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PS techniques

The techniques listed from Table 12.10 to Table 12.11 are rated according to the scheme shown in Table 12.9. [Pg.222]

Ratings Efficiency rating, % Operating cost/yr, EUR/t VOC Installation cost, EUR/t VOC [Pg.222]

Emissions Available techniques Cost Efficiency Remarks [Pg.222]

Storage Minimise level variation L M Only for integrated sites [Pg.222]

Emissions Available teehniques Cost Efficiency Remark [Pg.223]


Fig.18a-b. Scanning electron micrographs on cryo fractured surfaces of a macroporous epoxy prepared with 6 wt % hexane via the Cl PS technique showing a narrow size distribution b macroporous epoxy prepared with 7.5 wt % hexane via the CIPS technique showing a narrow size distribution. Reprinted from Polymer, 37(25). J. Kiefer, J.G. Hilborn and J.L. Hedrick, Chemically induced phase separation a new technique for the synthesis of macroporous epoxy networks p 5719, Copyright (1996), with permission from Elsevier Science... [Pg.195]

The PS-4 ultrasonic examination system provides many new features, which allows the operator to perform several inspections simultaneously. Both pulse-echo and time-of-flight-diffraction technique can be applied together with storage of digital A-scan data at the same time. [Pg.872]

A successful modification to the technique involves delayed pulsed-field extraction which allows discrimination between zero and near-zero kinetic energy electrons. About 1 ps after the laser pulse has produced photoelectrons, a small voltage pulse is applied. This has the effect of amplifying the differences in fhe velocities of fhe phofoelecfrons and allows easy discrimination befween fhem as a resulf of fhe differenf times of arrival af fhe defector. In fhis way only fhe elections which originally had zero kinetic energy following ionization can be counted to give fhe ZEKE-PE specfmm. [Pg.403]

The film is fibrillated mechanically by mbbing or bmshing. Immiscible polymers, such as polyethylene or polystyrene (PS), may be added to polypropylene to promote fibrillation. Many common fiber-texturing techniques such as stuffer-box, false-twist, or knife-edge treatments improve the textile characteristics of slit-film fibers. [Pg.320]

Anionic polymerization, if carried out properly, can be truly a living polymerization (160). Addition of a second monomer to polystyryl anion results in the formation of a block polymer with no detectable free PS. This technique is of considerable importance in the commercial preparation of styrene—butadiene block copolymers, which are used either alone or blended with PS as thermoplastics. [Pg.517]

An optical detector with appropriate electronics and readout. Photomultiplier tubes supply good sensitivity for wavelengths in the visible range, and Ge, Si, or other photodiodes can be used in the near infrared range. Multichannel detectors like CCD or photodiode arrays can reduce measurement times, and a streak camera or nonlinear optical techniques can be used to record ps or sub-ps transients. [Pg.383]

The main experimental techniques used to study the failure processes at the scale of a chain have involved the use of deuterated polymers, particularly copolymers, at the interface and the measurement of the amounts of the deuterated copolymers at each of the fracture surfaces. The presence and quantity of the deuterated copolymer has typically been measured using forward recoil ion scattering (FRES) or secondary ion mass spectroscopy (SIMS). The technique was originally used in a study of the effects of placing polystyrene-polymethyl methacrylate (PS-PMMA) block copolymers of total molecular weight of 200,000 Da at an interface between polyphenylene ether (PPE or PPO) and PMMA copolymers [1]. The PS block is miscible in the PPE. The use of copolymers where just the PS block was deuterated and copolymers where just the PMMA block was deuterated showed that, when the interface was fractured, the copolymer molecules all broke close to their junction points The basic idea of this technique is shown in Fig, I. [Pg.223]

The techniques described above have been used to demonstrate that failure can occur by (1) simple chain pull-out, (2) chain scission close to the interface, or (3) chain scission within one of the blocks (typically PS). The transition from chain pull-out to scission is essentially controlled by molecular weight whilst the location of the scission seems to depend on the entanglement density. Fig. 2 shows the transition between (2) and (3) as E is increased. [Pg.223]

Following the release of WASH-1400, the techniques were disseminated by the authors and interpreters through publications, lectures, and workshops. Many organizations set up in-housc PS. groups, and the nucleus of the organization that had produced the Reactor Safety Study coiKinucd at the NRC. [Pg.4]

It is evident from these results that the interactive properties of the investigated SEC PS/DVB or DVB gels are very different. Because polar electroneutral macromolecules of PMMA were more retained from a nonpolar solvent (toluene) than from polar ones (THF, chloroform), we conclude that the dipol-dipol interactions were operative. Columns No. 1 and No. 2 were very interactive and can be applied successfully to LC techniques that combine exclusion and interaction (adsorption) mechanisms. These emerging techniques are LC at the critical adsorption point (18), the already mentioned LC under limiting conditions of adsorption (15,18), and LC under limiting conditions of desorption (16). In these cases, the adsorptivity of the SEC columns may even be advantageous. In most conventional SEC applications, however, the interactive properties of columns may cause important problems. In any case, interactive properties of SEC columns should be considered when applying the universal calibration, especially for medium polar and polar polymers. It is therefore advisable to check the elution properties of SEC columns before use with the... [Pg.455]

This procedure can now be repeated with a base D that is slightly weaker than C, using C as the reference. In this stepwise manner, a series of p determinations can be made over the acidity range from dilute aqueous solution to highly concentrated mineral acids. Table 8-18 gives pS bh+ values determined in this way for nitroaniline bases in sulfuric and perchloric acid solutions. This technique of determining weak base acidity constants is called the overlap method, and the series of p kBH+ values is said to be anchored to the first member of the series, which means that all of the members of the series possess the same standard state, namely, the hypothetical ideal 1 M solution in water. [Pg.448]

As these block copolymers were synthesized using the anionic polymerization technique, their molecular weight distributions were narrow. The microspheres with narrower size distribution are better for well-ordered self-organization. Actually, all block copolymers synthesized for these works formed poly(4-vinyl pyridine) (P4VP) spheres in the PS matrices with narrow size distributions. [Pg.602]

The poly(styrene-b-isoprene) (P(S-b-IP)) and poly(-styrene-b-2-vinyl pyridine) (P(S-b-2VP)) block copolymers with narrow molecular weight distributions for blending with the microspheres were also synthesized using the additional anionic polymerization technique. The number-average molecular weights (Mns) and PS contents are also shown in Table 1. [Pg.602]

In the late 1940s, the demand for styrene homopolymers (PS) and styrene-acrylonitrile copolymers (SAN) was drastically reduced due to their inherent brittleness. Thus, the interest was shifted to multiphase high-impact polystyrene (HIPS) and rubber-modified SAN (ABS). In principle, both HIPS and ABS can be manufactured by either bulk or emulsion techniques. However, in actual practice, HIPS is made only by the bulk process, whereas ABS is produced by both methods [132,133]. [Pg.656]

An interesting and practically valuable result was obtained in [21] for PE + N2 melts, and in [43] for PS + N2 melts. The authors classified upper critical volumetric flow rate and pressure with reference to channel dimensions x Pfrerim y Qf"im-Depending on volume gas content

channel entrance (pressure of 1 stm., experimental temperature), x and y fall, in accordance with Eq. (24), to tp 0.85. At cp 0.80, in a very narrow interval of gas concentrations, x and y fall by several orders. The area of bubble flow is removed entirely. It appears that at this concentration of free gas, a phase reversal takes place as the polymer melt ceases to be a continuous phase (fails to form a continuous cluster , in flow theory terminology). The theoretical value of the critical concentration at which the continuous cluster is formed equals 16 vol. % (cf., for instance, Table 9.1 in [79] and [80]). An important practical conclusion ensues it is impossible to obtain extrudate with over 80 % of cells without special techniques. In other words, technology should be based on a volume con-... [Pg.119]

Two relatively new techniques, matrix assisted laser desorption ionization-lime of flight mass spectrometry (MALDI-TOF) and electrospray ionization (FS1), offer new possibilities for analysis of polymers with molecular weights in the tens of thousands. PS molecular weights as high as 1.5 million have been determined by MALDI-TOF. Recent reviews on the application of these techniques to synthetic polymers include those by Ilantoif54 and Nielen.555 The methods have been much used to provide evidence for initiation and termination mechanisms in various forms of living and controlled radical polymerization.550 Some examples of the application of MALDI-TOF and ESI in end group determination are provided in Table 3.12. The table is not intended to be a comprehensive survey. [Pg.143]

The SP-PLP817 18 and PS-PLP171 techniques involve following the monomer conversion induced by a single laser pulse or a sequence of laser pulses. These experiments are usually conducted at high pressure beeause rates of termination are lower and sensitivities are somewhat higher. 7... [Pg.238]


See other pages where PS techniques is mentioned: [Pg.267]    [Pg.184]    [Pg.154]    [Pg.236]    [Pg.130]    [Pg.625]    [Pg.222]    [Pg.1181]    [Pg.267]    [Pg.184]    [Pg.154]    [Pg.236]    [Pg.130]    [Pg.625]    [Pg.222]    [Pg.1181]    [Pg.800]    [Pg.1607]    [Pg.189]    [Pg.597]    [Pg.80]    [Pg.515]    [Pg.411]    [Pg.503]    [Pg.504]    [Pg.507]    [Pg.516]    [Pg.528]    [Pg.669]    [Pg.118]    [Pg.350]    [Pg.218]    [Pg.637]    [Pg.148]    [Pg.213]    [Pg.451]    [Pg.326]    [Pg.143]    [Pg.144]    [Pg.260]   


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