A Comparative Study of Electrochemical Kinetic Parameters by the Potential Step Method. Electrode Reactions of CyDTA and EDTA Complexes of Cu(II) at DME

By using the same current-time (I-t) curves, electrochemical kinetic parameters are determined by two methods, (a) using the ratio of current at a given potential to the diffusion-controlled limiting current and (b) curve fitting method, for the reduction of Cu(II)–CyDTA complex. The analysis by the method (a) shows that the rate determining step involves only one electron although the overall reduction of the complex involves two electrons suggesting thereby the stepwise reduction of the complex. The nature of I-t curves suggests the adsorption of intermediate species at the electrode surface. Under these circumstances more reliable kinetic parameters can be obtained by the method (a) compared to that of (b). Similar observations are found in the case of reduction of Cu(II)–EDTA complex.

Potential of bio-DME as a transportation fuel for India

This article discusses the potential of bio-dimethyl ether (DME) as a promising fuel for India in the transportation sector where a majority of imported petroleum in the form of diesel is used. Specifically, the suitability of DME in terms of its properties vis-a-vis those of diesel, ability to liquefy DME at low pressures similar to liquefied petroleum gas (LPG), and ease of production from renewable feedstock (biomass), and most importantly, very low emissions including near-zero soot levels are some of the features that make it an attractive option. A detailed review presents the state-of-the-art on various aspects such as estimates of potential bio-DME production, methods of synthesis of bio-DME, important physicochemical properties, fuel-injection system-related concerns (both conventional and common-rail system), fuel spray characteristics which have a direct bearing on the engine performance, and finally, exhaust emissions. Future research directions covering all aspects from production to utilization are summarized (C) 2010 American Institute of Physics. doi:10.1063/1.3489529]

Preparación, caracterización y discriminación de nuevos catalizadores en el proceso de síntesis de DME

El dimetiléter (DME) es un combustible limpio que puede obtenerse a partir de fuentes alternativas al petróleo. La obtención de DME en una etapa a partir de gas de síntesis sobre un catalizador bifuncional (proceso STD) ofrece ventajas termodinámicas sobre el proceso en dos etapas (se obtienen elevados valores de conversión de CO y rendimiento de DME) y permite la coalimentación de CO2. En este trabajo se lleva a cabo la preparación, caracterización, diseño y discriminación de nuevos catalizadores bifuncionales para el proceso STD.

Excrétion organique du phytoplancton et activité bacterienne hétérotrophe dans le Dôme de Guinée (Océan Atlantique Tropical Est)

Primary production rates in the Gulf the Guinea (east tropical Atlantic) were measured with in situ incubations. The extracellular organic carbon passed through 0.8 u pore size membrane filters averaged 29.5% of the carbon fixed by photosynthesis. These is a good linear correlation (r=0.86) between assimilation and organic excretion. The significance and limits of the method for the measurements of low rates of photosynthesis is discussed. The influence of ecological factors (nutrients, light and stability) cannot be demonstrated. The importance of bacterial regeneration processes by reutilization of algal extracellular products is assessed.

Zooplancton et micronecton dans la région du Dôme d'Angola en février-mars 1971 et rélation avec les thons

Diurnal variations and geographic distribution of zooplankton and micronekton are studied in the Angola Dome. The small zooplankton species (Copepodids, Copepods, Amphipods, Ostracods, Chaetognaths, etc.) undertake vertical migrations within a 100 m water layer. Most of the micronekton species are below this layer during the day and move towards the surface during the night. The whole region prospected is rich in zooplankton and micronekton species that are present in the upper 100 m layer during the day. Only the South-West region is poor. On the contrary, this latter region is abundant in species that migrate below this layer during the day. The authors think there are 3 main difficulties in establishing good relationships between micronekton and tunas distribution: 1 - inability of micronekton nets to catch the tunas preys; 2 - the great diversity of tunas food; and 3 - the too large delay between micronekton studies and those of stomach contents of tunas.

Variabilité, circulation et chlorophylle dans la région du Dôme d'Angola en février-mars 1971

In February-March 1971 the hydrological conditions off Angola did not display the thermal dome mapped by Mazeika's averages (1967). Cold water cells observed are connected at the surface to a sinuous boundary between low-salinity coastal waters and high-salinity tropical oceanic waters. That boundary coincides rather regularly with an area where trades and SW winds alternate; photosynthesis growths rapidly in a thermoclinal layer that rises until 10 m of the surface but never outcrops. Below a poor and permanent homogeneous surface layer, chlorophyll concentrations show a distribution which is typical of divergence areas. Geostrophical and measured currents show off a transient process in horizontal and vertical movements, however the general curvature of the circulation is propitious to upwelling. Oxygen oversaturations of about 110%, suggest a moderate potential primary production which confirms slowness and alternation of movements. Also, the regular range of the various chemical and biological levels and moderate chlorophyll concentrations suggest an ecosystem where nutrients supply rapidly equilibrate phytoplankton consumption and not at all a 'phytoplankton bloom' area as that which exists in coastal upwelling. Values of Richardson's number show that instability becomes visible at the bottom of the euphotic layer. An evaluation of the vertical motion is inferred by the peculiar distribution and diurnal alternance of the winds shows that 'doming' structures may be sustained by local meteorological events.

Synthesis, crystal structure and reactivity of (2,4-C7H11)(2)Yb center dot DME

(2,4-C7H11)(2)Yb . DME was synthesized by the reaction of YbCl3 with K(2,4-C7H11)(2,4-dimethylpentadienyl potassium), and the single crystal X-ray diffraction showed that the complex exists in a cis- staggered conformation. Thf crystal of the compound belongs to the monoclinic space group P2(1)/n with a = 0.675 2 (1) nm, b = 1.490 6 (1) nm, c = 1.529 3 (2) nm, beta = 97.55 (2)degrees, V = 1.977 79 (4) nm(3), Z = 4, F(000) = 735.8 e, mu = 49.49 cm(-1), R = 0.033 and R-w = 0.032. The title complex can be used as a catalyst for the polymerization of methyl methacrylate (MMA).

Studies on organolanthanide complexes .58. Syntheses of 1,1'-(3-oxa-pentamethylene)dicyclopentadienyl divalent organolanthanides (Ln=Sm, Yb) and X-ray molecular structure of O(CH2CH2C5H4)(2)Yb(DME)

The compounds O(CH2CH2C5H4)(2)Ln(THF)(2) [Ln = Sm(1), Yb(2)] were synthesized by the reduction of O(CH2CH2C5H4)(2)LnCl with sodium metal in tetrahydrofuran (THF) at room temperature. Recrystallization of 2 from dimethoxyethane (DME) produced the single-crystal O(CH2CH2C5H4)(2)Yb(DME) (3) whose structure has been determined by an X-ray diffraction study. The crystals are orthorhombic, space group Pcab, with a = 14.168(4), b = 13.541(6), c = 19.314(8) Angstrom, Z = 8, D-calc. = 1.66 g cm(-3).

Synthesis and crystal structure of (eta(8)-C8H8)Gd(eta(5)-C6H5CH2C5H4)center dot DME

LnCl(3) reacted with C6H5CH2C5H4Na in THF (tetrahydrofuran) in the ratio 1.1 at room temperature for 1 h giving C(6)H(5)CH(2)C(6)H(4)LnCl(2) . nTHF, which reacted with C8H8K2/THF and the crystals obtained were recrystallized in DME to yield the title complex. The crystal structure of (C8H8) Ln (C6H5CH2C5H4). DME was determined revealing that the Gd complex has one conformation. One benzylcyclopentadienyl (eta(5)), one cyclooctatetraenyl (eta(8)) and the two oxygen atoms of DME (dimethoxyethane) are coordinated to Gd with the effective coordination number of 10.

配合物[Li(DME)_3][(t-BuCp)_2Nd(NPh_2)_2]·(1/2)DME的合成及晶体结构

1990年,Schumann,H.等报道了用双(环戊=烯基)稀土甲基化物与二苯胺进行交换反应制得了[Li(THF)_4][Cp_2Sm(NPh_2)_2],并测定了相应配合物镥的结构。但是,到目前为止,类似的轻稀土配合物尚未报道。这里,我们以双(叔丁基环戊二烯基)氯化钛为前体,与等当量的二苯胺基锂反应,制得了阴离子型配合物[Li(DME)_3][(t—BUCP)_2Nd(NPh_2)_2]·1/2DME,并测定了其单晶结构。

〔Li（DME）_3〕〔（η~5－MeCp）Nd（t－Bu）_3〕的合成及其对

将ＭｅＣｐＮｄＣｌ２·２ＬｉＣ１·ｎＴＨＦ和２摩尔ｔ－ＢｕＬｉ于四氢呋喃和戊烷混合溶剂中反应，合成得到一种新的阴离子型配合物〔Ｌｉ（ＤＭＥ）３〕〔（η５－ＭｅＣｐ）Ｎｄ（ｔ－Ｂｕ）３〕，用元素分析，红外光谱等作了表征，配合物溶于苯乙烯，可单独引发苯乙烯本体聚合，得无规聚苯乙烯。