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The effect of heavy metals on dinitrogen fixation by Rhizobium-white clover in a range of long-term sewage sludge amended and metal-contaminated soils.

An investigation was conducted to determine whether effective strains of Rhizobium leguminosarum biovar. trifolii capable of symbiotic N2 fixation with white clover (Trifolium repens) were present in a range of metal-contaminated soils. A number of historically sewage-amended sites (including experimental, pasture grassland and arable sites) were selected and compared with highly contaminated samples from abandoned heavy metal mines. Many sites had metal concentrations above the limits established by the UK Government, based on those developed by the European Commission (EC) for sludge-amended soils. Acetylene reduction activity (ARA) was used to screen the samples for effective N2 fixation. When the host plant was indigenous to the sward, rhizobia were found in the nodules and in the soil rhizosphere at all the sites tested. They were shown to be capable of effective symbiosis and N2 fixation, even though metal concentrations greatly exceeded the soil metal limits in some cases. However, nodulation failed to occur in some cases where T. repens was not indigenous to metal-contaminated soils. This indicated either that an ineffective rhizobial population was present, or that effective cells were absent from the soil. The influence of individual metals on ARA could not be determined conclusively because of the confounding effects of soil physicochemical variability and the presence of different metals at high concentrations together in the soil. However, Cd concentrations appeared to be particularly important in determining the presence of effective ARA in soils with no indigenous clover. In contrast to previous studies, the results presented here suggest that heavy metals may have had a quantitative effect on the free-living population of rhizobia, rather than a genetic effect.

Journal Article↗

Massive wear of an incompatible metal-on-metal articulation in total hip arthroplasty.

We report on a case of massive wear because of an incompatible metal-on-metal combination. In a 62-year-old man, a cobalt-chromium (CoCr) inlay and a stainless steel head were paired by accident. Because of persistent pain, revision surgery was performed 7 months later. Histologic analysis of the surrounding tissue revealed massive metallosis. The wear volume was increased by a factor of 18 for the head and 2 for the cup compared with normal metal-on-metal articulation. The serum concentrations of chromium and cobalt were increased by a factor of 20 and 4 over levels of a healthy population, respectively. Incompatible metal-on-metal combinations should be revised immediately. In case of delayed diagnosis, no metal-on-metal articulation should be implanted because of the high volume of metal in the human body.

Aged↗

Isothermal titration calorimetric procedure to determine protein-metal ion binding parameters in the presence of excess metal ion or chelator.

Determination of binding parameters for metal ion binding to proteins usually requires preceding steps to remove protein-bound metal ions. Removal of bound metal ions from protein is often associated with decreased stability and inactivation. We present two simple isothermal titration calorimetric procedures that eliminate separate metal ion removal steps and directly monitor the exchange of metal ions between buffer, protein, and chelator. The concept is to add either excess chelator or metal ion to the protein under investigation and subsequently titrate with metal ion or chelator, respectively. It is thereby possible in the same experimental trial to obtain both chelator-metal ion and protein-metal ion binding parameters due to the different thermodynamic "fingerprints" of chelator and protein. The binding models and regression routines necessary to analyze the corresponding binding isotherms have been constructed. Verifications of the models have been done by titrations of mixtures of calcium chelators (BAPTA, HEDTA, and EGTA) and calcium ions and they were both able to account satisfactorily for the observed binding isotherms. Therefore, it was possible to determine stoichiometric and thermodynamic binding parameters. In addition, the concept has been tested on a recombinant alpha-amylase from Bacillus halmapalus where it proved to be a consistent procedure to obtain calcium binding parameters.

Bacillus↗

Four-year study of cobalt and chromium blood levels in patients managed with two different metal-on-metal total hip replacements.

BACKGROUND: Metal-on-metal total hip prostheses will produce a certain amount of wear debris. This results in increased whole-blood metal levels, which may cause adverse effects. It is not known to what extent the problem has been overcome by advances in alloy technology. METHODS: In 259 patients who with total hip replacement, blood cobalt and chromium concentrations were measured with atomic absorption spectrophotometry over a period of four years after arthroplasty. Of the patients enrolled in the study, 131 had been managed with a METASUL cobalt-chromium alloy metal-on-metal bearing combination, while 128 had been given a SIKOMET-SM21 cobalt-chromium alloy metal-on-metal combination. The control group consisted of 31 age- and gender-matched subjects. RESULTS: Compared with the controls, all the patients had higher cobalt and chromium levels. Cobalt concentrations were up to 50 times higher, while chromium concentrations were up to 100 times higher. CONCLUSIONS: Both systems showed evidence, in the whole-blood samples, of wear debris production by the implants. Therefore, patients managed with metal-on-metal bearing combinations should be carefully monitored in order to ensure that any local or systemic complications are detected early on.

Arthroplasty, Replacement, Hip↗

Progressive bilateral pelvic osteolysis in a patient with McKee-Farrar metal-metal total hip prostheses.

As accumulating evidence indicates that polyethylene plays a central role in periprosthetic osteolysis, there is a renewed interest in alternatives such as metal-metal bearings. Several long-term studies report encouraging results with the McKee-Farrar total hip arthroplasty, but there is a paucity of data on the incidence, severity, and pathogenesis of osteolysis in metal-metal bearing total hip arthroplasties. This study presents a patient who had progressive bilateral pelvic osteolysis associated with his McKee-Farrar metal-metal total hip prostheses. His left hip was revised after 13.5 years of service. The tissues revealed no gross metal staining and fewer inflammatory constituents than are typically found in metal-polyethylene bearing hips. His right hip was still functioning after 22.5 years of service, although the acetabular component was loose by that point. An arthrogram of this hip demonstrated communication of the joint with the iliac osteolysis. The development of osteolysis in both hips followed a pattern similar to that seen in metal-polyethylene total hip arthroplasties. Bearing wear could not be detected in either of the hips. Accumulating evidence indicates that particulate debris of appropriate size and number is capable of fueling periprosthetic inflammation. Specific to this study, consideration should be given to particles of cobalt-chromium alloy, polymethyl methacrylate bone-cement, and barium sulfate. Other factors that should be considered are increased joint fluid pressure, soluble inflammatory mediators, and the effective joint space. When bone becomes part of the effective joint space, it is exposed to particulate debris, soluble factors, and potentially increased joint fluid pressures, which may promote localized bone resorption. It must be kept in mind that the development of osteolysis is multifactorial. Although bearings with better wear characteristics are desirable, the elimination of polyethylene will not eliminate osteolysis.

Arthroplasty, Replacement, Hip↗

Comparison of metallothionein concentrations and tissue distribution of trace metals in crabs (Pachygrapsus marmoratus) from a metal-rich estuary, in and out of the reproductive season.

Crabs, Pachygrapsus marmoratus, were sampled in June 1997 and February 1998 from two sites (at the mouth and 25 km upstream) in the metal-rich Gironde estuary, France. Gills and hepatopancreas were analysed for metal (Cd, Cu, Zn) and metallothionein (MT) contents, in order to examine the influence of both biological and environmental factors on the physico-chemical forms of detoxified metal storage in the crabs. The concentrations of MT and both cytosolic and insoluble metals were not greatly different between males and females, and the influence of organ weights was also minimal. Intersite differences were observed, probably resulting from the gradient of salinity in the estuary, which interacts with both the chemical speciation and bioavailability of metals, and the general protein metabolism of the crabs. Seasonal changes were also important, probably in interaction with the moult and reproductive cycles. In February, concentrations of insoluble metals were generally higher than in June, in both organs, suggesting that essential metals, particularly Zn, are stored during winter then remobilised during the breeding season. The natural variability in the concentrations of MT often concealed any relationship with accumulated metal concentrations. Thus MT in crabs cannot be considered as a useful biomarker of metal pollution.

Animals↗

Spectroscopic and structural study of metal-metal bonded metalloporphyrinic derivatives: the case of rhodium-indium.

The synthesis and spectroscopic characterization of heterometallic porphyrinate derivatives containing rhodium-indium metal-metal bonds are reported. The investigated compounds are represented by the formula [(Porph)RhIn(Porph')], where Porph and Porph' are OEP, TPP, beta-Cl(4)TPP, beta-Cl(8)TPP, or TPyP. UV-Visible spectroscopy of the title complexes confirms the presence of a strong pi-pi interaction between the macrocycles in each derivative and denotes the effect of the nontransition metal in their optical features. For comparison purposes, a new bimetallic complex with a rhodium-thallium metal-metal bond is also presented. According to (1)H and (13)C NMR data, we were able to distinguish two major NMR regions: the endo- between the metal-metal bonded macrocycles and the exo-, which are characteristic features of porphyrinic complexes at very close proximity. X-ray absorption spectroscopy (XAS) structural characterization of Rh-In bond was performed on the [(OEP)RhIn(OEP)] complex, in the fluorescence mode, and we essentially focused on the metal-metal distance determination. Finally, the distance of 2.543(3) A was deduced from the X-ray structure of a new [(TPP)RhIn(TPyP)] derivative.

Journal Article↗

Enhancement of metal-metal coupling at a considerable distance by using 4-pyridinealdazine as a bridging ligand in polynuclear complexes of rhenium and ruthenium.

Novel polynuclear complexes of rhenium and ruthenium containing PCA (PCA = 4-pyridinecarboxaldehyde azine or 4-pyridinealdazine or 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene) as a bridging ligand have been synthesized as PF(6-) salts and characterized by spectroscopic, electrochemical, and photophysical techniques. The precursor mononuclear complex, of formula [Re(Me(2)bpy)(CO)(3)(PCA)](+) (Me(2)bpy = 4,4'-dimethyl-2,2'-bipyridine), does not emit at room temperature in CH(3)CN, and the transient spectrum found by flash photolysis at lambda(exc) = 355 nm can be assigned to a MLCT (metal-to-ligand charge transfer) excited state [(Me(2)bpy)(CO)(3)Re(II)(PCA(-))](+), with lambda(max) = 460 nm and tau < 10 ns. The spectral properties of the related complexes [[Re(Me(2)bpy)(CO)(3)}(2)(PCA)](2+), [Re(CO)(3)(PCA)(2)Cl], and [Re(CO)(3)Cl](3)(PCA)(4) confirm the existence of this low-energy MLCT state. The dinuclear complex, of formula [(Me(2)bpy)(CO)(3)Re(I)(PCA)Ru(II)(NH(3))(5)](3+), presents an intense absorption in the visible spectrum that can be assigned to a MLCT d(pi)(Ru) --> pi(PCA); in CH(3)CN, the value of lambda (max) = 560 nm is intermediate between those determined for [Ru(NH(3))(5)(PCA)](2+) (lambda(max) = 536 nm) and [(NH(3))(5)Ru(PCA)Ru(NH(3))(5)](4+) (lambda(max) = 574 nm), indicating a significant decrease in the energy of the pi-orbital of PCA. The mixed-valent species, of formula [(Me(2)bpy)(CO)(3)Re(I)(PCA)Ru(III)(NH(3))(5)](4+), was obtained in CH(3)CN solution, by bromine oxidation or by controlled-potential electrolysis at 0.8 V in a OTTLE cell of the [Re(I),Ru(II)] precursor; the band at lambda(max) = 560 nm disappears completely, and a new band appears at lambda(max) = 483 nm, assignable to a MMCT band (metal-to-metal charge transfer) Re(I) --> Ru(III). By using the Marcus-Hush formalism, both the electronic coupling (H(AB)) and the reorganization energy (lambda) for the metal-to-metal intramolecular electron transfer have been calculated. Despite the considerable distance between both metal centers (approximately 15.0 Angstroms), there is a moderate coupling that, together with the comproportionation constant of the mixed-valent species [(NH(3))(5)Ru(PCA)Ru(NH(3))(5)](5+) (K(c) approximately 10(2), in CH(3)CN), puts into evidence an unusual enhancement of the metal-metal coupling in the bridged PCA complexes. This effect can be accounted for by the large extent of "metal-ligand interface", as shown by DFT calculations on free PCA. Moreover, lambda is lower than the driving force -DeltaG degrees for the recombination charge reaction [Re(II),Ru(II)] --> [Re(I),Ru(III)] that follows light excitation of the mixed-valent species. It is then predicted that this reverse reaction falls in the Marcus inverted region, making the heterodinuclear [Re(I),Ru(III)] complex a promising model for controlling the efficiency of charge-separation processes.

Journal Article↗

Direct electrical measurement of the conversion of metal acetates to metal sulfides by hydrogen sulfide.

Copper acetate and related metal salt films react directly with hydrogen sulfide at room temperature to form metal sulfides, resulting in conductivity changes as large as 108. The observed changes in conductivity are related to the solubility product constant (Ksp) and the difference in conductivity between the metal salt and the resulting metal sulfide. A smaller Ksp indicates a more stable metal sulfide and, therefore, greater metal salt reactivity. Polyaniline nanofiber/metal salt composites were also examined and show metal sulfide conversion with changes in resistance up to 106. The direct electrical measurement of the conversion of metal salt to metal sulfide has the potential to be the basis of a new type of sensitive, thin-film chemical sensor.

Journal Article↗

Photodissociation of metal-silicon clusters: encapsulated versus surface-bound metal.

Metal-silicon cluster cations of the form MSi(n)+ (M = Cu, Ag, Cr) are produced in a molecular beam with pulsed laser vaporization. These species are mass-selected in a reflectron time-of-flight spectrometer and studied with laser photodissociation at 532 and 355 nm. For the noble metals copper and silver, photodissociation of the n = 7 and 10 clusters proceeds primarily by the loss of metal atoms, indicating that the metal is not located within the interior of silicon cages, and that metal-silicon bonding is weaker than silicon-silicon bonding. Chromium-silicon clusters for n = 7 also lose primarily the metal atom, but at n = 15 and 16 these dissociate via the loss of silicon, producing smaller metal-silicon species. This behavior is consistent with stronger metal-silicon bonding and encapsulated metal structures, as suggested previously by theory. MSi6(+) cations are produced efficiently in all of these photodissociation processes, indicating that these species have enhanced stability compared to other small clusters. Improved values are obtained for the ionization potentials of Si7 and Si10.

Letter↗

Metal-metal bonding in molecular actinide compounds: electronic structure of [M2X8](2-) (M = U, Np, Pu; X = Cl, Br, I) complexes and comparison with d-block analogues.

Density functional and multiconfigurational (ab initio) calculations have been performed on [M(2)X(8)](2-) (X = Cl, Br, I) complexes of 4d (Mo, Tc, Ru), 5d (W, Re, Os), and 5f (U, Np, Pu) metals in order to investigate general trends, similarities and differences in the electronic structure and metal-metal bonding between f-block and d-block elements. Multiple metal-metal bonds consisting of a combination of sigma and pi interactions have been found in all species investigated, with delta-like interactions also occurring in the complexes of Tc, Re, Np, Ru, Os, and Pu. The molecular orbital analysis indicates that these metal-metal interactions possess predominantly d(z2) (sigma), d(xz) and d(yz) (pi), or d(xy) and d(x2-y2) (delta) character in the d-block species, and f(z3) (sigma), f(z2x) and f(z2y) (pi), or f(xyz) and f(z) (delta) character in the actinide systems. In the latter, all three (sigma, pi, delta) types of interaction exhibit bonding character, irrespective of whether the molecular symmetry is D(4h) or D(4d). By contrast, although the nature and properties of the sigma and pi bonds are largely similar for the D(4h) and D(4d) forms of the d-block complexes, the two most relevant metal-metal delta-like orbitals occur as a bonding and antibonding combination in D(4h) symmetry but as a nonbonding level in D(4d) symmetry. Multiconfigurational calculations have been performed on a subset of the actinide complexes, and show that a single electronic configuration plays a dominant role and corresponds to the lowest-energy configuration obtained using density functional theory.

Journal Article↗

Exposure to chromium, cobalt and molybdenum from metal-on-metal total hip replacement and hip resurfacing arthroplasty.

BACKGROUND: All metal implants--and metal-on-metal bearings in particular--corrode and cause a release of metal ions. Because cobalt and chromium have been shown to be carcinogenic and mutagenic in human and animal models, systemic toxicity and cancer risk are considered to be possible disadvantages of the metal-on-metal articulation. This study was designed to investigate the serum concentration profiles of chromium, cobalt and molybdenum after implantation of a Birmingham hip resurfacing arthroplasty (BHR) and a cementless total hip replacement with a 28-mm Metasul articulation (MTHR), over the first 2 years after implantation. METHODS: We analyzed profiles of metal ion serum levels in 111 patients implanted with a BHR, in 74 patients implanted with an MTHR, and in 130 implant-free probands control subjects using atomic absorption spectrophotometry. RESULTS: Chromium and cobalt concentrations (in microg/L) of all BHR and MTHR patients differed significantly from those of control subjects (chromium: < 0.25; cobalt: 0.25). The median chromium and cobalt concentrations in BHR patients had increased to 5.1 and 4.3 microg/L 2 years after surgery. Concentrations in BHR patient exceeded those in the unilateral MTHR patients. Molybdenum serum concentrations hardly changed over time in either group and were not significantly different from the concentrations seen in the control subjects. INTERPRETATION: During the first 2 years after surgery, the Birmingham hip resurfacing arthroplasty leads to a significantly greater increase in serum chromium and cobalt levels than the 28-mm metal-on-metal MTHR. Observation of patients over a longer period will be necessary in order to evaluate any chronic adverse effects to the system due to elevated chromium and cobalt serum concentrations.

Aged↗

Medium-term results of a modern metal-on-metal system in total hip replacement.

Since 1988, metal-on-metal articulation from cobalt-chromium-molybdenum alloy was reintroduced into hip arthroplasty as an alternative to metal-on-polyethylene or ceramic-on-polyethylene components. Modular joint surfaces were developed for the second generation metal-on-metal articulation using newly introduced and proven prosthetic implants. Since 1990, 78 patients with 78 uncemented total hip replacements were followed up in a prospective study. The mean followup was 60 months. Three patients were lost to followup. The average age of the patients at the time of surgery was 48.8 years. Thirty-three patients had been operated on previously. No early infections occurred; one late infection occurred after 3 years. Dislocation of the prosthesis occurred in one patient who was lost to followup. In two patients ectopic ossifications were removed 17 and 27 months postoperatively. At revision surgery no metallosis could be identified. At the last followup examination, the Harris hip score was 96.8 points on average. There was no evidence that the metal-on-metal articulation gave rise to new problems or complications. Metal-on-metal articulation reduced wear considerably in the authors' previous experience. It is hoped that foreign body reactions are reduced significantly so that an alternative for total hip replacement in younger and active patients will be available.

Adolescent↗

Comparative strength of metal-ceramic and metal-composite bonds after extended thermocycling.

The relative strengths of ceramic-to-metal and composite-to-metal bonds were compared after prolonged thermocycling. A total of 104 cast discs were produced from a gold alloy (Pontor LFC). A ceramic material (Duceragold) was fused to 24 discs to assess the strength of the metal-ceramic bond. An indirect composite material (New Metacolor Infis) was bonded to the remaining discs after surface preparation by Rocatec tribochemical coating, tin plating and priming with a phosphate conditioner [10-methacryloyloxydecyl dihydrogen phosphate (MDP), Cesead II], priming with a thione conditioner (V-Primer) or no treatment (unprimed control). Shear bond strengths were determined before and after thermocycling at 20,000 and 100,000 cycles. Pre-thermocycling bond strengths were ranked in the order: metal-ceramic (40.5 MPa); Rocatec treatment (33.1 MPa) and tin plating-MDP (31.0 MPa); V-Primer (20.9 MPa); and control (11.9 MPa). The bond strengths of the first three groups were not significantly different after 20,000 thermocycles, whereas those of the V-Primer and control groups were significantly reduced. After extended thermocycling (100,000 cycles) the metal-ceramic group had the highest mean shear bond strength (28.5 MPa; P < 0.05), followed by the Rocatec (23.9 MPa) and tin plating-MDP (22.1 MPa) groups. The metal-ceramic bond was the most durable, although its strength was reduced by 29.6% after extended thermocycling. On the basis of these results, we recommend the Rocatec and tin plating-MDP systems for composite-to-metal bonding. Metal-ceramic bonding, however, is superior to metal-composite bonding within the limitation of the current experiment.

Analysis of Variance↗

Toxicity of metal mixtures to a tropical freshwater alga (Chlorella sp): the effect of interactions between copper, cadmium, and zinc on metal cell binding and uptake.

The individual and combined effects of copper, cadmium, and zinc on the cell division rate of the tropical freshwater alga Chlorella sp. were determined over 48 to 72 h. Metal mixtures were prepared based on multiples of their single-metal median effective concentration (EC50) values, i.e., toxic units (TU) using a triangular mixture design with five toxicant levels (0, 0.75, 1.0, 1.25, and 1.5 TU). Single-metal EC50 values after a 72-h exposure were 0.11, 0.85, and 1.4 microM for copper, cadmium, and zinc, respectively. Significant interactions were observed for all metal combinations after 48 and 72 h. An equitoxic mixture of Cu + Cd was more than concentration additive (synergistic) to the growth of Chlorella sp., while combinations of Cu + Zn, Cd + Zn, and Cu + Cd + Zn were all less than concentration additive or were antagonistic. To determine the effect of each metal on the uptake of the other, extracellular (membrane-bound) and intracellular metal concentrations, both alone and in mixtures, were compared. The increased growth inhibition observed for mixtures of Cu + Cd was due to higher concentrations of cell-bound and intracellular copper in the presence of cadmium compared with copper alone (i.e., cadmium-enhanced copper uptake). In contrast, both extra- and intracellular cadmium concentrations were reduced in the presence of copper. In mixtures of Cu + Zn, copper also inhibited the binding and cellular uptake of zinc, which resulted in decreased toxicity. Zinc had no appreciable effect on the uptake of copper by Chlorella sp. Our results suggest that all three metals share some common uptake and transport sites on Chlorella cells and that copper out competes both cadmium and zinc for cell binding. Determination of metal cell distribution coefficients (K(d)) confirmed that K(d) values for cadmium and zinc in single-metal exposures decreased in the presence of copper.

Cadmium↗

Role of metal ions in Escherichia coli alkaline phosphatase. A study of the metal-water interaction by nuclear relaxation rate measurements on water protons.

The binding of metal to alkaline phosphatase from Escherichia coli and the binding of water and orthophosphate to the Me-2+-enzyme binary complex have been examined by water proton relaxation rate (PRR) measurements. Titration of the three paramagnetic metals, Mn2+, Cu2+, and Co2+, into apoalkaline phosphatase and the titrations of apoenzyme into metal have been carried out. Analysis of the spin-lattice relaxation rates for these titrations and of Scatchard binding curves derived from these results, as well as EPR data, show four tight manganese sites, between two and three tight copper sites, or four cobalt sites per enzyme dimer of molecular weight 80,000. The multiple sites for each metal are indistinguishable by these magnetic resonance techniques. Both the spin-lattice- and spin-spin-relaxation rates exhibit a negative temperature coefficient, showing that these processes are not exchange-limited. From a frequency dependence study of T-1 and from the T-1:T-2 ratio measured at 220 MHz, correlation times from the water-enzyme complexes have been estimated. For H20-Mn-2+-alkaline phosphatase, gamma c equals 1.55 times 10-9 s; for H20-Cu-2+ -alkaline phosphatase, gamma c equals 1.82 times 10-s; and for the cobalt complex, gamma c equals 1.0 times 10-12 s at 4 degrees. Assuming 1 water molecule bound per metal site, these correlation times correspond to the following water-metal distances: gamma (A) is 4.0 A for Mn-2+-H20, 3.4 A for Cu-2+-H20, and 2.8 A for Co-2+-H20. Thus, water is shown to bind directly to the metal atoms of alkaline phosphatase. The correlation between the length of the water-metal bond and the relative activity of the various metalloenzymes support the importance of this binding in the monophosphoesterase reaction catalyzed by alkaline phosphatase. Addition of excess orthophosphate to any of the water-metalloenzyme complexes does not displace an exchangeable water molecule from the metal site. The Mn-PO-4 distance which we have reported earlier (Zukin, R.S., Hollis, D.P., and Gray, G.A. (1973) Biochem. Biophys. Res. Commun. 53, 238) to be 7.3 A is consistent with this finding and suggests a model in which Pi binds to Mn-2+-alkaline phosphatase through a water bridge.

Alkaline Phosphatase↗

[Application of electroforming for coronal restorations. Metal frame for porcelain fused to metal crowns].

Today, it has been quite important to realize that the esthetic factor the coronal restration is more emphasized in dental practice. It is popular to use porcelain as a dental material for the Coronal restoration and the technique is pretty much stabilized. Because of the color itself and its great affinity to the human body. Mostly used technique is the porcelain fused-to metal crown. However, there are various disadvantages relating to this technique. On the other hand. The electroforming technique has some great characteristics that is producing the complex shape with less difficulty, and the improvement of it's final surface. It also has the ability for reduplication. Overall, metal frame can be constracted on the same working model without a duplication of it. Therefore, it is possible to make the procedure extremely simple. Here, the author has done some experiments with the newly developed electroforming apparatus for constructing the Coronal restoration. The purpose of the experiments are to apply all these great advantages of the system to dental prosthodontics field. One characteristic of the equipment is the diffusion of current distribution by the cathode rotary system. The other one is the circulation of electrolyte for reducing the diffusion layer. Firstly, the author operated the electroposition with Ni on the three different standard models of abutment teeth, in order to determine the possibility of making a metal frame and the relationship between the shape of the abutment teeth and the current. Next experiment was to investigate if it's possible to apply the metal frame, constructed by the apparatus, to porcelain fused-to metal crown by again determining the relationship between the electropositioned metal and the porcelain. The results were obtained as follows. 1. It was possible to construct a metal frame for the porcelain fused-to metal crown by the method. 2. The minimum electroposition time was approximately 35-40 min. with a high current density. 3. The thickness of the metal frame did not effect the current, however it barely effected the shape of the abutment teeth. 4. The tensile strength by shear was approximately 150 kg/cm2. 5. There was no evident that the current has any effects on tensile strength.

Crowns↗

[The shear bond strength of porcelain and base metal alloys for metal-ceramic crown (VI)].

The popularity of base metal alloy for porcelain fused to a metal crown and bridges has increased recently because of lower price, superior yield strength and modulus of elasticity (rigidity). The use of these alloys give them the potential advantage of thinner coping with less material and the required rigidity for long-span fixed partial dentures. The addition of beryllium to base metal alloys increases fluidity and improves casting fit. Beryllium also controls surface oxidation and bonding strength. Oxidation heat treatment of the metal is used to remove entrapped air, eliminate organic material and form the metal oxidized layer. The bonding agent and gold bonding agent also affect the bonding strength between porcelain and metal alloys. Four commercially available ceramic base alloys (two alloys contain beryllium element, another two do not) are studied. The purposes of this investigation are to test the shear bond strength between porcelain and metal alloy under different conditions (oxidized layer removed or not, gold bonding agent and uniseal bonding agent used in combination, separately or not at all). The following results were obtained: 1. Whether the oxidized layer was removed or not did not have a significant effect on the bond strength of porcelain (p > 0.05). 2. When different metal alloys was used, Wiron 88 alloy showed significantly the best bond strength of all alloys tested (p < 0.05). 3. When different bonding agent were used, the combination of bonding agent and gold bonding agent showed the best bond strength of all bonding agents tested. It showed a significantly higher bonding strength than opaque layer and gold bonding agent. 4. Vita porcelain powder showed a significantly higher bond strength than did Unibond porcelain (p < 0.05). 5. When opaque layer was used and when no bonding agent was used, the porcelain powder significantly affected the bond strength (p < 0.0001). The Vita porcelain showed a significantly higher bond strength than did Unibond porcelain. Wiron 88 alloy showed significantly the high bond strength than Rexillium III alloy (p < 0.05). 6. When bonding agent was used, the porcelain powder and alloy significantly affected bond strength. The Vita porcelian showed a significantly higher bond strength than did Unibond porcelain. Wiron 88 alloy showed significantly the best bond strength than other alloys Wiron (p < 0.05). 7. When bonding agent and gold bonding agent were used, the porcelain powder significantly affected the bond strength (p < 0.05). The Vita porcelain showed a significantly higher bond strength than did Unibond porcelain (p < 0.05). 8. When gold bonding agent was used, there was not any bond strength between metal and powder.

Crowns↗