Recycling and depolymerization of waste polyethylene terephthalate bottles by alcohol alkali hydrolysis

In this work,a novel alcohol alkali hydrolysis method was explored for the preparation of terephthalic acid(TPA)from waste polyethylene terephthalate(PET).First,a series of single factor experiments on the depolymerization rate of waste PET bottles and the yield of TPA were conducted to determine the optimized experimental conditions,in terms of reaction time,reaction temperature,dosage of ethylene glycol and sodium bicarbonate,amount of distilled water and stirring rate.Then IR spectra and elemental analysis were carried out for the characterization of obtained product.Under optimal experimental conditions,over 98%PET can be depolymerized into the target product(TPA)and the purity and yield of TPA are over 97%and 94%,respectively.Both the experimental and analytical results support a feasible process for the preparation of TPA from waste PET.It is expected that this alcohol alkali hydrolysis method can promise an effective way for the sustainable recycling of waste PET.

Decomposition of Cellulose by Continuous Near-Critical Water Reactions

A pilot-scale apparatus for continuous supercritical and near-critical water reaction was set up. A high-pressure slurry supplying system was developed to feed the solid material-water slurries. The apparatus features temperature up to 600℃, pressure up to 40MPa, residence time from 24s to 15min, maximum amount of slurry supply of 2.4 L·h-1, maximum solid content of slurry up to 10%(by mass) for cellulose from Merck, and resistance to corrosion. Long-time runs of decomposition of cellulose were carried out and steady runs were confirmed. Kinetics of cellulose decomposition was studied. The apparent activation energy evaluated was 147kJ·mol-1. In addition, a new three-step pathway for cellulose hydrolysis was proposed. The derived kinetic equation is in good agreement with the experimental data.

Antioxidation Activities of Low-Molecular-Weight Gelatin Hydrolysate Isolated from the Sea Cucumber Stichopus japonicus

Gelatin extracted from the body wall of the sea cucumber （Stichopus japonicus） was hydrolyzed with flavourzyme. Low-molecular-weight gelatin hydrolysate （LMW-GH） of 700-- 1700 Da was produced using an ultrafiltration membrane bioreaetor system. Chemiluminescence analysis revealed that LMW-GH scavenges high free radicals in a concentration-dependent manner; IC50 value for superoxide and hydroxyl radicals was 442 and 285 μgmL-1, respectively. LMW-GH exhibited excellent inhibitory characteristics against melanin synthesis and tyrosinase activity in B16 cells. Furthermore, LMW-GH notably increased in- traeellular glutathione （GSH）, which in turn suppressed melanogenesis. LMW-GH performs antioxidation activity, holding the potential of being used as a valuable ingredient in function foods, cosmetics and pharmaceuticals or nutriceuticals.

CoFe_2O_4/CdS nanocomposite:Preparation,characterisation,and application in sonocatalytic degradation of organic dye pollutants

A magnetic CoFe2O4/Cd S nanocomposite was prepared via one-step hydrothermal decomposition of cadmium diethanoldithiocarbamate complex on the surface of CoFe2O4 nanoparticles at a low temperature of 200 ℃.The nanocomposite was characterised by X-ray diffraction（XRD）,Fourier transform infrared spectroscopy（FT-IR）,scanning electron microscopy,energy-dispersive X-ray spectroscopy（EDX）,UV-visible spectroscopy,transmission electron microscopy（TEM）,N2 gas sorption analysis,X-ray photoelectron spectroscopy（XPS）,and vibrating sample magnetometry.The FT-IR,XRD,EDX and XPS results confirmed the formation of the CoFe2O4/Cd S nanocomposite.Based on the TEM analysis,the CoFe2O4/Cd S nanocomposite constituted nearly uniform,sphere-like nanoparticles of ～20 nm in size.The optical absorption spectrum of the CoFe2O4/Cd S nanocomposite displayed a band gap of 2.21 e V,which made it a suitable candidate for application in sono/photocatalytic degradation of organic pollutants.Accordingly,the sonocatalytic activity of the CoFe2O4/Cd S nanocomposite was evaluated towards the H2O2-assisted degradation of methylene blue,rhodamine B,and methyl orange under ultrasonic irradiation.The nanocomposite displayed excellent sonocatalytic activity towards the degradation of all dyes examined—the dyes were completely decomposed within 5–9 min.Furthermore,a comparison study revealed that the CoFe2O4/Cd S nanocomposite is a more efficient sonocatalyst than pure Cd S;thus,adopting the nanocomposite approach is an excellent means to improve the sonoactivity of Cd S.Moreover,the magnetic properties displayed by the CoFe2O4/Cd S nanocomposite allow easy retrieval of the catalyst from the reaction mixture for subsequent uses.

Biodiversity of Indigenous Amylolytic and Cellulolytic Bacteria in Sago Waste Product at Susupu, North Moluccas

People at Susupu, North Moluccas prepare the sago （Metroxylon sago） in traditionally way for consumption. The residue of processed sago usually thrown away on the ground, so it was caused pollution. Some amylolytic bacteria species and cellulolytic bacteria species could be founded in sago waste product. The purpose of this research are：1 ） to identify the indigenous amylolytic bacteria species in sago waste product; 2） to identify the indigenous cellulolytic bacteria species in sago waste product; 3） to test the amylum hydrolysis ability of each amylolytic bacteria species; 4） to test the cellulose hydrolysis ability of each cellulolytic bacteria species. This research was conduct at the Microbiology laboratory, Biology Department-FMIPA-State University of Malang and the Microbiology laboratory-Faculty of Medicine-Brawijaya University. The research samples are sago waste product from Susupu, North Moluccas. The samples were grinded and diluted in nutrient broth, and then the suspension was diluted gradually until 10^-10. The suspension was inoculated 0.1 mL each on nutrient agar medium in 37℃ during 1 × 24 h. Each bacteria colony that grows on the medium were isolated and determined to know which one were the amyloliytic bacteria and the cellulolytic bacteria. The amylum hydrolysis index of each amylolytic bacteria species were counted as well as the cellulose hydrolysis index of each cellulolytic bacteria species. Each amylolytic bacteria and cellulolytic bacteria species were identified. This research result shows that： 1） there are 5 indigenous amylolytic bacteria species, i.e., Bacillus mycoides, Bacillus cereus, Bacillus licheniformis, Bacillus alvei and Serratia liquefaciens; 2） there are 4 indigenous cellulolytic bacteria species, i.e., Serratia liquefaciens, Acinetobacter iwofii, Bacillus licheniformis and Bacillus cereus; 3） Serratia liquefaciens has the highest amylum hydrolysis index, i.e., 3.08; 4） Acinetobacter iwoffii has the highest cellulose hydrolysis index, i.e., 2.01.

Resistivity in Formation and Decomposition of Natural Gas Hydrate in Porous Medium

A new one-dimensional system for resistivity measurement for natural gas hydrate(NGH)exploitation is designed,which is used to study the formation and decomposition processes of NGH.The experimental results verify the feasibility of the measurement method,especially in monitoring the nucleation and growth of the NGH. Isovolumetric formation experiment of NGH is performed at 2°C and 7.8 MPa.Before the NGH formation,the initial resistivity is measured to be 4-7Ω·m,which declines to the minimum value of 2-3Ω·m when NGH begins to nucleate after the pressure is reduced to 3.3 MPa.As the NGH grows,the resistivity increases to a great extent,and finally it keeps at 11-13Ω·m,indicating the completion of the formation process.The NGH decomposition experiment is then performed.When the outlet pressure decreases,NGH begins to decompose,accordingly,the resistivity declines gradually,and is at 5-9Ω·m when the decomposition process ends,which is slightly higher than the resistivity value before the formation of NGH.The occurrence and distribution uniformity of NGH are determined by the distribution and magnitude of the resistivity measured on an one-dimensional sand-packed model.This study tackles the accurate estimation for the distribution of NGH in porous medium,and provides an experimental basis for further study on NGH exploitation in the future.

Synthesis and application of covalent triazine framework/graphene hybrids for photocatalysis

In recent years,photocatalysis with efficient,low-cost and stable metal-free catalysts is one of the most promising technologies for non-polluting energy production and resource-economic environment purifying.Benefiting from the molecularly precise backbones,regular and homogeneous porosity,lightelement composition,nitrogen-rich system with unique electronic band structure of two-dimensional(2D)covalent triazine framework(CTF),as well as the huge specific surface area,superior thermal conductivity,excellent carrier mobility and mechanical properties of 2D graphene,CTF/graphene hybrid-based photocatalysts show great application potential in the field of photocatalysis.In this review,the recent development in synthesis of CTF/graphene hybrid-based photocatalysts,and their applications in photocatalytic water splitting for hydrogen production and photocatalytic degradation of pollutants are summarized.Firstly,we briefly describe the molecular structures,physicochemical properties,and synthetic strategies for CTF/graphene hybrid-based photocatalysts including solution mixing method,in-situ polymerization method and sol-gel method.We further assess the impact of different preparation methods on the structure,morphology,and interacting model between CTF and graphene in CTF/graphene hybrids.Following the various preparation process for CTF/graphene hybrid-based photocatalysts,these methods are analyzed and compared regarding their merits and demerits.Secondly,the functions of CTF/graphene hybrid-based photocatalysts obtained from different synthesis approaches that enhance the catalytic activity for photocataLytic hydrogen evolution and photocatalytic degradation of pollutants are discussed from the three aspects of light harvesting,charge separation and transfer,and surface catalysis.Particular focus has been placed on the catalytic mechanisms of CTF/graphene hybridbased photocatalysts for enhanced photocatalytic hydrogen evolution and improved photocatalytic degradation of pollutants.Then the rational manipulation of selection and building units of CTF,connecting bonds between CTF and graphene,dimensions and pore structures of CTF/graphene hybrids in design of CTF/graphene hybrid-based photocatalysts is discussed,aiming to inspire critical thinking about the effective strategies for modification of photocatalysts rather than the development of novel materials.In the end,the challenges and some future trends of CTF/graphene hybrids as advanced photocatalysts are also discussed from three aspects:catalysts design,performance stability and reaction mechanism.The approaches offer potential solutions to address the challenges of largescale production,catalyst activity and stability in the further research and development of new types of metal-free hybrid photocatalysts with high efficiency.

厌氧消化数学模型ADM1的研究及应用进展

自2002年国际水协厌氧消化工艺数学模型课题组推出厌氧消化模型ADM1以来,随着研究与应用的深入,该模型不断发展完善,已经被证明是指导厌氧消化工艺设计与模拟、预测厌氧消化过程及结果的可靠工具。总结了近年ADM1在生化反应动力学、不同反应器类型、不同发酵底物、厌氧消化微生物种群等方面的拓展与改进研究,简单介绍了该模型在厌氧消化实际工程中的应用及模型存在的缺陷和不足。

Nickel-coated silicon photocathode for water splitting in alkaline electrolytes

Photoelectrochemical （PEC） water splitting is a promising approach to harvest and store solar energy [1]. Silicon has been widely investigated for PEC photoelectrodes due to its suitable band gap （1.12 eV） matching the solar spectrum [2]. Here we investigate employing nickel both as a catalyst and protecting layer of a p-type silicon photocathode for photoelectrochemical hydrogen evolution in basic electrolytes for the first time. The silicon photocathode was made by depositing 15 nm Ti on a p-type silicon wafer followed by 5 nm Ni. The photocathode afforded an onset potential of -0.3 V vs. the reversible hydrogen electrode （RHE） in alkaline solution （1 M KOH）. The stability of the Ni/Ti/p-Si photocathode showed a 100 mV decay over 12 h in KOH, but the stability was significantly improved when the photocathode was operated in potassium borate buffer solution （pH ≈ 9.5）. The electrode surface was found to remain intact after 12 h of continuous operation at a constant current density of 10 mA/cm^2 in potassium borate buffer, suggesting that Ni affords good protection of Si based photocathodes in borate buffers.

Preparation of nano-TiO_2 photocatalysts and their decomposition activity in phenol-contaminated water

ZiO2 was prepared by the hydrolyzation method in （NH4）2SO4-modified TiCl4 solution, and TiO2 photocatalysts were obtained by accelerating the precipitation of TiO2 powder in a high-temperature water bath. The photocatalysts were characterized by Brunauer-Emmett-Teller （BET）, X-ray diffraction （XRD）, Raman spectrum and UV-Vis （Ultraviolet-Visible） spectrometry techniques, and the photocatalytic activity in phenol-contaminated water was investigated. The results showed that photocatalysts calcined at 400 ℃ had a specific surface area of 138.2 m^2/g and an average particle size of 9 nm, and a significant increase in thermal stability of anatase phase. At the calcination temperature of 700 ~C, the crystal form of TiO2 started to change into rutile （anatase： 97%, rutile： 3%）. The activity of TiO2 photocatalysts prepared with （NH4）2SO4-modified TIC14 solution was markedly stronger than that without （NH4）2SOg-modified TIC14 solution. Maximal photocatalytic activity was observed at the mole ratio of Ti：（NH4）2SO4= 1：2, the water-bath temperature of 90℃ and the calcination temperature of 700 ℃.

Improved water-splitting performances of CuW_(1-x)Mo_xO_4 photoanodes synthesized by spray pyrolysis

CuW（1-x）MoxO4 solid solution of CuWO4 and CuMoO4, which is a copper-based multi-component oxide semiconductor, possesses much narrower band gap than CuWO4. In theory, it can absorb a larger part of the visible spectrum, widening the use of solar spectroscopy and obtaining a higher photo-to-chemical conversion efficiency. In this study, CuW（1-x）MoxO4 thin-film photoanodes on conducting glass were prepared using a simple and low-cost spray pyrolysis method. The resulting CuW（1-x）MoxO4 photoanodes perform higher photocurrent than CuWO4 photoanodes under AM 1.5 G simulated sunlight illumination（100 m W cm^（-2））in 0.1 mol L^（-1） phosphate buffer at pH 7. Combined with IPCE and Mott-Schottky analysis, the enhancement of the photocurrent is due to the improvement of photon utilization and the increase of carrier concentration with the incorporation of Mo atoms. Moreover, with the optimal Mo/W atomic ratio,the photocurrent density increases obviously from 0.07 to 0.46 m A cm^（-2） at 1.23 V（RHE） bias. In addition, compared with particle-assembled thin-film photoanodes prepared by solidphase reaction and drop-necking treatment, the photoanodes prepared by spray pyrolysis have obvious advantages in terms of reducing resistance and facilitating charge transport.

MODELING AND ANALYSIS OF SALT TRANSPORT IN THE SINGLE CYLINDRICAL ROOT WITH FINITE LENGTH

A mathematical model for salt transport by a cylindrical root in an infinite extent of soil is derived and solved analytically by asymptotic matching of the inner and outer solutions. By asymptotic analysis it is shown that the salt solution uptake by a single cylindrical root in the absence of competition does not influence the overall salt concentration in the soil even when the soil moisture concentration is less than full saturation.

Break-down criterion for the water-wave equation

We study the break-down mechanism of smooth solution for the gravity water-wave equation of infinite depth. It is proved that if the mean curvature κ of the free surface Σt, the trace（V, B） of the velocity at the free surface, and the outer normal derivative ？P/？n of the pressure P satisfy sup t∈[0,T]｜｜κ（t）｜｜Lp∩L^2＋∫0^T｜｜（▽V, ▽B）（t）｜｜L∞^6dt〈＋∞,inf （t,x,y）∈[0,T]×Σ_t- P/ n（t, x, y）≥c0,for some p 〉 2d and c_0〉 0, then the solution can be extended after t = T.

Numerical Algorithm Based on Quintic Nonpolynomial Spline for Solving Third-Order Boundary Value Problems Associated with Draining and Coating Flows

A numerical algorithm is developed for the approximation of the solution to certain boundary value problems involving the third-order ordinary differential equation associated with draining and coating flows. The authors show that the approximate so- lutions obtained by the numerical algorithm developed by using uonpolynomial quintic spline functions ave better than those produced by other spline and domain decomposition methods. The algorithm is tested on two problems associated with draining and coating flows to demonstrate the practical usefulness of the approach.