensive because processes that otherwise had to be controlled separately are now controlled by a single processing step, i.e., by guiding the electrolyte fluid through the ion exchanger. Also, with the method according to the invention, measurement and control steps can be eliminated because the bath composition no longer must to be monitored with expensive processes. Therefore, processing steps and costs can be eliminated. Further, the lifetime of an electrolyte is no longer limited by the problematic conditions described elsewhere herein because its composition can be kept substantially constant. The improved consistency in composition, and thus quality, of the electrolyte results in fewer quality defects for the deposited films. Furthermore, the feature according to the invention of using an ion exchanger for care and maintenance of an electrolyte is also advantageous due to the regenerability of the ion exchanger, so that the method has a low material expense and thus is also cost effective.
  • the method according to the invention can be used for the maintenance of any electrolyte for which an ion composition and/or concentration can be adjusted by means of an ion exchanger.
  • the ion exchanger exchanges undesired ions that negatively influence the quality of the electrolyte with ions that need to be replenished in the bath.
  • the ion exchanger preferably contains counterions that are present in the electrolyte and that are needed to maintain bath quality. In this way, the ion exchanger can be advantageously regenerated after use.
  • the method according to the invention is used to maintain acidic gold electrolytes.
  • the disadvantages for gold electrolytes during operations are the build up of potassium ions and the increase in electrolyte pH.
  • the precise maintenance of the pH, and thus the hydrogen ion concentration, is a determinative factor, particularly for gold electrolytes.
  • the present invention can reduce or eliminate the excessive addition of inorganic or organic acids for the purpose of pH control, by providing such control through the use of an ion exchanger. As these additives can be substantially eliminated, so too is the negative influence on bath quality from the undesired deposits that they cause.
  • the principle of ion exchange is used with the present invention in an extremely advantageous way, wherein one type of ion can be easily exchanged with another, so that the ions negatively influencing the bath quality of the electrolyte, such as potassium ions for acidic gold baths, can be exchanged with counterions positively influencing the bath quality, such as hydrogen ions for acidic gold baths.
  • a cation exchanger is preferably used for control. More preferably, an acidic cation exchanger is a used to perform the care and maintenance of an acidic gold electrolyte.
  • the cations contained in the electrolyte can be exchanged with hydrogen ions of the cation exchanger.
  • the potassium ions that are disadvantageous for the operation of the bath are exchanged with hydrogen ions that are necessary in order to prevent an increase in the pH. Therefore, two essential problems in the operation of an electrolyte bath, particularly those of an acidic gold electrolyte, are solved in an uncomplicated way by means of the method according to the invention.
  • potassium ions which produce a shortened lifetime for the bath due to an increase in density of the bath, are removed from the electrolyte. They are preferably exchanged with hydrogen ions that advantageously replace the hydrogen ions reduced by the electrolysis. This process acts against the tendency for the pH of an electrolyte to increase during operation. In this way, the addition of greater amounts of inorganic or organic acids can be substantially eliminated. This further prevents the otherwise occurring precipitation of potassium salt, e.g., potassium sulfate, according to the acids that are used.
  • potassium salt e.g., potassium sulfate
  • the ion exchanger is occasionally regenerated when the matrix becomes loaded with ions which are problematic to an electrolyte.
  • the ion exchanger becomes loaded with the problematic cations.
  • ion exchange is a reversible process in which the problematic cations may be eluted out of a cation exchanger treatment with acid and water can transform a cation exchanger back to its original state loaded with hydrogen ions.
  • the ion exchanger has a long service life and enjoys essentially unlimited use. This leads to a valuable cost reduction, especially in the operation of a gold bath.
  • the composition of the electrolyte bath is held substantially constant, whereby the lifetime of the electrolyte bath is not limited.
  • continuously determined amounts of electrolyte can be removed from the electrolyte bath by means of transport devices and guided through the appropriate ion exchanger.
  • Electrolyte column effluent that is depleted of potassium ions, in the case of the maintenance of an acidic gold bath, and which has been enriched with an essentially equivalent amount of hydrogen ions can be fed back to the electrolyte bath. Flushing is preferably performed to regenerate an ion exchanger matrix loaded with potassium ions, wherein the ions captured from the electrolyte are eluted and, in turn, the matrix is loaded with hydrogen ions.
  • the column is alternately washed with diluted acid and water to elute the ions captured from the electrolyte. After flushing, the column is again ready for use.
  • the means and steps are to be adapted to the ion exchanger that is used.
  • gold is generally recovered from flushings that have settled out, from rejected electrolytes, and from defective tools. Because gold ions can also be captured in the matrix of an ion exchanger, an eluate may comprise gold ions can be fed into other flushing solutions, or the like, which perform a gold recovery. Gold recovery can be performed, e.g., by means of highly basic anionic exchanger resin or electrolysis cells.
  • the method according to the invention also allows the setting of additional fine adjustments.
  • small pH value deviations that cannot be regulated by means of the ion exchanger are regulated by means that supplement the ion exchanger.
  • the relevant process variables of the electrolyte are measured by means of measurement devices, compared with the desired target values, and appropriate means are automatically started.
  • the flow rate of the electrolyte fluid through the ion exchanger can be increased, a fine adjustment of pH, which cannot be done by the ion exchanger, can be performed by means of an inorganic or organic acid, and further, possible drag-out losses are supplemented.
  • measurement devices can determine the amount of floating particles, and, if necessary, filtration can be done by means of filter systems.
  • the invention proposes a device for the care and maintenance of an electrolyte, particularly an acidic gold electrolyte, which comprises measurement devices that measure the relevant process variables of the electrolyte to be maintained in the form of actual values, as well as storage devices that store the target values of the relevant process variables of the electrolyte to be maintained, as well as at least one calculation unit that compares the measured actual value with the stored target value and a control unit that controls the means in order to adjust the actual value of the electrolyte to the target value.
  • the device may optionally comprise: an ion exchanger that exchanges the ions negatively influencing the bath quality from the electrolyte with its own counterions that are also present in the electrolyte and that are required for good electrolyte quality; transport devices that guide the electrolyte fluid to the ion exchanger as well as back into the electrolyte bath; and, flushing devices to regenerate a loaded ion exchanger.
  • an ion exchanger that exchanges the ions negatively influencing the bath quality from the electrolyte with its own counterions that are also present in the electrolyte and that are required for good electrolyte quality
  • transport devices that guide the electrolyte fluid to the ion exchanger as well as back into the electrolyte bath
  • flushing devices to regenerate a loaded ion exchanger.
  • less complex devices that exhibit substantially constant operating parameters and that can function without measurement, storage, and calculation units are also included within the scope of the invention.
  • the methods of the present invention can be adapted to a wide range of different electrolytes; they should neither be interpreted as being restricted to the care and maintenance of acidic gold baths nor to other processes in which pH would otherwise rise.
  • the methods according to the invention are also well-suited to maintaining a substantially constant composition and ion concentration of alkali electrolytes. Only the corresponding parameters, e.g., of the ion exchanger, which, e.g., can be a basic anionic exchanger, the flushing steps, and the regeneration, etc., must be adapted.
  • This non-restrictive example demonstrates the effectiveness of the method according to the invention for the maintenance of an acidic gold electrolyte.
  • an aqueous electrolyte was used that contained as essential components citric acid/potassium citrate, a cobalt (II) citrate complex, formic acid/potassium formate, as well as a gold complex (potassium gold cyanide).
  • citric acid/potassium citrate a cobalt (II) citrate complex
  • formic acid/potassium formate as well as a gold complex (potassium gold cyanide).
  • a gold complex gold gold cyanide
  • the ion exchanger reduced the potassium concentration from 75 g/L to 59 g/L and reduced the pH from 5.0 to 4.7.
  • the stability of the gold cyanide complex was not negatively influenced. No other significant ions were observed to be retained in the matrix of the ion exchanger in subsequent tests.
  • the selectivity is particularly advantageous in that no ions are removed from the electrolyte that must be replaced at great cost, such as gold ions.
  • the ion exchanger resin was regenerated with 5% sulfuric acid. Multiple repetitions of the test showed that the method functions consistently with good results, and, due to its regenerability, the ion exchanger showed essentially no aging effects.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Automation & Control Theory (AREA)
  • Treatment Of Water By Ion Exchange (AREA)
  • Electrolytic Production Of Metals (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
  • Control Of Non-Electrical Variables (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Water Treatment By Electricity Or Magnetism (AREA)
US10/104,127 2001-03-24 2002-03-22 Maintenance of an electrolyte Abandoned US20020166772A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01107350.9 2001-03-24
EP01107350A EP1243673A1 (de) 2001-03-24 2001-03-24 Wartung eines Elektrolyten

Publications (1)

Publication Number Publication Date
US20020166772A1 true US20020166772A1 (en) 2002-11-14

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Family Applications (1)

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US10/104,127 Abandoned US20020166772A1 (en) 2001-03-24 2002-03-22 Maintenance of an electrolyte

Country Status (8)

Country Link
US (1) US20020166772A1 (ja)
EP (1) EP1243673A1 (ja)
JP (1) JP2002322600A (ja)
KR (1) KR20020075825A (ja)
CN (1) CN1306072C (ja)
PL (1) PL352752A1 (ja)
RU (1) RU2002107327A (ja)
SG (1) SG111051A1 (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1816237A1 (de) * 2006-02-02 2007-08-08 Enthone, Inc. Verfahren und Vorrichtung zur Beschichtung von Substratoberflächen

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* Cited by examiner, † Cited by third party
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CN101453037B (zh) * 2007-11-30 2011-04-20 比亚迪股份有限公司 一种锂离子电池有机电解液的精制方法
US8889912B2 (en) 2011-12-30 2014-11-18 E I Du Pont De Nemours And Company Process for preparing 1,6-hexanediol
US8865940B2 (en) 2011-12-30 2014-10-21 E I Du Pont De Nemours And Company Process for preparing 1,6-hexanediol
EP2797868A4 (en) 2011-12-30 2015-08-12 Du Pont PROCESS FOR PRODUCING HEXANEDIOLS
JP2015509088A (ja) 2011-12-30 2015-03-26 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company 1,6−ヘキサンジオールを調製する方法
WO2013101970A1 (en) 2011-12-30 2013-07-04 E. I. Du Pont De Nemours And Company Production of 5-hydroxymethyl-2-furfural from levoglucosenone
EP2797904A4 (en) 2011-12-30 2015-08-05 Du Pont PREPARATION OF TETRAHYDROFURAN-2, 5-DIMETHANOL FROM ISOSORBIDE
US9018423B2 (en) 2012-04-27 2015-04-28 E I Du Pont De Nemours And Company Production of alpha, omega-diols
US8859826B2 (en) 2012-04-27 2014-10-14 E I Du Pont De Nemours And Company Production of alpha, omega-diols
US8846984B2 (en) 2012-04-27 2014-09-30 E I Du Pont De Nemours And Company Production of α,ω-diols
KR101681194B1 (ko) * 2015-11-16 2016-12-12 대영엔지니어링 주식회사 전착도장 품질관리방법

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3865701A (en) * 1973-03-06 1975-02-11 American Chem & Refining Co Method for continuous high speed electroplating of strip, wire and the like

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Publication number Priority date Publication date Assignee Title
US3637473A (en) * 1969-07-03 1972-01-25 Engelhard Min & Chem Method for electroplating gold
JPS58177499A (ja) * 1982-04-08 1983-10-18 Sannou Tokin Kk 電気メツキ液の不純物除去装置
JPS6152400A (ja) * 1984-08-20 1986-03-15 Nippon Mining Co Ltd 銀めつきの方法
JPS63223200A (ja) * 1987-03-13 1988-09-16 Nippon Mining Co Ltd 金めつき液の再生方法
US5393416A (en) * 1993-01-26 1995-02-28 Henkel Corporation Apparatus for maintaining a stable bath for an autodeposition composition by periodically separating particular metal ions from the composition
KR100240470B1 (ko) * 1993-04-22 2000-01-15 에모또 간지 주석도금액의회수재생방법

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3865701A (en) * 1973-03-06 1975-02-11 American Chem & Refining Co Method for continuous high speed electroplating of strip, wire and the like

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1816237A1 (de) * 2006-02-02 2007-08-08 Enthone, Inc. Verfahren und Vorrichtung zur Beschichtung von Substratoberflächen
WO2007088008A2 (de) 2006-02-02 2007-08-09 Enthone Inc. Verfahren und vorrichtung zur beschichtung von substratoberflächen
WO2007088008A3 (de) * 2006-02-02 2008-04-17 Enthone Verfahren und vorrichtung zur beschichtung von substratoberflächen
US20090324804A1 (en) * 2006-02-02 2009-12-31 Enthone Inc. Method and device for coating substrate surfaces

Also Published As

Publication number Publication date
CN1382836A (zh) 2002-12-04
EP1243673A1 (de) 2002-09-25
KR20020075825A (ko) 2002-10-07
RU2002107327A (ru) 2004-03-20
JP2002322600A (ja) 2002-11-08
SG111051A1 (en) 2005-05-30
CN1306072C (zh) 2007-03-21
PL352752A1 (en) 2002-10-07

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Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HENDRIKS, JAN J.M.;WEEL, JOSEPHUS H.M.;REEL/FRAME:013143/0582;SIGNING DATES FROM 20020621 TO 20020624

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