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The aim of the present paper to compare the cleaning treatments of paper samples exposed to artificial aging, toluene and isopropyl alcohol gel in cleaning wax stains.

In total, paper samples were made from wood pulp. They had a deterioration phenomenon represented in the stains of the paraffin wax, so two types of cleaning were used: A traditional method using a toluene solution and another new method using isopropanol gel by a cotton swap in a circular movement until the completion of the cleaning process. Then, all paper samples were treated with toluene and isopropanol to handle the second artificial aging and detect how the samples were affected by artificial aging. For identifying the efficacy of these materials in removing paraffin wax stains, a range of examinations and analyses were used, such as universal serial bus, scanning electron microscope, infrared analysis (IR), pH analysis, color change analysis. Moreover, these results were compared with the standard sample’s results.

The results of examinations and analyses proved that the use of toluene affected the paper samples. Their effects were twice as weak, fragile and degraded paper fibers compared to isopropanol gel. Therefore, the isopropanol gel is preferred for paper cleaning to the toluene solution.

This paper highlights the efficiency of isopropyl alcohol gel in cleaning wax stains from historical paper supports.

A number of resins have recently been introduced by Cray Valley Products to meet market demands for new components for flexographic, gravure and screen inks. This article summarises the basic characteristics of these resins and gives a selection of starting point formulations.

Until comparatively recently, in the practice of gel permeation chromatography it has been customary to use porous gel beads that have an average diameter in the range between 75 and 100 microns, and which are packed into columns up to 4ft long and having an inside diameter of approximately 0.3in, in order to achieve a separation. A working pressure in the region of 40 psi is normal for each of these columns when eluted with solvents such as toluene or tetrahydrofuran (THF) at ambient temperature. Therefore, a pump that is capable of producing a steady pulseless flow at around 300 psi is sufficient to meet the working requirements of a combination of up to seven such GPC columns. At the customary flow rate of 1cm3 min‐1 a chromatograph equipped as described would produce a GPC scan of whole polymer in about 3 hours.

This research aims to investigate how adaptability potential analysis in collaborative manufacturing networks can be used to enhance resilience when addressing innovative production challenges that require change initiatives.

A literature review on collaborative adaptive systems showed a lack of solutions to adapt production to an unpredicted product within a network. A framework is proposed for evaluating the adaptability of collaborative networks and providing inter-system adaptation recommendations. We demonstrate the applicability of this approach through an illustrative experimentation involving a cosmetic company seeking to produce a new product, hydroalcoholic gels in the context of collaborative networks.

The experimentation demonstrates that the adaptability analysis based on ontology can help different manufacturing systems make decisions based on their state and limits of capabilities. Also, our adaptation recommendations may help understand the economic impacts of collaboration for different scenarios before launching.

The research scope does not extend to the consideration of quantity and operational aspects. Additionally, the reconfigurability aspects within each manufacturing system, such as the reordering of layout sequences, have not been addressed yet.

The results allow organizations to compare resilience states from an individual and collaborative perspective, enabling them to make informed decisions about new production opportunities and effectively navigate the changing manufacturing landscape.

This research combines capability-based analysis and a collaborative network perspective to streamline decision-making for systems facing new production demands. It provides new insights into effectual decision-making, empowering organizations to skilfully manage unexpected challenges and identify suitable partners accordingly.

The purpose of this paper was to protect carbon steel from corrosion with self–aggregated, eco-friendly, water-soluble hyperbranched polyamide-ester (Hb-PAE).

Hb-PAE was synthesized through bulk polycondensation reaction between maleic anhydride and di-isopropanol amine. Complete structural analysis for the obtained polymer was performed using Fourier Transfer Infra-Red Spectroscopy, 1H NMR, Thermal gravimetric analysis (TGA) and differential scanning calorimetry, and the molar mass was measured using gel permeation chromatography/refractive index. For this study, the surface activity of Hb-PAE with hydroxyl end groups was investigated. Surface tension of 1.0 × 10−6 to 0.1M of both Hb-PAE/H₂O and Hb-PAE/1N HCl systems was measured, and the critical aggregation concentration (CAC) in both systems was determined. Hb-PAE was examined as a corrosion inhibitor for plain carbon steel in both neutral (distilled water) and acidic (1N HCl) media. The corrosion of the steel was studied quantitatively by measuring its weight loss in both media in the absence and presence of Hb-PAE. The surface morphology of the exposed steel test samples was examined using scanning electron microscopy.

It was found that Hb-PAE inhibited corrosion of steel around the CAC, and its corrosion inhibition efficiency was increased by increasing its concentration.

The research can provide a reference for the relationship between the aggregation concentration of the prepared Hb-PAE with its corrosion inhibition efficiency on plain carbon steel. Hb-PAE as a corrosion inhibitor is environmentally acceptable, economical and readily available.

The purpose of this study is to evaluate the effectiveness of alginate as a vehicle to protect coenzyme Q10 in liposomes.

Encapsulation efficiency and stability were conducted at varying temperatures (20, 30, 40°C) for 5 d and at exposure to simulated gastric conditions (pH 2) for 2 h. The content of coenzyme Q10 was determined using HPLC (LC/MS). Cytotoxicity and phagocytosis of mouse macrophages (RAW264.7) was determined.

Results showed that thermostability was strongly improved by alginate complex formation with liposomes. Moreover, alginate could maintain coenzyme Q10 at a significantly higher level in simulated gastric pH for at least 2 h (p<0.00).

This allowed a higher amount of coenzyme Q10 remaining to be absorbed in the small intestine. Alginate not only showed no toxic effect on mouse macrophages but also activated their proliferation and phagocytosis ability.

As a consequence, alginate could be applied as an aid to encapsulation stability and immunostimulating potency.

The effects of catalysts used to promote the reaction of epoxy‐anhydride mixtures was studied by Nuss (77) using a GPC technique. It was demonstrated that when the polymerisation reaction occuring in an identical system was monitored, in the presence of different catalysts, the relationship between the apparent molecular size distribution and the lapsed time of the curing reaction was a function of the catalyst employed.

Resins used in surface coatings are mostly polymers of one sort or another and although they differ in a number of ways from the high polymers used to make plastics and synthetic fibres, they nevertheless show some of those properties peculiar to polymers. One of the things that distinguishes polymers from ‘ordinary’ organic compounds is the fact that instead of all the molecules having the same characteristic molecular weight, the molecules present have a variety of molecular weights (because they contain different numbers of monomer units). Instead of talking about a polymer's ‘molecular weight’ therefore, we have to talk about its average molecular weight and its molecular weight distribution.

An efficient protocol for the isolation of high molecular weight DNA from dry powdered samples of turmeric including market samples is described which will help in PCR based detection of adulteration in marketed turmeric powders. The method involves a modified CTAB (3 per cent) procedure with 2 M NaCl, 0.3 per cent β‐mercaptoethanol coupled with purification of DNA in 30 per cent polyethylene glycol (8000). The yield of the DNA obtained from the samples varied from 2 to 4 μg/g tissue. The DNA obtained from the five different samples were consistently amplifiable (RAPD primers).

The paper's aim is to show the development of materials and methods which allow freeform fabrication of macroscopic Zn‐air electrochemical batteries. Freedom of geometric design may allow for new possibilities in performance optimization.

The authors have formulated battery materials which are compatible with solid freeform fabrication (SFF) while retaining electrochemical functionality. Using SFF processes, they have fabricated six Zn‐air cylindrical batteries and quantitatively characterized them and comparable commercial batteries. They analyze their performance in light of models from the literature and they also present SFF of a flexible two‐cell battery of unusual geometry.

Under continuous discharge to 0.25 V/cell with a 100 Ω load, the cylindrical cells have a specific energy and power density in the range of 40‐70 J/g and 0.4‐1 mW/cm², respectively, with a mass range of 8‐18 g. The commercial Zn‐air button cells tested produce 30‐750 J/g and 7‐9 mW/cm² under the same conditions, and have a mass range of 0.2‐2 g. The two‐cell, flexible Zn‐air battery produces a nominal 2.8 V, open‐circuit.

The freeform‐fabricated batteries have ∼10 percent of the normalized performance of the commercial batteries. High‐internal contact resistance, loss of electrolyte through evaporation, and inferior catalyst reagent quality are possible causes of inferior performance. Complicated material preparation and battery fabrication processes have limited the number of batteries fabricated and characterized, limiting the statistical significance of the results.

Performance enhancement will be necessary before the packaging efficiency and design freedom provided by freeform‐fabricated batteries will be of practical value.

The paper demonstrates a multi‐material SFF system, material formulations, and fabrication methods which together allow the fabrication of complete functional Zn‐air batteries. It provides the first quantitative characterization of completely freeform‐fabricated Zn‐air batteries and comparison to objective standards, and shows that highly unusual, functional battery designs incorporating flexibility, multiple cells, and unusual geometry may be freeform fabricated.