Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Electroplating”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 307 records · Page 17Linked to original sources
PubMed2001

Toxicity evaluation of sewage sludges in Hong Kong.

Anaerobically digested sewage sludges collected from four wastewater treatment plants located in Sha Tin, Tai Po, Yuen Long, and Shek Wu Hui in Hong Kong were subjected to chemical characterization and toxicity testing to provide preliminary assessment of their suitability for land application. All sewage sludges were slightly alkaline with pH range of 8.3-8.7. Electrical conductivity (EC; 0.69 dS m(-1)) and soluble NH4-N content (996 mg kg(-1)) of sewage sludge from Yuen Long were lower than that of other plants. Concentrations of heavy metals were determined as total, extractable, and water-soluble fraction using mixed acid digestion, DTPA (pH 7.3), and distilled water, respectively. Yuen Long sludge was most polluted with Zn and Cr higher than the pollutant concentration limits listed in Part 503 of USEPA, owing to the effluent coming from the tannery industry. High concentration of Ni was found in sludge from Sha Tin that originated mainly from the electroplating industry. DTPA-extractable Zn contents were high in sludges from Yuen Long (1247 mg kg(-1)) and Shek Wu Hui (892 mg kg(-1)), while 3.7 mg kg(-1) of DTPA-extractable Cr was found in Yuen Long sludge. Metal speciation of sludges showed that Pb was major in residual phase while Cu, Cr, and Ni in organic and residual phases, and Zn did not show any dominant chemical phase. The sludge extracts did not exert significant adverse effect on seed germination of Brassica chinensis (Chinese cabbage), but Yuen Long sludge caused a reduction in root growth. In view of its lower EC and soluble ammonia contents, the high concentration of Zn and Cr in Yuen Long sludge would likely be responsible for this adverse effect on root growth. Therefore, Yuen Long sludge would likely have a more serious impact on soil quality and plant growth as compared to other sludges. This would require further verification from greenhouse and field experiments.

Ammonia↗
PubMed1998

A simple, low-cost and fast Peltier thermoregulation set-up for electrophysiology.

Most of the parameters recorded in electrophysiology are strongly temperature dependent. In order to control temperature fluctuations we have built a system that ensures an accurate thermoregulation of the recording chamber. Temperature of physiological preparations can be changed relatively quickly (about 8 degrees C/min) and with a good accuracy (+/- 0.5 degrees C) without inducing thermal oscillations. Contrary to other thermoregulating devices, the temperature regulation is not carried out through the perfused medium but directly at the bottom of the chamber where a 3-cm2 Peltier element has been placed. The element is driven by a dedicated electronic device which controls the amount and the direction of the current flowing across the Peltier thermocouple. All construction details and the appropriate electrical circuits are provided. Using this home-made device, the steady-state chamber temperature could be precisely monitored with a resolution of +/- 0.1 degrees C in a range of 0-40 degrees C. This set-up was tested in experiments designed to evaluate the temperature dependence of synaptic transmission in the Torpedo nerve electroplate synapses and of calcium currents recorded from isolated nerve cells. This low-cost method is suitable for a wide range of applications.

Animals↗
PubMed2002

Sample preparation for the determination of 241Am in sediments utilizing gamma-spectroscopy.

This paper describes a procedure developed to separate americium-241 from the bulk of a sample by coprecipitation followed by high sensitivity gamma-counting of the concentrate in a well-type detector. It enables the measurement of 241Am at low concentrations, e.g. fallout levels in soils and sediments, or where large sample sizes are not available. The method is much faster and more reliable than those involving separation from other alpha-emitters, electroplating and alpha-spectrometry. A number of tracer experiments was performed in order to optimize the conditions for coprecipitation of 241Am from sediment leachates. The general outline of the determination of americium is also given.

Americium↗
PubMed1997

Implementation of a continuous-flow stirred bioreactor system in the bioremediation of heavy metals from industrial waste water.

The industrial applicability of immobilized non-viable yeast biomass (Saccharomyces cerivisiae) in continuous-flow stirred bioreactors was tested with respect to metal removal from electroplating effluent solutions containing Cu, Cd, Cr, Ni and Zn in excess of the stipulated water quality criteria. Two systems, a dual bioreactor and triple bioreactor system in series, were tested and compared regarding their efficiency of metal removal. The system containing two bioreactors linked in series provided a more efficient solution to the problem. The introduction of a third bioreactor into the system had a marginal effect on the amount of metal removed. Subsequent to treatment within the bioreactors the levels of Cu, Cr and Ni in the effluent complied with the stipulated drinking water quality criteria and, although in excess of these criteria only 18% of the initial Zn and 17% of the Cd remained in solution.

Journal Article↗
PubMed2000

A new method to control electrolytes pH by circulation system in electrokinetic soil remediation.

To simultaneously avoid a decrease of electro-osmotic flow by hydrogen ions and to increase heavy metal precipitation due to hydroxide ions, simulated electrokinetic remediation was conducted in saturated kaolinite specimens loaded with lead(II) using an electrolyte circulation method to control electrolyte pH. At an electrolyte circulation rate of 1.1 ml/min, it was possible to increase the anolyte pH from 2 to 4 and decrease the catholyte pH from 12 to 8. Using electrolyte circulation, it was observed that the rate of decrease of clay pH due to the change of electrolyte pH was reduced. As a result, the operable period was extended and the removal efficiency for lead(II) was also increased. It was observed that most of the effluent lead(II) from the cathode compartment was electroplated onto the cathode and that residual effluent lead(II) did not precipitate onto, or adsorb to, the clay at the anode compartment during circulation. Therefore, there was no need to treat the electrolyte because there was virtually no effluent from the cathode compartment in the circulation system. It was also found that the electrolyte volume required to sustain the electrolytic reaction was sufficient for the whole electrokinetic remediation process.

Electrochemistry↗
PubMed2002

Chloride influence on the incorporation of Cr(2)O(3) and NiO in clinker: a laboratory evaluation.

Co-incinerating wastes in cement rotary kilns may introduce elements not usually found in the raw material into the process or even increase the quantity of some minor elements. Chromium and nickel are present in some electroplating sludges. These wastes are hazardous and must be treated and disposed of in a controlled landfill. The objective of this work was to study the incorporation of chromium and nickel oxides when they were added to clinker raw meal. The clinker raw meal used in this study was prepared by mixing pure compounds in the ratio that made it possible to obtain the same phases of an industrial Portland clinker at the end of the heating process. Twelve samples were prepared by adding 0.05, 0.1, 0.3, 0.5, 0.8 and 1.0wt.% of Cr(2)O(3) and 0.05, 0.1, 0.3, 0.5, 0.8 and 1.0wt.% of NiO to the base charge. Also, four more samples were prepared with additions of 0.6% Cr(2)O(3) and 0.1% NaCl, 0.7% Cr(2)O(3) and 0.1% KCl, 0.8% NiO and 0.1% NaCl and 0.8% NiO and 0.1% KCl. In order to study the Cr and Ni incorporation, thermogravimetric (TG) tests were performed, as well as tests in an assembled experimental device. The products were characterized by X-ray fluorescence chemical analysis, microprobe analyses by energy disperse scanning (EDS) and leaching tests. The results showed that the chromium and nickel added were incorporated into the clinker, even when chlorides were present.

Chromium Compounds↗
PubMedDate not supplied

New purification protocol for actinide measurement in excreta based on calixarene chemistry.

The determination of actinides concentration level in excreta, mainly urine is currently carried out to monitor people potentially exposed to alpha emitters. To measure actinides in such samples, specific analytical protocols have been set up. The chemical purification uses different chromatographic columns to selectively separate the actinides and each fraction, after electroplating, is measured by alpha spectrometry. To reach 1 mBq l(-1) of U, Pu or Am using these protocols, 6 days equally distributed between the chemical purification and the measurement are necessary. The protocol proposed here is based on a single extractant, the 1,3,5-trimethoxy-2,4,6-tricarboxy-p-tert-butylcalix[6]arene, used to selectively separate U, Pu and Am from the urinary matrix prior to be measured. Using this analytical protocol, U and Pu are quantitatively and selectively recovered in two different acidic backextraction solutions whereas Am is quantitatively and selectively recovered in the organic phase. Furthermore, the purification stage is considerably shortened. The uranium and plutonium amounts are measured in aqueous phases using alpha spectrometry or inductively coupled plasma-mass spectrometry, whereas Am is measured in the organic phase using alpha liquid scintillation (photon/electron-rejecting alpha liquid scintillation).

Actinoid Series Elements↗
PubMed2001

Cyclotron production of no-carrier-added palladium-103 by bombardment of rhodium-103 target.

Electroplated rhodium foil was employed as the target for cyclotron production of palladium-103. An electrodissolution apparatus was found better than other dissolution methods in terms of personnel shielding and palladium-103 yield. The ion-exchange column chromatography method was simple and effective for the purification of palladium-103 and the final stripping agent of NH4Cl + NH3(1:1) was more efficient than other agents.

Brachytherapy↗
PubMedDate not supplied

Cross-section measurements of the nuclear reactions natZn(d,x)64Cu, 66Zn(d,alpha)64Cu and 68Zn(p,alphan)64Cu for production of 64Cu and technical developments for small-scale production of 67Cu via the 70Zn(p,alpha)67Cu process.

The radionuclides 64Cu (T1/2=12.7h) and 67Cu (T1/2=61.9h) are useful in internal therapy. In connection with production of 64Cu, excitation functions of the reactions natZn(d,x)64Cu, 66Zn(d,alpha)64Cu and 68Zn(p,alphan)64Cu were measured radiochemically using the stacked-foil technique. From the measured data, the thick target yields of 64Cu were calculated and compared with experimental data available in the literature. The three investigated processes are discussed in comparison to the commonly used 64Ni(p,n)64Cu reaction for the production of 64Cu. As regards 67Cu production, the technical feasibility of the 70Zn(p,alpha)67Cu process was investigated. An electroplated isotopically enriched 70Zn target was developed which can withstand slanting beams of 20MeV protons of currents up to 20 microA. Methods for chemical separation of 67Cu and efficient recovery of the enriched target material were worked out. The method is suitable only for small-scale production of 67Cu.

Copper Radioisotopes↗
PubMed2003

Planar microcoil-based microfluidic NMR probes.

Microfabricated small-volume NMR probes consisting of electroplated planar microcoils integrated on a glass substrate with etched microfluidic channels are fabricated and tested. 1H NMR spectra are acquired at 300 MHz with three different probes having observed sample volumes of respectively 30, 120, and 470 nL. The achieved sensitivity enables acquisition of an 1H spectrum of 160 microg sucrose in D2O, corresponding to a proof-of-concept for on-chip NMR spectroscopy. Increase of mass-sensitivity with coil diameter reduction is demonstrated experimentally for planar microcoils. Models that enable quantitative prediction of the signal-to-noise ratio and of the influence of microfluidic channel geometry on spectral resolution are presented and successfully compared to the experimental data. The main factor presently limiting sensitivity for high-resolution applications is identified as being probe-induced static magnetic field distortions. Finally, based on the presented model and measured data, future performance of planar microcoil-based microfluidic NMR probes is extrapolated and discussed.

Electronics↗
PubMed2000

Iridium-based electrocatalytic systems for the determination of insulin.

Two electrochemical catalytic systems for the determination of insulin were developed. The homogeneous system was based on the oxidation of insulin by chloro complexes of iridium(IV). Kinetic studies revealed that the aquation of iridium complexes activated them toward the oxidation of insulin in acidic solutions; e.g., the rate constant was equal to 25, 900, and 8,400 L mol(-1) s(-1) for the oxidation of insulin by the IrCl62-, Ir(H2O)CI5-, and Ir(H2O)2Cl4 complexes, respectively. The inertness of the iridium complexes argued for the outer-sphere mechanism of the homogeneous oxidation reaction. Electroplating of aquated iridium complexes on the glassy carbon electrode resulted in the formation of the iridium oxide (IrOx) surface film, which was used in the heterogeneous detection system for insulin. The catalytic activity of the IrOx film toward insulin oxidation was ascribed to a combination of electron-transfer mediation and oxygen transfer which was related to the acid/base chemistry of the film. The IrOx film electrode was used as an amperometric detector for flow injection analysis of insulin in pH 7.40 phosphate buffer. Linear least-squares calibration curves over the range 0.05-0.50 microM (five points) had slopes of 35.2 +/- 0.4 nA microM(-1) and correlation coefficients of 0.999. The detection limit for insulin was 20 nM using the criterion of a signal of 3 times the peak-to-peak noise. The advantageous properties of the detector based on the IrOx film are its inherent stability at physiological pH, high catalytic activity toward insulin oxidation, and simplicity of preparation.

Algorithms↗
PubMed1989

Measurement of nanomolar dopamine diffusion using low-noise perfluorinated ionomer coated carbon fiber microelectrodes and high-speed cyclic voltammetry.

Several improvements in the fabrication and use of carbon fiber voltammetric microelectrodes (CFVMs) are described. These procedures did not involve oxidative treatment, but resulted in sensitivities and selectivities approaching those of treated CFVMs, without the inherent slow response times associated with the latter electrodes. To accomplish this we reduced CFVM noise by (1) improving the adhesive seal between the 8 microns o.d. carbon fiber and the glass insulation using vacuum, (2) snapping rather than cutting or beveling the fiber to be flush with the glass, and (3) using a concentrated electrolyte solution to make electrical contact with the fiber. System noise was reduced by digital smoothing and signal averaging. Selectivity of the CFVMs for dopamine over ascorbate was enhanced to better than 2000:1 by coating with Naflon, a perfluorinated cation exchange polymer, using a low (+0.5 V vs Ag/AgCl) electroplating potential. This low voltage also prevented electrode surface oxidation. To demonstrate the performance of our CFVMs, we used them in conjunction with high-speed cyclic voltammetry to accurately measure the diffusion coefficient of iontophoretically released dopamine at concentrations as low as 35 nM over distances of less than 200 microns in agarose gel.

Diffusion↗
PubMed2003

Selective electroless and electrolytic deposition of metal for applications in microfluidics: fabrication of a microthermocouple.

This paper describes a general strategy for the fabrication of a microthermocouple based on the spatially defined electroless deposition of metal, followed by annealing and electroplating. We present scanning electron microscopy and atomic force microscopy characterizations of the deposition and annealing process, as well as the performance of the microfabricated Ni-Ag thermocouple. The temperature-voltage curve for this Ni-Ag microthermocouple is linear over the range 0-50 degrees C with a slope of 61.9 degrees C mV(-1). The sensitivity of our temperature measurement, which is limited by the uncertainty of our calibration curve, is approximately 1 degrees C. The optimum figure of merit (Z(opt)) is 1.0 x 10(-5) for this type of Ag-Ni thermocouple. We have fabricated microthermocouples ranging in size from 50 to 300 microm. The microthermocouple was integrated into microchannels and used to measure the in-channel temperature rise caused by the following: (1) a simple acid-base reaction, HCl + NaOH --> H2O + NaCl, and (2) an enzyme-catalyzed biochemical reaction, H2O2 + catalase --> H2O + 1/2 O2. We have also profiled the temperature increase in the presence of electroosmotic flow for a 100-, 200-, and 300-microm channel.

Journal Article↗
PubMed2004

Durable microfabricated high-speed humidity sensors.

We describe a durable microfabricated humidity sensor made of interdigitated rhodium electrodes on a silicon substrate covered with a sensing film of Nafion perfluorosulfonate ionomer. Rhodium electrodes are much less prone to oxidative degradation compared to previously described gold electrode-based sensors. Even with dc excitation, Rh electrode sensors exhibit excellent long-term response stability. It has been found that low-amplitude (+/-1 V) square wave excitation can prolong the usability of gold electrode-based sensors to at least several months; however, this mode of interrogation cannot provide subsecond response times. Rhodium deposition on the microsensors is much more difficult than that of gold. We were able to attain crack-free Rh deposits by adaptation of pulsed electroplating techniques. At excitation voltages of >2 V dc, the Rh sensors respond to moisture with 10 <--> 90% rise and fall times of 30-50 ms. These are the fastest microfabricated water vapor sensors reported to date. We demonstrate applications as a breath monitor. Such sensors should also be of utility in atmospheric eddy measurements. Short-term repeatability is better than 0.6% RSD (n = 7).

Biosensing Techniques↗
PubMed2004

A microfabricated device for subcellular organelle sorting.

We report a microfabricated field flow fractionation device for continuous separation of subcellular organelles by isoelectric focusing. The microdevice provides fast separation in very small samples while avoiding large voltages and heating effects typically associated with conventional electrophoresis-based devices. The basis of the separation is the presence of membrane proteins that give rise to the effective isoelectric points of the organelles. Simulations of isoelectric focusing of mitochondria in microchannels are used to assess design parameters, such as dimensions and time scales. In addition, a model of Joule heating effects in the microdevice during operation indicates that there is no significant heating, even without active cooling. The device is fabricated using a combination of photolithography, thin-film metal deposition/patterning, and electroplating techniques. We demonstrate that in the microfluidic devices, mitochondria from cultured cells migrate under the influence of an electric field into a focused band in less than 6 min, consistent with model predictions. We also illustrate separation of mitochondria from whole cells and nuclei as well as the separation of two mitochondrial subpopulations. When automated and operated in parallel, these microdevices should facilitate high-throughput analysis in studies requiring separation of organelles.

Cell Fractionation↗
PubMed2000

Determination of selenium(IV) by a photooxidized 3,3'-diaminobenzidine/perfluorinated polymer mercury film electrode

A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.

Journal Article↗
PubMedDate not supplied

A heavy metal biotrap for wastewater remediation using poly-gamma-glutamic acid.

Poly-gamma-glutamic acid (gamma-PGA) obtained from Bacillus licheniformis ATCC 9945 was evaluated as a potential biosorbent material for use in the removal of heavy metals from aqueous solution. Copper (Cu(2+)) was chosen as the model heavy metal used in these studies since it is extensively used by electroplating and other industries, has been the model for many other similar studies, and can be easily assayed through a number of convenient methods. Cu(2+)-gamma-PGA binding parameters under varying conditions of pH, temperature, ionic strength, and in the presence of other heavy metal ions were determined for the purified biopolymer using a specially designed dialysis apparatus. Applying the Langmuir adsorption isotherm model showed that gamma-PGA had a copper capacity approaching 77.9 mg/g and a binding constant of 32 mg/L (0.5 mM) at pH 4.0 and 25 degrees C. Cu(2+)-gamma-PGA adsorption was relatively temperature independent between 7 and 40 degrees C, while an increase in ionic strength led to a decrease in metal ion binding. Cd(2+) and Zn(2+) ions compete with Cu(2+) for binding sites on the gamma-PGA biopolymer. Metal uptake by gamma-PGA was further tested using a tangential flow filtration apparatus in a diafiltration mode in which metal was continually processed through a dilute solution of gamma-PGA without allowing for equilibrium to be established. The circulating polymer solution was able to complex metal as well as successfully prevent passage of unbound copper ions present in solution through the membrane. Using 500 mL of a 0.2% gamma-PGA solution, up to 97% of a 50 mg/L copper sulfate solution processed at a flow rate of 115 mL/min was retained by the polymer. For a 10 mg/L solution of Cu(2+) as copper sulfate, filtrate concentrations of Cu(2+) never rose above 0.6 mg/L while processing 2.5 L of dilute copper sulfate.

Cations↗
PubMed2001

Hydrogen peroxide effects on chromium oxidation state and solubility in four diverse, chromium-enriched soils.

High concentrations of H2O2 are being tested for in situ oxidation and remediation of buried organic contaminants in soils and groundwater. Peroxide is being considered as a direct chemical oxidant in Fenton-type reactions or as a source of oxidizing equivalents in bioremediation schemes. How H2O2 affects the oxidation state and solubility of Cr(III) and Cr(VI), common co-contaminants with organic chemicals, is explored here in four chemically diverse soils containing elevated levels of Cr. Soil contaminated with soluble Cr(VI) from chromite ore processing residue and soil containing high levels of recently reduced Cr (III) from electroplating waste both released dissolved Cr(VI) after single applications of up to 24 mM H2O2. In no case was there evidence that H202 reduced preexisting Cr(VI) to Cr(III), even though this would be allowed thermodynamically. Chromate in the leachates exceeded the U.S. EPA drinking water standard for total dissolved Cr (2 microM) by a factor of 10-1000. Anaerobic conditions in an organic-rich, tannery waste-contaminated soil protected Cr(III) from oxidation and mobilization. Mineral forms of Cr in serpentinitic soil near a former chromite mine also resisted oxidation on the time scale of days. Mobilization of Cr(VI) could be a hazardous consequence of using H2O2 for in situ remediation of chemically complex wastes, but H2O2 could prove attractive for ex situ treatment (i.e., soil washing). This paper demonstrates marked differences among Cr-contaminated soils in their capacity to release Cr(VI) upon chemical treatment with H2O2.

Carcinogens, Environmental↗