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.     

Chemical changes in polyvinyl fluoride during the process of fibre-spinning

Conclusions The change in some properties of polyvinyl fluoride during the process of fibre spinning has been investigated.It has been found that during the process of converting PVF powder into fibre, the degree of polymer crystallinity plus its resistance to thermal and thermooxidative degradation is increased; depending on the spinning regime, the densities and physicomechanical properties of PVF fibres are different.Translated from Khimicheskie Volokna, No. 4, pp. 34–35, July–August, 1984.     

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.     

Coal liquefaction using a hydrogenated creosote oil solvent: H-atom transfer from hydrogen donor components in the solvent

The presence of hydroaromatic, hydrogen donor components in a coal-derived solvent is one of the more important factors in the successful operation of a non-catalytic coal liquefaction process. Various hydrogen donor species present in a hydrogenated creosote oil have been identified. Their rate of disappearance under conditions that are consistent with a short residence time coal liquefaction process has been used to rank the reactivities of the various hydrogen donors. 1,2,3,10b-Tetrahydrofluoranthene was found to be an exceptional donor while 4,5-dihydropyrene, the hexahydropyrenes and 9,10-dihydrophenanthrene were found to be quite active. Sym.-octahydrophenanthrene and 2a,3,4,5-tetrahydroacenaphthene exhibited moderate activity. Tetralin and the four methyltetralin isomers were found to be unreactive under the coal liquefaction conditions employed.     

Unsaturated polyesters. II. Structure and properties of polyester resins based on cinnamylsuccinic acid

Unsaturated Polyester resins were prepared by the reaction of cinnamylsuccinic acid with saturated diols, namely, ethylene, diethylene, propylene, dipropylene, tetramethylene, and hexamethylene glycols, and the unsaturated diols, namely, 1,4-butene- and 1,4-butynediols. All the polyester resins obtained have been characterized and were found to cure with styrene, with relatively low conversions. The properties of the cured polyesters in the form of films were determined. IR and ¹H-NMR spectroscopy were used for both qualitative and quantitative analyses of the polyesters and their hydrolyzate products, after curing with styrene.