Application of a Technofunctional Caseinate Hydrolysate to Replace Surfactants in Ice Cream

There is a demand for a clean label of ice cream in the food industry. To meet this requirement, alternative surfactants and hydrocolloids without an additive number have to be found. Here, a caseinate hydrolysate with improved interfacial properties was investigated as such an additive. Replacing only the surfactant resulted in ice cream characteristics, comparable to using a commercial emulsifier (INS 472b). Thus, a clean labeling of the surfactant using this hydrolysate is possible. By contrast, replacing the hydrocolloid additionally led to an unfavorable ice cream texture and stability.     

Reconfiguring flexible machine modules of a PCB assembly line

Assembly of electronic components to Printed Circuit Boards (PCB) is a complicated manufacturing process and therefore its control is usually divided into several subtasks which are handled separately. We consider the combined task of determining a machine configuration and line balancing for a single assembly line of interconnected, reconfigurable machine modules and one PCB type in production. The modules can be tailored to the needs of each PCB type by suitable assignments for placement heads, nozzles and feeders. Out of these, the component-to-machine assignment appears to be most difficult and we propose five different solution methods for it; brute force, random, greedy, local search and genetic algorithm. The genetic algorithm outperformed the other methods in practical test.     

Aerobic Oxidation of Benzylic Alcohols in Water by 2,2,6,6‐Tetramethylpiperidine‐1‐oxyl (TEMPO)/Copper(II) 2‐N‐Arylpyrrolecarbaldimino Complexes

Novel copper(II) 2‐N‐arylpyrrolecarbaldimine‐based catalysts for the aerobic oxidation of benzylic alcohols mediated by the 2,2,6,6‐tetramethylpiperidine‐1‐oxyl (TEMPO) radical are reported. The catalytic activity for both synthesized and in situ made complexes in alkaline water solutions was studied revealing high efficiency and selectivity (according to GC selectivity always >99%) for both of these catalytic systems. For example, quantitative conversion of benzyl alcohol to benzaldehyde can be achieved with the in situ prepared bis[2‐N‐(4‐fluorophenyl)‐pyrrolylcarbaldimide]copper(II) catalysts in 2 h with atmospheric pressure of O₂ at 80 °C. Interestingly, these catalysts can utilize dioxygen as well as air or hydrogen peroxide as the end oxidants, producing water as the only by‐product.     

Electrochemical reduction of oxygen on thin-film Pt electrodes in acid solutions

The electrochemical reduction of oxygen on thin-film platinum electrodes in 0.1 M HClO₄ and 0.05 M H₂SO₄ solutions has been investigated using the rotating disk electrode (RDE) method. Thin films of Pt (0.25-20 nm thick) were prepared by vacuum evaporation onto glassy carbon substrate. The surface morphology of Pt films was examined by transmission electron microscopy (TEM). The specific activity of O₂ reduction was higher in HClO₄ and decreased with decreasing film thickness. In H₂SO₄, the specific activity was lower and appeared to be independent of the Pt loading. The values of Tafel slopes close to −120 mV dec⁻¹ in high current density range and −60 mV dec⁻¹ in low current density range were obtained for all electrodes in both solutions, indicating that the mechanism of O₂ reduction is the same for thin-film electrodes as for bulk Pt. The number of electrons transferred per O₂ molecule was close to four for all thin Pt films studied.     

Nitroxide‐mediated synthesis of styrenic‐based segmented and tapered block copolymers using poly(lactide)‐functionalized TEMPO macromediators

Poly(styrene)‐poly(lactide) (PS‐PLA), poly (tert‐butyl styrene)‐poly(lactide) (PtBuS‐PLA) diblocks, and poly(tert‐butyl styrene)‐poly(styrene)‐poly(lactide) (PtBuS‐PS‐PLA) segmented and tapered triblocks of controlled segment lengths were synthesized using nitroxide‐mediated controlled radical polymerization. Well‐defined PLA‐functionalized macromediators derived from hydroxyl terminated TEMPO (PLA_T) of various molecular weights mediated polymerizations of the styrenic monomers in bulk and in dimethylformamide (DMF) solution at 120–130°C. PS‐PLA and PtBuS‐PLA diblocks were characterized by narrow molecular weight distributions (polydispersity index (M_w/M_n) < 1.3) when using the PLA_T mediator with the lowest number average molecular weight M_n= 6.1 kg/mol while broader molecular weight distributions were exhibited (M_w/M_n = 1.47‐1.65) when using higher molecular weight mediators (M_n = 7.4 kg/mol and 11.3 kg/mol). Segmented PtBuS‐PS‐PLA triblocks were initiated cleanly from PtBuS‐PLA diblocks although polymerizations were very rapid with PS segments ～ 5–10 kg/mol added within 3–10 min of polymerization at 130°C in 50 wt % DMF solution. Tapering from the PtBuS to the PS segment in semibatch mode at a lower temperature of 120°C and in 50 wt % DMF solution was effective in incorporating a short random segment of PtBuS‐ran‐PS while maintaining a relatively narrow monomodal molecular weight distribution (M_w/M_n ≈ 1.5). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Tunable microwave devices using low-sintering-temperature screen-printed barium strontium titanate (BST) thick films

A tunable microwave phase shifter composed of a low-sintering-temperature, screen-printable barium strontium titanate (BST) film and silver metallization was fabricated on an alumina substrate and co-fired at 900 °C for 3 h. The dielectric properties of the films were characterized in a frequency range of 0.8–8 GHz using scattering parameter measurements and a quasi-static coplanar waveguide transmission line model. The temperature dependency of the films was measured through capacitance measurements in a frequency range of 0.5–2.5 GHz. The figure of merit (phase shift/dB of insertion loss) of the phase shifter was found to be 14.6 at 3 GHz with an applied bias field strength of 2.5 V/μm. The performance of the phase shifter is briefly discussed and compared with other phase shifters fabricated by direct screen-printing of BST films.     

Membrane evaluation for the treatment of acidic clear filtrate

The total effluent load of a paper mill can be significantly decreased by recycling of purified clear filtrate (CF) back to paper-making process. The CF treated with membranes can be reused, for instance, as wire section shower water and in the dilution of chemicals. The main requirements for a membrane in CF treatment are high filtration capacity, high retention of turbidity and low fouling tendency. Previous studies have shown that the regenerated cellulose (RC) ultrafiltration (UF) membrane C30F (current trade name UC030T) is especially suitable for the treatment of paper mill process waters. Every paper-making process is, however, different. Thus, filtration experiments are required in order to find the most optimal membrane for the treatment of a certain process water. In this study the best membrane for the treatment of acidic clear filtrate (ACF) was searched. The performance of the C30F membrane was compared with five UF and three microfiltration (MF) membranes. The results revealed that in addition to the C30F membrane, also some other membranes produced high filtration capacity with ACF (approximately 200 L/(m²h bar)). All the tested membranes also retained over 90% of turbidity. The extremely hydrophilic C30F membrane had, however, lower fouling tendency compared to the other tested membranes. Therefore, it was concluded that the C30F membranes were the best possible membrane for the ACF treatment.     

Chemoenzymatic Asymmetric Synthesis of Pyridine-Based α-Fluorinated Secondary Alcohols

Fluoro-substituted and heteroaromatic compounds are valuable intermediates for a variety of applications in pharma- and agrochemistry and synthetic chemistry. This study investigates the chemoenzymatic preparation of chiral alcohols bearing a heteroaromatic ring with an increasing degree of fluorination in α-position. Starting from readily available picoline derivatives prochiral α-halogenated acyl moieties were introduced with excellent selectivity and 64–95 % yield. The formed carbonyl group was subsequently reduced to the corresponding alcohols using the alcohol dehydrogenase from Lactobacillus kefir, yielding an enantiomeric excess of 95–>99 % and up to 98 % yield.     

Partial electrode method for loss and physical parameter determination of piezoceramics: Simplification,error investigation and applicability

The IEEE standard to determine physical parameters of piezoceramics has been utilized for decades by many researchers, yet it omits presence of important loss factors and possesses serious deficits that restrict accurate parameter determination. To resolve these issues, the partial electrode (PE) method was previously proposed, though the focus has been merely made on development of the method itself. In this study, we provide method simplification and more detailed analysis. The omission of unnecessary samples greatly boosts experiment and analysis process. To prove that the PE method is reliable, possible causes of errors were investigated; it is shown that they were either negligibly small or can be resolved with proper calibration. Furthermore, Applicability of PE method to various types of piezoceramic materials and compatibility with impedance analyzers are shown. Finally, PE method is proved to be reliable and can be alternative to IEEE Standard on Piezoelectricity.     

美卓超滤膜技术——提高水和涂料的循环利用率

造纸行业日趋承受着节水、节能以及环保的压力。也就是说,造纸企业必须寻找新技术,将注意力转移到生产中的整个水质和高效的原料回收系统上。