Specific Surface Properties Research Articles

Research progress of nanoscale zero-valent iron in synergistic combinations of denitrifying bacteria for nitrate removal

Nitrate (NO3--N) is a common inorganic nitrogen pollutant in water. Excessive NO3--N can lead to water eutrophication and threaten human health. Nanoscale zero-valent iron (nZVI) has attracted much attention in NO3--N removal due to its high specific surface and excellent electron donor properties. The combination of nZVI and denitrifying bacteria (DNB) demonstrates high efficiency in converting NO3--N into N2. This approach not only substantially enhances the removal rate of NO3--N but also exhibits superior environmental sustainability compared with conventional chemical denitrification methods. Accordingly, it holds substantial promise for mitigating NO3--N pollution and warrants further exploration in the pollution control. Therefore, it is necessary to understand the interaction mechanism between nZVI and DNB for NO3--N removal. This paper details the factors affecting the removal of NO3--N by nZVI combined with DNB, reviews the latest research progress in this field, elaborates on the interaction mechanism between nZVI and DNB for NO3--N removal, and discusses the challenges and future research directions of NO3--N removal by nZVI combined with DNB. This review aims to provide a theoretical basis for the development of efficient approaches for the remediation of NO3--N pollution.

Diatoms in Focus: Chemically Doped Biosilica for Customized Nanomaterials.

Diatoms are photosynthetic microalgae widely diffused around the globe and well adapted to thrive in diverse environments. Their success is closely related to the nanostructured biosilica shell (frustule) that serves as exoskeleton. Said structures have attracted great attention, thanks to their hierarchically ordered network of micro- and nanopores. Frustules display high specific surface, mechanical resistance and photonic properties, useful for the design of functional and complex materials, with applications including sensing, biomedicine, optoelectronics and energy storage and conversion. Current technology allows to alter the chemical composition of extracted frustules with a diverse array of elements, via chemical and biochemical strategies, without compromising their valuable morphology. We started our research on diatoms from the viewpoint of material scientists, envisaging the possibilities of these nanostructured silica shells as a general platform to obtain functional materials for several applications via chemical functionalization. Our first paper in the field was published in ChemPlusChem ten years ago. Ten years later, in this Perspective, we gather the most recent and relevant functional materials derived from diatom biosilica to show the growth and diversification that this field is currently experiencing, and the key role it will play in the near future.

Improving the Bioactivity and Antibiofilm Properties of Metallic Implant Materials via Controlled Surface Microdeformation.

Although metallic implants provide most of the required properties for bone-related applications, especially orthopedic implants, insufficient osseointegration, which may lead to loosening of the implant or prolonged healing time, is still an issue to be resolved. Osseointegration can be improved via application of various surface treatments on the metal surface. The current study focuses on a novel surface microdeformation method, which enables the formation of controlled surface patterns of various parameters. With this purpose, a surface microdeformation procedure was applied on 316L stainless steel surfaces, forming four different patterns which affected various surface parameters such as roughness, surface energy, dislocation activities close to the surface, and wettability. Static immersion tests in a simulated body fluid (SBF) environment showed that modifying the surface parameters via controlled surface patterning promoted the formation of a stable oxide layer and calcium-phosphate (CaP) deposition on the metal surfaces, improving bioactivity. Moreover, the higher amount of CaP deposition and oxide layer formation on the modified surfaces led to reduced ion release, which contributed to improved corrosion resistance. Finally, the effect of the formed surface patterns on antibiofilm formation was investigated via incubation with C. albicans for 24 h, which exhibited that microdeformation patterns remarkably inhibited the biofilm formation. Throughout the experiments, certain patterns yielded outstanding results among the four patterns formed. Overall, it was concluded that forming controlled patterns on stainless steel surfaces via surface microdeformation significantly contributed to the metal's biocompatibility via improving bioactivity, corrosion resistance, and antibiofilm formation properties. Especially, the specific surface properties such as increased surface energy, high surface roughness, and dislocation density close to the metal surface as well as increased hydrophilicity obtained via forming the pattern with relatively deeper and narrowly spaced indents yielded the most promising outcomes. These methodologies constitute novel approaches to be used while designing new methodologies for the surface modification of metallic implant materials for improved osseointegration.

Exploration of the adsorption and desorption performance of volatile organic compounds by activated carbon with different shapes based on fixed-bed experiments

Activated carbon (AC) has been widely used in volatile organic compounds (VOCs) treatment of industrial exhaust gases. Rather than modifying specific pore size distributions and surface properties, altering the shape of AC offers a more feasible approach to enhance its adsorption performance. This study investigates the adsorption-desorption performance of two different shaped ACs with highly similar properties for the removal of VOCs. The clover-shaped AC (CSAC) has a 27.46% lower internal void fraction and a 39.10% higher external void fraction compared to cylindrical AC (CAC), resulting in denser packing and longer contact time with VOCs. Adsorption experiments showed the CSAC has 40% longer adsorption breakthrough (BT) times for ethanol, ethyl acetate, and n-hexane on average, and 20% higher saturation adsorption capacity per unit volume. CSAC also has higher partition coefficients, with the highest values for ethanol, ethyl acetate, and n-hexane being 0.0187, 0.0382, and 0.0527 mol kg−1·Pa−1, respectively. The desorption process for selected VOCs is non-spontaneous and endothermic. Optimal desorption conditions were identified as an inlet space velocity of 3535 h−1, a desorption temperature of 150 °C, and a pulsed inlet method. To investigate the possibility of the application of CSAC in real-world scenarios, xylene was chosen as a representative industrial VOC. Results showed CSAC has 20% higher BT time and saturation adsorption capacity for xylene compared to CAC under different bed heights. The desorption efficiency for xylene on both ACs is below 40%. With increasing xylene inlet concentration, the mass transfer zone (MTZ) height initially increases but stabilizes beyond 1704 mg m−3. At identical bed heights, the MTZ height of CSAC is 29% shorter than CAC, indicating a higher bed utilization efficiency.

Properties and mechanism of uranium adsorption on single-sided fluorinated graphene: A first-principles study

Functionalized two-dimensional materials have been widely explored as possible candidates to adsorb radioactive nuclide due to their large specific surface and tunable properties. In this work, single-sided fluorinated graphene (ssFG) with different fluorinated rates have been predicted to be an effective adsorbent for uranium atoms using density functional theory (DFT) simulations. The linear response method was used to obtain a more accurate Hubbard U value (3.1 eV) of the 5f orbital of the uranium atom. Our calculated results show that uranium atoms were energetically favorable adsorbed on the C2F, C6F, C8F ssFGs, and their adsorption energies are 3.45, 1.20, and 1.12 eV, respectively. The electronic analysis, such as the density of states, charge transfer and differential charge density suggest that the uranium atom has the strongest chemisorption with the substrate C2F. C2F also exhibits excellent performance in terms of the adsorption capacity of uranium atoms. In addition, the critical temperature for the adsorption-desorption transition of uranium atoms was predicted to be 632 K by the adsorption rate equation. The results suggest that ssFG, especially C2F, was a promising material for uranium adsorption, have promising application in nuclear waste disposal, extraction of uranium from seawater, uranium detection, etc.

Optimizing TPU performance: The role of mold temperature on injection molding of TPU

AbstractThis study explores the influence of mold temperatures below 60°C on thermoplastic polyurethane (TPU) properties during injection molding, focusing on phase separation and its impact on mechanical, thermal, and viscoelastic properties. Using a combination of micro‐indentation, temperature scanning stress relaxation, and conventional characterization methods, the research highlights how increased mold temperatures promote more distinct phase separation, enhancing mechanical stability and physical properties. The novel use of micro‐indentation revealed a gradient in material stiffness from the surface to the core of injection‐molded samples, attributed to differential cooling rates and shear forces, which affect phase separation and crystallinity of the hard domains. These insights are critical for applications requiring specific surface properties and underscore the importance of understanding the interplay between chemical composition and processing conditions for optimizing TPU properties. Furthermore, the paper shows that tensile testing, differential scanning calorimetry, and Shore hardness cannot quantify the effects of mold temperatures below 60°C. The research highlights the influence and importance of chemical composition, rheological history, and thermal history on the properties of TPU.

Nanoparticles for stimulation of neutrophil extracellular trap-mediated immunity.

Neutrophil extracellular traps (NETs) have been identified as triggers for a self-limited inflammatory reaction upon contact with nanoparticles within our bodies. This typically results in entrapping potentially harmful nano- or micro-objects following an immune burst. The demand for potent adjuvants has led to research on particulate-based adjuvants, particularly those that act via NET formation. Various particles, including hydrophobic nanoparticles, needle-like microparticles, and other natural and artificial crystals, have been shown to induce NET formation, eliciting a robust humoral and cellular immune response toward co-injected antigens. The NET formation was found to be the basis of the efficient use of alum as a vaccine adjuvant. Thus, nanoparticles with specific surface properties serve as NET-stimulating adjuvants. In this mini-review, we aim to summarize the current knowledge about the surface properties of particulate objects and the molecular pathways involved in inducing NET formation by neutrophils. Additionally, we discuss the potential use of nanoparticles for activating neutrophils in the tissues and the exploitation of such activation for enhancing vaccine adjuvants.

Catalytic conversion of volatiles over homologous char: Distinct interaction patterns at different temperatures

Char produced at specific pyrolysis temperatures has specific surface properties, which is also expected to have specific interaction patterns with volatiles produced at the same temperature. In this study, the char produced at varied temperatures was used for catalyzing conversion of homogenous volatiles generated at the same temperature. The aim was to explore the change of properties of char catalyst via volatiles-char interaction, which was almost equivalent to the evolution of property of char in pyrolysis. The results suggested that the char-300 (the number refers to temperature (°C) for production of char) and char-450 retained abundant oxygen-containing functionalities, rendering them superior activity for cracking of aliphatics and aromatics, producing less bio-oil with a lower abundance of π-conjugated structures but more gases (especially over char-450, increased by 57.8%). Char-600 and char-750, with a lower abundance of oxygen-containing functionalities, were not that active for cracking or interaction with volatiles, and their properties were also not changed that much. In comparison, the spent char-300 and char-450 experienced remarkable dehydrogenation and deoxygenation via interaction with volatiles, resulting in overall net weight loss, increased carbon content as well as enhanced thermal stability, aromatic degree, and carbon crystallinity. The biggest change of char-600 and char-750 could be the filling of pores with volatiles-derived deposits. The characterization of catalytic pyrolysis with in-situ IR technique also confirmed that the char-300 showed higher capability than char-750 for catalyzing conversion –OH and CO via varied reaction routes.

In situ synergistic reduced graphene oxide-boron carbon nitride nanosheet heterostructures for high-performance fabric-based supercapacitors.

We develop a new type of heterostructure nanocomposite made of reduced graphene oxide-boron carbon nitride nanosheets (rGO-BCN) by B-C covalent bonds. The rGO-BCN nanocomposite delivers a large specific surface and excellent electrochemical properties, and is then constructed into flexible fabric-based high-performance supercapacitor electrodes based on the microfluidic electrospinning technology.

A Spinel Metal Oxide (Ni–Fe–O) Decorated Glassy Carbon Electrode as a Sensitive Sensor for the Electrochemical Detection of Fenitrothion

Fenitrothion is a widely prescribed pesticide in agriculture to control penetrating, chewing, and sucking pests on various crops. The electrochemical analytical technique is the obvious choice for establishing a fast, simple, cheap, and sensitive method for fenitrothion analysis. Nickel-iron spinel is an ideal material for electrode modification due to its good electrochemical catalytic properties, high specific surface properties of the nanoparticles, and target trapping ability of the metal hydroxyl sites. Therefore, this work intends to improve the detection of fenitrothion in the environmental matrix by adopting an electrochemical sensor. Herein, NiFe2O4 material was prepared in terms of the hydrothermal synthesis method. Its electrocatalytic performance in fenitrothion detection was evaluated. The synthesized NiFe2O4 was characterized using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The electrocatalytic performance of the electrode modified by NiFe2O4 was studied through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). It was observed that the fabricated electrochemical sensor based on NiFe2O4 modified electrode exhibited higher electrocatalytic activity towards fenitrothion, resulting in a wide linear range of detection with a low limit of detection (LOD) of 1 × 10−8 mol l−1.

Preparation of high-efficiency titanium ion immobilized magnetic graphite nitride nanocomposite for phosphopeptide enrichment

BackgroundProtein phosphorylation has been implicated in life processes including molecular interaction, protein structure transformation, and malignant disease. An in-depth study of protein phosphorylation may provide vital information for the discovery of early biomarkers. Mass spectrometry (MS)-based techniques have become an important method for phosphopeptide identification. Nevertheless, direct detection remains challenging because of the low ionization efficiency of phosphopeptides and serious interference from non-phosphopeptides. There is a great need for an efficient enrichment strategy to analyze protein phosphorylation prior to MS analysis. ResultsIn this study, a novel nanocomposite was prepared by introducing titanium ions into two-dimensional magnetic graphite nitride. The nanocomposite was combined with immobilized metal ion affinity chromatography (IMAC) and anion-exchange chromatography mechanisms for phosphoproteome research. The nanocomposite had the advantages of a large specific surface (412.9 m2 g−1), positive electricity (175.44 mV), and excellent magnetic property (35.7 emu g−1). Moreover, it presented satisfactory selectivity (α-casein:β-casein:bovine serum albumin = 1:1:5000), a low detection limit (0.02 fmol), great recyclability (10 cycles), and high recovery (92.8%). The nanocomposite demonstrated great practicability for phosphopeptides from non-fat milk, human serum, and saliva. Further, the nanocomposite was applied to enrich phosphopeptides from a more complicated specimen, A549 cell lysate. A total of 890 phosphopeptides mapping to 564 phosphoproteins were successfully detected with nano LC-MS. SignificanceWe successfully designed and developed an efficient analysis platform for phosphopeptides, which includes protein digestion, phosphopeptide enrichment, and MS detection. The MS-based enrichment platform was further used to analyze phosphopeptides from complicated bio-samples. This work paves the way for the design and preparation of graphite nitride-based IMAC materials for phosphoproteome analysis.

Removal of per- and polyfluoroalkyl substances by activated hydrochar derived from food waste: Sorption performance and desorption hysteresis

Carbonaceous materials, derived from waste biomass, have proven to be a viable and appealing alternative for removing emerging micro-pollutants, such as per- and polyfluoroalkyl substances (PFAS). To assess the feasibility and efficacy of using material derived from food waste to alleviate PFAS pollution, this study prepared activated hydrochar (AHC) for sorbing ten PFAS, including five perfluoroalkyl carboxylic acids (PFCA; C4–C8), three perfluoroalkyl sulfonic acids (PFSA; C4, C6, C8), and two emerging PFAS, namely hexafluoropropylene oxide dimer acid (commercial name GenX, an alternative to perfluorooctanoic acid (PFOA)) and 6:2 fluorotelomer sulfonic acid (6:2 FTS). The results demonstrated that AHC possessed a relatively high specific surface area (207 m2/g) and hydrophobic surface properties. At environmentally relevant concentrations (40 μg/L), the sorption partition coefficients (log Kd) of PFAS on AHC ranged from 2.33 to 6.49 L/kg. Notably, GenX exhibited a lower log Kd value (2.33 L/kg) than PFOA (3.88 L/kg). The AHC showed favorable sorption performance for all tested PFAS, with log Kd values surpassing other reported sorbents (e.g., 0.83 for GenX on pyrochar, and 2.83 for PFOA on commercial biochar). Additionally, desorption hysteresis was observed for all PFAS, except for PFOA, and was particularly pronounced in PFBA, GenX, and 6:2 FTS at high initial concentrations, with Hysteresis Index (HI) values varying from 0.31 to 1.45, 0.68 to 1.88, and 0.51 to 1.85, respectively. Given its robust sorption capacity and desorption hysteresis toward PFAS, AHC is expected to be a favorable candidate for remediating PFAS-contaminated water. This study underscores, for the first time, the potential of food waste-derived hydrochar as an efficient sorbent for alleviating PFAS contamination, and further study is needed to investigate the sorption and desorption behaviors of PFAS on AHC at various environmental conditions.

Material matters: exploring the interplay between natural biomaterials and host immune system

Biomaterials are widely used for various medical purposes, for instance, implants, tissue engineering, medical devices, and drug delivery systems. Natural biomaterials can be obtained from proteins, carbohydrates, and cell-specific sources. However, when these biomaterials are introduced into the body, they trigger an immune response which may lead to rejection and failure of the implanted device or tissue. The immune system recognizes natural biomaterials as foreign substances and triggers the activation of several immune cells, for instance, macrophages, dendritic cells, and T cells. These cells release pro-inflammatory cytokines and chemokines, which recruit other immune cells to the implantation site. The activation of the immune system can lead to an inflammatory response, which can be beneficial or detrimental, depending on the type of natural biomaterial and the extent of the immune response. These biomaterials can also influence the immune response by modulating the behavior of immune cells. For example, biomaterials with specific surface properties, such as charge and hydrophobicity, can affect the activation and differentiation of immune cells. Additionally, biomaterials can be engineered to release immunomodulatory factors, such as anti-inflammatory cytokines, to promote a tolerogenic immune response. In conclusion, the interaction between biomaterials and the body’s immune system is an intricate procedure with potential consequences for the effectiveness of therapeutics and medical devices. A better understanding of this interplay can help to design biomaterials that promote favorable immune responses and minimize adverse reactions.

Facile prepared microfluidic chip for multiplexed digital RT-qPCR test.

The chip-based digital polymerase chain reaction (PCR) is an indispensable technique for amplifying and quantifying nucleic acids, which has been widely employed in molecular diagnostics at both fundamental and clinical levels. However, the previous designs have yet to achieve widespread application due to limitations in complex chip fabrication, pretreatment procedures, special surface properties, and low throughput. This study presents a facile digital microfluidic chip driven by centrifugal force for digital PCR analysis. Interestingly, regardless of the hydrophilicity or hydrophobicity of the inner chip surface, an efficient digitization process can be achieved. PCR reagents introduced into the inlet can be allocated to 9600 microchambers and subsequently isolated by the immiscible phase (silicone oil). The centrifugal priming approach offers a facile means to achieve high-throughput analysis. The design was further employed for the quantification of nucleic acids using digital PCR. The calculated result exhibited a strong correlation with the measured value at the concentrations from 1 copy/μL to 1000 copies/μL (R2 =0.99). Additionally, the chip also allowed digital multiplexed analysis, thereby indicating its potential for multi-target detection applications.

Advanced surface engineering of titanium materials for biomedical applications: From static modification to dynamic responsive regulation.

Titanium (Ti) and its alloys have been widely used as orthopedic implants, because of their favorable mechanical properties, corrosion resistance and biocompatibility. Despite their significant success in various clinical applications, the probability of failure, degradation and revision is undesirably high, especially for the patients with low bone density, insufficient quantity of bone or osteoporosis, which renders the studies on surface modification of Ti still active to further improve clinical results. It is discerned that surface physicochemical properties directly influence and even control the dynamic interaction that subsequently determines the success or rejection of orthopedic implants. Therefore, it is crucial to endow bulk materials with specific surface properties of high bioactivity that can be performed by surface modification to realize the osseointegration. This article first reviews surface characteristics of Ti materials and various conventional surface modification techniques involving mechanical, physical and chemical treatments based on the formation mechanism of the modified coatings. Such conventional methods are able to improve bioactivity of Ti implants, but the surfaces with static state cannot respond to the dynamic biological cascades from the living cells and tissues. Hence, beyond traditional static design, dynamic responsive avenues are then emerging. The dynamic stimuli sources for surface functionalization can originate from environmental triggers or physiological triggers. In short, this review surveys recent developments in the surface engineering of Ti materials, with a specific emphasis on advances in static to dynamic functionality, which provides perspectives for improving bioactivity and biocompatibility of Ti implants.

The Role of Particle Size and Shape on the Recovery of Copper from Different Electrical and Electronic Equipment Waste

The increasing world population and the development of technology have boosted the demand for electrical and electronic equipment (EEE). Equipment that has completed its life cycle causes serious damage to the environment due to its toxic components. In addition, it contains many more base metals (copper, aluminum, nickel, lead, tin, etc.) and precious metals (silver, gold, palladium, platinum, etc.) compared with a run of mine ore. Recycling these values with an economic and environmental understanding will ensure sustainability and prevent the rapid depletion of natural resources. Specific gravity, magnetic, electrostatic, optical, surface, thermal, and other property differences between particles as well as the shape, size, and distribution of individual particles directly determine the success of the recycling process. By determining the behavior of the particles during enrichment and producing grains suitable for enrichment with better performance in the size reduction stage, the quality of the concentrate to be subjected to the final chemical/metallurgical treatment will be enhanced. The main aim of this study is to reveal the effect of particle size and shape properties on the recovery of valuable metals from two different waste electrical and electronic equipment (WEEE) sources, end-of-life printed circuit boards and waste electric wires, using environmentally friendly, easier-to-use, and cost-effective mechanical, physical, and physiochemical processes. Deciding on the most suitable enrichment process after detailed characterization of the products obtained from different comminution equipment and their particle size and shape directly affected the amount, content, and recovery of the final concentrate.

Scanning Strategies in Laser Surface Texturing: A Review.

Laser surface texturing (LST) is one of the most promising technologies for controllable surface structuring and the acquisition of specific physical surface properties needed in functional surfaces. The quality and processing rate of the laser surface texturing strongly depend on the correct choice of a scanning strategy. In this paper, a comparative review of the classical and recently developed scanning strategies of laser surface texturing is presented. The main attention is paid to maximal processing rate, precision and existing physical limitations. Possible ways of further development of the laser scanning strategies are proposed.

Effect of Chain Structure on the Various Properties of the Copolymers of Fluorinated Norbornenes with Cyclooctene.

Fluorinated polymers are attractive due to their special thermal, surface, gas separation, and other properties. In this study, new diblock, multiblock, and random copolymers of cyclooctene with two fluorinated norbornenes, 5-perfluorobutyl-2-norbornene and N-pentafluorophenyl-exo-endo-norbornene-5,6-dicarboximide, are synthesized by ring-opening metathesis copolymerization and macromolecular cross-metathesis in the presence of the first- to third-generation Grubbs' Ru-catalysts. Their thermal, surface, bulk, and solution characteristics are investigated and compared using differential scanning calorimetry, water contact angle measurements, gas permeation, and light scattering, respectively. It is demonstrated that they are correlated with the chain structure of the copolymers. The properties of multiblock copolymers are generally closer to those of diblock copolymers than of random ones, which can be explained by the presence of long blocks capable of self-organization. In particular, diblock and multiblock fluorine-imide-containing copolymers show a tendency to form micelles in chloroform solutions well below the overlap concentration. The results obtained may be of interest to a wide range of researchers involved in the design of functional copolymers.

Catalytic oxidation of Bisphenol A with Co3+ rich spinel Co3O4: Performance evaluation with peroxymonosulfate activation and mineralization mechanism

Bisphenol A (BPA) is a toxic substance that is released into the environment mainly from paint, polymer, plastics and pharmaceutical industries. In this study, spinel Co3O4 consisting of Co2+/(Co3+)2O4 nanospheres with excellent specific surface properties were systematically synthesized via a simple hydrothermal approach preceded by calcination. The as-synthesized Co3O4 spinels were used for peroxymonosulfate (PMS) activation to reduce the bisphenol A (BPA). The effects of operating parameters including PMS dosage, initial pH, catalyst dosage, and co-existing ions were detected during the BPA degradation. It was observed that at neutral pH, the nano-Co3O4/PMS system effectively degrades the BPA (∼92%) with very low cobalt leaching and excellent recyclability. Control experiment analysis confirms the magnificent performance of the Co3O4/PMS system and the synergistic interaction between Co3O4 and PMS. Various characterization techniques were used to determine the thermal, textural and structural properties. A chemical quenching study confirmed that both hydroxyl radicals (•OH) and sulfate radicals (SO4•−) promotes BPA oxidation. The chloride (Cl-) ions and dihydrogen phosphate ions (H2PO4-) have little inhibition effect while adding humic acid (HA) and HCO3- inhibits the BPA oxidation. Separation techniques such as high-performance liquid chromatography (HPLC) coupled with mass spectroscopy (MS) were used to identify the oxidative by-products and the mineralization pathway of BPA reduction. First-order pseudo-kinetics were observed for BPA degradation. However, the power law model also fits nth-order kinetics models.

Heterogeneous Surface Reaction Analysis of Non-Thermal Plasma-Enhanced Spherical MOx/(Ce0.7Ti0.3)O2 Catalyst Desulfurization: Effects of Plasma and MOx Loading on Surface Oxygen Defects

Homogeneous gas-phase plasma reactions and heterogeneous surface reactions are involved in non-thermal plasma-enhanced catalysis, along with a very complicated strengthening mechanism. In this study, we supported CuO, Co3O4, Fe2O3, or NiO on a hydrothermally synthesized spherical (Ce0.7Ti0.3)O2 catalyst, analyzed its active sites, and examined how plasma affects the catalyst surface and influences heterogeneous surface reactions. Loading CuO onto the catalyst led to increases of 5.85 and 13.51% in the proportions of surface Ce3+ and surface O vacancies, respectively. The CuO-loaded catalyst exhibited a significantly higher redox capacity than the other catalysts at 250–290 °C, which promotes SO2 desorption and surface reactions at low temperatures. Treatment with plasma led to increases in the active-to-lattice-oxygen ratio on the catalyst surface (by 19.12%), the defect-induced D-band to F2g band (ID/IF2g) ratio (by 0.443), and the D-band intensity (by a factor of 3.5). Significantly more defects that adsorb plasma-generated oxygen radicals (O* and O2*) and O3, which subsequently oxidize adsorbed pollutant molecules, are present on the catalyst surface. In general, the special surface properties of the spherical CuO/(Ce0.7Ti0.3)O2 catalyst are applicable to a broad number of non-thermal plasma-enhanced catalytic oxidation scenarios.