CA2037594A1 - Electrolytic graining - Google Patents
Electrolytic grainingInfo
- Publication number
- CA2037594A1 CA2037594A1 CA002037594A CA2037594A CA2037594A1 CA 2037594 A1 CA2037594 A1 CA 2037594A1 CA 002037594 A CA002037594 A CA 002037594A CA 2037594 A CA2037594 A CA 2037594A CA 2037594 A1 CA2037594 A1 CA 2037594A1
- Authority
- CA
- Canada
- Prior art keywords
- aluminium
- electrolyte
- sheets
- alternating current
- graining
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N3/00—Preparing for use and conserving printing surfaces
- B41N3/03—Chemical or electrical pretreatment
- B41N3/034—Chemical or electrical pretreatment characterised by the electrochemical treatment of the aluminum support, e.g. anodisation, electro-graining; Sealing of the anodised layer; Treatment of the anodic layer with inorganic compounds; Colouring of the anodic layer
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/02—Etching
- C25F3/04—Etching of light metals
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A method of electrolytically graining aluminium, aluminium alloy or aluminium laminate, desirably in a substantially uniform manner, in particular for use as a lithographic printing plate substrate, is disclosed wherein the graining is effected using a square wave alternating current.
A method of electrolytically graining aluminium, aluminium alloy or aluminium laminate, desirably in a substantially uniform manner, in particular for use as a lithographic printing plate substrate, is disclosed wherein the graining is effected using a square wave alternating current.
Description
2 ~
ELECTROLYTIC GRAINING
This invention relates to the electrolytic graining of aluminium, aluminium alloys and aluminium lamina~es and mo.re par~icularly, but not exclusively, is concerned with the electrolytic graining of aluminium, alumini.um alloys or aluminium laminates in the production of substrates suitable for use in the manufacture of radiation sensitive plates in lithographic printing plate production.
Radiation sensitive plates of the type with which this invention is concerned conventionally consist of a substrate onto which is coated a radiation sensitive composition. Image-wise exposure of the plate to radiation causes the coating to change its characteristics in the areas struck by radiation so that the coating may be selectivel~ removed from the substrate in the non-image areas by application of a suitable developer to leave aprinting image (or etch resistant axea) on the substrate. In the case of the so-called negative-working devices, it is the non-radiation struck areas of the coating which are removed. Those parts of the coating which are not removed and which thus form the printing image are ordinarily water-repellent and ink-receptive and those parts of the substrate revealed on development are ordinarily water-receptive and ink-repellent.
It will be apparent that the surface of the substrate should be such that the printing image can ~trongly adhere thereto and ~ 25 such that i~ iB readily wettable with water. It is known to ; improve the adhesion of the printing image and to improve the wetting characteristics of the non-image areas by roughening (conventionally referred to as graining) -the substrate before applying the radiation sensitive coating.
The coarseness or surface roughness of the grained substrate can be characterised, for example, by measurement of a centre line average (CLA).
The type of grain required for the substrate of a radiation sensitive printing plate for lithographic printing plate production depends upon the requirements of the final printing plate. Thus a fine grain - i.e. shallow depressions - results in better reproduction of half-tones whereas a coarse grain - i.e. deep depressions - results in the non-image areas having better wetting characteristics. In either case however it is important that the depressions are evenly spaced over the substrate surface and that they are close enough together so that peaks, rather than plateaux, are formed between the depressions.
It is known to grain substrates in lithographic printing plate production by electrolytic techniques. Graining is normally effected by immersing the substrates in a suitable electrolyte and subjecting them to a sine waveform alternating current.
Conventionally, hydrochloric acid has been used as the electrolyts for graining aluminium and aluminium alloy substrates.
However, when using hydrochloric acid it is difficult to obtain a fine homogeneou~ grain and it is therefore nece~sary carefully to control the acid concentration of the electrolyte in order to ensure consiætent results. This is particularly the case when aluminium alloys such as 3103 aluminium manganese alloy are used as the substrate. The use of such alloys for -the substra-te can be ~ ~ ~ r~
particularly advantageous due to their increased resistance to tearing and cracking and to tempera-~ures in excess of 200C which are used to harden the image on the printing plate and thus to increase the printing run leng~h.
It is known to grain aluminium substrates using a~ the electrolyte a mixture of hydrochloric and phosphoric acids. Whilst this method can result in an even grain, an excessive amount of smut is produced on the substrate which can cause the radiation sensitive coating of the plate to become insolubilised during storage of the plate. Thus the smu~ has normally to he removed.
A further disadvantage of using a hydrochloric acid/phosphoric acid mixture as electrolyte is that the process is inflexible in respect of the type of grain which can be produced.
; The use of hydrochloric acid or hydrochloric acid/phosphoric acid mixtures is further disadvantageous when using certain aluminium alloys since both these elec~rolytes attack the impurities in the alloy and thus cause pi~ting of khe surface.
It is also known to use as the electrolyte hydrochloric acid in combination with monocarboxylic acids having between 1 and 4 carbon atoms. By this method aluminium and aluminium alloy substrates having a fine homogeneous grain structure can be producedO However, complicated analytical techniques are required to monitor the relative amounts of hydrochloric acid and monocarboxylic acid. Moreover, the use of additives to the hydrochloric acid electrolyte such as monocarboxylic acids can be environmentally undesirable.
~7~
It is an object of the present invention to provide a method of electrolytically graining aluminium and aluminium alloys and aluminium laminates which results in a fine homogeneous grain structure and which obviates the need for complex chemical analysis of the electrolyte.
It has surprisingly been found that in the electrolytic graining of aluminium, aluminium alloys or aluminium laminates, a fine homogeneous grain structure can be achieved by the use of an alternating current having a square waveform rather than the conventional alternating current having a sine waveform.
Accordingly the present invention provides a method of electrolytically graining a sheet of aluminium, aluminium alloy or aluminium laminate which comprises immersing the sheat in an aqueous electrolyte and passing an alternating current through the electrolyte wherein the alternating current has a square waveform.
Generally hydrochloric acid is used, and the concentration of hydrochloric acid in the electrolyte will be from 3 to 20~ and the electrolytic graining may preferably be effected at a voltage of, for example, SV to 45V, particularly preferably from lOV to 35V
for 15 seconds to 4 minutes to give a surface roughness characterised by a centre line average (CLA), as measured, for example, by a Rank Taylor Hobson Talysurf 10, of from 0.3 to 1~0 microns. The electrolyte may be at any suitable temperature but preferably from 25 to 34C. An alternative to the above is to use nitric acid in which case concentrations of between 5 and 30gl~l may he used.
~ ~ 3 ~
The frequency of the alternating square wave current will preferably be from 20 ko lOOHz and particularly preferably from 40 to 70Hz. The voltage in each half cycle can be chosen as desired within the preferred range. The preferred ratios of the voltaye in the positive and negative half cycles are within the range of from 1:2 to 1:1, positive : negative. It is also possible to vary the time period of each half-cycle whilst maintaining the fr~quency within the preferred range. The preferred range for the ratio of the time periods in the positive and negative half cycles is from 1:2 to 1:1, positive : negative.
The graining may be effected by immersing the aluminium, a].uminium alloy or aluminium laminate sheet in the electrolyte, the square waveform alternating current being passed ~hrough the electrolyte using the sheet as an electrode. A second similar sheet may be used as the second electrode. Alternatively the graining may be effected as a continuous process by passing a continuous web of aluminium/ aluminium alloy or aluminium laminate through the electrolyte. In this case the electrodes used to introduce the square waveform alternating current may, for example, be carbon electrodes located near to the web.
After graining, the aluminium, aluminium alloy or aluminium laminate may be anodised in a suitable electrolyte, preferably using direct current. Thereafter the grained surface (or the grained and anodised surface, as the case may be) of the sheet may be coated with a radiation sensitive composition to form a radiation sensitive plate. The radiation sensitive composition may be a positive working composi~ion such as a mix~ure of a quinone diazode and a novolak resin or a negative working composition, such as a photopolymerisable resin. The radiation sensitive pla~e may then be imagewise exposed and suitably processed to produce a lithographic printing plate.
For a better understanding of tha invention, and to show how the same may be carried in~o effect, reference will be made, by way of example only, to the following figures in which:-Figures la and lb illustrate the waveform associated respectively with a sine waveform and a square waveform alternating current, Figures 2 to 5 are electron micrographs of electrolytically grained sheets of 3103 grade aluminium-manganPse alloy, of which Fiqure 2 shows a sheet of the alloy grained in accordance with the present invention, Figure 3 shows a sheet of the alloy grained in hydrochloric acid electrolyte, using a sine wavefoxm alternating current, Figure 4 shows a sheat of the alloy grained in hydrochloric acid electrolyte with added monocarboxylic acid using a sine waveform alternating current, and Figure S shows a sheet of the alloy graîned in hydrochloric acid electrolyte with added monocarboxylic acid using a square waveform alternating current.
Figures 6 to 9 are electron micrographs of electrolytically grained sheet of 1050 grade aluminium, of which Figure 6 shows a sheet of the aluminium grained in accordance with the present invention, Figure 7 æhows a sheet of the zluminium grained in hydrochloric acid electrolyte using a sine waveform alternating current, Figure 8 shows a sheet of the aluminium grained in hydrochloric acid electrolyte with added mono~arboxylic acid using a sine wa~eform alternating current, and Figure 9 shows a sheet of the aluminium grained in hydrochloric acid electrolyte with added monocarboxylic acid using a square waveform alternating current.
10It can be appreciated that Figures 2 to 9, inclusive, are best represented by photographs of the surface of the sheets described.
The following examples illustrate the invention:-Sheets of 3103 grade aluminium-manganese alloy were degreased 15in 10 to 20gl~l sodium hydroxide for 30s ak 35 to 40C and rinsed.
The sheets were then elec~rolytically grained using hydrochloric acid at a concentration of 7gl~l and a tempexature of 26 to 28C and using a s~uare waveform alternating current at an applied voltage of 16 to 18V and at a frequency of 50Hz. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one sheet is shown in Figure 2.
CO~PARATIVE~EXAMPLE 1 Sheets of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Example 1, but using a sine waveform alternating current. The resulting grained sheets had a CLA of 0.~
to 0.8 microns. Part of the su.rface of one sheet is shown in Figure 3.
~ ~ f3 r~ 5; ~ 4L
COMD ~
Sheets of 3103 grade aluminium-manganese alloy were degreased and rinsed as in Example 1. The sheets were then elec~rolytically grained using an electrolyte comprising 8 to 10gl~1 hydrochloric acid and 15 to 30gl~l of a monocarboxylic acid at a temperature of 26 to 28C and using a sine waveform alternating current at an applied voltage of 16 to 18V and frequency of 50Hz. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one of the sheets is shown in Figure 4.
She~ts of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Comparative Example 2, but using a square waveform a.lternating current. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one of the sheets is shown in Figure 5.
Sheets of 1050 grade aluminium (99.5%Al) were degreased, rinsed and grained using the same conditions as Example 1. Part of the surface of one of the sheets is shown in Figure 6.
Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Comparative Example 1. Part of the surface of one of the sheets is shown in Figure 7.
Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Compara~ive Example 2. Part of the surface of one of the sheetæ is shown in Figure 8.
~,~3~
COMPARATIVE EXAM,P E 6 Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Comparative Example 3. Part of the surface of one of the sheets is shown in Figure 9.
Sheets of 3103 grade aluminium-manganese alloy were degreased in 10 to 20gl-~ sodium hydroxide for 30 seconds at 35 to 40C and rinsed. The sheets were then electrolytically grained using nitric acid at a concentration of 16gl~l and a temperature of 26-28C. A
square waveform at a frequency of 50 Hz and voltage of 18-~OV was used. The resulting grained sheets had a CLA of O.6 to O.8 microns.
COMPARATIVF: EXA~lPLE 7 Sheets of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Example 7, but using a sine waveform. The resulting grained sheets had a CLA of O.6 to O.8 microns.
Comparison of Figure 2 with Figure 3 and Figure 6 with Figure 7 clearly shows that when using a standard hydrochloric acid electrolyte in the grain,ing of aluminium or aluminium alloys the use of a square waveform alternating current instead of the conventional sine waveform results in a significantly finer and more homogeneous substrate surface.
Comparison of Figures 2 and 6 with Figures 4 and 8 respectively demonstrates that the grained aluminium or alumini~
alloy substrate obtained by use of a standard hydrochloric acid electrolyte with a square waveform alternating current has an equally fine and homogeneous surface as that obtained by use of a mixed hydrochloric acid/monocarboxylic acid electrolyte and a ~ine waveform alternating current. Furthermore it can be seen from Figures 5 and 9 that no further advantage is gained by using a mixed hydrochloric acid/monocarboxylic acid electrolyte with a square waveform alternating current. Moreover, such a method is disadvantageous because of the technical complexity of monitoring the relative hydrochloric acid and monocarboxylic acid concentrations.
. .
~, , . - .
.. . ' ' . ' ~ :
ELECTROLYTIC GRAINING
This invention relates to the electrolytic graining of aluminium, aluminium alloys and aluminium lamina~es and mo.re par~icularly, but not exclusively, is concerned with the electrolytic graining of aluminium, alumini.um alloys or aluminium laminates in the production of substrates suitable for use in the manufacture of radiation sensitive plates in lithographic printing plate production.
Radiation sensitive plates of the type with which this invention is concerned conventionally consist of a substrate onto which is coated a radiation sensitive composition. Image-wise exposure of the plate to radiation causes the coating to change its characteristics in the areas struck by radiation so that the coating may be selectivel~ removed from the substrate in the non-image areas by application of a suitable developer to leave aprinting image (or etch resistant axea) on the substrate. In the case of the so-called negative-working devices, it is the non-radiation struck areas of the coating which are removed. Those parts of the coating which are not removed and which thus form the printing image are ordinarily water-repellent and ink-receptive and those parts of the substrate revealed on development are ordinarily water-receptive and ink-repellent.
It will be apparent that the surface of the substrate should be such that the printing image can ~trongly adhere thereto and ~ 25 such that i~ iB readily wettable with water. It is known to ; improve the adhesion of the printing image and to improve the wetting characteristics of the non-image areas by roughening (conventionally referred to as graining) -the substrate before applying the radiation sensitive coating.
The coarseness or surface roughness of the grained substrate can be characterised, for example, by measurement of a centre line average (CLA).
The type of grain required for the substrate of a radiation sensitive printing plate for lithographic printing plate production depends upon the requirements of the final printing plate. Thus a fine grain - i.e. shallow depressions - results in better reproduction of half-tones whereas a coarse grain - i.e. deep depressions - results in the non-image areas having better wetting characteristics. In either case however it is important that the depressions are evenly spaced over the substrate surface and that they are close enough together so that peaks, rather than plateaux, are formed between the depressions.
It is known to grain substrates in lithographic printing plate production by electrolytic techniques. Graining is normally effected by immersing the substrates in a suitable electrolyte and subjecting them to a sine waveform alternating current.
Conventionally, hydrochloric acid has been used as the electrolyts for graining aluminium and aluminium alloy substrates.
However, when using hydrochloric acid it is difficult to obtain a fine homogeneou~ grain and it is therefore nece~sary carefully to control the acid concentration of the electrolyte in order to ensure consiætent results. This is particularly the case when aluminium alloys such as 3103 aluminium manganese alloy are used as the substrate. The use of such alloys for -the substra-te can be ~ ~ ~ r~
particularly advantageous due to their increased resistance to tearing and cracking and to tempera-~ures in excess of 200C which are used to harden the image on the printing plate and thus to increase the printing run leng~h.
It is known to grain aluminium substrates using a~ the electrolyte a mixture of hydrochloric and phosphoric acids. Whilst this method can result in an even grain, an excessive amount of smut is produced on the substrate which can cause the radiation sensitive coating of the plate to become insolubilised during storage of the plate. Thus the smu~ has normally to he removed.
A further disadvantage of using a hydrochloric acid/phosphoric acid mixture as electrolyte is that the process is inflexible in respect of the type of grain which can be produced.
; The use of hydrochloric acid or hydrochloric acid/phosphoric acid mixtures is further disadvantageous when using certain aluminium alloys since both these elec~rolytes attack the impurities in the alloy and thus cause pi~ting of khe surface.
It is also known to use as the electrolyte hydrochloric acid in combination with monocarboxylic acids having between 1 and 4 carbon atoms. By this method aluminium and aluminium alloy substrates having a fine homogeneous grain structure can be producedO However, complicated analytical techniques are required to monitor the relative amounts of hydrochloric acid and monocarboxylic acid. Moreover, the use of additives to the hydrochloric acid electrolyte such as monocarboxylic acids can be environmentally undesirable.
~7~
It is an object of the present invention to provide a method of electrolytically graining aluminium and aluminium alloys and aluminium laminates which results in a fine homogeneous grain structure and which obviates the need for complex chemical analysis of the electrolyte.
It has surprisingly been found that in the electrolytic graining of aluminium, aluminium alloys or aluminium laminates, a fine homogeneous grain structure can be achieved by the use of an alternating current having a square waveform rather than the conventional alternating current having a sine waveform.
Accordingly the present invention provides a method of electrolytically graining a sheet of aluminium, aluminium alloy or aluminium laminate which comprises immersing the sheat in an aqueous electrolyte and passing an alternating current through the electrolyte wherein the alternating current has a square waveform.
Generally hydrochloric acid is used, and the concentration of hydrochloric acid in the electrolyte will be from 3 to 20~ and the electrolytic graining may preferably be effected at a voltage of, for example, SV to 45V, particularly preferably from lOV to 35V
for 15 seconds to 4 minutes to give a surface roughness characterised by a centre line average (CLA), as measured, for example, by a Rank Taylor Hobson Talysurf 10, of from 0.3 to 1~0 microns. The electrolyte may be at any suitable temperature but preferably from 25 to 34C. An alternative to the above is to use nitric acid in which case concentrations of between 5 and 30gl~l may he used.
~ ~ 3 ~
The frequency of the alternating square wave current will preferably be from 20 ko lOOHz and particularly preferably from 40 to 70Hz. The voltage in each half cycle can be chosen as desired within the preferred range. The preferred ratios of the voltaye in the positive and negative half cycles are within the range of from 1:2 to 1:1, positive : negative. It is also possible to vary the time period of each half-cycle whilst maintaining the fr~quency within the preferred range. The preferred range for the ratio of the time periods in the positive and negative half cycles is from 1:2 to 1:1, positive : negative.
The graining may be effected by immersing the aluminium, a].uminium alloy or aluminium laminate sheet in the electrolyte, the square waveform alternating current being passed ~hrough the electrolyte using the sheet as an electrode. A second similar sheet may be used as the second electrode. Alternatively the graining may be effected as a continuous process by passing a continuous web of aluminium/ aluminium alloy or aluminium laminate through the electrolyte. In this case the electrodes used to introduce the square waveform alternating current may, for example, be carbon electrodes located near to the web.
After graining, the aluminium, aluminium alloy or aluminium laminate may be anodised in a suitable electrolyte, preferably using direct current. Thereafter the grained surface (or the grained and anodised surface, as the case may be) of the sheet may be coated with a radiation sensitive composition to form a radiation sensitive plate. The radiation sensitive composition may be a positive working composi~ion such as a mix~ure of a quinone diazode and a novolak resin or a negative working composition, such as a photopolymerisable resin. The radiation sensitive pla~e may then be imagewise exposed and suitably processed to produce a lithographic printing plate.
For a better understanding of tha invention, and to show how the same may be carried in~o effect, reference will be made, by way of example only, to the following figures in which:-Figures la and lb illustrate the waveform associated respectively with a sine waveform and a square waveform alternating current, Figures 2 to 5 are electron micrographs of electrolytically grained sheets of 3103 grade aluminium-manganPse alloy, of which Fiqure 2 shows a sheet of the alloy grained in accordance with the present invention, Figure 3 shows a sheet of the alloy grained in hydrochloric acid electrolyte, using a sine wavefoxm alternating current, Figure 4 shows a sheat of the alloy grained in hydrochloric acid electrolyte with added monocarboxylic acid using a sine waveform alternating current, and Figure S shows a sheet of the alloy graîned in hydrochloric acid electrolyte with added monocarboxylic acid using a square waveform alternating current.
Figures 6 to 9 are electron micrographs of electrolytically grained sheet of 1050 grade aluminium, of which Figure 6 shows a sheet of the aluminium grained in accordance with the present invention, Figure 7 æhows a sheet of the zluminium grained in hydrochloric acid electrolyte using a sine waveform alternating current, Figure 8 shows a sheet of the aluminium grained in hydrochloric acid electrolyte with added mono~arboxylic acid using a sine wa~eform alternating current, and Figure 9 shows a sheet of the aluminium grained in hydrochloric acid electrolyte with added monocarboxylic acid using a square waveform alternating current.
10It can be appreciated that Figures 2 to 9, inclusive, are best represented by photographs of the surface of the sheets described.
The following examples illustrate the invention:-Sheets of 3103 grade aluminium-manganese alloy were degreased 15in 10 to 20gl~l sodium hydroxide for 30s ak 35 to 40C and rinsed.
The sheets were then elec~rolytically grained using hydrochloric acid at a concentration of 7gl~l and a tempexature of 26 to 28C and using a s~uare waveform alternating current at an applied voltage of 16 to 18V and at a frequency of 50Hz. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one sheet is shown in Figure 2.
CO~PARATIVE~EXAMPLE 1 Sheets of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Example 1, but using a sine waveform alternating current. The resulting grained sheets had a CLA of 0.~
to 0.8 microns. Part of the su.rface of one sheet is shown in Figure 3.
~ ~ f3 r~ 5; ~ 4L
COMD ~
Sheets of 3103 grade aluminium-manganese alloy were degreased and rinsed as in Example 1. The sheets were then elec~rolytically grained using an electrolyte comprising 8 to 10gl~1 hydrochloric acid and 15 to 30gl~l of a monocarboxylic acid at a temperature of 26 to 28C and using a sine waveform alternating current at an applied voltage of 16 to 18V and frequency of 50Hz. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one of the sheets is shown in Figure 4.
She~ts of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Comparative Example 2, but using a square waveform a.lternating current. The resulting grained sheets had a CLA of 0.6 to 0.8 microns. Part of the surface of one of the sheets is shown in Figure 5.
Sheets of 1050 grade aluminium (99.5%Al) were degreased, rinsed and grained using the same conditions as Example 1. Part of the surface of one of the sheets is shown in Figure 6.
Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Comparative Example 1. Part of the surface of one of the sheets is shown in Figure 7.
Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Compara~ive Example 2. Part of the surface of one of the sheetæ is shown in Figure 8.
~,~3~
COMPARATIVE EXAM,P E 6 Sheets of 1050 grade aluminium were degreased, rinsed and grained using the same conditions as Comparative Example 3. Part of the surface of one of the sheets is shown in Figure 9.
Sheets of 3103 grade aluminium-manganese alloy were degreased in 10 to 20gl-~ sodium hydroxide for 30 seconds at 35 to 40C and rinsed. The sheets were then electrolytically grained using nitric acid at a concentration of 16gl~l and a temperature of 26-28C. A
square waveform at a frequency of 50 Hz and voltage of 18-~OV was used. The resulting grained sheets had a CLA of O.6 to O.8 microns.
COMPARATIVF: EXA~lPLE 7 Sheets of 3103 grade aluminium-manganese alloy were degreased, rinsed and grained as in Example 7, but using a sine waveform. The resulting grained sheets had a CLA of O.6 to O.8 microns.
Comparison of Figure 2 with Figure 3 and Figure 6 with Figure 7 clearly shows that when using a standard hydrochloric acid electrolyte in the grain,ing of aluminium or aluminium alloys the use of a square waveform alternating current instead of the conventional sine waveform results in a significantly finer and more homogeneous substrate surface.
Comparison of Figures 2 and 6 with Figures 4 and 8 respectively demonstrates that the grained aluminium or alumini~
alloy substrate obtained by use of a standard hydrochloric acid electrolyte with a square waveform alternating current has an equally fine and homogeneous surface as that obtained by use of a mixed hydrochloric acid/monocarboxylic acid electrolyte and a ~ine waveform alternating current. Furthermore it can be seen from Figures 5 and 9 that no further advantage is gained by using a mixed hydrochloric acid/monocarboxylic acid electrolyte with a square waveform alternating current. Moreover, such a method is disadvantageous because of the technical complexity of monitoring the relative hydrochloric acid and monocarboxylic acid concentrations.
. .
~, , . - .
.. . ' ' . ' ~ :
Claims (12)
1. A method of electrolytically graining an aluminium containing substrate which method comprises providing one member selected from the group comprising aluminium sheets, aluminium alloy sheets and aluminium laminate sheets, immersing the said sheet in an aqueous electrolyte and passing an alternating current through the said electrolyte wherein the alternating current has a square waveform.
2. A method according to claim 1 wherein the electrolyte contains hydrochloric acid, at a concentration in the range of from 3 to 20 g/l.
3. A method according to claim 1 wherein the electrolyte contains nitric acid in the concentration range of from 5-30gl-1.
4. A method according to claim 1 wherein the graining is effected at a voltage in the range of from 5 to 45V.
5. A method according to claim 1, wherein the graining is effected for from 15 seconds to 4 minutes.
6. A method according to claim 1, wherein the frequency of said alternating current lies within the range 20 to 100Hz.
7. A method according to claim 1, wherein said square waveform has both a positive and a negative half cycle and wherein the ratio of the voltages in said positive and negative half cycles is in the range of from 1:1 to 1:2.
8. A method according to claim 1, wherein said square waveform has positive and negative half cycles having a temporal ratio in the range of from 1:2 to 1:1.
9. A method according to claim 1 wherein at least one electrode comprises a sheet of aluminium, aluminium alloy or aluminium laminate.
10. A method according to claim 1 where a continuous web of aluminium, aluminium alloy or aluminium laminate is passed through the electrolyte.
11. A method according to claim 1 including a stage in which the grained surface is anodised.
12. A method according to claim 1 including a final stage comprising coating the substrate with a radiation sensitive composition.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909005035A GB9005035D0 (en) | 1990-03-06 | 1990-03-06 | Improvements in or relating to electrolytic graining |
| GB9005035.2 | 1990-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2037594A1 true CA2037594A1 (en) | 1991-09-07 |
Family
ID=10672117
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002037594A Abandoned CA2037594A1 (en) | 1990-03-06 | 1991-03-05 | Electrolytic graining |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0445959A1 (en) |
| JP (1) | JPH0770800A (en) |
| AU (1) | AU7197691A (en) |
| BR (1) | BR9100958A (en) |
| CA (1) | CA2037594A1 (en) |
| CS (1) | CS58091A3 (en) |
| FI (1) | FI910745A7 (en) |
| GB (1) | GB9005035D0 (en) |
| HU (1) | HUT57129A (en) |
| IE (1) | IE910722A1 (en) |
| NO (1) | NO910882L (en) |
| ZA (1) | ZA911605B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4412678A (en) * | 1979-06-18 | 1983-11-01 | Turco Manufacturing Co. | Saddle for bar and bar-type weight |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2358194B (en) * | 2000-01-17 | 2004-07-21 | Ea Tech Ltd | Electrolytic treatment |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59215500A (en) * | 1983-05-19 | 1984-12-05 | Fuji Photo Film Co Ltd | Electrolytic treatment method |
| JPH0729507B2 (en) * | 1987-10-30 | 1995-04-05 | 富士写真フイルム株式会社 | Method for producing aluminum support for printing plate |
| JPH0798430B2 (en) * | 1988-03-31 | 1995-10-25 | 富士写真フイルム株式会社 | Method for producing aluminum support for printing plate |
-
1990
- 1990-03-06 GB GB909005035A patent/GB9005035D0/en active Pending
-
1991
- 1991-02-15 FI FI910745A patent/FI910745A7/en not_active Application Discontinuation
- 1991-02-27 AU AU71976/91A patent/AU7197691A/en not_active Abandoned
- 1991-02-27 EP EP91301602A patent/EP0445959A1/en not_active Withdrawn
- 1991-03-05 ZA ZA911605A patent/ZA911605B/en unknown
- 1991-03-05 CA CA002037594A patent/CA2037594A1/en not_active Abandoned
- 1991-03-05 HU HU91713A patent/HUT57129A/en unknown
- 1991-03-05 IE IE072291A patent/IE910722A1/en unknown
- 1991-03-05 BR BR919100958A patent/BR9100958A/en not_active Application Discontinuation
- 1991-03-06 NO NO91910882A patent/NO910882L/en unknown
- 1991-03-06 CS CS91580A patent/CS58091A3/en unknown
- 1991-03-06 JP JP3067886A patent/JPH0770800A/en not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4412678A (en) * | 1979-06-18 | 1983-11-01 | Turco Manufacturing Co. | Saddle for bar and bar-type weight |
Also Published As
| Publication number | Publication date |
|---|---|
| HUT57129A (en) | 1991-11-28 |
| HU910713D0 (en) | 1991-09-30 |
| GB9005035D0 (en) | 1990-05-02 |
| NO910882L (en) | 1991-09-09 |
| ZA911605B (en) | 1991-12-24 |
| NO910882D0 (en) | 1991-03-06 |
| FI910745A0 (en) | 1991-02-15 |
| BR9100958A (en) | 1991-11-05 |
| JPH0770800A (en) | 1995-03-14 |
| CS58091A3 (en) | 1992-04-15 |
| FI910745L (en) | 1991-09-07 |
| IE910722A1 (en) | 1991-09-11 |
| AU7197691A (en) | 1991-09-12 |
| FI910745A7 (en) | 1991-09-07 |
| EP0445959A1 (en) | 1991-09-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |