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Abstract: The conceptual design of a coal gasification system for the production of hydrogen is undertaken here using the PRO-II Simulation program. The operating conditions for the gasifier were tuned to between 1200 °C–1500 °C, 15 atm–30 atm and to a feed molar ratio of C:H2O:O2 = 1:0.5–1:0.25–0.5. The refinery temperature and pressure were kept at 550 °Cand 24.5 atm. The syngas produced goes to water gas shift (WGS) reactors operated at 400 °C, 24 atm (HTS) and 250 °C, 23.5 atm (LTS). The production of hydrogen was found to be independent of the concentration of steam in the feed. However, when other operating conditions are constant, the hydrogen output changes dramatically with changes to the concentration of O2 in the feed. The optimal operating conditions for the production of hydrogen by the gasification of Drayton coal were found to be: 1500 °C, 25 atm and a feed ratio C:H2O:O2 = 1:0.58:0.43. [ABSTRACT FROM AUTHOR]

The purpose of this research was to assess the acylation reactions of peptides, salmon calcitonin (sCT), human parathyroid hormone 1–34 (hPTH1–34) and leuprolide, in poly(lactic-co-glycolic acid) (PLGA) microspheres. Capillary electrophoresis (CE) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) were used for determining and monitoring peptide acylation and quantitating acylation products in the degrading PLGA microspheres. In the degrading PLGA microspheres of sCT and hPTH1–34, the acylation products were observed and determined to be adducts with glycolic acid units from degradable PLGA polymer by MALDI-TOF MS. In the microsphere of leuprolide, however, the acylation product was not observed even after 28 days of incubation at the release medium, which represents the different stabilities among peptides according to the primary structure. As the leuprolide contains tyrosine and serine having hydroxyl group of nucleophilic amino acids, the acylation reaction of peptide is shown to be mainly due to the primary amino groups of N-terminus or lysine residue. The complementary use of CE and MALDI-TOF MS will be useful for searching the counter measures as well as determining the peptide acylation in the manufactured formulations on the market. [Copyright &y& Elsevier]

• Propose a new water lean amine solvent for CO 2 capture. • The low regeneration energy of K 2 Sol is demonstrated through pilot plant operation. • K 2 Sol presents superior performances about cyclic capacity and thermal stability. • GPBO is used as a new way to optimize operating conditions in pilot-scale testing. • K 2 Sol requires only 65% of regeneration energy of MEA. The development of new amine solvents without the major drawbacks of conventional amines is crucial to industrial applications of CO 2 capture. This paper presents a water-lean CO 2 capture solvent having a low regeneration energy and low degradation. The water-lean solvent, K 2 Sol, is a sterically hindered diamine; because of the hindered amine site, K 2 Sol easily forms bicarbonate, resulting in a high absorption capacity. The minimum solvent regeneration energy is obtained using Gaussian process Bayesian optimization (GPBO) and bench-scale pilot plant experiments. GPBO finds the optimal solution using the input and output relationship of experiments; thus, expensive first-principle model construction can be avoided. According to the pilot plant experiment, the optimal regeneration energies of monoethanolamine (MEA) and K 2 Sol are 4.3 and 2.8 GJ/t CO 2 , respectively, indicating that K 2 Sol requires only 65% of the regeneration energy of MEA. Fewer than 30 experiments are required to find the optimal pilot plant operation for both the MEA and K 2 Sol experiments. We also describe the superior properties of K 2 Sol in terms of the CO 2 loading, cyclic capacity, regeneration temperature, and degradation. [ABSTRACT FROM AUTHOR]

• We studied flocculation of microalgae- and clay-containing suspensions. • Investigations were done in different microalgal growth phases. • A two-class flocculation kinetic model and Bayesian calibration were applied. • Effect of organic matter secreted by algae on flocculation kinetics was evaluated. • Distinct flocculation mechanisms were identified in different microalgal growth phases. Interplays between microalgae and clay minerals enhance biologically mediated flocculation, thereby affecting the sedimentation and transportation of suspended particulate matter (SPM) in water and benthic environments. This interaction forms larger flocs with a higher settling velocity and enhances SPM sinking. The aim of this study was to investigate the flocculation kinetics of microalgae and clay in suspension and to elucidate the mechanisms associated with such interactions. Standard jar test experiments were conducted using various mixtures of kaolinite and microalgal samples from batch cultures (Chlorella vulgaris) to estimate biologically mediated flocculation kinetics. The organic matter (OM) composition secreted by the microalgae was characterized using a liquid chromatography - organic carbon detection system, and quantitative analysis of transparent exopolymer particles was conducted separately. A two-class flocculation kinetic model, based on the interaction between flocculi and flocs, was also adopted to quantitatively analyze the experimental data from flocculation. Results from the flocculation kinetic tests and OM analyses, in association with other data analyses (i.e., floc size distribution and flocculation kinetic model), showed that flocculation increased with OM concentration during the growth phase (10–20 d). However, on day 23 during the early stationary phase, flocculation kinetics started decreasing and substantially declined on day 30, even though the amount of OM (mainly biopolymers) continued to increase. Our results indicate that an adequate quantity of biopolymers produced by the microalgal cells in the growth phase enhanced floc-to-floc attachment and hence flocculation kinetics. In contrast, an excessive quantity of biopolymers and humic substances in the stationary phase enhanced the formation of polymeric backbone structures and flocculation via scavenging particles but simultaneously increased steric stabilization with the production of a large number of fragmented particles. [Display omitted] [ABSTRACT FROM AUTHOR]

Abstract: The solubility of carbon dioxide in room temperature ionic liquids (RTILs), dialkylimidazolium dialkylphosphates, was measured at 313–333K and at pressures close to atmospheric pressure, from which Henry''s law coefficients, standard Gibbs free energy, enthalpy, and entropy changes of solvation were derived. The CO2 solubility in the dialkylimidazolium dialkylphosphate was found to increase with increasing chain length of the alkyl groups on the cation and/or the anion as was similarly found in other RTILs. Among various dialkylimidazolium dialkylphosphates tested, 1-ethyl-3-methylimidazolium diethylphosphate ([EMIM][Et2PO4]) and 1-butyl-3-methylimidazolium dibutylphosphate ([BMIM][Bu2PO4]) exhibited the comparable or better capability of dissolving CO2 in comparison with that of [BMIM][BF4], but their absorption capacities were still lower than that of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM][Tf2N]). [Copyright &y& Elsevier]