Quantification of response time in poly(vinyl alcohol)–metal complex thermochromic polymeric systems

Thermochromic poly(vinyl alcohol) (PVA)‐based material was synthesized and an extensive study of its thermochromic behavior with respect to response time was carried out. It was observed that it is possible to manipulate the response time by keeping control over chemical and physical parameters. The response time, which is the most important property of a smart material, has in this case been found to be very much influenced by rate of heat transfer into the material. Different compositions of the thermochromic material and their corresponding response time with respect to rate of heat transfer were studied and correlated. First, a theoretical equation was derived and later on it was experimentally verified to quantify the response time in PVA–metal complex‐based thermochromic systems. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4832–4834, 2006     

取代水杨醛Schiff碱金属配合物催化氧化脱硫性能

以水杨醛类Schiff碱为配体,与Co(NO_3)_2、Cu(NO_3)_2反应合成6种Salen(M)型配合物Ⅰ～Ⅵ。以1-己硫醇、二丁基硫醚和2-甲基噻吩为模型化合物配制模拟油体系,考察了配合物Ⅰ～Ⅵ的催化氧化脱硫性能,并分析了配合物结构与氧化脱硫性能的关系。结果表明,6种配合物在75 min时的总脱硫效果为Ⅵ>Ⅴ>Ⅳ>Ⅰ>Ⅲ>Ⅱ,Ⅵ的总脱硫率为31.9%。对1-己硫醇及二丁基硫醚脱除效果最佳的是Ⅴ,脱除率分别为74.2%和65.1%;对2-甲基噻吩脱除效果最好的是Ⅰ,脱除率为26.8%。构效关系研究表明,中心金属离子与O_2的配位能力越强,配体的共轭体系越大、电子云密度越高,配合物的脱硫性能越好;通过IR和离子色谱对单一硫化物模拟油体系氧化前后的产物进行分析发现,硫化物氧化后皆生成相应的砜类或亚砜类,且1-己硫醇和二丁基硫醚被进一步氧化生成SO_3~(2–)或SO_4~(2–)。     

金属阳极电解槽修订标准释义

对HG/T 2471-1993《隔膜法电解槽金属阳极涂层》和HG 2951-1988（原GB 9844-88）《隔膜法金属阳极电解槽制造技术条件》标准的修订版HG/T 2471-2001《电解槽金属阳极涂层》和HG/T 2951-2001《隔膜法金属阳极电解槽》进行了技术性解释。公布了按照HG/T 2471-2001《电解槽金属阳极涂层》要求对产品质量达标企业的型式检验结果。     

富氢气氛中CO的选择性氧化——碱金属助剂对Pt/γ-Al2O3催化剂性能的影响

研究了碱金属助剂对Pt/γ-Al₂O₃催化剂选择性氧化富氢气氛中CO性能的影响。结果表明，碱金属助剂的引入对Pt/γ-Al₂O₃的催化性能有不同程度的改变，其中添加Na和K后，能明显提高低温下的CO转化率。     

Microwave assisted ultrafast synthesis of graphene oxide based magnetic nano composite for environmental remediation

We have successfully synthesized multi-layer graphene oxide and graphene oxide based magnetic nanocomposite (M/GO) by microwave-assisted modified Hummers’ method for removal of toxic lead (Pb²⁺) and cadmium (Cd²⁺) ions from aqueous solution. The X-ray diffraction spectra of synthesized graphene oxide and M/GO confirm increased interlayer spacing along c-axis. Raman spectra revealed the good quality of synthesized GO and M/GO. The wrinkles were seen in the SEM images of synthesized graphene oxide. The presence of conjugated double bond (CC) and carbonyl (CO) were confirmed by using the UV–Vis spectroscopic spectra. Brunauer–Emmett–Teller (BET) analysis showed high (126 m²/g) surface area M/GO composite which accounts for large number of active binding sites for the adsorption of heavy metal ions. The adsorption studies revealed that Pb²⁺ ions were efficiently adsorbed on GO sheets. Interestingly, M/GO showed better adsorption for cadmium ions.     

罩面金属氟碳涂料的配方设计及应用

介绍了氟碳金属涂料和氟碳罩面清漆的参考配方、生产工艺,探讨了罩面金属氟碳涂料配方的设计及喷涂效果,表明金属氟碳漆罩清漆效果良。     

我国木质素油田化学品的发展现状

本文综述了我国木质素类（碱木质素或木质素磺酸盐）油田化学品的最新进展，其中包括钻井液处理剂、油井水泥添加剂、堵水剂、调剖剂、稠油降粘剂和表面活性剂驱油的牺牲剂。目前我国木质素类堵水剂、调剖剂和稠油降粘剂的研究和应用方面已达到或超过世界先进水平，改性木质素磺酸盐的研究也接近国际先进水平，但钻井处理剂和水泥添加剂仅为美国的1／9，许多木质素化学品仍为空白。因此，这些油田化学品仍然是吸引人去研究的课题，期望不久的将来会有较大的进展。     

基于优进策略的遗传算法对重油热解模型参数的估计

针对常规遗传算法全局寻优效率偏低的弱点，提出了一种优进策略，用以改进常规遗传算法。该策略将从繁衍过程中获取进化信息，自适应地改进子代分布，适时引入确定性操作，以提高全局寻优性能。提出的相关技术包括维持种群的多样性、改进交叉算子、增加Powell寻优算子等。实例测试表明这种优进策略效果良好，并已成功地应用于重油热解三集总动力学复杂数学模型的非线性参数估计。     

纳米层状双金属氢氧化物的制备及结构表征

采用恒定pH 12±0.2,按n(Mg2+)∶n(Al3+)∶n(OH-)∶n(CO2-3)=6∶2∶16∶1配制溶液,采用一步反应液相法,制备纳米层状双金属氢氧化物(LDH)粉体.为了获得无团聚、分散均匀的纳米粉体,探讨了溶剂置换干燥、真空干燥、常压干燥对纳米LDH粉体形成团聚的影响;用X射线衍射仪、透射电镜、红外光谱仪和元素分析仪对样品的物相、形貌、粒径和组成进行了表征.结果表明,溶剂置换干燥能够有效防止纳米粉体形成硬团聚,样品分散性好,呈针状形态,长50 nm,宽5 nm.     

Chemistry of organosulphur compound types occurring in heavy oil sands: 3. Reaction of thiophene and tetrahydrothiophene with vanadyl and nickel salts

As part of a study of the chemistry of the steam-stimulated recovery of heavy oils, the hydrolysis and subsequent desulphurization of tetrahydrothiophene and thiophene by aqueous solutions of vanadyl and nickel salts was investigated. Vanadyl sulphate and vanadyl chloride were shown to behave very differently, emphasizing that these salts have different molecular species in aqueous solutions.