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
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
  • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
  • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
  • C23C22/34—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B22—CASTING; POWDER METALLURGY
  • B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
  • B22D11/00—Continuous casting of metals, i.e. casting in indefinite lengths
  • B22D11/12—Accessories for subsequent treating or working cast stock in situ
  • B22D11/124—Accessories for subsequent treating or working cast stock in situ for cooling
  • B22D11/1245—Accessories for subsequent treating or working cast stock in situ for cooling using specific cooling agents
• • 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
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
  • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
  • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
  • C23C22/48—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 not containing phosphates, hexavalent chromium compounds, fluorides or complex fluorides, molybdates, tungstates, vanadates or oxalates
  • C23C22/56—Treatment of aluminium or alloys based thereon
• • 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
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
  • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
  • C23C22/68—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous solutions with pH between 6 and 8

Definitions

• the invention includes a method for reducing corrosion in cooling and process water, which can lead to an entry of acids into the system, e.g. B. in continuous casting plants of the steel industry.
• the entry of silicon tetrafluoride and HF in the spray zones resulting from fluoride burn-off of the casting powder leads to a drop in the pH value in the spray water and to corrosion of system parts.
• the object of the invention was to provide an effective method for reducing corrosion without having the disadvantages of the known methods.
• a method should be made available which is not very critical with regard to a pH increase and at the same time allows a quick adaptation to changing operating conditions.
• the invention relates to a method for reducing the corrosiveness of cooling or process water, in which there is a lowering of the pH due to an entry of acids, characterized in that at least one water-soluble salt with a buffering effect is added to the cooling or process water added.
• water-soluble is understood to mean that at least 1 g of the salt dissolves in 1 liter of water at 20 ° C.
• the water-soluble salt with a buffering effect is preferably used in the form of an aqueous solution, since this can simply be metered in via metering pumps.
• the cooling or process water in the reservoir and in the piping system is at least 5 times as large, preferably at least 10 times as large and in particular at least 20 times as large as the amount of cooling or process water in the work area.
• the method is particularly suitable for such a device.
• the method can also be carried out in such a way that the cooling or process water is conducted in a continuous system which comprises a piping system and a working area.
• the cooling or process water is not circulated, but is drained off after a single use.
• “Working area” is understood to mean that area of the device in which the cooling or process water has its technically intended effect. This can be, for example, the area in which the cooling or process water exchanges heat or substances with the ambient air or with other substrates
• it can be a cooling device in which the cooling or process water absorbs heat from this heat by direct or indirect contact with a medium to be cooled.An example of this is the evaporation zone of a cooling tower, but this can also be an area act by bringing the cooling or process water into contact with warm substrate surfaces in order to cool them, for example in the case of continuous casting plants in the steel industry, where the cooling or process water is sprayed onto metal surfaces to be cooled.
• the cooling or process water In the work area, the cooling or process water usually not only comes into contact with the intended substrate, but also with the ambient air. Therefore, the cooling or process water in this area absorbs foreign matter either directly from the substrate surface or from the ambient air. These can be gaseous, solid or liquid in nature. This chemical absorption changes the chemical composition of the cooling or process water. In the example given above, the entry of acidic substances leads to a drop in the pH value in the cooling or process water. As a result, its corrosiveness to the materials of the device and possibly also to the substrate is undesirably increased.
• the drop in pH is counteracted by metering a water-soluble salt with a buffering effect into the cooling or process water.
• a water-soluble salt is buffered Effect metered into the pipe system at a point that is seen in the flow direction of the cooling or process water in front of the work area. Accordingly, it is not necessary to change the chemical composition of the entire cooling or process water, the main amount of which is in the reservoir, by adding the salt with a buffering effect. Rather, you only change the composition of that part of the cooling or process water that subsequently enters into a mass exchange with the environment in the work area.
• the water-soluble salt with a buffering effect is dosed, based on experience, in proportion to the amount of water that flows through the work area. For example, per m 3 of cooling or process water that flows through the work area, a quantity of salt with a buffering effect determined by experience can be metered in. Accordingly, one embodiment of the method according to the invention is that the water-soluble salt with a buffering effect is metered in as a function of the amount of cooling or process water which flows through the working area within a predetermined time interval.
• the dosage amount of the salt with a buffering effect can be made dependent on the currently determined need. This can apply to the entire addition of the salt with a buffering effect. However, one can also proceed in such a way that a basic amount of salt with a buffering effect is metered in proportion to the amount and additionally a fine metering is carried out on the basis of the currently determined need.
• the procedure is preferably such that the value of at least one guide variable in the cooling or process water is measured continuously or discontinuously and the water-soluble salt with a buffering action is metered in as a function of the value of the guide variable.
• the value of the guide variable is expediently measured either in the work area itself, in a sample of the cooling or process water taken in the work area or in that part of the line system which is located behind the work area in the direction of flow of the cooling or process water.
• a sample can be taken in the work area by either draining off part of the cooling or process water and discarding it after measuring the guide variable or by returning it to the work area or the pipe system.
• the guide variable can be selected, for example, from the pH value, the fluoride ion concentration and the acid capacity of the cooling or process water.
• the water-soluble salt with a buffering effect is added when the pH value falls below a predetermined threshold value.
• This threshold value to be determined depending on the material properties of the device and / or the substrate can be, for example, in the range from 4 to 7, in particular from 5 to 6. If the value falls below the threshold value, either salt with a buffering effect is added until the threshold value is exceeded again, or an amount of salt with a buffering effect is added, which depends on the difference between the threshold value and the pH actually measured.
• the fluoride ion concentration can be selected as the guide variable. As mentioned in the introduction, this is the case, for example, with continuous casting plants in the steel industry.
• the acid input is then proportional to the increase in the fluoride ion concentration.
• the water-soluble salt with a buffering effect can be metered in if the fluoride ion concentration exceeds a predetermined threshold value, which can be, for example, in the range from 40 to 300 mg / 1, in particular in the range from 60 to 200 mg / 1. In this case, it is particularly advantageous to determine the deviation of the fluoride ion concentration from the predetermined threshold value and to add the salt with a buffering effect depending on the amount of this deviation.
• the acid capacity of the cooling or process water is selected as the guide variable. This is defined by the amount (in millimoles) of strong monobasic acid that has to be added to one liter of the water in order to Lower the value to 4.3. It is expressed in millimoles of acid added per liter of water.
• the water-soluble salt with a buffering effect is metered in when the acid capacity falls below a predetermined threshold. This can be, for example, in the range from 0.1 to 1 millimole / l, in particular from 0.3 to 0.7 millimole / l.
• the proportionality factor is preferably determined empirically again.
• any water-soluble salt (as defined above) that is known to have a buffering effect can be selected as the salt with a buffering effect.
• the water-soluble salt with a buffering effect can be selected from hydrogen carbonates, carbonates, borates, orthophosphates and polyphosphates.
• Such salts are preferably selected which are selected from alkali, alkaline earth and ammonium salts, preferably from sodium salts for reasons of cost and the environment.
• preferred salts with a buffering action are, in particular, alkali or ammonium salts, especially the sodium salts, with hydrogen carbonate, carbonate, borate, orthophosphate or polyphosphate ions.
• the method according to the invention is particularly suitable for reducing the corrosiveness of cooling or process water from continuous casting plants in the steel industry.
• a preferred embodiment of the invention consists in additionally preventing the deposition of calcium fluoride in the cooling or process water by additionally adding to the cooling or process water at least one further water-soluble salt which contains at least one of the following ions: magnesium cations, cations trivalent metals, anions of oligo- or polyphosphate.
• at least one further water-soluble salt which contains at least one of the following ions: magnesium cations, cations trivalent metals, anions of oligo- or polyphosphate.
• magnesium cations cations trivalent metals
• anions of oligo- or polyphosphate there is a water-soluble salt with magnesium cations to. More detailed information on special embodiments and preferred addition amounts can be found in the aforementioned DE 100 64412, to which reference is hereby expressly made.
• additives known for this area of application can be added to the cooling or process water.
• examples of these are scale inhibitors, corrosion inhibitors and dispersants.
• examples of such additives are polymers or copolymers of unsaturated carboxylic acids, such as, for example, acrylic acid, methacrylic acid and / or maleic acid, which can additionally carry phosphonic or phosphinic acid groups.
• polyamino acids such as polyaspartic acid are known.
• polymeric molecules or ions such as aminoalkylenephosphonic acids, phosphonocarboxylic acids, geminal diphosphonic acids, which are not capable of forming chelate complexes are known for this purpose. Selected examples are contained in DE 10064412 already mentioned.
• the pH value is continuously measured in the spray water of a continuous casting plant by means of a pH electrode, and the metering pump for the water-soluble, buffering salts is started when the temperature falls below a predetermined threshold. If the threshold value is exceeded, the metering is stopped again.
• the threshold value here is usually in the pH range between 4 and 7, preferably in the pH range from 5 to 6.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Mechanical Engineering (AREA)
• General Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Materials Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Preventing Corrosion Or Incrustation Of Metals (AREA)
• Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
• Heat Treatments In General, Especially Conveying And Cooling (AREA)

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• 2002
  • 2002-06-17 DE DE10227040A patent/DE10227040A1/de not_active Withdrawn
• 2003
  • 2003-06-10 AU AU2003236726A patent/AU2003236726A1/en not_active Abandoned
  • 2003-06-10 AT AT03735588T patent/ATE324954T1/de not_active IP Right Cessation
  • 2003-06-10 WO PCT/EP2003/006041 patent/WO2003106074A2/fr not_active Application Discontinuation
  • 2003-06-10 DE DE50303211T patent/DE50303211D1/de not_active Expired - Lifetime
  • 2003-06-10 EP EP03735588A patent/EP1513634B1/fr not_active Expired - Lifetime
  • 2003-06-10 ES ES03735588T patent/ES2263003T3/es not_active Expired - Lifetime

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