Bio-Inspired Lotus-Fiber-like Spiral Hydrogel Bacterial Cellulose Fibers.

Hydrogel materials with high water content and good biocompatibility are drawing more and more attention now, especially for biomedical use. However, it still remains a challenge to construct hydrogel fibers with enough strength and toughness for practical applications. Herein, we report a bio-inspired lotus-fiber-mimetic spiral structure hydrogel bacterial cellulose fiber with high strength, high toughness, high stretchability, and energy dissipation, named biomimetic hydrogel fiber (BHF). The spiral-like structure endows BHF with excellent stretchability through plastic deformation and local failure, assisted by the breaking-reforming nature of the hydrogen bonding network among cellulose nanofibers. With the high strength, high stretchability, high energy dissipation, high hydrophilicity, porous structure, and excellent biocompatibility, BHF is a promising hydrogel fiber for biomedicine. The outstanding stretchability and energy dissipation of BHF allow it to absorb energy from the tissue deformation around a wound and effectively protect the wound from rupture, which makes BHF an ideal surgical suture.

Cryoprotectant choice and analyses of freeze-drying drug suspension of nanoparticles with functional stabilisers.

Freeze-drying is an effective way to improve long-term physical stability of nanosuspension in drug delivery applications. Nanosuspension also known as suspension of nanoparticles. In this study, the effect of freeze-drying with different cryoprotectants on the physicochemical characteristics of resveratrol (RSV) nanosuspension and quercetin (QUE) nanosuspension was evaluated. D-α-tocopheryl polyethylene glycol succinate (TPGS) and folate-modified distearoylphosphatidyl ethanolamine-polyethylene glycol (DSPE-PEG-FA) were selected as functional stabilisers formulated nanosuspension which were prepared by anti-solvent precipitation method. RSV nanoparticle size and QUE nanoparticle size were about 210 and 110 nm, respectively. The AFM and TEM results of nanosuspension showed uniform and irregular shape particles. After freeze-drying, the optimal concentration of four cryoprotectants was determined by the particle size of re-dispersed nanoparticles. The dissolution profile of drug nanoparticle significantly showed approximately at a 6-8-fold increase dissolution rate. Moreover, TPGS and DSPE-PEG-FA stabilised RSV nanosuspension and QUE nanosuspension samples showed better effect on long-term physical stability.

Application of waste derived magnetic acid-base bifunctional CoFe/biochar/CaO as an efficient catalyst for biodiesel production from waste cooking oil.

The loss of active components, weak acid resistance, and low recover efficiency of common Ca-based catalysts limited its further development and application. In this study, to effectively produce biodiesel from waste cooking oil (WCO), a green and recyclable magnetic acid-base bifunctional CoFe/biochar/CaO catalyst was prepared from sargassum and river snail shell waste via hydrothermal method. The catalysts' structure and properties were investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), CO2/NH3 temperature programmed desorption (CO2/NH3 TPD), etc., The prepared catalyst mainly consisted of the carbon skeleton, CoFe alloy, and CaO. CoFe alloy provided catalyst's ferromagnetism for magnetic separation as well as acid sites for transesterification of WCO. Ca and other metal species with nanoscale (∼5.64 nm) were dispersively anchored on sargassum biochar surface, thereby leading to good catalytic activity (99.21% biodiesel yield) and stability (91.70% biodiesel yield after the 5th cycle). In addition, response surface methodology-Box-Behnken design (RSM-BBD) revealed the optimal operational conditions were 16:1 methanol/oil molar ratio, 3 wt% catalyst dosage, 73 °C for 157 min. The maximum biodiesel yield predicted value was 98.29% and the experimental value was 99.21%, indicating good satisfaction of the established model. Moreover, the quality of WCO biodiesel met the ASTM D6751 standards. This study benefits magnetic waste-derived acid-base bifunctional catalysts for the disposal of WCO towards sustainable biodiesel production.

From cellulose to tar: Analysis of tar formation pathway with distinguishing the primary and secondary reactions.

Tar problem seriously hinders the development of biomass gasification. The tar formation of biomass is greatly influenced by cellulose. In this work, PY-GC/MS was employed for providing a precise insight into the formation of primary and secondary products, and a tar contribution index was introduced to evaluate the potential of tar formation from different origins. Combined with statistical analysis and corroboration by DFT analysis, key intermediates for tar formation are recognized, and corresponding influence is confirmed. A new framework from cellulose to tar was built. The secondary reaction acts a more important role for tar formation. The aromatic precursors and high-activity small-molecular gases are two key compounds responding to tar formation, and the existence of high-activity small-molecular gases could significantly reduce the energy barrier during tar formation. For furans, the energy barrier can be reduced from 100.2 kcal/mol to 74.2 kcal/mol in the presence of ethylene.

Biodiesel production in a magnetically fluidized bed reactor using whole-cell biocatalysts immobilized within ferroferric oxide-polyvinyl alcohol composite beads.

Magnetic whole-cell biocatalysts (MWCBs) constructed by immobilizing Bacillus subtiliscells within ferroferric oxide-polyvinyl alcohol composite beads were developed and employed to transesterify waste frying oil to biodiesel in a magnetically fluidized bed reactor (MFBR). Effective variables including biocatalysts concentration, reactant flow rate, magnetic field intensity and temperature were evaluated to enhance the transesterification. By coupling MFBR with MWCBs, continuous biodiesel production was achieved. Response surface methodology and Box-Behnken design were employed to predict the optimal conditions and the maximum biodiesel yield reached 89.0 ± 0.6% after 48 h under the optimized conditions. Furthermore, MWCBs displayed satisfactory stability and reusability in MFBR and still maintained a biodiesel yield of more than 82.5% after 10 cycles. Lastly, the fuel properties of the obtained biodiesel met the ASTM and EN standards. The present study revealed that the route of producing biodiesel over MWCBs in the MFBR system showed great potential for industrialization.

Conversion of plastic waste into fuels: A critical review.

Plastic wastes have posed serious threats to the environment, including decrease of soil nutrient effectiveness and agricultural production as well as emerge of ecological instability. Fuel conversion from plastic waste is regarded as a promising strategy for its disposal and energy utilization. Plastic wastes can be converted into target fuels by adjusting cracking of chemical bonds. Currently, numerous technologies regarding fuel conversion from plastic wastes have been reported, including conventional pyrolysis, novel heat treatment and advanced oxidation. However, systematic summary and comparative analysis of different technologies are still scarcely reported. In this review, fuel conversion from plastic wastes was summarized comprehensively, highlighting novel heat treatment and advanced oxidation technologies reported in recent years. Furthermore, the superiority and drawbacks of each technology were analyzed, and future prospects of technology application were proposed. With lower reaction temperature and higher-value fuel, novel heat treatment of plastics is more popular than traditional one. Advanced oxidation can be controlled to convert plastics into fuels under room temperature and pressure, guiding the new normal in energy utilization of plastic wastes. This review aims to provide inspiration for energy utilization of solid waste, addressing the issues of white pollution and energy shortage.

Double-edged effects of polyvinyl chloride addition on heavy metal separation and biochar production during pyrolysis of Cd/Zn hyperaccumulator.

Pyrolysis is a promising technique to achieve the sustainable utilization of heavy metal hyperaccumulator derived from phytoremediation of contaminated soils. To investigate the feasibility of synergistic treatment of hyperaccumulator and plastic waste (i.e. polyvinyl chloride, PVC), co-pyrolysis of Sedum alfredii and different mass percentages of PVC (5-25 wt%) was conducted at 300-900 °C in the present study. High pyrolysis temperature and low PVC addition amount (5 wt%) effectively promoted the volatilization of Cd and Zn from S. alfredii, while high PVC addition amount (15 wt% and 25 wt%) caused a significant suppression effect at insufficient pyrolysis temperatures. After PVC addition, the yields of biochar increased by 5.18-37.19% as compared with the theoretical values. However, the concentrations of Cd and Zn leached from biochar significantly elevated with increasing PVC addition amount, indicating that the addition of PVC improved the mobility of Cd and Zn in biochar. Moreover, S. alfredii derived biochars showed considerable sorption capacity for Cd (87.6-198.3 mg/g). These results imply that the addition of PVC has double-edged effects on heavy metal separation and biochar production during pyrolysis of Cd/Zn hyperaccumulator, and low PVC addition amount and sufficient pyrolysis temperature are beneficial for the further utilization of biochar.

Assessment of biomass demineralization on gasification: From experimental investigation, mechanism to potential application.

Considering the advantages (e.g. agglomeration mitigation) and disadvantages (e.g. inorganic species catalysis removal) of biomass demineralization, it is valuable to investigate its effects on gasification performance, thus assessing its necessity prior to performing gasification. To accomplish this, corn straw (CS) was demineralized to different degrees with H2O and HCl, respectively. H2O and HCl demineralization behaved different abilities to inorganic species removal. Cellulose and hemicelluloses content decreased, while lignin content increased, especially with HCl demineralization. The experiments were investigated by using a bench-scale downdraft fixed-bed gasifier at 600-800 °C and were further analyzed via thermogravimetric coupled with Fourier transform infrared spectrometry. Demineralization demonstrated a positive effect on gasification at lower temperatures (600-700 °C) for a dominant effect of lignin content and an insignificant effect of inorganic species removal. However, the catalysis of inorganic species increased as the temperature increased, resulting in the highest H2 (11.30 vol%) and CO (16.02 vol%) production of raw CS compared to demineralized CS at 800 °C. Inorganic species had a dual positive effect on CO generation, promoting both CO2 and char generation leading to a higher CO yield following Boundouard reaction, and increasing the formation of active intermediates thus producing more CO. These effects enhanced when the gasification temperature increased. Additionally, inorganic species catalyzed the aromatic rings rearrangement to generate more H2O, thus driving the endothermic Primary water-gas to produce H2. This was also positively correlated with gasification temperature. Therefore, raw CS demonstrated higher H2 and CO production than demineralized CS at a higher gasification temperature. Moreover, the promotion effect of inorganic species on thermal devolatilization of methoxyl groups and Methanation reaction led to the higher CH4 production of raw CS. This research clarifies the effects of biomass demineralization on its gasification and suggests the potential application.

In vitro and in vivo evaluation of poly (acrylic acid) modified mesoporous silica nanoparticles as pH response carrier for ß-elemene self-micro emulsifying.

The strategy of formulating poorly soluble actives as liquid self-micro emulsifying drug delivery system (SMEDDS) has been explored in more than a thousand research papers. However, there have been a limited number of reports on pH sensitive solid SMEDDS. This study explored the feasibility of using poly (acrylic acid) modified mesoporous silica nanoparticles (MSNs-PAA) as a pH-mediated solid SMEDDS carrier for ß-elemene. This SMEDDS was optimized using a central composite design-response surface methodology, pseudo ternary phase diagrams, and studies of the preliminary stability. MSNs-PAA was synthesized and used for loading ß-elemene SMEDDS. Ele/MSNs-PAA was capable of pH-sensitive release of ß-elemene. In addition to structural analyses, the morphological and stability of this SMEDDS was also investigated. In comparison of the ß-elemene solution and the SMEDDS, the Ele/MSNs-PAA demonstrated improved Cmax, AUC and MRT after oral administration. These results suggested that the MSNs-PAA could be further developed as a promising approach for the pH sensitive release of ß-elemene SMEDDS with enhanced oral bioavailability.