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Split care

Collaborative care has many definitions. It does not refer to split care, which usually implies that the physician treats the biological part of the patient by prescribing medication, and the therapist does the rest. Although split care may be attractive in terms of cost and ease for the provider, it is inadequate care. Patients need their therapist and physician to communicate, particularly in the creation and maintenance of a treatment plan. [Pg.4]

It is crucial in quantitative GC to obtain a good separation of the components of interest. Although this is not critical when a mass spectrometer is used as the detector (because ions for identification can be mass selected), it is nevertheless good practice. If the GC effluent is split between the mass spectrometer and FID detector, either detector can be used for quantitation. Because the response for any individual compound will differ, it is necessary to obtain relative response factors for those compounds for which quantitation is needed. Care should be taken to prevent contamination of the sample with the reference standards. This is a major source of error in trace quantitative analysis. To prevent such contamination, a method blank should be run, following all steps in the method of preparation of a sample except the addition of the sample. To ensure that there is no contamination or carryover in the GC column or the ion source, the method blank should be run prior to each sample. [Pg.215]

The total worldwide consumption of AOS in 1990 was of the order of 85,000 tonnes [12] split between household products (55,000 tonnes) toiletries and personal care products (20,000 tonnes), and industrial and institutional uses (10,000 tonnes). The worldwide consumption of all synthetic detergents in 1990 was as follows (1) anionics (3,390,000 tonnes), cationics (815,000 tonnes), and nonionics (910,000 tonnes). From the total of 5,115,000 tonnes, AOS consumption accounts for 1.5%. [Pg.365]

A remarkable splitting of the two signals in the F-spectra of P2O3F4 is observed, when traces of difluorophosphoric acid are carefully excluded and the spectrum is scanned at very slow speed (777). The doublet is split into two triplets symmetrical to each other with the intensity ratio 1 2 5, which is in accordance with the AA XX A" a" expectation spectrum (777). The F-spectra of F2P(S)- 0—P(S)p2 can be interpreted in the same way the normally appearing doublet of lines splits into two symmetrical nonets at very slow scan speeds (777). [Pg.78]

Genuine iron(V) is a very rare oxidation state. In the preparation of iron oxides (and of other solid-state materials), the intended iron(V) disproportionates mostly into an iron(lll) fraction and two parts of an iron(Vl) fraction [276]. The only example of an iron(V) oxide for which the Mbssbauer parameters are known [185] is La2Li-FeOs- A low isomer shift of = —0.41 mm s was observed at room temperature with practically zero quadmpole splitting [277], which was taken as a proof that iron is accommodated in octahedral FeOg sites surrounded by six Li ions. Although repeatedly cited, it seems that the spectra have never been published, and the data must therefore be considered with care. [Pg.438]

FTIR in multiply hyphenated systems may be either off-line (with on-line collection of peaks) [666,667] or directly on-line [668,669]. Off-line techniques may be essential for minor components in a mixture, where long analysis times are required for FT-based techniques (NMR, IR), or where careful optimisation of the response is needed. In an early study a prototype configuration comprised SEC, a triple quadrupole mass spectrometer, off-line evaporative FTIR with splitting after UV detection see Scheme 7.12c [667]. Off-line IR spectroscopy (LC Transform ) provides good-quality spectra with no interferences from the mobile phase and the potential for very high sensitivity. Advanced approaches consist of an HPLC system incorporating a UV diode array, FTIR (using an ATR flow-cell to obtain on-flow IR spectra), NMR and ToF-MS. [Pg.524]

In the parathion studies and the more recent DDT studies, the fruits were split in half by cutting axially one third through the fruit with a broad-bladed knife and then twisting the blade to one side. The core and pulp, exclusive of the part touched by the knife blade, were carefully scraped out with sharpened melon bailers. [Pg.130]

The splitting of the Bt—Bl MOs into bonding and anti-bonding MOs is taken care of by the average parameter... [Pg.77]

Dealing with batch size restrictions is slightly more elaborate. Two new variables need to be defined, one of them being integer. In each period tthe current campaign quantity (K, + Xjt) is split into two variables. One of them (Rjt) counts the number of full batches already produced in the current campaign and the second one (Sjt) takes the rest. This is done by constraints (11.15) and (11.16). The latter one takes care that no more than a full batch is contained in slack variables Sjt nor any rest remains if production of another campaign starts. Finally, (11.17) and (11.18) state the domain of the variables Rjt and Sjt. [Pg.257]

Care must be taken, however, in how such products are labeled. Results of the 1991 Euro-barometer survey, for instance, reported an interesting finding related to labeling biotechnology products. Results indicated that the way biotechnology products are labeled influenced both perceptions of and attitudes toward such products. The survey was conducted using a split... [Pg.140]

The mean values (A ) begin to split with each other at a density where U a becomes finite. We d like to make a comment here. One may be surprised to see their value of O(GeV), coming from our parameter choice. However, what we d like to reveal here is not their realistic values but a possibility of color magnetic superconductivity and its qualitative features. More realistic study, of course, is needed by carefully checking our approximations, especially the contact interaction and the sharp cutoff at the Fermi surface. [Pg.253]

The prime drawback with the nitrone traps, is the relative paucity of information immediately available from the spectra of the derived spin adducts. For example, with few exceptions the spin adducts of PBN [7] give six-line spectra with resolved splittings only from nitrogen and from the / proton. Identification of spin adducts must then be by careful comparison of the magnitude of the hyperfine splittings with those found for reference nitroxides... [Pg.19]


See other pages where Split care is mentioned: [Pg.289]    [Pg.289]    [Pg.2277]    [Pg.204]    [Pg.314]    [Pg.386]    [Pg.183]    [Pg.459]    [Pg.316]    [Pg.191]    [Pg.148]    [Pg.463]    [Pg.96]    [Pg.97]    [Pg.36]    [Pg.181]    [Pg.102]    [Pg.107]    [Pg.368]    [Pg.416]    [Pg.53]    [Pg.191]    [Pg.96]    [Pg.264]    [Pg.233]    [Pg.510]    [Pg.162]    [Pg.20]    [Pg.191]    [Pg.75]    [Pg.225]    [Pg.168]    [Pg.229]    [Pg.37]    [Pg.117]    [Pg.332]    [Pg.57]    [Pg.27]    [Pg.242]   
See also in sourсe #XX -- [ Pg.4 , Pg.289 ]




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