熔融制样-X射线荧光光谱法测定钨精矿中主次组分

本文采用熔融制样-X射线荧光光谱法测定钨精矿中的主次组分(WO_3、Fe_2O_3、MnO_2、CaO、SiO_2)。采用熔融制样,消除样品的颗粒效应与矿物效应;以D.Jongh数学模式对谱线干扰和基体效应进行校正,得到满意的工作曲线。结果表明方法重复性和再现性良好,相对标准偏差为0.154%~1.900%,样品的测定值与认定值基本一致,回收率为92.50%~106.00%。该方法能满足日常分析工作的要求。     

气相色谱-微池电子捕获检测法同时检测饮用水中多种有机污染物

本文建立了气相色谱-微池电子捕获检测法(GC-μECD),同时测定生活饮用水中百菌清、七氯、滴滴涕、六六六、林丹、六氯丁二烯、溴氰菊酯、1,1-二-氯苯、1,2-二氯苯、三氯苯、六氯苯11种有机氯,马拉硫磷、对硫磷、甲基对硫磷、毒死蜱、乐果、敌敌畏6种有机磷,以及硝基苯、2,4,6-三硝基甲苯、1,3-二硝基苯、邻,间,对硝基氯苯、2,4-二硝基氯苯,2,4-二硝基甲苯6种硝基苯类有机物的分析方法.样品经萃取后,采用OV-1701色谱柱(30 m×0.25 mm×0.25μtm)程序升温进行分离,用微池电子捕获检测器(μECD)进行检测,通过保留时间定性,外标法定量.结果表明该方法分离效果好,灵敏度高,选择性强,简便、快速、准确,能够满足同时测定生活饮用水中上述23种有机化合物的需要.     

POSS-modified PEG adhesives for wound closure

PEG-related adhesives are limited in clinical use because they are easy to swell and cannot support the cell growth.In this study,we produced a series of POSS-modified PEG adhesives with high adhesive strength.Introduction of inorganic hydrophobic POSS units decreased the swelling of the adhesives and enhanced cell adhesion and growth.The in vitro cytotoxicity and in vivo inflammatory response experiments clearly demonstrated that the adhesives were nontoxic and possessed excellent biocompatibility.Compared with the sutured wounds,the adhesive-treated wounds showed an accelerated healing process in wounded skin model of the Bama miniature pig,demonstrating that the POSS-modified PEG adhesive is a promising candidate for wound closure.     

Fiber-reinforced three-dimensional graphene aerogels for electrically conductive epoxy composites with enhanced mechanical properties

To enhance the mechanical properties of three-dimensional graphene aerogels with aramid fibers,graphene/organic fiber aerogels are prepared by chemical reduction of graphene oxide in the presence of organic fibers of poly(p-phenylene terephthalamide)(PPTA) and followed by freeze-drying. Thermal annealing of the composite aerogels at 1300 ° C is adopted not only to restore the conductivity of the reduced graphene oxide component but also to convert the insulating PPTA organic fibers to conductive carbon fibers by the carbonization. The resultant graphene/carbon fiber aerogels(GCFAs) exhibit high electrical conductivities and enhanced compressive properties, which are highly efficient in improving both mechanical and electrical performances of epoxy composites. Compared to those of neat epoxy, the compressive modulus, compressive strength and energy absorption of the electrically conductive GCFA/epoxy composite are significantly increased by 60%, 59% and 131%, respectively.     

苯酰亚胺结构对PET阻燃抗熔滴及抑烟的贡献

通过本体聚合方法合成了一系列侧链含苯酰亚胺结构的聚对苯二甲酸乙二酯(PET)共聚酯.研究发现,苯酰亚胺单元的引入不仅提高了共聚酯的玻璃化转变温度(T_g)和高温成炭性,并且大大降低了共聚酯高温下的热分解速率.随着苯酰亚胺含量的增加,共聚酯表现出更高的氧指数(LOI)值和更好的阻燃抗熔滴效果.锥形量热测试结果表明,苯酰亚胺结构的引入可以有效地降低共聚酯的峰值热释放速率(p-HRR)、峰值烟释放速率(p-RSR)和总烟释放量(TSR).通过对纯PET和共聚酯燃烧测试后残炭的结构和形貌分析,发现苯酰亚胺结构有助于共聚酯形成石墨化程度更高的致密炭层,这些炭层起到隔热隔氧和抑制有机可燃烟气挥发的作用,在不引入传统阻燃剂的情况下,赋予共聚酯很好的本征阻燃性及抑烟性.     

具有高灵敏性且稳定可重复的正温度系数效应的PVDF/CF导电复合材料

以碳纤维(CF)为填料,聚偏氟乙烯(PVDF)为基体,通过熔融共混法制备PVDF/CF导电复合材料.所得复合材料具有显著的正温度系数(PTC)效应,温度上升到聚合物熔点附近时,电阻率对温度变化敏感.在转折温度区间(155.5~171.0oC,(35)(28)15.5oC)内,其体积电阻率的增加速率约为1.3×105?cm K-1.在不同CF含量下,复合材料表现出不同的PTC行为.随着CF含量的增加,其峰值电阻略有下降.高导电粒子含量下,无负温度系数(NTC)效应.在冷却循环过程,导电网络的重构性良好.复合材料即使经过多次热循环,依然表现出良好的PTC特性重现性.     

非光滑半无限多目标优化问题的对偶性北大核心CSCD

研究了一个非光滑半无限多目标优化问题(简记为SIMOP)并讨论它的对偶性.本文重点考虑此SIMOP的Mond-Weir型半无限多目标对偶问题,通过对目标函数和约束函数的某种组合赋予Clarke-凸性假设,获得了弱/强/逆对偶结论.文章的一些结论是比较新的,并推广了已有文献的一些结果.     

Enhanced hydrogen evolution reaction in Sr doped BiFeO_3 by achieving the coexistence of ferroelectricity and ferromagnetism at room temperature

The perovskite transition metal oxide(TMO) has been considered in electrocatalysis for the modern clean energy technologies as its high electrochemical activity and low cost. The atomic scale engineering to the local stoichiometry of single crystal TMO provides a clue of the relation between electronic structure and catalytic performance. Here we report a hydrogen evolution reaction(HER) activity enhancement ~ 1761% of Bi_0.85Sr_0.15FeO_3 compared to the pure BiFeO_3. By the systemic investigation of the Sr doping level of Bi_1-xSr_xFeO_3(BSFO), it is found that the HER enhancement originates from the improvement of ferromagnetism of BSFO without obvious scarification of the ferroelectricity at the room temperature. The multiple ferroic orderings in BSFO are beneficial for HER activity, which offers the strengthen of hybridization of Fe 3d and O2 p orbitals from the view of ferromagnetism, and the assistance of electron drift by spontaneous electric polarization. Our study not only affords the strategy of developing multiple ferroic orderings in TMO, but also facilitates the atomic scale understanding of the improved HER activity.     

Nitrogen-rich metal-organic framework mediated Cu-N-C composite catalysts for the electrochemical reduction of CO2

Cu-based MOFs,i.e.,HKUST-1,etc.,have been pertinently chosen as the pristine materials for CO₂ ER due to the unique ability of copper for generation hydrocarbon fuel.However,the limited conductivity and stability become the stumbling-block that prevents the development of it.The exploring of MOFsderived M-C materials starts a new chapter for the MOFs precursors,which provides a remarkable electronic connection between carbon matrix and metals/metal oxides.N-doped M-N-C with extensive M-N sites scattering into the carbon matrix are more popular because of their impressive contribution to catalytic activity and specific product selectivity.Nevertheless,Cu-N-C system remained undeveloped up to now.The lack of ideal precursor,the sensitivity of Cu to be oxidized,and the difficulties in the synthesis of small size Cu nanoparticles are thus known as the main barriers to the development of Cu-N-C electrocatalysts.Herein,a nitrogen-rich Cu-BTT MOF is employed for the derivation of N-doped Cu-N-CT composite electrocatalysts by the pyrolyze method.High-temperature pyrolysis product of Cu-N-C1100exhibits the best catalytic activity for productions of CO(-0.6 V vs.RHE,jCO=0.4 mA/cm²)and HCOOH(-0.9 V vs.RHE,jHCOOH=1.4 mA/cm²).     

Synergy of a hierarchical porous morphology and anionic defects of nanosized Li4Ti5O12 toward a high-rate and large-capacity lithium-ion battery

Exploring electrode materials with a high volumetric energy density and high rate capability remains of a great challenge for nanosized-Li₄Ti₅O₁₂(LTO)batteries.Here,hierarchical porous Ti³⁺-C-N-Br co-doped LTO(LTOCPB-CC)is synthesized using carboxyl-grafted nanocarbon(CC)and cetylpyridinium bromide(CPB)as combined structure-directing agents.Ti⁴⁺-O-CPB/Li⁺-CC is designed as a new molecular chelate,in which CPB and CC promote the uniform mixing of Li⁺and Ti⁴⁺and control the morphology of TiO₂ and the final product.The defects(oxygen vacancies and ion dopants)formed during the annealing process increase the electron/hole concentration and reduce the band gap,both of which enhance the n-type electron modification of LTO.As-prepared LTOCPB-CC has a large specific surface area and high tap density,as well as a high electronic conductivity(2.84×10^-4 S cm^-1)and ionic conductivity(3.82×10^-12cm² s^-1),which are responsible for its excellent rate capability(157.7 mA h g^-1 at 20 C)and stable long-term cycling performance(0.008% fade per cycle after 1000 cycles at 20 C).