US1939799A - Lead of high resistance against the action of hot sulphuric acid - Google Patents

Lead of high resistance against the action of hot sulphuric acid Download PDF

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Publication number
US1939799A
US1939799A US419455A US41945530A US1939799A US 1939799 A US1939799 A US 1939799A US 419455 A US419455 A US 419455A US 41945530 A US41945530 A US 41945530A US 1939799 A US1939799 A US 1939799A
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Prior art keywords
lead
sulphuric acid
action
resistance against
high resistance
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Expired - Lifetime
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US419455A
Inventor
Wallis Theodor
Falek Oskar
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IG Farbenindustrie AG
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IG Farbenindustrie AG
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C11/00Alloys based on lead

Definitions

  • the resistance of lead against the action of hot sulphuric acid may be improved by addition of copper or silver, a fact which may be explained by reference to the higher degree of fineness of the crystalline structure and to the prevention of recrystallization by formation of an eutectic mixture.
  • the quantity of added metal amounts to 0.06 to 0.1 per cent; in the case of silver, essentially greater quantities are required.
  • the hardness and therewith the brittleness is increased which is undesired in the case of soft lead.
  • nickel and selenium may be used instead of copper preferably nickel and selenium.
  • a leadnickel alloy may be made containing 2 to 3 per cent of nickel, from which alloy the calculated quantity is added to the fused lead to be improved.

Description

Patented Dec. 19, 1933 LEAD OF HIGH RESISTANCE AGAINST THE ACTION OF HOT SULPHURIC ACID Theodor Wallis, Dessau-Ziebigk in Anhalt, and
Oskar Falek, Wiederitzsch, near Leipzig, Germany, assignors' to I. G. Farbenindustrie Aktiengesellschaft, Frankfort on the Main, Germany No Drawing. Application January 8, 1930, Serial No.8 419,455, and in Germany November 12, 192
1 Claim.
Our present invention relates to new alloys of lead. One of its objects is to provide a lead of high resistance against the action of hot sul-' phuric acid and more particularly it relates to a lead containing nickel and selenium in a distinct proportion. It is a continuation-in-part of our co-pending application Serial No. 361,248,
filed May 7, 1929.
The whole crux of our invention can well be exemplified by brief discussion of the prior art and by the table following hereafter and showing the superiority of our new alloys over others known in the art.
It is well known that the resistance of lead against the action of hot sulphuric acid may be improved by addition of copper or silver, a fact which may be explained by reference to the higher degree of fineness of the crystalline structure and to the prevention of recrystallization by formation of an eutectic mixture. As found by many researches, for this purpose in case of copper the quantity of added metal amounts to 0.06 to 0.1 per cent; in the case of silver, essentially greater quantities are required. When adding these commensurably great quantities of additional metals to the lead, the hardness and therewith the brittleness is increased which is undesired in the case of soft lead.
Now we have found that instead of copper preferably nickel and selenium may be used.
In contradistinction to the lead alloys mentioned above and containing copper or silver, our lead alloys do not shown an increased brittleness, the melting point of our mixtures lying only slightly below that of pure lead. The higher resistance against the action of sulphuric acid of different commercial lead brands improved according to our invention, may well be seen from the following table showing the action of boiling concentrated sulphuric acid on balls of lead of about 20 grams weight and of 7 square centimeters surface. The tests were carried out in such a manner that the sulphuric acid was kept in a continuous circulation for 30 minutes. Under these conditions unimproved brands of lead were rapidly attached and completely dissolved.
The following table shows the resistance of lead alloyed according to our invention in comparison to lead alloys containing only nickel. The decrease in weight of the test balls given by percentage is the average of a plurality of tests indicated in the last column.
Table Percentage tie; N be crease m um r Alloy containing weight of tests alter 30 minutes Percen Commercial lead without addition 100. 0 3 Commercial 1ead+0.03% Ni 55. 0 5 Commercial lead-{003% Ni 55. 0 3 Commercial lead+0.0l% N1+0.02% Se... 14. 0 2 Commercial lead-l-0.02% Ni+0.l% 8a..-- 7. 5 4
The quantity of nickel and selenium, which is necessary to obtain an unobjectionable result is dependent from the variety and quantity of the impurities contained in the lead serving as starting material. It does not surpass 0.05 per cent of nickel and 0.1 per cent of selenium. The selection of the improving material is influenced by the temperature, by the concentration and in some cases by the impurities contained in the sulphuric acid which is allowed to come in contact with our new lead alloys. The optimal result may be found in each case by a simple experiment.
The alloying process is carried out in the known manner. Thus, for instance, previously, a leadnickel alloy may be made containing 2 to 3 per cent of nickel, from which alloy the calculated quantity is added to the fused lead to be improved.
What we claim is:--
Soft lead alloy of high resistance against the action of hot concentrated sulphuric acid containing nickel in an amount of about 0.01 to about 0.05 per cent and selenium in an amount from 0.01 to 0.1 per cent, the balance consisting of commercial soft lead.
, THEODOR WALLIS.
OSKAR FALEK.
US419455A 1928-11-12 1930-01-08 Lead of high resistance against the action of hot sulphuric acid Expired - Lifetime US1939799A (en)

Applications Claiming Priority (1)

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DE1939799X 1928-11-12

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2620367A (en) * 1947-12-04 1952-12-02 Chloride Electrical Storage Co Lead-acid accumulator
US2729602A (en) * 1952-07-29 1956-01-03 George Robert Van Houten Electrodeposition of bright zinc plate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2620367A (en) * 1947-12-04 1952-12-02 Chloride Electrical Storage Co Lead-acid accumulator
US2729602A (en) * 1952-07-29 1956-01-03 George Robert Van Houten Electrodeposition of bright zinc plate

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