Synthesis of TiO2 nanopellet by TiCl4 as a precursor for degradation of RhodamineB

In the present investigation in order to promote TiO₂ pellet structure and its photocatalytic activity, two new precursors were synthesized in the powder and sol forms, using sol–gel method with precipitation of TiCl₄. Since TiO₂ pellets are normally synthesized by the commercial TiO₂ powder (DegussaP25), in this investigation and in the first step a new synthesized TiO₂ powder was produced and compared with DegussaP25. Subsequently, two types of pellet were made by the new synthesized powder and titania sol. The characterization of the synthesized TiO₂ powder and pellet were performed by XRD, FT-IR, scanning electron microscopy (SEM) and atomic force microscopy (AFM). The result showed that by the new procedure utilized here, without using any additive not only the surface area of the produced TiO₂ powder has been increased, but also the crystalline phase is completely in the anatase form. It was also found that the synthesized pellets by the sol precursor had better morphological structure than the synthesized pellets by theTiO₂ powder (either DegussaP25 or new synthesized powder). Ultimately, in order to evaluate photocatalytic activity of TiO₂ powders and pellet, degradation of RhodamineB was tested.     

Editable Supercapacitors with Customizable Stretchability Based on Mechanically Strengthened Ultralong MnO2 Nanowire Composite

Although some progress has been made on stretchable supercapacitors, traditional stretchable supercapacitors fabricated by predesigning structured electrodes for device assembling still lack the device‐level editability and programmability. To adapt to wearable electronics with arbitrary configurations, it is highly desirable to develop editable supercapacitors that can be directly transferred into desirable shapes and stretchability. In this work, editable supercapacitors for customizable shapes and stretchability using electrodes based on mechanically strengthened ultralong MnO₂ nanowire composites are developed. A supercapacitor edited with honeycomb‐like structure shows a specific capacitance of 227.2 mF cm^?2 and can be stretched up to 500% without degradation of electrochemical performance, which is superior to most of the state‐of‐the‐art stretchable supercapacitors. In addition, it maintains nearly 98% of the initial capacitance after 10 000 stretch‐and‐release cycles under 400% tensile strain. As a representative of concept for system integration, the editable supercapacitors are integrated with a strain sensor, and the system exhibits a stable sensing performance even under arm swing. Being highly stretchable, easily programmable, as well as connectable in series and parallel, an editable supercapacitor with customizable stretchability is promising to produce stylish energy storage devices to power various portable, stretchable, and wearable devices.     

金属氧化物和分子筛在CO2环加成中的研究进展

二氧化碳（CO2）是主要的温室气体,同时也是一种廉价、无毒且可再生的一碳资源,因此将CO2转化为有价值的精细化学品可有效减缓气候变化、助力实现碳中和。CO2与环氧化物的环加成反应具有高原子经济、高选择性、低污染等优点,其产物环状碳酸酯可作为锂离子电池电解质、聚合物材料前体以及精细化学品中间体,应用前景广阔。氧化物因具有结构多样、可调性强等优点在CO2与环氧化物的环加成反应中的应用引起了广泛的关注。文章综述了两种典型且成本低廉、易于规模化生产的氧化物——金属氧化物与分子筛催化CO2与环氧化物的环加成反应的研究进展,重点分析了反应机理以及催化剂的应用。今后的研究重点是高性能无助剂的非均相催化剂的开发以及催化机理的探究。     

VOx薄膜的制备、电阻-温度特性及结构研究

VO2是一种热致相变材料.发生相变时,VO2的电阻、红外光透过率、反射率都会发生显著变化.采用直流反应磁控溅射法,通过改变氧氩比(O2:Ar)、工作气压、衬底温度等制备工艺参数,研究了工艺参数对VOx薄膜的结构、电阻-温度性能的影响.结果表明,当氧氩比为1.0:15、工作气压为2.0Pa时,制备的薄膜中VO2的含量较多;衬底温度为250℃时,制备的VOx薄膜的电阻一温度突变性能最佳.     

基于响应曲面法的超临界CO2萃取油基钻屑油相工艺优化

目的对超临界CO₂萃取油基钻屑中油相工艺参数进行优化。 方法采用响应曲面法对影响超临界CO₂萃取工艺的重要参数进行具体实验并根据实验结果进行数值模拟,通过模拟得出萃取时间、压力、温度和超临界CO₂流量等参数的优化数据。 结果响应曲面分析了各变量之间对萃取效果的影响,基于萃取数据建立了二次多项式模型,能够较好地拟合实验结果,得出最佳萃取条件为萃取压力25 MPa、温度323.15 K、时间90 min和流量25.0 L/h。 结论通过具体实验数据结合响应曲面法得出了最佳萃取条件,在该条件下油类最大去除率为95.22%。利用气相色谱仪-质谱联用仪(GC-MS)分析萃取物前后性状未发生明显变化,该方法能够更好地实现固液分离和资源回收。      

SO_4~（2－）／ZrO_2超强酸催化剂的结构表征

用ＢＥＴ法分析了制备条件对ＳＯ＿４￣（２－）／ＺｒＯ＿２超强酸催化剂的比表面和孔结构的影响，用ＳＥＭ观察了催化剂的表面形貌。结果表明，引人ＳＯ＿４￣（２－）后催化剂的比表面和比表面的热稳定性都增大了，在Ｈ＿２ＳＯ＿４浓度为１．０ｍｏｌ／１和焙烧温度约７７３Ｋ时催化剂的比表面较大。制备Ｚｒ（ＯＨ）＿４时用浓氨水得到的催化剂的比表面、平均孔径和孔体积都较大。ＳＯ＿４￣（２－）／ＺｒＯ＿２催化剂的孔为平均孔径３－５ｎｍ的中孔。ＳＥＭ结果表明，ＳＯ＿４￣（２－）／ＺｒＯ＿２催化剂的表面为很不平整的蜂窝状。     

事故氯处理装置的改进

山东华阳农药化工集团氯碱厂烧碱生产装置扩能的同时,事故氯处理装置由石灰水吸收事故氯改造为碱液吸收。改造后高效、安全、环保。     

Exploring the Effects of the Interaction of Carbon and MoS2 Catalyst on CO2 Hydrogenation to Methanol

Hydrogenation of CO₂ to form methanol utilizing green hydrogen is a promising route to realizing carbon neutrality. However, the development of catalyst with high activity and selectivity to methanol from the CO₂ hydrogenation is still a challenge due to the chemical inertness of CO₂ and its characteristics of multi-path conversion. Herein, a series of highly active carbon-confining molybdenum sulfide (MoS₂@C) catalysts were prepared by the in-situ pyrolysis method. In comparison with the bulk MoS₂ and MoS₂/C, the stronger interaction between MoS₂ and the carbon layer was clearly generated. Under the optimized reaction conditions, MoS₂@C showed better catalytic performance and long-term stability. The MoS₂@C catalyst could sustain around 32.4% conversion of CO₂ with 94.8% selectivity of MeOH for at least 150 h.     

Control of sonoluminescence signal in deionized water using carbon dioxide

Megasonic cleaning is routinely employed in semiconductor industry for cleaning of wafers. However, the method also results in damage to wafer features and such damage has been proposed to arise from transient, imploding cavities formed during megasonic processing. Transient cavitation is associated with the release of light, a phenomenon called sonoluminescence (SL) and the extent of damage has been shown to correlate with the intensity of SL. Control of sonoluminescence may therefore allow control of damage during megasonic processing of wafers. In this study, the ability of carbon dioxide to quench sonoluminescence generation in deionized water exposed to megasonic field of varying power density and duty cycle has been systematically investigated. It has been found that CO₂ is not only incapable but also a potent inhibitor of sonoluminescence, providing a potential means for selective alleviation of the violent effects of transient cavitation in process fluids. A novel chemical method has been established for in situ release of CO₂ from NH₄HCO₃ through a pH induced shift in the carbonic acid equilibria in deionized water. Using this method, a precisely controlled, progressive decrease in SL of air saturated deionized water through addition of NH₄HCO₃ has been demonstrated. It has been determined that 130 ppm of released CO₂ is sufficient for complete inhibition of sonoluminescence generated in air saturated deionized water.