Pore Structure and Gas Content Characteristics of Lower Jurassic Continental Shale Reservoirs in Northeast Sichuan, China.

The Jurassic shale in the northeastern Sichuan Basin is one of the main target intervals for continental shale gas exploitation. Research on the pore structure and gas-bearing properties of shales is the key issue in target interval optimization. Through core observation, geochemistry, bulk minerals, scanning electron microscopy, nitrogen adsorption, and isothermal adsorption experiments, various lithofacies with different pore structure characteristics were clarified. In addition, the factors that control gas-bearing properties were discussed, and a continental shale gas enrichment model was finally established. The results show that the Jurassic continental shale in the northeastern Sichuan Basin can be classified into six lithofacies. Organic pores, intergranular pores, interlayer pores in clay minerals, intercrystalline pores in pyrite framboids, and dissolution pores can be observed in shale samples. Pore structures varied in different shale lithofacies. The contact angle of shales is commonly less than 45°, leading to complex wettability of pores in the shales. Free gas content is mainly controlled by the organic matter (OM) content and the brittleness in the Jurassic shale. The adsorbed gas content is mainly controlled by the OM content, clay mineral type, and water saturation of the shales. The enrichment mode of the Lower Jurassic continental shale gas in the northeastern Sichuan Basin is established. Paleoenvironments control the formation of organic-rich shales in the center part of lakes. The "baffle" layer helps the confinement and high pressure, and the complex syncline controls the preservation, forming the enrichment pattern of the complex syncline-central baffle layer.

Monolithic Structure-Optical Fiber Sensor with Temperature Compensation for Pressure Measurement.

In this paper, an optical fiber pressure sensor cascading a diaphragm-assisted Fabry-Perot interferometer (FPI) and a fiber Bragg grating (FBG) is proposed and demonstrated. The sensor comprises an optical fiber, a fused-silica ferrule, and a fused-silica diaphragm. We use a femtosecond laser firstly to fabricate a pit on the end face of the ferrule and then investigate the laser heat conduction welding and deep penetration welding technology for manufacturing the seepage pressure sensor of the all-fused-silica material. We develop a sensor based on a monolithic structured FPI without adhesive bonding by means of all-laser-welding. The pressure characteristics of the sensor have good linearity at different temperatures. Also, the monolithic structured sensor possesses excellent resolution, hysteresis, and long-term stability. The environmental temperature obtained by the FBG is employed to compensate for the difference in seepage pressure at different temperatures, and the difference in seepage pressure responses at different temperatures is shown to be very small after temperature compensation.

Seismic Evidence for a Geosuture between the Yangtze and Cathaysia Blocks, South China.

South China, composed of the Yangtze and Cathaysia Blocks and the intervening Jiangnan orogenic belt, has been central to the debate on the tectonic evolution of East Asia. Here we investigate the crustal structure and composition of South China from seismic data employing the H-k stacking technique. Our results show that the composition and seismic structure of the crust in the Jiangnan orogenic belt are identical to those of the Cathaysia Block. Our data reveal a distinct contrast in the crustal structure and composition between the two flanks of the Jiujiang-Shitai buried fault. We propose that the Jiujiang-Shitai buried fault defines a geosuture between the Yangtze and Cathaysia Blocks, and that the felsic lower crust of the Cathaysia Block and the Jiangnan orogenic belt may represent fragments derived from the Gondwana supercontinent.

Synthesis of chiral aminophosphines from chiral aminoalcohols via cyclic sulfamidates.

Protic aminophosphines with multiple chiral centers were synthesized in good yields and high purity by the nucleophilic ring-opening of N-protected cyclic sulfamidates with metal phosphides, followed by hydrolysis and deprotection. This synthetic approach is clean, scalable, and high yielding. The method provides an efficient alternative route for the synthesis of chiral aminophosphines.

Aminophosphine ligands R(2)P(CH(2))(n)NH(2) and ruthenium hydrogenation catalysts RuCl(2)(R(2)P(CH(2))(n)NH(2))(2).

The aminophosphine ligands R(2)P(CH(2))(2)NH(2) and R(2)P(CH(2))(3)NH(2) (R = Ph, (i)Pr, (t)Bu) were isolated in good to excellent yields from the reaction of LiPR(2) with Cl(CH(2))(2)N(TMS)(2) and Cl(CH(2))(3)N(TMS)(2), respectively, followed by hydrolysis. This approach allows fine tuning of the ligands' stereoelectronic properties through the variation of the substituents on the phosphine. The aminophosphine ligands were used to prepare the ruthenium complexes RuCl(2)(R(2)P(CH(2))(2)NH(2))(2) and RuCl(2)(R(2)P(CH(2))(3)NH(2))(2) by reacting a 2:1 mixture of the respective ligand and [RuCl(2)(cod)](n) in an appropriate solvent. The resulting complexes were found to be excellent catalysts for the hydrogenation of ketones and imines.

Highly active iridium catalysts for the hydrogenation of ketones and aldehydes.

The pressure hydrogenation capabilities of the iridium pincer complexes IrH2Cl[((i)Pr2PC2H4)2NH] (1) and IrH3[((i)Pr2PC2H4)2NH] (2) are described and compared to related results obtained previously in transfer hydrogenation. Complex 1 was shown to act as a convenient air-stable entry point to the active catalyst 2, in the presence of base and hydrogen gas. The catalysts are active in a range of solvents, including CH2Cl2 and CHCl3, in contrast to related ruthenium systems. This class of iridium complexes is very effective for the direct hydrogenation of a wide range of carbonyl compounds including ketones, diketones, alpha,beta-unsaturated ketones and aldehydes. A catalytic cycle is proposed for this system which involves an ionic heterolytic bifunctional hydrogenation mechanism.

A modular design of ruthenium catalysts with diamine and BINOL-derived phosphinite ligands that are enantiomerically-matched for the effective asymmetric transfer hydrogenation of simple ketones.

A method is reported for making a potentially very wide series of ruthenium hydrido chloro complexes with diamine and readily-prepared diphosphinite ligand modules as precatalysts for the asymmetric transfer hydrogenation of simple ketones to give chiral alcohols in good yield and enantioselectivity.

Applications of ruthenium hydride borohydride complexes containing phosphinite and diamine ligands to asymmetric catalytic reactions.

[reaction: see text] A series of novel trans-ruthenium hydride borohydride complexes with chiral phosphinite and diamine ligands were synthesized. They can be used in the asymmetric transfer hydrogenation of aryl ketones, including base-sensitive ones, to give chiral alcohols in moderate to good enantioselectivities (up to 94% ee). They are also efficient catalysts for the Michael addition of malonates to enones with enantioselectivities of up to 90%. This kind of catalyst allows a one-pot tandem Michael addition/H(2) hydrogenation protocol to build structures with multiple chiral centers.

Ru-catalyzed highly enantioselective hydrogenation of beta-alkyl-substituted beta-(acylamino)acrylates.

Highly enantioselective hydrogenation of beta-alkyl-substituted (E)-beta-(acylamino)-acrylates catalyzed by Ru((R)-Xyl-P-Phos)(C(6)H(6))Cl(2) complex (cat. 1c) was achieved in up to 99.7% ee. Moderate to good enantioselectivities in the hydrogenation of corresponding (Z)-isomers in the presence of [Rh((R)-Xyl-P-Phos)(COD)]BF(4) (cat. 2c) were also obtained. The results demonstrated that the electronic and steric properties of the dipyridylphosphine ligands as well as the different transition metal ions have significant influences on the catalytic properties in the hydrogenation of beta-(acylamino)acrylates.