摘要：On the basis of single factor tests, the effect of trace elements—Fe2+, Co2+ and Ni2+ ions—on biological methane production from heavy oil was investigated by the response surface method. A three-level Box-Behnken design was employed to study the relationship between the independent variables and the dependent variable by applying initial Fe2+, Co2+ and Ni2+ concentration as the independent variables(factors) and using the methane production after 270 days of cultivation as the dependent variable(response). A prediction model of quadramatic polynomial regression equation was obtained. The results showed that the methane production could be as high as 240.69 μmol after optimization compared with 235.74 μmol obtained under un-optimized condition. Furthermore, the microbial communities before and after biodegradation were analyzed by PCR-DGGE method. The dominant bands were recovered and sequenced. Three strains were obtained; the strain T1 has 97% similarity with Bacillus thermoamylovorans, the strain H3 has 97% similarity with Bacillus thermoamylovorans and the strain H4 has 99% similarity with Bacillus vietnamensis.

摘要：This work develops a heuristic method for the design of batch water-using networks of multiple contaminants with regeneration unit based on the concepts of concentration potential. A water-using network involving regeneration unit can be formed by adding the regenerated stream(s) into the network involving reuse only. In the design procedure of the network operated in a single batch mode, time is take n as the primary factor a nd con centration potentials as the secondary one. For the networks operated in a repeated mode, the design procedure is similar to that for continuous processes, besides designing the storage tanks with the rules proposed. Continuous regeneration unit is selected in this work. With the proposed method, the network structure corresponding to the minimum freshwater consumption can be obtained. It is shown that the method proposed in this article is simple, effective and has clear engineering meaning.

摘要：In this paper, the mixture of dimethyl carbonate, ethyl methyl carbonate and diethyl carbonate was separated by middle-vessel batch distillation with feeding in middle-vessel and process control characteristics were researched. The steady state simulation results in Aspen Plus were exported to Aspen Dynamics. Then control effect of liquid level control with HighSelector, composition control(structure1, structure2) and temperature control(proportional action, proportional integration action) were proposed. Composition control structure 2 and temperature control with PI action were investigated to achieve a good control effect.

摘要：An interesitng class of organicA-π-D-π-A dyes based on an N,N,N＇,N＇-tetraphenylbenzidine（TPD） unit as donor was designed and synthesized for dye-sensitized solar cells（DSSCs）. TPD-4-based DSSCs gave a short circuit photocurrent density（Jsc） of 16.67 mA/cm2, a open circuit voltage（Voc） of 0.635 V and a fill factor（f/） of 0.68, achieving a solar-to-electricity conversion efficiency（r/） of 7.22% in preliminary tests. The N3-sensitized device gave an η value of 8.02% with a Jsc of 18.81 mA/cm2, a Voc of 0.630 V and anffof 0.68 under the same conditions. The incident photo-to-current efficiency（IPCE） values above 70% observed in a range of 460 to 600 nm with a maximum value of 80% at 500 nm indicate that the TPD-4-based DSSC shows a high performance. Under the same conditions, the DSSC based on N3 provided the IPCE values above 70% in a range of 490 to 580 nm with a maximum value of 76% at 500 nm. Both further optimization of the device processing and structural modification of these dyes are an- ticipated to make the device give even better performances.

摘要：This paper is focused on investigation of coordination polymers constructed by Cu(II)and rigid pyridyl ligands,such as 4,4'-bipyridyl-1,2,4-triazole(Hpytz)and 1,10-phenanthroline(phen)from a mononuclear precursor[Cu(DMF)_(4)(NCS)_(2)](1).As expected,the complex was self-assembled with phen to form a 1D double-stranded chain of[Cu(phen)(μ-SCN)_(2)]∞(2),with Hpytz to form 1D zigzag chain of[Cu_(2)(μ-Hpytz)_(2)(NCS)_(2)(DMF)_(2)(μ-SCN)_(2)]∞(3)in which thiocyanate anion linked the Cu-μ-Hpytz-Cu chain into an infinite 2D network via weak Cu…S *** treat 3 with the bridged anion dca,a novel 3D framework[Cu(μ-Hpytz)(μ-dca)(μ-SCN)]∞(4)was obtained in which Cu-μ-Hpytz-Cu chain is preserved and both thiocyanate anion and dicyanamide(dca)act as bridging *** addition,complex 3 was applied as a metal catalyst in polymerization of MMA in aqueous solution at room temperature.

摘要：Tuning the electronic properties of single atom catalysts(SACs)between the central metal and the neighboring surface atoms has emerged as an efficient strategy to boost catalytic efficiency and metal *** we describe a simple and efficient approach to create atomically dispersed palladium atoms supported over defect-containing porous ceria nanorod containing palladium up to 0.26 wt.%.The existence of singly dispersed palladium atoms is confirmed by spherical aberration correction electron microscopy and extended X-ray absorption fine structure *** catalyst shows excellent efficiency in hydrodehalogenation reactions at low H2 pressure under mild conditions,along with satisfactory recyclability and *** functional theory(DFT)calculations reveal that the high activity stems from the spatial isolation of palladium atoms and the modified electronic structure of palladium confined in defect-containing ceria *** work may lay the foundation for the facile creation of single atom catalysts within the synthetic community and shed light on the possibility for scale-up production.

摘要：Chemoselective hydrodeoxygenation of vanillin is of great importance in converting biomass into high value-added ***,we describe a facile photochemical route to access palladium single atoms and clusters supported on silicoaluminophosphate-31(SAPO-31)as a highly active,chemoselective,and reusable catalyst for hydrodeoxygenation of *** by aberration-corrected high-angle annular dark-field scanning transmission electron microscopy,extended X-ray absorption fine structure measurement,and CO-absorbed diffuse reflectance infrared Fourier transform spectroscopy reveal the atomically dispersed palladium single atoms and clusters are loosely bonded and randomly dispersed,without forming strong palladium-palladium metallic bonding,over the SAPO-31 *** catalyst,with a full metal availability to the reactants,exhibits exceptional catalytic activity(TOF:3,000 h^(−1),Yield:>99%)in the hydrodeoxygenation of vanillin toward 2-methoxy-4-methylphenol(MMP)under mild conditions(1 atm,80°C,30 min),along with excellent stability,scalability(up to 100-fold),and wide substrate *** superior catalytic performance can be attributed to the synergistic effect of the positively charged palladium single atoms and fully exposed clusters,as well as the strong metal-support *** work may offer a new avenue for the design and synthesis of fully exposed metal catalysts with targeted functionalities.

摘要：Due to their capability of reversibly accepting multi lithium ions,polyoxometalates(POMs)have been widely regarded as promising candidates for electrochemical lithium ***,the insulating nature of POMs hinders fast migration kinetics of lithium within the bulk of these ***,we propose the introduction of a local electric field surrounding the POM nanoparticles consisting of Mn and V where the concomitant Coulomb forces can accelerate the migration of lithium *** rationally hybridizing POMs with MXene nanosheets,the imbalanced charge distribution emerging at their interface produces the local electric field,thereby leading to a 250-fold increase of lithium diffusion *** this regard,a capacitive contribution as high as 81.7%at 1.0 mV sis ***,the POM nanoparticles could densely assemble on the surface of MXene nanosheets,offering highly packed electrodes and thus high volumetric *** to the improved lithiumion transfer kinetics,the POMs/MXenes composites are paired with activated carbon to produce lithium-ion capacitors which could offer a high energy density of 195.5 W h kgand a large power capability of 3800 W *** findings in this work could build a clear relationship between materials with different conductivities for designing electrode materials.

摘要：高熵合金近年来在电催化领域广受关注.由于其四大“核心效应”,即高熵效应、晶格畸变效应、迟滞扩散效应和鸡尾酒效应,高熵合金在诸多电催化反应中展现出了优异的活性和选择性.然而在已报道的文献综述中,有关其优异性能的理解以及合理设计的系统性总结仍然具有局限性.本文不仅综述了高熵合金电催化剂的特点和设计准则,还对其应用的最新进展进行了系统性的归纳整理,对高熵合金未来的发展具有指导意义.首先我们从多个角度阐明了高熵合金作为一种优异电催化剂的原因,包括其出色的机械性能、可优化的结构和组成、大量具有高本征活性的活性位点,以及出色的稳定性.为了进一步深入对高熵合金电催化剂的理解,我们还从设计准则、元素选择,以及理论计算预测材料性质等角度,详细介绍了高熵合金的合理设计.随后,我们介绍了高熵合金电催化剂在电解水、有机小分子氧化、燃料电池和碳/氮基转化反应的最新研究进展,其中还包括了一系列理论计算和原位表征在理解催化反应机理方面的应用.最后,我们展望了高熵合金电催化剂在未来发展中面临的挑战和机遇.

摘要：A series of quaternary ammonium ionic liquids(ILs)were synthesized and employed as catalysts for the production of poly(isosorbide carbonate)(PIC)from diphenyl carbonate and isosorbide via a melt polycondensation *** relationship between the anions of the ILs and the catalytic activities was investigated,and the readily‐prepared IL tetraethylammonium imidazolate(TEAI)was found to exhibit the highest catalytic *** optimizing the reaction conditions,a PIC with a weight‐average molecular weight(Mw)of25600g/mol was obtained,in conjunction with an isosorbide conversion of92%.As a means of modifying the molecular flexibility and thermal properties of the PIC,poly(aliphatic diol‐co‐isosorbide carbonate)s(PAIC)s were successfully synthesized,again using TEAI,and polymers with Mw values ranging from29000to112000g/mol were obtained.13C NMR analyses determined that the PAIC specimens had random microstructures,while differential scanning calorimetry demonstrated that each of the PAICs were amorphous and had glass transition temperatures ranging from50to115°*** analyses found Td‐5%values ranging from316to332°C for these *** on these data,it is evident that the incorporation of linear or cyclohexane‐based diol repeating units changed the thermal properties of the PIC.