Effect of oxide interactions on chromium speciation transformation during simulated municipal solid waste incineration.

Chromium released during municipal solid waste incineration (MSWI) is toxic and carcinogenic. The removal of chromium from simulated MSWI flue gas by four sorbents (CaO, bamboo charcoal (BC), powdered activated carbon (PAC), and Al2O3) and the effects of four oxides (SiO2, Al2O3, Fe2O3, and CaO) on chromium speciation transformation were investigated. The results showed that the removal rates of total Cr by the four sorbents were Al2O3 < CaO < PAC < BC, while the removal rates of Cr(VI) by the four sorbents were Al2O3 < PAC < BC < CaO. CaO had a strong oxidizing effect on Cr(III), while BC and PAC had a better-reducing effect on Cr(VI). SiO2 was better for the reduction of Na2CrO4 and K2CrO4 above 1000°C due to its strong acidity, and the addition of CaO significantly inhibited the reduction of Cr(VI). MgCrO4 decomposed above 700°C to form MgCr2O4, and the reaction between MgCrO4 and oxides also existed in the form of a more stable trivalent spinel. Furthermore, when investigating the effect of oxides on the oxidation of Cr(III) in CrCl3, it was discovered that CaO promoted the conversion of Cr(III) to Cr(VI), while the presence of chlorine caused chromium to exist in the form of Cr(V), and increasing the content of CaO and extending the heating time facilitated the oxidation of Cr(III). In addition, silicate, aluminate, and ferrite were generated after the addition of SiO2, Al2O3, and Fe2O3, which reduced the alkalinity of CaO and had an important role in inhibiting the oxidation of Cr(III). The acidic oxides can not only promote the reduction of Cr(VI) but also have an inhibitory effect on the oxidation of Cr(III) ascribed to alkali metals/alkaline earth metals, and the proportion of acidic oxides can be increased moderately to reduce the generation of harmful substances in the hazardous solid waste heat treatment.

Intraperitoneal administration of carcinoembryonic antigen-directed chimeric antigen receptor T cells is a robust delivery route for effective treatment of peritoneal carcinomatosis from colorectal cancer in pre-clinical study.

BACKGROUND AIMS: Peritoneal carcinomatosis (PC) from colorectal cancer (CRC) is a highly challenging disease to treat. Systemic chimeric antigen receptor (CAR) T cells have shown impressive efficacy in hematologic malignancies but have been less effective in solid tumors. We explored whether intraperitoneal (i.p.) administration of CAR T cells could provide an effective and robust route of treatment for PC from CRC. METHODS: We generated second-generation carcinoembryonic antigen (CEA)-specific CAR T cells. Various animal models of PC with i.p. and extraperitoneal metastasis were treated by i.p. or intravenous (i.v.) administration of CEA CAR T cells. RESULTS: Intraperitoneally administered CAR T cells exhibited superior anti-tumor activity compared with systemic i.v. cell infusion in an animal model of PC. In addition, i.p. administration conferred a durable effect and protection against tumor recurrence and exerted strong anti-tumor activity in an animal model of PC with metastasis in i.p. or extraperitoneal organs. Moreover, compared with systemic delivery, i.p. transfer of CAR T cells provided increased anti-tumor activity in extraperitoneal tumors without PC. This phenomenon was further confirmed in an animal model of pancreatic carcinoma after i.p. administration of our newly constructed prostate stem cell antigen-directed CAR T cells. CONCLUSIONS: Taken together, our data suggest that i.p. administration of CAR T cells may be a robust delivery route for effective treatment of cancer.

Hypoxia-Responsive CAR-T Cells Exhibit Reduced Exhaustion and Enhanced Efficacy in Solid Tumors.

Expanding the utility of chimeric antigen receptor (CAR)-T cells in solid tumors requires improving their efficacy and safety. Hypoxia is a feature of most solid tumors that could be used to help CAR-T cells discriminate tumors from normal tissues. In this study, we developed hypoxia-responsive CAR-T cells by engineering the CAR to be under regulation of hypoxia-responsive elements and selected the optimal structure (5H1P-CEA CAR), which can be activated in the tumor hypoxic microenvironment to induce CAR-T cells with high polyfunctionality. Hypoxia-responsive CAR T cells were in a "resting" state with low CAR expression under normoxic conditions. Compared with conventional CAR-T cells, hypoxia-responsive CAR-T cells maintained lower differentiation and displayed enhanced oxidative metabolism and proliferation during cultivation, and they sowed a capacity to alleviate the negative effects of hypoxia on T-cell proliferation and metabolism. Furthermore, 5H1P-CEA CAR-T cells exhibited decreased T-cell exhaustion and improved T-cell phenotype in vivo. In patient-derived xenograft models, hypoxia-responsive CAR-T cells induced more durable antitumor activity than their conventional counterparts. Overall, this study provides an approach to limit CAR expression to the hypoxic tumor microenvironment that could help to enhance CAR T-cell efficacy and safety in solid tumors. SIGNIFICANCE: Engineering CAR-T cells to upregulate CAR expression under hypoxic conditions induces metabolic reprogramming, reduces differentiation, and increases proliferation to enhance their antitumor activity, providing a strategy to improve efficacy and safety.

Efficient Hg0 catalytic removal by direct S-scheme heterostructure of two-dimensional Bi2MoO6 (2 0 0)/g-C3N4 nanosheets under visible light.

The gaseous elemental mercury (Hg0) emitted from coal-fired flue gas is extremely harmful to the atmospheric environment and human health. In this study, a 2D/2D Bi2MoO6(2 0 0)/g-C3N4 heterojunction photocatalyst was synthesized and exhibited a high visible-light driven Hg0 removal efficiency up to 99.5% in an atmosphere consisting of N2, O2 (6%), CO2 (12%), NO (100 ppm), SO2 (800 ppm), and H2O (5%). The introduction of surfactant CTAB led to further exposure of the highly active (2 0 0) crystal facet of Bi2MoO6, with a higher reactive oxygen species ratio than the original mainly exposed (1 3 1) crystal facet, and inhibited the agglomeration of Bi2MoO6, thereby greatly reducing the micro-thickness and improving the specific surface area. The smaller thickness effectively promoted the separation of photoinduced carriers and the speed of transfer to the interface. Additionally, through EPR characterization and work function calculation, we observed that the change in the exposed crystal facet regulated the Fermi level of Bi2MoO6 nanosheets, altering the direction of the built-in electric field at the interface with g-C3N4. This formation of an S-scheme 2D/2D Bi2MoO6(2 0 0)/g-C3N4 heterostructure further facilitated the recombination of unintentional carriers and strengthened the separation and catalysis of effective photogenerated carriers. To a certain extent, this work provides a guidance for the research of photocatalysis to achieve efficient and sustainable mercury removal from coal-fired flue gas.

Evaluation of the kinetics of direct aqueous mineral carbonation of wood combustion ash using modified shrinking core models.

The direct aqueous mineral carbonation of wood combustion ash (WCA), which is a representative high-calcium waste from combustion process, was systematically investigated by varying complex operating conditions, including reaction time, liquid-to-solid ratio (L/S), CO2 concentration, and particle size. The WCA exhibited high CO2 sequestration characteristics with an optimal carbonation efficiency of 76.4%, corresponding to a CO2 sequestration capacity of 0.314 g CO2/g WCA. In addition to solid carbonates, dry residues from liquid products with high potassium contents are potential feedstocks for quality potash fertilizer. Modified shrinking core models based on diffusion-controlled mechanism were proposed to evaluate the carbonation process. The theoretical framework assumes a contracting interface mechanism where active CaO reacts with CO2 to form a product layer. The effective diffusion coefficient of CO2 through the product layer decreases over time, giving deficient carbonation efficiency. The newly proposed models corresponding to different geometrical dimensions provided more perfect fit to the experimental data when compared with the most commonly used kinetic equations. The low apparent activation energy of the carbonation reaction demonstrated the diffusion-controlled mechanism. This work is useful for improving the economics and feasibility of bioenergy carbon capture and storage (CCS) technology chain.

Retention of trace elements in coal-fired flue gas by a novel heterogeneous agglomeration technology.

Heterogeneous agglomeration (HA) is a very potential technology for coal-fired flue gas treatment. In this paper, the distribution and migration mechanisms of trace elements (TEs) such as Se, As and Pb in CFPPs were studied on a 30,000 m3/hr pilot-scale experimental platform. The influences of HA on the removal efficiency of gaseous and particulate TEs were well analyzed. The results showed that Se, As and Pb were enriched in fly ash, and their sensitivity to particle size is quite different. The content of Se was the highest in PM1, reaching 193.04 mg/kg at the electrostatic precipitator (ESP) outlet. The average particle size of the total dust before ESP increased significantly from 21.686 to 62.612 µm after injecting the heterogeneous agglomeration adsorbent, conducive to its further removal by ESP. In addition, the concentrations of gaseous Se, As and Pb in the flue gas decreased after adsorbent spray, and accordingly, their contents in the hierarchical particles increased, indicating that the adsorbent could effectively promote the adsorption of gaseous trace elements in fly ash and reduce the possibility of their escape to the atmosphere. Total concentrations of Se, As and Pb emitted by wet flue gas desulfurization (WFGD) are 0.223, 0.668 and 0.076 µg/m3, which decreased by 59.98%, 47.69% and 90.71%, respectively. Finally, a possible HA mechanism model was proposed, where chemical adsorption, physical condensation and collision agglomeration of gaseous TEs and fine particles with adsorbent droplets occurred to form larger agglomerates.

Two-dimensional heterostructures for photocatalytic CO2 reduction.

The photocatalysis conversion of CO2 into fuels has become an encouraging method to address climate and energy issues as a long-term solution. Single material suffers poor yield due to low light energy utilization and high recombination rate of photoinduced electron-hole pairs. It is an efficient approach to construct heterojunction through two or three materials to improve the photocatalytic performance. Recently, 2D-based heterojunction is getting popular for outstanding properties, such as special light collecting structure to enhance light harvest, intimate interface to facilitate charge transfer and separation, and large specific surface area to provide abundant reactive sites. Recently, some new 2D-based heterostructures materials (both structure and composition) have been developed with excellent performance. 2D materials exert structural and functional advantages in these fine composite photocatalysts. In this review, the literatures about the photocatalytic conversion of CO2 are mainly summarized based on overall structure, interface type and material type of 2D-based heterojunction, with special attention given to the preparation, characterization, structural advantages and reaction mechanism of novel 2D-based heterojunction. This work is in hope of offering a basis for designing improved composite photocatalyst for CO2 photoreduction.

A critical review on lead migration, transformation and emission control in Chinese coal-fired power plants.

Coal is widely utilized as an important energy source, but coal-fired power plant was considered to be an important anthropogenic lead emission source. In the present study, the distribution characteristics of lead in coal and combustion by-products are reviewed. Specifically, lead is mainly transferred to ash particles and the formation and migration mechanisms of particulate lead are summarized. Also, targeted measures are proposed to control the formation of fine particulate lead as well as to increase the removal efficiency during the low-temperature flue gas clean process. In detail, interactions between gaseous lead and some coal-bearing minerals or added adsorbents could obviously suppress the formation of fine particulate lead. On the other hand, some efforts (including promoting capture of fine particles, reducing resistivity of particles and strengthening the gas-liquid contact) could be made to improve the fine particulate lead removal capacity. Notably, the formation mechanism of fine particulate lead is still unclear due to the limitations of research methods. Some differences in the removal principles of fine particles and particulate lead make the lead emission precisely control a great challenge. Finally, the environmental potential risk of lead emission from flue gas and ash residues is addressed and further discussed.

Fate and emission behavior of heavy metals during hazardous chemical waste incineration.

The fate and emission behavior of heavy metals (As, Cd, Co, Cr, Cu, Ni, Pb, Se, and Zn) from a hazardous chemical waste incinerator were systematically explored. The results show that the main components of incineration fly ashes and slags contain minerals such as salt, plagioclase, pyroxene, gypsum, calcite, and slaked lime. The elements As, Cd, Pb, and Se are enriched in the fly ash particles during flue gas condensation. Co and Ni are more likely to be deposited in the rotary kiln slag and cooling tower slag owing to their lower volatility. Zn, Cr, and Cu are usually volatilized into the flue gas as oxides or chlorides are condensed and enriched in the slag of the cooling tower during the flue gas cooling process. The content of As, Cd, Pb, Ni, Cr, and Se increase with decreasing fly ash particle size. After the flue gas purification equipment was employed, the concentration of particulate metals significantly reduced. In the exhaust flue gas, the concentrations of Cu and Zn are 29.85 and 28.47 µg/m3, those of As, Cr, Ni, Pb, and Se range from 2.54 to 9.25 µg/m3, and those of Co and Cd are 0.42 and 0.13 µg/m3, respectively.

Influence of SO3 on the MnOx/TiO2 SCR catalyst for elemental mercury removal and the function of Fe modification.

Elemental mercury (Hg0) is a highly hazardous pollutant of coal combustion. The low-temperature SCR catalyst of MnOx/TiO2 can efficiently remove Hg0 in coal-burning flue gas. Considering its sulfur sensitivity, the effect of SO3 on the catalytic efficiency of MnOx/TiO2 and Fe modified MnOx/TiO2 for Hg0 removal was investigated comprehensively for the first time. Characterizations of Hg-TPD and XPS were conducted to explore the catalytic mechanisms of Hg0 removal processes under different conditions. Hg0 removal efficiency of MnOx/TiO2 was inhibited irreversibly from 92% to approximately 60% with the addition of 50 ppm SO3 at 150 â„ƒ, which resulted from the transformation of Mn4+ and chemisorbed oxygen to MnSO4. The existence of H2O would intensify the inhibitory effect. The inhibition almost disappeared and even converted to promotion as the temperature increased to 250 â„ƒ and above. Fe modification on MnOx/TiO2 improved the Hg0 removal performance in the presence of SO3. The addition of SO3 caused only a slight inhibition of 1.9% on Hg0 removal efficiency of Fe modified MnOx/TiO2 in simulated coal-fired flue gas, and the efficiency maintained good stability during a 12 h experimental period. This work would be conducive to the future application of MnOx/TiO2 for synergistic Hg0 removal.

A review on removal of mercury from flue gas utilizing existing air pollutant control devices (APCDs).

Mercury is a highly toxic heavy metal pollutant. It is of great significance to develop cost-effective mercury pollution control technologies of coal-fired flue gas. Among various mercury from flue gas removal methods, the application of existing air pollution control devices (APCDs) to remove mercury from flue gas is one of the most valuable methods because it doesn't need to install additional mercury removal equipment, reducing the cost of mercury removal. This review summarizes the recent progress of mercury from flue gas removal by APCDs (e.g., SCR denitration device, WFGD system and dust removal device). SCR denitration device can achieve partial removal of mercury in flue gas through combined with WFGD system, but easy inactivation and poor sulfur/water/heavy metals resistance of SCR catalyzers are still the main problems. WFGD systems can remove most of Hg2+ (80%-95%), but have low treatment ability for Hg0. Various oxidants can effectively oxidize Hg0 into Hg2+. However, traditional oxidants have high prices and secondary pollution due to the formation of by-products. Fabric filters (FFs), electrostatic precipitators (ESPs) and hybrid fabric filters (HFs) can all control the emission of mercury in the flue gas to a certain extent, especially can effectively remove most of HgP and part of Hg2+, but has low removal capacity for Hg0. Compared with ESP, FF has better capture efficiency for Hg2+ and Hg0, and a combination of ESP and FF, that is HF, can effectively improve the mercury removal capacity.

Enhanced photocatalytic Hg0 oxidation activity of iodine doped bismuth molybdate (Bi2MoO6) under visible light.

The application of photocatalytic Hg0 oxidation under visible light is an up-and-coming method to solve the problem of energy shortage and environmental pollution. In this work, iodine doped Bi2MoO6 nanomaterials were prepared by one-step solvothermal method. The photocatalytic oxidation efficiency was greatly improved by iodine doping from 35.5% to 95.2% in the N2 + 4% O2 atmosphere under visible light. The main reason was that iodine doping decreased the band gap of the catalyst, expanded the optical response range and intensity, sped up the separation rate of photoinduced carriers and reduced the recombination rate. In addition, the flue gas components of SO2 and NO played a promoting role in mercury removal. Iodine doped Bi2MoO6 had good stability and still maintained high mercury removal efficiency after 5 cycles. Density functional theory (DFT) calculations and experiments demonstrated that iodine doping changed the valence band and conduction band of the catalyst, making superoxide ions, hydroxyl radicals and photoinduced hole become the active species of the catalytic reaction.

Condensation and adsorption characteristics of gaseous selenium on coal-fired fly ash at low temperatures.

Gaseous selenium is of high saturated vapor pressure, making its retention in solid phases quite difficult during coal combustion. The selenium transformation from gaseous form into solid phases at low temperatures can be essential to control selenium emission. To understand the migration of SeO2 (g) on ash particles in the low-temperature zone, this study investigated the speciation of selenium in fly ash and simulated the physical retention of SeO2 (g) on fly ash. The results demonstrated that there was a large proportion of physically-bound Se in the fly ash of pulverized-coal-fired boiler (22.62 %-58.03%), while the content of physically-bound Se in fly ash of circulated fluidized-bed boiler was lower (∼6%). The physically-bound Se was formed through selenium condensation and physical adsorption. The decrease of temperature or the increase of cooling rate could promote the transformation of gaseous selenium to solid phase and the presence of HCl might suppress SeO2 transformation into Se in the condensation process. Meanwhile the compositions of fly ash had a great influence on the selenium adsorption process. Among typical coal-fired ash components, mullite showed the best performance in the selenium capture in the temperature range of 90-200 °C, contributing to the high content of physically-adsorbed selenium in PC fly ash. These findings provided new ideas for improving the removal rate of volatile selenium.

Comparative study on fuel characteristics and pyrolysis kinetics of corn residue-based hydrochar produced via microwave hydrothermal carbonization.

Corn residues are an important source of bioenergy. Due to their highly diverse lignocellulosic structures, the hydrochar produced from microwave-assisted carbonization of different corn residues may have distinct fuel properties and pyrolysis kinetics. This study comprehensively investigated the effect of processing temperature on the basic fuel properties of hydrochar and examined the pyrolysis behavior of hydrochar as a precursor through kinetic analysis. The results indicate that the fuel quality of corn straw hydrochar prepared by microwave-assisted hydrothermal carbonization at 230 °C was significantly improved over that of its feedstock, with a higher heating value of approximately 20.7 MJ/kg. Hydrochar prepared by microwave-assisted hydrothermal carbonization of corn cob at 230 °C presents noticeable environmental advantages because it contains the lowest ash and nitrogen contents (0.5% and 0.5%, respectively) and lower sulfur content (0.05%). Moreover, regarding the kinetic modeling, the Doyle and Coats-Redfern models, which are both first-order and single-step kinetic models, were identified as satisfactory in interpreting the key pyrolysis kinetic parameters. Additionally, the microwave-assisted hydrothermal process increased the apparent activation energy of hydrochar due to the increase in crystallinity and the increase in the number of CC and CO bonds.

Photo- and thermo-catalytic mechanisms for elemental mercury removal by Ce doped commercial selective catalytic reduction catalyst (V2O5/TiO2).

The elemental mercury was catalytically removed by V2O5/TiO2 and Ce doped V2O5/TiO2 catalysts under the UV irradiation at 30-160 °C to determine whether the catalysts could simultaneously have both thermo- and photo-catalytic activities. The physicochemical properties of catalysts were characterized by XRD, SEM, EDX, BET, XPS, UV-visible, PER and EIS. The experimental results demonstrated that V2O5/TiO2 and Ce-doped catalysts possessed both thermo- and photo-catalytic reactivities. A suitable reaction temperature (120 °C) and UV light had promoting effects on mercury removal efficiency. In addition, owing to the high oxidation capability as well good oxygen storage performance of Ce4+, Ce doping could greatly improve the mercury removal properties of the catalyst, reduce the inhibition of SO2 and make NO the component with enhanced effect. Ce doping also had the capability of enhancing the light absorption intensity in the UV region as well as the separation rate of photoinduced carriers. Finally, DFT calculations of V-Ti and Ce-V-Ti for Hg0 removal were investigated to further verify the experimental conclusion.

A novel spin-valley-coupled nodal-ring semimetal in single-layer Ta2C3.

Nodal-ring semimetals with band crossing are the new type of quantum materials that have attracted considerable interest from scholars for research. In general, the spin-orbit coupling (SOC) effect opens a band gap at the Dirac point. Therefore, finding 2D nodal-ring semimetals with resistance to SOC has more challenges. Based on first-principles calculations, we propose here that the two-dimensional (2D) Ta2C3 monolayer is a novel nodal-ring semimetal. In particular, Ta2C3 forms six closed rings in the Brillouin zone (BZ) with SOC, which originates from the dxy,x2-y2 orbitals of Ta and the pz orbitals of C. The nodal-ring bands at the K point in Ta2C3 exhibits characteristics of valley splitting and spin polarization due to the breaking of inversion symmetry and SOC. The masximal spin-splitting at the K point is as large as 268.87 meV and 61.90 meV for the conduction band minimum (CBM) and valence band maximum (VBM), respectively. The massless Dirac fermions in the non-equivalent valley have the opposite Berry curvature and spin moment. Therefore, 2D Ta2C3 is novel spin-valley-coupled nodal-ring semimetal. In addition, we found interesting negative differential resistance effects when calculating its transport properties. Our results not only provide an ideal platform for studying the combination of new physical properties, spintronics and valleytronics, but also open the way for designing low-power and fast-transport electronic devices.

Insights into the mechanism of lead species adsorption over Al2O3 sorbent.

Al2O3 is regarded as an effective sorbent to capture lead from flue gas. The adsorption behaviors of different species of lead (Pb, PbO, PbCl and PbCl2) on the Al2O3 surfaces were explored based on density functional theory. The results show that the chemisorption mechanism is responsible for the adsorption of lead species on the Al2O3 surface. The high reactivity of Pb adsorption on the α-Al2O3 (110) surface is mainly attributed to the existence of unsaturated Al atoms. The Al hollow sites are identified as the effectively active sites for Pb adsorption on the (110) surface. The adsorption energies of different species of lead on the Al-terminated (110) surface are in the range of - 4.20 to - 6.30 eV. PbO adsorption at the Al hollow site of the Al-terminated (110) surface shows the highest adsorption energy (- 6.30 eV), suggesting that Al2O3 prefers to capture PbO among different species of lead. The strong interactions of PbO, PbCl and PbCl2 molecules with the unsaturated Al atoms of the α-Al2O3 (110) surface are responsible for PbO, PbCl and PbCl2 capture by Al2O3. Al2O3 has a good ability to capture different species of lead, and the adsorption capacity follows the order: PbO > Pb > PbCl > PbCl2.

Reversed selectivity of photocatalytic CO2 reduction over metallic Pt and Pt(II) oxide cocatalysts.

The chemical state of Pt in cocatalysts has a major influence on the activity and selectivity of the photocatalytic reduction of CO2; however, the underlying mechanism is unclear owing to the co-existence of different Pt chemical states and mutual transformation between them. In this study, PtO/TiO2 catalysts were prepared through photodeposition and Pt/TiO2 was prepared by the photoreduction of PtO/TiO2 to avoid interference arising from co-existing Pt forms and different loading amounts. These catalysts exhibited completely reversed selectivity for CO and CH4 production during CO2 photoreduction: PtO/TiO2 tended to produce CO (100%), whereas Pt/TiO2 favored the production of CH4 (66.6%). By combining experimental analysis and theoretical calculations, the difference in selectivity was ascribed to the different charge transfer/separation and CO/H adsorption properties of PtO/TiO2 and Pt/TiO2. Photoelectric and photoluminescence (PL) analysis showed that Pt was more advantageous to the photogenerated carrier separation compared with PtO, which was conducive to the multi-electron CH4 reduction reaction. Fourier transform-infrared spectroscopy, temperature-programmed desorption/temperature-programmed reduction, and density functional theory calculations indicated that the adsorption of CO and hydrogen on Pt was stronger than that on PtO, which favored the further reduction of CO to CH4. Based on the above results, a mechanism was proposed to explain the reversed selectivity of the photocatalytic reduction of CO2 over Pt/TiO2 and PtO/TiO2.

CD9, a potential leukemia stem cell marker, regulates drug resistance and leukemia development in acute myeloid leukemia.

BACKGROUND: Leukemia stem cells (LSCs) are responsible for the initiation, progression, and relapse of acute myeloid leukemia (AML). Therefore, a therapeutic strategy targeting LSCs is a potential approach to eradicate AML. In this study, we aimed to identify LSC-specific surface markers and uncover the underlying mechanism of AML LSCs. METHODS: Microarray gene expression data were used to investigate candidate AML-LSC-specific markers. CD9 expression in AML cell lines, patients with AML, and normal donors was evaluated by flow cytometry (FC). The biological characteristics of CD9-positive (CD9+) cells were analyzed by in vitro proliferation, chemotherapeutic drug resistance, migration, and in vivo xenotransplantation assays. The molecular mechanism involved in CD9+ cell function was investigated by gene expression profiling. The effects of alpha-2-macroglobulin (A2M) on CD9+ cells were analyzed with regard to proliferation, drug resistance, and migration. RESULTS: CD9, a cell surface protein, was specifically expressed on AML LSCs but barely detected on normal hematopoietic stem cells (HSCs). CD9+ cells exhibit more resistance to chemotherapy drugs and higher migration potential than do CD9-negative (CD9-) cells. More importantly, CD9+ cells possess the ability to reconstitute human AML in immunocompromised mice and promote leukemia growth, suggesting that CD9+ cells define the LSC population. Furthermore, we identified that A2M plays a crucial role in maintaining CD9+ LSC stemness. Knockdown of A2M impairs drug resistance and migration of CD9+ cells. CONCLUSION: Our findings suggest that CD9 is a new biomarker of AML LSCs and is a promising therapeutic target.

Mercury species and potential leaching in sludge from coal-fired power plants.

Wet flue gas desulfurization (WFGD) sludge, generated from the WFGD effluent treatment process, is suitable for multiple uses in various industries. However, risk assessments of its utilization are limited. Systematic study of Hg species occurrences, partitioning and risks of leaching is required, and these concerns were addressed in the present study. Hg temperature-programmed decomposition (Hg-TPD) and an improved European Community Bureau of Reference (BCR) method indicated residual Hg in WFGD sludge was related to HgS, and the content of this fraction was from 2 to 3%. HgCl2, HgO and HgSO4 were assigned to the water/acid-soluble fractions, and reducible Hg was related to Fe species in the sludge. Leachate evaluation of the WFGD sludge indicated potentially high Hg leaching risk. WFGD sludge with higher Hg concentrations and smaller particulate diameters exhibited greater leaching potential. Leaching of Hg from WFGD sludge in China into the environment was estimated at 7.46 t/yr.