Adhesive Joint Durability Assessed Using Open-faced Peel Specimens

This paper presents an investigation of the durability of two aluminum-epoxy adhesive systems by means of open-faced peel specimens. A peel analysis model was used to determine the fracture energy from the peel data. Both wet and dry peel tests were conducted in order to distinguish between the reversible and the permanent effects of water. The effects of water on the cohesive properties of the adhesives were also assessed by tension tests. It was found that, for the two-part epoxy adhesive, which plasticized to a large extent, the peel testing should be carried out in a dry state to assess the interfacial weakening. It was also observed that the two-part adhesive was much stiffer in the dry, degraded state, and it was important to take account of such permanent changes in the cohesive properties associated with water uptake when determining the fracture energy from the peel data. In contrast, the one-part epoxy system did not suffer from appreciable cohesive changes, either reversible or permanent. In this case, both wet and dry failure loci were interfacial, and some of the interfacial damage was found to be reversible. Finally, surface analyses of the peel failure surfaces were carried out, and the formation of micro-debonds was identified as a possible mechanism of degradation for the two-part system.     

Peeling of Acrylic Pressure Sensitive Adhesives: Cross-Linked versus Uncross-Linked Adhesives

In this paper we analyze the adhesive properties of two kinds of adhesives, determined by a 90[ddot] peeling test on a Pyrex^TM substrate. Simultaneously, we observe the mechanisms of flow at the peeling front. An uncross-linked acrylic pressure-sensitive adhesive is used, whereas the second one, of the same class, is slightly cross-linked. The mechanisms of peeling are compared with the ones of our previous study (Benyahia et al [8]) and are found to be identical in the case of uncross-linked adhesives. On the other hand, we find new regimes of flow when the adhesive is cross-linked.

To investigate these differences further, we determine the rheometrical properties of the adhesives in dynamic shear tests and in uniaxial elongational experiments. Furthermore, surfaces are characterized.

A discussion of the peeling curves is finally presented, showing the combined effects of the rheological properties and the surface ones. Conditions for predicting the type of regimes and transitions are also investigated.     

Sorption Isotherms and Drying Characteristics of Tomato Peel Isolated from Tomato Pomace

Tomato peel was separated from pomace by sedimentation and dried in cabinet and fluidized-bed dryer at 50–70°C using 4–12 kg/m²tray load. The drying of tomato peel took place under the falling rate period and the drying behavior was well described by Page's model with coefficient of determination greater than 0.99 and standard error of 0.003–0.016. A fluidized-bed dryer was much more efficient than a cabinet dryer to dry tomato peel. The moisture adsorption isotherms of tomato peel were obtained by equilibrating above saturated salt solutions of known a _w (0.113–0.92) at 20–60°C. The data were analyzed using fifteen sorption models based on coefficient of determination, standard error, and residual plots. Modified Henderson was the best model for tomato peel with coefficient of determination >0.99, standard error <0.210, and a scattered residual plot. The net isostearic heat of sorption, estimated using the Clausius-Clapeyron equation, was 0.74–23.23 kJ/mol at 2.0–2.5% moisture content (dry basis).     

Preparation and characterization of modified telechelic natural rubber-based pressure-sensitive adhesive

Telechelic natural rubber (TNR) was prepared by the use of potassium persulfate and propanal at 70 °C and various degradation times from 0 to 30 h. These samples were then grafted by maleic anhydride (MA) in toluene solution before modification with 3-amino-1,2,4-triazole (ATA) to produce modified TNRs (AMTNRs). Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) was used to identify the chemical compositions. Carboxyl and hydroxyl groups of TNRs were clearly observed, due to chain scission, oxidation, and modified chain ends. The viscosities of TNRs were dropped greatly after 5 h and then decreased slowly as a function of degradation time. ATR-FTIR spectra of AMTNRs showed amide bonds between ATA and MA groups, and then the multiple hydrogen bonding arrays were formed. The glass transition temperatures (T_g) of AMTNRs were determined by differential scanning calorimetry. The T_g of AMTNR_0 moved to a higher temperature of –55 °C after modification by ATA, confirming the formation of multiple hydrogen bonding arrays. However, the T_g of AMTNR_5 to AMTNR_30 decreased slightly due to chain scission in the degradation process. The adhesive properties of AMTNR-based pressure-sensitive adhesive were evaluated by a Lloyd adhesion tester. The tack of AMTNRs depended on wettability whereas peel and shear strengths were responded by a combination between wettability and multiple hydrogen bonding arrays.     

MODIFIED PLANTAIN PEEL AS CELLULOSE-BASED LOW-COST ADSORBENT FOR THE REMOVAL OF 2,6-DICHLOROPHENOL FROM AQUEOUS SOLUTION: ADSORPTION ISOTHERMS,KINETIC MODELING,AND THERMODYNAMIC STUDIES

In this study, the feasibility of using modified plantain peel to remove 2,6-dichlorophenol from iaqueous solutions was investigated under batch mode. The effects of physical factors such as initial 2,6-dichlorophenol concentration, contact time, biosorbent particle size, biosorbent dosage and temperature on the removal process were evaluated. The results showed that biosorption of 2,6-dichlorophenol was dependent on these factors. The equilibrium biosorption data were analyzed by the Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich (D-R) adsorption isotherm models. The four tested isotherm models provided good fits to the experimental data obtained at 30°C; however, the Freundlich isotherm model provided the best correlation (R² = 0.9874) of the experimental data. The maximum monolayer biosorption capacity (Q _max ) was found to be 14.25 mg/g. The biosorption kinetics data of 2,6-dichlorophenol were analyzed by pseudo-first-order, pseudo-second-order, Elovich, intraparticle diffusion, and liquid film diffusion models. The five kinetic models fitted well to the biosorption kinetic data; however, the pseudo-second-order kinetic model gave the best fit when the biosorption mechanism was controlled by film diffusion. Thermodynamic quantities such as standard Gibbs free energy (ΔG°), standard enthalpy (ΔH°), standard entropy change of biosorption (ΔS°), and activation energy (E_a) were evaluated, and it was found that the biosorption process was spontaneous, feasible, endothermic in nature and of dual nature, physisorption and chemisorption; however, the physisorption process was dominant. Therefore, modified plantain peel has potential for application as an effective bioadsorbent for removal of 2,6-dichlorophenol from aqueous solution.     

Influence of metallic substrate surface engineering on peel resistance of adhesively bonded polymer film

The peel resistance of adhesively bonded polymer films to a stainless steel sheet substrate (SSSS) with different engineered surface characteristics was examined in two different loading directions and for two different peel speeds. The SSSS was laminated with two thin polymeric adherends using two different pressure-sensitive adhesives. The SSSS surface was altered by grinding and knurling techniques before lamination and the effects of surface alterations on peel resistance were compared with peel resistance of the adherend from as-received SSSS with a bright annealed surface condition. For ground surface, an increase in adherend peel resistance was observed and the increase was attributed to increase in contact area between the adhesive and SSSS surface. For knurled surfaces which involved deeper and less frequent grooves, however, a decrease in peel resistance was observed. This was attributed to a more complex stress state at the peel front in the SSSS groove region during peeling. An increase in peel speed enhanced the peel resistance from both ground and knurled surfaces.     

Photocrosslinking of solvent-based acrylic pressure-sensitive adhesives (PSA) by the use of selected photoinitiators type I

This study investigated the photocrosslinking of solvent-based acrylic pressure-sensitive adhesives (PSA) containing selected photoinitiators type I, known as α-cleavage photoinitiators. Photocrosslinking of PSA, especially of acrylic PSA, is well established crosslinking process using the UV radiation technology. UV-initiated crosslinking of acrylic PSA allows the synthesis of the wide range of UV-crosslinkable PSA with the interesting features. Especially, the important balances of properties such as adhesive and cohesive strength which are typically critical for the application performance can be achieved by this technology. The selection of suitable photoinitiator plays an important role to obtain the optimum properties of acrylic PSA including tack, peel adhesion, and shear strength. In this study, the investigations on different saturated conventional photoinitiators of type I for solvent-based PSA were carried out. The effects of photoinitiator concentration, UV crosslinking time and UV dose on the tack, peel strength, and shear strength were explored in detail for guiding the choice of photoinitiators to fabricate advanced PSA for industrial usage.     

Sawtooth-shaped stringiness with front frame formation for polyacrylic pressure-sensitive adhesives with two different molecular structures

The formation of sawtooth-shaped stringiness during 90° peeling was investigated using crosslinked poly(n-butyl acrylate–acrylic acid) and poly(2-ethylhexyl acrylate–acrylic acid) random copolymers with an acrylic acid content of 5 wt.% and different crosslinking degrees as pressure-sensitive adhesives (PSAs). The gel fraction was measured by toluene extraction of PSA, and it increased with crosslinker content for both systems. The observed stringiness was sawtooth-shaped, but there were three different types; both the typical sawtooth shape and the frame formed at the front tip with interfacial failure, and the sawtooth shape formed with cohesive failure. The change in the stringiness shape was affected strongly by the gel fraction of PSA. The peel rate under constant peel load was measured and revealed that the peel rate was lowest upon formation of the front frame type. A good relation was found between peel rate and peel strength, with a greater peel strength upon formation of the front frame type. The concentrated stress at the peeling tip is released by progress of peeling and deformation of the adhesive layer (stringiness) for no frame type. On the other hand, the sufficient interfacial adhesion delays the progress of peeling, and the applied larger stress causes cavitation in the PSA layer for front frame type. The formed cavity grows and the front frame type formed as a result. That is, internal deformation occurred preferentially over peeling. In order to improve the peel strength, the front frame type is the most useful stringiness shape.     

采用石墨电极制备多孔硅工艺研究

采用石墨电极作为阴极,通过向腐蚀溶液中添加适量65％(质量分数wt％,下同)浓硝酸,以电化学腐蚀法在单晶硅片表面制备出多孔硅微结构.实验表明,随着腐蚀时间的增加,衡量多孔硅表面形貌的粗糙度和颗粒度指标值呈周期性增减变化;在电流密度为10 mA/cm2的阳极腐蚀参数下,将单晶硅片腐蚀1875秒制备的多孔硅样品的粗糙度和颗粒度值相对较大,原子力显微镜(AFM)和扫描电子显微镜(SEM)检测结果表明其硅柱最大高度、颗粒最大直径和平均直径分别达到470 nm、1693.590nm、489.954nm.     

Evaluation of pressure-sensitive tape adhesion and backing directionality by excimer laser methods

The effects of 248 nm KrF excimer laser irradiation on a pressure-sensitive adhesive tape bonded to a glass substrate were investigated as a possible method to evaluate the quality of adhesion, as well as the directionality induced during manufacture. The model pressure-sensitive tape consisted of biaxially-oriented polypropylene (PP) tape coated with a hot-melt rubber resin. Analysis of the front-shot experiments, which were performed by irradiation through the PP backing, allowed correlation between the excimer laser irradiation-induced detachment and the peel adhesion strength. For this purpose, peel tests were performed before and after laser shots. The directionality induced during manufacture resulted in a more ablated area in the strength direction than in the transverse direction when the bonded tapes were irradiated with an elliptically-shaped laser beam above the ablation threshold. A correlation was found between the detachment bubbles created by irradiation below the ablation threshold and their respective peel adhesion values, which allows us to evaluate the quality of adhesion for pressure-sensitive tapes. Thus, a method to evaluate the quality of adhesion using an excimer laser is proposed based on the findings of this work.