[go: up one dir, main page]

EP0037221B1 - Verfahren und Zusammensetzung zur Verhinderung der Korrosion von Metalloberflächen in wässrigen Lösungen - Google Patents

Verfahren und Zusammensetzung zur Verhinderung der Korrosion von Metalloberflächen in wässrigen Lösungen Download PDF

Info

Publication number
EP0037221B1
EP0037221B1 EP81301199A EP81301199A EP0037221B1 EP 0037221 B1 EP0037221 B1 EP 0037221B1 EP 81301199 A EP81301199 A EP 81301199A EP 81301199 A EP81301199 A EP 81301199A EP 0037221 B1 EP0037221 B1 EP 0037221B1
Authority
EP
European Patent Office
Prior art keywords
water
chromate
polymer
soluble
aqueous medium
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.)
Expired
Application number
EP81301199A
Other languages
English (en)
French (fr)
Other versions
EP0037221A1 (de
Inventor
Frederick Gottlieb Vogt
Patricia Timpano Sparrell
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.)
BetzDearborn Europe Inc
Original Assignee
Betz Europe 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
Priority claimed from US06/134,813 external-priority patent/US4329250A/en
Priority claimed from US06/134,812 external-priority patent/US4297317A/en
Application filed by Betz Europe Inc filed Critical Betz Europe Inc
Publication of EP0037221A1 publication Critical patent/EP0037221A1/de
Application granted granted Critical
Publication of EP0037221B1 publication Critical patent/EP0037221B1/de
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids

Definitions

  • the present invention relates to a method and a composition for reducing corrosion of metal surfaces in contact with aqueous systems.
  • Chromates are widely referred to in the literature, and their effectiveness in reducing the rate of corrosion of metallic surfaces exposed to corroding aqueous mediums is well known. However, if used in low concentrations these inhibitors can cause considerable pitting and tuberculation. Indeed, if added in insufficient quantities to stop metal surface attach altogether, corrosion can become so severely localized and the intensity of attack so intense that perforations may occur more extensively than if no inhibitor treatment had been added.
  • U.S. Patent 4, 209, 398 discloses a water treatment composition
  • a water treatment composition comprising a polymer containing a structural unit that is derived from a monomer having an ethylenically unsaturated bond and one or more carboxyl radicals, at least a portion of which radicals have been modified.
  • Compounds such as inorganic phosphates, phosphonic acids, organic phosphoric acid esters and polyvalent metal salts are combined with the polymer for treating the particular system.
  • the polymer may be used in combination with conventional corrosion inhibitors for iron, steel, copper, copper alloys or other metals, conventional scale and contamination inhibitors, metal ion sequestering agents and other conventional water treating agents.
  • corrosion inhibitors there are can be enumerated chromates, bichromates, tungstate, molybdates, nitrites, borates, silicates, oxycarboxylic acids, amino acids, catechols, aliphatic amino surface active agents, benzotriazole, and mercaptobenzotriazole.
  • U.S. Patent 3,658,710 discloses a method of removing tubercles of corrosion from a substrate and inhibiting scale formation using organic polymers and silica and/or chromium compounds.
  • a second polymer, such as an organic phosphonate may also be used.
  • a chromate-based corrosion inhibitor for metal surfaces exposed to a corroding aqueous medium consists essentially of (i) water-soluble chromate and (ii) a particular type of water-soluble polymer comprised of units derived from acrylic acid or derivatives thereof (AA) and 2-hydroxy-propyl acrylate units (HPA).
  • AA acrylic acid or derivatives thereof
  • HPA 2-hydroxy-propyl acrylate units
  • methods according to the present invention would comprise the use of zinc-free corrosion inhibitor treatments comprising components (i) and (ii) as defined above.
  • methods according to the present invention would comprise the use of zinc-free and phosphate free corrosion inhibitors comprising the noted components (i) and (ii).
  • the present invention relates to a corrosion inhibitor treatment comprising water-soluble chromate AA/HPA wherein the chromate is added in an amount of less than 5 parts of active chromate per million parts of aqueous medium.
  • the present invention is considered to have applicability to any aqueous system. It is particularly useful in cooling water systems. Accordingly, the present invention will hereinafter be described as it relates to cooling water systems.
  • AA acrylic acid compound
  • the polymers are considered, more broadly, to have a mole ratio of AA:HPA of from about 1:4 to 36:1. This mole ratio is preferably 1:1 to 11:1, and most preferably 1:1 to 5:1.
  • the only criteria that is considered to be of importance with respect to mole ratios is that the copolymer should be water-soluble. As the proportion of hydroxylated alkyl acrylate moieties increases, the solubility of the copolymer decreases. It is noted that, from an efficacy point of view, the polymers having a mole ratio of AA:HPA of 1:1 to 5:1 are considered the best.
  • the polymers preferably have a molecular weight of from 1,000 to 50,000 with from 2,000 to 6,000 being most preferred.
  • the polymers utilized in accordance with the invention can be prepared by vinyl addition polymerization or by treatment of an acrylic acid or salt polymer. More specifically, acrylic acid or derivatives thereof or their water soluble salts, e.g., sodium, potassium, ammonium, etc. can be copolymerized with the hydroxy alkyl acrylate under standard copolymerization conditions utilizing free radical initiators such as benzoyl peroxide, azobisisobutyronitrile or redox initiators such as ferrous sulfate and ammonium persulfate. The molecular weight of the resulting copolymer can be controlled utilizing standard chain control agents such as secondary alcohols (isopropanol), mercaptans, halocarbons, etc. Copolymers falling within the scope of the invention are commercially available from, for example, National Starch Company.
  • the 2-hydroxypropyl acrylate can be prepared by reacting acrylic acid with propylene oxide.
  • the polymers of the invention may also be prepared by reacting a polyacrylic acid or derivative thereof with an appropriate amount of propylene oxide. The reaction takes place at the COOH or COM group of the units to provide the hydroxylated propyl acrylate unit.
  • the polymer prepared either by copolymerization of AA with hydroxypropyl acrylate (HPA) or reaction of AA with propylene oxide would be composed primarily of units having the structural formulas: wherein M is as earlier defined. It is noted that in aqueous solution with hydroxypropyl acrylate unit is in equilibrium with a minor amount of 1-methyl-2-hydroxyethyl acrylate.
  • chromate compounds which could be used in practicing methods according to the present invention are described in U.S. 2,900,222 to Kahler et al. These compounds would include alkali metals or any water-soluble compound that contains hexavalent chromate and provides chromate radical in water solutions.
  • Illustrative water-soluble chromate compounds are sodium chromate dihydrate, sodium chromate anhydrous, sodium chromate tetrahydrate, sodium chromate hexahydrate, sodium chromate decahydrate, potassium dichromate, potassium chromate, ammonium dichromate and chromic acid.
  • the amount of each constituent added to the cooling water would, of course, be, an effective amount for the purpose and would depend on such factors as the nature and severity of the corrosion problem being treated and the temperature and pH of the cooling water.
  • active polymer As little as about 0.5 part per million parts of cooling water (ppm) should be effective, while about 2 ppm is the preferred lower limit. Based on economic considerations, the polymer could be fed in amount as high as about 200 ppm, with about 50 ppm being the preferred upper limit.
  • ppm part per million parts of cooling water
  • active chromate that is, active hexavalent chromate ion
  • active chromate ion as little as about 0.5 ppm should be effective.
  • the upper limit would depend on such factors as cost and toxicity and is less than 5 ppm.
  • chromate and the polymer may however be added to the aqueous system separately or together.
  • the treatment is preferably used as an aqueous solution.
  • the constitutes are combined by simply adding them to water. Should long-term stability problems be experienced, a two-barrel treatment may be more desirable. Of course, the constituents could be combined in any relative proportions in dry form.
  • compositions according to the present invention could vary widely and preferably comprise, on a weight basis:
  • the cooling water it is possible for the cooling water to have a pH of about 5.5 to 9.5. More commonly, the pH is about 6.5 to 8.5, with about 6.5 to 7.5 being most common.
  • Corrosion rate was determined by weight loss measurement. Prior to immersion, coupons were scrubbed with a mixture of trisodium phosphate-pumice, rinsed with water, rinsed with isopropyl alcohol and then air dried. Weight measurement to the nearest milligram was made. At the end of one day, a weighed coupon was removed and cleaned. Cleaning consisted of immersion into a 50% solution of HCI for approximately 20 seconds, rinsing with tap water, scrubbing with a mixture of trisodium phosphate-pumice until clean and then rinsing with tap water and isopropyl alcohol. When dry, a second weight measurement to the nearest milligram was made. At the termination of tests, the remaining coupon was removed, cleaned and weighed.
  • the results of these tests are reported below in TABLE 1 in terms of per cent (%) corrosion inhibition of various treatments as compared to an untreated control test.
  • the polymer tested was an acrylic acid/hydroxypropyl acrylate copolymer (AA/HPA) having a mole ratio of AA to HPA of 3:1 and a nominal molecular weight of 6000.
  • the chromate compound used was sodium dichromate dihydrate. The amounts of chromate reported are active chromate dosages in ppm, and the pH of the test water was 8. The corrosion rates are reported in mils per year (mpy) and millimetres per year (mmpy).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Chemical Treatment Of Metals (AREA)

Claims (9)

1. Verfahren zur Verringerung der Korrosion von Metalloberflächen, die mit einem wäßrigen Medium in Berührung stehen, gekennzeichnet, durch Zugabe zu diesem wäßrigen Medium einer für den Zweck wirksamen Menge eines zinkfreien und phosphatfreien
. i) wasserlöslichen Chromats und
ii) wasserlöslichen Polymers, umfassend Einheiten, die abgeleitet sind von Acrylsäure oder wasserlöslichen Salzen davon und Einheiten von 2-Hydroxypropyl-acrylat, wobei die Einheiten des Polymers die folgenden Formeln besitzen
Figure imgb0010
wobei R Wasserstoff oder eine niedere Alkylgruppe mit 1 bis 3 Kohlenstoffatomen bedeutet, R, OH, NH2 oder OM ist, wobei M ein wasserlösliches Kation bedeutet, und das Molverhältnis x:y der erstgenannten zu den letztgenannten Einheiten 1:4 bis 36:1 beträgt, und das Chromat und das Polymer entweder getrennt oder zusammen zugesetzt werden und das wasserlösliche Chromat in einer Menge von 0,5 bis weniger als 5 Teile aktives Chromat pro Millionen Teile des wäßrigen Mediums zugesetzt wird.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß das Polymer Molekulargewicht von 1 000 bis 50 000 hat.
3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß das Molverhältnis x:y 1:1 bis 11:1 beträgt.
4. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, daß das wasserlösliche Polymer in einer Menge von 0,5 bis 200 Teilen Polymer pro Millionen Teile des wäßrigen Mediums zugesetzt wird.
5. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, daß das wäßrige Medium Kühlwasser ist.
6. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, daß die Komponenten (i) und (ii) zusammen zu dem wäßrigen Medium zugesetzt werden.
7. Mittel zur Verringerung der Korrosion von Metalloberflächen, die mit einem wäßrigen Medium in Berührung stehen, dadurch gekennzeichnet, daß das Mittel zinkfrei und phosphatfrei ist und in Kombination enthält
i) wasserlösliches Chromat und
ii) wasserlösliches Polymer wie in einem der Ansprüche 1 bis 3 definiert.
8. Mittel nach Anspruch 7, dadurch gekennzeichnet, daß, bezogen auf das Gewicht, das Chromat 1 bis 99% und das Polymer 1 bis 99%, bezogen auf die Gesamtmenge an wasserlöslichem Chromat und wasserlöslichem Polymer ausmacht.
9. Mittel nach Anspruch 7 oder 8, dadurch gekennzeichnet, daß es eine stabile wäßrige Lösung der Komponenten (i) und (ii) ist.
EP81301199A 1980-03-28 1981-03-20 Verfahren und Zusammensetzung zur Verhinderung der Korrosion von Metalloberflächen in wässrigen Lösungen Expired EP0037221B1 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US06/134,813 US4329250A (en) 1980-03-28 1980-03-28 Low level chromate-based corrosion inhibition in aqueous mediums
US06/134,812 US4297317A (en) 1980-03-28 1980-03-28 Low level chromate-based corrosion inhibition in aqueous mediums
US134812 1980-03-28
US134813 1987-12-18

Publications (2)

Publication Number Publication Date
EP0037221A1 EP0037221A1 (de) 1981-10-07
EP0037221B1 true EP0037221B1 (de) 1984-07-25

Family

ID=26832698

Family Applications (1)

Application Number Title Priority Date Filing Date
EP81301199A Expired EP0037221B1 (de) 1980-03-28 1981-03-20 Verfahren und Zusammensetzung zur Verhinderung der Korrosion von Metalloberflächen in wässrigen Lösungen

Country Status (5)

Country Link
EP (1) EP0037221B1 (de)
AU (1) AU533121B2 (de)
CA (1) CA1147137A (de)
DE (1) DE3164965D1 (de)
NZ (1) NZ194191A (de)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2643422A1 (de) * 1976-09-21 1978-03-30 Kurita Water Ind Ltd Wasserbehandlungsmittel und verfahren zur behandlung von wasser

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1255964A (en) * 1968-02-28 1971-12-08 Grace W R & Co Composition and method for inhibiting scaling in aqueous systems
US3658710A (en) * 1971-01-13 1972-04-25 W E Zimmie Inc Method of removing tubercles using organic polymers and silica and/or chromium compounds
US4183772A (en) * 1978-01-30 1980-01-15 Union Carbide Corporation Composition and method for coating metal surfaces

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2643422A1 (de) * 1976-09-21 1978-03-30 Kurita Water Ind Ltd Wasserbehandlungsmittel und verfahren zur behandlung von wasser

Also Published As

Publication number Publication date
EP0037221A1 (de) 1981-10-07
CA1147137A (en) 1983-05-31
AU533121B2 (en) 1983-11-03
AU5955780A (en) 1981-10-01
DE3164965D1 (en) 1984-08-30
NZ194191A (en) 1983-05-10

Similar Documents

Publication Publication Date Title
EP0033417B1 (de) Verfahren und Zusammensetzung zur Korrosionsverhinderung
AU617792B2 (en) Method for controlling corrosion using molybdate compositions
JP2916000B2 (ja) ある種のホスホノメチルアミン類を用いる水性系における腐食の抑制
EP0142929B1 (de) Wasserlösliche Polymere und deren Anwendung
CA1222749A (en) Process of inhibiting corrosion of metal surfaces and/or deposition of scale thereon
JPS60118295A (ja) 用水処理用ポリマーとその使用方法
US4033896A (en) Method of corrosion inhibition and compositions therefor
US4446046A (en) Poly (alkenyl) phosphonic acid and methods of use thereof
JP3205563B2 (ja) ある種のホスホノメチルアミン類を用いる水性系における腐食の抑制
EP0277412B1 (de) Korrosionsinhibierung von Eisenmetallen
EP0396243A1 (de) Korrosioninhibierung in wässrigen Systemen
JPH0141705B2 (de)
EP0488538B1 (de) Korrosionsverhinderung
EP0037221B1 (de) Verfahren und Zusammensetzung zur Verhinderung der Korrosion von Metalloberflächen in wässrigen Lösungen
US4297317A (en) Low level chromate-based corrosion inhibition in aqueous mediums
US4329250A (en) Low level chromate-based corrosion inhibition in aqueous mediums
EP0017373B1 (de) Stabile Zusammensetzungen zur Verwendung als Korrosionsinhibitoren und Verfahren zur Korrosionsverhütung in wässrigen Systemen
KR100297807B1 (ko) 금속의부식방지용수처리제조성물
JP4089648B2 (ja) 腐食防止方法
AU617791B2 (en) Method and compositions for controlling corrosion in low and high hardness water
CA1181196A (en) Isopropenyl phosphonic acid copolymers and methods of use thereof
EP0363439A1 (de) Behandlung von wassersystemen zur vorbeugung von korrosion und kesselstein
JPS6296683A (ja) 水系における金属類のスケ−ル抑制を兼ねた腐食防止剤
KR850000599B1 (ko) 부식방지 조성물
JPS59193282A (ja) 金属表面の状態調整方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): BE DE FR GB IT NL

17P Request for examination filed

Effective date: 19810810

ITF It: translation for a ep patent filed
GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): BE DE FR GB IT NL

REF Corresponds to:

Ref document number: 3164965

Country of ref document: DE

Date of ref document: 19840830

ET Fr: translation filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19850328

Year of fee payment: 5

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19860331

Year of fee payment: 6

BERE Be: lapsed

Owner name: BETZ EUROPE INC.

Effective date: 19870331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19871001

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19871130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19871201

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Effective date: 19890331

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19890331

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19900320

GBPC Gb: european patent ceased through non-payment of renewal fee