The possibility of using bacteria to drill metallic surfaces has been demonstrated using Staphylococcus sp., a facultative anaerobic bacterium, isolated from corroded copper piping. The experiment involved exposure of copper coupons (25 mm x 15 mm x 3 mm) to a culture of Staphylococcus sp. for a maximum period of 7 days. Coupons exposed to sterile bacterial growth medium were used as controls. Exposed coupons were removed intermittently and observed microscopically for the extent of drilling. The total pit area and volume on these coupons were determined using image analysis. The results showed that both the biomachined area and volume increased with the duration of coupon exposure. In the drilling experiment, a copper thin film 2 microm thick was perforated by this bacterium within a period of 7 days. In conclusion, the results suggested that bacteria can be used as a tool for machining metallic surfaces.
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http://dx.doi.org/10.1080/08927010902985300 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Chemistry, McGill University, Montréal, Québec H3A 0G4, Canada.
Metal powders are crucial precursors for manufacturing surfaces through thermal spraying, cold spraying, and 3D printing methods. However, surface oxidation of these precursors poses a challenge to the coherence of the metallic materials during manufacturing processes. Herein, we introduce a method for surface modification of copper powder with N-heterocyclic carbenes (NHCs) using mechanochemistry to mitigate surface oxidation.
View Article and Find Full Text PDFInorg Chem
January 2025
Beijing Spacecrafts Manufacturing Factory, Beijing 100094, P. R. China.
The rapid upsurge of metal-organic frameworks (MOFs) has sparked profound interest in their potential as proton conductors for proton exchange membrane fuel cells. However, proton-conducting behaviors of hydrophobic MOFs remain poorly understood compared with their hydrophilic counterparts, largely due to the absence of a microscopic phase separation structure akin to that found in Nafion membranes. Herein, we demonstrate a strategy for regulating the structures and proton conductivities of MOFs by separately incorporating hydrophobic -C(CF)- group alongside hydrophilic -O- and -SO- groups into organic ligands as linkers.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
January 2025
Qingdao Qingli Environmental Protectionquipmen Co, LTD, Jiaozhou, 266300, China.
With the growing demand for nickel in the stainless steel and battery industries, conventional methods of extracting nickel from ores face challenges such as high production costs and environmental concerns. This study proposes a new process for the recovery of nickel metal and the production of nickel-iron alloys from nickel-bearing scrap. The reduction rates of nickel and iron oxides were investigated by optimizing the roasting temperature, time, and C/O ratio, and the process was optimized using response surface methodology (RSM).
View Article and Find Full Text PDFInorg Chem
January 2025
NUPOM Lab, Chemistry, School of Natural and Environmental Sciences, Newcastle University, Newcastle upon Tyne NE1 7RU, U.K.
An understanding of proton transfer and migration at the surfaces of solid metal oxides and related molecular polyoxometalates (POMs) and metal alkoxides is crucial for the development of reactivity involving protonation or the absorption/binding of water. In this work, the hydrolysis of alkoxido Ti- and Sn-substituted Lindqvist [(MeO)MWO] (M = Ti, ; M = Sn, ) and Keggin [(MeO)MPWO] (M = Ti, ; M = Sn, ) type polyoxometalates (POMs) to hydroxido derivatives and subsequent condensation to μ-oxido species has been investigated in detail to provide insight into proton transfer reactions in these molecular metal oxide systems. Solution NMR studies revealed the dependence of reactions not only on the nature of the heteroatom (Ti or Sn) but also on the type of lacunary (W or PW) POM and also on the solvent (MeCN or DMSO).
View Article and Find Full Text PDFACS Nano
January 2025
Creative Research Initiative Center for Nanospace-confined Chemical Reactions (NCCR), Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Unlike homogeneous metal complexes, achieving absolute control over reaction selectivity in heterogeneous catalysts remains a formidable challenge due to the unguided molecular adsorption/desorption on metal-surface sites. Conventional organic surface modifiers or ligands and rigid inorganic and metal-organic porous shells are not fully effective. Here, we introduce the concept of "ligand-porous shell cooperativity" to desirably reaction selectivity in heterogeneous catalysis.
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