Modeling and surface texturing on surface roughness in machining LaPO4–Y2O3 composite

In this work, lanthanum phosphate with a 20% yttria (LaPO₄/Y₂O₃) composite prepared by an Aqueous Sol–Gel process is machined using an Abrasive Water Jet Machine (AWJM). The machinability of this composite is studied by varying the input parameters namely Jet Pressure (JP), Stand-Off Distance (SOD), and Traverse Speed (TS) on Surface finish. Garnet of 80 mesh size is used as an abrasive with a flow rate of 85?g/min. The microstructural characterization study reveals the presence of new element YPO₄. This element enhances the machinability and reduced porosity in the composite. Microscopy examinations on the machined surface reveals that partial overlapping at low JP, poor surface finish at high JP and SOD, forged deficiency at maximum SOD and TS. The minimum levels of all input parameters are influenced to obtain acceptable Ra. Atomic Force Microscopy (AFM) on the kerf surface shows micro wear track and peaks. The Multiple Regression Analysis (MRA) is developed for Ra to check the adequacy. From the Analysis of Variance (ANOVA), SOD has a significant effect on Ra with a contribution of 53%. The influence of JP and TS on Ra is found to be 31% and 15%, respectively.     

海上稠油油田蒸汽吞吐产量确定新方法

针对目前蒸汽吞吐产量预测模型假设条件简单、普适性差等问题,一般采用测试法和类比法综合确定海上稠油油田蒸汽吞吐初期产量。由于目前海上油田通常只开展常规测试,无法直接获得热采开发初期产量。笔者提出海上稠油油田蒸汽吞吐初期产量确定新方法,建立蒸汽吞吐相对于常规开发的初期产量倍数预测模型,通过蒸汽吞吐产量倍数,将常规测试确定的产量转化为蒸汽吞吐产量。研究表明,蒸汽吞吐初期产量倍数主要受储集层渗透率、原油黏度、注入强度、蒸汽干度等因素影响,利用正交试验设计和多元回归等方法,建立海上稠油油田蒸汽吞吐初期产量倍数与油藏地质参数及注入参数之间的非线性预测模型,该模型经实际生产数据验证,预测误差小于5%,可靠性高,能够为海上稠油油田蒸汽吞吐初期产量的确定提供依据。     

ZSM-5沸石膜用于生物油的脱水分离及其再生过程研究

在水热条件下通过无模板剂法合成了连续的ZSM-5沸石膜，并将其用于生物油的渗透汽化以进行高效脱水分离。ZSM-5沸石膜在强酸性、多组分的生物油体系中保持了很好的化学稳定性和优异的分离选择性，但在分离过程中面临着较强的膜污染问题，导致了膜通量的大幅下降。ZSM-5沸石膜的再生研究表明，膜的渗透通量随着再生温度的升高而逐渐提高。当再生温度为220℃时，ZSM-5沸石膜的渗透通量可以恢复至初始的88%。再生的机理研究表明，ZSM-5沸石膜中大量的晶内孔在生物油体系中极易被污染，从而导致渗透通量迅速下降；而相对较大的晶间孔却难以被完全堵塞，水分子在被污染的ZSM-5沸石膜中主要通过晶间孔进行渗透。上述结果表明，通过合理调控ZSM-5沸石膜的晶间孔的数量和尺寸大小可有效提升ZSM-5沸石膜在生物油中的渗透汽化脱水分离性能。     

氧化石墨烯杂化分子印迹复合膜制备及性能研究

采用改进的Hummers法，通过冷冻干燥制备了氧化石墨烯(GO)。以辛弗林盐酸盐为模板分子，水溶性的丙烯酰胺为功能单体，离子液体(溴代1-丁基-3-甲基咪唑)为致孔剂，把GO加入聚合液中，制备了GO杂化的分子印迹复合膜(GO-MIM)。利用透射电镜、扫描电镜、X射线衍射和红外光谱等方法对GO及GO-MIM进行了表征。通过将分子印迹膜技术与GO相结合，明显提高了分子印迹膜的力学性能。吸附及渗透实验表明，GO-MIM可在纯水溶剂体系，对辛弗林盐酸盐具有很好的选择性吸附能力和优先透过能力，体现了明显的分子印迹效果。     

氮酮与薄荷醇联用对5-氟尿嘧啶的促透作用

目的：以5-氟尿嘧啶（5-FU）为模型药物，对氮酮和薄荷醇的促透特性进行比较，并探讨两种促透剂合用时的促透效果。方法：在离体透皮实验装置上进行透皮试验，由浓度计算累积透过量，运用倍量法对氮酮与薄荷醇联用的效果进行评价。结果： 浓度为0.25%、0.50%、1.00%、2.00%的氮酮对5-FU均有促透作用，与空白对照组相比，差异具有统计学意义（P<0.01）；浓度为0.25%、0.50%、1.00%、2.00%的薄荷醇对5-FU也有明显的促透作用，与空白对照相比，差异具有统计学意义（P<0.01）；用倍量法对两种药物联用的作用进行评价分析时，二者联用未显示有协同作用。结论：氮酮和薄荷醇对（5-FU）均有促透作用，但二者以相同浓度合用时，未有明显的协同作用。     

纳滤法制备高纯度雪莲果低聚果糖及其结构表征

采用纳滤分离技术以雪莲果为原料纯化低聚果糖，通过Box-Behnken中心组合设计（CCD）及响应面分析（RSM）建立预测低聚果糖纯度的二次多项数学模型，优化分离纯化工艺。结果表明：操作压力0.15 MPa，循环流量5.3 mL/min，pH值2.7时，纯化倍数为5，实际低聚果糖纯度为95.1%，达到P级产品标准。通过应用HPLC-MS、IR、¹H NMR及¹³C NMR等对雪莲果低聚果糖组分的纯度、组成、结构进行表征，结果表明：分离纯化得到的雪莲果低聚果糖由蔗果三糖、蔗果四糖和蔗果五糖组成，纯度为95.1%，平均包含5个果糖单元，主要是由β-呋喃构型的果糖组成。     

Fabrication of magnetically recoverable Fe3O4/CdS/g-C3N4 photocatalysts for effective degradation of ciprofloxacin under visible light

Photocatalytic technology is an environmentally safe method of eliminating organic pollutants and antibiotics in wastewater. In this research, the performance of Fe₃O₄/CdS/g-C₃N₄ (FCN) photocatalyst for degradation of antibiotics was studied. The composite photocatalysts with different concentrations of g-C₃N₄ were prepared. FCN has better photocatalytic activity than degradation dyes in removal of antibiotics under visible light. This indicates that FCN could effectively hinder the recombination of carriers, and the addition of g-C₃N₄ increases the optical response range of CdS. At the same time, the introduction of Fe₃O₄ magnetic nanoparticles overcomes the problem of difficulty in recovery of the powder photocatalyst. The photocatalytic activity is not reduced to any significant after three cycles of use.     

Influence of Different Additives on the Interaction of Quinolone Antibiotic Drug with Surfactant: Conductivity and Cloud Point Measurement Study

Conductometric and cloud point (CP) measurement studies have been performed to investigate the interaction of tetradecyltrimethylammonium bromide (TTAB) and Triton® X-100 (TX-100) with ciprofloxacin hydrochloride (CFH) in different solvents over the temperature range of 295.15–315.15 K. CFH is used for the treatment of various bacterial infections. The observed critical micelle concentration (CMC) values of TTAB were found to be reduced in the presence of electrolytes (Na₂SO₄/Na₃PO₄), and this reduction proceeds with the elevation of salt concentration. The order of the CMC of TTAB follows the trend: > >. The observed CMC values of TTAB were found to increase with increasing temperature and decrease with increasing concentration of CFH in aqueous medium. The values of Gibbs free energy of micellization () for the TTAB/TTAB + CFH mixture were found to be negative, implying spontaneous micellization. The estimated CP of TX-100 decreases with increasing concentration of TX-100 in aqueous medium. The CP values first decrease with increasing concentration of CFH and then increase at higher concentration of CFH almost in all cases investigated. The values of free energy of clouding were found to be positive in all cases studied implying that phase separation of TX-100 was nonspontaneous. The other thermodynamic parameters associated with the micellization of TTAB and the phase separation of TX-100 were estimated and explained.     

基于综合赋权与集对分析的煤炭企业安全评价

安全评价是发现系统风险,提高生产安全性的有效手段。运用集对分析理论对煤炭企业生产安全性进行分析与评价。根据SHEL模型,结合煤炭企业实际对生产中的风险因素进行分析,确定了煤炭企业安全评价指标体系;将熵权法与超标倍数赋权法相组合来确定各评价指标的综合权重,基于集对分析理论构建了煤炭企业安全评价模型。将构建的指标体系和评价模型在平煤集团5个生产矿井进行了应用,结果显示,利用集对分析得到的评价结果与实际情况基本吻合。     

Size-dependent separation of graphene oxide by deformation of packed-gel in a chromatographic column

ABSTRACT

A deformable gel-packed chromatographic column was used to separate as-synthesized graphite oxide with different sizes. The synthesized gel (56 µm) was deformed by pressure of the fluid flow and the gaps in the gels showed a range of sizes. A suspension of graphene oxide (0.1 g/L, 10 mL) was injected, and graphene oxide in the elution had a size at 0.56 μm and 0.14 μm, whereas in half upper and bottom domain of the gel layer graphene oxide had a size at 33 µm and 2.9 µm, respectively, demonstrating that graphene oxide suspension was separated by size through gel layer.