#mytweet via Instagram: Exploring User Behaviour across Multiple Social Networks

We study how users of multiple online social networks (OSNs) employ and share information by studying a common user pool that use six OSNs - Flickr, Google+, Instagram, Tumblr, Twitter, and YouTube. We analyze the temporal and topical signature of users' sharing behaviour, showing how they exhibit distinct behaviorial patterns on different networks. We also examine cross-sharing (i.e., the act of user broadcasting their activity to multiple OSNs near-simultaneously), a previously-unstudied behaviour and demonstrate how certain OSNs play the roles of originating source and destination sinks.Comment: IEEE/ACM International Conference on Advances in Social Networks Analysis and Mining, 2015. This is the pre-peer reviewed version and the final version is available at http://wing.comp.nus.edu.sg/publications/2015/lim-et-al-15.pd

Synthesis and structure of the inclusion complex {NdQ[5]K@Q[10](H₂O)4}·4NO₃·20H₂O

Heating a mixture of Nd(NO₃)₃·6H₂O, KCl, Q[10] and Q[5] in HCl for 10 min affords the inclusion complex {NdQ[5]K@Q[10](H₂O)₄}·4NO₃·20H₂O. The structure of the inclusion complex has been investigated by single crystal X-ray diffraction and by X-ray Photoelectron spectroscopy (XPS)

Slow pyrolysis of metal(loid)-rich biomass from phytoextraction: characterisation of biomass, biochar and bio-oil

Plants have successfully been used for phytoextraction of metal contaminated soils, however the use of these plants for energy production has been a subject of debates due to the potential conversion of the metals in the plants into airborne respirable particles. The aim of this study was to investigate the deportment of metal(loid)s during pyrolysis of a biomass cultivated in a highly contaminated soil in order to engineer best practice environmental approach for utilization of this biomass. A heavy metal(loid) contaminated mangrove (Avicennia marina var. australasica) biomass was used as a feedstock in this study. The biomass was subjected to slow pyrolysis under the heating rate of 60 ℃/min and different pyrolysis temperatures. Inductively coupled plasma mass spectrometry, thermogravimetric analysis, Fourier-transform infrared spectroscopy, X-ray fluorescence spectroscopy and gas chromatography–mass spectrometry were introduced to characterise the biomass, biochar and bio-oil samples. Results showed that biochar yield decreased from 57.4 % to 35.3 % with the increase in pyrolysis temperature from 300 to 700 ℃. Heavy metal(loid)s (chromium, manganese, iron, copper, zinc, arsenic and lead) were mainly bound in the biochar produced at 300 ℃, while the recovery decreased substantially with the increase of pyrolysis temperature. Phenols, carboxylic acids and alcohols were the dominant compounds in all bio-oil samples. This study suggested further requirements of biochar quality and environmental risk assessment to provide a safe and value-added way of phytoextraction residual applications

Investigating the effect of Cu/zeolite on deoxygenation of bio-oil from pyrolysis of pine wood

Pyrolysis is one of the significant technologies that can utilize lignocellulose biomass to produce different bioenergy fuels, such as bio-oil, pyrolytic gases and bio-char. The application of pyrolysis has been extensively studied to produce bio-oil, which is foreseen as the potential transportation fuel in the near future. However, the presence of oxygenated compounds, such as phenols and alcohols in bio-oil makes it highly acidic and unstable for a suitable transportation fuel. These oxygenated compounds can be converted to refinable hydrocarbons by using different catalysts. Therefore, this study aimed to prepare a catalyst that is Cu10%-zeolite and investigated its deoxygenation activity for bio-oil produced from pyrolysis of pine wood sawdust. The catalyst was prepared by a wet-impregnation method. Subsequently, the catalyst was characterized by X-ray diffraction and transmission electron microscopy. Furthermore, the catalyst was applied for in-situ (catalyst: biomass=5) and ex-situ catalytic pyrolysis (catalyst: biomass=3) and the results were compared with those from sole zeolite support. The pyrolysis process was carried out at a heating rate of 100 °C/min to a final temperature of 700 °C and the composition of bio-oil was examined by gas chromatography-mass spectroscopy. The results revealed that Cu-zeolite showed significant deoxygenation activity for bio-oil as compared to zeolite or without any catalyst. Evidently, Cu-zeolite after in-situ pyrolysis produced bio-oil with 20.9% aromatic hydrocarbons and 7.5% aliphatic hydrocarbons, which were approximately 80% and several times higher than with only zeolite, respectively. Meanwhile the concentration of alcohols was reduced from 47.5% to 5%. On the other hand, bio-oil produced from ex-situ catalytic pyrolysis was enriched with 41.6% aromatic hydrocarbons while only 1% alcohols were present in bio-oil. This promising deoxygenation activity can be ascribed to Cu-zeolite’s catalytic activity that converted phenol and alcohols to refinable hydrocarbons via various reactions, such as dehydration, decarboxylation and decarbonylation

Supramolecular drug inclusion complex constructed from cucurbit[7]uril and the hepatitis B drug Adefovir

The interaction between cucuribit[7]uril (Q[7]) and Adefovir (ADV) has been studied in aqueous solution by 1H NMR spectroscopy, electronic absorption spectroscopy, Isothermal Titration Calorimetry and mass spectrometry. The results revealed that an inclusion complex was formed via encapsulation of the purine rings of the guest ADV, while the phosphonomethoxyethyl group was prevented from entering the cavity. ITC data revealed that the formation of this 1:1 inclusion complex is mainly driven by favourable enthalpy changes. Studies investigating the release of ADV from the inclusion complex revealed enhanced rates under acidic conditions, although the rates were slower than observed for the free guest under the same conditions. Thermal stability studies indicated that the included form of ADV was more stable that the free form

A hemicyanine and cucurbit[n]uril inclusion complex: competitive guest binding of cucurbit[7]uril and cucurbit[8]uril

The interaction between the hemicyanine indole derivative H and the cucubit[n]urils Q[7] and Q[8] has been studied using 1H NMR and UV spectroscopy as well as by fluorescence experiments. Competitive studies on the inclusion of H by Q[7] and Q[8] have also been conducted, and reveal that on changing the size of the Q[n] cavity, the binding behaviour can be very different