Enantioselective Additions of Aryltitanium Tris(isopropoxide) to Ketones: Structure of [(i‐PrO)2Ti{μ‐(S)‐BINOLate}(μ‐O‐i‐Pr)TiPh(O‐i‐Pr)2], Study of Mechanistic and Stereochemical Insights

Aryl addition reactions of ArTi(O‐i‐Pr)₃ to aromatic, heteroaromatic, or α,β‐unsaturated ketones are described, producing tertiary alcohols in good to excellent enantioselectivities of up to 97% ee. The structure of the dititanium complex [(i‐PrO)₂Ti{μ‐(S)‐BINOLate}(μ‐O‐i‐Pr)TiPh(O‐i‐Pr)₂] [(S)‐ 4 ] that simultaneously bears a chiral directing ligand and a nucleophile is reported. Complex (S)‐ 4 possesses a pocket structure and has been illustrated as the key active species for addition reactions of both aldehydes and ketones. Mechanistic and stereochemical insights concerning addition reactions of organometallic reagents to organic carbonyls are rationalized based on the pocket structure and pocket size of (S)‐ 4 .     

Enhancement of Palmarumycins C12 and C13 Production in Liquid Culture of Endophytic Fungus Berkleasmium sp. Dzf12 after Treatments with Metal Ions

The influences of eight metal ions (i.e., Na⁺, Ca²⁺, Ag⁺, Co²⁺, Cu²⁺, Al³⁺, Zn²⁺, and Mn⁴⁺) on mycelia growth and palmarumycins C₁₂ and C₁₃ production in liquid culture of the endophytic fungus Berkleasmium sp. Dzf12 were investigated. Three metal ions, Ca²⁺, Cu²⁺ and Al³⁺ were exhibited as the most effective to enhance mycelia growth and palmarumycin production. When calcium ion (Ca²⁺) was applied to the medium at 10.0 mmol/L on day 3, copper ion (Cu²⁺) to the medium at 1.0 mmol/L on day 3, aluminum ion (Al³⁺) to the medium at 2.0 mmol/L on day 6, the maximal yields of palmarumycins C₁₂ plus C₁₃ were obtained as 137.57 mg/L, 146.28 mg/L and 156.77 mg/L, which were 3.94-fold, 4.19-fold and 4.49-fold in comparison with that (34.91 mg/L) of the control, respectively. Al³⁺ favored palmarumycin C₁₂ production when its concentration was higher than 4 mmol/L. Ca²⁺ had an improving effect on mycelia growth of Berkleasmium sp. Dzf12. The combination effects of Ca²⁺, Cu²⁺ and Al³⁺ on palmarumycin C₁₃ production were further studied by employing a statistical method based on the central composite design (CCD) and response surface methodology (RSM). By solving the quadratic regression equation between palmarumycin C₁₃ and three metal ions, the optimal concentrations of Ca²⁺, Cu²⁺ and Al³⁺ in medium for palmarumycin C₁₃ production were determined as 7.58, 1.36 and 2.05 mmol/L, respectively. Under the optimum conditions, the predicted maximum palmarumycin C₁₃ yield reached 208.49 mg/L. By optimizing the combination of Ca²⁺, Cu²⁺ and Al³⁺ in medium, palmarumycin C₁₃ yield was increased to 203.85 mg/L, which was 6.00-fold in comparison with that (33.98 mg/L) in the original basal medium. The results indicate that appropriate metal ions (i.e., Ca²⁺, Cu²⁺ and Al³⁺) could enhance palmarumycin production. Application of the metal ions should be an effective strategy for palmarumycin production in liquid culture of the endophytic fungus Berkleasmium sp. Dzf12.     

Design of a europium-activated lithium-silicate cyan phosphor via cation substitution

Lithium-containing silicates have been considered as a considerable alternative for luminescent materials. In this study, a novel cyan-emitting phosphor, Na₃LiHf₂Si₃O₁₂: Eu²⁺, was successfully synthesized via cationic substitution with Na₄Hf₂Si₃O₁₂: Eu²⁺ as the initial model. The crystal structure, morphology, and luminescence performance of Na_4-xLi_xHf₂Si₃O₁₂: Eu²⁺ were investigated in detail. The substitution of Li⁺ for Na⁺ site causes a significant blue-shift of the emission band in the range of 550–500 nm and a smaller full width at half maximum. As a result, a cyan phosphor Na₃LiHf₂Si₃O₁₂: Eu²⁺ that can be effectively excited by near-ultraviolet and high-energy beams is obtained. The mechanism of emission regulation was proposed based on the transformation of crystal structure and luminescence performance. In addition, the thermal quenching and cathodoluminescence behaviors were also studied. The results show that cation substitution is an effective method to design new lithium-containing silicate phosphors.     

Metal modified (Ni,Ce, Ta) Ti/SnO2–Sb2O5–RuO2 electrodes for enhanced electrochemical degradation of Orange G

Journal of Applied Electrochemistry - Ni, Ce, and Ta modified Ti/SnO2–Sb2O5–RuO2 anodes were first prepared by thermal decomposition strategy and applied for Orange G degradation to...     

Rheology,mechanical, and thermal properties of core–shell silicon-acrylic copolymer emulsion films and its application on surface sizing: role of silane coupling agent

With the assistance of polymerisable maleate surfactant and costabilizer, core–shell emulsions with poly(butyl acrylate) core (PBA) and poly(butyl acrylate–styrene–methacryloxypropyl trimethoxysilane) shell (PSBM) were prepared through seeded emulsion polymerization. Effects of MPTS on rheological, mechanical, and thermal properties were investigated. Simultaneously, the emulsions were utilized as paper surface sizing agents, and corresponding properties were studied. It was found that the emulsion possessed viscoelastistic nature and changed from viscous to elastic with MPTS addition. At the same time, enhanced internal network strength among particles was detected, which was weakened when MPTS concentration was 8%. The tensile strength and thermal stability of copolymer films were therefore increased accordingly. However, decrease in tensile strength, elongation at break and thermal properties was observed with higher MPTS concentration due to weakened interaction among different shells. It was also found that glass transition temperature (T _g) did not influence greatly by MPTS, and two phases corresponding to core and shell copolymer were observed with low degree of microphase separation. Furthermore, the interaction between polymer and fiber was improved, resulting in improved sizing degree, ring crush strength, surface strength, and folding strength. While the surface strength and folding endurance decreased due to the increase of brittleness with higher crosslinking degree.     

速溶高蛋白花生晶的研制

本文根据营养学原理及水剂法花生加工工艺研制优质营养食品。利用花生、蔗糖等原料生产速溶高蛋白花生晶,这是一种优质、新型的植物蛋白饮料。本文详细地介绍了速溶高蛋白花生晶研制的理论依据,生产配方及方法。     

永磁直驱型风电机组两类故障的穿越技术

为了提高永磁直驱型风电机组的并网性能,分析永磁直驱型风电机组的基本结构,讨论应用于永磁直驱型风电机组的各种低电压穿越技术,变桨距控制,增加功率开关器件的额定容量,网侧加装辅助变流器,STATCOM运行模式控制,不同位置加装撬棒Crowbar耗能元件,加装超级电容器,储能电池或超级电容器与储能电池组合,连接点出现事故性不对称故障时,改进网侧变流器的控制策略,配合撬棒Crowbar保护电路控制机组的功率平衡,实现不对称故障穿越。文中分析的各种故障穿越技术为后续永磁直驱型风电机组并网能力的提高有一定的理论指导。     

某新建污水处理站环境影响分析

以某污水处理工程站为例,为了污水达标排放,满足公司可持续发展要求,促进经济、社会和环境的协调发展,在分析该项目的特点的基础上,对新建污水处理站的清洁生产及环境经济损益进行评价,并提出了有效的减轻环境影响的对策措施,为污水处理站建设项目环境影响评价提供参考。     

Preparation and characterization of biodegradable polymer blends from poly(3‐hydroxybutyrate)/poly(vinyl acetate)‐modified corn starch

Biodegradable polymer blends prepared by blending poly(3‐hydroxybutyrate) (PHB) and corn starch do not form intact films due to their incompatibility and brittle behavior. For improving their compatibility and flexibility, poly(vinyl acetate) (PVAc) was grafted from the corn starch to prepare the PVAc‐modified corn starch (CSV). The resulting CSV consisted of 47.2 wt% starch‐g‐PVAc copolymer and 52.8 wt% PVAc homopolymer and its structure was verified by FT‐IR analysis. In comparison with 35°C of the neat PVAc, the glass transition temperature (T_g) of the grafted PVAc chains on starch‐g‐PVAc was higher at 44°C because of the hindered molecular mobility imposed from starch on the grafted PVAc. After blending PHB with the CSV, structure and thermal properties of the blends were investigated. Only a single T_g was found for all the PHB/CSV blends and increased with increasing the CSV content. The T_g‐composition dependence of the PHB/CSV blends was well‐fitted with the Gordon‐Taylor equation, indicating that the CSV was compatible with the PHB. In addition, the presence of the CSV could raise the thermal stability of the PHB component. It was also found that the presence of the PHB and PVAc components would not hinder the enzymatic degradation of the corn starch by α‐amylase. POLYM. ENG. SCI., 55:1321–1329, 2015. © 2015 Society of Plastics Engineers     

Circulating Organ-Specific MicroRNAs Serve as Biomarkers in Organ-Specific Diseases: Implications for Organ Allo- and Xeno-Transplantation

Different cell types possess different miRNA expression profiles, and cell/tissue/organ-specific miRNAs (or profiles) indicate different diseases. Circulating miRNA is either actively secreted by living cells or passively released during cell death. Circulating cell/tissue/organ-specific miRNA may serve as a non-invasive biomarker for allo- or xeno-transplantation to monitor organ survival and immune rejection. In this review, we summarize the proof of concept that circulating organ-specific miRNAs serve as non-invasive biomarkers for a wide spectrum of clinical organ-specific manifestations such as liver-related disease, heart-related disease, kidney-related disease, and lung-related disease. Furthermore, we summarize how circulating organ-specific miRNAs may have advantages over conventional methods for monitoring immune rejection in organ transplantation. Finally, we discuss the implications and challenges of applying miRNA to monitor organ survival and immune rejection in allo- or xeno-transplantation.