Study on the Effect of an Intermittent Ventilation Strategy on Controlling Formaldehyde Concentrations in Office Rooms

Material emission and ventilation are two aspects influencing indoor air quality. In this study, a model predictive control (MPC) strategy is proposed for intermittent ventilation system in office buildings, to achieve a healthy indoor environment. The strategy is based on a dynamic model for predicting emissions of volatile organic compounds (VOCs) from materials. The key parameters of formaldehyde from panel furniture in the model are obtained by an improved C-history method and large-scale chamber experiments. The effectiveness of the determined key parameters is validated, which are then used to predict the formaldehyde concentration variation and the pre-ventilation time in a typical office room. In addition, the influence of some main factors (i.e., vacant time, loading ratio, air change rate) on the pre-ventilation time is analyzed. Results indicate that the pre-ventilation time of the intermittent ventilation system ranges from several minutes to several hours. The pre-ventilation time decreases exponentially with the increase in the vacant time, the air change rate, and with the decrease in the loading ratio. When the loading ratio of the furniture is 0.30 m2/m3 and the vacant time is 100 days, the required pre-ventilation time approaches zero. Results further reveal that an air change rate of 2 h−1 is the most effective means for rapid removal of indoor formaldehyde for the cases studied. The proposed strategy should be helpful for achieving effective indoor pollution control.

Manipulating spatial alignment of donor and acceptor in host-guest MOF for TADF

Thermally activated delayed fluorescence (TADF) was achieved when electron-rich triphenylene (Tpl) donors (D) were confined to a cage-based porous MOF host (NKU-111) composed of electron-deficient 2,4,6-tri(pyridin-4-yl)-1,3,5-triazine (Tpt) acceptor (A) as the ligand. The spatially-separated D and A molecules in a face-to-face stacking pattern generated strong through-space charge transfer (CT) interactions with a small singlet-triplet excited states energy splitting (∼0.1 eV), which enabled TADF. The resulting Tpl@NKU-111 exhibited an uncommon enhanced emission intensity as the temperature increased. Extensive steady-state and time-resolved spectroscopic measurements and first-principles simulations revealed the chemical and electronic structure of this compound in both the ground and low-lying excited states. A double-channel (T1, T2) intersystem crossing mechanism with S1 was found and explained as single-directional CT from the degenerate HOMO-1/HOMO of the guest donor to the LUMO + 1 of one of the nearest acceptors. The rigid skeleton of the compound and effective through-space CT enhanced the photoluminescence quantum yield (PLQY). A maximum PLQY of 57.36% was achieved by optimizing the Tpl loading ratio in the host framework. These results indicate the potential of the MOFs for the targeted construction and optimization of TADF materials.

Electrocatalytic Degradation of Sulfameth Thiadiazole by GAC@Ni/Fe Three-Dimensional Particle Electrode

In this work, GAC@Ni/Fe particle electrodes were prepared and employed for the degradation of Sulfamethylthiadiazole (SMT) by three-dimensional electrocatalytic technology.The effects of particle electrode bi-metal loading ratio, cell voltage, particle electrode dosage, electrode plate spacing and SMT initial concentration on SMT removal were studied.In addition, GAC@Ni/Fe particle electrode was analyzed by the scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS) and Fourier transform infrared spectrometer (FTIR) to characterize . which indicated that a significant amount of Iron-nickel oxide were formed on the surface of GAC@Ni/Fe particle electrode.The results indicated that when the nickel-iron loading ratio is 1:1, the SMT removal effect is the best, and the removal rate can reach 90.89% within 30 minutes,Compared with the granular activated carbon without bimetal, the removal efficiency is increased by 37.58%. The degradation of SMT in the GAC@Ni/Fe particle three-dimensional electrode reactor is the joint result of both direct oxidation and indirect oxidation. The contribution rates of direct oxidation of anode and particle electrode and indirect oxidation of ·OH in the degradation are 32%, 27% and 41%, respectively. Based on the intermediate detected by ultra high liquid chromatography and the calculation of bond energy of SMT molecule by Gauss software，the degradation pathway of SMT in the GAC@Ni/Fe three-dimensional electrode reactor is proposed. This research provides a green, healthy and effective method for removing sulfonamide micro-polluted wastewater.

Effects of CoMo/γ-Al2O3 Catalysts on Product Hydrocarbon and Phenol Distribution during Hydrodeoxygenation of Oxidized Bio-Oil in a Batch Reactor

Hydrodeoxygenation is an essential process for producing liquid transportation fuels. In this study, the effects of CoMo/γ-Al2O3 catalysts form and loading ratio on the hydrodeoxygenation upgrading of bio-oil were investigated in a batch reactor. Raw bio-oil was first oxidized with hydrogen peroxides and oxone to obtain the oxidized bio-oil with reduced levels of aldehydes and ketones, increasing the organic liquid yield during hydrodeoxygenation by suppressing the coke formation. CoMo/γ-Al2O3 was selected as the catalyst because of its low cost and commercial availability. The effect of the reduction and sulfidation of CoMo/γ-Al2O3 catalyst on the hydrodeoxygenation of the oxidized bio-oil was compared. The effect of the catalyst loading ratio on bio-oil hydrodeoxygenation using sulfided CoMo/γ-Al2O3 catalysts was also investigated. The research results showed that the sulfided CoMo/γ-Al2O3 catalyst facilitated the formation of hydrocarbons, while the reduced CoMo/γ-Al2O3 catalyst produced more phenols in the organic liquids. Moreover, a high sulfided catalyst loading ratio promoted the formation of hydrocarbons.

Mechanism Study of Thermally Induced Anti-Tumor Drug Loading to Engineered Human Heavy-Chain Ferritin Nanocages Aided by Computational Analysis

Diverse drug loading approaches for human heavy-chain ferritin (HFn), a promising drug nanocarrier, have been established. However, anti-tumor drug loading ratio and protein carrier recovery yield are bottlenecks for future clinical application. Mechanisms behind drug loading have not been elaborated. In this work, a thermally induced drug loading approach was introduced to load anti-tumor drug doxorubicin hydrochloride (DOX) into HFn, and 2 functionalized HFns, HFn-PAS-RGDK, and HFn-PAS. Optimal conditions were obtained through orthogonal tests. All 3 HFn-based proteins achieved high protein recovery yield and drug loading ratio. Size exclusion chromatography (SEC) and transmission electron microscopy (TEM) results showed the majority of DOX loaded protein (protein/DOX) remained its nanocage conformation. Computational analysis, molecular docking followed by molecular dynamic (MD) simulation, revealed mechanisms of DOX loading and formation of by-product by investigating non-covalent interactions between DOX with HFn subunit and possible binding modes of DOX and HFn after drug loading. In in vitro tests, DOX in protein/DOX entered tumor cell nucleus and inhibited tumor cell growth.

Effectiveness of Ethyl Formate as a Fumigant of Blattella germanica and Periplaneta americana (Blattodea: Ectobiidae, Blattidae) in Cross-Border Trade Transportation

Cockroaches cause problems as pests not only locally in residential areas but also internationally, as they can disperse across borders in transport vessels. We investigated the effects of the ethyl formate (EF) fumigant on all developmental stages of Blattella germanica and Periplaneta americana. For B. germanica eggs, the hatching inhibition rate increased directly proportionately with the increasing treatment concentration of EF, but the 100% control was not observed. P. americana eggs did not show any fumigation effect, even after exposure to 60 mg/L of fumigant in a 12 L desiccator. Adults and nymphs of the two species showed various fumigation effects dependent on the concentration in the 12 L desiccator. When EF was applied at the lethal concentration for 99% mortality (LCT99) values of 35 mg/L for 4 h (78.5 mg·h/L) and 60 mg/L for 2 h (70.8 mg·h/L), respectively, adults and nymphs of both species had 100% mortality in a 0.65 m3 fumigation chamber with a 20% loading ratio. However, no significant difference from the control was observed in the egg stage of either species of cockroach. The results of this experiment indicate that EF can be used as a fumigant for cross-border transport vessels if the control period occurs during the cockroach developmental stage and continuous refumigation is performed.

Correlation between Fractal Dimension and Areal Surface Parameters for Fracture Analysis after Bending-Torsion Fatigue

This paper investigates the fracture surface topography of two steel and aluminum alloys subject to bending-torsion fatigue loadings, as well as their susceptibility to fatigue performance and failure mechanisms. Using fracture surface topography data analysis, elements with different geometries were elaborated. A correlation between the fractal dimension, other selected parameters of surface topography such as areal Sx, and fatigue loading conditions was found. Distinctions in particular regions of cracks were also recognized through proving the correctness and universality of the total fracture surface method. The influence of fatigue loading parameters on the surface topography of fatigue fractures was demonstrated. For the analyzed cases, results show that the fractal dimension and standard surface topography parameters represent a correlation between them and loading conditions. As a single parameter, the appropriate loading ratio cannot be outright calculated with fractal dimension, but can be estimated with some approximation, taking into account additional assumptions.

g-C3N4/MoS2 Heterojunction for Photocatalytic Removal of Phenol and Cr(VI)

In this study, molybdenum disulfide (MoS2) decorated on graphitic carbon nitride (g-C3N4) heterostructure catalysts at various weight ratios (0.5%, 1%, 3%, 10%, w/w) were successfully prepared via a two-step hydrothermal synthesis preparation method. The properties of the synthesized materials were studied by X-ray diffraction (XRD), attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FT-IR), UV–Vis diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM) and N2 porosimetry. MoS2 was successfully loaded on the g-C3N4 forming heterojunction composite materials. N2 porosimetry results showed mesoporous materials, with surface areas up to 93.7 m2g−1, while determined band gaps ranging between 1.31 and 2.66 eV showed absorption over a wide band of solar light. The photocatalytic performance was evaluated towards phenol oxidation and of Cr (VI) reduction in single and binary systems under simulated sunlight irradiation. The optimum mass loading ratio of MoS2 in g-C3N4 was 1%, showing higher photocatalytic activity under simulated solar light in comparison with bare g-C3N4 and MoS2 for both oxidation and reduction processes. Based on scavenging experiments a type-II photocatalytic mechanism is proposed. Finally, the catalysts presented satisfactory stability (7.8% loss) within three catalytic cycles. Such composite materials can receive further applications as well as energy conversion.

Synthesis of Nano-ZnO/Diatomite Composite and Research on Photoelectric Application

The key to the commercialization of sustainable energy conversion technologies is the development of high-performance catalysts. The discovery of a stable, efficient, and low-cost multi-function catalyst is key. We used a simple green precipitation method to load diatomite nanozinc oxide particles onto a diatomite substrate. The ZnO is nano-sized. This precipitation method produces ZnO nanoparticles in situ on diatomite. The catalyst degraded 90% of a Methylene blue solution and also degraded gaseous benzene and acetone. Not only can the catalyst be used for the organic degradation of wastewater, but it also has the potential to degrade volatile organic compounds. Photocatalytic efficiency is closely related to the generation and separation of photosynthetic electrons and holes. The effective suppression of the composite rate of photoliving carriers, and thus improvement of the photocatalytic activity, has become a key research area. At present, At present, photocatalysis is an effective technology to inhibit photocarrier synthesis, which is often studied in sewage treatment. Photocatalytic water treatment reduces the combination of photoelectrons and holes by applying an external bias, thus improving the quantum efficiency for the complete mineralization of organic pollutants. The composite catalyst was used for oxygen and hydrogen extraction reactions, and a comparison of the catalysts with various loading ratios showed that the electrolysis water activity of the in situ loaded catalyst is due to pure ZnO, and the efficiency is highest when the loading ratio is 10%. This work provides new methods for the design and further optimization of the preparation of electrolytic aqueous catalysts.

Equilibrium & kinetic studies of reactive extraction of trans-aconitic acid using sunflower oil with tri-n-octylamine

In order to design an efficient extraction system for the separation of biochemically produced trans-aconitic acid (TAH) from fermentation broth; equilibrium and kinetics of reactive extraction of TAH from aqueous solutions was investigated using tri-n-octylamine (TOA) as an extractant and sunflower oil as a diluent. Through the equilibrium studies stoichiometry (acid, extractant) of complex formations was determined with the help of loading ratio. Formation of (1, 1), (2, 1), & (3, 1) stoichiometry complexes were observed having complexation constants values 179.73 kmol−1 m3, 9512.58 kmol−2 m6, and 614,407.02 kmol−3 m9, respectively. Kinetics experiments were performed in Lewis type stirred cell and results confirmed that reaction between TAH and TOA in sunflower oil fall in regime 1, i.e. slow reaction occurring in bulk organic phase. The overall order of reaction is pseudo first order with rate constant (K mn ) 1.78 × 10−5 (kmol m−3)−0.71 s−1 and physical mass transfer coefficient (K l ) 4.22 × 10−5 m s−1.