Effects of desertification on permafrost environment in Qinghai-Tibetan Plateau.

Soil thermal state exerts an important role in soil physicochemical properties, nutrient content, soil carbon losses, and hydrological processes in cold regions. In the Qinghai-Tibet Plateau, desertification and aeolian sand accumulation greatly change the surface cover types and simultaneously alter the surface energy budget. However, the quantification of their impacts on the soil thermal state hasn't been studied methodically. Here, a laboratory experiment was conducted to investigate the impact of surface cover types, including bare surface, grass-coved surface, dry and wet (3%) aeolian sand-covered surface, on underlying soil thermal state. Our results demonstrate that there is a reciprocal relationship between environment change and permafrost degradation. The amount of heat entering the active layer was determined by the surface cover types and soil water content. Using the bare surface case as a reference, vegetation layer acted as a buffer to reduce the amount of heat propagation downwards the ground by 20% and to lower the near surface temperature by 0.7 °C. In contrast, dry aeolian sand acted as an insulation layer and warmed the ground by about 2 °C. Also, wet aeolian sand with high thermal conductivity facilitated the heat exchange with the atmosphere and warmed the ground about 1.5 °C. Our results have implications for thermal and hydrological processes in the atmosphere-ground-permafrost system and thermal stability of infrastructure under the effect of the desertification and aeolian sand accumulation. The hydrothermal interaction of desertification and permafrost needs to be quantified in the further study through long-term field observations and a fully-coupled water flow and heat transport model under a changing climate.

Storage Stability of Volatile Organic Compounds from Petrochemical Plant of China in Different Sample Bags.

According to the emission characteristics of volatile organic compounds (VOCs) in the petrochemical plants of China, the storage stability of VOCs for two different bags, polyester aluminum (PEA) and polyvinyl fluoride (PVF), was investigated in this study by comparing the adsorption of gas samples. A series of experiments were carried out to study the impact of different factors of sampling in the petrochemical industry. The results showed that the C2∼C3 substances can be adsorbed by the Tedlar bag, and after being refilled with pure nitrogen, the VOCs adsorbed previously by the bag material can be released. The aromatic hydrocarbon VOCs with larger molecular weight had a relatively lower recovery rate than the smaller molecular weights. And the average recovery of PEA airbags was significantly better than that of PVF airbags for storing stationary VOCs in the refinery of China. More kinds of substances can be detected in the airbags that had been added with helium protective gas, and it had a higher recovery rate for both kinds of simple bags after 24 hours of storage time, which indicated that the airbags without protective gas had adsorbed these substances.

Synergetic effect between adsorption and photodegradation on rGO/TiO2/ACF composites for dynamic toluene gaseous removal.

The toluene poses a serious threat to the atmospheric environment and human health. Herein, the reduced graphene oxide (rGO)/TiO2 immobilized on the activated carbon fiber (ACF) are fabricated by ultrasonic assisted sol-gel impregnation method to photodegrade dynamic toluene. Characterizations of rGO/TiO2/ACF composites reveal that the majority of graphene oxide (GO) is reduced to rGO and rGO/TiO2 is evenly loaded onto the ACF surface in the form of a smooth film. Furthermore, the photoelectrochemical experiments demonstrate both rGO and ACF can enhance significantly the separation efficiency of electron-hole pairs. The maximum removal efficiency of rGO/TiO2/ACF-0.75% can be up to 85% under ultraviolet irradiation. The rGO/TiO2/ACF exhibits more excellent adsorption and photodegradation activity for dynamic toluene than both rGO/TiO2 and ACF due to the synergetic effect rather than a simple linear combination of the rGO/TiO2 and ACF for toluene conversion. The possible photodegradation pathway is proposed according to intermediates measured by GC-MS, and adsorption coupling photocatalytic mechanisms are discussed.

Research on the effect of wall corrosion and rim seal on the withdrawal loss for a floating roof tank.

Storage tanks are important parts of volatile organic compound (VOC) fugitive emission sources of the petrochemical industry; the floating roof tank is the main oil storage facility at present. Based on the mechanism of withdrawal loss and the type of rim seal, octane and gasoline were taken as the research objects. A model instrument for simulating the oil loading process by the 316 stainless steel and A3 carbon steel as the test piece was designed, and the film thickness was measured by wet film thickness gauge to investigate the influence of the corrosion of the tank wall and rim seal on the withdrawal loss for floating roof tanks. It was found that withdrawal loss was directly proportional to the shell factor, and the oil thickness of the octane and gasoline increased with the strength of the wall corrosion with the same wall material and rim seal. Compared with the untreated test piece, the oil film thickness of the octane/gasoline was increased by 7.04~8.57 µm/13.14~21.93 µm and 5.59~11.49 µm/11.61~25.48 µm under the corrosion of hydrochloric acid for 32 and 75 h, respectively. The oil film thickness of octane and gasoline decreased with the increasing of the rim seal, and the oil film thickness of the octane decreased by 11.97~28.90% and 37.32~73.83% under the resilient-filled seal and the double seal, respectively. The gasoline dropped by 11.97~31.18% and 45.98~75.34% under the resilient-filled seal and the double seal, respectively. In addition, the tank surface roughness reduced the compression of the rim seal on the tank wall, and the effect of scraping decreased. The API withdrawal loss formula for a floating roof tank was recommended to take into account the effect of the rim seal to improve the accuracy of the loss evaluation. Finally, some measures of reducing the withdrawal loss were proposed.

On-line measurement of propofol using membrane inlet ion mobility spectrometer.

The concentration of propofol in patient's exhaled air is an indicator of the anesthetic depth. In the present study, a membrane inlet ion mobility spectrometer (MI-IMS) was built for the on-line measurement of propofol. Compared with the direct sample introduction, the membrane inlet could eliminate the interference of moisture and improve the selectivity of propofol. Effects of membrane temperature and carrier gas flow rate on the sensitivity and response time have been investigated experimentally and theoretically. Under the optimized experimental conditions of membrane temperature 100 °C and carrier gas flow rate 200 mL min(-1), the calculated limit of detection (LOD) for propofol was 1 ppbv, and the calibration curve was linear in the range of 10-83 ppbv with a correlation coefficient (R(2)) of 0.993. Finally, the propofol concentration in an anaesthetized mouse exhaled air was monitored continuously to demonstrate the capability of MI-IMS in the on-line measurement of propofol in real samples.

Note: Design and construction of a simple and reliable printed circuit board-substrate Bradbury-Nielsen gate for ion mobility spectrometry.

A less laborious, structure-simple, and performance-reliable printed circuit board (PCB) based Bradbury-Nielsen gate for high-resolution ion mobility spectrometry was introduced and investigated. The gate substrate was manufactured using a PCB etching process with small holes (Φ 0.1 mm) drilled along the gold-plated copper lines. Two interdigitated sets of rigid stainless steel spring wire (Φ 0.1 mm) that stands high temperature and guarantees performance stability were threaded through the holes. Our homebuilt ion mobility spectrometer mounted with the gate gave results of about 40 for resolution while keeping a signal intensity of over 0.5 nano-amperes.

[A novel gas chromatography detector based on ion mobility spectrometry technology and its application].

Ion mobility spectrometry (IMS) is an attractive detector of gas chromatography (GC) due to its high sensitivity, short response time, and comparatively low cost. The hyphenated GC-IMS instrument can simultaneously provide high separation ability of GC and high sensitivity of IMS. In this paper, one setup of a GC-IMS instrument is introduced. The parameters of IMS as the GC detector were evaluated and studied with respect to the resolution and sensitivity including temperature, total voltage and drift gas flow rate. Under the optimal conditions, GC-IMS was used to detect iodomethane, 1,2-dichloroethane, tetrachloromethane and dibromomethane and the detection limits were 2, 0.02, 1 and 0.1 ng, respectively. And the linear ranges of two orders of magnitude were achieved. As the detector of gas chromatography, IMS can provide more information for compound identification because of its second dimensional separation and can realize selective detection of different compounds.

Bipolar ionization source for ion mobility spectrometry based on vacuum ultraviolet radiation induced photoemission and photoionization.

A novel bipolar ionization source based on a commercial vacuum-UV Kr lamp has been developed for ion mobility spectrometry (IMS), which can work in both negative and positive ion mode. Its reactant ions formed in negative ion mode were predominantly assigned to be O(3)(-)(H(2)O)(n), which is different from that of the (63)Ni source with purified air as carrier and drift gases. The formation of O(3)(-)(H(2)O)(n) was due to the production of ozone caused by ultraviolet radiation, and the ozone concentration was measured to be about 1700 ppmv by iodometric titration method. Inorganic molecules such as SO(2), CO(2), and H(2)S can be easily detected in negative ion mode, and a linear dynamic range of 3 orders of magnitude and a limit of detection (S/N = 3) of 150 pptv were obtained for SO(2). Its performance as a negative ion source was investigated by the detection of ammonium nitrate fuel oil explosive, N-nitrobis(2-hydroxyethyl)amine dinitrate, cyclo-1,3,5-trimethylene-2,4,6-trinitramine, and pentaerythritol tetranitrate (PETN) at 150 degrees C. The limit of detection was reached at 45 pg for PETN, which was much lower than the 190 pg using (63)Ni ion mobility spectrometry under the same experimental condition. Also, its performance as an ordinary photoionization source was investigated in detecting benzene, toluene, and m-xylene.