Об индивидуальном учете вытеснения токов ротора при расчетах группового самозапуска асинхронных электродвигателей собственных нужд ТЭС

The paper considers the possibility to make calculation of group self-starting of asynchronous electric motors being TPS auxiliaries with the help of generalized (averaged) dependences Kr{s), Kx{s) which are equal for all electric motors involved in self-starting process and which makes it possible to take into account displacement of rotor current. Generalized dependences have been obtained on the basis of individual dependences using method of least squares with due account of utilization of these or that characteristics. The paper provides results of the calculations in respect of individual and averaged characteristics of a number of motors. It is concluded that there is possibility to use averaged characteristics for calculation of motor group self-starting.В статье рассматривается возможность выполнения расчетов группового самозапуска с использованием для учета вытеснения токов ротора обобщенных (усредненных) зависимостей Kr{s), Kx{s). одинаковых для всех электродвигателей, участвующих в самозапуске. Обобщенные зависимости получены на базе индивидуальных зависимостей методом наименьших квадратов с учетом частот использования тех или иных характеристик. Приводятся результаты расчетов по индивидуальным и усредненным характеристикам для группы двигателей и делается заключение о возможности использования усредненной характеристики для расчета группового самозапуска

Transition metal-nitrogen-carbon catalysts for oxygen reduction reaction in neutral electrolyte

© 2016 The Authors Platinum group metal-free (PGM-free) catalysts based on M-N-C types of materials with M as Mn, Fe, Co and Ni and aminoantipyrine (AAPyr) as N-C precursors were synthesized using sacrificial support method. Catalysts kinetics of oxygen reduction reaction (ORR) was studied using rotating ring disk electrode (RRDE) in neutral pH. Results showed that performances were distributed among the catalysts as: Fe-AAPyr>Co-AAPyr>Mn-AAPyr>Ni-AAPyr. Fe-AAPyr had the highest onset potential and half-wave potential. All the materials showed similar limiting current. Fe-AAPyr had an electron transfer involving 4e− with peroxide formed lower than 5%. Considering H2O2 produced, it seems that Co-AAPyr, Mn-AAPyr and Ni-AAPyr follow a 2×2e− mechanism with peroxide formed during the intermediate step. Durability test was done on Fe-AAPyr for 10,000cycles. Decrease of activity was observed only after 10,000cycles

Iron based catalysts from novel low-cost organic precursors for enhanced oxygen reduction reaction in neutral media microbial fuel cells

© 2016 The Royal Society of Chemistry. Two iron-based platinum group metal-free catalysts for the oxygen reduction reaction (ORR) were synthesized from novel and low cost organic precursors named niclosamide and ricobendazole. These catalysts have been characterized, incorporated in a gas diffusional electrode and tested in "clean" conditions as well as in operating microbial fuel cell (MFC) for 32 days. Both catalysts demonstrated unprecedented performance yielding a power density 25% higher than that of platinum (Pt) and roughly 100% higher than activated carbon (AC) used as a control. Durability tests were performed and showed that Pt-based cathodes lost their activity within the first week of operation, reaching the level of the supporting AC-based electrode. Fe-ricobendazole, however, demonstrated the highest performance during the long-term study with a power density of 195 ± 7 μW cm-2 (day 2) that slightly decreased to 186 ± 9 μW cm-2 at day 29. Fe-niclosamide also outperformed Pt and AC but the power density roughly decreased with 20% for the 32 days of the study. Accelerated poisoning test using S2- as pollutant showed high losses in activity for Pt. Fe-niclosamide suffered higher losses compared to Fe-ricobendazole. Importantly, Fe-ricobendazole represents a 55-fold cost reduction compared to platinum

Three-dimensional graphene nanosheets as cathode catalysts in standard and supercapacitive microbial fuel cell

© 2017 The Authors Three-dimensional graphene nanosheets (3D-GNS) were used as cathode catalysts for microbial fuel cells (MFCs) operating in neutral conditions. 3D-GNS catalysts showed high performance towards oxygen electroreduction in neutral media with high current densities and low hydrogen peroxide generation compared to activated carbon (AC). 3D-GNS was incorporated into air-breathing cathodes based on AC with three different loadings (2, 6 and 10mgcm−2). Performances in MFCs showed that 3D-GNS had the highest performances with power densities of 2.059±0.003Wm-2, 1.855±0.007Wm-2 and 1.503±0.005Wm-2 for loading of 10, 6 and 2mgcm−2 respectively. Plain AC had the lowest performances (1.017±0.009Wm-2). The different cathodes were also investigated in supercapacitive MFCs (SC-MFCs). The addition of 3D-GNS decreased the ohmic losses by 14–25%. The decrease in ohmic losses allowed the SC-MFC with 3D-GNS (loading 10mgcm−2) to have the maximum power (Pmax) of 5.746±0.186Wm-2. At 5mA, the SC-MFC featured an “apparent” capacitive response that increased from 0.027±0.007F with AC to 0.213±0.026F with 3D-GNS (loading 2mgcm−2) and further to 1.817±0.040F with 3D-GNS (loading 10mgcm−2)

Influence of platinum group metal-free catalyst synthesis on microbial fuel cell performance

© 2017 The Authors Platinum group metal-free (PGM-free) ORR catalysts from the Fe-N-C family were synthesized using sacrificial support method (SSM) technique. Six experimental steps were used during the synthesis: 1) mixing the precursor, the metal salt, and the silica template; 2) first pyrolysis in hydrogen rich atmosphere; 3) ball milling; 4) etching the silica template using harsh acids environment; 5) the second pyrolysis in ammonia rich atmosphere; 6) final ball milling. Three independent batches were fabricated following the same procedure. The effect of each synthetic parameters on the surface chemistry and the electrocatalytic performance in neutral media was studied. Rotating ring disk electrode (RRDE) experiment showed an increase in half wave potential and limiting current after the pyrolysis steps. The additional improvement was observed after etching and performing the second pyrolysis. A similar trend was seen in microbial fuel cells (MFCs), in which the power output increased from 167 ± 2 μW cm−2 to 214 ± 5 μW cm−2. X-ray Photoelectron Spectroscopy (XPS) was used to evaluate surface chemistry of catalysts obtained after each synthetic step. The changes in chemical composition were directly correlated with the improvements in performance. We report outstanding reproducibility in both composition and performance among the three different batches

Enhancement of microbial fuel cell performance by introducing a nano-composite cathode catalyst

© 2018 The Authors Iron aminoantipyrine (Fe-AAPyr), graphene nanosheets (GNSs) derived catalysts and their physical mixture Fe-AAPyr-GNS were synthesized and investigated as cathode catalysts for oxygen reduction reaction (ORR) with the activated carbon (AC) as a baseline. Fe-AAPyr catalyst was prepared by Sacrificial Support Method (SSM) with silica as a template and aminoantipyrine (AAPyr) as the organic precursor. 3D-GNS was prepared using modified Hummers method technique. The Oxygen Reduction Reaction (ORR) activity of these catalysts at different loadings was investigated by using rotating ring disk (RRDE) electrode setup in the neutral electrolyte. The performance of the catalysts integrated into air-breathing cathode was also investigated. The co-presence of GNS (2 mg cm−2) and Fe-AAPyr (2 mg cm−2) catalyst within the air-breathing cathode resulted in the higher power generation recorded in MFC of 235 ± 1 μW cm−2. Fe-AAPyr catalyst itself showed high performance (217 ± 1 μW cm−2), higher compared to GNS (150 ± 5 μW cm−2) while AC generated power of roughly 104 μW cm−2

Microbial fuel cells: From fundamentals to applications. A review

© 2017 The Author(s) In the past 10–15 years, the microbial fuel cell (MFC) technology has captured the attention of the scientific community for the possibility of transforming organic waste directly into electricity through microbially catalyzed anodic, and microbial/enzymatic/abiotic cathodic electrochemical reactions. In this review, several aspects of the technology are considered. Firstly, a brief history of abiotic to biological fuel cells and subsequently, microbial fuel cells is presented. Secondly, the development of the concept of microbial fuel cell into a wider range of derivative technologies, called bioelectrochemical systems, is described introducing briefly microbial electrolysis cells, microbial desalination cells and microbial electrosynthesis cells. The focus is then shifted to electroactive biofilms and electron transfer mechanisms involved with solid electrodes. Carbonaceous and metallic anode materials are then introduced, followed by an explanation of the electro catalysis of the oxygen reduction reaction and its behavior in neutral media, from recent studies. Cathode catalysts based on carbonaceous, platinum-group metal and platinum-group-metal-free materials are presented, along with membrane materials with a view to future directions. Finally, microbial fuel cell practical implementation, through the utilization of energy output for practical applications, is described