我国高端石化材料在新能源领域的应用及市场研究

近年来,在能源向多元化、绿色化、低碳化转型的大背景下,我国以风能、光伏、氢能产业为代表的新能源领域快速发展,同时带动了相应领域高端石化材料的需求增长。但目前相关材料自给率较低,部分关键高端材料仍依赖进口,具有较大国产化潜力。该文通过拆解新能源领域主要部件结构、评估用材单耗并结合行业规模发展趋势,对我国新能源用材种类与规模进行测算。预计到2030年,我国风、光、氢新能源产业将以年均20%左右的速度增长,对高端石化材料的需求规模将从2022年的230余万吨增长至2030年的近450万吨。

石化新材料产业发展探讨——以惠州市为例

本文基于石化产业规划和区域发展的红利政策,介绍了石化新材料发展的有利背景,分析了产业面临的诸如同质化发展、资源环境约束等现实问题。以惠州市产业发展和布局为例,介绍了石化新材料的总体发展思路。最后给出了石化产业差异化发展,划定红线明确招商图谱,坚持政府配套市场为主的政策建议。

生物降解高分子材料研究应用进展

介绍了生物降解材料的特点及降解作用机理,重点讨论天然高分子材料和化学合成高分子材料的研究应用进展,并对生物降解材料的发展前景进行了展望和论述。

Nitrogen⁃doped 3D graphene⁃carbon nanotube network for efficient lithium storage

A 3D nitrogen⁃doped graphene/multi⁃walled carbon nanotube(CS⁃GO⁃NCNT)crosslinked network mate⁃rial was successfully synthesized utilizing chitosan and melamine as carbon and nitrogen sources,concomitant with the incorporation of multi⁃wall carbon nanotubes and employing freeze drying technology.The material amalgamates the merits of 1D/2D hybrid carbon materials,wherein 1D carbon nanotubes confer robustness and expedited elec⁃tron transport pathways,while 2D graphene sheets facilitate rapid ion migration.Furthermore,the introduction of nitrogen heteroatoms serves to furnish additional active sites for lithium storage.When served as an anode material for lithium⁃ion batteries,the CS⁃GO⁃NCNT electrode delivered a reversible capacity surpassing 500 mAh·g^(-1),mark⁃edly outperforming commercial graphite anodes.Even after 300 cycles at a high current density of 1 A·g^(-1),it remained a reversible capacity of up to 268 mAh·g^(-1).

甲控乙供材料管理模式在大型工程建设项目中的应用

文章结合新疆独山子石化公司千万吨炼油和百万吨乙烯工程对普通大宗材料的管理控制情况,提出甲控乙供材料管理模式在大型工程项目建设中推广应用的必要性,具体阐述了这种管理模式的概念、特点、运行措施和取得的效果,并结合实际运行情况提出了相关注意事项。

Synthesis of Cu_2O/reduced graphene oxide composites as anode materials for lithium ion batteries

A facile way was used to synthesize Cu2O/reduced graphene oxide （rGO） composites with octahedron-like morphology in aqueous solution without any surfactant. TEM images of the obtained Cu2O/rGOs reveal that the Cu2O particles and rGO distribute hierarchically and the primary Cu2O particles are encapsulated well in the graphene nanosheets. The electrochemical performance of Cu2O/rGOs is enhanced compared with bare Cu2O when they are employed as anode materials for lithium ion batteries. The Cu2O/rGO composites maintain a reversible capacity of 348.4 mA？h/g after 50 cycles at a current density of 100 mA/g. In addition, the composites retain 305.8 mA？h/g after 60 cycles at various current densities of 50, 100, 200, 400 and 800 mA/g.

Enhanced photocatalytic performance of cementitious material with TiO_2@Ag modified fly ash micro-aggregates

A TiO2 photocatalyst is coated on the surface of a zeolite fly ash bead（ZFAB） to improve its dispersability and exposure degree in a cement system.The application of Ag particles in TiO2/ZFAB modified cementitious materials is to further enhance the photocatalytic performance.Various Ag@TiO2/ZFAB modified cementitious specimens with different Ag dosages are prepared and the characteristics and photocatalytic performance of the prepared samples are investigated.It is observed that the multi-level pore structure of ZFAB can improve the exposure degree of TiO2 in a cement system and is also useful to enhance the photocatalytic efficiency.With an increment of the amounts of Ag particles in the TiO2/ZFAB modified cementitious samples,the photocatalytic activities increased first and then decreased.The optimal Ag@TiO2/ZFAB modified cementitious sample reveals the maximum reaction rate constant for degrading benzene（9.91×10^-3 min^-1）,which is approximately 3 and 10 times higher than those of TiO2/ZFAB and TiO2 modified samples,respectively.This suggests that suitable Ag particles coupled with a ZFAB carrier could effectively enhance the photocatalytic effects and use of TiO2 in a cement system.Thus,ZFAB as a carrier could provide a potential method for a high efficiency engineering application of TiO2 in the construction field.

Preparation of uniform flower-like CuO and flower-like CuO/graphene composite and their application in lithium ion batteries

Flower-like CuO and flower-like CuO/graphene composite were prepared successfully by hydrothermal method. They were characterized by X-ray diffraction, scanning electron microscopy, nitrogen adsorption, temperature-programmed reduction, and thermogravimetric analysis. It is found that the flower-like CuO microspheres, which are composed of CuO nanosheets, possess an average diameter of 4.2 μm and a Brunauer–Emmett–Teller surface area of 12.6 m2/g. Compared with the flower-like CuO, the obtained flower-like CuO/graphene composite shows an enhanced electrochemical performance with a higher capacity of 603 mA-h/g at 0.1 C rate and 382 mA-h/g at 1 C rate, and exhibits a better cycle stability with a high capacity retention of 95.5 % after 50 cycles even though at 1 C rate.

Effect of WS_2 addition on electrical sliding wear behaviors of Cu-graphite-WS_2 composites

Four kinds of Cu-based composites with different mass ratios of graphite and WS2 as lubricants were fabricated by hot-pressing method. Electrical sliding wear behaviors of the composites were investigated using a block-on-ring tribometer rubbing against Cu-5%Ag alloy ring. The results demonstrated that 800 ~C was the optimum sintering temperature for Cu-graphite-WS2 dual-lubricant composites to obtain the best comprehensive properties of mechanical strength and lubrication performance. Contact voltage drops of the Cu-based composites increased with increasing the mass ratio of WS2 to graphite. The Cu-based composite with 20% graphite and 10% WS2 showed the best wear resistance due to the excellent synergetic lubricating effect of graphite and WS2. The reasonable addition of WS2 into the Cu-graphite composite can remarkably improve the wear resistance without much rise of electrical energy loss which provides a novel principle of designing suitable sliding electrical contact materials for industrial applications.

Three-dimensional MoS_2/reduced graphene oxide aerogel as a macroscopic visible-light photocatalyst

Photocatalysis is regarded as an ideal technology for solving the urgent environmental and energy issues that we face today.Among the reported photocatalysts,molybdenum disulfide（MoS2） is very promising for applications in hydrogen production and pollutant photodegradation.However,its lack of active sites and the difficulty of recovering catalysts in powder form have hindered its wide application.Here,we report the successful preparation of a macroscopic visible-light responsive MoS2/reduced graphene oxide（MoS2/RGO） aerogel.The obtained MoS2/RGO aerogel exhibits enhanced photocatalytic activity towards hydrogen production and photoreduction of Cr（Ⅵ） in comparison with the MoS2 powder.In addition,the low density（56.1 mg/cm^3） of the MoS2/RGO aerogel enables it to be used as an efficient adsorption material for organic pollutants.Our results demonstrate that this very promising multifunctional aerogel has potential applications in environmental remediation and clean energy production.

Magnetic and microwave absorbing properties of M-type barium ferrite/graphene oxide composite microwave absorber

In order to improve the absorbing properties of M- type barium ferrite absorbing materials, M-type barium ferrite/graphene oxide composites with different graphene oxide contents were synthesized by the sol-gel autocombustion method. X-ray diffraction （XRD）, a scanning electronic microscopy （ SEM ）, a physical properties measurement system （PPMS-9）, and a vector network analyzer were used to analyze their structure, surface morphology, magnetic and absorbing properties, respectively. The results show that the absorbing band of the composite absorbing material is widened and the absorbing strength is increased compared with the pure M-type barium ferrite. The sample with the content of doped graphene oxide of 3% has the minimum reflectivity at 10 to 18 GHz frequencies. Hence, the doped graphene oxide effectively improves the absorbing properties of M-type barium ferrite.

Ultrasonic synthesis of CoO/graphene nanohybrids as high performance anode materials for lithium-ion batteries

A facile ultrasonic method was used to synthesize CoO/graphene nanohybrids by employing Co4（CO）12 as a cobalt precursor. The nanohybrids were characterized by SEM, TEM and XPS, and the results show that CoO nanoparticles （3-5 nm） distribute uniformly on the surface of graphene. The CoO/graphene nanohybrids display high performance as an anode material for lithium-ion battery, such as high reversible lithium storage capacity （650 mA-h/g after 50 cycles, almost twice that of commercial graphite anode）, high coulombic efficiency （over 95%） and excellent cycling stability. The extraordinary performance arises from the structure of the nanohybrids： the nanosized CoO particles with high dispersity on conductive graphene substrates are beneficial for lithium-ion insertion/extraction, shortening diffusion length for lithium ions and improving conductivity, thus the lithium storage performance was improved.

In situ synthesis of a nickel boron oxide/graphdiyne hybrid for enhanced photo/electrocatalytic H_(2) evolution

Developing highly active catalysts for photo/electrocatalytic water splitting is an attractive strategy to produce H2 as a renewable energy source.In this study,a new nickel boron oxide/graphdiyne(NiBi/GDY)hybrid catalyst was prepared by a facile synthetic approach.Benefitting from the strong electron donating ability of graphdiyne,NiBi/GDY showed an optimized electronic structure containing lower valence nickel atoms and demonstrated improved catalytic performance.As expected,NiBi/GDY displayed a high photocatalytic H2 evolution rate of 4.54 mmol g^(-1)h^(-1),2.9 and 4.5 times higher than those of NiBi/graphene and NiBi,respectively.NiBi/GDY also displayed outstanding electrocatalytic H2 evolution activity in 1.0 M KOH solution,with a current density of 400 mA/cm^(2)at an overpotential of 478.0 mV,which is lower than that of commercial Pt/C(505.3 mV@400 mA/cm^(2)).This work demonstrates that GDY is an ideal support for the development of highly active catalysts for photo/electrocatalytic H2 evolution.

Preparation and characteristics of porous ceramics

Pyrophyllite is always used for making porous ceramics. In order to design the preparation technics of porous ceramics with pyrophyllite reasonably we must know the classifications, characteristics, properties and applications of porous ceramics. The classification and characteristics of porous ceramics are reviewed in this article; and several common preparations with their advantages and disadvantages are also introduced. The authors discussed the problems existing in researching and developing process for porous ceramics, and forecasted the development prospect of porous ceramics.

Conversion of coal gangue into alumina, tobermorite and TiO_2-rich material

A large amount of coal gangue from coal mining and processing is regarded as waste and usually stockpiled directly. In order to recycle the valuable elements from the coal gangue, an integrated process is proposed. The process consists of three steps: 1concentrating alumina from the coal gangue via activation roasting followed by alkali leaching of Si O2 which produces alumina concentrate for alumina extraction by the Bayer process; 2) synthesizing tobermorite whiskers from the filtrated alkali liquo containing silicate via a hydrothermal method and reusing excess caustic liquor; and 3) enriching titanium component from the Baye process residue by sulfuric acid leaching. Alumina concentrate with 69.5% Al_2O_3 and mass ratio of alumina to silica(A/S) of 5.9pure 1.1 nm tobermorite whisker and TiO_2-rich material containing 33% TiO_2 are produced, respectively, with the optimal parameters Besides, the actual alumina digestion ratio of alumina concentrate reaches 80.4% at 270 oC for 40 min in the Bayer process.

Synthesis of graphene/tourmaline/TiO_2 composites with enhanced activity for photocatalytic degradation of 2-propanol

We report the construction of a graphene/tourmaline/TiO2(G/T/TiO2)composite system with enhanced charge‐carrier separation,and therefore enhanced photocatalytic properties,based on tailoring the surface‐charged state of graphene and/or by introducing an external electric field arising from tourmaline.A simple two‐step hydrothermal method was used to synthesize G/T/TiO2composites and poly(diallyldimethylammonium chloride)‐G/T/TiO2composites.In the photocatalytic degradation of2‐propanol(IPA),the catalytic activity of the composite containing negatively charged graphene was higher than of the composite containing positively charged graphene.The highest acetone evolution rate(223?mol/h)was achieved using the ternary composite with the optimum composition,i.e.,G0.5/T5/TiO2(0.5wt%graphene and5wt%tourmaline).The involvement of tourmaline and graphene in the composite is believed to facilitate the separation and transportation of electrons and holes photogenerated in TiO2.This synergetic effect could account for the enhanced photocatalytic activity of the G/T/TiO2composite.A mechanistic study indicated that O2??radicals and holes were the main reactive oxygen species in photocatalytic degradation of IPA.

Photocatalytic degradation of Brilliant Green dye using CdSe quantum dots hybridized with graphene oxide under sunlight irradiation

CdSe quantum dots(QDs)hybridized with graphene oxide(GO)are synthesized by a facile chemical precipitation method.The absorption of the CdSe/GO nanocomposite is increased with a significantblue shift with respect to CdSe QDs.The specific surface area of the CdSe/GO nanocomposite is10.4m2/g,which is higher than that of CdSe QDs(5m2/g).The PL intensity of the CdSe/GO nanocomposite is lower than that of the CdSe QDs owing to the inhibition of the recombination of electron‐hole pairs in the composite.In Raman analysis,the two bands of the CdSe/GO nanocomposite are shifted to higher wavenumbers with respect to graphene oxide,which is attributed to electron injection that is induced by CdSe QDs into graphene oxide.Using the Brilliant Green dye,the photocatalytic reduction efficiency of CdSe QDs and the CdSe/GO nanocomposite under sunlight irradiation for90min are approximately81.9%and95.5%,respectively.The calculated photodegradation rate constants for CdSe QDs and the CdSe/GO nanocomposite are0.0190min–1and0.0345min–1,respectively.The enhanced photocatalytic activity of the CdSe/GO nanocomposite can be attributed to the high specific surface area and the reduction of electron‐hole pair recombination because of the introduction of graphene oxide.

Thermal Oxidative Degradation and Ageing Performance of Silicone Rubber Filled with Attapulgite

The natural attapulgite(NAPT)was disaggregated by high-pressure homogenization technology combined with extrusion process to prepare the attapulgite with disaggregated rod crystal bundles(DAPT)and large specific surface area of 133.7 m^(2)/g.NAPT and DAPT were incorporated into the silicone rubber to obtain the composite NAPTSR and DAPT-SR by mechanical blending method,respectively.After thermal oxidative ageing at 300℃ for 0.5 h,temperature for the 5%weight loss increased greatly from 385℃ of the neat silicone rubber to 396-399℃ with addition of NAPT and DAPT.NAPT and DAPT enhanced the interaction between the filler nanoparticles and rubber matrix thus inhibited the nanoparticle agglomeration.The conservation rate of the side methyl group in NAPT-SR and DAPT-SR was greatly improved after ageing.Therefore,the thermal oxidative degradation and ageing performance of the silicone rubber composites was significantly reinforced.Moreover,DAPT could greatly restrain the growth of nanoparticles after ageing.Therefore,DAPT-SR showed the better retention of tensile strength(40.6%),elongation at break(34.9%)and tear strength(30.1%)compared with the corresponding mechanical properties of the neat silicone rubber(10.6%,7.4%,and 5.0%)after ageing.

Thermo-mechanical properties of mullite–zirconia composites derived from reaction sintering of zircon and sillimanite beach sand: Effect of CaO

Mullite–zirconia composites containing 20% zirconia（mass fraction） were prepared by reaction sintering route utilizing Indian coastal zircon flour and sillimanite beach sand. 4%-12% of CaO（mole fraction） with respect to zirconia was used as additive. The effect of additive on densification, microstructure as well as various mechanical and thermo-mechanical properties was studied. Incorporation of CaO reduced the densification temperature of the composites to 1550 ℃ compared to 1600 ℃（for CaO free samples）. CaO formed small amount of liquid phase（calcium aluminosilicate）, which facilitated sintering. Average grain size of the composites decreased up to 4% CaO addition, afterwards grain size increased with further addition of CaO. Samples with 4% CaO exhibited ～225 MPa of flexural strength, ～6 MPa·m^1/2 of fracture toughness and significant improvement in thermal shock resistance. CaO stabilized the tetragonal zirconia phase and thus improved the mechanical properties.

Facile preparation of sepiolite@LDH composites for the visible-light degradation of organic dyes

Sepiolite@LDH(Sep@LDH)composites were designed and prepared based on the assembly of layered double hydroxides(LDH)on acidified sepiolites(Sep)for the simultaneous photocatalytic degradation of methyl orange(MO)and methylene blue(MB).The structure,morphology,texture,optical properties,and photocatalytic performance of the prepared Sep@LDH were studied in detail.Among the Sep@LDH composites,Sep4@LDH(4.0 g Sep)exhibited the highest photocatalytic activity under visible‐light irradiation,which could be attributed to its large surface area,high crystallinity,and plentiful active sites on its surface.The photodegradation of the dyes followed a pseudo first‐order kinetic model(Langmuir‐Hinshelwood model),indicating that the copious and homogeneous active sites on the surface of the composites contributed to the high photocatalytic activity.The photodegradation mechanism was studied by examining the active species(^-OH,h+,and·O2^-anions)using appropriate scavengers.It was found that·OH radicals played a critical role in the photocatalytic process of MO and MB,where the generation of·OH radicals occurred on the electron/hole(e^-/h+)pairs on the surface of the Sep@LDH composites.