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MY'STORY

The MOVE Fire

This is a personal recollection on the Move fire on May 13, 1985 Philadelphia police fired thousands of rounds at the MOVE house, city officials approved dropping an explosive device on the roof, the resulting fire was allowed to burn, 11 people—including five children—died, and 61 homes were destroyed. Philadelphia City Council later called it a “brutal attack carried out by the City of Philadelphia on its own citizens” and acknowledged that no individual faced criminal consequences for the bombing. One timeline correction worth preserving for the BHP record: the major previous MOVE-police confrontation was August 8, 1978, about seven years before the bombing, not a year or two earlier. Officer James Ramp was killed, other police and firefighters were wounded, nine MOVE members were later convicted, and television cameras recorded police beating Delbert Africa during his arrest. The 1985 MOVE Commission later specifically criticized city planners for failing to adequately use lessons from that 1978 confrontation. And that actually strengthens the point you’re making: 1985 did not happen without precedent or institutional memory. There had already been a deadly confrontation with MOVE, years of conflict, negotiations and police involvement before Osage Avenue.

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BLACK FACTS
The Truths They Never Taught You...

Shirley Chisholm — Unbought and Unbossed

In 1968 Shirley Chisholm became the first Black woman elected to the United States Congress. In 1972 she launched a campaign for the Democratic presidential nomination, breaking another political barrier.

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BHP gathered finds from its connected research sources. Showing the 4 strongest Black History matches.
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Wikipedia

Non-ferrous extractive metallurgy

Electrowinning of copper

Non-ferrous extractive metallurgy is one of the two branches of extractive metallurgy which pertains to the processes of reducing valuable, non-iron metals from ores or raw material.[1][2][3] Metals like zinc, copper, lead, aluminium as well as rare and noble metals are of particular interest in this field,[1] while the more common metal, iron, is considered a major impurity.[4][5] Like ferrous extraction, non-ferrous extraction primarily focuses on the economic optimization of extraction processes in separating qualitatively and quantitatively marketable metals from its impurities (gangue).[6]

Any extraction process will include a sequence of steps or unit processes for separating highly pure metals from undesirables in an economically efficient system. Unit processes are usually broken down into three categories: pyrometallurgy, hydrometallurgy, and electrometallurgy. In pyrometallurgy, the metal ore is first oxidized through roasting or smelting. The target metal is further refined at high temperatures and reduced to its pure form. In hydrometallurgy, the object metal is first dissociated from other materials using a chemical reaction, which is then extracted in pure form using electrolysis or precipitation. Finally, electrometallurgy generally involves electrolytic or electrothermal processing. The metal ore is either distilled in an electrolyte or acid solution, then magnetically deposited onto a cathode plate (electrowinning); or smelted then melted using an electric arc or plasma arc furnace (electrothermic reactor).[7]

Another major difference in non-ferrous extraction is the greater emphasis on minimizing metal losses in slag. This is widely due to the exceptional scarcity and economic value of certain non-ferrous metals which are, inevitably, discarded during the extraction process to some extent.[6] Thus, material resource scarcity and shortages are of great concern to the non-ferrous industry. Recent developments in non-ferrous extractive metallurgy now emphasize the reprocessing and recycling of rare and non-ferrous metals from secondary raw materials (scrap) found in landfills.[8][9]

History

[edit]

Prehistory of non-ferrous extractive metallurgy

[edit]

In general, prehistoric extraction of metals, particularly copper, involved two fundamental stages: first, the smelting of copper ore at temperatures exceeding 700 °C is needed to separate the gangue from the copper; second, melting the copper, which requires temperatures exceeding its melting point of 1080 °C.[10] Given the available technology at the time, accomplishing these extreme temperatures posed a significant challenge. Early smelters developed ways to effectively increase smelting temperatures by feeding the fire with forced flows of oxygen.[4]

Copper extraction in particular is of great interest in archeometallurgical studies since it dominated other metals in Mesopotamia from the early Chalcolithic until the mid-to-late sixth century BC.[11][12] There is a lack of consensus among archaeometallurgists on the origin of non-ferrous extractive metallurgy. Some scholars believe that extractive metallurgy may have been simultaneously or independently discovered in several parts of the world. The earliest known use of pyrometallurgical extraction of copper occurred in Belovode, eastern Serbia, from the late sixth to early fifth millennium BC.[10] However, there is also evidence of copper smelting in Tal-i-Iblis, southeastern Iran, which dates back to around the same period.[13] During this period, copper smelters used large in-grown pits filled with coal, or crucibles to extract copper, but by the fourth millennium BC this practice had begun to phase out in favor of the smelting furnace, which had a larger production capacity. From the third millennium onward, the invention of the reusable smelting furnace was crucial to the success of large-scale copper production and the robust expansion of the copper trade through the Bronze Age.[4]

The earliest silver objects began appearing in the late fourth millennium BC in Anatolia, Turkey. Prehistoric silver extraction is strongly associated with the extraction of the less valuable metal, lead; although evidence of lead extraction technology predates silver by at least 3 millennia.[14][15] Silver and lead extractions are also associated because the argentiferous (silver-bearing) ores used in the process often contain both elements.

In general, prehistoric silver recovery was broken down into three phases: First, the silver-lead ore is roasted to separate the silver and lead from the gangue. The metals are then melted at high temperature ( greater than 1100 °C) in the crucible while air is blown over the molten metal (cupellation). Finally, lead is oxidized to form lead monoxide (PbO) or is absorbed into the walls of the crucible, leaving the refined silver behind.

The silver-lead cupellation method was first used in Mesopotamia between 4000 and 3500 BC. Silver artifacts, dating around 3600 BC, were discovered in Naqada, Egypt. Some of these cast silver artifacts contained less than 0.5% lead, which strongly indicates cupellation.[14]

Early to late Anglo-Saxon cupellation

[edit]
Medieval smelting plant

Cupellation was also being used in parts of Europe to extract gold, silver, zinc, and tin by the late ninth to tenth century AD. Here, one of the earliest examples of an integrated unit process for extracting more than one precious metal was first introduced by Theophilus around the twelfth century. First, the gold-silver ore is melted down in the crucible, but with an excess amount of lead. The intense heat then oxidizes the lead which reacts quickly and binds with the impurities in the gold-silver ore. Since both gold and silver have low reactivity with the impurities, they remain behind once the slag is removed. The last stage involves parting, in which the silver is separated from the gold. First the gold-silver alloy is hammered into thin sheets and placed into a vessel. The sheets were then covered in urine, which contains sodium chloride (NaCl). The vessel is then capped and heated for several hours until the chlorides bind with the silver, creating silver chloride (AgCl). Finally, the silver chloride powder is then removed and smelted to recover the silver, while the pure gold remains intact.[5]

Hydrometallurgy in Chinese antiquity

[edit]

During the Song dynasty, Chinese copper output from domestic mining was in decline and the resulting shortages caused miners to seek alternative methods for extracting copper. The discovery of a new “wet process” for extracting copper from mine water was introduced between the eleventh and twelfth century, which helped to mitigate their loss of supply.

Similar to the Anglo-Saxon method for cupellation, the Chinese employed the use of a base metal to extract the target metal from its impurities. First, the base metal, iron, is hammered into thin sheets. The sheets are then placed into a trough filled with “vitriol water” i.e., copper mining water which is then left to steep for several day. The mining water contains copper salts in the form of copper sulfate CuSO
4
. The iron then reacts with the copper, displacing it from the sulfate ions, causing the copper to precipitate onto the iron sheets, forming a "wet" powder. Finally, the precipitated copper is collected and refined further through the traditional smelting process. This is the first large-scale use of a hydrometallurgical process.[16]

See also

[edit]

References

[edit]
  1. ^ a b Gosh, A., and H.S. Ray. Principles of Extractive Metallurgy. 2nd Ed. New Delhi: New Age International Ltd, 1991. pp 1-10.
  2. ^ Reardon, Arthur C. Metallurgy for the Non-Metallurgist. 2nd Ed. U.S.: ASM International, 2011. Pp. 11.
  3. ^ Habashi, F. (2005). "Mining, Metallurgy, and the Industrial Revolution Part 3". CIM Bulletin. 98 (1091): 81–82.
  4. ^ a b c Potts, D. T. (2012). A Companion to the Archaeology of the Ancient Near East. John Wiley & Sons. pp. 300–302. ISBN 978-1-4051-8988-0.
  5. ^ a b Nakamura, Takashi (2007). "Present Status and Issues of Non-Ferrous Extractive Metallurgy". Journal of MMIJ. 123 (12): 570–574. doi:10.2473/journalofmmij.123.570. ProQuest 33106898.
  6. ^ a b Waseda, Yoshio.The Structure and Properties of Oxide Melts: Application of Basic Science to Metallurgical Processing. Singapore: World Scientific Publishing, 1998. Pp. 174.
  7. ^ Mathur, V.N.S.. "Waste Management in Mineral Industries-Some Considerations." Proceedings of the International Conference on Environmental Management in Metallurgical Industries: EMMI 2000. Ed. R.C. Gupta. New Delhi: Allied Publisher Ltd., 2000. 87. Web. 21 Apr. 2013.
  8. ^ Gordon, R. B.; Bertram, M.; Graedel, T. E. (31 January 2006). "Metal stocks and sustainability". Proceedings of the National Academy of Sciences of the United States of America. 103 (5): 1209–1214. doi:10.1073/pnas.0509498103. PMC 1360560. PMID 16432205.
  9. ^ Djokic, Sasa; Djokic, Biljana (February 2005). Metallic secondary raw materials recycling strategy in Serbia. EPD Congress 2005 as held at the 2005 TMS Annual Meeting. San Francisco. ProQuest 28530773.
  10. ^ a b Radivojević, Miljana; Rehren, Thilo; Pernicka, Ernst; Šljivar, Dušan; Brauns, Michael; Borić, Dušan (November 2010). "On the origins of extractive metallurgy: new evidence from Europe". Journal of Archaeological Science. 37 (11): 2775–2787. Bibcode:2010JArSc..37.2775R. doi:10.1016/j.jas.2010.06.012.
  11. ^ Killick, David (December 2009). "Cairo to Cape: The Spread of Metallurgy Through Eastern and Southern Africa". Journal of World Prehistory. 22 (4): 399–414. doi:10.1007/s10963-009-9025-3. S2CID 162458882.
  12. ^ Forbes, R.J. Studies in Ancient Technology:Volume 4 of Studies in Ancient Technology Series. Vol 9. The Netherlands: Brill, 1964. 84-104.
  13. ^ Thornton, C.P.; Rehren, Th. (January 2007). "Report on the First Iranian Prehistoric Slag Workshop". Iran. 45 (1): 315–318. doi:10.1080/05786967.2007.11869198. S2CID 192248709.
  14. ^ a b Gale, N. H.; Stos-Gale, Z. A. (November 1981). "Cycladic Lead and Silver Metallurgy". The Annual of the British School at Athens. 76: 169–224. doi:10.1017/S0068245400019523. JSTOR 30103034. S2CID 137377867.
  15. ^ Yener, K.A., and H. Ozbal. "Bolkardağ Mining District Survey of Silver and Lead in Ancient Anatolia." Proceedings of the 24th International Archaeometry Symposium, (1986), pp. 309-317 Published by: The Smithsonian Institution Press.
  16. ^ Needham, Joseph, and Peter J. Golas. Science and Civilization in China. Vol. 13. Cambridge: Cambridge University Press, 1999, pp. 88,378-382. ISBN 978-0521580007

Source: Wikipedia. Article content is retrieved live through the MediaWiki API.

Wikipedia

Non-ferrous extractive metallurgy

Non-ferrous extractive metallurgy is one of the two branches of extractive metallurgy which pertains to the processes of reducing valuable, non-iron metals from ores or raw material. Metals like zinc, copper, lead, aluminium as well as rare and noble metals are of particular interest in this field, while the more common metal, iron, is considered a major impurity. Like ferrous extraction, non-ferrous extraction primarily focuses on the economic optimization of extraction processes in separating qualitatively and quantitatively marketable metals from its impurities (gangue). Any extraction process will include a sequence of steps or unit processes for separating highly pure metals from undesirables in an economically efficient system. Unit processes are usually broken down into three categories: pyrometallurgy, hydrometallurgy, and electrometallurgy. In pyrometallurgy, the metal ore is first oxidized through roasting or smelting. The target metal is further refined at high temperatures and reduced to its pure form. In hydrometallurgy, the object metal is first dissociated from other materials using a chemical reaction, which is then extracted in pure form using electrolysis or precipitation. Finally, electrometallurgy generally involves electrolytic or electrothermal processing. The metal ore is either distilled in an electrolyte or acid solution, then magnetically deposited onto a cathode plate (electrowinning); or smelted then melted using an electric arc or plasma arc furnace (electrothermic reactor). Another major difference in non-ferrous extraction is the greater emphasis on minimizing metal losses in slag. This is widely due to the exceptional scarcity and economic value of certain non-ferrous metals which are, inevitably, discarded during the extraction process to some extent. Thus, material resource scarcity and shortages are of great concern to the non-ferrous industry. Recent developments in non-ferrous extractive metallurgy now emphasize the reprocessing and recycling of rare and non-ferrous metals from secondary raw materials (scrap) found in landfills.

MORE →
Wikipedia

Mobilization of non-ferrous metals

The mobilization of non-ferrous metals was an event in Second World War France, starting in 1941. During it Nazi Germany requisitioned a large amount of non-ferrous metals for its armament factories, including tin, lead, nickel and copper. With the collaboration of the Vichy regime and under the cover-story of supporting French agriculture, the population was invited to donate such metals, while church bells and many statues were melted down. Some curators estimate that around 1700 statues were destroyed on the Vichy regime's orders, including more than 100 in Paris.

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Wikipedia

Non-ferrous metal

In metallurgy, non-ferrous metals are metals or alloys that do not contain iron (allotropes of iron, ferrite, and so on) in appreciable amounts. Generally more costly than ferrous metals, non-ferrous metals are used because of desirable properties such as low weight (e.g. aluminium), higher conductivity (e.g. copper), non-magnetic properties or resistance to corrosion (e.g. zinc). Some non-ferrous materials are also used in the iron and steel industries. For example, bauxite is used as flux for blast furnaces, while others such as wolframite, pyrolusite, and chromite are used in making ferrous alloys. Important non-ferrous metals include aluminium, copper, lead, tin, titanium, and zinc, and alloys such as brass. Precious metals such as gold, silver, and platinum and exotic or rare metals such as mercury, tungsten, beryllium, bismuth, cerium, cadmium, niobium, indium, gallium, germanium, lithium, selenium, tantalum, tellurium, vanadium, and zirconium are also non-ferrous. They are usually obtained through minerals such as sulfides, carbonates, and silicates. Non-ferrous metals are usually refined through electrolysis.

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Wikipedia

British Non-Ferrous Metals Research Association

The British Non-Ferrous Metals Research Association (officially abbreviated as B.N.F.M.R.A. but commonly as BNF) was a research group active the United Kingdom during the 20th century, bringing together public and privately funded research into metallurgy. It was formed in January 1920 by members of the British Non-Ferrous Metals Federation, which represented the commercial interests of British manufacturers of coppers and copper alloys, lead, zinc and other non-ferrous metals and their alloys, latterly including titanium. The BNF's function was to furthern scientific development and facilitate collaborative research. It was headquartered in Birmingham while its most prominent laboratory was in London; the laboratories were grouped into specialties. It was partially funded by the Department of Scientific and Industrial Research (DSIR). The BNF was involved in numerous critical research projects during the Second World War, including the development of nuclear weapons. In 1990, it bought Fulmer Research Laboratories, which was permanently shuttered two years later. During the late 1990s, it was revealed that an BNF employee, Melita Norwood, had been leaking classified documents to the Soviet Union.

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TOPIC OF THE DAY

Greenwood / Black Wall Street

Before the 1921 destruction of Tulsa’s Greenwood District, Black residents had created a remarkable center of business and community life. The district included stores, professional offices, entertainment venues and homes owned by Black citizens. Understanding Greenwood means learning what was built—not only what was burned.

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TRIVIA QUESTION OF THE DAY

Which Supreme Court case ruled state-sponsored public-school segregation unconstitutional?

Brown v. Board of Education in 1954.