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Tuesday, December 07, 2010

Industry urged to take precautions with triclosan

source cosmetics design-europe.com

By Andrew McDougall, 03-Dec-2010

Following various studies on the use of the antibacterial agent triclosan in consumer products, including oral care, experts are urging companies to remove it from their formulations as a precaution.

Elizabeth Salter Green, director of ChemTrust, a health and environmental body, explained that on a precautionary basis the chemical may not be safe to use at any level.

“It is important to stress that triclosan is not a dioxin, however concerns are that under certain circumstances it can develop the ability to disrupt hormones,” she told CosmeticsDesign-Europe.com.

Found in many consumer products

Triclosan is an ingredient added to many consumer products as an antibacterial ingredient.

It may be found in products such as antibacterial soaps and body washes, toothpastes, and some cosmetics. It is regulated by the U.S. Food and Drug Administration (FDA), and the European Union.

At this time, the FDA does not have evidence that triclosan added to antibacterial soaps and body washes provides extra health benefits over soap and water. However it stated that in 1997, reviewed extensive effectiveness data on triclosan in Colgate Total toothpaste showing that triclosan in this product was effective in preventing gingivitis.

Salter Green suggested that whilst one toxin may be harmless in a product individually, they may be dangerous if reacting together, suggesting that if there was no benefit for the toxin, it should be left out of the formulation.

Removed from GSK’s oral products

Oral care giant, GlaxoSmithKline, has removed triclosan from its Aquafresh and Sensodyne toothpastes, as well as its Corsodyl mouthwash, according to the University of Florida which has performed a study on the ingredient in sheep.

“If one eats the right foods and maintains correct dental hygiene, then triclosan, or other antibacterial agents are not needed,” explained Salter Green.

In the study by the University of Florida, researchers found that levels of triclosan were potentially damaging to the unborn foetus, if ingested by the carrying mother.

“We know it's a problem. But we just don't know how much of a problem. Triclosan can affect blood flow to the uterus, meaning the baby’s brain does not get the oxygen it needs,” said Professor Margaret James, who is the lead-author of the present study.

Discussing this particular study, Salter Green mentioned that a developing foetus in the uterus is extremely sensitive, and may be affected by disrupted hormone affecting brain development, metabolism, or the reproductive system.

Although this test was carried out on sheep, she explained that if the triclosan disrupts the hormone activity in an animal, whilst not being 100 per cent comparable, preserved hormonal evolution would suggest possible dangers to humans, and that the agent should be avoided if possible purely from a precautionary level.

comment

after wide spread use in sanitizers an increase in dioxine levels was experienced, leading to the conclusion that under some circumstances dioxines may be formed from triclosan.

FDA-fact sheet triclosan


What is triclosan?

Triclosan is an ingredient added to many consumer products to reduce or prevent bacterial contamination. It may be found in products such as clothing, kitchenware, furniture, and toys. It also may be added to antibacterial soaps and body washes, toothpastes, and some cosmetics—products regulated by the U.S. Food and Drug Administration (FDA).

What is known about the safety of triclosan?

Triclosan is not currently known to be hazardous to humans. But several scientific studies have come out since the last time FDA reviewed this ingredient that merit further review.

Animal studies have shown that triclosan alters hormone regulation. However, data showing effects in animals don’t always predict effects in humans. Other studies in bacteria have raised the possibility that triclosan contributes to making bacteria resistant to antibiotics.

In light of these studies, FDA is engaged in an ongoing scientific and regulatory review of this ingredient. FDA does not have sufficient safety evidence to recommend changing consumer use of products that contain triclosan at this time.

Does triclosan provide a benefit in consumer products?

For some consumer products, there is clear evidence that triclosan provides a benefit. In 1997, FDA reviewed extensive effectiveness data on triclosan in Colgate Total toothpaste. The evidence showed that triclosan in this product was effective in preventing gingivitis.

For other consumer products, FDA has not received evidence that the triclosan provides an extra benefit to health. At this time, the agency does not have evidence that triclosan in antibacterial soaps and body washes provides any benefit over washing with regular soap and water.

What consumers should know:

  • Triclosan is not known to be hazardous to humans.
  • FDA does not have sufficient safety evidence to recommend changing consumer use of products that contain triclosan at this time.
  • In light of questions raised by recent animal studies of triclosan, FDA is reviewing all of the available evidence on this ingredient’s safety in consumer products. FDA will communicate the findings of its review to the public in spring 2011.
  • At this time, FDA does not have evidence that triclosan added to antibacterial soaps and body washes provides extra health benefits over soap and water. Consumers concerned about using hand and body soaps with triclosan should wash with regular soap and water.
  • Consumers can check product labels to find out whether products contain triclosan.

How can I tell if there is triclosan in a product that I am using?

Antibacterial soaps and body washes, and toothpastes are considered over-the-counter drugs. If an over-the-counter drug contains triclosan, it will be listed as an ingredient on the label, in the Drug Facts box. If a cosmetic contains triclosan, it will be included in the ingredient list on the product label.

What is FDA doing to evaluate the safety of triclosan?

We are engaged in an ongoing scientific and regulatory review of the safety of triclosan in FDA-regulated products. We also have partnered with other Federal Agencies to study the effects of this substance on animal and environmental health (see http://www.epa.gov/oppsrrd1/REDs/factsheets/triclosan_fs.htm; http://www.epa.gov/endo/).

FDA is working to incorporate the most up-to-date data and information into the regulations that govern the use of triclosan in consumer products. FDA will communicate the findings of its review to the public in spring 2011.

This article appears on FDA's Consumer Updates page, which features the latest on all FDA-regulated products.

Date Posted: April 8, 2010

Friday, December 03, 2010

new interest in surfactant enhanced soil clean-up

In the last years I only sporadically observed new abstracts on this topic.
In the latest issue of clu-in.org I found several of them. It seems interest in this topic is revitalizing.

the first is not associated with surfactants I think

ADVANCED METHODOLOGIES FOR THE TREATMENT OF HYDROCARBON CONTAMINATED SLUDGES FROM SOIL WASHING PROCESSES

Garcia Frutos, F.J., O. Escolano, R. Perez, A. Rubio, A. Gimeno, M.D. Fernandez, M. Babin, G. Carbonell, C. Perucha, and J. Laguna. First Spanish National Conference on Advances in Materials Recycling and Eco-Energy, Madrid, 12-13 November 2009. Paper S02-6, p 49-52, 2009

Fine products (silt-clay fractions) in sludge from soil washing plants following bulk soil treatment usually are highly contaminated. These fractions commonly are committed to landfill disposal or thermal destruction (in the case of organic contaminants). This paper presents the results of preliminary physical-chemical and bioremediation treatability tests carried out on a hydrocarbon-heavy sludge sample after bulk soil processing in a soil washing plant. To date, best results were obtained in two bioremediation processes tested at lab scale—landfarming and bioreactors—which decreased hydrocarbon levels by better than 50% in two months and one month, respectively. http://digital.csic.es/bitstream/10261/18607/1/S02_6.pdf

comment: reducing the very high contamination with spending time and money by only 50 % is really not worse the effort.


ULTRASOUND ASSISTED SOIL WASHING FOR REMOVAL OF DIESEL WITH SURFACTANT
Cho, S.-H., Y. Son, J. Cha, S.-G. Nam, M. Lim, and J. Khim, Korea Univ.
Proceedings of Symposium on Ultrasonic Electronics, Vol 30, p 147-148, 2009 [18-20 November 2009, Paper 1P4-31]

Mechanical mixing generally is a key process in conventional soil washing, sometimes accompanied by injection of anionic or non-ionic surfactants to enhance mass transfer of pollutants from soil to aqueous phase. Tests of the application of ultrasound to the washing process indicate a significant increase in removal efficiency. When the washing water or slurry was irradiated with ultrasound, cavitation events occurred, and sonochemical and sonophysical effects were induced. Sonophysical effects, such as micro jet and micro streaming, could enhance mass transfer of organic/inorganic pollutants from soil phase to aqueous phase. This paper describes the conduct and results of a study undertaken to compare an ultrasonic soil washing process with a conventional mechanical soil washing treatment to gain a better understanding of the mechanisms of each process. http://www.use-jp.org/USE2010/proceedings/USE09/pdf/1P4-31.pdf


TREATMENT OF FUEL-OIL CONTAMINATED SOILS BY BIODEGRADABLE SURFACTANT WASHING FOLLOWED BY FENTON-LIKE OXIDATION
Tsai, T.T. and C.M. Kao (National Sun Yat-Sen Univ., Taiwan); R.Y. Surampalli (U.S. EPA, Kansas City, KS); S. H. Liang (National Sun Yat-Sen Univ.).
Journal of Environmental Engineering, Vol 135 No 10, p 1015-1024, 2009

A bench-scale study was conducted to develop a two-stage remedial system consisting of surfactant washing followed by a Fenton-like oxidation process to remediate fuel-oil contaminated soils. The researchers also evaluated the effects of residual surfactant and soil organic matter (SOM) on the efficiency of Fenton-like oxidation; the effect of potassium dihydrogen phosphate (KH2PO4) addition on the stability of H2O2 and oxidation efficiency; and the possible oxidation products after the oxidation process. In the surfactant washing stage, a biodegradable surfactant, Simple Green (SG) at 50 g/L, was applied to flush fuel-oil contaminated soil having initial total petroleum hydrocarbons (TPHs) concentration of 50,000 mg/kg. Washing with 45 pore volumes (PVs) of SG followed by 25 PVs of deionized water achieved 90% TPH removal, dropping the soil TPH concentration from 50,000 to 4,950 mg/kg. In the Fenton-like oxidation stage at initial soil TPH concentration of ~4,950 mg/kg, TPH removal efficiency increased significantly with increased H2O2 concentrations. There was evidence that residual SG and SOM can compete with TPH for oxidants and thereby decrease oxidation efficiency; hence, an oxidation-sorption-desorption-oxidation scheme for soil TPH was observed in this experiment due to the initial sorption of TPH on SOM. Addition of 2.2 mM of KH2PO4 increased the stability and half-life of H2O2 but decreased TPH removal efficiency. The oxidation potential of the Fenton-like process was insufficient to oxidize fuel oil completely to nontoxic end products. The by-products observed after the oxidation process contained carboxyl groups with molecular weights similar to their parent compounds. Results indicate that the two-stage remedial system shows promise for future treatment of fuel-oil contaminated soil.

REMEDIATION OF DDT-CONTAMINATED SOIL USING OPTIMIZED MIXTURES OF SURFACTANTS AND A MIXING SYSTEM
Ghazali, M., E. McBean, H. Shen, W. Anderson, and P.-A. Dastous.
Remediation Journal, Vol 20 No 4, p 119-132, 2010

A surfactant-aided soil washing technique was studied as an alternative method for remediation of DDT-contaminated clayey soil. The ex situ process used both nonionic and anionic surfactants. A mixture of 1% nonionic surfactant (Brij 35) and 1% anionic surfactant (SDBS) removed more than 50% of DDT from soil in a flow-through system, whereas individual surfactants or other combinations of the surfactants exhibited lower removal efficiency. The use of a mixing system improved the soil washing process. A combination of 2% Brij 35 and 0.1% SDBS was found to be optimum, removing 70 to 80% of DDT. Prewashing the soil with tap water decreased the adsorption of surfactants to soil particles by 30 to 40%, and postwashing recovered 90% of the surfactants.


BENCH SCALE TREATABILITY STUDIES OF CONTAMINATED SOIL USING SOIL WASHING TECHNIQUE

Gupta, M.K., R.K. Srivastava, and A.K. Singh.
E-Journal of Chemistry, Vol 7 No 1, p 73-80, 2010

Surfactant washing is an ex situ process. The excavated contaminated soil can be heaped on plastic liners or other impermeable barriers and irrigated with washing solutions such as surfactant; alternatively, batch washing of the contaminated soil can be conducted in tanks or lined pits using continuous flows washing in countercurrent or normal modes. The authors applied soil washing using plain water enhanced with surfactants to a study of the remediation of soil contaminated with engine lubricant oil or a heavy metal. The engine oil was used at different percentages (by dry weight of the soil) to contaminate the soil artificially. The geotechnical properties of the soil underwent large modifications after mixing with the oil. Sorption experiments were conducted with cadmium metal in an aqueous medium at different initial concentrations of the metal and at varying pH values of the sorbing medium. For the remediation of contaminated soil matrices, a nonionic surfactant was used for the restoration of geotechnical properties of the soil samples contaminated with lubricant oil, while an anionic surfactant was employed to desorb cadmium from the contaminated soil matrix. The surfactant for soil contaminated with lubricant oil was able to restore properties up to 98% of those of virgin soil, while up to 54% cadmium was desorbed from the contaminated soil matrix in surfactant-aided desorption experiments. http://www.e-journals.in/PDF/V7N1/73-80.pdf

comment: As nonionic surfactant Triton X-100, as anionic Sodium Dodecyl Sulfate, selection seems to be based on scholarly aspects.
In my experience for mineral oil contaminated soil a mixture of anionic/nonionic works best, e.g. 3 parts Na Alkyl benzene sulfonate / 7 parts Synperonic 91/4



ELECTROKINETIC REMOVAL OF PETROLEUM HYDROCARBON FROM RESIDUAL CLAYEY SOIL FOLLOWING A WASHING PROCESS

Jeon, C.-S., J.-S. Yang, K.-J. Kim, and K. Baek.
CLEAN — Soil, Air, Water, Vol 38 No 2, Feb 2010

A study was conducted of total petroleum hydrocarbon (TPH) removal from residual clayey soil using an electrokinetic process following a washing procedure. Eight electrokinetic experiments were carried out to investigate the characteristics of TPH removal. When 0.1 M MgSO4 or 0.1 M NaOH was used as an electrolyte, the electric current increased rapidly within the first 100 or 200 h, respectively. A negatively charged soil surface resulted in a more negative zeta potential and greater electroosmotic flow toward the cathode. The accumulated electroosmotic flow was higher when using 0.1 M NaOH as the anolyte-purging solution than when using 0.1 M MgSO4. Although the energy consumption for the two purging solutions was similar, the efficiencies of TPH removal when 0.1 M MgSO4 and 0.1 M NaOH with surfactant were used were 0 and 39, respectively, because the electroosmotic flow rate increased with TPH removal efficiency. When 5 isopropyl alcohol was used as a circulation solution, the electric current increased, but the TPH removal was similar to that using water. In terms of energy consumption, the use of a surfactant-enhanced electrokinetic process with NaOH as electrolyte was effective in removing TPHs from low-permeability soil. http://onlinelibrary.wiley.com/doi/10.1002/clen.200900190/pdf


REMOVAL OF HIGH CONCENTRATIONS OF POLYCYCLIC AROMATIC HYDROCARBONS FROM CONTAMINATED SOIL BY BIODIESEL
Jinbao Wu, Zongqiang Gong, Liyan Zheng, Yanli Yi, Jinghua Jin, Xiaojun Li and Peijun Li
Frontiers of Environmental Science & Engineering in China, [online prior to print publication] 2010
Solubilizing experiments were carried out to evaluate the ability of biodiesel to remove PAHs from highly contaminated manufactured gas plant (MGP) and PAH-spiked soils alongside applications of hydroxypropyl-beta-cyclodextrin (HPCD) and tween 80 as comparisons. Biodiesel displayed the highest solubilities for phenanthrene (420.7 mg/L), pyrene (541.0 mg/L), and benzo(a)pyrene (436.3 mg/L). These corresponded to several-fold increases relative to 10% HPCD and tween 80. Biodiesel showed a good efficiency for PAH removal from the spiked and MGP soils for both low- and high-molecular-weight PAHs at high concentrations. Biodiesel was a more effective agent for PAH removal from the spiked soils compared with HPCD and tween 80; it achieved over 77.9% removal of individual PAHs. Tween 80 also showed comparable capability with biodiesel for PAH solubilization at a concentration of 10% for the spiked soils. Biodiesel solubilized a wider range of PAHs than HPCD and tween 80 for the MPG soils. At PAH concentrations of 229.6 and 996.9 mg/kg, biodiesel removed >80% of total PAHs. The investigators observed a significant difference between PAH removals from the spiked and field MGP soils: PAH removals from the MGP soil by HPCD and tween 80 were much lower than those from the spiked soil. These results demonstrate the potential for utilizing biodiesel for remediation of highly PAH-contaminated soil.

comment: Though biodiesel worked best (I experienced the same), it works when used as 100 %. Clean-up of biodiesel for recycling proved difficult, with activated carbon it will be costly. For PAH extraction I would suggest a combination of about 1 part carboxymethyl cellulose / 9 Part Synperonic 91/4.


WASHING OF FIELD WEATHERED CRUDE OIL CONTAMINATED SOIL WITH AN ENVIRONMENTALLY COMPATIBLE SURFACTANT, ALKYL POLYGLUCOSIDE
Han, M., G. Ji, and J. Ni, Peking Univ., Beijing, China.
Chemosphere, Vol 76 No 5, p 579-86, 2009
Weathered crude oil-contaminated soils are much more difficult to remediate than those freshly contaminated. Although surfactant-enhanced ex situ soil washing can be used to remediate the weathered soils, surfactant toxicity is a major concern. A class of green surfactants, alkyl polyglucosides (APGs), was tested for washing field-weathered soils with relatively high oil concentration (123 mg/g dry soil) from an oilfield in China. APG1214, characterized with a longer alkyl chain, was more effective than APG0810 for removing crude oil. Addition of inorganic sodium salts to the APG1214 solution further improved crude oil removal efficiency. Washing parameters (temperature, washing time, agitation speed, and solution/soil ratio) were investigated, further optimized, and integrated with an orthogonal design. Under optimum conditions, removal efficiency reached 97%. GC/MS analysis showed that the proportion of small n-alkanes (C(16) to C(23)) in residual crude oil gradually increased, which helped to interpret the oil removal mechanism. Removal of large n-alkanes was achieved from the synergy between APG1214 and inorganic salts, which was the opposite of the effect when they were added separately. This study presents a promising technique for remediation of weathered crude oil-contaminated soils with ecologically compatible surfactant and provides guidelines for its practical application.

Friday, July 23, 2010

Asphaltene stability - nonscanning NIR technique: World Congress on Emulsion 2010

Contribution to the 5th world congress on emulsion CME
12 - 14 October, Lyon, France

A comparative study of asphaltene precipitation/flocculation by a new non-scanning NIR-technique in accordance with ASTM D 7061

St. Küchler, T. Sobisch, A. Uhl, D. Lerche

LUM

Rudower Chaussee 29 (OWZ) 12489 Berlin / Germany

info@lum-gmbh.de, www.lum-gmbh.com


Abstract

Asphaltenes and its derivatives, which are present in crude oil emulsions , may create severe technical and economical problems when they precipitate. Especially the flocculation of asphaltenes in heavy fuel oils may cause severe problems, including reservoir plugging, fouling of production facilities, altering wettability and poisoning refinary catalysts. Therefore the prediction and prevention of asphaltene flocculation is a crucial task for technical and laboratory staff in R&D, QC and production.

From the various methods that have been suggested over the years to serve this task the ASTM D 7061-05a has become an industrial standard to quantify and predict asphaltene flocculation in crude oils and heavy fuels.

In this contribution a non-scanning NIR-technique will be applied to measure asphaltene stability according to ASTM D 7061-05a by space and time resolved extinction (transmission) profiles (STEP-Technology). This apparatus (LUMiReader®, LUM GmbH) has the capability to measure simultaneously in 3 channels at tontrolled temperature up to 60°C.

Nine different crude oils with and without inhibitor were studied.

For direct comparison the same samples have been analyzed by the scanning apparatus described in the ASTM D 7061-05a.

The Separability Numbers, calculated from the measurements with the non-scanning NIR-apparatus, range from 0.2 to 15 showing a very good reproducibility and a very good agreement with the scanning technique. The applied non-scanning NIR-apparatus therefore is able to serve the broad spectra of crude oils in the market.


Keywords: Crude oil, heavy fuel oil, Induced Phase Separation of Asphaltene, Separability Number, STEP-Technology

test for long term stability - bottom focused back scattering World Congress on Emulsion 2010

Contribution to the 5th world congress on emulsion CME
12 - 14 October, Lyon, France

Easing formulation of emulsions and test for long term stability using bottom focussed back scattering

T. Sobisch, U. Rietz, D. Lerche

LUM

Rudower Chaussee 29 (OWZ) 12489 Berlin / Germany

info@lum-gmbh.de, www.lum-gmbh.com

Abstract

Selection of efficient emulsifiers, their optimum concentration and of the processing conditions is a demanding and time consuming process. Evaluation of emulsion stability can be eased when focussing on the changes in droplet concentration right at the bottom part of the emulsion samples. Furthermore the level of the back scattering signal is directly related to the dispersion degree. Thus the initial back scattering signal can be used to compare emulsification quality and to detect loss in dispersity due to aging.

A new multisample approach using light backscattering signals is presented. It allows for fast measurement of stability and/or demixing phenomena and separation kinetics of up to 8 different samples simultaneously, by monitoring the concentration change in a very small region of interest at the bottom of the sample cell.

The method was applied to trace the optimum emulsifier concentrations for silicone oil emulsions to evaluate the influence of processing intensity. Further the method was used to detect the very first changes of sample dispersity after accelerated aging.

Results demonstrate that bottom focussed back scattering can be applied as tool in every day formulation work and that during accelerated aging tests the method can serve as a sensitive measure of loss of dispersion integrity.

Keywords: formulation, emulsifier selection, processing conditions, accelerated aging, bottom focussed back scattering


Inclined creaming, speeding-up stability evaluation - World Congress on Emulsion 2010

-->Contribution to the 5th world congress on emulsion CME
12 - 14 October, Lyon, France


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Speeding up the evaluation of emulsion stability during normal storage conditions
T. Sobisch, D. Lerche
LUM
Rudower Chaussee 29 (OWZ) 12489 Berlin / Germany

Abstract
The principle of inclined settling is often used in separation technology to increase capacity and efficiency of settling aggregates. The Boycott effect is also applied in clinical tests to speed-up the evaluation of blood samples.
To answer the question whether this approach can also be used to speed up the evaluation of emulsion stability tests were carried out with colloidal stable emulsions (stable against aggregation and coalescence) and flocculated emulsions.
The LUMiReader instrument (LUM, Germany) can measure space and time resolved extinction (transmission) profiles (STEP technology) in multiple channels using near infrared (NIR) or visible light. This way it measures changes in turbidity and the movement of the boundary towards the supernatant. Even more the angle of inclination can be varied between 0 and 30° from the vertical.
Investigations on creaming as function of angel of inclination were carried out on nonflocculated silicone oil-in-water emulsions varying the oil concentration and on flocculated silicone oil-in-water emulsions at different electrolyte concentration.
The same principle behaviour as in case of monodisperse colloidal stable silica was found for the polydisperse colloidal stable (nonflocculated) emulsion. In this case ‘inclined creaming’ proceeds. At 30° inclination the creaming can be accelerated by a factor of about 9, i.e. the necessary time for stability evaluation can be shortened accordingly.
The creaming rate dependence on inclination is rather unpredictable for flocculated network forming emulsions. A maximum in creaming rate was observed around 25° inclination. In case of the emulsion with 0.5 M NaCl this relates to an enhancement factor of over 25, however, for 0.75 M NaCl it is only slightly higher than 1.
Keywords: enhanced creaming, Boycott effect, emulsion stability, creaming velocity, salt induced flocculation

Rapid emulsifier selection, emulsion stability, reformulation - World Congress on Emulsion 2010

Contribution to the 5th world congress on emulsion CME
12 - 14 October, Lyon, France

Rapid emulsifier selection and evaluation of emulsion stability for reformulation


T. Sobisch, D. Lerche, LUM

Rudower Chaussee 29 (OWZ) 12489 Berlin / Germany

info@lum-gmbh.de, www.lum-gmbh.com


Abstract


Selection of emulsifiers and evaluation of emulsion stability is a frequent task. This relates to practical issues like formulation of emulsions, optimization of preparation conditions, quality control, shelf life estimation and breaking of emulsions. Due to European legislation (REACH) many companies are facing the problem to replace proven components in their formulations (low volume speciality compounds or problematic chemicals). This also applies to emulsifiers and emulsion based products.

A multisample technique based on analytical centrifugation is presented which allows for an accelerated study of creaming, sedimentation and of separation of oil and water phases. Not only information on the extent of phase separation is provided but also the kinetics are measured directly in-situ.

The method was applied to check for alternatives to nonyl phenol based surfactants as emulsifiers for silicone oil emulsions. Different commercial products were evaluated. It proved to be a very efficient screening method, which can be also applied in every day formulation work.

Due to the multisample approach one centrifugal run with 12 different samples was sufficient to identify more environmentally benign emulsifiers with identical or better performance. In a second run the efficiency of emulsifier combinations was tested. The primary destabilization mechanism for all emulsions was creaming, however, most emulsions showed phase inversion when a critical phase ratio was reached inside the cream layer. By increasing the polarity of the alternative emulsifiers the risk of phase inversion could be rigorously reduced.

Keywords: reformulation, REACH, emulsifier selection, silicon oil-in-water emulsions, creaming kinetics, analytical centrifugation


Surfactant adsorption kinetics - emulsion stability, World Congress on Emulsion 2010

Contribution to the 5th world congress on emulsion CME
12 - 14 October, Lyon, France

Interrelation between surfactant adsorption kinetics, interfacial rheology and emulsion stability

T. Sobisch1, N. Mucic2, J. Krägel2, A.V. Makievski3, R. Miller² and D. Lerche1

1 LUM GmbH, Rudower Chaussee 29 (OWZ) 12489 Berlin / Germany
info@lum-gmbh.de, www.lum-gmbh.com
² MPI für Kolloid- und Grenzflächenforschung, Am Mühlenberg 1, 14424 Potsdam / Germany
3 SINTERFACE Technologies, Volmerstrasse 5, 12489 Berlin / Germany


Abstract
The right choice of emulsifier is an ongoing challenge in emulsion technology. The time scale of the emulsification process has a strong impact on the emulsifier efficiency, which can only become effective if the adsorption kinetics are fast enough to avoid coalescence of freshly formed droplets. Additionally, the interfacial rheology at the oil-water interface determines the final emulsion stability.
The interrelation between surfactant adsorption kinetics, interfacial rheology and emulsion stability was investigated in model systems paraffin oil / water / nonionic surfactants, where the EO-chain length was varied.
The kinetics and thermodynamic properties of the surfactants at the oil/water interface were measured by using drop profile analysis tensiometry. The same tool is applied for the investigation of the interfacial dilational rheology by recording the interfacial tension response to harmonic area compressions-expansions of the studied drop.
Emulsions were prepared with a dissolver type homogenizer. Stability of emulsions was investigated as function of time of processing, surfactant concentration and HLB value using multisample analytical centrifugation. Not only the extent of phase separation but also the kinetics are directly measured in-situ.
Emulsion stability increases with time of emulsification. The emulsifier with 5 EO units is far more effective than that with 12 EO units. Adsorption equilibrium at the interface is reached in seconds. The kinetics of adsorption show clearly a depletion effect of surfactant molecules from the aqueous phase, which is especially pronounced for the emulsifier with 5 EO units. Nevertheless, at higher surfactant concentration the interfacial tension is lower for the more lipophilic surfactant.


Keywords: emulsion stability, adsorption layer properties, analytical centrifugation, emulsion preparation, emulsifier selection, oil-in-water

Monday, June 28, 2010

Characterization of the dispersion properties of carbon nanotubes in ionic liquids by the separation behaviour in the centrifugal field


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Characterization of the dispersion properties of carbon nanotubes in ionic liquids by the separation behaviour in the centrifugal field


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T. Sobisch, D. Lerche
LUM Berlin/Germany www.LUM-gmbh.com
Y. Korth, C. Friedrich
Albert-Ludwigs-Universität Freiburg/Germany www.fmf.uni-freiburg.de
Scope
Carbon nanotubes are considered as nano materials with a broad application potential, e.g. as filler, in electronic devices and batteries. The relatively good dispersibility in ionic liquids is an interesting approach.
Carbon nanotubes in ionic liquids tend to form extended inter-tangled fibre networks, however, for efficient application a high degree of dispersion is required.
In this study dispersions of different multiwalled carbon nanotube products in 1-butyl-3-methyl-imidazoliniumtetrafluoroborat (BMIBF4) were characterized by multisample analytical centrifugation with high resolution photometric detection. Based on the sedimentation/consolidation behaviour pronounced differences in the degree of network formation and in the packing density were identified. The size distribution of the products was also determined by multisample analytical centrifugation.
Carbon nanotube dispersions [1]
Raw materials














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Fig. 1 Overview over materials used and below related TEM pictures
The 3 different products used differ largely in material properties and morphology (Fig. 1)


Dispersion preparation
In a first step the nanotubes were dispersed in ethanol by sonication. After adding BMIBF4 sonication was repeated and in a third step the ethanol was evaporated. Dispersions of 1 % m/m were prepared. For the centrifugal analysis dispersions were further diluted to 0.1 % m/m.
Method of multisample analytical centrifugation
Time and space resolved detection of light transmission (STEP-Technology) combined with multisample analytical centrifugation (LUMiSizer, LUM, Germany, [2-4]) was applied, which measures concentration changes inside the sample by high resolution photometric detection (see Fig. 2).






















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Fig. 2 Measurement scheme of the multisample analytical centrifuge. Local changes are detected during centrifugation. The distribution of transmission is recorded over the whole sample length at predefined time intervals.
Up to 12 different samples can be analysed at the same time at constant or variable centrifugal acceleration up to 2300 g. The shape and progression of the transmission profiles contain the information on the dispersion properties. The transmission profiles (Fig. 4) are representative for the distribution of particle concentration inside the sample (low transmission means high, high transmission means low particle concentration). Based on this, sedimentation and clarification kinetics, the dependence between packing density and pressure, as well as the velocity and particle size distribution can be obtained. Polycarbonate cells with an optical path length of 2.1 mm were used.


Results and discussion
Size distributions























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Fig. 3 Comparison of the cumulative intensity weighted distribution of the 3 products.
The particle size is obtained as equivalent particle diameter according to the hydrodynamic diameter of spherical particles. Therefore the large asymmetry of the nanotubes will have a pronounced impact on these results. Nevertheless, it can be seen that the Nanocyl product has a narrower distribution and lacks the coarse fraction present in the two other products.


Separation behaviour as function of raw material


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Fig. 4 Transmission profiles obtained during 2 hours centrifugation at 2300 g as function of the raw material used (first profile after 10 seconds in red, last profile after 2 hours in green).
As obvious from Fig. 4 the evolution of transmission profiles during centrifugation can be used as finger print to distinct the 3 products. All 3, especially Nanocyl, exhibit a different behaviour.
The transmission profiles depict the transmission as function of the position inside the sample given as distance from the centre of rotation.
In case of Nanocyl sharp vertical profiles are obtained showing that all particles move with identical velocity. The distance between the consecutive profiles is narrowing due to the resistance to compaction is increasing with the packing density obtained. This is characteristic for a flocculated particle network, in this case for a network of entangled nanotubes. For the other 2 products there is no sharp sedimentation front, instead the transmission is gradually decreasing towards the cell bottom. This relates to a polydisperse sedimentation, the particles or aggregates/agglomerates move with different velocity. It can be further noticed that for these two dispersions sediment (range of minimum transmission close to the bottom) is formed instantaneously followed by a gradual increase of transmission in the supernatant. Therefore, it can be concluded that there is a fast settling of aggregates/agglomerates followed by the separation of fines.
On a closer look for Polytech&Net one can observe a gradual compression of the instantaneously formed sediment (particle network).
According to the sediment height the order of packing density is:
Nanocyl <>
From the comparison of the transmission profiles it can be concluded that the Iolitek has the highest dispersibility, Nanocyl has a pronounced tendency to form an entangled network.


Influence of the degree of ultrasonication on separation kinetics

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Fig. 5 Separation kinetics as function of intensity of sonication for the centrifugation of 0.1 % dispersion of Nanocyl in BMIBF4 at 2300 g.
For Nanocyl the intensity of sonication during dispersion was varied, abbreviated as CE.10.42, CE.10.43, CE.65.45 (amplitude and duration: 10 % 5 min / 10 % 8 min / 65% 16 min). Fig. 5 exhibits the related separation kinetics (movement of the boundary supernatant/dispersion with time). Increasing the sonication intensity the separation slows down and the equilibrium sediment height increases (difference between position of the cell bottom and the position of the boundary towards the sediment), i.e. the packing density decreases.


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Fig. 6 Compression-dilation kinetics of the sediment formed after 2 hours centrifugation in Nanocyl dispersions as function of sonication intensity. The centrifugal acceleration was increased step-wise and then decreased.
As shown in Fig. 6 sediments formed in case of Nanocyl (compacted particle network) exhibit elastic behaviour. The packing density calculated from sediment volume and particle concentration decreases with intensity of sonication.
References
[1] Y. Korth, PhD thesis Rheologische und morphologische Eigenschaften von Fasernetzwerken
Freiburg i. Breisgau, Univ., Diss., 2010
[2] D. Lerche, Dispersion stability and particle characterisation by sedimentation kinetics in a centrifugal field
J. Dispersion Sci. Technol. 23, 5, 699 ‑ 709 (2002)
[3] G.G. Badolato, F. Aguilar, H.P. Schuchmann, T. Sobisch and D. Lerche, Evaluation of long term stability of model emulsions by multisample analytical centrifugation,
Progr. Colloid Polym. Sci. 134 66–73 (2008)
[4] T. Sobisch and D. Lerche, Thickener performance traced by multisample analytical centrifugation
Colloids & Surfaces A 331 114-118 (2008)