The efficient removal of perfluorooctanoic acid (PFOA) from contaminated water remains a challenge due to the very stable carbon?fluorine bonds in perfluorinated compounds.In this experiment,nanosecond pulsed dielectric barrier discharge (DBD) plasma was used to degrade PFOA,a difficult?to?degrade organic pollutant in water,and the effects of discharge parameters such as discharge atmosphere,discharge power,gas flow rate,and liquid flow rate,as well as the reaction conditions,on the removal rate of PFOA were investigated in the reaction.The experimental results showed that under the conditions of the discharge atmosphere of argon,discharge power of 11.84 W,gas flow rate of 3.33 L/min,and liquid flow rate of 0.28 L/min,DBD had a better degradation effect on PFOA,and the removal rate could reach more than 94.0% after 60 min of reaction.Combined with emission spectroscopy and free radical burst analysis,it was determined that e^-,?OH,H₂O₂, and O₃ were the main active species to break the molecular structure of PFOA and realize the efficient degradation of the reactants,and thus could provide an effective solution for the removal of PFOA in water.

Anthraquinone dyes are the second most significant dyes in the dye industry after azo dyes.Nitroanthraquinone prepared by the nitration of anthraquinone,is one of the important raw materials for the synthesis of various types of anthraquinone dyes.In this study,a microreactor with excellent heat and mass transfer properties was utilized to investigate the continuous?flow nitration process of anthraquinone.The effects of key process parameters such as reaction temperature,volume flow rate,molar ratio of nitric acid to anthraquinone,anthraquinone concentration,residence time,and sulfuric acid intensity on the nitration process were examined.The results showed that the competition between mono? and di?nitrification reactions during anthraquinone nitrification was significant, and the adjustment of process parameters would significantly affect the ratio of mono? and di?nitrification products while promoting the conversion rate of anthraquinone.The full use of the advantages of microreactors to precisely regulate the process parameters is an effective measure to improve the selectivity of the target nitration product.

Plastics are synthetic or natural polymers that are widely used in industrial fields and daily life due to its good durability and plasticity.Among plastics,polyethylene terephthalate (PET) is the most commonly used.Polyethylene terephthalate (PET) is one of the commonly used plastics,which is widely used in many fields.PET is difficult to be degraded under natural circumstances without artificial treatment,which brings serious burden to the ecosystems,so the issue of degradation and regeneration of PET plastics has become a hot issue globally.Many methods such as photodegradation,thermal degradation,biodegradation,etc.,have been developed to degrade plastics.Among them,biodegradation is considered as environmental friendly and highly efficient method.Thus,the design and transformation of PET degradation has become a key issue.The main methods for degrading plastics at the present stage,the common enzymes used for degrading PET by biodegradation methods and the modification methods of PET degrading enzymes are reviewed,to provide a theoretical basis for the rapid degradation and regeneration of PET.

Aiming at the problems of slow generation rate,low storage capacity and harsh generation conditions of CO₂ during the hydrate generation process,bimetallic Cu and Al?loaded graphene oxide materials were used as additives for the kinetic characterisation of CO₂ hydrate generation.Firstly,the prepared GO?Cu?Al material was characterized by TEM,EDS,XPS,and stability analysis.Secondly,experiments were conducted on the kinetics of CO₂ hydrate formation under 274.15 K and 3.0 MPa.The effects of different additive concentrations on the induction time,reaction time, gas consumption,and gas storage capacity of CO₂ hydrate formation were analyzed,and a comparison was made between monometallic and bimetallic supported materials.The results show that bimetallic Cu and Al can be uniformly loaded onto graphene oxide with good stability.At 274.15 K,3.0 MPa,and a concentration of 50 \mathrm{\mu } \mathrm{g} / \mathrm{g} ,the induction time of CO₂ hydrate is 85 min, the reaction time is 170 min, the gas consumption is 0.216 mol,and the gas storage capacity is 123.81 cm³/cm³.Compared with pure water system,the induction time and reaction time are shortened by about \mathrm{1}/\mathrm{4} and \mathrm{1}/\mathrm{7} respectively,and the gas consumption and storage capacity are correspondingly improved.Compared with the monometallic loading system，the maximum induction time is shortened by about \mathrm{1}/\mathrm{2} , the maximum reaction time is shortened by about \mathrm{1}/\mathrm{5} , and the gas storage capacity is significantly improved.

Cobalt?based catalyst is regarded as a suitable choice for Fischer?Tropsch synthesis (FTS) due to its high activity and strong C—C bond formation ability. FTS reaction mechanism of Co?based catalysts was summarised, and the structure of the active phase as well as the conformational relationship between additives and catalytic performance were analysed. For clarifying the role of catalyst supports, the promotion of FTS reaction via regulating metal?carrier interaction was also summarized. Specially, the direct synthesis of liquid fuel by coupling metal Co with zeolite catalyst was discussed, and the reaction route for liquid fuel and the character of as?used bifunctional catalyst were focused.

Graphite phase carbon nitride(g?C₃N₄), as an environmentally benign semiconductor material, has good application prospects in photocatalysis. However, the disadvantages of pure g?C₃N₄ such as small specific surface area and difficult separation of photogenerated carriers will limit its photocatalytic performance, which will restrict its large?scale application.From the synthetic methods and modification strategies, the research progress of g?C₃N₄ photocatalysts by researchers in recent years is reviewed, and the development of g?C₃N₄ photocatalysts in the fields of degradation of pollutants in water treatment, H₂ and H₂O₂ production is summarised, and it can be found that the performance of the modified g?C₃N₄ photocatalysts has been greatly improved.Finally,the development direction of g?C₃N₄ photocatalyst is prospected.

Aerogel is a solid material with the smallest density and lightest weight in the world at present. Its unique three?dimensional network structure makes it widely used. Cellulose aerogels not only have the characteristics of high porosity and high specific surface area of aerogels, but also can be degraded by microorganisms and be compatible with other substances, which is a new energy suitable for sustainable development. The preparation process of cellulose aerogel—sol gel process and hydrogel drying process are described. In addition, the applications of cellulose aerogel in oil?water separation, heat insulation, phase change, supercapacitor, biomedicine and other aspects are also introduced, and its development is prospected.

In order to achieve high ionic conductivity and good alkaline resistance of Polysulfone?based AEMs, chloromethylated polysulfone was prepared by green method, and crown ether?functionalized polysulfone membranes with different triethylamine and amino crown ether contents were then prepared using amino crown ether as cross?linking agent and metal ions and triethylamine as cationic groups followed by crown ether functional polysulfone membrane with triethylamine and triethylamine as cationic groups(PSF?CE _X ?QA_1?X ).The effect of the addition of polyethylene glycol on the membrane properties was explored by introducing the low molecular weight polyethylene glycol (PEG) into the above polysulfone cross?linking membrane.The results shown that the presence of hydrophilic polyethylene glycol helps to facilitate the formation of ordered ion channels in the membrane.The conductivity and alkali?resistant stability of PSF?CE _X ?QA_1?X ?PEG were improved compared to PSF?CE _X ?QA_1?X membrane.Among them, the electrical conductivity of PSF?CE_0.1?QA_0.9?PEG at 80 ℃ is 56.78 mS/cm,which can retain 85% of the original conductivity after alkaline resistance test.In addition,PSF?CE _X ?QA_1?X ?PEG has good dimensional and thermal stability.

The modification of waterborne polyurethane(WPU) coating can be improved, and the nanocomposite particles can be added to WPU coating, and its mechanical properties and ultraviolet resistance can be improved.GO was synthesized by modified Hummers method, nano?ZnO/CeO₂ by copprecipitation, and nano?GO?ZnO/CeO₂ by in situ polymerization.It was also characterised by FT?IR,TEM,SEM,XRD,etc.,and the effect of nano?GO?ZnO/CeO₂ doping on the performance of WPU was explored.The results showed that nano?GO?ZnO/CeO₂ was composed of hybrid particles formed by ZnO and CeO₂ of cubic crystal fluorite structure on the GO surface. Compared with the pure WPU film,the fracture tensile strength and elongation at break of the WPU film with the addition of a mass fraction of 0.6% nano?GO?ZnO/CeO₂ increased by 43.1% and 47.0%.After 168 h of UV aging experiments,the modified membrane absorbed 15.4% of water,increased the tensile strength at break by 328.0% and the elongation at break by 39.0%.It shows that nano?GO?ZnO/CeO₂ can effectively improve the mechanical properties and UV aging resistance of WPU after film formation.

Surface?enhanced Raman spectroscopy (SERS) is an important spectroscopic method with the advantages of high sensitivity, simplicity, fast detection and good selectivity. The performance of SERS is highly dependent on the properties of the enhanced substrate. Cellulose is one kind of the most abundant biopolymer in the world, which is inexpensive, readily available, renewable and environmental friendly. Therefore, cellulosic materials are usually employed to prepare SERS substrate. In this review, the enhancement mechanism of SERS was firstly disscussed, and then the fabrication of cellulose SERS substrates were introduced. The applications of cellulose SERS substrates were reviewed in biological analysis, water quality assessment, food safety and environmental pollution, and dye identification.

Organic polymer membranes have been widely used for wastewater treatment.Due to occurrence of irreversible membrane contamination,the replacement of the membrane after the performance decay leads to the generation of a large number of discarded membranes.How to realize the reuse of these waste polymer films has important economic and environmental value.In this study,a carbonaceous material with both ultramicroporous,mesoporous,and macroporous structures was prepared by a simple pyrolysis remodeling reaction using waste hollow fiber membranes as a template.The differences in the adsorption performance of the waste membrane?derived activated carbon and commercial activated carbon were investigated based on the structural characterizations of the carbonaceous materials.The kinetic and thermodynamic processes for the adsorption removal of typical aromatic hydrocarbon organic contaminants and antibiotics from water were investigated.It was found that the the waste membrane carbon with hierarchical pore structure had a higher removal capacity for aromatic hydrocarbon organic pollutants than commercial carbon,while the adsorption performance for antibiotics such as ciprofloxacin,carbamazepine and sulfadiazine was lower than that of commercial carbon.

This article conducts research on the injection production well patterns under different injection production conditions through two methods: physical simulation and numerical simulation. On the core scale, a reservoir physical simulation model was prepared based on similarity criteria. It was found that the higher the permeability of the physical model was, the lower the overall pressure value was and the smaller the average pressure drop after shutdown. As the viscosity of crude oil increases, the overall pressure of the model increases, and the reduction in pressure during adjustment becomes more pronounced. As the decrease in flow rate increases, the decrease in pressure regulation significantly increases. According to the numerical simulation results, due to the obstruction of the fault, there is no connectivity on both sides, resulting in different energy replenishment on both sides. As the mining progresses, the pressure difference decreases from 0.35 MPa in the initial stage to around 0.15 MPa.When both sides of the fault of the adjustment well are one injection and two extractions, the pressure difference between the two sides of the fault exists with the extension of the development time, but converges again in the late production period.While both sides of the fault of the adjustment well are one injection and two extractions and one injection and four extractions, the difference between the two sides of the fault pressure system increases with the extension of the development time. The research of this paper is of great significance to drilling of adjustment wells in the "Double High" oilfield.

Rising levels of nitrate and nitrogen in water bodies pose a potential threat to aquatic ecosystems and human health. Therefore, it is urgent to solve the problem of excessive nitrate in water bodies. Fe(NO₃)₃·9H₂O, Co(NO₃)₂·6H₂O, reed biochar, NH₃·H₂O was used as raw material, and co?precipitation method was used to load cobalt?iron layered bimetals onto reed biochar to prepare Co/Fe?LDH@BC for adsorption of excess nitrate nitrogen in water. The experimental results showed that Co/Fe?LDH@BC could effectively adsorb nitrate nitrogen in water, and its adsorption capacity was 88.52 mg/g. The adsorption kinetic model conforms to the pseudo?second?order kinetic model, and the isotherm conforms to the Langmuir isotherm model, indicating that the adsorption reaction is spontaneous and endothermic, which mainly involves four reaction mechanisms: ion exchange, ligand exchange, electrostatic attraction and hydrogen bonding. In addition, Co/Fe?LDH@BC has a strong affinity for nitrate nitrogen in most water bodies where coexisting anions are present, making it suitable for practical applications.

Aromaticity is one of the important chemical properties of aromatic compounds. Clarifying the aromaticity of a clearly ring?conjugated system is crucial for understanding the chemical reactivity and stability of the system. A detailed study of the aromaticity, one?photon absorption (OPA), two?photon absorption (TPA) spectra, and electron transfer properties of Kekulene was carried out through quantum chemical calculations and wave function analysis. The aromaticity of different benzene rings in the molecule was quantitatively analyzed through multicenter bond indices and AV1245 indices. The aromaticity of Kekulene was studied through various methods such as electron localization function (ELF), localized orbital locator (LOL), magnetic susceptibility current, and isotropic chemical shielding surface (ICSS). The electron transfer processes of OPA and TPA transitions were visualized through charge difference density (CDD) analysis. The results showed that the aromaticity of rings 1 and 2 was significantly stronger than that of rings 3 and 4. The π electrons of ELF and LOL can be highly delocalized on both sides of the first ring and form a loop. The OPA spectrum has excited states with higher transition dipole moments, which are more likely to become intermediate states in the TPA process. The research results can provide effective theoretical methods and application approaches for the aromaticity of different systems.

γ?Al₂O₃ is commonly used as a carrier for catalysts, and the physicochemical properties of its surface greatly influence the catalytic reaction. The exposed Al coordination environment can be regulated by adjusting the morphology of γ?Al₂O₃ carriers by changing the synthesis method and synthesis conditions. The energy of the exposed crystal lattice of carriers with different morphologies is different, which will directly affect the acidity of the carrier and the interaction between active metals, and active metals and carriers, thus creating different loading sites of active metals. Carrier morphology control is an effective way to regulate the structure of the active components. The regulation of the support morphology of the propane dehydrogenation catalyst will affect the catalytic performance. The research progress of γ?Al₂O₃ support was reviewed from the aspects of preparation method, morphology control, and its influence on propane dehydrogenation catalyst.

For the deep removal of CO from hydrogen?rich gas,the preparation of catalysts with better CO?Prox catalytic performance is a current research hotspot.CuO/NiO?CeO₂ catalysts were prepared by stepwise impregnation method,and the catalysts were characterized by XRD,BET,H₂?TPR and HR?TEM to investigate the effects of molar loading of metal Cu+Ni (metal loading) on the catalysts' structure,reduction properties and their CO?Prox performance.The results showed that Cu/Ni?O?Ce solid solutions were all formed in CuO/NiO?CeO₂ catalysts.The catalytic activity is mainly related to the content of Cu species highly dispersed on the carrier surface as well as to the content of the solid solution.Among them,the catalyst with a metal loading of 8% had a higher content of Cu species highly dispersed on the carrier surface and a higher content of solid solutions,and the catalyst exhibited better catalytic activity.Under the CO/H₂/CO₂/O₂/Ar atmosphere,a reaction temperature of 130 °C,an oxygen excess coefficient of 1.2,and a mass?air velocity of 20 266 mL/（g·h）,the CO conversion was 95.9%,and the CO oxidation selectivity was 86.3%.

Cu_0.7Mn_0.3Al_2.5 ternary solid solution spinel catalysts were prepared by ball milling method using copper nitrate as the copper source, proposed thin alumina as the aluminium source, citric acid as the additive, and manganese acetate as the third component to partially replace copper. With the help of characterisation techniques such as XRD, BET, H₂?TPR and XPS, the crystalline phase structure, weaving properties, reducing properties and surface cation states and distributions of Cu_0.7Mn_0.3Al_2.5 were investigated. The catalytic performance of Cu_0.7Mn_0.3Al_2.5 in methanol steam reforming (MSR) for hydrogen production with a sustained release feature was scrutinized, and a comparison was made with CuAl_2.5 binary spinel and Cu_0.7Zn_0.3Al_2.5 ternary spinel catalysts. The results showed that compared with CuAl_2.5 and Cu_0.7Zn_0.3Al_2.5, the Cu_0.7Mn_0.3Al_2.5 exhibited the maximum contraction of the unit cell, resulting in a smaller unit cell constant. The catalyst had smaller crystalline size and higher specific surface area. The catalyst showed an aluminium?rich state, but with a higher percentage of Cu in the surface spinel phase, which made the reduction under H₂ atmosphere more difficult, and exhibited a better slow?release catalytic performance in MSR hydrogen production. Under the conditions of a reaction temperature of 265 °C, n（H₂O）/n（CH₃OH） =2, and mass flow rate of 2.25 h^-1, a stable conversion rate of 84% was achieved for 40 hours. The study provided valuable data reference for the development of efficient copper?based sustained?release catalysts.

Solving the sensitivity of concrete to admixture dosage and concrete shrinkage has always been a technical challenge eagerly awaited in the construction industry.A new type of ester polycarboxylate superplasticizer monomer (ACPEG) was synthesizeduses by 3?methyl?3?butenoxyacetic acid (MBA) as the priming agent.The relative molecular mass (M_w) of ACPEG was determined to be 2 389 by an multi?angle laser dispersion spectrumeig scattering instrument,indicating the formation of a polyether monomer structure.The results showed that ACPEG has a unique advantage of low polymerization activity,allowing for the one?step synthesis of superplasticizers at 40 ℃ without risk of explosion.The superplasticizer synthesized from ACPEG exhibited a water?reducing rate of 37.4%,segregation rate of 10.8%,bleeding rate of 6.2% at 1 hour,and surface tension of 35.67 mN/m. Although slightly inferior to superplasticizers synthesized from ester?type monomers (MAPEG) in terms of workability,ACPEG outperformed superplasticizers synthesized from methallyl polyethylene glycol ethers (IPEG) and isoprene polyethylene glycol ethers (TPEG) in concrete slump,bleeding distance,segregation rate,workability,and shrinkage reduction effects.

Under alkaline conditions,the aldehyde group is introduced into dibenzo?18?crown?6 (DB18C6) with the help of chloroform (CHCl₃) to prepare dimethyl dibenzo?18?crown?6 (DDB18C6).Then,using DDB18C6 and soluble deacetylated chitin (CTS) as raw materials,Schiff reaction was used to synthesize a grafted crown ether CTS membrane with an increasing mass fraction of small molecule crown ethers,which was named C _a ?CTS membrane (a=m(DDB18C6)/m(C _a ?CTS membrane）).The C _a ?CTS membrane is ion exchanged in alkali solution.The C _a ?CTS membrane absorbs K⁺ through the oxygen hole structure,and then the C _a ?CTSK membrane is prepared.Eeach stage the sample membrane was subjected to structural characterization and performance testing.The results show that with the increase of the crown ether grafting degree,the thermal stability of CTS can be improved;when a=0.20,the grafting degree of C_0.20?CTSK membrane can reach 43.91%,the water absorption rate can reach 168.6%,the IEC value is 1.38 mmol/g. At a temperature of 70 ℃,the conductivity of C_0.20?CTSK membrane can reach 46.8 mS/cm; the introduction of grafting of crown ether improves the alkali resistance stability of this series of membranes. After the C _a ?CTSK series membranes are soaked in 6 mol/L KOH solution for 480 hours, the conductivity decreases only 4.0%.

The Biological seepage studies the seepage of biofluids in living organisms and fluids containing microorganisms in non?biological porous media.The mass transfer diffusion osmosis phenomenon of a porous bioelastomer material,poly(glycidyl sebacate) (PGS),implanted into human soft tissues was simulated.The pore structure of the PGS material was characterised by N₂ adsorption?desorption and the scaffold model with different pore numbers and pore diameters was designed using the multi?physics field simulation software?COMSOL to investigate the effects of pore and pore diameter parameters on blood osmosis when the pore size was constant.COMSOL was used to design the adapted PGS stent models,numerically simulate the characteristics of the blood flow when blood flowed through the PGS stent,and analyse the kinetic viscosity and the shear rate of the blood field with the theory of fluid dynamics.Comparative analyses of seepage pressure and diffusion at different blood inlet velocities were carried out. The results show that the PGS material is a material that tends to be mesoporous.When the blood flows inside the porous scaffold, the kinetic viscosity varies with the shear rate,indicating that the blood seepage inside the scaffold is a kind of non?Newtonian fluid seepage.The diffusion speed of the blood inside the porous scaffold is different under different inlet velocities and the larger the inlet velocity is,the higher the pressure,and the faster the mass transfer diffusion speed will be.