Optimization of Internet of Things Remote Desktop Protocol for Low-Bandwidth Environments Using Convolutional Neural Networks.

This paper discusses optimizing desktop image quality and bandwidth consumption in remote IoT GUI desktop scenarios. Remote desktop tools, which are crucial for work efficiency, typically employ image compression techniques to manage bandwidth. Although JPEG is widely used for its efficiency in eliminating redundancy, it can introduce quality loss with increased compression. Recently, deep learning-based compression techniques have emerged, challenging traditional methods like JPEG. This study introduces an optimized RFB (Remote Frame Buffer) protocol based on a convolutional neural network (CNN) image compression algorithm, focusing on human visual perception in desktop image processing. The improved RFB protocol proposed in this paper, compared to the unoptimized RFB protocol, can save 30-80% of bandwidth consumption and enhances remote desktop image quality, as evidenced by improved PSNR and MS-SSIM values between the remote desktop image and the original image, thus providing superior desktop image transmission quality.

Characteristics, application and modeling of solid amine adsorbents for CO2 capture: A review.

In recent years, global warming has become an important topic of public concern. As one of the most promising carbon capture technologies, solid amine adsorbents have received a lot of attention because of their high adsorption capacity, excellent selectivity, and low energy cost, which is committed to sustainable development. The preparation methods and support materials can influence the thermal stability and adsorption capacity of solid amine adsorbents. As a supporting material, it needs to meet the requirements of high pore volume and abundant hydroxyl groups. Industrial and biomass waste are expected to be a novel and cheap raw material source, contributing both carbon dioxide capture and waste recycling. The applied range of solid amine adsorbents has been widened from flue gas to biogas and ambient air, which require different research focuses, including strengthening the selectivity of CO2 to CH4 or separating CO2 under the condition of the dilute concentration. Several kinetic or isotherm models have been adopted to describe the adsorption process of solid amine adsorbents, which select the pseudo-first order model, pseudo-second order model, and Langmuir isotherm model most commonly. Besides searching for novel materials from solid waste and widening the applicable gases, developing the dynamic adsorption and three-dimensional models can also be a promising direction to accelerate the development of this technology. The review has combed through the recent development and covered the shortages of previous review papers, expected to promote the industrial application of solid amine adsorbents.

Biodrying with the hot-air aeration system for kitchen food waste.

Biodrying is a promising method that produces bio-stabilized output with minimum pretreatment requirements. In this study, a hot-air supply system was added to the traditional biodrying process for kitchen waste, which showed significant reduction in moisture content in 5 days (maximum reduction of 37.45%). A series of experiments was conducted to optimize the hot-air biodrying system utilizing different aeration rates, temperatures, and mixing ratios of feedstock to bulking agents. The results showed that a 65 °C aeration temperature led to the highest water removal rate and low volatile solids consumption rate, with the biodrying index reaching 4.9 g water per gram of volatile solids. On the other hand, evaluation of the overall biodrying efficiency based on the weight loss and bio-stabilization showed that intermittent aeration temperature at 55 °C performed best, offering suitable conditions for water evaporation and bio-degradation. In combination with a flow rate of 0.8 L/kg*min and 1:1 mixing ratio, these conditions resulted in the maximum volatile solids consumption of 26.26% in 5 days. The volatile solids consumption and 34.47% water removal rate of the trial had contributed to a total of 64.13% weight loss. The weight loss was even higher than that of a conventional biodrying system which was conducted for more than 14 days.

Carrier Tuning in ZnSnN2 by Forming Amorphous and Microcrystalline Phases.

ZnSnN2 (ZTN), an earth-abundant element semiconductor, is a potential candidate for photovoltaic applications. However, the excessively high n-type carrier concentration caused by intrinsic defects hinders its progress. In this work, a series of Zn1± xSnN2 thin films are fabricated by RF-magnetron sputtering deposition. The zinc-rich composition is found to promote the crystallization of ZTN. As a main source of n-type carriers in the zinc-rich thin films, the interstitial Zn dominates the change of carrier concentration with an increase in the Zn/Sn ratio. Near the stoichiometric ratio, amorphous ZTN (a-ZTN) thin films are fabricated, and the n-type carrier concentration is suppressed to 1016 cm-3. With an increase in the Zn/Sn ratio from 0.9 to 1.3, the n-type carrier concentration can be tuned in the range 1016-1019 cm-3, accompanied by the phase-transition from a-ZTN to microcrystalline ZTN (µc-ZTN). For the a-ZTN thin film, the carrier mobility reaches up to 7 cm2 V-1 s-1, and the photoresponse covers almost the whole visible band. The above properties demonstrate that a-ZTN and µc-ZTN are potential candidates for photovoltaic applications.

Methionine sulfoxide reductase B1 regulates proliferation and invasion by affecting mitogen-activated protein kinase pathway and epithelial-mesenchymal transition in u2os cells.

Methionine sulfoxide reductase B1 (MsrB1), a member of the selenoprotein family and contributes significantly to the reduction of methionine sulfoxides produced from reactive oxygen species (ROS). However, few studies have examined the role of MsrB1 in tumors. Here We tested the proliferation and invasion in MsrB1 knockdown u2os cells under H2O2/thioredoxin. As shown in our result, knockdown of MsrB1 inhibited the proliferation of u2os cells and regulates mitogen-activated protein kinase (MAPK) pathway by down-regulation of Erk, MeK phosphorylation and p53 expression in u2os cells. In a xenograft tumorigenicity mice, MsrB1 knockdown effectively inhibited tumor growth. Furthermore, MsrB1 knockdown resulted in migration and invasion reducement of u2os cells. MsrB1 regulates epithelial-mesenchymal transition (EMT) via affecting cytoskeleton by increasing E-cadherin expression and decreasing N-cadherin, TGF-ß1, slug, fibronectin, vimentin, c-myc, snail and ß-catenin expressions. In vivo, MsrB1 shRNAi can inhibit lung metastasis in metastasis model. In conclusion, MsrB1 regulates proliferation and invasion of u2os cells by affecting MAPK pathway and EMT, and MsrB1 gene may be a novel therapeutic target against tumors.

Interfacial defects induced electronic property transformation at perovskite SrVO3/SrTiO3 and LaCrO3/SrTiO3 heterointerfaces.

Unravelling the atomic structure and chemical species of interfacial defects is critical to understanding the origin of interfacial properties in many heterojunctions. Here, by combining advanced transmission electron microscopy, spectroscopy and first-principles calculations, we demonstrate interfacial Ti diffusion in SrVO3/SrTiO3 and LaCrO3/SrTiO3 heterointerfaces and uncover that the interfacial defects induce a significant change in electronic properties by showing an electronic transformation from the insulating state to metallic state at SrVO3/SrTiO3 heterointerfaces due to the hybridization of interfacial Ti d, O p and V d, and a metallic to insulating state transformation at LaCrO3/SrTiO3 because of Ti-Cr mixing induced charge redistribution in the interfacial layer.

Synergistic effects of intrinsic cation disorder and electron-deficient substitution on ion and electron conductivity in La1-xSrxCo0.5Mn0.5O3-δ (x = 0, 0.5, and 0.75).

The effects of intrinsic cation disorder and electron-deficient substitution for La1-xSrxCo0.5Mn0.5O3-δ (LSCM, x = 0, 0.5, and 0.75) on oxygen vacancy formation, and their influence on the electrochemical properties, were revealed through a combination of computer simulation and experimental study. First-principles calculations were first performed and found that the tendency of the oxygen vacancy formation energy was Mn(3+)-O*-Mn(4+) < Co(2+)-O*-Co(3+) < Co(2+)-O*-Mn(4+), meaning that antisite defects not only facilitate the formation of oxygen vacancy but introduce the mixed-valent transition-metal pairs for high electrical conductivity. Detailed partial density of states (PDOS) analysis for Mn on Co sites (MnCo) and Co on Mn sites (CoMn) indicate that Co(2+) is prone to being Co(3+) while Mn(4+) is prone to being Mn(3+) when they are on antisites, respectively. Also it was found that the holes introduced by Sr tend to enter the Co sublattice for x = 0.5 and then the O sublattice when x = 0.75, which further promotes oxygen vacancy formation, and these results are confirmed by both the calculated PDOS results and charge-density difference. On the basis of microscopic predictions, we intentionally synthesized a series of pure LSCM compounds and carried out comprehensive characterization. The crystal structures and their stability were characterized via powder X-ray Rietveld refinements and in situ high-temperature X-ray diffraction. X-ray photoelectron spectroscopy testified to the mixed oxidation states of Co(2+)/Co(3+) and Mn(3+)/Mn(4+). The thermal expansion coefficients were found to match the Ce0.8Sm0.2O2-δ electrolyte well. The electrical conductivities were about 41.4, 140.5, and 204.2 S cm(-1) at doping levels of x = 0, 0.5, and 0.75, and the corresponding impedances were 0.041, 0.027, and 0.022 Ω cm(2) at 850 °C, respectively. All of the measured results testify that Sr-doped LaCo0.5Mn0.5O3 compounds are promising cathode materials for intermediate-temperature solid oxide fuel cells.

Broadband down-conversion for silicon solar cell by ZnSe/phosphor heterostructure.

Down-conversion is a feasible way to improve conversion efficiency of silicon solar cell. However, the width of excitation band for down-converter based on trivalent lanthanide ions is still not satisfying. Here, we designed and fabricated a heterostructural down-converter composed of Y2O3: [(Tb³âº-Yb³âº), Li⁺] quantum cutting phosphor and ZnSe. The ZnSe phase was used to absorb the incident light with energy larger than its bandgap, and transfer the energy to Tb³âº-Yb³âº quantum cutting couple. Short-wavelength incident light was finally converted into a strong Yb³âº emission at about 1000 nm, locating at the maximal spectral response of silicon solar cell. The excitation band of the down-conversion covers a wide region of 250-550 nm. Benefiting from the energy match between ZnSe bandgap and 7F6→5D4 absorption of Tb³âº ions, the bandwidth of down-conversion is almost maximized.

Mitigating heavy metal volatilization during thermal treatment of MSWI fly ash by using iron(III) sulfate as a chlorine depleting agent.

In the thermal treatment of municipal solid waste incineration fly ash (FA), the presence of chlorides leads to the pronounced volatilization of heavy metals at high temperature, making heavy metals stabilization challenging. Conventional washing processes struggle to remove chlorides completely, and even minor residual chlorides can lead to significant heavy metal volatilization. This study innovatively applied iron(III) sulfate as a chlorine depleting agent, which can form FeCl3 (boiling point 316 °C) and volatilize to remove the residual chlorides at below 500 °C, thus preventing the chlorination and volatilization of heavy metals at 600-1000 °C. Using water-washed FA to produce lightweight aggregate (LWA) preparation, after adding iron(III) sulfate, the volatilization rates of Pb and Cd at 1140 °C decreased to 5.4% and 9.3%, respectively, a reduction of 82.8% and 84.1% compared to before its addition. The LWA met standard requirements in both performance and heavy metal leaching toxicity. The mechanism was further studied through thermodynamic equilibrium calculations and heating experiments of pure chemicals. This study presents novel approaches and insights for suppressing the volatilization of heavy metals in FA at high temperature, thereby promoting the advancement of thermal treatment techniques and the safe, resourceful disposal of FA.

A review on the evaluation models and impact factors of greenhouse gas emissions from municipal solid waste management processes.

The total amount of global municipal solid waste (MSW) will reach 3.5 billion tons by 2050, thereby bringing tremendous environmental pressure, especially global warming. Large amounts of greenhouse gases (GHGs) have been released during MSW management (MSWM). Accounting for GHG emissions is a prerequisite for providing recommendations on appropriate treatment options to mitigate emissions from MSWM systems. There are many methods involved in estimating emissions. This paper summarizes the computing models commonly used in each process of the integrated MSWM system and emphasizes the influence of parameters and other factors. Compared with other disposal methods, landfilling has the highest emissions, commonly estimated using first-order decay (FOD) methods. Emission reduction can be realized through waste to energy (WtE) and resource recovery measures. IPCC is commonly used for calculating direct emissions, while LCA-based models can calculate emissions including upstream and downstream processes, whose results depend on assumptions and system boundaries. The estimation results of models vary greatly and are difficult to compare with each other. Besides, large gaps exist between the default emission factors (EFs) provided by models and those F measured in specific facilities. These findings provide a systematic view for a bettering understanding of MSW emissions as well as the estimating methods and also reveal the key points that need be developed in the future.

Impacts of seasonal variation on volatile fatty acids production of food waste anaerobic fermentation.

This study aims to investigate the influence of seasonal variations on Volatile fatty acids (VFAs) production from food waste (FW) and to quantify their impact. Results of batch experiments with external pH control indicated that the properties of FW exhibited significant seasonal variations and were markedly different from kitchen waste (KW). The spring group demonstrated the highest VFA concentration and VFA/SCOD, at 31.24 g COD/L and 92.20 % respectively, which were 1.22 and 1.27 times higher than those observed in the summer season. The combined proportion of acetic acid and butyric acid accounted for 81.10 % of the total VFAs in spring, suggesting the highest applicability to the carbon source. The VFA content of all seasonal groups in descending order was butyric acid, propionic acid and acetic acid. Carbohydrates, along with spicy and citrusy substances, promoted the conversion of total VFA and butyric acid, while proteins and lipids favored the production of acetic acid and propionic acid.

Comprehensive study of recycling municipal solid waste incineration fly ash in lightweight aggregate with bloating agent: Effects of water washing and bloating mechanism.

Recycling into lightweight aggregate (LWA) by sintering is a promising technology for disposal of municipal solid waste incineration fly ash (FA). In this study, FA and washed FA (WFA) were combined with bentonite and SiC (bloating agent) to make LWA. The performance was comprehensively studied by hot-stage microscopy and laboratory preparation experiments. Water washing and increased FA/WFA improved LWA bloating extent, while shorten the bloating temperature range. Water washing also increased the 1 h-water absorption rate of LWA, making it harder to meet the standard. Excessive FA /WFA usage (70 wt%) will prevent LWA from bloating. For the goal of recycling more FA, mixture with 50 wt% WFA could prepare LWA that meet standard GB/T 17431 at 1140-1160 °C. After water washing, the ratio of Pb, Cd, Zn, and Cu stabilized in LWA increased by 279 %, 410 %, 458 %, and 109 % for 30 wt% FA/WFA addition, and 364 %, 554 %, 717 %, and 697 % for 50 wt% FA/WFA addition, respectively. The change of liquid phase content and viscosity at high temperature were determined using the thermodynamic calculations and chemical compositions. The bloating mechanism was further investigated by integrating these two properties. To obtain accurate results of the bloat viscosity range (2.75-4.44 log Pa·s) for high CaO systems, the composition of the liquid phase should be taken into account. The liquid phase viscosity required for bloating start was proportional to the liquid phase content. With temperature increasing, bloating would end when viscosity drops to 2.75 log Pa·s or liquid phase content reach 95 %. These findings provided further understanding of the heavy metal stabilization during LWA production and the bloating mechanism of high CaO content systems, and could contribute to the feasibility and sustainability of recycling FA and other CaO-rich solid wastes into LWA.

Analysis of enrichment, correlation, and leaching patterns of rare earth elements in coal fly ash assisted by statistical measures.

Coal fly ash (CFA) is a typical industrial solid waste, which has recently been reported to contain rare earth elements (REEs). REEs are important materials in many industrial fields. Therefore, extracting REEs from CFA becomes a win-win strategy to both make full use of CFA and reclaim REEs. However, the stable crystalline structure of CFA is hard to break, which limits the extraction of REEs. The inter-correlation and the leaching patterns of the REEs in CFA also remain unclear. In this work, REEs were enriched by desilication, and the correlation and the influences of multiple acids of the leached REEs were investigated. It was found that desilication could increase the leachable amount of REEs from 137.37 ppm to 346.12 ppm. The light rare earth elements (LREEs) were less inter-correlated than heavy rare earth elements (HREEs) and desilication enhanced the leaching of LREEs more than that of HREEs. The ratio and type of the leaching acids both influenced the extraction of REEs from CFA: HCl and HF played important roles in the extraction from the untreated CFA while HNO3 and HF were more decisive for the desilicated CFA. In addition, we used statistical analysis to quantificationally confirm that desilication and acids both significantly influenced the extraction of REEs. This work provides evidence for the enrichment of REEs in CFA and acid choosing when leaching REEs from CFA.

A green and multi-win strategy for coal fly ash disposal by CO2 fixation and mesoporous silica synthesis.

Coal combustion provides plenty of energy, along with enormous coal fly ash (CFA) and CO2 emission. CFA could be recycled for mesoporous silica synthesis, but expensive templates are usually needed. In this work, we proposed a multi-win strategy using CO2 as the precipitator and template. Mesoporous silica powders, with a maximum specific surface area of 355.45 m2/g, a pore volume of 0.73 cm3/g, and an average pore size of around 7.67 nm, were synthesized. The influences of silicon concentration, CO2 flow rate, and ultrasound were investigated. In addition, the Na2CO3 by-product was produced with a purity of over 92 %. By averagely calculating, 1 ton CFA could generate 285 kg mesoporous silica and 1.02 t crude Na2CO3. Around 433 kg of CO2 could be absorbed. Therefore, multi-goals of CFA disposal, CO2 storage, and valuable silica materials production were realized, and the study could pave the way for large-scale industrial applications.

Recycling municipal solid waste incineration fly ash in super-lightweight aggregates by sintering with clay and using SiC as bloating agent.

Municipal solid waste incineration (MSWI) fly ash is classified as hazardous waste and requires proper treatments. Sintering of MSWI fly ash for the production of lightweight aggregate (LWA) is a promising treatment technology, while the dependence on natural bloating clay to produce high quality LWA has limited its wide application. In this study, by using SiC as a bloating agent, normal clay could be used to produce super-lightweight aggregate (bulk density <500 kg/m3) with MSWI fly ash. Effects of SiC addition amount, sintering temperature and duration on LWA performance were studied. The results showed that LWA with SiC addition of 0.1-0.5 wt% had significant expansion at sintering temperature of 1120 °C-1160 °C. The optimal conditions were 0.3 wt% SiC addition and sintering at 1120 °C for 30 min, and the bulk density could reach 212 kg/m3 with other properties meeting the LWA standard (GB/T 17431.1-2010). Further, the heavy metal leaching toxicity was significantly decreased after sintering and met the MSWI fly ash utilization standard (HJ 1134-2020). The X-ray diffraction results revealed the formation of a complex diopside-based phase after sintering. This study provides a new approach for recycling MSWI fly ash in LWA without dependence on specific clay resources, and makes this technology wider applicability.

Insights into the Critical Role of Abundant-Porosity Supports in Polyethylenimine Functionalization as Efficient and Stable CO2 Adsorbents.

The emerging polyethylenimine (PEI)-functionalized solid adsorbents have witnessed significant development in the implementation of CO2 capture and separation because of their decent adsorption capacity, recyclability, and scalability. As an indispensable substrate, the importance of selecting porous solid supports in PEI functionalization for CO2 adsorption was commonly overlooked in many previous investigations, which instead emphasized screening amine types or developing complex porous materials. To this end, we scrutinized the critical role of different commercial porous supports (silica, alumina, activated carbon, and polymeric resins) in PEI impregnation in this study, taking into account multiple perspectives. Hereinto, the present results identified that abundant larger pore structures and surface functional groups were conducive to loading a considerable amount of PEI molecules. Various supports after PEI functionalization had great differences in adsorption capacities, amine efficiencies, and the corresponding optimal temperatures. In addition, more attention was paid to the role of porous supports in long-term stability during the consecutive adsorption-regeneration cycles, while N2 and CO2 purging as regeneration strategies, respectively. Especially, CO2-induced degradation due to urea species formation was specifically recognized in a SiO2-based adsorbent, which would induce serious concerns in CO2 cyclic capture. On the other side, we also confirmed that adopting conventional porous supports, for example, HP20, could achieve superior adsorption performance (above 4 mmol CO2/g) and cyclic stability (around 1% loss after 30 cycles) rather than the ones synthesized through complex approaches, which ensured the availability and scalability of PEI-functionalized CO2 adsorbents.

Effectively Promoting Activity and Stability of a MnCo2O4-Based Cathode by In Situ Constructed Heterointerfaces for Solid Oxide Fuel Cells.

The development of multiphase composite electrocatalysts plays a key role in achieving the efficient and durable operation of intermediate-temperature solid oxide fuel cells (IT-SOFCs). Herein, a self-assembled nanocomposite is developed as the oxygen reduction reaction (ORR) catalyst for IT-SOFCs through a coprecipitation method. The nanocomposite is composed of a doped (Mn0.6Mg0.4)0.8Sc0.2Co2O4 (MMSCO) spinel oxide (84 wt %), an orthorhombic perovskite phase (11.3 wt %, the spontaneous combination of PrO2 additives and spinel), and a minor Sc2O3 phase (4.7 wt %). The surface of the (Mn0.6Mg0.4)0.8Sc0.2Co2O4 phase is activated by the self-assembled nanocoating with many heterogeneous interfaces. Thence, the ORR kinetics is obviously accelerated and an area-specific resistance (ASR) of ∼0.11 Ω cm2 is obtained at 750 °C. Moreover, a single cell with the cathode shows a peak power density (PPD) of 1144.1 mW cm-2 at 750 °C, much higher than that of the cell with the MnCo2O4 cathode (456.2 mW cm-2). An enhanced stability of ∼120 h (0.8 A cm-2, 750 °C) is also achieved, related to the reduced thermal expansion coefficient (13.9 × 10-6 K-1). The improvement in ORR kinetics and stability can be attributed to the refinement of grains, the formation of heterointerfaces, and the enhancement of mechanical compatibility.

SNHG1 knockdown upregulates miR-376a and downregulates FOXK1/Snail axis to prevent tumor growth and metastasis in HCC.

Long non-coding RNAs (lncRNAs), microRNAs (miRNAs or miRs), and genes are emerging players in cancer progression. In the present study, we explored the roles and interactions of oncogenic lncRNA small nucleolar RNA host gene 1 (SNHG1), miR-376, forkhead box protein K1 (FOXK1), and Snail in hepatocellular carcinoma (HCC). Expression of SNHG1, miR-376, and FOXK1 in HCC was characterized in clinical HCC tissues of 75 patients with HCC. The interactions between SNHG1 and miR-376 and between miR-376 and FOXK1 were predicted and confirmed by dual-luciferase reporter gene and RNA immunoprecipitation assays. Overexpression and knockdown experiments were performed in HCC cells to examine the effects of the SNHG1/miR-376/FOXK1/Snail axis on viability, apoptosis, invasiveness, and migrating abilities. Their effects on tumor growth and metastasis were validated in nude mouse models. SNHG1 and FOXK1 were upregulated, and miR-376a was downregulated in HCC. SNHG1 knockdown contributed to suppression of HCC cell viability, invasion, and migration properties and promotion of apoptosis. SNHG1 could competitively bind to miR-376a to upregulate its target gene FOXK1, which upregulated Snail. SNHG1 knockdown delayed cancer progression both in vitro and in vivo by upregulating miR-376a and downregulating FOXK1 and Snail. SNHG1 knockdown exerts anti-tumor activity in HCC, suggesting a therapeutic target.

Methionine Sulfoxide Reductase B1 Regulates Hepatocellular Carcinoma Cell Proliferation and Invasion via the Mitogen-Activated Protein Kinase Pathway and Epithelial-Mesenchymal Transition.

Methionine sulfoxide reductase B1 (MsrB1) is a member of the selenoprotein family, which contributes to the reduction of methionine sulfoxides produced from reactive oxygen species (ROS) by redox processes in energy pathways. However, few studies have examined the role of MsrB1 in human hepatocellular carcinoma (HCC). We observed that MsrB1 is highly expressed in HCC tissues and that its expression correlated with the prognoses of patients with HCC after hepatectomy. In vitro, knockdown of MsrB1 inhibits HCC cell growth by MTT and EdU proliferation assay, and MsrB1 interference enhances H2O2/trx-induced apoptosis. We observed that phosphorylation of the key proteins of the MAPK pathway, namely, ERK, MEK, and p53, was inhibited, but PARP and caspase 3 were increased, thus infecting mitochondrial integrity. In vivo, MsrB1 knockdown effectively inhibited tumor growth. Furthermore, MsrB1 knockdown reduced HCC cell migration and invasion in a transwell assay through inhibition of cytoskeletal rearrangement and spread. This change was linked to epithelial-mesenchymal transition (EMT) inhibition resulting from increases in E-cadherin expression and decreases in expression in TGF-ß1, Slug, MMP-2/9, and so on. MsrB1 regulates HCC cell proliferation and migration by modulating the MAPK pathway and EMT. Thus, MsrB1 may be a novel therapeutic target with respect to the treatment of HCC.

HBV-specific CD4+ cytotoxic T cells in hepatocellular carcinoma are less cytolytic toward tumor cells and suppress CD8+ T cell-mediated antitumor immunity.

In East Asia and sub-Saharan Africa, chronic infection is the main cause of the development of hepatocellular carcinoma, an aggressive cancer with low survival rate. Cytotoxic T cell-based immunotherapy is a promising treatment strategy. Here, we investigated the possibility of using HBV-specific CD4+ cytotoxic T cells to eliminate tumor cells. The naturally occurring HBV-specific cytotoxic CD4+ and CD8+ T cells were identified by HBV peptide pool stimulation. We found that in HBV-induced hepatocellular carcinoma patients, the HBV-specific cytotoxic CD4+ T cells and cytotoxic CD8+ T cells were present at similar numbers. But compared to the CD8+ cytotoxic T cells, the CD4+ cytotoxic T cells secreted less cytolytic factors granzyme A (GzmA) and granzyme B (GzmB), and were less effective at eliminating tumor cells. In addition, despite being able to secrete cytolytic factors, CD4+ T cells suppressed the cytotoxicity mediated by CD8+ T cells, even when CD4+ CD25+ regulator T cells were absent. Interestingly, we found that interleukin 10 (IL-10)-secreting Tr1 cells were enriched in the cytotoxic CD4+ T cells. Neutralization of IL-10 abrogated the suppression of CD8+ T cells by CD4+ CD25- T cells. Neither the frequency nor the absolute number of HBV-specific CD4+ cytotoxic T cells were correlated with the clinical outcome of advanced stage hepatocellular carcinoma patients. Together, this study demonstrated that in HBV-related hepatocellular carcinoma, CD4+ T cell-mediated cytotoxicity was present naturally in the host and had the potential to exert antitumor immunity, but its capacity was limited and was associated with immunoregulatory properties.