Phosphoric acid fuel cells temperature

Phosphoric Acid Fuel Cell. Concentrated phosphoric acid is used for the electrolyte ia PAFC, which operates at 150 to 220°C. At lower temperatures, phosphoric acid is a poor ionic conductor (see Phosphoric acid and the phosphates), and CO poisoning of the Pt electrocatalyst ia the anode becomes more severe when steam-reformed hydrocarbons (qv) are used as the hydrogen-rich fuel. The relative stabiUty of concentrated phosphoric acid is high compared to other common inorganic acids consequentiy, the PAFC is capable of operating at elevated temperatures. In addition, the use of concentrated (- 100%) acid minimizes the water-vapor pressure so water management ia the cell is not difficult. The porous matrix used to retain the acid is usually sihcon carbide SiC, and the electrocatalyst ia both the anode and cathode is mainly Pt. 

Medium-temperature phosphoric acid fuel cells (PAFCs). The electrolyte is 85 to 95% phosphoric acid the working temperatures are 180 to 200°C. Such systems were used to build numerous autonomous power plants with an output of up to about 250 kW, and even some with an output of up to 4 MW, in the United States, Japan, and other countries. 

In applications where Nafion is not suitable, at temperatures above 200 °C with feed gas heavily contaminated with CO and sulfur species, a phosphoric acid fuel cell (PAFC)-based concentrator has been effective [15]. Treating the gas shown in Table 1, a H2 product containing 0.2% CO, 0.5%CO2 and only 6 ppm H2S was produced. The anode electrode was formed from a catalyst consisting basically of Pt-alloy mixed with 50% PTFE on a support of Vulcan XC-72 carbon. The cathode was... 

There are six different types of fuel cells (Table 1.6) (1) alkaline fuel cell (AFC), (2) direct methanol fuel cell (DMFC), (3) molten carbonate fuel cell (MCFC), (4) phosphoric acid fuel cell (PAFC), (5) proton exchange membrane fuel cell (PEMFC), and (6) the solid oxide fuel cell (SOFC). They all differ in applications, operating temperatures, cost, and efficiency. 

Phosphoric acid fuel cell (PAFC) working at 180-200 °C vfith a porous matrix of PTFE-bonded silicon carbide impregnated with phosphoric acid as electrolyte, conducting by the H cation. This medium-temperature fuel cell is now commercialized by ONSI (USA), mainly for stationary applications. 

Fuel cells can be broadly classified into two types high temperature fuel cells such as molten carbonate fuel cells (MCFCs) and solid oxide polymer fuel cells (SOFCs), which operate at temperatures above 923 K and low temperature fuel cells such as proton exchange membrane fuel cells (PEMs), alkaline fuel cells (AFCs) and phosphoric acid fuel cells (PAFCs), which operate at temperatures lower than 523 K. Because of their higher operating temperatures, MCFCs and SOFCs have a high tolerance for commonly encountered impurities such as CO and CO2 (CO c)- However, the high temperatures also impose problems in their maintenance and operation and thus, increase the difficulty in their effective utilization in vehicular and small-scale applications. Hence, a major part of the research has been directed towards low temperature fuel cells. The low temperature fuel cells unfortunately, have a very low tolerance for impurities such as CO , PAFCs can tolerate up to 2% CO, PEMs only a few ppm, whereas the AFCs have a stringent (ppm level) CO2 tolerance. 

Phosphoric Acid Fuel Cell. This cell demonstrates the possibilities of using very concentrated phosphoric acid to allow the temperature of the solution to be raised to about 200-205 °C without the need for high-pressure equipment. The higher temperature makes it possible to produce large amounts of free steam for the re-forming of natural gas to the hydrogen upon which most development has been based. 

Phosphoric acid fuel cells (PAFC) with concentrated H3P04 (in silicon carbide matrices) electrolyte, which transports H+ cations, generated at the anode, to an ambient-air-exposed cathode, where they are electro-oxidised to water at moderate temperatures. 

Alkaline fuel cells (AFC) — The first practical -+fuel cell (FC) was introduced by -> Bacon [i]. This was an alkaline fuel cell using a nickel anode, a nickel oxide cathode, and an alkaline aqueous electrolyte solution. The alkaline fuel cell (AFC) is classified among the low-temperature FCs. As such, it is advantageous over the protonic fuel cells, namely the -> polymer-electrolyte-membrane fuel cells (PEM) and the - phosphoric acid fuel cells, which require a large amount of platinum, making them too expensive. The fast oxygen reduction kinetics and the non-platinum cathode catalyst make the alkaline cell attractive. 

Phosphoric-acid fuel cell (PAFC) — In PAFCs the -> electrolyte consists of concentrated phosphoric acid (85-100%) retained in a silicon carbide matrix while the -> porous electrodes contain a mixture of Pt electrocatalyst (or its alloys) (-> electrocatalysis) supported on -> carbon black and a polymeric binder forming an integral structure. A porous carbon paper substrate serves as a structural support for the electrocatalyst layer and as the current collector. The operating temperature is maintained between 150 to 220 °C. At lower temperatures, phosphoric acid tends to be a poor ionic conductor and poisoning of the electrocatalyst at the anode by CO becomes severe. 

Several types of fuel cells have been developed and are classified according to the electrolytes used alkaline fuel cells, molten carbonate fuel cells, phosphoric acid fuel cells (PAFCs), PEMFCs, and solid oxide fuel cells (SOFCs). As shown in Figure 1.3, the optimum operation temperatures of these fuel cells are different, and each type has different advantages and disadvantages. 

Development of supported Pt electrocatalysts came as a result of intensive research on fundamental and applied aspects of electrocatalysis [especially for kinetically difficult oxygen reduction reaction (ORR)] fueled by attempts at commercialization of medium-temperature phosphoric acid fuel cells (PAFCs) in the late 1960s and early 1970s. Dispersion of metal crystallites in a conductive carbon support resulted in significant improvements in all three polarization zones (activation, ohmic, and... 

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