Electrochemical hydrogen storage characteristics of Ti_(0.10)Zr_(0.15)V_(0.35)Cr_(0.10)Ni_(0.30)-10% LaNi_3 composite and its synergetic effect

Hydrogen storage composite alloy Ti0.10Zr0.15V0.35Cr0.10Ni0.30–10% LaNi3 was prepared by two-step arc-melting to improve the electro-catalytic activity and the kinetic performance of Ti-V-based solid solution alloy. The electrochemical properties and synergetic effect of the composite alloy electrode were systematically investigated by using X-ray diffractometry, field emission scanning electron microscopy, energy-dispersive spectrometry, electrochemical impedance spectroscopy and galvanostatic charge/discharge test. It is found that the main phase of the composite alloy is composed of V-based solid solution phase with a BCC structure and C14 Laves phase with hexagonal structure, while the secondary phase is formed in the composite alloy. The comprehensive electrochemical properties of the composite alloy electrode are significantly improved. The activation cycle number, the maximum discharge capacity and the low temperature dischargeability of the composite alloy are 5 cycles, 362.5 mA-h/g and 65.84% at 233 K, respectively. It is suggested that distinct synergetic effect occurs in the activation process, composite process, cyclic process and discharge process at a low or high temperature under different current densities, in the charge–transfer resistance and exchange current density.

Synergetic effect between non-thermal plasma and photocatalytic oxidation on the degradation of gas-phase toluene: Role of ozone

In this study, a hybrid process using non‐thermal plasma (NTP) and photocatalytic oxidation (PCO) was adopted for the degradation of gas‐phase toluene using TiO2 as the photocatalyst. To discover the synergetic effect between NTP and PCO, the performances of both sole (O3, UV, NTP, and PCO) and combined (O3 + TiO2, O3 + UV, NTP + UV, O3 + PCO, and NTP + PCO) processes were investigated from different perspectives, such as the toluene removal efficiency, selectivity of COx, mineralization rate, ozone utilization, and the generation of by‐products. The toluene removal efficiency of the combined NTP + PCO process was 80.2%, which was much higher than that of a sole degradation process such as NTP (18.8%) and PCO (13.4%). The selectivity of CO2 and the ozone utilization efficiency also significantly improved. The amount of by‐products in the gas phase and the carbon‐ based intermediates adsorbed on the catalyst surface dramatically reduced. The improvement in the overall performances of the combined NTP + PCO process was mainly ascribed to the efficient utilization of ozone in the photocatalytic oxidation, and the ozone further acting as an electron acceptor and scavenger, generating more hydroxyl radicals and reducing the recombination of electron‐ hole pairs.

Degradation of 4-Chlorophenol Solution by Synergetic Effect of Dual-frequency Ultrasound with Fenton Reagent

4-Chlorophenol (4-CP) solution was treated by dual-frequency ultrasound inconjunction with Fenton reagent, and obvious improvement in the 4-CP degradation rate was observedin this advanced oxidation process. Experimental results showed that ultrasonic intensity,saturating gas and pH value affected greatly the 4-CP removal rate. Among four different saturatinggases (Ar, O_2, air and N_2), 4-CP degradation with Ar-saturated solution was the best. However, inthe view of practical wastewater treatment, using oxygen as the saturating gas would be moreeconomical. The addition of Fenton reagent followed the first-order kinetics and increased the 4-CPdegradation rate. The 4-CP removal rate increased by around 126% within 15 min treatment. Thesynergetic effect of dual-frequency ultrasound with Fenton reagent on 4-CP degradation was obviouslyobserved.

Synergetic effect between sulfurized Mo/γ-Al_2O_3 and Ni/γ-Al_2O_3 catalysts in hydrodenitrogenation of quinoline

An evidence for the synergetic effect between the stacked bed of Mo/γ-Al2O3 and Ni/γ-Al2O3 in the hydrodenitrogenation （HDN） reaction of quinoline has been provided in this paper. The synergism factor decreases when the reaction temperature increases （280？340 ？C）. The synergetic effect leads to improve the hydrogenation activity for the stacked bed compared with the single Mo/γ-Al2O3 bed, which may be attributed to the generation of hydrogen spillover on the Ni/γ-Al2O3 catalyst.

Synergetic Effects of UV/Fe^(3+) Combined with Electrocatalysis for p-Nitrophenol Degradation

Synergetic effects for p-nitrophenol degradation were observed in the combination of two-advanced oxidation processes, UV/Fe3+ and electrocatalysis. The enhancement of removal rate for p-nitrophenol and COD was around 123% and 278%, respectively. The possible contributions for the synergetic effects were the electrochemically regeneration of ferric ion and the role of the oxygen that formed on the anode.

Synergetic effect of nitrogen‐doped carbon catalysts for high‐efficiency electrochemical CO_(2) reduction

The use of carbon‐based materials is an appealing strategy to solve the issue of excessive CO_(2) emis‐sions.In particular,metal‐free nitrogen‐doped carbon materials(mf‐NCs)have the advantages of convenient synthesis,cost‐effectiveness,and high conductivity and are ideal electrocatalysts for the CO_(2) reduction reaction(CO_(2)RR).However,the unclear identification of the active N sites and the low intrinsic activity of mf‐NCs hinder the further development of high‐performance CO_(2)RR electrocat‐alysts.Achieving precise control over the synthesis of mf‐NC catalysts with well‐defined active N‐species sites is still challenging.To this end,we adopted a facile synthesis method to construct a set of mf‐NCs as robust catalysts for CO_(2)RR.The resulting best‐performing catalyst obtained a Far‐adaic efficiency of CO of approximately 90%at−0.55 V(vs.reversible hydrogen electrode)and good stability.The electrocatalytic performance and in situ attenuated total reflectance surface‐enhanced infrared absorption spectroscopy measurements collectively revealed that graphitic and pyridinic N can synergistically adsorb CO_(2) and H_(2)O and thus promote CO_(2) activation and protonation.

Synergetic effects for p-nitrophenol abatement using a combinedactivated carbon adsorption-electrooxidation process

A novel fluidized electrochemical reactor that integrated advanced electrochemical oxidation with activated carbon (AC) fluidization in a single cell was developed to model pollutant p-nitrophenol (PNP) abatement. AC fluidization could enhance COD removal by 22%-30%. In such a combined process, synergetic effects on PNP and COD removal was found, with their removal rate being enhanced by 137.8% and 97.8%, respectively. AC could be electrochemically regenerated and reused, indicating the combined process would be promising for treatment of biorefractory organic pollutants.

Synergetic effects of NaAlH_4-TiF_3 co-additive on dehydriding reaction of Mg(AlH_4)_2

The effects of NaA1H4, TiF3 and NaA1H4-TiF3 co-additive on dehydriding reaction of Mg（A1H4）2 are systematically investigated. The on- set dehydrogenation temperature of the co-doped Mg（A1H4）2 composites decreased to 74 ℃, which is about 59 ℃ lower than that of pure Mg（A1H4）2. The dehydrogenation kinetics of NaA1H4-TiF3 co-doped Mg（A1H4）2 sample was also improved, which released about 94% hydrogen within 48 min, but no visible hydrogen was released from pure Mg（A1H4）2 under the same conditions. The activation energy of co-doped Mg（A1H4）2 was 85.6 kJ.mol-t, which was significantly lower than that of additive-free Mg（A1H4）2 sample. The synergetic effects of NaA1H4 and TiF3 on the dehydrogenation performance of Mg（A1H4）2 were confirmed. In addition, a possible catalytic mechanism is discussed, regarding the different roles of NaA1H4 and TiF3 on Mg（A1H4）2.

Modeling the Synergetic Effect of Various Factors on Chloride Transport in Nonsaturated Concrete

Diffusion has been systematically described as the main mechanism of chloride transport in reinforced concrete（RC） structure, especially when the concrete is in a saturated state. However, the single mechanism of diffusion is not able to describe the actual chloride ingress in the nonsaturated concrete. Instead, it is dominated by the interaction of diffusion and convection. With the synergetic effects of various factors taken into account, this study aimed to modify and develop an analytical convection- diffusion coupling model for chloride transport in nonsaturated concrete. The model was verified by simulation of laboratory tests and field measurement. The results of comparison study demonstrate that the analytical model developed in this study is efficient and accurate in predicting the chloride profiles in the nonsaturated concrete.

Synergetic effects of lanthanum,nitrogen and phosphorus tri-doping on visiblelight photoactivity of TiO_2 fabricated by microwave-hydrothermal process

Effects of La, N, and P doping on the structural, electronic and optical properties of TiO_2 synthesized from TiCl_4 hydrolysis via a microwave-hydrothermal process were investigated by X-ray diffraction, transmission electron microscopy, N_2 adsorption-desorption isotherm, X-ray photoelectron spectroscopy, electron paramagnetic resonance, UV-vis absorbance spectroscopy, photoelectrochemical measurements, and photoluminescence spectroscopy. The results showed that the presence of La in the tri-doped TiO_2 played a predominant role in inhibiting the recombination of the photogenerated electrons and holes. The existence of the substitutional N, interstitial N, and oxygen vacancies in TiO_2 lattices led to the band gap narrowing. It was P-doping rather than La or N doping that played a key role in inhibiting both anatase-to-rutile phase transformation and crystal growth, in stabilizing the mesoporous textural properties, and in increasing the content of surface bridging hydroxyl. Moreover, the tri-doping significantly enhanced the surface Ti^（4＋）-O^（2-）-Ti^（4＋）-O^（-·） species. All above-mentioned factors cooperated to result in the enhanced photoactivity of the tri-doped TiO_2. As a result, it exhibited the highest photoactivity towards the degradation of 4-chlorophenol（4-CP） under visible-light irradiation among all samples, which was much superior to commercial P25 TiO_2.

Enhancing oxygen reduction reaction of Pt-Co/C nanocatalysts via synergetic effect between Pt and Co prepared by one-pot synthesis

Designing highly active and durable electrocatalysts towards oxygen reduction reaction(ORR)plays a paramount importance for proton exchange membrane fuel cells.Pt-based binary alloys Pt-M(M=3d-transition metals)possessing excellent electronic and geometric properties have received increasing interests as highly active electrocatalysts.Herein,we report a series of Pt_(x)Co/C(x=1,2,3)catalysts by a facile one-pot soft-chemistry method.In the acidic conditions,the mass activities of PtCo/C,Pt_(2)Co/C and Pt_(3)Co/C are 0.526,0.462 and 0.441 A·mgPt^(-1),which are 2.60,2.31 and 2.22 times higher than that of Pt/C(0.200 A·mgPt^(-1)),respectively.The specific activities of PtCo/C,Pt_(2)Co/C and Pt_(3)Co/C are 706.59,679.41 and 801.83μA·cm^(-2),which are accordingly 2.89,2.76 and 3.28 times higher than that of Pt/C(244.75μA·cm^(-2)).Notably,Pt_(3)Co/C shows a remarkable durability.After 5000 cycles of the accelerated durability testing,the mass activity and specific activity of Pt_(3)Co/C catalyst are 2.47 and 3.80 times higher than that of the commercial Pt/C,respectively.The improved ORR activity and durability can be ascribed to the synergistic interaction between Pt and Co.

Synergetic effect of thermo-photocatalytic oxidation of benzene on Pt-TiO_2/Ce-MnO_x

Pt-TiO2/Ce-MnOx catalysts were obtained by depositing TiO2 and platinum, respectively, on the Ce-Mn oxides prepared by co-precipitation method. The phases of CeO2 and anatase TiO2 were observed in the catalysts from X-ray diffraction （XRD） patterns. X-ray photoelectron spectroscopy （XPS） revealed that lattice oxygen and surface active oxygen were found to be the major components of O 1 s. The experiment results showed that the kinetic constant of thermo-photocatalysis was 7.6 times of the kinetic constant of single photocatalysis, and was 2.29 times of the kinetic constant sum of photocatalytic and thermal catalytic reaction.

Enhanced photoelectric conversion efficiency of dye-sensitized solar cells by the synergetic effect of NaYF_4:Er^(3+)/Yb^(3+) and g-C_3N_4

TiO2-NaYF4：Er^3＋/Yb^3＋-C3N4 composite photoanodes were successfully designed for the first time. The photoelectric conversion efficiency of TiO2-NaYF4：Er^3＋/Yb^3＋ C3N4 composite cell can result an efficiency of 7.37%, which is higher than those of pure TiO2 cell and TiO2-C3N4 composite cell. The enhancement of the efficiency can be attributed to the synergetic effect of NaYF4：Er^3＋/Yb^3＋ and C3N4. Elec- trochemical impedance spectroscopy analysis revealed that the interfacial resistance of the TiO2-dyelI3^-/I^- electrolyte interface of TiO2-NaYF4：Er^3＋/Yb^3＋-C3N4 composites cell was much smaller than that of pure TiO2 cell. In addition, the TiO2-NaYF4：Er^3＋/Yb^3＋-C3N4 composite cell had longer electron recombination time and shorter electron transport time than that of pure TiO2 cell.

Electrochemical characteristics and synergetic effect of Ti_(0.10)Zr_(0.15)V_(0.35)Cr_(0.10)Ni_(0.30)-10 wt.%LaNi_5 hydrogen storage composite electrode

In order to improve performance of Ti-V-based solid solution alloy, electrochemical characteristics and synergetic effect of Ti0.10Zr0.15V0.35Cr0.10Ni0.30-10 wt.%LaNi5 hydrogen storage composite electrode prepared by two-step arc-melting were investigated system-atically. X-ray diffractometry （XRD） and scanning electron microscopy-energy dispersive spectroscopy （SEM-EDS） showed that the main phase of composite alloy was composed of V-based solid solution phase with a BCC structure and C14 Laves phase with hexagonal structure, while secondary phase also existed in the composite alloy. The results showed that electrochemical characteristics of the composite alloy elec-trode were significantly improved. It was suggested that synergetic effect appeared in the maximum discharge capacity of the composite alloy, synergetic effect of the discharge capacity appeared in the activation process, in the composite process, in the cyclic process, in the discharge process at low/high temperature and at different current densities, and synergetic effect existed in the charge-transfer resistance and in the ex-change current density, which seemed to be related to formation of the secondary phase.

Influence of H_(2)S and NH_(3) on biogas dry reforming using Ni catalyst:a study on single and synergetic effect

Biogas is a renewable biomass energy source mainly composed of CH4 and CO_(2).Dry reforming is a promising technology for the high-value utilization of biogas.Some impurity gases in biogas can not be completely removed after pretreatment,which may affect the performance of dry reforming.In this study,the influence of typical impurities H_(2)S and NH_(3) on dry reforming was studied using Ni/MgO catalyst.The results showed that low concentration of H_(2)S in biogas could cause serious deactivation of catalyst.Characterization results including EDS,XPS and TOF-SIMS confirmed the adsorption of sulfur on the catalyst surface,which was the cause of catalyst poisoning.We used air calcination method to regenerate the sulfur-poisoned catalysts and found that the regeneration temperature higher than 500℃could help catalyst recover the original activity.NH_(3)in the concentration range of 50–10000 ppm showed a slight inhibitory effect on biogas dry reforming.The decline rate of biogas conversion efficiency increased with the increase of NH_(3) concentration.This was related to the reduction of oxygen activity on catalyst surface caused by NH_(3).The synergetic effect of H_(2)S and NH_(3)in biogas was investigated.The results showed that biogas conversion decreased faster under the coexistence of H_(2)S and NH_(3)than under the effect of H_(2)S alone,so as the surface oxygen activity of catalyst.Air calcination regeneration could also recover the activity of the deactivated catalyst under the synergetic effect of H_(2)S and NH_(3).

Stratosphere-troposphere synergetic effect on the extreme low-temperature event over China in late November 2022

In late November 2022,most regions in China were hit by a strong northwest-path cold wave,bringing a high-hazard extreme low-temperature event(ELTE).Several parts of Northwest China experienced extremely low temperatures and record-breaking snow depths.A stratosphere-troposphere synergetic effect was suggested to be closely related to the ELTE according to a diagnostic analysis.On the one hand,the concurrent establishment of two blockings in Europe-Northeast Atlantic and North Pacific led to a polar vortex split at the tropopause,and the Arctic Oscillation phase subsequently turned negative.An airflow with high potential vorticity(PV)was squeezed out of the Arctic.Meanwhile,a high-PV air that originated from the lower stratospheric Arctic was conveyed southwards to the western Siberian Plain along the sloping isentropic surface.This condition triggered a tropospheric response in which the East Asia trough deepened due to the intensified cyclonic circulation induced by the high-PV intrusion.On the other hand,downward propagation of stratospheric anomalies accompanied by stratospheric polar vortex displacement and split was observed in mid-and late November,respectively.Changes in stratospheric circulation contributed to enhanced blockings over Europe-Northeast Atlantic in the lower stratosphere or upper troposphere.As a result,the inverted omega-shaped circulation pattern was formed in the middle to upper troposphere,and it consisted of the intensified East Asia trough and two blockings in the upstream and downstream regions.The high-PV air upstream of the East Asia trough was advected to China,which directly led to the outbreak of the ELTE.The establishment of double blockings and the displacement or split of the stratospheric polar vortex can be efficient signals for cold-event prediction in China.This study provides novel insights into the cause of ELTEs under warming climates in the future.

Synergetic strengthening mechanism of ultrasound combined with calcium fluoride towards vanadium extraction from low-grade vanadium-bearing shale

The effect and mechanism of ultrasound and CaF_(2) on vanadium leaching from vanadium-bearing shale were investigated systematically.In consideration of the enhancement for vanadium recovery,the combination of ultrasound and CaF_(2)(66.28%) exerts more evident effects than ultrasound(26.97%) and CaF_(2)(60.35%) alone,demonstrating the synergetic effect of ultrasound and CaF_(2).Kinetic analysis manifests that the product layer diffusion controls vanadium leaching in ultrasound system without CaF_(2),however product layer diffusion and interfacial reaction is the rate-controlling step for vanadium leaching in other three leaching systems.The combination of ultrasound and CaF_(2) notably decreases the activation energy(E_(a)) from 62.03 to 27.61 kJ/mol,nevertheless individual CaF_(2) only reduces the E_(a) to 50.70 kj/mol.X-ray diffraction and fourier transform infrared spectrometer analyses show that the decomposition degree of the vanadium-bearing mica structure is the most significant in ultrasound and CaF_(2) system,proving the highest release degree of vanadium.Specific surface area and pore distribution combined with scanning electron microscope analyses reveal that the action of ultrasound and CaF_(2) would provide higher specific surface area,more abundant pores structure and cracks for the particles,which further prompts the rapid diffusion of H^(+),F^(-)and HF,and achieves the conspicuous improvement of vanadium leaching recovery.

Synergetic photo-epoxidation of propylene with molecular oxygen over bimetallic Au–Ag/TS-1 photocatalysts

Au-Ag bimetallic nanoparticle‐supported microporous titanium silicalite‐1catalysts were prepared via a hydrothermal‐immersion method,and their structures were examined.These materials serve as efficient catalysts for the photosynthesis of propylene oxide via the epoxidation of propene.The Au/Ag mass ratio and reaction temperature were demonstrated to have significant effects on the catalytic activity and selectivity of propylene oxide.The optimal formation rate(68.3μmol/g·h)and selectivity(52.3%)toward propylene oxide were achieved with an Au:Ag mass ratio of4:1.Notably,the strong synergistic effect between Au and Ag resulted in superior photocatalysis of the bimetallic systems compared with those of the individual systems.A probable reaction mechanism was proposed based on the theoretical and experimental results.

Recent Advances on Porous Materials for Synergetic Adsorption and Photocatalysis

Porous photocatalysts are promising materials capable of simultaneously adsorbing and oxidizing/reducing target species,showing great potentials in environmental remediation and energy generation.This review offered a comprehensive overview of the recent progress in design,fabrication,and applications of porous photocatalysts,including carbon-based semiconductors,metal oxides/sulfides,metal–organic frameworks,and adsorbent–photocatalyst hybrids.The fundamental understanding of the structure–performance relationships of porous materials together with the in-depth insights into the synergetic effects between adsorption and photocatalysis was presented.The strategies to further improve the photocatalytic activity of porous photocatalysts were proposed.This review would provide references and outlooks of constructing efficient porous materials for adsorptive and photocatalytic removal of pollutants and energy production.

Synergetic Inactivation of Microorganisms in Drinking Water by Short-term Free Chlorination and Subsequent Monochloramination

Objective To introduce synergetic inactivation of microorganisms in drinking water by short-term free chlorination for less than 15 minutes followed by monochloramination. Methods Indicator microorganisms such as Escherichia coli, Staphylococcus aureus, Candida albicans, and spores of Bacillus subtilis were used to assess the efficiency of sequential chlorination and free chlorination. Results The sequential chlorination was more efficient in inactivating these microorganisms than free chlorination, indicating that synergy was provided by free chlorine and monochloramine. Ammonia addition time, temperature and pH had influences on this synergy. Conclusion The possible mechanism of this synergy might involve three aspects： free chlorine causing sublethal injury to microorganisms and monochloramine further inactivating them; different ability of free chlorine and monochloramine to penetrate and inactivate microorganism congeries; and higher concentration of residual chlorine in sequential chlorination than in free chlorination.