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Focusing on the uncontrolled discharge of organic dyes, a known threat to human health and aquatic ecosystems, this work employs a dual-functional catalyst approach, by immobilizing a synthesized bismuth sulfur iodide (BiSI) into a poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) polymeric matrix for multifunctional water remediation. The resulting BiSI@PVDF nanocomposite membrane (NCM), with 20 wt% filler content, maintains a highly porous structure without compromising morphology or thermal properties. Demonstrating efficiency in natural pH conditions, the NCM removes nearly all Rhodamine B (RhB) within 1 h, using a combined sonophotocatalytic process. Langmuir and pseudo-second-order models describe the remediation process, achieving a maximum removal capacity (Qmax) of 72.2 mg/g. In addition, the combined sonophotocatalysis achieved a degradation rate ten and five times higher (0.026 min-1) than photocatalysis (0.002 min-1) and sonocatalysis (0.010 min-1). Furthermore, the NCM exhibits notable reusability over five cycles without efficiency losses and efficiencies always higher than 90%, highlighting its potential for real water matrices. The study underscores the suitability of BiSI@PVDF as a dual-functional catalyst for organic dye degradation, showcasing synergistic adsorption, photocatalysis, and sonocatalysis for water remediation.

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The rampant upsurge of organic pollutants in aqueous media has become one of the major concerns nowadays. Finding non-specific catalysts that can target a wide range of organic pollutants is a key challenge. Eco-friendly oxidative radicals, such as promoted by peroxymonosulfate (PMS), are necessary for efficient water decontamination. We propose a multicomponent composite catalyst for activating PMS using a dual strategy of sonophotocatalysis. The composite integrates cobalt ferrite and Cu- or Ce-doped SnO2, with the at. % of doping metal and the mixture ratio carefully balanced. The top-performing architectures were able to decompose rhodamine B (20 ppm), a representative pollutant, in under 3 min and achieve over 70% mineralization in just 5 min. The synthesized nanocomposites demonstrated exceptional sonophotocatalytic performance, even when treating complex and diverse multipollutant solutions (80 ppm), achieving over 75% mineralization after 150 min. Considering their high stability and reusability, the proposed CoFe2O4/Cu- and Ce-doped SnO2 materials are among the state-of-the-art heterogeneous catalysts for mineralizing organic pollutants through PMS activation.

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Catalytic conversion of lignin to value-added aromatic compounds is still an open challenge, since the selective cleavage of the linkages interconnecting the aromatic molecules, especially the ß-O-4 ones, is not efficiently achieved yet. Herein, novel titania-based nanostructured materials were synthesized using low-power-low-frequency ultrasound that demonstrated high efficiency for the selective cleavage of Cα-Cß bond of ß-O-4 linkages of lignin-inspired model compounds. Going a step ahead, experiments of sonophotocatalytic valorization of 2-phenoxy-1-phenylethanol were contacted for the first time, where the exposure to ultrasound leading to better conversion and selectivity towards the desired products in the case of the novel ultrasound-synthesized nano-photocatalyst. Mechanistic insights showcased that photogenerated holes are the main active species in the catalytic process. In general, this research work provides a green, effective, and cost-effective approach for the selective and efficient catalytic lignin valorization.

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The health of all living organisms is greatly influenced by the quality of the water. Therefore, developing cost-effective, eco-friendly, and easily accessible methods is desperately needed to meet the high global demand for clean water. Recently, nanozyme-based dye degradation methods have been promising for the remediation of water pollution. In this work, peroxidase-mimic Co3O4/TiO2 nanocomposite was synthesized and characterized for its size, morphology, and crystalline structure. Colorimetric assay results showed that the peroxidase-like activity of the Co3O4/TiO2 nanocomposite was considerably enhanced compared to the pure Co3O4 NPs and TiO2 NPs. Besides excellent enzyme-mimic activity, the higher sonophotocatalytic dye degradation capability of the nanocomposite after immobilization on zeolite (Co3O4/TiO2@Ze) was also demonstrated. Under optimal conditions (pH = 5.0, 25 °C), 0.1 g/L of catalyst was able to degrade 100 % of methylene blue (MB) with 600 µM in the presence of 30 µM H2O2 within 12 min. GC/MS analysis and toxicity studies revealed less toxic metabolite production after treatment of MB with sonophotocatalytic Co3O4/TiO2@Ze. Modeling of MB degradation using artificial neural networks (ANN) with a 5:6:1 topology was successfully performed, and the results confirmed the fitness of theoretical and experimental outputs according to the calculated correlation coefficient values. The prepared nanocomposite could thus be used as a promising and highly effective catalyst for the removal of organic dyes from polluted water.

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Palm oil mill effluent (POME) is regarded as deleterious to the environment, primarily owing to the substantial volume of waste it produces during palm oil extraction. In terms of contaminant composition, POME surpasses the pollutant content typically found in standard municipal sewage, therefore releasing it without treatment into water bodies would do irreparable damage to the environment. Main palm oil mills are normally located in the proximity of natural rivers in order to take advantage of the cheap and abundant water source. The same rivers are also used as a water source for many villages situated along the river banks. As such, it is imperative to degrade POME before its disposal into the water bodies for obvious reasons. The treatment methods used so far include the biological processes such as open ponding/land application, which consist of aerobic as well as anaerobic ponds, physicochemical treatment including membrane technology, adsorption and coagulation are successful for the mitigation of contaminants. As the above methods require large working area and it takes more time for contaminant degradation, and in consideration of the strict environmental policies as well as palm oil being the most sort of vegetable oil in several countries, numerous researchers have concentrated on the emerging technologies such as advanced oxidation processes (AOPs) to remediate POME. Methods such as the photocatalysis, Fenton process, sonocatalysis, sonophotocatalysis, ozonation have attained special importance for the degradation of POME because of their efficiency in complete mineralization of organic pollutants in situ. This review outlines the AOP technologies currently available for the mineralization of POME with importance given to sonophotocatalysis and ozonation as these treatment process removes the need to transfer the pollutant while possibly degrading the organic matter sufficiently to be used in other industry like fertilizer manufacturing.

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Nanoparticles of NiLaxFe2-xO4 ferrite spinel incorporated in a SiO2 matrix were synthesized via a sol-gel method, followed by annealing at 200, 500, and 800 °C. The resulting materials were characterized via XRD, AFM, and BET techniques and evaluated for photocatalytic activity. The XRD diffractograms validate the formation of a single-phase cubic spinel structure at all temperatures, without any evidence of secondary peaks. The size of crystallites exhibited a decrease from 37 to 26 nm with the substitution of Fe3+ with La3+ ions. The lattice parameters and crystallite sizes were found to increase with the rise in La3+ content and annealing temperature. Isotherms were employed to calculate the rate constants for the decomposition of malonate precursors to ferrites and the activation energy for each ferrite. All nanocomposites have pores within the mesoporous range, with a narrow dispersion of pore sizes. The impact of La content on sonophotocatalytic activity was evaluated by studying Rhodamine B degradation under visible light irradiation. The results indicate that the introduction of La enhances nanocomposite performance. The prepared Ni-La ferrites may have potential application for water decontamination.

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Designing a heterostructure nanoscale catalytic site to facilitate N2 adsorption and photogenerated electron transfer would maximize the potential for photocatalytic activity and N2 reduction reactions. Herein, we have explored the interfacial TiO2 nanograins between the Ti3C2TxMXene-WS2 heterostructure and addressed the beneficial active sites to expand the effective charge transfer rate and promote sonophotocatalytic N2 fixation. Benefiting from the interfacial contact and dual heterostructure interface maximizes the photogenerated carrier separation between WS2 and MXene/TiO2. The sonophotocatalytic activity of the MXene@TiO2/WS2 hybrid, which was assessed by examining the photoreduction of N2 with ultrasonic irradiation, was much higher than that of either sonocatalytic and photocatalytic activity because of the synergistic sonocatalytic effect under photoirradiation. The Schottky junction between the MXene and TiO2 on the hybrid MXene/TiO2-WS2 heterostructure resulted in the sonophotocatalytic performance through effective charge transfer, which is 1.47 and 1.24 times greater than MXene-WS2 for nitrogen fixation and pollutant degradation, respectively. Under the sonophotocatalytic process, the MXene/TiO2-WS2 heterostructure exhibits a decomposition efficiency of 98.9 % over tetracycline in 90 min, which is 5.46, 1.73, and 1.10 times greater than those of sonolysis, sonocatalysis, and photocatalysis, respectively. The production rate of NH3 on MXene/TiO2-WS2 reached 526 µmol g-1h-1, which is 3.17, 3.61, and 1.47 times higher than that of MXene, WS2, and MXene-WS2, respectively. The hybridized structure of MXene-WS2 with interfacial surface oxidized TiO2 nanograins minimizes the band potential and improves photocarrier use efficiency, contributing directly to the remarkable catalytic performance towards N2 photo fixation under visible irradiation under ultrasonic irradiation. This report provides the strategic outcome for the mass carrier transfer rate and reveals a high conversion efficiency in the hybridized heterostructure.

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A cost effective and environmentally benign ultrasonic method has been developed for the synthesis of InVO4 (InV), In2S3 (InS) and the InVO4/In2S3 heterostructure (InV/InS). All the designed materials were evaluated for their structural, morphological, spectroscopic, and electrochemical characterizations. Materials were examined for photocatalytic, sonocatalytic, and sonophotocatalytic degradation of carbofuran (CBF) and diazinon (DZN) pesticides under visible light. InV/InS showed enhanced degradation of CBF and DZN when compared to InV and InS. Photocatalytic degradation was accelerated by ultrasonication and found to degrade 97 and 98 % of CBF and DZN in 60 and 70 min, respectively. The reaction conditions, like pH, catalyst dosage, acoustic intensity, and ultrasound power, were carefully optimized. Electron spin resonance (ESR) spectroscopy shows the generation of superoxide radical anion and hydroxyl radicals as reactive species during photoredox reaction. The CBF and DZN degradation intermediates were analyzed using liquid chromatography mass spectroscopy (LC-MS) that shows the mineralization of the CBF and DZN to CO2 and H2O. The effect of Cl-, and PO43- were examined towards degradation of CBF and DZN under optimal conditions in the presence of InV/InS. The degradation of CBF and DZN is decreased in presence of Cl-, CO32- and NO3- but PO43- ions does not show any effect on degradation. The bandgap and Mott-Schottky results suggest the existence of type-II heterostructure between InV and InS through the interface. The synthesis of heterostructure and degradation of pesticides utilizes ultrasonic waves, which prove their multiple applications and attract researchers towards the effective use of sonication.

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The photocatalytic technique has drawn far-ranging interests in addressing the current issues; however, its property suffers from the limited visible light response and rapid recombination of carriers. To address these issues, two specific approaches have been proposed to enhance the photocatalytic activity: (1) ultrasound-assisted synthesis has been utilized to prepare photocatalysts, resulting in refined grain size, increased specific surface area, and reduced photogenerated carrier recombination; (2) sonophotocatalysis and piezoelectric enhanced photocatalysis have been developed to accelerate the reaction, which utilizes the synergism between ultrasound and light. On one side, sonophotocatalysis generates cavitation bubbles which induce more reactive radicals for redox reactions. On the other side, ultrasound induces deformation of the piezoelectric material structure, which changes the internal piezoelectric potential and improves the photocatalytic performance. Currently, intensive efforts have been devoted to related research and great progress has been reached with applications in pollutant degradation, new energy production, and other fields. This work starts by elucidating the fundamental concept of ultrasound-assisted photocatalyst synthesis and photocatalysis. Then, the synergistic behavior between ultrasonic and light in ultrasonic-assisted photocatalysis has been thoroughly discussed, including pollutant degradation, water splitting, and bacterial sterilization. Finally, the challenge and outlook are investigated and proposed.

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Due to water shortage and increased water pollution, various methods are being explored to improve water quality by treating contaminants. Sonophotocatalysis is a combination of two individual water treatment processes i.e., photocatalysis and sonocatalysis. With advantages including shorter reaction times and enhanced activity, this technique shows possible futuristic applications as an efficient water treatment technology. Herein, background insight on sonophotocalysis as a water and wastewater treatment technique as well as the general mechanism of activity is explained. The commonly used catalysts for sonophotocatalytic applications as well as their synthesis pathways are also briefly discussed. Additionally, the utilisation of sonophotocatalysis for the disinfection of various microbial species as well as treatment of wastewater pollutants including organic (dyes, pharmaceuticals and pesticides) and inorganic species (heavy metals) is deliberated. This review also gives a critical analysis of the efficiency, enhancement strategies as well as challenges and outlooks in this field. It is thus intended to give insight to researchers in the context of facilitating future developments in the field of water treatment, and advancing sonophotocatalysis towards large-scale implementation and commercialization.

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Organic dyes play vital roles in the textile industry, while the discharge of organic dye wastewater in the production and utilization of dyes has caused significant damage to the aquatic ecosystem. This review aims to summarize the mechanisms of photocatalysis, sonocatalysis, and sonophotocatalysis in the treatment of organic dye wastewater and the recent advances in catalyst development, with a focus on the synergistic effect of ultrasound and light in the catalytic degradation of organic dyes. The performance of TiO2-based catalysts for organic dye degradation in photocatalytic, sonocatalytic, and sonophotocatalytic systems is compared. With significant synergistic effect of ultrasound and light, sonophotocatalysis generally performs much better than sonocatalysis or photocatalysis alone in pollutant degradation, yet it has a much higher energy requirement. Future research directions are proposed to expand the fundamental knowledge on the sonophotocatalysis process and to enhance its practical application in degrading organic dyes in wastewater.

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In this study, humic acid (HA) enhanced 17ß-estradiol (17ß-E2) degradation by Er3+-CdS/MoS2 (ECMS) was investigated under ultrasonic and light conditions. The degradation reaction rate of 17ß-E2 was increased from (14.414 ± 0.315) × 10-3 min-1 to (122.677 ± 1.729) × 10-3 min-1 within 90 min sonophotocatalytic (SPC) reaction with the addition of HA. The results of quenching coupled with chemical probe experiments indicated that more reactive intermediates (RIs) including reactive oxygen species (ROSs) and triplet-excited states were generated in the HA-enhanced sonophotocatalytic system. The triplet-excited states of humic acid (3HA*), hydroxyl radical (•OH), and superoxide radical (•O2-) were the dominant RIs for 17ß-E2 elimination. In addition, the energy- and electron-transfer process via coexisting HA also account for 12.86% and 29.24% contributions, respectively. The quantum yields of RIs in the SPC-ECMS-HA system followed the order of 3HA* > H2O2 > 1O2 > â€¢O2-> •OH. Moreover, the spectral and fluorescence characteristics of HA were further analyzed during the sonophotocatalytic reaction process. The study expanded new insights into the comprehension of the effects of omnipresent coexisting HA and RIs formation for the removal of 17ß-E2 during the sonophotocatalytic process.

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Treatment of real textile industry effluent using photocatalysis, sonocatalysis, sonophotocatalysis and H2O2 assisted sonophotocatalysis have been studied based on the use of Ce-TiO2 nanocatalyst synthesized using sonochemical co-precipitation method. Characterization studies of the obtained catalyst revealed crystallite size as 1.44 nm with particles having spherical morphology. A shift of the absorption edge to the visible light range was also observed in UV-Vis diffuse reflectance spectra (UV-DRS) analysis. The effects of different operational parameters viz catalyst dose (0.5 g/L-2 g/L), temperature (30 °C-55 °C) and pH (3-12) on the COD reduction were studied. The reduction in the COD was higher at lower pH and the optimum temperature established was 45 °C. It was also elucidated that the required catalyst dose was lesser in combined sonophotocatalysis when compared with individual photocatalysis and sonocatalysis. Combination of processes and addition of oxidants increased the COD reduction with the sonophotocatalytic oxidation combined with H2O2 treatment showing the best results for COD reduction (84.75%). The highest reduction in COD for photocatalysis was only 45.09% and for sonocatalysis, it was marginally higher at 58.62%. The highest reduction in COD achieved by sonophotocatalysis was 64.41%. Toxicity tests coupled with Liquid Chromatography Mass Spectrometry (LC-MS) analysis revealed that there were no additional toxic intermediates added to the system during the treatment. Kinetic study allowed establishing that generalized kinetic model fits the experimental results well. Overall, the combined advanced oxidation processes showed better results than the individual processes with higher COD reduction and lower requirement of the catalyst.

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Over the past several decades, the increase in industrialization provoked the discharge of harmful pollutants into the environment, affecting human beings and ecosystems. ZnO-based photocatalysts seem to be the most promising photocatalysts for treating harmful pollutants. However, fast charge carrier recombination, photo corrosion, and long reaction time are the significant factors that reduce the photoactivity of ZnO-based photocatalysts. In order to enhance the photoactivity of such photocatalysts, a combined process i.e., sonocatalysis + photocatalysis = sonophotocatalysis was used. Sonophotocatalysis is one of several different AOP methods that have recently drawn considerable interest, as it produces high reactive oxygen species (ROS) which helps in the oxidation of pollutants by acoustic cavitation. This combined technique enhanced the overall efficiency of the individual method by overcoming its limiting factors. The current review aims to present the theoretical and fundamental aspects of sonocatalysis and photocatalysis along with a detailed discussion on the benefits that can be obtained by the combined process i.e., US + UV (sonophotocatalysis). Also, we have provided a comparison of the excellent performance of ZnO to that of the other metal oxides. The purpose of this study is to discuss the literature concerning the potential applications of ZnO-based sonophotocatalysts for the degradation of pollutants i.e., dyes, antibiotics, pesticides, phenols, etc. That are carried out for future developments. The role of the produced ROS under light and ultrasound stimulation and the degradation mechanisms that are based on published literature are also discussed. In the end, future perspectives are suggested, that are helpful in the development of the sonophotocatalysis process for the remediation of wastewater containing various pollutants.

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This study is the first to explore the possibility of utilizing CuCr LDH decorated on reduced graphene oxide (rGO) and graphene oxide (GO) as sonophotocatalysts for the degradation of dimethyl phthalate (DMP). CuCr LDH and its nanocomposites were successfully fabricated and characterized. Scanning electron microscopy (SEM) along with high-resolution transmission electron microscope (HRTEM) both evidenced the formation of randomly oriented nanosheet structures of CuCr LDH coupled with thin and folded sheets of GO and rGO. The impact of diverse processes on the degradation efficiency of DMP in the presence of the so-prepared catalysts was compared. Benefiting from the low bandgap and high specific surface area, the as-obtained CuCr LDH/rGO represented outstanding catalytic activity (100 %) toward 15 mg L-1 of DMP within 30 min when subjected to light and ultrasonic irradiations simultaneously. Radical quenching experiments and visual spectrophotometry using an O-phenylenediamine revealed the crucial role of hydroxyl radicals compared to holes and superoxide radicals. Overall, outcomes disclosed that CuCr LDH/rGO is a stable and proper sonophotocatalyst for environmental remediation.

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A comparison study examines six different metal oxides (CuO, ZnO, Fe3O4, Co3O4, NiO, and α-MnO2) for the degradation of malachite green dye using four distinct processes. These processes are as follows: sonocatalysis (US/metal oxide), sonocatalysis under ultra-violet irradiation (US/metal oxide/UV), sonocatalysis in the presence of hydrogen peroxide (US/metal oxide/H2O2), and a combination of all these processes (US/metal oxide/UV/H2O2). The effective operating parameters, such as the dosage of metal oxide nanoparticles (MONPs), the type of the process, and the metal oxides' efficiency order, were studied. At the same reaction conditions, the sonophotocatalytic is the best process for all six MOsNPs, CuO was the better metal oxide than other MOsNPs, and at the sonocatalysis process, ZnO was the best metal oxide in other processes. It was found that the metal oxide order for sonocatalytic process is CuO > α-MnO2 ≥ ZnO > NiO ≥ Fe3O4 ≥ Co3O4 within 15-45 min. The order of (US/metal oxide/UV) process is ZnO ≥ NiO ≥ α-MnO2 > Fe3O4 ≥ CuO ≥ Co3O4 within 5-40 min. The order of (US/ MOsNPs/ H2O2) process is ZnO ≥ CuO ≥ α-MnO2 ≥ NiO > Co3O4 > Fe3O4 within 5-20 min. The maximum removal efficiency order of the sonophotocatalytic process is ZnO ≥ CuO > α-MnO2 > NiO > Fe3O4 ≥ Co3O4 within 2-8 min. The four processes degradation efficiency was in the order US/MOsNPs ˂ US/MOsNPs/UV ˂ US/MOsNPs/H2O2 ˂ (UV/Ultrasonic/MOsNPs/H2O2). Complete degradation of MG was obtained at 0.05 g/L MONPs and 1 mM of H2O2 using 296 W/L ultrasonic power and 15 W ultra-violet lamp (UV-C) within a reaction time of 8 min according to the MOsNPs type at the same sonophotocatalytic/H2O2 reaction conditions. The US/metal oxide/UV/H2O2 process is inexpensive, highly reusable, and efficient for degrading dyes in colored wastewater.

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In this study, the photocatalytic activity of ZnO was effectively improved via its combination with spinel cobalt ferrite (SCF) nanoparticles. The catalytic performance of ZnO@SCF (ZSCF) was investigated in coupling with UV irradiation and ultrasound (US), as a heterogeneous sono-photocatalytic process, for the decontamination of phenanthrene (PHE) from contaminated soil. Soil washing tests were conducted in a batch environment, after extraction assisted by using Tween 80. Several characterization techniques such as XRD, FESEM-EDS, BET, TEM, UV-vis DRS, PL and VSM were utilized to determine the features of the as-prepared catalysts. ZSCF showed an excellent catalytic activity toward degradation of PHE in the presence of US and UV with a significant synergic effect. It was found that more than 93% of PHE (35 mg/L) and 87.5% of TOC could be eliminated by the integrated ZSCF/US/UV system under optimum operational conditions (pH: 8.0, ZSCF: 1.5 g/L, UV power: 6.0 W and US power: 70 W) within 90 min of reaction. After five times of use, ZSCF illustrated good reusability in the decontamination of PHE (87%) and TOC (79%). Quenching tests revealed the contribution of h+, HO• and e- species during PHE degradation over ZSCF/UV/US and an S-scheme photocatalytic mechanisms was proposed for the possible charge transfer routes under the ZSCF system. This study provides the important role of SCF in enhancing the ZnO photocatalytic activity due to its high performance, easy recovery and excellent durability, which it make an efficient and promising catalyst in environmental clean-up applications.

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The structure, morphology, and sonophotocatalytic activity of Ni-Zn-Co ferrite nanoparticles, embedded in a SiO2 matrix and produced by a modified sol-gel method, followed by thermal treatment, were investigated. The thermal analysis confirmed the formation of metal succinate precursors up to 200 °C, their decomposition to metal oxides and the formation of Ni-Zn-Co ferrites up to 500 °C. The crystalline phases, crystallite size and lattice parameter were determined based on X-ray diffraction patterns. Transmission electron microscopy revealed the shape, size, and distribution pattern of the ferrite nanoparticles. The particle sizes ranged between 34 and 40 nm. All the samples showed optical responses in the visible range. The best sonophotocatalytic activity against the rhodamine B solution under visible irradiation was obtained for Ni0.3Zn0.3Co0.4Fe2O4@SiO2.

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Sono-photo-catalysis (SPC) has been regarded as a promising route for hydrogen evolution from water splitting due to the sono-photo-synergism, whereas its current performance (∼µmol g-1 h-1) is yet far from expectation. Herein, we give the first demonstration that the intrinsically coupled thermal effects of light and ultrasound, which is normally underestimated or neglected, can simultaneously reshape the photo- and sono-catalytic activities for hydrogen evolution and establish a higher degree of synergy between light and ultrasound in SPC even on the traditional Pt-TiO2 catalyst. A high-efficient hydrogen evolution rate of 225.04 mmol g-1 h-1 with light-to­hydrogen efficiency of 0.89% has been achieved in thermally-enhanced SPC, which is an order of magnitude higher than that without thermal effects. More impressively, the increase of synergy index up to 53% has been achieved. Through experiments and theoretical calculations, the thermally-enhanced sono-photo-synergism is attributed to the sono-photo-thermo-modulated structural optimization of defect-rich TiO2 support and deaggregated Pt species with functional complementary lattice facets, which optimizes not only the thermodynamic properties by enhancing light harvesting and the charge redox power, but also the kinetic properties by accelerating the net efficiency of charge separation and the whole processes of water splitting, including the dissociation of water molecules on high-index (200) Pt facets and production of H∗ intermediates on defect-rich TiO2-x support and low-index (111) Pt facets. This study exemplifies that coupling light- and ultrasonic-induced thermal effects in SPC system could enhance the synergy between light and ultrasound by modulating catalyst structure to achieve double optimization of thermodynamic and kinetic properties of SPC hydrogen evolution.

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Acetamiprid (ACE), a neonicotinoid pesticide widely used in pest control, was found in high concentrations in soils, rivers, and lakes. In the present study, ACE degradation was investigated using visible light driven photocatalysis over nitrogen-graphene oxide (N-GO) and palladium-graphene oxide (Pd-GO)-doped ZnO photocatalysts combined with ultrasonication implemented either as a pretreatment (sonolysis) or operated simultaneously with photocatalysis (sonophocatalysis). The effectiveness of the two ACE degradation processes was determined separately. The sonolysis pretreatment allowed reaching almost 40% acetamiprid conversion within 30 min of reaction. Pursuing with the photodegradation reaction in the presence of N-GO-ZnO and Pd-GO-ZnO resulted in a maximum conversion of 98% of ACE within 5 h. As for the sonophotocatalysis process, the reaction time was shortened from 5 to 2 h with 100% acetamiprid conversion. In addition, the photocatalysts were shown to keep their activity even after 5 sonophotocatalytic cycles, thus proving their reusability. Supplementary Information: The online version contains supplementary material available at 10.1007/s11270-022-05867-4.