Search results for "Molar mass"
showing 10 items of 239 documents
Role of lignin and sodium carbonate on the swelling behavior of black liquor droplets during combustion
2018
AbstractA partial removal of lignin from black liquor (BL) by carbonation and lignin precipitation was studied. In lignin-lean BL droplets during combustion in a laboratory furnace at 800°C in stagnant air, the maximum swelling was decreased. This observation was interpreted as showing that the lignin content decrement is due mainly to removal of higher molar mass (HMM) lignin and that the Na2CO3content of the BL is increased. Stepwise precipitation experiments with industrial softwood and hardwood kraft BLs by carbonation (resulting in pH decrement from 13 to 9) indicated that a fraction of HMM lignin (MM >10 kDa) with a higher amount of carbohydrates precipitated more prominently and e…
Chemometric Study on Alkaline Pre-treatments of Wood Chips Prior to Pulping
2016
Alkaline pre-treatments were performed for the production of organics-containing effluents from silver/white birch (Betula pendula/pubescens) and Scots pine (Pinus sylvestris) chips prior to chemical pulping. Pre-treatment conditions were varied with respect to time (from 30 min to 120 min), temperature (130 °C and 150 °C), and alkali charge (1, 2, 3, 4, 6, and 8% of NaOH on oven-dried wood). The analytical data (total content, weight average molar mass, and molar mass distribution) on dissolved lignin were subjected to principal component analysis to examine the relationship between molar mass and molar mass distributions in lignin removed from different wood species under varying alkaline…
A critical evaluation of Amicon Ultra centrifugal filters for separating proteins, drugs and nanoparticles in biosamples
2015
Amicon(®) Ultra centrifugal filters were critically evaluated for various sample preparations, namely (a) proteome fractionation, (b) sample cleanup prior to liquid chromatography mass spectrometry (LC-MS) measurement of small molecules in cell lysate, and (c) separating drug-loaded nanoparticles and released drugs for accurate release profiling in biological samples. (a) Filters of supposedly differing molar mass (MM) selectivity (10, 30, 50 and 100K) were combined to attempt fractionation of samples of various complexity and concentration. However, the products had surprisingly similar MM retentate/filtrate profiles, and the filters were unsuited for proteome fractionation. (b) Centrifuga…
Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminum Alkyls, 6. Polymerization of Primary and Tertiary Acrylates
1998
The kinetics of the polymerization of n-butyl acrylate initiated by lithiated ester enolates in the presence of aluminum alkyls was investigated in toluene and in toluene/Lewis base mixed solvents at −78 °C. In pure toluene, curved time−conversion plots, incomplete monomer conversion, and broad molecular weight distributions (Mw/Mn ≈ 2) are observedin the absence of aluminum alkyls the molecular weight distributions are significantly broader (Mw/Mn > 14). High monomer conversions and narrower molecular weight distributions (Mw/Mn ≈ 1.5) are obtained when using Lewis bases (e.g., methyl pivalate) as cosolvents. The polymerization of tert-butyl acrylate rapidly reaches full monomer conversion…
Kinetics and mechanism of group transfer polymerization of N-butyl acrylate catalyzed by Hgl2 /(CH3 )3 Sil in toluene
1994
The group transfer polymerization (GTP) of n-butyl acrylate (nBuA) using 1-methoxy-1-(trimethylsiloxy)-2-methyl-1-propene (MTS) as an initiator, mercuric iodide (HgI2) as a catalyst in toluene at room temperature gives a very good control of molecular weight and narrow molecular weight distribution. (Mw/Mn < 1.2). Kinetic studies in this system reveal that this reaction is rather slow, half-lives being in the range of hours. The kinetic order of the apparent rate constant of propagation with respect to initiator and catalyst concentrations were found to be near to unity. However, the first-order time-conversion plots exhibit considerable induction periods. Upon addition of trimethylsilyl io…
Adsorptionseffekte als Fehlerquellen bei Lichtzerstreuungsmessungen
1956
Es werden die Einflusse der Adsorption von Hochpolymeren aus den Losungen auf Lichtzerstreuungsmessungen untersucht. Zunachst wird die Adsorption aus Losung an Glaswolle und Glaspulver in verschiedenen Losungsmitteln gemessen. Es zeigt sich, das sowohl Konzentrationserniedrigung, bestimmt im Differentialrefraktometer, wie auch eine Abnahme des Molekulargewichtes, aus der Lichtzerstreuung bestimmt, infolge selektiver Adsorption auftreten. Beim Schutteln der Losungen tritt als weiterer Effekt ein Abbau der Kettenmolekule ein. Beim Filtrieren von Losungen nehmen durch Adsorption im Filter Konzentration und Molekulargewicht ab. Die Abnahme wachst mit der Feinheit des Filters, d. h. mit seiner O…
Accelerated Solvent Extraction and Pulsed Electric Fields for Valorization of Rainbow Trout (Oncorhynchus mykiss) and Sole (Dover sole) By-Products: …
2021
Fishery by-products are rich in biologically active substances and the use of green and efficient extraction methods to recover these high-added-value compounds is of particular importance. In this study, head, skin and viscera of rainbow trout and sole were used as the target matrices and accelerated solvent extraction (ASE) (45–55 °C, 15 min, pH 5.2–6.8, 103.4 bars) and pulsed electric fields (PEF) (1–3 kV/cm, 123–300 kJ/kg, 15–24 h) were applied as extraction technologies. The results showed that ASE and PEF significantly increased the protein extract efficiency of the fish by-products (p < 0.05) by up to 80%. SDS-PAGE results showed that ASE and PEF treatments changed the molecular size…
Continuous fractionation of poly[(dimethylimino)decamethylene bromide] and molecular weight dependence of the glass transition
1995
30 g of the ionene poly[(dimethylimino)decamethylene bromide] were fractionated by a continuous counter-current extraction method (CPF) using ethylene glycol monoethyl ether as the solvent and diisopropyl ether as the non-solvent component. The efficiency of the separation was checked by viscometry and gel-permeation chromatography (GPC) measurements. Eight fractions of different molar mass were prepared for differential scanning calorimetry (DSC) experiments. With bromide as counter-ion, the glass transition temperature of the ionene increases from ca. 60 to 85°C as the intrinsic viscosity of this material (in 0,4 M aqueous solutions of KBr at 25°C) rises from ca. 14 to 22 mL/g. When bromi…
The use of utraviolet-visible spectrophotometry in the determination of average properties of nonylphenol ethylene oxide condensates
1983
Ultraviolet spectrophotometry is usd in the determination of average molecular weight (M), average degree of polymerization (X), the hydrophilic-lipophilic balance (HLB) and ethylene oxide percentage of nonylphenol ethylene oxide condensates. The method is based on determination of the absorptivity a, expressed in g lt-1 cm−1, from the absorbances measured at 275 nm for a series of dilutions of an aqeuous ethanolic solution (60:40, v/v/) of a given product, followed by numerical interpolation of this value in the expression a = f(HLB), log a = f(log M), and log a = f(log X). These expressions are obtained from reference samples or samples previously analyzed. The proposed method gives relat…
Membranes Directly Prepared from Solutions of Unsubstituted Cellulose
2005
Summary: Starting from 5 wt.-% solutions of a prehydrolysis kraft pulp ( = 135 kg · mol−1) in the mixed solvent (dimethylacetamide + 7 wt.-% LiCl) we have prepared cellulose membranes on different supports according to the phase inversion process using above all acetone (AC) and 2-propanol as precipitants. In this context we have studied the phase behavior of the quasiternary system (DMAc+LiCl)/AC/cellulose. The obtained membranes are mechanically stable and in their mechanical and separation properties on the whole comparable to membranes consisting of regenerated cellulose. With respect to gas separation the ideal selectivity of CO2 in combination with N2 and O2 turns out to be opposite f…