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Second draft

International Allelopathy Society (IAS). Article 2, IAS Constitution (draft), Second Newsletter 1998, http // www2.uca.es/dept/quimica organica/ias/newslett2.htm draft International Allelopathy Society. Department of Biochemistry, Oklahoma State University, Stillwater, Oklahoma, US A, 1998. [Pg.138]

The draft standard was then developed so that it was possible to classify both types of film in separate groups. The first being a Classical film, the second a Wide Latitude film. The density range of the standard covered from D=2.0 to D=4.0. A radiographer would expect the contrast to be higher at D=4.0 than the contrast at D=2.0. [Pg.422]

The steam generator is a balanced draft, controlled circulation, multichamber unit which incorporates NO control and final burnout of the fuel-rich MHD combustion gases. The MHD generator exhaust is cooled in a primary radiant chamber from about 2310 to 1860 K in two seconds, and secondary air for afterburning and final oxidation of the gas is introduced in the secondary chamber where seed also condenses. Subsequent to afterburning and after the gas has been cooled down sufftciendy to soHdify condensed seed in the gas, the gas passes through the remaining convective sections of the heat recovery system. [Pg.425]

AH discussion of the post-1965 era must begin with the Restatement (Second) of Torts, Section 402A. The person responsible for this section was Dean William Prosser, who became the reporter for American Law Institute s Restatement (Second) of Torts at a time when change was on the horizon in the field of products HabiUty. His initiative in drafting Section 402A provided the courts with a ready-made formulation for the adoption of strict tort HabiUty. Entitled "Special Liabihty of Seller of Product for Physical Harm to the User or Consumer," Section 402A reads as follows ... [Pg.98]

Bunker-fuel specifications for merchant vessels are described by ASTM D 2069, Standard Specification for Marine Fuels. Deep draft vessels carry residual (e.g., No. 6 fuel oil) or distillate-residual blend for main propulsion, plus distillate for start-up, shutdown, maneuvering, deck engines, and diesel generators. Main-propulsion fuel is identified principally by its viscosity in centistokes at 373 K. Obsolete designations include those based on Redwood No. 1 seconds at 100°F (311 K) (e.g., "MD 1500 ) and the designations "Bunker A for No. 5 fuel oil and "Bunker B and "Bunker C for No. 6 fuel oil in the lower-and upper-viscosity ranges, respectively. [Pg.2363]

Cenrers for Disease Control and Prevention. Draft guidelines for preventing the transmission of tuberculosis in health-care facilities, second edition Notice of comment period, federal Register, vol. 58, no. 195 (October 12, 1993), 52809-52854. [Pg.1011]

Following are two versions of a PSM team s mission statement. The first Is a draft prepared in advance of such a team s first meeting the second reflects group consensus and is designed for dissemination to company employees. [Pg.54]

The decentralised procedure can be used in cases where the product has never been authorised in any of the Member States, and the applicant wishes to obtain a license in a number of states simultaneously. The applicant must submit applications with the complete dossier to the Competent Authorities of each of the Member States where authorisation is desired. A single Member State should be chosen as the reference state to undertake the scientific assessment ofthe complete dossier, while the other states are designated as concerned states. The review process has many parallels vhth the centralised procedure, in that similar time lines exist, the reference State plays the role ofthe rapporteur, and the concerned States replace the CHMP. Once all States have validated that the dossiers are complete, the reference State is allowed 70 days to review the dossier and prepare a preliminary assessment report, which is circulated to the concerned Member States and the applicant. Comments from the concerned Member States and applicant responses are collected so that by day 120 the reference State may issue a draft assessment report together vhth draft SPC, label and leaflet texts. The clock may be stopped until requested responses from the applicant are received. The application then enters the second step in the assessment process, during which all the concerned Member States consider the... [Pg.121]

The time to assemble the implementation team would ideally be prior to researching and designing the implementation proposal. This is has two main advantages first, a proposal that comes from a group is often more believable and secondly, you can share the preparation work if you are working as a team rather than on your own. If the team was not formed prior to drafting the implementation proposal, this should be your first task after it has been passed. [Pg.215]

The discovery of two new elements started a frenetic race to find more. Actinium was soon unearthed (Debierne 1900) and many other substances were isolated from U and Th which also seemed to be new elements. One of these was discovered somewhat fortuitously. Several workers had noticed that the radioactivity of Th salts seemed to vary randomly with time and they noticed that the variation correlated with drafts in the lab, appearing to reflect a radioactive emanation which could be blown away from the surface of the Th. This Th-emanation was not attracted by charge and appeared to be a gas, °Rn, as it turns out, although Rutherford at first speculated that it was Th vapor. Rutherford swept some of the Th-emanation into a jar and repeatedly measured its ability to ionize air in order to assess its radioactivity. He was therefore the first to report an exponential decrease in radioactivity with time, and his 1900 paper on the subject introduced the familiar equation dN/dt = - iN, as well as the concept of half-lives (Rutherford 1900a). His measured half-life for the Th emanation of 60 seconds was remarkably close to our present assessment of 55.6 seconds for °Rn. [Pg.663]

Two different series of experiments were carried out. In one series, the three draft tube velocities were maintained essentially constant while the aeration to downcomers was varied. One of the three draft tube velocities was purposely increased to simulate possible unbalanced operation conditions in an actual industrial plant in the second series of experiments. Each experiment was characterized by solid particle velocity in each downcomer, the pressure drop across each draft tube, and the pressure drop across each downcomer. [Pg.261]

However, for small scale equipment, Cheng (1993) and Xu (1993) measured the circulation times of a single tagged particle in a 150 mm diameter fluidized bed coater with a draft tube and found that typical circulation times were between 2-10 seconds. Robinson and Waldie (1978) made similar measurements in a 6" diameter conventional spouted bed and found mean circulation times in the range of 3-6 seconds. [Pg.344]

Murder is a crime in every country in the world, but it s no crime in the world-at-large because the Second Circuit Court of Appeals never said so. Ask Senator Taft. He never took the trouble to call it murder before anyway, so now he says How can you call it murder after the war is over The charges are very badly drafted, Joe. We should have charged excusable larceny and justified, premeditated killing. That s the kind of theory they ll be happy with."... [Pg.110]

The first Frenchman to go to Berlin was welcome in Dearborn, too. He wrote a second letter to Edsel Ford twelve days after the first letter, enclosing an audit of profits accruing from his expanded business— 1,600,000 francs. The cash position of the firm was weak in dollars, because of world restrictions imposed by the United States Treasury. "But, as you know, our gold standard has been replaced by another standard which, in my opinion, is a draft on the future, not only in France and Europe, but, maybe, in the world."... [Pg.254]

The typical deliverables of a development cycle (see Pattern 15.13, Interpreting Models for Clients) are not individual completed documents from the linear life cycle. More usually, they might be first draft requirements GUI mockup client feedback second draft requirements critical core code version 1 requirements modified to what we find we can achieve ... [Pg.304]

Careful scrutiny of their publications, draft manuscripts, correspondence, record books, idea and plan books along with marginal notes made on their copies of various journal articles has resulted in an hypothesis that is too long to be elaborated in its entirety. A few bits and pieces will suffice for now. First of all, Osborne and Mendel believed their own experimental results and conclusions to be more correct than others unless the others agreed with them completely (not an unusual phenomenon). Second, they were convineed that Hopkins experiments were of too short a duration to truly compare his results with theirs in which p. f. m. had been used as a successful supplement for up to 80 days. Third, Osborne and Mendel were convineed of the purity of the diets they used. They prepared most of the proteins in their own labs in addition to the p. f. m. It must have been with some reluctance that they finally admitted that commerical lactose or even some of their home-made lactose carried growth promoters. [Pg.90]

Harmonization of pharmacopeial standards as a practical matter began at the International Congresses of Pharmacy between 1865 and 1910 [2], but the first formal attempt can be traced to 1902. Both USP President Horatio C. Wood, M.D., and Frederick M. Power, Ph.D., an American chemist of the Wellcome Chemical Research Laboratories of London, were appointed by the U.S. Secretary of State as delegates to represent the United States government at the International Conference for the Unification of the Formulae for Heroic Medicines, a conference of 19 countries from Europe and North America [3]. The second conference occurred in 1918. The 3rd in 1925 was attended by 31 countries from all continents except Asia and Australia. They drafted a new International Convention, which came in force in 1929. It revised the 1902 agreements on 77 heroic medicines and introduced the concept of maximum dose. It also requested that the League of Nations create a permanent secretariat of pharmacopeias [4]. Andrew G. DuMez, Ph.D., represented the USP, and was officially appointed by the U.S. Public Health Service to represent the United States at this conference [4,5]. An expert committee of the League of Nations planned a third conference for 1938, but it was never convened because of World War II [2]. [Pg.76]

The TGD has been revised and the second edition was published in 2003 (EC 2003). However, the human health risk characterization part was not included in this second edition. A final draft version of the human health risk characterization part was released in 2005 with a detailed guidance on, among others, the main issues to be included in derivation of the reference MOS (MOSref), which is analogous to an overall assessment factor. The individual factors contributing to the MOSref are described separately and guidance is given on how to combine these into the MOSref. The guidance provided in this draft version has been extensively used in relation to the risk assessment of prioritized substances carried out since the draft version was released however, this version is not publicly available. [Pg.220]

Stage 3 Pubhcation of fhe draft text in the forum of each pharmacopoeia Pharmeuropa (Ph Eur), Japanese Pharmacopoeial Forum (JP) and Pharmacopoeial Forum (USP) Comments received and consohdated Preparation of a second draft text ( Stage 3 draft )... [Pg.560]


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See also in sourсe #XX -- [ Pg.80 ]




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