Pervaporation performance of oligosilylstyrene-polydimethylsiloxane membrane for separation of organics from water

A novel silicone rubber was prepared by crosslinking silylstyrene-oligomer containing -SiH groups with divinyl-polydimethylsiloxane using Karstedt's catalyst at room temperature. Membranes cast from this silicone rubber were found capable of separating chlorinated hydrocarbons and aromatics from water containing trace amount of the organics through pervaporation (PV). Synthesis of this silylstyrene-oligomer, crosslinking it to divinyl-polydimethylsiloxane to produce the silicone rubber and preparation of membranes from this rubber are discussed. PV test results are presented.     

Influence of organics on the structure of water adsorbed on activated carbons

The influence of organics on the structure of water adsorbed on activated carbons was studied using adsorption of nitrogen, benzene, and water, and by (1)H NMR spectroscopy with freezing out of bulk water with the presence of benzene-d(6) or chloroform-d. It was found that interactions of water with the activated carbon surface depend on both structural characteristics (contributions of micro- and mesopores, pore size distributions) of adsorbents and chemical properties (changed by oxidation or reduction) of the adsorbents. Moreover, the interfacial behavior of water is affected by water-insoluble organics such as benzene and chloroform. Changes in the Gibbs free energy of water adsorbed on carbons exposed to air, water, chloroform-d, or benzene-d(6) are related to textural properties of adsorbents and the degree of their oxidation. Since chloroform-d and benzene-d(6) are strongly adsorbed on activated carbons and immiscible with water they replace a significant portion of adsorbed water in micropores, on the walls of mesopores, and in the transport pores of carbons causing changes in the Gibbs free energy and other characteristics of water.     

On the modification of solid adsorbents with volatile organics II. The role of the layer adsorbed

Summary This paper presents a continuation of our research dedicated to solid-adsorbent surface modification with what are commonly regarded as volatile and easily eluted organic compounds. Two porous adsorbents were used: natural zeolite (clinoptilolite) and alumina, while the adsorbates employed were n-hepatane and benzene. The results show that a simple injection of volatile adsorbate greatly alters the solid surface adsorption properties. The consequences of volatile modifier application are discussed on the grounds of adsorption isotherms determined at 313K. Possible implications to the tailor made adsorbents are outlined as well.Part I, J. Chromatogr.442, 105 (1988)     

Pervaporation characteristics of cross-linked poly(dimethylsiloxane) membranes for removal of various volatile organic compounds from water

The permeation and separation characteristics of volatile organic compounds (VOCs), such as chloroform, benzene, and toluene, from water by pervaporation through cross-linked poly(dimethylsiloxane) membranes prepared from poly(dimethylsiloxane) dimethylmethacrylate macromonomer (PDMSDMMA) and divinyl compounds, such as ethylene glycol dimethylmethacrylate (EGDM), divinyl benzene (DVB), divinyl siloxane (DVS), and divinyl perfluoro-n-hexane (DVF) are described. When aqueous solutions containing 0.05 wt.% VOCs were permeated through cross-linked PDMSDMMA membranes, these membranes showed high VOC/water selectivity and permeability. Both VOC/water selectivity and permeability were affected significantly by the divinyl compound. Furthermore cross-linked PDMSDMMA membranes showed the highest chloroform/water selectivity. The VOC/water selectivity was mainly governed by the sorption selectivity rather than the diffusion selectivity. However, the difference in the selectivity between different types of VOCs depended on differences in the diffusivity of permeants. With increasing downstream pressure, the VOC/water selectivity of all cross-linked PDMSDMMA membranes increased, but the permeability decreased. A PDMSDMMA–DVF membrane exhibited a normalized permeation rate of 1.9 × 10⁻⁵ kg m/m² h and a separation factor for chloroform/water of 4850, yielding a separation index of 9110. The pervaporation characteristics of the cross-linked PDMSDMMA membranes are discussed based on their chemical and physical structures as well as the chemical and physical properties of the permeants.     

Modification of solids with volatile organics III: Natural zeolites

Summary The effect of pre-adsorbed benzene and ethanol on the adsorptive properties of natural zeolite (clinoptilolite) has been studied by gas-solid chromatography. It has been shown that modification of the solid surface by volatile organics has a significant influence on the adsorptive properties. The modification is of the same order as the more difficult modification by inorganics, as illustrated here by clinoptilolite modification with Co²⁺. Energy distribution of surface adsorptive sites appears to be continuous and confirms previous finding that only a small proportion of active sites is responsible for most adsorbate retention. Part II reference [4]     

Determination of volatile organics in drinking water with USEPA method 524.2 and the ion trap detector

New drinking water regulations require the monitoring of eight volatile organic compounds that have established maximum contaminant levels (MCLs) and 51 other volatile organics for which MCLs are not established. A laboratory analytical method (Method 524.2) for the determination of 58 of these compounds is investigated, and precision and accuracy data are obtained. The method uses a standard inert gas purge extraction, isolation of the volatile organics on a three-stage solid-phase trap, thermal desorption into a gas chromatograph, separation with a fused-silica capillary column, and identification and measurement with a relatively low cost, benchtop ion trap detector that functions as a mass spectrometer. At a concentration of 2 micrograms/L (2 parts per billion), the grand mean measurement accuracy for 54 compounds was 95% of the true value with a mean relative standard deviation (RSD) of 4%. At 0.2 micrograms/L (200 parts per trillion), the grand mean measurement accuracy for 52 compounds was 95% of the true value with a mean RSD of 3%.     

Determination of the partial pressure of single low volatile compounds in mixtures

A new measuring system for the determination of the vapour pressure of single compounds in mixtures is introduced. A coupling system consisting of a quadrupol mass spectrometer and a vapour pressure balance was used for these measurements. Some calibration measurements and investigations of mixtures are discussed.     

Determination of the partial pressure of single low volatile compounds in mixtures

A new measuring system for the determination of the vapour pressure of single compounds in mixtures is introduced. A coupling system consisting of a quadrupol mass spectrometer and a vapour pressure balance was used for these measurements. Some calibration measurements and investigations of mixtures are discussed.     

Substrate temperature effects on film chemistry in plasma depositions of organics. II. Polymerizable precursors

The influence of substrate temperature during plasma deposition on the chemistry of the organic films formed was examined. Plasma ionization of precursor gases that are polymerizable by conventional mechanisms was studied. Film chemistry was analyzed by x-ray photoelectron spectroscopy (XPS). Monomers that polymerize by a free radical mechanism [2-hydroxyethyl methacrylate (HEMA) and hexafluorobutadiene (HFB)] form more regular polymers (i.e. with less molecular rearrangement) by plasma deposition at low substrate temperatures than monomers that polymerize by ionic mechanisms [ethylene oxide (EO) and tetrahydrofuran (THF)]. In all cases, lowering the substrate temperature during deposition produces films with elemental composition virtually identical to that of the precursor gas. Comparison of high-resolution XPS spectra of the deposited films with those for model polymers suggests that functional groups in the monomers used to generate the plasma are incorporated to a greater extent at low substrate temperatures. The effect of plasma power on the degree of precursor structure retention obtained when reduced substrate temperatures are employed was also examined. Plasma deposition of HEMA at low substrate temperatures and low plasma power produces thin films which are, by core level XPS, indistinguishable from HEMA polymerized by conventional methods. EO and THF films coated at low substrate temperatures on glass, polyethylene, or polytetrafluoroethylene varied widely in surface chemistry due to differences in film uniformity. Film quality (uniformity) is enhanced for these low reactivity precursors by pretreating substrates with an argon plasma. © 1992 John Wiley & Sons, Inc.     

Influence of pressure on the properties of chromatographic columns. II. The column hold-up volume

The effect of the local pressure and of the average column pressure on the hold-up column volume was investigated between 1 and 400 bar, from a theoretical and an experimental point of view. Calculations based upon the elasticity of the solids involved (column wall and packing material) and the compressibility of the liquid phase show that the increase of the column hold-up volume with increasing pressure that is observed is correlated with (in order of decreasing importance): (1) the compressibility of the mobile phase (+1 to 5%); (2) in RPLC, the compressibility of the C18-bonded layer on the surface of the silica (+0.5 to 1%); and (3) the expansion of the column tube (<0.001%). These predictions agree well with the results of experimental measurements that were performed on columns packed with the pure Resolve silica (0% carbon), the derivatized Resolve-C18 (10% carbon) and the Symmetry-C18 (20% carbon) adsorbents, using water, methanol, or n-pentane as the mobile phase. These solvents have different compressibilities. However, 1% of the relative increase of the column hold-up volume that was observed when the pressure was raised is not accounted for by the compressibilities of either the solvent or the C18-bonded phase. It is due to the influence of the pressure on the retention behavior of thiourea, the compound used as tracer to measure the hold-up volume.     

Influence of reaction medium composition on enzymatic synthesis of galactooligosaccharides and lactulose from lactose concentrates prepared from whey permeate

The paper presents the results of investigations into the technological possibilities of controlling the transgalactosylation process of lactose in permeate after whey ultrafiltration in order to improve the efficiency of galactooligosaccharides or lactulose synthesis. The synthesis efficiency was influenced by the selection of a β-galactosidase preparation, substrate concentration and, in the synthesis of lactulose, also by the ratio of lactose and fructose added to the reaction mixture. The obtained synthesis efficiency of GOS and, most of all, of lactulose (65 g L⁻¹), may be found satisfactory. The study also resulted in a proposed GOS or lactulose concentrates (concentrated or dried) production technology using permeate after ultrafiltration of milk or whey as lactose sources. Presented at the 35th International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 26–30 May 2008.     

Pervaporation of water from aqueous sulfuric acid at elevated temperatures using Nafion membranes

The concentration of sulfuric acid by pervaporation has been studied using Nafion-112^® and Nafion-117^® membranes, which have been characterized in terms of flux, permeability, and separation factor at 100 and 120 °C. Feed acid concentrations investigated ranged from 40 to over 80 wt%. In general, water fluxes ranged from 100 to 8000 g/m² h, depending on feed acid concentration and separation factors as high as 10⁴ were observed. Membrane stability was probed using dynamic mechanical analysis that revealed an increase in the temperature at which the α transition is observed, which corresponds to the glass transition (T_g) of the hydrophilic domain, upon use, suggesting embrittlement of the polymer structure. Further studies showed that the embrittlement was due to an interaction with the acid and was not induced by the operating temperature.     

Chiral sulphonated phosphines : II. Influence of water on the enantioselectivity in the reduction of dehydro-aminoacids

For the reduction of dehydro aminoacids in various media with rhodium complexes containing chiral ligands, a linear correlation of log %S/%R with the solvophobicity parameter S_p has been observed. The decrease in enantioselectivity in water is due to the high interfacial energy of this solvent.     

Removal of organics from produced water by reverse osmosis using MFI-type zeolite membranes

Separation of an organics/water mixture was carried out by reverse osmosis using an α-alumina-supported MFI-type zeolite membrane. The organic rejection performance is strongly dependent on the ionic species and dynamic size of dissolved organics. The membrane showed high rejection efficiency for electrolytes such as pentanoic acid. An organic rejection of 96.5% with a water flux of 0.33 kg m⁻² h⁻¹ was obtained for 100 ppm pentanoic acid solution at an operation pressure of 2.76 MPa. For non-electrolyte organics, separation efficiency is governed by the molecular dynamic size; the organics with larger molecular dynamic size show higher separation efficiency. The zeolite membrane gives an organic rejection of 99.5% and 17% for 100 ppm toluene and 100 ppm ethanol, respectively, with a water flux of 0.03 kg m⁻² h⁻¹, 0.31 kg m⁻² h⁻¹ at an operation pressure of 2.76 MPa. It was observed that organic rejection and water flux were affected by the organic concentration. As pentanoic acid concentration increased from 100 ppm to 500 ppm, both organic rejection and water flux decreased slightly.     

Isolation and preconcentration of volatile organic compounds from water

Methods for the isolation and/or concentration of volatile organic compounds from water samples for trace organic analysis by gas chromatography are reviewed. The following basic groups of methods are discussed: liquid-liquid extraction, adsorption on solid sorbents, extraction with gas (gas stripping and static and dynamic headspace techniques) and membrane processes. The theoretical bases of these methods are discussed. Experimental arrangements for the isolation and/or concentration of volatile compounds from water are presented and discussed with respect to their efficiency. The applicability of the described methods to the isolation and/or concentration of various organic compounds from waters of various origins is discussed.     

Analytical isolation, separation and identification of mutagens from nonvolatile organics of drinking water

A general procedure has been developed for the concentration/fractionation of mutagenic residue organics from small, less than 50L, and large, to 1200L, volumes of drinking water obtained from a variety of sources. This procedure features concentration of the residue organics chromatographically by passage of the water through XAD-2 and XAD-7 resins in specially designed columns, details of which are given. The residue organics are eluted from the resins via organic solvents, followed by solvent removal and subsequent bioassay for mutagenicity. Then the residue organics are fractionated via a coupled bioassay/analytical fractionation method which progressively focuses to the bioactive constituents of the complex mixture of residue organics. In this report, results for the optimal operation and validation of the concentration system are given, using drinking water derived from an industrially polluted river system, a wilderness river system and a major aquifer system. The predominant type of mutagenesis observed for the residue organics isolated from these samples was direct-acting to the Salmonella tester strain, TA98, which was decreased by the addition of the metabolic activation system from the livers of rats previously treated with Arochlor 1254. Some TA100 direct-acting mutagenesis was observed for all samples. Fractionation of the residue organics indicated the mutagens to be nonpolar. Samples of residue organics collected over a period of a year from each type of drinking water showed no discernable pattern of mutagenesis versus season. The methodologies described in this paper provide a comprehensive approach for the concentration/isolation of residue organics from drinking water for studies to identify biohazardous compounds and to characterize these compounds biologically.     

Sampling and analysis of volatile organics emitted from wastewater treatment plant and drain system of an industrial science park

Volatile organic compounds (VOCs) were monitored in the different sections of a wastewater treatment plant (WWTP), the outlet of both the WWTP and rainfall water, and the downstream of the WWTP joining the river in the area or vicinity of an industrial science park located in Hsinchu, Taiwan. Levels of VOCs were determined by collecting air samples over several sampling points and analyzed using gas chromatography. Among VOCs identified in the drainage and effluent system in each season, acetone, isopropanol (IPA) and dimethyl sulfide (DMS) were the major emission species and maximum concentrations were 400.4, 22.8 and 641.2 ppbv, respectively. The ambient air and wastewater sample analysis from neighboring wastewater streams identified pollutants being discharged from unaccounted sources other than the industrial park. According to the 24 h semi-continuous monitoring data (27/7/2002-29/7/2002), the total VOC concentration was an average of 93 ppbv (acetone contributed ∼78%) with a dramatic variation during the day and night. The emission rate of measured VOCs estimated using fixed box model projected an average of 2-4 μg m⁻² h⁻¹) during the day and 9-17 μg m⁻² h⁻¹ during the night. In addition, the isopleth maps show that the acetone and DMS emissions influence adversely the nearby residential area located at less than 100 m downwind from the plant. Eventually, based on this study, an on-line monitoring and alerting system could be built for a long-term performance, and with regular information on the varying pollutants over time construction of a green strategy and creation of a sustainable environment can be achieved.     

Influence of hydrostatic pressure on water absorption of polyoxymethylene: experiment and molecular dynamics simulation

This work experimentally investigated the influence of hydrostatic pressure on the water absorption of polyoxymethylene, followed by analyzing its micro‐mechanism via molecular dynamics simulation. Tests results show that the polyoxymethylene water absorption decreases with the increase in hydrostatic pressure when the latter is within 0–3.0 MPa; it subsequently increases with the increase in hydrostatic pressure in the range of 3.0–5.0 MPa. Simulation of water molecules diffusion on polyoxymethylene surface shows that water molecules diffuse into polyoxymethylene surface during an equilibration run, and water molecule displacement value of maximum relative concentration gives almost the same characteristics: firstly decreases and then increases with the increase of hydrostatic pressure. Simulation of water molecule diffusion inside polyoxymethylene suggests the following: (i) water molecules vibrate from the interior to the edge of polyoxymethylene cell during the equilibration run, and (ii) water diffusion coefficient in polyoxymethylene gives trend of firstly decreasing and then increasing with the increase of hydrostatic pressure. Copyright © 2016 John Wiley & Sons, Ltd.