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101.
The yellowing of white and pastel coloured textiles and garments has been a problem for many years in the textile industry. In the last 15 years much evidence has been published which suggests that a large proportion of storage yellowing is attributable not to the yellowing of fibre substrate or textile finish but to the yellowing of phenolic antioxidants which migrate onto the textiles from polyethylene and polypropylene packaging. These mobile phenolic compounds interact with atmospheric pollutants, particularly oxides of nitrogen, to give yellow compounds. A brief outline of the problems of yellowing is given, together with the identification of the yellow substances produced by BHT (2,6-di-tert-butyl-4-methyl phenol) and possible mechanisms of their formation. Prophylactic measures that can be taken by the garment manufacturer and finisher to prevent or minimise yellowing are also discussed. 相似文献
102.
Bobby L. Wilson Rudolph R. Schwarzer Callista O. Chukwuenye 《Microchemical Journal》1982,27(4):558-563
This paper reports the development of a field electrode method for the determination of total sulfide in water. The method involves the use of preweighed sodium sulfide crystals in the standardization process. Sodium sulfide crystals were weighed and sealed in air-tight plastic volumetric flasks. Standards were prepared in the field by adding a sulfide antioxidant buffer to the flasks containing the sulfide crystals and diluting it to mark with deionized deaerated water. Standards of lower concentration were prepared by serial dilutions of first standards.The results of the reproducibility determination revealed that sulfide concentrations as low as 6 ppb could be measured with a reproducibility of better than ±10%.Water samples were collected from a series of lakes in Fort Bend County, Texas (near Houston) and analyzed for sulfide content. The sulfide ion concentrations of these samples were determined directly in the field by use of an Orion Model 407A/F specific meter equipped with a silver/sulfide ion selective electrode in conjunction with a double junction reference electrode. 相似文献
103.
Budarin VL Clark JH Tavener SJ Wilson K 《Chemical communications (Cambridge, England)》2004,(23):2736-2737
The reaction of localised C[double bond, length as m-dash]C bonds on the surface of activated carbons has been shown to be an effective method of chemical modification especially using microwave-assisted reactions. 相似文献
104.
Three theories which have been proposed to explain the observed shortening of a single bond when it is adjacent to a double bond are discussed. Possible predictions from these theories are examined, especially for comparison with various quantities measurable by microwave spectroscopy. It is concluded that the steric theory is probably untenable, that some conjugation appears necessary to explain observed barries to internal rotation, and that it is difficult to find testable predictions from the hybridization theory. 相似文献
105.
Li AC Alton D Bryant MS Shou WZ 《Rapid communications in mass spectrometry : RCM》2005,19(14):1943-1950
Bioanalytical support of plasma pharmacokinetic (PK) studies for drug discovery programs primarily involves the quantitative analysis of dosed compounds using liquid chromatography/atmospheric pressure ionization tandem mass spectrometry (LC/MS/MS) operated in selected reaction monitoring (SRM) mode. However, there is a growing need for information on the metabolism of new chemical entities (NCEs), in addition to the time-concentration profiles from these studies. In this paper, we present a novel approach to not only quantify parent drugs with SRM, but also simultaneously screen for metabolites using a hybrid triple quadrupole/linear ion trap (QqQ(LIT)) instrument. This was achieved by incorporating both the conventional SRM-only acquisition of parent compounds and the SRM-triggered information-dependent acquisition (IDA) of potential metabolites within the same scan cycle during the same LC/MS/MS run. Two test compounds were used to demonstrate the applicability of this approach. Plasma samples from PK studies were processed by simple protein precipitation and the supernatant was diluted with water before injection. The fast scanning capability of the linear ion trap allowed for the information-dependent acquisition of metabolite MS/MS spectra (<1 s/scan), in addition to the collection of adequate data points for SRM-only channels. The MS/MS spectra obtained from potential metabolites in post-dose samples correlated well with the spectra of the parent compounds studied, therefore providing additional confirmatory structure information without the need for repetitive analyses. Relative quantitative time-concentration profiles of identified metabolites were also obtained. Furthermore, this articulated SRM+SRM-IDA approach generated equivalent quantitative results for parent compounds to those obtained by conventional SRM-only analysis. This approach has been successfully used to support discovery PK screening programs. 相似文献
106.
107.
Richard M. Wilson 《Combinatorica》1984,4(2-3):247-257
This paper contains a proof of the following result: ifn≧(t+1)(k?t?1), then any family ofk-subsets of ann-set with the property that any two of the subsets meet in at leastt points contains at most \(\left( {\begin{array}{*{20}c} {n - t} \\ {k - t} \\ \end{array} } \right)\) subsets. (By a theorem of P. Frankl, this was known whent≧15.) The bound (t+1)(k-t-1) represents the best possible strengthening of the original 1961 theorem of Erdös, Ko, and Rado which reaches the same conclusion under the hypothesisn≧t+(k?t) \(\left( {\begin{array}{*{20}c} k \\ t \\ \end{array} } \right)^3 \) . Our proof is linear algebraic in nature; it may be considered as an application of Delsarte’s linear programming bound, but somewhat lengthy calculations are required to reach the stated result. (A. Schrijver has previously noticed the relevance of these methods.) Our exposition is self-contained. 相似文献
108.
The effects of the administration of a single dose of the model nephrotoxin mercuric chloride (2.0 mg kg(-1), subcutaneous) to male Wistar-derived rats on the urinary metabolite profiles of a range of endogenous metabolites has been investigated using (1)H NMR and HPLC-MS. Urine samples were collected daily for 9 days from both dosed and control animals. Analysis of these samples revealed marked changes in the pattern of endogenous metabolites as a result of HgCl(2) toxicity. Peak disturbances in the urinary metabolite profiles were observed (using both NMR and HPLC-MS) at 3 days post dose. Thereafter the urinary metabolite profile gradually returned to a more normal composition. Markers of toxicity identified by (1)H NMR spectroscopy were raised concentrations of lactate, alanine, acetate, succinate, trimethylamine (TMA), and glucose. Reductions in the urinary excretion of citrate and alpha-ketoglutarate were also seen. Markers identified by HPLC-MS, in positive ion mode, were kynurenic acid, xanthurenic acid, pantothenic acid and 7-methylguanine which decreased after dosing. In addition an ion at m/z 188, probably 3-amino-2-naphthoic acid, was observed to increase after dosing. As well as these identified compounds other ions at m/z 297 and 267 decreased after dosing. In negative ion mode a range of sulfated compounds were observed, including phenol sulfate and benzene diol sulfate, which decreased after dosing. As well as the sulfated components an unidentified glucuronide at m/z 326 was also observed to decrease after dosing. The results of this study demonstrate the complementary nature of the NMR and MS-based techniques for metabonomic analysis. 相似文献
109.
In vivo and ex vivo studies of fluorescence from endogenous and exogenous molecules in tissues and cells are common for applications such as detection or characterization of early disease. A systematic determination of the excitation-emission matrices (EEM) of known and putative endogenous fluorophores and a number of exogenous fluorescent photodynamic therapy drugs has been performed in solution. The excitation wavelength range was 250-520 nm, with fluorescence emission spectra collected in the range 260-750 nm. In addition, EEM of intact normal and adenomatous human colon tissues are presented as an example of the relationship to the EEM of constituent fluorophores and illustrating the effects of tissue chromophore absorption. As a means to make this large quantity of spectral data generally available, an interactive database has been developed. This currently includes EEM and also absorption spectra of 35 different endogenous and exogenous fluorophores and chromophores and six photosensitizing agents. It is intended to maintain and extend this database in the public domain, accessible through the Photochemistry and Photobiology website (http://www.aspjournal. com/). 相似文献
110.
Ernst Berger David W. T. Griffith Gerhard Schuster Stephen R. Wilson 《Mikrochimica acta》1988,95(1-6):239-241
The use of an integrating sphere for the measurement of absorption spectra of thin films is described. The thin film (for example a rare gas matrix) is grown directly on the inside surface of the sphere. Multiple reflections inside the integrating sphere lead to significant enhancement of weak absorptions of the film, increasing the sensitivity of such measurements. 相似文献