Common-duct series-cell electrolyzer with anomalous gas production rate

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Common-duct series-cell electrolyzer with anomalous gas production rate tero.ranta@bigfoot.com Ver 1.1 6 th Sept 2005 - +

Electrolyzer The electrolyzer shown in Figure 1 is based on the common duct series-cell electrolyzer concept originally developed and patented by William Rhodes, Ernest Spirig, Yull Brown and later refined by Bob Boyce, George Wiseman, etc It uses an alkaline electrolyte to split distilled water into hydrogen and oxygen components very efficiently. The produced hydrogen and oxygen gasses are not separated to separate containers, but kept mixed. The produced oxyhydrogen gas is a stoichiometric mixture of hydrogen (2 parts vol.) and oxygen (1 part vol.) and can be combusted in vacuum. The combination of series-cell topology and keeping the gasses mixed seems to produce anomalous amount of gas (up to 200%) at a given current level compared to the values predicted by Faraday s law. The electrolyzer runs fairly cool, at about 30-50 C depending on the current and electrolyte. It is possible that the gas produced by this device is not conventional diatomic H 2 /O 2 gas but rather mono-atomic H/O gas. It seems that for highest anomalous gas production it is essential that electrolyte in each compartment is not allowed to contact the electrolyte in other compartmens. No level equalization holes should be drilled that are permantly below the electrolyte level to prevent bypass current leakage. Level equalization in this design is achieved by temporarily turning the electrolyzer 90 degrees to allow the electrolyte levels to equalize through the gas vent holes in the plates. The electrolyzer shown in this report has ~120% Faraday efficiency when powered by pure DC. It is known that similar designs exist that can reach better than 180% Faraday efficiency and the work is ongoing to reach these levels. Pulsing or modulation of the input voltage waveform could increase the performance further. The electrolyzer has 7 cells with a target input voltage of about 12.9-14.1Vdc depending on temperature. This makes the cell voltage about 1.85-2.0V. - +12..14Vdc @ 5-10A + Plate spacing 3mm, active plate area ~170cm^2 per side Gas vent hole in each plate Gas output, water input valve Electrolyte level ~20mm below gas vent hole PVC end plate Stainless steel electrodes Electrolyte in each compartment is FULLY isolated from other compartments, there are no electrolyte level equalization holes drilled in the plates Soft transparent PVC spacers rings Figure 1. Series cell electrolyzer cross-section

Electrolyzer construction The eight electrolyzer plates (Figure 2) are about 0.8mm thick 160mm x 200 mm stainless steel (304 grade). A 10mm gas vent hole is drilled in each plate. The electrolyte level is always about 25mm below the gas vent hole. There are no liquid level equalization holes in the plates below the liquid level to prevent current leakage between cells that reduces efficiency. The two end plates have a small SS piece welded for electrical contact. After taking the picture the plates were sanded with an orbital sander to expose clear metal and then cross-hatch pattern was engraved on the plates with a rough file attached to a wooden block. This is to increase the active surface area of the plates and seems necessary for ultra high efficiency. Other methods to increase plate area exist as well. Figure 2. Stainless steel electrolyzer plates (8 total) Nine spacers (Figure 3) are cut out of 3mm thick soft and transparent PVC sheet with a knife. The wall thickness is 12mm. The PVC sheet is originally designed for door material for large room-size refrigerators. The small square PVC blocks were meant to keep proper distance between SS plate centers, but they turned out to be unnecessary and were not used.

Figure 3. Soft PVC spacers rings The end plates (Figure 4) were cut out of 12mm thick PVC plate. The size of the plates was 200mm x 240mm. Eight 8mm holes were drilled for M8 size stainless steel through-bolts. A ¼ pipe thread was tapped in a 11.8mm gas vent hole. A valve and gas hose connector was epoxy glued to the ¼ tapped hole in both plates. Other thread sealants may not be compatible with the electrolyte so it s best to use epoxy or teflon tape. The valve was lined up with gas vent hole in SS plates. Figure 4. PVC end plates with gas valves attached

The first stainless steel plate and one PVC spacer ring are shown in Figure 5. There is a PVC spacer ring also between the PVC end plate and first SS plate. A 35mm piece of 8mm ID 12mm OD rubber hose is slid over the bolts to isolate the bolts from the plates and hold the plates in place. Note that it would have made more sense to drill the gas vent hole to the upper left corner of the plates, so that draining the all of the electrolyte out of the electrolyzer would have been easier. It would also have made sense to drill another gas vent hole in the upper right corner to allow free air flow between the plates when the electrolyzer is turned 90 degrees for electrolyte level equalization. Figure 5. First SS plate in place with the PVC spacer shown A side view of the cell stack with several SS plates and PVC spacer rings in place is shown in Figure 6. Note the soft PVC sheet material in the background with the cut outline drawn with a permanent overhead transparent marker pen.

Figure 6. Partly assembled cell stack The finished electrolyzer is shown in Figure 7. The two PVC end plates are clamped together with 70mm long M8 stainless steel bolts with Nyloc nuts. After initial tightening I submerged the electrolyzer in hot tap water (about 60 C) with the gas vent valves closed. This softened the PVC gaskets and allowed the stack to be tightened up even further to provide an excellent seal. Note that the 12mm PVC plates are quite soft and some bulging is visible. Two additional bolts would have been useful to equalize the bolt forces more evenly around the plates. Figure 7. Assembled stack

Faraday s law and electrolyzer efficiency: Faraday s Law of Electrolysis states that it takes 1 F = 96485.31 As = 26.8 Ah to produce 0.75*22.4141 liters = 16.8 liters of H 2 /O 2 gas in STP. It has 2 parts H 2 and one part O 2 by volume as the gas is produced by splitting H 2 O. This corresponds to a current consumption of 1.594 A per liter per hour = 1.594 Ah/l per one cell. Each cell in series configuration produces this amount, so it must be multiplied by the amount of cells in series. If the cell produces more gas than predicted by Faraday s law, the cell has Faraday or current efficiency over 100%. Stated the other way passing one amp through one cell would produce 0.627 liters of gas per hour, or 0.627 l/ah according to Faraday s Law. The Faraday or current efficiency is the amount of gas produced by a certain current in a single cell compared to Faraday s law. It can be calculated as follows: 1.594 F η I = = 1. 594, where F = flow [liters per hour], I = current [A] and n = number of cells I /( F / n) I n in series. The thermoneutral cell voltage is ~1.48 V, which means the voltage at which all input energy for the electrolysis process comes from the electrical input energy. At 1.23 V (reversible cell potential) part of the energy comes from ambient heat and electrolyzer is about 120% voltage efficient. Note that 100% efficient hydrogen oxygen fuel cell would produce 1.23V. The thermoneutral voltage of ~1.48V is considered to be the 100% voltage and power efficient electrolysis. That is, if the electrolyzer is 100% Faraday efficient, 1.48V across one cell produces 100% power efficient electrolysis. Burning the produced gas will release exactly the same amount of energy that was used in making the gas. The 100% power or wattage efficient electrolyzer would consume 1.48 V * 1.594 Ah/l = 2.36 Wh / l. That is it consumes 2.36 Watts for each liter per hour it produces. Note that the heat of combustion of the hydrogen gas contained in the electrolytic gas is also 2.36 Wh/l. To calculate power efficiency you don t need to take into account the number of cells. The total power efficiency is the amount of gas produced by a certain power in the whole electrolyzer compared to what a 100% efficient conventional electrolyzer would produce: = 2.36 F η I = 2. U I / F 36 U I, where F = flow [liters per hour], I = current [A] and U = voltage [V], The electrolyzer might be over 100% efficient at either current efficiency, or power efficiency or both. If the Faraday efficiency is over 100% it might imply that the produced gas is not conventional H 2 /O 2. In the literature the electrolyzer efficiency is usually defined as the ratio of the thermoneutral voltage (1.48V) to the cell voltage. At 2.0V cell voltage it would imply an efficiency of 74%, which is incorrect if the Faraday efficiency is higher than 100%. It seems that the practical lower limit for the cell voltage at 3mm electrode spacing is about 1.9-2.0V at a practical current density of about 0.3-0.5 A/sq. in. If the Faraday efficiency is 200%, this would imply lowest achievable total power efficiency would be about 1.5Wh/l. It should also be noted that the Faraday or current efficiency over 100% implies an overunity gas production mechanims, while the power or wattage efficiency is only an indicator of the how low the cell voltage is.

Output measurements: Run #7: (3 rd Aug 2005) Electrolyte drain-cleaner grade 93% pure Potassium Hydroxide or KOH pellets in medical grade purified water. Concentration 28% KOH and 72% water by weight. 500 grams of electrolyte (about 450ml volume) was mixed and poured into the electrolyzer. The electrolyzer was allowed to run without collecting gasses for a few hours. During this time the electrolyte temperature stabilized at 45C while the ambient temperature was 17C. The gas production rate was measured by collecting the gas in a 0.5L coke bottle filled with water. The weight of the bottle with water was measured. The bottle filled with water was turned upside down while partly submerged in a cold water bath. The gas was allowed to bubble through the water bath to the bottle and the time was measured. After removing the gas hose and stopping the timer the cap of the bottle was screwed on while still under water and the weight of the bottle filled partly with water and partly with gas was measured. The weight difference between start and end weights was recorded, as the weight difference in grams corresponds to the volume of produced gas in milliliters. The production rate was found to be 475ml in 30 seconds, which corresponds to 57 LPH (liters per hour). The cell was powered by a current limited (11A limit) battery charger. The voltage across the electrolyzer and the current were measured with Fluke True-RMS multimeter. Oscilloscope was used to make sure that voltage and current waveforms were pure DC without any ripples. The voltage and current across the electrolyzer were measured to be 12.9 V and 11 A during the gas collection. Thus the input power was 141.9 W. The Faraday efficiency was determined by dividing the current consumption of the cell by the amount of gas produced by one cell. It is 11A / (57LPH/7) = 1.18 Ah / liter per cell. This is about 118% efficient, or produces 18% more gas than according to Faraday s Law. The power efficiency was determined by dividing the total power consumption by the amount of gas produced. This is 141.9W / 57 LPH = ~2.49 Wh/l. This corresponds to about 94.8% power efficiency. Discussion: It is known at least two similar 7-cell series electrolyzers exist that are able to produce about 90 LPH at 13.8Vdc and 11A. These numbers correspond to a Faraday efficiency of 186% and total power efficiency of 140%. The electrolyzer in shown this report currently produces 57LPH at 11A, but it should be possible to get this up to 90LPH. The work is ongoing to improve the performance.