Electrode plastic

A method was described for the determination of nonionic surfactants containing poly(oxyethylene) chains with sodium tetraphenylborate, based on the precipitatiOTi of ternary compounds in the presence of bivalent metal ions (barium salts). Titrations were monitored potentiometricaUy with a simple PVC membrane-coated aluminum wire electrode plasticized with 2,4-dinitrophenyloctyl ether. " ... 

One example of a liquid-based ion-selective electrode is that for Ca +, which uses a porous plastic membrane saturated with di-(n-decyl) phosphate (Figure 11.13). As shown in Figure 11.14, the membrane is placed at the end of a nonconducting cylindrical tube and is in contact with two reservoirs. The outer reservoir contains di-(n-decyl) phosphate in di- -octylphenylphosphonate, which soaks into the porous membrane. The inner reservoir contains a standard aqueous solution of Ca + and a Ag/AgCl reference electrode. Calcium ion-selective electrodes are also available in which the di-(n-decyl) phosphate is immobilized in a polyvinyl chloride... 

The principal uses of PCTFE plastics remain in the areas of aeronautical and space, electrical/electronics, cryogenic, chemical, and medical instmmentation industries. AppHcations include chemically resistant electrical insulation and components cryogenic seals, gaskets, valve seats (56,57) and liners instmment parts for medical and chemical equipment (58), and medical packaging fiber optic appHcations (see Fiber optics) seals for the petrochemical /oil industry and electrodes, sample containers, and column packing in analytical chemistry and equipment (59). 

The zinc electrolyte contains ca 60 kg/m zinc as sulfate and ca 100 kg/m free sulfuric acid. It is electrolyzed between electrodes suspended vertically in lead or plastic-lined, eg, poly(vinyl chloride), concrete tanks. The insoluble anodes are made of lead with small amounts of silver. The anodic... 

Until the end of World War II, coal tar was the main source of these aromatic chemicals. However, the enormously increased demands by the rapidly expanding plastics and synthetic-fiber industries have greatly outstripped the potential supply from coal carbonization. This situation was exacerbated by the cessation of the manufacture in Europe of town gas from coal in the eady 1970s, a process carried out preponderantly in the continuous vertical retorts (CVRs), which has led to production from petroleum. Over 90% of the world production of aromatic chemicals in the 1990s is derived from the petrochemical industry, whereas coal tar is chiefly a source of anticorrosion coatings, wood preservatives, feedstocks for carbon-black manufacture, and binders for road surfacings and electrodes. 

Separator s a physical barrier between the positive and negative electrodes incorporated into most cell designs to prevent electrical shorting. The separator can be a gelled electrolyte or a microporous plastic film or other porous inert material filled with electrolyte. Separators must be permeable to ions and inert in the battery environment. 

To complete the assembly of a cell, the interleaved electrode groups are bolted to a cov er and the cover is sealed to a container. Originally, nickel-plated steel was the predominant material for cell containers but, more recently plastic containers have been used for a considerable proportion of pocket nickel-cadmium cells. Polyethylene, high impact polystyrene, and a copolymer of propylene and ethylene have been the most widely used plastics. 

Cell Construction. Nickel—2iac batteries are housed ia molded plastic cell jars of styrene, SAN, or ABS material for maximum weight savings. Nickel electrodes can be of the siatered or pocket type, however, these types are not cost effective and several different types of plastic-bonded nickel electrodes (78—80) have been developed. 

Nickel—2iiic batteries containing a vibrating zinc anode lias been reported (83). In this system zinc oxide active material is added to the electrol 1 e as a slurry. During charge the anode substrates are vibrated and the zinc is electroplated onto the surface in a unifomi mamier. Tlie stationary positive electrodes (nickel) are encased in a thin, open plastic netting which constitutes the entire separator system. 

Self-baked carbon electrodes are those whose shapes are formed in situ (33). The carbonaceous mixture is placed into a hoUow tube-shaped metal casing. The upper end receives the unbaked mixture as a soHd block, small particles, or warm plastic paste. The casing contains inwardly-projecting longitudinal perforated fins that become surrounded by baked carbon as the casing is incrementally moved downward and through the contact plates. Casing and carbon are consumed in this furnace. 

The obtained results exhibit the efficacy of using the mentioned ionic pairs as electrode-active substances for plasticized ionoselective electrodes. 

The sufficient selectivity to a principal component is the most important condition determining the possibility of ion-selective electrodes (ISEs) practical appliances. In this work, the relationship between the potentiometric selectivity of alkylammonium-selective electrodes and factors such as the nature of plasticizer, ion-exchanger and substitution degree of cationic nitrogen atoms of the principal and foreign ions, is discussed. 

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