Quantitative analysis and risk assessment to full-size microplastics pollution in the coastal marine waters of Hong Kong.

Given the potential risk to the ecosystem, attention has increased in recent decades to the contamination of the aquatic environment by microplastics (MPs). Due to the limitations of conventional analysis methods of MPs, little is known about the size distribution and abundance of a full-size MPs from 1 µm to 5 mm. The present study quantified MPs with size ranges of 50 µm - 5 mm and 1-50 µm in the coastal marine waters from twelve locations in Hong Kong using fluorescence microscopy and flow cytometry respectively, during the end of wet (September 2021) and dry (March 2022) seasons. The average abundance of MPs with size ranges of 50 µm - 5 mm and 1-50 µm from twelve sampling locations marine surface waters were found ranging from 27 to 104 particles L-1 and 43,675-387,901 particles L-1 in the wet season respectively, and 13-36 particles L-1 and 23,178-338,604 particles L-1 in the dry season respectively. Significant temporal and spatial variations of small MPs abundance might be observed at the sampling locations, which were contributed by the influences of the estuary of Pearl River, sewage discharge points, land structure, and other anthropogenic activities. Based on the MPs abundance information, ecological risk assessment was conducted and revealed that the small MPs (< 10 µm) in coastal marine surface waters may pose potential health risks to aquatic organisms. Additional risk assessments are needed in order to determine whether or not the MPs exposure would cause health risks to the public.

Hydrogenolysis-Isomerization of Waste Polyolefin Plastics to Multibranched Liquid Alkanes.

Upcycling of waste polyolefin plastics still meets with economic and technological challenges in practice. In this work, the catalytic hydrogenolysis-isomerization of nondegradable polyolefin plastic waste to high-value gasoline, diesel, and light lubricants with highly branched chain is achieved over a bifunctional Rh/Nb2 O5 catalyst under relatively mild conditions. Owing to the high efficiency of metallic Rh active sites, the dehydrogenation/hydrogenation of long carbon chains of polyolefins is enhanced. With the assistance of strong Brønsted acidity of Nb2 O5 , the cleavage of C-C bonds, skeletal rearrangements, as well as the ß-scission of alkylcarbenium ions occurs, which boosts the one-step solvent-free catalytic hydrogenolysis and isomerization of polyolefins. In addition, the preliminary economic analysis shows that this technology is economical, feasible, and has great potential in accelerating the transition to a circular plastics economy for sustainable development.

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production.

A method for facile synthesis of nanostructured catalysts supported on carbon nanotubes with atomically dispersed cobalt and nitrogen dopant is presented herein. The novel strategy is based on a facile one-pot pyrolysis treatment of cobalt (II) acetylacetonate and nitrogen-rich organic precursors under Ar atmosphere at 800 °C, resulting in the formation of Co- and N- co-doped carbon nanotube with earthworm-like morphology. The obtained catalyst was found to have a high density of defect sites, as confirmed by Raman spectroscopy. Here, cobalt (II) nanoparticles were stabilized on the atomically dispersed cobalt- and nitrogen-doped carbon nanotubes. The catalyst was confirmed to be effective in the catalytic hydrolysis of ammonia borane, in which the turnover frequency was 5.87 mol H2·molCo-1·min-1, and the specific hydrogen generation rate was determined to be 2447 mL H2·gCo-1·min-1. A synergistic function between the Co nanoparticle and the doped carbon nanotubes was proposed for the first time in the catalytic hydrolysis of ammonia borane reaction under a mild condition. The resulting hydrogen production with its high energy density and minimal refueling time could be suitable for future development as energy sources for mobile and stationary applications such as road trucks and forklifts in transport and logistics.

Techno-economic evaluation of a biorefinery applying food waste for sophorolipid production - A case study for Hong Kong.

This study evaluates the techno-economic feasibility of sophorolipid (SL) production process that co-utilizes food waste, glucose and oleic acid as substrates. Two variables are considered in terms of (a) Plant construction: Purchasing equipment either from the US or Mainland China and (b) Production: to produce SL crystals (about 97% active) or a concentrated SL liquid/syrup (about 78% active). Hence, four scenarios are generated: Scenario I: equipment made in the USA + SL crystals; Scenario II: equipment made in the USA + SL syrup; Scenario III: equipment made in China + SL crystals; Scenario IV: equipment made in China + SL syrup. It is found that all scenarios are economically feasible and Scenario I has the highest net profit. Scenario III has the highest internal rate of return, net present value and the shortest payback period at a 7% discount rate. Finally, comparison of food waste-related techno-economic studies was conducted.

A review on high catalytic efficiency of solid acid catalysts for lignin valorization.

It is imminent to develop renewable resources to replace fossil-derived energies as fossil resources are on the brink of exhaustion. Lignin is one of the major components of lignocellulosic biomass, which is a natural amorphous three-dimensional polymer with abundant C-O bonds and aromatic structure. Hence, valorization of lignin into high value-added liquid fuels and chemicals is regarded as a promising strategy to mitigate fossil resource shortages. Solid acid catalysts are extensively studied due to environmentally friendly in terms of the ease of separation, recovery and reduced amount of wastes. Hence, this review focuses on summarizing the recent progress of catalytic valorization of lignin over different kinds of solid acid catalysts including zeolites, heteropolyacids, metal oxides, amorphous SiO2-Al2O3, metal phosphates, and Lewis acid. Based on reviewing of current progress of lignin conversion, the challenges and future prospects are emphasized.

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether.

We herein present a method for the synthesis of HNbWO6, HNbMoO6, HTaWO6 solid acid nanosheet modified Pt/CNTs. By varying the weight of various solid acid nanosheets, a series of Pt/xHMNO6/CNTs with different solid acid compositions (x = 5, 20 wt%; M = Nb, Ta; N = Mo, W) have been prepared by carbon nanotube pretreatment, protonic exchange, solid acid exfoliation, aggregation and finally Pt particles impregnation. The Pt/xHMNO6/CNTs are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and NH3-temperature programmed desorption. The study revealed that HNbWO6 nanosheets were attached on CNTs, with some edges of the nanosheets being bent in shape. The acid strength of the supported Pt catalysts increases in the following order: Pt/CNTs < Pt/5HNbWO6/CNTs < Pt/20HNbMoO6/CNTs < Pt/20HNbWO6/CNTs < Pt/20HTaWO6/CNTs. In addition, the catalytic hydroconversion of lignin-derived model compound: diphenyl ether using the synthesized Pt/20HNbWO6 catalyst has been investigated.

Recent advancement in lignin biorefinery: With special focus on enzymatic degradation and valorization.

With the intensive development of lignocellulosic biorefineries to produce fuels and chemicals from biomass-derived carbohydrates, lignin was generated at a large quantity every year. Therefore, lignin has received increasing attention as an abundant aromatics resource in terms of research and development efforts for value-added chemicals production. In this review, studies about lignin degradation especially the crucial enzymes involved and the reaction mechanism were substantially discussed, which provided the molecular basis of lignin biodegradation. Then, the latest improvements in lignin valorization by biological methods were summarized and case studies about value-added compounds from lignin were introduced. Afterwards, challenges, opportunities and prospects regarding biorefinery of lignin were presented.

Synthesis of Sea Urchin-Like NiCo2O4 via Charge-Driven Self-Assembly Strategy for High-Performance Lithium-Ion Batteries.

In this study, hydrothermal synthesis of sea urchin-like NiCo2O4 was successfully demonstrated by a versatile charge-driven self-assembly strategy using positively charged poly(diallydimethylammonium chloride) (PDDA) molecules. Physical characterizations implied that sea urchin-like microspheres of ~ 2.5 µm in size were formed by self-assembly of numerous nanoneedles with a typical dimension of ~ 100 nm in diameter. Electrochemical performance study confirmed that sea urchin-like NiCo2O4 exhibited high reversible capacity of 663 mAh g-1 after 100 cycles at current density of 100 mA g-1. Rate capability indicated that average capacities of 1085, 1048, 926, 642, 261, and 86 mAh g-1 could be achieved at 100, 200, 500, 1000, 2000, and 3000 mA g-1, respectively. The excellent electrochemical performances were ascribed to the unique micro/nanostructure of sea urchin-like NiCo2O4, tailored by positively charged PDDA molecules. The proposed strategy has great potentials in the development of binary transition metal oxides with micro/nanostructures for electrochemical energy storage applications.

A comprehensive review of anaerobic digestion of organic solid wastes in relation to microbial community and enhancement process.

Organic solid wastes (OSWs) should be regarded as valuable resources rather than dead-end landfill waste that causes public health and odor concerns. Anaerobic digestion (AD) is an ideal approach for managing organic solid waste issues and involves using a group of anaerobic microorganisms to transform OSWs into useful products. In this review, over 100 publications related to AD of OSWs have been compiled, discussed, and analyzed. A comprehensive analysis of the environmental and safety impacts of AD, its key environmental factors, co-digestion, and pretreatment, as well as the AD of OSWs by various anaerobic microbes uncovered by high throughput sequencing-based approaches, is presented. The purpose of this review is to provide an outline of the current knowledge of AD processes from a multi-angle perspective. A comprehensive understanding of AD of OSWs and genome-enabled biology development could be helpful for providing up-to-date knowledge of AD, developing it, overcoming its drawbacks and, ultimately, improving global waste control for more efficient environmental management. © 2018 Society of Chemical Industry.

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area.

We demonstrate a method for the synthesis of NixNb1-xO catalysts with sponge-like and fold-like nanostructures. By varying the Nb:Ni ratio, a series of NixNb1-xO nanoparticles with different atomic compositions (x = 0.03, 0.08, 0.15, and 0.20) have been prepared by chemical precipitation. These NixNb1-xO catalysts are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. The study revealed the sponge-like and fold-like appearance of Ni0.97Nb0.03O and Ni0.92Nb0.08O on the NiO surface, and the larger surface area of these NixNb1-xO catalysts, compared with the bulk NiO. Maximum surface area of 173 m2/g can be obtained for Ni0.92Nb0.08O catalysts. In addition, the catalytic hydroconversion of lignin-derived compounds using the synthesized Ni0.92Nb0.08O catalysts have been investigated.

Enhanced activity and stability of La-doped CeO2 monolithic catalysts for lean-oxygen methane combustion.

Effective utilization of coal bed methane is very significant for energy utilization and environment protection. Catalytic combustion of methane is a promising way to eliminate trace amounts of oxygen in the coal bed methane and the key to this technology is the development of high-efficiency catalysts. Herein, we report a series of Ce1-xLaxO2-δ (x = 0-0.8) monolithic catalysts for the catalytic combustion of methane, which are prepared by citric acid method. The structural characterization shows that the substitution of La enhance the oxygen vacancy concentration and reducibility of the supports and promote the migration of the surface oxygen, as a result improve the catalytic activity of CeO2. M-Ce0.8La0.2O2-δ (monolithic catalyst, Ce0.8La0.2O2-δ coated on cordierite honeycomb) exhibits outstanding activity for methane combustion, and the temperature for 10 and 90% methane conversion are 495 and 580 °C, respectively. Additionally, Ce0.8La0.2O2-δ monolithic catalyst presents excellent stability at high temperature. These Ce1-xLaxO2-δ monolithic materials with a small amount of La incorporation therefore show promises as highly efficient solid solution catalysts for lean-oxygen methane combustion. Graphical abstract ᅟ.

Synthesis of chiral aminophosphines from chiral aminoalcohols via cyclic sulfamidates.

Protic aminophosphines with multiple chiral centers were synthesized in good yields and high purity by the nucleophilic ring-opening of N-protected cyclic sulfamidates with metal phosphides, followed by hydrolysis and deprotection. This synthetic approach is clean, scalable, and high yielding. The method provides an efficient alternative route for the synthesis of chiral aminophosphines.

Scope and limitations of the base-catalyzed phospha-peterson P=C bond-forming reaction.

Phosphaalkenes (MesP=CRR': R = R' = Ph (1a); R = R' = 4-FC6H4 (1b); R = Ph, R' = 4-FC6H4 (1c); R = R' = 4-OMeC6H4 (1d); R = Ph, R' = 4-OMeC6H4 (1e); R = Ph, R' = 2-pyridyl (1f)) are prepared from the reaction of MesP(SiMe3)2 and O=CRR' in the presence of a trace of KOH or NaOH. The base-catalyzed phospha-Peterson reaction is quantitated by NMR spectroscopy, and isolated yields of phosphaalkene between 40 and 70% are obtained after vacuum distillation and/or recrystallization. The asymmetrically substituted phosphaalkenes (1c, 1e, 1f) form as 1:1 mixtures of E and Z isomers; however, X-ray crystallography reveals that the E isomers crystallize preferentially. Interestingly, E-1e and E-1f readily isomerize in solution in the dark, although the rate of isomerization is much faster when samples are exposed to light. X-ray crystal structures of 1b, E-1e, and E-1f reveal that the P=C bond lengths (average of 1.70 A) are in the long end of the range typically found in phosphaalkenes (1.61-1.71 A). Attempts to prepare isolable P-adamantyl phosphaalkenes following this route were unsuccessful. Although AdP=CPh2 (2a) is detected by 31P NMR spectroscopy, attempts to isolate this species afforded the 1,2-diphosphetane (AdPCPh2)2 (3a), which was characterized by X-ray crystallography.

A convenient synthesis of new isolable phosphaalkenes using the base-induced rearrangement of secondary vinylphosphines.

The secondary vinylphosphines Ar(F)P(H)C(R)[double bond]CH(2) [2a, Ar(F) = 2,6-(CF(3))(2)C(6)H(3), R = CH(3); 2b, Ar(F) = 2,6-(CF(3))(2)C(6)H(3), R = C(6)H(5); 2c, Ar(F) = 2,4,6-(CF(3))(3)C(6)H(2), R = CH(3)] were prepared by treating the corresponding dichlorophosphine Ar(F)PCl(2) (1) with H(2)C[double bond]C(R)MgBr. In the presence of catalytic base (DBU or DABCO) the vinylphosphines (2a-c) undergo quantitative 1,3-hydrogen migration over 3 d to give stable and isolable phosphaalkenes Ar(F)P=C(R)CH(3) (3a, Ar(F) = 2,6-(CF(3))(2)C(6)H(3), R = CH(3); 3b, Ar(F) = 2,6-(CF(3))(2)C(6)H(3), R = C(6)H(5); 3c, Ar(F) = 2,4,6-(CF(3))(3)C(6)H(2), R = CH(3)). Under analogous conditions, only 90% conversion is observed in the base-catalyzed rearrangement of MesP(H)C(CH(3))[double bond]CH(2) to MesP[double bond]C(CH(3))(2). Presumably, the increase in acidity of the P-H group when electron-withdrawing groups are employed (i.e. 2a-c) favors quantitative rearrangement to the phosphaalkene tautomer (3a-c). Thus, the double-bond migration reaction is a convenient and practical method of preparing new phosphaalkenes with C-methyl substituents.

The addition polymerization of a p=c bond: a route to new phosphine polymers.

Addition polymerization, the most general method of preparation for organic polymers, has successfully been extended to P=C bonds. The polymerization of a phosphaalkene has been initiated by thermolysis or with alkyllithium reagents. The unprecedented poly(methylenephosphine)s are easily oxidized using oxygen or sulfur to give air stable macromolecules. A molecular weight (M(w)) of 35000 g/mol for the poly(methylenephosphine sulfude) was estimated by light-scattering GPC.

Highly Chlorinated, Brominated, and Iodinated Icosahedral Carborane Anions: 1-H-CB(11)X(11)(-), 1-CH(3)-CB(11)X(11)(-) (X = Cl, Br, I); 1-Br-CB(11)Br(11)(-).

Direct chlorination of 1-CH(3)-CB(11)H(11)(-) in glacial acetic acid gave the highly chlorinated carborane anion 1-CH(3)-CB(11)Cl(11)(-), and treatment of 1-CH(3)-CB(11)H(11)(-) with ICl in triflic acid afforded the highly iodinated carborane anion 1-CH(3)-CB(11)I(11)(-). Under similar or more vigorous reaction conditions, however, the reaction of 1-CH(3)-CB(11)H(11)(-) with Br(2) in triflic acid did not proceed to completion. The highly brominated carborane anion 1-CH(3)-CB(11)Br(11)(-) was achieved via a sealed-tube reaction. This new method has led to the isolation of 1-H-CB(11)X(11)(-) (X = Cl, Br, I) and 1-Br-CB(11)Br(11)(-) in high yield. The lithiation of 1-H-CB(11)X(11)(-) resembles that of its parent anion CB(11)H(12)(-). Treatment of these lithio species with methyl iodide gave the methylated carborane anions 1-CH(3)-CB(11)X(11)(-). These new weakly coordinating anions were fully characterized by (1)H, (13)C, and (11)B NMR, IR, and negative-ion MALDI MS spectroscopy. Some were further confirmed by single-crystal X-ray analysis.