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Different [sup.13]C NMR methods of determining triad distributions in two poly(ethylene-co-1-hexene) copolymers are examined using high signal-to-noise ratio [sup.13]C NMR spectra of the copolymers dissolved in deuterated 1,2,4 trichlorobenzene at 398 K. This examination includes a comparison of three integration techniques. The experimental impact of decoupler sidebands and significantly nonequal [sup.13]C NOE values are examined. A least-squares regression analysis technique for solving for triad mole fractions is tested and appears to be more reliable than two published algebraic expressions (and other expressions examined in the work reported here). The resultant triad mole fractions are compared to sequence distribution parameters expected by Bernoullian and first-order Markovian statistical models. On the basis of [sup.13] C NMR-determined average reactivity ratios, the copolymer designated sample B (5.3 mol % 1-hexene) appears to be a Bernoullian copolymer resulting from a single-site catalytic system. The copolymer designated sample S (3.6 mol % 1-hexene overall) is better described as a mixture of polyethylene and a Bernoullian copolymer with 6.4 mol % 1-hexene content, and thus appears to result from a multisite catalytic system.

The hydroxyl groups and 'physisorbed' water moieties of the pseudo-boehmite (Al2O3.2.05H2O) compound was analyzed via solid-state nuclear magnetic resonance (SSNMR) after successive dehydration treatments. SSNMR analysis of the high-surface-area boehmite during exposure to various heating temperatures indicated the loss of 'physisorbed' water protons in aluminum-coordinated hydroxyls in the clustered Al2OH sites. Furthermore, the less distorted nature of the 5-coordinated AlO4OH species favored the condensation of the isolated AlOH groups.

Phosphorus-31 nuclear magnetic resonance (31P NMR) was used to explore the decomposition of chlorpyrifos (an organothiophosphate pesticide) sorbed at high concentration (typically 2-10 wt %) on partially hydrated montmorillonite clays in four different cation-exchanged forms (Ca2+, Cu2+, Zn2+, and Al3+). Solid-state 31P NMR (using magic-angle spinning and cross polarization or direct polarization) and liquid-solution 31P NMR of DMSO and acetone extracts indicate that chlorpyrifos is initially physisorbed, appearing by solid-state 31P NMR to exhibit significant motion on the molecular level, which results in almost liquidlike solid-state spectra. Over periods ranging from hours to years, the signals due to unreacted chlorpyrifos diminish and are replaced by new 31P NMR peaks resulting from hydrolysis, isomerization, mineralization, and oxidation reactions. The 31P NMR signal characteristics indicate that these decomposition products are much more tightly bound to the clay than is chlorpyrifos. Partially hydrated Cu(II)- and Al-montmorillonites most effectively catalyzed chlorpyrifos decomposition (but with different product distributions); Ca-montmorillonites (and, as previously shown, kaolin) were least effective. Solid-state13C and 27Al NMR spectra were less useful for following the decomposition of chlorpyrifos than those obtained by 31P NMR. Pesticide loading levels (1-10% w/w) that are very much higher than those typically found in the environment were used to facilitate 31P NMR detection of less-than-dominant decomposition species. [ABSTRACT FROM AUTHOR]

Phosphorus-31 nuclear magnetic resonance (31P NMR) was used to follow the decomposition of chlorpyrifos (an organothiophosphate pesticide) adsorbed on soil, humic acid, partially hydrated kaolin clay, and partially hydrated montmorillonite clay at high concentration (typically 2-10 wt %). Solid-state 31P NMR (using magic-angle spinning and cross polarization or direct polarization) and liquid-solution 31P NMR of DMSO and acetone extracts indicate that chlorpyrifos is initially physisorbed, appearing by solid-state 31P NMR to exhibit significant motion on the molecular level, which results in almost liquidlike solid-state spectra. Over periods ranging from hours to years, the signals due to unreacted chlorpyrifos sorbed on the clays diminish and are replaced by new 31P NMR peaks resulting from hydrolysis, isomerization, mineralization, and oxidation reactions. The 31P NMR signal characteristics indicate that these decomposition products are much more tightly bound to the clay than is chlorpyrifos. Solid-state 31C and 27Al NMR spectra were less useful for following the decomposition of chlorpyrifos than those obtained by 31P NMR. Solid-state 31P NMR results indicate that a chlorpyrifos loading level of 10% by weight, used in some of the samples to facilitate 31P NMR detection of less-than-dominant decomposition products, exceeds the adsorption capacity of the soil, humic acid, and kaolinite tested, but not Ca2+-exchanged montmorillonite. This pattern is consistent with intercalation into the montmorillonite, but only surface adsorption on kaolinite. [ABSTRACT FROM AUTHOR]

The decomposition of methyl parathion (an organothiophosphate pesticide) sorbed on partially hydrated kaolin and montmorillonite clays (in Ca2+ Cu2+, Zn2+, and Al3+ forms) at high concentration (typically 1-10 wt %) has been examined by nuclear magnetic resonance (NMR), using solid-state 31P NMR (based on magic-angle spinning and cross polarization or direct polarization) and liquid- state 31P NMR of DMSO and acetone extracts. The results indicate that methyl parathion is initially physisorbed, appearing by solid-state 31P NMR to exhibit substantial molecular-level motion. The signals due to unreacted methyl parathion diminish and are replaced by new 31P NMR peaks resulting from hydrolysis, isomerization, and oxidation reactions over periods ranging from hours to years. 31P NMR characteristics indicate that these decomposition products are much more tightly bound to the clay than is methyl parathion. Methyl parathion decomposition is most effectively catalyzed by partially hydrated Cu(II)- and Al-montmorillonites (but with different product distributions); Ca-montmorillonite and kaolin were least effective. [ABSTRACT FROM AUTHOR]

Different 13C NMR methods of determining triad distributions in two poly(ethylene-co-1-hexene) copolymers are examined using high signal-to-noise ratio 13C NMR spectra of the copolymers dissolved in deuterated 1,2,4- trichlorobenzene at 398 K. This examination includes a comparison of three integration techniques. The experimental impact of decoupler sidebands and significantly nonequal 13C NOE values are examined. A least-squares regression analysis technique for solving for triad mole fractions is tested and appears to be more reliable than two published algebraic expressions (and other expressions examined in the work reported here). The resultant triad mole fractions are compared to sequence distribution parameters expected by Bernoullian and first-order Markovian statistical models. On the basis of 13C NMR- determined average reactivity ratios, the copolymer designated sample B (5.3 mol % 1-hexene) appears to be a Bernoullian copolymer resulting from a single-site catalytic system. The copolymer designated sample S (3.6 mol %1-hexene overall) is better described as a mixture of polyethylene and a Bernoullian copolymer with 6.4 mol % 1-hexene content, and thus appears to result from a multisite catalytic system. [ABSTRACT FROM AUTHOR]