scholarly journals Correlation between Surface Energy and Adhesion Force of Polyethylene/Paperboard: A Predictive Tool for Quality Control in Laminated Packaging

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Danielle M. F. Madeira ◽  
Osvaldo Vieira ◽  
Luís Antonio Pinheiro ◽  
Benjamim de Melo Carvalho

Poor adhesion continues to be a problem for manufacturers of laminated packaging. Therefore, the aim of this research was to study the effect of flame treatment, the type of coating, and starch application on the adhesion force of polyethylene/paperboard. The force of adhesion was determined using the peel test method; the paper surface energy was assessed by contact angle analysis; and paperboard roughness was determined by profilometer. The flame treatment did not affect the surface roughness but significantly increased the paperboard surface energy. The paperboard coated with polar latex showed much higher surface energy than the paperboard coated with nonpolar latex. The adhesion force of polyethylene presented a linear correlation to the surface energy of the paperboard. Therefore, the surface energy of paperboard is an excellent indication of its adhesion force to polyethylene, and this represents a very reliable and practical method in terms of quality control in the paper industry for producing laminated packages.

2015 ◽  
Vol 54 (3) ◽  
pp. 749-753 ◽  
Author(s):  
Maria M. Traczewski ◽  
Jennifer Deane ◽  
Daniel Sahm ◽  
Steven D. Brown ◽  
Laurent Chesnel

Test parameter variations were evaluated for their effects on surotomycin MICs. Calcium concentration was the only variable that influenced MICs; therefore, 50 μg/ml (standard for lipopeptide testing) is recommended. Quality control ranges forClostridium difficile(0.12 to 1 μg/ml) andEggerthella lenta(broth, 1 to 4 μg/ml; agar, 1 to 8 μg/ml) were approved by the Clinical and Laboratory Standards Institute based on these data.


2014 ◽  
Vol 36 (2) ◽  
pp. 246-252 ◽  
Author(s):  
Tereza Cristina de Carvalho ◽  
Camila Ribeiro de Souza Grzybowski ◽  
Osvaldo de Castro Ohlson ◽  
Maristela Panobianco

The tetrazolium test is part of internal programs of seed quality control because it allows a quick, reliable and accurate assessment of seed viability. The purpose of this study was to determine, among the various methodologies suggested in the literature, a practical and efficient procedure for carrying out the tetrazolium test in sorghum seeds, with a view toward a rapid estimate of their viability. Four seed lots of the simple hybrid Buster were used, testing two forms of seed pre-conditioning (direct immersion in water and between moistened paper towels); two types of preparation (longitudinal cut of the seed through the embryo with immersion of one of the halves in the tetrazolium solution or placement of the two halves on filter paper moistened with tetrazolium solution); two forms of staining (on paper and with direct immersion in the solution) and three concentrations of tetrazolium solution (0.1%, 0.5% and 1.0%). The tetrazolium test may be efficiently conducted for sorghum seeds through pre-conditioning between paper towels for 18 hours at 20 ºC, with immersion staining of one half of the seed in tetrazolium solution at 0.1% for three hours at 40 ºC.


2021 ◽  
Vol 7 ◽  
Author(s):  
Bastian Poerschke ◽  
Stanislav N. Gorb ◽  
Clemens F. Schaber

Dynamic adhesion is a key ability for animals to climb smooth surfaces. Spiders evolved, convergent to geckos, a dry adhesive system made of setae branching into smaller microtrichia ending as spatulae. Several previous studies concentrated either on the whole adhesive claw tuft on the spider´s foot that consists of attachment setae or on the single adhesive contact elements, the microtrichia with spatula-shaped tips. Here, the adhesion of single setae of the spider Cupiennius salei was examined and the morphology of the pretarsus and the fine structure of the setae were studied in further detail. Using individual setae fixed to force sensing cantilevers, their adhesion at different contact angles with a glass substrate was measured as well as their adhesive performance on substrates with different roughness and on smooth surfaces with different surface energies. The results show an individual variability of the adhesive forces corresponding to the seta morphology and especially to the seta tip shape. The tip shapes of the setae vary largely even in neighboring setae of the pretarsal claw tuft that comprises approximately 2,400 setae. Regarding surface energy of the substrate, the adhesion force on hydrophobic polytetrafluoroethylene was 30% of that on a hydrophilic glass substrate, which points to the importance of both van der Waals interactions and hydrogen bonds in spider adhesion.


MRS Advances ◽  
2018 ◽  
Vol 3 (57-58) ◽  
pp. 3379-3390 ◽  
Author(s):  
Saaketh R. Narayan ◽  
Jack M. Day ◽  
Harshini L. Thinakaran ◽  
Nicole Herbots ◽  
Michelle E. Bertram ◽  
...  

ABSTRACTThe effects of crystal orientation and doping on the surface energy, γT, of native oxides of Si(100) and Si(111) are measured via Three Liquid Contact Angle Analysis (3LCAA) to extract γT, while Ion Beam Analysis (IBA) is used to detect Oxygen. During 3LCAA, contact angles for three liquids are measured with photographs via the “Drop and Reflection Operative Program (DROP™). DROP™ removes subjectivity in image analysis, and yields reproducible contact angles within < ±1°. Unlike to the Sessile Drop Method, DROP can yield relative errors < 3% on sets of 20-30 drops. Native oxides on 5 x 1013 B/cm3 p- doped Si(100) wafers, as received in sealed, 25 wafer teflon boats continuously stored in Class 100/ISO 5 conditions at 24.5°C in 25% controlled humidity, are found to be hydrophilic. Their γT, 52.5 ± 1.5 mJ/m2, is reproducible between four boats from three sources, and 9% greater than γT of native oxides on n- doped Si(111), which averages 48.1 ± 1.6 mJ/m2 on four 4” Si(111) wafers. IBA combining 16O nuclear resonance with channeling detects 30% more oxygen on native oxides of Si(111) than Si(100). While γT should increase on thinner, more defective oxides, Lifshitz-Van der Waals interactions γLW on native oxides of Si(100) remain at 36 ± 0.4 mJ/m2, equal to γLW on Si(111), 36 ± 0.6 mJ/m2, since γLW arises from the same SiO2 molecules. Native oxides on 4.5 x 1018 B/cm3 p+ doped Si(100) yield a γT of 39 ± 1 mJ/m2, as they are thicker per IBA. In summary, 3LCAA and IBA can detect reproducibly and accurately, within a few %, changes in the surface energy of native oxides due to thickness and surface composition arising from doping or crystal structure, if conducted in well controlled clean room conditions for measurements and storage.


2020 ◽  
Vol 103 (4) ◽  
pp. 1140-1147
Author(s):  
Isaac Lee ◽  
Jennie Vo ◽  
Quanyin Gao ◽  
Piyush Purohit ◽  
Veronica Zarraga ◽  
...  

Abstract Background A quantitative NMR (qNMR) method can provide rapid analysis compared to chromatographic methods. Sample preparation steps are relatively simpler and run time is shorter. Rapid analysis methods for release tests in quality control laboratories are very important for laboratory efficiency. Here, we describe a single-laboratory validation study for a rapid qNMR analysis of L-arginine, L-citrulline, and taurine in powdered and tablet dietary supplement products. Objectives This validation work is to provide documented evidence for the qNMR method validity as well as method performance. Methods The method used Bruker 400 MHz high-resolution proton NMR spectroscopy for simultaneous determination of L-arginine, L-citrulline, and taurine contents in dietary supplement product 1 (powder) and dietary supplement product 2 (tablet). The absolute NMR quantitation is based on a principle of universal proton response intensity correlation with the number of protons in each target analyte (amino acids) vs. that of a reference standard (maleic acid). Results The test method performance was validated with dietary supplement-1 (powder) and dietary supplement-2 (tablet). The linearity of the method was studied from about 360 mg/g to about 675 mg/g of L-arginine; from about 15 mg/g to about 30 mg/g of L-citrulline; and from about 20 mg/g to about 40 mg/g of taurine in dietary supplement-1, and from about 15 mg/g to about 30 mg/g of taurine in dietary supplement-2. The coefficients of determination (R2) are 1.0000 for L-arginine, 0.9967 for L-citrulline, and 0.9995 for taurine in dietary supplement-1 and 0.9903 for taurine in dietary supplement-2. The accuracies measured from the sample matrices are 102%, 101%, and 100% average recoveries for 80%, 100%, and 120% concentration levels of L-arginine, 105%, 105%, and 103% average recoveries for 80%, 100%, and 120% concentration level of L-citrulline, and 101%, 102%, and 100% average recoveries of taurine for 80%, 100%, 120% concentration levels in dietary supplement-1; and 95, 98%, and 93% average recoveries of taurine for 80%, 100%, 120% concentration levels in dietary supplement-2, respectively. The precisions (RSD) are 1% for L-arginine, 5% for L-citrulline, and 2% for taurine in dietary supplement -1, respectively; and 4% for taurine in dietary supplement-2. The ruggedness of the test method is within 2%, 4%, and 2% for L-arginine, L-citrulline, and taurine for dietary supplement -1, respectively, and within 4% for dietary supplement-2. The method is specific for the quantitation of each nutrient with no background interference from the matrix for the proton peaks of L-arginine, L-citrulline, taurine, and maleic acid (standard). Conclusions The test method is proven to be specific, precise, accurate, rugged, and suitable for intended quantitative analysis of L-arginine, L-citrulline, and taurine in powdered and tablet finished products. Highlights The simultaneous determination of all three nutrients of L-arginine, L-citrulline, and taurine using proton NMR provides rapid analysis for quality control release tests that is more efficient versus that of two HPLC methods. Previously, our laboratory was using one HPLC method to analyze L-arginine and L-citrulline while using a second HPLC method to analyze taurine. That approach required two HPLC instruments and two analysts for parallel analysis that takes 2 days using volatile and flammable solvents for extraction and chemical derivatization. This rapid NMR method can analyze the sample “as is” with results obtained in less than 4 h, and is efficient, safe, and environmentally friendly. The initial higher NMR instrument investment versus two HPLC instruments is rewarded with high returns for continued quality control tests.


2003 ◽  
Vol 782 ◽  
Author(s):  
Jin-Hyung Lee ◽  
Hyun-Woo Lim ◽  
Jin-Goo Park ◽  
Eun-Kyu Lee ◽  
Yangsun Kim

ABSTRACTHot embossing has been widely accepted as an alternative to photolithography in generating patterns on polymer substrates. The optimization of embossing process should be accomplished based on polymer surface properties. Therefore, in this paper, polymers with different surface characteristic were selected and the surface properties of each polymers such as surface energy and adhesion force were investigated by contact angle and AFM. Based on these results, the imprinted nano patterns were compared. Silicon molds with nano size patterns were fabricated by e-beam direct writing. Molds were coated with self-assembled monolayer (SAM) of (1, 1, 2, 2H –perfluorooctyl)-trichlorosilane to reduce the stiction between molds and polymer substrates. For embossing, pressure of 500 psi, embossing time of 5 min and temperature of above transition temperature were applied. Mr-I 8010 polymer (Micro Resist Technology), Polymethylmethacrylate (PMMA 495k) and LOR (polyaliphatic imide copolymer) were used as substrate for hot embossing process development in nano size. These polymers were spun coated on the Si wafer with the thickness of 150 nm. The nano size patterns obtained by hot embossing were identified by atomic force microscopy without breaking the pattern and compared based on the polymer surface properties. The mr-I 8010 which has the lowest surface energy and adhesion force shows the best demolding property.


2020 ◽  
Vol 36 ◽  
pp. 101522
Author(s):  
Aslan Alamdari ◽  
Jeongwoo Lee ◽  
Myoeum Kim ◽  
Md. Omar Faruk Emon ◽  
Ali Dhinojwala ◽  
...  

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