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PubMed1975

Properties and specificity of the major anionic trypsin-like enzyme in the keratinolytic larvae of the webbing clothes moth.

The major form of the trypsin-like proteinases from the larvae of the webbing clothes moth Tineola bisselliella has been further purified and some of its properties investigated. It differs from bovine trypsin in several respects. It is anionic at neutral pH, is very stable at alkaline pH, has no requirement for calcium ions for this stability and is very sensitive to urea. It resembles vertebrate trypsins in its complete inhibition by diisopropylfluorophosphate, its pH optimum of 8.5 for hydrolysis of benzoyl-arginine p-nitroanilide and its cleavage specificity against glucagon and the beta-chain of S-carboxymethyl insulin.

Amino Acids↗

PubMed1976

Properties of the major carboxypeptidase in the larvae of the webbing clothes moth, Tineola bisselliella.

The larvae of the webbing clothes moth, Tineola bisselliella contain two carboxypeptidases (EC 3.4.12-) and one of these has been purified by preparative polyacrylamide gel electrophoresis. Its pH optimum for the hydrolysis of N-benzyloxycarbonyl-glycyl-leucine was pH 7.5-7.7 and its molecular weight as judged by gel filtration was 72 000. It is strongly inhibited by disopropylfluorophosphate, thiol reagents and some metal cations and also by 1:10 phenanthroline but not EDTA. Km and V values for the hydrolysis of 13 N-acyl dipeptides were determined. The enzyme has a strong preference for neutral aliphatic amino acid residues and does not hydrolyse C-terminal proline, arginine or lysine. It is a true carboxypeptidase, requiring an L-amino acid in the C-terminal position, with a free carboxyl group and hydrolysing peptide substrates consecutively from the C-terminal end. Dipeptides are cleaved much more slosly than tripeptides or N-acyl dipeptides.

Animals↗

PubMed1991

Application of polymyxin-coated polyester cloth to the semi-quantitation of Salmonella in processed foods.

A rapid and economical semi-quantitative test for Salmonella cells in foods is proposed. Food samples containing different levels of Salmonella cells were homogenized and serially diluted in enrichment broths and then incubated for about 20 h at 37 degrees C. The presence of Salmonella cells in each dilution was assayed by capturing deoxycholate-extracted Salmonella lipopolysaccharides on a sheet of polymyxin-coated polyester cloth, followed by colorimetric detection with an anti-Salmonella antibody-enzyme conjugate. The minimum dilutions which resulted in no detectable growth were correlated with the extent of Salmonella contamination in the food samples.

Colorimetry↗

PubMed1995

Effects of high levels of selenite and Escherichia coli on enrichment of Salmonella and detection of Salmonella by polymyxin-cloth enzyme immunoassay.

The effect of various concentrations of selenite on the recovery of Salmonella typhimurium and Escherichia coli was examined in a rich medium containing 0.5% cholate. For heat-injured S. typhimurium, longer preincubation periods were required for recovery in higher concentrations of selenite. When 0.7% selenite was added to 6-h preincubated cultures of heat-injured cells, S. typhimurium was fully recovered while E. coli, whether heat-injured or uninjured, did not recover when present at numbers at less than 2 x 10(7) colony forming units (CFU). The polymyxin-cloth enzyme immunoassay detected S. typhimurium grown from a small number (as low as 1 CFU) of cells in the presence of a large excess of E. coli.

Cholic Acid↗

PubMed1996

The impact of health education to promote cloth filters on dracunculiasis prevalence in the northern region, Ghana.

This paper describes a health education intervention which was conducted during the 1990 dry season in 3 study villages in the Northern Region of Ghana, to reduce dracunculiasis prevalence in that area by promoting the use of cloth filters for drinking water and avoidance of water contact by sufferers. The impact of the intervention in reducing dracunculiasis prevalence was examined by comparing the period prevalence of infection in 1990 and 1991. The findings demonstrate that the intervention had a measurable but limited impact on dracunculiasis prevalence. Face-to-face health education was successful in persuading 56% of households to buy filters. Ownership of at least one filter for every 10 people in the household was associated with a reduction of at least 20% in the risk of dracunculiasis.

Adult↗

PubMed2005

Adsorption kinetics and isotherms of pesticides onto activated carbon-cloth.

Adsorption of pesticides ametryn, aldicarb, dinoseb and diuron from aqueous solution onto high specific area activated carbon-cloth was studied. Kinetics of adsorption was followed by in situ UV-spectroscopy and the data were treated according to various rate models. The extent of adsorption was determined at the end of 125 min adsorption period. Rate constants and the extent of adsorption for the four pesticides were found to follow the order: dinoseb > ametryn > diuron > aldicarb. Adsorption isotherms were derived at 25 degrees C on the basis of batch analysis. Isotherm data were treated according to Langmuir and Freundlich models. The fits of experimental data to these equations were examined. The types of interactions between the surface and pesticide molecules were discussed.

2,4-Dinitrophenol↗

PubMed2006

Adsorption of dyes onto activated carbon cloth: using QSPRs as tools to approach adsorption mechanisms.

The present study aimed to investigate the adsorption of dyes onto activated carbon cloths. Kinetics and isotherms were studied based on results of batch reactors to constitute databases for the adsorption rates and capacities of 22 commercial dyes. Added to a qualitative analysis of experimental results, quantitative structure property relationships (QSPRs) were used to determine the structural features that influence most adsorption processes. QSPRs consisted of multiple linear regressions correlating adsorption parameters with molecular connectivity indices (MCIs) as molecular descriptors. Results related to adsorption kinetics showed that the size of molecules was the significant feature, the high order MCIs involved in QSPRs indicating the influence of a critical size on adsorption rate. Improved statistical fits were obtained when the database was divided according to the chemical classes of dyes. As regards to adsorption isotherms, their particular form led to the use of saturation capacity as the adsorption parameter. By contrast with adsorption kinetics, molecular overcrowding seemed to be of less influence on adsorption equilibrium. In this case, MCIs included in the QSPR were more related to details of the molecular structure. The robustness of the QSPR assessed for azo dyes was studied for the other dyes. Although the small size of the database limited predictive ability, features relevant to the influence of the database composition on QSPRs have been highlighted.

Adsorption↗

PubMed2005

Adsorption behaviors of some phenolic compounds onto high specific area activated carbon cloth.

Adsorption of phenol, hydroquinone, m-cresol, p-cresol and p-nitrophenol from aqueous solutions onto high specific area activated carbon cloth has been studied. The effect of ionization on adsorption of these ionizable phenolic compounds was examined by studying the adsorption from acidic, basic and natural pH solutions. Kinetics of adsorption was followed by in situ UV spectroscopy over a period of 90 min. First-order rate law was found to be valid for the kinetics of adsorption processes and the rate constants were determined. The highest rate constants were obtained for the adsorption from solutions at the natural pH. The lowest rate constants were observed in basic solutions. The rate constants decreased in the order p-nitrophenol approximately m-cresol>p-cresol>hydroquinone approximately phenol. Adsorption isotherms were derived at 30 degrees C and the isotherm data were treated according to Langmuir, Freundlich and Tempkin isotherm equations. The goodness of fit of experimental data to these isotherm equations was tested and the parameters of equations were determined. The possible interactions of compounds with the carbon surface were discussed considering the charge of the surface and the possible ionization of compounds at acidic, basic and natural pH conditions.

Adsorption↗

PubMed2006

Adsorption of aromatic organic acids onto high area activated carbon cloth in relation to wastewater purification.

Adsorption of aromatic organic acids: benzoic acid (BA), salicylic acid (SA), p-aminobenzoic acid (pABA) and nicotinic acid (NA), onto high area activated carbon cloth from solutions in 0.4 M H(2)SO(4), in water at natural pH, in 0.1 M NaOH and also from solutions having pH 7.0 were studied by in situ UV-spectroscopic technique. The first-order rate law was found to be applicable for the kinetic data of adsorption. The rates and extents of adsorption of the organic acids were the highest from water or 0.4 M H(2)SO(4) solutions and the lowest from 0.1 M NaOH solution. The order of rates and extents of adsorption of the four organic acids in each of the four solutions (0.4 M H(2)SO(4), water, solution of pH 7.0 and 0.1 M NaOH) was determined as SA>BA>NA approximately pABA. These observed orders were explained in terms of electrostatic, dispersion and hydrogen bonding interactions between the surface and the adsorbate species, taking the charge of the carbon surface and the adsorbate in each solution into account. Adsorption of BA in molecular form or in benzoate form was analyzed by treating the solution as a mixture of two components and applying Lambert-Beer law to two-component system. The adsorption isotherm data of the systems studied were derived at 30 degrees C and fitted to Langmuir and Freundlich equations.

4-Aminobenzoic Acid↗

PubMed2006

Kinetic and equilibrium studies on the removal of acid dyes from aqueous solutions by adsorption onto activated carbon cloth.

Removal of acid dyes Acid Blue 45, Acid Blue 92, Acid Blue 120 and Acid Blue 129 from aqueous solutions by adsorption onto high area activated carbon cloth (ACC) was investigated. Kinetics of adsorption was followed by in situ UV-spectroscopy and the data were treated according to pseudo-first-order, pseudo-second-order and intraparticle diffusion models. It was found that the adsorption process of these dyes onto ACC follows the pseudo-second-order model. Adsorption isotherms were derived at 25 degrees C on the basis of batch analysis. Isotherm data were treated according to Langmuir and Freundlich models. The fits of experimental data to these equations were examined.

Acids↗

PubMed2002

Adsorption of cadmium by activated carbon cloth: influence of surface oxidation and solution pH.

The surface of activated carbon cloth (ACC), based on polyacrylonitrile fibre as a precursor, was oxidised using nitric acid, ozone and electrochemical oxidation to enhance cadmium ion exchange capacity. Modified adsorbents were physically and chemically characterised by pH titration, direct titration, X-ray photoelectron spectroscopy, elemental analysis, surface area and porosimetry, and scanning electron microscopy. BET surface area decreased after oxidation, however, the total ion exchange capacity increased by a factor of approximately 3.5 compared to the commercial as-received ACC. A very significant increase in cadmium uptake, by a factor of 13, was observed for the electrochemically oxidised ACC. Equilibrium sorption isotherms were determined at pH 4, 5 and 6 and these showed that cadmium uptake increased with increasing pH. There was clear evidence of physical damage to ozone-oxidised fibre, however, acid and electrochemically oxidised samples were completely stable.

Adsorption↗

PubMed2003

Improvement in capacitive deionization function of activated carbon cloth by titania modification.

Activated carbon cloth (ACC) was modified by the reaction between polar groups on its surface and metal alkoxides of titanium, silicon, aluminum and zirconium to enhance its capacitive deionization (CDI) performance. Incorporated state of metals and surface property of modified ACC were deduced from surface analysis results obtained using FE-SEM, XRD, XPS and zeta-potential meter. Titania was highly dispersed on the ACC surface with tetrahedral coordination, and the incorporated titania was effective to decrease physical adsorption of NaCl and to increase electric field adsorption, resulting in a significant enhancement of CDI performance. The negligible contribution of silica, alumina and zirconia modifications suggested that the small oxidation-reduction potential of titania was responsible for the enhancement of the electric field adsorption. Reversibility of adsorption and desorption operation on titania-modified ACC were also discussed relating to its CDI function.

Adsorption↗

PubMed1997

Acid-base regulation, alpha-stat, and the emperor's new clothes.

Considerable time and effort have been expended to determine the most appropriate technique for management of a patient's acid-base status during hypothermic cardiopulmonary bypass. A critical question is whether to maintain plasma pH at 7.4 regardless of temperature (pH-stat) or to permit a relative alkalosis as the patient is cooled (alpha-stat). Until recently, there has been a remarkable lack of evidence in the literature for a consistent physiological benefit provided by one protocol over the other. The alpha-stat versus pH-stat controversy has taken on the characteristics of the emperor's new clothes, with alpha-stat winning by default because of theoretical arguments and because it was technically easier to perform. Part of the explanation is the realization that cellular mechanisms are capable of maintaining intracellular pH despite fluctuations in extracellular conditions. The prevailing plasma pH does have strong influence over cerebral blood flow, even to the point of overriding normal autoregulatory mechanisms. Recent evidence suggests that cerebral blood flow variations between alpha-stat and pH-stat conditions have important implications for patient outcomes.

Acid-Base Equilibrium↗

PubMedDate not supplied

Further insights into the persistence of transferred fibres on outdoor clothes.

This study was conducted to assess persistence of fibres on items of outdoor clothes in normal wear situations. The persistence of acrylic and wool fibres transferred on 23 recipient garments was examined in relation to: time of wear; features of the recipient garment (fibre composition, surface structure and texture); conditions of wear (public transport used or not), and; their location on the recipient. After 8 hours of wear more than 75% of transferred fibres were lost during 8-10 hours of wear. After 16 hours of wear no more than 10%, most often up to 5%, of fibres remained. Fibres were lost at higher rate when public transport was used. The persistence of fibres depended more on the surface structure and texture of the recipient garment and the location of donor fibres rather than on the type of fibre.

Journal Article↗

PubMedDate not supplied

A study in relation to the random distribution of four fibre types on clothing (incorporating a review of previous target fibre studies).

A new target fibre study was undertaken building upon eight previous published studies, which are reviewed here. Fifty-eight items of outer clothing, obtained from households across England, were taped and searched for three types of commonly occurring fibres and one less common fibre type. The tapes were examined using a combination of automatic and manual searching. Any fibres similar to the target fibres were removed and examined using microspectrophotometry, comparison microscopy, thin layer chromatography (TLC) and fourier transform infrared spectroscopy (FTIR) where applicable. One polyester fibre, four acrylic fibres and eleven wool fibres were found that matched the three commonly occurring target fibre samples. None of the less common polyester fibres were found. One item had six matching wool fibres and another had the polyester fibre and an acrylic fibre recovered from it. The remaining eight fibres were each recovered from individual items. The results suggest that finding a large number of fibres that match a control is unlikely to happen by chance, which supports the findings of the previous target fibre studies.

Journal Article↗

PubMed1985

An examination of teat drying with disinfectant impregnated cloths on the bacteriological quality of milk and on the transfer of Streptococcus agalactiae before milking.

Total bacterial counts of the milk from individual cows were measured for three groups of ten winter housed cows at three milkings. The teats were either (i) left unwashed or (ii) washed with disinfected water (60 ppm available iodine) and dried with individual paper towels or (iii) washed with plain water and then dried with a single fabric cloth impregnated with a polymeric bisguanide and a quaternary ammonium compound. The mean total bacterial counts/ml for the groups were 5820, 2108 and 1116 respectively. Treatments (ii) and (iii) were also compared for their ability to prevent the inter-teat transfer of bacteria. Before teat washing and drying, one teat of each cow was deliberately contaminated with Streptococcus agalactiae. Significantly fewer teats (5/30) became contaminated with Str. agalactiae when treatment (iii) was used for teat washing and drying compared with treatment (ii) (20/30).

Animals↗

PubMed2004

Activated carbon fiber cloth electrothermal swing adsorption system.

Capture and recovery of hazardous air pollutants (HAPs) and volatile organic compounds (VOCs) from gas streams using physical adsorption onto activated carbon fiber cloth (ACFC) is demonstrated on the bench-scale. This system is regenerated electrothermally, by passing an electric current directly through the ACFC. The adsorbate desorbs from the ACFC, rapidly condenses on the inside walls of the adsorber, and then drains from the adsorber as a pure liquid. Rapid electrothermal desorption exhibits such unique characteristics as extremely low purge gas flow rate, rapid rate of ACFC heating, rapid mass transfer kinetics inherent to ACFC, and in-vessel condensation. An existing system was scaled up 500%, and the new system was modeled using material and energy balances. Adsorption isotherms using methyl ethyl ketone (MEK) and ACFC were obtained while electricity passed through the ACFC and at temperatures above MEK's boiling point. These isotherms agreed within 7% to Dubinin-Radushkevich modeled isotherms that were extrapolated from independently determined gravimetric measurements obtained at lower temperatures. Energy and material balances for the electrothermal desorption of organic vapors and ACFC agree to within 7% of experimentally measured values. These results allow the modeling of electrothermal desorption of organic vapors from gas streams with in-vessel condensation to optimize operating conditions of the system during regeneration of the adsorbent.

Adsorption↗

PubMed2005

Microwave-swing adsorption to capture and recover vapors from air streams with activated carbon fiber cloth.

Adsorption with regeneration is a desirable means to control the emissions of organic vapors such as hazardous air pollutants (HAPs) and volatile organic compounds (VOCs) from air streams as it allows for capture, recovery, and reuse of those VOCs/HAPS. Integration of activated-carbon fiber-cloth (ACFC) adsorbent with microwave regeneration provides promise as a new adsorption/ regeneration technology. This research investigates the feasibility of using microwaves to regenerate ACFC as part of a process for capture and recovery of organic vapors from gas streams. A bench-scale fixed-bed microwave-swing adsorption (MSA) system was built and tested for adsorption of water vapor, methyl ethyl ketone (MEK), and tetrachloroethylene (PERC) from an airstream and then recovery of those vapors with microwave regeneration. The electromagnetic heating behavior of dry and vapor-saturated ACFC was also characterized. The MSA system successfully adsorbed organic vapors from the airstreams, allowed for rapid regeneration of the ACFC cartridge, and recovered the water and organic vapors as liquids.

Adsorption↗