Low Reaction Rate Research Articles

Efficacy and safety of Xiaofeng powder in the treatment of chronic urticaria: A systematic review and meta-analysis.

Chronic urticaria is a group of skin diseases characterized by pruritus and/or vascular oedema and belongs to the category of "addictive rash" in Traditional Chinese Medicine, and its aetiology is closely related to wind evil. Antihistamines are often used in treatment. Although they have certain effects, they also easily cause disease recurrence. Xiaofeng powder treats this disease has a significant effect in improving the disease state and reducing the recurrence rate. However, there is a lack of evidencebased research. This study to systematically evaluate the clinical efficacy of modified Xiaofeng powder in the treatment of chronic urticaria (CU). Computer searches of Chinese databases such as China National Knowledge Infrastructure, China Scientific Journal Database, China Biomedical Literature Database, and WanFang Date and foreign databases such as PubMed and the Web of Science were performed. We retrieved published clinical randomized controlled trials of Xiaofeng powder in the treatment of CU from the establishment of the databases to November 2023. The data were extracted from clinical trials that met the inclusion criteria of this study, and the quality was evaluated through the Cochrane Handbook of Systematic Reviews 5.1.0. Finally, a meta-analysis was performed using RevMan 5.3 statistical software. A total of 11 randomized controlled trials involving 1076 patients were included. The cure rate odds ratio (OR) and 95% confidence interval (CI; shown in brackets) were 2.11 [1.45, 3.07]; the total effective rate OR and CI were 2.42 [1.60, 3.68]; the recurrence rate OR and CI were 0.22 [0.15, 0.34]; the adverse reaction rate OR and CI were 0.23 [0.12, 0.45]; and the mean weighted mean difference (MD) and 95% CI (shown in brackets) of itching degree, wind mass size, wind mass number and wind mass duration in symptom and sign integrals were -0.70 [-0.73, 0.67], -0.64 [-0.96, 0.31], , -0.72 [-1.23, 0.22], and -0.68 [-1.13, 0.23], , respectively. The clinical efficacy of modified Xiaofeng powder in the treatment of CU is better than that of antihistamine drugs, with lower adverse reaction and recurrence rates and higher safety. However, the quality of clinical research included is relatively low, and findings need to be confirmed by high-quality research.

Impact of Pickering Emulsions Composition on Lipase Catalyzed Peroxyacetic Acid Synthesis

AbstractDue to the need for environmental protection and sustainability, there has been a rising need to replace the traditionally harsh oxidative functionalization process, which is essential for syntheses of various organic compounds, by biocatalysis. However, the investigated alternative processes are still challenged with enzyme instability and/or low specific reaction rate. Due to these still existing challenges and the recognition of Pickering emulsions as an efficient platform for continuous biphasic biocatalysis, the first, enzymatic step of the lipase catalyzed oxidative functionalization was investigated in bioactive Pickering emulsions. The study focused on the impact of Pickering emulsion composition such as the volume phase fraction, type and concentration of the nanoparticles and enzymes on continuous peroxyacetic acids synthesis. The type of nanoparticles used and Candida antarctica lipase B concentration significantly impacted the process while the other named parameters only had a marginal influence.

Dramatic change in the properties of magnetite-modified MOF particles depending on the synthesis approach

Iron-containing metal–organic frameworks are promising Fenton catalysts. However, the absence of additional modifiers has proven difficult due to the low reaction rates and the inability to manipulate the catalysts. We hypothesize that the production of iron oxide NPs in the presence of a metal-organic framework will increase the rate of the Fenton reaction and lead to the production of particles that can be magnetically manipulated without changing the structure of the components. A comprehensive approach lead to a metal organic framework using the example of MIL-88b (Materials of Institute Lavoisier) modified with iron oxides NPs: formulation of iron oxide in the presence of MIL-88b and vice versa. The synthesis of MIL-88b consists of preparing a complexation compound with the respective structure and addition of terephthalic acid. The synthesis of MIL-88b facilitates to control the topology of the resulting material. Both methods for composite formulation lead to the preservation of the structure of iron oxide, however, a more technologically complex approach to obtaining MIL-88b in the presence of Fe3O4 suddenly turned out to be the more efficient for the release of iron ions.

Boosting nitrate electroreduction reactivity with a 3D Cu-Pd bimetallic flow-through electrode

NO3− pollution in water and wastewater is a pressing global environmental issue, leading to the deterioration of water quality and an increased risk to human health. Herein, we present a three-dimensional (3D) flow-through electrode composed of electrodeposited Cu-Pd bimetallic catalysts on a nickel foam. The Cu-Pd bimetallic particles exhibited cluster-like shapes on the surface of the nickel foam. This electrode design enhanced the electrochemical activity of the NF/Cu63Pd37 electrode for NO3− reduction, as evidenced by linear sweep voltammetry (LSV) measurements. By tailoring the Cu-Pd ratio (Cu:Pd 0.63:0.37), the NF/Cu63Pd37 electrode showed the highest reactivity of NO3− reduction and selectivity (43.1 %) toward N2. Importantly, the NF/Cu63Pd37 electrode not only achieved over 99 % NO3− removal but also exhibited a higher kinetic rate constant of 1.44 h−1 in the flow-through mode. In contrast, in the flow-by mode, NO3− removal was 67.5 % with a lower reaction rate constant of 0.30 h−1. Furthermore, the NF/Cu63Pd37 electrode exhibited a reduced energy consumption (EEO) of 6.86 kWh m−3 order−1 in the flow-through mode, contrasting with 13.66 kWh m−3 order−1 in the flow-by mode. Moreover, the results also demonstrated successful NO3− remediation across various initial pH values (pH 3, 6, 9, and 11) and NO3− concentrations (100, 200, and 300 mg L−1). The results of this study highlight that the 3D Cu-Pd bimetallic flow-through electrode, with its high reactivity in reducing NO3−, marks a significant advancement in efficiently treating nitrate-contaminated water.

The Impact of Activating Agents on Non-Enzymatic Nucleic Acid Extension Reactions.

Non-enzymatic template-directed primer extension is increasingly being studied for the production of RNA and DNA. These reactions benefit from producing RNA or DNA in an aqueous, protecting group free system, without the need for expensive enzymes. However, these primer extension reactions suffer from a lack of fidelity, low reaction rates, low overall yields, and short primer extension lengths. This review outlines a detailed mechanistic pathway for non-enzymatic template-directed primer extension and presents a review of the thermodynamic driving forces involved in entropic templating. Through the lens of entropic templating, the rate and fidelity of a reaction are shown to be intrinsically linked to the reactivity of the activating agent used. Thus, a strategy is discussed for the optimization of non-enzymatic template-directed primer extension, providing a path towards cost-effective in vitro synthesis of RNA and DNA.

Photoresponsive CHA-Integrated Self-Propelling 3D DNA Walking Amplifier within the Concentration Localization Effect of DNA Molecular Framework Enables Highly Efficient Fluorescence Bioimaging.

While three-dimensional (3D) DNA walking amplifiers hold considerable promise in the construction of advanced DNA-based fluorescent biosensors for bioimaging, they encounter certain difficulties such as inadequate sensitivity, premature activation, the need for exogenous propelling forces, and low reaction rates. In this contribution, a variety of profitable solutions have been explored. First, a catalytic hairpin assembly (CHA)-achieved nonenzymatic isothermal nucleic acid amplification is integrated to enhance sensitivity. Subsequently, one DNA component is simply functionalized with a photocleavage-bond to conduct a photoresponsive manner, whereby the target recognition occurs only when the biosensor is exposed to an external ultraviolet light source, overcoming premature activation during biodelivery. Furthermore, a special self-propelling walking mechanism is implemented by reducing biothiols to MnO2 nanosheets, thereby propelling forces that are self-supplied to a Mn2+-reliant DNAzyme. By carrying the biosensing system with a DNA molecular framework to induce a unique concentration localization effect, the nucleic acid contact reaction rate is notably elevated by 6 times. Following these, an ultrasensitive in vitro detection performance with a limit of detection down to 2.89 fM is verified for a cancer-correlated microRNA biomarker (miRNA-21). Of particular importance, our multiple concepts combined 3D DNA walking amplifier that enables highly efficient fluorescence bioimaging in live cells and even bodies, exhibiting a favorable application prospect in disease analysis.

Evaluation of Mixing Effect on Coupled Heat Release and Transfer Performance of a Novel Segregated Solid Rocket Motor

The effect of mixing on coupled heat release and transfer performance of a novel segregated solid motor is numerically evaluated with a transient two-dimensional combustion model. The results show that vortex structures are formed and evolved in the combustion chamber. Quantitative calculation of the mixing effect shows the inhomogeneous distribution of oxidant and fuel species. The well-mixing area is located in a narrow belt-like coupled combustion region near the burning surface of the propellant. Heat transfer coefficient decreases greatly due to lower combustion reaction rate and enlarged flow channel area. Heat transfer coefficients near the two ends of the propellant grain are higher than other parts due to the influence of vortex mixing. Raising the inlet mass flow rate leads to enhanced mixing and heat transfer, which results in a lower temperature and regression rate of the propellant with combustion time. Temperature and oxidation rates of H2 and CO are unevenly distributed in the boundary layer of coupled combustion. Increasing the mass flux of inlet oxidizer gas leads to a higher combustion heat release rate. Therefore, the gas-phase temperature increases significantly. The heat release rate reaches the maximum near the ends of the propellant grain, where vortex mixing strengthens the coupled combustion process in the motor.

A carbon quantum dot-decorated g-C3N4 composite as a sulfur hosting material for lithium-sulfur batteries.

Although lithium-sulfur (Li-S) batteries have attracted strong consideration regarding their fundamental mechanism and energy applications, the inferior cycling performance and low reaction rate caused by the "shuttling effect" and the sluggish reaction kinetics of lithium polysulfides (LiPSs) impede their practical application. In this work, graphitic C3N4 (g-C3N4) assembled with highly-dispersed nitrogen-containing carbon quantum dots (CQDs) is designed as a cooperative catalyst to accelerate the reaction kinetics of LiPS conversion, the precipitation of Li2S during discharging, and insoluble Li2S decomposition during the charging process. Meanwhile, the introduction of CQDs improves the conductivity of the g-C3N4 substrate, showing great significance for the construction of high-performance electrocatalysts. As a result, the as-obtained composite shows efficient adsorption and electrochemical conversion of LiPSs, and the Li-S batteries assembled with CQDs/g-C3N4 exhibit an initial specific capacity of 1300.0 mA h g-1 at the current density of 0.1C and retain 582.3 mA h g-1 after 200 cycles. The electrode with the modified composite displays a greater capacity contribution of Li2S precipitation (175.7 mA h g-1), indicating an enhanced catalytic activity of g-C3N4 decorated by CQDs. The rational design of CQDs/g-C3N4 as a sulfur host could be an effective strategy for developing high performance Li-S batteries.

Comparison between effects of mini-implant anchorage and face-bow anchorage in orthodontics for children.

To study the values of mini-implant anchorage in orthodontics for children in the mixed dentition stage, 78 children in the mixed dentition stage who had accepted orthodontic treatment in our hospital from January 2020 to January 2021 were enrolled into this study. All children were treated with straight-wire appliance. According to their anchorages, children were divided into observation group and control group based on the random number table. Children in the control group used face-bow to control the anchorages and children in the observation group used mini-implants to control the anchorages. After treatment, the upper central incisor convex distance difference, inclination angle of the upper central incisor, displacement of the molar, gingival health, masticatory function, treatment effect and adverse reaction rate of children in two groups were compared. One year after treatment, compared with children in the control group, children in the observation group had smaller the upper central incisor convex distance difference, inclination angle of the upper central incisor, displacement of the molar, small scores of plaque index (PLI), bleeding index (BI) and gingival index (GI), stronger biting force and higher masticatory efficiency, lower adverse reaction rate during treatment, better treatment effect, higher satisfaction of orthodontic treatment. And differences of all the above indexes were statistically significant (p < 0.05). Mini-implant anchorages have good stability and directive force, and have certain values in orthodontics for children in the mixed dentition stage.

Fondaparinux Results in Similar Pregnancy Outcomes with Lower Adverse Reaction Rates Compared to Low Molecular Weight Heparin in Chinese Recurrent Miscarriage Women.

Fondaparinux inhibits thrombin generation by inactivating factor Xa, which has the potential to treat recurrent miscarriage (RM). However, more clinical evidence is required to support its application in Chinese women with RM. This research aimed to compare the live birth rate, gestational weeks at delivery, birth weight, Apgar score of newborns, and adverse reaction rates between fondaparinux and low molecular weight heparin (LMWH) in Chinese women with RM. Totally, 132 women with RM treated with fondaparinux or LMWH were included in this retrospective study. According to the corresponding treatment, women with RM were divided into the fondaparinux cohort (N = 45) and LMWH cohort (N = 87). The live birth rate was 68.9% in the fondaparinux cohort and 56.3% in the LMWH cohort, which was not different between the two cohorts (P = 0.161). Multivariable logistics regression analysis suggested that only previous miscarriage times (≥ 4 times vs. < 4 times) were independently related to a lower possibility of live birth in women with RM (odds ratio = 0.431, P = 0.036). It was also observed that gestational weeks at delivery (38.1 ± 1.4 vs. 37.7 ± 1.7 weeks) (P = 0.258), birth weight (2,923.7 ± 355.0 vs. 2,807.8 ± 334.0 g) (P = 0.144), and Apgar score of newborns (9.8 ± 0.5 vs. 9.6 ± 0.8) (P = 0.175) were not different between the fondaparinux cohort and LMWH cohort. Inspiringly, the total adverse reaction rate was reduced in the fondaparinux cohort vs. the LMWH cohort (20.0% vs. 37.9%) (P = 0.036). Fondaparinux results in similar pregnancy outcomes with lower adverse reaction rates compared to LMWH in Chinese women with RM.

Tailoring C-H amination activity via modification of the triazole-derived carbene ligand.

Two new C,O-bidentate chelating triazolylidene-phenolate ligands were synthesized that feature a diisopropylphenyl (dipp) and an adamantyl (Ad) substituent respectively on the triazole scaffold. Subsequent metalation afforded iron(II) complexes [Fe(C^O)2] that are active catalysts for the intramolecular C-H amination of organic azides. When compared to the parent complex containing a triazolylidene with a mesityl substituent (Mes) the increased steric bulk led to slightly lower activity (TOFmax = 23 h-1vs. 30 h-1), however selectivity towards pyrrolidine formation increases from 92% up to >99%. Kinetic studies indicate that the mechanism is similar in all three complexes and includes a half-order dependence in [Fe(C^O)2], congruent with the involvement of a dimetallic catalyst resting state within this catalyst class. Structural analysis suggests that enhanced bulkiness disfavors N2 loss and nitrene formation, yet shields the nitrene from intermolecular processes and thus favors intramolecular nitrene insertion into the C-H bond. This model rationalizes the high selectivity and the lower reaction rate observed with dipp and with Ad substituents on the ligand.

Magnetic recoverable Ag3PO4/Fe3O4/γ-Fe2O3 nanocomposite

The use of nanomaterials in water treatment is an alternative for the development of new systems to optimize the purification process. Heterogeneous photocatalysis is used for the treatment of wastewaters contaminated with recalcitrant pollutants that cannot be removed with conventional wastewater treatment techniques. Silver phosphate (Ag3PO4) can be used in visible-light driven photocatalysis. An important challenge of heterogeneous photocatalysis is to find a proper support for the photocatalysts to reduce the expense associated with the separation and reuse of these materials. However, the immobilization of the catalyst leads to lower reaction rates because the exposed surface area decreases and the material used as support can also interfere. In the last years, the use of magnetic materials to support photocatalysts has attracted special attention because it allows high surface areas to be exposed. Only few authors have reported the use of Ag3PO4/magnetic nanocomposites for photocatalysis and these need to be continued to improve their efficiency. In this work we synthesized Ag3PO4 and supported it on ferromagnetite (Fe3O4). In this study, Fe3O4 was synthesis following the Massart’s method. Ag3PO4 was synthesised over Fe3O4 from the reaction between silver nitrate (AgNO3) and disodium hydrogen phosphate (Na2HPO4). For characterization, DRS, SEM, XRD and magnetization studies were carried out. Ag3PO4 was synthesised and satisfactorily supported over magnetite (Fe3O423). The photodegradation of 10 mg·L−1 of methylene blue was achieved, although the apparent reaction rate constant was slightly lower for the magnetic composite than for bare Ag3PO4. This is explained because the composite contained 48% of the active Ag3PO4 material, as depicted form XRD studies.

Early Failure Detection for CO2 Reduction Electrolyzers Via in-Line Electrochemical Impedance Spectroscopy

The electrochemical CO2 reduction reaction (CO2RR) presents the opportunity to produce chemical feedstocks and fuels directly from CO2. Recent achievements in energy efficiency and current density are approaching the targets required for commercial viability; however, stability remains more than two orders of magnitude below the required 80,000 h. In CO2RR there is a challenge to distinguish the cause of failure among many possibilities. Failure can result from initial setup (e.g. over or under compression of the membrane and electrodes), gradual degradation of components (e.g. cathode and anode catalyst restructuring and dissolution), accumulation of products or byproducts (e.g. alcohols or salt accumulation), or immediate failures (e.g. a hole in the membrane or a short circuit). These failure modes must be addressed to reach the targeted stability needed for the wide-scale adoption of this technology. Early identification and mitigation of these failures would increase the electrolyzer lifetime and the commercial viability of CO2RR electrolyzers.Current techniques to characterize failures of the electrolyzer rely on post-mortem analysis of cell components. The analysis of individual components after operation may not accurately reflect their state in operando. There are techniques that are capable of analyzing the cell in operation (e.g. XAS, Raman, and TEM), but these typically require modified cell architectures and are operated at lower reaction rates. To effectively diagnose failure, the analysis technique should be applied to electrolyzers operating under realistic conditions.Here we implement an in-line real-time electrochemical impedance spectroscopy (EIS) technique to monitor CO2RR electrolyzers during operation. EIS is a non-destructive technique that can provide continuous information on the performance of specific components within the electrolyzer. We characterize common failure modes, such as poor compression, salt formation, catalyst degradation, and short circuits, and their identifying changes to the EIS response. We extract key electrochemical parameters from the EIS response and use them to develop a framework to identify and prevent the most common failure modes. Among other applications, this framework allowed for the detection of anode catalyst degradation 11 h before other indicators, such as cell voltage or product selectivity. This technique and framework can be applied to monitor CO2 electrolyzers as they are scaled and stacked.

Influence of ground quartz sand finesses on the formation of poorly ordered calcium silicate hydrate prepared by dynamically hydrothermal synthesis

This study aimed to prepare poorly ordered calcium silicate hydrate (C-S-H) via the hydrothermal synthesis method, using ground quartz sand powder and lime as starting materials. The fineness of quartz sand powder under different grinding time and varied grinding aids content was investigated. It further affected the formation of calcium silicate hydrate. Results showed that the main synthesized product was crystalline dicalcium silicate hydrate (C2SH) with a small amount of C-S-H when quartz sand was ground to 29.95 µm for D50, attributed to the coarse particle size with a low silica reaction rate. Increasing the grinding time and grinding aid content of quartz sand improved the silica reaction rate and accelerated the formation of calcium silicate hydrate. Adding 1‰ grinding aid content would greatly improve the grinding efficiency, and the particle size of quartz sand powder was greatly reduced to the smallest value recorded in this study (D50 was 21.08 µm), which was beneficial to the transformation of C-S-H from C2SH. Meanwhile, C-S-H underwent a change from having a flocculated morphology to a needle-like, short-rod-like and fibrous morphology.

Hydraulic retention time optimization achieved unexpectedly high nitrogen removal rate in pilot-scale anaerobic/aerobic/anoxic system for low-strength municipal wastewater treatment

Applications of post-denitrification processes are subjected to low reaction rates caused by a lack of carbon resources. To offer a solution for reaction rate promotion, this research found a pilot-scale anaerobic/aerobic/anoxic bioreactor treating 55–120 m3/d low-strength municipal wastewater for 273 days. A short hydraulic retention time (HRT, 5–6 h) and a high nitrogen removal rate (63.2 ± 9.3 g-N/m3·d) were achieved using HRT optimization. The effluent total nitrogen concentration was maintained at 5.8 ± 1.4 mg/L while operating at a high nitrogen loading rate of 86.2 ± 12.8 g-N/m3·d. The short aeration (1.25–1.5 h) minimized the Glycogen loss. The endogenous denitrification rate increased to above 1.0 mg/(g-VSS·h). The functional genus Ca. Competibacter enriched to 2.3 %, guaranteeing the efficient post-denitrification process. Dechloromonas rose to 1.1 %, aiding in the synchronous phosphorus removal. These findings offered fresh insights into AOA processes to achieve energy/cost-saving wastewater treatment.

Enhanced photo-electrochemical reduction of CO2 into methanol at CuInS2/CuFeO2 thin-film photocathodes with synergistic catalysis of oxygen vacancy and S–O bond

The low reaction rate and poor selectivity to target products have largely limited the application of photo-electrochemical CO2 reduction. Herein we introduce oxygen vacancy (Vo) and S–O bond into CuInS2/CuFeO2 (CIS/CFO) composite thin-film catalysts by tuning the composition of precursor solution during the electrodeposition process. Vo causes the formation of unique S–O bond at CIS/CFO interface. Vo improves the visible-light absorption performance and enhances *CO adsorption on catalyst surface. S–O bond improves Vo stability, increases the carrier lifetime, and reduces the energy barrier. When polyvinyl alcohol concentration in the precursor solution is 12 mg mL−1, the resulted 12CIS/CFO-Vo-SO thin-film photocathode provides methanol yield of 0.31 mM at −0.700 V (vs saturated calomel electrode) within 1 h, which is twice of that at CIS/CFO thin-film photocathode, and Faradaic efficiency as high as 90 %. This synergistic catalysis strategy provides an innovative route for improving the photo-electrochemical performance of catalysts.

The Effect of Ignition Procedure on Flashback of Hydrogen-Enriched Flames

Abstract The impact of different ignition sequences on the ignition dynamics of CH4-H2 flames in a bluff body burner is investigated at atmospheric conditions. Experiments are performed over a wide range of operating conditions covering pure methane injection (PH0) to pure hydrogen injection (PH100). A perforated plate of total porosity σ=0.17 is positioned at the outlet of the combustion chamber to increase the chamber back pressure and trigger transient flashback during ignition. Time-series of pressure, OH* chemiluminescence and OH-PLIF images of the propagating flame branch are recorded simultaneously to characterize the ignition process. Two ignition procedures are investigated. For ignition procedure A, designated as an early ignition procedure, the spark is initiated before fuel injection. For ignition procedure B, designated as a late ignition, the spark is only activated after the fuel injection. The impact of the fuel air mixing on the final stabilization state is investigated by changing the fuel delivery time (dt) before the initial spark. Three different time delays are considered dt = 1, 3, and 5 s. The final state of the flame is found to be highly sensitive to the selected ignition procedure and increasing dt favors the occurrence of flashback. At constant power, the magnitude of the pressure peak is driven by a competition between the fuel mass flowrate at the moment of ignition and the high reactivity of hydrogen, which shifts the flammability limit toward lower equivalence ratios, hence generating a lower reaction rate. For procedure A, the peak of the chamber over pressure shows a nonmonotonic growth for increasing levels of H2 in the fuel blend, while it linearly increases for procedure B. Experiments are then conducted at a fixed injection flow velocity Ub = 5 m s–1 and fixed laminar burning velocity Sl0=0.25 m s–1 by varying the level of hydrogen enrichment. For procedure A, the over pressure amplitude decreases with increasing the hydrogen enrichment leading to a soft ignition for all CH4-H2 blends. Under ignition procedure B, the amplitude of the over pressure reached during ignition is found to be relatively unaffected by the hydrogen concentration, but the flame stabilization mode shows a strong dependence to both the level of H2-enrichment and fuel delivery time dt. OH* as well as OH-PLIF images reveal that the trajectory of the flame leading point changes as dt increases. The different dynamics of the flame leading points is likely to be the cause the different types of stabilization modes observed.

Analysis of the Efficacy of Triamcinolone Acetonide Combined with Ranibizumab in the Treatment of Fundus Diseases

Objective: To analyze the effect of triamcinolone acetonide combined with ranibizumab in patients with fundus diseases. Methods: 100 patients with fundus diseases admitted from January 2018 to January 2023 were selected. The patients were separated into two groups according to the random number table method, with 50 cases in the control group (treated with ranibizumab), and 50 cases in the observation group (treated with triamcinolone acetonide combined with ranibizumab). The clinical effects of both treatment regimens were compared. Results: The time taken for symptom disappearance of the observation group was shorter than that of the control group (P &lt; 0.05). The observation group had higher naked-eye visual acuity (4.18 ± 0.89) compared to the control group. Besides, the observation group also had lower intraocular pressure (14.19 ± 1.33 mmHg) and retinal thickness (283.14 ± 3.29 μm), with (P &lt; 0.05) compared to the control group. Moreover, the observation group had a lower adverse reaction rate and a higher quality of life (P &lt; 0.05). Conclusion: The application of triamcinolone acetonide combined with ranibizumab treatment can quickly relieve the clinical symptoms of patients with fundus disease, improve visual acuity, intraocular pressure, and retinal thickness, with low adverse reaction rate and better prognosis and quality of life.

Heterogeneous catalysts, reaction kinetics, and reactor designs for methanol production from carbon dioxide: A critical review

AbstractThe process of preparing methanol from carbon dioxide is one of the ways to solve the environmental problems caused by greenhouse gases, the problem of fossil energy depletion, and the problem of fuel exhaust emissions. However, after decades of development, the process of preparing methanol from carbon dioxide is still unable to achieve large‐scale industrialization. This critical review sharply points out the problems and obstacles that need to be solved urgently on the industrialization road of carbon dioxide methanol preparation process and summarizes its progress. The problems faced by the methanol production industry from carbon dioxide are first the thermodynamic constraints, second the lower reaction rate and conversion effect, and finally the energy loss. In order to solve these problems, this paper first introduces the active sites, structural effects, and dynamic changes of copper‐based catalysts, as well as the unique reaction mechanism and doping modification of indium‐based catalysts. Zinc and zirconium promoters and some metal oxide supports can form unique interactions with active components to improve the catalytic performance of the catalyst. Next, various kinetic models and applications of methanol production from carbon dioxide are summarized, which is an important bridge linking laboratory and industrialization; the advantages and disadvantages of fixed bed reactor and paddle reactor were compared. Finally, the full text is summarized and prospected.

Synergistic effect of characteristics of raw materials on controlling the mechanical properties of fly ash-based geopolymers

This study investigates the macro- and micro-characteristics of the geopolymers to verify the feasibility of prediction of compressive strength via quantitatively adjusting the amorphous phase content (APC) and particle size distribution (PSD) of raw material. The optimization of PSD through the sieving method does not reach the intended compressive strength compared to the reference, while controlling APC by partly replacing fly ash with slag achieves the expected target. The critical reasons are well explained by the micro properties of geopolymers. The sieving process leads to the reduction in the porosity but has little effect on the Si/Al molar ratio and APC of geopolymers, which is related to the heterogeneous distribution of active constituents of fly ash. By contrast, the addition of slag significantly enhances the microstructure of geopolymers, especially by the interaction between C-A-S-H and N-A-S-H gel. As a result, the compressive strength is primarily determined by the micro index MCa, proved by the mutual positive correlation. Besides, given the low reaction rate of fly ash in the geopolymerization and relevant experimental results, the modified formula that only uses the APC and specific gravity (G20°C) of powder raw materials to establish the relationship with compressive strength owns a better linear dependence and probably more appropriate for the prediction of mechanical properties of fly ash-based geopolymers.