US38283A - Improvement in the manufacture of white lead - Google Patents
Improvement in the manufacture of white lead Download PDFInfo
- Publication number
- US38283A US38283A US38283DA US38283A US 38283 A US38283 A US 38283A US 38283D A US38283D A US 38283DA US 38283 A US38283 A US 38283A
- Authority
- US
- United States
- Prior art keywords
- lead
- manufacture
- white lead
- ore
- improvement
- 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 - Lifetime
Links
- 229910000004 White lead Inorganic materials 0.000 title description 20
- 238000004519 manufacturing process Methods 0.000 title description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 14
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 14
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 8
- 150000001242 acetic acid derivatives Chemical class 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 230000001264 neutralization Effects 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000003723 Smelting Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 239000004328 sodium tetraborate Substances 0.000 description 4
- 235000010339 sodium tetraborate Nutrition 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- QVQLCTNNEUAWMS-UHFFFAOYSA-N Barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N Boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L Magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 241001062472 Stokellia anisodon Species 0.000 description 2
- 235000015450 Tilia cordata Nutrition 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 241000282485 Vulpes vulpes Species 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium(0) Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 229910001864 baryta Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 235000010338 boric acid Nutrition 0.000 description 2
- 229960002645 boric acid Drugs 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 231100000078 corrosive Toxicity 0.000 description 2
- 231100001010 corrosive Toxicity 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 235000014380 magnesium carbonate Nutrition 0.000 description 2
- 239000011776 magnesium carbonate Substances 0.000 description 2
- 239000004579 marble Substances 0.000 description 2
- 229910052573 porcelain Inorganic materials 0.000 description 2
- 230000001376 precipitating Effects 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 230000001105 regulatory Effects 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 238000004017 vitrification Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/54—Reclaiming serviceable parts of waste accumulators
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G21/00—Compounds of lead
- C01G21/14—Carbonates
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/84—Recycling of batteries or fuel cells
Definitions
- pigment white lead meaning pure white lead
- Thequantity of acid which I employ in the process depends entirely upon the percentage of lead in tions as to form a subacetate of lead-that is tosay, the acid supersaturated withlead.
- the liquor obtained in this manner is brightened by passing it through animal charcoal or other decoloriziu g matter, and then precipitated with carbonic acid.
- the liquor is allowed to percolate through a large holder, and meets the gas, which is introduced at the bottom of the said holder by means of a series of pipes.
- the excess of oxide in the subacetate is thus thrown down as carbonate of lead, which is allowed to settle.
- the liquor is then drawn 0d", and the precipitate washed.
- the vapor from the acid itself If used, then it must be applied to the wet calcined ore through perforations in the manner described in the former process.
- the calcined ore in a wet state must be placed in an apparatus supplying the place of the condenser in the ordinary process of distilling wood.
- borax a solution of borax into the lead by grinding or other available means, either produced from an alkaline boraie or otherwise from boracic acid.
- the strength of the solution will depend upon the nature of the pigments to be treated. For practical purposes I prefer the refined borax of commerce, and to introduce it at the last stage of washing.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
UNITED STATES PATENT OFFICE.
THOMAS OOBLEY, OF LONDON, ENGLAND.
Specification forming part of Letters Patent No. 38,283, dated April 28, 1863.
['0 all whom it may concern.-
Be it known that I, 'Iuorms OoBLEY, of the city of London, Great Britain, have invented certain Improvements in the Manufacture of White Lead, (meaniu g carbonates of lead 5 and I do hereby declare that the following is a description of my invention sutiicient to enable those skilled in the art to practice it-that is to say:
Having first ground or crushed the ore to be acted upon, I then put it upon a simply-constructed furnace consisting of a surface of tireclay tiles, iron plates, or otherwise, and carefully roast it, regulating the heat as much as possible, so as not to form insoluble compounds by the vitrification or other reducing in fluences. It I am about to form pigment white lead, meaning pure white lead, I treat the roasted ore, in the first instance to form the standard lye, with the acetic acid of commerce, (where theore is very impure with a solution of the neutral acctate,) either in a gaseous or liquid form, the latter obtainable either by decomposition of alkaline acetates or acetatesformed from the earthy bases ofvaporized acetic acid, in which case the vapor or gas is introduced by means of a pipe from an apparatus for that purpose into a closed tank or vessel, which is divided into two parts by means of a finely-perforated diaphragm, upon which the roasted ore is placed, and which is kept wet in ordertocondense the vapor. Thequantity of acid which I employ in the process depends entirely upon the percentage of lead in tions as to form a subacetate of lead-that is tosay, the acid supersaturated withlead. The liquor obtained in this manner is brightened by passing it through animal charcoal or other decoloriziu g matter, and then precipitated with carbonic acid. I propose to obtain my carbonic acid by decomposing carbonaceous matters or from by-products given ofi' in the manufacture of silicate of soda, from carbonate of baryta or carbonate of soda, or of chloride of barium, or by the decomposition of marble, limestone, dolomite, magnesite, or any other of the alkaline carbonates, either obtained by the direct application of the said carbon ates, or by double decomposition, or from the carbonates or protocarbonates of iron or other available metallic carbonate;
When I use carbonic acid I always prefer to apply it in a heated state, and,furthermore, to purify it before use by passing it through a solution of copper or lead, or by any other well-known means. The method I adopt for bringing the carbonic acid into combination with the liquid, so as to cause precipitatiom'is,
as follows:- The liquor is allowed to percolate through a large holder, and meets the gas, which is introduced at the bottom of the said holder by means of a series of pipes. The excess of oxide in the subacetate is thus thrown down as carbonate of lead, which is allowed to settle. The liquor is then drawn 0d", and the precipitate washed. Then to render it into an oxiearbonate, or partiallyso, in which form it corresponds with the lead made by the corrosive process, I make use of a caustic alkaline lye possessing great affinity for carbonic acidas baryt-a or lime or any other alkaline earth-to withdraw a certain amount of earbonic acid, which is preferably efl'ected by boiling it in the same lye. After being dried in the ordinary manner it is then ready for market. I now treat the neutral liquor with a fresh supply of ore prepared as before until a subacetate is again formed, and again I precipitate as before, and continue charging and precipitating alternately. Hence the cost of the acetic acid becomes nominal, as I only use it asacarrier.
In producing white lead, which is used by potters, porcelain manufacturers, color-makers, and others, I employ a cheaper course of obtaining acetic acid-that is to say, I use the crude pyroligneous acid of commerce as a liquid, or the vapor of the said acid, or pyroligneous gas produced from dry distillation of wood, or a solution of the brown neutral. acetate. In this process I take the pyroligneous liquor and mix the ore with it, taking the latter warm from the calcining-furnace, using the necessary proportions of each. I then allow it to.stand, lixiviate itwith hot water, brighten it as before described, then precipitate it in the manner before mentioned. If the vapor from the acid itself is used, then it must be applied to the wet calcined ore through perforations in the manner described in the former process. When pyroligneous gases are used the calcined ore in a wet state must be placed in an apparatus supplying the place of the condenser in the ordinary process of distilling wood.
The liquor obtained by any of the last-de- 'potters or glazing lead greater flexibility, I
introduce a solution of borax into the lead by grinding or other available means, either produced from an alkaline boraie or otherwise from boracic acid. The strength of the solution will depend upon the nature of the pigments to be treated. For practical purposes I prefer the refined borax of commerce, and to introduce it at the last stage of washing.
I am aware that it is not new to make carbonate of lead by precipitation from the basic acetates. Neitherisitnew to make clichy-white by precipitation from a basic salt of lead by means of carbonic acid, nor to precipitate from solutions of native ores a leaden sponge, processes all of which are well known, and may be found describedin Mnspratts Chemistry. My process difl'ers from these, inasmuch as I do not use the metal or basic acetates or litharge to precipitate from. Neither do I employ the ore to produce a metallic sponge; but, having first pulverized or crushed the ore, I obtain directly therefrom a pure white lead by the process as above described. The advantages of this method of mauufacture are numerous and important. Isave the cost of making metallic lead or litharge from the ores and the time required to oxidize the former. I can use ore carbonates which are too poor to smelt. In smelting poor carbonates there is a very great loss of metal; but by using them in my process all the lead is saved, being taken up direct in white lead, and Iain enabled not only to save time, but to use ores otherwise of no value or too poor for smelting,
producing at low cost of manufacture a very fine and high-colored white lead.
Having now described the natureof my invention and how the same is carried into operation and the results obtained, I wish it understood that what I claim is I 1. The manufacture of white lead from crushed or ground native ore carbonates of lead by the process set forth, or by means substantially the same.
2. The method of treating precipitated white lead with acaustic alkaline solution for the purpose of producing an oxicarbonate of lead, by which it is rendered more amorphous and less crystalline and the covering properties of the lead are largely increased.
TH. OOBLEY.
Witnesses:
"SAML. ARGHBUTT,
THOS. Fox,
12 Oopthall Court, London.
Publications (1)
Publication Number | Publication Date |
---|---|
US38283A true US38283A (en) | 1863-04-28 |
Family
ID=2107856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US38283D Expired - Lifetime US38283A (en) | Improvement in the manufacture of white lead |
Country Status (1)
Country | Link |
---|---|
US (1) | US38283A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3933973A (en) * | 1973-10-16 | 1976-01-20 | Sherritt Gordon Mines Limited | Treatment of lead sulphide bearing material |
US20170195859A1 (en) * | 2015-12-30 | 2017-07-06 | Hubbell Incorporated | Power outlet having availability notification |
-
0
- US US38283D patent/US38283A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3933973A (en) * | 1973-10-16 | 1976-01-20 | Sherritt Gordon Mines Limited | Treatment of lead sulphide bearing material |
US20170195859A1 (en) * | 2015-12-30 | 2017-07-06 | Hubbell Incorporated | Power outlet having availability notification |
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