Prevention of protein denaturation during exposure to sterilization temperatures

Firefly luciferase exposed to a temperature of 135 degrees C for 36 hours re tained up to 40 percent of its original activity. Prerequisites for heat stability were the use of a molecular sieve (Seph adex G-25 or Biogel P-300) and a high vacuum (5 x 10(-4) mm-Hg). These studies present a possible solution to the problem of sterilization for exobiologi cal experiments.     

Manganese oxide octahedral molecular sieves: preparation, characterization, and applications

A thermally stable 3 x 3 octahedral molecular sieve corresponding to natural todorokite (OMS-1) has been synthesized by autoclaving layer-structure manganese oxides, which are prepared by reactions of MnO(4)(-) and Mn(2+) under markedly alkaline conditions. The nature and thermal stability of products depend strongly on preparation parameters, such as the MnO(4)(-)/Mn(2+) ratio, pH, aging, and autoclave conditions. The purest and the most thermally stable todorokite is obtained at a ratio of 0.30 to 0.40. Autoclave treatments at about 150 degrees to 180 degrees C for more than 2 days yield OMS-1, which is as thermally stable (500 degrees C) as natural todorokite minerals. Adsorption data give a tunnel size of 6.9 angstroms and an increase of cyclohexane or carbon tetrachloride uptake with dehydration temperature up to 500 degrees C. At 600 degrees C, the tunnel structure collapses. Both Lewis and Br?nsted acid sites have been observed in OMS-1. Particular applications of these materials include adsorption, electrochemical sensors, and oxidation catalysis.     

Supported iron nanoparticles as catalysts for sustainable production of lower olefins

Lower olefins are key building blocks for the manufacture of plastics, cosmetics, and drugs. Traditionally, olefins with two to four carbons are produced by steam cracking of crude oil-derived naphtha, but there is a pressing need for alternative feedstocks and processes in view of supply limitations and of environmental issues. Although the Fischer-Tropsch synthesis has long offered a means to convert coal, biomass, and natural gas into hydrocarbon derivatives through the intermediacy of synthesis gas (a mixture of molecular hydrogen and carbon monoxide), selectivity toward lower olefins tends to be low. We report on the conversion of synthesis gas to C(2) through C(4) olefins with selectivity up to 60 weight percent, using catalysts that constitute iron nanoparticles (promoted by sulfur plus sodium) homogeneously dispersed on weakly interactive α-alumina or carbon nanofiber supports.     

分离CH4/CO2吸附剂优选及其工艺参数研究

选用5A分子筛、13X分子筛和硅胶作为吸附剂,采用变压吸附法进行脱除沼气中CO2试验,考察不同的吸附压力条件下CH4/CO2分离的效果,并对三种吸附剂的吸附性能进行分析和比较.结果表明,5A分子筛在0.7 Mpa下脱除CO2效果最好,获得CH4含量最大为90%~92%.5A分子筛在流量22.1 L·min-1的穿透时间约为200 s,获得CH4浓度最大,平均纯度为83.5%;脱附时间为560 s,再生效果较好     

A high-efficiency power cycle in which hydrogen is compressed by absorption in metal hydrides

A high-efficiency power cycle is proposed in which molecular hydrogen gas is used as a working fluid in a regenerative closed Brayton cycle. The hydrogen gas is compressed by an absorption-desorption cycle on metal hydride (FeTiH(x)) beds. Low-temperature solar or geothermal heat (temperature about 100 degrees C) is used for the compression process, and high-temperature fossil fuel or nuclear heat (temperature about 700 degrees C) supplies the expansion work in the turbine. Typically, about 90 percent of the high-temperature heat input is converted to electricity, while about 3 kilowatts of low-temperature heat is required per kilowatt of electrical output.     

分子筛吸附净化天然气实验研究

为了减少天然气温室气体排放,保护大气环境,对于小型LNG装置,建议采用分子筛吸附法脱水脱硫,提出了预处理模块化的概念.实验测定了天然气在复合吸附床（3A＋13X分子筛）上的动态透出曲线和分子筛脱硫的透出曲线,采用竞争吸附理论对各吸附模块进行了优化组合与配置.预处理模块的吸附顺序一般为＂先脱水再脱硫最后脱碳＂,而脱附顺序为＂先脱碳再脱硫最后脱水＂.对于不同产地不同气质的天然气,预处理模块化工艺可以适应对各种气源进行液化的苛刻要求.     

Enhanced c2 yields from methane oxidative coupling by means of a separative chemical reactor

Of the processes for converting natural gas into a more useful chemical feedstock, the oxidative coupling of methane to form ethane and ethylene (C(2)) has perhaps been the most intensively investigated in recent years, but it has proved extremely difficult to obtain C(2) yields in excess of 20 to 25%. Methane oxidative coupling was carried out in a separative chemical reactor that simulated a countercurrent chromatographic moving-bed. This reaction gives 65% methane conversion, 80% C(2) selectivity, and a C(2) yield slightly better than 50% with Sm(2)O(3) catalyst at approximately 1000 K.     

Silkworm Bombyx mori L.: Nature of Diapause Factor

The diapause factor which is responsible for the induction of embryonic diapause in the silkworm (Bombyx mori L.) was isolated from the heads of female moths. It was extracted with 80 percent ethanol or 80 percent methanol and was heat-stable and not dialyzable. Since the active material was precipitated with ammonium sulfate and lost when incubated with proteolytic enzymes, it is highly probable that the diapause factor is a protein or a complex molecule containing peptide bonds. Molecular sieve techniques revealed two species of the diapause factor. The molecular weight of the smaller species lies between 5,000 and 10,000.     

Venting of carbon dioxide-rich fluid and hydrate formation in mid-okinawa trough backarc basin

Carbon dioxide-rich fluid bubbles, containing approximately 86 percent CO(2), 3 percent H(2)S, and 11 percent residual gas (CH(4) + H(2)), were observed to emerge from the sea floor at 1335- to 1550-m depth in the JADE hydrothermal field, mid-Okinawa Trough. Upon contact with seawater at 3.8 degrees C, gas hydrate immediately formed on the surface of the bubbles and these hydrates coalesced to form pipes standing on the sediments. Chemical composition and carbon, sulfur, and helium isotopic ratios indicate that the CO(2)-rich fluid was derived from the same magmatic source as dissolved gases in 320 degrees C hydrothermal solution emitted from a nearby black smoker chimney. The CO(2)-rich fluid phase may be separated by subsurface boiling of hydrothermal solutions or by leaching of CO(2)-rich fluid inclusion during posteruption interaction between pore water and volcanogenic sediments.     

气刺微割技术在GT1更新胶树上使用试验小结

气刺微割技术在GT1胶树上的试验结果表明,在GT1更新胶树上采用S/4U d3+ETG、每周期5刀的刺激方式,株净增产率达61.1%,增产效果显著。在提高割胶速度、减少耗皮等方面有明显优势。两割年试验分析认为,在计划更新的GT1胶树上采用气刺微割采胶技术对挖掘胶树潜力具有较好的推广价值。     

玉米闽单88高产制种综合农艺措施的数学模型

采用二次回归旋转设计方法,研究了玉米闽单 ８８ 主要栽培因子（密度、 Ｎ 肥、 Ｐ 肥、 Ｋ 肥）与制种产量的关系,通过微机对模型进行模拟,得出各因子对制种产量效应的主次关系及２ 因子搭配的产量效应．通过频数分析,筛选出指定产量水平下的最佳农艺措施组合方案,建立了闽单８８ 在三明红黄壤条件下的高产制种数学模型     

Atmospheric trace gases in antarctica

Trace gases have been measured, by electron-capture gas chromatography and gas chromatography-mass spectrometry techniques, at the South Pole (SP) in Antarctica and in the U.S. Pacific Northwest (PNW) ( approximately 45 degrees N) during January of each year from 1975 to 1980. These measurements show that the concentrations of CCl(3)F, CCl(2)F(2), and CH(3)CCl(3) have increased exponentially at substantial rates. The concentration of CCl(3)F increased at 12 percent per year at the SP and at 8 percent per year in the PNW; CCl(2)F(2) increased at about 9 percent per year at both locations, and CH(3)CCl(3) increased at 17 percent per year at the SP and 11.6 percent per year at the PNW site. There is some evidence that CCl(4) ( approximately 3 percent per year) and N(2)O (0.1 to 0.5 percent per year) may also have increased. Concentrations of nine other trace gases of importance in atmospheric chemistry are also being measured at these two locations. Results of the measurements of CHClF(2)(F-22), C(2)Cl(3)F(3)(F-113), SF(6), C(2)-hydrocarbons, and CH(3)Cl are reported here.     

Coking- and sintering-resistant palladium catalysts achieved through atomic layer deposition

We showed that alumina (Al(2)O(3)) overcoating of supported metal nanoparticles (NPs) effectively reduced deactivation by coking and sintering in high-temperature applications of heterogeneous catalysts. We overcoated palladium NPs with 45 layers of alumina through an atomic layer deposition (ALD) process that alternated exposures of the catalysts to trimethylaluminum and water at 200°C. When these catalysts were used for 1 hour in oxidative dehydrogenation of ethane to ethylene at 650°C, they were found by thermogravimetric analysis to contain less than 6% of the coke formed on the uncoated catalysts. Scanning transmission electron microscopy showed no visible morphology changes after reaction at 675°C for 28 hours. The yield of ethylene was improved on all ALD Al(2)O(3) overcoated Pd catalysts.     

A chemically functionalizable nanoporous material

Although zeolites and related materials combine nanoporosity with high thermal stability, they are difficult to modify or derivatize in a systematic way. A highly porous metal coordination polymer [Cu3(TMA)2(H2O)3]n (where TMA is benzene-1,3,5-tricarboxylate) was formed in 80 percent yield. It has interconnected [Cu2(O2CR)4] units (where R is an aromatic ring), which create a three-dimensional system of channels with a pore size of 1 nanometer and an accessible porosity of about 40 percent in the solid. Unlike zeolites, the channel linings can be chemically functionalized; for example, the aqua ligands can be replaced by pyridines. Thermal gravimetric analysis and high-temperature single-crystal diffractometry indicate that the framework is stable up to 240 degreesC.     

Toward separation and purification of olefins using dithiolene complexes: an electrochemical approach

The complex Ni[S2C2(CF3)2]2 reacts with light olefins, including ethylene and propylene, selectively and reversibly. The reaction is not poisoned by hydrogen gas, carbon monoxide, acetylene, or hydrogen sulfide, which are commonly present in olefin streams, presumably because olefin binding occurs through the sulfur ligand rather than the metal center. The reversible reaction of olefins with Ni[S2C2(CN)2]2n (n = 0, -1, -2) can be controlled electrochemically, where the oxidation state-dependent binding and release of olefins are fast on the electrochemical time scale. The observed tolerance to poisons and controllable electrochemical reactivity present an alternative approach to the separation of olefins from complex streams.     

Dense-gas chromatography of nonvolatile substances of high molecular weight

Working at pressures of up to 2000 atmospheres, more than ten times higher than in previous gas chromatography, we used the solvent power of dense gases to enable migration of chromatographic substances of molecular weights as high as 400,000. Carotenoids, corticol steroids, sterols, nucleosides, amino acids, carbohydrates, and several polymers have been caused to migrate, separated, and detected in NH(3) and CO(2) carrier gases at temperatures of 140 degrees and 40 degrees C, just above the respective critical points. Previously such compounds either defied separation by gas chromatography or had to be chromatographed as their more volatile derivatives.     

Enhanced ethylene and ethane production with free-radical cracking catalysts

A series of free-radical catalysts have been discovered that increase the yield of highly valuable olefins from the cracking of low molecular weight paraffins. For example, catalytic cracking of n-butane, isobutane, and propane over manganese or iron supported on magnesium oxide (MgO) gave product distributions different from those given by thermal (free-radical) cracking or cracking over traditional acid catalysts. With n-butane and propane feeds, the products from catalytic cracking included large amounts of ethylene and ethane; with isobutane feed, propylene was the major product. Physical characterization of the MgO-supported catalyst showed the manganese to be in a 2+ oxidation state in the reduced catalyst and a 4+ oxidation state in the fully oxidized catalyst. Manganese was also shown to be uniformly distributed in the support material with very little enrichment at the surface. Matrix isolation of the gasphase radicals from n-butane feed showed that ethyl and methyl radicals were produced over the active catalysts. In the thermal process, only methyl radicals were produced. The mechanism of the catalytic reaction appears to be selective formation of primary carbanions at the catalyst surface followed by electron transfer and release of primary hydrocarbon radicals to the gas phase.     

Electron-microprobe analyses of phases in lunar samples

In fine (type A) and coarse-grained (type B) Apollo 11 lunar volcanic rocks clinopyroxenes are extremely inhomogeneous. Ferrosilite-rich areas in type B rocks have decomposed to submicron vermicular intergrowths of clinopyroxene-fayalite-cristobalite(?). Plagioclase has normal zoning with K(2)O up to 0.5 percent in rims. Ilmenites are relatively homogeneous with low mgo(0.1 to 2 percent) and high zro(2) (up to 0.26 percent). Metal phase in troilite has <0.02 percent nickel. The breccias (type C) and fines (type D) containing 0.09 to 10.52 percent Ti0(2.) Rare metal fragments with meteorite-like compositions occur in breccias and fines. Gross similarities between euctites and Apollo 11 volcanic rocks indiacate similar evolutionary environments, but detailed mineralogical differences suggest either separate origins or if eucrites are lunar, chemical inhomogeneities on the lunar surface.     

A pure enzyme catalyzing penicillin biosynthesis

Isopenicillin N synthetase (cyclase) has been purified to homogeneity from Cephalosporium acremonium strain C-10. The enzyme has a molecular weight of 40,000 to 42,000 and yields a single band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The enzyme was purified in 10 percent yield by a combination of protamine sulfate and ammonium sulfate precipitations, gel filtration, and ion-exchange high-performance liquid chromatography. The purified enzyme can be stabilized with sucrose and stored at -20 degrees C for several weeks without any loss in activity.     

Apollo lunar module engine exhaust products

Organic combustion products generated by the lunar module descent engine, which burns a 1:1 mixture of unsymmetrical dimethylhydrazine fuel and nitrogen tetroxide oxidizer, have been analyzed. The major gaseous combustion products found were ammonia, water, carbon monoxide, nitrous oxide, oxygen, carbon dioxide, and nitric oxide. The minor products were acetylene, hydrogen cyanide, ethylene, formaldehyde, propadiene, ketene, cyanous acid, hydrazoic acid, various methylamines, acetaldehyde, methyl nitrite, formic acid, nitrous acid, butadiyne, nitrilohydrazines, nitromethane, and nitrosohydrazines with other oxidized derivatives of unsymmetrical dimethylhydrazine and hydrazine. The ion intensities of the various species in all mass spectra were estimated as the following concentrations: the gases (NH(3), H(2)O, CO, NO, O(2), CO(2), and NO(2)), 87.7 percent; compounds of C, H, and O, 6.0 percent; and compounds of C, H, and N (with traces of O), 5.8 percent.