Cavitation in Superfluid Helium Possibly Arising from Penning Ionization of Dimers

We have perforated a series of experiments to study cavitation in superfluid helium into which electrons are injected by field-emission from a sharp tip. The injected electrons force open small cavities in the liquid (“electron bubble”). These objects explode at a critical negative pressure P _c, and in previous experiments we have studied the cavitation that resugts from these explosions. In the present experiments we have detected cavitation events that occur before a negative pressure as large as P _c is reached. We suggest that these events may arise from a process in which two neutral helium dimers interact and an electron is injected into the liquid through Penning ionization.     

Direct synthesis of copper faujasite

Copper containing faujasite has been successfully prepared for the first time using a direct synthesis method. Faujasite type zeolite can be prepared in the presence of copper species by tuning the synthesis conditions. Ammonium hydroxide was used to form a copper complex that was later mixed with the reacting gel. Sodium is required to obtain copper faujasite. The complete elimination of sodium ions from the starting gel produces amorphous material. Crystallization took place at 358 K for 11 days. Crystallization temperature of 373 K produces ANA type zeolite as an impurity. Increasing by two times the amount of copper complex added to the reacting gel increases the crystallization time of Cu-FAU from 11 to 20 days (the crystallization rate decreases). The copper containing faujasite obtained was characterized by XRD, FESEM, EDX, EPR, FT-IR, TPR, and BET. According to the XRD pattern only FAU type zeolite was obtained. According to TPR experiments, the reduction temperature for Cu²⁺ ions present in Cu-FAU prepared by direct synthesis was 70 K more than for Cu-FAU prepared by ion-exchange. This difference can be due to the different location of the copper ions in the supercages or in the sodalite cages of the faujasite.     

Purification and some properties of a xylanase from Aspergillus sydowii MG49

Aspergillus sydowii MG49 produces a 30-kDa exosplitting xylobiohydrolase during growth on xylan. A specific chemical modification and substrate protection analysis of purified xylanase provided evidence that tryptophan and carboxy and amino groups are present at the catalytic site of this enzyme. Thermal inactivation of the xylanase occurs because of irreversible polymolecular aggregation, which is slower in the presence of glycerol.     

Screen‐printed biosensor for allergens

Allergen levels in indoor environments, leading to many diseases, eg asthma, rhinitis and conjunctivitis, affect a large and increasing fraction of the population. A quite effective and inexpensive method of a rough but very rapid overall assessment of total allergen level in the environment has been developed. The method involved estimation of protein in allergen extracts by screen‐printed electrodes using two different techniques. The biosensor comprised a rhodinised carbon working electrode, a silver/silver chloride reference electrode and a carbon counter electrode. In the first method the enzyme protease reacted with allergen protein to release amino acid, which produced hydrogen peroxide in the presence of amino acid oxidase. This was detected amperometrically. The second method used potassium bromide as electrolyte and the electrode was subjected to dual potential. Bromine, released due to electrolysis at higher potential, was consumed by the allergen protein at lower potential. In the first method, a unique technique was used to microencapsulate the enzyme protease and immobilise it on the surface of the electrode by in‐situ polymerisation to avoid contact with the amino acid oxidase. A total of seven allergens were tested and the results gave a good correlation with the standard protein measurement method. Environmental specimens from indoors, schools and workplaces can be evaluated for the aeroallergens produced by dust mites, animal hairs, cockroach debris, pollens, etc as a means of determining the exposure risk. Copyright © 2005 Society of Chemical Industry     

Fatty acids from Macoma sp. of bivalve mollusc

Fatty acids of the total lipids of flesh and hepatopancreas of Macoma sp. have been determined. The level of 20:5w3 (ca 17%), a biologically important fatty acid, was found to be considerably high. Other major component fatty acids were 16:0, 16:1, 18:1 and 22:4w6. High levels of 22:5w6 (8%), 22:5w3 (8%) and 22:6w3 (ca 15%) were found in flesh lipid. Nonsaponifiables were also high (28–30%). Alkyl ether acyl glycerols were found in flesh (1.3%) and hepatopancreas (3.8%).     

Microstructural Investigation on Failure of Internal Drive Shaft

17-4 PH stainless steel is used as internal drive shaft material in liquid engine pumps. One of the drive shafts failed during operation. The shaft pieces were in contact for short duration after failure, which has resulted in abrasion of fractured surfaces. Samples from the location of failure were taken, and investigation of the failure was carried out using optical and scanning electron microscopy. The microstructural analysis of the material and fractographic analysis of the fractured surface show that the failure was caused by excessive torsion.     

Detecting nondeterminacy in parallel programs

Methods and tools for detecting nondeterminacy in programs for shared-memory multiprocessors are discussed. The approach described divides the debugging chore into two phases. The first phase uses tools that automatically detect nondeterminacy to debug synchronization errors, assuming it is decided at the outset to make the parallel program determinate. At the end of this phase, it is known that the program is determinate, that timing differences will not affect results, and the debugging sessions are repeatable. In the second phase, an interactive break-point debugger is used to find arithmetic and logical errors. The proposed tools fall into two groups: those that statically analyze the source program and those that analyze an execution trace of the program     

ENVIRONMENTAL TOBACCO SMOKE REMOVAL CAPABILITY OF ACTIVATED CARBON

Removal of gaseous and vapor constituents of environmental tobacco smoke (ETS) by activated carbons in a packed bed arrangement was studied under dynamic conditions and was compared with that by silica gel and molecular sieve 13X. ETS is a mixture of sidestream smoke and exhaled mainstream smoke, and it consists of various organic and inorganic compounds, trace heavy metals, and particulate matters. Due to the complex nature of ETS-air mixture, its removal from indoors is a challenging task. For experimentation in a laboratory, the ETS was produced from a specially designed smoking apparatus that simulated the puffng of a cigarette by a person. Air containing ETS was passed through a bed containing about 25 grams of activated carbon at room temperature. The flow rate of air-ETS mixture through the bed was 4000 cm3/min. The relative humidity of the air was 50% and contained about 35 to 40 ppm of hydrocarbons as measured as methane-equivalent. The number of particles in the inlet air stream were in the range of 30,000 to 35,000 particles/cm3. About 60% of hydrocarbons present in ETS were removed at these operating conditions for a period of about 70 hours. Based on 15 adsorption and regeneration cycles, it was noted that the carbon bed did not loose its capacity for ETS significantly as indicated by the BET surface area and water adsorption data. At the beginning of an adsorption cycle, the carbon bed captured a significant number of particles. However, the bed rapidly lost its particle capture effciency as the experiment progressed. The number of particles in the outlet air stream was found to be the same as that of the inlet stream within five minutes.     

Application of Rachinger''s method to separate overlapped doublets in the X-ray photoelectron spectrum

Rachinger's method of separating ₁ and ₂ doublets in X-ray emission spectra is applied for the first time to separate the superimposed doublets due to spin-orbit coupling. This method has been applied to separate closely lying doublets such as (Ag 4p_3/2and Ag 4p_1/2, (Ni 3p_3/2and Ni 3p_1/2) and (Cu 3p_3/2and Cu 3p_1/2). The intensities ratios of the separated peaks are measured and compared with the ratios obtained from a first-order calculation. An excellent agreement between the measured and calculated ratios are obtained. Residual background intensities compared with the estimated values are found to agree within certain uncertainties.