Enantio-selective preparation of (S)-1-phenylethanol by a novel marine GDSL lipase MT6 with reverse stereo-selectivity

We previously functionally characterized a novel marine microbial GDSL lipase MT6 and identified that the stereo-selectivity of MT6 was opposite to that of other common lipases in trans-esterification reactions.Herein,we have investigated the use of MT6 in stereo-selective biocatalysis through direct hydrolysis reactions.Notably,the stereo-selectivity of MT6 was also demonstrated to be opposite to that of other common lipases in hydrolysis reactions.Parameters,including temperature,organic co-solvents,pH,ionic strength,catalyst loading,substrate concentration,and reaction time,affecting the enzymatic resolution of racemic 1-phenylethyl acetate were further investigated,with the e.e.of the final（S）-l-Phenylethanol product and the conversion being 97%and 28.5%,respectively,after process optimization.The lengths of side chains of 1-phenylethyl esters greatly affected the stereo-selectivity and conversion during kinetic resolutions.MT6 is a novel marine microbial GDSL lipase exhibiting opposite stereo-selectivities than other common lipases in both trans-esterification reactions and hydrolysis reactions.

Effects of Main Parameters on Rheological Properties of Oil-Coal Slurry

Oil-coal slurry prepared in coal direct liquefaction is a dispersed solid-liquid suspension system. In this paper, some factors such as solvent properties, solid concentrations and temperatures, which affect viscosity change of oil-coal slurry, were studied. The viscosity of coal slurry was measured using rotary viscometer, and the rheological properties have been investigated. The viscosity and rheological curves were plotted and regressed, respectively. The results show that the coal slurry behaves a pseudoplastic and thixotropic property. The rheological type of coal slurry was ascertained and its rheological equations were educed. The oil-coal slurry changes to non-Newtonian fluid from Newtonian fluid with the increasing of solid concentration.

Directed Molecular Evolution of Nitrite Oxido-reductase by DNA-shuffling

Objective To devellop directly molecular evolution Of nitrite oxido-reductase using DNA-shuffling technique because nitrobacteria grow extremelly slow and are unable to nitrify effectively inorganic nitrogen in wastewater treatmem. Methods The norB gene coding the ntitrite oxido-reductase in nitrobacteria was cloned and sequenced. Then, directed molecular evolution of nitrite oxido-reductase was developed by DNA-shuffling of 15 norB genes from different nitrobacteria. Results After DNA-shuffling with sexual PeR and staggered extension process PCR, the sequence was differem from its parental DNA fragmems and the homology ranged from 98% to 99%. The maximum nitrification rate of the modified bacterium of X16 by DNA-shuffling was up to 42.9 mg/L.d, which was almost 10 times higher than that of its parental bacteria. Furthermore, the modified bacterium had the same characteristics of its parental bacteria of E. coli and could grow rapidly in normal cultures. Conclusion DNA-shuffling was successfully used to engineer E. coli, which had norB gene and could degrade inorganic nitrogen effectively.

Effects of different factors during the de-silication of diaspore by direct flotation

Most of the bauxite resources in China are kaolinite-diaspore bauxite of middle to low grade, with a fine dissemination, and are difficultly separated. Direct flotation de-silication has been shown to be an effec- tive method for de-silication of diaspore. In this study the effect of different factors, including pulp tem- perature, density, pH value, depressant, and collector dosage, on direct flotation of diaspore were investigated by laboratory experiments. The optimum conditions were identified and the flotation perfor- mance was improved. The results show that under optimum conditions （a pulp temperature around 40℃, a pulp density from 30% to 33g, a pH value from 9.0 to 10.0, an air flow rate of 0.5 m3/（m2 rain）, a dispersant level from 35 to 70 g/t, and a collector level around 1000 g/t） an AI/Si ratio of 6.97 is obtained starting from an initial Al/Si ratio of about 4.71. The recovery of A1203 under these conditions was 86.94%.

Direct Z-scheme photochemical hybrid systems:Loading porphyrin-based metal-organic cages on graphitic-C_(3)N_(4) to dramatically enhance photocatalytic hydrogen evolution

The rational design of photochemical molecular device(PMD)and its hybrid system has great potential in improving the activity of photocatalytic hydrogen production.A series of Pd6L3 type metal-organic cages,denoted as MOC-Py-M(M=H,Cu,and Zn),are designed for PMDs by combining metalloporphyrin-based ligands with catalytically active Pd^(2+)centers.These metal-organic cages(MOCs)are first successfully hybridized with graphitic carbon nitride(g-C_(3)N_(4))to form direct Z-scheme heterogeneous MOC-Py-M/g-C_(3)N_(4)(M=H,Cu,and Zn)photocatalysts via π-πinteractions.Benefiting from its better light absorption ability,the MOC-Py-Zn/g-C_(3)N_(4) catalyst exhibits high H_(2) production activity under visible light(10348μmol g^(-1) h^(-1)),far superior to MOC-Py-H/g-C_(3)N_(4) and MOC-Py-Cu/g-C_(3)N_(4).Moreover,the MOC-Py-Zn/g-C_(3)N_(4) system obtains an enhanced turn over number(TON)value of 32616 within 100 h,outperforming the homogenous MOC-Py-Zn(TON of 507 within 100 h),which is one of the highest photochemical hybrid systems based on MOC for visible-light-driven hydrogen generation.This confirms the direct Z-scheme heterostructure can promote effective charge transfer,expand the visible light absorption region,and protect the cages from decomposition in MOC-Py-Zn/g-C_(3)N_(4).This work presents a creative example that direct Z-scheme PMD-based systems for effective and persistent hydrogen generation from water under visible light are obtained by heterogenization approach using homogeneous porphyrin-based MOCs and g-C_(3)N_(4) semiconductors.

Efficiency of Land Utilizationand Urbanization Progress of China

Urbanization is a process that is undergoing all over the world, which will speed up in the forthcoming years, especially in China as the boom of economy. On average, urbanization level is not only depended on the speed, but theefficiency, particularly efficiency of using land resource which affects urbanization directly. This paper provided status quo of land resource utilization efficiency, indictors, methods and factors, and illustrated the reference of well land utilization, aiming at fostering urbanization in China.

Treatment of methanol wastewater with two-stage and two-phase anaerobic process

The two-stage and two-phase anaerobic process (TSTP) composed of hydrolytic acidification reactor,first-order and second-order external circulation anaerobic reactors (EC) was taken to treat methanol wastewater. Test results show that TSTP process is quick start-up in 51 d, and the maximum VFA of hydrolytic acidification reactor effluent reaches 876 mg/L. Under the condition of volume loading of 6.56 kgCOD/m3·d, COD removal rate of the first-order EC reactor is about 85%, and under the condition of volume loading of 1.02 kgCOD/m3·d, COD removal rate of the second-order EC reactor is about 50%. When the inflow COD of TSTP process is between 7000-11000 mg/L, its effluent COD is lower than 600 mg/L. In the biological conversion process of methanol into methane,the production of acetic acids as an intermediate product can be ignored and the direct production of methane from methanol is predominant.

水化条件对La_2O_3水化特性的影响

针对我国目前La(OH)_3粉体制备工艺复杂、能耗大、成本高等特点,以La_2O_3为原料,研究了采用直接水化法制备La(OH)_3粉体的工艺过程,考察了不同水化条件对水化过程和转化率的影响;分析了不同水化条件下水化过程中温升曲线和转化率的变化;提出了La_2O_3直接水化制备La(OH)_3合理工艺条件。实现了整个工艺过程无废、低能耗、低成本、连续化和清洁化。

Mechanocaloric materials for solid-state cooling

This article reviews the up-to-date progress in mechanocaloric effect and materials near ambient temperature. For elastocaloric materials, we focus on directly measured temperature change and its entropy origin in nonmagnetic and magnetic shape memory alloys. In terms of barocaloric materials, change in magnetic state, volume and shift of transition temperature due to hydrostatic pressure are systematically compared. We propose advantages and challenges of elastocaloric materials for solidstate cooling. Strategies to enhance elastocaloric and mechanical stability under long-term mechanical cycles are presented. Finally, we conclude with an outlook on the prospect of elastocaloric cooling application.