Research on the Effects of Environmental Factors on the Emission of Volatile Organic Compounds from Plastic Track.

The volatile organic compounds (VOCs) released from a plastic track can cause stimulation and damage to the human body; the temperature, relative humidity (RH) and air exchange rate (AER) have a significant impact on the release of VOCs from materials. In this study, we used a 0.1 m3 environmental chamber; a qualitative and quantitative analysis of VOCs released from a plastic track was conducted by gas chromatography-mass spectrometry with a temperature range of 23-60 °C, RH of 5-65% and AER of 0.5-1.5 h-1. The formation rate, the speciation, the nature of the main compounds and the mass concentration of VOCs under different environmental conditions were determined. It is shown that with the increase of temperature, the concentration of some main VOCs gradually increased and the Calkane and Coxygenated organic compounds were larger by 736.13 µg·m-3 and 984.22 µg·m-3 at 60 °C, respectively. Additionally, with the increase of RH, the concentration of different VOCs gradually increased. Nonetheless, the change in RH had no effect on the concentration percentage of different VOCs in the total VOC. With the increase in AER, the concentration of different main VOCs significantly declined, as did the VOC detection rate. When the AER was increased from 0.5 h-1 to 1.5 h-1, the Calkane decreased by 206.74-254.21 µg·m-3 and Coxygenated organic compounds decreased by 73.06-241.82 µg·m-3, and the number of non-detected VOC monomers increased from 1 to 7-12 species. The conclusion is that the increase in temperature and RH can promote the emission of VOCs from a plastic track, while increasing AER significantly reduces the concentrations of VOCs. Environmental temperature mainly causes the changes in the concentrations of different VOCs, and RH is a main factor leading to the variation in the detection rate of main VOCs. Overall, the release of VOCs from a plastic track is affected by environmental temperature, AER and RH in sequence. Through this paper, we clarify the effects of ambient temperature, RH and AER on the emission of VOCs from a plastic track, and furthermore, we determine the release characteristics of plastic track VOCs.

Solution-processable carbon dots with efficient solid-state red/near-infrared emission.

Carbon dots (CDs) emerge as promising luminescent materials for potential applications in optoelectronics on basis of their merits including low cost, eco-friendliness and strong, color-tunable photoluminescence (PL). However, the research on solid-state emissive CDs is still at the primary stage because of the aggregation-caused quenching (ACQ) of PL and their poor film-formation ability. In this work, we produce CDs with branched-polyethylenimine (b-PEI) chemically functionalized on the surfaces. The thus newly synthesized P-CDs successfully overcome the bottleneck of ACQ effect and display efficient red and NIR emission in aggregate state. Under the excitation of 520 nm, a strong red emission (maxima of 640 nm) with a high photoluminescence quantum yield (PLQY) of 21% was observed for the P-CDs in neat film. Moreover, this design strategy endows the P-CDs with good film-formation ability via solution spin-coating, which significantly increases its value for the film-based optoelectronic devices.

R6G molecule induced modulation of the optical properties of reduced graphene oxide nanosheets for use in ultrasensitive SPR sensing.

A proper understanding of the role that molecular doping plays is essential to research on the modulation of the optical and electronic properties of graphene. The adsorption of R6G molecules onto defect-rich reduced graphene oxide nanosheets results in a shift of the Fermi energy and, consequently, a variation in the optical constants. This optical variation in the graphene nanosheets is used to develop an ultrasensitive surface plasmon resonance biosensor with a detection limit of 10(-17) M (0.01 fM) at the molecular level. A density functional theory calculation shows that covalent bonds were formed between the R6G molecules and the defect sites on the graphene nanosheets. Our study reveals the important role that defects play in tailoring the properties and sensor device applications of graphene materials.

Metabolic Engineering of Escherichia coli for Poly(3-hydroxybutyrate) Production under Microaerobic Condition.

The alcohol dehydrogenase promoter PadhE and mixed acid fermentation pathway deficient mutants of Escherichia coli were employed to produce poly(3-hydroxybutyrate) (P3HB) under microaerobic condition. The E. coli mutant with ackA-pta, poxB, ldhA, and adhE deletions accumulated 0.67 g/L P3HB, up to 78.84% of cell dry weight in tube cultivation. The deletion of pyruvate formate-lyase gene pflB drastically decreased P3HB production and P3HB content to 0.09 g/L and 24.44%, respectively. Overexpressing pflB via the plasmid in its knocked out mutant restored cell growth and P3HB accumulation, indicating the importance of the pyruvate formate-lyase in microaerobic carbon metabolism. The engineered E. coli BWapld (pWYC09) produced 5.00 g/L P3HB from 16.50 g/L glucose in 24 h batch fermentation, and P3HB production yield from glucose was 0.30 g/g, which reached up to 63% of maximal theoretical yield.

A switch of the oxidation state of graphene oxide on a surface plasmon resonance chip.

Controlling the assembly and manipulating the oxidation state of graphene nanosheets on surfaces are of essential importance for application of graphene-related optical and biosensing devices. In this study, we assemble a graphene oxide (GO) film on a surface plasmon resonance chip surface and then convert it to reduced graphene by an in situ electrochemical method. The mechanism and application of surface-enhanced Raman spectroscopy and DNA sensing from graphene-based substrates are investigated. The average thickness and dielectric constant of GO are varied significantly with the switch of its oxidation state. Electrochemical reduction decreases the distance between carbon atoms and the gold surface by removing the spacer of oxygen functional groups. The electromagnetic field of the graphene surface is therefore enhanced, resulting in an enhancement of the Raman signal. A p doping of electrochemically reduced GO (ERGO) that occurred from changes in the graphene electronic structure through interaction between gold and ERGO is also observed during electrochemical reduction. The GO and ERGO substrates perform different interaction abilities with single- and double-stranded DNA. This work may be valuable for graphene-related research works on optoelectronics and biosensors.

Photo-assisted preparation and patterning of large-area reduced graphene oxide-TiO(2) conductive thin film.

A mild photo-assisted reduction method was developed to fabricate large-area, uniform reduced graphene oxide-TiO(2) films and micropatterns on various substrates in air at room temperature from a composite insulating film of graphene oxide sheets and TiO(2) nanoparticles, with a conductivity (0.5-2 Omega cm) comparable to chemically reduced graphene.