群体感应抑制控制膜生物污染的研究进展

水中微生物及其代谢产物沉积吸附在膜表面,进而生长繁殖,形成了膜生物污染。膜生物污染的控制已经成为学者们研究的热点之一,而基于驱散群体感应体系对膜生物污染进行控制是国内外新兴的研究课题之一。本文综述了传统的膜生物污染控制方法,并阐述了基于驱散群体感应体系控制膜生物污染的研究新进展,并提出前景展望。     

牛田洋生产基地水产养殖的水质净化技术研发

牛田洋生产基地水产养殖的水质,经过研究和检测,其溶解氧、BOD,及Cr、Cd、Ph、Zn等金属离子的质量浓度,超过《渔业水质标准》（GB11607—89）的几十倍甚至几百倍,其水质远远低于渔业水质标准,从而大大影响了牛田洋区域的水产品产量和质量。针对牛田洋的水质情况以及现有养殖水质的净化技术,提出以下两种解决方案：一是植物净化法,在鱼塘内种植芦荻、茭白以及沉水植物轮叶黑藻、金鱼藻等来净化鱼塘水。二是采用水质净化的组合工艺：网栏（格筛）-混凝沉降（PAC＋PFS=I：1）-生物膜（生物滤池,塑料滤料）-后混凝沉降（PAC＋PFS=1：1）-砂滤（石英砂）-消毒（漂白粉）。     

无线传感器网络中一种基于覆盖的环簇路由算法

提出了一种基于覆盖的环簇路由算法CRAC。该算法利用Sink节点以广播环域坐标的方式将网络分为若干环域,并根据应用需求的服务质量计算各环域的覆盖划分以确定轮换簇,各轮换簇交替休眠以降低网络能耗。网络各环域根据能耗均衡方程确定其是否为发送环,将采集的数据并行传送到传输路径后汇聚至发送环,再由LEADER节点发送至Sink节点。仿真实验结果表明,该算法大幅度降低了网络的通信时延和能耗,延长了网络的生存时间,使节点能量均衡下降。     

绿色合成分子筛的研究进展

分子筛由于具有规则的孔道结构、适宜的酸性、良好的热和水热稳定性等特点,广泛应用于吸附、分离、离子交换及催化等领域。传统水热法制备分子筛因需要使用大量溶剂和有机模板剂,存在合成效率低、生产成本高、污染环境等一系列问题。近年来,随着"绿色化学"理念的深入人心,开发绿色、可持续的分子筛制备路线备受关注,逐渐成为该领域的研究热点。本文主要从水热法、离子热法、干胶法以及无溶剂法等几个方面,对国内外分子筛绿色合成的最新研究进展进行综述,并归纳比较上述合成方法的优缺点。最后,提出目前绿色合成分子筛过程中存在的问题,展望其未来发展前景。     

Tunable structure and intensive upconversion photoluminescence for Ho3+-Yb3+ codoped bismuth titanate composite synthesized by sol-gel-combustion (SGC) method

Ho³⁺ and Yb³⁺ codoped bismuth titanate (BTO) composite powders with infrared to visible upconversion luminescence (UCL) function were prepared by SGC method. The effects of Ho³⁺ and Yb³⁺ doping content on the structure and property were investigated for BTO: xHo, 0.2 Yb (x = 0, 0.02, 0.04, 0.06, 0.08, 0.1) and BTO: 0.02Ho, yYb (y = 0.1, 0.2, 0.3, 0.5, 0.7, 0.9) samples. All the samples include three bismuth titanate phases (Bi₄Ti₃O₁₂, Bi₂Ti₂O₇, and Bi₂₀TiO₃₂), and the phase proportion can be tuned by changing Ho³⁺ and Yb³⁺ doping content. These powders are well crystalized with honeycomb-like microscopic structure, and with good absorption for 233 nm, 310 nm and 975 nm wavelength. The band gap can be tuned from 3.53 eV to 4.03 eV when increasing Yb³⁺ content from y = 0 to y = 0.9. A strong 530–580 nm green emission band and a relative weak 630–690 nm red one corresponding to Ho³⁺: ⁵S₂ → ⁵I₈ and ⁵F₅ → ⁵I₈ transitions appear in the UCL spectra for all the BTO: Ho, Yb samples when pumped at 980 nm. The emission intensities can well be tuned with various Ho³⁺ and Yb³⁺ content. The optimal UCL was obtained in BTO: 0.02Ho, 0.5 Yb for all the prepared samples. The energy transfer mechanism is analyzed by building a two-photon energy transfer model, which is proved by the relationship between emission intensities and pumping power measurement. The concentration quenching of Ho³⁺ is caused by cross relaxation of CR₁ and CR₂ (Ho: ⁵F₄, ⁵S₂ + ⁵I₈ → ⁵I₄ + ⁵I₇) and by CR₃ (Ho: ⁵F₄, ⁵S₂ + Yb: ²F_7/2 → Ho: ⁵I₆ + Yb: ²F_5/2) for Yb³⁺ quenching. The mean luminescence lifetime (τ_m) from Ho: ⁵S₂ decreases monotonously with the increase of Ho³⁺ and Yb³⁺ content.     

Insight into the vacancy effects on mechanical and electronic properties of Tantalum Silicide

The effects of the vacancies on the structural stability, elastic constants, elastic moduli, brittle-to-ductile transition and electronic properties of Tantalum Silicide (TaSi₂) are investigated in detail by first-principles calculations. The values of vacancy formation energy confirm that the perfect TaSi₂ and TaSi₂ with different atomic vacancies can exhibit the structural stability at ground state. It is found that Ta atom vacancies are more stable than Si atom vacancies in TaSi₂ with vacancies. The elastic constants and elastic moduli describe the mechanical behavior for TaSi₂ and TaSi₂ with vacancies. The different atomic vacancies weaken the elastic stiffness for TaSi₂. But the values of B/G confirm that the brittle-to-ductile transition occurs with different atomic vacancies for TaSi₂. Although these vacancies make the shear and volume deformation resistance of TaSi₂ weaker, they obviously improve the brittle behavior of TaSi₂. The difference charge density and electronic structures are calculated to discuss and analyze the structural stability and mechanical properties for the perfect TaSi₂ and TaSi₂ with vacancies.     

Effect of K2O content on breakdown strength and energy-storage density in K2O-BaO-Nb2O5-SiO2 glass-ceramics

Phase evolution, dielectric properties, breakdown strength, and energy-storage performance were studied by varying K₂O content in K₂O-BaO-Nb₂O₅-SiO₂ glass-ceramics. It was found that dielectric loss with the increase of K₂O content increases owing to the un-crystallized K₂O into the glass network, while dielectric breakdown strength firstly increases and then decreases due to the competition between two physical mechanisms, i.e., interfacial polarization and bridging-oxygen bond broken by the non-bridging oxygen ions. With the increase of K₂O content, energy-storage density firstly increased up to 12.06±0.69 J/cm³ with a high breakdown strength of 1973 kV/cm, and then decreased. Also, the discharged efficiency is obtained as a high value of 92% from P-E hysteresis loops.     

Functional Characteristics of Oleogel Prepared from Sunflower Oil with β-Sitosterol and Stearic Acid

β‐Sitosterol (Sit) and stearic acid (SA) were combined at varying ratios (w/w) and added to sunflower oil (SFO) at the concentration of 20 g/100 g oil for preparing edible fat‐like oleogel. The oleogel was characterized using an optical microscope, Fourier transform infrared spectroscopy (FTIR), X‐ray diffractometer (XRD), differential scanning calorimeter, and texture analyzer. The oil‐binding capacity, melting temperature, and firmness of the oleogel increased with the increase in the amount of SA in the gelator combination (Sit:SA, w/w). The microscopic analysis showed that the gel network formed based on the crystallization and self‐organization of gelator molecules, and both gelators showed an independent crystalline behavior in the oleogel. In addition, the FTIR spectra showed that the gel network formed via physical entanglements and was stabilized by non‐covalent interactions such as hydrogen bonding. Furthermore, XRD diffraction patterns indicated high lateral packing of molecular layers in oleogel prepared with the Sit and SA combination compared with oleogel prepared with a single gelator. On the other hand, for studying the effect of varying concentrations of gelator combinations, the Sit3:SA2 (w/w) combination was added to SFO at concentrations of 10, 15, 20, 25, and 30 g/100 g oil. Specific characteristics such as the oil‐binding capacity and firmness of the oleogel improved as the concentration of the gelator combination (Sit3:SA2) increased from 10 up to 30 g/100 g oil. Therefore, it can be concluded that the saturated fat alternative oleogel can be prepared from SFO with a specific Sit and SA combination ratio and concentration.     

Structures and Properties of New Cadmium(II) and Copper(II) Metal–Organic Frameworks Based on Flexible Bridged 1,4-bi(1H-imidazol-1-yl)butane Ligand

Two new metal–organic frameworks (MOFs) based on cadmium(II) ions, 1,2-benzenedicarboxylic acid (BDC), flexible ligand 1,4-bi(1H-imidazol-1-yl)butane (BIIM), coordinated water molecules, [(BIIM)(BDC)(H₂O)Cd]_3n (1) and copper(II) ions, BIIM, coordinated water, free thiophene-2,5-dicarboxylate (TDC), free water, {[(BIIM)₄(H₂O)₄Cu₂]·(TDC)₂·(H₂O)₁₂}_n (2) are prepared and characterized by X-ray diffraction, thermal gravimetric analysis (TGA), infrared (IR) spectrum and the photoluminescence property for complex (1). The X-ray diffraction analysis reveals that the structures of complexes 1 and 2 are 2D structures through the C–H···π stacking interactions (for 1) and the BIIM bridging connections (for 2). The IR spectrum for 1 and 2 are presented in the paper, for 1, the strong peaks at 1399 and 1573 cm^?1 are owing to the carboxylic CO₂ ^? symmetry and asymmetry stretching vibrations of BDC. The features of the IR spectrum are consistent with the single crystal structures. The TGA reveal the water is the first lost material from complex, then the ligands removed, and finally the residues of these two complexes are the metal oxide.     

Preparation and Characterization of K_n|Ga(H_2O)MW_(11)O_(39)|·xH_2O

In this paper the heteropoly complexes K_n[Ga(H_20)MW_(11)O_39)]·xH_20 [M=Cu(Ⅱ), Co(Ⅱ), Cr(Ⅲ),Fe(Ⅲ), Mn(Ⅳ)] have been prepared in this laboratory firstly. The products were characterized by chemicalanalysis, ionexchange, IR, UV and X-ray powder diffraction.