CaCO3 scaling in AISI 316 stainless steel tubes – effect of thermal and hydraulic parameters on the induction time and growth rate

Calcium Carbonate (CaCO₃) is predominantly present in cooling water which is commonly used as a coolant in many industrial processes. It has inverse solubility characteristics i.e., it is less soluble in warm water, resulting in the deposition of scale on heat transfer surfaces. An experimental study was carried out to determine the effect of tube surface temperature, Reynolds number, tube diameter and salt concentration on the induction time of CaCO₃ scaling. It was observed that tube surface temperature, Reynolds number and tube diameter had no effect on the onset time of scaling, whereas salt concentration and tube surface roughness had a profound influence on the induction period. The data collected from the experiments were used to develop dimensionless fouling resistance models for estimation and prediction purposes. Received on 22 December 1997     

Facile Oxidation Approach to Amend Surface Chemistry of Carbon Particles for Augmented Dispersion in Epoxy Matrix

Russian Journal of Applied Chemistry - Surface chemistry of carbon black (CB) plays a major role towards its dispersion in liquid media. In this study a simple approach of surface modification has...     

Magnetic nanoparticle-based cancer nanodiagnostics

Diagnosis facilitates the discovery of an impending disease. A complete and accurate treatment of cancer depends heavily on its early medical diagnosis. Cancer, one of the most fatal diseases world-wide, consistently affects a larger number of patients each year. Magnetism, a physical property arising from the motion of electrical charges, which causes attraction and repulsion between objects and does not involve radiation, has been under intense investigation for several years. Magnetic materials show great promise in the application of image contrast enhancement to accurately image and diagnose cancer. Chelating gadolinium (Gd Ⅲ) and magnetic nanoparticles (MNPs) have the prospect to pave the way for diagnosis, operative management, and adjuvant therapy of different kinds of cancers. The potential of MNP-based magnetic resonance (MR) contrast agents (CAs) now makes it possible to image portions of a tumor in parts of the body that would be unclear with the conventional magnetic resonance imaging (MRI). Multiple functionalities like variety of targeting ligands and image contrast enhancement have recently been added to the MNPs. Keeping aside the additional complexities in synthetic steps, costs, more convoluted behavior, and effects in-vivo, multifunctional MNPs still face great regulatory hurdles before clinical availability for cancer patients. The trade-off between additional functionality and complexity is a subject of ongoing debate. The recent progress regarding the types, design, synthesis, morphology, characterization, modification, and the in-vivo and in-vitro uses of different MRI contrast agents, including MNPs, to diagnose cancer will be the focus of this review. As our knowledge of MNPs' characteristics and applications expands, their role in the future management of cancer patients will become very important. Current hurdles are also discussed, along with future prospects of MNPs as the savior of cancer victims.     

Cyclometalated Iridium (III) complexes: Recent advances in phosphorescence bioimaging and sensing applications

The phosphorescence bioimaging and sensing applications of Iridium (III) complexes, in particular to subcellular organelle staining as well as sensing of biologically important analytes, have been reviewed here. The bioimaging applications of the metal complexes provide an attractive alternative to fluorescent organic compounds in the construction of biosensors and biolabels because of having certain advantages.     

Magnetic nanoparticle-based cancer therapy

Nanoparticles(NPs) with easily modified surfaces have been playing an important role in biomedicine.As cancer is one of the major causes of death,tremendous efforts have been devoted to advance the methods of cancer diagnosis and therapy.Recently,magnetic nanoparticles(MNPs) that are responsive to a magnetic field have shown great promise in cancer therapy.Compared with traditional cancer therapy,magnetic field triggered therapeutic approaches can treat cancer in an unconventional but more effective and safer way.In this review,we will discuss the recent progress in cancer therapies based on MNPs,mainly including magnetic hyperthermia,magnetic specific targeting,magnetically controlled drug delivery,magnetofection,and magnetic switches for controlling cell fate.Some recently developed strategies such as magnetic resonance imaging(MRI) monitoring cancer therapy and magnetic tissue engineering are also addressed.     

Impact of Long‐Wavelength Ultraviolet A1 and Visible Light on Light‐Skinned Individuals

Solar radiation is known to be a major contributor to the development of skin cancer. Most sunscreen formulations, including those with broad spectrum, offer minimal protection in long‐wavelength ultraviolet A1 (UVA1; 370–400 nm) and visible light (VL; 400–700 nm) domain. There is limited information regarding the impact of this broad waveband (VL + UVA1, 370–700 nm) on those with light skin. In this study, ten healthy adult subjects with Fitzpatrick skin phototypes I–III were enrolled. On day 0, subjects' lower back was exposed to a VL + UVA1 dose of 480 J cm^?2. A statistically significant increase in erythema immediately after irradiation compared with subjects' baseline nonirradiated skin was observed. Clinically perceptible erythema with VL + UVA1 is a novel finding since the erythemogenic spectrum of sunlight has primarily been attributed to ultraviolet B and short‐wavelength ultraviolet A (320–340 nm). The results emphasize the need for protection against this part of the solar spectra and warrant further investigation.     

Correction to: Evaluation of accuracy dependence of Raman spectroscopic models on the ratio of calibration and validation points for non-invasive glucose sensing

Analytical and Bioanalytical Chemistry - The authors would like to bring to the reader’s attention that the Clarke error grid plot presented in Fig. 3 was generated using codes...     

Dipole and Combo Optical Solitons in Birefringent Fibers in the Presence of Four-Wave Mixing

The ultimate theme of this study is to develop dipole and combo optical solitons in birefringent fibers (BF) along with the effect of four-wave mixing (4WM). Two types of rough mediums are used which are Kerr law and parabolic law. Ansatz method of Choudhuri is applied to obtain dark in the bright (dipole) soliton solutions providing bright background for the propagation of optical dark pulse. Ansatz method of Li is applied to obtain combo soliton solutions providing bright solitary wave and dark solitary wave solutions. These results also exist to hold in non-Kerr media with higher order dispersion.     

Nuclear magnetic resonance and optical absorption spectroscopic studies on paramagnetic praseodymium(III) complexes with beta-diketone and heterocyclic amines

The optical absorption spectra of [Pr(acac)(3)(H(2)O)(2)].H(2)O, [Pr(acac)(3)phen.H(2)O] and [Pr(acac)(3)bpy] (where acac is the anion of acetylacetone, phen is 1,10-phenanthroline and bpy is 2,2'-bipyridyl) have been analyzed in the visible region in a series of non-aqueous solvents (methanol, ethanol, isopropanol, chloroform, acetonitrile and pyridine). The complexes display four non-hypersensitive 4f-4f transitions ((3)P(2), (3)P(1)+(1)I(6), (3)P(0) and (1)D(2)) from the (3)H(4) ground state. The band shape of the transitions shows remarkable changes upon dissolving in different solvents. Distinctively different band shapes have been observed for phen and bpy complexes. The phen is more effective in producing changes and the splitting of the bands is more pronounced in phen complex since it is a stronger ligand and leads to stronger Pr-N(phen) bond. The splitting of the bands is indicative of partaking of f-orbitals in bonding. The NMR signals of heterocyclic amines have been shifted to high fields while the resonances due to acetylacetone moiety have moved to low fields which is the consequence of change in geometry of the complexes upon coordination of the heterocyclic amines and reflects the importance of geometric factor (3cos(2)theta-1) in changing sign of the shift and to a good approximation the shifts arise predominantly from the dipolar mechanism. The phen complexes have narrower line width than bpy complexes. The line broadening in the case of bpy complexes is suggestive of exchange between inter-converting forms. The bpy possesses some degree of rotational freedom about C(6)-C(6') bond and the two pyridine rings undergo scissoring motion with respect to each other.