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1.
Understanding the sources and composition of organic aerosol (OA) in indoor environments requires rapid measurements, since many emissions and processes have short timescales. However, real-time molecular-level OA measurements have not been reported indoors. Here, we present quantitative measurements, at a time resolution of five seconds, of molecular ions corresponding to diverse aerosol-phase species, by applying extractive electrospray ionization mass spectrometry (EESI-MS) to indoor air analysis for the first time, as part of the highly instrumented HOMEChem field study. We demonstrate how the complex spectra of EESI-MS are screened in order to extract chemical information and investigate the possibility of interference from gas-phase semivolatile species. During experiments that simulated the Thanksgiving US holiday meal preparation, EESI-MS quantified multiple species, including fatty acids, carbohydrates, siloxanes, and phthalates. Intercomparisons with Aerosol Mass Spectrometer (AMS) and Scanning Mobility Particle Sizer suggest that EESI-MS quantified a large fraction of OA. Comparisons with FIGAERO-CIMS shows similar signal levels and good correlation, with a range of 100 for the relative sensitivities. Comparisons with SV-TAG for phthalates and with SV-TAG and AMS for total siloxanes also show strong correlation. EESI-MS observations can be used with gas-phase measurements to identify co-emitted gas- and aerosol-phase species, and this is demonstrated using complementary gas-phase PTR-MS observations.  相似文献   
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The T1 of a hyperpolarized site in solution is a key parameter that determines the time‐window in which its NMR signals are observable. For 13C sites adjacent to protons, 1H‐decoupling has been shown to increase the hyperpolarized signal resolution and SNR. Additionally, polarization transfer to protons has shown utility in increasing the sensitivity of detection. However, 1H‐decoupling could lead to a change in the decay rate of a hyperpolarized 13C site. Here we tested this possible effect in a case where the protons are directly bound to an sp3 hyperpolarized 13C site (using [1,2‐13C2]choline) and 1H‐decoupling was applied continuously throughout the hyperpolarized decay measurement. We found that 1H‐decoupling did not lead to any significant changes in the 13C polarization decay time but did result in the expected collapse of J‐coupling and produced sharper signals. This result suggested that 1H‐decoupling did not affect the decay rate of hyperpolarized sp3 13C sites. The deuterium‐substitution approach (using [1,1,2,2‐D4,1‐13C]choline) showed a dramatic prolongation of T1. Upper bounds on the T1 of all investigated sites were calculated.  相似文献   
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正位于上海的江森自控亚太总部是创新设计、可持续性和智能科技的领先典范。晋思建筑事务所上海和芝加哥办公室与拥有领先建筑技术和解决方案的江森自控携手合作,创建了世界级的总部大楼和企业园区,最大限度地减少了对自然环境的影响,增强了建筑的美观度与功能性,力求达到最高水平的入住舒适度。由于其前瞻性设计、智能节能解决方案以及对可持续发展承诺,该总部赢得了国际金融公司-世界银行集团  相似文献   
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Two donor–acceptor (D–A) polymers are obtained by coupling difluoro- and dichloro-substituted forms of the electron-deficient unit BDOPV and the relatively weak donor moiety dichlorodithienylethene (ClTVT). The conductivity and power factors of doped devices are different for the chlorinated and fluorinated BDOPV polymers. A high electron conductivity of 38.3 and 16.1 S cm−1 are obtained from the chlorinated and fluorinated polymers with N-DMBI, respectively, and 12.4 and 2.4 S cm−1 are obtained from the chlorinated and fluorinated polymers with CoCp2, respectively, from drop-cast devices. The corresponding power factors are 22.7, 7.6, 39.5, and 8.0  µ W m−1 K−2, respectively. Doping of PClClTVT with N-DMBI results in excellent air stability; the electron conductivity of devices with 50 mol% N-DMBI as dopant remained up to 4.9 S m−1 after 222 days in the air, the longest for an n-doped polymer stored in air, with a thermoelectric power factor of 9.3  µ W m−1 K−2. However, the conductivity of PFClTVT-based devices can hardly be measured after 103 days. These observations are consistent with morphologies determined by grazing incidence wide angle X-ray scattering and atomic force microscopy.  相似文献   
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Wahman DG  Henry AE  Katz LE  Speitel GE 《Water research》2006,40(18):3349-3358
Three mixed-culture nitrifier sources degraded low concentrations (25-450 microg/L) of four trihalomethanes (THMs) (trichloromethane (TCM) or chloroform, bromodichloromethane (BDCM), dibromochloromethane (DBCM), tribromomethane (TBM) or bromoform) commonly found in treated drinking water. Individual THM rate constants (k1THM) increased with increasing THM bromine-substitution with TBM>DBCM>BDCM>TCM and were comparable to previous studies with the pure culture nitrifier, Nitrosomonas europaea. A decrease in temperature resulted in a decrease in both ammonia and THM degradation rates with ammonia rates affected to a greater extent than THM degradation rates. The significant effect of temperature indicates that seasonal variations in water temperature should be a consideration for technology implementation. Product toxicity, measured by transformation capacity (T(c)), was similar to that observed with N. europaea. Because both rate constants and product toxicities increase with increasing THM bromine-substitution, a water's THM speciation is an important consideration for process implementation during drinking water treatment. Even though a given water is kinetically favored, the resulting THM product toxicity may not allow stable treatment process performance.  相似文献   
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We show that if a language L has a 4-round, black-box, computational zero-knowledge proof system with negligible soundness error, then [`(L)] ? MA\bar{L}\in \mathsf{MA}. Assuming the polynomial hierarchy does not collapse, this means in particular that NP-complete languages do not have 4-round zero-knowledge proofs with black-box simulation.  相似文献   
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