CARBOHYDRATE POLYMERS
·
2016
·
IF 4.219
Honghua Jia,Tingting Shao,Chao Zhong,Hengxiang Li,Min Jiang,Hua Zhou,Ping Wei
In this paper, we produced hemicellulosic hydrolysate from corncob by tetrabutylammonium hydroxide (TBAH) extraction and dilute acid hydrolysis combined, further evaluating the feasibility of the resultant corncob hemicellulosic hydrolysate used in xylitol production by Candida tropicalis . Optimized conditions for corncob hemicellulose extraction by TBAH was obtained via response surface methodology: time of 90 min, temperature of 60 °C, liquid/solid ratio of 12 (v/w), and TBAH concentration of 55%, resulting in a hemicellulose extraction of 80.07% under these conditions. The FT-IR spectrum of the extracted corncob hemicellulose is consistent with that of birchwood hemicellulose and exhibits specific absorbance of hemicelluloses at 1380, 1168, 1050, and 900 cm −1 . In addition, we found that C. tropicalis can ferment the resulting corncob hemicellulosic hydrolysate with pH adjustment and activated charcoal treatment leading to a high xylitol yield and productivity of 0.77 g/g and 2.45 g/(L h), respectively.
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高影响因子
WATER AIR AND SOIL POLLUTION
·
2016
·Vol. 227
·期 9
·1-11
·
IF 1.551
Wu Hailu,Xu Kaiqin,He Xiaojuan,Wang Xinze
Three macrophyte species, Typha augustifolia ( T. augustifolia ), Phragmites australis ( P. australis ), and Acorus calamus L. ( A. calamus L.), have been grown in hydroponic cultivation systems fed with synthetic wastewater. The experiment was designed as 3 × 2 factorial, with three species and two ratios of NH 4
+ /NO 3
− so as to investigate the nitrogen transformation and nitrogen removal capacity of each species. The nitrogen removal mechanism was further disclosed by comparing biomass production, nitrogen mass balance, and root exudates of the three plant species under different NH 4
+ /NO 3
− ratios. The results indicated there exists a linear relationship, with positive significance ( r = 0.946, p < 0.05), between plant biomass and total nitrogen (TN) removal efficiency; in other words, biomass could best reflect plant ability to remove nitrogen. It is also found that NH 4
+ /NO 3
− ratio could influence plant biomass and root exudates significantly. Additionally, the hydrogen donor and source of energy in denitrification happened in this research were mainly organic acids and soluble sugars, accounting for approximately 50 % of the composition in root exudates.
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CARBOHYDRATE POLYMERS
·
2015
·
IF 4.074
Chao Zhong,Chunming Wang,Fan Huang,Fengxue Wang,Honghua Jia,Hua Zhou,Ping Wei
A nanoscale catalyst, solid acid SO 4 2− /Fe 2 O 3 with both Lewis and Brønsted acidity was found to effectively hydrolyze hemicellulose while keeping cellulose and lignin inactive, and selective hydrolysis of hemicellulose from wheat straw by this catalyst was also confirmed. The factors that significantly affected hydrolysis process were investigated with response surface methodology, and the optimum conditions for time, temperature, and ratio of wheat straw to catalyst (w/w) were calculated to be 4.10 h, 141.97 °C, and 1.95:1, respectively. A maximum hemicellulose hydrolysis yield of 63.5% from wheat straw could be obtained under these conditions. In addition, the catalyst could be recycled six times with high activity remaining.
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高影响因子
GREEN CHEMISTRY
·
2015
·Vol. 17
·期 7
·4053-4060
·
IF 8.02
Jiang Deng,Tianyi Xiong,Fan Xu,Mingming Li,Chuanlong Han,Yutong Gong,Haiyan Wang,Yong Wang
Hierarchically porous carbons (HPCs) show great potential in energy storage due to their high surface area as well as short ion transport path derived from the interconnected porous framework. However, most existing protocols highly rely on nanocasting and soft-templating, which usually make the use of specific raw materials and thus their industrial application unfeasible. It still remains a big challenge to build HPCs from crude biomass, which is abundant on the earth, through a simple one-pot approach. Inspired by leavening of bread, we design a strategy to fabricate HPCs with three-dimensional (3D) hierarchical pores consisting of macro, meso, and micropores. The “leavening method” is conducted simply by mixing the biomass with KHCO3 followed by elevated temperature treatment. Besides the well-defined hierarchical structure, the as-prepared HPCs also exhibit notably large specific areas (up to 1893 m2 g−1). It is noteworthy that this “leavening” strategy is widely applicable to most of the biomass derivatives and biomass, including glucose, cellulose, chitin, starch, rice straw, bamboo, etc. When evaluated as supercapacitor electrode materials in two-electrode test systems, the as-prepared HPCs exhibit an excellent electrochemical performance: a specific capacitance of 253 F g−1, with almost no capacitance loss after 10 000 cycles.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2014
·
IF 2.235
Jiahe Yan,Yucui Hou,Shuhang Ren,Muge Niu,Weize Wu
Because of its controllable and recoverable properties, the H2O–SO2 system was studied as a reaction medium to hydrolyze corn cob to produce chemicals by a two-step treatment. The results indicated that, after the first-step treatment of corn cob, 27.0% xylose, 3.3% glucose, and 3.2% arabinose could be obtained at 140 °C for 1.5 h with 0.024 g/cm3 SO2; after the second-step treatment, 8.6% glucose could be obtained at 190 °C for 0.5 h with 0.048 g/cm3 SO2. The total yield of products by the two-step treatment of corn cob was 48.4%, which was greater than that obtained by the one-step treatment, 32.4% at 190 °C for 0.5 h with 0.048 g/cm3 SO2. Furthermore, the degradation products obtained from the two-step treatment were less than those obtained from the one-step treatment. More importantly, after the reaction, SO2 could be swept by stream stripping and reused.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2017
·
IF 9.446
Hu Li,Wenfeng Zhao,Zhen Fang
Liquid furanic hydrocarbons, a class of biomass-based fuels and chemicals, are typically required to achieve moderate product selectivity and yield under harsh conditions (e.g., high temperature and H 2 pressure) involving multi-step processes over different catalysts. In this study, a single-step catalytic process was developed for direct conversion of various saccharides to furanic biofuels such as 2,5-dimethylfuran and 2-methylfuran with high yields (>95%) at 110–130 °C. The negatively charged hydride (H − ) of readily available polymethylhydrosiloxane (PMHS) acting as green H-donor over hydrophobic Pd nanoparticles did not obstruct upstream reactions (e.g., hydrolysis, isomerization and dehydration) for the in situ formation of furanic aldehydes/alcohols from sugars, and could selectively facilitate the subsequent hydrodeoxygenation of carbonyl and hydroxyl groups other than the furanic ring in one pot, as clarified by deuterium-labeling study. Importantly, the unreduced Pd(II) nanocatalysts also exhibited comparable performance in the selective hydrodeoxygenation reaction. Moreover, the catalytic strategy was extended to various carboxides for quantitative production of corresponding furanic/aromatic hydrocarbons at room temperature that were more pronounced than previously reported results, and the optimal Pd/MIL-53(Al) coated with polydimethylsiloxane (Pd/MIL-53(Al)-P) was highly stable with little deactivation and Pd leaching for at least five consecutive cycles.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Xichuang Cheng,Chi Feng,Zhiqiang Li,Weiwei Zhang,Li Ji,Kun Wang,Jianxin Jiang
Lignocellulosic biomass, being a renewable carbon-based resource, holds paramount practical significance in terms of its comprehensive conversion and utilization for effectively substituting petroleum-based energy sources. Herein, we present a sustainable and environmental-friendly vanillic acid (VA) pretreatment approach for efficient and comprehensive utilization of sugarcane bagasse (SCB). The xylo -oligosaccharides (XOS) DP2-6 yield of 60.4 % (wt.% of xylan) was achieved under the conditions of 180 °C/15 min/6% VA (wt.% of SCB), while lignin condensation was simultaneously inhibited in this initial biorefinery stage. Subsequently, the enzymatic saccharification of the pretreatment residue was significantly enhanced due to the reduced cellulase adsorption of lignin. Lignin structural characterization demonstrated that VA could effectively incorporate to the lignin structure, resulting in the lignin exhibiting high preservation of β -O-4′ linkages (39.38/100 Ar), low molecular weight (2410 Da), abundant phenolic hydroxyl groups (3.70 mmol/g), and less degree of condensation (0.33). Importantly, the resulting less-condensed lignin (LCL) could effectively undergo melt-blending with poly(butylene adipate- co -terephthalate) (PBAT) owing to its low glass transition temperature, thereby facilitating the establishment of enhanced intermolecular interactions (π–π interaction and hydrogen bond) between LCL and PBAT. These interactions enhanced the plasticization of PBAT on LCL, and as a result, the prepared P/LCL 30 composite film possessed excellent tensile properties without requiring lignin modification or additional additives. The study presents a straightforward and efficient biorefinery conversion strategy for lignocellulosic biomass, wherein hemicellulose was degraded into XOS, cellulose was enzymatically hydrolyzed to glucose, and the remaining lignin with lower condensation was utilized as a filler of PBAT composite film.
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ENERGY
·
2024
·
IF 9
Bingbing Qiu,Jicheng Shi,Wei Hu,Yanfang Wang,Donghui Zhang,Huaqiang Chu
Hydrothermal liquefication of biomass to produce high-quality chemicals and liquid fuels is considered as a renewable and sustainable technology. Herein, a one-step hydrothermal method was used to prepare microcrystalline cellulose supported carbon-based catalyst PTA-BC with the activation factor of phosphotungstic acid. It was demonstrated by Py-FTIR, NH 3 -TPD and XPS that PTA-BC is not only rich in functional groups but also contains Brønsted acid sites (hydroxyl groups) and Lewis acid sites (C C, carboxyl groups). After experimental optimization, the optimum yield of furfural obtained from xylose catalyzed by PTA-BC was 81.02% at the reaction temperature of 180 °C and the reaction time of 20 min. The results show that PTA-BC contains –COOH, –OH and C C as catalytic sites and that the synergistic effect of these functional groups. The nature of the reaction solvent, appropriate reaction temperature and residence time are the main reasons for the good catalytic performance. This work provides a promising way for the synthesis of solid acid catalyst, which has a wide application prospect for the production of furfural.
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ENERGY & FUELS
·
2024
·
IF 5.2
Bo Wang,Wen Cai,Huai Liu,Rui Zhang,Wenlong Jia,Junhua Zhang,Lincai Peng
Catalytic hydrogenation of carbohydrates over the Raney Ni catalyst is an important industrial process to produce valuable polyols. However, this process generally encounters challenges such as harsh reaction conditions, low catalytic activity, and catalyst deactivation. In this contribution, metallic nickel-rich nickel borides (NiBO-nKH2PO4) were successfully constructed via a simple chemical reduction method with potassium dihydrogen phosphate (KH2PO4) as the buffering agent and sodium borohydride (NaBH4) as the reducing reagent. Especially, the obtained NiBO-10KH2PO4 afforded quantitative sorbitol yield from the catalytic hydrogenation of glucose under mild reaction conditions within 1 h (80 °C and 1 MPa H2). Compared with the reported literature for the production of sorbitol from glucose, the developed NiBO-10KH2PO4 catalyst circumvents the use of a high hydrogen pressure and reaction temperature while delivering excellent catalytic performance and stability. Moreover, the experimental analysis demonstrated that the obtained nickel borides, with the assistance of KH2PO4, possessed abundant metallic nickel species, which favored the adsorption and activation of hydrogen molecules and thus largely promoted the hydrogenation of glucose. This work provides new insights into the rational design of practical nickel-based catalysts for the efficient catalytic hydrogenation of carbohydrates.
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JOURNAL OF MEMBRANE SCIENCE
·
2024
·
IF 8.4
Xinxin Wei,Xuelin Wang,Kaiming Fan,Yanling Liu,Shengji Xia
The acid-accepting and gas-generating properties, along with the formation of extensive nanovoids, make CaCO 3 nanoparticles attractive as sacrificial nanofillers for fabricating thin-film composite (TFN) nanofiltration membranes. However, challenges such as severe agglomeration and limited acid etching efficiency of the nanoparticles hinder the pursuit of superior membrane performance. In this study, the dispersion and compatibility of CaCO 3 nanoparticles within the membrane matrix were improved by modifying them with a polydopamine (PDA) coating. The abundant phenolic hydroxyl groups of PDA enhanced the hydrophilicity and negative charges of membrane surface. Additionally, the PDA capsule increased the etching extent of the CaCO 3 nanoparticles by improving the nanoparticle dispersion and generating additional acid, which created sufficient water channels within the polyamide layer. It was demonstrated that incorporating 45 μg/cm 2 of PDA-modified CaCO 3 nanoparticles doubled the water permeance to 16.7 LMH/bar, while maintaining a low molecular weight cut-off of 249 Da and achieving rejections over 90 % for five types of per- and polyfluorinated substances. The PDA modification also overcame the membrane stability issue caused by the agglomerated CaCO 3 nanoparticles. This study provides a novel strategy for applying properly modified self-etching nanofillers in TFN membrane development, showing great potential for water treatment applications.
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STARCH-STARKE
·
2024
·
IF 2.6
Lian Li,Jia Zheng,Li Yao,Hong Wang,Yiyi Lv,Guichun Huang,Shuyi Qiu,Xiangyong Zeng,Chaoyang Wei
Baijiu distillers' grain is a solid waste after the fermentation of grains, and their high added value and deep processing and utilization require further study. This study uses the enzyme and microwave coassisted method to extract Baijiu distillers' grain polysaccharides (DGPs). Through optimization of the single-factor test and response surface methodology (RSM), the optimal conditions are solid–liquid ratio 1:30, enzyme time 50 min, enzyme temperature 50 °C, enzyme pH 5.0, microwave time 6 min, and microwave power 480 W, with a maximum DGP yield of 3.98% ± 0.03. DGP is purified by DEAE-Sepharose cellulose ion exchange chromatography to obtain four fractions, namely DGP-1, DGP-2, DGP-3, and DGP-4; the molecular weights are 2224.05, 90.99, 1478.16, and 346.19 kDa, respectively, and the main monosaccharide components are Man and Glc. The antioxidant assay shows that the four kinds of DGPs have different free radical scavenging capacities, among which DGP-2, DGP-3, and DGP-4 have good antioxidant activities. Therefore, DGP can be used as a potential natural antioxidant.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Weikang Ling,Jiliang Ma,Min Hong,Runcang Sun
Photocatalytic CO 2 reduction and biomass selective oxidation have considerable practical implications in addressing environmental challenges. However, developing efficient photocatalyst is the key to realize the mass-market applications. Herein, an MoS 2 @GCN S-scheme heterojunction, rich in sulfur vacancies (Sv), was fabricated by a dicyandiamide-blowing and calcination strategy using NH 4 Cl as the gas template. With the synergistic effects of Sv and the S-scheme charge migration mechanism, the 30%-Sv-MoS 2 @GCN demonstrated exceptional performance, showcasing a CO evolution rate of 68.3 μmol g −1 h −1 and a xylonic acid yield of 64.2%, without using any sacrificial agents. The formation of Sv was confirmed through electron paramagnetic resonance (EPR) analysis. The S-scheme charge transfer mechanism of the Sv-MoS 2 @GCN heterojunction was verified by in-situ X-ray photoelectron spectroscopy (XPS) spectra, EPR analysis, and density functional theory (DFT) calculations. This study establishes a framework for enhancing photocatalytic CO 2 reduction and biomass selective oxidation by regulating charge transfer through sensible structural design.
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