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Poly(2,6-diphenyl-1,4-phenylene oxide) (P30) is obtained from the polymerization of 2,6-dimethylphenol. In comparison to 2,6-dimethylphenol, the oxidation potential of 2,6-diphenylphenol is higher. Higher temperatures of polymerization are necessary.  [Pg.152]

P30 shows a glass transition temperature of 230°C and a melting temperature of 480°C. In contrast to PPE it readily crystallizes from the melt. It shows and exeellent thermal stability both in nitrogen and in air. [Pg.152]

Due to its high melting point, P30 cannot be processed by injection molding or extrusion teehniques. However, P30 ean be fabricated by solution casting techniques into films or by wet spin techniques into fibers. On orientation or heat treatment, these materials beeome insoluble. [Pg.152]

Commonly, PPE has a number average molecular weight of 3,000 0,000 Dalton. PPE is essentially an amorphous polymer, when cooled from the melt. It is soluble in chloroform, benzene, and toluene. Some properties of neat PPE are shown in Table 4.6. However, PPE is used mostly as a blend for the sake of processability. Properties of a PPE/PS are given in Table 4.7. [Pg.152]

Melt Mass-Flow Rate (MFR) 9.2 g/lOmin ASTM D1238 [Pg.153]


It is indicated in moderate to severe, acute or chronic pain and in painful diagnostic procedures and surgery arthralgia, dental pain, musculoskeletal pain, pain associated with fractures, dislocation and other related type of pain. [Pg.79]

CHEMICAL-SPECIFIC HEALTH CONSULTATION TREMOLITE ASBESTOS AND OTHER RELATED TYPES OF ASBESTOS... [Pg.375]

In whole plants, leaf chloroplasts convert cadaverine directly into lupanine (21) without releasing free intermediates in a channeled process involving membrane-associated enzymes (Kinghom and Balandrm, 1984). It is possible that matrine (26) and other related types of quinolizidine alkaloids are synthesized by a similar channeled process (Kinghom and Balandrin, 1984 Wink, 1987). [Pg.556]

Figure B3.1.5. Probability (as a fimction of angle) for finding the seeond eleetron in He when both eleetrons are loeated at the maximum in the Is orbital s probability density. The bottom line is that obtained using a Hylleraas-type fiinetion, and the other related to a highly-eorrelated multieonfigurational wavefLinetion. After [22],... Figure B3.1.5. Probability (as a fimction of angle) for finding the seeond eleetron in He when both eleetrons are loeated at the maximum in the Is orbital s probability density. The bottom line is that obtained using a Hylleraas-type fiinetion, and the other related to a highly-eorrelated multieonfigurational wavefLinetion. After [22],...
Even further complications are to be expected for general systems of the type (3). These are related to the approximation of the slowly varying solution components and other related quantities of (3) for k —> oo by the corresponding solution of the constrained system DAE... [Pg.282]

Assoeiate s degree or the equivalent in industrial hygiene, health physies, industrial safety, or other related field (work experienee ean be substituted if the amount and type eorrespond appropriately to projeet needs and are approved as appropriate)... [Pg.35]

The optical activity of quartz and certain other materials was first discovered by Jean-Baptiste Biot in 1815 in France, and in 1848 a young chemist in Paris named Louis Pasteur made a related and remarkable discovery. Pasteur noticed that preparations of optically inactive sodium ammonium tartrate contained two visibly different kinds of crystals that were mirror images of each other. Pasteur carefully separated the two types of crystals, dissolved them each in water, and found that each solution was optically active. Even more intriguing, the specific rotations of these two solutions were equal in magnitude and of opposite sign. Because these differences in optical rotation were apparent properties of the dissolved molecules, Pasteur eventually proposed that the molecules themselves were mirror images of each other, just like their respective crystals. Based on this and other related evidence, in 1847 van t Hoff and LeBel proposed the tetrahedral arrangement of valence bonds to carbon. [Pg.97]

Compounds with Sc, Y, lanthanoids and actinoids are of three types. Those with composition ME have the (6-coordinated) NaCl structure, whereas M3E4 (and sometimes M4E3) adopt the body-centred thorium phosphide structure (Th3P4) with 8-coordinated M, and ME2 are like ThAsi in which each Th has 9 As neighbours. Most of these compounds are metallic and those of uranium are magnetically ordered. Full details of the structures and properties of the several hundred other transition metal-Group 15 element compounds fall outside the scope of this treatment, but three particularly important structure types should be mentioned because of their widespread occurrence and relation to other structure types, namely C0AS3,... [Pg.555]

Examples with other Pirkle-type CSPs have also been described [139, 140]. In relation to polysaccharides coated onto silica gel, they have shown long-term stability in this operation mode [141, 142], and thus are also potentially good chiral selectors for preparative SFC [21]. In that context, the separation of racemic gliben-clamide analogues (7, Fig. 1-3) on cellulose- and amylose-derived CSPs was described [143]. [Pg.12]

Two types of chlorination processes are used for the different kinds of raw material. The first process is a reductive process by which oxide-type raw materials in the form of ores or concentrates are chlorinated. The essence of this process is the interaction with chlorine gas in the presence of coal or other related material. [Pg.6]

A theoretical explanation for such an anomalous phenomenon in certain nonalternant hydrocarbons has first been attempted, in case of pentalene, by Boer-Veenendaal and Boer followed by Boer-Veenen-daal et Snyder and Nakajima and Katagiri for other related nonalternant hydrocarbons. By making allowance for the effects of <7-bond compression, these authors have shown that a distorted structure resembling either of the two Kekule-type structures is actually energetically favored as compared with the apparently-full symmetrical one. [Pg.6]

An interesting application of the photodynamic properties of porphyrins is their possible use in the treatment of certain types of cancer, a procedure called cancer phototherapy. Tumors often take up more porphyrins than do normal tissues. Thus, hematopor-phyrin or other related compounds are administered to a patient with an appropriate mmor. The mmor is then exposed to an argon laser, which excites the porphyrins, producing cytotoxic effects. [Pg.273]

The cloned DNA can be used as a probe in one of several types of hybridization reactions to detect other related or adjacent pieces of DNA, or it can be used to quantitate gene products such as mRNA. [Pg.412]

A thorough insight into the comparative photoelectrochemical-photocorrosion behavior of CdX crystals has been motivated by the study of an unusual phenomenon consisting of oscillation of photocurrent with a period of about 1 Hz, which was observed at an n-type CdTe semiconductor electrode in a cesium sulfide solution [83], The oscillating behavior lasted for about 2 h and could be explained by the existence of a Te layer of variable width. The dependence of the oscillation features on potential, temperature, and light intensity was reported. Most striking was the non-linear behavior of the system as a function of light intensity. A comparison of CdTe to other related systems (CdS, CdSe) and solution compositions was performed. [Pg.229]

This paper does not aim to give a full account of all types and all consequences of MMCT. We try to present data and phenomena which originate mainly from the solid-state field, but which can be connected to and may be of use in other, related fields. Unfortunately this exchange of ideas on MMCT between the several fields in which they are of importance is not very common. [Pg.155]


See other pages where Other Related Types is mentioned: [Pg.545]    [Pg.124]    [Pg.152]    [Pg.277]    [Pg.112]    [Pg.640]    [Pg.545]    [Pg.124]    [Pg.152]    [Pg.277]    [Pg.112]    [Pg.640]    [Pg.62]    [Pg.261]    [Pg.259]    [Pg.126]    [Pg.249]    [Pg.41]    [Pg.366]    [Pg.7]    [Pg.715]    [Pg.67]    [Pg.41]    [Pg.366]    [Pg.309]    [Pg.29]    [Pg.97]    [Pg.85]    [Pg.186]    [Pg.221]    [Pg.158]    [Pg.246]    [Pg.280]    [Pg.324]    [Pg.208]    [Pg.49]    [Pg.118]    [Pg.317]    [Pg.50]    [Pg.70]   


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