Highly efficient photocatalyst fabricated from the recycling of heavy metal ions in wastewater for dye degradation.

Water pollution and energy crisis are becoming global and strategic issues that people are closely concerned about. Green and energy-saving photocatalytic technology is developing rapidly in solving global energy crises and environmental pollution problems. Therefore, we propose the "kill two birds with one stone" strategy to design efficient photocatalysts for dye wastewater treatment by utilizing heavy metal ions in wastewater. The adsorption properties of Mordenite (MOR) were utilized to removal heavy metal ions (Cd2+ and Zn2+) from waste water, and the adsorbed heavy metal ions were dried and sulfurized to obtain CdS/ZnS/MOR(ZnCdM). Then, g-C3N4 was ultrasonically dispersed and composited with ZnCdM by self-assembly, 25 wt% ZnCdCM photocatalytic material was obtained with a degradation rate of 99.8% in 1.5 h for Rhodamine B(RhB). It was found that MOR can provid adequate support for active substances, and the surface of MOR with smaller sizes of CdS nanoparticles, ZnS nanoparticles and g-C3N4 nanosheets, which increased the specific surface area of the materials and improved the reactivity. The porous structure of MOR is favorable for the enrichment of RhB, and the electric field effect of MOR leads to the decrease of the photogenerated carrier complex rate in the semiconductor, which increases the catalytic efficiency. In addition, the double Z charge transfer mechanism formed by CdS, ZnS, g-C3N4 is favorable for separating photogenerated carriers. These synergistic effects improved the photocatalytic efficiency. This strategy will be a green and promising solution to water pollution and energy crisis.

In situ growth of hierarchical phase junction CdS on a H-mordenite zeolite for enhanced photocatalytic properties.

A kind of cadmium sulfide (CdS) nanocomposite with different crystalline phases was grown on the surface of H-mordenite zeolite (HMOR) by a chemical liquid-phase co-precipitation method. In this work, 2 wt% CdS@HMOR photocatalytic material with the coexistence phase (hexagonal phase and cubic phase) of cadmium sulfide was grown on the surface of HMOR by controlling the reaction temperature and ammonia concentration. Photocatalytic degradation of methylene blue (MB) was used as an index to detect the photocatalytic performance of materials. The results indicated that the photocatalytic degradation efficiency of the system with HMOR was significantly improved in comparison to that without HMOR (CdS, 40.34%, 0.2578 h-1). It was found that 2 wt% CdS@HMOR had the best photocatalytic activity. The degradation rate of MB was 84.15% in 2 h, and the degradation rate constant was 0.8884 h-1. When 1.5 ml H2O2 was introduced into the system, the degradation rate of MB was increased to 98.98%, and the degradation rate constant was 1.9976 h-1. SEM, HRTEM, PL, EIS and photocurrent showed that the cubic and hexagonal phases of CdS were in contact with each other on the HMOR surface, forming a good electron transport. By XRD, XPS and SEM tests, the results of materials after four cycles of reactions showed that the structure of the 2 wt% CdS@HMOR was still stable. Therefore, HMOR may provide a good support for CdS, and the synergistic effect between them is beneficial for the occurrence of photocatalytic reactions. HMOR can act as an electron receptor to inhibit the recombination of carriers. The homo-junction between different phases of CdS on the surface of HMOR is beneficial to the separation of photo-induced carriers. These results indicate that the construction of phase heterojunctions on zeolites and the synergism among them are a method for improving the photocatalytic activity.

Defect-Guided Synthesis of Hierarchical Sn-B-Beta Zeolite with Highly Exposed Sn Sites.

Selectively anchoring active centers on the external surface for forming highly exposed acid sites is a highly desirable but challenging task in zeolite catalyst synthesis. Herein, a defect-guided etching-regrowth strategy is rationally designed for facilely positioning Sn Lewis acid sites on the outer surface of the Sn-B-Beta while fabricating a bifunctional hierarchical structure. The synthesis was conducted by hydrothermal treatment of the as-made B-Beta (uncalcined), which has intrinsic defects of the BEA structure, with Sn source and basic organic structure directing agent (SDA). Under a moderate SDA concentration, with blocked micropore channels, such SDA-triggered etching-regrowth will proceed along the defect defined pathway, which ensures Sn selectively anchored on the external surface. Moreover, this methodology has exclusively introduced tetrahedrally coordinated framework Sn with open Sn sites as the predominated species. Mono- and disaccharide isomerizations in ethanol over different Sn-Beta catalysts proved the prominent advantages of the hierarchical structure with highly exposed and synergetic acid sites.

Butanol production from acid hydrolyzed corn fiber with Clostridium beijerinckii mutant.

Sulfuric acid treated corn fiber hydrolysate (SACFH) inhibited cell growth and the production of butanol (4.7±0.2 g/L) by Clostridium beijerinckii IB4 in P2 medium. Optimal medium components were determined using fractional factorial design. NH4HCO3, FeSO4·7H2O and CaCO3 were demonstrated to be significant components in the production of butanol. The Box-Behnken design and a corresponding quadratic model were used to predict medium components (NH4HCO3 1.96 g/L, FeSO4·7H2O 0.26 g/L and CaCO3 3.15 g/L) and butanol yield (9.5 g/L). The confirmation experiment, under the predicted optimal conditions, yielded a butanol level of 9.5±0.1g/L. This study indicates that the Box-Behnken design is an effective approach for screening the optimal medium components required for the production of butanol. It also demonstrates that SACFH, which has high levels of inhibitors such as furan and phenolic compounds, may be used as a renewable carbon source in the production of biofuels.

Butanol production from hemicellulosic hydrolysate of corn fiber by a Clostridium beijerinckii mutant with high inhibitor-tolerance.

A Clostridium beijerinckii mutant RT66 with considerable inhibitor-tolerance obtained by continuous culture was used for butanol production from non-detoxified hemicellulosic hydrolysate of corn fiber treated with dilute sulfuric acid (SAHHC). In fed-batch fermentation, 1.8L of diluted SAHHC containing 10 g/L of reducing sugar was provided during the acidogenic phase and 0.2L of concentrated SAHHC containing 300 g/L of reducing sugar was provided during the solventogenic phase. The mutant produced a total amount of solvents of 12.9 g/L, which consisted of 3.1 g/L of acetone, 9.3 g/L of butanol and 0.5 g/L of ethanol. A solvent yield of 0.35 g/g sugar and a productivity of 0.18 g/L h in 72 h were achieved. The remarkable inhibitor-tolerance of C. beijerinckii RT66 demonstrates that this may be an excellent strain for butanol production from ligocellulosic materials.

Clostridium beijerinckii mutant with high inhibitor tolerance obtained by low-energy ion implantation.

Clostridium beijerinckii mutant strain IB4, which has a high level of inhibitor tolerance, was screened by low-energy ion implantation and used for butanol fermentation from a non-detoxified hemicellulosic hydrolysate of corn fiber treated with dilute sulfuric acid (SAHHC). Evaluation of toxicity showed C. beijerinckii IB4 had a higher level of tolerance than parent strain C. beijerinckii NCIMB 8052 for five out of six phenolic compounds tested (the exception was vanillin). Using glucose as carbon source, C. beijerinckii IB4 produced 9.1 g l(-1) of butanol with an acetone/butanol/ethanol (ABE) yield of 0.41 g g(-1). When non-detoxified SAHHC was used as carbon source, C. beijerinckii NCIMB 8052 grew well but ABE production was inhibited. By contrast, C. beijerinckii IB4 produced 9.5 g l(-1) of ABE with a yield of 0.34 g g(-1), including 2.2 g l(-1) acetone, 6.8 g l(-1) butanol, and 0.5 g l(-1) ethanol. The remarkable fermentation and inhibitor tolerance of C. beijerinckii IB4 appears promising for ABE production from lignocellulosic materials.