The enhancement mechanism of hydrogen photoproduction in Chlorella protothecoides under nitrogen limitation and sulfur deprivation

The aim of this study was to understand the enhancement mechanism of H₂ photoproduction in Chlorella protothecoides under simultaneous nitrogen limitation and sulfur deprivation (LNS). Nitrogen limitation (LN) rather than sulfur deprivation significantly inhibited relative variable fluorescence at K-step (W_K) and J-step (V_J), photochemical efficiency of PSII (photosystem II), F_v/F_m, during the process of incubation in the light. Under such conditions, photosynthetic O₂ evolution decreased and the anaerobiosis was established after 12 h of incubation. The algae generated large amounts of H₂ under nitrogen limitation but generated only trace amounts under sulfur deprivation. Obviously, nitrogen limitation rather than sulfur deprivation was the decisive factor that induced H₂ photoproduction in C. protothecoides under LNS. The LNS culture generated much more H₂ than the LN culture in the presence of DCMU during incubation, suggesting that a PSII-independent electron source contributed many more electrons for transfer to hydrogenase in the LNS culture. PSII electron transport includes linear electron flow (LEF) and cyclic electron flow (CEF) of PSII in C. protothecoides. In the PSII-dependent electron source for H₂ photoproduction, PSII supplies electrons to hydrogenase through the LEF. The LNS culture showed much higher LEF and lower CEF than the LN culture during the H₂ photoproduction phase, as indicated by the large lower quantum yield of PSII electron transport (Φ_PSII) in the LNS culture in the presence of DCMU. Therefore, compared with nitrogen limitation, simultaneous nitrogen limitation and sulfur deprivation enhanced H₂ photoproduction in C. protothecoides mainly due to enhanced PSII-dependent and -independent electron sources.     

An evaluation of alkylthiols and dialkyl disulfides on deactivation of Cu/Zn catalyst in hydrogenation of dodecyl methyl ester to dodecanol

Deactivation of co-precipitated Cu/Zn catalyst caused by exposure to either alkylthiols or dialkyl disulfides in catalytic hydrogenation of dodecyl methyl ester to dodecanol is explored in a stirred batch reactor. Catalytic activity decrement is highly dependent on levels of poisons, types of thiols/disulfides, chain length of alkanes. XRD, EDS and XPS are employed to characterize the fresh and spent Cu/Zn catalysts. It is evident that sulfuric species prefer to attack zinc oxide, forming chemically adsorbed Zn-SR at low sulfur levels, and ZnS is formed in the highly reductive atmosphere before sulfuric species attacking copper (forming Cu₇S₄ or Cu₃₁S₁₆).     

Removal of sulfur compounds from utility pipelined synthetic natural gas using modified activated carbons

Synthetic natural gas (SNG), which is produced from petroleum and distributed via pipeline in Honolulu by The Gas Company, was analyzed using a gas chromatograph equipped with a sulfur chemiluminescence detector (GC/SCD). Hydrogen sulfide (H₂S), methyl mercaptan (MM), ethyl mercaptan (EM), dimethylsulfide (DMS), dimethyl disulfide (DMDS), tetrahydrothiophene (THT), ethyl disulfide (EDS), and one unidentified compound (UN1) were detected. Among these sulfur compounds, THT is added as an odorant and was present in the highest concentration.A commercial activated carbon (Calgon OLC plus 12X30) was modified by oxidation and impregnation methods and the resulting materials were evaluated for their ability to adsorb sulfur compounds present in SNG. The evaluation results indicate that all of the modification methods can improve the retention of individual sulfur compounds or the total sulfur capacity compared with the untreated virgin carbon. It is also found that activated carbons impregnated with metal impurities have different selectivity for sulfur compounds. Cu and Zn loaded carbons had the highest capacity for H₂S removal, Fe loaded carbon was more efficient for DMS removal (the most difficult S compound to remove), and carbon oxidized by HNO₃ was the best for THT removal.Based on these findings, a composite sorbent consisting of Cu loaded and Fe loaded carbons was designed and tested. The test results indicate that the composite sorbent had improved performance in the removal of individual sulfur compound. A linear programming model was used to design a composite sorbent optimized to minimize the required sorbent mass based on a 1-kW scale fuel cell system service target. Validation tests showed that the optimized sorbent required less of the individual modified carbon components than when they were individually used for the same sulfur removal target.     

Sulfur addition to aldimines: thioamides,not thiaziridines,as products; revision of an old report

The reaction of 4-(phenylimino)butan-2-ol with ammonium polysulfide in refluxing EtOH yields 3-hydroxy-N-phenylbutanethioamide as the only isolated product. The structure has been established by single-crystal X-ray diffraction. Treatment of N-benzylidenamines with ammonium polysulfide has proven a general method for the preparation of thiobenzamides.     

Characterization and suitability of polyphenols-based formulas to replace sulfur dioxide for storage of sparkling white wine

The sparkling wine protection against air is of interest for maintaining its sensorial profile and it is achieved through the use of antioxidants while disgorging. Sulfur dioxide (SO₂) is commonly added, but its amount should be limited due to human health problems. The suitability of three polyphenols-based commercial formulas containing plant gallic and ellagic acids extracted from grape (Vitis vinifera L.) (AO1), plant ellagic acid and gum arabic (AO2), and plant gallic, ellagic acids and Saccharomyces cerevisiae cell-wall fractions (AO3) was evaluated after 7 months storage (at 15 °C and 25 °C) of disgorged sparkling white wine. The phenolic composition of these formulas was investigated through spectrophotometric measurements. Moreover, the phenols were characterized and quantified by HPLC-MS analyses. The sotolon concentration and the absorbance values at 420 nm were determined in wines. The HPLC-MS analysis showed that the formula AO1 mainly contained gallotannins, ellagic tannins and flavan-3-ols, while AO2 had high levels of flavan-3-ols and gallotannins. Flavan-3-ols were the only phenols found in AO3. The addition of these formulas increased the yellow hue. Sotolon was higher than the perception threshold in the samples with AO2 and at trace amount in the samples with both AO1 and AO3 only stored at 25 °C. The tested antioxidant formulas seemed to be less effective of SO₂ for the storage of sparkling white wine. However, the investigation of phenolics in antioxidant formulas could be helpful for the proper choice of a potential substitute of SO₂ due to increase interest in sulfur-free wine production.     

Relation of anodic and cathodic performance to pH variations in membraneless microbial fuel cells

One-compartment (membraneless) microbial fuel cells (MFCs) are effective tools to test new bio-technology at a laboratory level. More efforts in MFC design and materials are necessary to move from laboratory tests to real applications.     

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase Mercury Removal

Sulfur was impregnated onto activated carbon fibers (ACFs) through H2S oxidation catalyzed by the sorbent surface in a fixed-bed reactor. By changing the temperature and duration of the sulfur impregnation process, ACFs with different sulfur contents were developed. Characterization of ACFs before and after sulfur impregnation was conducted by surface area analysis, energy dispersive X-ray analysis, thermogravimetric analysis, X-ray photoelectron spectroscopy, and temperature programmed desorption. Vapor phase mercury adsorption experiments were carried out in a fixed-bed reactor. Sulfur was impregnated mainly as elemental sulfur and the amount of sulfur deposited on the ACF increased with an increase in impregnation temperature. Higher temperature leads to more uniform sulfur distribution inside the sorbent pores. The impregnation process can be explained by a combination of pore filling and monolayer adsorption, with the former mechanism predominating at low temperatures. In the absence of sulfur, the mercury adsorption capacity can be correlated with surface area and pore volume.     

苯基异硫腈钴（I）配合物的合成与结构及性质

本文报导了三－三苯基膦氧化钴（Ｉ）与过量的异硫氰酸苯酯反应，依据快原子轰击质谱（ＦＡＢ－ＭＳ），证实生成物的结构为四员钴杂环配合物。该配合物不稳定，容易脱硫，生成苯基异腈钴（Ⅱ）配合物。     

关于如何对低硫灰口铸铁进行孕育处理的探讨

研究了低硫情况下电炉熔炼如何改进孕育效果的方法．研究表明，对含硫较低铸铁的孕育方法的改进，不一定非要通过补硫或改善孕育剂的方法来实现；通过增加原有孕育剂的数量、改进孕育方法同样能改善孕育效果．