Academic literature on the topic 'Nickel'

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Journal articles on the topic "Nickel"

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Dai, Shu Juan, and Yao Liu. "The Experiment Study on Making Ultrafine Superfine Nickel Powder by N2H4–KHB Reduction and H2 Reduction." Advanced Materials Research 295-297 (July 2011): 677–80. http://dx.doi.org/10.4028/www.scientific.net/amr.295-297.677.

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The N2H4–KHB reduction then CH3OH watering and H2 reduction system was used to make superfine nickel powder by using nickel sulfate as material.The superfine nickel powder of the specific surface area of the nickel powde being 4.24m2/g, spheric shape with grain size 0.5-0.9μm,nickel content being over 99.5%,The toll nichel recovery being over 99.5% was made on the condition of reaction temperature 60°C, reaction time 150-180min,pH 8.0-8.5,[Ni]=1.25M,N2H4/Ni=1.35(mol ratio),sodium hexametaphosphate of 1.5‰ as additive,the dosage of KHB of 8.37×10-3g/g Ni and washing by carbinol,reducing by H2.
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Chan, K. C., N. S. Qu, and D. Zhu. "Crystallographic Texture in Pulse Current Electroforming of Nickel." Textures and Microstructures 30, no. 1-2 (January 1, 1997): 43–53. http://dx.doi.org/10.1155/tsm.30.43.

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Nickel deposits are rather seldom randomly oriented; they usually exhibit a column-like orientation with a definite [hkl] axis along the electric field direction in the electroforming process. However, up to present, most of the studies in electroforming nickels are still using a nickel sulfate bath which is now not commonly used in precise-electroforming or micro-electroforming. In this paper, an experimental investigation on the effect of pulse current on texture in micro-electroforming nickel has been carried out using a nickel sulphamate bath. It was reported that strong and weak [100] texture were formed at different pulse current conditions. These phenomena were considered to be related to the change of the amount of inhibiting chemical species at different conditions.
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Tritjahjono, Rahmad Imbang. "Synthesis of nanocrystalline nickel via pulsed current electrodeposition in additive-free deposition bath and comparison of nanoscale characterization." Eastern-European Journal of Enterprise Technologies 1, no. 12 (127) (February 28, 2024): 13–19. http://dx.doi.org/10.15587/1729-4061.2024.298302.

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An experimental investigation on synthesis of nanocrystalline nickels by pulsed current electrodeposition has been carried out in an additive-free Watts bath employing nickel-sulphate solution with similar nickel ion concentrations. Aluminum was used as a substrate. It demonstrated the advantage of easier removal process of electrodeposited nanocrystalline nickel from its substrate. Whereas the use of high-purity nickel anode was intended to replace nickel ions, which decreased during electrodeposition. Different peak current densities of 450, 750 and 1000 mA/cm2 were applied. A pulsed current was set at a similar pulse pattern of on-time and off-time of 1 ms and 9 ms respectively. The shorter on-time demonstrated the ability to limit ion deposition, which was related to the formation of finer grains. The off-time arrangement was targeted to ensure that the ion mobility had completely stopped. Higher current density demonstrated a dominant impact on deposits, generating a higher nucleation rate that is related to depositing nanocrystalline nickel. A peak current density of 1000 mA/cm2 produced grain sizes in the nanoscale regime. Without any additional additive, nanocrystalline nickel was successfully yielded. Investigation of grain size obtained from the 1000 mA/cm2 has been conducted by extracting full width at half maximum peak intensity (FWHM) revealed from X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM) exhibited consistent results of 22 nm and 25.4±3.4 nm, respectively. It is also evidence of the significant role of pulsed current density. In inclusion, nanocrystalline nickel can be synthesized in an electrodeposition bath without any addition of additives
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Nusamara, Arlyn Annabel, Virginia Virginia, and Matthew Mikha Sebastian Matondang. "Mechanism for Settlement of International Trade Disputes in the Case of the European Union's Lawsuit Against Indonesia Regarding Nickel Mining." AURELIA: Jurnal Penelitian dan Pengabdian Masyarakat Indonesia 3, no. 2 (July 1, 2024): 1408–14. http://dx.doi.org/10.57235/aurelia.v3i2.2730.

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Nickel, a naturally formed metal element, has a shiny shape and a sparkling white color. On some islands in Indonesia, nickel is still abundantly found, such as in Sulawesi, which is a hub of mining industry, especially in Morowali and North Morowali. Besides, it is also found on several other islands, like Maluku North (Halmahera), Papua, and Kalimantan. In addition, total nickel exports by 2022 rose to $5.97 billion. Following the entry into force of a policy banning the export of crude nickel seeds on January 1, 2020, Indonesian nickle exports have increased. However, the EU opposed the policy and sued Indonesia to the World Trade Organization (WTO) in early 2021. Indonesia was found to have violated article X.1 of the GATT on violation of regulatory transparency obligations, article 3.1 (b) of the Subsidy Agreement and the Contract Act on Prohibited Subsidies, and article XI.1 of GATT concerning export and import bans. The aim of the filed lawsuit is to maintain the balance of international trade and encourage more environmentally friendly mining practices. However, the impact is a decrease in foreign investment in the nickel sector.
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Faisal, Faisal Danu Tuheteru, Asrianti Arif Asrianti, and Fauzi Rajab Fauzi. "Potential of Nickel (Ni) Phytoremediation of Adaptive Species on Revegetation Land, PT. Vale Indonesia (Tbk). Pomalaa Site Kolaka Regency." Jurnal Wasian 4, no. 2 (December 30, 2017): 89–96. http://dx.doi.org/10.62142/z842hp80.

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This research aimed to determinate the type of adaptive plant and its potential of phytoremediations on nickel revegetation land, PT. Vale Indonesia Tbk. Pomalaa site Kolaka Regency. The research was carried out in March - October 2016, with stages of explation and identification of adaptive plant species as well as analysis of nicel leaves and soil content using HNO3 or HClO4 method and (AAS) Atomic Absorbtion Spectrophotometry test. 12 types of adaptive plants from 12 genera and 10 family. That grow naturally on nickel revegetation land PT. Vale Indonesia Tbk. site Pomalaa. Species from tree habitus thet freguently found, namely Gymnostoma sumatrana, Sarcotheca celebica, Parinaria corymbosa, Timonius celebicus, Weinnmania fraxinea, Alstonia macrophylla. Based on analysis result, there four species that was categorized as low acummulator Nepenthes maxima, Cheilanthes tenuifolia, Timonius celebicus, Sarcotheca celebica. The highest absorber is S. celebica with nickel content 595 mg/kg dry weight leaves. S. celebica potential to be developed as nickel phytoremedian.
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Murphy, Michael. "Nickel and nickel alloys." Metal Finishing 94, no. 2 (February 1996): 24–26. http://dx.doi.org/10.1016/s0026-0576(96)93839-8.

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Murphy, Michael. "Nickel and nickel alloys." Metal Finishing 95, no. 2 (February 1997): 26. http://dx.doi.org/10.1016/s0026-0576(97)94207-0.

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Bunga', Dicaprio Resen, Frans Phengkarsa, and Desi Sandy. "Karakteristik Beton Mutu Tinggi Dengan Komposisi Slag dan Agregat Halus Batu Gamping." Paulus Civil Engineering Journal 3, no. 2 (June 2, 2021): 141–48. http://dx.doi.org/10.52722/pcej.v3i2.247.

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In general, fine aggregate and coarse aggregate as the main components of concrete come from nature so that one day it will run out, alternative substitutes are needed. One of the alternative materials is Nickel Slag. Nickel slag is a type of rock dumped from the nickel industry. Limestone is also used as an alternative to fine aggregate. This study aims to determine the strength of concrete and the relationship between the characteristics of the concrete using nickeI sIag and limestone as a substitute for fine aggregate to the quality of the concrete. As for the variations of 0%, 10% and 20% and the percentage of using limestone as a substitute for fine aggregate is 10%. The method of mixing the concrete uses the SNI-03-2834-2000 method with a planned concrete quality of 42Mpa. From this research, it was found that the compressive strength of concrete with variations of 0%, 10% and 20% were respectively 42.360 MPa, 42.347 MPa and 41.781 MPa, the split tensile strength test with variations of 0%, 10% and 20% respectively was equal to 3.94 MPa, 3.064 MPa and 2.293 MPa and the flexural strength testing with variations of 0%, 10% and 20% were respectively 4.242 MPa, 4.068 MPa and 3.179 MPa. The relationship of split tensile strength for the variation of Nickel Slag variations 0%, 10%, and 20% is 9,242%, 7,178%, and 7% of the compressive strength, respectively, the relationship of split tensile strength for the variation of Nickel Slag variations 0%, 10%, and 20% of 0.65, 0.62, and 0.57 of compressive strength, respectively. From the resuIts of the study, it was concIuded that the concrete mixture with nickel and limestone slag substitution resulted in a decrease in strength as the percentage of nickel slag substitution increased.
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Syed-Hassan, Syed Shatir A., and Siti Nor Izuera Nor-Azemi. "Gasification of Nickel-Preloaded Oil Palm Biomass with Air." Bulletin of Chemical Reaction Engineering & Catalysis 11, no. 3 (October 11, 2016): 262. http://dx.doi.org/10.9767/bcrec.11.3.566.262-272.

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<p>This study experimentally investigates the gasification of nickel-preloaded oil palm biomass as an alternative catalytic approach to produce clean syngas. To eliminate the use of catalyst support, nickel was added directly to the oil palm mesocarp fiber via ion-exchange using an aqueous solution of nickel nitrate. Nickel species was found to disperse very well on the biomass at a nano-scale dispersion. The presence of the finely dispersed nickels on biomass enhanced syngas production and reduced tar content in the producer gas during the air gasification of biomass. It is believed that nickel particles attached on the biomass and its char promote the catalytic cracking of tar on their surface and supply free radicals to the gas phase to enhance the radical-driven gas-phase reactions for the reforming of high molecular weight hydrocarbons. The unconsumed nickel-containing char shows great potential to be re-utilised as a catalyst to further enhance the destruction of tar components in the secondary tar reduction process. Copyright © 2016 BCREC GROUP. All rights reserved</p><p><em>Received: 12<sup>nd</sup> September 2015; Revised: 10<sup>th</sup> January 2016; Accepted:16<sup>th</sup> January 2016</em></p><p><strong>How to Cite</strong>: Syed-Hassan, S.S.A., Nor-Azemi, S. (2016). Gasification of Nickel-Preloaded Oil Palm Biomass with Air.<em> Bulletin of Chemical Reaction Engineering &amp; Catalysis</em>, 11 (3): 262-272 (doi:10.9767/bcrec.11.3.566.262-272)</p><p><strong>Permalink/DOI</strong>: <a href="http://doi.org/10.9767/bcrec.11.3.566.262-272">http://doi.org/10.9767/bcrec.11.3.566.262-272</a></p>
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Sirwa . A. Qadir and C. N. Fathulla. "PHYSIOLOGICAL AND ANATOMICAL RESPONSES OF COMMON BEAN (PHASEOLUS VULGARIS L.) TO NICKLE NANOPARTICLES FOLIAR SPRAY." IRAQI JOURNAL OF AGRICULTURAL SCIENCES 55, Special (January 25, 2024): 80–89. http://dx.doi.org/10.36103/ijas.v55ispecial.1887.

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Nickel is an essential nutrient for plant growth with low concentrations, its excessive amounts in soil above threshold values could be cause in toxicity. The main objectives of the present research were to determine the effects of nickel nanoparticles foliar spray with 20, 40 and 70 nm diameter on the physiological characters and anatomical aspects of Phaseolus vulgaris L. plants. Lowest reduction significantly (P < 0.01) in root and shoot biomass was recorded due to in 70 nm; the measurements 0.08 and 0.05 g per plant and highest root: shoot; 0.65 as compared with control treatment. As well as the lowest conserved water content; 40% was observed in size 70 nm. While in size 40 nm Nickle nanoparticles increased chlorophyll a, b, total and carotenoids pigment contents. When the nickel nanoparticles size increased, the shoot and root tissue Ni concentrations also increased. However, the rate of Ni in root was greater than that observed in the shoot. While the Mn, Fe, Cu and Zn levels decreased due to applying nickel nanoparticles. The size of nanoparticles effects on the anatomical characteristics or structures such as stem, and leaf, also effects on the size of stomata.
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Dissertations / Theses on the topic "Nickel"

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El, Allam Driss. "Les enthalpies de formation des alliages liquides : palladium-nickel, palladium-gallium, palladium-indium, nickel-gallium, nickel-indium, palladium-nickel-gallium et paladium-nickel-indium." Aix-Marseille 1, 1989. http://www.theses.fr/1989AIX11239.

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A l'aide d'un calorimetre tres haute temperature (1000c
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Lehmberg, Claudia Erdmuthe. "Structure of nickel-iron and nickel-zinc electrodeposits." Thesis, Sheffield Hallam University, 1998. http://shura.shu.ac.uk/3118/.

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Electrodeposited nickel-iron and nickel-zinc alloys have been studied using `direct' methods e. g. XRD, microscopy, EDX and GDOES on coatings having different thicknesses and deposited on different substrates. The work has confirmed and extended the ideas of Finch et al. (2, 51), Piontelli et al. (3) and Pangarov (49.120, 121) applicable to alloy deposition. It has shown that a better understanding, particularly of the initial deposition stages, can be obtained by considering crystallographic, energy and electrochemical aspects in combination rather than individually. Initially alloy is deposited on a `foreign' substrate but subsequently the growing alloy itself serves as the `substrate'. Similarly `old' crystallites have to compete for growth with `newly' nucleated ones as the deposit develops. The three stages of growth observed in nickel-iron and nickel-zinc are discussed. Crystallographic strain, resulting from mismatch between substrate and deposit structures and the presence of impurities, along with the energies required to produce different structures are considered to play a major role in determining structure during alloy deposition. Competition for discharge between hydrogen and metallic ions at the changing deposit surface, including changes in its electrochemical nature are considered. In addition possible effects resulting from adsorbed species, including co-discharged hydrogen as well as other species such as hydroxyl ions or precipitated hydroxides are discussed. Whereas during initial nucleation the original substrate is the dominating influence, in the later stages the electrolytic parameters determine the structure of the deposit. If the structure of the outer deposit differs markedly from that of the deposit during the initial stages, then a transitional growth stage may be involved. The structures of deposits studied in the present work tended to be fine grained in the initial stages but developed coarser columnar structures due to selected grain growth with favoured grains becoming broader during the intermediate and final stages of growth.
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Wang, Shangyu. "Electrochemical properties of nanocrystalline nickel and nickel-molybdenum alloys." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq22500.pdf.

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Abraham, Matthias. "Electrodeposition and characterisation of nanocrystalline nickel and nickel alloys." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269947.

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Hankin, Anna. "Electrochemical recovery of nickel from nickel sulfamate plating effluents." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9241.

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Acidic aqueous nickel(II) sulfamate solutions are widely used for industrial nickel electroplating. The finite lifetimes of these baths are caused by the hydrolysis of sulfamate ions to ammonium ions which raise the stress in the nickel deposits. Spent solutions require treatment to recover the NiII, typically present at ca. 10³ mol m-³ , because consent concentrations for discharge to sewers are ca. 2x10-² mol m-³ . The aim of this project was to develop an electrochemical process and suitable control methods for treating the concentrated effluents by electrodeposition of NiII. The electrochemical reactor designed with a nickel mesh cathode, a Pt/Ti oxygen-evolving anode, and a cation-permeable membrane, was operated at constant current in batch-recycle mode. Elemental nickel was electrodeposited onto the cathode from the catholyte-effluent, separated from the aqueous sodium sulfate anolyte by the membrane, which prevented the oxidation of the sulfamate ions in the effluent and thus restricted the anodic reaction to the evolution of O2. Experiments with this system demonstrated that NiII could be recovered at current efficiencies greater than 90 % if the catholyte-effluent pH was maintained in the range 2.5 - 4.5 and if the magnitude of the applied current was regulated to be smaller than the mass transport limited NiII reduction current. Continuous additions of NaOH into the anolyte during reactor operation effectively decreased the rate of proton migration through the membrane from anolyte to catholyte and prevented the catholyte pH decreasing, so minimising the hydrogen evolution rate, the primary cause of the current efficiency always being less than 100 %. Increase in catholyte pH to values above 4.5 occured when effluents were contaminated with iron(III), present as either Fe2O3 or Fe(OH)3, the reduction of which consumed protons and caused cathode passivation due to formation of Ni(OH)2. The magnitude of the applied current was adjusted during the NiII depletion process to ensure it did not exceed the mass transport limited value for a given solution flow rate at any time. km(NiII) values, used to predict the limiting current densities, were derived from results of separate experiments in which mass transport limited reduction current densities of hexacyanoferrate(III) ions were measured as a function of flow rate in alkaline solution. Using these control methods, which were optimised using a reactor model incorporating mass balances, NiII concentrations in the effluent could be decreased by over 90 %. Using the typically measured average current efficiency of 95 % and the cell potential difference, typically 4.5 V in the presence of a Pt/Ti mesh anode, the specific electrical energy consumption was evaluated as ca. 4 300 kW h (tonne Ni)-¹, equivalent to ca. $650 (tonne Ni)-¹, which is two orders of magnitude lower than the price of elemental nickel, currently $22k tonne-¹. A micro-kinetic model was developed to describe the reduction mechanisms of nickel(II) and protons, considered as sequential one-electron charge transfers via separate adsorbed intermediates, as functions of electrode potential, ion concentrations and mass transport rates. This was coupled with the reactor model to facilitate predictions of reactor performance, based on the kinetic rate coe fficients and transfer coefficients. In order to determine these kinetic parameters the kinetics of nickel(II) and proton / water reduction were measured in sulfamate solutions on a rotating Ni disc electrode and on a Au EQCM as a function of NiII concentration, bulk pH, electrode potential and rotation rate.
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Woodcock, Thomas George. "The crystallographic texture and morphology of nickel oxide layers grown on textured nickel and nickel alloy substrates." Thesis, University of Birmingham, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289750.

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GIRON, JEAN-CHRISTOPHE. "Couches minces d'hydroxyde de nickel et d'oxydes mixtes nickel/lithium et nickel/sodium. Application aux systemes electrochromes." Paris 6, 1994. http://www.theses.fr/1994PA066373.

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La premiere partie de ce memoire est consacree a l'etude, par effet mirage, des flux ioniques mis en jeu lors de l'oxydo-reduction, dans une solution alcaline, d'un film d'hydroxyde de nickel electrodepose. La seconde partie concerne la croissance par ablation laser et par pulverisation magnetron de films d'oxydes mixtes nickel/lithium et nickel/sodium. Leur structure, leurs proprietes electrochimiques et leurs caracteristiques electrochromes ont ete etudiees par diverses techniques (diffraction x, microscopie electronique en transmission, spectroscopie infrarouge a transformee de fourier, xps, voltammetrie cyclique,). Finalement, un dispositif electrochrome incorporant un film d'oxyde de tungstene et un film d'oxyde mixte nickel/lithium a ete realise et ses performances ont ete caracterisees
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Meyer, Ralf Joachim. "Computersimulationen martensitischer Phasenübergänge in Eisen-Nickel- und Nickel-Aluminium-Legierungen." [S.l. : s.n.], 1998. http://deposit.ddb.de/cgi-bin/dokserv?idn=958804702.

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Piers, Newbery A. "Electric arc spray forming of nickel alloys and nickel aluminides." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359486.

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Lain, M. J. "Electrocatalytic hydrogenation on in-situ electrodeposited nickel and nickel alloys." Thesis, University of Southampton, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356694.

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Books on the topic "Nickel"

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F, Hertel R., Maass T, Müller V. R, World Health Organization, United Nations Environment Programme, International Labour Organisation, and International Program on Chemical Safety., eds. Nickel. Geneva: World Health Organization, 1991.

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Stimola, Aubrey. Nickel. New York: Rosen Pub. Group, 2007.

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Sibley, Scott F. Nickel. [Washington, D.C.?]: Dept. of the Interior, Bureau of Mines, 1985.

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Philippines. Lands Geological Survey Division., ed. Nickel. Quezon City: Lands Geological Survey Division, Mines and Geosciences Bureau, Dept. of Environment and Natural Resources, 2005.

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Kaschube, Wilfried. Reaktionen von Magnesiumdiorganylen mit Nickel(O)- [Nickel-] und Nickel(II)-Verbindungen [Nickel-Verbindungen]. [s.l.]: [s.n.], 1987.

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International Program on Chemical Safety., International Labour Organisation, World Health Organization, and United Nations Environment Programme, eds. Nickel, nickel carbonyl, and some nickel compounds health and safety guide. Geneva: World Health Organization, 1991.

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Campbell, R. Wright. Plugged nickel. New York: Pocket Books, 1988.

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Sa, Paulo de. Le nickel. Paris: Economica, 1990.

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Bird, Brad. Nickel trip. Winnipeg: Pemmican Publications, 2004.

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W, Smith C. Buffalo nickel. New York: Pocket Books, 1990.

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Book chapters on the topic "Nickel"

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Howard-White, F. B. "In the Heart of the Earth." In Nickel, 1–5. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-1.

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Howard-White, F. B. "The Metallurgist comes into his own." In Nickel, 167–77. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-14.

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Howard-White, F. B. "New Growth of the Nickel Industry." In Nickel, 186–96. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-16.

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Howard-White, F. B. "The Continuing Search." In Nickel, 210–29. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-18.

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Howard-White, F. B. "Here was a Material Second to None." In Nickel, 91–103. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-9.

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Howard-White, F. B. "‘I have called it Nickel’." In Nickel, 23–34. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-4.

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Howard-White, F. B. "The Bottom falls out of the Nickel Market." In Nickel, 157–66. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-13.

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Howard-White, F. B. "An Unparalleled Demand." In Nickel, 144–56. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-12.

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Howard-White, F. B. "Civilisation Dawns." In Nickel, 6–14. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-2.

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Howard-White, F. B. "A Time for Expansion." In Nickel, 178–85. London: Routledge, 2023. http://dx.doi.org/10.4324/9781032638836-15.

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Conference papers on the topic "Nickel"

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Song, Quansheng, C. H. Chiu, and S. L. I. Chan. "Nanocrystalline Nickel Hydroxide in Pasted Nickel Electrodes for Rechargeable Nickel Batteries." In 2006 International Conference on Nanoscience and Nanotechnology. IEEE, 2006. http://dx.doi.org/10.1109/iconn.2006.340567.

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Nakagawa, Hiroki, Noriyuki Takano, and Hiroki Yamamoto. "Stress analysis of nickel with nickel hydride." In FRACTURE AND DAMAGE MECHANICS: Theory, Simulation and Experiment. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0034136.

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DeMar, Peter J. "Nickel-Iron." In INTELEC 2011 - 2011 33rd International Telecommunications Energy Conference. IEEE, 2011. http://dx.doi.org/10.1109/intlec.2011.6099771.

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Beckman, J. P., and D. A. Woodford. "Intergranular Sulfur Attack in Nickel and Nickel-Base Alloys." In Superalloys. TMS, 1988. http://dx.doi.org/10.7449/1988/superalloys_1988_795_804.

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Rashidifar, Mahsa, Sara Darbari, and Yaser Abdi. "Characterization of humidity sensor based on nickel-MoS2-nickel." In 2020 28th Iranian Conference on Electrical Engineering (ICEE). IEEE, 2020. http://dx.doi.org/10.1109/icee50131.2020.9260786.

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Holden, C. A., R. L. Opila, H. H. Law, and G. R. Crane. "Wear resistance of nickel and nickel phosphorus alloy electrodeposits." In Electrical Contacts, 1988., Proceedings of the Thirty Fourth Meeting of the IEEE Holm Conference on Electrical Contacts. IEEE, 1988. http://dx.doi.org/10.1109/holm.1988.16105.

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Han, Joon Kuy, Hyoungshick Kim, and Simon S. Woo. "Nickel to Lego." In CCS '19: 2019 ACM SIGSAC Conference on Computer and Communications Security. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3319535.3363264.

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Zhang, Futao, Lu Xu, Jin-Qi Xie, Matthew M. F. Yuen, Xian-Zhu Fu, Rong Sun, and Ching-Ping Wong. "Electroless deposition of nickel conductive patterns using nickel-ion catalysts." In 2017 18th International Conference on Electronic Packaging Technology (ICEPT). IEEE, 2017. http://dx.doi.org/10.1109/icept.2017.8046578.

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Subagja, Rudi, Iwan Setiawan, and Januar Irawan. "Nickel dissolution from nickel matte into the aqueous sulfuric acid solutions." In 1ST INTERNATIONAL SEMINAR ON ADVANCES IN METALLURGY AND MATERIALS (i-SENAMM 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0017385.

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Neira, John Bernardo Vilca, Dener Martins dos Santos, Marcelo Breda Mourão, and Cyro Takano. "NICKEL RECOVERY BY CARBOTHERMIC REDUCTION FROM SLUDGE GENERATED DURING NICKEL PRODUCTION." In 7th Japan-Brazil Syposium on Dust Processing-Energy-Environment and 1st International Seminar On Self-Reducing and Cold Bonded Agglomeration. São Paulo: Editora Blucher, 2008. http://dx.doi.org/10.5151/5463-5463-0028.

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Reports on the topic "Nickel"

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Jacobson, Joyce. Perfluorodiethoxymethane on nickel and nickel oxide surfaces. Office of Scientific and Technical Information (OSTI), March 1994. http://dx.doi.org/10.2172/10147931.

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Van Rythoven, Adrian. Critical mineral: Nickel. Montana Bureau of Mines and Geology, May 2024. http://dx.doi.org/10.59691/eogn7509.

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Sopok, Samuel. Determination of Nickel, Nickel Chloride Hexahydrate and Boric Acid in Nickel Sulfamate Plating Solutions by Titration. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada420005.

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Hulbert, L. J. Sedimentary nickel sulphides. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/207972.

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Eckstrand, O. R. Nickel-copper sulphide. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/208042.

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Compere, A. L., W. L. Griffith, H. W. Hayden, J. S. Jr Johnson, and D. F. Wilson. Contaminated nickel scrap processing. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/41314.

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Zimmerman, A. H., and G. A. To. Porosity Characteristics of Nickel Sinter. Fort Belvoir, VA: Defense Technical Information Center, February 2005. http://dx.doi.org/10.21236/ada430971.

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Steffani, C., and M. Meltzer. Electroless nickel recycling via electrodialysis. Office of Scientific and Technical Information (OSTI), April 1995. http://dx.doi.org/10.2172/72881.

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Hsuan, H., M. Bitter, K. W. Hill, S. Grek, B. von Goeler, D. Johnson, L. C. Johnson, S. Sesnic, C. P. Bhalla, and K. R. Karim. Satellite spectra of heliumlike nickel. Office of Scientific and Technical Information (OSTI), February 1987. http://dx.doi.org/10.2172/6637118.

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Eckstrand, O. R., and D. J. Good. World distribution of nickel deposits. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2000. http://dx.doi.org/10.4095/211370.

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