scholarly journals Evaluation of High Molecular Weight of Chitosan as a Replacer of Sodium Nitrite on the Physico-Chemical Properties and Microbial Changes of Low-fat Sausages During Refrigerated Storage

2006 ◽  
Vol 48 (4) ◽  
pp. 563-574 ◽  
1978 ◽  
Vol 126 (1) ◽  
pp. 1-22 ◽  
Author(s):  
Kazuo Sutoh ◽  
Keiko Sutoh ◽  
Trudy Karr ◽  
William F. Harrington

1990 ◽  
Vol 63 (03) ◽  
pp. 499-504 ◽  
Author(s):  
A Electricwala ◽  
L Irons ◽  
R Wait ◽  
R J G Carr ◽  
R J Ling ◽  
...  

SummaryPhysico-chemical properties of recombinant desulphatohirudin expressed in yeast (CIBA GEIGY code No. CGP 39393) were reinvestigated. As previously reported for natural hirudin, the recombinant molecule exhibited abnormal behaviour by gel filtration with an apparent molecular weight greater than that based on the primary structure. However, molecular weight estimation by SDS gel electrophoresis, FAB-mass spectrometry and Photon Correlation Spectroscopy were in agreement with the theoretical molecular weight, with little suggestion of dimer or aggregate formation. Circular dichroism studies of the recombinant molecule show similar spectra at different pH values but are markedly different from that reported by Konno et al. (13) for a natural hirudin-variant. Our CD studies indicate the presence of about 60% beta sheet and the absence of alpha helix in the secondary structure of recombinant hirudin, in agreement with the conformation determined by NMR studies (17)


2019 ◽  
Vol 19 (1) ◽  
pp. 139-163 ◽  
Author(s):  
Chunlin Li ◽  
Quanfu He ◽  
Julian Schade ◽  
Johannes Passig ◽  
Ralf Zimmermann ◽  
...  

Abstract. Following wood pyrolysis, tar ball aerosols were laboratory generated from wood tar separated into polar and nonpolar phases. Chemical information of fresh tar balls was obtained from a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) and single-particle laser desorption/resonance enhanced multiphoton ionization mass spectrometry (SP-LD-REMPI-MS). Their continuous refractive index (RI) between 365 and 425 nm was retrieved using a broadband cavity enhanced spectroscopy (BBCES). Dynamic changes in the optical and chemical properties for the nonpolar tar ball aerosols in NOx-dependent photochemical process were investigated in an oxidation flow reactor (OFR). Distinct differences in the chemical composition of the fresh polar and nonpolar tar aerosols were identified. Nonpolar tar aerosols contain predominantly high-molecular weight unsubstituted and alkyl-substituted polycylic aromatic hydrocarbons (PAHs), while polar tar aerosols consist of a high number of oxidized aromatic substances (e.g., methoxy-phenols, benzenediol) with higher O : C ratios and carbon oxidation states. Fresh tar balls have light absorption characteristics similar to atmospheric brown carbon (BrC) aerosol with higher absorption efficiency towards the UV wavelengths. The average retrieved RI is 1.661+0.020i and 1.635+0.003i for the nonpolar and polar tar aerosols, respectively, with an absorption Ångström exponent (AAE) between 5.7 and 7.8 in the detected wavelength range. The RI fits a volume mixing rule for internally mixed nonpolar/polar tar balls. The RI of the tar ball aerosols decreased with increasing wavelength under photochemical oxidation. Photolysis by UV light (254 nm), without strong oxidants in the system, slightly decreased the RI and increased the oxidation state of the tar balls. Oxidation under varying OH exposure levels and in the absence of NOx diminished the absorption (bleaching) and increased the O : C ratio of the tar balls. The photobleaching via OH radical initiated oxidation is mainly attributed to decomposition of chromophoric aromatics, nitrogen-containing organics, and high-molecular weight components in the aged particles. Photolysis of nitrous oxide (N2O) was used to simulate NOx-dependent photochemical aging of tar balls in the OFR. Under high-NOx conditions with similar OH exposure, photochemical aging led to the formation of organic nitrates, and increased both oxidation degree and light absorption for the aged tar ball aerosols. These observations suggest that secondary organic nitrate formation counteracts the bleaching by OH radical photooxidation to eventually regain some absorption of the aged tar ball aerosols. The atmospheric implication and climate effects from tar balls upon various oxidation processes are briefly discussed.


2020 ◽  
Vol 40 (2) ◽  
pp. 136-142 ◽  
Author(s):  
Homa Maleki ◽  
Hossein Barani

AbstractThe stereocomplex formation is a promising method to improve the properties of poly(lactide) (PLA)-based products due to the strong interaction of the side-by-side arrangement of the molecular chains. Recently, electrospinning method has been applied to prepare PLA stereocomplex, which is more convenient. The objective of the current study is to make stereocomplexed PLA nanofibers using electrospinning method and compare their properties and structures with pure poly(l-lactide) (PLLA) fibers. The stereocomplexed fibers were electrospun from a blend solution of high molecular weight PLLA and poly(d-lactide) (1:1 ratio). The morphology of the obtained electrospun fibers was examined by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Differential scanning calorimetry was applied to study their thermal properties and crystallinity. Fourier transform infrared spectroscopy (FTIR) test was conducted on the samples to characterize their chemical properties. The SEM and AFM images indicated that smooth uniform fibers with a cylindrical structure were produced. Besides, the FTIR results and thermal properties confirmed that only stereocomplex crystallites formed in the resulting fibers via the electrospinning method.


1982 ◽  
Vol 30 (8) ◽  
pp. 2951-2957 ◽  
Author(s):  
AKIRA KATO ◽  
YOSHINOBU TAKAKURA ◽  
MITSURU HASHIDA ◽  
TOSHIKIRO KIMURA ◽  
HITOSHI SEZAKI

1930 ◽  
Vol 3 (3) ◽  
pp. 511-515
Author(s):  
H. Staudinger ◽  
H. F. Bondy

Abstract On the basis of earlier experiments with synthetic materials, compounds of high molecular weight are not composed of a single substance, but consist of a mixture of homologous polymers. The individual members of a polymeric homologous series differ very little in physical and chemical properties, and therefore a mixture of polymeric homologous products such as is obtained in the polymerization of the monomer cannot as a rule be decomposed into simple compounds by means of solvents, but merely into mixtures of products of low and high molecular weight. Such separations have been carried out, for example, in the case of polyvinylace-tates, polystyrols, polyindenes, polyanetholes, and polyethyleneoxides. On the basis of these experiments it was assumed that natural products of high molecular weight likewise consist of a mixture of polymeric homologs. Thus purified rubber, for example, according to our views is not such a completely homogeneous hydrocarbon that all the molecules have the same length, but consists of a mixture of perhaps 100 or more polymeric homologs. Pummerer's decomposition of rubber into sol,- and gel-rubber, according to our experiments, is due to the fact that rubber consists of easily soluble polyprenes and difficultly soluble polyprenes, all belonging to the same polymeric homologous series. Of course there is the possibility that, in forming compounds of high molecular weight, nature produced primary molecules of uniform size, and that the mixture of polymeric homologs was formed only later through decomposition. In that case the natural products would differ in constitution from the synthetic material. They would not be polymerically uniform but completely uniform compounds in the sense of classical organic chemistry. The fact that in life processes methods are possible which we cannot realize in the laboratory is well known. Such a finding would not, of course, contradict our former view that natural products, such as rubber and balata, are of high molecular weight in the sense of classical structural chemistry. Our former work has indicated a similar structure for rubber and gutta-percha. Here it is simply a question whether or not the macromolecules of these natural products have a uniform length. In order to reach a decision, we first of all investigated balata, since it is prepared pure more easily than rubber. It was made from balata latex which was supplied to us through the courtesy of the management of the Norddeutsche Seekabelwerke, Nordenham." The balata thus obtained is a flocculent, cellulose-like mass, which looks like gutta-percha and crystallizes like it.


2021 ◽  
Author(s):  
shuang han ◽  
Juan Hong ◽  
Qingwei Luo ◽  
Hanbing Xu ◽  
Haobo Tan ◽  
...  

<p>Hygroscopic properties of 23 organic compounds with different physico-chemical properties including carboxylic acids, amino acids, sugars and sugar alcohols were measured using a Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA). We converted our experimental GF data of organics at 90% RH to κ to facilitate the comparison and we find that organic compounds with different molecular functionality present quite different hygroscopicity. Compounds with extra functional groups usually show higher hygroscopicity compared to their parental molecular compounds. Moreover, some compounds share the same molecular structure or functionality but vary differently in hygroscopicity. In general, the hygroscopicity of organics increase with functional groups in the following order: (-CH3/-NH2) < (-OH) < (-COOH/C=C/C=O). For highly soluble organics, the hygroscopicity decreases with molecular weight; while for slightly soluble organics which are not fully dissolved in aerosol droplets, their hygroscopicity can be divided into two categories. One is non-hygroscopic compounds, which may not fully deliquesce in the aerosol droplets. The other is moderate hygroscopic compounds, of which the hygroscopicity is mainly limited by their water solubility. Moreover, the hygroscopicity of organic compounds generally increased linearly with O:C ratios, although some of them have the same O:C ratio of but with different hygroscopicity. The experimental determined hygroscopicity are also compared with model predictions using the Extended Aerosol Inorganics Model (E-AIM) and the UManSysProp at 10-90% RH. Both models poorly represent the hygroscopic behavior of some organics, which may due to that the phase transition and intermolecular interactions are not considered in the simulations.</p>


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