GB1588808A – Zinc alloy and galvanisation process
– Google Patents
GB1588808A – Zinc alloy and galvanisation process
– Google Patents
Zinc alloy and galvanisation process
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Publication number
GB1588808A
GB1588808A
GB40363/77A
GB4036377A
GB1588808A
GB 1588808 A
GB1588808 A
GB 1588808A
GB 40363/77 A
GB40363/77 A
GB 40363/77A
GB 4036377 A
GB4036377 A
GB 4036377A
GB 1588808 A
GB1588808 A
GB 1588808A
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United Kingdom
Prior art keywords
steel
galvanisation
steels
content
weight
Prior art date
1976-10-01
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
GB40363/77A
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Individual
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1976-10-01
Filing date
1977-09-28
Publication date
1981-04-29
1977-09-28
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filed
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1981-04-29
Publication of GB1588808A
publication
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patent/GB1588808A/en
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Expired
legal-status
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Classifications
C—CHEMISTRY; METALLURGY
C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
C22C—ALLOYS
C22C18/00—Alloys based on zinc
C22C18/04—Alloys based on zinc with aluminium as the next major constituent
C—CHEMISTRY; METALLURGY
C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
C22C—ALLOYS
C22C18/00—Alloys based on zinc
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
C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
C23C2/06—Zinc or cadmium or alloys based thereon
Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
Y10T428/00—Stock material or miscellaneous articles
Y10T428/12—All metal or with adjacent metals
Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
Y10T428/12771—Transition metal-base component
Y10T428/12785—Group IIB metal-base component
Y10T428/12792—Zn-base component
Y10T428/12799—Next to Fe-base component [e.g., galvanized]
Description
PATENT SPECIFICATION ( 11) 1 588 808
0 ( 21) Application No 40363/77 ( 22) Filed 28 Sep 1977 ( 19) 00 X ( 31) Convention Application No 7629545 ( 32) Filed 1 Oct 1976 in 2 d i 00 ( 33) France (FR) G ( 44) Complete Specification Published 29 Apr 1981
U ( 51) INT CL C 22 C 18/00 C 23 C 1/02 ( 52) Index at Acceptance C 7 A B 249 B 25 Y B 275 B 277 B 289 B 309 B 316 B 319 B 31 Y B 339 B 349 B 35 Y B 367 B 389 B 399 B 419 B 439 B 44 Y B 453 B 455 B 457 B 46 X B 46 Y B 519 B 539 B 549 B 559 B 610 B 613 B 616 B 619 B 621 B 624 B 627 B 62 X B 630 B 633 B 661 B 663 B 665 B 667 B 669 B 66 X B 670 C 7 F 1 G 3 2 A 2 Q 2 Z 1 2 Z 3 3 E 4 K G 3 ( 54) ZINC ALLOY AND GALVANISATION PROCESS ( 71) I, NOEL DREULLE, a French Citizen of 5 Rue Fourques, 59500 Douai, Nord, France, do hereby declare the invention for which I pray that a patent may be granted to me, and the method by which it is to be performed, to be particularly described in and by the following statement:-
The invention relates to an alloy intended for the immersion galvanisation of steels and 5 also to an immersion galvanisation process utilising this alloy.
Immersion galvanisation is conventionally effected in a bath of molten zinc containing about 0 1 to 1 5 % of lead The zinc used is generally a zinc of commercial purity corresponding to the standards AFNOR NFA 55101 of April 1955, classes Z 6 or Z 7 For example, a Z 7 zinc contains 0 15 % of Cd, 0 02 % of Fe, and 0 002 % of Cu as tolerated 10 impurities The actual galvanisation is generally preceded by operations of degreasing, pickling by immersion in hydrochloric acid containing a corrosion inhibitor, and fluxing or deposition of a coating of flux of the zinc chloride or ammonium type The coating of zinc is considered satisfactory if the appearance is white, smooth, relatively glossy, and obviously adherent, and has a thickness of about 70 microns 15 It has been found that conventional hot-dip galvanisation of the relatively recent building steels which contain more than 0 01 % of silicon gives poor results, the zinc coatings appearing greyish, indicating the formation of fragile intermetallic compounds, and being of abnormal thickness ( 200 to 300 Rm and more), and of poor adherence both as regards the thickness of the coatings and as regards their fragility 20 Steels in the state they are produced using modern continuous casting processes can be classified by their silicon content into the following categories:
effervescent steels (Si < 0 01 %) semi-calmed steels ( 0 01 % < Si < 0 10 %) calmed steels (Si-015 %) 25 high silicon content steels (Si > 0 20 %) Actually, the conventional classification and terminology for siliconcontaining steels is poorly defined, and the content limits of the silicon contents of calmed steels and semi-calmed steels vary according to the source of manufacture.
The thickness and crystalline state of zinc coatings produced by hot dip galvanisation are 30 closely linked with the kinetics of the reaction between iron and zinc, which is modified by the presence of silicon Moreover, iron-zinc reactivity is not proportional to the silicon content Effervescent steels are galvanised without difficulty, but semicalmed steels are highly reactive and the coatings obtained are thick and not very adherent Calmed steels are substantially more reactive than effervescent steels, but substantially less reactive than 35 semi-calmed steels Finally, steels containing more than 0 2 % of silicon are very highly reactive.
This has the result that steels containing silicon cannot be galvanised by conventional immersion processes If parts of regular shape and composition are treated, it certainly does not appear impossible to develop galvanisation processes giving suitable coatings on these 40 parts if parameters such as immersion time in the galvanisation bath, temperature of the bath, nature of the flux, rate of cooling, and so on are carefully regulated Thus, high-strength silicon steel bolts can be galvanised, but in general it is not possible for operating conditions for different parts to be controlled in an economically viable manner.
This is particularly true of jobbing galvanisation, where the galvaniser has to coat parts 5 having a composition which is not known to him and which moreover varies with the type of part, the customer, and so on.
It is known that the addition to galvanisation baths of aluminium in amounts ranging from 100 to 5000 ppm by weight reduces the reactivity of the zinc in relation to silicon steels.
The coatings obtained are thinner, more adherent, and more satisfactory in appearance 10 Nevertheless, it is found that the coatings obtained are not free from bare patches It is assumed that the alumina formed by oxidation of the aluminium combines with the flux and covers the steel in places, thus preventing the zinc-iron reaction from taking place.
The present invention relates to an aluminium-containing galvanisation alloy which does not have these shortcomings 15 An object of the present invention is to provide a galvanisation alloy suitable equally for steels containing less than 0 01 % of silicon and for steels in which the silicon content is as high as at least 0 2 %.
According to the present invention there is provided an alloy suitable for the galvanisation of steels by an immersion galvanisation process, including galvanisation of 20 steels containing silicon, the alloy consisting essentially of zinc of commercial purity and having a lead content of from 1000 to 20000 ppm by weight, an aluminium content of from to 5000 ppm by weight, a magnesium content of from 10 to 1000 ppm by weight and a tin content of from 300 to 20000 ppm by weight.
The invention is based on a finding that the presence of tin in the zinc alloy greatly 25 reduces the number of bare patches in the resultant coating of zinc alloy Similarly, the presence of magnesium makes it possible to obtain coatings entirely without bare patches.
The simultaneous presence of tin and magnesium gives more reliable results and increases the life of the galvanisation bath, the tin making up for any magnesium which might disappear through oxidation 30 The preferred contents by weight are from 300 to 600 ppm of aluminium, from 20 to 200 ppm of magnesium and from 1000 to 3000 ppm of tin.
Excellent results have been obtained with an alloy containing substantially 600 ppm of aluminium, 10 () ppm of magnesium, and 2500 ppm of tin, the parts being by weight in all cases 35 In another aspect, the invention relates to an immersion galvanisation process utilising the alloys mentioned above, wherein after degreasing, rinsing pickling in concentrated hydrochloric acid containing a corrosion inhibitor, and rinsing, pickling is effected in concentrated hydrochloric acid without inhibitor, followed by rinsing, and after conventional fluxing and drying the parts are immersed in the molten galvanisation bath incorporating 40 the alloy of the invention.
Excellent results have been obtained with a first pickling with 6 N hydrochloric acid containing a corrosion inhibitor, and a second pickling with hydrochloric acid of a concentration of 6 to 12 N without inhibitor.
The present invention will now be illustrated, by way of example only, with reference to 45 the accompanying drawings, in which:
Figure 1 shows a graph on which the thickness of a coating of zinc (deposited on silicon-containing steels using a conventional hot dip galvanisation bath) is plotted against the silicon content of the steel; Figure 2 is a diagram of the stages of conventional hot dip galvanisation; 50 Figure 3 is a diagram of the galvanisation stages in a preferred embodiment of the present invention.
Considering the graph of Figure 1, which shows on the abscissa the silicon content of the steel and on the ordinate the thickness of a deposit expressed in arbitrary units of mass zinc deposited per unit of surface, it is found that, if the thickness of coating on a steel 55 containing less than O 01 %’ of silicon is taken as unity, the thickness increases as the silicon content increases, until it reaches a maximum value at about 0 05 % silicon, the maximum though not precisely known exceeding 6 and then decreases to a minimum value at about 0.16 W/ silicon, the minimum value being about 2 5, and finally increases regularly It will be realised that the irregularity of the thickness of the deposits obtained is greater, the greater 60 the slope of the Curve Since excessive thickness of the coating is due to the rapid formation of fragile intermetallic compounds, it will he realised that irregularities of thickness lead to deficiencies in the adherence of the coating.
The curve in Figure 1 also shows the serious difficulties arising with conventional galvanisation baths in the coating of parts having different silicon contents If in fact it is 65 1 588 808 3 1588-808 3 conceivable to develop a galvanisation process for parts having a known, constant silicon content by adjusting the temperature of the bath to modify the rate of formation of intermetallic compounds, and correspondingly adjusting the immersion time and rate of cooling of the coated part so as to stabilise the thickness of intermetallic compounds, this development would need numerous experiments, which can be justified only for very large 5 homogeneous series.
It is known that the presence of aluminium reduces the reactivity of the iron-zinc pair It is also known that the presence of aluminium in amounts of from 100 to 5000 ppm in the zinc reduces the reactivity of silicon steels in relation to zinc Conventional galvanisation baths to which aluminium has been added within the range indicated above give as a rule 10 smooth, white, glossy coatings without excessive thicknesses Unfortunately, the coatings obtained in such baths have bare spots These bare spots are attributed to the formation of alumina through the oxidation of aluminium, this alumina being entrained by the flux which covers the part to be galvanised and forming an adherent skin on the steel, which the molten zinc will not wet 15 In the course of studies of the galvanisation of silicon steels which led to the present invention it was determined that the addition of two metals to galvanisation baths containing the above-mentioned amounts of aluminium made it possible to reduce or eliminate bare patches due to the presence of aluminium.
By adding tin to the bath a spectacular reduction of the number of bare spots is achieved 20 The effect, which is noticeable starting from 50 ppm of tin in the bath, becomes significant above 300 ppm Above 20,000 ppm of tin in the bath the coatings contain tin in excessive proportions The most interesting results are obtained with tin contents of from 1000 to 3000 ppm Although the exact mechanism of the reaction of tin in the galvanisation has not been elucidated, it seems probable that the tin increases the fluidity of the molten zinc and 25 also the ability of steels to be wetted by zinc, thereby facilitating the elimination of flux contaminated with alumina Zinc baths containing aluminium and tin in the contents previously mentioned permit the galvanisation of silicon steel parts with less than 10 % of defective parts.
By adding magnesium to a zinc bath containing aluminium, bare spots are practically 30 completely eliminated Magnesium starts to be effective in amounts of the order of 10 ppm.
Since magnesium is more readily oxidisable than aluminium, it is very probable that it reduces the formation of alumina, while magnesia reacts with the flux to form magnesium chloride, a compound which does not substantially modify the fluidity of the flux at the temperature of the galvanisation bath, provided that it is present in small amounts Thus, a 35 magnesium content of 1000 ppm in the bath should not be exceeded, because if it is the formation of magnesia by oxidation of magnesium is excessive The best results have been obtained with magnesium contents of from 20 to 200 ppm, for which the disappearance of the magnesium by oxidation is not excessively rapid and without the bath containing a troublesome excess of magnesia 40 Tests have also been shown that in galvanisation baths tin and magnesium practically do not react with one another, at least at the contents indicated above, so that the stabilising actions of these two metals do not counteract one another By adding magnesium and tin to galvanisation baths containing aluminium within the limits of the contents mentioned above, durable and stable galvanisation baths are obtained If in fact the magnesium 45 content falls below the effective content as the result of oxidation, tin acts as a stabiliser and the bath remains utilisable.
Tests have shown that the alloys for galvanisation baths which gave the best results in respect of effectiveness and long life contained from 300 to 600 ppm of aluminium, from 20 to 200 ppm of magnesium, and from 1000 to 3000 ppm of tin in addition to zinc of Z 6 or Z 7 50 quality (standard AFNOR NFA 55101, April, 1955) and lead in the usual contents of 1000 to 15000 ppm A standard alloy contains substantially 600 ppm of aluminium, 100 ppm of magnesium, and 2500 ppm of tin These alloys in particular have been found capable of very wide use, giving equivalent results under similar operating conditions with effervescent steels containing less than 0 01 % of silicon, with semi-calmed steels containing from 0 02 to 55 0.10 % of silicon, calmed steels containing 0 15 % of silicon, and steels containing more than 0.2 % of silicon.
Figure 2 shows a conventional surface preparation process which comprises degreasing, rinsing, pickling with concentrated hydrochloric acid to which a corrosion inhibitor has been added, rinsing, fluxing, and drying In order to facilitate the use of the alloys 60 according to the invention in an immersion galvanisation process it is advantageous to make the operating conditions for the actual galvanisation more flexible and to supplement the steps shown in Figure 2 The surface preparation process with the additional steps is illustrated in the diagram of Figure 3 Between the rinsing following pickling in hydrochloric acid containing an inhibitor there is interposed pickling in concentrated 65 1 588 808 hydrochloric acid without inhibitor, followed by rinsing This pickling has the object of completing the cleaning of the steel by dissolving from 2 to 3 microns of steel from the surface of the part.
The concentration of the hydrochloric acid in the first pickling is advantageously 6 N, whereas the concentration of the acid in the second pickling is preferably from 6 to 12 N 5 The invention is also illustrated by the following comparative examples.
EXAMPLE 1
Immersion galvanisation of a steel containing 0 06 % of silicon A control is galvanised in a conventional bath of Z 6 Z 7 zinc after conventional surface 10 preparation (in accordance with the diagram in Figure 2) A similar specimen is galvanised in a bath containing 600 ppm of aluminium, 100 ppm of magnesium, and 2500 ppm of tin in addition to the Z 6 Z 7 zinc, after surface preparation in accordance with the diagram in Figure 3 (first pickling in 6 N H Cl with inhibitor for 45 minutes, second pickling in 12 N HCI without inhibitor for 5 minutes) The characteristics of the coatings are given in Table I 15 TABLE I
Characteristics Specimen Control 20 Appearance: colour white grey-black gloss glossy/matt marbled matt roughness smooth rough 25 Adherence good poor (fragile) Thickness 70-90 llm 200-300 plm (very 30 (normal) thick) EXAMPLE 2
Immersion galvanisation of a steel containing 0 1 % of Si A control is galvanised in a conventional bath of Z 6, Z 7 zinc; a similar specimen is 35 galvanised in the same bath as the specimen of Example 1 Surface preparations are identical, in accordance with the conventional diagram of Figure 2 The characteristics of the coatings are shown in Table 11.
TABLE II 40
Characteristics Specimen Control Appearance: colour white grey 45 gloss glossy/matt matt, marbled roughness smooth rough Adherence good poor 50 Thickness 70-90 plm 150-250 plm (very (normal) thick) The fact that it is possible for steels having silicon contents within a range extending from less than O 01 % to more than O 2 %’/ to be subjected to immersion galvanisation practically by the same operational processes, utilising the galvanisation alloys and the processes of the invention, is found extremely advantageous, particularly for jobbing galvanisation It then becomes possible for batches of parts whose composition is not known to the operator to be 60 galvanised simultaneously and in the same bath, and the range of operation does not need to be modified when different parts have to be galvanised.
Claims (10)
WHAT I CLAIM IS:-
1 An alloy suitable for the galvanisation of steels by an immersion galvanisation process including galvanisation of steels containing silicon, which alloy is essentially 65 1 588 808 composed of zinc of commercial purity and has a lead content of 1000 to 20000 p p m by weight, an aluminium content of from 100 to 5000 p p m by weight, a magnesium content of from 10 to 1000 p p m by weight and a tin content of from 300 to 20000 p p m by weight.
2 An alloy according to Claim 1, in which the magnesium content is from 20 to 200 5 p.p m by weight.
3 An alloy according to Claim 1 or Claim 2, in which the tin content is from 1000 to 3000 p p m by weight.
4 An alloy according to any one of Claims 1 to 3, having an aluminium content of from 300 to 600 p p m, a magnesium content of from 20 to 200 p p m and a tin content of from 10 1000 to 3000 p p m, all parts being parts by weight.
An alloy according to Claim 4, having an aluminium content of 600 p p m, a magnesium content of 100 p p m and a tin content of 2500 p p m, all parts being parts by weight.
6 An alloy according to Claim 1, substantially as described in Example 1 or Example 2 15
7 An immersion galvanisation process for galvanising steels, including steels containing silicon, which process includes the steps of:
a) degreasing the steel to be galvanised and then rinsing the steel; b) pickling the steel with concentrated hydrochloric acid containing a corrosion inhibitor and then rinsing the steel; 20 c) pickling the steel in concentrated hydrochloric acid containing no inhibitor, followed by rinsing the steel; d) fluxing the steel and then drying it; and e) immersing the steel in a molten bath of an alloy as claimed in any of Claims 1 to 6.
8 A process according to Claim 7, wherein the concentration of hydrochloric acid in 25 step (b) is about 6 N and that in step (c) is from 6 to 12 N.
9 A process for galvanising steels according to Claim 7, substantially as hereinbefore described with reference to, and as illustrated in, the accompanying drawings.
A process for galvanising steels according to Claim 7, substantially as described in Example 1 or Example 2 30 11 Galvanised steel when prepared by a process as claimed in any one of claims 7 to
10.
PAGE, WHITE & FARRER, Chartered Patent Agents, 27 Chancery Lane, 35 London WC 2 A 1 NT.
Agents for the Applicant.
Printed for Her Majesty’s Stationery Office, by Croydon Printing Company Limited Croydon Surrey, 1981.
Published by The Patent Office, 25 Southampton Buildings, London, WC 2 A IAY, from which copies may be obtained.
GB40363/77A
1976-10-01
1977-09-28
Zinc alloy and galvanisation process
Expired
GB1588808A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
FR7629545A
FR2366376A1
(en)
1976-10-01
1976-10-01
ALLOY INTENDED FOR THE QUENCH GALVANIZATION OF STEELS, INCLUDING STEELS CONTAINING SILICON, AND GALVANIZATION PROCESS SUITABLE FOR THIS ALLOY
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GB1588808A
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GB1588808A
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1981-04-29
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GB40363/77A
Expired
GB1588808A
(en)
1976-10-01
1977-09-28
Zinc alloy and galvanisation process
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US4168972A
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JPS6043430B2
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AU
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AU512897B2
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(1)
BE859280A
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CA1106651A
(en)
DE
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DE2743655C3
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ES462702A1
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FI61044C
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FR
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FR2366376A1
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GB
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IT1091229B
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FR7629545A
patent/FR2366376A1/en
active
Granted
1977
1977-09-19
IE
IE1909/77A
patent/IE45591B1/en
unknown
1977-09-19
ZA
ZA00775604A
patent/ZA775604B/en
unknown
1977-09-20
US
US05/834,975
patent/US4168972A/en
not_active
Expired – Lifetime
1977-09-23
IT
IT69103/77A
patent/IT1091229B/en
active
1977-09-26
YU
YU02281/77A
patent/YU228177A/en
unknown
1977-09-28
ES
ES462702A
patent/ES462702A1/en
not_active
Expired
1977-09-28
NL
NL7710576A
patent/NL7710576A/en
not_active
Application Discontinuation
1977-09-28
DE
DE2743655A
patent/DE2743655C3/en
not_active
Expired
1977-09-28
GB
GB40363/77A
patent/GB1588808A/en
not_active
Expired
1977-09-28
FI
FI772861A
patent/FI61044C/en
not_active
IP Right Cessation
1977-09-29
CA
CA287,921A
patent/CA1106651A/en
not_active
Expired
1977-09-29
SE
SE7710912A
patent/SE441104B/en
unknown
1977-09-30
AU
AU29278/77A
patent/AU512897B2/en
not_active
Expired
1977-09-30
MX
MX776445U
patent/MX4217E/en
unknown
1977-09-30
BE
BE181378A
patent/BE859280A/en
not_active
IP Right Cessation
1977-09-30
NO
NO773351A
patent/NO144706C/en
unknown
1977-10-01
JP
JP52118526A
patent/JPS6043430B2/en
not_active
Expired
1979
1979-04-10
US
US06/028,919
patent/US4238532A/en
not_active
Expired – Lifetime
1982
1982-09-06
YU
YU02009/82A
patent/YU200982A/en
unknown
Cited By (27)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
GB2227255A
(en)
*
1988-11-08
1990-07-25
Lysaght John
Galvanizing with compositions including tin
GB2227255B
(en)
*
1988-11-08
1993-04-07
Lysaght John
Galvanizing with compositions including tin
US5480731A
(en)
*
1992-03-27
1996-01-02
The Louis Berkman Company
Hot dip terne coated roofing material
US5397652A
(en)
*
1992-03-27
1995-03-14
The Louis Berkman Company
Corrosion resistant, colored stainless steel and method of making same
GB2288410B
(en)
*
1992-03-27
1996-01-17
Berkman Louis Co
Coated substrate
US5395703A
(en)
*
1992-03-27
1995-03-07
The Louis Berkman Company
Hot dip terne coated roofing material
US6811891B2
(en)
1992-03-27
2004-11-02
The Louis Berkman Company
Corrosion-resistant coated metal and method for making the same
US6794060B2
(en)
1992-03-27
2004-09-21
The Louis Berkman Company
Corrosion-resistant coated metal and method for making the same
US6652990B2
(en)
1992-03-27
2003-11-25
The Louis Berkman Company
Corrosion-resistant coated metal and method for making the same
US5491036A
(en)
*
1992-03-27
1996-02-13
The Louis Berkman Company
Coated strip
GB2288410A
(en)
*
1992-03-27
1995-10-18
Berkman Louis Co
Coated substrate
US6080497A
(en)
1992-03-27
2000-06-27
The Louis Berkman Company
Corrosion-resistant coated copper metal and method for making the same
GB2265389A
(en)
*
1992-03-27
1993-09-29
Berkman Louis Co
Hot-dip coating of steel with tin based alloy with preliminary pickling
GB2265389B
(en)
*
1992-03-27
1996-01-17
Berkman Louis Co
Coated substrate
US5667849A
(en)
1992-03-27
1997-09-16
The Louis Berkman Company
Method for coating a metal strip
US5314758A
(en)
*
1992-03-27
1994-05-24
The Louis Berkman Company
Hot dip terne coated roofing material
US5520964A
(en)
*
1992-03-27
1996-05-28
The Louis Berkman Company
Method of coating a metal strip
US5491035A
(en)
*
1992-03-27
1996-02-13
The Louis Berkman Company
Coated metal strip
US5354624A
(en)
*
1992-07-15
1994-10-11
The Louis Berkman Company
Coated copper roofing material
US5492772A
(en)
*
1993-04-05
1996-02-20
The Louis Berkman Company
Building material coating
US5455122A
(en)
*
1993-04-05
1995-10-03
The Louis Berkman Company
Environmental gasoline tank
US5597656A
(en)
*
1993-04-05
1997-01-28
The Louis Berkman Company
Coated metal strip
US5695822A
(en)
1993-04-05
1997-12-09
The Louis Berkman Company
Method for coating a metal strip
US5470667A
(en)
*
1993-04-05
1995-11-28
The Louis Berkman Company
Coated metal strip
US5429882A
(en)
*
1993-04-05
1995-07-04
The Louis Berkman Company
Building material coating
US5401586A
(en)
*
1993-04-05
1995-03-28
The Louis Berkman Company
Architectural material coating
US5489490A
(en)
*
1993-04-05
1996-02-06
The Louis Berkman Company
Coated metal strip
Also Published As
Publication number
Publication date
FR2366376A1
(en)
1978-04-28
NO144706B
(en)
1981-07-13
FI61044B
(en)
1982-01-29
YU200982A
(en)
1983-12-31
NO773351L
(en)
1978-04-04
AU2927877A
(en)
1979-04-05
US4238532A
(en)
1980-12-09
SE7710912L
(en)
1978-04-02
YU228177A
(en)
1983-04-30
MX4217E
(en)
1982-02-04
SE441104B
(en)
1985-09-09
CA1106651A
(en)
1981-08-11
DE2743655C3
(en)
1980-10-16
ES462702A1
(en)
1978-06-01
NL7710576A
(en)
1978-04-04
DE2743655B2
(en)
1980-02-28
BE859280A
(en)
1978-03-30
AU512897B2
(en)
1980-11-06
FI61044C
(en)
1982-05-10
JPS6043430B2
(en)
1985-09-27
IE45591B1
(en)
1982-10-06
US4168972A
(en)
1979-09-25
ZA775604B
(en)
1978-07-26
FI772861A
(en)
1978-04-02
FR2366376B1
(en)
1980-11-07
IE45591L
(en)
1978-04-01
NO144706C
(en)
1981-10-21
DE2743655A1
(en)
1978-04-06
JPS5343630A
(en)
1978-04-19
IT1091229B
(en)
1985-07-06
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Legal Events
Date
Code
Title
Description
1981-07-15
PS
Patent sealed [section 19, patents act 1949]
1988-05-18
PCNP
Patent ceased through non-payment of renewal fee
