Abstract  Summary At present, there is an increasing demand for trace gas analytical information, especially in several fields of environmental protection, such as protection of workers from exposure to hazardous substances in work place atmospheres, ambient and indoor air pollution, or gaseous exhalations from polluted soils, waters, or waste deposits. Though the existing powerful trace analytical tools are in principle capable of answering the questions related to these problems, they cannot satisfy the information demand. This is mainly due to the fact that most of these analytical tools are to be used in the course of rather sophisticated multistep procedures which are time consuming and claim high personnel qualification and, thus, are too expensive for large scale application. This difficulty can be overcome by the development of simple one-step procedures based on low price ready-for-use sampling units which can be processed with a minimum of manpower input and, in addition, provide information of the required reliability. One possible way to this goal may be based on the measurement of caloric effects associated with the decomposition of the products resulting during the sampling step from a gas-solid reaction between the traces to be analyzed and suitable solid state reagents. Starting from properly prepared text gas mixtures, the gas-solid reactions of numerous amines, alcohols, aldehydes, ketones, hydrocarbons and halogenated hydrocarbons with several metal complexes and with reagents capable of forming clathrates have been investigated by means of thermoanalytical methods, mainly by means of differential scanning calorimetry (DSC). The results show that in many cases the very simple thermoanalytical evaluation enables both qualitative identification and quantification of the gas traces under concern with satisfying selectivity. These reaction may serve, therefore, as a promising basis for further development of fast, simple and reliable trace gas analysis using thermoanalytical methods.

Abstract  The thermodynamic parameters of mixed micelle formation (Lambda(mic)G degrees, Lambda(mic)H degrees, Lambda(mic)S degrees) have been determined for a series of mixed micelles consisting of two isomeric hexanediols (1,2-hexanediol and 1,6-hexanediol) in sodium dodecylsulfate micellar solutions. The enthalpies of micellization were determined directly from isoperibol solution calorimetry. Gibbs energies and entropies of micelle formation were obtained from the application of the charged pseudo-phase model of micelle formation to the calorimetric critical micelle concentration values. The location of the alcohols in the micellar palisade layer has been determined from two-dimensional nuclear Overhauser enhancement spectroscopy (NOESY) experiments. The calorimetric titration data indicates that the placement of the hydroxyl groups on the six carbon backbone greatly affects the energetics of the micelle formation process. From the NMR data, the location of the cosurfactant in the micelle has been determined. These results indicate that the locus of solubilization affects the subtle balance of forces responsible for the formation of the mixed aggregates.

Abstract  The gemini surfactant N-N'bis(dimethyldodecyl)-1,4-butanediammonium dibromide (12-4-12) was synthesized and its critical micelle concentrations (CMCs) and degree of counterion dissociation (alpha) in aqueous solutions in the presence of alkanols viz ethanol, isomeric butyl alcohols, 1-hexanol and alkanediols (ethanediol, 1,4-butanediol, 1,2-hexanediol, 2,5-hexanediol 1,6-hexanediol, and 1,8-octanediol) determined from electrical conductivity are reported. While ethanol, ethanediol, 1,4-butanediol showed an increase in CMC, a decrease was seen for isomeric butyl alcohols, 1-hexanol, isomeric hexanediols and 1,8-octanediol. For butyl alcohols the CMC decrease showed the trend 1 degrees>2 degrees>3 degrees in C(6) diols, 1,2-hexanediol exerted more decrease as compared to 2,5-hexanediol and 1,6-hexanediol.The results are explained on the basis of the structure and hydrophobicity of alcohols that determine their effect as cosolvent or cosurfactant (partitioning in micelles). Two-dimensional nuclear overhauser enhancement spectroscopy (2D-NOESY) was used to examine the location for 1-butanol and 1,4-butanediol in micellar systems as representative additives from alkanols and alkanediols showing CMC decreasing and increasing effect respectively. (C) 2011 Elsevier B.V. All rights reserved.

Abstract  Microemulsions (mu E) were prepared with palm fatty acid methyl esters (PFAME) as solvents, and stabilised by ethoxylated non-ionic surfactants, i.e., Dehydol LS 7 and Dehydol LS 2 as S-A and S-B with the hydrophilic-lipophilic balance (HLB) values at similar to 12.8 and similar to 7.3, respectively. The co-surfactants chosen were 1,2-hexanediol, 1,2-butanediol, 1,2-ethanediol and glycerol. The effects of the co-surfactants on the partial ternary phase diagrams were studied at 10%, 15%, 20%, 25%, 30% and 40% (w/w) concentrations. The ratio of PFAME to water was either 25:75 or 50:50. The mixtures were agitated vigorously, and then kept at ambient temperature (25 degrees C) for one to two days. The emulsions (two-phase), the mu E and liquid crystalline phases were observed using polarised light. In addition, the physical stability of the mu E solutions was determined at 45 degrees C over a period of one month. The effects of the co-surfactants on the ternary phase systems for PFAME/non-ionic surfactants/water were studied and mapped out at 25 degrees C and 45 degrees C, respectively.

Abstract  Liquid-liquid equilibria for hexafluorophosphate ionic liquids with 1-alkyl-3-methylimidazolium family of cations: 1-butyl-3-methylimidazolium, [bmim](+), 1-hexy1-3-methylimidazolium, [hmim](+), 1-octyl-3methylimidazolium, [omim](+) with polyhydric alcohols: 1,2-ethanediol, 1.2-propanediol, 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 1,5-pentanediol have been measured using the cloud point method. The influence of different characteristics of alcohols and ILs, including cation alkyl chain length, alcohol chain length, and relative position of the both OH groups in alcohol were studied. In general, the same type of the phase behavior is observed in all cases showing upper critical solution temperature but the impact of the above-mentioned factors is highly diversified. (c) 2011 Elsevier B.V. All rights reserved.

Abstract  Nickel supported on a variety of supports was evaluated in the batchwise hydrogenolysis of high-crystalline cellulose under hydrothermal conditions. The supports examined included Al2O3, kieselguhr, TiO2, SiO2, activated carbon (AC), ZnO, ZrO2 and MgO. All tested catalysts can effectively convert cellulose while the choice of supports plays a critical role in the product distribution and selectivity. The Ni catalysts favour the formation of industrially attractive 1,2-alkanediols such as 1,2-propanediol, ethylene glycol, 1,2-butanediol and 1,2-hexanediol. It was found that the bifunctional ZnO-supported Ni catalysts displayed superior activities and the best result was obtained on 20% Ni/ZnO which exhibited complete conversion of cellulose with up to 70.4% total glycol yields. The mechanism of the reaction involved was tentatively proposed by identifying the products formed.

Abstract  Aliphatic, linear dicarboxylic acids and branched dicarboxylic acids are the subject of this article. These dibasic acids are referred to by their trivial names, IUPAC system or by adding the suffix “dicarboxylic acid“ to the name of the hydrocarbon skeleton. For example a 10‐carbon atom dibasic acid is designated sebacic acid, decanoic or 1,8‐octane‐dicarboxylic acid. Physical and chemical properties of the most common dibasic acids are discussed. Manufacture and uses for glutaric acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, dodecanoic acid, brassylic acid and C‐19, C‐20, and C‐22 dicarboxylic acids are given. These diacids are intermediates for the manufacture of diesters, polyesters, and polyamides. These derivatives have many applications ,eg, as plasticizing agents, lubricants, heat‐transfer fuids, inks and coatings, insecticides. Azaleic acid is used in acne preparations. Toxicities and environmental concerns are also discussed.

Abstract  The study reports pig-skin permeation and skin accumulation of miconazole nitrate (MCZ) from positively charged microemulsions containing water, 1-decanol/1-dodecanol (2:1, w/w), lecithin and/or decyl polyglucoside at different weight ratios, propylene glycol, 1,2 hexanediol and a cationic charge-inducing agent (stearylamine (ST), L-alanine benzyl ester (ALAB) or cetyltrimethylammonium bromide (CTAB)). Zeta-potential values of the positively charged microemulsions ranged from 14.2 to 37.5 mV and mean droplet size from 6.0 to 16.8 nm. In vitro pig-skin permeation of MCZ after a single 24 h application was negligible for all microemulsions; accumulation from positively charged microemulsions was nearly twice that from their negatively charged counterparts. The increased accumulation might be ascribed to the interaction between positive microemulsive systems and negatively charged skin sites; no significant difference was observed among the various cationic charge-inducing agents. Skin accumulation from the microemulsion containing most lecithin was lower than those of other microemulsions; this was ascribed to the phase transformation from microemulsion to a liquid crystal system after skin contact. These results suggest that positively charged microemulsions could be used to optimize drug targeting without a concomitant increase in systemic absorption; ALAB, an ester of a natural aminoacid, is an appropriate cationic charge-inducing agent. (C) 2007 Elsevier B.V. All rights reserved.

Abstract  The aim of the current study was to investigate the effect of different co-surfactants on the phase behaviour of the pseudoternary system water:ethyl oleate:nonionic surfactant blend (sorbitan monolaurate/polyoxyethylene 20 sorbitan mono-oleate). Four aliphatic alcohols (1-propanol, 1-butanol, 1-hexanol and 1-octanol) and four 1,2-alkanediols (1,2-propanediol. 1,2-pentanediol, 1,2-hexanediol and 1,2-octanediol) were used. The co-surfactant-free system forms two different colloidal structures, a water-in-oil microemulsion (w/o ME) and lamellar liquid crystals (LC) and two coarse dispersions, water-in-oil (w/o EM) and oil-in-water (o/w EM) emulsions. Microemulsion region area (%ME), liquid crystalline region area (%LC), amount of amphiphile blend required to produce a balanced microemulsion (%AMPH) and amount of water solubilised (%W)were used as assessment criteria to evaluate the co-surfactants. Seven calculated physico-chemical descriptors were used to represent the different co-surfactants. 1-butanol, 1,2-hexanediol and 1,2-octanediol produced balanced MEs capable of solubilising a high percentage of both oil and water. A similarity was observed between the descriptors attributed to I-butanol and 1,2-hexanediol. The requirements of a co-surfactant molecule to produce a balanced microemulsion were: HLB Value 7.0-8.0, a carbon backbone of 4-6 atoms, percentage carbon of 60-65%, percentage oxygen of 20-30%, log P value 0.2-0.9 and log 1/S (S: aqueous solubility) close to zero. (C) 2000 Elsevier Science B.V. All rights reserved.

Abstract  A straight-chain alcohol or diol additive in the mobile phase was used to modify and improve the HPLC separation of organic acids and bases. Incorporation of 2% 1-butanol, 1% 1,2-hexanediol, or 0.25% 1,2-octanediol into an aqueous mobile phase greatly improved the separation of alkane carboxylic acids on a silica C18 column, both in terms of separation time and peak shape. When 1.5% 1-hexanol, 0.09% 1-decanol or 0.01% 1-dodecanol was added to an acetonitrile-water (30:70) mobile phase, much sharper peaks and better resolution were obtained for aromatic bases separated on an underivatized polystyrene-divinylbenzene column. The mobile phase additive is believed to coat the stationary phase surface by a dynamic equilibrium. The coated surface is more hydrophilic and facilitates the efficient partitioning of analytes between the mobile and stationary phases.

Abstract  Droplet evaporation of multicomponent droplets is essential for various physiochemical applications, e.g., in inkjet printing, spray cooling, and microfabrication. In this work, we observe and study the phase segregation of an evaporating sessile binary droplet, consisting of a miscible mixture of water and a surfactantlike liquid (1,2-hexanediol). The phase segregation (i.e., demixing) leads to a reduced water evaporation rate of the droplet, and eventually the evaporation process ceases due to shielding of the water by the nonvolatile 1,2-hexanediol. Visualizations of the flow field by particle image velocimetry and numerical simulations reveal that the timescale of water evaporation at the droplet rim is faster than that of the Marangoni flow, which originates from the surface tension difference between water and 1,2-hexanediol, eventually leading to segregation.

Abstract  Some polyols show micellar behavior in aqueous solutions at concentrations greater than the critical micellar concentration (cmc). The 1,2-alkanediols (C(n)H(2n+2)O2 with n=5,6,7), the 1,2,3-alkanetriols (C(n)H(2n+2)O3 with n=7,8,9), and the geminated alkanetriols (C(n)H(2n+2)O3 with n=8 and 9) are investigated by microcalorimetric techniques. Only the 1,2-hexanediol (n=6), the 1,2,3-octanetriol (n=8), and the 2,2-dihydroxymethyl 1-heptanol (n=9) possess, in aqueous solutions, an organized structure above the critical micellar concentration (cmc). The 1,2-pentanediol (n=5) and the 1,2,3-heptanetriol (n=7) would form weak associations, whereas the 2,2-dihydroxymethyl 1-hexanol (n=8) does not form any associations even at large concentration. The 1,2-heptanediol (n=7), being only very slightly soluble even at a temperature of 30 degrees C, could not be studied. The 1,2,3-nonanetriol (n=9) is not soluble at temperatures between 20 and 35 degrees C. The critical micellar concentrations are determined by specific heat capacity methods. The passage from the dispersed environment to the organized environment gives a constant quantity of specific heat capacities (about 50 JK(-1)mol(-1)) only for the 1,2-hexanediol (n=6), the 1,2,3-octanetriol (n=8) and the 2,2-dihydroxymethyl 1-heptanol (n=9), which form true micelles. Structural effects of these systems are discussed.

Abstract  Legumes such as alfalfa (Medicago sativa L.), barrel medic (Medicago truncatula), white sweet clover (Melilotus alba) and fenugreek (Trigonella graecum), normally accumulate (-)-medicarpin and its malonated glucose conjugate as natural inhibitors of fungal pathogens. These plants also accumulate the biosynthetic precursor formononetin as well as the malonated glycoside. We were interested in developing a robust high-throughput method to quantitate the levels of these two isoflavonoids, both free and conjugated, in legume root extracts, for use in screening for mutant plants accumulating altered levels of these compounds. Capillary electrophoresis was examined as an alternative to current high-performance liquid chromatography (HPLC) methods to generate isoflavonoid profiles. The developed assay used micellar electrokinetic capillary chromatography (MEKC) to provide the required selectivity in complex root extracts. The addition of 1,2-hexanediol to the sodium dodecyl sulfate (SDS) electrolyte provided improved resolution of adjacent isoflavonoids. We examined the role of several factors including sample preparation, buffer composition, buffer pH, and organic component in the injected sample. The use of capillaries with longer path lengths were also examined to increase sensitivity. A comparison of results obtained using MEKC and HPLC showed good correlation in the relative amounts of the isoflavonoids studied.

Abstract  PURPOSE: To report an unusual case of Demodex folliculitis presenting as periocular vesiculopustular rash.

DESIGN: Case report.

RESULTS: A 68 year-old woman presented with a unilateral periocular rash that was initially treated by her primary ophthalmologist with topical steroids and antivirals. Slit-lamp examination revealed severe bilateral blepharitis, right greater than left, with waxy sleeves around the eyelashes. The diagnosis of Demodex infestation was considered. Treatment with daily lid scrub with polyhexamethylene biguanide (PHMB), 1,2-hexanediol and 1,2-octanediol (OCuSOFT PLUS) and erythromycin ointment twice a day resulted in complete resolution of the symptoms after 4 weeks.

CONCLUSIONS: Ophthalmologists should be aware of Demodex and consider it in the differential diagnosis of periocular skin lesions.

Abstract  The slow, non-mediated transmembrane movement of the lipid probes lysophosphatidylcholine, NBD-phosphatidylcholine and NBD-phosphatidylserine in human erythrocytes becomes highly enhanced in the presence of 1-alkanols (C2-C8) and 1,2-alkane diols (C4-C8). Above a threshold concentration characteristic for each alcohol, flip rates increase exponentially with the alcohol concentration. The equieffective concentrations of the alcohols decrease about 3-fold per methylene added. All 1-alkanols studied are equieffective at comparable calculated membrane concentrations. This is also observed or the 1,2-alkane diols, albeit at a 5-fold lower membrane concentration. At low alcohol concentrations, flip enhancement is reversible to a major extent upon removal of the alcohol. In contrast, a residual irreversible flip acceleration is observed following removal of the alcohol after a treatment at higher concentrations. The threshold concentrations to produce irreversible flip acceleration by 1-alkanols and 1,2-alkane diols are 1.5- and 3-fold higher than those for flip acceleration in the presence of the corresponding alcohols. A causal role in reversible flip-acceleration of a global increase of membrane fluidity or membrane polarity seems to be unlikely. Alcohols may act by increasing the probability of formation of transient structural defects in the hydrophobic barrier that already occur in the native membrane. Membrane defects responsible for irreversible flip-acceleration may result from alterations of membrane skeletal proteins by alcohols.

Abstract  Microemulsions (mu E) were prepared with palm fatty acid esters (PFAME) as solvents stabilised by fatty alcohol ethoxylates (hydrophilic-lipophilic balance, HLB value similar to 12.8), and 1,2 hexanediol as a co-surfactant. The effects of co-surfactant on the ternary phase systems were studied only at 10, 15, 20, 25, and 30% (w/w) of surfactant concentrations. The ratio of PFAME/water was chosen at 30:70 only. The mixtures were mixed vigorously and then kept at ambient temperature (25 degrees C) for few days. The emulsions (two-phase), mu E and liquid crystalline phases were observed using the polarised light. In addition, the physical stability (accelerated test/month at 45 degrees C),conductivity and viscosity for mu E solutions were measured. The effects of co-surfactant on the ternary phase systems for PFAME/non-ionic surfactant/water were constructed at 25 and 45 degrees C. The result showed that larger mu E region was formed with PFAME 1 than the PFAME 2 at 30:70 ratio of oil to water. The minimum concentration of surfactant for producing clear, low viscosity and thermodynamically stable mu E solutions was 10% (w/w) for both PFAME 1 and PFAME 2 at 25C. However, the concentration of co-surfactant used to produce mu E solutions was 12.5% for PFAME 1 but was 30% (w/w) for PFAME 2. Furthermore, the conductivity and viscosity measurements indicated types of mu E, that is, O/W or W/O formed.

Abstract  Microemulsions formed with water, isopropyl myristate, PHS-PEO-PHS polymeric surfactant, and alkanediol have been investigated using small-angle X-ray scattering (SAXS) and conductivity at 25 degreesC. Isopropyl myristate has a low solubility in water; however, this molecule has some polar character because of its ester group. The conductivities of samples with some added NaCl (used here to increase the conductivity sensitivity) are low, but compared to the conductivity of water/alkanediol mixtures, the values are high for most of the samples. The X-ray scattering curves show a correlation peak if the water content is high enough. A two-phase model for the invariant calculation fits the experimental results reasonably well provided that the partition of the oil between the polar and nonpolar phases is taken into account. This partition can be obtained from the ternary water/isopropyl myristate/alkanediol system, which has some mutual-solubility regions. A hard-sphere model can be fitted to the SAXS scattering data. The volume fractions fitted from this model deviate from the volume fractions of the low-polarity phase, indicating that the structure of most of the samples is of the bicontinuous type.

Abstract  To study the potential for delayed Type IV dermal sensitivity of a new preservative system containing 1,2-hexanediol and caprylyl glycol, 200-subject repeat insult patch tests were performed with a 15% mixture of 1,2-hexanediol and caprylyl glycol (equal parts of the 2 ingredients) in carbomer gel and a cosmetic formulation at an actual use concentration. No delayed Type IV hypersensitivity reactions were observed.

Abstract  Using biomass-derived ethylene glycol (bio-EG) to synthesize poly(ethylene terephthalate) (PET) is of notable significance for alleviating the dependence on fossil energy resources. Bio-EG readily contains a small amount of miscellaneous diols, which derive from the side reactions in the catalytic conversion of biomass. To disclose the effects of miscellaneous diols on the synthesis and properties of PET, EG feedstock containing four 1,2-diols, i.e., 1,2-propylene glycol, 1,2-butanediol, 1,2-pentanediol, and 1,2-hexanediol at 0-10% concentrations was used for the synthesis of PET. The molecular weights, intrinsic viscosities, and thermal and mechanical properties of obtained PET materials were measured. It was found that when the overall content of miscellaneous diols in EG was lower than 5%, the molecular weights and thermal properties of the prepared PET materials were very similar to that of PET synthesized from pure EG. The miscellaneous diols were less likely to be incorporated into PET resin because of the steric hindrance of the alkyl group in diols to the esterification and polycondensation reactions. Instead, they preferred to undergo dehydration reactions to form low-boiling-point aldehydes and hemiacetals, which could be removed from the reaction system during the reactions. Three bio-EG samples at purities of 99.9, 98.5, and 95.8 wt % were used for the bio-PET synthesis. Transparent and colorless bio-PET samples were obtained, demonstrating that the presence of miscellaneous diols does not have negative effects on the color quality of PET. The physical properties of bio-PET prepared with bio-EG at a purity of higher than 98 wt % were nearly the same as those of PET derived from pure EG. At a lower bio-EG purity of 95.8 wt %, the tensile strength of the obtained bio-PET sample was slightly decreased. The comprehensive results of property characterization show that bio-PET materials prepared with bio-EG at purity higher than 95 wt % could be used as widely as the conventional petro-PET resin without notable deterioration in their performance.

Abstract  The ruthenium aqua complexes [cp*Ru(OH2)(N-N)](OTf) (cp* = [small eta]5-pentamethylcyclopentadienyl, N-N = 2,2[prime or minute]-bipyridine, phen = 1,10-phenanthroline, OTf- = trifluoromethanesulfonate) and the acetonitrile complex [cpRu(CH3CN)(bipy)](OTf) (cp = [small eta]5-cyclopentadienyl) are water-, acid-, and thermally stable (200 [degree]C) catalysts for the hydrogenation of aldehydes and ketones in sulfolane solution. In the presence of HOTf as a co-catalyst, they effect the deoxygenation of 1,2-hexanediol to 1-hexanol and hexane. Glycerol is deoxygenated to 1-propanol in up to 18% yield and under more forcing conditions completely deoxygenated to propene. The structure of the acetonitrile pro-catalyst [cpRu(CH3CN)(bipy)](OTf) has been determined by X-ray crystallography (space group P[1 with combining macron] (a = 9.3778(10) A; b = 10.7852(10) A; c = 11.1818(13) A; [small alpha] = 101.718(5)[degree]; [small beta] = 114.717(4)[degree]; [gamma] = 102.712(5)[degree]; R = 3.95%).

Abstract  1,2-Hexanediol (1,2-HD) and 1,2,3-octanetriol (1,2,3-OT) are known to self-associate in a manner very similar to that of conventional surfactants to give rise to micellelike aggregates (Hajii, S.; et al. J. Phys. Chem. 1989, 93, 4819). This paper reports on fluorescence probing, with pyrene as a probe, of these aggregates and on a study of the kinetics of monomer exchange between aggregates and bulk phase by means of the ultrasonic relaxation method in the frequency range 0.5-100 MHz. Thus the polarity sensed by pyrene solubilized in the aggregates is lower than for conventional nonionic surfactants of the C(n)E(m) type. The critical micellization concentrations determined by fluorescence probing are in agreement with the reported values. The ultrasonic relaxation amplitude A and frequency f(R) have been found to vary with concentration as expected from the expressions derived for conventional surfactants on the basis of the Aniansson and Wall treatment for the kinetics of surfactant exchange. The full use of these expressions permitted us to obtain the values of the rate constants kappa+ kappa-for the incorporation of a surfactant monomer into, and the dissociation of a monomer from, a micelle, respectively, as well as the standard deviation characterizing the distribution of micelle aggregation numbers (polydispersity) and the volume change upon incorporation. These results are discussed and compared to those obtained for conventional surfactants.

Abstract  A series of ruthenium complexes of the general composition [(eta(6) -arene)(N boolean AND N)Ru(X)] (Y)(n), (arene = p-Me-Pr-i-C6H4, C6Me6; N boolean AND N = bipy, phen, 6,6'-diamino-2,2'-bipyridine, 2,9-diamino-1,10-phenanthroline; X=Cl, H, H2O; Y=Cl, OTf) was synthesized and the new compounds exhaustively structurally characterized by standard techniques (NMR, IR, elemental analysis, single-crystal X-ray crystallography). The single-crystal X-ray structures of [(p-Me-Pr-i-C6H4)Ru(dabipy)Cl][CI] (3CI[CI]), [(p-Me-Pr-i-C6H4)Ru(daphen)CI][CI] (4CI[CI]), [(C6Me6)Ru(dabipy)CI][CI] (7CI[CI]), [(C6Me6)Ru(daphen)CI][CI] (8CI[OTf]), [(p-Me-Pr-i-C6H4)Ru(bipy)(H2O)][OTf](2) (1O[OTf](2)), [(p-Me-Pr-i-C6H4)Ru(dabipy)(H2O)][OTf](2) (3O[OTf](2)), [(p-Me-Pr-i-C6H4)Ru(dabipy)(H2O)][SO4] (3O[SO4]), [(P-Me-(PrC6H4)-Pr-i)-Ru(daphen)(H2O)][OTf](2) (4O[OTf](2)), [(C6Me6)Ru(daphen)(MeOH)][OTf](2) (8(MeOH)[OTf](2)), [(p-Me-Pr-i-C6H4)Ru(dabipy)(H)][OTf] (3H[OTf]), [(p-Me-Pr-i-C6H4)Ru(daphen)(H)][OTf] (4H[OTf]), [(C6Me6)Ru(dabipy-BH2-OTf)(H)] (7H[-NH2-BH2-OTf]) have been determined. Under 750-1100 psi (5-7.5 MPa) of hydrogen pressure at 110 degrees C in the presence of acid and water in sulfolane solvent the aquo complexes form active catalysts for the selective deoxygenation of terminal diols, notably 1,2-hexanediol, to the corresponding primary alcohol, i.e., 1-hexanol in up to 60% yield. The presence of amino functions on the ortho-positions of the chelating ligands results in lower catalyst activity. Under the same reaction conditions the catalysts fail to convert glycerol to GC-detectable products. At the higher temperatures (T> 150 degrees C) possibly required for glycerol activation the catalysts show increasing decomposition with increasing temperature. (C) 2007 Elsevier B.V. All rights reserved.

Abstract  The inhibition effect of the surfactants 1,2-hexanediol (HD), 1,2,3-octanetriol (OT); 1,2,3-nonanetriol (NT); and 3,7-dimethyl-1,2,3,6,7-octanepentol (DOP) on the corrosion of iron in 1 M hydrochloric acid (HCl) was studied, Results obtained from gravimetric methods showed inhibition efficiencies increased with increasing surfactant concentrations and attained a maximum around their critical micellar concentration (cmc). A comparative study of corrosion inhibition of surfactants indicated DOP was the best inhibitor, Polarization measurements showed DOP was a cathodic type-inhibitor and acted on the cathodic reaction without modifying the mechanism of the hydrogen evolution reaction. DOP appeared to function through a general adsorption mode following the Langmuir adsorption isotherm The effect of temperature on the corrosion behavior of iron in both 1 M HCl and 1 M HCl with addition of various concentrations of DOP was studied in the temperature range from 18 degrees C to 48 degrees C, The associated activation corrosion and free adsorption energies were determined.