Impact of storage at room temperature on the properties of CiP solutions

This work reports the analysis of cleaning solutions used in cleaning in place (CiP) and the changes that occur during storage at room temperature. Tests were performed on different solutions used to clean brewhouse vessels and a mash filter in a local brewery. The solutions were collected from CiP tanks after regeneration and were stored for three months in darkness at room temperature. Over time, the physical, chemical and microbiological parameters of the cleaning solutions were analysed. At the end of the study, the solutions were evaluated in terms of surface wetting and cleaning capability. The results showed that storage of the solutions at room temperature contributed to the agglomeration of particulates into larger conglomerates that may contribute to clarification of cleaning solutions by sedimentation. However, other parameters of the stored CiP solutions did not change. © 2019 The Institute of Brewing & Distilling     

植酸/植酸钠在食品工业上的应用研究进展

植酸/植酸钠广泛存在于谷类、豆类和油料作物等中,应用非常广泛,在食品工业上可用作食品抗氧化剂、抑菌剂、护色剂、螯合剂和保鲜剂等。本文简述了植酸/植酸钠的结构、组成和理化特性,并且综述其在食品工业中的应用与研究进展。重点介绍了植酸/植酸钠在果蔬制品、饮料、发酵食品、酿造酒、油脂和脂肪制品、水产品、肉制品、焙烤制品和面制品等加工中的应用及研究进展。同时探讨了目前植酸/植酸钠在食品工业应用中存在的问题及解决对策,并对其发展趋势进行展望。指出目前高纯度植酸和固体植酸的生产成本较高,将来可以在植酸的色谱层析分离材料上进行改进。同时,为了增加植酸在油溶性食品中的应用范围,可以通过植酸的改性或借助于乳化、微乳化技术制备植酸/植酸钠的乳液和微乳液产品,是将来的发展方向。     

The use of long-chain plant polyprenols as a means to modify the biological properties of new biodegradable polyurethane scaffolds for tissue engineering. A pilot study

Microporous membranes for tissue engineering were produced from new biodegradable polyurethane based on hexamethylene diisocyanate, poly(ε-caprolactone) diol and 1,4:3,6-dianhydro-d-sorbitol. The interconnected pores had an average size in the range of 5–100 μm. The tensile strength at break, the Young’s modulus and elongation at break of the membranes were 3.2 ± 0.3 MPa, 25.2 ± 1.5 MPa and 190 ± 12%, respectively, while nonporous foils from the same polymers had a tensile strength at break of 40 ± 2 MPa, a Young’s modulus of 91 ± 6 MPa, and an elongation at break of 370 ± 10%. The membranes were incubated for 10 days in a 2.65 vol% solution of long-chain plant polyprenol in n-hexane to promote their interaction with cells and tissues. The polyprenol was isolated from leaves of Magnolia cobus and was a mixture of prenol-10 and prenol-11. The prenol-impregnated membranes and nonimpregnated membranes (control) were tested in cell culture to assess whether impregnation has a beneficial effect on cell-material interaction. The cells used in the test were chondrocytes isolated from the articular-epiphyseal cartilage of leg bones of 5-day-old inbred LEW rats. The time of culture was 2 and 5 weeks. Both, the nonimpregnated and impregnated polyurethane membranes supported attachment and growth of rat chondrocytes. The cells firmly attached to the surface of the microporous membranes, invaded the pores and maintained the round shape characteristic for chondrocyte-like-morphology. Abundant fibrillar extracellular matrix produced by the cells resembled the network formed by chondrocytes in vivo. The cells produced relatively more extracellular matrix in the membranes impregnated with polyprenol than in the control membranes. Impregnation of polyurethane scaffolds with biologically active amphiphilic polyprenols may be a route to facilitate the cell–material interaction.     

Relating nutrient and herbicide fate with landscape features and characteristics of 15 subwatersheds in the Choptank River watershed

Excess nutrients and agrochemicals from non-point sources contribute to water quality impairment in the Chesapeake Bay watershed and their loading rates are related to land use, agricultural practices, hydrology, and pollutant fate and transport processes. In this study, monthly baseflow stream samples from 15 agricultural subwatersheds of the Choptank River in Maryland USA (2005 to 2007) were characterized for nutrients, herbicides, and herbicide transformation products. High-resolution digital maps of land use and forested wetlands were derived from remote sensing imagery. Examination of landscape metrics and water quality data, partitioned according to hydrogeomorphic class, provided insight into the fate, delivery, and transport mechanisms associated with agricultural pollutants. Mean Nitrate-N concentrations (4.9 mg/L) were correlated positively with percent agriculture (R² = 0.56) and negatively with percent forest (R² = 0.60). Concentrations were greater (p = 0.0001) in the well-drained upland (WDU) hydrogeomorphic region than in poorly drained upland (PDU), reflecting increased denitrification and reduced agricultural land use intensity in the PDU landscape due to the prevalence of hydric soils. Atrazine and metolachlor concentrations (mean 0.29 μg/L and 0.19 μg/L) were also greater (p = 0.0001) in WDU subwatersheds than in PDU subwatersheds. Springtime herbicide concentrations exhibited a strong, positive correlation (R² = 0.90) with percent forest in the WDU subwatersheds but not in the PDU subwatersheds. In addition, forested riparian stream buffers in the WDU were more prevalent than in the PDU where forested patches are typically not located near streams, suggesting an alternative delivery mechanism whereby volatilized herbicides are captured by the riparian forest canopy and subsequently washed off during rainfall. Orthophosphate, CIAT (6-chloro-N-(1-methylethyl)-1,3,5-triazine-2,4-diamine), CEAT (6-chloro-N-ethyl-1,3,5-triazine-2,4-diamine), and MESA (2-[(2-ethyl-6-methylphenyl) (2-methoxy-1-methylethyl)amino]-2-oxoethanesulfonic acid) were also analyzed. These findings will assist efforts in targeting implementation of conservation practices to the most environmentally-critical areas within watersheds to achieve water quality improvements in a cost-effective manner.     

Thioether–Polyglycidol as Multivalent and Multifunctional Coating System for Gold Nanoparticles

Thiofunctional polymers are the established standard for the coating and biofunctionalization of gold nanoparticles (AuNPs). However, the nucleophilic and oxidative character of thiols provokes polymeric crosslinking and significantly limits the chemical possibilities to introduce biological functions. Thioethers represent a chemically more stable potential alternative to thiols that would offer easier functionalization, yet a few studies in the literature report inconclusive data regarding the efficacy of thioethers to stabilize AuNPs in comparison to thiols. A systematic comparison is presented of mono‐ versus multivalent thiol‐ and thioether‐functional polymers, poly(ethylene glycol) versus side chain functional poly(glycidol) (PG) and it is shown that coating of AuNPs with multivalent thioether‐functional PG leads to superior colloidal stability, even under physiological conditions and after freeze‐drying and resuspension, as compared to thiol analogs at comparable polymer surface coverages. In addition, it is shown that a wide range of functional groups can be introduced in these polymers. Using diazirine functionalization as example, it is demonstrated that proteins can be covalently immobilized, and that conjugation of antibodies via this strategy enables efficient targeting and laser‐irradiation induced killing of cells.     

Synthesis and activity of zirconocene catalysts supported on silica-type sol-gel carrier for ethylene polymerization

Summary Synthesis and activity of bis(cyclopentadienyl)zirconium dichloride catalyst supported on unconventional silica-type material obtained in sol-gel process and activated by organoaluminium co-catalyst were studied. The effect of support modification conditions (thermal dehydration and/or modification by organoaluminium compound) and a type of co-catalyst on an activity of the catalytic system in ethylene polymerization and properties of resulting polymers were investigated and compared with results obtained earlier for vanadium catalysts supported on mentioned sol-gel carrier. The most appropriate method of the sol-gel silica-type support preparation is thermal pre-treating (200°C) followed by modification with AlEt₂Cl. Metallocene catalyst supported on such sol-gel product and activated by MAO appeared to be most active among studied systems. Studied Cp₂ZrCl₂/MAO supported on silica-type sol-gel carrier allow to obtain polyethylene (at 50°C polymerization temperature) with yield up to 30·10⁶ g/(mol_Zr·h), molecular weight below 300 000 and MWD=2−4. Received: 4 September 2000/Revised version: 3 January 2001/Accepted: 3 January 2001     

Synthesis and catalytic properties for olefin polymerization of new vanadium complexes containing silsesquioxane ligands with different denticity

A series of new vanadium‐silsesquioxanes ( 2a ? 2d ) was prepared by reacting VCl₄ with not fully condensed silsesquioxanes (having from one to four silanol groups) and evaluated as pre‐catalysts in olefin polymerization. The activation of 2a ? 2d with EtAlCl₂ generated highly active catalysts for ethylene polymerization, yielding high molar mass polymers with narrow dispersity. Ultra‐high molar mass polyethylenes, M _w up to 4 × 10⁶ g mol^?1, were obtained with methylaluminoxane and Al(i Bu)₃/[Ph₃C][B(C₆F₅)₄] as activators. Upon treatment with methylaluminoxane and boron compounds, all vanadium pre‐catalysts were active in 1‐octene polymerization as well, and produced isotactic‐rich poly(1‐octene)s with moderate monomer conversion (up to 23%). The polymerization parameters were optimized and the effect of the silsesquioxane structure on the catalytic activity and polymer properties was studied. © 2017 Society of Chemical Industry     

Synthesis of linear polysiloxanes with electron-donating organophosphorus pendant groups by kinetically controlled ring-opening polymerization

Six-membered ring siloxane monomers containing a phosphorus electron-donating groupR=–CH₂CH₂PPh₂ (1), –CH₂CH₂P(S)Ph₂ (2), and –CH₂CH₂P(O)Ph₂ (3) were synthesized. The anionic ring-opening polymerization of these monomers with kinetic control of products has been studied using tetrahydrofuran (THF) as solvent and lithium silanolates as initiators. The polymerization leads to a high molecular weight linear polymer with a very good yield in the case of2 and with a fairly good yield in the case of1 and3. The presence of the phosphorus group enhances the cyclization and broadens the molecular weight distribution of the linear polymer. This effect is relatively weak for the thiophosphinoyl group. At least in the case of the polymer obtained from2, phosphorus groups are distributed uniformly in the macromolecule, however, their arrangement along the chain is not regular. The interaction of polymers obtained from monomers1, 2, and3 with some electrophiles such as alkyl or silyl halides was demonstrated to lead to generation of polyelectrolytes.     

Properties of anionic polymerized ε‐caprolactam in the presence of carbon nanotubes

The results of the investigations of the relations between structure, physical and usage properties of polyamide 6 (PA6) reinforced with multiwall carbon nanotubes (MWNTs) are presented. A method of in situ anionic bulk polymerization of ε‐caprolactam in the presence of MWNTs was used for the preparation of reinforced PA6. The polymerization product was crushed, and the pellets of PA6 and PA6/MWNTs composites were injection molded to produce the standard test specimens for various measurements. The surface morphology (SEM), thermal (DSC, TGA, DMTA), and mechanical properties (tensile strength, Charpy's notched impact strength) of these materials were examined. Some differences between our specimens and those obtained by hydrolytic polymerization of ε‐caprolactam (CL) were found. It was found that a small amount of carbon nanotube decreases the crystallinity degree of PA6 matrix in the composites. The thermal stability was higher than that for neat PA6. DMTA results showed that the magnitudes of the storage modulus are higher for the PA6/MWNTs composites than for the unmodified PA6 in the temperature range between ?90 and 200°C. The tensile strength and tensile modulus are higher compared with the neat PA6. The elongation at break showed no noticeable change in the range of MWNTs loading considered, while the Charpy's notched impact strength slightly decreased. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Reactive polymeric microspheres: Catalytic reduction of a nitrobenzene derivative

Polymeric microspheres have been demonstrated as a potentially useful vehicle for targeted delivery applications. In this work we report on the preparation of polymer microspheres capable of performing specific reaction chemistry. The microspheres are modified with silver nanoparticles in a two‐step reaction. The first step involves formation of the microsphere by UV‐induced polymerization of pyrrole and the second step is the reduction of silver cations to metallic silver in situ. The resulting Ag‐decorated microspheres were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, energy dispersive X‐ray, and thermogravimetry analysis. The catalytic reaction behavior of the decorated microspheres was illustrated through the reduction reaction of m‐nitrobenzene sulfonate acid in the presence of sodium borohydride. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43653.