Solvents history

Generally, with careful attention to coal history, solvent history, and solvent properties, the solvent extraction of coal may be a useful technique for application to coal science. Studies of the extraction process itself and the related solvent swelling can provide insights into coal matrix structure only with careful, well thought out, and reproducible analyses. The data may also provide detailed and valuable information about the chemical species present in both extract and raw coal. 

WAXS data for as-cast blends showed that crystal melting peaks for PCL (relative to PCL contents) were nearly constant there was a small increase in crystallinity on addition of CAB in line with DSC data. On thermal cycling to 237 °C there was a massive loss of PCL crystallinity as solvent history was lost and the blend took on its own properties, consistent with DSC and differential thermal analysis data. It was noted that in as-cast blends one of the crystal diffraction peaks decreased in relative intensity. This effect was attributed (possibly) to distortion of unit cell dimensions, an effect found elsewhere in paracrystalUne materials. 

Throughout the history of the development of fats and oils, many wet chemical methods have been developed to assess the quaUty of the raw materials and products. As sophisticated instmmentation develops, many of the wet methods are being replaced. Particular attention is being given to methods that eliminate the use of solvents which cause an environmental disposal problem. Many in-line sensors are also being developed to allow corrections of critical parameters to be made more quickly in the process. 

Most by-product acetylene from ethylene production is hydrogenated to ethylene in the course of separation and purification of ethylene. In this process, however, acetylene can be recovered economically by solvent absorption instead of hydrogenation. Commercial recovery processes based on acetone, dimetbylform amide, or /V-metby1pyrro1idinone have a long history of successfiil operation. The difficulty in using this relatively low cost acetylene is that each 450, 000 t/yr world-scale ethylene plant only produces from 7000 9000 t/yr of acetylene. This is a small volume for an economically scaled derivatives unit. 

A crystalline or semicrystalline state in polymers can be induced by thermal changes from a melt or from a glass, by strain, by organic vapors, or by Hquid solvents (40). Polymer crystallization can also be induced by compressed (or supercritical) gases, such as CO2 (41). The plasticization of a polymer by CO2 can increase the polymer segmental motions so that crystallization is kinetically possible. Because the amount of gas (or fluid) sorbed into the polymer is a dkect function of the pressure, the rate and extent of crystallization may be controUed by controlling the supercritical fluid pressure. As a result of this abiHty to induce crystallization, a history effect may be introduced into polymers. This can be an important consideration for polymer processing and gas permeation membranes. 

World capacity and demand for tetrachloroethylene were approximately 1100 and 845 thousand metric tons ia 1974, respectively. Although demand iacreased iato the mid-1980s, siace then demand for tetrachloroethylene has decreased significantly as a result of the phaseout of chlorofluorocarbons, the use of more efficient dry-cleaning equipment, and iacreased reclamation of waste solvent. World capacity and demand as of 1988 are provided ia Table 2 Several United States manufacturers have shut down faciUties ia the last fifteen years. Current manufacturers and their capacities are Hsted ia Table 3. United States production and sales history is shown ia Table 4. 

Latex Adhesive Applications. Polychloroprene latex adhesives have a long history of use in foil laminating adhesives, facing adhesives, and constmction mastics. Increasingly stringent restrictions on the emission of photoreactive solvents has heightened interest in latex compounds for broader apphcations, particularly contact bond adhesives. Table 10 makes a general comparison of solvent and latex contact bond adhesives (158). 

H. T. Kohlbrand, Case History of a Deflagration Involving an Organic Solvent/Oxygen System Below its Flash Point, Paper presented at AlChE Loss Prevention Symposium, San Diego, Aug. 1990. 

Ionic liquids may be viewed as a new and remarkable class of solvents, or as a type of materials that have a long and useful history. In fact, ionic liquids are both, depending on your point of view. It is absolutely clear though, that whatever ionic liquids are, there has been an explosion of interest in them. Entries in Chemical Abstracts for the term ionic liquids were steady at about twenty per year through 1995, but had grown to over 300 in 2001. The increased interest is clearly due to the realization that these materials, formerly used for specialized electrochemical applications, may have greater utility as reaction solvents. 

The early history of ionic liquid research was dominated by their application as electrochemical solvents. One of the first recognized uses of ionic liquids was as a solvent system for the room-temperature electrodeposition of aluminium [1]. In addition, much of the initial development of ionic liquids was focused on their use as electrolytes for battery and capacitor applications. Electrochemical studies in the ionic liquids have until recently been dominated by work in the room-temperature haloaluminate molten salts. This work has been extensively reviewed [2-9]. Development of non-haloaluminate ionic liquids over the past ten years has resulted in an explosion of research in these systems. However, recent reviews have provided only a cursory look at the application of these new ionic liquids as electrochemical solvents [10, 11]. 

Figure 7 Effect of shearing history on swelling ratio for HP LDPE sample (A) Brabender worked at 190°C (A) solvent treated sample. Source Ref. 39.

Polylactides, 18 Poly lactones, 18, 43 Poly(L-lactic acid) (PLLA), 22, 41, 42 preparation of, 99-100 Polymer age, 1 Polymer architecture, 6-9 Polymer chains, nonmesogenic units in, 52 Polymer Chemistry (Stevens), 5 Polymeric chiral catalysts, 473-474 Polymeric materials, history of, 1-2 Polymeric MDI (PMDI), 201, 210, 238 Polymerizations. See also Copolymerization Depolymerization Polyesterification Polymers Prepolymerization Repolymerization Ring-opening polymerization Solid-state polymerization Solution polymerization Solvent-free polymerization Step-grown polymerization processes Vapor-phase deposition polymerization acid chloride, 155-157 ADMET, 4, 10, 431-461 anionic, 149, 174, 177-178 batch, 167 bulk, 166, 331 chain-growth, 4 continuous, 167, 548 coupling, 467 Friedel-Crafts, 332-334 Hoechst, 548 hydrolytic, 150-153 influence of water content on, 151-152, 154... 

In a case-control study of pesticide factory workers in Brazil exposed to methyl parathion and formulating solvents, the incidence of chromosomal aberrations in lymphocytes was investigated (De Cassia Stocco et al. 1982). Though dichlorodiphenyltrichloroethane (DDT) was coformulated with methyl parathion, blood DDT levels in the methyl parathion-examined workers and "nonexposed" workers were not significantly different. These workers were presumably exposed to methyl parathion via both inhalation and dermal routes however, a dose level was not reported. The exposed workers showed blood cholinesterase depressions between 50 and 75%. However, the baseline blood cholinesterase levels in nonexposed workers were not reported. No increases in the percentage of lymphocytes with chromosome breaks were found in 15 of these workers who were exposed to methyl parathion from 1 week to up to 7 years as compared with controls. The controls consisted of 13 men who had not been occupationally exposed to any chemical and were of comparable age and socioeconomic level. This study is limited because of concomitant exposure to formulating solvents, the recent history of exposure for the workers was not reported, the selection of the control group was not described adequately, and the sample size was limited. 

In November 1997, Ferrari (France) invited Solvay to help them to solve a problem of recycling PVC coated textile for light mobile structures, especially ones used for shortterm applications (advertising). The Vinyloop is aphysical recycling process making use of an organic solvent to separate the PVC compound from the other materials in a PVC composite. It is a closed loop process the solvent is completely recycled. Aspects outlined include history and a description of the process, precipitated PVC compound evaluation and financial data... 

This very truncated survey of the history of the study of ligand substitution studies brings us to the present and the question of future directions. Although this review predominantly deals with solvent exchange and monodentate ligand substitution processes, the ideas ex-... 

If the solute is heat sensitive, and can be extracted in to a lower boiling solvent, to reduce the heat history during recovery. 

The divalent Co(salen) complex (69a) is one of the most versatile and well-studied Co coordination compounds. It has a long and well-documented history and we shall not restate this here. Recent applications of (69a) as both a synthetic oxygen carrier and as a catalyst for organic transformations are described in Sections 6.1.3.1.2 and 6.1.4.1 respectively. Isotropic shifts in the HNMR spectrum of low-spin Co(salphn) (69b) were investigated in deuterated chloroform, DMF, DMSO, and pyridine.319 Solvent-dependent isotropic shifts indicate that the single unpaired electron, delocalized over the tetradentate 7r-electron system in CHCI3, is an intrinsic property of the planar four-coordinate complex. The high-spin/low-spin equilibrium of the... 

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