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Solid-acid catalysts functionalized with catalytic groups have attracted intense interest for converting cellulose into soluble products. However, design of solid-7 acid catalysts has been guided by molecular level interactions and the actual mechanism of cellulose-solid-acid catalyst particles adsorption remains unknown. Here, colloidal stability theory, DLVO, is used to rationalize the design of solid acids for targeted cellulose adsorption. In nearly all cases, an energy barrier, arising from electrostatic repulsion and much larger than the energy associated with thermal fluctuations, prevents close contact between the solid acid and cellulose. Polymer-based solid-acid substrates such as polystyrene and Nafion are especially ineffective as their interaction with cellulose is dominated by the repulsive electrostatic force. Carbon and metal oxides have potential to be effective for cellulose-solid-acid interaction as their attractive van der Waals interaction can offset the repulsive electrostatic interaction. The effects of reactor temperature and shear force were evaluated, with the finding that reactor temperature can minimize the catalyst-cellulose interaction barrier, promoting coagulation, but that the shear force in a typical laboratory reactor cannot. We have evaluated strategies for enhancing cellulose-catalyst interaction and conclude that raising reaction temperature or synthesizing acid/base bifunctional catalysts can effectively diminish electrostatic repulsion and promote cellulose-catalyst coagulation. The analysis presented here establishes a rational method for designing solid acid catalysts for cellulose hydrolysis.

Aluminium-selective ion optical sensor based on covalently attached lumogallion methacrylate was synthesized and investigated in this study. Lumogallion based derivatives were copolymerized with various methacrylate monomers via a simple one step free radical polymerization to produce a "self-plasticized" copolymer. We demonstrate that covalently attached lumogallion moieties provide adequate functionality to the optical film thus achieving a very simple, one component sensing membrane. Fluorescence experiments demonstrated excellent sensitivity towards aluminium (III) ions with the detection limits found at 4.8 × 10 -12  M. Furthermore, proposed sensor displays high selectivity towards aluminium over a number of biologically relevant cations. Moreover, the synthesized copolymer was used for the fabrication of nanoparticles that exhibit strong fluorescence upon contact with aluminium (III) ions. It is anticipated that lumogallion-based copolymers may form the basis for the development of highly sensitive and robust aluminium selective sensors capable of in situ measurements., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Although IUPAC has recommended a probabilistic approach to determining limit of detection (LOD) based on false-positive and false-negative rates for more than 20 years, the LOD definition for ion-selective electrodes (ISEs) long predates these recommendations and conflicts substantively with them. Although it is well known that the ISE LOD definition does not follow best practice, it continues to be used due to simplicity and a lack of available methods for estimating LOD for nonlinear sensors. Here, we use ISEs as a model system for estimation of LOD for nonlinear sensors that is consistent with broad IUPAC recommendations and justified using statistical theory. Using freely available software, the new approach and updated definition is demonstrated through theory, simulation, and an environmental application. The results show that the current LOD definition for ISEs performs substantially worse than the proposed definition when assessed against IUPAC recommendations, including ignoring sensor noise and LOD uncertainty, leading to bias of an order of magnitude or more. Further, the environmental application shows that the new definition, which includes estimates of LOD uncertainty, allows more objective assessment of sensor response and fitness for purpose. The growing demand for ultrasensitive sensors that operate in complex matrices has pushed the boundaries of traditional calibration approaches. These sensors often operate near their limit of detection (LOD), with additional challenges created if their response is nonlinear. These challenges are amplified when assessing new sensors, since they may be less reproducible and noisier than benchmark techniques.

Novel solid-contact iodide-selective electrodes based on covalently attached 1,2,3 triazole ionic liquid (IL) were prepared and investigated in this study. Triazole-based IL moieties were synthesized using click chemistry and were further copolymerized with lauryl methacrylate via a simple one-step free radical polymerization to produce a "self-plasticized" copolymer. The mechanical properties of the copolymer are suitable for the fabrication of plasticizer-free ion-selective membrane electrodes. We demonstrate that covalently attached IL moieties provide adequate functionality to the ion-selective membrane, thus achieving a very simple, one-component sensing membrane. We also demonstrate that the presence of iodide as the counterion in the triazole moiety has direct influence on the membrane's functionality. Potentiometric experiments revealed that each electrode displays high selectivity toward iodide anions over a number of inorganic anions. Moreover, the inherent presence of the iodide in the membrane reduces the need for conditioning. The nonconditioned electrodes show strikingly similar response characteristics compared to the conditioned ones. The electrodes exhibited a near Nernstian behavior with a slope of -56.1 mV per decade across a large concentration range with lower detection limits found at approximately 6.3 × 10(-8) M or 8 ppb. These all-solid-state sensors were utilized for the selective potentiometric determination of iodide ions in artificial urine samples in the nanomolar concentration range.

For organic semiconductors to find ubiquitous electronics applications, the development of new materials with high mobility and air stability is critical. Despite the versatility of carbon, exploratory chemical synthesis in the vast chemical space can be hindered by synthetic and characterization difficulties. Here we show that in silico screening of novel derivatives of the dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]thiophene semiconductor with high hole mobility and air stability can lead to the discovery of a new high-performance semiconductor. On the basis of estimates from the Marcus theory of charge transfer rates, we identified a novel compound expected to demonstrate a theoretic twofold improvement in mobility over the parent molecule. Synthetic and electrical characterization of the compound is reported with single-crystal field-effect transistors, showing a remarkable saturation and linear mobility of 12.3 and 16 cm(2) V(-1) s(-1), respectively. This is one of the very few organic semiconductors with mobility greater than 10 cm(2) V(-1) s(-1) reported to date.

(1)H MAS solid-state NMR methods are applied to elucidate the conduction mechanism of an anhydrous proton conducting triazole-functionalized polysiloxane. At temperatures below T = 260 K, hydrogen bonding between neighboring heterocycles is observed and a dimer formation can be excluded. From the temperature dependence of (1)H MAS NMR spectra, different dynamic processes of the triazole ring contributing to the proton conduction process are qualitatively and quantitatively analyzed and detailed insight into the conduction mechanism and temperature-dependent structural changes is obtained. Although the dynamics processes on the molecular level are qualitatively in good agreement with the findings from macroscopic conductivity measurements, temperature-dependent factors on mesoscopic scales beyond the local molecular mobility influence the macroscopic conductivity and hamper quantitative interpretation.