Selective Far Infrared Heating System—Spectral Manipulation. II

Spectral manipulation of infrared radiation for selective heating of food components was done using a far infrared (FIR) heating system. The incident FIR radiation was controlled in the specific spectral regions using three bandpass optical filters in ranges of 2.5-2.96 µm (filter A), 3.15-3.67 µm (filter B), and 5.45-12.23 µm (filter C). Pure soybean protein and starch powder were used to test the validity of the selective IR heating system in the three different bandpass ranges. Based on the heat flux ratio between soy protein and starch, in relation to the applied spectral conditions, a simulation model was developed and validated.     

红外辐射加热技术在涂层固化中的设计应用

简述了红外辐射加热技术在涂装行业中的应用状况;结合具体设计案例阐述红外辐射加热元件功率选择、布置方式、结构设计、运行环境等设计要点,通过优化设计实现红外加热元件空间上的立体可调;最终获得很好的固化温度曲线及涂层固化效果。     

Study on the Far Infrared Ray Emission Property and Adsorption Performance of Bamboo Charcoal/Polyvinyl Alcohol Fiber

In this study, bamboo charcoal materials were blended into polyvinyl alcohol (PVA) solution in various proportions to prepare bamboo charcoal/PVA fibers. A series of estimation was executed to discuss the performance of above fibers such as far infrared ray emission, heat preservation, deodorization of ammonia gas, and the adsorption of methylene blue. The spectrum of far infrared ray of bamboo charcoal/PVA fiber revealed that the average emission rate between 8–14 μm wavelengths increased with the increase in the bamboo charcoal content. From the heat preservation test, it is obvious that the surface temperature of bamboo charcoal/PVA fiber also increased with the increase in the bamboo charcoal content. This increase in content in the fiber specimen achieved a superior adsorption performance for ammonia gas and methylene blue.     

Selective Catalytic Reduction of NO by Ammonia over Raney‐Ni Supported Cu‐ZSM–5 I. Catalyst Activity and Stability

Composite materials containing Raney Ni and Cu‐ZSM‐5 are highly active catalysts for the selective catalytic reduction (SCR) of NO by NH₃. Their catalytic properties were studied with particular attention to the influence of moisture and SO₂ in the feed, and to effects of catalyst shaping operations. Composite materials (16–20 wt‐% zeolite) were prepared by mixing the components, with different degree of segregation in the resulting pressed particles, or by growing ZSM‐5 crystallites on the surface of leached Raney Ni, which were then exchanged with Cu ions. Catalytic tests were performed with 1000 ppm NO, 1000 ppm NH₃, 2 % O₂ in He, at 3–6.5 · 10⁵ h^–1 (related to zeolite component). With physical mixtures, the catalytic behaviour strongly depended on the mixing strategy, particles containing both Ni and zeolite being inferior to mixed Ni‐only and zeolite‐only particles. The SCR activity was promoted by 2 % H₂O in the feed, SO₂ (200 ppm) was a moderate poison at low temperatures, but indifferent or slightly promoting at high temperatures. A catalyst prepared from ZSM‐5 grown on Raney Ni, which was ranked intermediate in dry feed, was promoted to excellent performance in H₂O and SO₂ containing feed at T > 700 K and was stable for 38 h at 845 K. The results suggest that SCR catalysts containing highly active zeolites should be produced avoiding shaping operations e.g. by use of zeolite crystallites grown on wire packings.     

Microwave Heating Effects Rapid and Selective Decarboalkoxylation of Mono‐Alkylated Malonates and β‐Ketoesters

Brief microwave irradiation of mono‐alkylated malonates and β‐ketoesters at 160–200 °C in wet DMF induces smooth and selective decarboalkoxylation. Observations suggest that this reaction occurs by nucleophilic attack of water at the ester carbonyl carbon (hydrolysis) followed by decarboxylation of the resulting acid. The process occurs despite the absence of traditional acid, base or nucleophile catalysts or reagents.     

Heating/Drying Using Particulate Medium : A Review Part I. General and Heat transfer parameters

ABSTRACT

This paper presents an Overview of particulate medium drying and heat treating of cereal grains. While the conventional air drying of grains is well documented, studies on the drying of grains using heated granular medium do not appear to exist. The scientific study of the different aspects of drying with a heated granular medium began in the early 1970's. Progress on the utilization of particle-to-particle heat transfer was slow as evidenced by the fact that there is no commercial dryer using the method as of today.

The first section of this paper deals with conduction heating and how it led to the use of granular medium in heating the grain. Starting with the earliest work on conduction heating reported by Kelly ( 1939), the developments in the heating of grain using granular media is discussed. For decades since Kelly's report, work in the subject area dealt mostly with the theoretical aspects of solid-to-solid heat transfer. Thus, in the succeeding section of the paper, heat transfer parameters and mechanisms involved in the process are thoroughly investigated.     

Heating/Drying Using Particulate Medium : A Review Part I. General and Heat transfer parameters

This paper presents an Overview of particulate medium drying and heat treating of cereal grains. While the conventional air drying of grains is well documented, studies on the drying of grains using heated granular medium do not appear to exist. The scientific study of the different aspects of drying with a heated granular medium began in the early 1970's. Progress on the utilization of particle-to-particle heat transfer was slow as evidenced by the fact that there is no commercial dryer using the method as of today.

The first section of this paper deals with conduction heating and how it led to the use of granular medium in heating the grain. Starting with the earliest work on conduction heating reported by Kelly ( 1939), the developments in the heating of grain using granular media is discussed. For decades since Kelly's report, work in the subject area dealt mostly with the theoretical aspects of solid-to-solid heat transfer. Thus, in the succeeding section of the paper, heat transfer parameters and mechanisms involved in the process are thoroughly investigated.     

Hydrodynamics of disturbed flow and erosion—corrosion. Part I — Single-phase flow study

Numerical simulations of turbulent flow have been used to determine the flow structure in a sudden pipe expansion, in order to explain the effects of disturbed flow on mass transfer controlled erosion–corrosion. Previously determined rates of mass transfer through the liquid boundary layer have been directly related to the predicted levels of near-wall turbulence. When rust films are present, the turbulent fluctuations affect both the mass transfer through the boundary layer and the removal of the film. The determining resistance to mass transfer, under the conditions examined, was that of the rust film.     

Blends of modified epoxy resin and carboxyl‐terminated polybutadiene. I

Six blend samples were prepared by the physical mixing of epoxidized resole (EDR) with different weight ratios of carboxyl‐terminated polybutadiene (CTPB) liquid rubber ranging from 0 to 25 wt % in intervals of 5 wt %. The formation of various reaction products during the curing of unblended EDR and CTPB‐blended EDR were studied with Fourier transform infrared spectroscopy. The curing time at 100°C for the blend sample containing 15 wt % CTPB was the least among all of the blend samples. This blend sample, also, showed the highest initial degradation temperature, as obtained from thermogravimetric analysis thermograms, which indicated that it was the most thermally stable matrix system. The films of coatings based on the blend of EDR with 15 wt % CTPB offered the highest resistance toward different concentrations of acids and alkalis compared to the films having 5, 10, 20, and 25 wt % CTPB in the EDR/CTPB blends. Solvents showed almost the same behavior as acids and alkalis for these films except for hydrocarbon solvents such as mineral turpentine oil, toluene, and xylene. The resistance toward these solvents was poor and slightly inferior to those found with EDR unblended with CTPB. The tensile, flexural, and impact strengths of the molded specimens derived from the EDR/CTPB blends initially increased up to 15 wt % CTPB addition in the blend and then decreased, whereas the elongation at break remained constant for all blend compositions. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1802–1808, 2006     

Flame-retarding materials—I. Syntheses and flame-retarding property of alkylphosphate-type polyols and corresponding polyurethanes

In this research, oligomeric polyalkyl phosphate-type polyols (P% = 14–17) were synthesized from ethylene glycol or 1,4-butanediol (PBE or PBB) by means of butyl phosphorodichloridate, which was prepared from phosphorus oxychloride and butanol. These polyols were then reacted with isocyanate to form the corresponding polyurethanes (PETD and PBTD). These polyols were characterized by FTIR, ¹H-NMR, and ³¹P-NMR, and the thermal stabililties were measured by thermogravimetry analysis. The degradation phenomena were traced by FTIR and interpreted in terms of the degradation and formation of bonds. The corresponding polyurethanes were also characterized by FTIR and ¹H-NMR, and their thermal stability was also studied by thermogravimetry analysis. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 1635–1643, 1998     

De Novo Design,Synthesis and Evaluation of Benzylpiperazine Derivatives as Highly Selective Binders of Mcl‐1

Considerable efforts have been made to the development of small‐molecule inhibitors of antiapoptotic B‐cell lymphoma 2 (Bcl‐2) family proteins (such as Bcl‐2, Bcl‐x_L, and Mcl‐1) as a new class of anticancer therapies. Unlike general inhibitors of the entire family, selective inhibitors of each member protein can hopefully reduce the adverse side effects in chemotherapy treatments of cancers overexpressing different Bcl‐2 family proteins. In this study, we designed four series of benzylpiperazine derivatives as plausible Bcl‐2 inhibitors based on the outcomes of a computational algorithm. A total of 81 compounds were synthesized, and their binding affinities to Bcl‐2, Bcl‐x_L, and Mcl‐1 measured. Encouragingly, 22 compounds exhibited binding affinities in the micromolar range (K_i<20 μM ) to at least one target protein. Moreover, some compounds were observed to be highly selective binders to Mcl‐1 with no detectable binding to Bcl‐2 or Bcl‐x_L, among which the most potent one has a K_i value of 0.18 μM for Mcl‐1. Binding modes of four selected compounds to Mcl‐1 and Bcl‐x_L were derived through molecular docking and molecular dynamics simulations. It seems that the binding affinity and selectivity of these compounds can be reasonably interpreted with these models. Our study demonstrated the possibility for obtaining selective Mcl‐1 inhibitors with relatively simple chemical scaffolds. The active compounds identified by us could be used as lead compounds for developing even more potent selective Mcl‐1 inhibitors with potential pharmaceutical applications.     

Design and In vitro Evaluation of Branched Peptide Conjugates: Turning Nonspecific Cytotoxic Drugs into Tumor‐Selective Agents

The use of peptide receptors as targets for tumor‐selective therapies was envisaged years ago with the findings that receptors for different endogenous regulatory peptides are overexpressed in several primary and metastatic human tumors, and can be used as tumor antigens. Branched peptides can retain or even increase, through multivalent binding, the biological activity of a peptide and are very resistant to proteolysis, thus having a markedly higher in vivo activity compared with the corresponding monomeric peptides. Oligo‐branched peptides, containing the human regulatory peptide neurotensin (NT) sequence, have been used as tumor‐specific targeting agents. These peptides are able to selectively and specifically deliver effector units, for cell imaging or killing, to tumor cells that overexpress NT receptors. Results obtained with branched NT conjugated to different functional units for tumor imaging and therapy indicate that branched peptides are promising novel multifunctional targeting molecules. This study is focused on the role of the releasing pattern of drug‐conjugated branched NT peptides. We present results obtained with oligo‐branched neurotensin peptides conjugated to 6‐mercaptopurin (6‐MP), combretastain A‐4 (CA4) and monastrol (MON). Drugs were conjugated to oligo‐branched neurotensin through different linkers, and the mode‐of‐release, together with cytotoxicity, was studied in different human cancer cell lines. The results show that branched peptides are very promising pharmacodelivery options. Among our drug‐armed branched peptides, NT4–CA4 was identified as a candidate for further development and evaluation in preclinical pharmacokinetic and pharmacodynamic studies. This peptide–drug exhibits significant activity against pancreas and prostate human cancer cells. Consequently, this derivative is of considerable interest due to the high mortality rates of pancreas neuroendocrine tumors and the high incidence of prostate cancer.     

Selective reduction of NO by NH3 over manganese–cerium mixed oxides: Relation between adsorption, redox and catalytic behavior

Manganese–cerium mixed oxide catalysts with different molar ratio Mn/(Mn + Ce) (0, 0.25, 0.50, 0.75, 1) were prepared by citric acid method and investigated concerning their adsorption behavior, redox properties and behavior in the selective catalytic reduction of NO_x by NH₃. The studies based on pulse thermal analysis combined with mass spectroscopy and FT-IR spectroscopy uncovered a clear correlation between the dependence of these properties and the mixed oxide composition. Highest activity to nitrogen formation was found for catalysts with a molar ratio Mn/(Mn + Ce) of 0.25, whereas the activity was much lower for the pure constituent oxides. Measurements of adsorption uptake of reactants, NO_x (NO, NO₂) and NH₃, and reducibility showed similar dependence on the mixed oxide composition indicating a clear correlation of these properties with catalytic activity. The adsorption studies indicated that NO_x and NH₃ are adsorbed on separate sites. Consecutive adsorption measurements of the reactants showed similar uptakes as separate measurements indicating that there was no interference between adsorbed reactants. Mechanistic investigations by changing the sequence of admittance of reactants (NO_x, NH₃) indicated that at 100–150 °C nitrogen formation follows an Eley–Rideal type mechanism, where adsorbed ammonia reacts with NO_x in the gas phase, whereas adsorbed NO_x showed no significant reactivity under conditions used.     

Design,Synthesis, and Biological Evaluation of Tetrahydro‐β‐carboline Derivatives as Selective Sub‐Nanomolar Gelatinase Inhibitors

Targeting matrix metalloproteinases (MMPs) is a pursued strategy for treating several pathological conditions, such as multiple sclerosis and cancer. Herein, a series of novel tetrahydro‐β‐carboline derivatives with outstanding inhibitory activity toward MMPs are present. In particular, compounds 9 f , 9 g , 9 h and 9 i show sub‐nanomolar IC₅₀ values. Interestingly, compounds 9 g and 9 i also provide remarkable selectivity toward gelatinases; IC₅₀=0.15 nm for both toward MMP‐2 and IC₅₀=0.63 and 0.58 nm , respectively, toward MMP‐9. Molecular docking simulations, performed by employing quantum mechanics based partial charges, shed light on the rationale behind binding involving specific interactions with key residues of S1′ and S3′ domains. Taken together, these studies indicate that tetrahydro‐β‐carboline represents a promising scaffold for the design of novel inhibitors able to target MMPs and selectively bias gelatinases, over the desirable range of the pharmacokinetics spectrum.     

Design,Synthesis, and Biological Evaluation of 3‐Benzazepin‐1‐ols as NR2B‐Selective NMDA Receptor Antagonists

Cleavage and reconstitution of a bond in the piperidine ring of ifenprodil ( 1 ) leads to 7‐methoxy‐2,3,4,5‐tetrahydro‐1H‐3‐benzazepin‐1‐ols, a novel class of NR2B‐selective NMDA receptor antagonists. The secondary amine 7‐methoxy‐2,3,4,5‐tetrahydro‐1H‐3‐benzazepin‐1‐ol ( 12 ), which was synthesized in six steps starting from 2‐phenylethylamine 3 , represents the central building block for the introduction of several N‐linked residues. A distance of four methylene units between the basic nitrogen atom and the phenyl residue in the side chain results in high NR2B affinity. The 4‐phenylbutyl derivative 13 (WMS‐1405, K_i=5.4 nM ) and the conformationally restricted 4‐phenylcyclohexyl derivative 31 (K_i=10 nM ) represent the most potent NR2B ligands of this series. Whereas 13 shows excellent selectivity, the 4‐phenylcyclohexyl derivative 31 also interacts with σ₁ (K_i=33 nM ) and σ₂ receptors (K_i=82 nM ). In the excitotoxicity assay the phenylbutyl derivative 13 inhibits the glutamate‐induced cytotoxicity with an IC₅₀ value of 360 nM , indicating that 13 is an NMDA antagonist.     

Electrochemical behaviour of the antimony electrode in sulphuric acid solutions—I. Corrosion processes and anodic dissolution of antimony

The corrosion processes at open circuit conditions and in the active dissolution region of antimony, at low anodic overpotentials, have been studied in sulphuric acid solutions. It was established that antimony dissolution at open circuit is coupled to oxygen reduction, which occurs via the hydrogen peroxide route. The rate of antimony dissolution was found to increase linearly with increasing acid concentration. Based on potentiodynamic, galvanodynamic and steady-state measurements as well as ac impedance data possible mechanisms for the corrosion processes at open circuit as well as for the dissolution of antimony in the active region are proposed and discussed.     

Blends of polyamide 6, polycarbonate,and poly(propylene oxide). I. Reactive compatibilization–morphology relationships

The relationship between reactive compatibilization and morphology of the polyamide 6–polycarbonate (PA6–PC) and polyamide 6–polycarbonate–poly(pro-pylene oxide) (PA6–PC–PPO) blends were investigated by means of torque values, scanning electron microscopy, and Fourier transform infrared spectroscopy. The micrographs show that the blends processed for a long period of time presented a PC domain of smaller size and better adherence between the phases than the blends processed for a short period of time. This fact can be related with the presence of the block copolymer of PA6–PC synthesized in situ by the reaction of PA6 and PC and depend on temperature and mixing time. The presence of PPO does not impede the formation of copolymer but interferes on the size of the domain. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 857–864, 1998     

Design,Synthesis, and Biological Evaluation of Coumarin Derivatives Tethered to an Edrophonium‐like Fragment as Highly Potent and Selective Dual Binding Site Acetylcholinesterase Inhibitors

A large series of substituted coumarins linked through an appropriate spacer to 3‐hydroxy‐N,N‐dimethylanilino or 3‐hydroxy‐N,N,N‐trialkylbenzaminium moieties were synthesized and evaluated as acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors. The highest AChE inhibitory potency in the 3‐hydroxy‐N,N‐dimethylanilino series was observed with a 6,7‐dimethoxy‐3‐substituted coumarin derivative, which, along with an outstanding affinity (IC₅₀=0.236 nM ) exhibits excellent AChE/BChE selectivity (SI>300 000). Most of the synthesized 3‐hydroxy‐N,N,N‐trialkylbenzaminium salts display an AChE affinity in the sub‐nanomolar to picomolar range along with excellent AChE/BChE selectivities (SI values up to 138 333). The combined use of docking and molecular dynamics simulations permitted us to shed light on the observed structure–affinity and structure–selectivity relationships, to detect two possible alternative binding modes, and to assess the critical role of π–π stacking interactions in the AChE peripheral binding site.