Lipid production in Porphyridium cruentum grown under different culture conditions

Autotrophic growth of Porphyridium cruentum under 18:12 h and 12:12 h light:dark cycles showed the maximum cell concentration of 2.1 g-dry wt./L, whereas the specific growth rate, 0.042 (1/h), at 18:6 h is faster than that of 12:12 h, 0.031 (1/h), respectively. The highest lipid accumulation level, 19.3 (%, w/w), was achieved at 12:12 h cycle. Under dark cultivation condition with 10 g/L of glucose, the lipid accumulation in the cell was 10.9 (%, w/w), whereas the heterotrophic growth with glycerol as the carbon resource showed low level of cell concentration and lipid production, compared to that of glucose. The glucose was decided to be a suitable carbon resource for the heterotrophic growth of P. cruentum. The lipids from P. cruentum seemed be feasible for biodiesel production, because over 30% of the lipid was C₁₆–C_18:1. The cultivation time and temperature were important factors to increase the maximum cell concentration. Extending the cultivation time helps maintain the maximum cell concentration, and higher lipid accumulation was achieved at 25 °C, compared to 35 °C. The fed-batch cultures showed that, under the light condition, the specific production rate was slightly decreased to 0.4% lipid/g-dry wt./day at the later stage, whereas, under the dark condition, the specific production rate was maintained to be a maximum value of 1.1% lipid/g-dry wt./day, even in the later stage of cultivation. The results indicate that the heterotrophic or 12:12 h cyclic mixotrophic growth of P. cruentum could be used for the production of biodiesel in long-term fed-batch cultivation of P. cruentum.     

Prevalence and antimicrobial resistance of Campylobacter jejuni and Campylobacter coli isolated from raw chicken meat and human stools in Korea

Prevalence of Campylobacter in raw chicken meat and human stools and subsequent antibiotic resistance profiles of the pathogenic isolates obtained from 2000 through 2002 were investigated. Campylobacter jejuni and Campylobacter coli were isolated from 570 of the 923 raw chicken meat samples collected from traditional markets, large retail stores, or department stores in Korea, resulting in the isolation rate of 61.8%. A total of 579 Campylobacter isolates were obtained from raw chicken (36.3% for C. jejuni and 26.4% for C. coli) with the average population of 335.6 CFU/g. From 513 human stool samples, 15 isolates of Campylobacter were detected. Seasonal variation in the quantification of C. coli was not noticeable throughout the year, while the isolation rate of C. jejuni was the highest in September through October (840 CFU/g) followed by that of July through August and May through June in decreasing order, showing a significant seasonal effect (P < 0.05). Contamination of Campylobacter was more severe in raw chicken meat sold in traditional markets than in those sold in large retail stores and department stores. Prevalence of Campylobacter in raw chicken sold in traditional markets was significantly influenced by seasonal changes (P < 0.05), whereas the samples obtained from other places was less affected by the seasonal changes. Susceptibilities of the 594 chicken isolates to ciprofloxaxin, chloramphenicol, erythromycin, kanamycin, nalidixic acid, and tetracycline were determined by an E-test. Campylobacter isolates were the most resistant to nalidixic acid (91.4%) followed by ciprofloxaxin (87.9%), tetracycline (87.2%), kanamycin (30.6%), erythromycin (19.4%), and chloramphenicol (1.3%). Human isolates showed a similar resistance to the six antibiotics tested. The proportion of Campylobacter isolates with multidrug resistance to four or more antimicrobials obtained from 2000 through 2002 ranged from 28 to 43.5%, indicating that it could be a serious health-threatening factor. This study suggests that it is prudent to establish an effective National Monitoring Program in Korea for the prevention and control of Campylobacter spp.     

Experimental study on self-excitations in nitrogen-diluted laminar lifted butane flames

Laminar lifted butane flames diluted with nitrogen have been investigated experimentally to determine distinctive self-excitation regimes in the flame stability maps and also to elucidate the individual self-excitation characteristics. Self-excitations of lift-off height are classified into five regimes in laminar free-jet lift-off butane flames diluted with nitrogen: a stationary lifted regime (regime I), a heat-loss-induced self-excitation (regime II), a buoyancy-induced self-excitation due to flame flicker as well as a heat-loss-induced self-excitation (III), a combined form of an oscillation prior to blow-out and a heat-loss-induced oscillation (regime IV), and a combined form of an buoyancy-induced self-excitation and a heat-loss-induced oscillation as well as an additional buoyancy-driven self-excitation due to flame flicker (regime V). Extremely low-frequency (<0.1 Hz) self-excitation is caused by conductive heat loss from the premixed wings to the trailing diffusion flame and can be explained by a proposed mechanism. It is also found that the flame oscillation prior to flame blow-out is also caused by buoyancy and also significantly affected by the conductive heat loss from the premixed wings to the trailing diffusion flame, thereby showing that the frequency with nozzle exit velocity increases in the triple-flame propagation mode and then decreases in the flame-front propagation mode. Characterization of the individual self-excitation mode is presented and also discussed with Strouhal numbers and its relevant parameters through the analysis of power spectrum for temporal variation of lift-off height.     

Multigroup pin power reconstruction with two-dimensional source expansion and corner flux discontinuity

A pin power reconstruction method that is readily applicable to multigroup problems with superior accuracy is presented for applications involving rectangular fuel assemblies. It employs a two-dimensional (2D), fourth order Legendre expansion of the source distribution that naturally leads to a group-decoupled, 2D semi-analytic solution of the neutron diffusion equation. The four surface average currents and four corner fluxes are used as the boundary conditions to uniquely specify the homogenous solution. The corner fluxes and source expansion coefficients are iteratively determined using the condition of corner point balance and the orthogonal property of the Lengedre functions. Corner discontinuity is incorporated in the calculation of the corner fluxes which turns out to be very effective in the cases of enrichment zoning. The accuracy of the proposed method is assessed by performing the two-step core calculations for the L336C5, C5G7MOX, and MOX core transient benchmark problems and then by comparing with the direct whole-core transport solutions. The results indicate that the proposed method is as accurate as the fully analytic method and works well irrespective the number of groups. However, it is also noted that somewhat larger errors are inevitable at the peripheral assemblies near the reflector in which the error associated with a prioi generation of the homogenized cross-sections and form functions is not trivial.     

Effect of metal-sulfide additives on electrochemical properties of nano-sized Fe2O3-loaded carbon for Fe/air battery anodes

In the present study, K₂S and Bi₂S₃ were used as additives in electrolytes and electrodes, respectively. The effects of these additives on the electrochemical properties of nano-sized Fe₂O₃-loaded carbon electrodes were investigated using cyclic voltammetry (CV), galvanostatic cycling performance and scanning electron microscopy (SEM), along with electron dispersive spectroscopy (EDS). The results showed that both K₂S and Bi₂S₃ significantly reduced hydrogen evolution and benefited the Fe₂O₃-loaded carbon electrode, such as by retarding passivation and improving the discharge capacity. The effects of metal sulfide additives depended on the carbon used. For Bi₂S₃ additive, all carbons provided larger capacities than acetylene black (AB) while AB gave greater capacity than other carbons when K₂S was used.     

Improved performance of molten carbonate fuel cells with (Li/Na)2CO3 electrolytes by using BYS coated cathode at low operating temperatures

In order to improve the stack life time of MCFCs, it is necessary to reduce the operating temperature of MCFCs below 600 °C, because reduced operating temperature minimizes electrolyte loss due to evaporation and corrosion. However, at the low operating temperature below 600 °C, the cell performance of MCFCs with (Li/Na)₂CO₃ electrolyte is too low to operate the fuel cell stack and system. In this study, we have performed wettability control of the liquid molten carbonate electrolyte by coating NiO cathodes with poor wetting property of the mixed ionic and electronic conductor (MIEC) such as BYS (Bi_1.5Y_0.3Sm_0.3O_3-δ). From experiments with symmetrical cells, each polarization component with various temperatures and gas conditions were studied. To investigate effects of the BYS coated cathode on the performance of MCFCs, a 100 cm² single cell of MCFCs was employed. The performance of a 100 cm² single cell with BYS coated cathode was better than that with conventional cathode by a factor of 1.84, because BYS coated cathode reduces activation polarization and mass transfer resistance greatly.     

Enhanced heat transfer performance of alumina sponge-like nano-porous structures through surface wettability control in nucleate pool boiling

For several decades, a porous surface has been recognized as an efficient medium to increase boiling performance in a nucleate boiling regime. Most feasible porous surfaces have been studied in millimeter and micron-sized domains. It has been believed that a higher wall superheat is required to commence incipient nucleate boiling under a submicron regime. In this study, we demonstrate that a significantly enhanced pool boiling heat transfer is observed in a submicron regime through three dimensionally interconnected hybrid pores: the Alumina sponge-like nano-porous structure (ASNPS). The structural uniqueness of the ASNPS leads to an enlarged surface area, increases the potential number of the active nucleation site density, and improves the vapor–liquid menisci through the reentrant pore. Simultaneously, by changing the surface wettability with a hydrophobic self-assembled monolayer (SAM) coating, the number of active nucleation site density is improved. Eventually, the combination of the ASNPS and hydrophobic SAM coating can achieve substantial heat transfer coefficient (HTC) enhancement in the nucleate boiling. Also, the thickness of the ASNPS is a critical issue to adequately augment the HTC in pool boiling. The thickness of the ASNPS is optimized by examining the boiling performance of the ASNPS fabricated in different amounts of anodizing times. A classical mechanistic model from literature was modified and compared with the experimentally obtained data. The modified mechanistic model – with the combination of forced-convection and thin liquid film evaporation – showed reasonable predictions.     

Electrochemical hydrogen discharge of high-strength low alloy steel for high-pressure gaseous hydrogen storage tank: Effect of discharging temperature

Hydrogen discharge technique of high-strength low alloy steel for high-pressure gaseous hydrogen storage tank was developed by using an electrochemical technique. The electrochemical hydrogen discharge of high-strength low alloy steel were investigated in a deaerated borate buffer solution (0.3 M H₃BO₃ + 0.074 M N₂B₄O₇, pH = 8.4). By applying a potential of +630 mV_SCE which is higher than the hydrogen equilibrium potentials and lower than the pitting potential, the oxidation reaction of metal (Fe → Fe²⁺ + 2e⁻) is limited and oxidation reaction of the hydrogen (H₂ + 2OH⁻ → 2H₂O + 2e⁻) was induced simultaneously. Thus, the pre-charged hydrogen inside the specimen was eliminated effectively without any damage to the specimen. The electrochemical hydrogen discharge method was performed at 25 °C, 50 °C and 75 °C. The efficiency of hydrogen discharge was accelerated with increasing temperature because the exchange current density of hydrogen is increased with temperature.     

Self-sustained operation of a kWe-class kerosene-reforming processor for solid oxide fuel cells

In this paper, fuel-processing technologies are developed for application in residential power generation (RPG) in solid oxide fuel cells (SOFCs). Kerosene is selected as the fuel because of its high hydrogen density and because of the established infrastructure that already exists in South Korea. A kerosene fuel processor with two different reaction stages, autothermal reforming (ATR) and adsorptive desulfurization reactions, is developed for SOFC operations. ATR is suited to the reforming of liquid hydrocarbon fuels because oxygen-aided reactions can break the aromatics in the fuel and steam can suppress carbon deposition during the reforming reaction. ATR can also be implemented as a self-sustaining reactor due to the exothermicity of the reaction. The kW_e self-sustained kerosene fuel processor, including the desulfurizer, operates for about 250 h in this study. This fuel processor does not require a heat exchanger between the ATR reactor and the desulfurizer or electric equipment for heat supply and fuel or water vaporization because a suitable temperature of the ATR reformate is reached for H₂S adsorption on the ZnO catalyst beds in desulfurizer. Although the CH₄ concentration in the reformate gas of the fuel processor is higher due to the lower temperature of ATR tail gas, SOFCs can directly use CH₄ as a fuel with the addition of sufficient steam feeds (H₂O/CH₄ ≥ 1.5), in contrast to low-temperature fuel cells. The reforming efficiency of the fuel processor is about 60%, and the desulfurizer removed H₂S to a sufficient level to allow for the operation of SOFCs.