Platinum plating

Electrolysis cell. This is shown in Fig. VI, 31, 1 and is almost self-explanatory. The cylindrical cell of Pyrex glass (6" long by 2 " diameter) is cooled by immersion in a cooling bath. The electrodes consist of two platinum plates (4 cm. X 2-5 cm. X 0-3 mm.), which are placed about 2 mm. apart. The temperature of the electrolyte is maintained at 30-35° by means of the internal cooling coil and also by immersion of the cell in ice-water. A current of 1 5-2 0 amperes is passed until the electrolyte becomes slightly alkaline, which normally takes about 20-50 per cent, longer than the calculated time on the basis of the current and the amounts of acid employed. It is advantageous to reverse the direction of the current occasionally. 

Pla.tinum, Platinum plating has found appHcation in the production of platinised titanium, niobium, or tantalum anodes which are used as insoluble anodes in many other plating solutions (see Metalanodes). Plating solutions were often based on platinum "P" salt, which is diamminedinitroplatiniim (IT). A dinitroplatinite sulfate—sulfuric acid bath has been used to plate direcdy onto titanium (129). This bath contains 5 g/L of the platinum salt, pH adjusted to 2.0 with sulfuric acid. The bath is operated at 40°C at 10—100 A/m. Other baths based on chloroplatinic acid have been used in both acid and alkaline formulations the acid bath uses 20 g/L of the platinum salt and 300 g/L hydrochloric acid at 65° C and 10—200 A/m. The alkaline bath uses 10 g/L of the platinum salt, 60 g/L of ammonium phosphate and ammonium hydroxide to give a pH of 2.5—9.0. The alkaline bath can be plated directly onto nickel-base alloys acid baths require a gold strike on most metals. 

Platin-plattierung,/. platinum plating, -reihe, /. platinum series, -rhodium, n. platinum-rh ium. -rohr, n.,-rohre,/. platinum tube, -rtickstand, m. platinum residue, -salmiak, m. ammonium chloroplatinate, -salz, n. platinum salt, -sand, m. sand for cleaning platinum, -saure, /. platinic acid, -schale. 

Characteristics of established platinum plating baths have recently been reviewed . Advantages have been claimed for new baths based on the complex tetrammineplatinum(ii) cation. ... 

If it is desired to use the biamperometric method for detecting the end point, then the calomel electrode and also the silver rod (if used) must be removed and replaced by two platinum plates 1.25 cm x 1.25 cm. The potentiometer (or pH meter) used to measure the e.m.f. must also be removed, and one of the indicator electrodes is then joined to a sensitive galvanometer fitted with a variable shunt. The indicator circuit is completed through a potential divider... 

Apparatus. Set up the apparatus as in Section 14.10 with two small platinum plates connected to apparatus for the amperometric detection of the end point. 

Place the prepared copper acetate solution in the beaker and add 10 mL of 20 per cent potassium iodide solution. Set the stirrer in motion and add distilled water, if necessary, until the platinum plate electrode is fully immersed. Use a saturated calomel reference electrode, and carry out the normal potentiometric titration procedure using a standard sodium thiosulphate solution as titrant. 

Similarly to quantitative determination of high surfactant concentrations, many alternative methods have been proposed for the quantitative determination of low surfactant concentrations. Tsuji et al. [270] developed a potentio-metric method for the microdetermination of anionic surfactants that was applied to the analysis of 5-100 ppm of sodium dodecyl sulfate and 1-10 ppm of sodium dodecyl ether (2.9 EO) sulfate. This method is based on the inhibitory effect of anionic surfactants on the enzyme system cholinesterase-butyryl-thiocholine iodide. A constant current is applied across two platinum plate electrodes immersed in a solution containing butyrylthiocholine and surfactant. Since cholinesterase produces enzymatic hydrolysis of the substrate, the decrease in the initial velocity of the hydrolysis caused by the surfactant corresponds to its concentration. Amounts up to 60 pg of alcohol sulfate can be spectrometrically determined with acridine orange by extraction of the ion pair with a mixture 3 1 (v/v) of benzene/methyl isobutyl ketone [271]. 

The apparatus used for studying the photoelectrochemical behavior (11) of the Ti02 film electrode is shown in Figure 5- Platinum plate of 35x25 mm and saturated calomel electrode (S.C.E.) were employed as a counter and a reference electrode, respectively. A 500 W Xenon lamp was used for illuminating the Ti02 electrode. 

Adsorption of sodium poly(styrenesulfonate) from aqueous NaCl solutions onto a platinum plate at 25 °C was studied by ellipsometry as functions of molecular weight and concentration of NaCl. 

For homopolyelectrolyte, we first studied the ellipsometric measurement of the adsorption of sodium poly(acrylate) onto a platinum plate as a function of added sodium bromide concentration (5). We measured the effect of electrolyte on the thickness of the adsorbed layer and the adsorbances of the polyelectrolyte. It was assumed that the Donnan equilibrium existed between the adsorbed layer and the bulk phase. The thickness was larger and the adsorbance of the polyelectrolyte was lower for the lower salt concentration. However, the data on the molecular weight dependence of both the adsorbance and the thickness of the adsorbed polyelectrolyte have been lacking compared with the studies of adsorption of nonionic polymers onto metal surfaces (6-9). 

The aim of this paper is to offer experimental results for the molecular weight dependence of adsorption of polystyrene-sulfonate) onto a platinum plate from aqueous NaCl solution at 25 °C. Measurements of poly(styrenesulfonate) adsorption were carried out by ellipsometry. The dependences of molecular weight and added salt concentration on the thickness of the adsorbed layer and also the adsorbances of polymer and salt are examined. 

The platinum plate (Ishifuku Metal Co. Japan) was cleaned by soaking in a hot concentrated aqueous HNO3-H2SO4 (1 1) mixture, washed thoroughly with distilled water, and then dried in a dust free box. 

A) trough, (B) blades, (C) platinum plate(Wilhelmy plate), (D) water circulating oudet,... 

Suda and coworkers described the anodic oxidation of 2-silyl-l,3-dithianes which have two sulfur atoms on the carbon adjacent to silicon [42], In this case, however, the C Si bond is not cleaved, but the C-S bonds are cleaved to give the corresponding acylsilanes (Scheme 12). Although the detailed mechanism has not been clarified as yet, the difference in the anode material seems to be responsible for the different pathway of the reaction. In fact, a platinum plate anode is used in this reaction, although a carbon anode is usually used for the oxidative cleavage of the C-Si bond. In the anodic oxidation of 2-silyl-l,3-dithianes the use of a carbon anode results in a significant decrease in the yield of acylsilanes. The effects of the nature of the solvent and the supporting electrolyte may also be important for the fate of the initially formed cation radical intermediate. Since various 2-alkyl-2-silyl-l,3-dithianes can be readily synthesized, this reaction provides a convenient route to acylsilanes. 

Excessive corrosion of platinum-plated titanium electrodes in the presence of fluorine-containing anolyte feed streams improvements in plating techniques are expected to solve this problem but have not yet been demonstrated. 

Pairs of platinum plate (2x5 cm) were set in a cell with 1 mm spacing as the working and the auxiliary electrode (Figure 2). Reference electrode was Ag/AgCl. The solution (50 ml) of phenol (0.005 mol) and electrolyte (0.01 mol) such as tetraethylammonium bromide and tetraethylammonium perchrolate was kept under nitrogen atmosphere in the cell. The electrolysis was carried out with constant potential or current density (10 mA/cm2) which was supplied by a potentiogalva-... 

Thus, by using very thin plates with thickness 0.1 to 0.002 mm, one can measure surface tension with very high sensitivity. In practice, by using very thin platinum plates of well-known dimension (length = 1.00 or 2.00 cm), one can calibrate the apparatus with pure liquids, such as water and ethanol. The buoyancy correction is made very small (and negligible) by using a very thin plate and dipping the plate as little as possible. 

The wetting of water on a platinum plate is achieved very satisfactorily by using commercially available plates that are roughened. This property produces almost complete wetting that is, 0 = 0. 

I. 4-methoxyacetophenone (30 //moles) was added as an internal standard. The reaction was stopped after 2 hours by partitioning the mixture between methylene chloride and saturated sodium bicarbonate solution. The aqueous layer was twice extracted with methylene chloride and the extracts combined. The products were analyzed by GC after acetylation with excess 1 1 acetic anhydride/pyridine for 24 hours at room temperature. The oxidations of anisyl alcohol, in the presence of veratryl alcohol or 1,4-dimethoxybenzene, were performed as indicated in Table III and IV in 6 ml of phosphate buffer (pH 3.0). Other conditions were the same as for the oxidation of veratryl alcohol described above. TDCSPPFeCl remaining after the reaction was estimated from its Soret band absorption before and after the reaction. For the decolorization of Poly B-411 (IV) by TDCSPPFeCl and mCPBA, 25 //moles of mCPBA were added to 25 ml 0.05% Poly B-411 containing 0.01 //moles TDCSPPFeCl, 25 //moles of manganese sulfate and 1.5 mmoles of lactic acid buffered at pH 4.5. The decolorization of Poly B-411 was followed by the decrease in absorption at 596 nm. For the electrochemical decolorization of Poly B-411 in the presence of veratryl alcohol, a two-compartment cell was used. A glassy carbon plate was used as the anode, a platinum plate as the auxiliary electrode, and a silver wire as the reference electrode. The potential was controlled at 0.900 V. Poly B-411 (50 ml, 0.005%) in pH 3 buffer was added to the anode compartment and pH 3 buffer was added to the cathode compartment to the same level. The decolorization of Poly B-411 was followed by the change in absorbance at 596 nm and the simultaneous oxidation of veratryl alcohol was followed at 310 nm. The same electrochemical apparatus was used for the decolorization of Poly B-411 adsorbed onto filter paper. Tetrabutylammonium perchlorate (TBAP) was used as supporting electrolyte when methylene chloride was the solvent. 

Fig. 3.22. Arrangement of the leads inside the conductivity cell shown in Fig. 3.23. Cu copper wire, Sd soldered joint, W tungsten wire, SW spot-weld, Pt platinum wire, S soda glass sleeve, SS silver-soldered joint, P borosilicate glass arm fused to the cell, PtP platinum plate electrodes held together with lead glass beads L.

If a solution of ammonio chloride be electrolyzed, the negative electrode being mercury and the positive a platinum plate, the mercury is observed to swell up, owing to the forma Uon of a spongy metallic mass. 

The 3-in.-square platinum plates are welded to a heavy platinum wire that protrudes through one of the holes cut in the glass lid. Heavy copper wire (No. 10) is used to connect the electrodes to the source of current. 

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