Nickel measurement

Measurements of the amount of nickel in your blood, feces, and urine can be used to estimate your exposure to nickel. More nickel was found in the urine of workers who were exposed to nickel compounds that dissolve easily in water (soluble) than in the urine of workers exposed to compounds that are hard to dissolve (less-soluble). This means that it is easier to tell if you have been exposed to soluble compounds than less-soluble compounds. The nickel measurements do not accurately predict potential health effects from exposure to nickel. More information on medical tests can be found in Chapters 2 and 6. 

This value is the lowest reliable detectable concentration of nickel measurable by the methods recommended by NIOSH (1977). 

The molybdenum dispersion also depends on the phosphorus content of the catalyst. Atanasova et al. (68, 87) reported that the dispersion of molybdenum and nickel, measured by X-ray photoelectron spectroscopy (XPS), shows a steep increase due to the presence of phosphorus at low loadings. The dispersion of molybdenum in NiMoP/Al catalysts increases further as a result of calcination, whereas that of nickel decreases. In contrast, Sajkowski et al. (83) reported, on the basis of an extended X-ray absorption fine structure (EXAFS) investigation, that phosphorus does not affect the size of the polymolybdate species, Mangnus et al. (31) inferred that the stacking of molybdates does not increase as a result of the addition of phosphorus since the height of a temperature-programmed reduction (TPR) peak at 400°C due to the reduction of deposited multilayered molybdenum oxo-species was found to be independent of the phosphorus content. However, Chadwick el al. (60) concluded from XPS measurements that the dispersion of molybdenum decreases upon addition of phosphorus. 

After calcination (air at 300 °C for 2 h) and reduction (H2 at 400 °C for 2 h) the carbon nanotubes decorated with nickel metal were obtained. The concentration of nickel measured by ICP-MS was 20 wt.%. The TEM micrograph of the sample reduced under flowing hydrogen at 400°C unambiguously proved that the nickel phase was exclusively located on the outer walls of the carbon nanotubes with a particle mean diameter of about 40-50 nm [12]. It should be noted that despite the low reactivity of the exposed basal planes of the carbon nanotubes the nickel particles were well dispersed without formation of aggregates. 

A piece of nickel measuring 6" x 4" is immersed in deaerated water having a pH of 8.0. The solubility product Ni(OH)2 is 1.6 X 10" . Determine the potential of nickel in the given conditions and state whether nickel would corrode or not. 

This paper deals with the control of weld depth penetration for cylinders in gold-nickel alloy and tantalum. After introducing the experimental set-up and the samples description, the study and the optimization of the testing are presented for single-sided measurements either in a pulse-echo configuration or when the pump and the probe laser beams are shifted (influence of a thermal phenomenon), and for different kind of laser impact (a line or a circular spot). First, the ultrasonic system is used to detect and to size a flat bottom hole in an aluminium plate. Indeed, when the width of the hole is reduced, its shape is nearly similar to the one of a slot. Then, the optimization is accomplished for... 

Marcus P, Teissier A and Oudar J 1984 The influence of sulfur on the dissolution and the passivation of a nickel-iron alloy. 1. Electrochemical and radiotracer measurements Corrosion Sc . 24 259... 

In the practical applications of Raney nickel it is more convenient to measure the catalyst than to weigh it. The product, prepared as above, contains about 0-6 g. of the catalyst per millilitre of settled material a level teaspoonful is about 3 g. of nickel. 

Analysis of Trace or Minor Components. Minor or trace components may have a significant impact on quaHty of fats and oils (94). Metals, for example, can cataly2e the oxidative degradation of unsaturated oils which results in off-flavors, odors, and polymeri2ation. A large number of techniques such as wet chemical analysis, atomic absorption, atomic emission, and polarography are available for analysis of metals. Heavy metals, iron, copper, nickel, and chromium are elements that have received the most attention. Phosphoms may also be detectable and is a measure of phosphoHpids and phosphoms-containing acids or salts. 

Standard commercial iastmmentation and control devices are used ia fluorine systems. Pressure is measured usiag Bourdon-type gauges or pressure transducers. Stainless steel or Monel constmction is recommended for parts ia contact with fluoriae. Standard thermocouples are used for all fluorine temperature-measuriag equipment, such as the stainless-steel shielded type, iaserted through a threaded compression fitting welded iato the line. For high temperature service, nickel-shielded thermocouples should be used. 

Fig. 7. Comparison of relaxation strengths at 1000 h as measured by residual stress of various steels and nickel alloys (34). To convert MPa to psi, multiply...

Nickel Carbonyl The extremely toxic gas nickel carbonyl can be detected at 0.01 ppb by measuring its chemiluminescent reaction with ozone in the presence of carbon monoxide. The reaction produces excited nickel(II) oxide by a chain process which generates many photons from each pollutant molecule to permit high sensitivity (315). 

Another anomalous property of some nickel—iron aHoys, which are caHed constant-modulus aHoys, is a positive thermoelastic coefficient which occurs in aHoys having 27—43 wt % nickel. The elastic moduH in these aHoys increase with temperature. UsuaHy, and with additions of chromium, molybdenum, titanium, or aluminum, the constant-modulus aHoys are used in precision weighing machines, measuring devices, and osciHating mechanisms (see Weighing AND proportioning). 

Tetrakisligand nickel(0) complexes have tetrahedral stmctures. Electronic stmctures have been studied and conformational analysis performed. Quantitative equiUbria measurements of the ligands in these complexes imply a dominant role for ligand steric effects when the complexes are employed as catalysts (94). 

Nickel carbonyl should be used in totally enclosed systems or under good local exhaust. Plants and laboratories where nickel carbonyl is used should make use of air-monitoring devices, alarms should be present in case of accidental leakage, and appropriate personal respiratory protective devices should be readily available for emergency uses. Monitoring of urinary nickel levels is useful to help determine the severity of exposure and identify appropriate treatment measures. Some large-scale users of nickel carbonyl maintain a supply of sodium diethyldithiocarbamate, or Antabuse, a therapeutic agent, on hand for use in case of overexposure. 

Receptor models are powerful tools for source apportionment of particulates because a vast amount of particulate species characterization data have been collected at many sampling sites worldwide, and because many aerosol species are primary pollutants. Most of the information available is for elemental concentrations, eg, lead, nickel, and alurninum, although more recent measurements have provided data on concentrations of ionic species and carbonaceous compounds. At a sampling (or receptor) site, the aerosol mass concentration of each species i is... 

If the source fingerprints, for each of n sources are known and the number of sources is less than or equal to the number of measured species (n < m), an estimate for the solution to the system of equations (3) can be obtained. If m > n, then the set of equations is overdetermined, and least-squares or linear programming techniques are used to solve for L. This is the basis of the chemical mass balance (CMB) method (20,21). If each source emits a particular species unique to it, then a very simple tracer technique can be used (5). Examples of commonly used tracers are lead and bromine from mobile sources, nickel from fuel oil, and sodium from sea salt. The condition that each source have a unique tracer species is not often met in practice. 

The methods of choice for beryUium oxide in beryUium metal are inert gas fusion and fast neutron activation. In the inert gas fusion technique, the sample is fused with nickel metal in a graphite cmcible under a stream of helium or argon. BeryUium oxide is reduced, and the evolved carbon monoxide is measured by infrared absorption spectrometry. BeryUium nitride decomposes under the same fusion conditions and may be determined by measurement of the evolved nitrogen. Oxygen may also be determined by activation with 14 MeV neutrons (20). The only significant interferents in the neutron activation technique are fluorine and boron, which are seldom encountered in beryUium metal samples. 

In the presence of 6-iodo-l-phenyl-l-hexyne, the current increases in the cathodic (negative potential going) direction because the hexyne catalyticaHy regenerates the nickel(II) complex. The absence of the nickel(I) complex precludes an anodic wave upon reversal of the sweep direction there is nothing to reduce. If the catalytic process were slow enough it would be possible to recover the anodic wave by increasing the sweep rate to a value so fast that the reduced species (the nickel(I) complex) would be reoxidized before it could react with the hexyne. A quantitative treatment of the data, collected at several sweep rates, could then be used to calculate the rate constant for the catalytic reaction at the electrode surface. Such rate constants may be substantially different from those measured in the bulk of the solution. The chemical and electrochemical reactions involved are... 

Plate Thickness. Thickness of the plate should always be specified as should the locations on the work where the thickness is to be measured. Generally, thicker deposits perform better, but there are notable exceptions. Mating parts, eg, fasteners having fine machine threads, are not usable if over plated. Machine-threads are usually plated to 10 p.m or less, depending on tolerances. Additionally, gold-plate over nickel does not solder well if too thick thus, gold is usually 1—2 pm or less. Chromium, plated for decorative purposes from the conventional chromic acid bath, tends to macrocrack above about 0.7—1.0 pm. 

K. Parker, Internal Stress Measurements of Electroless Nickel Coatings by the Rigid Strip Method, ASTM STP 947, American Society for Testing and Materials, Philadelphia, Pa., 1987. 

---