Changes In Surface pH Research Articles

Can ocean iron fertilization mitigate ocean acidification?

Ocean iron fertilization has been proposed as a method to mitigate an- thropogenic climate change, and there is continued commercial interest in using iron fertilization to generate carbon credits. It has been further speculated that ocean iron fertilization could help mitigate ocean acidification. Here, using a global ocean car- bon cycle model, we performed idealized ocean iron fertilization simulations to place an upper bound on the effect of iron fertilization on atmospheric CO2 and ocean acidification. Under the IPCC A2 CO2 emission scenario, at year 2100 the model simulates an atmospheric CO2 concentration of 965 ppm with the mean surface ocean pH 0.44 units less than its pre-industrial value of 8.18. A globally sustained ocean iron fertilization could not diminish CO2 concentrations below 833 ppm or reduce the mean surface ocean pH change to less than 0.38 units. This maximum of 0.06 unit mitigation in surface pH change by the end of this century is achieved at the cost of storing more anthropogenic CO2 in the ocean interior, furthering acidifying the deep- ocean. If the amount of net carbon storage in the deep ocean by iron fertilization produces an equivalent amount of emission credits, ocean iron fertilization further acidifies the deep ocean without conferring any chemical benefit to the surface ocean.

Environmental green chemistry applications of nanoporous carbons

Influence of surface properties of nanoporous carbons on activity and selectivity during the photooxidation of 4-chlorophenol on UV-irradiated TiO2 was performed. Characterization by infrared spectroscopy, X-ray photoelectronic spectroscopy and X-ray absorption near edge structure spectroscopy confirm the presence of a contact interface between both solids and suggest the coordination of some functional organic groups of the carbon surface, mainly ethers and carboxylic acids, to metallic centre Ti+4 in TiO2. Changes in surface pH of carbons from basic to neutral or acid remarkably increase the production of 4-chlorocathecol by a factor of 22 on TiO2–Carbon in comparison of TiO2 alone. A scheme of interaction between TiO2 and carbon is proposed to the increased photoactivity of TiO2 and a reaction mechanism for the different intermediate products detected is also proposed. Results showed that TiO2–Carbon can be used as an alternative photocatalyst for environmental green chemistry and selective organic synthesis applications.

Alteration of bacterial surface electrostatic potential and pH upon adhesion to a solid surface and impacts to cellular bioenergetics

In our previous study [Hong Y, Brown DG (2009) Appl Environ Microbiol 75(8):2346-2353], the adenosine triphosphate (ATP) level of adhered bacteria was observed to be 2-5 times higher than that of planktonic bacteria. Consequently, the proton motive force (Delta p) of adhered bacteria was approximately 15% greater than that of planktonic bacteria. It was hypothesized that the cell surface pH changes upon adhesion due to the charge-regulated nature of the bacterial cell surface and that this change in surface pH can propagate to the cytoplasmic membrane and alter Delta p. In the current study, we developed and applied a charge regulation model to bacterial adhesion and demonstrated that the charge nature of the adhering surface can have a significant effect on the cell surface pH and ultimately the affect the ATP levels of adhered bacteria. The results indicated that the negatively charged glass surface can result in a two-unit drop in cell surface pH, whereas adhesion to a positively charged amine surface can result in a two-unit rise in pH. The working hypothesis indicates that the negatively charged surface should enhance Delta p and increase cellular ATP, while the positively charged surface should decrease Delta p and decrease ATP, and these results of the hypothesis are directly supported by prior experimental results with both negatively and positively charged surfaces. Overall, these results suggest that the nature of charge on the solid surface can have an impact on the proton motive force and cellular ATP levels.

Abrupt sea surface pH change at the end of the Younger Dryas in the central sub-equatorial Pacific inferred from boron isotope abundance in corals (Porites)

Abrupt sea surface pH change at the end of the Younger Dryas in the central sub-equatorial Pacific inferred from boron isotope abundance in corals (Porites)

Modelling surface pH and emissions of hydrogen sulphide, ammonia, acetic acid and carbon dioxide from a pig waste lagoon

Pig slurry is a source of atmospheric pollutants. Emissions of basic and acidic compounds, such as hydrogen sulphide (H2S) from slurry are largely dependent on surface pH. In a storage system, the pH at the surface changes over time due to volatilisation of ammonia (NH3), carbon dioxide (CO2) and acetic acid (HAc). In this article, a gas emission–pH (GE–pH) coupled model is proposed to describe the release of H2S, NH3, CO2 and HAc from pig slurry. The GE–pH model accounts for changes in pH and concentration of buffer components in the surface layer due to volatilisation. The model was applied to calculate gaseous emissions from an undisturbed pig waste lagoon. The predicted pH at the surface layer in the undisturbed slurry lagoon increased over time from 8.0 (initial pH in the homogenised slurry) up to 8.64. H2S emissions predicted by the GE–pH coupled model (7.61 ± 0.56 μg m−2 min−1) showed a good agreement with measured data (5.92 ± 3.90 μg m−2 min−1) compared to previous gaseous models in which changes in surface pH caused by emission of NH3, CO2 and HAc were not considered (126.01 ± 1.53 μg m−2 min−1). This improvement supports the idea that emissions of important acidic and basic gases (such as CO2 and NH3), and changes in buffer component concentrations and pH at the surface layers due to volatilisation of these gases, should be taken into account when modelling the emissions of a specific (acidic or basic) target gas, such as H2S.

Eco-friendly TiO2–AC Photocatalyst for the Selective Photooxidation of 4-Chlorophenol

The influence of surface pH of activated carbon on selectivity of TiO2 during the photooxidation of 4-chlorophenol on UV-irradiation was studied. Chlorine substitution by p-hydroxylation yielding hydroquinone in equilibrium with benzoquinone and o-hydroxylation to 4-chlorocathecol were detected as the main intermediates in the photooxidation of 4CP. Changes in surface pH of carbons from basic to closely neutral induce a remarkably increase in the production of 4-chlorocatechol by a factor of 22 on TiO2–AC in comparison of TiO2 alone. A mechanism of interaction between both solids is proposed to explain changes both in photoactivity and photoselectivity of TiO2. In conclusion, results showed that TiO2–AC can be used as an alternative green photocatalyst in organic synthesis.

Relative CO 2 /NH 3 selectivities of AQP1, AQP4, AQP5, AmtB, and RhAG

The water channel aquaporin 1 (AQP1) and certain Rh-family members are permeable to CO(2) and NH(3). Here, we use changes in surface pH (pH(S)) to assess relative CO(2) vs. NH(3) permeability of Xenopus oocytes expressing members of the AQP or Rh family. Exposed to CO(2) or NH(3), AQP1 oocytes exhibit a greater maximal magnitude of pH(S) change (DeltapH(S)) compared with day-matched controls injected with H(2)O or with RNA encoding SGLT1, NKCC2, or PepT1. With CO(2), AQP1 oocytes also have faster time constants for pH(S) relaxation (tau(pHs)). Thus, AQP1, but not the other proteins, conduct CO(2) and NH(3). Oocytes expressing rat AQP4, rat AQP5, human RhAG, or the bacterial Rh homolog AmtB also exhibit greater DeltapH(S)(CO(2)) and faster tau(pHs) compared with controls. Oocytes expressing AmtB and RhAG, but not AQP4 or AQP5, exhibit greater DeltapH(S)(NH(3)) values. Only AQPs exhibited significant osmotic water permeability (P(f)). We computed channel-dependent (*) DeltapH(S) or P(f) by subtracting values for H(2)O oocytes from those of channel-expressing oocytes. For the ratio DeltapH(S)(CO(2))*/P(f)*, the sequence was AQP5 > AQP1 congruent with AQP4. For DeltapH(S)(CO(2))*/DeltapH(S)(NH(3))*, the sequence was AQP4 congruent with AQP5 > AQP1 > AmtB > RhAG. Thus, each channel exhibits a characteristic ratio for indices of CO(2) vs. NH(3) permeability, demonstrating that, like ion channels, gas channels can exhibit selectivity.

Micro‐shear bond strengths and etching efficacy of a two‐step self‐etching adhesive system to fluorosed and non‐fluorosed enamel

The purpose of this study was to evaluate the micro-shear bond strengths and the etching efficacy of a two-step self-etching adhesive system to fluorosed and non-fluorosed enamel. The extracted teeth, obtained from Australian and Japanese patients, were classified according to the severity of fluorosis, using the Thylstrup & Fejerskov index (TFI). Australian teeth were classified as mildly fluorosed (TFI = 1-3), whereas Japanese teeth were classified as non-fluorosed (TFI = 0). Resin composite was bonded to 20 enamel samples using Clearfil SE bond. The bonded samples were stressed at a crosshead speed of 1 mm min(-1) to determine the micro-shear bond strength. To examine the etching efficacy of primer on fluorosed and non-fluorosed enamel, the enamel-surface pH values were directly measured using a micro pH sensor. The non-fluorosed enamel showed significantly higher bond strengths compared with the fluorosed enamel. There was a statistical difference between fluorosed and non-fluorosed enamel regarding the surface pH change before and after application of the Clearfil SE bond primer. The results from this study suggest that water fluoridation has an effect on the acid resistance of enamel surfaces when treated with a two-step self-etching adhesive system and that this effect leads to reduced bond strengths.

Changes in soil mineral nitrogen, nitrogen leached, and surface pH under annual and perennial pasture species

Soil mineral nitrogen (N) profiles during the growing season and changes in total soil N and available N after 3–4 years were examined under 9 different pasture swards containing annual legumes, lucerne (Medicago sativa L.), or one of 4 perennial grasses at 2 sites representative of the low and medium rainfall belt of south-eastern Australia. The effect of the presence of phalaris (Phalaris aquatica L.) or lucerne on the spatial variation in surface pH was also measured. The 9 pastures were subterranean clover (Trifolium subterraneum L.), subterranean clover with annual weeds, yellow serradella (Ornithopus compressus L.), lucerne, phalaris, cocksfoot (Dactylis glomerata L.), lovegrass (Eragrostis curvula (Schrader) Nees), wallaby grass (Austrodanthonia richardsonii (Cashm.) H.P. Linder), and a mixture of lucerne, phalaris, and cocksfoot. All the perennial treatments were sown with subterranean clover. Available mineral N values in the surface 0.10 m of soil following summer rainfall were substantially higher in pure subterranean clover or serradella (Ornithopus compressus L.) swards (24–50 μg N/g) than those containing a mixture of subterranean clover and perennials (9–20 μg N/g). Apparent leaching of soil nitrate down the profile during winter was greatest in annual pasture treatments and least in swards containing perennials. Soil pH(CaCl2) at the 0–0.10 m depth varied with proximity to perennial plants and was significantly higher (+0.2–1.1 pH units) near the base of perennial plants than in gaps between the perennials or in annual-only swards. Available mineral N to 1.0 m before cropping at the end of the pasture phase was highest following subterranean clover (175–344 kg N/ha) and serradella (202–316 kg N/ha) at both sites. Available N was lowest (91–143 kg N/ha) following perennial grass–clover swards at the drier site where the annual legume content was lower, but perennial grass–clover swards produced larger soil N values (147–219 kg N/ha) at the higher rainfall site. Removal of the pasture in August–September compared with November in the year before cropping increased available N at the time of sowing by an average of 44% (51 kg N/ha) at the drier site and 43% (74 kg N/ha) at the wetter site. Incorporating perennial pasture species in swards was found to be advantageous in reducing nitrate leaching and preventing a decline in surface soil pH; however, available soil N to following crops could be lower if the annual legume content of perennial grass-based pastures declined due to competition from the perennial species.

The impact of Manuka honey dressings on the surface pH of chronic wounds

Chronic non healing wounds have an elevated alkaline environment. The acidic pH of Manuka honey makes it a potential treatment for lowering wound pH, but the duration of effect is unknown. Lowering wound pH can potentially reduce protease activity, increase fibroblast activity and increase oxygen release consequently aiding wound healing. The aim of this study was to analyse the changes in surface pH and size of non healing ulcers following application of Manuka honey dressing after 2 weeks. The study was an open label, non randomised prospective study. Patients presenting consecutively with non healing chronic superficial ulcers, determined by aetiology and no reduction in wound size in previous 3 weeks. Single pH measurements recorded using Blueline 27 glass surface electrode and R 315 pH meter set (Reagecon/Alkem, Co. Clare Ireland). Area determined using Visitrak (Smith & Nephew, Mull, UK) digital planimetry. Apinate (Manuka honey) (Comvita, Slough, UK) applied to wounds for 2 weeks after which wounds re-evaluated. Eight males and nine females with 20 ulcers (3 bilateral) were included: venous, 50% (n = 10); mixed aetiology, 35% (n = 7); arterial, 10% (n = 2) and pressure ulcer, 5% (n = 1). Reduction in wound pH after 2 weeks was statistically significant (P < 0.001). Wounds with pH >or= 8.0 did not decrease in size and wounds with pH <or= 7.6 had a 30% decrease in size. A reduction in 0.1 pH unit was associated with an 8.1% reduction in wound size (P < 0.012). The use of Manuka honey dressings was associated with a statistically significant decrease in wound pH and a reduction in wound size. Elevated pH readings at the start were associated with minimal reduction in size. Surface wound pH measurements may contribute to objective wound assessments, but further research is necessary to determine its exact contribution.

Deciphering PiT transport kinetics and substrate specificity using electrophysiology and flux measurements

Members of the SLC20 family or type III Na(+) -coupled P(i) cotransporters (PiT-1, PiT-2) are ubiquitously expressed in mammalian tissue and are thought to perform a housekeeping function for intracellular P(i) homeostasis. Previous studies have shown that PiT-1 and PiT-2 mediate electrogenic P(i) cotransport when expressed in Xenopus oocytes, but only limited kinetic characterizations were made. To address this shortcoming, we performed a detailed analysis of SLC20 transport function. Three SLC20 clones (Xenopus PiT-1, human PiT-1, and human PiT-2) were expressed in Xenopus oocytes. Each clone gave robust Na(+)-dependent (32)P(i) uptake, but only Xenopus PiT-1 showed sufficient activity for complete kinetic characterization by using two-electrode voltage clamp and radionuclide uptake. Transport activity was also documented with Li(+) substituted for Na(+). The dependence of the P(i)-induced current on P(i) concentration was Michaelian, and the dependence on Na(+) concentration indicated weak cooperativity. The dependence on external pH was unique: the apparent P(i) affinity constant showed a minimum in the pH range 6.2-6.8 of approximately 0.05 mM and increased to approximately 0.2 mM at pH 5.0 and pH 8.0. Xenopus PiT-1 stoichiometry was determined by dual (22)Na-(32)P(i) uptake and suggested a 2:1 Na(+):P(i) stoichiometry. A correlation of (32)P(i) uptake and net charge movement indicated one charge translocation per P(i). Changes in oocyte surface pH were consistent with transport of monovalent P(i). On the basis of the kinetics of substrate interdependence, we propose an ordered binding scheme of Na(+):H(2)PO(4)(-):Na(+). Significantly, in contrast to type II Na(+)-P(i) cotransporters, the transport inhibitor phosphonoformic acid did not inhibit PiT-1 or PiT-2 activity.

Surface potential distribution over a zinc/steel galvanic couple corroding under thin layer of electrolyte

In this study, surface potential and surface pH changes over a zinc/steel galvanic couple corroding in artificial seawater (ASW) at 60 and 90% RH have been investigated. The results from surface potential and surface pH measurements were substantiated by the surface observation of the corroded sample during and after the corrosion test. The potential difference over the zinc and steel surface in 90% RH was very low (less than 200 mV) showing that whole steel surface was under galvanic protection. On the other hand, in 60% RH, after several days of corrosion the potential difference between the zinc coating and the steel surface was very high (more than 500 mV) and hence the galvanic protection was limited to interface region. The X-ray analysis of the sample corroded in 60% RH has shown that the zinc corrosion products were deposited on the steel surface near the interface, the same region has shown a low pH compared to than in other part of the steel surface. This led to conclude that with the progress of corrosion, the coating surface of zinc coated steel acidifies by the hydrolysis reaction of the dissolved zinc ions, and the iron surface showed the alkalinity by the oxygen reduction reaction. Moreover, the parts of the steel surface covered with zinc corrosion products had developed relatively less noble potential than other parts indicating that zinc corrosion products took a role to protect the base steel against corrosion. It was assumed that this behavior was related to a combination of the water absorbing capability of zinc corrosion products and adsorption of zinc ion on the steel surface due to low pH.

Interaction of piroxicam and meloxicam with DMPG/DMPC mixed vesicles: Anomalous partitioning behavior

Small unilamellar vesicles (SUVs) formed from a mixture of dimyristoylphosphatidylcholine (zwitterionic lipid with bulkier headgroup) and dimyristoylphosphatidylglycerol (anionic lipid with relatively smaller headgroup) allows better modulation of the physical properties of lipid bilayers compared to SUVs formed by a single type of lipid, providing us with a better model system to study the effect of membrane parameters on the partitioning of small molecules. Membrane parameter like packing of the vesicles is more pronounced in the gel phase and hence the study was carried out in the gel phase. Mixed vesicles formed from DMPG and DMPC with the mole percent ratio of 100:0, 90:10 and 80:20 were used for this study. As examples of polar solutes, piroxicam and meloxicam, two Non Steroidal Anti-inflammatory Drugs (NSAIDs) were chosen. The pH was adjusted to 2.8 in order to eliminate the presence of anionic forms of the drugs that would not approach the vesicles containing negatively charged DMPG (50% deprotonated at pH 2.8). Surface potential measured by using TNS (2,6- p-toluidinonaphthalene sulfonate, sodium salt) as surface charge sensitive probe showed no significant changes in the surface electrostatics in increasing DMPC content from 0 to 20%. Transmission electron microscopy (TEM) was used to characterize SUVs of different composition at pH 2.8. The average diameter of the mixed vesicles was found to be smaller than that formed by DMPG and DMPC alone. Partition coefficient ( K P) of piroxicam and meloxicam was measured using intrinsic fluorescence of these molecules. K P value of piroxicam decreases with increase in DMPC content whereas it increases with DMPC content in case of meloxicam. This anomalous behavior of partitioning is unexpected since there was no significant change in surface pH of the vesicles and has been explained in terms of lipid packing and water penetration in the lipid bilayer.

A new method for gaining insight into the chemistry of drying mineral surfaces using ATR-FTIR

Although it is understood that the chemical environment at a drying surface is likely to be quite different from that at a fully hydrated surface, the difficulty of quantitative measurement has meant that this potentially crucial aspect of surface chemistry has gone largely overlooked. As a result, most of our understanding comes from measurement before and after drying, with a gray region of speculation in between. An interesting natural example is the paradoxical reduction of Mn oxides in moist soils as they dry, because drying is usually considered an oxidative process. This phenomenon indicates that important chemical changes are occurring during drying and an approach is needed to probe the chemistry of drying surfaces. Here we show the suitability of attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy for real-time, in situ investigation of the drying solid–water interface, using the change in surface pH as an example. This was achieved by adsorbing thymol blue pH indicator (p K a = 1.65 ) onto a natural Mn-rich clay and observing the real-time pH change, which dropped from pH 5 to below pH 1.65 with the removal of free water from the surface.

Visible and subclinical skin changes in male and female dispatch department workers of newspaper printing plants

BACKGROUND AND PROBLEM: Wet work and skin exposure to detergents or solvents are well-established causes of irritant hand dermatitis. In contrast, physical irritation of the skin as another potential cause of occupational hand dermatitis has been investigated less. Our study included 71 individuals exposed to physical irritation during work in the dispatch department of two newspaper printing plants. Clinical examination and measurements of transepidermal water loss (TEWL), capacitance and skin surface pH of the skin of hands and forearms was performed. Erythema and/or scaliness of the hands were unexpectedly common: 26 of the 38 female inlay workers, 11 of the 13 male inlay workers and 15 of the 20 male machine operators were affected, compared to 18 of 28 printers exposed to solvents who had been investigated in a previous study. A significantly higher skin surface pH on the hands (P < 0.05) and, less pronounced, on the forearms (P > 0.05) was found in females. There was no association between domestic skin exposure, according to questionnaire data, and the bioengineering results. Skin cleansing and skin care differed between male and female workers, but were again not associated with the outcomes. The point prevalence of skin changes in dispatch department workers in the present study is unexpectedly high, which points to the importance of physical irritation by paper dust. Significant differences in bioengineering parameters between male and female inlay workers were found only for skin surface pH at the exposed back of hands. Future studies should (i) try to elucidate the role of skin surface pH changes and (ii) pay more attention to physical trauma to the skin.

Short communication: Teat skin pH.

Changes in teat skin surface pH were studied over 12 wk in 99 lactating Holstein cows. Half the udder of each cow routinely received postmilking disinfection, and the other half served as control. Measures of pH were made on all teats at weekly intervals. Teat skin pH was affected by treatment but not week. Mean teat skin pH measures were: 7.18 (+/- 0.64) and 7.53 (+/- 0.46) for treatment and control teats. In study II, pH teat skin measures were made hourly on 16 cows, starting 2 h before milking, immediately before a milking, immediately after a milking, and for 2 h postmilking. Teat skin pH was significantly lower for treatment teats and was lower for all teats postmilking.

Basipetal propagation of gravity-induced surface pH changes along primary roots of Lepidium sativum L.

While there is ample evidence for a role of auxin in root gravitropism, the seeming rapidity of gravi-induced changes in electrical parameters has so far been an argument against auxin being a primary signal in gravitropic signal transmission. To address this problem, we re-investigated the effect of gravistimulation on membrane voltages of Lepidium sativum L. and Vigna mungo L. root cells. In our hands, gravistimulation did not induce changes in membrane voltage in cells of the root cap statenchyma, root meristem or apical elongation zone that can be correlated with the orientation of the cells relative to the gravity vector. While these results challenge a model of rapid electrically based signal transmission, there is evidence for a slower signal propagation along gravistimulated L. sativum roots. Using multiple proton-selective microelectrodes to simultaneously measure surface pH on opposite root flanks at different distances from the root tip, we observed gravi-induced asymmetric pH changes at the surface of all investigated root zones. Upon gravistimulation, the surface pH decreased on the physically upper root flank and increased on the lower flank. The pH asymmetry appeared first [2.1+/-0.4 min (mean +/- SD) after tilting] at the root cap and then - with incrementing lag times - at the meristem (after 2.5+/-0.3 min at 300 micro m from root tip; after 3.7+/-0.4 min at 700 micro m) and apical elongation zone (4.8+/-0.5 min at 1,000 micro m), suggesting a basipetal progression of differential surface acidification at a rate of 250-350 micro m min(-1), consistent with reported auxin transport rates.

Aluminium-induced growth inhibition is associated with impaired efflux and influx of H+ across the plasma membrane in root apices of squash (Cucurbita pepo).

It is generally understood that the inhibition of growth of root apices is the initial effect caused by aluminium (Al) toxicity. The correlation between impaired H+-fluxes across the plasma membrane (PM) and Al-induced growth inhibition, Al accumulation and callose formation in root apices of squash (Cucurbita pepo L. cv. Tetsukabuto) is reported here. The root inhibition was dependent on Al concentration, and the duration of exposure, with the damage occurring preferentially in regions with high Al accumulation and callose formation. Using the fluorescent Al indicator (Morin), Al was localized in the cell walls of the root-tip cells after 3 h and in the whole root-tip cells after 6 h of the Al treatment (50 micro M). The inhibition of H+-pumping rate in the highly purified PM vesicles obtained from the Al-treated apical root portions (1 cm) coincided with the inhibition of root growth under Al stress. Furthermore, H+-ATPase activity of PM vesicles prepared from the control root apices was strongly inhibited by Al in vitro in a dose-dependent manner. Approximately 50% inhibition was observed when PM vesicles were preincubated at Al concentration as low as 10 micro M followed by the enzyme assay in the medium without Al. Using the pH indicator (bromocresol purple), it is shown that surface pH of the control (0 Al) root apices was strongly alkalized from the starting pH of 4.5 in a time-dependent manner. By contrast, the surface pH changed only slightly in the Al-treated root apices. The changes in surface pH mediated by altered dynamics of H+ efflux and influx across the root tip PM play an important role in root growth as affected by Al.

The use of chitosan gels as matrices for electrically-modulated drug delivery

This study evaluated and characterized the use of chitosan gels as matrices for electrically modulated drug delivery. Chitosan gels were prepared by acetylation of chitosan and subsequently hydrated to facilitate further studies. After determining the degree of deacetylation, hydrated and unhydrated gel formulations were characterized for their microviscosity and compression strength. In the electrification studies, gel mass variation, surface pH changes, and later, release-time profiles for neutral (hydrocortisone), anionic (benzoic acid), and cationic (lidocaine hydrochloride) drug molecules from hydrated chitosan gels were monitored in response to different milliamperages of current as a function of time. Hydrated gels had very similar microviscosity while exhibiting differences in the gel strength, results which are not inconsistent as they pertain to different aspects of the gel. The cumulative gel mass loss and rate of gel mass loss increased with an increase in the milliamperage (mA) of the applied current. Gel syneresis — principally involving electroosmosis and gel collapse — was pronounced, particularly at higher mAs and for chitosan gels with lower degrees of acetylation. The surface pH values of the gels were lower at the anode and higher at the cathode, in accordance with reports in the literature. The release of the model drugs from the gel matrix was in the order benzoic acid>hydrocortisone>lidocaine, which is consistent with the electrokinetically competing forces that are involved in these gels. Adequate characterization of electrical effects on formulation matrices, such as chitosan gels, is critical to the development of effective and reliable electrically modulated drug delivery systems.

The Effect of Heat Treatment and Surface Roughness on the Zincate Treatment of Aluminium Alloy 6082

SUMMARYThe effect of heat treatment and surface roughness on the zincate treatment of aluminium alloy 6082 was investigated using scanning electron microscopy, electrochemical measurement and surface profilometry. It has been found that the heat treatment of the alloy has a smalt effect on the ease of zincate plating. The zinc coverage is incomplete at grain boundaries of aged samples. Surface roughness has a greater effect: on rougher surfaces, the zinc preferentially grows on peaks rather than in the valleys: the effect is consistent with a lower open circuit potential during plating. The roughness effect is explained in terms of the transport of zinc to the surface and local pH changes.