Drying cellulose triacetate in a dryer with a vibrational fluidized bed

Conclusions The process of drying cellulose triacetate in a vibrating bed has been studied.For final drying of cellulose triacetate before solution, it is recommended to use an industrial specimen of a unit with a vibrating bed having a capacity of 2700 kg/h.This assembly can be used to dry other fibre-forming disperse polymeric materials containing strongly bound moisture.Translated from Khimicheskie Volokna, No. 3, pp. 49–51, May–June, 1984.     

N.m.r. line shape-relaxation correlation analysis of bitumen and oil sands

The first results of the analysis of bitumen and oil sands using the recently developed n.m.r. spingrouping technique are presented. The n.m.r. relaxation experiments were carried out on bitumen, and on natural and dried oil sands samples. The results indicate that the spin-grouping can resolve and quantify several components of the samples studied. The bitumen and bitumen fraction of the oil sands are resolved according to their spin-spin relaxation times into three major groups: solid-like (rigid), solid-like (mobile) and semi-liquid. The water in the oil sands exists in two different environments. Tentatively one environment is assigned to be the bridges between the sand grains, while the other is assigned to be the clay surface. One can conclude that with spin grouping of complex mixtures the decomposition (in which components are resolved according to their dynamic state) is possible. The accuracy of such resolution is of the order of a few per cent.     

Effect of process distillation on mutagenicity and cell-transformation activity of solvent-refined,coal-derived liquids

Blended SRC-II process streams, representing a full boiling range distillate material, were fractionally distilled into non-overlapping 50 °F cuts with boiling points between 300 and 850 °F. Another set of 18 distillate cuts were obtained with boiling points ranging between 138 and 1055 °F. Distillate cuts were assayed for mutagenic activity using the histidine reversion assay with Salmonella typhimurium strains TA98, TA100, TA1535 and TA1537, as well as for mammalian-cell transformation activity in the Syrian hamster embryo test, and DNA damage in the prophage induction assay. Samples were also separated into chemical class fractions by alumina column chromatography and analysed by high resolution gas chromatography so that the chemical composition of the cuts could be related to their relative activity in the different assays. In the mammalian cell transformation and microbial mutagenicity assays, significant activity was found almost exclusively in distillate cuts with components boiling > 700 °F, with the highest activity in the transformation assay observed for cuts > 800 °F. All of the distillate cuts showed increased levels of DNA damage as expressed by lambda prophage induction in Escherichia coli 8177. However, the greatest activity was associated with distillate cuts with boiling points in the 800 °F + range. Chemical analysis of the 50 °F distillate cuts showed a variety of polycyclic aromatic hydrocarbons (PAH) and amino-PAH compounds to be present in the distillate cuts boiling > 700 °F and essentially absent from cuts boiling < 700 °F. The sample set of non-overlapping (50 °F) cuts were reblended according to the proportions of each cut found in the original blend material. These reblended composites were then assayed to compare their activity with that predicted from the activities of the component distillate cuts. The reblending experiments indicated the microbial mutagenicity response was essentially additive. Mammalian cell transformation activities were non-additive, indicating a compositional effect on the expression of transforming agents in the complex mixture.     

Summary of discussion on ‘Sciences related to pitch and coke usage in carbon manufacture’

This article is a brief summary of the Discussion session held after the presentation of the preceding papers at the conference organized by the Industrial Carbon and Graphite Group of the Society of Chemical Industry, London, March 1984.     

Effect of catalysts on the reaction between a cycloaliphatic diisocyanate (H-MDI) and n-butanol

Kinetics of the reaction between bis(4-isocyanatocyclohexyl)methane, H-MDI, and n-butanol was studied in toluene at 100°C. Effects of various catalysts, such as Hg(CH₃COO)₂, Zn(CH₃COO)₂ · 2H₂O, SnCl₄ · 5H₂O, and dibutyltindilaurate on the reaction rate and kinetics were also investigated. Reactions were followed by determining the unreacted isocyanate as a function of reaction time, using the standard dibutylamine back titration method. All catalysts seem to be very effective in increasing of the rate of the reaction compared to the uncatalyzed system. Depending on the initial stoichiometric ratio of (NCO) and (OH) and the concentration of the catalyst used, it seems possible to have preferential catalysis of the primary reaction between (NCO) and (OH) over the side reactions.     

Formation and Properties of Calcium Aluminosilicate Glasses

The glass-forming region for calcium aluminosilicate glasses has been determined. A number of properties of these glasses (thermal expansion coefficient, glass transformation and dilatometric softening temperature, and refractive index) have been studied. The results of these measurements suggeq that the structures of these glasses may not as closely resemble those of alkali aluminosilicate glasses as is commonly assumed. Evidence is presented which suggests that the binary calcium aluminate glasses may be phase separated.     

Phase Studies Concerning Sintering in Aluminas Doped with Ti4+

Previous solid state analyses of sintering in Ti⁴⁺-doped-commercial alumina are shown to be in error because a liquid phase exists in the appropriate region of the Al₂O₃−TiO₃−Na₂Ophase diagram at least by 1350^°C, a temperature lower than that at which "solid state" studies were conducted. It is suggested that liquid-phase sintering is a much more common occurrence than was realized formerly.     

Physical and chemical characteristics of butterfat fractions obtained by crystallization from molten fat

Both summer and winter butterfats were fractionated using a laboratory procedure which was designed to simulate a commercial fractionation process. The process is based on a slow, controlled cooling of the melted fat, a short stabilization time at the fractionation temperature, and separation of the crystals from the liquid oil by vacuum filtration using a stainless steel perforated disc. Fractionation temperatures of 29, 26, 23 and 19 C for winter butterfat and 29 and 19 C for summer butterfat were used to obtain solid and liquid fractions at each temperature. Three replications at each temperature showed good reproducibility of results. The fractions were characterized by their fatty acid and triglyceride compositions, melting and crystallization behavior, iodine value, peroxide value and melting point. Presented at the AOCS meeting in Philadelphia in May 1985.