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Dried porosity

Macroporous resins are also called macroreticular. Macroporous resins have a measurable porosity. It does not disappear when the resin is dry. Porosity is more dependent on the solvent used when manufacturing the copolymer than on the degree of cross-linking. [Pg.376]

Similarly, we polymerized the same mixture used for the preparation of capillary columns in glass vials and used the product for mercury intrusion porosimetry. Since we found that a strong correlation exists between the "dry" porous properties of the monoliths and their chromatographic performance, even dry porosity measurements may be used to tailor column performance. [Pg.234]

General hydrodynamic theory for liquid penetrant testing (PT) has been worked out in [1], Basic principles of the theory were described in details in [2,3], This theory enables, for example, to calculate the minimum crack s width that can be detected by prescribed product family (penetrant, excess penetrant remover and developer), when dry powder is used as the developer. One needs for that such characteristics as surface tension of penetrant a and some characteristics of developer s layer, thickness h, effective radius of pores and porosity TI. One more characteristic is the residual depth of defect s filling with penetrant before the application of a developer. The methods for experimental determination of these characteristics were worked out in [4]. [Pg.613]

Prepare a solution of 41 g. of anhydrous palladium chloride (1) in 10 ml. of concentrated hydrochloric acid and 25 ml. of water (as in A). Add all at once 60 ml. of 6iV-sulphuric acid to a rapidly stirred, hot (80°) solution of 63 1 g. of A.R. crystallised barium hydroxide in 600 ml. of water contained in a 2-htre beaker. Add more 6iV-sulphuric acid to render the suspension just acid to htmus (5). Introduce the palladium chloride solution and 4 ml. of 37 per cent, formaldehyde solution into the hot mechanically stirred suspension of barium sulphate. Render the suspension slightly alkaline with 30 per cent, sodium hydroxide solution, continue the stirring for 5 minutes longer, and allow the catalyst to settle. Decant the clear supernatant hquid, replace it by water and resuspend the catalyst. Wash the catalyst by decantation 8-10 times and then collect it on a medium - porosity sintered glass funnel, wash it with five 25 ml. portions of water and suck as dry as possible. Dry the funnel and contents at 80°, powder the catalyst (48 g.), and store it in a tightly stoppered bottle. [Pg.951]

Fig. 22. Performance cut diameter predictions for typical dry packed bed particle collectors as a function of bed height or depth, packing diameter and packing porosity (void area) S. Bed irrigation increases collection efficiency or decreases cut diameter (271). SoHd lines, = 25 mm dashed lines,... Fig. 22. Performance cut diameter predictions for typical dry packed bed particle collectors as a function of bed height or depth, packing diameter and packing porosity (void area) S. Bed irrigation increases collection efficiency or decreases cut diameter (271). SoHd lines, = 25 mm dashed lines,...
Suspension polymerization of VDE in water are batch processes in autoclaves designed to limit scale formation (91). Most systems operate from 30 to 100°C and are initiated with monomer-soluble organic free-radical initiators such as diisopropyl peroxydicarbonate (92—96), tert-huty peroxypivalate (97), or / fZ-amyl peroxypivalate (98). Usually water-soluble polymers, eg, cellulose derivatives or poly(vinyl alcohol), are used as suspending agents to reduce coalescence of polymer particles. Organic solvents that may act as a reaction accelerator or chain-transfer agent are often employed. The reactor product is a slurry of suspended polymer particles, usually spheres of 30—100 pm in diameter they are separated from the water phase thoroughly washed and dried. Size and internal stmcture of beads, ie, porosity, and dispersant residues affect how the resin performs in appHcations. [Pg.386]

The printing of newspapers is conducted at very high speeds, often reaching 3000 feet per miaute. AH three printing processes utilize similar quaHty newsptint which, essentiaHy, is made of groundwood or thermomechanical pulp. Presses are fed a continuous web of newsptint that unwiads from a feed roUer. Inks dry by absorption of Hquid iato the porosity of the substrate. Some evaporation of water ia a flexo pubHcation ink can accelerate the dryiag process. [Pg.249]

DRI can be produced in pellet, lump, or briquette form. When produced in pellets or lumps, DRI retains the shape and form of the iron oxide material fed to the DR process. The removal of oxygen from the iron oxide during direct reduction leaves voids, giving the DRI a spongy appearance when viewed through a microscope. Thus, DRI in these forms tends to have lower apparent density, greater porosity, and more specific surface area than iron ore. In the hot briquetted form it is known as hot briquetted iron (HBI). Typical physical properties of DRI forms are shown in Table 1. [Pg.424]

Soda. Ash Roasting. Some of the first processes to recover selenium on a commercial basis were based on roasting of copper slimes with soda ash to convert both selenium and tellurium to the +6 oxidation state. Eigure 1 shows flow sheets for two such processes. Slimes are intensively mixed with sodium carbonate, a binder such as bentonite, and water to form a stiff paste. The paste is extmded or peUetized and allowed to dry. Care in the preparation of the extmdates or pellets is required to ensure that they have sufficient porosity to allow adequate access to the air required for oxidation. [Pg.327]

Two more recent appHcations for amorphous siHcas are expected to grow to large volumes. Precipitated siHcas are used ia the manufacture of separator sheets placed between cells ia automotive batteries. Their function is to provide a controlled path for the migration of conductive ions as a result of the porosity of the siHca particles. Additionally, both precipitated siHcas and aerogels are being developed for use ia low temperature iasulation, where the low thermal conductivity of the dry siHca powders makes them useful ia consumer products such as refrigerators (83). [Pg.481]

Tape can be cast on a stainless steel table or belt, glass plate, or a Mylar, Teflon, or ceUulose acetate film carrier. The tape should adhere to the carrier sufficiently to prevent curling, but should be easily removable. In a continuous casting process, the tape is dried by air flowing 1—2 m/min counter to the casting direction. A typical dry green tape contains approximately 35 vol % organics, 50% ceramic powder, and 15% porosity. [Pg.309]


See other pages where Dried porosity is mentioned: [Pg.146]    [Pg.146]    [Pg.2767]    [Pg.250]    [Pg.1]    [Pg.3]    [Pg.4]    [Pg.5]    [Pg.52]    [Pg.342]    [Pg.530]    [Pg.52]    [Pg.57]    [Pg.224]    [Pg.149]    [Pg.376]    [Pg.378]    [Pg.532]    [Pg.151]    [Pg.40]    [Pg.42]    [Pg.366]    [Pg.125]    [Pg.543]    [Pg.543]    [Pg.9]    [Pg.19]    [Pg.125]    [Pg.330]    [Pg.487]    [Pg.491]    [Pg.109]    [Pg.249]    [Pg.251]    [Pg.555]    [Pg.555]    [Pg.576]    [Pg.174]    [Pg.309]    [Pg.205]   
See also in sourсe #XX -- [ Pg.280 ]




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