Relative humidity , solvent

Precipita.tlon. An ink may also be caused to dry by precipitation of its binder rather than by evaporation of solvent. This can be accompHshed by a dding a diluent, such as water in the form of steam or humidity, to a hygroscopic solvent ink system, which causes the solubiHty of the resin in the ink film to decrease sharply and causes it to precipitate when its tolerance for the diluent is reached. Eurther drying is accompHshed by absorption of the solvents into the stock and then by evaporation. Another form of precipitation setting is the quick-set mechanism. This utilizes resins held in solution in a relatively poor solvent, by means of a small amount of an exceUent solvent (called a sweetener) blended with it. When the ink film is printed on the paper, an amount of the solvents is absorbed reducing the content of the sweetener solvent to a point which causes the resins to precipitate and the ink to set. 

Relative humidity can have a significant impact on drying behavior and film quahty. Water-based formulations that perform weU when apphed under dry conditions may be deficient under high humidity apphcation conditions. The rate of water evaporation is much slower at high humidity, but solvent evaporation continues. This results in solvent depletion during the critical phases of film formation and consequent poor film development. 

Effective antistatic agents must act at a relative humidity below 40%, preferably below 15%. The agent must form a film on various surfaces and be apphed from a solution or dispersion in water or other inexpensive solvents. The antistatic agent must not interfere with subsequent processing of the product, impair the hand, or affect color, odor, appearance, and performance properties of the substrate. It should be nontoxic and nonflammable. 

Crystallisable polymers have also been prepared from diphenylol compounds containing sulphur or oxygen atoms or both between the aromatic rings. Of these the polycarbonates from di-(4-hydroxyphenyl)ether and from di-(4-hydroxy-phenyl)sulphide crystallise sufficiently to form opaque products. Both materials are insoluble in the usual solvents. The diphenyl sulphide polymer also has excellent resistance to hydrolysing agents and very low water absorption. Schnell" quotes a water absorption of only 0.09% for a sample at 90% relative humidity and 250°C. Both the sulphide and ether polymers have melting ranges of about 220-240°C. The di-(4-hydroxyphenyl)sulphoxide and the di-(4-hydroxy-phenyl)sulphone yield hydrolysable polymers but whereas the polymer from the former is soluble in common solvents the latter is insoluble. 

If you are considering recovering solvent from air, is the relative humidity of the air low enough to allow adsorption ... 

In a process in which benzene is used as a solvent, it is evaporated into dry nitrogen. The resulting mixture at a temperature of 297 K and a pressure of 101.3 kN/m2 has a relative humidity of 60%. It is desired to recover 80% of the benzene present by cooling to 283 K and compressing to a suitable pressure. What must this pressure be ... 

Three test batches of a chemical were manufactured with the intention of validating the process and having a new product to offer on the market. Samples were put on stability under the accepted ambient (25°C, 60% relative humidity) and accelerated (= stress 40°C, 75% rh) conditions cf. Section 4.20. One of the specification points related to the yellowish tinge imparted by a decomposition product, and an upper limit of 0.2 AU was imposed for the absorption of the mother liquor (the solvent mixture from which the crystalline product is precipitated) at a wavelength near 400 nm. 

Polymorphs are different crystal forms of the same compound [55], They are usually prepared by crystallization of the drug from different solvents under diverse conditions. However, exposure to changes in temperature, pressure, relative humidity, and comminution which are encountered in processes such as drying, granulation, milling, and compression may also lead to polymorphic transformations. 

The curves in Fig. 10 were drawn for the particular instance of a volatile solute dissolved in a volatile solvent, such as would exist for the acetone-chloroform system (whose diagram is very nearly like that of Fig. 10B). For many nonvolatile solutes, it not possible to trace smooth partial pressure curves across the entire range of mole fractions. This is especially true for aqueous salt solutions, where at a certain concentration of solute the solution becomes saturated. Any further addition of crystalline solute to the system does not change the mole fraction in the liquid phase, and the partial pressure of water thereafter remains constant, in accord with the phase rule. This phenomenon permits the use of saturated salt solutions as media to establish fixed relative humidity values in closed systems [12],... 

Self-assembly of the precursor components in the EISA process starts after evaporation of part of the volatile solvent, which progressively enriches the solution with respect to surfactant, precursor, and water. When their concentration in the deposited him achieves a certain critical level, mesostructure formation takes place. The latter is in equilibrium with the processing atmosphere. So the relative humidity, as well as the temperature during him deposition, represent some of the most important parameters influencing the mesostructure formation. 

This means that at higher temperatures the activity decreases, and that this decrease depends on both the solvent and the sorbent. There may even be an interaction between the temperature and the relative humidity, meaning that the effect of temperature is different at different relative humidities, since a is influenced by the general activity, which is partly controlled by the relative humidity. 

For a Taguchi approach to robustness the solvent composition is varied in the inner array, and the relative humidity and temperature in the outer array. The response is the resolution of noscapine and quinine. The data used in this example is a subset of the data set which is collected for this paper. The inner array consists of seven design points, the outer array of three. The three responses obtained at each setting of the inner array are combined to form a so-called signal-to-noise ratio. For maximization of the responses the following equation is [11] ... 

The results are given in Table 6.2. In this table on the left hand side the settings of the control factors (solvent composition) are given and on the upper site settings of the noise factors (temperature and relative humidity). Each of the combinations of control factor and noise factor settings results in one resolution. The signal-to-noise ratio S/N) summarizes the effect of noise factors for each of the control factors. 

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