Publications by authors named "Zhiping Du"

Selective non-catalytic reduction (SNCR) with NH as the reducing agent is widely used for the denitrification of flue gas in coal-fired boilers, where fly ash significantly influences the conversion of the residual NH that does not participate in denitrification. However, there have been few studies on the exact nature of this influence, particularly the adsorption and reaction mechanisms of NH on fly ash. In this study, temperature-programmed desorption (TPD) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) were used to study the mechanisms of NH adsorption and reactions over coal ash.

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Prenatal DEHP exposure can cause offspring neurodevelopmental toxicity, but the persistent effects of such exposure window are unclear. This study aimed to investigate the lasting neurobehavioral impact of DEHP on offspring following early exposure from GD9.5 (fetal neural tube closure) to GD16.

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Graphene oxide (GO) coating has recently been reported as a novel approach to increase membrane flux of membrane distillation (MD), yet the phenomena underlying the process are still not fully understood. In this study, a mathematical model based on capillary-film assumption was developed and validated with the results (R>0.99) from a series of MD experiments.

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The path planning of robot is of great significance for the logistics industry, which helps to improve the efficiency of warehousing, sorting and distribution. On the basis of ant colony algorithm, multi step search strategy is used instead of single step search strategy, pheromone update mechanism is redesigned, and path smoothing is configured to improve the performance of the algorithm. The experimental results show that the improved ant colony algorithm proposed in this paper can plan a shorter optimal path on the 16 * 16 grid logistics storage site, and the path length is saved by 9.

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Pseudocapacitive asymmetric supercapacitors are promising candidates for achieving high energy density in flexible energy storage devices. However, seeking suitable positive electrode materials that are compatible with negative electrode materials remains a considerable challenge. In the current study, a pseudocapacitive TiCT MXene used as negative electrodes is rationally compatible with redox-type VO as positive electrodes, resulting in the assembly of an all-pseudocapacitive TiCT MXene//VO asymmetric flexible energy storage device.

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Article Synopsis
  • The study investigates the relationship between phthalate exposure and obesity among elderly individuals in China, focusing on a sample from Lu'an, Anhui province.
  • Researchers analyzed urine samples for seven phthalate metabolites and used health metrics like body mass index and waist circumference to assess obesity.
  • Findings revealed that over half the participants were generally obese, and significant associations were found between several phthalate metabolites and both general and abdominal obesity, with variations noted between genders.
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Article Synopsis
  • The study examines 371 hazardous material (hazmat) transportation accidents in China from 2004-2018 to highlight the severe impacts on lives, the economy, and the environment due to these incidents.
  • It develops a comprehensive analysis framework to understand the key factors influencing hazmat accidents, incorporating adaptive data analysis techniques to enhance safety management practices.
  • By employing innovative methods like decision trees and F-N curve analysis, the study quantifies the relationships between hazmat properties and accident outcomes, providing actionable insights for reducing accident frequencies and risks in hazmat transportation.
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Co-metabolism is one of the effective approaches to increase the removal of refractory pollutants in microbial fuel cells (MFCs), but studies on the links between the co-substrates and biodegradation remain limited. In this study, four external carbon resources were used as co-substrates for phenol removal and power generation in MFC. The result demonstrated that acetate was the most efficient co-substrate with an initial phenol degradation of 78.

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During pregnancy, fetal thyroid hormones (THs) are dependent on maternal placental transport and their physiological level is crucial for normal fetal neurodevelopment. Earlier research has shown that Di-(2-ethylhexyl) phthalate (DEHP) disrupts thyroid function and THs homeostasis in pregnant women and fetuses, and affects placental THs transport. However, the underlying mechanisms are poorly understood.

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Development of sustainable routes to synthesize precious metal supported catalysts is of great importance because of their wide applications in the catalysis field. This paper reported a controllable and recyclable cation-assisted reduction route to fabricate a palladium nanoparticle supported catalyst. At 323 K, highly dispersed Pd/AlO-CAR was prepared through introducing M (M = Mn, Zn or Cu) ions to promote the reduction of HPdCl in ethylene glycol-water solution, and the residual filtrate after preparation could be recycled to prepare Pd/AlO catalysts.

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As one of the typical solid-wastes, FGD gypsum usually occupies land and causes resource waste and environmental pollution. Its high content of CaSO·2HO shows highly potential in synthesizing CaCO by incorporating CO. Nevertheless, the impurities in FGD gypsum have significant effects on polymorph of CaCO and the formation mechanism of CaCO polymorph during FGD gypsum carbonation was still unclear.

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We present the facile preparation of a superhydrophobic-oleophilic stainless steel mesh with excellent oil/water separation efficiency and resistance to corrosion through hydrofluoric (HF) acid etching, Ag nanoparticle coating, and stearic acid modification, to construct a superhydrophobic micro/nanohierarchical structure. The surface of the treated mesh exhibits superhydrophobicity, with a water contact angle of 152°, and superoleophilicity, with an oil contact angle of 0°. The effects of variation in the HF etching time and Ag nanoparticle coating on surface wettability were explored.

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Pickering emulsions exhibit outstanding stability, especially those prepared with Janus particles, whose desorption energy is expected to be up to 3-fold greater than emulsions of homogeneous particles from theoretical calculations. To the best of our knowledge, however, there remains no experimental proof of this behavior in practice. In this study, inorganic Janus nanoparticles were fabricated by regioselective modification of the separate side of SiO nanoparticles with a judiciously selected mixture of trimethoxysilylpropyldiethylenetriamine and n-octyltrimethoxysilane.

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To address the limitations of batch organic-aqueous biphasic catalysis, we develop a conceptually novel method termed Flow Pickering Emulsion, or FPE, to process biphasic reactions in a continuous flow fashion. This method involves the compartmentalization of bulk water into micron-sized droplets based on a water-in-oil Pickering emulsion, which are packed into a column reactor. The compartmentalized water droplets can confine water-soluble catalysts, thus "immobilizing" the catalyst in the column reactor, while the interstices between the droplets allow the organic (oil) phase to flow.

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Article Synopsis
  • Five polysiloxanes modified with butynediol-ethoxylate (PSi-EO) were synthesized through a two-step reaction process involving silicone oil preparation and hydrosilylation.
  • The chemical makeup of these compounds was verified using techniques like FT-IR and NMR.
  • Detailed studies on their surface activity showed that PSi-EO surfactants had low critical aggregation concentrations and surface tension, and they self-assembled into spherical aggregates in water, efficiently spreading on low-energy surfaces.
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Six novel siloxane-based surface-active ionic liquids (SAILs)--siloxane ammonium carboxylate [Si(n)N(2)-CA(1), (n = 3, 4)]--were designed and synthesized. Their melting points, surface activities, and self-aggregation behavior in aqueous solution were studied. The results showed that because of the bulky hydrophobic siloxane chains at the end of the tail, all six siloxane-based SAILs are room-temperature ionic liquids (RT-SAILs).

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A conceptually novel methodology is explored for in situ recycling of nanoparticle catalysts based on transforming a conventional organic/aqueous biphasic system into a Pickering emulsion/organic biphasic system (PEOBS). The suggested PEOBS exists as two phases, with the nanoparticle catalyst "anchored" in the Pickering emulsion phase, but is "continuous" between the organic phase and the continuous phase of the Pickering emulsion. Aqueous hydrogenations are used to evaluate the reaction performances of PEOBS, and the underlying principles of PEOBS are preliminarily elaborated.

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Adsorption and aggregation behaviors of novel tetrasiloxane-tailed gemini surfactants N,N'-ditetrasiloxane-N,N'-digluconamide oligo ethylene glycol diglycidyl (Si-m-Si, where m is the number of ethylene glycol of 1, 2, and 3) were investigasted using surface tension, bromophenol blue encapsulation, dynamic light scattering (DLS), and transmission electron microscope (TEM) methods. The static surface tension of the aqueous Si-m-Si solutions measured at the critical aggregate concentration (CAC) was observed to be lower than that of traditional hydrocarbon gemini surfactants. This suggests that these newly synthesized gemini surfactants are capable of forming a closely packed monolayer film at the air/aqueous solution interface.

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Grafted SMA containing poly(styrene-co-maleic anhydride)-g-(poly(ethylene glycol) monomethyl ether) (SMA-PEG) and its hydrophobically modified products poly(styrene-co-maleic anhydride)-g-(poly(ethylene glycol) monomethyl ether & dodecyl) (SMA-PEG+C(12)) and poly(styrene-co-maleic anhydride)-g-(dodecyl) (SMA-C(12)) were prepared using a single batch method. Their adsorption and rheology behavior was investigated using equilibrium surface tension and rheological techniques. The adsorption parameters, saturation surface excess concentration (Γ(max)), and the minimum area (A(min)) of these copolymers were evaluated.

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Three novel amphiphilic dicephalic (double-headed) surfactants containing oligo(ethylene-oxide)methyl-ether and a sugar moiety TGA-m (m = 1, 2, and 3) that incorporate a tetrasiloxane at the terminus of a hydrocarbon chain were designed and synthesized. Their surface activity and aggregation behavior in aqueous solution were systematically investigated by surface tension, dynamic light scattering (DLS), and transmission electron microscopy (TEM) techniques at 298 K. The surface tension measurements provided the critical aggregation concentration (CAC) and the surface tension at the CAC (γ(cac)).

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Four carbohydrate-modified siloxane surfactants, Si(n)N-GA and Si(n)N-LA (n = 3, 4), were designed and synthesized. Their surface activities, adsorption, and aggregation behavior in aqueous solution were investigated by surface tension measurements, dynamic light scattering (DLS) and transmission electron microscopy (TEM). Due to the bulky siloxane moiety at the end of hydrophobic chains, the surfactant solutions displayed low critical aggregation concentration (cac) and low surface tension.

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The comb-like surfactants, poly(styrene-co-maleic anhydride)-g-(poly(ethylene glycol) monomethyl ether), poly(St-co-MA)-g-(MPEG), have been prepared using a macromonomer approach to get controlled molecular structures. The macromonomer (MAMPEG) was obtained by esterification of poly(ethylene glycol) monomethyl ether with maleic anhydride. Poly(St-co-MA)-g-(MPEG) with various molar ratios of St to MAMPEG (R) were then constructed by radical copolymerization.

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The dynamic rheological properties of discontinuous cubic liquid crystal, formed by nonionic surfactant C(12-14)E(12), were investigated in the discrete and continuous patterns of raising temperature. In the discrete pattern, the discontinuous cubic phase appears in two types of viscoelastic behaviors under the melting points of cubic phase: elastic gel and viscoelastic liquid. When the discontinuous cubic phase begins to melt, it has the weak polymer-like viscoelasticity.

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The rate of shrinkage of air bubbles of initial radii, r, from 50 to 150 microm injected beneath a planar air-water interface has been measured. Bubbles were stabilized by 0.05 wt% protein in approximately 0.

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The rate of shrinkage of air bubbles, of initial radius from 50 to 200 microm, injected beneath a planar air-water interface has been measured. Bubbles were stabilized in solutions of 0.05 wt% gelatin or pure beta-lactoglobulin.

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